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11-OXO-PROSTA-5Z,12E,14Z-TRIEN-1-OIC ACID, also known as 11-oxo-prostanoic acid, is a type of prostaglandin, which is a group of lipids that have hormone-like effects in the body. This particular chemical is a derivative of prostaglandin E2 and is involved in various physiological processes, including inflammation, smooth muscle contraction, and blood pressure regulation. It is also believed to play a role in pain perception and fever response.
Used in Pharmaceutical Industry:
11-OXO-PROSTA-5Z,12E,14Z-TRIEN-1-OIC ACID is used as a therapeutic agent for the treatment of inflammatory conditions and cancer. Its involvement in physiological processes such as inflammation, smooth muscle contraction, and blood pressure regulation makes it a potential candidate for the development of drugs targeting these conditions.
Used in Research Applications:
11-OXO-PROSTA-5Z,12E,14Z-TRIEN-1-OIC ACID is used as a research tool for studying the role of prostaglandins in various physiological processes. Its involvement in inflammation, pain perception, and fever response makes it a valuable compound for investigating the mechanisms underlying these processes and identifying potential therapeutic targets.

596104-94-8

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596104-94-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 596104-94-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,9,6,1,0 and 4 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 596104-94:
(8*5)+(7*9)+(6*6)+(5*1)+(4*0)+(3*4)+(2*9)+(1*4)=178
178 % 10 = 8
So 596104-94-8 is a valid CAS Registry Number.

596104-94-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-(2-oct-2-enylidene-3-oxocyclopentyl)hept-5-enoic 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:596104-94-8 SDS

596104-94-8Downstream Products

596104-94-8Relevant academic research and scientific papers

Identification and Structural Analysis of New Nrf2 Activators by Mechanism-Based Chemical Transformation of 15-Deoxy-Δ12, 14-PGJ2

Kim, Kyeojin,Park, Jong-Min,Kim, Nam-Jung,Kim, Su-Jung,Moon, Hyunyoung,An, Hongchan,Lee, Jeeyeon,Park, Hyun-Ju,Surh, Young-Joon,Suh, Young-Ger

, p. 1900 - 1904 (2016)

Mechanism-based chemical transformation of 15-deoxy-Δ12, 14-PGJ2 (15d-PGJ2) resulted in a series of new NF-E2-related factor-2 (Nrf2) activators and detailed elucidation of the function of each electrophilic binding site. In addition, HO-1 expression resulting from Nrf2 activation through enhanced dissociation of the Keap1–Nrf2 complex by the new activators was proved.

Total Synthesis of Prostaglandin 15d-PGJ2 and Investigation of its Effect on the Secretion of IL-6 and IL-12

Egger, Julian,Fischer, Stefan,Bretscher, Peter,Freigang, Stefan,Kopf, Manfred,Carreira, Erick M.

supporting information, p. 4340 - 4343 (2015/09/15)

An efficient synthesis of 15-deoxy-Δ12,14-prostaglandin J2 (15d-PGJ2, 1) is reported. The route described allows for diversification of the parent structure to prepare seven analogues of 1 in which the positioning of electrophilic sites is varied. These analogues were tested in SAR studies for their ability to reduce the secretion of proinflammatory cytokines. It was shown that the endocyclic enone is crucial for the bioactivity investigated and that the conjugated ω-side chain serves in a reinforcing manner.

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