CHEBI:8350 - pradimicin B

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ChEBI Name pradimicin B
Definition A member of the class of prodimicins that is isolated from the cultured broth of Actinomadura hibisca No. P157-2 (ATCC 53557).
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C35H36N2O14
Net Charge 0
Average Mass 708.66530
Monoisotopic Mass 708.21665
InChI InChI=1S/C35H36N2O14/c1-10-6-17-22(28(42)19(10)33(46)37-11(2)34(47)48)21-15(27(41)32(17)51-35-31(45)30(44)24(36-4)12(3)50-35)9-16-23(29(21)43)26(40)14-7-13(49-5)8-18(38)20(14)25(16)39/h6-9,11-12,24,27,30-32,35-36,38,41-45H,1-5H3,(H,37,46)(H,47,48)/t11-,12-,24+,27+,30+,31-,32+,35+/m1/s1
SMILES CN[C@H]1[C@@H](C)O[C@@H](O[C@@H]2[C@@H](O)c3cc4C(=O)c5c(O)cc(OC)cc5C(=O)c4c(O)c3-c3c(O)c(C(=O)N[C@H](C)C(O)=O)c(C)cc23)[C@H](O)[C@H]1O
Metabolite of Species Details
Actinomadura hibisca (NCBI:txid68565) of strain ATCC 53557 See: DOI
Roles Classification
Biological Role(s): antimicrobial agent
A substance that kills or slows the growth of microorganisms, including bacteria, viruses, fungi and protozoans.
(via pradimicin )
antifungal agent
An antimicrobial agent that destroys fungi by suppressing their ability to grow or reproduce.
(via pradimicin )
bacterial metabolite
Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
(via pradimicin )
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ChEBI Ontology
Outgoing pradimicin B (CHEBI:8350) has functional parent D-alanine (CHEBI:15570)
pradimicin B (CHEBI:8350) is a L-alanine derivative (CHEBI:83943)
pradimicin B (CHEBI:8350) is a aromatic ether (CHEBI:35618)
pradimicin B (CHEBI:8350) is a monosaccharide derivative (CHEBI:63367)
pradimicin B (CHEBI:8350) is a polyketide (CHEBI:26188)
pradimicin B (CHEBI:8350) is a polyphenol (CHEBI:26195)
pradimicin B (CHEBI:8350) is a pradimicin (CHEBI:83230)
pradimicin B (CHEBI:8350) is a secondary alcohol (CHEBI:35681)
(2R)-2-({[(5S,6S)-5-{[(2S,3R,4S,5R,6R)-3,4-dihydroxy-6-methyl-5-(methylamino)tetrahydro-2H-pyran-2-yl]oxy}-1,6,9,14-tetrahydroxy-11-methoxy-3-methyl-8,13-dioxo-5,6,8,13-tetrahydrobenzo[a]tetracen-2-yl]carbonyl}amino)propanoic acid
Manual Xref Database
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Registry Numbers Types Sources
117704-66-2 CAS Registry Number ChemIDplus
4640809 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
2167304 PubMed citation Europe PMC
8478261 PubMed citation Europe PMC
Last Modified
28 November 2014