1002-19-3

Usage

Uses

Used in Medicinal Chemistry:
3-[(3-AMINO-3-OXOPROPYL)DITHIO]PROPANAMIDE is used as a compound of interest for its potential applications in medicinal chemistry, due to its unique structural features that may contribute to the development of new drugs.
Used in Drug Development:
3-[(3-AMINO-3-OXOPROPYL)DITHIO]PROPANAMIDE is used as a potential candidate in drug development, where its structural properties could be leveraged to create novel therapeutic agents.
Used in Organic Synthesis:
3-[(3-AMINO-3-OXOPROPYL)DITHIO]PROPANAMIDE is used as a building block in organic synthesis, where its amine and oxopropyl functional groups can be utilized to construct more complex molecules.
Used in Materials Science:
3-[(3-AMINO-3-OXOPROPYL)DITHIO]PROPANAMIDE is used as a potential component in materials science, where its chemical properties could be explored for the creation of new materials with specific characteristics.
Further research and investigation are necessary to fully understand the properties and potential uses of 3-[(3-Amino-3-oxopropyl)dithio]propanamide, as its applications in these fields are still being explored.

InChI:InChI=1/C6H12N2O2S2/c1-3(5(7)9)11-12-4(2)6(8)10/h3-4H,1-2H3,(H2,7,9)(H2,8,10)/p-2

Upstream product

• 75-15-0 carbon disulfide 
• 2935-95-7 β-Propiothiolactone 
• 1119-62-6 3,3'-dithiobis(propionic acid) 
• 1002-18-2 3-(2-chlorocarbonyl-ethyldisulfanyl)-propionyl chloride 
• 79-06-1 2-propenamide 
• 135468-50-7 3-(benzhydrylthio)propanamide 
• 1336-21-6 ammonium hydroxide 

Downstream Products

• 25629-58-7 5-chloroisothiazol-3(2H)-one 
• 26172-54-3 2-methyl-4-isothiazolin-3-one hydrochloride 
• 763-35-9 β-mercaptopropionamide 
• 14217-66-4 3-Chlorisothiazol 
• 1003-07-2 3-oxo-2,3-dihydroisothiazole 

Relevant academic research and scientific papers

Nitridoosmium(VI) and nitridoruthenium(VI) complexes of cysteine(2-) and related ligands

Anionic complexes of nitridoruthenium(VI) and nitridoosmium(VI) containing covalently bound N-acetyl-L-cysteinato, 3-sulfidopropionato, and 3-sulfidopropionamidato ligands have been synthesized to model the binding of δ-(L-α-aminoadipyl)-L-cysteinyl-D-val

TETRAHYDROPYRAZOLO-PYRAZINYL-DIHYDROIMIDAZOLONE OR TETRAHYDROPYRAZOLO-PYRIDINYL-DIHYDROIMIDAZOLONE COMPOUNDS AND METHODS OF USING SAME

The application relates to a compound of Formula (I) : or a pharmaceutically acceptable salt, hydrate, solvate, prodrug, stereoisomer, or tautomer thereof, which modulates the activity of GLP-1 receptor, a pharmaceutical composition comprising a compound of Formula (I), and a method of treating or preventing a disease in which GLP-1 receptor plays a role.

A 3 - chloroisothiazole chemical synthesis method

The invention relates to a chemical synthesis method of 3-chloroisothiazole. The chemical synthesis method takes 4,5- dithio-1,8-octanedioic acid as a material and simply synthesizes 3-chloroisothiazole by two-step reaction. The method is as follows: adding the 4,5- dithio-1,8-octanedioic acid into thionyl chloride, evaporating out thionyl chloride after reaction is ended, adding into ammonia water, controlling a temperature to generate 4,5- dithio-1,8-octanedioyl amine; dissolving phosphorus oxychloride in an organic solvent toluene, adding 4,5- dithio-1,8-octanedioyl amine, controlling the reaction temperature at a lower temperature, increasing the temperature for reaction after reacting for 48 hours to synthesize 3-chloroisothiazole. The chemical synthesis method disclosed by the invention is low in synthesis route cost, high in yield, simple and convenient to operate, and therefore, an efficient synthesis method is provided for synthesizing the compound.

Synthesis and antibacterial activity of 2-(4-substituted phenyl)-3(2H)-isothiazolones

Several new and known 2-(4-substituted phenyl)-3(2H)-isothiazolone derivatives with or without chloro substituent at C-5 position were synthesized and their in vitro antibacterial activity against selected Gram-negative and Gram-positive bacteria were eva

A General Synthesis of N-Substituted Isothiazol-3(2H)-ones

A general route to the synthesis of N-substituted isothiazol-3(2H)-ones (4a-i) is described which proceeds via trichloroacetic acid-mediated ring closure of N-substituted (Z)-3-(benzylsulfinyl)propenamides (15a-i).

ESTER PRODRUGS

This invention relates to ester prodrugs for alkanoic acid compounds useful as leukotriene antagonists, and pharmaceutical compositions containing such ester prodrug compounds. This invention also relates to methods of treating diseases in which leukotrienes are a factor by administration of an effective amount of the above compounds or compositions.

THIOPHENYL ALKANOIC ACIDS USEFUL AS LEUKOTRIENE ANTAGONISTS

This invention relates to alkanoic acid compounds having phenyl and thio substituents which are useful as leukotriene antagonists and pharmaceutical compositions containing such compounds. This invention also relates to treating diseases in which leukotrienes are a factor by administration of an effective amount of the above compounds or compositions.

Leukotriene antagonists

This invention relates to alkanoic acid compounds having phenyl and thio substituents which are useful as leukotriene antagonists and pharmaceutical compositions containing such compounds. This invention also relates to methods of treating diseases in which leukotrienes are a factor by administration of an effective amount of the above compounds or compositions.