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930636

Sigma-Aldrich

VH 032 amide-alkyl C5-acid

≥95%

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Synonym(s):
(S,R,S)-AHPC-CO-C5-acid, (S,R,S)-AHPC-amido-C5-acid, 6-{[(2S)-1-[(2S,4R)-4-hydroxy-2-({[4-(4-methyl-1,3-thiazol-5-yl)phenyl]methyl}carbamoyl)pyrrolidin-1-yl]-3,3-dimethyl-1-oxobutan-2-yl]carbamoyl}hexanoic acid, L-Prolinamide, N-(6-carboxy-1-oxohexyl)-3-methyl-L-valyl-4-hydroxy-N-[[4-(4-methyl-5-thiazolyl)phenyl],methyl]-, (4R)-
Empirical Formula (Hill Notation):
C29H40N4O6S
CAS Number:
Molecular Weight:
572.72
MDL number:
UNSPSC Code:
12352106
NACRES:
NA.21

ligand

VH032

Quality Level

Assay

≥95%

form

powder

functional group

carboxylic acid

storage temp.

2-8°C

SMILES string

C([C@@H](NC(CCCCCC(O)=O)=O)C(C)(C)C)(=O)N1[C@H](C(NCC2=CC=C(C=C2)C3=C(C)N=CS3)=O)C[C@@H](O)C1

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Information

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The current inhibitor-based approach to therapeutics has inherent limitations owing to its occupancy-based model: 1) there is a need to maintain high systemic exposure to ensure sufficient in vivo inhibition, 2) high in vivo concentrations bring potential for off-target side effects, and 3) there is
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Traditional pharmaceutical drug discovery is almost exclusively focused on directly controlling protein activity to cure diseases. Modulators of protein activity, especially inhibitors, are developed and applied at high concentration to achieve maximal effects. Thereby, reduced bioavailability and off-target effects can

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