192725-39-6
192725-39-6
Chemical Structure
Lopinavir Metabolite M-1
- CAS No.: 192725-39-6
- Formula:C37H46N4O6
- Molecular Weight:642.78
IUPAC Name: (S)-N-((2S,4S,5S)-5-(2-(2,6-dimethylphenoxy)acetamido)-4-hydroxy-1,6-diphenylhexan-2-yl)-2-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)-3-methylbutanamide
InChIKey: PSUMJBRVYHIASB-MEROQGEASA-N
SMILES: O=C(N[C@@H](CC1=CC=CC=C1)C[C@H](O)[C@@H](NC(COC2=C(C)C=CC=C2C)=O)CC3=CC=CC=C3)[C@H](C(C)C)N(C(N4)=O)CCC4=O
Biological Activity: Lopinavir Metabolite M-1, an active metabolite of Lopinavir, inhibits HIV protease with a Ki of 0.7 pM. Lopinavir Metabolite M-1 has antiviral activities in vitro[1][2].
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Lopinavir Metabolite M-1 | Lopinavir Metabolite M-1, an active metabolite of Lopinavir, inhibits HIV protease with a Ki of 0.7 pM. Lopinavir Metabolite M-1 has antiviral activities in vitro. | |||||||||||||||||||||
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References
- [1]. Sham HL, et, al. Synthesis and antiviral activities of the major metabolites of the HIV protease inhibitor ABT-378 (Lopinavir). Bioorg Med Chem Lett. 2001 Jun 4; 11(11): 1351-3. [Content Brief]
- [2]. Kumar GN, et, al. Potent inhibition of the cytochrome P-450 3A-mediated human liver microsomal metabolism of a novel HIV protease inhibitor by ritonavir: A positive drug-drug interaction. Drug Metab Dispos. 1999 Aug; 27(8): 902-8. [Content Brief]
Keywords
