D-eritadenine, 23918-98-1

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CODE181199 CODE181199
Product(s):
23918-98-1 D-Eritadenine ≥95%
D-Eritadenine is an adenosine analog and a potent, reversible inhibitor of S-adenosylhomocysteine hydrolase. Dietary administra

CAS Number:	23918-98-1	3D/inchi
FDA UNII:	41T27K4B9F
Nikkaji Web:	J16.032F
XlogP3:	-1.80 (est)
Molecular Weight:	253.21847000
Formula:	C9 H11 N5 O4
NMR Predictor:	Predict (works with chrome, Edge or firefox)

Category:natural substances and extractives

US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:

Google Scholar:	Search
Google Books:	Search
Google Scholar: with word "volatile"	Search
Google Scholar: with word "flavor"	Search
Google Scholar: with word "odor"	Search
Google Patents:	Search
US Patents:	Search
EU Patents:	Search
Pubchem Patents:	Search
PubMed:	Search
NCBI:	Search

Physical Properties:

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

Organoleptic Properties:

Odor and/or flavor descriptions from others (if found).

Cosmetic Information:

None found

Suppliers:

BOC Sciences

For experimental / research use only.

D-Eritadenine ≥95%

Odor: characteristic

Use: D-Eritadenine is an adenosine analog and a potent, reversible inhibitor of S-adenosylhomocysteine hydrolase. Dietary administra

Carbosynth

For experimental / research use only.

Eritadenine

Santa Cruz Biotechnology

For experimental / research use only.

D-Eritadenine ≥95%

Safety Information:


Hazards identification

Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements

Pictogram

Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined

Safety in Use Information:

Category:
natural substances and extractives
Recommendation for D-eritadenine usage levels up to:
	not for fragrance use.

Recommendation for D-eritadenine flavor usage levels up to:
	not for flavor use.

Safety References:

EPI System: View

AIDS Citations:Search

Cancer Citations:Search

Toxicology Citations:Search

EPA ACToR:Toxicology Data

EPA Substance Registry Services (SRS):Registry

Laboratory Chemical Safety Summary :159961

National Institute of Allergy and Infectious Diseases:Data

(2R,3R)-4-(6-aminopurin-9-yl)-2,3-dihydroxybutanoic acid

Chemidplus:0023918981

References:

	(2R,3R)-4-(6-aminopurin-9-yl)-2,3-dihydroxybutanoic acid
NIST Chemistry WebBook:	Search Inchi
Pubchem (cid):	159961
Pubchem (cas):	23918-98-1

Other Information:

(IUPAC):	Atomic Weights of the Elements 2011 (pdf)
Videos:	The Periodic Table of Videos
tgsc:	Atomic Weights use for this web site
(IUPAC):	Periodic Table of the Elements
CHEMBL:	View
HMDB (The Human Metabolome Database):	HMDB29895
FooDB:	FDB001137
VCF-Online:	VCF Volatile Compounds in Food
ChemSpider:	View

Potential Blenders and core components note

None Found

Potential Uses:

None Found

Occurrence (nature, food, other):note

mushroom shitake mushroom
Search PMC Picture

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)

Articles:

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.

Notes:

None found

D-eritadenine lentysine

Supplier Sponsors

Articles:

D-eritadenine
lentysine