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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T4118 | SB 271046 hydrochloride | SB 271046A | 5-HT Receptor |
SB 271046 hydrochloride (SB 271046A) is selective, orally active 5-HT6 antagonist (pKi values are 9.02-8.92, 6.35, 6.55, 6.27 at 5-HT6, 5-HT1A, 5-HT1D and D3, and 6.05, 5.95, 5.76, 5.73, 5.62, 5.55, 5.41, 5.39, 5.27 and ... | |||
T1579 | Mestranol | Devocin,Norquen,Menophase | Estrogen Receptor/ERR , Estrogen/progestogen Receptor |
Mestranol (Devocin), a semisynthetic estrogen, is used as an estrogen receptor agonist and must be demethylated to be biologically active. | |||
T1587 | Exemestane | EXE,FCE 24304,PNU155971 | Aromatase |
Exemestane (EXE) is an Aromatase Inhibitor. The mechanism of action of exemestane is as an Aromatase Inhibitor. | |||
T12678 | (Rac)-Telmesteine | 3-(Ethoxycarbonyl)thiazolidine-4-carboxylic acid,3-ethoxycarbonyl-1,3-thiazolidine-4-carboxylic acid,3,4-Thiazolidinedicarboxylic Acid 3-Ethyl Ester | Protease |
(Rac)-Telmesteine (3,4-Thiazolidinedicarboxylic Acid 3-Ethyl Ester) is an inhibitor of protease and is thus a suitable enzyme stabilizer. | |||
T71708 | Minamestane | Aromatase | |
Minamestane is a novel irreversible aromatase inhibitor.Minamestane induces time-dependent inhibition of human placental aromatase with a half-life of 4 minutes and a K of 59 nM.Minamestane has antitumor activity. | |||
TQ0295 | Coumestrol | Estrogen Receptor/ERR | |
Coumestrol that existed in soybean products suppresses the proliferation of ES2 cells (IC50: 50 μM). It exhibits activities against neurological disorders, cancers and autoimmune diseases. | |||
T12564 | Prudomestin | 3,5,7-Trihydroxy-4',8-dimethoxyflavone | Xanthine Oxidase |
Prudomestin (3,5,7-Trihydroxy-4',8-dimethoxyflavone) is a natural product isolated from the heartwood of Prunus domestica, with xanthine oxidase (XO) inhibitory activity with IC50 of 6 µM. | |||
T1536 | Promestriene | 3-propyl ethyl,17B-methyl estradiol,Promestriano | Estrogen/progestogen Receptor |
Promestriene (3-propyl ethyl) (INN) is a synthetic estrogen and glucocorticoid used topically in a 1% cream formulation. It is described as a tropic agent and antiseborrheic. | |||
T35772 | Emestrin | ||
Emestrin is a mycotoxin originally isolated from E. striata that has antimicrobial, immunomodulatory, and cytotoxic activities.1,2,3,4,5 It is active against the fungi C. albicans and C. neoformans, as well as the bacter... | |||
T28942 | Telomestatin | SOT 095,GM95,(R)-Telomestatin,GM 95,GM-95 | |
Telomestatin is an inhibitor of the telomerase, it induces the formation of basket-type G-quadruplex (G4) structures from hybrid-type G-quadruplexes in the telomeric region. | |||
T31485 | Dimestrol | ||
Dimestrol can induce DNA damage. | |||
T29886 | Almestrone | BA-38372,BA 38372,Ciba-38372,BA38372,Ciba 38372 | |
Almestrone (developmental code names Ba 38372, Ciba 38372), also known as 7α-methylestrone, is a synthetic, steroidal estrogen which was synthesized in 1967 but was never marketed. It is used as a precursor in the synthe... | |||
T68775 | Etamestrol | ||
Etamestrol is a synthetic, steroidal estrogen described as an ovulation inhibitor or hormonal contraceptive | |||
T33032 | Lynestrenol mixture with mestranol | ||
Lynestrenol mixture with mestranol is a bioactive chemical. | |||
T68720 | Plomestane | ||
Plomestane is a selective inhibitor of aromatization in human breast tissue and may provide a mechanism for controlling estrogen responsive processes. | |||
T24012 | Domesticine, (-)- | L-Domesticine | |
Domesticine, (-)- is an antagonist of alpha-1D-adrenoceptor. | |||
T20956 | Telmesteine | ||
Telmesteine is a mucolitic drug. | |||
TN5883 | 4'-O-Methylcoumestrol | 9-O-Methylcoumestrol | |
4'-O-Methylcoumestrol is a natural product from Glycyrrhiza pallidiflora Maxim. | |||
T82220 | Hedysarimcoumestan B | ||
Hedysarumcoumestan B, a natural product, is isolated from the roots of Hedysarum multijugum [1]. | |||
T35676 | 17β-hydroxy Exemestane | ||
17β-hydroxy Exemestane is the primary active metabolite of exemestane . It is formed by metabolism of exemestane by the cytochrome P450 (CYP) isoforms CYP1A and CYP4A11. 17β-hydroxy Exemestane is an aromatase inhibitor (... |