Exact Mass: 442.1376092
Exact Mass Matches: 442.1376092
Found 500 metabolites which its exact mass value is equals to given mass value 442.1376092,
within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error
0.01 dalton.
Lusitanicoside
Isolated from cherries (Prunus lusitanica). Lusitanicoside is found in sweet marjoram and fruits. Lusitanicoside is found in fruits. Lusitanicoside is isolated from cherries (Prunus lusitanica).
Cortisol 21-sulfate
Cortisol 21-sulfate is also known as Cortisol-21-sulfuric acid or 4-Pregnen-11,17,21-triol-3,20-dione 21-sulfate. Cortisol 21-sulfate is considered to be practically insoluble (in water) and acidic. Cortisol 21-sulfate is a steroid conjugate lipid molecule D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones
12-Dehydrotetracycline
The 12-dehydro derivative of tetracycline.
Methacycline
Methacycline is only found in individuals that have used or taken this drug. It is a broad-spectrum semisynthetic antibiotic related to tetracycline but excreted more slowly and maintaining effective blood levels for a more extended period. [PubChem]Methacycline, a tetracycline antibiotic, is a protein synthesis inhibitors, inhibiting the binding of aminoacyl-tRNA to the mRNA-ribosome complex. Methacycline inhibits cell growth by inhibiting translation. It binds to the 16S part of the 30S ribosomal subunit and prevents the amino-acyl tRNA from binding to the A site of the ribosome. The binding is reversible in nature. Tetracyclines also have been found to inhibit matrix metalloproteinases. This mechanism does not add to their antibiotic effects, but has led to extensive research on chemically modified tetracyclines or CMTs (like incyclinide) for the treatmet of rosacea, acne, and various types of neoplasms. J - Antiinfectives for systemic use > J01 - Antibacterials for systemic use > J01A - Tetracyclines > J01AA - Tetracyclines C784 - Protein Synthesis Inhibitor > C1595 - Tetracycline Antibiotic D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents C254 - Anti-Infective Agent > C258 - Antibiotic
Eltrombopag
B - Blood and blood forming organs > B02 - Antihemorrhagics > B02B - Vitamin k and other hemostatics COVID info from clinicaltrial, clinicaltrials, clinical trial, clinical trials C78275 - Agent Affecting Blood or Body Fluid Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS
(-)-Epicatechin 3-O-gallate
(-)-epicatechin-3-O-gallate is a gallate ester obtained by formal condensation of the carboxy group of gallic acid with the (3R)-hydroxy group of epicatechin. A natural product found in Parapiptadenia rigida. It has a role as a metabolite, an EC 3.2.1.1 (alpha-amylase) inhibitor and an EC 3.2.1.20 (alpha-glucosidase) inhibitor. It is a catechin, a gallate ester and a polyphenol. It is functionally related to a (-)-epicatechin and a gallic acid. (-)-Epicatechin gallate is a natural product found in Scurrula atropurpurea, Acacia omalophylla, and other organisms with data available. Isolated from tea and numerous other plant subspecies inc. rhubarb and grapes. Epicatechin 3-gallate is found in many foods, some of which are cucumber, muskmelon, black raspberry, and cashew nut. A gallate ester obtained by formal condensation of the carboxy group of gallic acid with the (3R)-hydroxy group of epicatechin. A natural product found in Parapiptadenia rigida. (-)-Epicatechin 3-O-gallate is found in almond. (-)-Epicatechin 3-O-gallate is isolated from tea and numerous other plant species including rhubarb and grapes. D004791 - Enzyme Inhibitors > D011480 - Protease Inhibitors D020011 - Protective Agents > D000975 - Antioxidants D000970 - Antineoplastic Agents (-)-Epicatechin gallate (Epicatechin gallate) inhibits cyclooxygenase-1 (COX-1) with an IC50 of 7.5 μM. (-)-Epicatechin gallate (Epicatechin gallate) inhibits cyclooxygenase-1 (COX-1) with an IC50 of 7.5 μM. (-)-Epicatechin gallate (Epicatechin gallate) inhibits cyclooxygenase-1 (COX-1) with an IC50 of 7.5 μM. (-)-Epicatechin gallate (Epicatechin gallate) inhibits cyclooxygenase-1 (COX-1) with an IC50 of 7.5 μM.
(-)-Catechin 3-O-gallate
(-)-catechin-3-O-gallate is a gallate ester obtained by formal condensation of the carboxy group of gallic acid with the (3R)-hydroxy group of (-)-catechin. It has a role as a metabolite. It is a gallate ester, a polyphenol and a member of flavans. It is functionally related to a (-)-catechin and a gallic acid. It is an enantiomer of a (+)-catechin-3-O-gallate. (-)-Catechin gallate is a natural product found in Rheum palmatum, Vitis vinifera, and other organisms with data available. A gallate ester obtained by formal condensation of the carboxy group of gallic acid with the (3R)-hydroxy group of (-)-catechin. (-)-Catechin 3-O-gallate is a polyphenol compound found in foods of plant origin (PMID: 20428313) (-)-Catechin gallate is a minor constituent in green tea catechins. (-)-Catechin gallate inhibits the activity of COX-1 and COX-2 enzymes. (-)-Catechin gallate is a minor constituent in green tea catechins. (-)-Catechin gallate inhibits the activity of COX-1 and COX-2 enzymes. (-)-Catechin gallate is a minor constituent in green tea catechins. (-)-Catechin gallate inhibits the activity of COX-1 and COX-2 enzymes. (-)-Catechin gallate is a minor constituent in green tea catechins. (-)-Catechin gallate inhibits the activity of COX-1 and COX-2 enzymes.
7-Galloylcatechin
7-Galloylcatechin is found in herbs and spices. 7-Galloylcatechin is isolated from roots of great burnet (Sanguisorba officinalis). Isolated from roots of great burnet (Sanguisorba officinalis). Catechin 7-gallate is found in tea and herbs and spices.
