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ChemicalBook--->CAS DataBase List--->1035557-09-5

1035557-09-5

1035557-09-5 Structure

1035557-09-5 Structure
IdentificationBack Directory
[Name]

A1-Phytoprostane-I Exclusive
[CAS]

1035557-09-5
[Synonyms]

A1-Phytoprostane-I
A1-Phytoprostane-I Exclusive
A1 Phytoprostane I,A-1-Phytoprostane-I,A1PhytoprostaneI
[Molecular Formula]

C18H28O4
[MOL File]

1035557-09-5.mol
[Molecular Weight]

308.41
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

DMF: 20 mg/ml; DMSO: 20 mg/ml; DMSO:PBS(pH7.2) (1:1): 0.5 mg/ml; Ethanol: 10 mg/ml
Safety DataBack Directory
[Symbol(GHS) ]


GHS02,GHS07
[Signal word ]

Danger
[Hazard statements ]

H225-H319-H336
[Precautionary statements ]

P210-P240-P241-P242-P243-P261-P264-P271-P280-P303+P361+P353-P304+P340-P305+P351+P338-P312-P337+P313-P370+P378-P403+P233-P403+P235-P405-P501
Hazard InformationBack Directory
[Description]

A1-Phytoprostane-I is a cyclopentenone isoprostane produced by the action of reactive oxygen species on α-linolenic acid in plants. There are two A1-phytoprostanes, both having the single ketone group on the ring structure. This isoform results from cyclization between carbons 9 and 13 of linolenic acid, as opposed to carbons 3 and 7 in A1-phytoprostane-II. A1-Phytoprostanes induce the expression of glutathione-S-transferase, increase phytoalexin biosynthesis, and trigger the expression of several genes involved in primary and secondary metabolism in plants.
[storage]

Store at -20°C
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