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4-(3-(4-benzylpiperidin-1-yl)-1-hydroxy-2-Methylpropyl)phenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

375856-62-5

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375856-62-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 375856-62-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,5,8,5 and 6 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 375856-62:
(8*3)+(7*7)+(6*5)+(5*8)+(4*5)+(3*6)+(2*6)+(1*2)=195
195 % 10 = 5
So 375856-62-5 is a valid CAS Registry Number.

375856-62-5Downstream Products

375856-62-5Relevant academic research and scientific papers

Method for preventing dyskinesias

-

, (2008/06/13)

Dyskinesias in humans are prevented by administering a therapeutically effective dose of a NR1A/2B site-selective NMDA receptor antagonist compound to a human.

Discovery of (R)-1-[2-hydroxy-3-(4-hydroxy-phenyl)-propyl]-4-(4-methyl-benzyl)-piperidin- 4-ol: A novel NR1/2B subtype selective NMDA receptor antagonist

Pinard, Emmanuel,Alanine, Alexander,Bourson, Anne,Buettelmann, Bernd,Gill, Ramanjit,Heitz, Marie-Paule,Jaeschke, Georg,Mutel, Vincent,Trube, Gerhard,Wyler, Rene

, p. 2173 - 2176 (2007/10/03)

Starting from Ro-25-6981 as a lead compound, highly potent and selective NR1/2B subtype selective NMDA receptor antagonists, with low activity at α1 adrenergic receptors were developed.

Phenylalkanolamine derivatives as antagonists of the NMDA receptor

-

, (2008/06/13)

Compounds of the formula ψψ ψ wherein ψ Ris hydrogen, hydroxy, or aryl lower alkyloxy; Xis hydrogen; Yis hydroxy or hydrogen; ψ or both X and Y taken together are oxygen; ψ Zis aryl lower alkyl; and mis an integer from 1 to 4 ψ or a diastereomer or an enantiomer thereof, except, the R,R diastereomer of formula I, wherein X is hydrogen, Y is hydroxy, R is benzyloxy, Z is benzyl, and m is 1, or pharmaceutically acceptable salts thereof, reduce adverse effects of toxic injury to central neurons and thus are useful in the treatment of ischemia, stroke, hypoxia and are NMDA receptor antagonists.ψ

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