Exact Mass: 272.033

Exact Mass Matches: 272.033

Found 500 metabolites which its exact mass value is equals to given mass value 272.033, within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error 0.01 dalton.

Naringenin

4H-1-Benzopyran-4-one, 2,3-dihydro-5,7-dihydroxy-2-(4-hydroxyphenyl)-, (2S)-

C15H12O5 (272.0685)


Naringenin is a flavorless, colorless flavanone, a type of flavonoid. It is the predominant flavanone in grapefruit, and is found in a variety of fruits and herbs. Naringenin has the skeleton structure of a flavanone with three hydroxy groups at the 4, 5, and 7 carbons. It may be found both in the aglycol form, naringenin, or in its glycosidic form, naringin, which has the addition of the disaccharide neohesperidose attached via a glycosidic linkage at carbon 7. Naringenin (not to be confused with naringin) is a flavanone that is considered to have a bioactive effect on human health as antioxidant, free radical scavenger, antiinflammatory, carbohydrate metabolism promoter, immunity system modulater. This substance has also been shown to repair DNA. Scientists exposed cells to 80 micomoles of naringenin per liter, for 24 hours, and found that the amount of hydroxyl damage to the DNA was reduced by 24 percent in that very short period of time. Unfortunately, this bioflavonoid is difficult to absorb on oral ingestion. Only 15\\\\\\\% of ingested naringenin will get absorbed, in the human gastrointestinal tract, in the best case scenario. A full glass of orange juice will supply about enough naringenin to achieve a concentration of about 0.5 micromoles per liter. Naringenin is a biomarker for the consumption of citrus fruits. (S)-naringenin is the (S)-enantiomer of naringenin. It has a role as an expectorant and a plant metabolite. It is a naringenin and a (2S)-flavan-4-one. It is a conjugate acid of a (S)-naringenin(1-). It is an enantiomer of a (R)-naringenin. Naringenin is a natural product found in Elaeodendron croceum, Garcinia multiflora, and other organisms with data available. See also: Naringin (related). Most widely distributed flavanone. Citrus fruits (grapefruit, oranges and pummelos) are especially good sources. Glycosides also widely distributed The (S)-enantiomer of naringenin. [Raw Data] CB070_Naringenin_pos_20eV_CB000030.txt [Raw Data] CB070_Naringenin_pos_10eV_CB000030.txt [Raw Data] CB070_Naringenin_pos_40eV_CB000030.txt [Raw Data] CB070_Naringenin_pos_30eV_CB000030.txt [Raw Data] CB070_Naringenin_pos_50eV_CB000030.txt [Raw Data] CB070_Naringenin_neg_10eV_000021.txt [Raw Data] CB070_Naringenin_neg_30eV_000021.txt [Raw Data] CB070_Naringenin_neg_50eV_000021.txt [Raw Data] CB070_Naringenin_neg_20eV_000021.txt [Raw Data] CB070_Naringenin_neg_40eV_000021.txt (±)-Naringenin. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=67604-48-2 (retrieved 2024-07-09) (CAS RN: 67604-48-2). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). (±)-Naringenin is a naturally-occurring flavonoid. (±)-Naringenin displays vasorelaxant effect on endothelium-denuded vessels via the activation of BKCa channels in myocytes[1]. (±)-Naringenin is a naturally-occurring flavonoid. (±)-Naringenin displays vasorelaxant effect on endothelium-denuded vessels via the activation of BKCa channels in myocytes[1]. Naringenin is the predominant flavanone in Citrus reticulata Blanco; displays strong anti-inflammatory and antioxidant activities. Naringenin has anti-dengue virus (DENV) activity. Naringenin is the predominant flavanone in Citrus reticulata Blanco; displays strong anti-inflammatory and antioxidant activities. Naringenin has anti-dengue virus (DENV) activity.

   

Chalconaringenin

2-Propen-1-one, 3-(4-hydroxyphenyl)-1-(2,4,6-trihydroxyphenyl)-, (2E)-

C15H12O5 (272.0685)


2,4,4,6-tetrahydroxychalcone is a member of the class of chalcones that is trans-chalcone substituted by hydroxy groups at positions 2 ,4, 4, and 6 respectively. It has a role as a metabolite, an anti-allergic agent and an anti-inflammatory agent. It is a polyphenol and a member of chalcones. It is functionally related to a trans-chalcone. Naringenin chalcone is a natural product found in Populus koreana, Populus tremula, and other organisms with data available. Isolated from tomato fruit cuticles. Chalconaringenin is found in many foods, some of which are cherry tomato, lettuce, greenthread tea, and lemon. A member of the class of chalcones that is trans-chalcone substituted by hydroxy groups at positions 2 ,4, 4, and 6 respectively. Chalconaringenin is found in garden tomato. Chalconaringenin is isolated from tomato fruit cuticle Naringenin chalcone. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=5071-40-9 (retrieved 2024-07-12) (CAS RN: 25515-46-2). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

   

Butein

2 inverted exclamation mark ,3,4,4 inverted exclamation mark -tetrahydroxy Chalcone

C15H12O5 (272.0685)


Butein is a chalcone that is (E)-chalcone bearing four additional hydroxy substituents at positions 2, 3, 4 and 4. It has a role as a tyrosine kinase inhibitor, an antioxidant, an EC 1.1.1.21 (aldehyde reductase) inhibitor, an antineoplastic agent, a geroprotector, a radiosensitizing agent, a hypoglycemic agent and a plant metabolite. It is a member of chalcones and a polyphenol. Butein is a natural product found in Dahlia pinnata, Calanticaria bicolor, and other organisms with data available. Butein is a flavonoid obtained from the seed of Cyclopia subternata. It is a specific protein tyrosine kinase inhibitor that induces apoptosis. (NCI) See also: Semecarpus anacardium juice (part of). A chalcone that is (E)-chalcone bearing four additional hydroxy substituents at positions 2, 3, 4 and 4. C471 - Enzyme Inhibitor > C1404 - Protein Kinase Inhibitor > C1967 - Tyrosine Kinase Inhibitor Butein, also known as 2,3,4,4-tetrahydroxychalcone, is a member of the class of compounds known as 2-hydroxychalcones. 2-hydroxychalcones are organic compounds containing chalcone skeleton that carries a hydroxyl group at the 2-position. Thus, butein is considered to be a flavonoid lipid molecule. Butein is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Butein is a bitter tasting compound found in broad bean, which makes butein a potential biomarker for the consumption of this food product. Butein is a chalcone of the chalconoids. It can be found in Toxicodendron vernicifluum (or formerly Rhus verniciflua), Dahlia, Butea (Butea monosperma) and Coreopsis It has antioxidative, aldose reductase and advanced glycation endproducts inhibitory effects. It is also a sirtuin-activating compound, a chemical compound having an effect on sirtuins, a group of enzymes that use NAD+ to remove acetyl groups from proteins. It turned out that buteins possess a high ability to inhibit aromatase process in the human body, for this reason, the use of these compounds in the treatment of breast cancer on the estrogen ground has been taken into account. The first attempts of sport pro-hormone supplementation with the use of buteins took place in Poland . Butein is a cAMP-specific PDE inhibitor with an IC50 of 10.4 μM for PDE4[1]. Butein is a specific protein tyrosine kinase inhibitor with IC50s of 16 and 65 μM for EGFR and p60c-src in HepG2 cells[2]. Butein sensitizes HeLa cells to Cisplatin through AKT and ERK/p38 MAPK pathways by targeting FoxO3a[3]. Butein is a SIRT1 activator (STAC). Butein is a cAMP-specific PDE inhibitor with an IC50 of 10.4 μM for PDE4[1]. Butein is a specific protein tyrosine kinase inhibitor with IC50s of 16 and 65 μM for EGFR and p60c-src in HepG2 cells[2]. Butein sensitizes HeLa cells to Cisplatin through AKT and ERK/p38 MAPK pathways by targeting FoxO3a[3]. Butein is a SIRT1 activator (STAC).

   

Pinobanksin

4H-1-BENZOPYRAN-4-ONE, 2,3-DIHYDRO-3,5,7-TRIHYDROXY-2-PHENYL-, (2R,3R)-

C15H12O5 (272.0685)


Pinobanksin is a trihydroxyflavanone in which the three hydroxy substituents are located at positions 3, 5 and 7. It has a role as an antimutagen, an antioxidant and a metabolite. It is a trihydroxyflavanone and a secondary alpha-hydroxy ketone. Pinobanksin is a natural product found in Populus koreana, Ozothamnus stirlingii, and other organisms with data available. Pinobanksin has apoptotic induction in a B-cell lymphoma cell line[1].

   

Garbanzol

4H-1-Benzopyran-4-one, 2,3-dihydro-3,7-dihydroxy-2-(4-hydroxyphenyl)-, (2R-trans)-

C15H12O5 (272.0685)


Garbanzol is a member of the class of dihydroflavonols that is (2S)-flavanone substituted by hydroxy groups at positions 3, 7 and 4. It has a role as an antimutagen and a metabolite. It is a trihydroxyflavanone, a member of dihydroflavonols, a secondary alpha-hydroxy ketone and a member of 4-hydroxyflavanones. Garbanzol is a natural product found in Pterocarpus marsupium, Brucea javanica, and other organisms with data available. See also: Pterocarpus marsupium wood (part of). A member of the class of dihydroflavonols that is (2S)-flavanone substituted by hydroxy groups at positions 3, 7 and 4. Garbanzol is found in Cicer arietinum (chickpea) and Capsella bursa-pastoris (shepherds purse).

   

Butin_(molecule)

4H-1-BENZOPYRAN-4-ONE, 2-(3,4-DIHYDROXYPHENYL)-2,3-DIHYDRO-7-HYDROXY-, (2S)-

C15H12O5 (272.0685)


Butin is a trihydroxyflavanone in which the three hydroxy substituents are located at positions 3, 4 and 7. It is found in Acacia mearnsii, Vernonia anthelmintica and Dalbergia odorifera and has a protective affect against oxidative stress-induced mitochondrial dysfunction. It has a role as an antioxidant, a protective agent and a metabolite. It is a trihydroxyflavanone and a member of 4-hydroxyflavanones. Butin is a natural product found in Dipteryx lacunifera, Acacia vestita, and other organisms with data available. A trihydroxyflavanone in which the three hydroxy substituents are located at positions 3, 4 and 7. It is found in Acacia mearnsii, Vernonia anthelmintica and Dalbergia odorifera and has a protective affect against oxidative stress-induced mitochondrial dysfunction. (-)-Butin is the S enantiomer of Butin. Butin is a major biologically active flavonoid isolated from the heartwood of Dalbergia odorifera, with strong antioxidant, antiplatelet and anti-inflammatory activities[1][2]. (-)-Butin is the S enantiomer of Butin. Butin is a major biologically active flavonoid isolated from the heartwood of Dalbergia odorifera, with strong antioxidant, antiplatelet and anti-inflammatory activities[1][2]. (-)-Butin is the S enantiomer of Butin. Butin is a major biologically active flavonoid isolated from the heartwood of Dalbergia odorifera, with strong antioxidant, antiplatelet and anti-inflammatory activities[1][2]. (-)-Butin is the S enantiomer of Butin. Butin is a major biologically active flavonoid isolated from the heartwood of Dalbergia odorifera, with strong antioxidant, antiplatelet and anti-inflammatory activities[1][2]. Butin is a major biologically active flavonoid isolated from the heartwood of Dalbergia odorifera, with strong antioxidant, antiplatelet and anti-inflammatory activities. Butin significantly alleviates myocardial infarction and improves heart function, together with prevents diabetes-induced cardiac oxidative damage in rat[1][2]. Butin is a major biologically active flavonoid isolated from the heartwood of Dalbergia odorifera, with strong antioxidant, antiplatelet and anti-inflammatory activities. Butin significantly alleviates myocardial infarction and improves heart function, together with prevents diabetes-induced cardiac oxidative damage in rat[1][2].

   

Toralactone

9,10-Dihydroxy-7-methoxy-3-methyl-1H-naphtho[2,3-c]pyran-1-one, 9CI

C15H12O5 (272.0685)


Toralactone is an organic heterotricyclic compound that is 9,10-dihydroxy-1H-benzo[g]isochromen-1-one substituted at positions 3 and 7 by methyl and methoxy groups respectively. It has a role as a plant metabolite. It is an organic heterotricyclic compound, a lactone, a member of phenols, an aromatic ether, a polyketide and a naphtho-alpha-pyrone. It is functionally related to a nor-toralactone. Toralactone is a natural product found in Senna obtusifolia and Senna tora with data available. An organic heterotricyclic compound that is 9,10-dihydroxy-1H-benzo[g]isochromen-1-one substituted at positions 3 and 7 by methyl and methoxy groups respectively. Isolated from seeds of Cassia tora (charota). Toralactone is found in coffee and coffee products, herbs and spices, and pulses. Toralactone is found in coffee and coffee products. Toralactone is isolated from seeds of Cassia tora (charota). Toralactone, isolated from Cassia obtusifolia, mediates hepatoprotection via an Nrf2-dependent anti-oxidative mechanism[1]. Toralactone, isolated from Cassia obtusifolia, mediates hepatoprotection via an Nrf2-dependent anti-oxidative mechanism[1].

   

7-ACA

(6R,7R)-3-(acetyloxymethyl)-7-amino-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

C10H12N2O5S (272.0467)


7beta-aminocephalosporanic acid is the alpha,beta-unsaturated monocarboxylic acid that is the active nucleus for the synthesis of cephalosporins and intermediates. It is functionally related to a cephalosporanic acid. It is a tautomer of a 7beta-aminocephalosporanic acid zwitterion. 7-Aminocephalosporanic acid has been reported in Apis cerana D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents > D002511 - Cephalosporins D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents > D047090 - beta-Lactams D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents > D007769 - Lactams

   

Rubrofusarin

InChI=1\C15H12O5\c1-7-3-10(16)14-12(20-7)5-8-4-9(19-2)6-11(17)13(8)15(14)18\h3-6,17-18H,1-2H

C15H12O5 (272.0685)


A member of the class of benzochromenones that is benzo[g]chromen-4-one carrying two additional hydroxy substituents at positions 5 and 6 as well as methyl and methoxy substituents at positions 2 and 8 respectively. An orange polyketide pigment that is a common intermediate in many different fungal biosynthetic pathways. CONFIDENCE Culture of Fusarium graminearum from DAOM

   

(Z)-4-(2-Hydroxy-5-sulfonatophenyl)-2-oxo-3-butenoate

(Z)-4-(2-Hydroxy-5-sulfonatophenyl)-2-oxo-3-butenoate

C10H8O7S (271.9991)


   

Glycinol

8,17-dioxatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]heptadeca-2(7),3,5,11(16),12,14-hexaene-5,10,14-triol

C15H12O5 (272.0685)


Constituent of soybean seedlings (Glycine max) and kudzu (Pueraria thunbergiana). Glycinol is found in many foods, some of which are scarlet bean, soy bean, gram bean, and pulses. Glycinol is found in gram bean. Glycinol is a constituent of soybean seedlings (Glycine max) and kudzu (Pueraria thunbergiana).

   

Licodione

1- (2,4-Dihydroxyphenyl) -3- (4-hydroxyphenyl) -1,3-propanedione

C15H12O5 (272.0685)


   

(±)-2'-Hydroxydihydrodaidzein

3-(2,4-dihydroxyphenyl)-7-hydroxy-3,4-dihydro-2H-1-benzopyran-4-one

C15H12O5 (272.0685)


(±)-2-hydroxydihydrodaidzein, also known as 2,4,7-trihydroxyisoflavanone, is a member of the class of compounds known as isoflavanones. Isoflavanones are polycyclic compounds containing an isoflavan skeleton which bears a ketone at position C4. Thus, (±)-2-hydroxydihydrodaidzein is considered to be a flavonoid lipid molecule (±)-2-hydroxydihydrodaidzein is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). (±)-2-hydroxydihydrodaidzein can be found in green bean, pulses, and yellow wax bean, which makes (±)-2-hydroxydihydrodaidzein a potential biomarker for the consumption of these food products. (±)-2-Hydroxydihydrodaidzein is found in pulses. (±)-2-Hydroxydihydrodaidzein is isolated from pods of Phaseolus vulgaris (kidney bean) and also from Phaseolus coccineus (scarlet runner bean).

