Home Pyridines 1161205-04-4
1161205-04-4,MFCD16618402
Catalog No.:AA000BLT

1161205-04-4 | N-(4-Chloro-3-methoxyphenyl)pyridine-2-carboxamide

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5mg
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$6.00   $4.00
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10mg
98%
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$8.00   $6.00
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25mg
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$13.00   $9.00
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50mg
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100mg
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  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA000BLT
Chemical Name:
N-(4-Chloro-3-methoxyphenyl)pyridine-2-carboxamide
CAS Number:
1161205-04-4
Molecular Formula:
C13H11ClN2O2
Molecular Weight:
262.6916
MDL Number:
MFCD16618402
SMILES:
COc1cc(ccc1Cl)NC(=O)c1ccccn1
Properties
Computed Properties
 
Complexity:
288  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
18  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
3  
XLogP3:
2.6  

Downstream Synthesis Route

[1]BioorganicandMedicinalChemistry,2013,vol.21,p.5955-5962

[2]JournalofMedicinalChemistry,2009,vol.52,p.4115-4118

[3]BioorganicandMedicinalChemistryLetters,2015,vol.25,p.3956-3960

[1]Cheung,ChiWai;LeendertPloeger,Marten;Hu,Xile[ChemicalScience,2018,vol.9,#3,p.655-659]

Literature

Title: Functional and pharmacological characteristics of metabotropic glutamate receptors 2/4 heterodimers.

Journal: Molecular pharmacology 20120901

Title: Discovery, synthesis, and structure-activity relationship development of a series of N-4-(2,5-dioxopyrrolidin-1-yl)phenylpicolinamides (VU0400195, ML182): characterization of a novel positive allosteric modulator of the metabotropic glutamate receptor 4 (mGlu(4)) with oral efficacy in an antiparkinsonian animal model.

Journal: Journal of medicinal chemistry 20111110

Title: Tricyclic thiazolopyrazole derivatives as metabotropic glutamate receptor 4 positive allosteric modulators.

Journal: Journal of medicinal chemistry 20110728

Title: Discovery, synthesis, and structure-activity relationship development of a series of N-(4-acetamido)phenylpicolinamides as positive allosteric modulators of metabotropic glutamate receptor 4 (mGlu(4)) with CNS exposure in rats.

Journal: Journal of medicinal chemistry 20110224

Title: Synthesis and evaluation of a series of heterobiarylamides that are centrally penetrant metabotropic glutamate receptor 4 (mGluR4) positive allosteric modulators (PAMs).

Journal: Journal of medicinal chemistry 20090723

Title: Engers DW, et al. Synthesis and evaluation of a series of heterobiarylamides that are centrally penetrant metabotropic glutamate receptor 4 (mGluR4) positive allosteric modulators (PAMs). J Med Chem. 2009 Jul 23;52(14):4115-8.

Title: Engers DW, et al. Discovery, synthesis, and structure-activity relationship development of a series of N-(4-acetamido)phenylpicolinamides as positive allosteric modulators of metabotropic glutamate receptor 4 (mGlu(4)) with CNS exposure in rats. J Med Chem. 2011 Feb 24;54(4):1106-10.

Title: Jantas D, et al. Neuroprotective effects of mGluR II and III activators against staurosporine- and doxorubicin-induced cellular injury in SH-SY5Y cells: New evidence for a mechanism involving inhibition of AIF translocation. Neurochem Int. 2015 Sep;88:124-37.

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