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About This Item
Empirical Formula (Hill Notation):
C26H32N3O5Cl
CAS Number:
Molecular Weight:
502.00
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352200
MDL number:
biological source
synthetic (organic)
Quality Segment
assay
≥90% (TLC)
form
solid
solubility
DMSO: 1 mg/mL, clear, colorless
storage temp.
−20°C
SMILES string
CC(C)C[C@H](NC(=O)CNC(=O)OCc1ccccc1)C(=O)N[C@@H](Cc2ccccc2)C(=O)CCl
InChI
1S/C26H32ClN3O5/c1-18(2)13-22(25(33)30-21(23(31)15-27)14-19-9-5-3-6-10-19)29-24(32)16-28-26(34)35-17-20-11-7-4-8-12-20/h3-12,18,21-22H,13-17H2,1-2H3,(H,28,34)(H,29,32)(H,30,33)/t21-,22-/m0/s1
InChI key
BRGPJZPHCVTNNI-VXKWHMMOSA-N
Biochem/physiol Actions
Cathepsin G inhibitor.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Related Content
Datasheet
Substrate binding site in bovine chymotrypsin A-gamma. A crystallographic study using peptide chloromethyl ketones as site-specific inhibitors.
D M Segal et al.
Biochemistry, 10(20), 3728-3738 (1971-09-28)