   

p-coumaroyltriacetic acid lactone

p-coumaroyltriacetic acid lactone

C15H12O5 (272.0685)


   

Dihydrogenistein

2,3-Dihydro-5,7-dihydroxy-3-(4-hydroxyphenyl)-4H-1-benzopyran-4-one

C15H12O5 (272.0685)


Dihydrogenistein is a metabolite of the soy isoflavone genistin (the glycoside conjugate of genistein) by intestinal bacteria. Isoflavones are one of the three major classes of phytoestrogens; phytoestrogens are a diverse group of plant-derived compounds that structurally and functionally mimic mammalian estrogen. The isoflavone genistin is one of the most prevalent in soy foods. They are biologically inactive; once ingested, they are cleaved by glucosidases to "aglycones", genistein. Epidemiological studies have associated high soy intake with a lowered risk for certain hormone-dependent disease. Many studies reveal that the incidence of prostate cancer and breast cancer is much lower in Asian people in comparison to people from the West and, and the prevailing contribution to this difference has been attributed to the diet. Soy foods and soy-derived products which contain abundant isoflavones are consumed in large quantities by Asian people. In vitro, isoflavone metabolites have dual functions: they can act as an estrogenic agonist or antagonist depending on the estrogen concentration. (PMID: 17499260, 16965913) [HMDB]. Dihydrogenistein is a biomarker for the consumption of soy beans and other soy products. Dihydrogenistein is a metabolite of the soy isoflavone genistin (the glycoside conjugate of genistein) by intestinal bacteria. Isoflavones are one of the three major classes of phytoestrogens; phytoestrogens are a diverse group of plant-derived compounds that structurally and functionally mimic mammalian estrogen. The isoflavone genistin is one of the most prevalent in soy foods. They are biologically inactive; once ingested, they are cleaved by glucosidases to "aglycones", genistein. Epidemiological studies have associated high soy intake with a lowered risk for certain hormone-dependent disease. Many studies reveal that the incidence of prostate cancer and breast cancer is much lower in Asian people in comparison to people from the West and, and the prevailing contribution to this difference has been attributed to the diet. Soy foods and soy-derived products which contain abundant isoflavones are consumed in large quantities by Asian people. In vitro, isoflavone metabolites have dual functions: they can act as an estrogenic agonist or antagonist depending on the estrogen concentration. (PMID: 17499260, 16965913). Dihydrogenistein is a biomarker for the consumption of soy beans and other soy products.

   

3-(Phenylsulfonyl)acrylophenone

1-Phenyl-3-(phenylsulfonyl)-2-propen-1-one; 3-(Phenylsulfonyl)acrylophenone

C15H12O3S (272.0507)


A sulfone that is 1-phenyl-2-propenone with a phenylsulfonyl group at position 3.

   

2,7,4'-trihydroxyisoflavanone

2,7-dihydroxy-3-(4-hydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-4-one

C15H12O5 (272.0685)


2,7,4-trihydroxyisoflavanone is a member of the class of compounds known as isoflavanols. Isoflavanols are polycyclic compounds containing a hydroxylated isoflavan skeleton. 2,7,4-trihydroxyisoflavanone is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). 2,7,4-trihydroxyisoflavanone can be found in a number of food items such as common mushroom, loganberry, sesbania flower, and allium (onion), which makes 2,7,4-trihydroxyisoflavanone a potential biomarker for the consumption of these food products.

   

6,7,4-Trihydroxyflavanone

6,7,4-Trihydroxyflavanone

C15H12O5 (272.0685)


   

2-epi-5-epi-Valiolone 7-phosphate

2-epi-5-epi-Valiolone 7-phosphate

C7H13O9P (272.0297)


A member of the class of cyclitols that is 2-epi-5-epi-valiolone carrying a phospho substituent at position 7.

   

6,7-Dichloro-l-tryptophan

6,7-Dichloro-l-tryptophan

C11H10Cl2N2O2 (272.0119)


A non-proteinogenic L-alpha-amino acid that is L-tryptophan in which the hydrogens at positions 6 and 7 on the indole ring have been replaced by chlorines.

   

5-Epi-valiolone 7-phosphate

5-Epi-valiolone 7-phosphate

C7H13O9P (272.0297)


A member of the class of cyclitols that is 5-epi-valiolone carrying a phospho substituent at position 7.

   

Naringenin

5,7-dihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-4-one

C15H12O5 (272.0685)


Naringenin is a trihydroxyflavanone that is flavanone substituted by hydroxy groups at positions 5, 6 and 4. It is a trihydroxyflavanone and a member of 4-hydroxyflavanones. 5,7-Dihydroxy-2-(4-hydroxyphenyl)chroman-4-one is a natural product found in Prunus mume, Helichrysum cephaloideum, and other organisms with data available. D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006727 - Hormone Antagonists > D004965 - Estrogen Antagonists A trihydroxyflavanone that is flavanone substituted by hydroxy groups at positions 5, 6 and 4. D005765 - Gastrointestinal Agents > D000897 - Anti-Ulcer Agents (±)-Naringenin is a naturally-occurring flavonoid. (±)-Naringenin displays vasorelaxant effect on endothelium-denuded vessels via the activation of BKCa channels in myocytes[1]. (±)-Naringenin is a naturally-occurring flavonoid. (±)-Naringenin displays vasorelaxant effect on endothelium-denuded vessels via the activation of BKCa channels in myocytes[1]. Naringenin is the predominant flavanone in Citrus reticulata Blanco; displays strong anti-inflammatory and antioxidant activities. Naringenin has anti-dengue virus (DENV) activity. Naringenin is the predominant flavanone in Citrus reticulata Blanco; displays strong anti-inflammatory and antioxidant activities. Naringenin has anti-dengue virus (DENV) activity.

   

Dihydrobaicalein

Dihydrobaicalein

C15H12O5 (272.0685)


Dihydrobaicalein is a PLK1 Inhibitor with an IC50 of 6.3 μM. Dihydrobaicalein also inhibits VRK2 and PLK2. Dihydrobaicalein is a natural product that can be isolated from Scutellaria scandens[1]. Dihydrobaicalein is a PLK1 Inhibitor with an IC50 of 6.3 μM. Dihydrobaicalein also inhibits VRK2 and PLK2. Dihydrobaicalein is a natural product that can be isolated from Scutellaria scandens[1].

   

Wittifuran X

Wittifuran X

C15H12O5 (272.0685)


   

2,3,4,6-Tetrahydroxychalcone

2,3,4,6-Tetrahydroxychalcone

C15H12O5 (272.0685)


   

Moracin J

5-(5-hydroxy-6-methoxy-1-benzofuran-2-yl)benzene-1,3-diol

C15H12O5 (272.0685)


Moracin J is found in fruits. Moracin J is isolated from Morus alba (white mulberry) infected with Fusarium solani. Isolated from Morus alba (white mulberry) infected with Fusarium solani. Moracin J is found in fruits.

   

5,7,3-Trihydroxyflavanone

5,7,3-Trihydroxyflavanone

C15H12O5 (272.0685)


   

1-Hydroxy-3,7-dimethoxyxanthone

3,7-Dimethoxy-1-hydroxy-9H-xanthene-9-one

C15H12O5 (272.0685)


1-Hydroxy-3,7-dimethoxyxanthone is found in alcoholic beverages. 1-Hydroxy-3,7-dimethoxyxanthone is isolated from Gentiana lutea (yellow gentian

   

4',5,8-Trihydroxyflavanone

5,8-dihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-4-one

C15H12O5 (272.0685)


4,5,8-Trihydroxyflavanone is found in green vegetables. 4,5,8-Trihydroxyflavanone is a constituent of Spinacia oleracea (spinach) Constituent of Spinacia oleracea (spinach). 4,5,8-Trihydroxyflavanone is found in green vegetables and spinach.

   

Fukiic acid

(2R,3S)-2-[(3,4-dihydroxyphenyl)methyl]-2,3-dihydroxybutanedioic acid

C11H12O8 (272.0532)


Fukiic acid is found in green vegetables. Fukiic acid is a hydrolysis produced from Petasites japonicus (sweet coltsfoot

   

3,4,9-Trihydroxypterocarpan

8,17-dioxatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]heptadeca-2(7),3,5,11(16),12,14-hexaene-5,6,14-triol

C15H12O5 (272.0685)


3,4,9-Trihydroxypterocarpan is found in alfalfa. 3,4,9-Trihydroxypterocarpan is isolated from fungus-infected leaves of Melilotus alba (white melilot). Isolated from fungus-infected leaves of Melilotus alba (white melilot). 3,4,9-Trihydroxypterocarpan is found in alfalfa, herbs and spices, and pulses.

   

Dihydronorwogonin

Dihydronorwogonin

C15H12O5 (272.0685)


   

3'-Hydroxydihydrodaidzein

3-(3,4-dihydroxyphenyl)-7-hydroxy-3,4-dihydro-2H-1-benzopyran-4-one

C15H12O5 (272.0685)


3-Hydroxydihydrodaidzein is a polyphenol metabolite detected in biological fluids (PMID: 20428313). A polyphenol metabolite detected in biological fluids [PhenolExplorer]

   

6-Hydroxydihydrodaidzein

6,7-dihydroxy-3-(4-hydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-4-one

C15H12O5 (272.0685)


6-Hydroxydihydrodaidzein is a polyphenol metabolite detected in biological fluids (PMID: 20428313). A polyphenol metabolite detected in biological fluids [PhenolExplorer]

   

8-Hydroxydihydrodaidzein

7,8-dihydroxy-3-(4-hydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-4-one

C15H12O5 (272.0685)


8-Hydroxydihydrodaidzein is a polyphenol metabolite detected in biological fluids (PMID: 20428313). A polyphenol metabolite detected in biological fluids [PhenolExplorer]

   

5-(Hydroxyphenyl)-gamma-valerolactone-O-sulphate

{3-[(5-oxooxolan-2-yl)methyl]phenyl}oxidanesulfonic acid

C11H12O6S (272.0355)


5-(Hydroxyphenyl)-gamma-valerolactone-O-sulphate belongs to the family of Substituted Benzenes. These are aromatic compounds containing a benzene substituted at one or more positions.

   

5-Carboxy-2'-deoxyuridine

4-hydroxy-1-[(2S,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-2-oxo-1,2-dihydropyrimidine-5-carboxylic acid

C10H12N2O7 (272.0644)


5-Carboxy-2-deoxyuridine is a metabolite of trifluridine. Trifluridine (also called trifluorothymidine or TFT) is an anti-herpesvirus antiviral drug, used primarily on the eye. It was sold under the trade name, Viroptic, by Glaxo Wellcome, now merged into GlaxoSmithKline. The brand is now owned by Monarch Pharmaceuticals, which is wholly owned by King Pharmaceuticals. (Wikipedia)

   

5-(4'-Hydroxyphenyl)-γ-valerolactone 4'-sulfate

{4-[(5-oxooxolan-2-yl)methyl]phenyl}oxidanesulphonic acid

C11H12O6S (272.0355)


   

(+)-1-(9-Fluorenyl)ethyl chloroformate

(+)-(3S,4S)-1-BENZYL-3-PYRROLIDINYLMETHYL1,4-DIHYDRO-2,6-DIMETHYL-4-(3-NITROPHENYL)-3,5-PYRIDINEDICARBOXYLATE

C16H13ClO2 (272.0604)


   

(2R)-5,7-Dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one

(2R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one

C15H12O5 (272.0685)


Isolated from Camellia sinensis (tea). Naringenin fructoside is found in tea.

   

7-Aminocephalosporanic acid

3-[(Acetyloxy)methyl]-7-amino-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

C10H12N2O5S (272.0467)


   

Butin

2-(3,4-dihydroxyphenyl)-7-hydroxy-3,4-dihydro-2H-1-benzopyran-4-one

C15H12O5 (272.0685)


   

Protosappanin A

5,14,15-trihydroxy-8-oxatricyclo[10.4.0.0²,⁷]hexadeca-1(16),2,4,6,12,14-hexaen-10-one

C15H12O5 (272.0685)


   

quinalizarin

1,2,5,8-tetrahydroxy-9,10-dihydroanthracene-9,10-dione

C14H8O6 (272.0321)


   

TUCARESOL

4-[(2-formyl-3-hydroxyphenoxy)methyl]benzoic acid

C15H12O5 (272.0685)


C78275 - Agent Affecting Blood or Body Fluid

   

Dibenzo(b,f)thiepin-3-methanol, 5,5-dioxide

14-(hydroxymethyl)-2lambda6-thiatricyclo[9.4.0.0^{3,8}]pentadeca-1(11),3,5,7,9,12,14-heptaene-2,2-dione

C15H12O3S (272.0507)


   

3,4',7-Trihydroxyflavanone

3,7-dihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-4-one

C15H12O5 (272.0685)


(2r,3r)-3,4,7-trihydroxyflavanone is a member of the class of compounds known as flavanonols. Flavanonols are compounds containing a flavan-3-one moiety, with a structure characterized by a 2-phenyl-3,4-dihydro-2H-1-benzopyran bearing a hydroxyl group and a ketone at the carbon C2 and C3, respectively (2r,3r)-3,4,7-trihydroxyflavanone is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). (2r,3r)-3,4,7-trihydroxyflavanone can be found in chickpea, common bean, and lima bean, which makes (2r,3r)-3,4,7-trihydroxyflavanone a potential biomarker for the consumption of these food products.

   

1,7-Dihydroxy-2,3-methylenedioxyxanthone

8,11-Dihydroxy-10H-[1,3]dioxolo[4,5-b]xanthen-10-one

C14H8O6 (272.0321)


1,7-Dihydroxy-2,3-methylenedioxyxanthone is a natural product found in Polygala fallax, Polygala arillata, and other organisms with data available.

