77979-22-7
Chemical Structure
Glyceocarpin
- CAS No.: 77979-22-7
- Formula:C20H20O5
- Molecular Weight:340.38
IUPAC Name: (6aS,11aS)-2-(3-methylbut-2-en-1-yl)-6H-benzofuro[3,2-c]chromene-3,6a,9(11aH)-triol
InChIKey: TUXXPRXOVFCNPC-VQTJNVASSA-N
SMILES: O[C@]12[C@](C=3C(OC1)=CC(O)=C(CC=C(C)C)C3)(OC=4C2=CC=C(O)C4)[H]
Biological Activity: Glyceocarpin is a phytoalexin and antibacterial agent naturally occurring in Glycine max, with weak antifungal activity. Glyceocarpin serves as the biosynthetic precursor of Glyceollins II (HY-N18032) and Glyceollins III. Glyceocarpin can be biosynthesized by the prenyltransferase and subsequent modification by cytochrome P450 enzymes. Glyceocarpin can be used for the study of soybean root and stem rot caused by Phytophthora sojae[1][2][3].
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Glyceocarpin | Glyceocarpin is a phytoalexin and antibacterial agent naturally occurring in Glycine max, with weak antifungal activity. Glyceocarpin serves as the biosynthetic precursor of Glyceollins II (HY-N18032) and Glyceollins III. Glyceocarpin can be biosynthesized by the prenyltransferase and subsequent modification by cytochrome P450 enzymes. Glyceocarpin can be used for the study of soybean root and stem rot caused by Phytophthora sojae. | |||||||||||||||||||||
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- [1]. Sun Y, et al. Elucidation and de novo reconstitution of glyceollin biosynthesis. Mol Plant. 2025;18(5):820-832. [Content Brief]
- [2]. Ingham JL, et al. Inducibly-formed isoflavonoids from leaves of soybean. Phytochemistry. 1981;20(5):1117-1121.
- [3]. Raytek LM, et al. At the roots of resistance. Nat Chem Biol. 2025 Jun 26;21:1473–1475.
Keywords
