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(1S,2R,5aS,7R,8aR,8bS)-2-{(1R)-1-[3,5-bis(trifluoromethyl)phenyl]ethoxy}-1-(4-fluorophenyl)-7-hydroxyoctahydrocyclopenta[a]pyrrolizin-5(1H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1254353-63-3

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1254353-63-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1254353-63-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,4,3,5 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1254353-63:
(9*1)+(8*2)+(7*5)+(6*4)+(5*3)+(4*5)+(3*3)+(2*6)+(1*3)=143
143 % 10 = 3
So 1254353-63-3 is a valid CAS Registry Number.

1254353-63-3Downstream Products

1254353-63-3Relevant academic research and scientific papers

Fused tricyclic pyrrolizinones that exhibit pseudo-irreversible blockade of the NK1 receptor

Morriello, Gregori J.,Chicchi, Gary,Johnson, Tricia,Mills, Sander G.,Demartino, Julie,Kurtz, Marc,Tsao,Zheng, Song,Tong, Xinchun,Carlson, Emma,Townson, Karen,Wheeldon, Alan,Boyce, Susan,Collinson, Neil,Rupniak, Nadia,Devita, Robert J.

supporting information; experimental part, p. 5925 - 5932 (2010/11/18)

Previously, we had disclosed a novel class of hNK1 antagonists based on the 5,5-fused pyrrolidine core. These compounds displayed subnanomolar hNK1 affinity along with good efficacy in a gerbil foot-tapping (GFT) model, but unfortunately they had low to moderate functional antagonist (IP-1) activity. To elaborate on the SAR of this class of hNK1 compounds and to improve functional activity, we have designed and synthesized a new class of hNK1 antagonist with a third fused ring. Compared to the 5,5-fused pyrrolidine class, these 5,5,5-fused tricyclic hNK1 antagonists maintain subnanomolar hNK1 binding affinity with highly improved functional IP-1 activity (1 binding affinity, off-target selectivity, pharmacokinetic profile and in vivo activity. Complete inhibition of agonist activity was observed at both 0 and 24 h in the gerbil foot-tapping model with an ID50 of 0.02 mpk at both 0 and 24 h, respectively.

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