   

Alternariol monomethyl ether

3,4-Dihydroxy-5-methoxy-6-methyldibenzo[a]pyrone

C15H12O5 (272.0685)


   

6-Methoxymicrominutinin

6-Methoxymicrominutinin

C15H12O5 (272.0685)


   

5,6-Dehydromethysticin

5,6-Dehydromethysticin

C15H12O5 (272.0685)


   

Corynesidone A

Corynesidone A

C15H12O5 (272.0685)


   

5,7,2-Trihydroxyflavanone

(2S)-5,7,2-Trihydroxyflavanone

C15H12O5 (272.0685)


   

XYLARIAQUINONE A

XYLARIAQUINONE A

C15H12O5 (272.0685)


   

Securixanthone B

Securixanthone B

C15H12O5 (272.0685)


   

5-Hydroxy-1,3-dimethoxyxanthone

5-Hydroxy-1,3-dimethoxyxanthone

C15H12O5 (272.0685)


   

5,7-Dihydroxydehydroiso-alpha-lapachone

5,7-Dihydroxydehydroiso-alpha-lapachone

C15H12O5 (272.0685)


   
   

4-Hydroxy-1,2-dimethoxy-xanthone

4-Hydroxy-1,2-dimethoxy-xanthone

C15H12O5 (272.0685)


   

Griseoxanthone C

Xanthen-9-one, 1,6-dihydroxy-3-methoxy-8-methyl-

C15H12O5 (272.0685)


   

4-Methoxyphenanthrene-2,3,6,7-tetrol

4-Methoxyphenanthrene-2,3,6,7-tetrol

C15H12O5 (272.0685)


   

1-Hydroxy-7-hydroxymethyl-6-methoxyxanthone

1-Hydroxy-7-hydroxymethyl-6-methoxyxanthone

C15H12O5 (272.0685)


   

Hibiscoquinone D

Hibiscoquinone D

C15H12O5 (272.0685)


   

Aplidioxin B

Aplidioxin B

C14H8O6 (272.0321)


   

8-Hydroxy-6-methoxy-3,5-dimethylnaphtho[2,3-b]furan-4,9-dione

8-Hydroxy-6-methoxy-3,5-dimethylnaphtho[2,3-b]furan-4,9-dione

C15H12O5 (272.0685)


   

Isopestacin

Isopestacin

C15H12O5 (272.0685)


   

1,8-Dimethoxy-2-hydroxyxanthone

1,8-Dimethoxy-2-hydroxyxanthone

C15H12O5 (272.0685)


   

7,8,4-Trihydroxyflavanone

7,8,4-Trihydroxyflavanone

C15H12O5 (272.0685)


   

EBENFURAN I

EBENFURAN I

C15H12O5 (272.0685)


   

2,4-Dimethoxy-3-hydroxyxanthone

2,4-Dimethoxy-3-hydroxyxanthone

C15H12O5 (272.0685)


   
   

2-hydroxy-1,7-dimethoxyxanthone

2-hydroxy-1,7-dimethoxyxanthone

C15H12O5 (272.0685)


   

4-hydroxy-2,3-dimethoxyxanthone

4-hydroxy-2,3-dimethoxyxanthone

C15H12O5 (272.0685)


   

Gnetofuran C

Gnetofuran C

C15H12O5 (272.0685)


   

Bhimamycin A

Bhimamycin A

C15H12O5 (272.0685)


   

3-Hydroxy-1,5-dimethoxyxanthone

3-Hydroxy-1,5-dimethoxyxanthone

C15H12O5 (272.0685)


   

2beta-5,7-Trihydroxyflavanone

2-beta-5,7-Trihydroxyflavanone

C15H12O5 (272.0685)


   

2,4,2,4-Tetrahydroxychalcone

2,4,2,4-Tetrahydroxychalcone

C15H12O5 (272.0685)


   

4,2,3,4-Tetrahydroxychalcone

4,2,3,4-Tetrahydroxychalcone

C15H12O5 (272.0685)


   

2-(1-hydroxyethyl)-6-methoxynaphtho[2,3-b]furan-4,9-dione

2-(1-hydroxyethyl)-6-methoxynaphtho[2,3-b]furan-4,9-dione

C15H12O5 (272.0685)


   

Butin

(S) -2- (3,4-Dihydroxyphenyl) -2,3-dihydro-7-hydroxy-4H-1-benzopyran-4-one

C15H12O5 (272.0685)


Butin, also known as (-)-butin or 7,3,4-trihydroxyflavanone, is a member of the class of compounds known as flavanones. Flavanones are compounds containing a flavan-3-one moiety, with a structure characterized by a 2-phenyl-3,4-dihydro-2H-1-benzopyran bearing a ketone at the carbon C3. Thus, butin is considered to be a flavonoid lipid molecule. Butin is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Butin can be found in mango, which makes butin a potential biomarker for the consumption of this food product. Butin may refer to: Butin is the mountain located in Pendro Butin (molecule), a flavanone Aleksandr Butin (born 1985), Russian professional football player Origny-le-Butin, a commune in the Orne department in northwestern France Butin, a village in Gătaia town, Timiş County, Romania . (-)-Butin is the S enantiomer of Butin. Butin is a major biologically active flavonoid isolated from the heartwood of Dalbergia odorifera, with strong antioxidant, antiplatelet and anti-inflammatory activities[1][2]. (-)-Butin is the S enantiomer of Butin. Butin is a major biologically active flavonoid isolated from the heartwood of Dalbergia odorifera, with strong antioxidant, antiplatelet and anti-inflammatory activities[1][2]. (-)-Butin is the S enantiomer of Butin. Butin is a major biologically active flavonoid isolated from the heartwood of Dalbergia odorifera, with strong antioxidant, antiplatelet and anti-inflammatory activities[1][2]. (-)-Butin is the S enantiomer of Butin. Butin is a major biologically active flavonoid isolated from the heartwood of Dalbergia odorifera, with strong antioxidant, antiplatelet and anti-inflammatory activities[1][2].

   

(±)-Naringenin

4,5,7-trihydroxyflavanone

C15H12O5 (272.0685)


(±)-Naringenin is a naturally-occurring flavonoid. (±)-Naringenin displays vasorelaxant effect on endothelium-denuded vessels via the activation of BKCa channels in myocytes[1]. (±)-Naringenin is a naturally-occurring flavonoid. (±)-Naringenin displays vasorelaxant effect on endothelium-denuded vessels via the activation of BKCa channels in myocytes[1].

   

7,3,5-Trihydroxyflavanone

7,3 inverted exclamation marka,5 inverted exclamation marka-Trihydroxyflavanone

C15H12O5 (272.0685)


7,3,5-Trihydroxyflavanone is a natural product found in Glycyrrhiza inflata with data available.

   

Wittifuran X

Wittifuran X

C15H12O5 (272.0685)


   

Naringenin chalcone

4,2,4,6-TETRAHYDROXYCHALCONE

C15H12O5 (272.0685)


Naringenin chalcone is an intermediate in flavonol biosynthesis and is spontaneously metabolized into naringenin (NAR) by chalcone isomerase. Naringenin chalcone has anti-inflammatory and antiallergic activities[1]. Naringenin chalcone is an intermediate in flavonol biosynthesis and is spontaneously metabolized into naringenin (NAR) by chalcone isomerase. Naringenin chalcone has anti-inflammatory and antiallergic activities[1].

   

1,3,6,8-tetrahydroxyanthraquinone

1,3,6,8-tetrahydroxyanthraquinone

C14H8O6 (272.0321)


A tetrahydroxyanthraquinonen that is 9,10-anthraquinone substituted by hydroxy groups at positions 1, 3, 6 and 8. It has been isolated from Chaetomium globosum and Leptographium wageneri.

   

Isotoralactone

Isotoralactone

C15H12O5 (272.0685)


   

Pinobanksin

(2R) -2,3-Dihydro-3beta,5,7-trihydroxy-2alpha-phenyl-4H-1-benzopyran-4-one

C15H12O5 (272.0685)


Pinobanksin is a trihydroxyflavanone in which the three hydroxy substituents are located at positions 3, 5 and 7. It has a role as an antimutagen, an antioxidant and a metabolite. It is a trihydroxyflavanone and a secondary alpha-hydroxy ketone. Pinobanksin is a natural product found in Populus koreana, Ozothamnus stirlingii, and other organisms with data available. A trihydroxyflavanone in which the three hydroxy substituents are located at positions 3, 5 and 7. Pinobanksin has apoptotic induction in a B-cell lymphoma cell line[1].

   

Pseudosindorin

3,5,2,4-Tetrahydroxychalcone

C15H12O5 (272.0685)


   

Isosalipurpol

(2E) -3- (4-hydroxyphenyl) -1- (2,4,6-trihydroxyphenyl) -2-Propen-1-one

C15H12O5 (272.0685)


   

Garbanzol

(2R,3R) -2,3-Dihydro-3,7-dihydroxy-2- (4-hydroxyphenyl) -4H-1-benzopyran-4-one

C15H12O5 (272.0685)


(2r,3r)-3,4,7-trihydroxyflavanone is a member of the class of compounds known as flavanonols. Flavanonols are compounds containing a flavan-3-one moiety, with a structure characterized by a 2-phenyl-3,4-dihydro-2H-1-benzopyran bearing a hydroxyl group and a ketone at the carbon C2 and C3, respectively (2r,3r)-3,4,7-trihydroxyflavanone is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). (2r,3r)-3,4,7-trihydroxyflavanone can be found in chickpea, common bean, and lima bean, which makes (2r,3r)-3,4,7-trihydroxyflavanone a potential biomarker for the consumption of these food products.

   

4-Hydroxydemethylmedicarpin

4-Hydroxydemethylmedicarpin

C15H12O5 (272.0685)


   

2-Hydroxydihydrodaidzein

2-Hydroxy-2,3-dihydrodaidzein

C15H12O5 (272.0685)


A hydroxyisoflavanone that is 2,3-dihydrodaidzein with an additonal hydroxy substituent at position 2.

   

Naringenin

(2S) -2,3-Dihydro-5,7-dihydroxy-2- (4-hydroxyphenyl) -4H-1-benzopyran-4-one

C15H12O5 (272.0685)


Annotation level-1 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.904 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.906 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.901 CONFIDENCE standard compound; ML_ID 50 (±)-Naringenin is a naturally-occurring flavonoid. (±)-Naringenin displays vasorelaxant effect on endothelium-denuded vessels via the activation of BKCa channels in myocytes[1]. (±)-Naringenin is a naturally-occurring flavonoid. (±)-Naringenin displays vasorelaxant effect on endothelium-denuded vessels via the activation of BKCa channels in myocytes[1]. Naringenin is the predominant flavanone in Citrus reticulata Blanco; displays strong anti-inflammatory and antioxidant activities. Naringenin has anti-dengue virus (DENV) activity. Naringenin is the predominant flavanone in Citrus reticulata Blanco; displays strong anti-inflammatory and antioxidant activities. Naringenin has anti-dengue virus (DENV) activity.

   

5,7,3-Trihydroxyflavanone

5,7,3-Trihydroxyflavanone

C15H12O5 (272.0685)


   

Dihydronorwogonin

5,7,8-Trihydroxyflavanone

C15H12O5 (272.0685)


   

methyl 5-chloro-2-(2-ethoxy-2-oxoethoxy)benzoate

methyl 5-chloro-2-(2-ethoxy-2-oxoethoxy)benzoate

C12H13ClO5 (272.0451)


   

ACon1_001828

ACon1_001828

C15H12O5 (272.0685)


   

3-(5-Acetyl-2-furyl)-5-methoxy-2-benzofuran-1(3H)-one

3-(5-Acetyl-2-furyl)-5-methoxy-2-benzofuran-1(3H)-one

C15H12O5 (272.0685)


[Raw Data] CB152_3-(5-Acetyl-2-furyl)-5-methoxy-2-benzofuran-1(3H)-one_neg_50eV_000030.txt [Raw Data] CB152_3-(5-Acetyl-2-furyl)-5-methoxy-2-benzofuran-1(3H)-one_neg_40eV_000030.txt [Raw Data] CB152_3-(5-Acetyl-2-furyl)-5-methoxy-2-benzofuran-1(3H)-one_neg_30eV_000030.txt [Raw Data] CB152_3-(5-Acetyl-2-furyl)-5-methoxy-2-benzofuran-1(3H)-one_neg_20eV_000030.txt [Raw Data] CB152_3-(5-Acetyl-2-furyl)-5-methoxy-2-benzofuran-1(3H)-one_neg_10eV_000030.txt [Raw Data] CB152_3-(5-Acetyl-2-furyl)-5-methoxy-2-benzofuran-1(3H)-one_pos_50eV_CB000057.txt [Raw Data] CB152_3-(5-Acetyl-2-furyl)-5-methoxy-2-benzofuran-1(3H)-one_pos_40eV_CB000057.txt [Raw Data] CB152_3-(5-Acetyl-2-furyl)-5-methoxy-2-benzofuran-1(3H)-one_pos_30eV_CB000057.txt [Raw Data] CB152_3-(5-Acetyl-2-furyl)-5-methoxy-2-benzofuran-1(3H)-one_pos_20eV_CB000057.txt [Raw Data] CB152_3-(5-Acetyl-2-furyl)-5-methoxy-2-benzofuran-1(3H)-one_pos_10eV_CB000057.txt

   

Microminutin

Microminutin

C15H12O5 (272.0685)


   

Calcium levulinate anhydrous

Calcium levulinate anhydrous

C10H16CaO6+2 (272.0573)


   

phenoxy radical VIII

phenoxy radical VIII

C15H12O5 (272.0685)


   
   
   

1-acetoxy-4-(5-penta-1,3-diynyl-thiophen-2-yl)-but-3-yn-2-ol|2-Hydroxy,1-Ac-4-[5-(1,3-Pentadiynyl)-7-thienyl]-3-butyn-1-ol

1-acetoxy-4-(5-penta-1,3-diynyl-thiophen-2-yl)-but-3-yn-2-ol|2-Hydroxy,1-Ac-4-[5-(1,3-Pentadiynyl)-7-thienyl]-3-butyn-1-ol

C15H12O3S (272.0507)


   

ventiloquinone L

ventiloquinone L

C15H12O5 (272.0685)


   
   

ACMC-20n4kl

ACMC-20n4kl

C15H12O5 (272.0685)


   

Anhydrojavanicin

Anhydrojavanicin

C15H12O5 (272.0685)


   

DTXSID80694527

DTXSID80694527

C15H12O5 (272.0685)


   
   

Anhydro-5-deoxyfusarubin

Anhydro-5-deoxyfusarubin

C15H12O5 (272.0685)


   

2,3,4,4-tetrahydroxychalcone

2,3,4,4-tetrahydroxychalcone

C15H12O5 (272.0685)


   

2-(1-Hydroxyethyl)-8-methoxynaphtho[2,3-b]furan-4,9-dione

2-(1-Hydroxyethyl)-8-methoxynaphtho[2,3-b]furan-4,9-dione

C15H12O5 (272.0685)


   

Methylnorlichexanthone

Methylnorlichexanthone

C15H12O5 (272.0685)


   

Protosappanin A

Protosappanin A

C15H12O5 (272.0685)


Protosappanin A (PTA), an immunosuppressive ingredient and major biphenyl compound isolated from Caesalpinia sappan L, suppresses JAK2/STAT3-dependent inflammation pathway through down-regulating the phosphorylation of JAK2 and STAT3[1]. Protosappanin A (PTA), an immunosuppressive ingredient and major biphenyl compound isolated from Caesalpinia sappan L, suppresses JAK2/STAT3-dependent inflammation pathway through down-regulating the phosphorylation of JAK2 and STAT3[1].

   

CHEMBL185138

CHEMBL185138

C15H12O5 (272.0685)


   

Canarione

Canarione

C14H8O6 (272.0321)


   

leptosphaerin D

leptosphaerin D

C15H12O5 (272.0685)


   

5-Hydroxy-1,2-dimethoxyxanthone

5-Hydroxy-1,2-dimethoxyxanthone

C15H12O5 (272.0685)


   

Hypostrepsilic acid

Hypostrepsilic acid

C15H12O5 (272.0685)


   

4,5,4,5-Bismethylendioxydipheno-2,2-chinon

4,5,4,5-Bismethylendioxydipheno-2,2-chinon

C14H8O6 (272.0321)


   

4-Hydroxyhydrangenol

4-Hydroxyhydrangenol

C15H12O5 (272.0685)


   

1,8-Dihydroxy-5-methoxy-3-methylxanthone

1,8-Dihydroxy-5-methoxy-3-methylxanthone

C15H12O5 (272.0685)


   

SCHEMBL16431388

SCHEMBL16431388

C13H8N2O5 (272.0433)


   

5-hydroxy-2-hydroxyisopropylnaphtho<2,3-b>furan-4,9-quinone

5-hydroxy-2-hydroxyisopropylnaphtho<2,3-b>furan-4,9-quinone

C15H12O5 (272.0685)


   

1,2,4,8-tetrahydroxyanthracene-9,10-dione

1,2,4,8-tetrahydroxyanthracene-9,10-dione

C14H8O6 (272.0321)


   

AKOS015906809

AKOS015906809

C15H12O5 (272.0685)


   

(+/-)-hydromacrophyllol A|hydramacrophyllol B

(+/-)-hydromacrophyllol A|hydramacrophyllol B

C15H12O5 (272.0685)


   

1H-Naphtho(2,3-c)pyran-1-one, 3,4-dihydro-9,10-dihydroxy-7-methoxy-3-methylene-

1H-Naphtho(2,3-c)pyran-1-one, 3,4-dihydro-9,10-dihydroxy-7-methoxy-3-methylene-

C15H12O5 (272.0685)


   
   

1,6-dihydroxy-5,7-dimethoxy-9H-fluoren-9-one|dengibsinin

1,6-dihydroxy-5,7-dimethoxy-9H-fluoren-9-one|dengibsinin

C15H12O5 (272.0685)


   
   

CHEMBL289256

CHEMBL289256

C15H12O5 (272.0685)


   

CHEMBL2029865

CHEMBL2029865

C15H12O5 (272.0685)


   

1,8-dihydroxy-3-methoxy-6-methylxanthone

1,8-dihydroxy-3-methoxy-6-methylxanthone

C15H12O5 (272.0685)


A member of the class of xanthones that is 9H-xanthen-9-one substituted by hydroxy groups at positions 1 and 8, a methoxy group at position 3 and a methyl group at position 6. It has been isolated from Microdiplodia species.