1-O-E-Cinnamoyl-(6-arabinosylglucose)
C20H26O11 (442.14750460000005)
1-O-E-Cinnamoyl-(6-arabinosylglucose) is found in fruits. 1-O-E-Cinnamoyl-(6-arabinosylglucose) is a constituent of Psidium guajava (guava)
[2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-3,4-dihydro-2H-chromen-5-yl] 3,4,5-trihydroxybenzoate
3-Galloylcatechin
Constituent of Bergenia crassifolia (Siberian tea). Catechin 3-gallate is found in many foods, some of which are macadamia nut (m. tetraphylla), tea, avocado, and pecan nut. 3-Galloylcatechin is found in almond. 3-Galloylcatechin is a constituent of Bergenia crassifolia (Siberian tea) (-)-Epicatechin gallate (Epicatechin gallate) inhibits cyclooxygenase-1 (COX-1) with an IC50 of 7.5 μM. (-)-Epicatechin gallate (Epicatechin gallate) inhibits cyclooxygenase-1 (COX-1) with an IC50 of 7.5 μM. (-)-Epicatechin gallate (Epicatechin gallate) inhibits cyclooxygenase-1 (COX-1) with an IC50 of 7.5 μM. (-)-Epicatechin gallate (Epicatechin gallate) inhibits cyclooxygenase-1 (COX-1) with an IC50 of 7.5 μM.
beta-D-Xylopyranosyl-(1->4)-alpha-L-rhamnopyranosyl-(1->2)-D-fucose
beta-D-Xylopyranosyl-(1->4)-alpha-L-rhamnopyranosyl-(1->2)-D-fucose is a constituent of desacylsaponins from the bark of Quillaja saponaria (soapbark tree). Constituent of desacylsaponins from the bark of Quillaja saponaria (soap-bark tree)
Epicatechin-3-gallate
3-[(2R)-2-Hydroxy-3-methyl-3-[(phosphonooxy)methyl]butanamido]propanoylcarnitine
C16H31N2O10P (442.17162360000003)
3-[(2R)-2-Hydroxy-3-methyl-3-[(phosphonooxy)methyl]butanamido]propanoylcarnitine is an acylcarnitine. More specifically, it is an 3-[(2R)-2-hydroxy-3-methyl-3-[(phosphonooxy)methyl]butanamido]propanoic acid ester of carnitine. Acylcarnitines were first discovered more than 70 year ago (PMID: 13825279). It is believed that there are more than 1000 types of acylcarnitines in the human body. The general role of acylcarnitines is to transport acyl-groups (organic acids and fatty acids) from the cytoplasm into the mitochondria so that they can be broken down to produce energy. This process is known as beta-oxidation. According to a recent review [Dambrova et al. 2021, Physiological Reviews], acylcarnitines (ACs) can be classified into 9 different categories depending on the type and size of their acyl-group: 1) short-chain ACs; 2) medium-chain ACs; 3) long-chain ACs; 4) very long-chain ACs; 5) hydroxy ACs; 6) branched chain ACs; 7) unsaturated ACs; 8) dicarboxylic ACs and 9) miscellaneous ACs. Short-chain ACs have acyl-groups with two to five carbons (C2-C5), medium-chain ACs have acyl-groups with six to thirteen carbons (C6-C13), long-chain ACs have acyl-groups with fourteen to twenty once carbons (C14-C21) and very long-chain ACs have acyl groups with more than 22 carbons. 3-[(2R)-2-Hydroxy-3-methyl-3-[(phosphonooxy)methyl]butanamido]propanoylcarnitine is therefore classified as a medium chain AC. As a medium-chain acylcarnitine 3-[(2R)-2-Hydroxy-3-methyl-3-[(phosphonooxy)methyl]butanamido]propanoylcarnitine is somewhat less abundant than short-chain acylcarnitines. These are formed either through esterification with L-carnitine or through the peroxisomal metabolism of longer chain acylcarnitines (PMID: 30540494). Many medium-chain acylcarnitines can serve as useful markers for inherited disorders of fatty acid metabolism. Carnitine octanoyltransferase (CrOT, EC:2.3.1.137) is responsible for the synthesis of all medium-chain (MCAC, C5-C12) and medium-length branched-chain acylcarnitines in peroxisomes (PMID: 10486279). The study of acylcarnitines is an active area of research and it is likely that many novel acylcarnitines will be discovered in the coming years. It is also likely that many novel roles in health and disease will be uncovered. An excellent review of the current state of knowledge for acylcarnitines is available at [Dambrova et al. 2021, Physiological Reviews].
Eltrombopag
B - Blood and blood forming organs > B02 - Antihemorrhagics > B02B - Vitamin k and other hemostatics COVID info from clinicaltrial, clinicaltrials, clinical trial, clinical trials C78275 - Agent Affecting Blood or Body Fluid Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS
Hydrocortisone phosphate
Indanthrene
Rondomycin
Piflufolastat F 18
C18H23FN4O8 (442.14998499999996)
Villol
Antibiotic RP 1551-3
C25H27ClO5 (442.15469220000006)
Pratensin A
Epicatechin-3-gallate
(-)-Epicatechin gallate (Epicatechin gallate) inhibits cyclooxygenase-1 (COX-1) with an IC50 of 7.5 μM. (-)-Epicatechin gallate (Epicatechin gallate) inhibits cyclooxygenase-1 (COX-1) with an IC50 of 7.5 μM. (-)-Epicatechin gallate (Epicatechin gallate) inhibits cyclooxygenase-1 (COX-1) with an IC50 of 7.5 μM. (-)-Epicatechin gallate (Epicatechin gallate) inhibits cyclooxygenase-1 (COX-1) with an IC50 of 7.5 μM.
(-)-Catechin gallate
(-)-Catechin gallate is a minor constituent in green tea catechins. (-)-Catechin gallate inhibits the activity of COX-1 and COX-2 enzymes. (-)-Catechin gallate is a minor constituent in green tea catechins. (-)-Catechin gallate inhibits the activity of COX-1 and COX-2 enzymes. (-)-Catechin gallate is a minor constituent in green tea catechins. (-)-Catechin gallate inhibits the activity of COX-1 and COX-2 enzymes. (-)-Catechin gallate is a minor constituent in green tea catechins. (-)-Catechin gallate inhibits the activity of COX-1 and COX-2 enzymes.
Regaloside B
C20H26O11 (442.14750460000005)
Regaloside B is a natural product found in Lilium auratum and Lilium brownii with data available. Regaloside B is a phenylpropanoid isolated from Lilium longiflorum. Regaloside B can inhibit the expression of iNOS and COX-2. Regaloside B has anti-inflammatory activity[1][2]. Regaloside B is a phenylpropanoid isolated from Lilium longiflorum. Regaloside B can inhibit the expression of iNOS and COX-2. Regaloside B has anti-inflammatory activity[1][2].
