ML 339 - ≥98%, mezcla de isómeros , CAS No.2080300-49-6

CAS: 2080300-49-6 Cat. No.: M288061 Fórmula: C₂₆H₃₂ClN₃O₅ Peso molecular: 502.00

GRADE & PURITY ≥98%, mixture of isomers

Synonyms

N-[(1R,3S,5S)-9-(2-((2-clorofenil)amino)-2-exoetil)-9-azabiciclo[3.3.1]nonan-3-il)-3,4,5-trimetoxibenzamida

Storage

Conservar a -20°C

Shipped In

Hielera + almohadillas de hielo

Descripción general

El ML339 es un antagonista selectivo del CXCR6 con una IC50 de 140 nM. El ML339 tiene una IC50 >79 μM para los receptores CXCR5, CXCR4, CCR6 y Apelina (APJ). El ML339 tiene potencial para avanzar en el campo de la investigación del cáncer de próstata

Specifications

Sinónimos

N-[(1R,3S,5S)-9-(2-((2-clorofenil)amino)-2-exoetil)-9-azabiciclo[3.3.1]nonan-3-il)-3,4,5-trimetoxibenzamida

Especificaciones y pureza

≥98%, mezcla de isómeros

Mecanismos bioquímicos y fisiológicos

Antagonista potente y selectivo del hCXCR6 (IC50= 140 nM); 100 veces menos activo en el receptor murino CXCR6 (IC50= 18μM). Muestra selectividad sobre los receptores CXCR5, CXCR4, CCR6 y APJ (IC50>79μM).

Condiciones de almacenamiento de almacenamiento

Conservar a -20°C

Enviado en

Hielera + almohadillas de hielo

Pureza

≥98%

Nombres e identificadores

Pubchem Sid

528765499

Sonrisas canónicas

COC1=CC(=CC(=C1OC)OC)C(=O)NC2CC3CCCC(C2)N3CC(=O)NC4=CC=CC=C4Cl

IUPAC Name

N-[(1S,5R)-9-[2-(2-chloroanilino)-2-oxoethyl]-9-azabicyclo[3.3.1]nonan-3-yl]-3,4,5-trimethoxybenzamide

InChIKey

SSPYAPRDKNCABY-YQQQUEKLSA-N

INCHI

1S/C26H32ClN3O5/c1-33-22-11-16(12-23(34-2)25(22)35-3)26(32)28-17-13-18-7-6-8-19(14-17)30(18)15-24(31)29-21-10-5-4-9-20(21)27/h4-5,9-12,17-19H,6-8,13-15H2,1-3H3,(H,28,32)(H,29,31)/t17?,18-,19+

Isómeros SMILES

COC1=CC(=CC(=C1OC)OC)C(=O)NC2C[C@H]3CCC[C@@H](C2)N3CC(=O)NC4=CC=CC=C4Cl

CAS alternativo

2579689-83-9

Peso molecular

502.00

Reaxy-Rn

61424938

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=61424938&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Clase Carboxylic acids and derivatives
      • Subclass Amino acids, peptides, and analogues
        • Level5 Amino acids and derivatives
          • Level6 Alpha amino acids and derivatives
            • Level7 Alpha amino acid amides

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Clase: Carboxylic acids and derivatives
• Subclass: Amino acids, peptides, and analogues
• Intermediate Tree Nodes: Amino acids and derivatives - Alpha amino acids and derivatives
• Direct Parent: Alpha amino acid amides
• Alternative Parents: Anilides Benzamides Phenoxy compounds N-arylamides Methoxybenzenes Anisoles Benzoyl derivatives Alkyl aryl ethers Chlorobenzenes Piperidines Aryl chlorides Trialkylamines Secondary carboxylic acid amides Azacyclic compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides Organochlorides
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Alpha-amino acid amide - Anilide - Benzamide - Benzoic acid or derivatives - Phenoxy compound - Anisole - Methoxybenzene - Benzoyl - N-arylamide - Phenol ether - Alkyl aryl ether - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Benzenoid - Monocyclic benzene moiety - Piperidine - Carboxamide group - Tertiary amine - Tertiary aliphatic amine - Secondary carboxylic acid amide - Azacycle - Organoheterocyclic compound - Ether - Organochloride - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Carbonyl group - Organohalogen compound - Amine - Aromatic heteropolycyclic compound
• Descripción: This compound belongs to the class of organic compounds known as alpha amino acid amides. These are amide derivatives of alpha amino acids.
• 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)

CXCR4 Tclin C-X-C chemokine receptor type 4 (3338 Activities)

Discover Target: CXCR4

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CCR6 Tchem C-C chemokine receptor type 6 (388 Activities)

Discover Target: CCR6

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CXCR6 Tchem C-X-C chemokine receptor type 6 (264 Activities)

Discover Target: CXCR6

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Solvent:DMSO, Max Conc. mg/mL: 50.2, Max Conc. mM: 100; Solvent:ethanol, Max Conc. mg/mL: 10.04, Max Conc. mM: 20
• Peso molecular: 502.000 g/mol
• XLogP3: 4.200
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 8
• Exact Mass: 501.203 Da
• Monoisotopic Mass: 501.203 Da
• Topological Polar Surface Area: 89.100 Ų
• Heavy Atom Count: 35
• Formal Charge: 0
• Complexity: 699.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 2
• 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