   

CHEMBL3422848

CHEMBL3422848

C15H12O5 (272.0685)


   

1-Hydroxy-2,3-dimethoxy-9H-xanthen-9-one

1-Hydroxy-2,3-dimethoxy-9H-xanthen-9-one

C15H12O5 (272.0685)


   

3-hydroxy-2,5-dimethoxyxanthone

3-hydroxy-2,5-dimethoxyxanthone

C15H12O5 (272.0685)


   

1,6-Dihydroxy-7,8-methylendioxy-xanthon|1,6-Dihydroxy-7,8-methylendioxyxanthon

1,6-Dihydroxy-7,8-methylendioxy-xanthon|1,6-Dihydroxy-7,8-methylendioxyxanthon

C14H8O6 (272.0321)


   

5-Deoxyanhydrofusarubin

5-Deoxyanhydrofusarubin

C15H12O5 (272.0685)


   

CHEBI:68126

CHEBI:68126

C15H12O5 (272.0685)


   

9-Dehydroxyeurotinone

9-Dehydroxyeurotinone

C15H12O5 (272.0685)


   

1-hydroxy-6,7-dimethoxyxanthone

1-hydroxy-6,7-dimethoxyxanthone

C15H12O5 (272.0685)


   

1-Hydroxy-6-methoxy-7-(hydroxymethyl)xanthone

1-Hydroxy-6-methoxy-7-(hydroxymethyl)xanthone

C15H12O5 (272.0685)


   

Corymbiferone C

Corymbiferone C

C15H12O5 (272.0685)


   

2,4,4,6-tetrahydroxychalcone

2,4,4,6-tetrahydroxychalcone

C15H12O5 (272.0685)


   

3,8-Dihydroxydehydroiso-alpha-lapachone

3,8-Dihydroxydehydroiso-alpha-lapachone

C15H12O5 (272.0685)


   

6-hydroxy-1,2-dimethoxyxanthone

6-hydroxy-1,2-dimethoxyxanthone

C15H12O5 (272.0685)


   

leptosphaerin E

leptosphaerin E

C15H12O5 (272.0685)


   

(+)-matteucen A|(3S,4R)-3,4-dihydro-4,6,8-trihydroxy-3-phenyl-isochromen-1-one

(+)-matteucen A|(3S,4R)-3,4-dihydro-4,6,8-trihydroxy-3-phenyl-isochromen-1-one

C15H12O5 (272.0685)


   

1-Hydroxy-2,4-dimethoxyxanthone

1-Hydroxy-2,4-dimethoxyxanthone

C15H12O5 (272.0685)


   

2-(4-Hydroxyphenyl)-2H-1-benzopyran-3,5,7-triol

2-(4-Hydroxyphenyl)-2H-1-benzopyran-3,5,7-triol

C15H12O5 (272.0685)


   

2,5,7-trihydroxyflavanone dibenzoylmethane tautomer

2,5,7-trihydroxyflavanone dibenzoylmethane tautomer

C15H12O5 (272.0685)


   

CHEMBL2029863

CHEMBL2029863

C15H12O5 (272.0685)


   

8-hydroxy-2-hydroxyisopropylnaphtho<2,3-b>furan-4,9-quinone|avicequinone D

8-hydroxy-2-hydroxyisopropylnaphtho<2,3-b>furan-4,9-quinone|avicequinone D

C15H12O5 (272.0685)


   

thunberginol F

thunberginol F

C15H12O5 (272.0685)


   

1-hydroxy-5,6-dimethoxyxanthone

1-hydroxy-5,6-dimethoxyxanthone

C15H12O5 (272.0685)


   

SCHEMBL3725569

SCHEMBL3725569

C13H8N2O5 (272.0433)


   

7-hydroxy-3-(hydroxymethyl)-1-methoxy-9h-xanthen-9-one

7-hydroxy-3-(hydroxymethyl)-1-methoxy-9h-xanthen-9-one

C15H12O5 (272.0685)


   
   

Rheoemodin

Rheoemodin

C14H8O6 (272.0321)


   

Securixanthone E

Securixanthone E

C15H12O5 (272.0685)


   

Thunberginol G

Thunberginol G

C15H12O5 (272.0685)


   

Thunberginol C

Thunberginol C

C15H12O5 (272.0685)


   

2-(prop-1-inyl)-5-(6-acetoxy-5-hydroxyhexa-1,3-diinyl)-thiophene

2-(prop-1-inyl)-5-(6-acetoxy-5-hydroxyhexa-1,3-diinyl)-thiophene

C15H12O3S (272.0507)


   

3-(beta-hydroxycinnamoyl)-4-hydroxy-6-methyl-2h-pyran-2-one

3-(beta-hydroxycinnamoyl)-4-hydroxy-6-methyl-2h-pyran-2-one

C15H12O5 (272.0685)


   

Autumnariniol

Autumnariniol

C15H12O5 (272.0685)


   

pogopyrone-A

pogopyrone-A

C15H12O5 (272.0685)


   

1,2-Dimethoxy-8-hydroxyxanthone

1,2-Dimethoxy-8-hydroxyxanthone

C15H12O5 (272.0685)


   

9H-Xanthen-9-one, 3-hydroxy-2,4-dimethoxy-

9H-Xanthen-9-one, 3-hydroxy-2,4-dimethoxy-

C15H12O5 (272.0685)


   

7-methanesulfonylmethyl-1,3-dimethyl-3,7-dihydro-purine-2,6-dione|alpha-<7-(1,3-Dimethylxanthinyl)>methylmethylsulfon

7-methanesulfonylmethyl-1,3-dimethyl-3,7-dihydro-purine-2,6-dione|alpha-<7-(1,3-Dimethylxanthinyl)>methylmethylsulfon

C9H12N4O4S (272.0579)


   

Roxburghinol

Roxburghinol

C15H12O5 (272.0685)


   

SCHEMBL151859

SCHEMBL151859

C15H12O5 (272.0685)


   

SCHEMBL14781369

SCHEMBL14781369

C15H12O5 (272.0685)


   

3,6,7-trihydroxyflavanone

3,6,7-trihydroxyflavanone

C15H12O5 (272.0685)


   

1-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-beta-D-ribo-1,5-dideoxy-hexofuranuronic acid|Uridin-7-carbonsaeure

1-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-beta-D-ribo-1,5-dideoxy-hexofuranuronic acid|Uridin-7-carbonsaeure

C10H12N2O7 (272.0644)


   

CHEMBL254528

CHEMBL254528

C15H12O5 (272.0685)


   

1,2,4,6-Tetrahydroxyanthracene-9,10-dione

1,2,4,6-Tetrahydroxyanthracene-9,10-dione

C14H8O6 (272.0321)


   

3-hydroxy-1,2-dimethoxy-9H-xanthen-9-one

3-hydroxy-1,2-dimethoxy-9H-xanthen-9-one

C15H12O5 (272.0685)


   

2,5,7-Trihydroxyflavanone

2,5,7-Trihydroxyflavanone

C15H12O5 (272.0685)


   

quinalizarin

quinalizarin

C14H8O6 (272.0321)


   

2-hydroxyliquiritigenin

2-hydroxyliquiritigenin

C15H12O5 (272.0685)


   

sappanol B

5,14,15-trihydroxy-8-oxatricyclo[10.4.0.02,7]hexadeca-1(16),2(7),3,5,12,14-hexaen-10-one

C15H12O5 (272.0685)


Protosappanin A is a member of catechols. It has a role as a metabolite. Protosappanin A is a natural product found in Alpinia japonica, Biancaea decapetala, and Biancaea sappan with data available. A natural product found in Caesalpinia sappan. Protosappanin A (PTA), an immunosuppressive ingredient and major biphenyl compound isolated from Caesalpinia sappan L, suppresses JAK2/STAT3-dependent inflammation pathway through down-regulating the phosphorylation of JAK2 and STAT3[1]. Protosappanin A (PTA), an immunosuppressive ingredient and major biphenyl compound isolated from Caesalpinia sappan L, suppresses JAK2/STAT3-dependent inflammation pathway through down-regulating the phosphorylation of JAK2 and STAT3[1].

   

2-Hydroxypinocembrin

2,5,7-trihydroxy-2-phenyl-2,3-dihydro-4H-chromen-4-one

C15H12O5 (272.0685)


2,5,7-trihydroxy-2-phenyl-2,3-dihydro-4H-chromen-4-one is a trihydroxyflavanone carrying the hydroxy groups at positions 2,5 and 7. It is a trihydroxyflavanone and a member of 2-hydroxyflavanones.

   

Thunberginol_C

Thunbergil C ;3,4-Dihydro-6,8-dihydroxy-3-(4-hydroxyphenyl)-1H-2-benzopyran-1-one

C15H12O5 (272.0685)


Thunberginol C is a natural product found in Hydrangea macrophylla and Hydrangea serrata with data available.

   

(+)-Butin

(+)-Butin

C15H12O5 (272.0685)


(+)-Butin is the R enantiomer of Butin. Butin is a major biologically active flavonoid isolated from the heartwood of Dalbergia odorifera, with strong antioxidant, antiplatelet and anti-inflammatory activities[1]. (+)-Butin is the R enantiomer of Butin. Butin is a major biologically active flavonoid isolated from the heartwood of Dalbergia odorifera, with strong antioxidant, antiplatelet and anti-inflammatory activities[1].

   

Djalonensone

6H-Dibenzo[b,d]pyran-6-one, 3,7(3,9 or 7,9)-dihydroxy-9(7 or 3)-methoxy-1-methyl-

C15H12O5 (272.0685)


Djalonensone is a benzochromenone that is alternariol in which the hydroxy group at position 9 has been converted into the corresponding methyl ether. A natural product found in Chaetomium globosum as well as being one of the two most important compounds belonging to the group of Altenaria mycotoxins. It has a role as an antifungal agent, a fungal metabolite and a mycotoxin. It is a benzochromenone and an aromatic ether. It is functionally related to an alternariol. Alternariol monomethyl ether is a natural product found in Sonneratia alba, Talaromyces diversus, and other organisms with data available. Alternariol methyl ether is an altertoxin, which is a mycotoxin of Alternaria fungi. Altertoxins are important contaminants in cereals, vegetables, and fruits, as well as in the ground, on wood or walls. Studies have shown altertoxins to be toxic, genotoxic, mutagenic, and carcinogenic. In particular, they have been associated with esophageal cancer in humans. (A2977, A2979) A benzochromenone that is alternariol in which the hydroxy group at position 9 has been converted into the corresponding methyl ether. A natural product found in Chaetomium globosum as well as being one of the two most important compounds belonging to the group of Altenaria mycotoxins.

   

Alternariol monomethyl ether_120111

Alternariol monomethyl ether_120111

C15H12O5 (272.0685)


   

3-(2,6-dihydroxyphenyl)-4-hydroxy-6-methyl-3H-2-benzofuran-1-one

NCGC00180098-02!3-(2,6-dihydroxyphenyl)-4-hydroxy-6-methyl-3H-2-benzofuran-1-one

C15H12O5 (272.0685)


   

1,6-dihydroxy-3-methoxy-8-methylxanthen-9-one

NCGC00380279-01!1,6-dihydroxy-3-methoxy-8-methylxanthen-9-one

C15H12O5 (272.0685)


   

5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one

NCGC00017346-06!5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one

C15H12O5 (272.0685)


   

7-methoxy-8-(3-methyl-5-oxo-2H-furan-4-yl)chromen-2-one

NCGC00384658-01!7-methoxy-8-(3-methyl-5-oxo-2H-furan-4-yl)chromen-2-one

C15H12O5 (272.0685)


   

6,8-dihydroxy-3-(4-hydroxyphenyl)-3,4-dihydroisochromen-1-one

NCGC00385856-01!6,8-dihydroxy-3-(4-hydroxyphenyl)-3,4-dihydroisochromen-1-one

C15H12O5 (272.0685)


   

6-hydroxy-1,5-dimethoxyxanthen-9-one

NCGC00384827-01!6-hydroxy-1,5-dimethoxyxanthen-9-one

C15H12O5 (272.0685)


   

3,7-dihydroxy-9-methoxy-1-methylbenzo[c]chromen-6-one

NCGC00380600-01!3,7-dihydroxy-9-methoxy-1-methylbenzo[c]chromen-6-one

C15H12O5 (272.0685)


   

2-(3,4-dihydroxyphenyl)-7-hydroxy-2,3-dihydrochromen-4-one

NCGC00180724-02!2-(3,4-dihydroxyphenyl)-7-hydroxy-2,3-dihydrochromen-4-one

C15H12O5 (272.0685)


   

7-Aminocephalosporanic acid

7-Aminocephalosporanic acid

C10H12N2O5S (272.0467)


D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents > D002511 - Cephalosporins D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents > D047090 - beta-Lactams D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents > D007769 - Lactams

   

3,4,7-Trihydroxyflavanone

3,4,7-Trihydroxyflavanone

C15H12O5 (272.0685)


Butin is a major biologically active flavonoid isolated from the heartwood of Dalbergia odorifera, with strong antioxidant, antiplatelet and anti-inflammatory activities. Butin significantly alleviates myocardial infarction and improves heart function, together with prevents diabetes-induced cardiac oxidative damage in rat[1][2]. Butin is a major biologically active flavonoid isolated from the heartwood of Dalbergia odorifera, with strong antioxidant, antiplatelet and anti-inflammatory activities. Butin significantly alleviates myocardial infarction and improves heart function, together with prevents diabetes-induced cardiac oxidative damage in rat[1][2].

   

3-(2,6-dihydroxyphenyl)-4-hydroxy-6-methyl-3H-2-benzofuran-1-one

3-(2,6-dihydroxyphenyl)-4-hydroxy-6-methyl-3H-2-benzofuran-1-one

C15H12O5 (272.0685)


   

7-methoxy-8-(3-methyl-5-oxo-2H-furan-4-yl)chromen-2-one

7-methoxy-8-(3-methyl-5-oxo-2H-furan-4-yl)chromen-2-one

C15H12O5 (272.0685)


   

Alternariol methyl ether

Alternariol monomethyl ether

C15H12O5 (272.0685)


CONFIDENCE Reference Standard (Level 1)

   

Flavanone base + 3O

Flavanone base + 3O

C15H12O5 (272.0685)


Annotation level-3

   

7-methoxy-8-(3-methyl-5-oxo-2H-furan-4-yl)chromen-2-one [IIN-based: Match]

NCGC00384658-01!7-methoxy-8-(3-methyl-5-oxo-2H-furan-4-yl)chromen-2-one [IIN-based: Match]

C15H12O5 (272.0685)


   

7-methoxy-8-(3-methyl-5-oxo-2H-furan-4-yl)chromen-2-one [IIN-based on: CCMSLIB00000846503]

NCGC00384658-01!7-methoxy-8-(3-methyl-5-oxo-2H-furan-4-yl)chromen-2-one [IIN-based on: CCMSLIB00000846503]

C15H12O5 (272.0685)


   

3-(2,6-dihydroxyphenyl)-4-hydroxy-6-methyl-3H-2-benzofuran-1-one_major

3-(2,6-dihydroxyphenyl)-4-hydroxy-6-methyl-3H-2-benzofuran-1-one_major

C15H12O5 (272.0685)


   

Naringenin_pos

Naringenin_pos

C15H12O5 (272.0685)


(±)-Naringenin is a naturally-occurring flavonoid. (±)-Naringenin displays vasorelaxant effect on endothelium-denuded vessels via the activation of BKCa channels in myocytes[1]. (±)-Naringenin is a naturally-occurring flavonoid. (±)-Naringenin displays vasorelaxant effect on endothelium-denuded vessels via the activation of BKCa channels in myocytes[1].

