Saquinavir Mesylate

For research use only. Not for therapeutic Use.

  • CAT Number: I001850
  • CAS Number: 149845-06-7
  • Molecular Formula: C38H50N6O5 • CH3SO3H
  • Molecular Weight: 767.00
  • Purity: ≥95%
Inquiry Now

Saquinavir Mesylate(Cat No.:I001850)is an antiretroviral drug used primarily in the treatment of HIV infection. It is a potent inhibitor of the HIV-1 protease enzyme, which is essential for the replication of the virus. By inhibiting this enzyme, Saquinavir Mesylate prevents the maturation of viral particles, reducing viral load and slowing disease progression. This compound is often used in combination with other antiretroviral therapies for optimized treatment. Its high purity and specificity make it a key component in the development of effective HIV management protocols.


Catalog Number I001850
CAS Number 149845-06-7
Synonyms

(2S)-N-[(2S,3R)-4-[(3S,4aS,8aS)-3-(tert-butylcarbamoyl)-3,4,4a,5,6,7,8,8a-octahydro-1H-isoquinolin-2-yl]-3-hydroxy-1-phenylbutan-2-yl]-2-(quinoline-2-carbonylamino)butanediamide;methanesulfonic acid

Molecular Formula C38H50N6O5 • CH3SO3H
Purity ≥95%
Target Metabolic Enzyme/Protease
Solubility 10 mM in DMSO
Storage Store at -20°C
IUPAC Name (2S)-N-[(2S,3R)-4-[(3S,4aS,8aS)-3-(tert-butylcarbamoyl)-3,4,4a,5,6,7,8,8a-octahydro-1H-isoquinolin-2-yl]-3-hydroxy-1-phenylbutan-2-yl]-2-(quinoline-2-carbonylamino)butanediamide;methanesulfonic acid
InChI InChI=1S/C38H50N6O5.CH4O3S/c1-38(2,3)43-37(49)32-20-26-14-7-8-15-27(26)22-44(32)23-33(45)30(19-24-11-5-4-6-12-24)41-36(48)31(21-34(39)46)42-35(47)29-18-17-25-13-9-10-16-28(25)40-29;1-5(2,3)4/h4-6,9-13,16-18,26-27,30-33,45H,7-8,14-15,19-23H2,1-3H3,(H2,39,46)(H,41,48)(H,42,47)(H,43,49);1H3,(H,2,3,4)/t26-,27+,30-,31-,32-,33+;/m0./s1
InChIKey IRHXGOXEBNJUSN-YOXDLBRISA-N
SMILES CC(C)(C)NC(=O)[C@@H]1C[C@@H]2CCCC[C@@H]2CN1C[C@H]([C@H](CC3=CC=CC=C3)NC(=O)[C@H](CC(=O)N)NC(=O)C4=NC5=CC=CC=C5C=C4)O.CS(=O)(=O)O
Reference

<p style=/line-height:25px/>
<br>[1]. Kaldor et al (1995) Isophthalic acid derivatives: amino acid surrogates for the inhibition of HIV-1 protease. Bioorg.Med.Chem.Lett. 5 721.
<br>[2]. Yerino GA, Halabe EK, Zini E, Feleder EC. Bioequivalence study of two oral tablet formulations containing saquinavir mesylate boosted with ritonavir in healthy male subjects. Arzneimittelforschung. 2011;61(8):481-7.
<br>[3]. Branham ML, Moyo T, Govender T. Preparation and solid-state characterization of ball milled saquinavir mesylate for solubility enhancement. Eur J Pharm Biopharm. 2012 Jan;80(1):194-202.
<br>[4]. Brouwers J, Vermeire K, Grammen C, Schols D, Augustijns P. Early identification of availability issues for poorly water-soluble microbicide candidates in biorelevant media: a case study with saquinavir. Antiviral Res. 2011 Aug;91(2):217-23.
<br>[5]. Knechten H, Lutz T, Pulik P, Martin T, Tappe A, Jaeger H. Safety and Efficacy in HIV-1-Infected Patients Treated with Ritonavir-Boosted Saquinavir Mesylate.
</p>

Request a Quote