DM-1451 - Moligand™ , Agonist of 5-HT 6 receptor;Agonist of 5-HT 7 receptor, CAS No.173456-49-0, Agonist of 5-HT 6 receptor;Agonist of 5-HT 7 receptor

CAS: 173456-49-0 Cat. No.: D609926 PubChem CID: 9847259

GRADE & PURITY Moligand™

Synonyms

7-(4-(4-(2,3-Dichloro-4-hydroxy-phenyl)piperazin-1-yl)butoxy)-3,4-dihydro-1H-quinolin-2-one | UNII-YS6K7Q8UP4 | YS6K7Q8UP4 | 2(1H)-Quinolinone, 7-(4-(4-(2,3-dichloro-4-hydroxyphenyl)-1-piperazinyl)butoxy)-3,4-dihydro- | GTPL267 | 7-(4-(4-(2,3-Dichloro-4-h

Storage

Room temperature

Specifications

Sinónimos

7-(4-(4-(2,3-Dichloro-4-hydroxy-phenyl)piperazin-1-yl)butoxy)-3,4-dihydro-1H-quinolin-2-one | UNII-YS6K7Q8UP4 | YS6K7Q8UP4 | 2(1H)-Quinolinone, 7-(4-(4-(2,3-dichloro-4-hydroxyphenyl)-1-piperazinyl)butoxy)-3,4-dihydro- | GTPL267 | 7-(4-(4-(2,3-Dichloro-4-h

Especificaciones y pureza

Moligand™

Condiciones de almacenamiento de almacenamiento

Room temperature

Grado

Moligand™

Tipo de acción

AGONIST

Mecanismo de acción

Agonist of 5-HT 6 receptor;Agonist of 5-HT 7 receptor

Nombres e identificadores

• Sonrisas canónicas: O=C1CCc2c(N1)cc(cc2)OCCCCN1CCN(CC1)c1ccc(c(c1Cl)Cl)O
• IUPAC Name: 7-[4-[4-(2,3-dichloro-4-hydroxyphenyl)piperazin-1-yl]butoxy]-3,4-dihydro-1H-quinolin-2-one
• InChIKey: YZIVLADPQQPFLO-UHFFFAOYSA-N
• INCHI: 1S/C23H27Cl2N3O3/c24-22-19(6-7-20(29)23(22)25)28-12-10-27(11-13-28)9-1-2-14-31-17-5-3-16-4-8-21(30)26-18(16)15-17/h3,5-7,15,29H,1-2,4,8-14H2,(H,26,30)
• Isómeros SMILES: C1CC(=O)NC2=C1C=CC(=C2)OCCCCN3CCN(CC3)C4=C(C(=C(C=C4)O)Cl)Cl
• PubChem CID: 9847259

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Clase Diazinanes
      • Subclass Piperazines

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Clase: Diazinanes
• Subclass: Piperazines
• Intermediate Tree Nodes: Not available
• Direct Parent: Phenylpiperazines
• Alternative Parents: N-arylpiperazines Hydroquinolones Hydroquinolines Aniline and substituted anilines Dialkylarylamines Dichlorobenzenes p-Aminophenols M-chlorophenols O-chlorophenols Phenol ethers 1-hydroxy-2-unsubstituted benzenoids Alkyl aryl ethers N-alkylpiperazines Aryl chlorides Lactams Trialkylamines Amino acids and derivatives Secondary carboxylic acid amides Azacyclic compounds Hydrocarbon derivatives Organic oxides Organochlorides Carbonyl compounds
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: N-arylpiperazine - Phenylpiperazine - Tetrahydroquinolone - Quinolone - Tetrahydroquinoline - Aminophenol - P-aminophenol - 1,2-dichlorobenzene - 3-halophenol - 2-halophenol - Aniline or substituted anilines - Dialkylarylamine - 3-chlorophenol - 2-chlorophenol - Phenol ether - Tertiary aliphatic/aromatic amine - Alkyl aryl ether - Chlorobenzene - 1-hydroxy-2-unsubstituted benzenoid - Halobenzene - N-alkylpiperazine - Phenol - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Benzenoid - Secondary carboxylic acid amide - Tertiary amine - Tertiary aliphatic amine - Carboxamide group - Amino acid or derivatives - Lactam - Ether - Carboxylic acid derivative - Azacycle - Organooxygen compound - Amine - Organochloride - Carbonyl group - Organohalogen compound - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteropolycyclic compound
• Descripción: This compound belongs to the class of organic compounds known as phenylpiperazines. These are compounds containing a phenylpiperazine skeleton, which consists of a piperazine 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

Objetivos asociados (humanos)

HTR7 Tclin 5-hydroxytryptamine receptor 7 (1 Activities)

Discover Target: HTR7

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

HTR6 Tchem 5-hydroxytryptamine receptor 6 (1 Activities)

Discover Target: HTR6

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

Mecanismos de acción