   

5,8,4-Trihydroxyflavanone

5,8,4-Trihydroxyflavanone

C15H12O5 (272.0685)


   

Dihydrobaicalein

Dihydrobaicalein

C15H12O5 (272.0685)


Dihydrobaicalein is a PLK1 Inhibitor with an IC50 of 6.3 μM. Dihydrobaicalein also inhibits VRK2 and PLK2. Dihydrobaicalein is a natural product that can be isolated from Scutellaria scandens[1]. Dihydrobaicalein is a PLK1 Inhibitor with an IC50 of 6.3 μM. Dihydrobaicalein also inhibits VRK2 and PLK2. Dihydrobaicalein is a natural product that can be isolated from Scutellaria scandens[1].

   

Asahina

4H-1-Benzopyran-4-one, 2,3-dihydro-5,7-dihydroxy-2-(4-hydroxyphenyl)-, (2S)-

C15H12O5 (272.0685)


D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006727 - Hormone Antagonists > D004965 - Estrogen Antagonists D005765 - Gastrointestinal Agents > D000897 - Anti-Ulcer Agents (±)-Naringenin is a naturally-occurring flavonoid. (±)-Naringenin displays vasorelaxant effect on endothelium-denuded vessels via the activation of BKCa channels in myocytes[1]. (±)-Naringenin is a naturally-occurring flavonoid. (±)-Naringenin displays vasorelaxant effect on endothelium-denuded vessels via the activation of BKCa channels in myocytes[1]. Naringenin is the predominant flavanone in Citrus reticulata Blanco; displays strong anti-inflammatory and antioxidant activities. Naringenin has anti-dengue virus (DENV) activity. Naringenin is the predominant flavanone in Citrus reticulata Blanco; displays strong anti-inflammatory and antioxidant activities. Naringenin has anti-dengue virus (DENV) activity.

   

Fukiic acid

(2R,3S)-2-[(3,4-dihydroxyphenyl)methyl]-2,3-dihydroxybutanedioic acid

C11H12O8 (272.0532)


   

1-Hydroxy-3,7-dimethoxyxanthone

3,7-Dimethoxy-1-hydroxy-9H-xanthene-9-one

C15H12O5 (272.0685)


   

Moracin J

5-(5-hydroxy-6-methoxy-1-benzofuran-2-yl)benzene-1,3-diol

C15H12O5 (272.0685)


   

3'-Hydroxydihydrodaidzein

3-(3,4-dihydroxyphenyl)-7-hydroxy-3,4-dihydro-2H-1-benzopyran-4-one

C15H12O5 (272.0685)


   

6-Hydroxydihydrodaidzein

6,7-dihydroxy-3-(4-hydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-4-one

C15H12O5 (272.0685)


   

8-Hydroxydihydrodaidzein

7,8-dihydroxy-3-(4-hydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-4-one

C15H12O5 (272.0685)


   

(-)-Glycinol

3,6a,9-Trihydroxypterocarpan

C15H12O5 (272.0685)


   

1-(4-BENZYLPIPERAZINO)-2-CHLOROPROPAN-1-ONE

1-(4-BENZYLPIPERAZINO)-2-CHLOROPROPAN-1-ONE

C11H14BrFN2 (272.0324)


   

tert-Butyl (3-chloro-2-nitrophenyl)carbamate

tert-Butyl (3-chloro-2-nitrophenyl)carbamate

C11H13ClN2O4 (272.0564)


   

1-tosyl-1H-benzo[d]imidazole

1-tosyl-1H-benzo[d]imidazole

C14H12N2O2S (272.0619)


   

Zolimidine

2-(4-methylsulfonylphenyl)imidazo[1,2-a]pyridine

C14H12N2O2S (272.0619)


A - Alimentary tract and metabolism > A02 - Drugs for acid related disorders > A02B - Drugs for peptic ulcer and gastro-oesophageal reflux disease (gord) C78276 - Agent Affecting Digestive System or Metabolism > C29701 - Anti-ulcer Agent

   

2,6-diamino-4-(2-fluorophenyl)-4H-thiopyran-3,5-dicarbonitrile

2,6-diamino-4-(2-fluorophenyl)-4H-thiopyran-3,5-dicarbonitrile

C13H9FN4S (272.0532)


   

1-(iodomethyl)-1,2,3,4-tetrahydronaphthalene

1-(iodomethyl)-1,2,3,4-tetrahydronaphthalene

C11H13I (272.0062)


   

1,2,3,4-TETRAHYDRO-2-(IODOMETHYL)-NAPHTHALENE

1,2,3,4-TETRAHYDRO-2-(IODOMETHYL)-NAPHTHALENE

C11H13I (272.0062)


   

4-CHLORO-2-(2-FLUORO-PHENYL)-5-METHYL-QUINAZOLINE

4-CHLORO-2-(2-FLUORO-PHENYL)-5-METHYL-QUINAZOLINE

C15H10ClFN2 (272.0517)


   

3-Boc-Amino-4-bromopyridine

3-Boc-Amino-4-bromopyridine

C10H13BrN2O2 (272.016)


   

Bromo(tert-butyl)methoxy(phenyl)silane

Bromo(tert-butyl)methoxy(phenyl)silane

C11H17BrOSi (272.0232)


   

3 7-DIHYDROXYFLAVONE HYDRATE

3 7-DIHYDROXYFLAVONE HYDRATE

C15H12O5 (272.0685)


   

3-(4-chlorophenyl)-7-hydroxychromen-4-one

3-(4-chlorophenyl)-7-hydroxychromen-4-one

C15H9ClO3 (272.024)


   

2-Bromo-4,5-diethoxybenzaldehyde

2-Bromo-4,5-diethoxybenzaldehyde

C11H13BrO3 (272.0048)


   

3-BROMO-4,5-DIETHOXY-BENZALDEHYDE

3-BROMO-4,5-DIETHOXY-BENZALDEHYDE

C11H13BrO3 (272.0048)


   

3-bromo-5-methoxy-4-propan-2-yloxybenzaldehyde

3-bromo-5-methoxy-4-propan-2-yloxybenzaldehyde

C11H13BrO3 (272.0048)


   

2,4-Diamino-6-pteridinemethanol hydrobromide

2,4-Diamino-6-pteridinemethanol hydrobromide

C7H9BrN6O (272.0021)


   

1-(2-methoxylphenyl)-piperazine monohydrobromide

1-(2-methoxylphenyl)-piperazine monohydrobromide

C11H17BrN2O (272.0524)


   

Morpholine,4-[(4-nitrophenyl)sulfonyl]-

Morpholine,4-[(4-nitrophenyl)sulfonyl]-

C10H12N2O5S (272.0467)


   

(4-METHOXY-PHENYLAMINO)-ACETICACIDHYDRAZIDE

(4-METHOXY-PHENYLAMINO)-ACETICACIDHYDRAZIDE

C12H11F3N2S (272.0595)


   

3-Bromo-1-adamantaneacetic acid

3-Bromo-1-adamantaneacetic acid

C12H17BrO2 (272.0412)


   

4-CHLORO-2-(2-FLUORO-PHENYL)-6-METHYL-QUINAZOLINE

4-CHLORO-2-(2-FLUORO-PHENYL)-6-METHYL-QUINAZOLINE

C15H10ClFN2 (272.0517)


   

3,5-bis(trifluoromethyl)benzhydrazide

3,5-bis(trifluoromethyl)benzhydrazide

C9H6F6N2O (272.0384)


   

4-BROMO-1-CHLORO-3,5-DIFLUOROBENZENE

4-BROMO-1-CHLORO-3,5-DIFLUOROBENZENE

C11H7F3N2O3 (272.0409)


   

Butanoic acid,4-[[4-(aminosulfonyl)phenyl]amino]-4-oxo-

Butanoic acid,4-[[4-(aminosulfonyl)phenyl]amino]-4-oxo-

C10H12N2O5S (272.0467)


   

2-(2,5-Dimethylphenyl)-1,1,1,3,3,3-hexafluoropropan-2-ol

2-(2,5-Dimethylphenyl)-1,1,1,3,3,3-hexafluoropropan-2-ol

C11H10F6O (272.0636)


   

Nitroscanate

4-Isothiocyanato-4-nitrodiphenyl ether

C13H8N2O3S (272.0256)


C254 - Anti-Infective Agent > C276 - Antiparasitic Agent > C250 - Antihelminthic Agent

   

2-methoxy-5-[5-(trifluoromethyl)tetrazol-1-yl]benzaldehyde

2-methoxy-5-[5-(trifluoromethyl)tetrazol-1-yl]benzaldehyde

C10H7F3N4O2 (272.0521)


   

methyl 4-phenoxycarbonyloxybenzoate

methyl 4-phenoxycarbonyloxybenzoate

C15H12O5 (272.0685)


   

1,4-bis(4-fluorophenyl)but-2-ene-1,4-dione

1,4-bis(4-fluorophenyl)but-2-ene-1,4-dione

C16H10F2O2 (272.0649)


   

5-METHOXY-[1,1-BIPHENYL]-3,3-DICARBOXYLIC ACID

5-METHOXY-[1,1-BIPHENYL]-3,3-DICARBOXYLIC ACID

C15H12O5 (272.0685)


   

5-METHOXY-[1,1-BIPHENYL]-3,4-DICARBOXYLIC ACID

5-METHOXY-[1,1-BIPHENYL]-3,4-DICARBOXYLIC ACID

C15H12O5 (272.0685)


   

1-BENZYL-3-METHYL-1H-THIENO[2,3-C]PYRAZOLE-5-CARBOXYLIC ACID

1-BENZYL-3-METHYL-1H-THIENO[2,3-C]PYRAZOLE-5-CARBOXYLIC ACID

C14H12N2O2S (272.0619)


   

ETHYL 4-HYDROXY-3-(METHYLTHIO)-4,5,6,7-TETRAHYDROBENZO[C]THIOPHENE-1-CARBOXYLATE

ETHYL 4-HYDROXY-3-(METHYLTHIO)-4,5,6,7-TETRAHYDROBENZO[C]THIOPHENE-1-CARBOXYLATE

C12H16O3S2 (272.0541)


   

tert-Butyl (5-bromopyridin-3-yl)carbamate

tert-Butyl (5-bromopyridin-3-yl)carbamate

C10H13BrN2O2 (272.016)


   

2-Bromo-4-boc pyridine

2-Bromo-4-boc pyridine

C10H13BrN2O2 (272.016)


   

3-(2-Bromo-4,5-dimethoxyphenyl)propanal

3-(2-Bromo-4,5-dimethoxyphenyl)propanal

C11H13BrO3 (272.0048)


   

3-(4-Bromo-2,5-dimethoxyphenyl)propanal

3-(4-Bromo-2,5-dimethoxyphenyl)propanal

C11H13BrO3 (272.0048)


   

3-(BENZO[D][1,3]DIOXOL-5-YL)-5-METHOXYBENZOIC ACID

3-(BENZO[D][1,3]DIOXOL-5-YL)-5-METHOXYBENZOIC ACID

C15H12O5 (272.0685)


   

METHYL 3-BROMO-5-ISOPROPOXYBENZOATE

METHYL 3-BROMO-5-ISOPROPOXYBENZOATE

C11H13BrO3 (272.0048)


   
   

Methyl 3,5-bis(trifluoromethyl)benzoate

Methyl 3,5-bis(trifluoromethyl)benzoate

C10H6F6O2 (272.0272)


   

2-[(2-chloroacetyl)amino]-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxamide

2-[(2-chloroacetyl)amino]-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxamide

C11H13ClN2O2S (272.0386)


   

3,5-bis(trifluoromethyl)benzamidoxime

3,5-bis(trifluoromethyl)benzamidoxime

C9H6F6N2O (272.0384)


   

5-Bromo-4-methoxy-2-(1-piperazinyl)pyrimidine

5-Bromo-4-methoxy-2-(1-piperazinyl)pyrimidine

C9H13BrN4O (272.0273)


   

(1S 4S)-2-(4-FLUOROPHENYL)-2 5-DIAZABI-&

(1S 4S)-2-(4-FLUOROPHENYL)-2 5-DIAZABI-&

C11H14BrFN2 (272.0324)


   

3-(4-Fluorophenyl)-2-thioxo-2,3-dihydro-4(1H)-quinazolinone

3-(4-Fluorophenyl)-2-thioxo-2,3-dihydro-4(1H)-quinazolinone

C14H9FN2OS (272.042)


   

4-BROMOACETOPHENONE DIETHYL ACETAL

4-BROMOACETOPHENONE DIETHYL ACETAL

C12H17BrO2 (272.0412)


   

2-(pyridin-2-ylmethoxy)aniline

2-(pyridin-2-ylmethoxy)aniline

C12H14Cl2N2O (272.0483)


   

Z-2-(2,3-Dichlorophenyl)methylene-3-oxobutanoic acid methyleater

Z-2-(2,3-Dichlorophenyl)methylene-3-oxobutanoic acid methyleater

C12H10Cl2O3 (272.0007)


   

2,4-Dichlorophenylboronic acid, pinacol ester

2,4-Dichlorophenylboronic acid, pinacol ester

C12H15BCl2O2 (272.0542)


   

3-(P-TOLYLOXY)PHTHALIC ACID

3-(P-TOLYLOXY)PHTHALIC ACID

C15H12O5 (272.0685)


   

(1S,4S)-2-(3-fluorophenyl)-2,5-diazabicyclo[2.2.1]heptane,hydrobromide

(1S,4S)-2-(3-fluorophenyl)-2,5-diazabicyclo[2.2.1]heptane,hydrobromide

C11H14BrFN2 (272.0324)


   

2-bromo-3-4-dimethoxypropiophenone

2-bromo-3-4-dimethoxypropiophenone

C11H13BrO3 (272.0048)


   

5-carboxy-2-deoxyuridine

5-carboxy-2-deoxyuridine

C10H12N2O7 (272.0644)


A nucleoside analogue that is 2-deoxyuridine in which the hydrogen at position 5 on the uracil ring is replaced by a carboxy group.

