Cobicistat

CHEMBL2095208 Phase 4 معتمد Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
776.0 g/mol
LogP
5.7
Phase
4

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

SVG PNG

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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 section for drug detail pages. Renders standard pharmacological database links plus the drug's data_sources field. #}

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.

إخلاء المسؤولية الطبية

This content is for educational and informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before making medication decisions.

Data sources: ChEMBL, PubChem, DailyMed.