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Drug Metabolite

Drug Metabolite

Drug metabolites are created when a drug is metabolized into a different form that still has therapeutic effects. Active metabolites can be produced by drug metabolism redox reactions like heteroatom dealkylations, hydroxylations, heteroatom oxygenations, reductions, and dehydrogenations. In some rare circumstances, conjugation reactions can also produce an active metabolite. 

Drug Metabolite related products

Structure Cat No. Product Name CAS No. Product Description
α-Hydroxy etizolam V107414 α-Hydroxy etizolam 64546-10-7 α-Hydroxyetizolam is the major metabolite of etizolam and has almost the same pharmacological potency as etizolam and has a high affinity for benzodiazepine receptors.
α-Hydroxy flualprazolam V107680 α-Hydroxy flualprazolam 37115-46-1 Alpha-hydroxyfluanilide is a benzodiazepine.
α-Hydroxy Montelukast V102990 α-Hydroxy Montelukast 2045402-27-3 α-Hydroxymontelukast (M7) is a metabolite of montelukast.
β-Nicotyrine V72246 β-Nicotyrine 487-19-4 β-Nicotyrine is a metabolite of Nicotine.
Δ2-cis-Hexadecenoic acid V102982 Δ2-cis-Hexadecenoic acid 2825-68-5 Δ2-cis-hexadecenoic acid is an unsaturated fatty acid and a hydrolysis product of lipopolysaccharide.
Δ9-THCQ V104573 Δ9-THCQ 860480-30-4 Δ9-THCQ (Δ9-tetrahydrocannabinol) is an oxidation byproduct of Δ9-THC.
ω-Hydroxy-DEET V72143 ω-Hydroxy-DEET 72236-22-7 ω-Hydroxy-DEET is a major metabolite of the insect repellent DEET.
二丙二醇单乙醚 V40039 4-Desmethyl Istradefylline 160434-48-0 4-Desmethyl Istradefylline is the demethylated metabolite of Istradefylline (KW-6002; Nourianz), which is an orally bioavailable adenosine A2A receptor (A2AR) antagonist approved for the treatment of PD (Parkinson's disease).
依折麦布Phenexy葡萄糖醛酸 V40057 Ezetimibe phenoxy glucuronide 190448-57-8 Ezetimibe phenoxy glucuronide (Ezetimibe glucuronide) is the bioactive metabolite of Ezetimibe and has anti-hyperlipoproteinemia effects.
去烷基l阿扎那韦 V19605 Des(benzylpyridyl) Atazanavir 1192224-24-0 Des(benzylpyridyl) Atazanavir (compound M1) is an N-dealkylated Atazanavir metabolite.
吗多明 V21871 Molsidomine 25717-80-0 Molsidomine is anorally bioactive and long acting vasodilator acting as anNO donor and annexin A2 inhibitor.
奥司他韦酸 V16457 Oseltamivir carboxylate (GS 4071; Ro 64 0802) 187227-45-8 Oseltamivir acid (GS 4071), the bioactive metabolite of Oseltamivir phosphate, is an orally bioavailable and selective inhibitor of influenza virus neuraminidase (IC50=2 nM), active against both influenza viruses A and B.
对乙酰氨基酚代谢产物 V30699 Acetaminophen metabolite 3-hydroxy-acetaminophen 37519-14-5 3-hydroxy-acetaminophen is a metabolite of Acetaminophen.
小檗红碱 V32638 Berberrubine chloride 15401-69-1 Berberrubine chloride, a potent metabolite of berberine, reduces symptoms of ulcerative colitis in animal models.
尼拉帕尼代谢物 M1 V3789 Niraparib metabolite M1 1476777-06-6 Niraparib metabolite M1 is a carboxylic acid metabolite of niraparib (MK4827; Zejula), which is a PARP1/2 inhibitor approved for cancer treatment.
尼群地平杂质B V40035 m-Nifedipine 21881-77-6 m-Nifedipine is an impurity of Nifedipine (Bay-1040; BAY-a-1040; Cordipin; Corinfar) which is an approved dihydropyridine calcium channel blocker (CCB) used as antihypertensive drug.
尿石素A V27881 Urolithin A 1143-70-0 Urolithin A isa microbial metabolite of ellagic acidin the gut and an inducer of mitophagy.
度他雄胺二氢 V40044 Dihydro Dutasteride 164656-22-8 Dihydro Dutasteride is an impurity generated during the production of Dutasteride (GI198745, GG745; GI-198745, GG-745;Avodart, Avidart), which is an approved anticancer medication and a 5-α reductase inhibitor.
度洛西汀杂质C V28672 Duloxetine metabolite Para-Naphthol Duloxetine 949095-98-1 Duloxetine metabolite Para-Naphthol Duloxetine is a metabolite of Duloxetine, which is a serotonin-norepinephrine reuptake inhibitor (SNRI)used for the treatment of major depressive disorder and generalized anxietydisorder (GAD),fibromyalgia and neuropathic pain.
恩扎鲁胺羧酸代谢物 V40125 Enzalutamide carboxylic acid 1242137-15-0 Enzalutamide carboxylic acid(also called MDV-3100 carboxylic acid)is a major inactive metabolite of Enzalutamide (MDV3100; Xtandi) which is a non-steroidal androgen-receptor (AR) antagonist approved for use as an anticancer drug.
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