Item 5 of 19 (back to results) previous next vomilenine An indole alkaloid that is vinorine bearing a hydroxy substituent at position 21.

Current search: 04. Bioactive Capabilities of Specific Chemicals : Oxidoreductases [EC:1] > Acting on paired donors, with incorporation or reduction of molecular oxygen [EC:1.14] × 08. Chemical Category: main group molecular entity [CHEBI:33579] > p-block molecular entity [CHEBI:33675] > carbon group molecular entity [CHEBI:33582] > organic molecular entity [CHEBI:50860] > heteroorganic entity [CHEBI:33285] > organonitrogen compound [CHEBI:35352] > organic amino compound [CHEBI:50047] × Select any link to see items in a related category. more general categories    information about this item 04. Bioactive Capabilities of Specific Chemicals   04. Bioactive Capabilities of Specific Chemicals  Oxidoreductases [EC:1] (1697)   Acting on the CH-NH group of donors [EC:1.5] (120)   With NAD or NADP as acceptor [EC:1.5.1] (77)   Vomilenine reductase [EC:1.5.1.32] (5)   vomilenine [CHEBI:16408] (1)  Acting on paired donors, with incorporation or reduction of molecular oxygen [EC:1.14] (587)   With NADH or NADPH as one donor, and incorporation of one atom of oxygen [EC:1.14.13] (391)   Vinorine hydroxylase [EC:1.14.13.75] (7)   vomilenine [CHEBI:16408] (1)  Transferases [EC:2] (1441)   Glycosyltransferases [EC:2.4] (334)   Hexosyltransferases [EC:2.4.1] (257)   Vomilenine glucosyltransferase [EC:2.4.1.219] (5)   vomilenine [CHEBI:16408] (1)  Hydrolases [EC:3] (824)   Glycosylases [EC:3.2] (112)   Glycosidases, i.e. enzymes hydrolysing O- and S-glycosyl compounds [EC:3.2.1] (81)   Raucaffricine beta-glucosidase [EC:3.2.1.125] (4)   vomilenine [CHEBI:16408] (1) 08. Chemical Category  08. Chemical Category  main group molecular entity [CHEBI:33579] (25650)   p-block molecular entity [CHEBI:33675] (25343)   pnictogen molecular entity [CHEBI:33302] (10027)   nitrogen molecular entity [CHEBI:51143] (7930)   organonitrogen compound [CHEBI:35352] (6705)   alkaloid [CHEBI:22315] (473)   indole alkaloid [CHEBI:38958] (144)   vomilenine [CHEBI:16408] (1)  organic amino compound [CHEBI:50047] (2472)   hemiaminal [CHEBI:73080] (13)   vomilenine [CHEBI:16408] (1)  chalcogen molecular entity [CHEBI:33304] (15225)   oxygen molecular entity [CHEBI:25806] (14414)   organooxygen compound [CHEBI:36963] (11352)   hemiaminal [CHEBI:73080] (13)   vomilenine [CHEBI:16408] (1)  organochalcogen compound [CHEBI:36962] (11874)   organooxygen compound [CHEBI:36963] (11352)   hemiaminal [CHEBI:73080] (13)   vomilenine [CHEBI:16408] (1)  carbon group molecular entity [CHEBI:33582] (23847)   organic molecular entity [CHEBI:50860] (23769)   heteroorganic entity [CHEBI:33285] (15197)   organonitrogen compound [CHEBI:35352] (6705)   alkaloid [CHEBI:22315] (473)   indole alkaloid [CHEBI:38958] (144)   vomilenine [CHEBI:16408] (1)  organic amino compound [CHEBI:50047] (2472)   hemiaminal [CHEBI:73080] (13)   vomilenine [CHEBI:16408] (1)  organochalcogen compound [CHEBI:36962] (11874)   organooxygen compound [CHEBI:36963] (11352)   hemiaminal [CHEBI:73080] (13)   vomilenine [CHEBI:16408] (1)  organic amino compound [CHEBI:50047] (2472)   hemiaminal [CHEBI:73080] (13)   vomilenine [CHEBI:16408] (1) ChEBI Compound Accession Identifier:   [CHEBI:16408] ChEBI Compound Description:   An indole alkaloid that is vinorine bearing a hydroxy substituent at position 21. ChEBI Compound Identification Number:   16408 ChEBI InChI Value:   InChI=1S/C21H22N2O3/c1-3-11-12-8-15-18-21(13-6-4-5-7-14(13)22-18)9-16(23(15)20(11)25)17(12)19(21)26-10(2)24/h3-7,12,15-17,19-20,25H,8-9H2,1-2H3/b11-3+/t12-,15-,16-,17?,19+,20+,21+/m0/s1 ChEBI InChIKey Value:   BERYBAUEDCRDKM-FDHUPVAHSA-N ChEBI Compound Name:   vomilenine ChEBI SMILES Value:   [H][C@@]12C[C@]3([H])N([C@H]4C[C@@]5([C@H](OC(C)=O)C14)c1ccccc1N=C35)[C@H](O)\C2=C\C ChEBI Substance ID:   22395980 ChEBI URL:   ChEBI:16408 ChemSpider ID:   NS Ontomatica Chemical Accession Key (OnChAKey):   BERYBAUEDCRDKM_FDHUPVAHSA_N_000_000000 PubChem Compound ID:   11953806