NCBI Taxonomy: 52497

Prangos pabularia (ncbi_taxid: 52497)

found 210 associated metabolites at species taxonomy rank level.

Ancestor: Prangos

Child Taxonomies: Prangos pabularia subsp. lamellata, Prangos pabularia subsp. cylindrocarpa

Umbelliferone

7-Hydroxy-2H-1-benzopyran-2-one

C9H6O3 (162.03169259999999)


Umbelliferone is a hydroxycoumarin that is coumarin substituted by a hydroxy group ay position 7. It has a role as a fluorescent probe, a plant metabolite and a food component. Umbelliferone is a natural product found in Ficus septica, Artemisia ordosica, and other organisms with data available. See also: Chamomile (part of). Occurs widely in plants including Angelica subspecies Phytoalexin of infected sweet potato. Umbelliferone is found in many foods, some of which are macadamia nut, silver linden, quince, and capers. Umbelliferone is found in anise. Umbelliferone occurs widely in plants including Angelica species Phytoalexin of infected sweet potat A hydroxycoumarin that is coumarin substituted by a hydroxy group ay position 7. [Raw Data] CB220_Umbelliferone_pos_50eV_CB000077.txt [Raw Data] CB220_Umbelliferone_pos_40eV_CB000077.txt [Raw Data] CB220_Umbelliferone_pos_30eV_CB000077.txt [Raw Data] CB220_Umbelliferone_pos_10eV_CB000077.txt [Raw Data] CB220_Umbelliferone_pos_20eV_CB000077.txt [Raw Data] CB220_Umbelliferone_neg_40eV_000039.txt [Raw Data] CB220_Umbelliferone_neg_10eV_000039.txt [Raw Data] CB220_Umbelliferone_neg_30eV_000039.txt [Raw Data] CB220_Umbelliferone_neg_20eV_000039.txt Umbelliferone. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=93-35-6 (retrieved 2024-07-12) (CAS RN: 93-35-6). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). Umbelliferone (7-Hydroxycoumarin), a natural product of the coumarin family, is a fluorescing compound which can be used as a sunscreen agent. Umbelliferone (7-Hydroxycoumarin), a natural product of the coumarin family, is a fluorescing compound which can be used as a sunscreen agent.

   

Isoimperatorin

7,4-[(3-methyl-2-butenyl)oxy]-7H-furo[3,2-g]-1-benzopyran-7-one

C16H14O4 (270.0892044)


Isoimperatorin is a member of the class of compounds known as psoralens. Psoralens are organic compounds containing a psoralen moiety, which consists of a furan fused to a chromenone to for 7H-furo[3,2-g]chromen-7-one. Isoimperatorin is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). Isoimperatorin can be found in a number of food items such as parsley, lime, wild celery, and parsnip, which makes isoimperatorin a potential biomarker for the consumption of these food products. Isoimperatorin is a non-carcinogenic (not listed by IARC) potentially toxic compound. If the compound has been ingested, rapid gastric lavage should be performed using 5\\\\% sodium bicarbonate. For skin contact, the skin should be washed with soap and water. If the compound has entered the eyes, they should be washed with large quantities of isotonic saline or water. In serious cases, atropine and/or pralidoxime should be administered. Anti-cholinergic drugs work to counteract the effects of excess acetylcholine and reactivate AChE. Atropine can be used as an antidote in conjunction with pralidoxime or other pyridinium oximes (such as trimedoxime or obidoxime), though the use of -oximes has been found to be of no benefit, or possibly harmful, in at least two meta-analyses. Atropine is a muscarinic antagonist, and thus blocks the action of acetylcholine peripherally (T3DB). D011838 - Radiation-Sensitizing Agents > D017319 - Photosensitizing Agents > D011564 - Furocoumarins Isoimperatorin is a methanolic extract of the roots of Angelica dahurica shows significant inhibitory effects on acetylcholinesterase (AChE) with the IC50 of 74.6 μM. Isoimperatorin is a methanolic extract of the roots of Angelica dahurica shows significant inhibitory effects on acetylcholinesterase (AChE) with the IC50 of 74.6 μM.

   

Imperatorin

InChI=1/C16H14O4/c1-10(2)5-7-19-16-14-12(6-8-18-14)9-11-3-4-13(17)20-15(11)16/h3-6,8-9H,7H2,1-2H

C16H14O4 (270.0892044)


Imperatorin is a member of the class of psoralens that is psoralen substituted by a prenyloxy group at position 8. Isolated from Angelica dahurica and Angelica koreana, it acts as a acetylcholinesterase inhibitor. It has a role as an EC 3.1.1.7 (acetylcholinesterase) inhibitor and a metabolite. Imperatorin is a natural product found in Allium wallichii, Ammi visnaga, and other organisms with data available. Imperatorin is found in anise. Imperatorin is present in Aegle marmelos (bael fruit) and seeds of Pastinaca sativa (parsnip).Imperatorin is a furocoumarin and a phytochemical that has been isolated from Urena lobata L. (Malvaceae). It is biosynthesized from umbelliferone, a coumarin derivative.Imperatorin has been shown to exhibit anti-hypertrophic and anti-convulsant functions (A7784, A7785).Imperatorin belongs to the family of Furanocoumarins. These are polycyclic aromatic compounds containing a furan ring fused to a coumarin moeity. See also: Angelica Dahurica Root (part of); Aegle marmelos fruit (part of); Ammi majus seed (part of) ... View More ... Imperatorin is found in anise. Imperatorin is present in Aegle marmelos (bael fruit) and seeds of Pastinaca sativa (parsnip).Imperatorin is a furocoumarin and a phytochemical that has been isolated from Urena lobata L. (Malvaceae). It is biosynthesized from umbelliferone, a coumarin derivative A member of the class of psoralens that is psoralen substituted by a prenyloxy group at position 8. Isolated from Angelica dahurica and Angelica koreana, it acts as a acetylcholinesterase inhibitor. D011838 - Radiation-Sensitizing Agents > D017319 - Photosensitizing Agents > D011564 - Furocoumarins Present in Aegle marmelos (bael fruit) and seeds of Pastinaca sativa (parsnip) INTERNAL_ID 2244; CONFIDENCE Reference Standard (Level 1) CONFIDENCE Reference Standard (Level 1); INTERNAL_ID 2244 Imperatorin is an effective of NO synthesis inhibitor (IC50=9.2 μmol), which also is a BChE inhibitor (IC50=31.4 μmol). Imperatorin is a weak agonist of TRPV1 with EC50 of 12.6±3.2 μM. Imperatorin is an effective of NO synthesis inhibitor (IC50=9.2 μmol), which also is a BChE inhibitor (IC50=31.4 μmol). Imperatorin is a weak agonist of TRPV1 with EC50 of 12.6±3.2 μM.

