Exact Mass: 324.1452494
Exact Mass Matches: 324.1452494
Found 386 metabolites which its exact mass value is equals to given mass value 324.1452494,
within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error
0.001 dalton.
Corylifolinin
Isobavachalcone is a member of the class of chalcones that is trans-chalcone substituted by hydroxy groups at positions 4, 2 and 4 and a prenyl group at position 3. It has a role as an antibacterial agent, a platelet aggregation inhibitor and a metabolite. It is a polyphenol and a member of chalcones. It is functionally related to a trans-chalcone. Isobavachalcone is a natural product found in Broussonetia papyrifera, Anthyllis hermanniae, and other organisms with data available. See also: Angelica keiskei top (part of). A member of the class of chalcones that is trans-chalcone substituted by hydroxy groups at positions 4, 2 and 4 and a prenyl group at position 3. Isobavachalcone (Corylifolinin) is derived from Psoralea corylifolia Linn. and is a potent inhibitor of Akt signaling pathway, which induces apoptosis in human cancer cells (Inhibits OVCAR-8 cell growth with an IC50 value of 7.92 μM). Isobavachalcone also induces Reactive Oxyen Species (ROS) generation in OVCAR-8 cells and has exhibit cancer anti-promotive and anti-proliferative activity[1]. Isobavachalcone (Corylifolinin) is derived from Psoralea corylifolia Linn. and is a potent inhibitor of Akt signaling pathway, which induces apoptosis in human cancer cells (Inhibits OVCAR-8 cell growth with an IC50 value of 7.92 μM). Isobavachalcone also induces Reactive Oxyen Species (ROS) generation in OVCAR-8 cells and has exhibit cancer anti-promotive and anti-proliferative activity[1]. Isobavachalcone (Corylifolinin) is derived from Psoralea corylifolia Linn. and is a potent inhibitor of Akt signaling pathway, which induces apoptosis in human cancer cells (Inhibits OVCAR-8 cell growth with an IC50 value of 7.92 μM). Isobavachalcone also induces Reactive Oxyen Species (ROS) generation in OVCAR-8 cells and has exhibit cancer anti-promotive and anti-proliferative activity[1].
Glabranin
Glabranin is a dihydroxyflavanone that is pinocembrin substituted by a prenyl group at position 8. It has a role as a plant metabolite. It is a dihydroxyflavanone and a (2S)-flavan-4-one. It is functionally related to a pinocembrin. Glabranin is a natural product found in Sophora tomentosa, Annona squamosa, and other organisms with data available. A dihydroxyflavanone that is pinocembrin substituted by a prenyl group at position 8. Saponin from licorice (Glycyrrhiza glabra). Glabranin B is found in tea and herbs and spices. Origin: Plant, Pyrans Glabranin. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=41983-91-9 (retrieved 2024-07-09) (CAS RN: 41983-91-9). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
Oxyphenbutazone
M - Musculo-skeletal system > M02 - Topical products for joint and muscular pain > M02A - Topical products for joint and muscular pain > M02AA - Antiinflammatory preparations, non-steroids for topical use M - Musculo-skeletal system > M01 - Antiinflammatory and antirheumatic products > M01A - Antiinflammatory and antirheumatic products, non-steroids > M01AA - Butylpyrazolidines S - Sensory organs > S01 - Ophthalmologicals > S01B - Antiinflammatory agents > S01BC - Antiinflammatory agents, non-steroids C78272 - Agent Affecting Nervous System > C241 - Analgesic Agent > C2198 - Nonnarcotic Analgesic D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents D002491 - Central Nervous System Agents > D000700 - Analgesics D000893 - Anti-Inflammatory Agents D018501 - Antirheumatic Agents Oxyphenbutazone is a Phenylbutazone (HY-B0230) metabolite, with anti-inflammatory effect. Oxyphenbutazone is an orally active non-selective COX inhibitor. Oxyphenbutazone selectively kills non-replicating Mycobaterium tuberculosis[1][2].
Dolasetron
Dolasetron is an antinauseant and antiemetic agent indicated for the prevention of nausea and vomiting associated with moderately-emetogenic cancer chemotherapy and for the prevention of postoperative nausea and vomiting. Dolasetron is a highly specific and selective serotonin 5-HT3 receptor antagonist. This drug has not shown to have activity at other known serotonin receptors, and has low affinity for dopamine receptors. D018377 - Neurotransmitter Agents > D018490 - Serotonin Agents > D012702 - Serotonin Antagonists D018373 - Peripheral Nervous System Agents > D001337 - Autonomic Agents D005765 - Gastrointestinal Agents > D000932 - Antiemetics D002491 - Central Nervous System Agents Dolasetron(MDL-73147) is a serotonin 5-HT3 receptor antagonist used to treat nausea and vomiting following chemotherapy.
(R)-Glabridin
(R)-Glabridin is found in herbs and spices. (R)-Glabridin is isolated from Glycyrrhiza glabra (licorice). Isolated from Glycyrrhiza glabra (licorice). (R)-Glabridin is found in tea and herbs and spices. C26170 - Protective Agent > C275 - Antioxidant > C306 - Bioflavonoid Glabridin is a natural isoflavan from Glycyrrhiza uralensis, binds to and activates PPARγ, with an EC50 of 6115 nM. Glabridin exhibits antioxidant, anti-bacterial, anti-nephritic, anti-diabetic, anti-fungal, antitumor, anti-inflammatory, antiosteoporotic, cardiovascular protective, neuroprotective and radical scavenging activities[1][2]. Glabridin is a natural isoflavan from Glycyrrhiza uralensis, binds to and activates PPARγ, with an EC50 of 6115 nM. Glabridin exhibits antioxidant, anti-bacterial, anti-nephritic, anti-diabetic, anti-fungal, antitumor, anti-inflammatory, antiosteoporotic, cardiovascular protective, neuroprotective and radical scavenging activities[1][2]. Glabridin is a natural isoflavan from Glycyrrhiza uralensis, binds to and activates PPARγ, with an EC50 of 6115 nM. Glabridin exhibits antioxidant, anti-bacterial, anti-nephritic, anti-diabetic, anti-fungal, antitumor, anti-inflammatory, antiosteoporotic, cardiovascular protective, neuroprotective and radical scavenging activities[1][2].
Phaseollidin
Phaseollidin is found in common bean. Phaseollidin is isolated from kidney bean Phaseolus vulgaris, mung bean Phaseolus aureus, rice bean Phaseolus calcaratus, papadi Dolichos biflorus, and hyacinth bean Lablab niger.
