![S-[N-(3-PHENYLPROPYL)(THIOCARBAMOYL)]-L-CYSTEINE](/img/137915-13-0.jpg "S-[N-(3-PHENYLPROPYL)(THIOCARBAMOYL)]-L-CYSTEINE")
| S-[N-(3-PHENYLPROPYL)(THIOCARBAMOYL)]-L-CYSTEINE Basic information |
| Product Name: | S-[N-(3-PHENYLPROPYL)(THIOCARBAMOYL)]-L-CYSTEINE |
| Synonyms: | S-[N-(3-PHENYLPROPYL)(THIOCARBAMOYL)]-L-CYSTEINE;S-(N-PHENYLPROPYLTHIOCARBAMOYL)-L-*CYSTE INE;S-(N-(3-phenylpropyl)(thiocarbamoyl))-cysteine;L-Cysteine (3-Phenylpropyl)carbaModithioate (ester);(2R)-2-amino-3-(3-phenylpropylcarbamothioylsulfanyl)propanoicaci;S-[N-(3-PHENYLPROPYL)(THIOCARBAMOYL)]-L-CYSTEINE USP/EP/BP |
| CAS: | 137915-13-0 |
| MF: | C13H18N2O2S2 |
| MW: | 298.42 |
| EINECS: | |
| Product Categories: | Amino Acids & Derivatives;Aromatics;Glutathione S-Transferase Agents;Sulfur & Selenium Compounds |
| Mol File: | 137915-13-0.mol |
| S-[N-(3-PHENYLPROPYL)(THIOCARBAMOYL)]-L-CYSTEINE Chemical Properties |
| Melting point | 224-225°C dec. |
| form | White solid |
| color | White |
| Safety Information |
| MSDS Information |
| S-[N-(3-PHENYLPROPYL)(THIOCARBAMOYL)]-L-CYSTEINE Usage And Synthesis |
| Chemical Properties | White Solid |
| Uses | 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. |
| Uses | 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. |
| S-[N-(3-PHENYLPROPYL)(THIOCARBAMOYL)]-L-CYSTEINE Preparation Products And Raw materials |
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