16,19-Secostrychnidine-10,16-dione, 21,22-epoxy-21,22-dihydro-4,14-dihydroxy-3-methoxy-19-methyl-, (21.alpha.,22.alpha.)-
N-L-gamma-glutamyl-S-sinapyl-L-cysteine
C19H26N2O8S (442.14097960000004)
15-O-??-D-Glucopyranosyl-11??,13-dihydrourospermal A
(+)-Catechin 4-O-gallate|4-O-(3,4,5-Trihydroxybenzoyl)-(2R,3S)-3,3,4,5,7-Pentahydroxyflavan
(1S,3R,5S,6S,8S,9S,10R,13R)-1-acetoxy-3-bromo-6-hydroxy-8,13-epoxylabd-14-ene
C22H35BrO4 (442.17185700000005)
8a-[4-(alpha-rhamnopyranosyl)-2-oxo-2,5-dihydro-furan-3-ylmethyl]-6-methyl-tetrahydro-furo[3,4-c]oxepine-1,8-dione
C20H26O11 (442.14750460000005)
(8Z)-decaene-4,6-diyn-1-O-beta-D-apiofuranosyl-(1->6)-beta-D-glucopyranoside
2,2-diamino-4,4-dioxo-4,4-(2-amino-3-oxo-3H-phenoxazine-1,9-diyl)-bis-butyric acid
C20H18N4O8 (442.11245879999996)
(+)-phrymarin II|1-acetoxy-2e-piperonyl-6e-[6-methoxypiperonyl]-3,7-dioxabicyclo[3.3.0]octane
(-)-sanguinolignan C|(8S,7S,8R)-7-acetoxy-3,4-methylenedioxy-3,4-dimethoxy-7-oxolignano-9,9-lactone
beta-D-glucopyranosyl phaseate|[1R-[1alpha,5alpha,8S*(2Z,4E)]]-1-O-[5-(8-hydroxy-1,5-dimethyl-3-oxo-6-oxabicyclo[3.2.1]oct-8-yl)-3-methyl-2,4-pentadienoyl]-beta-D-glucopyranose
2,3-Dimethoxy-14,15-dihydroxy-16,16-dimethyl-9,10-(epoxypropano)-5,11,13-trioxa-5H-benzo[4,5]cyclohepta[1,2-b]naphthalene-6(12H)-one
7,8-dihydroxy-6-[3-beta-D-glucopyranosyloxy-2(zeta)-hydroxy-3-methylbutyl]coumarin|skimminan
C20H26O11 (442.14750460000005)
3beta,4alpha-dihydroxy-4-beta-(chloromethyl)-8alpha-(4-hydroxymethacrylate)-11beta,13-dihydro-13-isopropyl-1alphaH,5alphaH,6betaH,7alphaH-guai-10(14)-en-6,12-olide|Diain
Dienestrol glucuronide|O1-[alpha,alpha-Di-((E)-aethyliden)-4-hydroxy-bibenzyl-4-yl]-beta-D-glucopyranuronsaeure|O1-[alpha,alpha-di-((E)-ethylidene)-4-hydroxy-bibenzyl-4-yl]-beta-D-glucopyranuronic acid
8-(4-Hydroxyphenylactyl),Me ester-6,8,15-Trihydroxy-2-oxo-1(10),3,11(13)-guaiatrien-12-oic acid|Methyl 2-oxo-6alpha,15-dihydroxy-8alpha-(p-hydroxyphenylacetoxy)-guaia-1(10),3,11-trien-5alphaH-12-oate
Glaberide I 4-O-beta-D-glucopyranoside
C20H26O11 (442.14750460000005)
(-)-(1R*,2S*,3S*,4S*,5R*,6R*)-2-O-acetyl-4-O-benzoyl-1-benzoyloxymethyl-1,6-epoxycyclohexan-2,3,4,5-tetrol|2-acetylrotepoxide B
7-O-Galloyltricetiflavan
A gallate ester obtained by the formal condensation of gallic acid with the hydroxy group at position 7 of 3,4,5,5,7-pentahydroxyflavan. Isolated from the leaves of Pithecellobium clypearia, it exhibits antiviral activity.
2R,3R-13-hydroxypterosin L 3-O-beta-D-glucopyranoside
4-((6-O-caffeoyl-beta-D-glucopyranosyl)oxy)-2-methylbutyric acid
C20H26O11 (442.14750460000005)
2-(3,4-Dimethoxyphenyl)-3,5-dimethoxy-7-(2-hydroxy-3-methyl-3-butenyloxy)-4H-1-benzopyran-4-one
BENZYL 2,3-DI-O-ACETYL-4,6-O-BENZYLIDEN-|A-D-GLUCOPYRANOSIDE
2-acetyl-3-[(E)-caffeoyl]-1-[(E)-p-coumaroyl]glycerol|Lasiocarpin B
Mulberrofuran H
Mulberrofuran H is a natural product found in Morus lhou, Morus mongolica, and Morus alba with data available.
3,4,17-trihydroxy-6,7-didehydro-aspidofractinine-1,3-dicarboxylic acid dimethyl ester|ent-(2S)-3alpha,4xi,17-Trihydroxy-6,7-didehydro-aspidofractinin-1,3beta-dicarbonsaeure-dimethylester|ent-(2S)-3alpha,4xi,17-trihydroxy-6,7-didehydro-aspidofractinine-1,3beta-dicarboxylic acid dimethyl ester|Kopsaporin
13beta,21-Dihydroxyeurycomanone|pasakbumin-D
C20H26O11 (442.14750460000005)
O-alpha-L-rhamnopyranosyl-(1-2)-O-alpha-L-rhamnopyranosyl-(1-5)-L-arabinose
5-O-trans-cinnamoyl beta-D-apiosyl(1->3)-alpha-D-glucopyranoside|visartiside D
C20H26O11 (442.14750460000005)
2-amino-5-[[1-(carboxymethylamino)-3-[(4-nitrophenyl)methylsulfanyl]-1-oxopropan-2-yl]amino]-5-oxopentanoic acid
RubioncolinC
Rubioncolin C is a natural product found in Rubia oncotricha with data available.
Rubipodanone A
Rubipodanone A, a naphthohydroquinone dimer, shows cytotoxicity against A549, BEL-7402, HeLa, HepG2, SGC-7901 and U251 cells. Rubipodanone A also shows obvious activating effect at 20 and 40 μM for NF-κB[1].
Yadanziolide B
C20H26O11 (442.14750460000005)
Yadanziolide B is a quassinoid that is 13,20-epoxypicras-3-ene substituted by hydroxy groups at positions 1, 6, 11, 12, 14, 15 and 21 and oxo groups at positions 2 and 16. Isolated from the ethanol extract of the stem of Brucea mollis, it exhibits cytotoxic activity. It has a role as an antineoplastic agent and a plant metabolite. It is a quassinoid, a delta-lactone, an enone, an organic heteropentacyclic compound, a heptol and a secondary alpha-hydroxy ketone. It derives from a hydride of a picrasane. Yadanziolide B is a natural product found in Brucea javanica and Brucea mollis with data available. A quassinoid that is 13,20-epoxypicras-3-ene substituted by hydroxy groups at positions 1, 6, 11, 12, 14, 15 and 21 and oxo groups at positions 2 and 16. Isolated from the ethanol extract of the stem of Brucea mollis, it exhibits cytotoxic activity.