Phaseollinisoflavan
Phytoalexin from Phaseolus vulgaris (kidney bean), other Phaseolus subspecies and Glycyrrhiza glabra (licorice). Phaseollinisoflavan is found in many foods, some of which are green bean, yellow wax bean, herbs and spices, and common bean. Phaseollinisoflavan is found in common bean. Phytoalexin from Phaseolus vulgaris (kidney bean), other Phaseolus species and Glycyrrhiza glabra (licorice
5-(galactosylhydroxy)-L-lysine
C12H24N2O8 (324.15325839999997)
Galactosylhydroxylysine is released during bone resorption and elevated in subjects with metabolic bone loss. Galactosylhydroxylysine is a sensitive and specific marker of bone resorption. (PMID 10222355).
dolasetron
A - Alimentary tract and metabolism > A04 - Antiemetics and antinauseants > A04A - Antiemetics and antinauseants > A04AA - Serotonin (5ht3) antagonists C78272 - Agent Affecting Nervous System > C66885 - Serotonin Antagonist > C94726 - 5-HT3 Receptor Antagonist D018377 - Neurotransmitter Agents > D018490 - Serotonin Agents > D012702 - Serotonin Antagonists D018373 - Peripheral Nervous System Agents > D001337 - Autonomic Agents C78272 - Agent Affecting Nervous System > C267 - Antiemetic Agent D005765 - Gastrointestinal Agents > D000932 - Antiemetics D002491 - Central Nervous System Agents Dolasetron(MDL-73147) is a serotonin 5-HT3 receptor antagonist used to treat nausea and vomiting following chemotherapy.
Bindarit
Bindarit has been used in trials studying the prevention and treatment of Coronary Restenosis and Diabetic Nephropathy. D004791 - Enzyme Inhibitors > D011500 - Protein Synthesis Inhibitors C29629 - Combination Medication > C29634 - Antirheumatic Preparation D000893 - Anti-Inflammatory Agents Bindarit (AF2838) is a selective inhibitor of the monocyte chemotactic proteins MCP-1/CCL2, MCP-3/CCL7, and MCP-2/CCL8, and no effect on other CC and CXC chemokines such as MIP-1α/CCL3, MIP-1β/CCL4, MIP-3/CCL23. Bindarit also has anti-inflammatory activity[1].
Valaciclovir
Valaciclovir (INN) or valacyclovir (USAN) is an antiviral drug used in the management of herpes simplex and herpes zoster (shingles). It is a prodrug, being converted in vivo to aciclovir. It is marketed by GlaxoSmithKline under the trade name Valtrex or Zelitrex. [Wikipedia] J - Antiinfectives for systemic use > J05 - Antivirals for systemic use > J05A - Direct acting antivirals > J05AB - Nucleosides and nucleotides excl. reverse transcriptase inhibitors D000890 - Anti-Infective Agents > D000998 - Antiviral Agents C471 - Enzyme Inhibitor > C29575 - DNA Polymerase Inhibitor C254 - Anti-Infective Agent > C281 - Antiviral Agent
(S)-5,7-Dihydroxy-6-prenylflavanone
(S)-5,7-Dihydroxy-6-prenylflavanone is found in herbs and spices. (S)-5,7-Dihydroxy-6-prenylflavanone is a constituent of Glycyrrhiza glabra (licorice). Constituent of Glycyrrhiza glabra (licorice). (S)-5,7-Dihydroxy-6-prenylflavanone is found in tea and herbs and spices.
(E)-2',4,4'-Trihydroxy-3-prenylchalcone
(E)-2,4,4-Trihydroxy-3-prenylchalcone is found in herbs and spices. (E)-2,4,4-Trihydroxy-3-prenylchalcone is a constituent of hairy root cultures of Glycyrrhiza glabra (licorice)
Moracin I
Isolated from Morus alba (white mulberry) infected with Fusarium solani. Moracin I is found in mulberry and fruits. Moracin I is found in fruits. Moracin I is isolated from Morus alba (white mulberry) infected with Fusarium solani.
6-(3-methylbut-2-en-1-yl)-8,17-dioxatetracyclo[8.7.0.0(2),.0(1)(1),(1)]heptadeca-2(7),3,5,11(16),12,14-hexaene-5,14-diol
5-(Galactosylhydroxy)-L-Lysine
C12H24N2O8 (324.15325839999997)
(2S,5R)-2,6-Diamino-5-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyhexanoic acid
C12H24N2O8 (324.15325839999997)
Component of collagen
4-Butyl-5-hydroxy-2-(4-hydroxyphenyl)-1-phenyl-1H-pyrazol-3(2H)-one
Bavachalcone
Isobavachalcone (Corylifolinin) is derived from Psoralea corylifolia Linn. and is a potent inhibitor of Akt signaling pathway, which induces apoptosis in human cancer cells (Inhibits OVCAR-8 cell growth with an IC50 value of 7.92 μM). Isobavachalcone also induces Reactive Oxyen Species (ROS) generation in OVCAR-8 cells and has exhibit cancer anti-promotive and anti-proliferative activity[1]. Isobavachalcone (Corylifolinin) is derived from Psoralea corylifolia Linn. and is a potent inhibitor of Akt signaling pathway, which induces apoptosis in human cancer cells (Inhibits OVCAR-8 cell growth with an IC50 value of 7.92 μM). Isobavachalcone also induces Reactive Oxyen Species (ROS) generation in OVCAR-8 cells and has exhibit cancer anti-promotive and anti-proliferative activity[1]. Isobavachalcone (Corylifolinin) is derived from Psoralea corylifolia Linn. and is a potent inhibitor of Akt signaling pathway, which induces apoptosis in human cancer cells (Inhibits OVCAR-8 cell growth with an IC50 value of 7.92 μM). Isobavachalcone also induces Reactive Oxyen Species (ROS) generation in OVCAR-8 cells and has exhibit cancer anti-promotive and anti-proliferative activity[1].
7-Hydroxy-2-(4-hydroxyphenyl)-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one
Bindarit
D004791 - Enzyme Inhibitors > D011500 - Protein Synthesis Inhibitors C29629 - Combination Medication > C29634 - Antirheumatic Preparation D000893 - Anti-Inflammatory Agents Bindarit (AF2838) is a selective inhibitor of the monocyte chemotactic proteins MCP-1/CCL2, MCP-3/CCL7, and MCP-2/CCL8, and no effect on other CC and CXC chemokines such as MIP-1α/CCL3, MIP-1β/CCL4, MIP-3/CCL23. Bindarit also has anti-inflammatory activity[1].
Ditazole
B - Blood and blood forming organs > B01 - Antithrombotic agents > B01A - Antithrombotic agents > B01AC - Platelet aggregation inhibitors excl. heparin C78275 - Agent Affecting Blood or Body Fluid > C1327 - Antiplatelet Agent
epsilon-Deoxy-fructosyl-lysine
C12H24N2O8 (324.15325839999997)
galactosyl hydroxylysine
C12H24N2O8 (324.15325839999997)
1,2-Diphenyl-3,5-dioxo-4-(3-hydroxybutyl)pyrazolidine
D-Valacyclovir
O-Galactosyl-5-hydroxylysine
C12H24N2O8 (324.15325839999997)
Bavachin
Bavachin is a natural product found in Broussonetia papyrifera, Cullen corylifolium, and other organisms with data available. Bavachin, a flavonoid first isolated from seeds of P. corylifolia, acts as a phytoestrogen that activates the estrogen receptors ERα and ERβ with EC50s of 320 and 680 nM, respectively. Bavachin, a flavonoid first isolated from seeds of P. corylifolia, acts as a phytoestrogen that activates the estrogen receptors ERα and ERβ with EC50s of 320 and 680 nM, respectively.