   

Osthol

InChI=1/C15H16O3/c1-10(2)4-7-12-13(17-3)8-5-11-6-9-14(16)18-15(11)12/h4-6,8-9H,7H2,1-3H

C15H16O3 (244.1099386)


Osthol, also known as 7-methoxy-8-(3-methylpent-2-enyl)coumarin, belongs to coumarins and derivatives class of compounds. Those are polycyclic aromatic compounds containing a 1-benzopyran moiety with a ketone group at the C2 carbon atom (1-benzopyran-2-one). Osthol is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). Osthol can be found in a number of food items such as wild celery, lemon, parsley, and wild carrot, which makes osthol a potential biomarker for the consumption of these food products. Osthol is an O-methylated coumarin. It is a calcium channel blocker, found in plants such as Cnidium monnieri, Angelica archangelica and Angelica pubescens . Osthole is a member of coumarins and a botanical anti-fungal agent. It has a role as a metabolite. Osthole is a natural product found in Murraya alata, Pentaceras australe, and other organisms with data available. See also: Angelica pubescens root (part of). D002317 - Cardiovascular Agents > D002121 - Calcium Channel Blockers D000077264 - Calcium-Regulating Hormones and Agents D049990 - Membrane Transport Modulators D007155 - Immunologic Factors Osthole (Osthol) is a natural antihistamine alternative. Osthole may be a potential inhibitor of histamine H1 receptor activity. Osthole also suppresses the secretion of HBV in cells. Osthole (Osthol) is a natural antihistamine alternative. Osthole may be a potential inhibitor of histamine H1 receptor activity. Osthole also suppresses the secretion of HBV in cells. Osthole (Osthol) is a natural antihistamine alternative. Osthole may be a potential inhibitor of histamine H1 receptor activity. Osthole also suppresses the secretion of HBV in cells.

   

beta-Sitosterol 3-O-beta-D-galactopyranoside

(2R,3R,4S,5S,6R)-2-(((3S,8S,9S,10R,13R,14S,17R)-17-((2R,5R)-5-Ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol

C35H60O6 (576.4389659999999)


Daucosterol is a steroid saponin that is sitosterol attached to a beta-D-glucopyranosyl residue at position 3 via a glycosidic linkage. It has bee isolated from Panax japonicus var. major and Breynia fruticosa. It has a role as a plant metabolite. It is a steroid saponin, a beta-D-glucoside and a monosaccharide derivative. It is functionally related to a sitosterol. It derives from a hydride of a stigmastane. Sitogluside is a natural product found in Ophiopogon intermedius, Ophiopogon jaburan, and other organisms with data available. beta-Sitosterol 3-O-beta-D-galactopyranoside is found in herbs and spices. beta-Sitosterol 3-O-beta-D-galactopyranoside is a constituent of Hibiscus sabdariffa (roselle) leaves. C308 - Immunotherapeutic Agent Daucosterol is a natural sterol compound. Daucosterol is a natural sterol compound.

   

Nonacosane

Nonacosane; Celidoniol, deoxy- (7CI); n-Nonacosane

C29H60 (408.469476)


Nonacosane, also known as CH3-[CH2]27-CH3, belongs to the class of organic compounds known as alkanes. These are acyclic branched or unbranched hydrocarbons having the general formula CnH2n+2 , and therefore consisting entirely of hydrogen atoms and saturated carbon atoms. Nonacosane is a very hydrophobic molecule, practically insoluble in water, and relatively neutral. Thus, nonacosane is considered to be a hydrocarbon lipid molecule. Nonacosane is a straight-chain hydrocarbon with a molecular formula of C29H60. Nonacosane has been identified within several essential oils. Nonacosane has been detected, but not quantified, in several different foods, such as peachs, ginkgo nuts, cauliflowers, arabica coffee, and lambsquarters. This could make nonacosane a potential biomarker for the consumption of these foods. Nonacosane occurs naturally and has been reported to be a component of a pheromone of Orgyia leucostigma, and evidence suggests it plays a role in the chemical communication of several insects, including the female Anopheles stephensi (a mosquito). It can also be prepared synthetically. It has 1,590,507,121 constitutional isomers. Nonacosane, also known as ch3-[ch2]27-ch3, is a member of the class of compounds known as alkanes. Alkanes are acyclic branched or unbranched hydrocarbons having the general formula CnH2n+2 , and therefore consisting entirely of hydrogen atoms and saturated carbon atoms. Thus, nonacosane is considered to be a hydrocarbon lipid molecule. Nonacosane can be found in a number of food items such as garden tomato (variety), papaya, brussel sprouts, and wild carrot, which makes nonacosane a potential biomarker for the consumption of these food products. Nonacosane occurs naturally and has been reported to be a component of a pheromone of Orgyia leucostigma, and evidence suggests it plays a role in the chemical communication of several insects, including the female Anopheles stephensi (a mosquito) . Nonacosane is a straight-chain alkane comprising of 29 carbon atoms. It has a role as a plant metabolite and a volatile oil component. Nonacosane is a natural product found in Euphorbia larica, Quercus salicina, and other organisms with data available. See also: Moringa oleifera leaf oil (part of). A straight-chain alkane comprising of 29 carbon atoms. Nonacosane, isolated from Baphia massaiensis, exhibits weak activities against E. coli, B. subtilis, P. aeruginosa and S. aureus[1]. Nonacosane, isolated from Baphia massaiensis, exhibits weak activities against E. coli, B. subtilis, P. aeruginosa and S. aureus[1].

   

(R)-Oxypeucedanin

7H-Furo[3,2-g][1]benzopyran-7-one, 4-((3,3-dimethyloxiranyl)methoxy)-, (S-)-

C16H14O5 (286.0841194)


(r)-oxypeucedanin, also known as hishigado or phosphine, is a member of the class of compounds known as psoralens. Psoralens are organic compounds containing a psoralen moiety, which consists of a furan fused to a chromenone to for 7H-furo[3,2-g]chromen-7-one (r)-oxypeucedanin is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). (r)-oxypeucedanin can be found in carrot, lemon, parsley, and wild carrot, which makes (r)-oxypeucedanin a potential biomarker for the consumption of these food products. (R)-Oxypeucedanin is a member of psoralens. 4-[(3,3-Dimethyloxiran-2-yl)methoxy]furo[3,2-g]chromen-7-one is a natural product found in Prangos latiloba, Citrus medica, and other organisms with data available. D011838 - Radiation-Sensitizing Agents > D017319 - Photosensitizing Agents > D011564 - Furocoumarins (R)-Oxypeucedanin is found in herbs and spices. (R)-Oxypeucedanin is isolated from Angelica glauc Oxypeucedanin is a furocoumarin derivative isolated from Angelica dahurica. Oxypeucedanin is a selective open-channel blocker, inhibits the hKv1.5 current with an IC50 value of 76 nM.?Oxypeucedanin prolongs cardiac action potential duration (APD), is a potential antiarrhythmic agent for atrial fibrillation[1]. Oxypeucedanin induces cell?apoptosis through inhibition of cancer cell migration[2]. Oxypeucedanin is a furocoumarin derivative isolated from Angelica dahurica. Oxypeucedanin is a selective open-channel blocker, inhibits the hKv1.5 current with an IC50 value of 76 nM.?Oxypeucedanin prolongs cardiac action potential duration (APD), is a potential antiarrhythmic agent for atrial fibrillation[1]. Oxypeucedanin induces cell?apoptosis through inhibition of cancer cell migration[2].