Pasakbumin D
C20H26O11 (442.14750460000005)
Pasakbumin D is a natural product found in Eurycoma longifolia with data available.
catechin gallate
(-)-Catechin gallate is a minor constituent in green tea catechins. (-)-Catechin gallate inhibits the activity of COX-1 and COX-2 enzymes. (-)-Catechin gallate is a minor constituent in green tea catechins. (-)-Catechin gallate inhibits the activity of COX-1 and COX-2 enzymes. (-)-Catechin gallate is a minor constituent in green tea catechins. (-)-Catechin gallate inhibits the activity of COX-1 and COX-2 enzymes. (-)-Catechin gallate is a minor constituent in green tea catechins. (-)-Catechin gallate inhibits the activity of COX-1 and COX-2 enzymes.
[(2R,3R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl] 3,4,5-trihydroxybenzoate
[(2S,3R)-2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-3,4-dihydro-2H-chromen-7-yl] 3,4,5-trihydroxybenzoate
C24H26O8_Spiro[furo[4,3,2-ij]pyrano[4,3:4,5]cyclohepta[1,2-f][2]benzopyran-7(9H),2-oxirane]-1,5,9,13(2H,3aH,11H)-tetrone, 5a,6,6a,13a,13b,13c-hexahydro-2,5a,11,11,13a-pentamethyl
C21H30O10_(2E,4E)-5-{6-[(beta-D-Glucopyranosyloxy)methyl]-1-hydroxy-2,6-dimethyl-4-oxo-2-cyclohexen-1-yl}-3-methyl-2,4-pentadienoic acid
C21H30O10_4-Allylphenyl 6-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranoside
Ala Cys Cys Phe
Ala Cys Phe Cys
Ala Cys Ser Tyr
C18H26N4O7S (442.15221260000004)
Ala Cys Tyr Ser
C18H26N4O7S (442.15221260000004)
Ala Asp His Thr
Ala Asp Thr His
Ala Glu His Ser
Ala Glu Ser His
Ala Phe Cys Cys
Ala His Asp Thr
Ala His Glu Ser
Ala His Ser Glu
Ala His Thr Asp
Ala Ser Cys Tyr
C18H26N4O7S (442.15221260000004)
Ala Ser Glu His
Ala Ser His Glu
Ala Ser Tyr Cys
C18H26N4O7S (442.15221260000004)
Ala Thr Asp His
Ala Thr His Asp
Ala Tyr Cys Ser
C18H26N4O7S (442.15221260000004)
Ala Tyr Ser Cys
C18H26N4O7S (442.15221260000004)
Cys Ala Cys Phe
Cys Ala Phe Cys
Cys Ala Ser Tyr
C18H26N4O7S (442.15221260000004)
Cys Ala Tyr Ser
C18H26N4O7S (442.15221260000004)
Cys Cys Ala Phe
Cys Cys Phe Ala
Cys Cys Met Ser
Cys Cys Ser Met
Cys Phe Ala Cys
Cys Phe Cys Ala
Cys Phe Ser Ser
C18H26N4O7S (442.15221260000004)
Cys Gly Thr Tyr
C18H26N4O7S (442.15221260000004)
Cys Gly Tyr Thr
C18H26N4O7S (442.15221260000004)
Cys His Pro Ser
C17H26N6O6S (442.16344560000005)
Cys His Ser Pro
C17H26N6O6S (442.16344560000005)
Cys Met Cys Ser
Cys Met Ser Cys
Cys Pro His Ser
C17H26N6O6S (442.16344560000005)
Cys Pro Ser His
C17H26N6O6S (442.16344560000005)
Cys Ser Ala Tyr
C18H26N4O7S (442.15221260000004)
Cys Ser Cys Met
Cys Ser Phe Ser
C18H26N4O7S (442.15221260000004)
Cys Ser His Pro
C17H26N6O6S (442.16344560000005)
Cys Ser Met Cys
Cys Ser Pro His
C17H26N6O6S (442.16344560000005)
Cys Ser Ser Phe
C18H26N4O7S (442.15221260000004)
Cys Ser Tyr Ala
C18H26N4O7S (442.15221260000004)
Cys Thr Gly Tyr
C18H26N4O7S (442.15221260000004)
Cys Thr Tyr Gly
C18H26N4O7S (442.15221260000004)
Cys Tyr Ala Ser
C18H26N4O7S (442.15221260000004)
Cys Tyr Gly Thr
C18H26N4O7S (442.15221260000004)
Cys Tyr Ser Ala
C18H26N4O7S (442.15221260000004)
Cys Tyr Thr Gly
C18H26N4O7S (442.15221260000004)
Asp Ala His Thr
Asp Ala Thr His
Asp Asp Gly His
Asp Asp His Gly
Asp Asp Pro Pro
C18H26N4O9 (442.16997060000006)
Asp Gly Asp His
Asp Gly His Asp
Asp His Ala Thr
Asp His Asp Gly
Asp His Gly Asp
Asp His Thr Ala
Asp Pro Asp Pro
C18H26N4O9 (442.16997060000006)
Asp Pro Pro Asp
C18H26N4O9 (442.16997060000006)
Asp Thr Ala His
Asp Thr His Ala
Glu Ala His Ser
Glu Ala Ser His
Glu Gly His Thr
Glu Gly Thr His
Glu His Ala Ser
Glu His Gly Thr
Glu His Ser Ala
Glu His Thr Gly
Glu Ser Ala His
Glu Ser His Ala
Glu Thr Gly His
Glu Thr His Gly
Mometasone Metabolite (Pregna-1,4-diene-3,20-dione, 9,21-dichloro-6,11,17-trihydroxy-16-methyl-, (6b
Mometasone Metabolite (Pregna-1,4-diene-3,20-dione, 9,21-dichloro-6,11,17-trihydroxy-16-methyl-, (6a
Phe Ala Cys Cys
Phe Cys Ala Cys
Phe Cys Cys Ala
Phe Cys Ser Ser
C18H26N4O7S (442.15221260000004)
Phe Ser Cys Ser
C18H26N4O7S (442.15221260000004)
Phe Ser Ser Cys
C18H26N4O7S (442.15221260000004)
Gly Cys Thr Tyr
C18H26N4O7S (442.15221260000004)
Gly Cys Tyr Thr
C18H26N4O7S (442.15221260000004)
Gly Asp Asp His
Gly Asp His Asp
Gly Glu His Thr
Gly Glu Thr His
Gly His Asp Asp
Gly His Glu Thr
Gly His Thr Glu
Gly Thr Cys Tyr
C18H26N4O7S (442.15221260000004)
Gly Thr Glu His
Gly Thr His Glu
Gly Thr Tyr Cys
C18H26N4O7S (442.15221260000004)
Gly Tyr Cys Thr
