CHEBI:34638 - chromomycin A3

ChEBI IDCHEBI:34638
ChEBI Namechromomycin A3
Stars
ASCII Namechromomycin A3
Last Modified28 July 2014
DownloadsMolfile
FormulaC57H82O26
Net Charge0
Average Mass1183.257
Monoisotopic Mass1182.50943
SMILES[H][C@@]1([C@H](OC)C(=O)[C@@H](O)[C@@H](C)O)Cc2cc3cc(O[C@H]4C[C@@H](O[C@@H]5C[C@@H](O)[C@@H](OC)[C@@H](C)O5)[C@@H](OC(C)=O)[C@@H](C)O4)c(C)c(O)c3c(O)c2C(=O)[C@H]1O[C@H]1C[C@@H](O[C@H]2C[C@@H](O[C@H]3C[C@](C)(O)[C@@H](OC(C)=O)[C@H](C)O3)[C@H](O)[C@@H](C)O2)[C@H](O)[C@@H](C)O1
InChIInChI=1S/C57H82O26/c1-21-34(79-40-19-37(53(26(6)75-40)77-28(8)59)82-38-16-33(61)52(70-11)25(5)74-38)15-31-13-30-14-32(54(71-12)51(68)46(63)22(2)58)55(50(67)44(30)49(66)43(31)45(21)62)83-41-18-35(47(64)24(4)73-41)80-39-17-36(48(65)23(3)72-39)81-42-20-57(10,69)56(27(7)76-42)78-29(9)60/h13,15,22-27,32-33,35-42,46-48,52-56,58,61-66,69H,14,16-20H2,1-12H3/t22-,23-,24-,25-,26-,27+,32+,33-,35-,36-,37-,38-,39+,40+,41+,42+,46+,47-,48-,52+,53+,54+,55+,56+,57+/m1/s1
InChIKeyZYVSOIYQKUDENJ-WKSBCEQHSA-N
Roles Classification
Biological Roles:
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.
antimicrobial agent  A substance that kills or slows the growth of microorganisms, including bacteria, viruses, fungi and protozoans.
ChEBI Ontology
Outgoing Relation(s)
chromomycin A3 (CHEBI:34638) is a chromomycin (CHEBI:51233)
IUPAC Name 
(1S)-1-C-[(2S,3S)-7-{[4-O-acetyl-2,6-dideoxy-3-O-(2,6-dideoxy-4-O-methyl-α-D-lyxo-hexopyranosyl)-β-D-lyxo-hexopyranosyl]oxy}-3-{[4-O-acetyl-2,6-dideoxy-3-C-methyl-α-L-arabino-hexopyranosyl-(1→3)-2,6-dideoxy-β-D-arabino-hexopyranosyl-(1→3)-2,6-dideoxy-β-D-arabino-hexopyranosyl]oxy}-5,10-dihydroxy-6-methyl-4-oxo-1,2,3,4-tetrahydroanthracen-2-yl]-5-deoxy-1-O-methyl-D-xylulose
Synonyms  Source
Chromomycin A3KEGG COMPOUND
ToyomycinKEGG COMPOUND
Aburamycin BKEGG COMPOUND
3B-O-(4-O-acetyl-2,6-dideoxy-3-C-methyl-α-L-arabinohexopyranosyl)-7-methylolivomycin DChemIDplus
Manual XrefsDatabases
C13569KEGG COMPOUND
D02062KEGG DRUG
C00018673KNApSAcK
Registry NumbersSources
Beilstein:6630334Beilstein
CAS:7059-24-7KEGG COMPOUND
CAS:7059-24-7ChemIDplus