   

Cnidin

4-[(3-Methyl-2-buten-1-yl)oxy]-7H-Furo[3,2-g][1]benzopyran-7-one; 7H-Furo[3,2-g][1]benzopyran-7-one, 4-[(3-methyl-2-butenyl)oxy]- (8CI,9CI); Isoimperatorin (6CI); 4-[(3-Methyl-2-buten-1-yl)oxy]-7H-furo[3,2-g][1]benzopyran-7-one

C16H14O4 (270.0892044)


Isoimperatorin is a member of the class of psoralens that is psoralen substituted by a prenyloxy group at position 5. Isolated from Angelica dahurica and Angelica koreana, it acts as a acetylcholinesterase inhibitor. It has a role as a metabolite and an EC 3.1.1.7 (acetylcholinesterase) inhibitor. Isoimperatorin is a natural product found in Ferulago sylvatica, Prangos trifida, and other organisms with data available. Isoimperatorin is a tumor necrosis factor antagonist isolated from Glehniae root or from Poncirus trifoliate Raf (L579). Furocoumarins, are phototoxic and photocarcinogenic. They intercalate DNA and photochemically induce mutations. Furocoumarins are botanical phytoalexins found to varying extents in a variety of vegetables and fruits, notably citrus fruits. The levels of furocoumarins present in our diets, while normally well below that causing evident acute phototoxicity, do cause pharmacologically relevant drug interactions. Some are particularly active against cytochrome P450s. For example, in humans, bergamottin and dihydroxybergamottin are responsible for the grapefruit juice effect, in which these furanocoumarins affect the metabolism of certain drugs. See also: Angelica archangelica root (part of). A member of the class of psoralens that is psoralen substituted by a prenyloxy group at position 5. Isolated from Angelica dahurica and Angelica koreana, it acts as a acetylcholinesterase inhibitor. D011838 - Radiation-Sensitizing Agents > D017319 - Photosensitizing Agents > D011564 - Furocoumarins Isoimperatorin is a methanolic extract of the roots of Angelica dahurica shows significant inhibitory effects on acetylcholinesterase (AChE) with the IC50 of 74.6 μM. Isoimperatorin is a methanolic extract of the roots of Angelica dahurica shows significant inhibitory effects on acetylcholinesterase (AChE) with the IC50 of 74.6 μM.

   

Spathulenol

1H-Cycloprop(e)azulen-7-ol, decahydro-1,1,7-trimethyl-4-methylene-, (1aR-(1aalpha,4aalpha,7beta,7abeta,7balpha))-

C15H24O (220.18270539999997)


Spathulenol is a tricyclic sesquiterpenoid that is 4-methylidenedecahydro-1H-cyclopropa[e]azulene carrying three methyl substituents at positions 1, 1 and 7 as well as a hydroxy substituent at position 7. It has a role as a volatile oil component, a plant metabolite, an anaesthetic and a vasodilator agent. It is a sesquiterpenoid, a carbotricyclic compound, a tertiary alcohol and an olefinic compound. Spathulenol is a natural product found in Xylopia aromatica, Xylopia emarginata, and other organisms with data available. See also: Chamomile (part of). A tricyclic sesquiterpenoid that is 4-methylidenedecahydro-1H-cyclopropa[e]azulene carrying three methyl substituents at positions 1, 1 and 7 as well as a hydroxy substituent at position 7. Spathulenol is found in alcoholic beverages. Spathulenol is a constituent of Salvia sclarea (clary sage).

   

Isopropyl beta-D-glucoside

2-(hydroxymethyl)-6-(propan-2-yloxy)oxane-3,4,5-triol

C9H18O6 (222.1103328)


Isopropyl beta-D-glucoside is found in herbs and spices. Isopropyl beta-D-glucoside is present in fenne Present in fennel. Isopropyl beta-D-glucoside is found in herbs and spices.

   

(S)-Auraptenol

8-(2-hydroxy-3-methylbut-3-en-1-yl)-7-methoxy-2H-chromen-2-one

C15H16O4 (260.1048536)


(s)-auraptenol belongs to coumarins and derivatives class of compounds. Those are polycyclic aromatic compounds containing a 1-benzopyran moiety with a ketone group at the C2 carbon atom (1-benzopyran-2-one) (s)-auraptenol is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). (s)-auraptenol can be found in citrus, which makes (s)-auraptenol a potential biomarker for the consumption of this food product. (S)-Auraptenol is found in citrus. (S)-Auraptenol is a constituent of Seville bitter orange (Citrus aurantium ssp. amara) oil

   

(E)-Suberenol

6-[(1E)-3-hydroxy-3-methylbut-1-en-1-yl]-7-methoxy-2H-chromen-2-one

C15H16O4 (260.1048536)


Isolated from Limonia acidissima (wood apple) and Citrus nobilis (king orange). (E)-Suberenol is found in many foods, some of which are beverages, sweet orange, citrus, and fruits. (E)-Suberenol is found in beverages. (E)-Suberenol is isolated from Limonia acidissima (wood apple) and Citrus nobilis (king orange

   

Oxypeucedanin hydrate

4-(2,3-dihydroxy-3-methylbutoxy)-7H-furo[3,2-g]chromen-7-one

C16H16O6 (304.0946836)


   

Loliolide

(6S,7aR)-6-hydroxy-4,4,7a-trimethyl-2,4,5,6,7,7a-hexahydro-1-benzofuran-2-one

C11H16O3 (196.1099386)


Loliolide, also known as (3s5r)-loliolide, is a member of the class of compounds known as benzofurans. Benzofurans are organic compounds containing a benzene ring fused to a furan. Furan is a five-membered aromatic ring with four carbon atoms and one oxygen atom. Loliolide is soluble (in water) and an extremely weak acidic compound (based on its pKa). Loliolide can be found in sunflower, tea, and wakame, which makes loliolide a potential biomarker for the consumption of these food products.

   

Heraclenin

9-{[(2S)-3,3-dimethyloxiran-2-yl]methoxy}-7H-furo[3,2-g]chromen-7-one

C16H14O5 (286.0841194)


Heraclenin is a member of the class of compounds known as psoralens. Psoralens are organic compounds containing a psoralen moiety, which consists of a furan fused to a chromenone to for 7H-furo[3,2-g]chromen-7-one. Heraclenin is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). Heraclenin can be found in carrot, lemon, and wild carrot, which makes heraclenin a potential biomarker for the consumption of these food products.