Glabridin
Glabridin is a member of the class of hydroxyisoflavans that is (R)-isoflavan substituted by hydroxy groups at positions 2 and 4 and a 2,2-dimethyl-2H-pyran group across positions 7 and 8 respectively. It has a role as an antiplasmodial drug. It derives from a hydride of a (R)-isoflavan. Glabridin is a natural product found in Ornithopus sativus, Glycyrrhiza glabra, and other organisms with data available. See also: Glycyrrhiza Glabra (part of). C26170 - Protective Agent > C275 - Antioxidant > C306 - Bioflavonoid Glabridin is a natural isoflavan from Glycyrrhiza uralensis, binds to and activates PPARγ, with an EC50 of 6115 nM. Glabridin exhibits antioxidant, anti-bacterial, anti-nephritic, anti-diabetic, anti-fungal, antitumor, anti-inflammatory, antiosteoporotic, cardiovascular protective, neuroprotective and radical scavenging activities[1][2]. Glabridin is a natural isoflavan from Glycyrrhiza uralensis, binds to and activates PPARγ, with an EC50 of 6115 nM. Glabridin exhibits antioxidant, anti-bacterial, anti-nephritic, anti-diabetic, anti-fungal, antitumor, anti-inflammatory, antiosteoporotic, cardiovascular protective, neuroprotective and radical scavenging activities[1][2]. Glabridin is a natural isoflavan from Glycyrrhiza uralensis, binds to and activates PPARγ, with an EC50 of 6115 nM. Glabridin exhibits antioxidant, anti-bacterial, anti-nephritic, anti-diabetic, anti-fungal, antitumor, anti-inflammatory, antiosteoporotic, cardiovascular protective, neuroprotective and radical scavenging activities[1][2].
Bavachalcone
Bavachalcone is a member of chalcones. Bavachalcone is a natural product found in Broussonetia papyrifera, Cullen corylifolium, and Sophora prostrata with data available. Bavachalcone is a compound isolated from psoralen. It is widely used in traditional Chinese medicine and has antibiotic and anti-cancer activities. Bavachalcone is a compound isolated from psoralen. It is widely used in traditional Chinese medicine and has antibiotic and anti-cancer activities.
Isobavachin
Isobavachin is a member of flavanones. Isobavachin is a natural product found in Brosimum acutifolium, Erythrina sigmoidea, and other organisms with data available. Isobavachin, an antioxidant isaolated from Psoralea corylifolia with a prenyl group at position 8 of ring A, promotes neuronal differentiation and the potential role of its protein prenylation[1][2]. Isobavachin, an antioxidant isaolated from Psoralea corylifolia with a prenyl group at position 8 of ring A, promotes neuronal differentiation and the potential role of its protein prenylation[1][2].
Calocarpin
Flemistrictin E
Flemistrictin F
6-Carboxy-5-hydroxy-2,2-dimethyl-7-(2-phenylethyl)chromene
1-(1,3-Benzodioxole-5-yl)-2,3-dimethyl-6,7-(methylenedioxy)-1,2,3,4-tetrahydronaphthalene
2-[[2-(3,5-dihydroxy-4-isopropyl-phenyl)-2-guanidino-acetyl]amino]acetic acid
Crotaramosmin
1-(2,5-dihydro-6,8-dihydroxy-3-methyl-1-benzoxepin-7-yl)-3-phenyl-1-propanone
4-Hydroxycordoin
A member of the class of chalcones that is trans-chalcone substituted by hydroxy groups at position 4 and 2 and a (3-methylbut-2-en-1-yl)oxy group at position 4. It has been isolated from Lonchocarpus neuroscapha.
NPE_325.1547_12.8
CONFIDENCE Tentative identification: most likely structure (Level 3); INTERNAL_ID 1101
1-(2,4-dihydroxyphenyl)-3-[4-(3-methylbut-2-enoxy)phenyl]prop-2-en-1-one
Me glycoside-4-O-alpha-L-Rhamnopyranosyl-L-rhamnose|Me glycoside-4-O-beta-L-Rhamnopyranosyl-L-rhamnose
1-O-beta-D-fructofuranosyl-2R,5R-dihydroxymethyl-3R,4R-dihydroxypyrrolidine
C12H24N2O8 (324.15325839999997)
dimethyl 2,4-diphenylcyclobutane-1,3-dicarboxylate
(E)-cinnamyl (E)-3,4-dimethoxycinnamate|(E)-cinnamyl (E)-O,O-dimethyl-caffeate|(E)-cinnamyl-(E)-O,O-dimethyl caffeate|cinnamyl 3,4-dimethoxycinnamate
5-(E)-propenyl-2-(2,4,5-trimethoxyphenyl)benzofuran|6-Demethoxy,5-methoxy-5-(1-Propenyl)-2-(2,4,6-trimethoxyphenyl)benzofuran
1,1,10-Trimethyl-3-hydroxy-7-isopropylanthracene-2,5,6(1H)-trione
1-[2,4-dihydroxy-5-(3-methylbut-2-enyl)phenyl]-3-(4-hydroxyphenyl)prop-2-en-1-one
2-(3,4-methylenedioxyphenyl)-5-(1,2-dihydroxypropyl)-3-methylbenzofuran
2,3-dihydro-3,7-dihydroxy-6-(3-methyl-2-butenyl)-2-phenyl-4h -1-benzopyran-4-one
2-(3,4-Dimethoxyphenyl)-3-methyl-7-(2-propenyl)benzofuran-5-ol
6-Methyl-2-oxo-tetrahydro-pyran-3-carbonsaeure-(N,N-diphenyl-hydrazid)|6-methyl-2-oxo-tetrahydro-pyran-3-carboxylic acid-(N,N-diphenyl-hydrazide)
2,2-Dimethyl-5-hydroxy-7-(2-phenylethyl)-2H-1-benzopyran-6-carboxylic acid
Sanggenofuran B
Sanggenofuran B is a natural product found in Morus cathayana with data available.
3-Ethyl-1,3-ethano-1,3-propanospiro[1H-indole-2(3H),2-piperidine]-9,10,11-trione
1-(4-hydroxy-3-methoxyphenyl)-7-phenyl-5-hydroxy-4,6-heptadiene-3-one
(E)-1-(5-hydroxy-2,2-dimethyl-3,4-dihydrochromen-8-yl)-3-(4-hydroxyphenyl)prop-2-en-1-one
5-Ethyl-7,12-ethano-6,5-(iminopropano)-6-hydroxy-2,3,4,5,6,7-hexahydro-1H-1-benzoazonine-13,17(7)-diene-2,16-dione
Me glycoside-3-O-alpha-L-Rhamnopyranosyl-L-rhamnose
3alpha-hydroxy-9(10->20)abeo-abieta-1,5,8,10(20),13-pentaene-7,11,12-trione
Methyl (3S,5S)-5-Hydroxy-3-(beta-D-glucopyranosyloxy)hexanoate|Methyl-(3S,5S)-5-hydroxy-3-(??-D-glucopyranosyloxy) hexanoate
1-(4-hydroxy-3-methoxyphenyl)-7-methoxy-2,3-dimethylnaphthalen-6-ol
(+-)-alpha-truxillic acid monoethyl ester|(+-)-alpha-Truxillsaeure-monoaethylester
licarinB
Licarin B is a natural product found in Magnolia kachirachirai, Licaria guianensis, and other organisms with data available. Licarin B, a nitric oxide production inhibitor extracted from the component of the seeds of Myristica fragrans, improves insulin sensitivity via PPARγ and activation of GLUT4 in the IRS-1/PI3K/AKT pathway[1][2][3]. Licarin B, a nitric oxide production inhibitor extracted from the component of the seeds of Myristica fragrans, improves insulin sensitivity via PPARγ and activation of GLUT4 in the IRS-1/PI3K/AKT pathway[1][2][3]. Licarin B, a nitric oxide production inhibitor extracted from the component of the seeds of Myristica fragrans, improves insulin sensitivity via PPARγ and activation of GLUT4 in the IRS-1/PI3K/AKT pathway[1][2][3]. Licarin B, a nitric oxide production inhibitor extracted from the component of the seeds of Myristica fragrans, improves insulin sensitivity via PPARγ and activation of GLUT4 in the IRS-1/PI3K/AKT pathway[1][2][3].
