SAH

Modify Date: 2024-01-02 15:26:05

SAH Structure
SAH structure
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 N/A
MSDS USA Flash Point 430.0±35.7 °C

 Use of SAH


SAH is an amino acid derivative and a modulartor in several metabolic pathways. It is an intermediate in the synthesis of cysteine and adenosine.

 Names

Name S-adenosyl-L-homocysteine
Synonym More Synonyms

 SAH Biological Activity

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
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
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

 Synthetic Route

 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
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