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eritadenine

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EntityQ15410938· pop 5· linked from 2 articles

eritadenine

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Also known as Lentinacin, Lentysine, D-Eritadenine

Eritadenine is a chemical compound found in shiitake mushrooms. Eritadenine is an inhibitor of S-adenosyl-L-homocysteine hydrolase (SAHH) and has hypocholesterolemic activity.

Chemical data

Formula
C9H11N5O4
Molecular weight
253.22 g/mol
IUPAC name
(2R,3R)-4-(6-aminopurin-9-yl)-2,3-dihydroxybutanoic acid
SMILES
C1=NC(=C2C(=N1)N(C=N2)C[C@H]([C@H](C(=O)O)O)O)N
InChIKey
LIEMBEWXEZJEEZ-INEUFUBQSA-N
XLogP
-1.8
Polar surface area
147 Ų
H-bond donors
4
H-bond acceptors
8
Formal charge
0

via PubChem

Drug data · ChEMBL

Molecule type
Small molecule

via ChEMBL · EBI

Wikidata facts

Mass
253.081
Show 5 more facts
chemical formula
C₉H₁₁N₅O₄
canonical SMILES
C1=NC2=C(C(=N1)N)N=CN2CC(C(C(=O)O)O)O
isomeric SMILES
C1=NC2=C(C(=N1)N)N=CN2C[C@H]([C@H](C(=O)O)O)O
subject has role
enzyme inhibitor
found in taxon
Agaricus bisporus
Sources (2)

via Wikidata · CC0

~1 min read

Encyclopedic overview

3 sections
Contents
  • Synthesis
  • References
  • External links

Eritadenine is a chemical compound found in shiitake mushrooms. Eritadenine is an inhibitor of S-adenosyl-L-homocysteine hydrolase (SAHH) and has hypocholesterolemic activity.

==Synthesis== The structure is a purine alkylated with an oxidized sugar fragment. thumb|center|700px|Eritadenine synthesis: Alternative synthesis: Ring opening of the protected lactone (1), derived from erythrose with sodium phthalimide gives the acid 2; hydrazinolysis (cf Gabriel synthesis) then leads to the amino acid 3. Displacement of chlorine in pyrimidine 4 by the amine function on 3 serves to attach the future imidazole nitrogen and the sugar-derived sidechain (5). The nitro group is then reduced by catalytic hydrogenation, the resulting primary amine is the most basic and is selectively formylated with formic acid. These strongly acidic conditions serve to remove the acetonide protecting group as well (6). Treatment with NaOH then serves to close the imidazole ring, forming eritadenine (7)

Excerpted from Wikipedia’s “eritadenine” article, available under the CC BY-SA 4.0 licence.

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