   

N-METHYL-N-([2-[4-(TRIFLUOROMETHYL)PHENYL]-1,3-THIAZOL-4-YL]METHYL)AMINE

N-METHYL-N-([2-[4-(TRIFLUOROMETHYL)PHENYL]-1,3-THIAZOL-4-YL]METHYL)AMINE

C12H11F3N2S (272.0595)


   

3-BROMO-5-METHYL-2-PROPOXYPHENYLBORONIC&

3-BROMO-5-METHYL-2-PROPOXYPHENYLBORONIC&

C10H14BBrO3 (272.0219)


   

3-BROMO-2-ISOPROPOXY-5-METHYLPHENYLBORO&

3-BROMO-2-ISOPROPOXY-5-METHYLPHENYLBORO&

C10H14BBrO3 (272.0219)


   

(3-Bromo-2-butoxyphenyl)boronic acid

(3-Bromo-2-butoxyphenyl)boronic acid

C10H14BBrO3 (272.0219)


   

2-Bromo-5-Boc-aminopyridine

2-Bromo-5-Boc-aminopyridine

C10H13BrN2O2 (272.016)


   

2-[2,5-bis(trifluoromethyl)phenyl]acetic acid

2-[2,5-bis(trifluoromethyl)phenyl]acetic acid

C10H6F6O2 (272.0272)


   

2,4-Bis(trifluoromethyl)phenylacetic acid

2,4-Bis(trifluoromethyl)phenylacetic acid

C10H6F6O2 (272.0272)


   

1,2,5,6-Tetrahydroxyanthraquinone

9,10-Anthracenedione,1,2,5,6-tetrahydroxy-

C14H8O6 (272.0321)


   

6-METHYL-1-(PHENYLSULFONYL)-1H-PYRROLO[2,3-B]PYRIDINE

6-METHYL-1-(PHENYLSULFONYL)-1H-PYRROLO[2,3-B]PYRIDINE

C14H12N2O2S (272.0619)


   

N-(4-Amino-2-chlorophenyl)phthalimide

N-(4-Amino-2-chlorophenyl)phthalimide

C14H9ClN2O2 (272.0353)


   

5-Formyluridine

5-Formyluridine

C10H12N2O7 (272.0644)


   

(6-BROMO-2-PYRIDINYL)-CARBAMICACID,1,1-DIMETHYLETHYLESTER

(6-BROMO-2-PYRIDINYL)-CARBAMICACID,1,1-DIMETHYLETHYLESTER

C10H13BrN2O2 (272.016)


   

3,4-Dinitrobenzophenone

3,4-Dinitrobenzophenone

C13H8N2O5 (272.0433)


   

Sulfadiazine sodium

Sulfadiazine sodium

C10H9N4NaO2S (272.0344)


C254 - Anti-Infective Agent > C29739 - Sulfonamide Anti-Infective Agent

   

4-(CYANOMETHYL)PHENYL 2-CHLORONICOTINATE

4-(CYANOMETHYL)PHENYL 2-CHLORONICOTINATE

C14H9ClN2O2 (272.0353)


   

3-Bromo-4-butoxybenzoic acid

3-Bromo-4-butoxybenzoic acid

C11H13BrO3 (272.0048)


   

4-Bromo-9,9-dimethyl-9H-fluorene

4-Bromo-9,9-dimethyl-9H-fluorene

C15H13Br (272.0201)


   

4-Oxo-1-(2,4,5-trifluorophenyl)cyclohexanecarboxylic acid

4-Oxo-1-(2,4,5-trifluorophenyl)cyclohexanecarboxylic acid

C13H11F3O3 (272.066)


   

6-(4-bromopiperidin-1-yl)-1,3,5-triazine-2,4-diamine

6-(4-bromopiperidin-1-yl)-1,3,5-triazine-2,4-diamine

C8H13BrN6 (272.0385)


   

2-(3,4-Dichlorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

2-(3,4-Dichlorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

C12H15BCl2O2 (272.0542)


   

2-(2-Amino-5-chlorophenyl)-1H-isoindole-1,3(2H)-dione

2-(2-Amino-5-chlorophenyl)-1H-isoindole-1,3(2H)-dione

C14H9ClN2O2 (272.0353)


   

4- Methyl-1-(phenylsulfonyl)-1 H-pyrrolo[2,3-b]pyridine

4- Methyl-1-(phenylsulfonyl)-1 H-pyrrolo[2,3-b]pyridine

C14H12N2O2S (272.0619)


   

2,6-diamino-4-(4-fluorophenyl)-4H-thiopyran-3,5-dicarbonitrile

2,6-diamino-4-(4-fluorophenyl)-4H-thiopyran-3,5-dicarbonitrile

C13H9FN4S (272.0532)


   

Tricyclo[3.3.1.13,7]decane-1-carboxylicacid, 3-bromo-5-methyl-

Tricyclo[3.3.1.13,7]decane-1-carboxylicacid, 3-bromo-5-methyl-

C12H17BrO2 (272.0412)


   

[3,5-Bis(trifluoromethyl)phenyl]acetic acid

[3,5-Bis(trifluoromethyl)phenyl]acetic acid

C10H6F6O2 (272.0272)


   

2-BENZO[1,3]DIOXOL-5-YL-6-CHLORO-IMIDAZO[1,2-A]PYRIDINE

2-BENZO[1,3]DIOXOL-5-YL-6-CHLORO-IMIDAZO[1,2-A]PYRIDINE

C14H9ClN2O2 (272.0353)


   

2,3,4,5,6-Pentafluorobenzophenone

2,3,4,5,6-Pentafluorobenzophenone

C13H5F5O (272.0261)


   

3-Bromoacetophenone diethyl ketal,

3-Bromoacetophenone diethyl ketal,

C12H17BrO2 (272.0412)


   

N2-(5-Fluoro-2,4-dinitrophenyl)-L-alaninamide

N2-(5-Fluoro-2,4-dinitrophenyl)-L-alaninamide

C9H9FN4O5 (272.0557)


   

5-methyl-1-(phenylsulfonyl)-1H-Pyrrolo[2,3-b]pyridine

5-methyl-1-(phenylsulfonyl)-1H-Pyrrolo[2,3-b]pyridine

C14H12N2O2S (272.0619)


   

3-Bromo-5-butoxybenzoic acid

3-Bromo-5-butoxybenzoic acid

C11H13BrO3 (272.0048)


   

3-Bromo-5-isobutoxybenzoic acid

3-Bromo-5-isobutoxybenzoic acid

C11H13BrO3 (272.0048)


   

4-Bromo-2-butoxybenzoic acid

4-Bromo-2-butoxybenzoic acid

C11H13BrO3 (272.0048)


   

2-Bromo-4-tert-butyl-6-nitroaniline

2-Bromo-4-tert-butyl-6-nitroaniline

C10H13BrN2O2 (272.016)


   

6-CHLORO-7-HYDROXY-4-PHENYL-2H-CHROMEN-2-ONE

6-CHLORO-7-HYDROXY-4-PHENYL-2H-CHROMEN-2-ONE

C15H9ClO3 (272.024)


   

2-(3,5-Dichlorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

2-(3,5-Dichlorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

C12H15BCl2O2 (272.0542)


   

2-Bromo-9,9-dimethylfluorene

2-Bromo-9,9-dimethylfluorene

C15H13Br (272.0201)


   

4-CHLORO-2-(4-FLUORO-PHENYL)-6-METHYL-QUINAZOLINE

4-CHLORO-2-(4-FLUORO-PHENYL)-6-METHYL-QUINAZOLINE

C15H10ClFN2 (272.0517)


   

N-Amino-N-pentylguanidine hydroiodide

N-Amino-N-pentylguanidine hydroiodide

C6H17IN4 (272.0498)


   

3,5-BIS(TRIFLUOROMETHYL)PHENYLDIMETHYLSILANE

3,5-BIS(TRIFLUOROMETHYL)PHENYLDIMETHYLSILANE

C10H10F6Si (272.0456)


   

5-tert-butoxycarbonylamino-2-chloro-nicotinic acid

5-tert-butoxycarbonylamino-2-chloro-nicotinic acid

C11H13ClN2O4 (272.0564)


   

Methyl 3-bromo-4-isopropoxybenzoate

Methyl 3-bromo-4-isopropoxybenzoate

C11H13BrO3 (272.0048)


   

4,4-BIS(METHYLTHIO)-2-PHENYL-1,3-BUTADIEN-1,1-DICARBONITRILE

4,4-BIS(METHYLTHIO)-2-PHENYL-1,3-BUTADIEN-1,1-DICARBONITRILE

C14H12N2S2 (272.0442)


   

4-bromo-2-(2-methylpropoxy)benzoic acid

4-bromo-2-(2-methylpropoxy)benzoic acid

C11H13BrO3 (272.0048)


   

Methyl 3-bromo-5-propoxybenzoate

Methyl 3-bromo-5-propoxybenzoate

C11H13BrO3 (272.0048)


   

diammonium tetraborate

diammonium tetraborate

B4H8N2O12 (272.0449)


   

sodium [(6-hydroxy-4-methyl-2-oxo-2H-1-benzopyran-7-yl)oxy]acetate

sodium [(6-hydroxy-4-methyl-2-oxo-2H-1-benzopyran-7-yl)oxy]acetate

C12H9NaO6 (272.0297)


   

5-(4-nitrophenyl)thieno[2,3-d]pyrimidin-4-amine

5-(4-nitrophenyl)thieno[2,3-d]pyrimidin-4-amine

C12H8N4O2S (272.0368)


   

1-(Phenylsulfonyl)-2-methyl-4-azaindole

1-(Phenylsulfonyl)-2-methyl-4-azaindole

C14H12N2O2S (272.0619)


   

3-(4-CHLORO-PHENYL)-IMIDAZO[1,2-A]PYRIDINE-8-CARBOXYLIC ACID

3-(4-CHLORO-PHENYL)-IMIDAZO[1,2-A]PYRIDINE-8-CARBOXYLIC ACID

C14H9ClN2O2 (272.0353)


   

Ethyl 6-phenylimidazo[2,1-b][1,3]thiazole-3-carboxylate

Ethyl 6-phenylimidazo[2,1-b][1,3]thiazole-3-carboxylate

C14H12N2O2S (272.0619)


   

(2-AMINO-PYRIDIN-3-YL)-ACETICACID

(2-AMINO-PYRIDIN-3-YL)-ACETICACID

C10H12N2O5S (272.0467)


   

1-(3,4-Dichlorophenyl)cyclohexanecarboxylic acid

1-(3,4-Dichlorophenyl)cyclohexanecarboxylic acid

C13H14Cl2O2 (272.0371)


   

(S)-1-Bromo-4-((3-methoxy-2-methylpropoxy)methyl)benzene

(S)-1-Bromo-4-((3-methoxy-2-methylpropoxy)methyl)benzene

C12H17BrO2 (272.0412)


   

2-AMINO-4,5-DI-THIOPHEN-2-YL-FURAN-3-CARBONITRILE

2-AMINO-4,5-DI-THIOPHEN-2-YL-FURAN-3-CARBONITRILE

C13H8N2OS2 (272.0078)


   

2-BENZENESULFONYLMETHYL-1H-BENZOIMIDAZOLE

2-BENZENESULFONYLMETHYL-1H-BENZOIMIDAZOLE

C14H12N2O2S (272.0619)


   

3-Chloro-7-hydroxy-4-phenyl-2H-chromen-2-one

3-Chloro-7-hydroxy-4-phenyl-2H-chromen-2-one

C15H9ClO3 (272.024)


   

4-chloro-2-(3-methoxyphenyl)-2H-chromene

4-chloro-2-(3-methoxyphenyl)-2H-chromene

C16H13ClO2 (272.0604)


   

tert-Butyl 4-bromo-2-hydroxybenzoate

tert-Butyl 4-bromo-2-hydroxybenzoate

C11H13BrO3 (272.0048)


   

3-BROMO-5-METHOXY-4-PROPOXY-BENZALDEHYDE

3-BROMO-5-METHOXY-4-PROPOXY-BENZALDEHYDE

C11H13BrO3 (272.0048)


   

5-chloro-3-phenyl-1-benzofuran-2-carboxylic acid

5-chloro-3-phenyl-1-benzofuran-2-carboxylic acid

C15H9ClO3 (272.024)


   

1,3-Butanedione,1-benzo[b]thien-3-yl-4,4,4-trifluoro-

1,3-Butanedione,1-benzo[b]thien-3-yl-4,4,4-trifluoro-

C12H7F3O2S (272.0119)


   

6-Chloro-4-hydroxyflavone

6-Chloro-4-hydroxyflavone

C15H9ClO3 (272.024)


   

4-(trifluoromethyl)umbelliferyl acetate

4-(trifluoromethyl)umbelliferyl acetate

C12H7F3O4 (272.0296)


   

(3-Bromo-5-isobutoxyphenyl)boronic acid

(3-Bromo-5-isobutoxyphenyl)boronic acid

C10H14BBrO3 (272.0219)


   

Morpholine,4-[(3-nitrophenyl)sulfonyl]-

Morpholine,4-[(3-nitrophenyl)sulfonyl]-

C10H12N2O5S (272.0467)


   

2-[(2-OXO-2-PHENYLETHYL)THIO]BENZOIC ACID

2-[(2-OXO-2-PHENYLETHYL)THIO]BENZOIC ACID

C15H12O3S (272.0507)


   

4-Chloro-2-(chloromethyl)-6,7-dimethoxyquinazoline

4-Chloro-2-(chloromethyl)-6,7-dimethoxyquinazoline

C11H10Cl2N2O2 (272.0119)


   

2-Bromo-N,N-diethyl-4-nitroaniline

2-Bromo-N,N-diethyl-4-nitroaniline

C10H13BrN2O2 (272.016)


   

2-BROMO-N-(TERT-BUTYL)-4-NITROANILINE

2-BROMO-N-(TERT-BUTYL)-4-NITROANILINE

C10H13BrN2O2 (272.016)


   

(1S,4S)-(-)-2-(4-FLUOROPHENYL)-2,5-DIAZABICYCLO[2.2.1]HEPTANE, HYDROBROMIDE

(1S,4S)-(-)-2-(4-FLUOROPHENYL)-2,5-DIAZABICYCLO[2.2.1]HEPTANE, HYDROBROMIDE

C11H14BrFN2 (272.0324)


   

4-phenyl-5-(trifluoromethyl)-2-thiophenecarboxylic acid

4-phenyl-5-(trifluoromethyl)-2-thiophenecarboxylic acid

C12H7F3O2S (272.0119)


   

4-(5-Chloro-1H-pyrrolo[2,3-b]pyridin-3-yl)benzoic acid

4-(5-Chloro-1H-pyrrolo[2,3-b]pyridin-3-yl)benzoic acid

C14H9ClN2O2 (272.0353)


   

3-(4-fluorophenoxy)-7-hydroxy-4h-1-benzopyran-4-on

3-(4-fluorophenoxy)-7-hydroxy-4h-1-benzopyran-4-on

C15H9FO4 (272.0485)


   

methyl 4-(3-bromopropoxy)benzoate

methyl 4-(3-bromopropoxy)benzoate

C11H13BrO3 (272.0048)


   

5-BENZYLOXY-ISOPHTHALIC ACID

5-BENZYLOXY-ISOPHTHALIC ACID

C15H12O5 (272.0685)


   

4-Bromo-N-(tert-butyl)-2-nitroaniline

4-Bromo-N-(tert-butyl)-2-nitroaniline

C10H13BrN2O2 (272.016)


   

5-BROMO-N-(TERT-BUTYL)-2-NITROANILINE

5-BROMO-N-(TERT-BUTYL)-2-NITROANILINE

C10H13BrN2O2 (272.016)


   

Methanone,bis(4-nitrophenyl)-

Methanone,bis(4-nitrophenyl)-

C13H8N2O5 (272.0433)


   

Ethyl (3-bromo-4-methoxyphenyl)acetate

Ethyl (3-bromo-4-methoxyphenyl)acetate

C11H13BrO3 (272.0048)


   

2,2-Bibenzothiazole,2,2,3,3-tetrahydro-

2,2-Bibenzothiazole,2,2,3,3-tetrahydro-

C14H12N2S2 (272.0442)


   

Glycine,N-[[4-(acetylamino)phenyl]sulfonyl]-

Glycine,N-[[4-(acetylamino)phenyl]sulfonyl]-

C10H12N2O5S (272.0467)


   

1-[3,5-bis(trifluoromethyl)phenyl]propan-1-ol

1-[3,5-bis(trifluoromethyl)phenyl]propan-1-ol

C11H10F6O (272.0636)


   

Butyl 5-bromo-2-hydroxybenzoate

Butyl 5-bromo-2-hydroxybenzoate

C11H13BrO3 (272.0048)


   

Ethyl 4-(2-bromoethoxy)benzoate

Ethyl 4-(2-bromoethoxy)benzoate

C11H13BrO3 (272.0048)


   

3-(2-fluorophenoxy)-7-hydroxychromen-4-one

3-(2-fluorophenoxy)-7-hydroxychromen-4-one

C15H9FO4 (272.0485)


   

Methyl 2-(2,3-dichlorobenzylidine)acetoacetate

Methyl 2-(2,3-dichlorobenzylidine)acetoacetate

C12H10Cl2O3 (272.0007)


