137915-13-0

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)
• CAS NO: 137915-13-0
• Molecular Formula: C₁₃H₁₈N₂O₂S₂
• Molecular Weight: 298.42
• Product Categories: Glutathione S-Transferase Agents;Amino Acids & Derivatives;Aromatics;Sulfur & Selenium Compounds
• Mol File: 137915-13-0.mol
• Article Data: 2

Chemical Properties

• Melting Point: 224-225°C dec.
• Boiling Point: 479.1 °C at 760 mmHg
• Flash Point: 243.5 °C
• Appearance: /
• Density: 1.29 g/cm³
• Vapor Pressure: 5.49E-10mmHg at 25°C
• Refractive Index: 1.636
• CAS DataBase Reference: S-[N-(3-PHENYLPROPYL)(THIOCARBAMOYL)]-L-CYSTEINE(CAS DataBase Reference)
• NIST Chemistry Reference: S-[N-(3-PHENYLPROPYL)(THIOCARBAMOYL)]-L-CYSTEINE(137915-13-0)
• EPA Substance Registry System: S-[N-(3-PHENYLPROPYL)(THIOCARBAMOYL)]-L-CYSTEINE(137915-13-0)

Safety Data

• Hazardous Substances Data: 137915-13-0(Hazardous Substances Data)

Usage

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.

InChI:InChI=1/C13H18N2O2S2/c14-11(12(16)17)9-19-13(18)15-8-4-7-10-5-2-1-3-6-10/h1-3,5-6,11H,4,7-9,14H2,(H,15,18)(H,16,17)/t11-/m0/s1

Upstream product

• 52-90-4 L-Cysteine 
• 2627-27-2 3-phenylpropyl isothiocyanate 
• 52-89-1 l-cysteine hydrochloride 

Relevant articles and documents

Phenylalkyl Isothiocyanate-Cysteine Conjugates as Glutathione S-Transferase Stimulating Agents

The develop analogues of phenylalkyl isothiocyanate with less toxicity and better biological activity, two water-soluble phenylalkyl isothiocyanate-cysteine conjugates, S--L-cysteine (1) and S--L