Drug Metabolite
Drug metabolite results when a drug is metabolized into a modified form which continues to produce effects. Drug metabolism redox reactions such as heteroatom dealkylations, hydroxylations, heteroatom oxygenations, reductions, and dehydrogenations can yield active metabolites, and in rare cases even conjugation reactions can yield an active metabolite.
All Product Categories
-
Drug Metabolite Related Products (2022)
Related Products (2022)
-
Antibodies (1)
-
Related Compound Screening Libraries (1)
-
Hexane-2,5-dione
0 ImagesHexane-2,5-dione (2,5-HD) is an orally active, CNS-penetrant cytotoxic agent. Hexane-2,5-dione reduces BCL-2 and β-catenin/TCF transcriptional activity, increases BAX and active caspase-3 expression, and promotes apoptosis. Hexane-2,5-dione causes an accumulation of neurofilaments within axons in rats. Hexane-2,5-dione can be used for the research of neurodegenerative diseases.
-
Triiodothyronine sulfate
0 ImagesTriiodothyronine sulfate is the main metabolite of thyroid hormone triiodothyronine (T3). Triiodothyronine is an active form of thyroid hormone, which binds to β1 thyroid hormone receptor (TRβ1), and activates its activity.
-
3-Phenoxybenzoic acid
0 ImagesSynonyms: 3-PBA3-Phenoxybenzoic acid is the metabolite of pyrethroid insecticides. 3-Phenoxybenzoic acid induces immunotoxicity and oxidative stress, and inhibits the phagocytic ability of macrophages.
-
Quercetin 7-glucuronide
0 ImagesSynonyms: Quercetin 7-O-β-glucuronide
-
Roflumilast N-oxide
0 ImagesRoflumilast N-oxide is a PDE type 4 inhibitor.
-
3,4-Dihydroxybenzeneacetic acid (Standard)
0 Images3,4-Dihydroxybenzeneacetic acid (Standard) is the analytical standard of 3,4-Dihydroxybenzeneacetic acid. This product is intended for research and analytical applications. 3,4-Dihydroxybenzeneacetic acid is the main neuronal metabolite of dopamine.
-
1'-Hydroxy bufuralol
0 ImagesCat. No.: HY-122277CAS No.: 57704-16-2Synonyms: Ro 03-74101'-Hydroxy bufuralol is the main metabolite of Bufuralol (HY-105124) by the cytochrome P450 isoenzymes 2D1 and 2D2 (CYP2D1/2). 1'-Hydroxy bufuralol can be used to determine CYP2D1/2 enzyme activity.
-
Zidovudine O-β-D-glucuronide sodium
0 ImagesSynonyms: 3'-Azido-3'-deoxythymidine β-D-glucuronide sodiumZidovudine O-β-D-glucuronide (3'-Azido-3'-deoxythymidine β-D-glucuronide) sodium is the glucuronide conjugate and metabolite of Zidovudine (HY-17413), which can be used to detect UGT2B7 activity. As a substrate, Zidovudine O-β-D-glucuronide sodium undergoes deconjugation via hydrolysis by immobilized β-glucuronidase to produce Zidovudine.
-
Homovanillic acid (Standard)
0 ImagesHomovanillic acid (Standard) (Vanilacetic acid (Standard)) is the analytical standard of Homovanillic acid (HY-N0384). This product is intended for research and analytical applications. Homovanillic acid (Vanilacetic acid) is a dopamine metabolite found to be associated with aromatic L-amino acid decarboxylase deficiency, celiac disease, growth hormone deficiency, and sepiapterin reductase deficiency.
-
Thyroxine sulfate
0 ImagesSynonyms: T4 SulfateThyroxine sulfate is a thyroid hormone metabolite.
-
Fludarabine triphosphate trisodium
0 ImagesCat. No.: HY-136650APurity: 99.93%Synonyms: F-ara-ATP trisodiumFludarabine triphosphate (F-ara-ATP) trisodium, the active metabolite of Fludarabine (HY-B0069), is a potent, noncompetitive and specific inhibitor of DNA primase, with an IC50 of 2.3 μM and a Ki of 6.1 μM. Fludarabine triphosphate trisodium inhibits DNA synthesis by blocking DNA primase and primer RNA formation. Fludarabine triphosphate trisodium inhibits ribonucleotide reductase and DNA polymerase and ultimately leads to cellular apoptosis.
