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Cat No. | Product Name | Synonyms | Targets |
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T7556 | Fadrozole hydrochloride | CGS 16949A | Aromatase |
Fadrozole hydrochloride (CGS 16949A) is a model aromatase inhibitor that has been shown to suppress estrogen production in the ovaries of fish. | |||
T25283 | Cytochrome P450 2C9 | Cyp2C9,Human cytochrome P450 2C9,Cytochrome P 450 2C9,S-Mephenytoin 4-hydroxylase | |
Cytochrome P450 2C9 is a cytochrome P-450 subtype that possesses specificity for acidic xenobiotics. It oxidizes a wide range of important clinical drugs under the categories of nonsteroidal anti-inflammatory agents, ant... | |||
TP2238 | Cytochrome P450 CYP1B1 (190-198) [Homo sapiens] | Others | |
Cytochrome P450 CYP1B1 (190-198) [Homo sapiens] is a small heme protein found loosely associated with the inner membrane of the mitochondrion. | |||
T117521 | 7-BFC | 7-Benzyloxy-4-(trifluoromethyl)coumarin,Y040-0031 | P450 |
7-BFC (7-Benzyloxy-4-(trifluoromethyl)coumarin) is a coumarin-like fluorescent substrate that serves as a biomarker for cytochrome P 450 and can be used to study CYP isoforms and cytochrome P 450 metabolism. | |||
T1597 | Proadifen hydrochloride | U-5446,RP-5171,SKF-525A | P450 |
Proadifen hydrochloride (RP-5171) is an inhibitor of drug metabolism and cytochrome P-450 enzyme system activity. | |||
T1378 | Tegafur | Fluorafur,FT-207,NSC 148958,FT 207 | Nucleoside Antimetabolite/Analog , DNA/RNA Synthesis |
Tegafur (FT 207) is a congener of the antimetabolite fluorouracil with antineoplastic activity. Tegafur is a prodrug that is gradually converted to fluorouracil in the liver by the cytochrome P-450 enzyme. | |||
T27918 | LY 43578 | LY-43578,LY43578 | P450 , Aromatase |
LY 43578 is an orally active aromatase inhibitor. LY43578 could inhibit O-demethylation of P-450-dependent p-nitroanisole and N-demethylation of ethylmorphine (IC50 of 0.3 and 5 μm, respectively) in rat liver microsomes.... | |||
T0120 | Voriconazole | UK-109496 | Antifection , Antifungal |
Voriconazole (UK-109496) is a triazole antifungal agent that specifically inhibits STEROL 14-ALPHA-DEMETHYLASE and CYTOCHROME P-450 CYP3A. | |||
T7696 | 3-Cyano-7-ethoxycoumarin | Others | |
3-Cyano-7-ethoxycoumarin is cytochrome P450 (CYP) isoforms CYP1A1 and CYP1A2 . | |||
T6686 | Sulconazole mononitrate | Exelderm,Sulconazole Nitrate,RS 44872 | Antibacterial , Antibiotic , Antifungal |
Sulconazole mononitrate (Exelderm) is the nitrate salt form of sulconazole, a synthetic imidazole derivative with the antifungal property. Sulconazole mononitrate inhibits fungal cytochrome P-450 sterol C-14 alpha-demeth... | |||
T5952 | Diniconazole | Rac-diniconazole | Antibacterial |
Diniconazole (Rac-diniconazole) is a fungicide. It is known as a plant hormone abscisic acid (ABA) catabolic inhibitor, and acts as a potent competitive inhibitor of recombinant Arabidopsis ABA 8'-hydroxylase, CYP707A3. | |||
T0922 | Zoxazolamine | NSC 24995,Contrazole | Others |
Zoxazolamine (NSC-24995) is a uricosuric and muscle relaxant. Zoxazolamine acts centrally as a muscle relaxant, but the mechanism of its action is not understood. | |||
T22229 | Acid Yellow 36 | Metanil Yellow | Others |
Acid Yellow 36 (Metanil Yellow) is an azo dye and a pH indicator. Acid Yellow 36 changes its color from red at pH 1.2 to yellow at pH 2.3. | |||
