Weight | 369.314 g/mol |
---|---|
Formula | C14H22Cl2N2O3S |
Hydrogen Acceptors | 4 |
Hydrogen Donors | 2 |
Aromatic Rings | 1 |
Rotatable Bonds | 9 |
TLCK hydrochloride (4238-41-9, 4272-74-6)
TLCK · Tosyllysine Chloromethyl Ketone · Tosyllysyl Chloromethane
Score:
#84 in Molecular and cellular biology
,
#2390 in Biochemistry
,
#4717 in Biology
,
#5995 in Chemistry
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- Nonlysosomal, pre-Golgi degradation of unassembled asialoglycoprotein receptor subunits: a TLCK- and TPCK-sensitive cleavage within the ER. (Journal of Cell Biology, 1991)
- Identification of the histidine residue at the active center of trypsin labelled by TLCK. (Biochemical and Biophysical Research Communications, 1967)
- Ethanol-Induced Apoptosis in Hepatoma Cells Proceeds via Intracellular Ca2+ Elevation, Activation of TLCK-Sensitive Proteases, and Cytochrome c Release (Experimental Cell Research, 2001)
- The Serine Protease Inhibitors, Tosylphenylalanine Chloromethyl Ketone and Tosyllysine Chloromethyl Ketone, Potently Inhibit pp70s6k Activation (Journal of Biological Chemistry, 1996)
- The site of action of N-alpha-tosyl-L-lysyl-chloromethyl-ketone (TLCK) on cloned cytotoxic T lymphocytes. (Journal of Immunology, 1983)
- Serine protease inhibitors N--Tosyl-L-Lysinyl-Chloromethylketone (TLCK) and N-Tosyl-L-Phenylalaninyl-Chloromethylketone (TPCK) are potent inhibitors of activated caspase proteases (Journal of Cellular Biochemistry, 2008)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - TLCK
- Tosyllysine Chloromethyl Ketone
- Tosyllysyl Chloromethane
- Chlorotosylamidoaminoheptanone
-
SMILESCC1=CC=C(C=C1)S(=O)(=O)NC(CCCCN)C(=O)CCl.Cl
-
InChIKeyYFCUZWYIPBUQBD-UHFFFAOYSA-N
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
P-TOLUENESULFONAMIDE
+
Reactant
(Alkylation of primary amines)
Reactant
+
Dichloromethane
(Grignard carbonyl)
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