[¹¹C]volinanserin - Moligand™ , Antagonist of 5-HT 2A receptor, CAS No.174792-03-1, Antagonist of 5-HT 2A receptor

CAS: 174792-03-1 Cat. No.: C613775 PubChem CID: 449851

GRAU & PUREZA Moligand™

Synonyms

GTPL3249 | MOLI001672 | MOLI000241 | Volinanserin C-11 | [11C]M100907 (PET ligand) | 8LEA6Q26BW | UNII-8LEA6Q26BW | (11C)-MDL100907 | (11C)-MDL-100907 | 11C-MDL100907 | [11C]volinanserin | [11C]MDL100907 | (R)-[2,3-di(methoxy)phenyl]-[1-[2-(4-fluorophenyl

Storage

Room temperature

Especificações

Sinónimos

GTPL3249 | MOLI001672 | MOLI000241 | Volinanserin C-11 | [11C]M100907 (PET ligand) | 8LEA6Q26BW | UNII-8LEA6Q26BW | (11C)-MDL100907 | (11C)-MDL-100907 | 11C-MDL100907 | [11C]volinanserin | [11C]MDL100907 | (R)-[2,3-di(methoxy)phenyl]-[1-[2-(4-fluorophenyl

Especificações e pureza

Moligand™

Condições de armazenamento de armazenamento

Room temperature

Grau

Moligand™

Tipo de ação

ANTAGONIST

Mecanismo de ação

Antagonist of 5-HT 2A receptor

Nomes e identificadores

Sorrisos canónicos

[11CH3]Oc1cccc(c1OC)[C@@H](C1CCN(CC1)CCc1ccc(cc1)F)O

IUPAC Name

(R)-[2,3-di(methoxy)phenyl]-[1-[2-(4-fluorophenyl)ethyl]piperidin-4-yl]methanol

InChIKey

HXTGXYRHXAGCFP-AVUPQLEMSA-N

INCHI

1S/C22H28FNO3/c1-26-20-5-3-4-19(22(20)27-2)21(25)17-11-14-24(15-12-17)13-10-16-6-8-18(23)9-7-16/h3-9,17,21,25H,10-15H2,1-2H3/t21-/m1/s1/i1-1

SMILES isoméricas

COC1=C(C=CC=C1O[11CH3])[C@@H](C2CCN(CC2)CCC3=CC=C(C=C3)F)O

PubChem CID

449851

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Classe Benzene and substituted derivatives
      • Subclass Methoxybenzenes

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: Benzene and substituted derivatives
• Subclass: Methoxybenzenes
• Intermediate Tree Nodes: Not available
• Direct Parent: Dimethoxybenzenes
• Alternative Parents: Phenethylamines Phenoxy compounds Anisoles Fluorobenzenes Aralkylamines Alkyl aryl ethers Piperidines Aryl fluorides Trialkylamines Secondary alcohols Azacyclic compounds Organopnictogen compounds Organofluorides Hydrocarbon derivatives Aromatic alcohols
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Dimethoxybenzene - O-dimethoxybenzene - Phenethylamine - Anisole - Phenoxy compound - Phenol ether - Alkyl aryl ether - Fluorobenzene - Halobenzene - Aralkylamine - Piperidine - Aryl fluoride - Aryl halide - Tertiary aliphatic amine - Tertiary amine - Secondary alcohol - Azacycle - Organoheterocyclic compound - Ether - Aromatic alcohol - Organofluoride - Organohalogen compound - Amine - Alcohol - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Organopnictogen compound - Organic nitrogen compound - Hydrocarbon derivative - Aromatic heteromonocyclic compound
• Descrição: This compound belongs to the class of organic compounds known as dimethoxybenzenes. These are organic aromatic compounds containing a monocyclic benzene moiety carrying exactly two methoxy groups.
• 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

Alvos associados (humanos)

HTR2A Tclin 5-hydroxytryptamine receptor 2A (0 Activities)

Discover Target: HTR2A

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

Mecanismos de ação