DRL-17822 - Moligand™, ≥98% , Inhibitor of Liver X receptor-α, CAS No.898911-09-6, Inhibitor of Liver X receptor-α

CAS: 898911-09-6 Cat. No.: D609972 Formule: C₃₀H₃₁F₆N₇ Poids moléculaire: 603.60 PubChem CID: 58689743

GRADE & PURITY Moligand™, ≥98%

Synonyms

3-[[[3,5-bis(trifluoromethyl)phenyl]methyl-(2-methyltetrazol-5-yl)amino]methyl]-N,N-bis(cyclopropylmethyl)-8-methylquinolin-2-amine | 2-(Bis(cyclopropylmethyl)amino)-N-((3,5-bis(trifluoromethyl)phenyl)methyl)-8-methyl-N-(2-methyl-2H-tetrazol-5-yl)-3-quino

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Vue d’ensemble

DRL-17822 is a Cholesteryl Ester Transfer Protein (CETP) inhibitor.

Specifications

Synonymes

3-[[[3,5-bis(trifluoromethyl)phenyl]methyl-(2-methyltetrazol-5-yl)amino]methyl]-N,N-bis(cyclopropylmethyl)-8-methylquinolin-2-amine | 2-(Bis(cyclopropylmethyl)amino)-N-((3,5-bis(trifluoromethyl)phenyl)methyl)-8-methyl-N-(2-methyl-2H-tetrazol-5-yl)-3-quino

Spécifications et pureté

Moligand™, ≥98%

Conditions de stockage de stockage

Store at -20°C

Expédié en

Ice chest + Ice pads

Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.

Grade

Moligand™

Type d'action

INHIBITOR

Mécanisme d'action

Inhibitor of Liver X receptor-α

Pureté

≥98%

Noms et identifiants

• Sourires canoniques: Cn1nnc(n1)N(Cc1cc2cccc(c2nc1N(CC1CC1)CC1CC1)C)Cc1cc(cc(c1)C(F)(F)F)C(F)(F)F
• IUPAC Name: 3-[[[3,5-bis(trifluoromethyl)phenyl]methyl-(2-methyltetrazol-5-yl)amino]methyl]-N,N-bis(cyclopropylmethyl)-8-methylquinolin-2-amine
• InChIKey: OCNBSSLDAIWTKS-UHFFFAOYSA-N
• INCHI: 1S/C30H31F6N7/c1-18-4-3-5-22-12-23(27(37-26(18)22)42(14-19-6-7-19)15-20-8-9-20)17-43(28-38-40-41(2)39-28)16-21-10-24(29(31,32)33)13-25(11-21)30(34,35)36/h3-5,10-13,19-20H,6-9,14-17H2,1-2H3
• Isomères SMILES: CC1=C2C(=CC=C1)C=C(C(=N2)N(CC3CC3)CC4CC4)CN(CC5=CC(=CC(=C5)C(F)(F)F)C(F)(F)F)C6=NN(N=N6)C
• PubChem CID: 58689743
• Poids moléculaire: 603.60

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Classe Quinolines and derivatives
      • Subclass Aminoquinolines and derivatives

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Classe: Quinolines and derivatives
• Subclass: Aminoquinolines and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Aminoquinolines and derivatives
• Alternative Parents: Trifluoromethylbenzenes Dialkylarylamines Benzylamines Aminopyridines and derivatives Imidolactams Tetrazoles Heteroaromatic compounds Azacyclic compounds Organofluorides Hydrocarbon derivatives Alkyl fluorides
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Aminoquinoline - Trifluoromethylbenzene - Dialkylarylamine - Benzylamine - Aminopyridine - Imidolactam - Benzenoid - Pyridine - Monocyclic benzene moiety - Heteroaromatic compound - Tetrazole - Azole - Tertiary amine - Azacycle - Alkyl fluoride - Organohalogen compound - Organofluoride - Organonitrogen compound - Hydrocarbon derivative - Organic nitrogen compound - Amine - Alkyl halide - Aromatic heteropolycyclic compound
• Description: This compound belongs to the class of organic compounds known as aminoquinolines and derivatives. These are organic compounds containing an amino group attached to a quinoline ring system.
• 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

Cibles associées (humaines)

NR1H3 Tchem Oxysterols receptor LXR-alpha (0 Activities)

Discover Target: NR1H3

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