C18H26N4O7S (442.15221260000004)
Gly Tyr Thr Cys
C18H26N4O7S (442.15221260000004)
His Ala Asp Thr
His Ala Glu Ser
His Ala Ser Glu
His Ala Thr Asp
His Cys Pro Ser
C17H26N6O6S (442.16344560000005)
His Cys Ser Pro
C17H26N6O6S (442.16344560000005)
His Asp Ala Thr
His Asp Asp Gly
His Asp Gly Asp
His Asp Thr Ala
His Glu Ala Ser
His Glu Gly Thr
His Glu Ser Ala
His Glu Thr Gly
His Gly Asp Asp
His Gly Glu Thr
His Gly Thr Glu
His Pro Cys Ser
C17H26N6O6S (442.16344560000005)
His Pro Ser Cys
C17H26N6O6S (442.16344560000005)
His Ser Ala Glu
His Ser Cys Pro
C17H26N6O6S (442.16344560000005)
His Ser Glu Ala
His Ser Pro Cys
C17H26N6O6S (442.16344560000005)
His Thr Ala Asp
His Thr Asp Ala
His Thr Glu Gly
His Thr Gly Glu
Met Cys Cys Ser
Met Cys Ser Cys
Met Ser Cys Cys
Pro Cys His Ser
C17H26N6O6S (442.16344560000005)
Pro Cys Ser His
C17H26N6O6S (442.16344560000005)
Pro Asp Asp Pro
C18H26N4O9 (442.16997060000006)
Pro Asp Pro Asp
C18H26N4O9 (442.16997060000006)
Pro His Cys Ser
C17H26N6O6S (442.16344560000005)
Pro His Ser Cys
C17H26N6O6S (442.16344560000005)
Pro Pro Asp Asp
C18H26N4O9 (442.16997060000006)
Pro Ser Cys His
C17H26N6O6S (442.16344560000005)
Pro Ser His Cys
C17H26N6O6S (442.16344560000005)
Ser Ala Cys Tyr
C18H26N4O7S (442.15221260000004)
Ser Ala Glu His
Ser Ala His Glu
Ser Ala Tyr Cys
C18H26N4O7S (442.15221260000004)
Ser Cys Ala Tyr
C18H26N4O7S (442.15221260000004)
Ser Cys Cys Met
Ser Cys Phe Ser
C18H26N4O7S (442.15221260000004)
Ser Cys His Pro
C17H26N6O6S (442.16344560000005)
Ser Cys Met Cys
Ser Cys Pro His
C17H26N6O6S (442.16344560000005)
Ser Cys Ser Phe
C18H26N4O7S (442.15221260000004)
Ser Cys Tyr Ala
C18H26N4O7S (442.15221260000004)
Ser Glu Ala His
Ser Glu His Ala
Ser Phe Cys Ser
C18H26N4O7S (442.15221260000004)
Ser Phe Ser Cys
C18H26N4O7S (442.15221260000004)
Ser His Ala Glu
Ser His Cys Pro
C17H26N6O6S (442.16344560000005)
Ser His Glu Ala
Ser His Pro Cys
C17H26N6O6S (442.16344560000005)
Ser Met Cys Cys
Ser Pro Cys His
C17H26N6O6S (442.16344560000005)
Ser Pro His Cys
C17H26N6O6S (442.16344560000005)
Ser Ser Cys Phe
C18H26N4O7S (442.15221260000004)
Ser Ser Phe Cys
C18H26N4O7S (442.15221260000004)
Ser Ser Ser Tyr
C18H26N4O9 (442.16997060000006)
Ser Ser Tyr Ser
C18H26N4O9 (442.16997060000006)
Ser Tyr Ala Cys
C18H26N4O7S (442.15221260000004)
Ser Tyr Cys Ala
C18H26N4O7S (442.15221260000004)
Ser Tyr Ser Ser
C18H26N4O9 (442.16997060000006)
Thr Ala Asp His
Thr Ala His Asp
Thr Cys Gly Tyr
C18H26N4O7S (442.15221260000004)
Thr Cys Tyr Gly
C18H26N4O7S (442.15221260000004)
Thr Asp Ala His
Thr Asp His Ala
Thr Glu Gly His
Thr Glu His Gly
Thr Gly Cys Tyr
C18H26N4O7S (442.15221260000004)
Thr Gly Glu His
Thr Gly His Glu
Thr Gly Tyr Cys
C18H26N4O7S (442.15221260000004)
Thr His Ala Asp
Thr His Asp Ala
Thr His Glu Gly
Thr His Gly Glu
Thr Tyr Cys Gly
C18H26N4O7S (442.15221260000004)
Thr Tyr Gly Cys
C18H26N4O7S (442.15221260000004)
Tyr Ala Cys Ser
C18H26N4O7S (442.15221260000004)
Tyr Ala Ser Cys
C18H26N4O7S (442.15221260000004)
Tyr Cys Ala Ser
C18H26N4O7S (442.15221260000004)
Tyr Cys Gly Thr
C18H26N4O7S (442.15221260000004)
Tyr Cys Ser Ala
C18H26N4O7S (442.15221260000004)
Tyr Cys Thr Gly
C18H26N4O7S (442.15221260000004)
Tyr Gly Cys Thr
C18H26N4O7S (442.15221260000004)
Tyr Gly Thr Cys
C18H26N4O7S (442.15221260000004)
Tyr Ser Ala Cys
C18H26N4O7S (442.15221260000004)
Tyr Ser Cys Ala
C18H26N4O7S (442.15221260000004)
Tyr Ser Ser Ser
C18H26N4O9 (442.16997060000006)
Tyr Thr Cys Gly
C18H26N4O7S (442.15221260000004)
Tyr Thr Gly Cys
C18H26N4O7S (442.15221260000004)
methacycline
J - Antiinfectives for systemic use > J01 - Antibacterials for systemic use > J01A - Tetracyclines > J01AA - Tetracyclines A tetracycline that is the 6-methylene analogue of oxytetracycline, obtained by formal dehydration at position 6. C784 - Protein Synthesis Inhibitor > C1595 - Tetracycline Antibiotic D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents C254 - Anti-Infective Agent > C258 - Antibiotic
Hydrocortisone phosphate
C147908 - Hormone Therapy Agent > C548 - Therapeutic Hormone > C1636 - Therapeutic Steroid Hormone C308 - Immunotherapeutic Agent > C574 - Immunosuppressant > C211 - Therapeutic Corticosteroid D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones
1-O-E-Cinnamoyl-(6-arabinosylglucose)
C20H26O11 (442.14750460000005)
b-D-Xylopyranosyl-(1->4)-a-L-rhamnopyranosyl-(1->2)-D-fucose
ST 21:3;O5;S
D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones
