Crixivan

Indinavir

Clinical data
Trade names	Crixivan
AHFS/Drugs.com	Monograph
MedlinePlus	a696028
License data	US FDA: Indinavir
Pregnancy category	US: C (Risk not ruled out)
Routes of administration	Oral
ATC code	J05AE02 (WHO)
Pharmacokinetic data
Bioavailability	~65%
Protein binding	60%
Metabolism	Hepatic via CYP3A4
Biological half-life	1.8 ± 0.4 hours
Identifiers
IUPAC name (2S)-1-[(2S,4R)-4-benzyl-2-hydroxy-4-{[(1S,2R)-2-hydroxy-2,3-dihydro-1H-inden-1-yl]carbamoyl}butyl]-N-tert-butyl-4-(pyridin-3-ylmethyl)piperazine-2-carboxamide
CAS Number	150378-17-9 Y
PubChem CID	5362440
DrugBank	DB00224 Y
ChemSpider	4515036 Y
UNII	9MG78X43ZT
KEGG	C07051 Y
ChEBI	CHEBI:44032 Y
ChEMBL	CHEMBL540914 N
NIAID ChemDB	005824
PDB ligand	MK1 (PDBe, RCSB PDB)
Chemical and physical data
Formula	C36H47N5O4
Molar mass	613.79 g/mol
3D model (JSmol)	Interactive image
SMILES CC(C)(C)NC(=O)[C@@H]1CN(CCN1C[C@H](C[C@@H](Cc2ccccc2)C(=O)N[C@H]3c4ccccc4C[C@H]3O)O)Cc5cccnc5
InChI InChI=1S/C36H47N5O4/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/h4-15,21,28-29,31-33,42-43H,16-20,22-24H2,1-3H3,(H,38,44)(H,39,45)/t28-,29+,31+,32-,33+/m1/s1 Y Key:CBVCZFGXHXORBI-PXQQMZJSSA-N Y
NY (what is this?)

Indinavir (IDV; trade name Crixivan, manufactured by Merck) is a protease inhibitor used as a component of highly active antiretroviral therapy to treat HIV/AIDS.

It is on the World Health Organization's List of Essential Medicines, a list of the most important medications needed in a basic health system.

Unfortunately, indinavir wears off quickly after dosing, so requires very precise dosing every eight hours to thwart HIV from forming drug-resistant mutations, including resistances to other protease inhibitors. It has restrictions on what sorts of food may be eaten concurrently. For these reasons it is now rarely used.

The most common side effects of indinavir include:

Indinavir inhibits urinary nitrous oxide production and may inhibit nitric oxide production. Treatment with this drug is frequently associated with renal abnormalities, sterile leukocyturia, and reduced creatinine clearance.

Indinavir impairs endothelial function in healthy HIV-negative men and may accelerate atherosclerotic disease.

The Food and Drug Administration (FDA) approved indinavir on March 13, 1996, making it the eighth antiretroviral drug approved. Indinavir is much more powerful than any prior antiretroviral drug; using it with dual NRTIs set a new standard for treatment of HIV/AIDS. Protease inhibitors changed the nature of AIDS from a terminal illness to a somewhat manageable one.

Increasingly, it is being replaced by newer drugs that are more convenient to take and less likely to promote virus resistance, such as darunavir or atazanavir.