| Weight | 222.266 g/mol |
|---|---|
| Formula | C7H14N2O4S |
| Hydrogen Acceptors | 5 |
| Hydrogen Donors | 4 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 7 |
L-cystathionine (56-88-2)
Cystathionine
Score:
#1237 in Biochemistry
,
#3072 in Biology
,
#3841 in Chemistry
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- H2S as a Physiologic Vasorelaxant: Hypertension in Mice with Deletion of Cystathionine -Lyase (Science, 2008)
- The natural history of homocystinuria due to cystathionine beta-synthase deficiency. (American Journal of Human Genetics, 1985)
- Mice deficient in cystathionine beta-synthase: animal models for mild and severe homocyst(e)inemia. (Proceedings of the National Academy of Sciences of the United States of America, 1995)
- Relative Contributions of Cystathionine -Synthase and -Cystathionase to H2S Biogenesis via Alternative Trans-sulfuration Reactions (Journal of Biological Chemistry, 2009)
- Elevation of serum cystathionine levels in patients with cobalamin and folate deficiency (Blood, 1993)
- H2S Biogenesis by Human Cystathionine -Lyase Leads to the Novel Sulfur Metabolites Lanthionine and Homolanthionine and Is Responsive to the Grade of Hyperhomocysteinemia (Journal of Biological Chemistry, 2009)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Cystathionine
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SMILESC(CSCC(C(=O)O)N)C(C(=O)O)N
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InChIKeyILRYLPWNYFXEMH-UHFFFAOYSA-N
- Pubchem - L-cystathionine
- Wikipedia - L-cystathionine
Cystathionine is an intermediate in the synthesis of cysteine. Cystathionine is produced by the transsulfuration pathway which converts homocysteine into cystathionine. The cystathionine is then used by the cystathionine gamma-lyase CTH, cysteine dioxygenase CDO, and cysteine sulfinic acid decarboxylase CSAD gene enzymes to produce hypotaurine and then taurine.
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L-cystathionine
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