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pyridin-2-yl-(4,5,6,8-tetrahydro-3-thia-1,7,8-triaza-cyclopenta[e]azulen-2-yl)-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1235325-16-2

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1235325-16-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1235325-16-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,5,3,2 and 5 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1235325-16:
(9*1)+(8*2)+(7*3)+(6*5)+(5*3)+(4*2)+(3*5)+(2*1)+(1*6)=122
122 % 10 = 2
So 1235325-16-2 is a valid CAS Registry Number.

1235325-16-2Downstream Products

1235325-16-2Relevant academic research and scientific papers

Tricyclic thiazolopyrazole derivatives as metabotropic glutamate receptor 4 positive allosteric modulators

Hong, Sang-Phyo,Liu, Kevin G.,Ma, Gil,Sabio, Michael,Uberti, Michelle A.,Bacolod, Maria D.,Peterson, John,Zou, Zack Z.,Robichaud, Albert J.,Doller, Darío

, p. 5070 - 5081 (2011/09/16)

There is an increasing amount of evidence to support that activation of the metabotropic glutamate receptor 4 (mGlu4 receptor), either with an orthosteric agonist or a positive allosteric modulator (PAM), provides impactful interventions in diseases such as Parkinson's disease, anxiety, and pain. mGlu4 PAMs may have several advantages over mGlu4 agonists for a number of reasons. As part of our efforts in identifying therapeutics for central nervous system (CNS) diseases such as Parkinson's disease, we have been focusing on metabotropic glutamate receptors. Herein we report our studies with a series of tricyclic thiazolopyrazoles as mGlu4 PAMs.

HETEROTRICYCLIC COMPOUNDS AS POSITIVE ALLOSTERIC MODULATORS OF METABOTROPIC GLUTAMATE RECEPTORS

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Page/Page column 34, (2010/08/04)

The present invention relates to novel compounds of Formula (I), wherein wherein X1, X2, Y, Z1, Z2, Z3, M and (A)m are defined as in Formula (I); invention compounds are modulators of metab

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