CGP 71683 - Moligand™, ≥98% , Antagonist of Y 5 receptor, CAS No.192321-23-6, Antagonist of Y 5 receptor

CAS: 192321-23-6 Cat. No.: C608510 Formula: C₂₆H₂₉N₅O₂S Peso molecolare: 475.61

GRADE & PURITY Moligand™, ≥98%

Synonyms

CGP 71683 | BDBM50166561 | L000175 | BRD-K31912990-003-01-0 | CGP71683 | cgp-71683a free base | CGP 71683A | E4901JA9JD | BDBM50089038 | UNII-E4901JA9JD | NCGC00165960-01 | BCP25968 | CHEBI:92555 | N-[[4-[[(4-aminoquinazolin-2-yl)amino]methyl]cyclohexyl]m

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Panoramica

CGP 71683 is a potent and highly selective non-peptide antagonist of the NPY Y(5) receptor in the study of obesity.

Specifications

Sinonimi

CGP 71683 | BDBM50166561 | L000175 | BRD-K31912990-003-01-0 | CGP71683 | cgp-71683a free base | CGP 71683A | E4901JA9JD | BDBM50089038 | UNII-E4901JA9JD | NCGC00165960-01 | BCP25968 | CHEBI:92555 | N-[[4-[[(4-aminoquinazolin-2-yl)amino]methyl]cyclohexyl]m

Specifiche e purezza

Moligand™, ≥98%

Condizioni di conservazione di stoccaggio

Store at -20°C

Spedito in

Ice chest + Ice pads

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Grado

Moligand™

Tipo di azione

ANTAGONIST

Meccanismo d'azione

Antagonist of Y 5 receptor

Purezza

≥98%

Nomi e identificatori

• Sorrisi canonici: Nc1nc(NCC2CCC(CC2)CNS(=O)(=O)c2cccc3c2cccc3)nc2c1cccc2
• IUPAC Name: N-[[4-[[(4-aminoquinazolin-2-yl)amino]methyl]cyclohexyl]methyl]naphthalene-1-sulfonamide
• InChIKey: UULIGRNKXHCLQN-UHFFFAOYSA-N
• INCHI: 1S/C26H29N5O2S/c27-25-22-9-3-4-10-23(22)30-26(31-25)28-16-18-12-14-19(15-13-18)17-29-34(32,33)24-11-5-7-20-6-1-2-8-21(20)24/h1-11,18-19,29H,12-17H2,(H3,27,28,30,31)
• Isomeri SMILES: C1CC(CCC1CNC2=NC3=CC=CC=C3C(=N2)N)CNS(=O)(=O)C4=CC=CC5=CC=CC=C54
• CAS alternativo: 192322-50-2
• Peso molecolare: 475.61

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Classe Naphthalenes
      • Subclass Naphthalene sulfonic acids and derivatives

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: Naphthalenes
• Subclass: Naphthalene sulfonic acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: 1-naphthalene sulfonic acids and derivatives
• Alternative Parents: 1-naphthalene sulfonamides Quinazolinamines Secondary alkylarylamines Aminopyrimidines and derivatives Organosulfonamides Imidolactams Heteroaromatic compounds Aminosulfonyl compounds Azacyclic compounds Primary amines Organopnictogen compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: 1-naphthalene sulfonamide - Naphthalene sulfonamide - 1-naphthalene sulfonic acid or derivatives - Quinazolinamine - Diazanaphthalene - Quinazoline - Aminopyrimidine - Secondary aliphatic/aromatic amine - Pyrimidine - Organosulfonic acid amide - Imidolactam - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Heteroaromatic compound - Sulfonyl - Aminosulfonyl compound - Secondary amine - Azacycle - Organoheterocyclic compound - Organic nitrogen compound - Amine - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Primary amine - Organonitrogen compound - Organosulfur compound - Aromatic heteropolycyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as 1-naphthalene sulfonic acids and derivatives. These are organic aromatic compounds that contain a naphthalene moiety that carries a sulfonic acid group (or a derivative thereof) at the 1-position. Naphthalene is a bicyclic compound that is made up of two fused benzene ring.
• 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

Obiettivi associati (umani)

NPY5R Tchem Neuropeptide Y receptor type 5 (1 Activities)

Discover Target: NPY5R

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

Proprietà chimiche e fisiche

• Peso molecolare: 475.600 g/mol
• XLogP3: 5.100
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 7
• Rotatable Bond Count: 7
• Exact Mass: 475.204 Da
• Monoisotopic Mass: 475.204 Da
• Topological Polar Surface Area: 118.000 Ų
• Heavy Atom Count: 34
• Formal Charge: 0
• Complexity: 751.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1