silahexocyclium - Moligand™ , Antagonist of M 1 receptor;Antagonist of M 2 receptor;Antagonist of M 3 receptor;Antagonist of M 4 receptor;Antagonist of M 5 receptor, CAS No.142173-06-6, Antagonist of M 1 receptor;Antagonist of M 2 receptor;Antagonist of M 3 receptor;Antagonist of M 4 receptor;Antagonist of M 5 receptor

CAS: 142173-06-6 Cat. No.: S613583 PubChem CID: 130169

GRADE & PURITY Moligand™

Synonyms

Q27088801 | GTPL331 | L001247 | 4-{[cyclohexyl(hydroxy)phenylsilyl]methyl}-1,1-dimethylpiperazin-1-ium | cyclohexyl-[(4,4-dimethylpiperazin-4-ium-1-yl)methyl]-hydroxy-phenylsilane | Piperazinium, 4-((cyclohexylhydroxyphenylsilyl)methyl)-1,1-dimethyl- | DT

Storage

Room temperature

Specifications

Synonymes

Q27088801 | GTPL331 | L001247 | 4-{[cyclohexyl(hydroxy)phenylsilyl]methyl}-1,1-dimethylpiperazin-1-ium | cyclohexyl-[(4,4-dimethylpiperazin-4-ium-1-yl)methyl]-hydroxy-phenylsilane | Piperazinium, 4-((cyclohexylhydroxyphenylsilyl)methyl)-1,1-dimethyl- | DT

Spécifications et pureté

Moligand™

Conditions de stockage de stockage

Room temperature

Grade

Moligand™

Type d'action

ANTAGONIST

Mécanisme d'action

Antagonist of M 1 receptor;Antagonist of M 2 receptor;Antagonist of M 3 receptor;Antagonist of M 4 receptor;Antagonist of M 5 receptor

Noms et identifiants

• Sourires canoniques: C[N+]1(C)CCN(CC1)C[Si](c1ccccc1)(C1CCCCC1)O
• IUPAC Name: cyclohexyl-[(4,4-dimethylpiperazin-4-ium-1-yl)methyl]-hydroxy-phenylsilane
• InChIKey: GBISIIAKUATURW-UHFFFAOYSA-N
• INCHI: 1S/C19H33N2OSi/c1-21(2)15-13-20(14-16-21)17-23(22,18-9-5-3-6-10-18)19-11-7-4-8-12-19/h3,5-6,9-10,19,22H,4,7-8,11-17H2,1-2H3/q+1
• Isomères SMILES: C[N+]1(CCN(CC1)C[Si](C2CCCCC2)(C3=CC=CC=C3)O)C
• PubChem CID: 130169

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Classe Diazinanes
      • Subclass Piperazines
        • Level5 N-alkylpiperazines
          • Level6 N-methylpiperazines

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Classe: Diazinanes
• Subclass: Piperazines
• Intermediate Tree Nodes: N-alkylpiperazines
• Direct Parent: N-methylpiperazines
• Alternative Parents: Alkylarylsilanes Benzene and substituted derivatives Tetraalkylammonium salts Trialkylamines Silanols Organoheterosilanes Organic metalloid salts Azacyclic compounds Organopnictogen compounds Organic oxygen compounds Hydrocarbon derivatives Organic cations
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: N-methylpiperazine - Alkylarylsilane - Benzenoid - Monocyclic benzene moiety - Tetraalkylammonium salt - Quaternary ammonium salt - Tertiary aliphatic amine - Tertiary amine - Organoheterosilane - Azacycle - Organic metalloid salt - Silanol - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Organic salt - Organosilicon compound - Organonitrogen compound - Amine - Organic cation - Aromatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as n-methylpiperazines. These are organic compounds containing a piperazine ring where the nitrogen ring atom carries a methyl 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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CHRM5 Tclin Muscarinic acetylcholine receptor M5 (1 Activities)

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CHRM3 Tclin Muscarinic acetylcholine receptor M3 (1 Activities)

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CHRM4 Tclin Muscarinic acetylcholine receptor M4 (1 Activities)

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CHRM2 Tclin Muscarinic acetylcholine receptor M2 (1 Activities)

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CHRM1 Tclin Muscarinic acetylcholine receptor M1 (1 Activities)

Discover Target: CHRM1

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