CAS 979-92-0|SAH
| Common Name | SAH | ||
|---|---|---|---|
| CAS Number | 979-92-0 | Molecular Weight | 384.411 |
| Density | 1.9±0.1 g/cm3 | Boiling Point | 787.5±70.0 °C at 760 mmHg |
| Molecular Formula | C14H20N6O5S | Melting Point | / |
| MSDS | USA | Flash Point | 430.0±35.7 °C |
Names
| Name | S-adenosyl-L-homocysteine |
|---|---|
| Synonym | More Synonyms |
SAH BiologicalActivity
| Description | SAH is an amino acid derivative and a modulartor in several metabolic pathways. It is an intermediate in the synthesis of cysteine and adenosine. |
|---|---|
| Related Catalog | Natural Products >>Acids and AldehydesResearch Areas >>Others |
| Target | Human Endogenous Metabolite |
| References | [1]. DE LA HABA G, et al. The enzymatic synthesis of S-adenosyl-L-homocysteine from adenosine and homocysteine. J Biol Chem. 1959 Mar;234(3):603-8. |
Chemical & Physical Properties
| Density | 1.9±0.1 g/cm3 |
|---|---|
| Boiling Point | 787.5±70.0 °C at 760 mmHg |
| Molecular Formula | C14H20N6O5S |
| Molecular Weight | 384.411 |
| Flash Point | 430.0±35.7 °C |
| Exact Mass | 384.121582 |
| PSA | 207.93000 |
| LogP | 0.15 |
| Appearance of Characters | crystalline |
| Vapour Pressure | 0.0±2.9 mmHg at 25°C |
| Index of Refraction | 1.839 |
| InChIKey | ZJUKTBDSGOFHSH-WFMPWKQPSA-N |
| SMILES | Nc1ncnc2c1ncn2C1OC(CSCCC(N)C(=O)O)C(O)C1O |
| Storage condition | −20°C |
| Water Solubility | 1 M HCl: soluble19.60 - 20.40mg/mL, clear to slightly hazy, colorless to faintly yellow |
Safety Information
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
|---|---|
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
| HS Code | 2934999090 |
Customs
| HS Code | 2934999090 |
|---|---|
| Summary | 2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
Articles93
More Articles| EZH2 modulates angiogenesis in vitro and in a mouse model of limb ischemia. Mol. Ther. 23(1) , 32-42, (2015) Epigenetic mechanisms may regulate the expression of pro-angiogenic genes, thus affecting reparative angiogenesis in ischemic limbs. The enhancer of zest homolog-2 (EZH2) induces thtrimethylation of l... | |
| Metabolomic profiles delineate potential role for sarcosine in prostate cancer progression. Nature 457(7231) , 910-4, (2009) Multiple, complex molecular events characterize cancer development and progression. Deciphering the molecular networks that distinguish organ-confined disease from metastatic disease may lead to the i... | |
| Characterization of RimO, a new member of the methylthiotransferase subclass of the radical SAM superfamily. Biochemistry 48(42) , 10162-74, (2009) RimO, encoded by the yliG gene in Escherichia coli, has been recently identified in vivo as the enzyme responsible for the attachment of a methylthio group on the beta-carbon of Asp88 of the small rib... |
Synonyms
| S-(5'-Adenosyl)-L-homocysteine |
| (2S)-adenosylhomocysteine |
| Adenosylhomocysteine |
| Adenosyl-L-homocysteine |
| AdenosylhoMocysteine-13C5 |
| (2S)-2-Amino-4-({[(2S,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxytetrahydro-2-furanyl]methyl}sulfanyl)butanoic acid (non-preferred name) |
| HOMOCYSTEINE,S-ADENOSYL |
| L-S-AdenosylhoMocysteine |
| s-adenosylhomocysteine |
| S-ADENOSYL-L-HOMOCYSTEINE |
| L-adenosyl-L-homocysteine |
| hpce |
| ADOHCY |
| 5'-DEOXY-S-ADENOSYL |