Bindarit
D004791 - Enzyme Inhibitors > D011500 - Protein Synthesis Inhibitors C29629 - Combination Medication > C29634 - Antirheumatic Preparation D000893 - Anti-Inflammatory Agents Bindarit (AF2838) is a selective inhibitor of the monocyte chemotactic proteins MCP-1/CCL2, MCP-3/CCL7, and MCP-2/CCL8, and no effect on other CC and CXC chemokines such as MIP-1α/CCL3, MIP-1β/CCL4, MIP-3/CCL23. Bindarit also has anti-inflammatory activity[1].
5,7-dihydroxy-8-(3-methylbut-2-enyl)-2-phenyl-2,3-dihydrochromen-4-one
7-hydroxy-2-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]-2,3-dihydrochromen-4-one
(E)-1-(2,4-dihydroxyphenyl)-3-[4-(3-methylbut-2-enoxy)phenyl]prop-2-en-1-one
Isobavachalcone
Isobavachalcone (Corylifolinin) is derived from Psoralea corylifolia Linn. and is a potent inhibitor of Akt signaling pathway, which induces apoptosis in human cancer cells (Inhibits OVCAR-8 cell growth with an IC50 value of 7.92 μM). Isobavachalcone also induces Reactive Oxyen Species (ROS) generation in OVCAR-8 cells and has exhibit cancer anti-promotive and anti-proliferative activity[1]. Isobavachalcone (Corylifolinin) is derived from Psoralea corylifolia Linn. and is a potent inhibitor of Akt signaling pathway, which induces apoptosis in human cancer cells (Inhibits OVCAR-8 cell growth with an IC50 value of 7.92 μM). Isobavachalcone also induces Reactive Oxyen Species (ROS) generation in OVCAR-8 cells and has exhibit cancer anti-promotive and anti-proliferative activity[1]. Isobavachalcone (Corylifolinin) is derived from Psoralea corylifolia Linn. and is a potent inhibitor of Akt signaling pathway, which induces apoptosis in human cancer cells (Inhibits OVCAR-8 cell growth with an IC50 value of 7.92 μM). Isobavachalcone also induces Reactive Oxyen Species (ROS) generation in OVCAR-8 cells and has exhibit cancer anti-promotive and anti-proliferative activity[1].
C20H20O4_6H-Benzofuro[3,2-c][1]benzopyran-3,9-diol, 6a,11a-dihydro-2-(3-methyl-2-buten-1-yl)-, (6aR,11aR)
C20H20O4_1,3-Benzenediol, 4-[3,4,8,9-tetrahydro-8-(1-methylethenyl)-2H-furo[2,3-h]-1-benzopyran-3-yl]
(E)-1-(2,4-dihydroxyphenyl)-3-[4-(3-methylbut-2-enoxy)phenyl]prop-2-en-1-one
4-(8-prop-1-en-2-yl-3,4,8,9-tetrahydro-2H-furo[2,3-h]chromen-3-yl)benzene-1,3-diol
4-(8-prop-1-en-2-yl-3,4,8,9-tetrahydro-2H-furo[2,3-h]chromen-3-yl)benzene-1,3-diol_major
amphotalide
C254 - Anti-Infective Agent > C276 - Antiparasitic Agent > C250 - Antihelminthic Agent
3-Ethyl-1,1,1,5,5,5-hexamethyl-3-trimethylsilanyloxy-trisiloxane
Glyoctamide
C78276 - Agent Affecting Digestive System or Metabolism > C29711 - Anti-diabetic Agent > C97936 - Sulfonylurea Antidiabetic Agent
1,1,3-TRIMETHYL-3-PHENYLINDAN-4,5-DICARBOXYLIC ACID
2-Piperazinyl-4-amino-6,7-dimethoxyquinazoline hydrochloride
1-(2-THIOPHEN-2-YL-IMIDAZO[1,2-A]PYRIDIN-3-YLMETHYL)-PIPERIDINE-4-CARBOXYLICACID
C12H28O6Si2 (324.14243480000005)
4-CHLORO-1-(TRIISOPROPYLSILYL)-1H-PYRROLO[2,3-B]PYRIDIN-5-OL
1-Tridecanol, phosphate, sodium salt
C13H27Na2O4P (324.14422720000005)
1-CYCLOHEXYL-2-(3-FURANYL)-1H-BENZIMIDAZOLE-5-CARBOXYLIC ACID, METHYL ESTER
N,N-dimethyl-1-(1,3,7,9-tetradeuteriophenothiazin-10-yl)propan-2-amine,hydrochloride
3-chloro-2-(4-morpholino)pyridine-4-boronic acid pinacol ester
Des(diethylaMinoethyl)-didesiodo-1-Methoxy AMiodarone
1H-BenziMidazole-7-carboxaMide, 2-[(2S)-2-Methyl-2-pyrrolidinyl]-, hydrochloride (1:2)
2,3,4,6,7,8,9,10-Octahydro-1H-pyrimido[1,2-a]azepin-5-ium 4-methy lbenzenesulfonate
((2S)-1-(-2-NITROVINYL)-2,3-DIPHENYLPYRROLIDIN-2-YL)METHANOL
4-(6-AMINO-5-NITRO-4-PYRIMIDINYL)-1-PIPERAZINECARBOXYLIC ACID 1,1-DIMETHYLETHYL ESTER
1,2,3,4-Butanetetrol,1-[5-[(2S,3R)-2,3,4-trihydroxybutyl]-2-pyrazinyl]-, (1R,2S,3R)-
C12H24N2O8 (324.15325839999997)
2-[(2-amino-6-oxo-3H-purin-9-yl)methoxy]ethyl 2-amino-3-methylbutanoate
1-[2-[2,5-Dimethyl-1-(phenylmethyl)-3-pyrrolyl]-2-oxoethyl]pyrrolidine-2,5-dione
6-Hydroxy-3-methyl-8-(2-phenylethyl)-2,5-dihydro-1-benzoxepine-7-carboxylic acid
7-(4-Hydroxy-3-methoxyphenyl)-1-(4-hydroxyphenyl)hepta-4,6-dien-3-one
7-Hydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one
5-[4-Tert-butylphenylsulfanyl]-2,4-quinazolinediamine
C18H20N4S (324.14086000000003)
Valacyclovir
J - Antiinfectives for systemic use > J05 - Antivirals for systemic use > J05A - Direct acting antivirals > J05AB - Nucleosides and nucleotides excl. reverse transcriptase inhibitors D000890 - Anti-Infective Agents > D000998 - Antiviral Agents C471 - Enzyme Inhibitor > C29575 - DNA Polymerase Inhibitor C254 - Anti-Infective Agent > C281 - Antiviral Agent
Ditazole
B - Blood and blood forming organs > B01 - Antithrombotic agents > B01A - Antithrombotic agents > B01AC - Platelet aggregation inhibitors excl. heparin C78275 - Agent Affecting Blood or Body Fluid > C1327 - Antiplatelet Agent
phaseollidin
Phaseollidin is a member of the class of compounds known as pterocarpans. Pterocarpans are benzo-pyrano-furano-benzene compounds, containing the 6H-[1]benzofuro[3,2-c]chromene skeleton. They are derivatives of isoflavonoids. Phaseollidin is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Phaseollidin can be found in a number of food items such as hyacinth bean, lima bean, yellow wax bean, and scarlet bean, which makes phaseollidin a potential biomarker for the consumption of these food products.
