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3-methyl-1-(2-n-propylphenyl)-1H-pyrazol-5-amine is a complex organic compound belonging to the pyrazole family. It is characterized by a pyrazole ring with a methyl group at the 3-position and a 2-n-propylphenyl group attached to the 1-position. This chemical is primarily used in the synthesis of pharmaceuticals and agrochemicals due to its potential biological activity. The compound's structure provides a foundation for further functionalization and modification, making it a valuable intermediate in the development of new drugs and chemical products. Its unique properties and reactivity make it an important molecule in the field of organic chemistry and medicinal chemistry.

1380573-87-4

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1380573-87-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1380573-87-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,0,5,7 and 3 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1380573-87:
(9*1)+(8*3)+(7*8)+(6*0)+(5*5)+(4*7)+(3*3)+(2*8)+(1*7)=174
174 % 10 = 4
So 1380573-87-4 is a valid CAS Registry Number.

1380573-87-4Downstream Products

1380573-87-4Relevant academic research and scientific papers

Pyrazole[3,4-e][1,4]thiazepin-7-one derivatives as a novel class of Farnesoid X Receptor (FXR) agonists

Marinozzi, Maura,Carotti, Andrea,Sansone, Emanuele,MacChiarulo, Antonio,Rosatelli, Emiliano,Sardella, Roccaldo,Natalini, Benedetto,Rizzo, Giovanni,Adorini, Luciano,Passeri, Daniela,De Franco, Francesca,Pruzanski, Mark,Pellicciari, Roberto

supporting information; experimental part, p. 3429 - 3445 (2012/07/30)

A virtual screening procedure was applied to the discovery of structurally diverse non-steroidal Farnesoid X Receptor (FXR) agonists. From 117 compounds selected by virtual screening, a total of 47 compounds were found to be FXR agonists, with 34 of them showing activity below a concentration of 20 μM. 1H-Pyrazole[3,4-e][1,4]thiazepin-7-one-based hit compound 7 was chosen for hit-to-lead optimization. A large number of 1H-pyrazole[3,4-e][1,4]thiazepin-7- one derivatives was designed, synthesized, and evaluated by a cell-based luciferase transactivation assay for their agonistic activity against FXR. Most of them exhibited low micromolar range of potency and very high efficacy.

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