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DINOR-12-OXO-PHYTODIENOIC ACID (dn-OPDA) is a bioactive compound belonging to the jasmonate family of signals, which plays a crucial role in plant defense mechanisms and stress responses. It is derived from the metabolism of polyunsaturated fatty acids and is involved in the regulation of various physiological processes in plants.
Used in Biological Study:
DINOR-12-OXO-PHYTODIENOIC ACID (dn-OPDA) is used as a signaling molecule in the biological study of loss of atypical kinases ABC1K7 and ABC1K8. It is responsible for altering the lipid composition of the chloroplast membrane in response to biotic and abiotic stress, thereby modifying membrane fluidity in Arabidopsis thaliana.
Used in Plant Defense Mechanisms:
DINOR-12-OXO-PHYTODIENOIC ACID (dn-OPDA) is used as a key component in plant defense mechanisms, where it helps in the regulation of stress responses and the activation of various physiological processes. This makes it an essential tool for understanding the complex interactions between plants and their environment.
Used in Agricultural Research:
In the agricultural research industry, DINOR-12-OXO-PHYTODIENOIC ACID (dn-OPDA) is used as a valuable resource for studying plant stress responses and developing strategies to improve crop resilience and productivity. Its role in modulating membrane fluidity and lipid composition makes it a promising candidate for the development of stress-tolerant crop varieties.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, the potential therapeutic applications of DINOR-12-OXO-PHYTODIENOIC ACID (dn-OPDA) could extend to the pharmaceutical industry, where it may be used as a lead compound for the development of novel drugs targeting various stress-related conditions. Its ability to modulate membrane fluidity and lipid composition could provide insights into the development of treatments for diseases associated with membrane dysfunction.

197247-23-7

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197247-23-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 197247-23-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,7,2,4 and 7 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 197247-23:
(8*1)+(7*9)+(6*7)+(5*2)+(4*4)+(3*7)+(2*2)+(1*3)=167
167 % 10 = 7
So 197247-23-7 is a valid CAS Registry Number.
InChI:InChI=1/C16H24O3/c1-2-3-5-9-14-13(11-12-15(14)17)8-6-4-7-10-16(18)19/h3,5,11-14H,2,4,6-10H2,1H3,(H,18,19)/b5-3-

197247-23-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name dinor-12-oxo Phytodienoic Acid

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:197247-23-7 SDS

197247-23-7Downstream Products

197247-23-7Relevant academic research and scientific papers

Verification of the versatility of the in vitro enzymatic reaction giving (+)-cis-12-Oxo-phytodienoic acid

Ito, Yusuke,Sasaki, Kento,Ogihara, Tsuyoshi,Kitaoka, Naoki,Takahahi, Kosaku,Matsuura, Hideyuki

, (2021/08/03)

Jasmonic acid (JA) is a plant hormone involved in the defense response against insects and fungi. JA is synthesized from α-linolenic acid (LA) by the octadecanoid pathway in plants. 12-oxo-Phytodienoic acid (OPDA) is one of the biosynthetic intermediates in this pathway. The reported stereo selective total synthesis of cis-(+)-OPDA is not very efficient due to the many steps involved in the reaction as well as the use of water sensitive reactions. Therefore, we developed an enzymatic method for the synthesis of OPDA using acetone powder of flax seed and allene oxide cyclase (PpAOC2) from Physcomitrella patens. From this method, natural cis-(+)-OPDA can be synthesized in the high yield of approximately 40%. In this study, we investigated the substrate specificity of the enzymatic synthesis of other OPDA analogs with successions to afford OPDA amino acid conjugates, dinor-OPDA (dn-OPDA), and OPDA monoglyceride, and it was suggested that the biosynthetic pathway of arabidopsides could occur via MGDG.

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