Exact Mass: 330.16784459999997
Exact Mass Matches: 330.16784459999997
Found 500 metabolites which its exact mass value is equals to given mass value 330.16784459999997,
within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error
0.01 dalton.
Carnosol
Carnosol is a naturally occurring phenolic diterpene found in rosemary (Rosemarinus officinalis, Labiatae). It has been known that an extract of rosemary leaves contains high antioxidative activity. Ninety percent of this antioxidative activity can be attributed to carnosol and carnosic acid. Carnosic acid is easily converted to carnosol by oxidation. Carnosol has multiple beneficial medicinal effects including anti-inflammatory, anti-microbial and anti-cancer activities in various disease models. Carnosol may possess important neuroprotective effects against rotenone-induced DA neuronal damage. Naturally occurring antioxidants reduce the risk of neurodegenerative diseases. In addition, carnosol and carnosic acid promoted the synthesis of nerve growth factor in glial cells. Carnosol-mediated neuroprotection in DA neurons is involved in the attenuation of caspase-3 activity, which was induced by rotenone. Furthermore, carnosol-mediated tyrosine hydroxylase (TH) increase, which is dependent on the Raf-mitogen-activated protein kinase (MEK)-extracellular signal-regulated kinase (ERK)1/2 signaling pathway, is responsible for the neuroprotection in SN4741 DA cells. (PMID: 17047462). Carnosol, a phenolic diterpene compound of the labiate herbs rosemary and sage, is an activator of the human peroxisome proliferator-activated receptor gamma (PPARgamma), a ligand activated transcription factor, belonging to the metazoan family of nuclear hormone receptors. Activation of PPARgamma increases the transcription of enzymes involved in primary metabolism, leading to lower blood levels of fatty acids and glucose. Hence, PPARgamma represents the major target for the glitazone type of drugs currently being used clinically for the treatment of type 2 diabetes. (PMID: 16858665). Bitter principle in Salvia carnosa, Salvia officinalis (sage), Salvia triloba (Greek sage) and Rosmarinus officinalis (rosemary). Nutriceutical with anticancer props. Carnosol is a diterpenoid. Carnosol is a natural product found in Podocarpus rumphii, Lepechinia salviae, and other organisms with data available.
Picrocrocin
Picrocrocin is a glycoside formed from glucose and safranal. It is found in the spice saffron, which comes from the crocus flower. Picrocrocin has a bitter taste and is the chemical most responsible for the taste of saffron. It is believed that picrocrocin is a degradation product of the carotenoid zeaxanthin (Wikipedia). Picrocrocin is a beta-D-glucoside of beta-cyclocitral; the precursor of safranal. It is the compound most responsible for the bitter taste of saffron. It is functionally related to a beta-cyclocitral. Picrocrocin is a natural product found in Crocus tommasinianus, Crocus sativus, and Crocus vernus with data available. Isolated from saffron (stamens of Crocus sativus). Food colour and flavouring ingredient Picrocrocin, an apocarotenoid found in Saffron. Picrocrocin shows anticancer effect. Picrocrocin exhibits growth inhibitory effects against SKMEL-2 human malignant melanoma cells[1]. Picrocrocin, an apocarotenoid found in Saffron. Picrocrocin shows anticancer effect. Picrocrocin exhibits growth inhibitory effects against SKMEL-2 human malignant melanoma cells[1].
Dicyclohexyl phthalate
CONFIDENCE standard compound; INTERNAL_ID 998; DATASET 20200303_ENTACT_RP_MIX500; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 10526; ORIGINAL_PRECURSOR_SCAN_NO 10521 CONFIDENCE standard compound; INTERNAL_ID 998; DATASET 20200303_ENTACT_RP_MIX499; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 10560; ORIGINAL_PRECURSOR_SCAN_NO 10557 CONFIDENCE standard compound; INTERNAL_ID 998; DATASET 20200303_ENTACT_RP_MIX500; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 10461; ORIGINAL_PRECURSOR_SCAN_NO 10459 CONFIDENCE standard compound; INTERNAL_ID 998; DATASET 20200303_ENTACT_RP_MIX499; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 10525; ORIGINAL_PRECURSOR_SCAN_NO 10523 CONFIDENCE standard compound; INTERNAL_ID 998; DATASET 20200303_ENTACT_RP_MIX499; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 10437; ORIGINAL_PRECURSOR_SCAN_NO 10436 CONFIDENCE standard compound; INTERNAL_ID 998; DATASET 20200303_ENTACT_RP_MIX500; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 10483; ORIGINAL_PRECURSOR_SCAN_NO 10481 CONFIDENCE standard compound; INTERNAL_ID 998; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3962; ORIGINAL_PRECURSOR_SCAN_NO 3958 CONFIDENCE standard compound; INTERNAL_ID 998; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3999; ORIGINAL_PRECURSOR_SCAN_NO 3998 CONFIDENCE standard compound; INTERNAL_ID 998; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3955; ORIGINAL_PRECURSOR_SCAN_NO 3952 CONFIDENCE standard compound; INTERNAL_ID 998; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3967; ORIGINAL_PRECURSOR_SCAN_NO 3965 CONFIDENCE standard compound; INTERNAL_ID 998; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3986; ORIGINAL_PRECURSOR_SCAN_NO 3983 CONFIDENCE standard compound; INTERNAL_ID 998; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3985; ORIGINAL_PRECURSOR_SCAN_NO 3982 CONFIDENCE standard compound; INTERNAL_ID 8270 CONFIDENCE standard compound; INTERNAL_ID 2506
Gibberellin A15
A C20-gibberellin that is the lactone form of gibberellin A15.