-
4-Carboxypyrazole
0 Images4-Carboxypyrazole is a pyrazole metabolite and a human liver alcohol dehydrogenase ligand. It is a metabolite of 4-methylpyrazole in mice and rats and does not inhibit the enzyme when methanol is used as a substrate. 4-Carboxypyrazole can be used in studies related to alcohol dehydrogenase metabolism.
-
Desacetyl bisacodyl
0 ImagesDesacetyl bisacodyl is the active metabolite of the laxative bisacodyl. Desacetyl bisacodyl induces epithelial Cl(-) secretion in rat colon and rectum. Desacetyl bisacodyl evokes several effects at the colon or rectum, including increased mucus and chloride secretion.
-
2-Carboxybenzaldehyde
0 Images2-Carboxybenzaldehyde (Phthalaldehydic acid) is a key intermediate metabolite in the biodegradation process of polycyclic aromatic hydrocarbons, and also a specific substrate for CBA reductase and NAD-dependent 2-carboxybenzaldehyde dehydrogenase. 2-Carboxybenzaldehyde undergoes regioselective reduction via CBA reductase in mammalian tissues to produce 2-hydroxymethylbenzoic acid. 2-Carboxybenzaldehyde is converted to phthalic acid by NAD-dependent dehydrogenase during bacterial degradation. 2-Carboxybenzaldehyde can be used in relevant research in fields such as organic synthesis.
-
3-(3-Sulfooxyphenyl)propanoic acid
0 Images3-(3-Sulfooxyphenyl) propanoic acid is a metabolite of Echinacoside (HY-N0020). It promotes neural, psychological and brain health, enhances the proliferation, function and activity of brain cells, and facilitates extinction learning. 3-(3-Sulfooxyphenyl) propanoic acid can be used in research related to anxiety disorders, post-traumatic stress disorder, extinction learning deficits, autism, as well as neurodegenerative diseases including Parkinson's disease and Alzheimer's disease.
-
Endoxifen hydrochloride
0 ImagesEndoxifen hydrochloride is a key active metabolite of Tamoxifen (TAM) with higher affinity and specificity to estrogen receptor that also inhibits aromatase activity. Endoxifen hydrochloride has the potential for breast cancer study.
-
N-Desmethylclozapine
0 ImagesSynonyms: Norclozapine; Desmethylclozapine; NormethylclozapineN-Desmethylclozapine is a major active metabolite of the atypical antipsychotic agent Clozapine. N-Desmethylclozapine is a potent, allosteric and partial M1 receptors agonist (EC50=115 nM) and is able to potentiate hippocampal N-methyl-d-aspartate (NMDA) receptor currents through M1 receptor activation. N-Desmethylclozapine is also a δ-opioid agonist.
-
3-O-Methyldopa-d3
0 ImagesSynonyms: 3-Methoxy-L-tyrosine-d3; 3-O-Methyl-L-DOPA-d33-O-Methyldopa-d3 (3-Methoxy-L-tyrosine-d3) is deuterium labeled 3-O-Methyldopa (HY-113468A). 3-O-Methyldopa (3-Methoxy-L-tyrosine) is a metabolite of L-DOPA (HY-N0304) that can cross the blood-brain barrier (BBB). 3-O-Methyldopa inhibits the astrocyte-mediated protective effect of L-DOPA (HY-N0304) on dopaminergic neurons. In addition, 3-O-Methyldopa has certain antidepressant and neuroprotective activities. 3-O-Methyldopa can be used in the research of nervous system diseases such as depression and Parkinson's disease.
-
Methotrexate metabolite
0 ImagesSynonyms: DAMPAMethotrexate metabolite (DAMPA) is an active metabolite of Methotrexate. Methotrexate is a Folic acid (HY-16637) antagonist, widely used as an immunosuppressant. Methotrexate metabolite is an antimalarial agent that inhibits parasite growth under physiological folic acid conditions, with IC50 values of 446 nM and 812 nM against folic acid-sensitive strains and highly resistant strains, respectively. Methotrexate metabolite exhibits pharmacokinetic characteristics of rapid clearance and extensive metabolism, with a mean clearance rate of 1.9 l/kg/h and a mean terminal half-life of 51 minutes. Methotrexate metabolite is promising for research in the field of inflammation.