dibutyl [(dipropoxyphosphinothioyl)thio]succinate
C18H35O6PS2 (442.16125800000003)
acetyl 4-[6-(4-acetyloxycarbonylphenoxy)hexoxy]benzoate
7-Amino-8-oxo-3-(cis-prop-1-enyl)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid diphenylmethyl ester hydrochloride
(1S,2S)-1,2-Bis(4-dimethylaminophenyl)-1,2-ethanediamine tetrahydrochloride
C18H30Cl4N4 (442.12244599999997)
1-Boc-4-[4-(3,4-dichlorophenoxy)piperidin-1-ylmethyl]piperidine
C22H32Cl2N2O3 (442.17898619999994)
2-benzofuran-1,3-dione,ethane-1,2-diol,furan-2,5-dione,3-(3-hydroxypropoxy)propan-1-ol
C20H26O11 (442.14750460000005)
Benzo[1,2-b:4,5-b]dithiophene, 2,6-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)
C22H28B2O4S2 (442.16150280000005)
Acepromazine maleate
C23H26N2O5S (442.15623460000006)
D002492 - Central Nervous System Depressants > D014149 - Tranquilizing Agents > D014150 - Antipsychotic Agents D002491 - Central Nervous System Agents > D011619 - Psychotropic Drugs > D014149 - Tranquilizing Agents D018377 - Neurotransmitter Agents > D015259 - Dopamine Agents > D018492 - Dopamine Antagonists D002491 - Central Nervous System Agents > D002492 - Central Nervous System Depressants C78272 - Agent Affecting Nervous System > C66883 - Dopamine Antagonist
(-)-1,1-bis((2s,4s)-2,4-diethylphosphotano)ferrocene
C24H36FeP2 (442.16415059999997)
TRIS(2,6-DIMETHOXYPHENYL)PHOSPHINE
C24H27O6P (442.15451720000004)
2,2-dimethylpropane-1,3-diol,1,3-dioxo-2-benzofuran-5-carboxylic acid,hexanedioic acid
C20H26O11 (442.14750460000005)
(s)-1-[(1r)-2-(diphenylphosphino)ferrocenyl]ethyldi-tert-butylphosphine
C24H36FeP2 (442.16415059999997)
2-[4-[(4-ethoxyphenyl)methylamino]phenyl]-1-ethylbenz[cd]indolium chloride
C28H27ClN2O (442.18118020000003)
6-chloro-3-indolyl-beta-d-glucuronide cyclohexylammonium salt
C20H27ClN2O7 (442.15067020000004)
Zuclopenthixol acetate
C24H27ClN2O2S (442.14816720000005)
D002492 - Central Nervous System Depressants > D014149 - Tranquilizing Agents > D014150 - Antipsychotic Agents D002491 - Central Nervous System Agents > D011619 - Psychotropic Drugs > D014149 - Tranquilizing Agents D002491 - Central Nervous System Agents > D002492 - Central Nervous System Depressants C78272 - Agent Affecting Nervous System > C29710 - Antipsychotic Agent
Telenzepine dihydrochloride
Telenzepine dihydrochloride is a selective and orally active muscarinic M1 receptor antagonist with a Ki of 0.94 nM. Telenzepine dihydrochloride inhibits gastric acid secretion and has antiulcer effects[1][2][3].
4-(4,6-dicyano-2-ethoxynaphthalen-1-yl)-3-ethoxynaphthalene-1,7-dicarbonitrile
C28H18N4O2 (442.14296879999995)
lithium 1-amino-9,10-dihydro-9,10-dioxo-4-[(2,4,6-trimethylphenyl)amino]anthracene-2-sulphonate
C23H19LiN2O5S (442.11746740000007)
Methyl 2-oxo-3-{[2-(5-oxo-2,5-dihydro-1,2,4-oxadiazol-3-yl)-4-biphenylyl]methyl}-2,3-dihydro-1H-benzimidazole-4-carboxylate
N-[(11bS)-4,5-Dihydro-3H-dinaphtho[2,1-c:1,2-e]azepin-2-yl]trifluoromethanesulfonamide
(3aR,4R,5R,6aS)- 5-(benzoyloxy)-4-[(1E,3S)-4-(3-chlorophenoxy)-3-hydroxy-1-buten-1-yl]hexahydro-2H-Cyclopenta[b]furan-2-one
Piflufolastat F-18
C18H23FN4O8 (442.14998499999996)
V - Various > V09 - Diagnostic radiopharmaceuticals > V09I - Tumour detection C1446 - Radiopharmaceutical Compound > C2124 - Radioconjugate
Verdinexor
C18H12F6N6O (442.09767339999996)
C254 - Anti-Infective Agent > C281 - Antiviral Agent
BRL 15572 hydrochloride
D018377 - Neurotransmitter Agents > D018490 - Serotonin Agents > D012702 - Serotonin Antagonists
(2E,4E)-5-[1-hydroxy-2,6-dimethyl-4-oxo-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]cyclohex-2-en-1-yl]-3-methylpenta-2,4-dienoic acid
(1-Tert-Butyl-5-Hydroxy-1h-Pyrazol-4-Yl)[6-(Methylsulfonyl)-4-Methoxy-2-Methyl-1,1-Biphenyl-3-Yl]methanone
C23H26N2O5S (442.15623460000006)
N-{2,4-Difluoro-3-[(5-Pyridin-3-Yl-1h-Pyrrolo[2,3-B]pyridin-3-Yl)carbonyl]phenyl}ethanesulfonamide
C21H16F2N4O3S (442.09111299999995)
3-[(2R)-2-Hydroxy-3-methyl-3-[(phosphonooxy)methyl]butanamido]propanoylcarnitine
C16H31N2O10P (442.17162360000003)
(E)-2-(4-(3-(2-Chloro-9H-thioxanthen-9-ylidene)propyl)piperazin-1-YL)ethyl acetate
C24H27ClN2O2S (442.14816720000005)
(4S,4aR,5S,5aR,12aR)-4-(dimethylamino)-5,10,11,12a-tetrahydroxy-6-methylidene-1,3,12-trioxo-4,4a,5,5a-tetrahydrotetracene-2-carboxamide
(-)-sanguinolignan C
A lignan isolated from the leaves of Piper sanguineispicum.