(2E)-4-{methyl[3-phenyl-3-(pyridin-2-yl)propyl]amino}-4-oxobut-2-enoic acid
2-Deamino-2-hydroxy-6-dehydroparomamine(2+)
C12H24N2O8+2 (324.15325839999997)
(2S,5R,6R)-6-(azepan-1-ylmethylideneamino)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 2,6-diamino-5-hydroxyhexanoate
C12H24N2O8 (324.15325839999997)
2,6-diamino-2-[3,4,5,6-tetrahydroxy-6-(hydroxymethyl)oxan-2-yl]hexanoic acid
C12H24N2O8 (324.15325839999997)
N-{5-[(dimethylamino)sulfonyl]-2-methylphenyl}cyclohexanecarboxamide
(-)-Phaseolin
A prenylated member of the class of pterocarpans and an organic heteropentacyclic compound that is 2,3,6b,12b-tetrahydro-1H,7H-chromeno[6,5:4,5]furo[3,2-c]chromen-10-ol in which both of the hydrogens at position 3 have been replaced by methyl groups (the R,R stereoisomer). It is found in found in the seeds of Phaseolus vulgaris (French bean) and in the stems of Erythrina subumbrans.
1-(2,6-diethylphenyl)-3-(1H-indazol-6-yl)thiourea
C18H20N4S (324.14086000000003)
[4-(8-fluoro-6-oxo-3,4,5,6-tetrahydro-1H-azepino[5,4,3-cd]indol-2-yl)phenyl]-N-methylmethanaminium
3-(5-Hydroxy-2,2-dimethylchromen-6-yl)-1-(4-hydroxyphenyl)propan-1-one
5,6-dihydroxy-1-[(2S)-4-phenylbutan-2-yl]indole-7-carboxamide
(Z)-1,2-Bis(fluorodimethylsilyl)-1,2-bis(trimethylsilyl)ethylene
G-29701
A metabolite of phenylbutazone obtained by hydroxylation at position 4 of one of the phenyl rings. Commonly used (as its hydrate) to treat pain, swelling and stiffness associated with arthritis and gout, it was withdrawn from the market 1984 following association with blood dyscrasis and Stevens-Johnson syndrome. M - Musculo-skeletal system > M02 - Topical products for joint and muscular pain > M02A - Topical products for joint and muscular pain > M02AA - Antiinflammatory preparations, non-steroids for topical use M - Musculo-skeletal system > M01 - Antiinflammatory and antirheumatic products > M01A - Antiinflammatory and antirheumatic products, non-steroids > M01AA - Butylpyrazolidines S - Sensory organs > S01 - Ophthalmologicals > S01B - Antiinflammatory agents > S01BC - Antiinflammatory agents, non-steroids C78272 - Agent Affecting Nervous System > C241 - Analgesic Agent > C2198 - Nonnarcotic Analgesic D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents D002491 - Central Nervous System Agents > D000700 - Analgesics D000893 - Anti-Inflammatory Agents D018501 - Antirheumatic Agents Oxyphenbutazone is a Phenylbutazone (HY-B0230) metabolite, with anti-inflammatory effect. Oxyphenbutazone is an orally active non-selective COX inhibitor. Oxyphenbutazone selectively kills non-replicating Mycobaterium tuberculosis[1][2].
Anzemet
D018377 - Neurotransmitter Agents > D018490 - Serotonin Agents > D012702 - Serotonin Antagonists D018373 - Peripheral Nervous System Agents > D001337 - Autonomic Agents D005765 - Gastrointestinal Agents > D000932 - Antiemetics D002491 - Central Nervous System Agents Dolasetron(MDL-73147) is a serotonin 5-HT3 receptor antagonist used to treat nausea and vomiting following chemotherapy.
(2S)-6-amino-2-{N-hydroxy[(3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]amino}hexanoic acid
C12H24N2O8 (324.15325839999997)
(-)-Phaseollinisoflavan
A member of the class of hydroxyisoflavans that is (3R)-3,4-dihydro-2H,2H-3,6-bichromene substituted by two methyl groups at positions 2 and 2 and hydroxy groups at positions 5 and 7 respectively.
(2z)-2-[(1-hydroxy-4-oxocyclohexyl)methyl]-3-[(4-methoxyphenyl)methyl]but-2-enedinitrile
(2s)-5-hydroxy-7-[(3-methylbut-2-en-1-yl)oxy]-2-phenyl-2,3-dihydro-1-benzopyran-4-one
5-methoxy-2,2-dimethyl-6-(3-methylbuta-1,3-dien-1-yl)pyrano[2,3-h]chromen-8-one
2-(4-hydroxy-2-methoxyphenyl)-5-(3-methylbut-2-en-1-yl)-1-benzofuran-6-ol
8-(7-hydroxy-3,4-dihydro-2h-1-benzopyran-3-yl)-2,2-dimethylchromen-5-ol
5,7-dihydroxy-8-(3-methylbut-1-en-1-yl)-2-phenyl-2,3-dihydro-1-benzopyran-4-one
(2e)-1-{2,6-dihydroxy-4-[(3-methylbut-2-en-1-yl)oxy]phenyl}-3-phenylprop-2-en-1-one
(1r,10r)-15-(3-methylbut-2-en-1-yl)-8,17-dioxatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]heptadeca-2,4,6,11(16),12,14-hexaene-5,14-diol
(2s,4r)-11-hydroxy-4-methyl-9-(2-phenylethyl)-6-oxatricyclo[5.4.0.0²,⁴]undeca-1(11),7,9-triene-10-carboxylic acid
4b,9-dihydroxy-7-methoxy-11,11-dimethyl-10h,10ah-benzo[b]fluoren-5-one
methyl 14-oxa-8,17-diazahexacyclo[10.7.1.0¹,⁹.0²,⁷.0¹³,¹⁵.0¹⁷,²⁰]icosa-2,4,6,9-tetraene-10-carboxylate
(4e,6e)-7-(4-hydroxy-3-methoxyphenyl)-1-(4-hydroxyphenyl)hepta-4,6-dien-3-one
