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ATB-337 is a hybrid molecule consisting of an H2S donor and the non-steroidal anti-inflammatory drug (NSAID) diclofenac. It is designed to combine the anti-inflammatory properties of diclofenac with the vasodilator and inflammatory modulating activity of hydrogen sulfide (H2S), potentially offering a more effective and safer alternative to traditional NSAIDs.
Used in Pharmaceutical Industry:
ATB-337 is used as an anti-inflammatory agent for its ability to inhibit COX-1 and COX-2 with similar efficacy as diclofenac, while also providing the additional benefits of H2S, such as vasodilation and modulation of inflammation.
Used in Gastrointestinal Protection:
ATB-337 is used as a gastrointestinal protective agent for its reduced potential to cause gastric damage compared to traditional NSAIDs like diclofenac. In rats, treatment with ATB-337 at the same dose as diclofenac did not cause significant gastrointestinal damage, making it a potentially safer option for long-term use.
Used in Inflammation Management:
ATB-337 is used as an inflammation management agent due to its ability to prevent leukocyte adherence to vascular endothelium and suppress the expression of pro-inflammatory mediators such as TNF-α, as well as adhesion molecules ICAM-1 and LFA-1. This suggests that ATB-337 may be more effective in managing inflammation than traditional NSAIDs alone.

912758-00-0

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912758-00-0 Usage

Biological Activity

atb-337 is a hybrid molecule of an h2s donor and the nsaid diclofenac [1].hydrogen sulfide (h2s) is a newly recognized signaling molecule with potent cytoprotective actions. hydrogen sulfide has been involved in mediating many physiological processes, such as the maintenance of gastrointestinal mucosal defense and repair. hydrogen sulfide also exerts many anti-inflammatory effects, including inhibition of leukocyte adherence to the vascular endothelium and leukocyte migration to sites of inflammation [2].oral administration of atb-337 did not produce any hemorrhagic erosions. oral administration of an equimolar dose of atb-337 produced > 90% less small intestinal damage and showed no significant effect on the hematocrit. in rats, administration of atb-337 (50 μmol/kg) showed no significant effect on leukocyte adherence. oral administration of atb-337 significantly increased plasma levels of h2s by > 40%. in a rat air pouch model, atb-337 (1 μmol/kg) suppressed cox-2 activity. in the rat, atb-337 inhibited thromboxane synthesis. atb-337 suppressed arachidonic acid–induced human platelet aggregation. pretreatment with atb-337 (10 μmol/kg) reduced paw swelling. atb-337 generated ~12nmol/min of h2s when it was incubated in buffer.

references

[1] wallace j l, caliendo g, santagada v, et al. gastrointestinal safety and anti-inflammatory effects of a hydrogen sulfide–releasing diclofenac derivative in the rat[j]. gastroenterology, 2007, 132(1): 261-271.[2] wallace j l. physiological and pathophysiological roles of hydrogen sulfide in the gastrointestinal tract[j]. antioxidants & redox signaling, 2010, 12(9): 1125-1133.

Check Digit Verification of cas no

The CAS Registry Mumber 912758-00-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,2,7,5 and 8 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 912758-00:
(8*9)+(7*1)+(6*2)+(5*7)+(4*5)+(3*8)+(2*0)+(1*0)=170
170 % 10 = 0
So 912758-00-0 is a valid CAS Registry Number.

912758-00-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name ATB-337

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:912758-00-0 SDS

912758-00-0Downstream Products

912758-00-0Relevant articles and documents

Modulation of angiogenesis by dithiolethione-modified NSAIDs and valproic acid

Isenberg,Jia,Field,Ridnour,Sparatore,Del Soldato,Sowers,Yeh,Moody,Wink,Ramchandran,Roberts

, p. 142 - 151 (2007)

Background and purpose: Angiogenesis involves multiple signaling pathways that must be considered when developing agents to modulate pathological angiogenesis. Because both cyclooxygenase inhibitors and dithioles have demonstrated anti-angiogenic properti

3H-1,2-DITHIOCYCLOPENTENE-3-THIOKETONE COMPOUNDS AND APPLICATION THEREOF

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Paragraph 0039; 0043, (2015/07/15)

The present invention relates to the field of medicaments, and in particular relates to 3H-1,2-dithiocyclopentene-3-thione compounds and application thereof. 3H-1,2-dithiocyclopentene-3-thione compounds disclosed by the invention have new structures shown in formula I or formula II. Proved by experiments, 3H-1,2-dithiocyclopentene-3-thione compounds can directly protect neurons in a cellular model, and can significantly restrain excessive inflammatory responses of brain inflammatory cells; and by using 3H-1,2-dithiocyclopentene-3-thione, focal ischemic cerebral infarct volumes of mice can be remarkably reduced in an animal model. Therefore, the invention provides the application of 3H-1,2-dithiocyclopentene-3-thione compounds and pharmaceutically acceptable salts thereof in the preparation of medicaments for preventing or treating cerebral apoplexy diseases.

HYDROGEN SULFIDE DERIVATIVES OF NON-STEROIDAL ANTI-INFLAMMATORY DRUGS

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Page/Page column 10, (2008/06/13)

The present invention relates to derivatives of non-steroidal anti-inflammatory drugs (NSAIDs) having improved anti-inflammatory properties useful in the treatment of inflammation, pain and fever. More particularly, NSAIDs are derivatized with a hydrogen

NEW ANTI-INFLAMMATORY COMPOUNDS

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Page/Page column 9-10, (2008/06/13)

The present invention relates to novel non steroidal anti-inflammatory compounds (NSAIDs) that release hydrogen sulfide (H2S). The present invention also provides methods for treating, preventing and/or reducing inflammation-associated diseases by releasing H2S in the cardiovascular, connective tissue, pulmonary, gastrointestinal, respiratory, urogenital, nervous, or cutaneous systems as well as infective diseases employing said compounds.

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