Bevenopran - ≥98% , Mu opioid receptor antagonist, CAS No.676500-67-7, Mu opioid receptor antagonist

CAS: 676500-67-7 Cat. No.: B646620 Summenformel: C₂₀H₂₆N₄O₄ Molekulargewicht: 386.44 PubChem CID: 10452732

GRADE & PURITY ≥98%

Synonyms

DS-10418 | UNII-IC58Q2EHPJ | 5-(2-Methoxy-4-(((2-(tetrahydro-2H-pyran-4-yl)ethyl)amino)methyl)phenoxy)pyrazine-2-carboxamide | 5-[2-Methoxy-4-[[[2-(tetrahydro-2H-pyran-4-yl)ethyl]amino]methyl]phenoxy]-2-pyrazinecarboxamide | BEVENOPRAN [WHO-DD] | Paeonifl

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Übersicht

Bevenopran is a peripheral μ-opioid receptor antagonist

In Vivo

Bevenopran is a peripheral μ-opioid receptor antagonist. Bevenopran is currently under investigation for the treatment of opioid-induced bowel dysfunction (OBD) . Bevenopran tends to increase bowel movement (BM) frequency, especially for 0.1 mg twice daily and 4 mg daily, respectively . MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Form:Solid

IC50& Target:μ-opioid receptor

Specifications

Synonyme

DS-10418 | UNII-IC58Q2EHPJ | 5-(2-Methoxy-4-(((2-(tetrahydro-2H-pyran-4-yl)ethyl)amino)methyl)phenoxy)pyrazine-2-carboxamide | 5-[2-Methoxy-4-[[[2-(tetrahydro-2H-pyran-4-yl)ethyl]amino]methyl]phenoxy]-2-pyrazinecarboxamide | BEVENOPRAN [WHO-DD] | Paeonifl

Spezifikationen & Reinheit

≥98%

Biochemische und physiologische Mechanismen

Bevenopran is a peripheral μ-opioid receptor antagonist.

Storage

Store at -20°C

Verschickt in

Ice chest + Ice pads

Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.

Aktionsart

ANTAGONIST

Mechanismus der Wirkung

Mu opioid receptor antagonist

Reinheit

≥98%

Produkteigenschaften

• ALogP: 1.1

Namen und Kennungen

• Pubchem Sid: 528763570
• Kanonisches Lächeln: COC1=C(C=CC(=C1)CNCCC2CCOCC2)OC3=NC=C(N=C3)C(=O)N
• IUPAC Name: 5-[2-methoxy-4-[[2-(oxan-4-yl)ethylamino]methyl]phenoxy]pyrazine-2-carboxamide
• InChIKey: ZGCYVRNZWGUXNQ-UHFFFAOYSA-N
• INCHI: 1S/C20H26N4O4/c1-26-18-10-15(11-22-7-4-14-5-8-27-9-6-14)2-3-17(18)28-19-13-23-16(12-24-19)20(21)25/h2-3,10,12-14,22H,4-9,11H2,1H3,(H2,21,25)
• Isomere SMILES: COC1=C(C=CC(=C1)CNCCC2CCOCC2)OC3=NC=C(N=C3)C(=O)N
• Alternative CAS-Nummer: 676500-67-7
• PubChem CID: 10452732
• Molekulargewicht: 386.44

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Klasse Organooxygen compounds
      • Subclass Ethers

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Klasse: Organooxygen compounds
• Subclass: Ethers
• Intermediate Tree Nodes: Not available
• Direct Parent: Diarylethers
• Alternative Parents: Pyrazinecarboxamides 2-heteroaryl carboxamides Phenylmethylamines Phenoxy compounds Anisoles Methoxybenzenes Benzylamines Alkyl aryl ethers Aralkylamines Oxanes Heteroaromatic compounds Primary carboxylic acid amides Amino acids and derivatives Dialkyl ethers Azacyclic compounds Oxacyclic compounds Dialkylamines Hydrocarbon derivatives Organic oxides
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Diaryl ether - Pyrazine carboxylic acid or derivatives - Pyrazinecarboxamide - Phenylmethylamine - 2-heteroaryl carboxamide - Phenol ether - Methoxybenzene - Phenoxy compound - Benzylamine - Anisole - Aralkylamine - Alkyl aryl ether - Pyrazine - Benzenoid - Monocyclic benzene moiety - Oxane - Heteroaromatic compound - Amino acid or derivatives - Carboxamide group - Primary carboxylic acid amide - Azacycle - Secondary aliphatic amine - Dialkyl ether - Carboxylic acid derivative - Oxacycle - Organoheterocyclic compound - Secondary amine - Organonitrogen compound - Amine - Hydrocarbon derivative - Organic oxide - Organic nitrogen compound - Aromatic heteromonocyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as diarylethers. These are organic compounds containing the dialkyl ether functional group, with the formula ROR', where R and R' are aryl groups.
• 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

Chemische und physikalische Eigenschaften

• Löslichkeit: DMSO : 125 mg/mL (323.47 mM; Need ultrasonic)
• Molekulargewicht: 386.400 g/mol
• XLogP3: 1.100
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 7
• Rotatable Bond Count: 9
• Exact Mass: 386.195 Da
• Monoisotopic Mass: 386.195 Da
• Topological Polar Surface Area: 109.000 Ų
• Heavy Atom Count: 28
• Formal Charge: 0
• Complexity: 475.000
• 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