2-[(chloroacetyl)(4-methoxyphenyl)amino]-N-(2-phenylethyl)-2-thien-2-ylacetamide
2-[(chloroacetyl)(3-methoxyphenyl)amino]-N-(2-phenylethyl)-2-thien-2-ylacetamide
4-methyl-N-(2-phenylphenyl)-3-(phenylsulfamoyl)benzamide
N-(3,4-dimethylphenyl)-2-[N-[(3,5-dimethyl-1H-pyrazol-4-yl)sulfonyl]-4-methoxyanilino]acetamide
C22H26N4O4S (442.16746760000007)
N-(3-methoxyphenyl)-1-[4-(1-tetrazolyl)phenyl]sulfonyl-3-piperidinecarboxamide
C20H22N6O4S (442.14231720000004)
5-tert-butyl-N-[[3-[(2,4-difluorophenoxy)methyl]-4-methoxyphenyl]methylideneamino]-1H-pyrazole-3-carboxamide
2-[[2-[4-(4-Chlorophenyl)-1-piperazinyl]-2-oxoethyl]thio]-3-ethyl-4-quinazolinone
2-[(3-ethyl-7-methyl-4-oxo-6,8-dihydro-5H-pyrido[2,3]thieno[2,4-b]pyrimidin-2-yl)thio]-N-(2-phenylethyl)acetamide
4-(2,3-dihydro-1,4-benzodioxin-6-yl)-3-[[2-(2-pyridinyl)-1-benzimidazolyl]methyl]-1H-1,2,4-triazole-5-thione
C23H18N6O2S (442.12118879999997)
3-[[[[3-[(4-Chlorophenyl)methyl]-2-methyl-4-oxo-6-quinazolinyl]amino]-oxomethyl]amino]propanoic acid ethyl ester
C22H23ClN4O4 (442.14077480000003)
1-Butyl-2-[(5-phenyl-2-oxazolyl)methylthio]-5-benzimidazolesulfonamide
3-[(4-methyl-1-piperazinyl)sulfonyl]-N-(4-phenyl-2-thiazolyl)benzamide
[4-methoxy-3-(4-morpholinylsulfonyl)phenyl]-(4-phenyl-3,6-dihydro-2H-pyridin-1-yl)methanone
C23H26N2O5S (442.15623460000006)
N-[2-(cyclopentylamino)-1-(5-methyl-2-furanyl)-2-oxoethyl]-N-[(4-fluorophenyl)methyl]-4-thiadiazolecarboxamide
C22H23FN4O3S (442.14748199999997)
8-[(1-tert-butyl-5-tetrazolyl)-thiomorpholin-4-ylmethyl]-3,6-dihydro-2H-[1,4]dioxino[2,3-g]quinolin-7-one
C21H26N6O3S (442.17870060000007)
[1-(2,1,3-Benzothiadiazol-4-ylsulfonyl)-3-piperidinyl]-(2-methyl-2,3-dihydroindol-1-yl)methanone
[5-(2-Furanyl)-7-(trifluoromethyl)-2-pyrazolo[1,5-a]pyrimidinyl]-[4-(2-pyridinyl)-1-piperazinyl]methanone
C21H17F3N6O2 (442.13650179999996)
2-Amino-5-oxo-4-phenyl-1-[3-(trifluoromethyl)phenyl]-4,6,7,8-tetrahydroquinoline-3-carboxylic acid methyl ester
[2-[(11S,17R)-11,17-dihydroxy-10,13-dimethyl-3-oxo-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-oxoethyl] dihydrogen phosphate
[4-[Bis(4-fluorophenyl)methyl]-1-piperazinyl]-(5-methyl-4-nitro-3-isoxazolyl)methanone
C22H20F2N4O4 (442.14525440000006)
(2E)-3-phenyl-2-propen-1-yl-6-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranoside
(1R,5S)-6-(4-chlorophenyl)sulfonyl-7-[4-(3-fluorophenyl)phenyl]-3,6-diazabicyclo[3.1.1]heptane
methyl (1S,3R)-2-(chloroacetyl)-1-[4-(methoxycarbonyl)phenyl]-2,3,4,4a,9,9a-hexahydro-1H-beta-carboline-3-carboxylate
2-chloro-N-[(2R,3R,6R)-2-(hydroxymethyl)-6-[2-(4-propyl-1-triazolyl)ethyl]-3-oxanyl]benzenesulfonamide
2-chloro-N-[(2S,3S,6S)-2-(hydroxymethyl)-6-[2-(4-propyl-1-triazolyl)ethyl]-3-oxanyl]benzenesulfonamide
N-[(1R,3R,4aR,9aS)-1-(hydroxymethyl)-3-[2-oxo-2-(2,2,2-trifluoroethylamino)ethyl]-3,4,4a,9a-tetrahydro-1H-pyrano[3,4-b]benzofuran-6-yl]-2-cyclopropylacetamide
N-[(1S,3R,4aS,9aR)-1-(hydroxymethyl)-3-[2-oxo-2-(2,2,2-trifluoroethylamino)ethyl]-3,4,4a,9a-tetrahydro-1H-pyrano[3,4-b]benzofuran-6-yl]-2-cyclopropylacetamide
N-[(1R,3S,4aS,9aR)-1-(hydroxymethyl)-3-[2-oxo-2-(2,2,2-trifluoroethylamino)ethyl]-3,4,4a,9a-tetrahydro-1H-pyrano[3,4-b]benzofuran-6-yl]-2-cyclopropylacetamide
[(3aS,4S,9bR)-8-[2-(2-fluorophenyl)ethynyl]-4-(hydroxymethyl)-5-methyl-3,3a,4,9b-tetrahydro-2H-pyrrolo[3,2-c]quinolin-1-yl]-(2-pyrazinyl)methanone
C26H23FN4O2 (442.18049499999995)
2-chloro-N-[(2S,3R,6S)-2-(hydroxymethyl)-6-[2-(4-propyl-1-triazolyl)ethyl]-3-oxanyl]benzenesulfonamide
2-chloro-N-[(2R,3S,6R)-2-(hydroxymethyl)-6-[2-(4-propyl-1-triazolyl)ethyl]-3-oxanyl]benzenesulfonamide
2-chloro-N-[(2S,3R,6R)-2-(hydroxymethyl)-6-[2-(4-propyl-1-triazolyl)ethyl]-3-oxanyl]benzenesulfonamide
2-chloro-N-[(2S,3S,6R)-2-(hydroxymethyl)-6-[2-(4-propyl-1-triazolyl)ethyl]-3-oxanyl]benzenesulfonamide
2-chloro-N-[(2R,3S,6S)-2-(hydroxymethyl)-6-[2-(4-propyl-1-triazolyl)ethyl]-3-oxanyl]benzenesulfonamide
2-chloro-N-[(2R,3R,6S)-2-(hydroxymethyl)-6-[2-(4-propyl-1-triazolyl)ethyl]-3-oxanyl]benzenesulfonamide
N-[(1S,3S,4aS,9aR)-1-(hydroxymethyl)-3-[2-oxo-2-(2,2,2-trifluoroethylamino)ethyl]-3,4,4a,9a-tetrahydro-1H-pyrano[3,4-b]benzofuran-6-yl]-2-cyclopropylacetamide
N-[(1R,3R,4aS,9aR)-1-(hydroxymethyl)-3-[2-oxo-2-(2,2,2-trifluoroethylamino)ethyl]-3,4,4a,9a-tetrahydro-1H-pyrano[3,4-b]benzofuran-6-yl]-2-cyclopropylacetamide
N-[(1S,3S,4aR,9aS)-1-(hydroxymethyl)-3-[2-oxo-2-(2,2,2-trifluoroethylamino)ethyl]-3,4,4a,9a-tetrahydro-1H-pyrano[3,4-b]benzofuran-6-yl]-2-cyclopropylacetamide