methyl gibberellin A9
Proparacaine Hydrochloride
C16H27ClN2O3 (330.17101019999996)
D002491 - Central Nervous System Agents > D002492 - Central Nervous System Depressants > D000777 - Anesthetics D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents C78272 - Agent Affecting Nervous System > C245 - Anesthetic Agent
Portuloside A
Portuloside A is found in green vegetables. Portuloside A is a constituent of Portulaca oleracea (purslane) Constituent of Portulaca oleracea (purslane). Portuloside A is found in green vegetables.
3,3',4,4'-Tetrahydroxy-5,5'-diisopropyl-2,2'-dimethylbiphenyl
3,3,4,4-Tetrahydroxy-5,5-diisopropyl-2,2-dimethylbiphenyl is found in herbs and spices. 3,3,4,4-Tetrahydroxy-5,5-diisopropyl-2,2-dimethylbiphenyl is a constituent of Thymus vulgaris (thyme). Constituent of Thymus vulgaris (thyme). 3,3,4,4-Tetrahydroxy-5,5-diisopropyl-2,2-dimethylbiphenyl is found in herbs and spices.
(1S,4R)-10-Hydroxyfenchone glucoside
(1S,4R)-10-Hydroxyfenchone glucoside is found in herbs and spices. (1S,4R)-10-Hydroxyfenchone glucoside is a constituent of Foeniculum vulgare (fennel). Constituent of Foeniculum vulgare (fennel). (1S,4R)-10-Hydroxyfenchone glucoside is found in herbs and spices.
Momilactone B
Momilactone B is found in cereals and cereal products. Momilactone B is a constituent of Oryza sativa (rice) Momilactone B is an allelopathic agent produced from the roots of rice (Oryza sativa L.) (100 mg from 200 kg dry rice husk). It has been shown to be produced in high concentrations by the roots of rice seedlings. The production of momilactone B has also been induced in response to infection by blast fungus (Pyricularia oryzae) or irradiated with UV light. More recently is has been shown to be a potential chemotherapeutic agent against human colon cancer. The second step is the cyclization of syn-CDP to 9 -pimara-7,15-diene. This step is initiated by the elimination of the diphosphate group, a type A cyclization. The genes encoding for the type A cyclase were found by Otomo et al. in 2004. It is suggested that OsKS4, located on chromosome 4 (14.3cM) is one of the genes responsible for phytoalexin biosynthesis. After UV-radiation, OsKS4 mRNA levels rise drastically in response to the attack. Constituent of Oryza sativa (rice)
Epijasminoside A
Epijasminoside A is a constituent of Saffron (Crocus sativus). Constituent of Saffron (Crocus sativus).
(1R,4R,5S)-5-Hydroxyfenchone glucoside
(1R,4R,5S)-5-Hydroxyfenchone glucoside is found in herbs and spices. (1R,4R,5S)-5-Hydroxyfenchone glucoside is a constituent of Foeniculum vulgare (fennel). Constituent of Foeniculum vulgare (fennel). (1R,4R,5S)-5-Hydroxyfenchone glucoside is found in herbs and spices.
6-Hydroxy-2-bornanone glucoside
6-Hydroxy-2-bornanone glucoside is found in herbs and spices. 6-Hydroxy-2-bornanone glucoside is a constituent of Foeniculum vulgare (fennel) Constituent of Foeniculum vulgare (fennel). 6-Hydroxy-2-bornanone glucoside is found in herbs and spices.
Yucalexin P15
Yucalexin P15 is found in root vegetables. Yucalexin P15 is a constituent of cassava roots (Manihot esculenta). Constituent of cassava roots (Manihot esculenta). Yucalexin P15 is found in root vegetables.
(4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside
(4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside is found in herbs and spices. (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside is a constituent of fruit of Carum carvi (caraway). Constituent of fruit of Carum carvi (caraway). (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside is found in herbs and spices.
(3b,4b,5b)-4,5-Epoxy-p-menth-1-en-3-ol 3-glucoside
(3b,4b,5b)-4,5-Epoxy-p-menth-1-en-3-ol 3-glucoside is a constituent of Carum ajowan (ajowan). Constituent of Carum ajowan (ajowan)
(1R,4S,6R)-6-Hydroxyfenchone glucoside
(1R,4S,6R)-6-Hydroxyfenchone glucoside is found in herbs and spices. (1R,4S,6R)-6-Hydroxyfenchone glucoside is a constituent of Foeniculum vulgare (fennel). Constituent of Foeniculum vulgare (fennel). (1R,4S,6R)-6-Hydroxyfenchone glucoside is found in herbs and spices.
Yucalexin P8
Yucalexin P10 is found in root vegetables. Yucalexin P10 is a constituent of cassava Manihot esculenta.
