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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
23 Results for "
cytochrome P450 3A
" in MedChemExpress (MCE) Product Catalog:
Products (23)
23 Results for "cytochrome P450 3A" in MCE Product Catalog:
13
13 Publications Verification
Synonyms: ABT-450; Veruprevir
Target:
Research Areas:
Paritaprevir (ABT-450) is a potent, orally active and antiviral non-structural protein 3/4A (NS3/4A) protease inhibitor with EC50s of 1 and 0.21 nM against HCV 1a and 1b, respectively. Paritaprevir is also a SARS-CoV 3CL pro inhibitor with an IC50 of 1.31 μM. Paritaprevir is metabolized primarily by cytochrome P450 (CYP) 3A. The plasma concentration and half-life of Paritaprevir can be enhanced by Ritonavir (a CYP450 inhibitor) .
12
Target:
Cobicistat is a potent and selective inhibitor of cytochrome P450 3A (CYP3A) enzymes with IC50s of 30-285 nM. Cobicistat is a pharmacokinetic enhancer which increases the overall absorption of several HIV medications.
6
Research Areas:
Pregnenolone 16α-carbonitrile is an orally active prototypical and effective rodent-PXR activator. Pregnenolone 16α-carbonitrile, a synthetic steroid, induces cytochrome P450 3A expression. Pregnenolone 16α-carbonitrile exhibits increased resistance to subsequent stressful insults .
1
1 Cited Publications
Target:
Research Areas:
LKY-047, a Decursin derivative, is a potent and selective reversible competitive cytochrome P45022J2 (CYP2J2) inhibitor with an IC50 of 1.7 μM. LKY-047 is inactive against other human P450s, such as CYPs 1A2, 2A6, 2B6, 2C8, 2C9, 2C19, 2D6, 2E1, and 3A .
1
1 Cited Publications
Cat. No.: HY-P74210
Purity: ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: CYP3A4; CYPIIIA3; Prev. CYP3A3; cytochrome P450, Subfamily IIIA (Niphedipine Oxidase), Polypeptide 3; cytochrome P450, Subfamily IIIA (Niphedipine Oxidase), Polypeptide 4; Taurochenodeoxycholate 6-Alpha-Hydroxylase; cytochrome P450, Family 3, Subfamily A,
Species:
Human
Source:
E. coli
Cat. No.: HY-174905
CAS No.: 2416858-84-7
Synonyms: QY201
Target:
Research Areas:
Quecitinib (QY201) is an orally active JAK1/TYK2 dual inhibitor. Quecitinib is also a substrate of cytochrome P450 3A and is mainly metabolized to mono-oxide and glucuronidation products. Quecitinib has favorable pharmacokinetic properties as well as safety. Quecitinib can be used in the research of atopic dermatitis and other autoimmune diseases .
Cat. No.: HY-117580
CAS No.: 13951-70-7
Synonyms: OH-PRED
Target:
Research Areas:
16α-Hydroxyprednisolone (OH-PRED) is a stereoselective metabolite of the 22(R) epimer of the glucocorticoid Budesonide (HY-13580). 16α-Hydroxyprednisolone formation is catalyzed by isoenzymes within the cytochrome P450 3A (CYP3A) subfamily. 16α-Hydroxyprednisolone formation can be inhibited by antibodies targeting the CYP3A subfamily .
Cat. No.: HY-154916
CAS No.: 139958-51-3
Synonyms: 13-DMT; 13-O-Demethyl FK 506
Target:
Research Areas:
13-O-Desmethyl tacrolimus (13-DMT; 13-O-Demethyl FK 506) is the major metabolite of Tacrolimus (HY-13756) formed via cytochrome P450 3A-mediated biotransformation. The ratio of 13-O-Desmethyl tacrolimus to Tacrolimus serves as a biomarker for myelotoxicity and hepatotoxicity .
