D-eritadenine

lentysine

CAS: 23918-98-1 C9 H11 N5 O4 MW: 253.21847000

Identification

NameD-eritadenine
CAS Number23918-98-1
FDA UNII41T27K4B9F
Molecular FormulaC9 H11 N5 O4
Molecular Weight253.21847000
Nikkaji NumberJ16.032F
XlogP3-1.80 (est)

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Soluble in water, 2.406e+004 mg/L @ 25 °C (est)

No sensory data available

Safety Information

Oral/Parenteral ToxicityNot determined
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categorynatural substances and extractives
Recommendation for D-eritadenine usage levels up tonot for fragrance use.
Recommendation for D-eritadenine flavor usage levels up tonot for flavor use.

BOC Sciences

Best of Chemicals Supplier

Quality supplier of research chemicals and biochemicals including inhibitors, building blocks, GMP Products, impurities and metabolites, APIs for Veterinary, Natural Compounds, ADCs, Stem Cell Molecul...

View All Website 1-631-485-4226 account@bocsci.com

Potential Uses

None Found

Natural Occurrence

mushroom shitake mushroom PMC

Synonyms

D-4-(6- amino-9H-purin-9-yl)-4-deoxyerythronic acid (2R,3R)-4-(6- aminopurin-9-yl)-2,3-dihydroxybutanoic acid D-erythro- eritadenine erythronic acid, 4-(6-amino-9H-purin-9-yl)-4-deoxy-, D- lentysine 9H- purine-9-butanoic acid, 6-amino-alpha,beta-dihydroxy-, (R-(R*,R*))- (9CI) PubMed: Efficacy of S-adenosylhomocysteine hydrolase inhibitors, D-eritadenine and (S)-DHPA, against the growth of Cryptosporidium parvum in vitro. PubMed: Characterization of S-adenosylhomocysteine hydrolase from Cryptosporidium parvum. PubMed: Structure and function of eritadenine and its 3-deaza analogues: potent inhibitors of S-adenosylhomocysteine hydrolase and hypocholesterolemic agents. PubMed: Inhibition of S-adenosylhomocysteine hydrolase by acyclic sugar adenosine analogue D-eritadenine. Crystal structure of S-adenosylhomocysteine hydrolase complexed with D-eritadenine. PubMed: High recombinagenic activities of three antiviral agents, adenine derivatives, in the Drosophila wing spot test. PubMed: Inhibition of phosphatase by open-chain nucleoside analogues in insects. PubMed: Disposition of homocysteine in rat hepatocytes and in nontransformed and malignant mouse embryo fibroblasts following exposure to inhibitors of S-adenosylhomocysteine catabolism. PubMed: The synergism of nucleoside antibiotics combined with guanine 7-N-oxide against a rhabdovirus, infectious hematopoietic necrosis virus (IHNV). PubMed: The effect of aliphatic adenine analogues on S-adenosylhomocysteine and S-adenosylhomocysteine hydrolase in intact rat hepatocytes.