CHEBI:84382 - chondramide C

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ChEBI Name chondramide C
ChEBI ID CHEBI:84382
Definition A chondramide formally obtained from N-[(2S,4E,6R,7R)-7-hydroxy-2,4,6-trimethyloct-4-enoyl]-L-alanyl-Nα-methyl-D-tryptophanyl-β-R-β-tyrosine by intramolecular condensation of the alcoholic hydroxy group with the carboxy group of the β-tyrosine residue. It is produced by strains of the myxobacterium, Chondromyces crocatus.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C35H44N4O6
Net Charge 0
Average Mass 616.74710
Monoisotopic Mass 616.32609
InChI InChI=1S/C35H44N4O6/c1-20-15-21(2)24(5)45-32(41)18-30(25-11-13-27(40)14-12-25)38-34(43)31(17-26-19-36-29-10-8-7-9-28(26)29)39(6)35(44)23(4)37-33(42)22(3)16-20/h7-15,19,21-24,30-31,36,40H,16-18H2,1-6H3,(H,37,42)(H,38,43)/b20-15+/t21-,22+,23+,24-,30-,31-/m1/s1
InChIKey NCRSWJPOFRASIF-HPUNWYTPSA-N
SMILES C[C@H]1OC(=O)C[C@@H](NC(=O)[C@@H](Cc2c[nH]c3ccccc23)N(C)C(=O)[C@H](C)NC(=O)[C@@H](C)C\C(C)=C\[C@H]1C)c1ccc(O)cc1
Metabolite of Species Details
Chondromyces crocatus (NCBI:txid52) 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): bacterial metabolite
Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
(via chondramide )
Application(s): antineoplastic agent
A substance that inhibits or prevents the proliferation of neoplasms.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing chondramide C (CHEBI:84382) has role antineoplastic agent (CHEBI:35610)
chondramide C (CHEBI:84382) has role bacterial metabolite (CHEBI:76969)
chondramide C (CHEBI:84382) is a chondramide (CHEBI:84384)
chondramide C (CHEBI:84382) is a indoles (CHEBI:24828)
chondramide C (CHEBI:84382) is a phenols (CHEBI:33853)
Incoming chondramide D (CHEBI:84383) has functional parent chondramide C (CHEBI:84382)
IUPAC Name
(4R,7R,10S,13S,15E,17R,18R)-4-(4-hydroxyphenyl)-7-(1H-indol-3-ylmethyl)-8,10,13,15,17,18-hexamethyl-1-oxa-5,8,11-triazacyclooctadec-15-ene-2,6,9,12-tetrone
Registry Numbers Types Sources
18855324 Reaxys Registry Number Reaxys
7404126 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
11722228 PubMed citation Europe PMC
18624308 PubMed citation Europe PMC
18624309 PubMed citation Europe PMC
8557566 PubMed citation Europe PMC
Last Modified
20 January 2015