T33110 | M 79193 | M79193,M-79193 | |
M 79193 induces total hepatic microsomal cytochrome P-450. | |||
T34990 | UK 39671 | ||
UK 39671 is an inhibitor of cytochrome P-450(CAM) inhibitor. | |||
T25591 | Lab 170250F | Lab-170250F,Lab170250F | |
Lab 170250F is a potent cytochrome P-450-obtusifoliol-14-demethylase inhibitor. | |||
T69553 | p,p'-DDMS | ||
p,p'-DDMS is a water soluble and highly specific inhibitor of cytochrome P-450 omega-hydroxylase. | |||
T31815 | Flumecinol | Zyxorin | |
Flumecinol is a hepatic enzyme (cytochrome P-450 monooxygenases) inducer. | |||
T69167 | Buthiobate | ||
Buthiobate is a fungicide which inhibits lanosterol 14 alpha-demethylation catalyzed by a cytochrome P-450. | |||
T19553 | RPR132595A | NPC | Others |
RPR132595A is an active CPT-11 metabolite, it is generated by cytochrome P-450 3A4 (CYP3A4). | |||
T78069 | RPR132595A hydrochloride | NPC hydrochloride | Drug Metabolite |
RPR132595A (NPC) hydrochloride, an active metabolite of CPT-11, is produced via cytochrome P-450 3A4 (CYP3A4) metabolism and is ultimately eliminated via urinary excretion [1]. | |||
T78135 | Nicotelline | Nicotellin | |
Nicotelline, also known as Nicotellin, is an alkaloid associated with nicotine and acts as a modest inhibitor of the enzyme human cDNA-expressed cytochrome P-450 2A6 (CYP2A6), which is responsible for coumarin 7-hydroxyl... | |||
T36666 | Dehydro Warfarin | ||
Dehydro warfarin is a metabolite of (±)-warfarin .1It is formed from (±)-warfarin by rat liver microsomes. 1.Kaminsky, L.S., Fasco, M.J., and Guengerich, F.P.Comparison of different forms of liver, kidney, and lung micro... | |||
T61259 | Valganciclovir | ||
Valganciclovir, the L-valyl ester of ganciclovir, is a prodrug effectively converted to ganciclovir in the body, serving as an antiviral medication for cytomegalovirus (CMV) infections. In vitro studies demonstrate that ... | |||
T38269 | Purfalcamine | ||
Purfalcamine is an orally active, selective Plasmodium falciparum calcium-dependent protein kinase 1 (PfCDPK1) inhibitor with an IC50 of 17 nM and an EC50 of 230 nM. Purfalcamine has antimalarial activity and causes mala... | |||
T35463 | (±)14(15)-EET | (±)14,15-EET,(±)14,15-EpETrE,(±)14(15)-EET | |
(±)14(15)-EET is a metabolite of arachidonic acid that is formed via epoxidation of arachidonic acid by cytochrome P450.[1],[2] It prevents increases in leukotriene B4, ICAM-1, and chemokine (C-C motif) ligand 1 (CCL2) i... |
Cat No. | Product Name | Synonyms | Targets |
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TN1078 | Seneciphylline | P450 , GST | |
Seneciphylline, one of the hepatotoxic pyrolizidine alkaloids, has mutagenic activity in Drosophila and their transfer into rat milk.Seneciphylline can significantly increased the activities of epoxide hydrase and glutat... | |||
T1011 | Itraconazole | R51211 | P450 , Hedgehog/Smoothened , Antibiotic , Autophagy , Antifungal |
Itraconazole (R51211) is a triazole antifungal agent that inhibits cytochrome P-450-dependent enzymes required for ERGOSTEROL synthesis. | |||
T40859 | 5-Hydroxy-8-methoxypsoralen | 5-Hydroxyxanthotoxin,5-Hydroxy-8-methoxypsoralen | |
5-Hydroxy-8-methoxypsoralen (5-Hydroxyxanthotoxin) is a metabolite derived from Xanthotoxin, which acts as a potent tricyclic furocoumarin suicide inhibitor of CYP (cytochrome P-450). It is employed as an agent for the t... |