
CAS 469-01-2: (+)-Pisatin
Formula:C17H14O6
InChI:InChI=1S/C17H14O6/c1-19-9-2-3-10-12(4-9)20-7-17(18)11-5-14-15(22-8-21-14)6-13(11)23-16(10)17/h2-6,16,18H,7-8H2,1H3/t16-,17+/m1/s1
InChI key:InChIKey=LZMRDTLRSDRUSU-SJORKVTESA-N
SMILES:O[C@@]12[C@@](C=3C(OC1)=CC(OC)=CC3)(OC=4C2=CC5=C(C4)OCO5)[H]
Synonyms:- (+)-(6aR,11aR)-Pisatin
- (+)-Pisatin
- (6aR,12aR)-3-Methoxy-6H-[1,3]dioxolo[5,6]benzofuro[3,2-c][1]benzopyran-6a(12aH)-ol
- (R,R)-Pisatin
- 6H-(1,3)Dioxolo(5,6)benzofuro(3,2-c)(1)benzopyran-6a(12aH)-ol, 3-methoxy-, (6aR-cis)-
- 6H-[1,3]Dioxolo[5,6]benzofuro[3,2-c][1]benzopyran-6a(12aH)-ol, 3-methoxy-
- 6H-[1,3]Dioxolo[5,6]benzofuro[3,2-c][1]benzopyran-6a(12aH)-ol, 3-methoxy-, (6aR,12aR)-
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Pisatin
CAS:Pisatin is an isoflavonoid compound, which is a type of phytoalexin commonly found in leguminous plants, particularly in peas. It is synthesized by these plants as a natural defense mechanism. In terms of its mode of action, Pisatin inhibits fungal growth by disrupting the integrity of fungal cell membranes, thereby interfering with the pathogen's cellular processes. Pisatin plays a crucial role in the plant's immune response, especially when the plant is under attack by fungal pathogens. Its production is triggered by microbial infection or environmental stress, acting swiftly to deter further invasion. This makes it an important subject of study for scientists interested in plant pathology and natural plant defense systems. Research into Pisatin not only enhances the understanding of plant immunity but also offers potential applications in agriculture. By studying Pisatin and its biosynthetic pathways, scientists can explore new methods for improving crop resistance against fungal diseases, ultimately aiding in the development of more resilient leguminous crops.Formula:C17H14O6Purity:Min. 95%Color and Shape:Beige PowderMolecular weight:314.29 g/mol