Cobicistat
A pharmacokinetic enhancer that inhibits CYP3A enzymes to boost blood levels of co-administered antiretroviral drugs without having intrinsic antiviral activity itself. It is used in combination HIV regimens as a booster, similar in function to ritonavir.
الوزن الجزيئي
776,0000 g/mol
LogP
5,70
TPSA
195,00 Ų
قاعدة ليبينسكي للخمسة
راسب
المجالات العلاجية
Pharmacokinetics (PK)
Pharmacodynamics (PD)
البنية ثنائية الأبعاد
Cite this structure
Embed this structure
SMILES
CC(C)c1nc(CN(C)C(=O)N[C@@H](CCN2CCOCC2)C(=O)N[C@H](CC[C@H](Cc2ccccc2)NC(=O)OCc2cncs2)Cc2ccccc2)cs1
InChI
InChI=1S/C40H53N7O5S2/c1-29(2)38-43-34(27-53-38)25-46(3)39(49)45-36(16-17-47-18-20-51-21-19-47)37(48)42-32(22-30-10-6-4-7-11-30)14-15-33(23-31-12-8-5-9-13-31)44-40(50)52-26-35-24-41-28-54-35/h4-13,24,27-29,32-33,36H,14-23,25-26H2,1-3H3,(H,42,48)(H,44,50)(H,45,49)/t32-,33-,36+/m1/s1
Molecular Formula
C40H53N7O5S2
HBD / HBA
3 / 10
الروابط القابلة للدوران
20
الذرات الثقيلة
54
No targets recorded
Target interaction data is not yet available for this drug.
No interactions recorded
Drug interaction data is not yet available for this compound.
No side effects recorded
Side effect data is not yet available for this drug.
الأسئلة الشائعة
A pharmacokinetic enhancer that inhibits CYP3A enzymes to boost blood levels of co-administered antiretroviral drugs without having intrinsic antiviral activity itself. It is used in combination HIV regimens as a booster, similar in function to ritonavir.
Yes, Cobicistat is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL2095208. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 25151504. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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