Item 4 of 52 (back to results) previous next (6S,9R)-vomifoliol A (6S)-vomifoliol with a R configuration for the hydroxy group at position 9.

Current search: 06. Name of Biological Source of Chemical: Plantae > Magnoliophyta > Magnoliopsida × 07. Part of Biological Source of Chemical: plant structure [PO:0009011] > multi-tissue plant structure [PO:0025496] > seed [PO:0009010] × Select any link to see items in a related category. more general categories    information about this item 03. Biological Effects of Specific Chemicals  03. Biological Effects of Specific Chemicals  biochemical uses [CHEBI:52206] (3306)   metabolite [CHEBI:25212] (2692)   secondary metabolite [CHEBI:26619] (2225)   (6S,9R)-vomifoliol [CHEBI:49164] (1)  toxin [CHEBI:27026] (45)   phytotoxin [CHEBI:38231] (17)   (6S,9R)-vomifoliol [CHEBI:49164] (1) 04. Bioactive Capabilities of Specific Chemicals   04. Bioactive Capabilities of Specific Chemicals  Oxidoreductases [EC:1] (1697)   Acting on the CH-OH group of donors [EC:1.1] (576)   With NAD or NADP as acceptor [EC:1.1.1] (507)   Vomifoliol dehydrogenase [EC:1.1.1.221] (5)   (6S,9R)-vomifoliol [CHEBI:49164] (1) 06. Name of Biological Source of Chemical  06. Name of Biological Source of Chemical  Plantae (1926)   Magnoliophyta (1872)   Liliopsida (183)   Poales (46)   Typhaceae (2)   Typha (2)   Typha latifolia (1)  Magnoliopsida (1649)   Sapindales (202)   Simaroubaceae (20)   Brucea (6)   Brucea javanica (6)  Solanales (56)   Solanaceae (39)   Solanum (6)   Solanum lyratum (3) 07. Part of Biological Source of Chemical  07. Part of Biological Source of Chemical  unspecified structure [PO:0000004] (703)  plant structure [PO:0009011] (1497)   whole plant [PO:0000003] (150)  multi-tissue plant structure [PO:0025496] (1114)   seed [PO:0009010] (82) 08. Chemical Category  08. Chemical Category  main group molecular entity [CHEBI:33579] (25650)   p-block molecular entity [CHEBI:33675] (25343)   carbon group molecular entity [CHEBI:33582] (23847)   organic molecular entity [CHEBI:50860] (23769)   lipid [CHEBI:18059] (3532)   isoprenoid [CHEBI:24913] (1402)   terpenoid [CHEBI:26873] (1099)   monoterpenoid [CHEBI:25409] (157)   fenchane monoterpenoid [CHEBI:36739] (14)   vomifoliol [CHEBI:28258] (7)   (6S)-vomifoliol [CHEBI:49156] (3)   (6S,9R)-vomifoliol [CHEBI:49164] (1)  isoprenoid [CHEBI:24913] (1402)   terpenoid [CHEBI:26873] (1099)   monoterpenoid [CHEBI:25409] (157)   fenchane monoterpenoid [CHEBI:36739] (14)   vomifoliol [CHEBI:28258] (7)   (6S)-vomifoliol [CHEBI:49156] (3)   (6S,9R)-vomifoliol [CHEBI:49164] (1) ChEBI Compound Accession Identifier:   [CHEBI:49164] ChEBI Compound Description:   A (6S)-vomifoliol with a R configuration for the hydroxy group at position 9. ChEBI Compound Identification Number:   49164 ChEBI InChI Value:   InChI=1S/C13H20O3/c1-9-7-11(15)8-12(3,4)13(9,16)6-5-10(2)14/h5-7,10,14,16H,8H2,1-4H3/b6-5+/t10-,13-/m1/s1 ChEBI InChIKey Value:   KPQMCAKZRXOZLB-KOIHBYQTSA-N ChEBI Compound Name:   (6S,9R)-vomifoliol ChEBI SMILES Value:   C[C@@H](O)\\C=C\\[C@@]1(O)C(C)=CC(=O)CC1(C)C ChEBI Substance ID:   49693467 ChEBI URL:   ChEBI:49164 ChemSpider ID:   4444115 Ontomatica Chemical Accession Key (OnChAKey):   KPQMCAKZRXOZLB_KOIHBYQTSA_N_000_000000 PubChem Compound ID:   5280462