Indinavir Sulfate
This sulfate salt of indinavir is the pharmaceutical formulation of this HIV protease inhibitor used in combination antiretroviral regimens. It blocks the HIV protease enzyme, preventing the assembly of mature, infectious HIV particles. It must be taken with careful attention to hydration due to the risk of kidney stones.
분자량
711.9000 g/mol
TPSA
201.00 Ų
치료 영역
작용 기전
Inhibits viral protease, an enzyme essential for cleaving polyprotein precursors into functional viral proteins required for viral maturation and infectivity.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Inhibits viral protease, an enzyme essential for cleaving polyprotein precursors into functional viral proteins required for viral maturation and infectivity.
2D 구조
Cite this structure
Embed this structure
SMILES
CC(C)(C)NC(=O)[C@@H]1CN(Cc2cccnc2)CCN1C[C@@H](O)C[C@@H](Cc1ccccc1)C(=O)N[C@H]1c2ccccc2C[C@H]1O.O=S(=O)(O)O
InChI
InChI=1S/C36H47N5O4.H2O4S/c1-36(2,3)39-35(45)31-24-40(22-26-12-9-15-37-21-26)16-17-41(31)23-29(42)19-28(18-25-10-5-4-6-11-25)34(44)38-33-30-14-8-7-13-27(30)20-32(33)43;1-5(2,3)4/h4-15,21,28-29,31-33,42-43H,16-20,22-24H2,1-3H3,(H,38,44)(H,39,45);(H2,1,2,3,4)/t28-,29+,31+,32-,33+;/m1./s1
Molecular Formula
C36H49N5O8S
HBD / HBA
6 / 11
회전 가능 결합
12
무거운 원자
50
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.
자주 묻는 질문
This sulfate salt of indinavir is the pharmaceutical formulation of this HIV protease inhibitor used in combination antiretroviral regimens. It blocks the HIV protease enzyme, preventing the assembly of mature, infectious HIV particles. It must be taken with careful attention to hydration due to the risk of kidney stones.
Inhibits viral protease, an enzyme essential for cleaving polyprotein precursors into functional viral proteins required for viral maturation and infectivity.
Yes, Indinavir Sulfate 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). CHEMBL1735. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 5462355. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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