VU 29 - Moligand™, ≥98% , Allosteric modulator of mGlu 5 receptor, CAS No.890764-36-0, Allosteric modulator of mGlu 5 receptor

CAS: 890764-36-0 Cat. No.: V286646 Formule: C₂₂H₁₆N₄O₃ Poids moléculaire: 384.39 PubChem CID: 11610682

QUALITÉ & PURETÉ Moligand™, ≥98%

Synonyms

BCP27694 | AKOS040745416 | DTXSID60469437 | GTPL6403 | VU29 | VU-29 | AKOS005266482 | NCGC00370929-02 | EX-A4560 | N-(1,3-diphenyl-1H-pyrazol-5-yl)-4-nitrobenzamide | N-(1,3-diphenyl-1H-pyrazol-5-yl)-4-nitro-benzamide | VU29;VU 29;DPAP | BDBM50187615 | N-

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Spécifications

Synonymes

BCP27694 | AKOS040745416 | DTXSID60469437 | GTPL6403 | VU29 | VU-29 | AKOS005266482 | NCGC00370929-02 | EX-A4560 | N-(1,3-diphenyl-1H-pyrazol-5-yl)-4-nitrobenzamide | N-(1,3-diphenyl-1H-pyrazol-5-yl)-4-nitro-benzamide | VU29;VU 29;DPAP | BDBM50187615 | N-

Spécifications et pureté

Moligand™, ≥98%

Mécanismes biochimiques et physiologiques

Potent allosteric potentiator at the rat mGlu5receptor (EC50= 9 nM); binds to the MPEP allosteric site (Ki app= 244 nM). Selective for mGlu5 over mGlu1and mGlu2receptors (EC50values are 557 nM and 1.51μM for mGlu1and mGlu2respectively). Potentiates both D

Conditions de stockage de stockage

Store at -20°C

Expédié en

Ice chest + Ice pads

Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.

Grade

Moligand™

Type d'action

ALLOSTERIC MODULATOR

Mécanisme d'action

Allosteric modulator of mGlu 5 receptor

Pureté

≥98%

Noms et identifiants

Pubchem Sid

528767661

Sourires canoniques

C1=CC=C(C=C1)C2=NN(C(=C2)NC(=O)C3=CC=C(C=C3)[N+](=O)[O-])C4=CC=CC=C4

IUPAC Name

N-(2,5-diphenylpyrazol-3-yl)-4-nitrobenzamide

InChIKey

KIALCSMRIHRFPL-UHFFFAOYSA-N

INCHI

1S/C22H16N4O3/c27-22(17-11-13-19(14-12-17)26(28)29)23-21-15-20(16-7-3-1-4-8-16)24-25(21)18-9-5-2-6-10-18/h1-15H,(H,23,27)

Isomères SMILES

C1=CC=C(C=C1)C2=NN(C(=C2)NC(=O)C3=CC=C(C=C3)[N+](=O)[O-])C4=CC=CC=C4

PubChem CID

11610682

Poids moléculaire

384.39

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Classe Azoles
      • Subclass Pyrazoles

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Classe: Azoles
• Subclass: Pyrazoles
• Intermediate Tree Nodes: Not available
• Direct Parent: Phenylpyrazoles
• Alternative Parents: Nitrobenzenes Benzamides Nitroaromatic compounds Benzoyl derivatives Heteroaromatic compounds Secondary carboxylic acid amides Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Azacyclic compounds Organooxygen compounds Organonitrogen compounds Organic zwitterions Organic salts Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Phenylpyrazole - Benzamide - Benzoic acid or derivatives - Nitrobenzene - Nitroaromatic compound - Benzoyl - Monocyclic benzene moiety - Benzenoid - Heteroaromatic compound - Carboxamide group - Organic nitro compound - C-nitro compound - Secondary carboxylic acid amide - Azacycle - Carboxylic acid derivative - Organic 1,3-dipolar compound - Organic oxoazanium - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic oxygen compound - Organic salt - Organic nitrogen compound - Organic oxide - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic zwitterion - Aromatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as phenylpyrazoles. These are compounds containing a phenylpyrazole skeleton, which consists of a pyrazole bound to a phenyl group.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Cibles associées (humaines)

GRM5 Tchem Metabotropic glutamate receptor 5 (2 Activities)

Discover Target: GRM5

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

GRM5 Tchem Metabotropic glutamate receptor 5 (5733 Activities)

Discover Target: GRM5

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

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Hdac6 Histone deacetylase 6 (222 Activities)

Discover Target: Hdac6

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rep Replicase polyprotein 1ab (378 Activities)

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Mécanismes d'action

Propriétés chimiques et physiques

• Solubilité: Solvent:DMSO, Max Conc. mg/mL: 38.44, Max Conc. mM: 100
• Poids moléculaire: 384.400 g/mol
• XLogP3: 4.600
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 4
• Exact Mass: 384.122 Da
• Monoisotopic Mass: 384.122 Da
• Topological Polar Surface Area: 92.700 Ų
• Heavy Atom Count: 29
• Formal Charge: 0
• Complexity: 561.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1