Ritonavir CAS NO:155213-67-5

Ritonavir CAS NO:155213-67-5

CAS NO: 155213-67-5
Molecular Formula: C37H48N6O5S2
Molecular Weight: 720.94
EINECS NO: 605-001-5
MDL NO: MFCD04115732/MFCD00927142
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Product Details

Product Description

Product Name: Ritonavir CAS NO:155213-67-5

 

 

Synonyms:

Norvir;

Ritonavir;

Liponavir Core;

Ritonavi;

ABT-538;

A-84538 ABT-538 Abbott 84538;

Norvi;

RITONA;

N-[(2S,4S,5S)-4-Hydroxy-1,6-diphenyl-5-{[(1,3-thiazol-5-ylmethoxy)carbonyl]amino}hexan-2-yl]-N-{[(2-isopropyl-1,3-thiazol-4-yl)methyl](methyl)carbamoyl}-L-valinamide;

(1E,2S)-N-[(2S,4S,5S)-4-Hydroxy-5-{(E)-[hydroxy(1,3-thiazol-5-ylmethoxy)methylene]amino}-1,6-diphenyl-2-hexanyl]-2-[(E)-(hydroxy{[(2-isopropyl-1,3-thiazol-4-yl)methyl](methyl)amino}methylene)amino]-3-methylbutanimidic acid;

1,3-Thiazol-5-ylmethyl-[(1S,2S,4S)-1-benzyl-2-hydroxy-4-({(2S)-3-methyl-2-[(methyl{[2-(1-methylethyl)-1,3-thiazol-4-yl]methyl}carbamoyl)amino]butanoyl}amino)-5-phenylpentyl]carbamate;

 

 

Chemical & Physical Properties

Appearance : White or almost white powder

Assay : ≥99%

Density: 1.239±0.1 g/cm3

Boiling Point: 947°C at 760 mmHg

Flash Point:526.6℃

Melting point:120-122℃

Solubility:DMSO: soluble10mg/mL (clear solution, warmed)

 

 

Norvir was launched in Germany, the UK and US for treatment of advanced HIV in combination with antiretroviral nucleoside analogs in a record 72 days by the FDA. It is an inhibitor of HIV aspartic protease which is critical in the processing of a propeptide into the gag, gag-pol gene products and the protease itself. This inhibition results in the release of non-infectous immature virus particles. It is greater than 500-fold more selective for viral aspartic protease than the human version, has good oral bioavailability and may increase the bioavailability of other protease inhibitors. Ritonavir was able to increase the CD4 and CD8 lymphocyte count as well as reduce viral RNA. It is more potent than saqunavir and comparible in potency to zidovudine and lamivudine.

 

Ritonivir is an HIV protease inhibitor (EC50 = 25 nM) that also inhibits CYP3A4, the primary cytochrome P450 isoform that metabolizes protease inhibitors. Through CYP3A4 inhibition, low doses of ritonivir can reduce the metabolism of concomitantly administered protease inhibitiors, enhancing their bioavailability and efficacy

 

 

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