   

2-Propanol,1,1,1,3,3,3-hexafluoro-, 2-benzoate

2-Propanol,1,1,1,3,3,3-hexafluoro-, 2-benzoate

C10H6F6O2 (272.0272)


   

Allyl 2,2,3,3,4,4,5,5-octafluoropentyl ether

Allyl 2,2,3,3,4,4,5,5-octafluoropentyl ether

C8H8F8O (272.0447)


   

3-(5-chloro-1-benzofuran-2-yl)benzoic acid

3-(5-chloro-1-benzofuran-2-yl)benzoic acid

C15H9ClO3 (272.024)


   

(2-BROMO-PYRIDIN-3-YL)-CARBAMIC ACID TERT-BUTYL ESTER

(2-BROMO-PYRIDIN-3-YL)-CARBAMIC ACID TERT-BUTYL ESTER

C10H13BrN2O2 (272.016)


   

(5-BROMO-2-METHOXY-PHENYL)-ACETIC ACID ETHYL ESTER

(5-BROMO-2-METHOXY-PHENYL)-ACETIC ACID ETHYL ESTER

C11H13BrO3 (272.0048)


   

ethyl 4,6,6-trichloro-3,3-dimethyl-hex-5-enoate

ethyl 4,6,6-trichloro-3,3-dimethyl-hex-5-enoate

C10H15Cl3O2 (272.0138)


   

(6E)-6-[(3-methoxyphenyl)methylidene]-7H-[1,3]thiazolo[3,2-a]pyrimidin-5-one

(6E)-6-[(3-methoxyphenyl)methylidene]-7H-[1,3]thiazolo[3,2-a]pyrimidin-5-one

C14H12N2O2S (272.0619)


   

6-[(3-methoxyphenyl)methyl]-[1,3]thiazolo[3,2-a]pyrimidin-5-one

6-[(3-methoxyphenyl)methyl]-[1,3]thiazolo[3,2-a]pyrimidin-5-one

C14H12N2O2S (272.0619)


   

tert-butyl (5-bromopyridin-2-yl)carbamate

tert-butyl (5-bromopyridin-2-yl)carbamate

C10H13BrN2O2 (272.016)


   

4-(2-Aminoethylthio)-2-(trifluoromethyl)quinoline

4-(2-Aminoethylthio)-2-(trifluoromethyl)quinoline

C12H11F3N2S (272.0595)


   

1-PYRIDIN-3-YL-1-TOSYLMETHYLISOCYANIDE

1-PYRIDIN-3-YL-1-TOSYLMETHYLISOCYANIDE

C14H12N2O2S (272.0619)


   

di-n-butyldifluorotin

di-n-butyldifluorotin

C8H18F2Sn (272.0398)


   

2-[3,5-bis-(Trifluoromethyl)phenyl]propan-2-ol

2-[3,5-bis-(Trifluoromethyl)phenyl]propan-2-ol

C11H10F6O (272.0636)


   

2-(2-HYDROXYETHYLAMINO)-N-(3-BROMOPHENYL)ACETAMIDE

2-(2-HYDROXYETHYLAMINO)-N-(3-BROMOPHENYL)ACETAMIDE

C10H13BrN2O2 (272.016)


   

5-[4-(Trifluoromethoxy)phenyl]furan-2-carboxylic Acid

5-[4-(Trifluoromethoxy)phenyl]furan-2-carboxylic Acid

C12H7F3O4 (272.0296)


   
   

3-Bromo-9,9-dimethylfluorene

3-Bromo-9,9-dimethylfluorene

C15H13Br (272.0201)


   

1-Bromo-9,9-dimethyl-9H-fluorene

1-Bromo-9,9-dimethyl-9H-fluorene

C15H13Br (272.0201)


   

1,3-dihydro-imidazol-2-one-5-(4-trifluoromethyl)phenyl-4-carboxylic acid

1,3-dihydro-imidazol-2-one-5-(4-trifluoromethyl)phenyl-4-carboxylic acid

C11H7F3N2O3 (272.0409)


   

2,6-dichloro-9-(oxan-2-yl)purine

2,6-dichloro-9-(oxan-2-yl)purine

C10H10Cl2N4O (272.0232)


   

5-(4-METHOXYPHENYL)PYRIDIN-2-YLAMINE DIHYDROCHLORIDE

5-(4-METHOXYPHENYL)PYRIDIN-2-YLAMINE DIHYDROCHLORIDE

C12H14Cl2N2O (272.0483)


   

9-(2-Bromoethyl)-9H-fluorene

9-(2-Bromoethyl)-9H-fluorene

C15H13Br (272.0201)


   

2-(2-CHLOROPHENYL)QUINAZOLINE-4(3H)-THIONE

2-(2-CHLOROPHENYL)QUINAZOLINE-4(3H)-THIONE

C14H9ClN2S (272.0175)


   

(E)-1-(2,4-Dihydroxyphenyl)-3-(3,5-dihydroxyphenyl)prop-2-en-1-one

(E)-1-(2,4-Dihydroxyphenyl)-3-(3,5-dihydroxyphenyl)prop-2-en-1-one

C15H12O5 (272.0685)


   

1-(3-Bromo-5-fluorophenyl)-4-methylpiperazine

1-(3-Bromo-5-fluorophenyl)-4-methylpiperazine

C11H14BrFN2 (272.0324)


   

2H-Pyrido[1,2-a]-1,3,5-triazine-2,4(3H)-dithione,3-(2-pyridinyl)-

2H-Pyrido[1,2-a]-1,3,5-triazine-2,4(3H)-dithione,3-(2-pyridinyl)-

C12H8N4S2 (272.019)


   

N-ISOBUTYL-N-[(1-METHYL-1H-PYRAZOL-4-YL)METHYL]-AMINE

N-ISOBUTYL-N-[(1-METHYL-1H-PYRAZOL-4-YL)METHYL]-AMINE

C11H13ClN2O4 (272.0564)


   
   

Ethyl 5-bromo-2-ethoxybenzoate

Ethyl 5-bromo-2-ethoxybenzoate

C11H13BrO3 (272.0048)


   

Ethyl 3-bromo-4-ethoxybenzoate

Ethyl 3-bromo-4-ethoxybenzoate

C11H13BrO3 (272.0048)


   

Methyl 3-bromo-4-propoxybenzoate

Methyl 3-bromo-4-propoxybenzoate

C11H13BrO3 (272.0048)


   

1-(4-CHLORO-PHENYL)-4-PHENYL-BUTANE-1,4-DIONE

1-(4-CHLORO-PHENYL)-4-PHENYL-BUTANE-1,4-DIONE

C16H13ClO2 (272.0604)


   
   

6-CHLORO-2-[(4-HYDROXYPHENYL)OXY]QUINOXALINE

6-CHLORO-2-[(4-HYDROXYPHENYL)OXY]QUINOXALINE

C14H9ClN2O2 (272.0353)


   

tert-Butyl (4-bromopyridin-2-yl)carbamate

tert-Butyl (4-bromopyridin-2-yl)carbamate

C10H13BrN2O2 (272.016)


   

1,4,5,8-Tetrahydroxyanthraquinone

1,4,5,8-Tetrahydroxy anthraquinone

C14H8O6 (272.0321)


   

3,3-Dinitrobenzophenone

3,3-Dinitrobenzophenone

C13H8N2O5 (272.0433)


   

6,8-DICHLORO-2H-CHROMENE-3-CARBOXYLIC ACID ETHYL ESTER

6,8-DICHLORO-2H-CHROMENE-3-CARBOXYLIC ACID ETHYL ESTER

C12H10Cl2O3 (272.0007)


   

4-Chloro-4-methoxychalcone

4-Chloro-4-methoxychalcone

C16H13ClO2 (272.0604)


   

5-[(tert-butoxycarbonyl)amino]-2-chloroisonicotinic acid

5-[(tert-butoxycarbonyl)amino]-2-chloroisonicotinic acid

C11H13ClN2O4 (272.0564)


   

2-METHYL-1-(PHENYLSULFONYL)-1H-PYRROLO[2,3-B]PYRIDINE

2-METHYL-1-(PHENYLSULFONYL)-1H-PYRROLO[2,3-B]PYRIDINE

C14H12N2O2S (272.0619)


   

3-Bromo-5-butoxyphenylboronic acid

3-Bromo-5-butoxyphenylboronic acid

C10H14BBrO3 (272.0219)


   

5-BROMO-2-(CYCLOHEXYLTHIO)PYRIMIDINE

5-BROMO-2-(CYCLOHEXYLTHIO)PYRIMIDINE

C10H13BrN2S (271.9983)


   

1-(3-(TRIFLUOROMETHOXY)PHENYL)-1H-PYRAZOLE-4-CARBOXYLIC ACID

1-(3-(TRIFLUOROMETHOXY)PHENYL)-1H-PYRAZOLE-4-CARBOXYLIC ACID

C11H7F3N2O3 (272.0409)


   

3-bromo-4-[(2-methylpropan-2-yl)oxy]benzoic acid

3-bromo-4-[(2-methylpropan-2-yl)oxy]benzoic acid

C11H13BrO3 (272.0048)


   

3-bromo-4-butan-2-yloxybenzoic acid

3-bromo-4-butan-2-yloxybenzoic acid

C11H13BrO3 (272.0048)


   

3-bromo-4-(propan-2-yloxymethyl)benzoic acid

3-bromo-4-(propan-2-yloxymethyl)benzoic acid

C11H13BrO3 (272.0048)


   

5-[2-(Trifluoromethoxy)phenyl]-2-Furoic Acid

5-[2-(Trifluoromethoxy)phenyl]-2-Furoic Acid

C12H7F3O4 (272.0296)


   

6-Methyl-2(propane-1-sulfonyl)-2H-thieno[3,2-D][1,2,3]diazaborinin-1-OL

6-Methyl-2(propane-1-sulfonyl)-2H-thieno[3,2-D][1,2,3]diazaborinin-1-OL

C9H13BN2O3S2 (272.0461)


   

3-(5-Amino-7-hydroxy-[1,2,3]triazolo[4,5-D]pyrimidin-2-YL)-benzoic acid

3-(5-Amino-7-hydroxy-[1,2,3]triazolo[4,5-D]pyrimidin-2-YL)-benzoic acid

C11H8N6O3 (272.0658)


   

(2R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one

(2R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one

C15H12O5 (272.0685)


D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006727 - Hormone Antagonists > D004965 - Estrogen Antagonists D005765 - Gastrointestinal Agents > D000897 - Anti-Ulcer Agents

   

(2R,3S)-2,4,7-trihydroxyisoflavanone

(2R,3S)-2,4,7-trihydroxyisoflavanone

C15H12O5 (272.0685)


A hydroxyisoflavanones that is isoflavanone bearing hydroxy groups at the 2, 7 and 4 positions, with R and S configurations at C-2 and C-3 respectively.

   

6-Hydroxy-2-[hydroxy-(4-hydroxyphenyl)methyl]-1-benzofuran-3-one

6-Hydroxy-2-[hydroxy-(4-hydroxyphenyl)methyl]-1-benzofuran-3-one

C15H12O5 (272.0685)


   

Dibenzo(b,f)thiepin-3-methanol, 5,5-dioxide

Dibenzo(b,f)thiepin-3-methanol, 5,5-dioxide

C15H12O3S (272.0507)


   

(5-chloropyridin-3-yl) 1H-indole-4-carboxylate

(5-chloropyridin-3-yl) 1H-indole-4-carboxylate

C14H9ClN2O2 (272.0353)


   

5-Chloropyridin-3-yl 1H-indole-5-carboxylate

5-Chloropyridin-3-yl 1H-indole-5-carboxylate

C14H9ClN2O2 (272.0353)


   

2-Hydroxy-6-[2-(4-hydroxyphenyl)-2-oxo-ethyl]benzoic acid

2-Hydroxy-6-[2-(4-hydroxyphenyl)-2-oxo-ethyl]benzoic acid

C15H12O5 (272.0685)


A monohydroxybenzoic acid that is 2-hydroxybenzoic acid substituted by a 2-(4-hydroxyphenyl)-2-oxoethyl group at position 6. It has been isolated from the roots of Scorzonera judaica.

   

Hydramacrophyllol A

Hydramacrophyllol A

C15H12O5 (272.0685)


An isobenzofuranone that is 2-benzofuran-1(3H)-one substituted by a hydroxy group at position 7 and a (S)-hydroxy(4-hydroxyphenyl)methyl group at position 3. It has been isolated from the roots of Scorzonera judaica.

   

Methanone, (4-chloro-5-hydroxy-3-benzofuranyl)phenyl-

Methanone, (4-chloro-5-hydroxy-3-benzofuranyl)phenyl-

C15H9ClO3 (272.024)


   

3-(difluoromethoxy)-N-(4,5-dihydrothiazol-2-yl)benzamide

3-(difluoromethoxy)-N-(4,5-dihydrothiazol-2-yl)benzamide

C11H10F2N2O2S (272.0431)


   

3-(2,6-Dihydroxyphenyl)-4-hydroxy-6-methylisobenzofuran-1(3H)-one

3-(2,6-Dihydroxyphenyl)-4-hydroxy-6-methylisobenzofuran-1(3H)-one

C15H12O5 (272.0685)


   

N-(3,4-Dichlorophenyl)-2-oxopyrrolidine-1-carboxamide

N-(3,4-Dichlorophenyl)-2-oxopyrrolidine-1-carboxamide

C11H10Cl2N2O2 (272.0119)


   

2-(2-Chloropyridin-4-Yl)-4-Methyl-1h-Isoindole-1,3(2h)-Dione

2-(2-Chloropyridin-4-Yl)-4-Methyl-1h-Isoindole-1,3(2h)-Dione

C14H9ClN2O2 (272.0353)


   

Toralactone

9,10-Dihydroxy-7-methoxy-3-methyl-1H-naphtho(2,3-c)pyran-1-one

C15H12O5 (272.0685)


Toralactone, isolated from Cassia obtusifolia, mediates hepatoprotection via an Nrf2-dependent anti-oxidative mechanism[1]. Toralactone, isolated from Cassia obtusifolia, mediates hepatoprotection via an Nrf2-dependent anti-oxidative mechanism[1].

   

1,3-Dihydroxy-6-methoxy-8-methyl-9-xanthenone

1,3-Dihydroxy-6-methoxy-8-methyl-9-xanthenone

C15H12O5 (272.0685)


   

1-Phenyl-3-(2,4,6-trihydroxyphenyl)propane-1,3-dione

1-Phenyl-3-(2,4,6-trihydroxyphenyl)propane-1,3-dione

C15H12O5 (272.0685)


   

(6R)-3-(acetoxymethyl)-7-ammonio-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

(6R)-3-(acetoxymethyl)-7-ammonio-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

C10H12N2O5S (272.0467)


   

2,4,7-Trihydroxyisoflavanone

2,4,7-Trihydroxyisoflavanone

C15H12O5 (272.0685)


   

3,8,9,10-Tetrahydroxy-6-methyl-1,4-dihydroanthracen-1-one

3,8,9,10-Tetrahydroxy-6-methyl-1,4-dihydroanthracen-1-one

C15H12O5 (272.0685)


   

(2S)-2-azaniumyl-3-(6,7-dichloro-1H-indol-3-yl)propanoate

(2S)-2-azaniumyl-3-(6,7-dichloro-1H-indol-3-yl)propanoate

C11H10Cl2N2O2 (272.0119)


   

methyl alpha-D-glucopyranoside 6-phosphate

methyl alpha-D-glucopyranoside 6-phosphate

C7H13O9P-2 (272.0297)


   

(2R,4R,5S,6R)-4,5-dihydroxy-6-(phosphonooxymethyl)oxane-2-carboxylic acid

(2R,4R,5S,6R)-4,5-dihydroxy-6-(phosphonooxymethyl)oxane-2-carboxylic acid

C7H13O9P (272.0297)


   

(2S,4R,5S,6R)-4,5-dihydroxy-6-(phosphonooxymethyl)oxane-2-carboxylic acid

(2S,4R,5S,6R)-4,5-dihydroxy-6-(phosphonooxymethyl)oxane-2-carboxylic acid

C7H13O9P (272.0297)


   

(Z)-1-(2,4-dihydroxyphenyl)-3-hydroxy-3-(4-hydroxyphenyl)prop-2-en-1-one

(Z)-1-(2,4-dihydroxyphenyl)-3-hydroxy-3-(4-hydroxyphenyl)prop-2-en-1-one

C15H12O5 (272.0685)


   

methyl beta-D-glucoside 6-phosphate

methyl beta-D-glucoside 6-phosphate

C7H13O9P-2 (272.0297)


   

(2,3,4,5-Tetrahydroxy-6-oxoheptyl) phosphate

(2,3,4,5-Tetrahydroxy-6-oxoheptyl) phosphate

C7H13O9P-2 (272.0297)


   

5-(4-Hydroxyphenyl)-gamma-valerolactone 4-sulfate

5-(4-Hydroxyphenyl)-gamma-valerolactone 4-sulfate

C11H12O6S (272.0355)


   

5-chloropyridin-3-yl 1H-indole-6-carboxylate

5-chloropyridin-3-yl 1H-indole-6-carboxylate

C14H9ClN2O2 (272.0353)


   

Hydramacrophyllol B

Hydramacrophyllol B

C15H12O5 (272.0685)


An isobenzofuranone that is 2-benzofuran-1(3H)-one substituted by a hydroxy group at position 7 and a (R)-hydroxy(4-hydroxyphenyl)methyl group at position 3. It has been isolated from the roots of Scorzonera judaica.

