NaturalProductMech

cladoniamide E

CHEBI:84370 EXACT SEEDED

An organic heteropentacyclic compound that is 7,12-dihydro-6H-pyrido[1,2-a:3,4-b']diindole substituted by chloro groups at positions 2 and 9, a hydroxy group and an N-methyl carbamyl group at position 6, a methoxy group at position 13, and an oxo group at position 7 (the 6R stereoisomer). It is isolated from the culture broth of Streptomyces uncialis.

Structure

Standard InChIKeyYOJVEXXBEGGPCU-OAQYLSRUSA-N
SMILESCNC(=O)[C@@]1(O)N2C3=C(C=C(Cl)C=C3)C(OC)=C2C2=C(C3=C(N2)C=CC(Cl)=C3)C1=O
Stereochemistryfully defined
Cross-referencesnpatlas:NPA02270, pubchem:25053149

Filing pathway

Alkaloids — computed by NPClassifier npclassifier.gnps2.org@2026-09-07, which is why it is pinned rather than recomputed. The gene cluster's asserted class is other, from MIBiG.

Producer organisms 1

A claim that this taxon makes the compound. The basis says what the evidence addressed — a knockout and a database assertion are not the same claim.

TaxonBasisClusterEvidence
Streptomyces uncialis
NCBITaxon:1048205
BGC_CORRELATED mibig:BGC0001334 PMID:21876764

Occurrences 2

Somebody found the compound in this organism and cited it. That is not a claim that the organism makes it, and nothing here promotes one to the other.

TaxonSourceReference
Streptomyces uncialis
NCBITaxon:1048205
LOTUS DOI:10.1021/OL801274C
Streptomyces uncialis
NCBITaxon:1048205
CHEBI PMID:18646774

Biosynthetic gene clusters 1

AccessionHostLocus evidenceGenome
mibig:BGC0001334 Streptomyces uncialis
NCBITaxon:1048205
CLUSTER_DEMONSTRATED genbank:JN165773.1

A locus claim and a taxon claim are different questions. Heterologous expression settles the first and leaves the second where the isolation report left it.

Provenance

Source conceptSourceVersion
BGC0001334MIBIG5
CHEBI:84370CHEBI3-star

This page is generated from data/natural_products/alkaloids/cladoniamide-e.yaml, which is generated from the committed inventories. Neither is edited by hand.