S-[N-BENZYL(THIOCARBAMOYL)]-L-CYSTEINE
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![S-[N-BENZYL(THIOCARBAMOYL)]-L-CYSTEINE structure](https://file.echemi.com/fileManage/upload/canonicalSmiles/20220811/935b099e139d4113974fd4f9f9ac89f3.png "S-[N-BENZYL(THIOCARBAMOYL)]-L-CYSTEINE")
S-[N-BENZYL(THIOCARBAMOYL)]-L-CYSTEINE
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CAS No:
35446-36-7
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Formula:
C11H14N2O2S2
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Chemical Name:
S-[N-BENZYL(THIOCARBAMOYL)]-L-CYSTEINE
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Synonyms:
s-(n-benzylthiocarbamoyl)cysteine;S-[N-BENZYL(THIOCARBAMOYL)]-L-CYSTEINE;L-Cysteine (PhenylMethyl)carbaModithioate;Uraton
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CAS No:
S-[N-BENZYL(THIOCARBAMOYL)]-L-CYSTEINE Use and Manufacturing
Induction of Glutathione S-transerase (GST) activity by anticarcinogenic compounds is believed to be a major mechanism for carcinogen detoxification. This compound has shown to induce Glutathione S- transerase activity in target organs of mice with no apparent toxic effects.
Computed Properties
Molecular Weight:270.4
XLogP3:-1
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:6
Exact Mass:270.04967004
Monoisotopic Mass:270.04967004
Topological Polar Surface Area:133
Heavy Atom Count:17
Complexity:268
Defined Atom Stereocenter Count:1
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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