4-({4-[(2,4,6-Trimethylphenyl)amino]-1,3,5-triazin-2-yl}amino)benzonitrile
(R)-4-(2-(2-(2-Methylpyrrolidin-1-yl)ethyl)benzofuran-5-yl)benzonitrile
D018377 - Neurotransmitter Agents > D018494 - Histamine Agents > D006633 - Histamine Antagonists
Pirsidomine
Gibberellin A15
Gibberellin a15 is a member of the class of compounds known as c19-gibberellin 6-carboxylic acids. C19-gibberellin 6-carboxylic acids are c19-gibberellins with a carboxyl group at the 6-position. Gibberellin a15 is practically insoluble (in water) and a weakly acidic compound (based on its pKa). Gibberellin a15 can be found in a number of food items such as winter squash, common pea, common wheat, and chayote, which makes gibberellin a15 a potential biomarker for the consumption of these food products.
meso-Dihydroguaiaretic acid
Meso-dihydroguaiaretic acid is a lignan that is 2,3-dimethylbutane substituted by 2-methoxyphenol groups at positions 1 and 4 respectively. It has been isolated from the bark of Machilus robusta. It has a role as a plant metabolite. It is a lignan and a member of guaiacols. Meso-dihydroguaiaretic acid is a natural product found in Kadsura angustifolia, Kadsura heteroclita, and other organisms with data available. See also: Larrea tridentata whole (part of). A lignan that is 2,3-dimethylbutane substituted by 2-methoxyphenol groups at positions 1 and 4 respectively. It has been isolated from the bark of Machilus robusta. Dihydroguaiaretic acid, is isolated from the fruits of Saururus chinensis with an anti-cancer activty[1]. Dihydroguaiaretic acid, is isolated from the fruits of Saururus chinensis with an anti-cancer activty[1].
(7Z)-Lobohedleolide
A cembrane diterpenoid isolated from Lobophytum hedleyi and Lobophytum. It exhibits anti-HIV-1 activity.
[1aS-[1aalpha,4alpha,4aalpha,5alpha(Z),9aS*]]-1a,2,4,4a,5,9-Hexahydro-4,4a,6-trimethyl-3H-oxireno[8,8a]naphtho[2,3-b]furan-5-yl ester 2-methyl-2-butenoic acid
[4S-(4alpha,4aalpha,5alpha,8abeta)]-4,4a,5,6,7,8,8a,9-Octahydro-3,4a,5-trimethyl-9-oxonaphtho[2,3-b]furan-4-yl ester 3-methyl-2-butenoic acid
dihydroguaiaretic acid
Dihydroguaiaretic acid, is isolated from the fruits of Saururus chinensis with an anti-cancer activty[1]. Dihydroguaiaretic acid, is isolated from the fruits of Saururus chinensis with an anti-cancer activty[1].
2alpha-(Angelyloxy)-9-oxo-10alphaH-furoeremophilane
6beta-Angeloyloxy-10alphaH-9-oxofuranoeremophilane
1,1,5-Trimethyl-2-hydroxymethyl-(5)-cyclohexene-(4)-one-O-beta-D-glucopyranoside
[4S-(4alpha,4aalpha,5alpha)]-4,4a,5,6,7,9-Hexahydro-3,4a,5-trimethyl-9-oxonaphtho[2,3-b]furan-4-yl ester 3-methylbutanoic acid
[4R-(4alpha,4aalpha,5beta)]-4,4a,5,6,7,9-Hexahydro-5-hydroxy-3,4a,5-trimethylnaphtho[2,3-b]furan-4-yl ester 3-methyl-2-butenoic acid
[1aR-(1aalpha,4beta,4abeta,5beta,9aS*)]-1a,2,4,4a,5,9-Hexahydro-4,4a,6-trimethyl-3H-oxireno[8,8a]naphtho[2,3-b]furan-5-yl ester 3-methyl-2-butenoic acid
8alpha-Isovaleryloxygazaniolide
3-(4-Geranyloxy-3-methoxyphenyl)-2-trans propenoic acid
11,12-Dihydroxy-6,8,11,13-abietatetraen-20-oic acid
4-decyl-3-hydroxy-5-oxooxolane-2,3-dicarboxylic acid
3-(5-hydroxyprenyl)-5-prenyl-7E-p-coumaric acid|3-<5-hydroxyprenyl>-5-prenyl-7E-p-coumaric acid
(1R,4R,5R)-5-hydroxybornan-2-one 5-O-beta-D-glucopyranoside
5b,6-epoxydecahydro-7-hydroxy-3-isopropyl-3a,5a-dimethyl-8-methylene-4H-pentaleno[1,6a-a]pentalene-4,5(5aH)-dione|crinipellin C|rel-(1aR,2S,3aR,4aR,7R,7aR,9aS,9bR)-octahydro-2-hydroxy-7a,9a-dimethyl-3-methylene-7-(1-methylethyl)-3H,8H-pentaleno[6a,1: 5,6]pentaleno[1,6a-b]oxirene-8,9(9aH)-dione
8beta,12:15,16-diepoxy-cis-ent-cleroda-13(16),14-dien-18alpha,6alpha-olide
(6R)-menthiafolic acid 6-O-beta-D-quinovoside|(6R)-menthiafolic acid-6-O-beta-D-quinovoside|menthiafolic acid 6-O-beta-D-quinovopyranoside
6,12-dihydroxyabieta-5,8,11,13-tetraene-7-one|fortunin F
(-)-10,13-dihydroxy-9-methyl-15-oxo-20-norkaur-16-en-18-ioc acid, gamma-lactone|13-hydroxy-15-oxozoapatlin
(15R)-12,16-epoxy-11,14-dihydroxy-8,11,13-abietatrien-7-one|hyptol
2,19;15,16-Diepoxy-neo-clerodan-3,13(16),14-trien-18-oic acid
(-)-cis-cleroda-1,3,13-trien-15,18-dioic acid-15,16-olide
2-Methoxy-6-(2-methoxy-4-propylphenoxy)-4-propylphenol
(-)-(4S,5S,8R,10R)-8,18-dihydroxy-12-oxo-abieta-9(11),13-dien-20-oic acid 18,20-lactone
An abietane diterpenoid isolated from the stem bark of Fraxinus sieboldiana.
