ZPCK

ZPCK
  • CAS No.:26049-94-5
Other grades of this product :
ZPCK Basic information
Product Name:ZPCK
Synonyms:SL-01;carbamicacid,[3-chloro-2-oxo-1-(phenylmethyl)propyl]-,phenylmethylester,(s;(S)-benzyl [1-benzyl-3-chloro-2-oxopropyl]carbamate;N-CBZ-L-PHENYLALANINE CHLOROMETHYL*KETON E;z-l-phe chloromethyl ketone;(S)-Penzyl [1-benzyl-3-chloro-2-oxopropyl]carbamate.;ZPCK, N-Carbobenzyloxy-L-phenylalanyl chloromethyl ketone;(3S)-1-Chloro-3-(benzyloxycarbonylamino)-4-phenyl-2-butanone
CAS:26049-94-5
MF:C18H18ClNO3
MW:331.79
EINECS:247-432-8
Product Categories:
Mol File:26049-94-5.mol
ZPCK Chemical Properties
Melting point 107-108 °C(lit.)
Boiling point 503.1±50.0 °C(Predicted)
density 1.1630 (rough estimate)
refractive index 1.6470 (estimate)
storage temp. -20°C
solubility Soluble in DMSO (up to 50 mg/ml) or in Ethanol (up to 15 mg/ml with warming).
pka10.74±0.46(Predicted)
form solid
color White
optical activity[α]23/D +30°, c = 1 in chloroform
Stability:Stable for 2 years from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20° for up to 1 month.
CAS DataBase Reference26049-94-5
EPA Substance Registry SystemBenzyl [(1S)-3-chloro-2-oxo-1-benzylpropyl]carbamate (26049-94-5)
Safety Information
Hazard Codes C
Risk Statements 34
Safety Statements 26-27-36/37/39-45
RIDADR UN 3261 8/PG 2
WGK Germany 3
HS Code 29225000
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
ZPCK Usage And Synthesis
DescriptionSL-01 (26049-94-5) inhibits the p53-MDM2 interaction (20 μM). Has also been shown to inhibit bovine chymotrypsin A-γ.
Chemical Propertieswhite powder
UsesZPCK's a peptidase from baker's yeast,and it is with esterase activities of carboxypeptidase Y.
UsesSL 01 is a prodrug of gemcitabine , the nucleoside analog used intravenously to treat various cancers that was designed for improved oral bioavailability. SL 01 can inhibit the growth of human non-small cell lung cancer NCI-H460 cells, colon cancer HCT-116 cells, and breast cancer MCF-7 cells (IC50s = 0.78, 0.92, and 0.64 μM, respectively), inducing apoptosis. In nude mice bearing NCI-H460, HCT-116, or MCF-7 cancer cell xenografts, SL 01 at 10-50 μM/kg has been shown to delay tumor growth.
UsesEnzyme inhibitor.
References1) Li et al. (2011), A cell-based high-throughput assay for the screening of small-molecule inhibitors of p53-MDM2 interaction; J. Biomol. Screening, 16 450
ZPCK Preparation Products And Raw materials

Welcome!

Please leave a message for us or use the following ways to contact us, we will reply to you as soon as possible, and provide you with the most sincere service, thank you.

  • NO. 18 ,Wujiang Road, Wulidian Street, Jiangbei District, Chongqing
  • +86-23-6139-8061 +86-13650506873
  • danny@chemdad.com sales@chemdad.com
  • www.chemdad.com
  • WhatsApp +86-13650506873

Name

phone

company

email

message

Payment methods
Google translate: 日本语日本语 한국어한국어 FrançaisFrançais DeutschDeutsch EspañaEspaña TürkiyeTürkiye