CHEBI:140442 - 12-epi-fischerindole U

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ChEBI Name 12-epi-fischerindole U
ChEBI ID CHEBI:140442
ChEBI ASCII Name 12-epi-fischerindole U
Definition A tetracyclic indole alkaloid that is produced by the Stigonematales genus of cyanobacteria.
Stars This entity has been manually annotated by the ChEBI Team.
Submitter Kristian Axelsen
Supplier Information
Download Molfile XML SDF
Formula C21H24N2
Net Charge 0
Average Mass 304.429
Monoisotopic Mass 304.19395
InChI InChI=1S/C21H24N2/c1-6-21(4)12-11-14-17(19(21)22-5)16-13-9-7-8-10-15(13)23-18(16)20(14,2)3/h6-10,14,17,19,23H,1,11-12H2,2-4H3/t14-,17-,19+,21+/m0/s1
InChIKey NEYJIGPAQAKWSI-QBGRRASTSA-N
SMILES C12=CC=CC=C1NC3=C2[C@]4([C@H]([C@](CC[C@@]4(C3(C)C)[H])(C)C=C)[N+]#[C-])[H]
Metabolite of Species Details
Hapalosiphon welwitschii (NCBI:txid1433842) of strain UTEX B 1830 See: PubMed
Roles Classification
Biological Role(s): bacterial metabolite
Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
(via alkaloid )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 12-epi-fischerindole U (CHEBI:140442) has role bacterial metabolite (CHEBI:76969)
12-epi-fischerindole U (CHEBI:140442) is a fischerindole alkaloid (CHEBI:141619)
12-epi-fischerindole U (CHEBI:140442) is a isocyanide (CHEBI:35353)
12-epi-fischerindole U (CHEBI:140442) is a organic heterotetracyclic compound (CHEBI:38163)
Synonyms Sources
(6aS,9S,10R,10aS)-9-ethenyl-10-isocyano-6,6,9-trimethyl-5H,6aH,7H,8H,10H,10aH-indeno[2,1-b]indole SUBMITTER
12-epi-fischerindole U UniProt
Manual Xref Database
CPD-20797 MetaCyc
View more database links
Registry Number Type Source
7144608 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
19035635 PubMed citation Europe PMC
25218740 PubMed citation Europe PMC
27348090 PubMed citation Europe PMC
28225144 PubMed citation Europe PMC
28288107 PubMed citation SUBMITTER
Last Modified
15 August 2018