(1R,7S,9aS)-7-decyl-octahydro-1H-quinolizin-1-ol - Moligand™ , Inhibitor of lanosterol synthase, CAS No.R609246, Inhibitor of lanosterol synthase

CAS: R609246 Cat. No.: R609246 PubChem CID: 44275335

GRADE & PURITY Moligand™

Synonyms

compound 4a

Storage

Room temperature

Specifications

Sinónimos

compound 4a

Especificaciones y pureza

Moligand™

Condiciones de almacenamiento de almacenamiento

Room temperature

Grado

Moligand™

Tipo de acción

INHIBITOR

Mecanismo de acción

Inhibitor of lanosterol synthase

Nombres e identificadores

• Sonrisas canónicas: CCCCCCCCCC[C@H]1CC[C@@H]2N(C1)CCC[C@H]2O
• IUPAC Name: (1R,7S,9aS)-7-decyl-octahydro-1H-quinolizin-1-ol
• InChIKey: ASQOQJYHIYYTEJ-GBESFXJTSA-N
• INCHI: 1S/C19H37NO/c1-2-3-4-5-6-7-8-9-11-17-13-14-18-19(21)12-10-15-20(18)16-17/h17-19,21H,2-16H2,1H3/t17-,18-,19+/m0/s1
• Isómeros SMILES: CCCCCCCCCC[C@H]1CC[C@H]2[C@@H](CCCN2C1)O
• PubChem CID: 44275335

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Clase Quinolizines

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Clase: Quinolizines
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Quinolizines
• Alternative Parents: Quinolizidines Piperidines Trialkylamines Secondary alcohols 1,2-aminoalcohols Azacyclic compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic heteropolycyclic compounds
• Substituents: Quinolizidine - Quinolizine - Piperidine - 1,2-aminoalcohol - Tertiary aliphatic amine - Tertiary amine - Secondary alcohol - Azacycle - Hydrocarbon derivative - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Amine - Alcohol - Organic nitrogen compound - Aliphatic heteropolycyclic compound
• Descripción: This compound belongs to the class of organic compounds known as quinolizines. These are compounds containing a quinolizine moiety, which consists of two fused pyridine rings sharing a nitrogen atom.
• 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)

LSS Tchem Lanosterol synthase (3 Activities)

Discover Target: LSS

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

Mecanismos de acción