N-[(1S,3R,4aR,9aS)-1-(hydroxymethyl)-3-[2-oxo-2-(2,2,2-trifluoroethylamino)ethyl]-3,4,4a,9a-tetrahydro-1H-pyrano[3,4-b]benzofuran-6-yl]-2-cyclopropylacetamide
(1S)-N-(2,4-difluorophenyl)-1-(hydroxymethyl)-7-methoxy-9-methyl-1-spiro[2,3-dihydro-1H-pyrido[3,4-b]indole-4,3-azetidine]carboxamide
6-[2-[4,6-Dihydroxy-2-methoxy-3-(3-methylbut-2-enyl)phenyl]acetyl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid
C20H26O11 (442.14750460000005)
6-[6-[(2-Carboxyacetyl)oxymethyl]-2,4,5-trihydroxyoxan-3-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid
C15H22O15 (442.09586620000005)
1-[(Z)-(1-acetyl-6-hydroxyspiro[3H-chromene-2,4-piperidine]-4-ylidene)amino]-3-(2-fluorophenyl)thiourea
C22H23FN4O3S (442.14748199999997)
2-[2-(2,5-difluoroanilino)-2-hydroxyethyl]sulfanyl-3-ethyl-7-phenyl-5H-pyrrolo[3,2-d]pyrimidin-4-one
C22H20F2N4O2S (442.12749640000004)
[[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] (3R)-3-isocyanobutanoate
3-[(4aS,12aR)-2-methyl-1,3,4,5,12,12a-hexahydropyrido[3,4-b]acridin-4a-yl]phenol;hydrate;hydrobromide
15-(1,3-Dihydroxy-3-methylbutyl)-4,18-dihydroxy-2-methoxy-7,9,13-trioxapentacyclo[10.8.0.03,10.04,8.014,19]icosa-1,3(10),5,11,14,16,18-heptaen-20-one
methyl (1R,9S,10R,11R,17S)-14-ethenyl-13-(2-hydroxyacetyl)oxy-12,21-dioxa-8,18-diazahexacyclo[9.9.1.01,9.02,7.09,17.010,15]henicosa-2,4,6-triene-10-carboxylate
(4R,4aR,5R,5aR,12aR)-4-(dimethylamino)-1,5,10,11,12a-pentahydroxy-6-methylidene-3,12-dioxo-4,4a,5,5a-tetrahydrotetracene-2-carboxamide
11,17-Dihydroxy-3,20-dioxopregn-4-en-21-yl hydrogen sulfate
D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones
cortisol 21-sulfate
A steroid sulfate obtained by the formal condensation of hydroxy group at position 21 of cortisol with sulfuric acid. D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones
S-adenosyl-S-carboxymethyl-L-homocysteine dizwitterion
A sulfonium betaine obtained by deprotonation of the carboxy groups and protonation of the amino group of S-adenosyl-S-carboxymethyl-L-homocysteine. Major microspecies at pH 7.3
12-dehydrotetracycline zwitterion
Zwitterionic form of 12-dehydrotetracycline arising from transfer of a proton from the 2-hydroxy group to the adjacent tertiary amino group.
PF-739
PF-739 is an orally active and non-selective activator of AMPK. PF-739 activates 12 heterotrimeric AMPK complexes and significantly reduces the level of glucose in plasma complexes[1][2].
2,3,7,12,15,16-hexahydroxy-17-(hydroxymethyl)-9,13-dimethyl-5,18-dioxapentacyclo[12.5.0.0¹,⁶.0²,¹⁷.0⁸,¹³]nonadec-9-ene-4,11-dione
C20H26O11 (442.14750460000005)
(2s,3r,4s,5s,6r)-6-({[(2s,3r,4r,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-3,4,5-trihydroxyoxan-2-yl (2e)-3-phenylprop-2-enoate
C20H26O11 (442.14750460000005)
2-({4,5-dihydroxy-6-methyl-2-[(3,4,5-trihydroxyoxolan-2-yl)methoxy]oxan-3-yl}oxy)-6-methyloxane-3,4,5-triol
4,6-dihydroxy-6-methyl-3,9-dimethylidene-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-octahydroazuleno[4,5-b]furan-2-one
4-{4-[4-(acetyloxy)-3-methoxyphenyl]-hexahydrofuro[3,4-c]furan-1-yl}-2-methoxyphenyl acetate
18,19-dimethoxy-13,14-dimethyl-20-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4,9,11(21),16,18-pentaen-12-yl acetate
23-hydroxy-17,18-dimethoxy-7,10-dioxa-4,14-diazaheptacyclo[10.8.3.2¹¹,¹⁴.0¹,¹³.0⁶,⁸.0⁶,²³.0¹⁵,²⁰]pentacosa-15(20),16,18-triene-21,24-dione
3,4,5-trihydroxy-6-{[(3,4,5-trihydroxyoxan-2-yl)oxy]methyl}oxan-2-yl 3-phenylprop-2-enoate
C20H26O11 (442.14750460000005)
(2s)-4-hydroxy-3-methylidene-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butan-2-yl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate
C20H26O11 (442.14750460000005)
(2s,3r,4r,5r,6s)-2-{[(2r,3r,4r,5r,6s)-4,5-dihydroxy-6-methyl-2-{[(2s,3r,4r,5s)-3,4,5-trihydroxyoxolan-2-yl]methoxy}oxan-3-yl]oxy}-6-methyloxane-3,4,5-triol
2-[(5-heptyl-7-hydroxy-4-oxochromen-2-yl)methyl]-3,4,6-trihydroxybenzoic acid
6-({[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-3,4,5-trihydroxyoxan-2-yl 3-phenylprop-2-enoate
C20H26O11 (442.14750460000005)
5-(6-hydroxy-1-benzofuran-2-yl)-2-{5-hydroxy-9-methyl-8-oxatricyclo[7.3.1.0²,⁷]trideca-2,4,6,10-tetraen-11-yl}benzene-1,3-diol
5,7-dihydroxy-3,6-dimethoxy-2-(4-methoxyphenyl)-4-oxochromen-8-yl 2-methylbut-2-enoate
2-[2-(4-{2-hydroxy-5-[2-(3-hydroxyphenyl)ethyl]phenoxy}phenyl)ethyl]benzene-1,4-diol
(2s)-1-(acetyloxy)-3-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}propan-2-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate
C20H26O11 (442.14750460000005)