15,16-epoxy-6alpha-hydroxy-cleroda-3,4,13(16),14-trien-12,10alpha,19-acetal|parvitexin C
6beta-tigloyloxy-furanoeremophil-1(10)-en-3beta-ol
ent-7-Oxo-6,7-secokaur-16-en-6,19-dicarbonsaeureanhydrid|Fujenal
8,9;15,16-Diepoxy-11-oxo-12-cleistanthen-17-al-(ent-8alpha,9alpha,14alphaH)-form
3-(5-methoxyprenyl)-5-prenyl-7E-p-coumaric acid|3-<5-methoxyprenyl>-5-prenyl-7E-p-coumaric acid
(-)-15,16-epoxy-cis-cleroda-1,13(16),14-trien-12-hydroxy-18-oic acid-18,6alpha-olide
1-O-beta-D-Glucopyranoside-1-Hydroxy-3,7-dimethyl-2,6-octadien-5-one|3,7-dimethyl-2(E),6-octadien-5-one-1-O-beta-D-glucoside
6-Ketone-(2alpha,6alpha)-2,6,11-Trihydroxy-7,9(11),13-abietatrien-12-one
6-Angloyl-(6beta,9beta)-Furanoeremophil-1(10)-ene-6,9-diol
11alpha-hydroxy-3-(1-hydroxy-1-methylethyl)-13beta-isopropyl-5-methyl-1,2,3beta,11,13,14beta-hexahydro-13,14-oxacyclopropa[a]phenalen-12-one|proinoid A
12(S)-hydroxy-15,16-epoxy-8(17),13(16),14-ent-labdatrien-20,19-olide
(+)-(5S,6S,7S,10R)-6,7,12-trihydroxyabieta-8,11,13-trien-20-oic acid 6,20-lactone
3,7-dimethyl-3(Z),6-octadien-5-one-1-O-beta-D-glucoside
6,12,15-trihydroxy-5,8,11,13-abietatetraen-7-one|6,12,15-trihydroxy-5,8,11,13-abietatetraene-7-one|6,12,15-trihydroxy-5,8,11,13-abietetriene-7-one
beta-D-glucopyranosyl 2,6,6-trimethylcyclohex-1-ene-1-carboxylate|jasminoside K
2,3-Dihydroxy-17beta-acetoxy-oestratrien-(1,3,5(10))|2-Hydroxy-oestradiol-monoacetat-(17beta)|Oestra-1,3,5(10)-trien-2,3,17beta-triol-17-acetat
3-Ac-(16alpha,17betaOH)-Estra-1,3,5(10)-triene-3,16,17-triol
7alpha-17(15-16)-Abeo-7,12-dihydroxy-8,12,16-abietatriene-11,14-dione
(7R,8R)-7-hydroxy-7-methyl-8-(2-oxoheptyl)-3-((E)-prop-1-enyl)-7,8-dihydro-6H-isochromen-6-one|monapurone A
(1E,6E)-xenica-1(9),6,13-triene-17,18:19,18-diolide
6beta-(2-methylbutanoyloxy)-9-oxo-1(10)-furanoeremophilene
3-(beta-D-Glucopyranosyloxymethyl)-2,4,4-trimethyl-2-cyclohexen-1-one|jasminoside E
1beta,12:15,16-diepoxy-cis-ent-cleroda-13(16),14-dien-18alpha,6alpha-olide
(-)-Borneol glucuronide|O1-((1S)-bornyl)-beta-D-glucopyranuronic acid|O1-((1S)-Bornyl)-beta-D-glucopyranuronsaeure
15-Ac-(15alpha,17beta)-Estra-1,3,5(10)-triene-3,15,17-triol
8,12-epoxy-2-[(senecioyl)oxy]eremophil-7,11-dien-9-one
1beta-senecioyloxy-5betaH,6alphaH,7alphaH,10alphaMe,11alphaH-eudesma-2,4(15)-dien-6,12-olide
8-hydroxy-alpha-thujone-(beta-D-glucopyranoside)|8-hydroxy-alpha-thujone-|8-O-beta-Glucopyranoside-8-Hyddroxy-3-thujanone
1-Aldehyde,8-O-beta-D-glucopyranoside-(E)-2-Methyl-6-methylene-2-octene-1,8-diol
(5S*,8S*,9R*,10S*)-11beta,12beta-epoxy-9alpha-hydroxy-19(4->3)abeo-abieta-3,13-diene-19,18-olide
jatrophodione A|rel-(1aR,3aR,7azeta,9S,9aS,9bR)-1a,2,3,3a,7a,9,9a,9b-octahydro-9-hydroxy-1,1,3a,6,9-pentamethyl-1H-cyclopropa[3,4]benz[1,2-f]azulene-5,8-dione
1,10a-Dihydroxy-3a,8,10b-trimethyl-8-vinyl-2,3,3a,4,9,10,10a,10b-octahydro-1H-phenanthro[10,1-bc]furan-6(8H)-one
