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TPCK

Basic information Safety Supplier Related

TPCK Basic information

Product Name:
TPCK
Synonyms:
  • L-1-TOSYLAMIDE-2-PHENYLETHYL-CHLOROMETHYL KETONE
  • L-1-P-TOSYLAMINO-2-PHENYLETHYL CHLOROMETHYL KETONE
  • L-1-CHLORO-3-(4-TOSYLAMIDO)-4-PHENYL-2-BUTANONE
  • L-1-CHLORO-3-TOSYLAMIDO-4-PHENYL-2-BUTANONE
  • L-1-4'-TOSYLAMINO-2-PHENYLETHYL CHLOROMETHYL KETONE
  • N-TOSYL-L-PHENYLALANINE CHLOROMETHYL KETONE
  • N-TOSYL-PHE-CHLOROMETHYLKETONE
  • N-TOSYLAMIDE PHENETHYL CHLOROMETHYLKETONE
CAS:
402-71-1
MF:
C17H18ClNO3S
MW:
351.85
EINECS:
206-954-6
Product Categories:
  • Apoptosis Inhibitors
Mol File:
402-71-1.mol
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TPCK Chemical Properties

Melting point:
106-108 °C(lit.)
Boiling point:
509.9±60.0 °C(Predicted)
Density 
1.1350 (rough estimate)
refractive index 
1.6100 (estimate)
storage temp. 
-20°C
solubility 
DMSO: >10 mg/mL stable for several months at 4°C.
form 
powder
pka
8.71±0.50(Predicted)
color 
white
BRN 
2895215
Stability:
Stable for 1 year from date of purchase as supplied. Solutions in DMSO may be stored at -20° for up to 3 months.
CAS DataBase Reference
402-71-1
EPA Substance Registry System
Benzenesulfonamide, N-[(1S)-3-chloro-2-oxo-1-(phenylmethyl)propyl]-4-methyl- (402-71-1)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
37/38-41
Safety Statements 
26-36
RIDADR 
UN 3335
WGK Germany 
3
RTECS 
XT5613500
10-19-21
TSCA 
Yes
HS Code 
29350090

MSDS

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TPCK Usage And Synthesis

Description

TPCK (402-71-1) is an irreversible inhibitor of the serine protease chymotrypsin.1 It also inhibits certain cysteine proteases (bromelain, ficin, papain).1 TPCK inhibited (IC50 = 5 μM) the mitogen-induced activation of pp70s6k, a mitogen-regulated serine/threonine kinase involved in the G1 to S phase transition of the cell cycle.2

Chemical Properties

white crystalline powder

Uses

N-α-Tosyl-L-phenylalanylchloromethane is a proteinase inhibitors with apoptotic function. Studies have shown that it induces caspase-dependent apoptosis in Epstein-Barr virus (EBV)-transformed human B cell lines with release of pro-apoptotic proteins from mitochondria. It also results in down-regulation of the anti-apoptotic proteins and caspase-dependent cleavage of two anti-apoptotic proteins. I t promotes dephosphorylation of p53 on serine residues.

Uses

N-α-Tosyl-L-phenylalanylchloromethane is a proteinase inhibitors with apoptotic function. Studies have shown that it induces caspase-dependent apoptosis in Epstein-Barr virus (EBV)-transformed human B cell lines with release of pro-apoptotic proteins from mitochondria. It also results in down-regulation of the anti-apoptotic proteins and caspase-dependent cleavage of two anti-apoptotic proteins. It promotes dephosphorylation of p53 on serine residues.

Definition

ChEBI: The N-tosyl derivative of L-phenylalanyl chloromethyl ketone.

Biochem/physiol Actions

Blocks the LPS- or cytokine-induced activation of nuclear factor κB (NFκB), which, in turn, blocks the induction of iNOS and COX-2 transcription. Blocks activation of pp70s6k by all mitogens. Blocks apoptosis cell lines by inhibiting the processing of caspases in some cell lines and to some stimuli. Also blocks apoptosis initiated by Taxol (in MCF-7 human breast carcinoma cells).

Safety Profile

Experimental reproductive effects. A flammable liquid. When heated to decomposition it emits toxic fumes of NOx, SOx, and Cl-.

References

1) Bond and Butler, (1987) Intracellular proteases; Annu. Rev. Biochem., 56 333 2) Grammer and Blenis (1996) The serine protease inhibitors, tosylphenylalanine chloromethylketone and tosyllysine chloromethylketone, potently inhibit pp70s6k activation; J. Biol. Chem., 271 23650

TPCKSupplier

J & K SCIENTIFIC LTD.
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010-82848833 400-666-7788
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jkinfo@jkchemical.com
Meryer (Shanghai) Chemical Technology Co., Ltd.
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4006608290; 18621169109
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market03@meryer.com
3B Pharmachem (Wuhan) International Co.,Ltd.
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821-50328103-801 18930552037
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3bsc@sina.com
TCI (Shanghai) Development Co., Ltd.
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021-67121386
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Sales-CN@TCIchemicals.com
Energy Chemical
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021-021-58432009 400-005-6266
Email
sales8178@energy-chemical.com