1-[(1's,2'r,3r,7'r,9's)-2-hydroxy-4'-oxa-12'-azaspiro[indole-3,10'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-6'-yl]ethanone
5-{6,7-dimethyl-2h,5h,6h,7h,8h-naphtho[2,3-d][1,3]dioxol-5-yl}-2h-1,3-benzodioxole
7-hydroxy-3-isopropyl-5,5,9-trimethylanthracene-1,2,6-trione
6-[9-(furan-2-yl)nona-2,4,6,8-tetraen-2-yl]-4-methoxy-3-methylpyran-2-one
2-[3-hydroxy-5-methoxy-4-(3-methylbut-2-en-1-yl)phenyl]-1-benzofuran-6-ol
(2s)-7-hydroxy-8-[(1z)-3-hydroxy-3-methylbut-1-en-1-yl]-2-phenyl-2,3-dihydro-1-benzopyran-4-one
5-[(1e)-prop-1-en-1-yl]-2-(2,4,6-trimethoxyphenyl)-1-benzofuran
ajuforrestine a
{"Ingredient_id": "HBIN014959","Ingredient_name": "ajuforrestine a","Alias": "NA","Ingredient_formula": "C20H20O4","Ingredient_Smile": "CC1=C(C2=CC(=O)C3=C(C4=C(C(=C3C2(CC1)C)O)OC=C4C)O)C","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "786","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}
anticancer diarylheptanoid pmv70p691-010
{"Ingredient_id": "HBIN016318","Ingredient_name": "anticancer diarylheptanoid pmv70p691-010","Alias": "NA","Ingredient_formula": "C20H20O4","Ingredient_Smile": "COC1=C(C=C2CCC3C(C2=C1)C=CC(O3)C4=CC=C(C=C4)O)O","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "1393","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}
avicennin
{"Ingredient_id": "HBIN017404","Ingredient_name": "avicennin","Alias": "NA","Ingredient_formula": "C20H20O4","Ingredient_Smile": "CC(=C)C=CC1=C(C2=C(C3=C1OC(=O)C=C3)OC(C=C2)(C)C)OC","Ingredient_weight": "324.4 g/mol","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "2035","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "5321265","DrugBank_id": "NA"}
bavachin
{"Ingredient_id": "HBIN017632","Ingredient_name": "bavachin","Alias": "NA","Ingredient_formula": "C20H20O4","Ingredient_Smile": "CC(=CCC1=CC2=C(C=C1O)OC(CC2=O)C3=CC=C(C=C3)O)C","Ingredient_weight": "324.4 g/mol","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "2172","TCMSP_id": "NA","TCM_ID_id": "6419","PubChem_id": "26436537","DrugBank_id": "NA"}
(10e,12r)-4-methoxy-2-oxatricyclo[13.2.2.1³,⁷]icosa-1(17),3(20),4,6,8,10,15,18-octaene-5,12-diol
(2s)-5,7-dihydroxy-6-(3-methylbut-2-en-1-yl)-2-phenyl-2,3-dihydro-1-benzopyran-4-one
{[(2s)-2-carbamimidamido-2-(3,5-dihydroxy-4-isopropylphenyl)-1-hydroxyethylidene]amino}acetic acid
tert-butyl 2-(9-hydroxy-10-oxophenanthren-9-yl)acetate
(2s)-5,7-dihydroxy-8-[(1e)-3-methylbut-1-en-1-yl]-2-phenyl-2,3-dihydro-1-benzopyran-4-one
{9-methoxy-5-methylnaphtho[2,3-b]furan-4-yl}methyl (2z)-2-methylbut-2-enoate
8-hydroxy-2-methyl-2-(4-methylpent-3-en-1-yl)benzo[g]chromene-5,10-dione
10-(3-methylbut-2-en-1-yl)-8,17-dioxatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]heptadeca-2,4,6,11,13,15-hexaene-5,14-diol
9-hydroxy-2,5,5-trimethyl-3,4,4a,12b-tetrahydro-6-oxatetraphene-7,12-dione
2-[4-hydroxy-2-methoxy-5-(3-methylbut-2-en-1-yl)phenyl]-1-benzofuran-6-ol
(2s)-7-hydroxy-2-(4-hydroxyphenyl)-6-(3-methylbut-2-en-1-yl)-2,3-dihydro-1-benzopyran-4-one
2-methoxy-4-{7-methoxy-3-methyl-5-[(1e)-prop-1-en-1-yl]-1-benzofuran-2-yl}phenol
(3r)-3-[(2s)-6-hydroxy-2-(prop-1-en-2-yl)-2,3-dihydro-1-benzofuran-5-yl]-3,4-dihydro-2h-1-benzopyran-7-ol
methyl (1r,12s,13s,15r,20s)-14-oxa-8,17-diazahexacyclo[10.7.1.0¹,⁹.0²,⁷.0¹³,¹⁵.0¹⁷,²⁰]icosa-2,4,6,9-tetraene-10-carboxylate
5-(prop-1-en-1-yl)-2-(2,4,6-trimethoxyphenyl)-1-benzofuran
13-hydroxy-4-methoxy-2-oxatricyclo[13.2.2.1³,⁷]icosa-1(17),3(20),4,6,8,15,18-heptaen-12-one
(3ar,5r,7r,9ar)-5-[(1r,3z)-1-chlorohex-3-en-5-yn-1-yl]-7-ethyl-2,2-dimethyl-3ah,4h,5h,7h,9ah-[1,3]dioxolo[4,5-d]oxocine
C18H25ClO3 (324.14921300000003)
5-[6-methoxy-7-(3-methylbut-2-en-1-yl)-1-benzofuran-2-yl]benzene-1,3-diol
1-(2,4-dihydroxyphenyl)-3-[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]prop-2-en-1-one
1-{5,5-dimethyl-3-oxo-4,13-diazatetracyclo[6.6.1.0²,⁶.0¹²,¹⁵]pentadeca-1(14),8(15),9,11-tetraen-4-yl}butane-1,3-dione
14-oxa-1,10-diazapentacyclo[15.3.1.0³,¹¹.0⁴,⁹.0¹²,¹⁸]henicosa-3(11),4,6,8,16-pentaene-12-carboxylic acid
(4as,12bs)-9-hydroxy-2,5,5-trimethyl-3,4,4a,12b-tetrahydro-6-oxatetraphene-7,12-dione
2,5,10-trimethoxy-3,8-dimethylcyclohepta[a]naphthalen-9-one
6-(3-methylbut-2-en-1-yl)-8,17-dioxatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]heptadeca-2(7),3,5,11,13,15-hexaene-5,14-diol
5-[(3s)-7-methoxy-3-methyl-5-[(1e)-prop-1-en-1-yl]-2,3-dihydro-1-benzofuran-2-yl]-2h-1,3-benzodioxole
6-hydroxy-3-methyl-8-(2-phenylethyl)-2,5-dihydro-1-benzoxepine-9-carboxylic acid
2-(3,4-dimethoxyphenyl)-3-methyl-7-(prop-2-en-1-yl)-1-benzofuran-5-ol
