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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
[Boiling point ]

489.2±45.0 °C(Predicted)
[density ]

1.115±0.06 g/cm3(Predicted)
[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
[pka]

4.78±0.10(Predicted)
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
[References]

[1] INGEBORG THOMA. Cyclopentenone isoprostanes induced by reactive oxygen species trigger defense gene activation and phytoalexin accumulation in plants[J]. The Plant Journal, 2003, 34 3: 363-375. DOI: 10.1046/j.1365-313x.2003.01730.x
[2] ULLRICH JAHN PRIV.-DOZ.?DR.  Thierry D Dr  Jean Marie Galano Dr. Beyond Prostaglandins—Chemistry and Biology of Cyclic Oxygenated Metabolites Formed by Free-Radical Pathways from Polyunsaturated Fatty Acids[J]. Angewandte Chemie International Edition, 2008, 47 32: 5894-5955. DOI: 10.1002/anie.200705122
[3] MARTIN J. MUELLER  Susanne B. Reactive electrophilic oxylipins: Pattern recognition and signalling[J]. Phytochemistry, 2009, 70 13: Pages 1511-1521. DOI: 10.1016/j.phytochem.2009.05.018
[4] KATHARINA DUECKERSHOFF . Impact of cyclopentenone-oxylipins on the proteome of Arabidopsis thaliana[J]. Biochimica et biophysica acta. Proteins and proteomics, 2008, 1784 12: Pages 1975-1985. DOI: 10.1016/j.bbapap.2008.09.003
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