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PD 135390

HCID 44153444
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Basic information

CAS
150351-31-8
Standard SMILES
C=CCS[C@@H](C(=O)NC(=O)[C@@H](N)Cc1ccccc1)N(C(CC1CCCCC1)C(O)CC(C(=O)NCCCC)C(C)C)S(=O)(=O)N1CCOCC1
InChIKey
AAAQSMBDXOUJHS-ITQWLJMDSA-N
Molecular formula
C37H61N5O7S2
Average molar mass
752 g/mol
Monoisotopic mass
751.40124165

Overview

structure given in first source

Names & identifiers

Preferred name
PD 135390
IUPAC
5-[[(1S)-2-[[(2S)-2-amino-3-phenylpropanoyl]amino]-2-oxo-1-prop-2-enylsulfanylethyl]-morpholin-4-ylsulfonylamino]-N-butyl-6-cyclohexyl-4-hydroxy-2-propan-2-ylhexanamide
English name
PD 135390
Molecular formula
C37H61N5O7S2
Molecular weight
752.04

Names & synonyms

PD-135390RefChem:170532150351-31-8PD 135390Glycinamide, N-(4-morpholinylsulfonyl)phenylalanyl-N-(4-((butylamino)carbonyl)-1-(cyclohexylmethyl)-2-hydroxy-5-methylhexyl)-2-(2-propenylthio)-DTXSID709339125-(N-{(1S)-2-{[(2S)-2-Amino-1-hydroxy-3-phenylpropylidene]amino}-2-oxo-1-[(prop-2-en-1-yl)sulfanyl]ethyl}morpholine-4-sulfonamido)-N-butyl-6-cyclohexyl-4-hydroxy-2-(propan-2-yl)hexanimidic acid5-[{2-[(2-Amino-1-hydroxy-3-phenylpropylidene)amino]-2-oxo-1-[(prop-2-en-1-yl)sulfanyl]ethyl}(morpholine-4-sulfonyl)amino]-N-butyl-6-cyclohexyl-4-hydroxy-2-(propan-2-yl)hexanimidic acid(Rac)-PD 135390Glycinamide, N-(4-morpholinylsulfonyl)phenylalanyl-N-[4-[(butylamino)carbonyl]-1-(cyclohexylmethyl)-2-hydroxy-5-methylhexyl]-2-(2-propenylthio)- (9CI)

Database identifiers

CAS
150351-31-8
PubChem CID
44153444
DTXSID
DTXSID70933912

Properties

Computed structural properties

XLogP
5.4
Topological polar surface area
205 Ų
Hydrogen bond donors
4
Hydrogen bond acceptors
11
Rotatable bonds
21
Heavy atoms
51
Formal charge
0
Complexity
1,180

Physicochemical properties

Density
1.21 · 1.21±0.1 g/cm3(Predicted)
pka
10.88 · 10.88±0.20(Predicted)

Chemistry & industry

Applications · 2 items

DescriptionPD 135390 is a novel HIV-1 protease inhibitors identified by rational selection. The human immunodeficiency virus (HIV-1), associated with the AIDS (acquired immunodeficiency syndrome) epidemic, encodes an aspartyl protease that is essential for polyprotein processing in the virus (Navia et al., 1989). It has been demonstrated that inactivation of the protease either catalytically or by an inhibitor prevents infectious virion formation (Kohl et al., 1988; Darke et al., 1989). The acquired knowledge of key molecular interactions occurring between inhibitors and aspartyl proteases, as well as the structural similarities between HIV-1 protease and human renin was used to rationally select candidates for HIV-1 screening from the pool of analogs designed as renin inhibitors. A minimal number of chosen compounds were tested in an HIV-1 protease assay system. Two structurally novel peptides emerged as potent enzymatic protease inhibitors. This study highlights the selection process and characterizes the antiviral properties of the two novel analogs.

Uses(Rac)-PD 135390 is a dipeptide and an HIV-1 protease inhibitor with an IC50 of 2 nM. (Rac)-PD 135390 can be utilized in antiviral research[1].

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