8,9-dihydroxy-7-methoxy-11,11-dimethyl-4bh,10h,10ah-benzo[b]fluoren-5-one
(1r,10r)-6-(3-methylbut-2-en-1-yl)-8,17-dioxatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]heptadeca-2(7),3,5,11,13,15-hexaene-5,14-diol
8-hydroxy-1-(hydroxymethyl)-3-methyl-5-(3-methylbut-2-en-1-yl)xanthen-9-one
5-hydroxy-2,8,8-trimethyl-6-[(1e)-3-methylbuta-1,3-dien-1-yl]pyrano[2,3-f]chromen-4-one
(11bs)-7,11-dihydroxy-4,4,9,11b-tetramethyl-1h-phenanthro[3,2-b]furan-6-one
2,6-dimethoxy-4-(prop-2-en-1-yl)phenyl (2e)-3-phenylprop-2-enoate
{9-methoxy-5-methylnaphtho[2,3-b]furan-4-yl}methyl 2-methylbut-2-enoate
(2e)-1-(5,7-dihydroxy-2,2-dimethyl-3,4-dihydro-1-benzopyran-8-yl)-3-phenylprop-2-en-1-one
1-(5,7-dihydroxy-2,2-dimethyl-3,4-dihydro-1-benzopyran-8-yl)-3-phenylprop-2-en-1-one
1-(4,5-dihydroxy-2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl)-3-phenylprop-2-en-1-one
5-hydroxy-2,8,8-trimethyl-6-(3-methylbuta-1,3-dien-1-yl)pyrano[2,3-f]chromen-4-one
3-phenyl-1-[2,4,6-trihydroxy-3-(3-methylbut-2-en-1-yl)phenyl]prop-2-en-1-one
2-[4-hydroxy-2-methoxy-3-(3-methylbut-2-en-1-yl)phenyl]-1-benzofuran-6-ol
1-(5-hydroxy-2,2-dimethylchromen-6-yl)-3-(4-hydroxyphenyl)propan-1-one
(4z,6e)-5-hydroxy-1-(4-hydroxy-3-methoxyphenyl)-7-phenylhepta-4,6-dien-3-one
8-[(3s)-7-hydroxy-3,4-dihydro-2h-1-benzopyran-3-yl]-2,2-dimethylchromen-5-ol
6-[(2e,4e,6e,8e)-9-(furan-2-yl)nona-2,4,6,8-tetraen-2-yl]-4-methoxy-3-methylpyran-2-one
5-[(2s,3s)-7-methoxy-3-methyl-5-[(1e)-prop-1-en-1-yl]-2,3-dihydro-1-benzofuran-2-yl]-2h-1,3-benzodioxole
(1s,10s)-4-(3-methylbut-2-en-1-yl)-8,17-dioxatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]heptadeca-2(7),3,5,11,13,15-hexaene-5,14-diol
(1s,12s,13s,16r,18r)-18-(hydroxymethyl)-16,18-dimethyl-17-oxapentacyclo[11.4.1.0¹,¹⁰.0³,⁸.0¹²,¹⁶]octadeca-3,5,7,10-tetraene-2,9-dione
(4bs,10ar)-4b,9-dihydroxy-7-methoxy-11,11-dimethyl-10h,10ah-benzo[b]fluoren-5-one
5-(prop-1-en-1-yl)-2-(2,4,5-trimethoxyphenyl)-1-benzofuran
5-hydroxy-2,2-dimethyl-7-(2-phenylethyl)chromene-6-carboxylic acid
13-hydroxy-6-isopropyl-12,12-dimethyltricyclo[9.4.0.0³,⁸]pentadeca-1,3(8),6,10,14-pentaene-4,5,9-trione
5-[(2r,3r)-7-methoxy-3-methyl-5-[(1e)-prop-1-en-1-yl]-2,3-dihydro-1-benzofuran-2-yl]-2h-1,3-benzodioxole
4-[(3r)-8,8-dimethyl-2h,3h,4h-pyrano[3,2-g]chromen-3-yl]benzene-1,3-diol
(2r)-5-hydroxy-2-(4-hydroxyphenyl)-6-(3-methylbut-2-en-1-yl)-2,3-dihydro-1-benzopyran-4-one
5-{7,8-dimethyl-2h,6h,7h,8h,9h-naphtho[1,2-d][1,3]dioxol-9-yl}-2h-1,3-benzodioxole
1-{2,6-dihydroxy-4-[(3-methylbut-2-en-1-yl)oxy]phenyl}-3-phenylprop-2-en-1-one
5-[(2s,3s)-7-methoxy-3-methyl-5-(prop-2-en-1-yl)-2,3-dihydro-1-benzofuran-2-yl]-2h-1,3-benzodioxole
3-benzyl-5-hydroxy-6-[(4-hydroxyphenyl)methyl]-1-methyl-3,6-dihydropyrazin-2-one
(3s,4ar,10bs)-3-(4-hydroxyphenyl)-9-methoxy-3h,4ah,5h,6h,10bh-benzo[f]chromen-8-ol
2-methoxy-4-[7-methoxy-3-methyl-5-(prop-2-en-1-yl)-1-benzofuran-2-yl]phenol
7,11-dihydroxy-4,4,9,11b-tetramethyl-1h-phenanthro[3,2-b]furan-6-one
(8e,13s)-13-hydroxy-4-methoxy-2-oxatricyclo[13.2.2.1³,⁷]icosa-1(17),3(20),4,6,8,15,18-heptaen-12-one
4-[2,3-diisocyano-4-(4-methoxyphenyl)but-2-en-1-yl]-4-hydroxycyclohexan-1-one
3-[2-(2h-1,3-benzodioxol-5-yl)-3-methyl-1-benzofuran-5-yl]butan-2-ol
2,5,11-trimethoxy-3,8-dimethylcyclohepta[a]naphthalen-9-one
(2s)-7-hydroxy-2-[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]-2,3-dihydro-1-benzopyran-4-one
1,4-dihydroxy-4b,7,8-trimethyl-2-(prop-2-en-1-yl)-5h-phenanthrene-3,6-dione
(2e)-1-[(4s)-4,5-dihydroxy-2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl]-3-phenylprop-2-en-1-one
7-hydroxy-8-(3-hydroxy-3-methylbut-1-en-1-yl)-2-phenyl-2,3-dihydro-1-benzopyran-4-one
18-(hydroxymethyl)-16,18-dimethyl-17-oxapentacyclo[11.4.1.0¹,¹⁰.0³,⁸.0¹²,¹⁶]octadeca-3,5,7,10-tetraene-2,9-dione
2-methoxy-4-[7-methoxy-3-methyl-5-(prop-1-en-1-yl)-1-benzofuran-2-yl]phenol
(13r)-13-hydroxy-6-isopropyl-12,12-dimethyltricyclo[9.4.0.0³,⁸]pentadeca-1,3(8),6,10,14-pentaene-4,5,9-trione
(2s)-7-hydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-en-1-yl)-2,3-dihydro-1-benzopyran-4-one
12-hydroxy-4-methoxy-2-oxatricyclo[13.2.2.1³,⁷]icosa-1(17),3(20),4,6,11,15,18-heptaen-10-one
11-hydroxy-4-methyl-9-(2-phenylethyl)-6-oxatricyclo[5.4.0.0²,⁴]undeca-1(11),7,9-triene-10-carboxylic acid
(1r,10r)-10-(3-methylbut-2-en-1-yl)-8,17-dioxatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]heptadeca-2,4,6,11,13,15-hexaene-5,14-diol
5-methoxy-2,2-dimethyl-6-[(1z)-3-methylbuta-1,3-dien-1-yl]pyrano[2,3-h]chromen-8-one
