A1-Phytoprostane-I Exclusive

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Company Name: Shanghai Hongye Biotechnology Co. Ltd  
Tel: 400-9205774
Email: sales@glpbio.cn
Products Intro: Product Name:A1-Phytoprostane-I
CAS:1035557-09-5
Purity:>98% Package:1mg;10mg;50mg;100mg;
Company Name: ChemeGen(Shanghai) Biotechnology Co.,Ltd.  
Tel: 18818260767
Email: sales@chemegen.com
Products Intro: Product Name:A1-Phytoprostane-I
CAS:1035557-09-5
Purity:98% Package:10 mg;50 mg;100 mg;500 mg;1 g;5 g;10 g
Company Name: MedBioPharmaceutical Technology Inc  
Tel: 021-69568360 18916172912
Email: order@med-bio.cn
Products Intro: Product Name:A1-Phytoprostane-I Exclusive
CAS:1035557-09-5
Purity:98% Package:500ug (solution); 100ug (solution); 1mg (solution) Remarks:Medbio
Company Name: TargetMol Chemicals Inc.  
Tel: 4008200310
Email: marketing@tsbiochem.com
Products Intro: Product Name:A1-Phytoprostane-I
CAS:1035557-09-5
Package:1mg/RMB 16400
Company Name: Shanghai Yifei Biotechnology Co. , Ltd.  
Tel: 021-65675885 18964387627
Email: customer_service@efebio.com
Products Intro: Product Name:A1-Phytoprostane-I Exclusive
CAS:1035557-09-5
Purity:95% Package:100μg;500μg;1mg
A1-Phytoprostane-I Exclusive Basic information
Product Name:A1-Phytoprostane-I Exclusive
Synonyms:A1-Phytoprostane-I Exclusive;A1-Phytoprostane-I;A1 Phytoprostane I,A-1-Phytoprostane-I,A1PhytoprostaneI;3-Cyclopentene-1-octanoic acid, 2-(3-hydroxy-1-penten-1-yl)-5-oxo-
CAS:1035557-09-5
MF:C18H28O4
MW:308.41
EINECS:
Product Categories:
Mol File:1035557-09-5.mol
A1-Phytoprostane-I    Exclusive Structure
A1-Phytoprostane-I Exclusive Chemical Properties
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
pka4.78±0.10(Predicted)
Safety Information
MSDS Information
A1-Phytoprostane-I Exclusive Usage And Synthesis
DescriptionA1-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.
A1-Phytoprostane-I Exclusive Preparation Products And Raw materials
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