   

Suberosin

7-Methoxy-6-(3-methylbut-2-en-1-yl)-2H-chromen-2-one

C15H16O3 (244.1099386)


Suberosin, also known as 7-methoxy-6-prenylcoumarin, belongs to coumarins and derivatives class of compounds. Those are polycyclic aromatic compounds containing a 1-benzopyran moiety with a ketone group at the C2 carbon atom (1-benzopyran-2-one). Suberosin is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). Suberosin can be found in lemon, mandarin orange (clementine, tangerine), and sweet orange, which makes suberosin a potential biomarker for the consumption of these food products. Suberosin, isolated from Plumbago zeylanica, exhibits anti-inflammatory and anticoagulant activity. Suberosin suppresses PHA-induced PBMC proliferation and arrested cell cycle progression from the G1 transition to the S phase through the modulation of the transcription factors NF-AT and NF-κB[1][2]. Suberosin, isolated from Plumbago zeylanica, exhibits anti-inflammatory and anticoagulant activity. Suberosin suppresses PHA-induced PBMC proliferation and arrested cell cycle progression from the G1 transition to the S phase through the modulation of the transcription factors NF-AT and NF-κB[1][2].

   

ent-Kauran-16-beta-ol

(1S,4R,9R,10R,13R,14R)-5,5,9,14-tetramethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-14-ol

C20H34O (290.2609514)


Ent-kauran-16-beta-ol is a member of the class of compounds known as kaurane diterpenoids. Kaurane diterpenoids are diterpene alkaloids with a structure that is based on the kaurane skeleton. Kaurane is a tetracyclic compound that arises by cyclisation of a pimarane precursor followed by rearrangement. It possesses a [3,2,1]-bicyclic ring system with C15-C16 bridge connected to C13, forming the five-membered ring D. Ent-kauran-16-beta-ol is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). Ent-kauran-16-beta-ol can be found in sunflower, which makes ent-kauran-16-beta-ol a potential biomarker for the consumption of this food product.

   

Suberosin

2H-1-Benzopyran-2-one, 7-methoxy-6-(3-methyl-2-butenyl)- (9CI)

C15H16O3 (244.1099386)


Suberosin is a member of the class of coumarins in which the coumarin ring is substituted at positions 6 and 7 by a 3-methylbut-2-en-1-yl group and a methoxy group, respectively. A natural product found in Citropsis articulata. It has a role as a plant metabolite and an anticoagulant. It is a member of coumarins and an aromatic ether. It is functionally related to a 7-demethylsuberosin. Suberosin is a natural product found in Zanthoxylum ovalifolium, Prangos bucharica, and other organisms with data available. A member of the class of coumarins in which the coumarin ring is substituted at positions 6 and 7 by a 3-methylbut-2-en-1-yl group and a methoxy group, respectively. A natural product found in Citropsis articulata. Suberosin, isolated from Plumbago zeylanica, exhibits anti-inflammatory and anticoagulant activity. Suberosin suppresses PHA-induced PBMC proliferation and arrested cell cycle progression from the G1 transition to the S phase through the modulation of the transcription factors NF-AT and NF-κB[1][2]. Suberosin, isolated from Plumbago zeylanica, exhibits anti-inflammatory and anticoagulant activity. Suberosin suppresses PHA-induced PBMC proliferation and arrested cell cycle progression from the G1 transition to the S phase through the modulation of the transcription factors NF-AT and NF-κB[1][2].

   

Prangenin

7H-Furo(3,2-g)(1)benzopyran-7-one, 9-((3,3-dimethyloxiranyl)methoxy)-, (R)- (9CI)

C16H14O5 (286.0841194)


Oxyimperatorin is a natural product found in Ferula sumbul, Angelica dahurica, and Ferula moschata with data available. Oxyimperatorin ((±)-Heraclenin) is a coumarin isolated from Angelica dahurica. Oxyimperatorin ((±)-Heraclenin) is a coumarin isolated from Angelica dahurica.

   

7-methoxy-2-oxo-2H-chromene-8-carbaldehyde

7-methoxy-2-oxo-2H-chromene-8-carbaldehyde

C11H8O4 (204.0422568)


   

Spathulenol

Spathulenol

C15H24O (220.18270539999997)


Constituent of Salvia sclarea (clary sage). Spathulenol is found in many foods, some of which are tarragon, spearmint, common sage, and tea.

   

Osthol

InChI=1/C15H16O3/c1-10(2)4-7-12-13(17-3)8-5-11-6-9-14(16)18-15(11)12/h4-6,8-9H,7H2,1-3H

C15H16O3 (244.1099386)


Osthole is a member of coumarins and a botanical anti-fungal agent. It has a role as a metabolite. Osthole is a natural product found in Murraya alata, Pentaceras australe, and other organisms with data available. See also: Angelica pubescens root (part of). A natural product found in Peucedanum ostruthium and Angelica pubescens. D002317 - Cardiovascular Agents > D002121 - Calcium Channel Blockers D000077264 - Calcium-Regulating Hormones and Agents D049990 - Membrane Transport Modulators D007155 - Immunologic Factors Origin: Plant, Coumarins Osthole (Osthol) is a natural antihistamine alternative. Osthole may be a potential inhibitor of histamine H1 receptor activity. Osthole also suppresses the secretion of HBV in cells. Osthole (Osthol) is a natural antihistamine alternative. Osthole may be a potential inhibitor of histamine H1 receptor activity. Osthole also suppresses the secretion of HBV in cells. Osthole (Osthol) is a natural antihistamine alternative. Osthole may be a potential inhibitor of histamine H1 receptor activity. Osthole also suppresses the secretion of HBV in cells.

   

Daucosterol

(2R,3R,4S,5S,6R)-2-(((3S,8S,9S,10R,13R,14S,17R)-17-((2R,5R)-5-Ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol

C35H60O6 (576.4389659999999)


Daucosterol is a steroid saponin that is sitosterol attached to a beta-D-glucopyranosyl residue at position 3 via a glycosidic linkage. It has bee isolated from Panax japonicus var. major and Breynia fruticosa. It has a role as a plant metabolite. It is a steroid saponin, a beta-D-glucoside and a monosaccharide derivative. It is functionally related to a sitosterol. It derives from a hydride of a stigmastane. Sitogluside is a natural product found in Ophiopogon intermedius, Ophiopogon jaburan, and other organisms with data available. A steroid saponin that is sitosterol attached to a beta-D-glucopyranosyl residue at position 3 via a glycosidic linkage. It has bee isolated from Panax japonicus var. major and Breynia fruticosa. C308 - Immunotherapeutic Agent Daucosterol is a natural sterol compound. Daucosterol is a natural sterol compound.

