Avenaol

General

Type : Strigolactone receptors ligand, Non-canonical strigolactone

Chemical_Nomenclature : (2R)-2-[(Z)-[(4S)-4-[(1R,3R,6R,7S)-3-hydroxy-1,5,5-trimethyl-2-oxo-7-bicyclo[4.1.0]heptanyl]-2-oxooxolan-3-ylidene]methoxy]-4-methyl-2H-furan-5-one

Canonical SMILES : CC1=CC(OC1=O)OC=C2C(COC2=O)C3C4C3(C(=O)C(CC4(C)C)O)C

InChI : InChI=1S\/C20H24O7\/c1-9-5-13(27-17(9)23)25-8-11-10(7-26-18(11)24)14-15-19(2,3)6-12(21)16(22)20(14,15)4\/h5,8,10,12-15,21H,6-7H2,1-4H3\/b11-8-\/t10-,12-,13-,14-,15-,20-\/m1\/s1

InChIKey : MZPHYCYAMMTPLA-VUFGVBPYSA-N

Other name(s) : (+)-Avenaol


MW : 376.4

Formula : C20H24O7

CAS_number :

PubChem : 102236949

UniChem : MZPHYCYAMMTPLA-VUFGVBPYSA-N

Target

Families : Avenaol ligand of proteins in family
RsbQ-like

References (4)

Title : Identification of 6-epi-heliolactone as a biosynthetic precursor of avenaol in Avena strigosa - Moriyama_2022_Biosci.Biotechnol.Biochem_86_998
Author(s) : Moriyama D , Wakabayashi T , Shiotani N , Yamamoto S , Furusato Y , Yabe K , Mizutani M , Takikawa H , Sugimoto Y
Ref : Biosci Biotechnol Biochem , 86 :998 , 2022
Abstract :
PubMedSearch : Moriyama_2022_Biosci.Biotechnol.Biochem_86_998
PubMedID: 35561745

Title : Molecular Transformation Based on an Innovative Catalytic System - Takemoto_2021_Chem.Pharm.Bull.(Tokyo)_69_819
Author(s) : Takemoto Y
Ref : Chem Pharm Bull (Tokyo) , 69 :819 , 2021
Abstract :
PubMedSearch : Takemoto_2021_Chem.Pharm.Bull.(Tokyo)_69_819
PubMedID: 34470946

Title : [Construction of All-cis-substituted Cyclopropane and Total Synthesis of Avenaol] - Yasui_2019_Yakugaku.Zasshi_139_1259
Author(s) : Yasui M
Ref : Yakugaku Zasshi , 139 :1259 , 2019
Abstract :
PubMedSearch : Yasui_2019_Yakugaku.Zasshi_139_1259
PubMedID: 31582609

Title : Lotuslactone, a non-canonical strigolactone from Lotus japonicus - Xie_2019_Phytochemistry_157_200
Author(s) : Xie X , Mori N , Yoneyama K , Nomura T , Uchida K , Akiyama K
Ref : Phytochemistry , 157 :200 , 2019
Abstract :
PubMedSearch : Xie_2019_Phytochemistry_157_200
PubMedID: 30439621