80971-95-5

Usage

Uses

Given the limited information provided, the potential uses of 3-Amino-3-(4-Cyanophenyl)propanoic Acid can only be hypothesized based on its chemical structure and functional groups. Here are some possible applications:
Used in Pharmaceutical Industry:
3-Amino-3-(4-Cyanophenyl)propanoic Acid could be used as a building block or intermediate in the synthesis of pharmaceutical compounds for [specific medical conditions or therapeutic areas], due to its reactive amino and carboxylic acid groups which can form various types of chemical bonds.
Used in Materials Science:
In the field of materials science, 3-Amino-3-(4-Cyanophenyl)propanoic Acid might be utilized as a component in the development of new materials with unique properties, such as polymers or composites, leveraging its aromatic cyanophenyl group for enhanced structural characteristics.
Used in Chemical Research:
As a niche compound, 3-Amino-3-(4-Cyanophenyl)propanoic Acid could serve as a subject of chemical research to explore its reactivity, potential reactions with other molecules, and its behavior under various conditions, contributing to the advancement of organic chemistry.

InChI:InChI=1/C10H10N2O2/c11-6-7-1-3-8(4-2-7)9(12)5-10(13)14/h1-4,9H,5,12H2,(H,13,14)

Upstream product

• 141-82-2 malonic acid 
• 105-07-7 4-cyanobenzaldehyde 

Downstream Products

• 80971-98-8 3-(4-Cyano-phenyl)-3-(naphthalene-2-sulfonylamino)-propionic acid 
• 288848-50-0 ethyl (+/-)-3-amino-3-(4-cyanophenyl)propanoate 
• 501015-22-1 (+/-)-3-(tert-butoxycarbonylamino)-3-(4-cyanophenyl)propanoic acid 
• 517905-92-9 (+/-)-3-(9-fluorenylmethoxycarbonylamino)-3-(4-cyanophenyl)propanoic acid 
• 288848-57-7 3-(4-cyanophenyl)-2,3-dihydro-1H-pyrrolizin-1-one 
• 288848-53-3 ethyl 3-(4-cyanophenyl)-3-(pyrrol-1-yl)propionate 
• 80972-06-1 N-[1-(4-Cyano-phenyl)-3-morpholin-4-yl-3-oxo-propyl]-4-methyl-benzenesulfonamide 
• 80972-52-7 4-[3-Morpholin-4-yl-1-(naphthalene-2-sulfonylamino)-3-oxo-propyl]-benzamidine; hydriodide 
• 80972-51-6 4-[1-(Naphthalene-2-sulfonylamino)-3-oxo-3-piperidin-1-yl-propyl]-benzamidine; hydriodide 
• 80972-54-9 3-(4-Carbamimidoyl-phenyl)-3-(naphthalene-2-sulfonylamino)-N-phenyl-propionamide; hydriodide 
• 80972-48-1 4-[3-Morpholin-4-yl-3-oxo-1-(toluene-4-sulfonylamino)-propyl]-benzamidine; hydriodide 
• 80972-53-8 N-Butyl-3-(4-carbamimidoyl-phenyl)-3-(naphthalene-2-sulfonylamino)-propionamide; hydriodide 
• 80972-47-0 4-[3-Oxo-3-piperidin-1-yl-1-(toluene-4-sulfonylamino)-propyl]-benzamidine; hydriodide 
• 80972-50-5 3-(4-Carbamimidoyl-phenyl)-N-phenyl-3-(toluene-4-sulfonylamino)-propionamide; hydriodide 

Relevant academic research and scientific papers

Structure activity relationships of αv integrin antagonists for pulmonary fibrosis by variation in aryl substituents

Antagonism of αvβ6 is emerging as a potential treatment of idiopathic pulmonary fibrosis based on strong target validation. Starting from an αvβ3 antagonist lead and through simple variation in the nature and position of the aryl substituent, the discovery of compounds with improved αvβ6 activity is described. The compounds also have physicochemical properties commensurate with oral bioavailability and are high quality starting points for a drug discovery program. Compounds 33S and 43E1 are pan αv antagonists having ca. 100 nM potency against αvβ3, αvβ5, αvβ6, and αvβ8 in cell adhesion assays. Detailed structure activity relationships with these integrins are described which also reveal substituents providing partial selectivity (defined as at least a 0.7 log difference in pIC50 values between the integrins in question) for αvβ3 and αvβ5.

New aromatase inhibitors. Synthesis and biological activity of aryl- substituted pyrrolizine and indolizine derivatives

We report herein the design and the synthesis of some aryl-substituted pyrrolizine and indolizine derivatives, on the basis of a hypothetical pharmacophore structure designed to fit the catalytic site of the human cytochrome P450 aromatase. The in vitro b