   

Imperatorin

Imperatorin

C16H14O4 (270.0892044)


Imperatorin is an effective of NO synthesis inhibitor (IC50=9.2 μmol), which also is a BChE inhibitor (IC50=31.4 μmol). Imperatorin is a weak agonist of TRPV1 with EC50 of 12.6±3.2 μM. Imperatorin is an effective of NO synthesis inhibitor (IC50=9.2 μmol), which also is a BChE inhibitor (IC50=31.4 μmol). Imperatorin is a weak agonist of TRPV1 with EC50 of 12.6±3.2 μM.

   

Umbelliferone

7-hydroxycoumarine

C9H6O3 (162.03169259999999)


Umbelliferone (7-Hydroxycoumarin), a natural product of the coumarin family, is a fluorescing compound which can be used as a sunscreen agent. Umbelliferone (7-Hydroxycoumarin), a natural product of the coumarin family, is a fluorescing compound which can be used as a sunscreen agent.

   

9-(2,3-dihydroxy-3-methylbutoxy)furo[3,2-g]chromen-7-one

NCGC00179981-03!9-(2,3-dihydroxy-3-methylbutoxy)furo[3,2-g]chromen-7-one

C16H16O6 (304.0946836)


   

4-(2,3-dihydroxy-3-methylbutoxy)furo[3,2-g]chromen-7-one

NCGC00169070-02!4-(2,3-dihydroxy-3-methylbutoxy)furo[3,2-g]chromen-7-one

C16H16O6 (304.0946836)


   

loliolide

2(4H)-Benzofuranone, 5,6,7,7a-tetrahydro-6-hydroxy-4,4,7a-trimethyl-, (6S-cis)-

C11H16O3 (196.1099386)


A natural product found in Brachystemma calycinum.

   

Isoimperatorin

Isoimperatorin

C16H14O4 (270.0892044)


D011838 - Radiation-Sensitizing Agents > D017319 - Photosensitizing Agents > D011564 - Furocoumarins Origin: Plant, Coumarins Isoimperatorin is a methanolic extract of the roots of Angelica dahurica shows significant inhibitory effects on acetylcholinesterase (AChE) with the IC50 of 74.6 μM. Isoimperatorin is a methanolic extract of the roots of Angelica dahurica shows significant inhibitory effects on acetylcholinesterase (AChE) with the IC50 of 74.6 μM.

   

Osthole

Osthole

C15H16O3 (244.1099386)


Annotation level-1

   

Heraclenin

Heraclenin

C16H14O5 (286.0841194)


Origin: Plant, Coumarins Heraclenin, a natural furanocoumarin, significantly inhibits T cell receptor-mediated proliferation in human primary T cells in a concentration-dependent manner by targeting nuclear factor of activated T-cells (NFAT)[1]. Heraclenin, a natural furanocoumarin, significantly inhibits T cell receptor-mediated proliferation in human primary T cells in a concentration-dependent manner by targeting nuclear factor of activated T-cells (NFAT)[1].

   

heraclenol

9-(2,3-dihydroxy-3-methylbutoxy)-2H-furo[3,2-g]chromen-2-one

C16H16O6 (304.0946836)


   

suberenol

6-[(1E)-3-hydroxy-3-methylbut-1-en-1-yl]-7-methoxy-2H-chromen-2-one

C15H16O4 (260.1048536)


   

Auraptenol

8-(2-hydroxy-3-methylbut-3-en-1-yl)-7-methoxy-2H-chromen-2-one

C15H16O4 (260.1048536)


   

Isopropyl b-D-glucoside

2-(hydroxymethyl)-6-(propan-2-yloxy)oxane-3,4,5-triol

C9H18O6 (222.1103328)


   

Spatulenol

1,7,7-trimethyl-4-methylidene-decahydro-1H-cyclopropa[e]azulen-1-ol

C15H24O (220.18270539999997)


   

Nonacosane

EINECS 211-126-2

C29H60 (408.469476)


Nonacosane, isolated from Baphia massaiensis, exhibits weak activities against E. coli, B. subtilis, P. aeruginosa and S. aureus[1]. Nonacosane, isolated from Baphia massaiensis, exhibits weak activities against E. coli, B. subtilis, P. aeruginosa and S. aureus[1].

   

Ostol

InChI=1\C15H16O3\c1-10(2)4-7-12-13(17-3)8-5-11-6-9-14(16)18-15(11)12\h4-6,8-9H,7H2,1-3H

C15H16O3 (244.1099386)


D002317 - Cardiovascular Agents > D002121 - Calcium Channel Blockers D000077264 - Calcium-Regulating Hormones and Agents D049990 - Membrane Transport Modulators D007155 - Immunologic Factors Osthole (Osthol) is a natural antihistamine alternative. Osthole may be a potential inhibitor of histamine H1 receptor activity. Osthole also suppresses the secretion of HBV in cells. Osthole (Osthol) is a natural antihistamine alternative. Osthole may be a potential inhibitor of histamine H1 receptor activity. Osthole also suppresses the secretion of HBV in cells. Osthole (Osthol) is a natural antihistamine alternative. Osthole may be a potential inhibitor of histamine H1 receptor activity. Osthole also suppresses the secretion of HBV in cells.

   

Ammidin

InChI=1\C16H14O4\c1-10(2)5-7-19-16-14-12(6-8-18-14)9-11-3-4-13(17)20-15(11)16\h3-6,8-9H,7H2,1-2H

C16H14O4 (270.0892044)


D011838 - Radiation-Sensitizing Agents > D017319 - Photosensitizing Agents > D011564 - Furocoumarins Imperatorin is an effective of NO synthesis inhibitor (IC50=9.2 μmol), which also is a BChE inhibitor (IC50=31.4 μmol). Imperatorin is a weak agonist of TRPV1 with EC50 of 12.6±3.2 μM. Imperatorin is an effective of NO synthesis inhibitor (IC50=9.2 μmol), which also is a BChE inhibitor (IC50=31.4 μmol). Imperatorin is a weak agonist of TRPV1 with EC50 of 12.6±3.2 μM.

   

482-45-1

7H-Furo(3,2-g)(1)benzopyran-7-one, 4-((3-methyl-2-butenyl)oxy)-

C16H14O4 (270.0892044)


D011838 - Radiation-Sensitizing Agents > D017319 - Photosensitizing Agents > D011564 - Furocoumarins Isoimperatorin is a methanolic extract of the roots of Angelica dahurica shows significant inhibitory effects on acetylcholinesterase (AChE) with the IC50 of 74.6 μM. Isoimperatorin is a methanolic extract of the roots of Angelica dahurica shows significant inhibitory effects on acetylcholinesterase (AChE) with the IC50 of 74.6 μM.

