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Bicyclo[3.1.0]hexane-6-carboxylic acid, 2-amino-2-cyano-4-methyl-, ethyl ester, is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

191399-80-1

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191399-80-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 191399-80-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,1,3,9 and 9 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 191399-80:
(8*1)+(7*9)+(6*1)+(5*3)+(4*9)+(3*9)+(2*8)+(1*0)=171
171 % 10 = 1
So 191399-80-1 is a valid CAS Registry Number.

191399-80-1Downstream Products

191399-80-1Relevant academic research and scientific papers

Methyl substitution of 2-aminobicyclo[3.1.0]hexane 2,6-dicarboxylate (LY354740) determines functional activity at metabotropic glutamate receptors: Identification of a subtype selective mGlu2 receptor agonist

Dominguez, Carmen,Prieto, Lourdes,Valli, Matthew J.,Massey, Steven M.,Bures, Mark,Wright, Rebecca A.,Johnson, Bryan G.,Andis, Sherri L.,Kingston, Ann,Schoepp, Darryle D.,Monn, James A.

, p. 3605 - 3612 (2005)

LY354740 (1) is a highly potent and selective agonist of metabotropic glutamate (mGlu) receptors 2 and 3. In the present study, we have prepared C3- and C4-methyl-substituted variants of rac-1, compounds 5, 9, and 13. Each of these racemic methyl-substituted analogues displaced specific binding of the mGlu2/3 receptor antagonist 3H-2S-2-amino-2-(1S,2S-2- carboxycycloprop-l-yl)-3-(xanth-9-yl)propanoic acid (3H-LY341495) from membranes expressing mGlu2 or mGlu3 receptor subtypes. Evaluation of the functional effects of this series on second messenger responses in cells expressing human mGlu2 or mGlu3 receptors revealed C3β-methyl analogue 5 to possess antagonist properties at both mGlu2 and mGlu3 receptors while C4β-methyl analogue 9 acts as a full agonist at each of these targets. Unexpectedly, we found that incorporation of a methyl substituent at the C4α-position as in analogue 13 results in a mixed mGlu2 agonist/mGlu3 antagonist pharmacological profile. All of the mGlu2 agonist and mGlu3 antagonist activity of rac-13 was found to reside in its resolved (+)-isomer.

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