13-hydroxy-14-isopropyl-7-oxo-8,11,13-podocarpatrien-19-oic acid|inumakiol G
mkapwanin|neo-clerodan-3,13-dien-16,15:18,19-diolide
(Z)-3,6-dimethyl-3-(beta-D-glucosylmethyl)cyclohept-4-enone
(1S*,2S*,12R*,13R*,3E,7E)-12,13-epoxy-11-oxocembra-3,7,15(17)-trien-16,2-olide|crassocolide N
3,4,15,16-diepoxy-cleroda-13(16),14-diene-12,17-olide
ent-11,12-dihydroxyabieta-7-oxo-8,11,13-trien-15-ol
12-hydroxy-7-oxo-dehydroabietic acid|liquiditerpenoic acid A
13-hydroxy-12-isopropyl-8,11,13-podocaratrien-18-oic acid|liquiditerpenoic acid B
(2-methylbutyryloxy)-isovaleryloxy-dehydrocostus|<2-methylbutyryloxy>-isovaleryloxy-dehydrocostus
5-alpha-Hydroxy-1,2-dehydro-5,10-dihydroprintzianic acid
1betaH,5betaH,6alphaH,7alphaH-11alpha-angeloyloxyguaia-3(4),10(14)-dien-6,7-olide
(1S,2S,3S,6E,7S,9R,10S,13R)-13-ethenyl-6-ethylidene-1,9,12,12-tetramethyl-4,8-dioxatetracyclo[8.3.1.02,9.03,7]tetradecane-5,11-dione|Pallavicinin
4-Me ether-(alphaE)-3-(10-Hydroxygeranyl)-p-coumaric acid
(ent-2alpha,5beta)-15,16-Epoxy-2-hydroxy-1(10),13(16),14-clerodatrien-18,19-olide
3beta-angeloyloxy-6alpha,14-epoxyfuranoereomphilane
1beta,16:15,16-diepoxy-cis-ent-cleroda-12,14-dien-18alpha,6alpha-olide
3,12-dioxo-15,16-epoxy-cleroda-13(16),14-dien-9-al
13-hydroxy-14-isopropyl-2-oxo-8,11,13-podocarpatrien-19-oic acid|inumakiol C
1,1-Dimethyl-5,6-dihydroxy-7-isopropyl-1,2,3,4,4a,10a-hexahydrophenanthrene-4a-carboxylic acid
3,4,18beta-cyclopropa-8beta-hydroxy-14-oxo-ent-abiet-13,15-en-16,12-olide|retusolide A
6beta-<2-methyl-2-vinylacetoxy>-furoeremophil-9-one
1,14-dioxo-4-hydroxycyatha-2,11-diene-12-carbaldehyde|cyrneine D
7-hydroxy-6-oxo-7,11,13-labdatrien-16,15-olide|hedychilactone D
(-)-(1beta,3Z,6beta,7E,9beta,20alpha)-6,20-dihydroxy-10-oxoverticilla-3,7,11-trien-18-al|cespihypotin Y
19-hydroxy-3-oxo-ent-labda-8(17),11,13-trien-16,15-olide
4,14-dihydroxy-1-oxocyatha-2,5(10),11-triene-12-carbaldehyde|cyrneine B
15-oxo-14,16H-seco-nidoresedic acid|15-oxo-14,16H-strictic acid
16-Ac-(16alpha,17betaOH)-Estra-1,3,5(10)-triene-3,16,17-triol
4-(3-Hydroxy-3-methylbutyl)-3,4,5-trimethoxybiphenyl|Tri-Me ether-3,4,5-Trihydroxy-4-(3-hydroxy-3-methylbutyl)biphenyl
1-[7,8-dihydro-7-hydroxy-7-methyl-8-oxo-3-(1E)-1-propenyl-6H-2-benzopyran]heptan-2-one|monarubrin
2-(4-Amino-4-carboxybutyrylamino)-6-oxodecanoic acid
TriptoquinoneB
Triptoquinone B is an abietane diterpenoid with formula C20H26O4, originally isolated from Tripterygium wilfordii. It has a role as a plant metabolite. It is a cyclic terpene ketone, a member of p-quinones, an abietane diterpenoid, a carbotricyclic compound, a tricyclic diterpenoid and a primary alcohol. Triptoquinone B is a natural product found in Tripterygium wilfordii and Tripterygium doianum with data available. An abietane diterpenoid with formula C20H26O4, originally isolated from Tripterygium wilfordii.