   

Oxypeucedanin

Oxypeucedanin

C16H14O5 (286.0841194)


A furanocoumarin that is 7H-furo[3,2-g][1]benzopyran-7-one substituted by a [(2S)-3,3-dimethyloxiran-2-yl]methoxy group at position 4. D011838 - Radiation-Sensitizing Agents > D017319 - Photosensitizing Agents > D011564 - Furocoumarins

   

2-(hydroxymethyl)-6-(propan-2-yloxy)oxane-3,4,5-triol

2-(hydroxymethyl)-6-(propan-2-yloxy)oxane-3,4,5-triol

C9H18O6 (222.1103328)


   

(+)-oxypeucedanin

(+)-oxypeucedanin

C16H14O5 (286.0841194)


A natural product found in Citrus hystrix.

   

(8s)-8-(prop-1-en-2-yl)-8h,9h-furo[2,3-h]chromen-2-one

(8s)-8-(prop-1-en-2-yl)-8h,9h-furo[2,3-h]chromen-2-one

C14H12O3 (228.0786402)


   

(5s)-2,4,4-trimethyl-5-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)cyclohex-2-en-1-one

(5s)-2,4,4-trimethyl-5-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)cyclohex-2-en-1-one

C16H26O7 (330.16784459999997)


   

8-[(2r)-2-hydroxy-3-methylbut-3-en-1-yl]-7-methoxychromen-2-one

8-[(2r)-2-hydroxy-3-methylbut-3-en-1-yl]-7-methoxychromen-2-one

C15H16O4 (260.1048536)


   

(2r,3s,4s,5r,6r)-2-(hydroxymethyl)-6-[(2,3,4-trimethylphenyl)methoxy]oxane-3,4,5-triol

(2r,3s,4s,5r,6r)-2-(hydroxymethyl)-6-[(2,3,4-trimethylphenyl)methoxy]oxane-3,4,5-triol

C16H24O6 (312.1572804)


   

(7ar)-1,1,7-trimethyl-4-methylidene-octahydrocyclopropa[e]azulen-7-ol

(7ar)-1,1,7-trimethyl-4-methylidene-octahydrocyclopropa[e]azulen-7-ol

C15H24O (220.18270539999997)


   

3-[(4,5-dihydroxy-3-{[3-hydroxy-2-methyl-4-({7-oxofuro[3,2-g]chromen-4-yl}oxy)butan-2-yl]oxy}-6-(hydroxymethyl)oxan-2-yl)oxy]-2-methylpyran-4-one

3-[(4,5-dihydroxy-3-{[3-hydroxy-2-methyl-4-({7-oxofuro[3,2-g]chromen-4-yl}oxy)butan-2-yl]oxy}-6-(hydroxymethyl)oxan-2-yl)oxy]-2-methylpyran-4-one

C28H30O13 (574.168633)


   

{3,4,5-trihydroxy-6-[(2-methyl-4-oxopyran-3-yl)oxy]oxan-2-yl}methyl acetate

{3,4,5-trihydroxy-6-[(2-methyl-4-oxopyran-3-yl)oxy]oxan-2-yl}methyl acetate

C14H18O9 (330.0950778)


   

7-methoxy-2-oxochromene-8-carbaldehyde

7-methoxy-2-oxo-8-chromenecarboxaldehyde; 2-keto-7-methoxy-chromene-8-carbaldehyde; 7-methoxy-2-oxo-chromene-8-carbaldehyde

C11H8O4 (204.0422568)


{"Ingredient_id": "HBIN013311","Ingredient_name": "7-methoxy-2-oxochromene-8-carbaldehyde","Alias": "7-methoxy-2-oxo-8-chromenecarboxaldehyde; 2-keto-7-methoxy-chromene-8-carbaldehyde; 7-methoxy-2-oxo-chromene-8-carbaldehyde","Ingredient_formula": "C11H8O4","Ingredient_Smile": "NA","Ingredient_weight": "204.18","OB_score": "21.4862191","CAS_id": "6724-42-1","SymMap_id": "SMIT05635","TCMID_id": "NA","TCMSP_id": "MOL003586","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}

   

3-{[(2s,3r,4s,5s,6r)-4,5-dihydroxy-3-{[(3r)-3-hydroxy-2-methyl-4-({7-oxofuro[3,2-g]chromen-4-yl}oxy)butan-2-yl]oxy}-6-(hydroxymethyl)oxan-2-yl]oxy}-2-methylpyran-4-one

3-{[(2s,3r,4s,5s,6r)-4,5-dihydroxy-3-{[(3r)-3-hydroxy-2-methyl-4-({7-oxofuro[3,2-g]chromen-4-yl}oxy)butan-2-yl]oxy}-6-(hydroxymethyl)oxan-2-yl]oxy}-2-methylpyran-4-one

C28H30O13 (574.168633)


   

3-{[(2s,3r,4s,5s,6r)-4,5-dihydroxy-3-{[3-hydroxy-2-methyl-4-({7-oxofuro[3,2-g]chromen-9-yl}oxy)butan-2-yl]oxy}-6-(hydroxymethyl)oxan-2-yl]oxy}-2-methylpyran-4-one

3-{[(2s,3r,4s,5s,6r)-4,5-dihydroxy-3-{[3-hydroxy-2-methyl-4-({7-oxofuro[3,2-g]chromen-9-yl}oxy)butan-2-yl]oxy}-6-(hydroxymethyl)oxan-2-yl]oxy}-2-methylpyran-4-one

C28H30O13 (574.168633)


   

2,4,4-trimethyl-5-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)cyclohexa-2,5-dien-1-one

2,4,4-trimethyl-5-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)cyclohexa-2,5-dien-1-one

C16H24O7 (328.1521954)


   

3-[(4,5-dihydroxy-3-{[3-hydroxy-2-methyl-4-({6-oxofuro[2,3-g]chromen-9-yl}oxy)butan-2-yl]oxy}-6-(hydroxymethyl)oxan-2-yl)oxy]-2-methylpyran-4-one

3-[(4,5-dihydroxy-3-{[3-hydroxy-2-methyl-4-({6-oxofuro[2,3-g]chromen-9-yl}oxy)butan-2-yl]oxy}-6-(hydroxymethyl)oxan-2-yl)oxy]-2-methylpyran-4-one

C28H30O13 (574.168633)


   

9-(2-hydroxy-3-methyl-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butoxy)furo[3,2-g]chromen-7-one

9-(2-hydroxy-3-methyl-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butoxy)furo[3,2-g]chromen-7-one

C22H26O11 (466.14750460000005)


   

3-{[(2s,3r,4s,5s,6r)-4,5-dihydroxy-3-{[(2s)-3-hydroxy-3-methyl-1-({7-oxofuro[3,2-g]chromen-4-yl}oxy)butan-2-yl]oxy}-6-(hydroxymethyl)oxan-2-yl]oxy}-2-methylpyran-4-one

3-{[(2s,3r,4s,5s,6r)-4,5-dihydroxy-3-{[(2s)-3-hydroxy-3-methyl-1-({7-oxofuro[3,2-g]chromen-4-yl}oxy)butan-2-yl]oxy}-6-(hydroxymethyl)oxan-2-yl]oxy}-2-methylpyran-4-one

C28H30O13 (574.168633)


