ASP8477 - Moligand™ , Inhibitor of Fatty acid amide hydrolase;Inhibitor of Fatty acid amide hydrolase-2, CAS No.A607780, Inhibitor of Fatty acid amide hydrolase;Inhibitor of Fatty acid amide hydrolase-2

CAS: A607780 Cat. No.: A607780 PubChem CID: 15950844

GRADE & PURITY Moligand™

Synonyms

ASP8477|ASP-8477|pyridin-3-yl 4-(phenylcarbamoyl)piperidine-1-carboxylate|W22BL56T55|906737-25-5|3-Pyridinyl 4-((phenylamino)carbonyl)-1-piperidinecarboxylate|3-Pyridinyl 4-[(phenylamino)carbonyl]-1-piperidinecarboxylate|1-Piperidinecarboxylic acid, 4-((p

Storage

Room temperature

Specifications

Synonyme

ASP8477 | ASP-8477 | pyridin-3-yl 4-(phenylcarbamoyl)piperidine-1-carboxylate | W22BL56T55 | 906737-25-5 | 3-Pyridinyl 4-((phenylamino)carbonyl)-1-piperidinecarboxylate | 3-Pyridinyl 4-[(phenylamino)carbonyl]-1-piperidinecarboxylate | 1-Piperidinecarboxylic acid, 4-((p

Spezifikationen & Reinheit

Moligand™

Storage

Room temperature

Note

Moligand™

Aktionsart

INHIBITOR

Mechanismus der Wirkung

Inhibitor of Fatty acid amide hydrolase;Inhibitor of Fatty acid amide hydrolase-2

Namen und Kennungen

• Kanonisches Lächeln: O=C(C1CCN(CC1)C(=O)Oc1cccnc1)Nc1ccccc1
• IUPAC Name: pyridin-3-yl 4-(phenylcarbamoyl)piperidine-1-carboxylate
• InChIKey: PLCMZPFTMOAGOE-UHFFFAOYSA-N
• INCHI: 1S/C18H19N3O3/c22-17(20-15-5-2-1-3-6-15)14-8-11-21(12-9-14)18(23)24-16-7-4-10-19-13-16/h1-7,10,13-14H,8-9,11-12H2,(H,20,22)
• Isomere SMILES: C1CN(CCC1C(=O)NC2=CC=CC=C2)C(=O)OC3=CN=CC=C3
• PubChem CID: 15950844

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Klasse Piperidines
      • Subclass Piperidinecarboxylic acids and derivatives

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Klasse: Piperidines
• Subclass: Piperidinecarboxylic acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Piperidinecarboxylic acids
• Alternative Parents: Piperidinecarboxamides Anilides N-arylamides Pyridines and derivatives Heteroaromatic compounds Carbamate esters Secondary carboxylic acid amides Azacyclic compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Piperidinecarboxamide - Piperidinecarboxylic acid - Anilide - N-arylamide - Monocyclic benzene moiety - Pyridine - Benzenoid - Heteroaromatic compound - Carbamic acid ester - Carboxamide group - Secondary carboxylic acid amide - Carboxylic acid derivative - Azacycle - Organic oxide - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Carbonyl group - Hydrocarbon derivative - Organic nitrogen compound - Aromatic heteromonocyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as piperidinecarboxylic acids. These are compounds containing a piperidine ring which bears a carboxylic acid 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

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FAAH2 Tchem Fatty-acid amide hydrolase 2 (1 Activities)

Discover Target: FAAH2

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

FAAH Tchem Fatty-acid amide hydrolase 1 (1 Activities)

Discover Target: FAAH

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