CHEBI:85997 - sangivamycin

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ChEBI Name sangivamycin
ChEBI ID CHEBI:85997
Definition A nucleoside analogue that is adenosine in which the nitrogen at position 7 is replaced by a carbamoyl-substituted carbon. It is a potent inhibitor of protein kinase C.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C12H15N5O5
Net Charge 0
Average Mass 309.27800
Monoisotopic Mass 309.10732
InChI InChI=1S/C12H15N5O5/c13-9-6-4(10(14)21)1-17(11(6)16-3-15-9)12-8(20)7(19)5(2-18)22-12/h1,3,5,7-8,12,18-20H,2H2,(H2,14,21)(H2,13,15,16)/t5-,7-,8-,12-/m1/s1
InChIKey OBZJZDHRXBKKTJ-JTFADIMSSA-N
SMILES NC(=O)c1cn([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)c2ncnc(N)c12
Roles Classification
Biological Role(s): protein kinase inhibitor
An EC 2.7.* (P-containing group transferase) inhibitor that interferes with the action of protein kinases.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing sangivamycin (CHEBI:85997) has functional parent adenosine (CHEBI:16335)
sangivamycin (CHEBI:85997) has role protein kinase inhibitor (CHEBI:37699)
sangivamycin (CHEBI:85997) is a nucleoside analogue (CHEBI:60783)
IUPAC Name
4-amino-7-β-D-ribofuranosyl-7H-pyrrolo[2,3-d]pyrimidine-5-carboxamide
Synonyms Sources
7-Deaza-7-carbamoyladenosine ChEBI
7-Deazaadenosine-7-carboxamide ChemIDplus
Registry Numbers Types Sources
18417-89-5 CAS Registry Number ChemIDplus
626355 Reaxys Registry Number Reaxys
626355 Beilstein Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
26024233 PubMed citation Europe PMC
3338987 PubMed citation Europe PMC
Last Modified
11 June 2015