![S-[N-Benzyl(thiocarbamoyl)]-L-cysteine (CAS 35446-36-7) - chemical structure image](https://media.scbt.com/product/s-n-benzyl-thiocarbamoyl--l-cysteine-35446-36-7-structure_17_24_b_172478.jpg)
![S-[N-Benzyl(thiocarbamoyl)]-L-cysteine (CAS 35446-36-7) - chemical structure image](https://media.scbt.com/product/s-n-benzyl-thiocarbamoyl--l-cysteine-35446-36-7-structure_17_24_t_172478.jpg "Molecular structure of S-[N-Benzyl(thiocarbamoyl)]-L-cysteine, CAS Number: 35446-36-7")
Molecular structure of S-[N-Benzyl(thiocarbamoyl)]-L-cysteine, CAS Number: 35446-36-7
S-[N-Benzyl(thiocarbamoyl)]-L-cysteine (CAS 35446-36-7)
Alternate Names:
L-Cysteine (Phenylmethyl)carbamodithioate
CAS Number:
35446-36-7
Molecular Weight:
270.37
Molecular Formula:
C11H14N2O2S2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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Induction of Glutathione S-transerase (GST) activity by anticarcinogenic compounds is believed to be a major mechanism for carcinogen detoxification. This compound induces Glutathione S-transerase activity in target organs of mice.
S-[N-Benzyl(thiocarbamoyl)]-L-cysteine (CAS 35446-36-7) References
Benson, A.M., et al.: Cancer Res., 38, 4486 (1978); Spanins, V.L., et al.: J. Natl. Cancer Inst., 68, 493 (1982); Lam, L.K.T., et al.: Nutr. Cancer, 12, 43 (1989); Zheng, G., et al.: J. Med. Chem., 35, 185 (1992)Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
S-[N-Benzyl(thiocarbamoyl)]-L-cysteine, 100 mg | sc-212810 | 100 mg | $300.00 |