3-(2,5-dihydroxy-6-methyl-3-propan-2-ylphenyl)-2-methyl-5-propan-2-ylbenzene-1,4-diol
1-(4-hydroxy-3-methoxyphenyl)-7-phenylheptane-3,5-diol
C16H26O7_(2,6,6-Trimethyl-4-oxo-2-cyclohexen-1-yl)methyl beta-D-glucopyranoside
C20H26O4_15-Hydroxy-7-oxoabieta-8(14),9(11),12-trien-18-oic acid
C20H26O4_(6E,10Z,14E)-6,14-Dimethyl-3-methylene-2-oxo-2,3,3a,4,5,8,9,12,13,15a-decahydrocyclotetradeca[b]furan-10-carboxylic acid
C20H26O4_2-Propenoic acid, 3-(4-hydroxy-3-methoxyphenyl)-, 1,7,7-trimethylbicyclo[2.2.1]hept-2-yl ester, (2E)
(4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl) (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate
7-[2-(furan-3-yl)ethyl]-5-hydroxy-7,8-dimethyl-5,6,6a,8,9,10-hexahydro-1H-benzo[d][2]benzofuran-3-one
(6E,10Z,14E)-6,14-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,12,13,15a-octahydrocyclotetradeca[b]furan-10-carboxylic acid
(1R,4aS,10aR)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-9-oxo-3,4,10,10a-tetrahydro-2H-phenanthrene-1-carboxylic acid
(1R,4aS,10aR)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-9-oxo-3,4,10,10a-tetrahydro-2H-phenanthrene-1-carboxylic acid_major
7-[2-(furan-3-yl)ethyl]-5-hydroxy-7,8-dimethyl-5,6,6a,8,9,10-hexahydro-1H-benzo[d][2]benzofuran-3-one_major
(4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl) (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate_major
Ala Gly Pro Ser
Ala Gly Ser Pro
Ala Pro Gly Ser
Ala Pro Ser Gly
Ala Ser Gly Pro
Ala Ser Pro Gly
Gly Ala Pro Ser
Gly Ala Ser Pro
Gly Gly Pro Thr
Gly Gly Thr Pro
Gly Pro Ala Ser
Gly Pro Gly Thr
Gly Pro Ser Ala
Gly Pro Thr Gly
Gly Ser Ala Pro
Gly Ser Pro Ala
Gly Thr Gly Pro
Gly Thr Pro Gly
Pergolide sulfoxide
C19H26N2OS (330.17657460000004)
Pro Ala Gly Ser
Pro Ala Ser Gly
Pro Gly Ala Ser
Pro Gly Gly Thr
Pro Gly Ser Ala
Pro Gly Thr Gly
Pro Ser Ala Gly
Pro Ser Gly Ala
Pro Thr Gly Gly
Ser Ala Gly Pro
Ser Ala Pro Gly
Ser Gly Ala Pro
Ser Gly Pro Ala
Ser Pro Ala Gly
Ser Pro Gly Ala
Thr Gly Gly Pro
Thr Gly Pro Gly
Thr Pro Gly Gly
4,4-(2,3-Dimethyl-1,4-butanediyl)bis(2-methoxyphenol)
methyl (E)-4-((3aS)-6-methoxy-1-methyl-5-oxo-2,3,5,8a-tetrahydropyrrolo[2,3-b]indol-3a(1H)-yl)-2-methylbut-2-enoate
Epijasminoside A
(1R,4R,5S)-5-Hydroxyfenchone glucoside
(1R,4S,6R)-6-Hydroxyfenchone glucoside
(1S,4R)-10-Hydroxyfenchone glucoside
6-Hydroxy-2-bornanone glucoside
Momilacton b
Yucalexin P15
Yucalexin P8
An organic heterotetracyclic compound that is ent-pimara-9(11),15-diene which is substituted by oxo groups at position 2 and 12, by a beta-epoxide at the 8,14 position, and by an alpha-hydroxy group at position 3.
(3b,4b,5b)-4,5-Epoxy-p-menth-1-en-3-ol 3-glucoside
(4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside
3,3,4,4-Tetrahydroxy-5,5-diisopropyl-2,2-dimethylbiphenyl
7-[2-(3-Furyl)ethyl]-5-hydroxy-7,8-dimethyl-6,6a,7,8,9,10-hexahydronaphtho[1,8a-c]furan-3(5H)-one
6-[(2E,6E)-7-(5-Hydroxy-3-methyl-2-oxo-3-cyclopenten-1-yl)-6-methyl-2,6-heptadien-2-yl]-3-methyl-5,6-dihydro-2H-pyran-2-one
(((4-(Prop-1-en-2-yl)-1,3-phenylene)bis(oxy))bis(methylene))dibenzene
Ethyl 4-{[dimethyl(2-methyl-2-propanyl)silyl]oxy}-2-naphthoate
Poly(oxy-1,2-ethanediyl), .alpha.-(carboxymethyl)-.omega.-(4-isooctylphenoxy)-, sodium salt
1-BOC-3-(4-TRIFLUOROMETHYL-PHENYLAMINO)-PYRROLIDINE
1-BOC-3-([(3-TRIFLUOROMETHYL-PHENYL)-AMINO]-METHYL)-AZETIDINE
1-BOC-3-([(4-TRIFLUOROMETHYL-PHENYL)-AMINO]-METHYL)-AZETIDINE
4-(2-Ethoxybenzamido)-1-methyl-3-n-propylpyrazole-5-carboxamide
4-(naphthalene-2-yl)phenyl boronic acid pinacol ester
C22H23BO2 (330.17910079999996)
TERT-BUTYL 4-(1,3-DIOXOISOINDOLIN-2-YL)PIPERIDINE-1-CARBOXYLATE
n-(tert-butoxycarbonyl)-3-(4-(1-pyrrolyl)phenyl)-l-alanine
ABT-239
ABT-239 is a novel, highly efficacious, non-imidazole?class of H3R antagonist and a transient receptor potential vanilloid type 1 (TRPV1) antagonist.?