   

2-{7-oxo-2h,3h-furo[3,2-g]chromen-2-yl}propyl 3-methylbut-2-enoate

2-{7-oxo-2h,3h-furo[3,2-g]chromen-2-yl}propyl 3-methylbut-2-enoate

C19H20O5 (328.13106700000003)


   

9-(2-hydroxy-3-methoxy-3-methylbutoxy)furo[3,2-g]chromen-7-one

9-(2-hydroxy-3-methoxy-3-methylbutoxy)furo[3,2-g]chromen-7-one

C17H18O6 (318.11033280000004)


   

2-(hydroxymethyl)-6-[(2,3,4-trimethylphenyl)methoxy]oxane-3,4,5-triol

2-(hydroxymethyl)-6-[(2,3,4-trimethylphenyl)methoxy]oxane-3,4,5-triol

C16H24O6 (312.1572804)


   

2,4,4-trimethyl-5-({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)cyclohexa-2,5-dien-1-one

2,4,4-trimethyl-5-({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)cyclohexa-2,5-dien-1-one

C16H24O7 (328.1521954)


   

9-{[(2r)-2-hydroxy-3-methylbut-3-en-1-yl]oxy}furo[3,2-g]chromen-7-one

9-{[(2r)-2-hydroxy-3-methylbut-3-en-1-yl]oxy}furo[3,2-g]chromen-7-one

C16H14O5 (286.0841194)


   

3-{[(2s,3r,4s,5s,6r)-4,5-dihydroxy-3-{[(3r)-3-hydroxy-2-methyl-4-({6-oxofuro[2,3-g]chromen-4-yl}oxy)butan-2-yl]oxy}-6-(hydroxymethyl)oxan-2-yl]oxy}-2-methylpyran-4-one

3-{[(2s,3r,4s,5s,6r)-4,5-dihydroxy-3-{[(3r)-3-hydroxy-2-methyl-4-({6-oxofuro[2,3-g]chromen-4-yl}oxy)butan-2-yl]oxy}-6-(hydroxymethyl)oxan-2-yl]oxy}-2-methylpyran-4-one

C28H30O13 (574.168633)


   

3-{[(2s,3r,4s,5s,6r)-4,5-dihydroxy-3-{[3-hydroxy-2-methyl-4-({7-oxofuro[3,2-g]chromen-4-yl}oxy)butan-2-yl]oxy}-6-(hydroxymethyl)oxan-2-yl]oxy}-2-methylpyran-4-one

3-{[(2s,3r,4s,5s,6r)-4,5-dihydroxy-3-{[3-hydroxy-2-methyl-4-({7-oxofuro[3,2-g]chromen-4-yl}oxy)butan-2-yl]oxy}-6-(hydroxymethyl)oxan-2-yl]oxy}-2-methylpyran-4-one

C28H30O13 (574.168633)


   

8-(prop-1-en-2-yl)-8h,9h-furo[2,3-h]chromen-2-one

8-(prop-1-en-2-yl)-8h,9h-furo[2,3-h]chromen-2-one

C14H12O3 (228.0786402)


   

9-{[(2s)-2-hydroxy-3-methylbut-3-en-1-yl]oxy}furo[3,2-g]chromen-7-one

9-{[(2s)-2-hydroxy-3-methylbut-3-en-1-yl]oxy}furo[3,2-g]chromen-7-one

C16H14O5 (286.0841194)


   

3-{[(2s,3r,4s,5s,6r)-4,5-dihydroxy-3-{[(2r)-3-hydroxy-3-methyl-1-({7-oxofuro[3,2-g]chromen-4-yl}oxy)butan-2-yl]oxy}-6-(hydroxymethyl)oxan-2-yl]oxy}-2-methylpyran-4-one

3-{[(2s,3r,4s,5s,6r)-4,5-dihydroxy-3-{[(2r)-3-hydroxy-3-methyl-1-({7-oxofuro[3,2-g]chromen-4-yl}oxy)butan-2-yl]oxy}-6-(hydroxymethyl)oxan-2-yl]oxy}-2-methylpyran-4-one

C28H30O13 (574.168633)


   

4-(2-hydroxy-3-methoxy-3-methylbutoxy)furo[3,2-g]chromen-7-one

4-(2-hydroxy-3-methoxy-3-methylbutoxy)furo[3,2-g]chromen-7-one

C17H18O6 (318.11033280000004)


   

6-(2,3-dihydroxy-3-methylbutyl)-7-methoxychromen-2-one

6-(2,3-dihydroxy-3-methylbutyl)-7-methoxychromen-2-one

C15H18O5 (278.1154178)


   

7-{[(2e,6e)-8-hydroxy-3,7-dimethylocta-2,6-dien-1-yl]oxy}chromen-2-one

7-{[(2e,6e)-8-hydroxy-3,7-dimethylocta-2,6-dien-1-yl]oxy}chromen-2-one

C19H22O4 (314.1518012)


   

6-[(2r)-2-hydroxy-3-methylbut-3-en-1-yl]-7-methoxychromen-2-one

6-[(2r)-2-hydroxy-3-methylbut-3-en-1-yl]-7-methoxychromen-2-one

C15H16O4 (260.1048536)


   

(2s)-3-hydroxy-3-methyl-1-({7-oxofuro[3,2-g]chromen-4-yl}oxy)butan-2-yl acetate

(2s)-3-hydroxy-3-methyl-1-({7-oxofuro[3,2-g]chromen-4-yl}oxy)butan-2-yl acetate

C18H18O7 (346.10524780000003)


   

9-[(2r)-2-hydroxy-3-methyl-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butoxy]furo[3,2-g]chromen-7-one

9-[(2r)-2-hydroxy-3-methyl-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butoxy]furo[3,2-g]chromen-7-one

C22H26O11 (466.14750460000005)


   

2,4,4-trimethyl-5-({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)cyclohex-2-en-1-one

2,4,4-trimethyl-5-({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)cyclohex-2-en-1-one

C16H26O7 (330.16784459999997)


   

2-{[1-(5-ethyl-6-methylheptan-2-yl)-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

2-{[1-(5-ethyl-6-methylheptan-2-yl)-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

C35H60O6 (576.4389659999999)


   

(8r)-8-(prop-1-en-2-yl)-8h,9h-furo[2,3-h]chromen-2-one

(8r)-8-(prop-1-en-2-yl)-8h,9h-furo[2,3-h]chromen-2-one

C14H12O3 (228.0786402)


   

(1ar,4ar,7s,7as,7br)-1,1,7-trimethyl-4-methylidene-octahydrocyclopropa[e]azulen-7-ol

(1ar,4ar,7s,7as,7br)-1,1,7-trimethyl-4-methylidene-octahydrocyclopropa[e]azulen-7-ol

C15H24O (220.18270539999997)


   

