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vidarabine phosphate

Structure via PubChem · Public domain (PubChem)

EntityQ6607436· pop 5· linked from 2 articles

vidarabine phosphate

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chemical compound

In the Vinony graph

Vinony's link graph records 2 inbound references to vidarabine phosphate, and connects out to deoxyribonucleotide, biochemistry and International Standard Serial Number.

Vinony files it under ECHA InfoCard ID from Wikidata and Nucleotides.

Vinony links it to 5 Wikipedia language editions.

Chemical data

Formula: C10H14N5O7P
Molecular weight: 347.22 g/mol
IUPAC name: [(2R,3S,4S,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl dihydrogen phosphate
SMILES: C1=NC(=C2C(=N1)N(C=N2)[C@H]3[C@H]([C@@H]([C@H](O3)COP(=O)(O)O)O)O)N
InChIKey: UDMBCSSLTHHNCD-UHTZMRCNSA-N
XLogP: -3.5
Polar surface area: 186 Å²
H-bond donors: 5
H-bond acceptors: 11
Formal charge: 0

via PubChem

Drug data · ChEMBL

Molecule type: Small molecule

via ChEMBL · EBI

Research

486 papers

CD19-Targeting CAR T Cells for Myositis and Interstitial Lung Disease Associated With Antisynthetase Syndrome.JAMA · 2023
[Vidarabine phosphate in the treatment of active chronic hepatitis B. A confirmed hope].La Revue du praticien · 1992
New anticancer agents.Cancer chemotherapy and biological response modifiers · 1991
5-Iodotubercidin inhibits SARS-CoV-2 RNA synthesis.Antiviral research · 2022
Fludarabine phosphate (Fludara).Journal of pediatric oncology nursing : official journal of the Association of Pediatric Oncology Nurses · 1992

Wikidata facts

Mass: 347.063

Show 4 more facts

canonical SMILES: C1=NC2=C(C(=N1)N)N=CN2C3C(C(C(O3)COP(=O)(O)O)O)O
chemical formula: C₁₀H₁₄N₅O₇P
isomeric SMILES: C1=NC2=C(C(=N1)N)N=CN2[C@H]3[C@H]([C@@H]([C@H](O3)COP(=O)(O)O)O)O
subject has role: antimetabolite

Sources (2)

via Wikidata · CC0

Available in 5 languages

via Wikidata sitelinks · CC0

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ECHA InfoCard ID from Wikidata Nucleotides