more general categories
information about this item
03. Biological Effects of Specific Chemicals
03. Biological Effects of Specific Chemicals
cyclomontanin A [CHEBI:65706] (1)
05. Industrial Uses
05. Industrial Uses
cyclomontanin A [CHEBI:65706] (1)
06. Name of Biological Source of Chemical
06. Name of Biological Source of Chemical
Annona montana (4)
07. Part of Biological Source of Chemical
07. Part of Biological Source of Chemical
seed [PO:0009010] (82)
08. Chemical Category
08. Chemical Category
cyclomontanin A [CHEBI:65706] (1)
cyclomontanin A [CHEBI:65706] (1)
cyclomontanin A [CHEBI:65706] (1)
cyclomontanin A [CHEBI:65706] (1)
cyclomontanin A [CHEBI:65706] (1)
cyclomontanin A [CHEBI:65706] (1)
cyclomontanin A [CHEBI:65706] (1)
cyclomontanin A [CHEBI:65706] (1)
cyclomontanin A [CHEBI:65706] (1)
ChEBI Compound Accession Identifier :
[CHEBI:65706]
ChEBI Compound Description :
A homodetic cyclic peptide composed of L-alanyl, L-tryptophyl, L-threonyl, L-prolylglycyl, L-leucyl and L-asparaginyl residues linked in a sequence. It is isolated from the seeds of Annona montana and has been shown to exhibit anti-inflammatory activity.
ChEBI Compound Identification Number :
65706
ChEBI InChI Value :
InChI=1S/C35H49N9O9/c1-17(2)12-23-32(50)42-25(14-27(36)46)31(49)39-18(3)30(48)41-24(13-20-15-37-22-9-6-5-8-21(20)22)33(51)43-29(19(4)45)35(53)44-11-7-10-26(44)34(52)38-16-28(47)40-23/h5-6,8-9,15,17-19,23-26,29,37,45H,7,10-14,16H2,1-4H3,(H2,36,46)(H,38,52)(H,39,49)(H,40,47)(H,41,48)(H,42,50)(H,43,51)/t18-,19+,23-,24-,25-,26-,29-/m0/s1
ChEBI InChIKey Value :
BJDACJTXTXRXOB-YOGBPHHOSA-N
ChEBI Compound Name :
cyclomontanin A
ChEBI SMILES Value :
[H][C@@]12CCCN1C(=O)[C@@]([H])(NC(=O)[C@H](Cc1c[nH]c3ccccc13)NC(=O)[C@H](C)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(C)C)NC(=O)CNC2=O)[C@@H](C)O
ChEBI Substance ID :
160709479
ChEBI URL :
ChEBI:65706
ChemSpider ID :
NS
Ontomatica Chemical Accession Key (OnChAKey) :
BJDACJTXTXRXOB_YOGBPHHOSA_N_000_000000
PubChem Compound ID :
25018458