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Substrate Report for: Heliolactone

General
Type Butenolide, Strigolactone receptors ligand
Chemical_Nomenclature methyl (E,2E)-2-[(4-methyl-5-oxo-2H-furan-2-yl)oxymethylidene]-4-(2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl)but-3-enoate
Canonical SMILES CC1=CC(OC1=O)OC=C(C=CC2C(=CC(=O)CC2(C)C)C)C(=O)OC
InChI InChI=1S/C20H24O6/c1-12-8-15(21)10-20(3,4)16(12)7-6-14(19(23)24-5)11-25-17-9-13(2)18(22)26-17/h6-9,11,16-17H,10H2,1-5H3/b7-6+,14-11+
InChIKey VPSDSSLYHQLBLR-WXGDJGGUSA-N
Other name(s)
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MW|360.4
Formula|C20H24O6
CAS_number|
PubChem|101882533
UniChem|VPSDSSLYHQLBLR-WXGDJGGUSA-N
IUPHAR|
Wikipedia|

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

References:
Search PubMed for references concerning: Heliolactone

2 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: Concise synthesis of heliolactone, a non-canonical strigolactone isolated from sunflower
    Yamamoto S, Atarashi T, Kuse M, Sugimoto Y, Takikawa H
    Ref: Biosci Biotechnol Biochem, 84:1113, 2020 : PubMed

            

    Title: Heliolactone, a non-sesquiterpene lactone germination stimulant for root parasitic weeds from sunflower
    Ueno K, Furumoto T, Umeda S, Mizutani M, Takikawa H, Batchvarova R, Sugimoto Y
    Ref: Phytochemistry, 108:122, 2014 : PubMed