979-92-0

979-92-0 structure
979-92-0 structure
  • Name: SAH
  • Chemical Name: S-adenosyl-L-homocysteine
  • CAS Number: 979-92-0
  • Molecular Formula: C14H20N6O5S
  • Molecular Weight: 384.411
  • Catalog: Biochemical Amino acids and their derivatives Cysteine derivative
  • Create Date: 2018-05-15 08:00:00
  • Modify Date: 2026-06-30 13:30:59
  • SAH is an amino acid derivative and a modulartor in several metabolic pathways. It is an intermediate in the synthesis of cysteine and adenosine.

Name S-adenosyl-L-homocysteine
Synonyms (S)-5'-(S)-(3-amino-3-cboxypropyl)-5'-thioadenosine
Butanedisulfonate Ademetionine Impurity
(2S)-adenosylhomocysteine
Adenosyl-L-hoMocysteine-13C5
Adenosyl-L-homocysteine
S-(5'-Adenosyl)-L-homocysteine;AdoHcy;S-(5'-Deoxyadenosine)-L-homocysteine
L-Homocysteine, S-(5'-deoxyadenosin-5'-yl)
S-(5'-deoxyadenosin-5'-yl)
5'-DEOXY-S-ADENOSYL-L-HOMOCYSTEINE //BP
SAH (S-Adenosyl-L-homocysteine)
S-(5′-Adenosyl)-L-homocysteine,5′-Deoxy-S-adenosyl-L-homocysteine, AdoHcy, S-(5′-Deoxyadenosine-5′)-L-homocysteine
S-(5'-Deoxyadenosin-5'-yl)-L-hoMocysteine-13C5
Adenosylhomocysteine
(S)-2-Amino-4-[[[(2S,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxy-2-tetrahydrofuryl]methyl]thio]butanoic Acid
5μ-Deoxy-S-adenosyl-L-homocysteine, AdoHcy, S-(5μ-Deoxyadenosine-5μ)-L-homocysteine
(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
S-(5′-Adenosyl)-L-homocysteine
SAH, 10 mM in DMSO
S-Adenosyl- L -homocysteine
S-adenosine-l-homocysteine
inhibit,SAH,Endogenous Metabolite,Inhibitor
L-adenosyl-L-homocysteine
S-(5'-DEOXYADENOSINE-5')-L-HOMOCYSTEINE
Adenosyl)- L -homocysteine
(S)-2-amino-4-((((2S,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl)thio)butanoic acid
L-S-AdenosylhoMocysteine-13C5
S-Adenosyl-L-Homocysteine (50 mg)
S-(5'-Deoxyadenosine)-L-homocysteine
5'-DEOXY-S-ADENOSYL
S-(5'-Adenosyl)-L-homocysteine
(2S)-2-amino-4-[[(2S,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxy-oxolan-2-yl]methylsulfanyl]butanoic acid
L-5'-S-(3-Amino-3-cboxypropyl)- 5'-thioadenosine
HOMOCYSTEINE, S-ADENOSYL
AdenosylhoMocysteine-13C5
S-(5''-Adenosyl)-L-homocysteine, Amino acid derivative
D4-S- (5'-Adenosyl)-L-homocysteine
5-( 3-AMINO.-3 CBOXYPROPYL) THIO ) -5-DEOXYADENOSINE
5'-Deoxy-S-Adenosyl-L-Homocystmine
S-ADENOSYL-L-HOMOCYSTEINE
S-ADENOSYL-L-HOMOCYSTEINE (ADENOSINE-13C10, )
S-Adenosyl-L-homocystein
hpce
S-((5-(6-amino-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl)homocysteine
S-(5'-Deoxyadenosin-5'-yl)-L-hoMocysteine
S-(5′-Adenosyl)- L -homocysteine
5-S'-[(S)-3-Amino-3-cboxypropyl]-5'-thioadenosine
S-Adenosyl-L-Homecysteine
SAH (S-Adenosylhomocysteine)
L-S-AdenosylhoMocysteine
s-adenosylhomocysteine
S-(5'-Adenosyl)-L-homocysteine dihydrate
5'-DEOXY-S-ADENOSYL-L-HOMOCYSTEINE
ADOHCY
Ademetionine 1,4-Butanedisulfonate Impurity 1
L-5'-S-(3-Amino-3-cboxypropyl)- 5'-thioadenosine-13C5
S-(5-Adenosyl)-L-Homocysteine extrapure
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.

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 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
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
HS Code 2934999090
Summary 2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%
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