4,4,5,5-Tetramethyl-2-(2-(naphthalen-2-yl)phenyl)-1,3,2-dioxaborolane
C22H23BO2 (330.17910079999996)
(R)-Piperazine-1,2,4-tricarboxylic acid 1,4-di-tert-butyl ester
1-BOC-3-([(2-TRIFLUOROMETHYL-PHENYL)-AMINO]-METHYL)-AZETIDINE
(S)-1,4-Bis(tert-butoxycarbonyl)piperazine-2-carboxylic acid
2-hydroxyethyl 2-methylprop-2-enoate,2-methylidenebutanoic acid,methyl 2-methylprop-2-enoate
tert-Butyl 2,7-diazaspiro[4.5]decane-2-carboxylate
Diethyl (4-isopropyl-3,5-dimethoxybenzyl)phosphonate
methyl(S)-7,9-dimethyl-5-((2-methyl-2H-tetrazol-5-yl)amino)-2,3,4,5-tetrahydro-1H-benzo[b]azepine-1-carboxylate
C16H22N6O2 (330.18041519999997)
1-fluoro-2-methyl-benzene; 1-fluoro-3-methyl-benzene; 1-fluoro-4-methyl-benzene
N-(4-Acetamido-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acrylamide
C17H23BN2O4 (330.17507880000005)
3,3,5,5-Tetramethyl-4,4’-di(2-hydoxethanyoxy)-bibenzene
(S)-3-(4-aminonaphthalen-1-yl)-2-((tert-butoxycarbonyl)amino)propanoic acid
Propoxycaine hydrochloride
C16H27ClN2O3 (330.17101019999996)
D002491 - Central Nervous System Agents > D002492 - Central Nervous System Depressants > D000777 - Anesthetics D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents C78272 - Agent Affecting Nervous System > C245 - Anesthetic Agent
Lobohedleolide
A cembrane diterpenoid isolated from Lobophytum hedleyi and Lobophytum. It exhibits anti-HIV-1 activity.
N-[4-(dimethylamino)phenyl]-3,4,5-trimethoxybenzamide
hedychilactone D
A labdane diterpenoid that is 7,11,13-labdatrien-16,15-olide substituted by a hydroxy group at position 7 and an oxo group at position 6. Isolated from the rhizomes of Hedychium spicatum, it exhibits cytotoxicity against the Colo-205 (Colo-cancer), A-431 (skin cancer), MCF-7 (breast cancer), A-549 (lung cancer) and Chinese hamster ovary cells (CHO).
L-N(omega)-Nitroarginine-(4R)-amino-L-proline amide
3-(2,5-Dihydroxy-6-methyl-3-propan-2-ylphenyl)-2-methyl-5-propan-2-ylbenzene-1,4-diol
6,14-Dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,12,13,15a-octahydrocyclotetradeca[b]furan-10-carboxylic acid
1-(4-Hydroxy-3-methoxyphenyl)-7-phenylheptane-3,5-diol
(S)-reticulinium(1+)
C19H24NO4+ (330.17052440000003)
An ammonium ion that is the conjugate acid of (S)-reticuline, arising from protonation of the tertiary amino group; major species at pH 7.3.
(7S)-salutaridinol(1+)
C19H24NO4+ (330.17052440000003)
Conjugate acid of (7S)-salutaridinol.
(R)-reticulinium(1+)
C19H24NO4+ (330.17052440000003)
The conjugate acid of (R)-reticuline; major species at pH 7.3.
4-[[(1S)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinolin-2-ium-1-yl]methyl]-2-methoxyphenol
C19H24NO4+ (330.17052440000003)
3-Hydroxy-3,20:6,18-diepoxypimara-7,15-dien-18-one
(1R,2R,5R,8R,9S,10S,11S)-11-methyl-6-methylidene-12-oxo-13-oxapentacyclo[9.3.3.15,8.01,10.02,8]octadecane-9-carboxylic acid
(E)-7-(6-hydroxy-2,5,7,8-tetramethyl-3,4-dihydrochromen-2-yl)hept-5-ene-2,4-dione
(-)-(5S,6S,7S,10R)-6,7,12-trihydroxyabieta-8,11,13-trien-20-oic acid 6,20-lactone
An abietane diterpenoid isolated from the stem bark of Fraxinus sieboldiana.
