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 No supplier information found for this compound.
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 Type Source
21210656 PubMed citation Europe PMC
Last Modified
26 May 2015