CHEBI:88275 - antelmycin

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ChEBI Name antelmycin
ChEBI ID CHEBI:88275
Definition A nucleoside antibiotic with anthelminthic properties that is isolated from Streptomyces longissimus.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C21H37N5O14
Net Charge 0
Average Mass 583.544
Monoisotopic Mass 583.23370
InChI InChI=1S/C21H37N5O14/c22-7-1-2-26(21(37)25-7)19-16(36)12(32)9(24)17(39-19)18(15(35)14(34)10(30)5(29)3-27)40-20-13(33)8(23)11(31)6(4-28)38-20/h1-2,5-6,8-20,27-36H,3-4,23-24H2,(H2,22,25,37)/t5-,6-,8+,9+,10-,11-,12+,13-,14+,15+,16-,17+,18-,19-,20+/m1/s1
InChIKey VQQSDVBOXQHCHU-SKPOXZENSA-N
SMILES O1[C@]([C@H](O[C@@H]2O[C@@H]([C@@H](O)[C@H](N)[C@H]2O)CO)[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO)([C@@H](N)[C@H](O)[C@@H](O)[C@@H]1N3C(=O)N=C(N)C=C3)[H]
Metabolite of Species Details
Streptomyces longissimus (NCBI:txid200596) See: PubMed
Bacillus methanolicus MGA3 (NCBI:txid796606) See: MetaboLights Study
Bacillus methanolicus MGA3 (NCBI:txid796606) See: PubMed
Roles Classification
Biological Role(s): nucleoside antibiotic

bacterial metabolite
Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
antimicrobial agent
A substance that kills or slows the growth of microorganisms, including bacteria, viruses, fungi and protozoans.
(via carbohydrate-containing antibiotic )
Application(s): anthelminthic drug
Substance intended to kill parasitic worms (helminths).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing antelmycin (CHEBI:88275) has functional parent cytosine (CHEBI:16040)
antelmycin (CHEBI:88275) has role anthelminthic drug (CHEBI:35443)
antelmycin (CHEBI:88275) has role bacterial metabolite (CHEBI:76969)
antelmycin (CHEBI:88275) has role nucleoside antibiotic (CHEBI:25605)
antelmycin (CHEBI:88275) is a N-glycosyl compound (CHEBI:21731)
antelmycin (CHEBI:88275) is a carbohydrate-containing antibiotic (CHEBI:23007)
antelmycin (CHEBI:88275) is a glycoside (CHEBI:24400)
antelmycin (CHEBI:88275) is a pyrimidone (CHEBI:38337)
INNs Sources
antelmicina ChemIDplus
antelmycin ChemIDplus
antelmycine ChemIDplus
antelmycinum ChemIDplus
Synonyms Sources
1-N-(2-O-(3-Amino-3-deoxy-beta-D-glucopyranosyl)-4-amino-4-deoxy-D-glycero-D-galacto-D-gluco-beta-D-undecapyranosyl)cytosine ChemIDplus
Anthelmycin KEGG DRUG
Antibiotic 33876 ChemIDplus
Hikizimycin ChemIDplus
L 33876 ChemIDplus
NSC 337588 KNApSAcK
Manual Xrefs Databases
C00018715 KNApSAcK
D02951 KEGG DRUG
US3143467 Patent
View more database links
Registry Numbers Types Sources
12706-94-4 CAS Registry Number ChemIDplus
12706-94-4 CAS Registry Number KEGG DRUG
4284256 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
14171214 PubMed citation Europe PMC
16196060 PubMed citation Europe PMC
371683 PubMed citation Europe PMC
4616934 PubMed citation Europe PMC
4754193 PubMed citation Europe PMC
5047747 PubMed citation Europe PMC
5572754 PubMed citation Europe PMC
903851 PubMed citation Europe PMC
Last Modified
07 June 2016