Inhibitor

Bibliography

Biblio print

Tree Display

AceDB Schema

XML Display

Feedback

Inhibitor Report for: 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
IUPHAR|
Wikipedia|

Target
Families | Avenaol ligand of proteins in family: RsbQ-like

References:
Search PubMed for references concerning: Avenaol

1 more
    Title: Identification of 6-epi-heliolactone as a biosynthetic precursor of avenaol in Avena strigosa
    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 : PubMed

            

    Title: Molecular Transformation Based on an Innovative Catalytic System
    Takemoto Y
    Ref: Chem Pharm Bull (Tokyo), 69:819, 2021 : PubMed

            

    Title: Lotuslactone, a non-canonical strigolactone from Lotus japonicus
    Xie X, Mori N, Yoneyama K, Nomura T, Uchida K, Akiyama K
    Ref: Phytochemistry, 157:200, 2019 : PubMed