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Substance Name: Tosyl-L-lysine chloromethylketone hydrochloride
RN: 4272-74-6
InChIKey: YFCUZWYIPBUQBD-ZOWNYOTGSA-N

Note

  • An inhibitor of SERINE ENDOPEPTIDASES. Acts as an alkylating agent and is known to interfere with the translation process.

Classification Code

  • Reproductive Effect

Molecular Formula

  • C14-H21-Cl-N2-O3-S.Cl-H

Molecular Weight

  • 369.311
 
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Names and Synonyms

Results Name

  • Tosyl-L-lysine chloromethylketone hydrochloride

Synonyms

  • (S)-N-(5-Amino-1-(chloroacetyl)pentyl)-4-methylbenzenesulfonamide monohydrochloride
  • Benzenesulfonamide, N-(5-amino-1-(chloroacetyl)pentyl)-4-methyl-, monohydrochloride, (S)-
  • EINECS 224-266-4
  • L-N-(5-Amino-1-(chloroacetyl)pentyl)-p-toluenesulfonamide hydrochloride
  • N-alpha-p-Tosyl-L-lysine chloromethyl ketone hydrochloride
  • TLCK hydrochloride
  • Tosyllysine chloromethylketone hydrochloride

Systematic Names

  • (S)-N-(5-Amino-1-(chloroacetyl)pentyl)-p-toluenesulphonamide monohydrochloride
  • Benzenesulfonamide, N-(5-amino-1-(chloroacetyl)pentyl)-4-methyl-, monohydrochloride, (S)-
  • p-Toluenesulfonamide, N-(5-amino-1-(chloroacetyl)pentyl)-, hydrochloride, L-

Registry Numbers

CAS Registry Number

  • 4272-74-6

System Generated Number

  • 0004272746

Molecular Formulas

Molecular Formula

  • C14-H21-Cl-N2-O3-S.Cl-H

Molecular Formula Fragments

  • C14-H21-Cl-N2-O3-S
  • Cl-H
  • COMPONENT

Structure Descriptors

InChI

1S/C14H21ClN2O3S.ClH/c1-11-5-7-12(8-6-11)21(19,20)17-13(14(18)10-15)4-2-3-9-16;/h5-8,13,17H,2-4,9-10,16H2,1H3;1H/t13-;/m0./s1

InChIKey

YFCUZWYIPBUQBD-ZOWNYOTGSA-N

Smiles

c1(ccc(cc1)C)S(=O)(=O)N[C@@H](CCCCN)C(=O)CCl.Cl