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2-[[3-[4-(2-methoxyphenyl)-1-piperazinyl]propyl]thio]-1-methyl-1H-benzimidazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1042976-36-2

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1042976-36-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1042976-36-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,2,9,7 and 6 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1042976-36:
(9*1)+(8*0)+(7*4)+(6*2)+(5*9)+(4*7)+(3*6)+(2*3)+(1*6)=152
152 % 10 = 2
So 1042976-36-2 is a valid CAS Registry Number.

1042976-36-2Downstream Products

1042976-36-2Relevant academic research and scientific papers

Synthesis of new arylpiperazinylalkylthiobenzimidazole, benzothiazole, or benzoxazole derivatives as potent and selective 5-HT1A serotonin receptor ligands

Siracusa, Maria A.,Salerno, Loredana,Modica, Maria N.,Pittalà, Valeria,Romeo, Giuseppe,Amato, Maria E.,Nowak, Mateusz,Bojarski, Andrzej J.,Mereghetti, Ilario,Cagnotto, Alfredo,Mennini, Tiziana

experimental part, p. 4529 - 4538 (2009/06/06)

A series of new compounds containing a benzimidazole, benzothiazole, or benzoxazole nucleus linked to an arylpiperazine by different thioalkyl chains was prepared. They were tested in radioligand binding experiments to evaluate their affinity for 5-HT1A and 5-HT2A serotonergic, α1 adrenergic, D1, and D2 dopaminergic receptors. Many of tested compounds showed an interesting binding profile; in particular, 36 displayed very high 5-HT1A receptor affinity and selectivity over all the other investigated receptors. Selected compounds, evaluated in functional assays, showed antagonistic or partial agonistic activity at 5-HT1A receptor. An extensive conformational research using both NMR and modeling techniques indicated that extended conformations predominated in vacuum, in solution and during interactions with 5-HT 1A receptor. Finally, the elaborated binding mode of selected compounds at 5-HT1A receptor was used to explain the influence of spacer length on ligands affinity.

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