Cat. No.: HY-10493R
CAS No.: 1004316-88-4
Synonyms: GS-9350 (Standard)
Target:
Cobicistat (Standard) is the analytical standard of Cobicistat. This product is intended for research and analytical applications. Cobicistat is a potent and selective inhibitor of cytochrome P450 3A (CYP3A) enzymes with IC50s of 30-285 nM. Cobicistat is a pharmacokinetic enhancer which increases the overall absorption of several HIV medications.
Cat. No.: HY-10493S
CAS No.: 2699607-48-0
Synonyms: GS-9350-d8
Cat. No.: HY-W700344
CAS No.: 172430-45-4
Synonyms: CVT-2514; RS-88390
Target:
Research Areas:
o-Desmethyl ranolazine (CVT-2514; RS-88390) is a metabolite of Ranolazine (HY-B0280), formed through metabolism of Ranolazine by enzymes of the cytochrome P450 (CYP) 3A family .
Cat. No.: HY-117580S
Synonyms: OH-PRED-d3
Cat. No.: HY-117580R
CAS No.: 13951-70-7
Synonyms: OH-PRED (Standard)
Target:
Research Areas:
16α-Hydroxyprednisolone (OH-PRED) (Standard) is the analytical standard of 16α-Hydroxyprednisolone. This product is intended for research and analytical applications. 16α-Hydroxyprednisolone is a stereoselective metabolite of the 22(R) epimer of the glucocorticoid Budesonide (HY-13580). 16α-Hydroxyprednisolone formation is catalyzed by isoenzymes within the cytochrome P450 3A (CYP3A) subfamily. 16α-Hydroxyprednisolone formation can be inhibited by antibodies targeting the CYP3A subfamily .
Cat. No.: HY-12594A
CAS No.: 1456607-71-8
Synonyms: ABT-450 dihydrate; Veruprevir dihydrate
Target:
Research Areas:
Paritaprevir (ABT-450) dihydrate is a potent, orally active and antiviral non-structural protein 3/4A (NS3/4A) protease inhibitor with EC50s of 1 and 0.21 nM against HCV 1a and 1b, respectively. Paritaprevir dihydrate is also a SARS-CoV 3CL pro inhibitor with an IC50 of 1.31 μM. Paritaprevir dihydrate is metabolized primarily by cytochrome P450 (CYP) 3A. The plasma concentration and half-life of Paritaprevir dihydrate can be enhanced by Ritonavir (a CYP450 inhibitor) .
Cat. No.: HY-12594R
CAS No.: 1216941-48-8
Synonyms: ABT-450 (Standard); Veruprevir (Standard)
Target:
Research Areas:
Paritaprevir (Standard) is the analytical standard of Paritaprevir. This product is intended for research and analytical applications. Paritaprevir (ABT-450) is a potent, orally active and antiviral non-structural protein 3/4A (NS3/4A) protease inhibitor with EC50s of 1 and 0.21 nM against HCV 1a and 1b, respectively. Paritaprevir is also a SARS-CoV 3CLpro inhibitor with an IC50 of 1.31 μM. Paritaprevir is metabolized primarily by cytochrome P450 (CYP) 3A. The plasma concentration and half-life of Paritaprevir can be enhanced by Ritonavir (a CYP450 inhibitor) .
Cat. No.: HY-P705910
Purity: ≥ 90%, as determined by reducing SDS-PAGE .
Synonyms: CYP3A5; Flavoprotein-Linked Monooxygenase; cytochrome P450 Family 3 Subfamily A Member 5; Aryl Hydrocarbon Hydroxylase; P450PCN3; Alternative Protein CYP3A5; CP35; Microsomal Monooxygenase; PCN3; Xenobiotic Monooxygenase; cytochrome P450, Subfamily IIIA (Niphedipine Oxidase), Polypeptide 5; Unspecific Monooxygenase; cytochrome P450, Family 3, Subfamily A, Polypeptide 5; cytochrome P450 HLp2; cytochrome P450-PCN3; cytochrome P450 3A; cytochrome P450 3A5; cytochrome P-450; CYPIIIA5; DKFZp686I18188; Uncharacterized Protein DKFZp686I18188
Species:
Human
Source:
E. coli
Cat. No.: HY-117580S2
Synonyms: OH-PRED-d5
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Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
