CHEBI:67811 - zorbamycin

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ChEBI Name zorbamycin
ChEBI ID CHEBI:67811
Definition A glycopeptide antibiotic found in Streptomyces flavoviridis.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C55H85N19O21S2
Net Charge 0
Average Mass 1412.50800
Monoisotopic Mass 1411.56088
InChI InChI=1S/C55H85N19O21S2/c1-19-32(71-45(74-43(19)60)24(12-30(59)77)66-13-22(56)44(61)83)48(86)72-33(39(25-14-63-18-67-25)93-53-41(37(81)35(79)21(3)91-53)94-52-38(82)40(95-54(62)89)36(80)28(15-76)92-52)49(87)69-23(8-11-75)34(78)20(2)46(84)73-42(55(4,5)90)50(88)65-10-7-31-68-27(17-96-31)51-70-26(16-97-51)47(85)64-9-6-29(57)58/h14,16,18,20-24,27-28,33-42,52-53,66,75-76,78-82,90H,6-13,15,17,56H2,1-5H3,(H3,57,58)(H2,59,77)(H2,61,83)(H2,62,89)(H,63,67)(H,64,85)(H,65,88)(H,69,87)(H,72,86)(H,73,84)(H2,60,71,74)/t20-,21-,22-,23+,24-,27+,28+,33-,34-,35+,36+,37-,38-,39-,40-,41-,42+,52+,53-/m0/s1
InChIKey UJKRUPHWCPAJIL-CPLCKGKLSA-N
SMILES C[C@@H]([C@H](O)[C@@H](CCO)NC(=O)[C@@H](NC(=O)c1nc(nc(N)c1C)[C@H](CC(N)=O)NC[C@H](N)C(N)=O)[C@@H](O[C@@H]1O[C@@H](C)[C@@H](O)[C@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](OC(N)=O)[C@@H]1O)c1c[nH]cn1)C(=O)N[C@H](C(=O)NCCC1=N[C@H](CS1)c1nc(cs1)C(=O)NCCC(N)=N)C(C)(C)O
Metabolite of Species Details
Streptomyces flavoviridis (NCBI:txid66889) of strain ATCC21892 See: PubMed
Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Biological Role(s): antimicrobial agent
A substance that kills or slows the growth of microorganisms, including bacteria, viruses, fungi and protozoans.
bacterial metabolite
Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing zorbamycin (CHEBI:67811) has role antimicrobial agent (CHEBI:33281)
zorbamycin (CHEBI:67811) has role bacterial metabolite (CHEBI:76969)
zorbamycin (CHEBI:67811) is a glycopeptide (CHEBI:24396)
Registry Numbers Types Sources
11042140 Reaxys Registry Number Reaxys
11056-20-5 CAS Registry Number ChemIDplus
Citation Waiting for Citations Type Source
21210656 PubMed citation Europe PMC
Last Modified
26 May 2015