   

6-Nitro-2-phenyl-1,2-benzothiazol-3-one

6-Nitro-2-phenyl-1,2-benzothiazol-3-one

C13H8N2O3S (272.0256)


   

1-Phenyl-3-(phenylsulfonyl)-2-propen-1-one

1-Phenyl-3-(phenylsulfonyl)-2-propen-1-one

C15H12O3S (272.0507)


   

5-Nitro-2-phenyl-1,2-benzothiazol-3-one

5-Nitro-2-phenyl-1,2-benzothiazol-3-one

C13H8N2O3S (272.0256)


   

5-chloropyridin-3-yl 1H-indole-2-carboxylate

5-chloropyridin-3-yl 1H-indole-2-carboxylate

C14H9ClN2O2 (272.0353)


   

2-(4,5,6,7-Tetrahydrothieno[2,3-c]pyridin-3-yl)-1,3-benzothiazole

2-(4,5,6,7-Tetrahydrothieno[2,3-c]pyridin-3-yl)-1,3-benzothiazole

C14H12N2S2 (272.0442)


   

3-(2-Furanylmethyl)-5-(2-methoxyethyl)-1,3,5-thiadiazinane-2-thione

3-(2-Furanylmethyl)-5-(2-methoxyethyl)-1,3,5-thiadiazinane-2-thione

C11H16N2O2S2 (272.0653)


   

5-chloropyridin-3-yl 1H-indole-7-carboxylate

5-chloropyridin-3-yl 1H-indole-7-carboxylate

C14H9ClN2O2 (272.0353)


   

4b,9b-dihydroxy-7,8-dihydro-6H-indeno[1,2-b]benzofuran-9,10-dione

4b,9b-dihydroxy-7,8-dihydro-6H-indeno[1,2-b]benzofuran-9,10-dione

C15H12O5 (272.0685)


   

(5E)-3-ethyl-5-(1H-indol-3-ylmethylidene)-1,3-thiazolidine-2,4-dione

(5E)-3-ethyl-5-(1H-indol-3-ylmethylidene)-1,3-thiazolidine-2,4-dione

C14H12N2O2S (272.0619)


   

2-(6-Imidazo[2,1-b]thiazolyl)acetic acid (phenylmethyl) ester

2-(6-Imidazo[2,1-b]thiazolyl)acetic acid (phenylmethyl) ester

C14H12N2O2S (272.0619)


   

2-(2-furanyl)-5,6,7,8-tetrahydro-3H-[1]benzothiolo[2,3-d]pyrimidin-4-one

2-(2-furanyl)-5,6,7,8-tetrahydro-3H-[1]benzothiolo[2,3-d]pyrimidin-4-one

C14H12N2O2S (272.0619)


   

(E)-2-(4-fluorostyryl)-5-(thiophen-2-yl)-1,3,4-oxadiazole

(E)-2-(4-fluorostyryl)-5-(thiophen-2-yl)-1,3,4-oxadiazole

C14H9FN2OS (272.042)


   

(E)-1-[5-(2-Chlorophenyl)furan-2-yl]-N-(1,2,4-triazol-4-yl)methanimine

(E)-1-[5-(2-Chlorophenyl)furan-2-yl]-N-(1,2,4-triazol-4-yl)methanimine

C13H9ClN4O (272.0465)


   

(7R)-3-(acetyloxymethyl)-7-amino-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

(7R)-3-(acetyloxymethyl)-7-amino-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

C10H12N2O5S (272.0467)


   

2-O-sulfo-3,4-di-O-methyl-alpha-L-rhamnose

2-O-sulfo-3,4-di-O-methyl-alpha-L-rhamnose

C8H16O8S (272.0566)


   

1-deoxy-D-altro-heptulose 7-phosphate(2-)

1-deoxy-D-altro-heptulose 7-phosphate(2-)

C7H13O9P-2 (272.0297)


   

(2R)-2,5,7-trihydroxy-2-phenyl-3H-chromen-4-one

(2R)-2,5,7-trihydroxy-2-phenyl-3H-chromen-4-one

C15H12O5 (272.0685)


   

(7-Hydroxy-1-oxoisochromen-3-yl)methyl hydrogen sulate

(7-Hydroxy-1-oxoisochromen-3-yl)methyl hydrogen sulate

C10H8O7S (271.9991)


   

[2-methoxy-4-[(E)-3-oxobut-1-enyl]phenyl] hydrogen sulfate

[2-methoxy-4-[(E)-3-oxobut-1-enyl]phenyl] hydrogen sulfate

C11H12O6S (272.0355)


   

6-(2,3-dichlorophenyl)-2-oxo-1H-1,2,4-triazin-2-ium-3,5-diamine

6-(2,3-dichlorophenyl)-2-oxo-1H-1,2,4-triazin-2-ium-3,5-diamine

C9H8Cl2N5O+ (272.0106)


   

(5-Hydroxy-2-methylchromen-2-yl)methyl hydrogen sulate

(5-Hydroxy-2-methylchromen-2-yl)methyl hydrogen sulate

C11H12O6S (272.0355)


   

1-(4-Methoxy-1-benzouran-5-yl)ethyl hydrogen sulate

1-(4-Methoxy-1-benzouran-5-yl)ethyl hydrogen sulate

C11H12O6S (272.0355)


   

(Z)-4-(2-hydroxy-5-sulfo-phenyl)-2-oxo-but-3-enoic Acid

(Z)-4-(2-hydroxy-5-sulfo-phenyl)-2-oxo-but-3-enoic Acid

C10H8O7S (271.9991)


   

2-(3-Chlorophenyl)-3-hydroxy-chromen-4-one

2-(3-Chlorophenyl)-3-hydroxy-chromen-4-one

C15H9ClO3 (272.024)


   

3-Hydroxy-7-chloroflavanone

3-Hydroxy-7-chloroflavanone

C15H9ClO3 (272.024)


   

2-Iodo-3-trimethylsiloxybutane

2-Iodo-3-trimethylsiloxybutane

C7H17IOSi (272.0093)


   

3-Chloromethyl-2-phenylchroman-4-one

3-Chloromethyl-2-phenylchroman-4-one

C16H13ClO2 (272.0604)


   

7beta-aminocephalosporanic acid zwitterion

7beta-aminocephalosporanic acid zwitterion

C10H12N2O5S (272.0467)


Zwitterionic form of 7beta-aminocephalosporanic acid.

   

5-(Hydroxyphenyl)-gamma-valerolactone-O-sulphate

5-(Hydroxyphenyl)-gamma-valerolactone-O-sulphate

C11H12O6S (272.0355)


   

1-[(2S,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-2,4-dioxopyrimidine-5-carboxylic acid

1-[(2S,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-2,4-dioxopyrimidine-5-carboxylic acid

C10H12N2O7 (272.0644)


   

7beta-aminocephalosporanic acid

7beta-aminocephalosporanic acid

C10H12N2O5S (272.0467)


The alpha,beta-unsaturated monocarboxylic acid that is the active nucleus for the synthesis of cephalosporins and intermediates.

   

adefovir(1-)

adefovir(1-)

C8H11N5O4P (272.0549)


A organophosphonate oxoanion obtained by removal of a proton from the phosphonate group of adefovir, a nucleoside reverse transcriptase inhibitor. It is the major microspecies at pH 7.3 (according to Marvin v 6.2.0.).

   

6,7-dichloro-L-tryptophan zwitterion

6,7-dichloro-L-tryptophan zwitterion

C11H10Cl2N2O2 (272.0119)


An L-alpha-amino acid zwitterion resulting from the transfer of a proton from the carboxy group to the alpha-amino group of 6,7-dichloro-L-tryptophan; major species at pH 7.3.

   
   

Aminocephalosporanic acid

Aminocephalosporanic acid

C10H12N2O5S (272.0467)


   

5,6-dihydroxy-2-methylcyclohexa[g]chromene-4,8,9-trione

5,6-dihydroxy-2-methylcyclohexa[g]chromene-4,8,9-trione

C14H8O6 (272.0321)


   

5,8-dihydroxy-2-methylcyclohexa[g]chromene-4,6,9-trione

5,8-dihydroxy-2-methylcyclohexa[g]chromene-4,6,9-trione

C14H8O6 (272.0321)


   

2-hydroxy-4-[5-(penta-1,3-diyn-1-yl)thiophen-2-yl]but-3-yn-1-yl acetate

2-hydroxy-4-[5-(penta-1,3-diyn-1-yl)thiophen-2-yl]but-3-yn-1-yl acetate

C15H12O3S (272.0507)


   

7β-aminocephalosporanic acid

7β-aminocephalosporanic acid

C10H12N2O5S (272.0467)


   

(2s)-2-[(4s)-4-[(1-hydroxyethylidene)amino]-3-oxo-1,2-oxazolidin-2-yl]-5-oxooxolane-2-carboxylic acid

(2s)-2-[(4s)-4-[(1-hydroxyethylidene)amino]-3-oxo-1,2-oxazolidin-2-yl]-5-oxooxolane-2-carboxylic acid

C10H12N2O7 (272.0644)


   

(2e)-3-(benzenesulfonyl)-1-phenylprop-2-en-1-one

(2e)-3-(benzenesulfonyl)-1-phenylprop-2-en-1-one

C15H12O3S (272.0507)


   

5-(4-chloro-3,5-dimethoxyphenyl)-3-hydroxyoxolan-2-one

5-(4-chloro-3,5-dimethoxyphenyl)-3-hydroxyoxolan-2-one

C12H13ClO5 (272.0451)


   

{5-[4-(furan-2-yl)but-3-en-1-yn-1-yl]thiophen-2-yl}methyl acetate

{5-[4-(furan-2-yl)but-3-en-1-yn-1-yl]thiophen-2-yl}methyl acetate

C15H12O3S (272.0507)


   

{5-[(3z)-4-(furan-2-yl)but-3-en-1-yn-1-yl]thiophen-2-yl}methyl acetate

{5-[(3z)-4-(furan-2-yl)but-3-en-1-yn-1-yl]thiophen-2-yl}methyl acetate

C15H12O3S (272.0507)


   

{5-[(3e)-4-(furan-2-yl)but-3-en-1-yn-1-yl]thiophen-2-yl}methyl acetate

{5-[(3e)-4-(furan-2-yl)but-3-en-1-yn-1-yl]thiophen-2-yl}methyl acetate

C15H12O3S (272.0507)


   

2,3,4-trihydroxyphenazine-1-carboxylic acid

2,3,4-trihydroxyphenazine-1-carboxylic acid

C13H8N2O5 (272.0433)


   

(3s)-3-amino-1-[(s)-amino(sulfoamino)phosphoryl]piperidin-2-one

(3s)-3-amino-1-[(s)-amino(sulfoamino)phosphoryl]piperidin-2-one

C5H13N4O5PS (272.0344)


   

(2r)-1-hydroxy-4-[5-(penta-1,3-diyn-1-yl)thiophen-2-yl]but-3-yn-2-yl acetate

(2r)-1-hydroxy-4-[5-(penta-1,3-diyn-1-yl)thiophen-2-yl]but-3-yn-2-yl acetate

C15H12O3S (272.0507)


   

(3r)-3-amino-1-[amino(sulfoamino)phosphoryl]piperidin-2-one

(3r)-3-amino-1-[amino(sulfoamino)phosphoryl]piperidin-2-one

C5H13N4O5PS (272.0344)


   

(3r,5s)-5-(4-chloro-3,5-dimethoxyphenyl)-3-hydroxyoxolan-2-one

(3r,5s)-5-(4-chloro-3,5-dimethoxyphenyl)-3-hydroxyoxolan-2-one

C12H13ClO5 (272.0451)


   

3-amino-1-[amino(sulfoamino)phosphoryl]piperidin-2-one

3-amino-1-[amino(sulfoamino)phosphoryl]piperidin-2-one

C5H13N4O5PS (272.0344)


   

2-[(3,4-dihydroxyphenyl)methyl]-2,3-dihydroxybutanedioic acid

2-[(3,4-dihydroxyphenyl)methyl]-2,3-dihydroxybutanedioic acid

C11H12O8 (272.0532)


   

2-(dichloromethyl)-6-[(1e,3e)-3-methylhexa-1,3-dien-1-yl]pyran-4-one

2-(dichloromethyl)-6-[(1e,3e)-3-methylhexa-1,3-dien-1-yl]pyran-4-one

C13H14Cl2O2 (272.0371)


   

2-[(4s)-4-[(1-hydroxyethylidene)amino]-3-oxo-1,2-oxazolidin-2-yl]-5-oxooxolane-2-carboxylic acid

2-[(4s)-4-[(1-hydroxyethylidene)amino]-3-oxo-1,2-oxazolidin-2-yl]-5-oxooxolane-2-carboxylic acid

C10H12N2O7 (272.0644)


   

8,11-dihydroxy-2h-[1,3]dioxolo[4,5-b]xanthen-10-one

8,11-dihydroxy-2h-[1,3]dioxolo[4,5-b]xanthen-10-one

C14H8O6 (272.0321)


   

(3s)-3-amino-1-[(r)-amino(sulfoamino)phosphoryl]piperidin-2-one

(3s)-3-amino-1-[(r)-amino(sulfoamino)phosphoryl]piperidin-2-one

C5H13N4O5PS (272.0344)


   

1-hydroxy-4-[5-(penta-1,3-diyn-1-yl)thiophen-2-yl]but-3-yn-2-yl acetate

1-hydroxy-4-[5-(penta-1,3-diyn-1-yl)thiophen-2-yl]but-3-yn-2-yl acetate

C15H12O3S (272.0507)


   

1,7-dihydroxy-9-oxoxanthene-3-carboxylic acid

1,7-dihydroxy-9-oxoxanthene-3-carboxylic acid

C14H8O6 (272.0321)


   

2,3,9-trihydroxyphenazine-1-carboxylic acid

2,3,9-trihydroxyphenazine-1-carboxylic acid

C13H8N2O5 (272.0433)


   

(2s)-2-hydroxy-4-[5-(penta-1,3-diyn-1-yl)thiophen-2-yl]but-3-yn-1-yl acetate

(2s)-2-hydroxy-4-[5-(penta-1,3-diyn-1-yl)thiophen-2-yl]but-3-yn-1-yl acetate

C15H12O3S (272.0507)