3-{[(2s,3r,4s,5s,6r)-4,5-dihydroxy-3-{[(3s)-3-hydroxy-2-methyl-4-({7-oxofuro[3,2-g]chromen-4-yl}oxy)butan-2-yl]oxy}-6-(hydroxymethyl)oxan-2-yl]oxy}-2-methylpyran-4-one

3-{[(2s,3r,4s,5s,6r)-4,5-dihydroxy-3-{[(3s)-3-hydroxy-2-methyl-4-({7-oxofuro[3,2-g]chromen-4-yl}oxy)butan-2-yl]oxy}-6-(hydroxymethyl)oxan-2-yl]oxy}-2-methylpyran-4-one

C28H30O13 (574.168633)


   

9-[(2-hydroxy-3-methylbut-3-en-1-yl)oxy]furo[3,2-g]chromen-7-one

9-[(2-hydroxy-3-methylbut-3-en-1-yl)oxy]furo[3,2-g]chromen-7-one

C16H14O5 (286.0841194)


   

6-(2-hydroxy-3-methylbut-3-en-1-yl)-7-methoxychromen-2-one

6-(2-hydroxy-3-methylbut-3-en-1-yl)-7-methoxychromen-2-one

C15H16O4 (260.1048536)


   

9-[(2r)-3-hydroxy-2-{[(3r)-3-hydroxy-2-methyl-4-({7-oxofuro[3,2-g]chromen-9-yl}oxy)butan-2-yl]oxy}-3-methylbutoxy]furo[3,2-g]chromen-7-one

9-[(2r)-3-hydroxy-2-{[(3r)-3-hydroxy-2-methyl-4-({7-oxofuro[3,2-g]chromen-9-yl}oxy)butan-2-yl]oxy}-3-methylbutoxy]furo[3,2-g]chromen-7-one

C32H30O11 (590.178803)


   

4-(2-hydroxy-3-methyl-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butoxy)furo[3,2-g]chromen-7-one

4-(2-hydroxy-3-methyl-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butoxy)furo[3,2-g]chromen-7-one

C22H26O11 (466.14750460000005)


   

9-(3-hydroxy-2-{[3-hydroxy-2-methyl-4-({7-oxofuro[3,2-g]chromen-9-yl}oxy)butan-2-yl]oxy}-3-methylbutoxy)furo[3,2-g]chromen-7-one

9-(3-hydroxy-2-{[3-hydroxy-2-methyl-4-({7-oxofuro[3,2-g]chromen-9-yl}oxy)butan-2-yl]oxy}-3-methylbutoxy)furo[3,2-g]chromen-7-one

C32H30O11 (590.178803)


   

3-[(4,5-dihydroxy-3-{[3-hydroxy-3-methyl-1-({7-oxofuro[3,2-g]chromen-4-yl}oxy)butan-2-yl]oxy}-6-(hydroxymethyl)oxan-2-yl)oxy]-2-methylpyran-4-one

3-[(4,5-dihydroxy-3-{[3-hydroxy-3-methyl-1-({7-oxofuro[3,2-g]chromen-4-yl}oxy)butan-2-yl]oxy}-6-(hydroxymethyl)oxan-2-yl)oxy]-2-methylpyran-4-one

C28H30O13 (574.168633)


   

8-[(2s)-2-hydroxy-3-methylbut-3-en-1-yl]-7-methoxychromen-2-one

8-[(2s)-2-hydroxy-3-methylbut-3-en-1-yl]-7-methoxychromen-2-one

C15H16O4 (260.1048536)


   

3-hydroxy-3-methyl-1-({7-oxofuro[3,2-g]chromen-4-yl}oxy)butan-2-yl acetate

3-hydroxy-3-methyl-1-({7-oxofuro[3,2-g]chromen-4-yl}oxy)butan-2-yl acetate

C18H18O7 (346.10524780000003)


   

6-[(3,3-dimethyloxiran-2-yl)(hydroxy)methyl]-7-methoxychromen-2-one

6-[(3,3-dimethyloxiran-2-yl)(hydroxy)methyl]-7-methoxychromen-2-one

C15H16O5 (276.0997686)


   

[(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-[(2-methyl-4-oxopyran-3-yl)oxy]oxan-2-yl]methyl acetate

[(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-[(2-methyl-4-oxopyran-3-yl)oxy]oxan-2-yl]methyl acetate

C14H18O9 (330.0950778)


   

9-[(2r)-2-hydroxy-3-methoxy-3-methylbutoxy]furo[3,2-g]chromen-7-one

9-[(2r)-2-hydroxy-3-methoxy-3-methylbutoxy]furo[3,2-g]chromen-7-one

C17H18O6 (318.11033280000004)


   

(1as,4as,7s,7ar,7bs)-1,1,7-trimethyl-4-methylidene-octahydrocyclopropa[e]azulen-7-ol

(1as,4as,7s,7ar,7bs)-1,1,7-trimethyl-4-methylidene-octahydrocyclopropa[e]azulen-7-ol

C15H24O (220.18270539999997)


   

4-[(2r)-2-hydroxy-3-methyl-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butoxy]furo[3,2-g]chromen-7-one

4-[(2r)-2-hydroxy-3-methyl-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butoxy]furo[3,2-g]chromen-7-one

C22H26O11 (466.14750460000005)


   

(2r,3s,4s,5r,6r)-2-(hydroxymethyl)-6-isopropoxyoxane-3,4,5-triol

(2r,3s,4s,5r,6r)-2-(hydroxymethyl)-6-isopropoxyoxane-3,4,5-triol

C9H18O6 (222.1103328)


   

3-{[(2s,3r,4s,5s,6r)-4,5-dihydroxy-3-{[(3r)-3-hydroxy-2-methyl-4-({6-oxofuro[2,3-g]chromen-9-yl}oxy)butan-2-yl]oxy}-6-(hydroxymethyl)oxan-2-yl]oxy}-2-methylpyran-4-one

3-{[(2s,3r,4s,5s,6r)-4,5-dihydroxy-3-{[(3r)-3-hydroxy-2-methyl-4-({6-oxofuro[2,3-g]chromen-9-yl}oxy)butan-2-yl]oxy}-6-(hydroxymethyl)oxan-2-yl]oxy}-2-methylpyran-4-one

C28H30O13 (574.168633)


   

3-{[(2s,3r,4s,5s,6r)-4,5-dihydroxy-3-{[3-hydroxy-3-methyl-1-({7-oxofuro[3,2-g]chromen-4-yl}oxy)butan-2-yl]oxy}-6-(hydroxymethyl)oxan-2-yl]oxy}-2-methylpyran-4-one

3-{[(2s,3r,4s,5s,6r)-4,5-dihydroxy-3-{[3-hydroxy-3-methyl-1-({7-oxofuro[3,2-g]chromen-4-yl}oxy)butan-2-yl]oxy}-6-(hydroxymethyl)oxan-2-yl]oxy}-2-methylpyran-4-one

C28H30O13 (574.168633)