(+)-(5S,6S,7R,10R)-6,7,12-trihydroxyabieta-8,11,13-trien-20-oic acid 6,20-lactone
An abietane diterpenoid isolated from the stem bark of Fraxinus sieboldiana.
2-[[[(1-Ethyl-3,5-dimethyl-4-pyrazolyl)methylamino]-oxomethyl]amino]benzoic acid methyl ester
N-tert-butyl-4-[3-(trifluoromethyl)-2-pyridinyl]-1-piperazinecarboxamide
2-[[4-(2-Methoxyanilino)-6-(1-pyrrolidinyl)-1,3,5-triazin-2-yl]amino]ethanol
C16H22N6O2 (330.18041519999997)
2-[[4-(3-Methoxyanilino)-6-(1-pyrrolidinyl)-1,3,5-triazin-2-yl]amino]ethanol
C16H22N6O2 (330.18041519999997)
2-[[4-(4-Methoxyanilino)-6-(1-pyrrolidinyl)-1,3,5-triazin-2-yl]amino]ethanol
C16H22N6O2 (330.18041519999997)
2-anilino-N-(3,5-dimethylphenyl)-2-phenylacetamide
1-[(5,7-Dimethyl-3-pyrazolo[1,5-a]pyrimidinyl)-oxomethyl]-4-piperidinecarboxylic acid ethyl ester
1-(3,4-Dihydroxybenzyl)-2,2-dimethyl-6-methoxy-7-hydroxy-1,2,3,4-tetrahydroisoquinoline-2-ium
C19H24NO4+ (330.17052440000003)
2-[(3S,6aS,8R,10aS)-3-hydroxy-1-(propylcarbamoyl)-3,4,6,6a,8,9,10,10a-octahydro-2H-pyrano[2,3-c][1,5]oxazocin-8-yl]acetic acid
2-[(3R,6aR,8R,10aR)-3-hydroxy-1-[oxo(propylamino)methyl]-3,4,6,6a,8,9,10,10a-octahydro-2H-pyrano[2,3-c][1,5]oxazocin-8-yl]acetic acid
2-[(3R,6aR,8S,10aR)-3-hydroxy-1-[oxo(propylamino)methyl]-3,4,6,6a,8,9,10,10a-octahydro-2H-pyrano[2,3-c][1,5]oxazocin-8-yl]acetic acid
N-[(3R,8Z,11R)-5,12-dioxo-3-phenyl-1-oxa-4-azacyclododec-8-en-11-yl]acetamide
2,6-Dimethyl-4-(2-pyridinyl)-3,4-dihydropyridine-3,5-dicarboxylic acid diethyl ester
2-[(3S,6aS,8S,10aS)-3-hydroxy-1-[oxo(propylamino)methyl]-3,4,6,6a,8,9,10,10a-octahydro-2H-pyrano[2,3-c][1,5]oxazocin-8-yl]acetic acid
(2E,4E,6E,8E)-9-[2-(hydroxymethyl)-6,6-dimethyl-3-oxocyclohex-1-en-1-yl]-3,7-dimethylnona-2,4,6,8-tetraenoic acid
(2E,4E,6E,8E)-9-[6-(hydroxymethyl)-2,6-dimethyl-3-oxocyclohex-1-en-1-yl]-3,7-dimethylnona-2,4,6,8-tetraenoic acid
(3aS,6Z,10E,14E,15aS)-6,14-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,12,13,15a-octahydrocyclotetradeca[b]furan-10-carboxylic acid
(3aS,6E,10E,14Z,15aS)-6,14-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,12,13,15a-octahydrocyclotetradeca[b]furan-10-carboxylic acid
(10E,14E)-6,7-Epoxy-6,10,14-trimethyl-3-methylene-3A,6,7,8,9,12,13,15A-octahydrocyclotetradeca(B)furan-2(3H),5(4H)-dione
1,1-Cyclopentanediacetic acid bis(trimethylsilyl) ester
C15H30O4Si2 (330.16825400000005)
3,3-Dimethyl-11-o-tolyl-2,3,4,5-tetrahydro-1H-dibenzo[b,e][1,4]diazepin-1-one
Picrocrocin
Picrocrocin is a beta-D-glucoside of beta-cyclocitral; the precursor of safranal. It is the compound most responsible for the bitter taste of saffron. It is functionally related to a beta-cyclocitral. Picrocrocin is a natural product found in Crocus tommasinianus, Crocus sativus, and Crocus vernus with data available. Picrocrocin, an apocarotenoid found in Saffron. Picrocrocin shows anticancer effect. Picrocrocin exhibits growth inhibitory effects against SKMEL-2 human malignant melanoma cells[1]. Picrocrocin, an apocarotenoid found in Saffron. Picrocrocin shows anticancer effect. Picrocrocin exhibits growth inhibitory effects against SKMEL-2 human malignant melanoma cells[1].
2,3,4,5-tetranor-prostaglandin FM
A prostanoid that is prostaglandin E2-UM in which the oxo group at position 9 has been reduced to the corresponding alcohol (alpha-configuration).