Name | S-sulfo-L-cysteine |
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Synonyms |
S-Sulfocysteine
S-sulpho-L-cysteine Cysteinyl-S-sulfonate S-Sulfo-L-cystein S-Sulphocysteine L-Cysteine S-sulfate (2R)-2-amino-3-sulfosulfanylpropanoic acid Cysteine-S-sulfonate S-Sulfo-L-cysteine Cysteine-S-sulfate Cysteinyl-S-sulfonic acid MFCD00133440 |
Description | L-Cysteine S-sulfate is a potent N-methyl-d-aspartate (NMDA) glutamatergic receptors agonist. L-Cysteine S-sulfate is the substrate for cystine lyase[1]. |
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Related Catalog | |
Target |
Human Endogenous Metabolite |
References |
Melting Point | 184-185ºC |
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Molecular Formula | C3H7NO5S2 |
Molecular Weight | 201.22100 |
Exact Mass | 200.97700 |
PSA | 151.37000 |
LogP | 0.71540 |
Index of Refraction | 1.604 |
Storage condition | −20°C |
Stability | Store in Freezer at -20°C |
Water Solubility | H2O: 20 mg/mL, clear, colorless |
Symbol |
![]() GHS07 |
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Signal Word | Warning |
Hazard Statements | H315-H319-H335 |
Precautionary Statements | P261-P305 + P351 + P338 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
Hazard Codes | Xi: Irritant; |
Risk Phrases | 36/37/38 |
Safety Phrases | 26-36 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
HS Code | 2930909090 |
~% 1637-71-4 |
Literature: Reitz et al. Journal of the American Chemical Society, 1946 , vol. 68, p. 1026,1030 |
~% 1637-71-4 |
Literature: Clarke Journal of Biological Chemistry, 1932 , vol. 97, p. 235,240,243,246 |
~% 1637-71-4 |
Literature: Uda, Narutoshi; Matoba, Yasuyuki; Kumagai, Takanori; Oda, Kosuke; Noda, Masafumi; Sugiyama, Masanori Antimicrobial Agents and Chemotherapy, 2013 , vol. 57, # 6 p. 2603 - 2612 |
~% 1637-71-4 |
Literature: Reitz et al. Journal of the American Chemical Society, 1946 , vol. 68, p. 1026,1030 |
~% 1637-71-4 |
Literature: Micheel; Bode Chemische Berichte, 1938 , vol. 71, p. 2653,2655 |
Precursor 6 | |
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DownStream 3 | |
HS Code | 2930909090 |
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Summary | 2930909090. other organo-sulphur compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0% |