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22744-13-4

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22744-13-4 Usage

Description

2-[4-(methoxycarbonyl)phenyl]-2-oxoethylidenediazenium is a chemical compound belonging to the diazeniumdiolate family. It functions as a nitric oxide donor, releasing nitric oxide upon decomposition in aqueous solutions. 2-[4-(methoxycarbonyl)phenyl]-2-oxoethylidenediazenium holds potential therapeutic applications due to nitric oxide's involvement in various physiological processes such as smooth muscle relaxation, vasodilation, and neurotransmission. The presence of a carbonyl group in the compound enables a controlled release of nitric oxide, making it a promising candidate for drug development in the treatment of cardiovascular diseases, pulmonary hypertension, and other conditions related to nitric oxide deficiency. However, further research is necessary to fully comprehend the potential benefits and limitations of this compound.

Uses

Used in Pharmaceutical Applications:
2-[4-(methoxycarbonyl)phenyl]-2-oxoethylidenediazenium is used as a therapeutic agent for the treatment of cardiovascular diseases, pulmonary hypertension, and other conditions related to nitric oxide deficiency. 2-[4-(methoxycarbonyl)phenyl]-2-oxoethylidenediazenium's ability to release nitric oxide in a controlled manner aids in addressing these health issues.
Used in Drug Development:
In the pharmaceutical industry, 2-[4-(methoxycarbonyl)phenyl]-2-oxoethylidenediazenium is used as a key compound in the development of new drugs targeting conditions associated with nitric oxide deficiency. Its controlled release of nitric oxide makes it a valuable asset in creating effective treatments for various medical conditions.
Used in Research and Development:
2-[4-(methoxycarbonyl)phenyl]-2-oxoethylidenediazenium is utilized as a research compound to further understand the role of nitric oxide in physiological processes and its potential applications in medicine. This knowledge can contribute to the development of novel therapeutic strategies and treatments for a range of health conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 22744-13-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,7,4 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 22744-13:
(7*2)+(6*2)+(5*7)+(4*4)+(3*4)+(2*1)+(1*3)=94
94 % 10 = 4
So 22744-13-4 is a valid CAS Registry Number.

22744-13-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (Z)-2-diazonio-1-(4-methoxycarbonylphenyl)ethenolate

1.2 Other means of identification

Product number -
Other names 4-diazoacetyl-benzoic acid methyl ester

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:22744-13-4 SDS

22744-13-4Relevant articles and documents

ONO-8430506: A Novel Autotaxin Inhibitor That Enhances the Antitumor Effect of Paclitaxel in a Breast Cancer Model

Hiramatsu, Atsushi,Hirooka, Yasuo,Hisaichi, Katsuya,Imagawa, Akira,Iwaki, Yuzo,Katoh, Makoto,Kobayashi, Juta,Komichi, Yuka,Maeda, Tatsuo,Matsumura, Naoya,Moriguchi, Hideki,Nakatani, Shingo,Nishiyama, Taihei,Ohhata, Akira,Okabe, Yasuyuki,Okada, Masahiro,Ota, Hiroto,Saga, Hiroshi,Sugiyama, Tetsuya,Watanabe, Toshihide,Yamamoto, Shingo

supporting information, p. 1335 - 1341 (2020/07/06)

Lysophosphatidic acid (LPA) is a bioactive lipid mediator that elicits a number of biological functions, including smooth muscle contraction, cell motility, proliferation, and morphological change. LPA is endogenously produced by autotaxin (ATX) from extracellular lysophosphatidylcholine (LPC) in plasma. Herein, we report our medicinal chemistry effort to identify a novel and highly potent ATX inhibitor, ONO-8430506 (20), with good oral availability. To enhance the enzymatic ATX inhibitory activity, we designed several compounds by structurally comparing our hit compound with the endogenous ligand LPC. Further optimization to improve the pharmacokinetic profile and enhance the ATX inhibitory activity in human plasma resulted in the identification of ONO-8430506 (20), which enhanced the antitumor effect of paclitaxel in a breast cancer model.

Synthesis and evaluation of a classical 2,4-diamino-5-substituted-furo[2,3-d]pyrimidine and a 2-amino-4-oxo-6-substituted-pyrrolo[2,3-d]pyrimidine as antifolates

Gangjee, Aleem,Yang, Jie,McGuire, John J.,Kisliuk, Roy L.

, p. 8590 - 8598 (2008/02/08)

Two classical antifolates, a 2,4-diamino-5-substituted furo[2,3-d]pyrimidine and a 2-amino-4-oxo-6-substituted pyrrolo[2,3-d]pyrimidine, were synthesized as potential inhibitors of dihydrofolate reductase (DHFR) and thymidylate synthase (TS). The synthese

[60]Fullerene as a substituent

Bagno, Alessandro,Claeson, Sofia,Maggini, Michele,Martini, Maria Luisa,Prato, Maurizio,Scorrano, Gianfranco

, p. 1015 - 1023 (2007/10/03)

The substituent effect of the dihydro[60]fullerenyl group and its hydrophobic parameters have been evaluated quantitatively. The substituent constant has been determined from the pK value of a fullerene-based, para-substituted benzoic acid 1 in 80% dioxan

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