5-[7-methoxy-3-methyl-5-(prop-1-en-1-yl)-2,3-dihydro-1-benzofuran-2-yl]-2h-1,3-benzodioxole
2-[(1r,7r,12r)-6,11,19-trioxapentacyclo[10.8.0.0²,¹⁰.0⁵,⁹.0¹³,¹⁸]icosa-2(10),3,5(9),13,15,17-hexaen-7-yl]propan-2-ol
(2r)-8-hydroxy-2-methyl-2-(4-methylpent-3-en-1-yl)benzo[g]chromene-5,10-dione
(3r)-7-hydroxy-3-methyl-3-(4-methylpent-3-en-1-yl)cyclohexa[f]chromene-9,10-dione
7-hydroxy-2-methoxy-8-(3-methylbut-2-en-1-yl)-9,10-dihydrophenanthrene-1,4-dione
(2r)-5,7-dihydroxy-6-(3-methylbut-2-en-1-yl)-2-phenyl-2,3-dihydro-1-benzopyran-4-one
(2r)-7-hydroxy-2-[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]-2,3-dihydro-1-benzopyran-4-one
(2s)-5-hydroxy-7-methoxy-8-(2-methylprop-1-en-1-yl)-2-phenyl-2,3-dihydro-1-benzopyran-4-one
15-(3-methylbut-2-en-1-yl)-8,17-dioxatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]heptadeca-2,4,6,11(16),12,14-hexaene-5,14-diol
(1s,13r)-13-ethyl-20-oxa-9,17-diazapentacyclo[11.7.0.0¹,¹⁷.0²,¹⁰.0³,⁸]icosa-2(10),3,5,7-tetraene-18,19-dione
1-[4-hydroxy-2-(prop-1-en-2-yl)-2,3-dihydro-1-benzofuran-5-yl]-3-(4-hydroxyphenyl)propan-1-one
(4br,10as)-8,9-dihydroxy-7-methoxy-11,11-dimethyl-4bh,10h,10ah-benzo[b]fluoren-5-one
8-[(3r)-7-hydroxy-3,4-dihydro-2h-1-benzopyran-3-yl]-2,2-dimethylchromen-5-ol
(3s,6s)-3-benzyl-5-hydroxy-6-[(4-hydroxyphenyl)methyl]-1-methyl-3,6-dihydropyrazin-2-one
(2r,11r)-17,17-dimethyl-4,12,18-trioxapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-1(13),5,7,9,14(19),20-hexaen-7-ol
5-[7-methoxy-3-methyl-5-(prop-2-en-1-yl)-2,3-dihydro-1-benzofuran-2-yl]-2h-1,3-benzodioxole
(8z,10e,12r)-4-methoxy-2-oxatricyclo[13.2.2.1³,⁷]icosa-1(17),3(20),4,6,8,10,15,18-octaene-5,12-diol
(1r,10s)-15-(3-methylbut-2-en-1-yl)-8,17-dioxatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]heptadeca-2,4,6,11(16),12,14-hexaene-5,14-diol
5-[6-methoxy-5-(3-methylbut-2-en-1-yl)-1-benzofuran-2-yl]benzene-1,3-diol
5-hydroxy-1-(4-hydroxy-3-methoxyphenyl)-7-phenylhepta-4,6-dien-3-one
(2s)-8-hydroxy-2-methyl-2-(4-methylpent-3-en-1-yl)benzo[g]chromene-5,10-dione
1-[(2r,6r)-5,5-dimethyl-3-oxo-4,13-diazatetracyclo[6.6.1.0²,⁶.0¹²,¹⁵]pentadeca-1(14),8(15),9,11-tetraen-4-yl]butane-1,3-dione
2-{6,11,19-trioxapentacyclo[10.8.0.0²,¹⁰.0⁵,⁹.0¹³,¹⁸]icosa-2(10),3,5(9),13,15,17-hexaen-7-yl}propan-2-ol
(1r,10r)-4-(3-methylbut-2-en-1-yl)-8,17-dioxatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]heptadeca-2(7),3,5,11,13,15-hexaene-5,14-diol
2-(4-hydroxy-2-methoxyphenyl)-5-(2-methylbut-3-en-2-yl)-1-benzofuran-6-ol
(4as,12br)-9-hydroxy-2,5,5-trimethyl-3,4,4a,12b-tetrahydro-6-oxatetraphene-7,12-dione
5-methoxy-2,2-dimethyl-6-[(1e)-3-methylbuta-1,3-dien-1-yl]pyrano[2,3-h]chromen-8-one
(12s,18s)-14-oxa-1,10-diazapentacyclo[15.3.1.0³,¹¹.0⁴,⁹.0¹²,¹⁸]henicosa-3(11),4,6,8,16-pentaene-12-carboxylic acid
5-hydroxy-7-methoxy-8-(2-methylprop-1-en-1-yl)-2-phenyl-2,3-dihydro-1-benzopyran-4-one
(4bs)-1,4-dihydroxy-4b,7,8-trimethyl-2-(prop-2-en-1-yl)-5h-phenanthrene-3,6-dione
5-(6-methoxy-1-benzofuran-2-yl)-2-(3-methylbut-2-en-1-yl)benzene-1,3-diol
5-(1-chlorohex-3-en-5-yn-1-yl)-7-ethyl-2,2-dimethyl-3ah,4h,5h,7h,9ah-[1,3]dioxolo[4,5-d]oxocine
C18H25ClO3 (324.14921300000003)
(2s,3r)-3-[2-(2h-1,3-benzodioxol-5-yl)-3-methyl-1-benzofuran-5-yl]butan-2-ol
2-hydroxy-5'-methyl-4'-oxa-12'-azaspiro[indole-3,10'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-ene-6'-carbaldehyde
5-[(1e)-prop-1-en-1-yl]-2-(2,4,5-trimethoxyphenyl)-1-benzofuran
8-(4-hydroxy-3-methoxyphenyl)-3-methoxy-6,7-dimethylnaphthalen-2-ol
3-hydroxy-17-methoxytricyclo[12.3.1.1²,⁶]nonadeca-1(18),2(19),3,5,14,16-hexaene-7,11-dione
(1's,2'r,3s,7'r,9's)-2-hydroxy-5'-methyl-4'-oxa-12'-azaspiro[indole-3,10'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-ene-6'-carbaldehyde
1-(5-hydroxy-2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl)-3-(4-hydroxyphenyl)prop-2-en-1-one
(4br,10ar)-8,9-dihydroxy-7-methoxy-11,11-dimethyl-4bh,10h,10ah-benzo[b]fluoren-5-one
5-[(5s,6s,7r)-6,7-dimethyl-2h,5h,6h,7h,8h-naphtho[2,3-d][1,3]dioxol-5-yl]-2h-1,3-benzodioxole
(4br,10ar)-4b,9-dihydroxy-7-methoxy-11,11-dimethyl-10h,10ah-benzo[b]fluoren-5-one
1-[(1's,2'r,3s,7'r,9's)-2-hydroxy-4'-oxa-12'-azaspiro[indole-3,10'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-6'-yl]ethanone
(11e)-12-hydroxy-4-methoxy-2-oxatricyclo[13.2.2.1³,⁷]icosa-1(17),3(20),4,6,11,15,18-heptaen-10-one
3-(4-hydroxyphenyl)-9-methoxy-3h,4ah,5h,6h,10bh-benzo[f]chromen-8-ol
(3ar,5r,7r,9ar)-5-[(1r,3e)-1-chlorohex-3-en-5-yn-1-yl]-7-ethyl-2,2-dimethyl-3ah,4h,5h,7h,9ah-[1,3]dioxolo[4,5-d]oxocine
C18H25ClO3 (324.14921300000003)