Oxtriphylline - 10mM in DMSO , Adenosine receptor antagonist, CAS No.4499-40-5, Adenosine receptor antagonist

CAS: 4499-40-5 Cat. No.: O424046 分子式: C₁₂H₂₁N₅O₃ 分子量: 283.33 EC番号: 224-798-7

GRADE & PURITY 10mM in DMSO

Synonyms

(2-Hydroxyethyl)trimethylammonium compound with theophylline | Choline thieophyllinate | OXTRIPHYLLINE [VANDF] | Sabidal | ETHANAMINIUM, 2-HYDROXY-N,N,N-TRIMETHYL-, SALT WITH 3,9-DIHYDRO-1,3-DIMETHYL-1H-PURINE-2,6-DIONE (1:1) | CHOLINE THEOPHYLLINATE [MAR

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

概要

N/A

Specifications

同義語

(2-Hydroxyethyl)trimethylammonium compound with theophylline | Choline thieophyllinate | OXTRIPHYLLINE [VANDF] | Sabidal | ETHANAMINIUM, 2-HYDROXY-N,N,N-TRIMETHYL-, SALT WITH 3,9-DIHYDRO-1,3-DIMETHYL-1H-PURINE-2,6-DIONE (1:1) | CHOLINE THEOPHYLLINATE [MAR

仕様と純度

10mM in DMSO

保管条件

Store at -80°C

入荷

Dry ice packs + Cold packs

この製品は冷冷この冷このこの製品の運送が必要です。地上およびその他の経済サービスは利用できません。

アクションタイプ

INHIBITOR

作用メカニズム

Adenosine receptor antagonist

名前と識別子

• パブケム・シド: 528766516
• カノニカル・スマイル: CN1C(=C2C(=NC=N2)N(C1=O)C)[O-].C[N+](C)(C)CCO
• IUPAC Name: 1,3-dimethyl-2-oxopurin-6-olate;2-hydroxyethyl(trimethyl)azanium
• InChIKey: SOELXOBIIIBLRJ-UHFFFAOYSA-M
• INCHI: 1S/C7H8N4O2.C5H14NO/c1-10-5-4(8-3-9-5)6(12)11(2)7(10)13;1-6(2,3)4-5-7/h3,12H,1-2H3;7H,4-5H2,1-3H3/q;+1/p-1
• 異性体SMILES: CN1C(=C2C(=NC=N2)N(C1=O)C)[O-].C[N+](C)(C)CCO
• 分子量: 283.33
• Reaxy-Rn: 4928440
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4928440&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • 分類 Imidazopyrimidines
      • Subclass Purines and purine derivatives

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• 分類: Imidazopyrimidines
• Subclass: Purines and purine derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Xanthines
• Alternative Parents: Purinones Alkaloids and derivatives Cholines Pyrimidones Tetraalkylammonium salts Heteroaromatic compounds Imidazoles Ureas 1,2-aminoalcohols Azacyclic compounds Organic salts Organic oxides Hydrocarbon derivatives Organic zwitterions Organopnictogen compounds Primary alcohols
• Molecular Framework: Not available
• Substituents: Xanthine - Purinone - Alkaloid or derivatives - Choline - Pyrimidone - Pyrimidine - Azole - Imidazole - Quaternary ammonium salt - Tetraalkylammonium salt - Heteroaromatic compound - Urea - 1,2-aminoalcohol - Azacycle - Alkanolamine - Amine - Organopnictogen compound - Organic oxygen compound - Primary alcohol - Organooxygen compound - Organonitrogen compound - Alcohol - Organic nitrogen compound - Organic oxide - Organic zwitterion - Organic salt - Hydrocarbon derivative - Aromatic heteropolycyclic compound
• 説明: This compound belongs to the class of organic compounds known as xanthines. These are purine derivatives with a ketone group conjugated at carbons 2 and 6 of the purine moiety.
• 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

作用メカニズム

化学的性質と物理的性質

• 分子量: 283.330 g/mol
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 2
• Exact Mass: 283.164 Da
• Monoisotopic Mass: 283.164 Da
• Topological Polar Surface Area: 91.600 Ų
• Heavy Atom Count: 20
• Formal Charge: 0
• Complexity: 415.000
• 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: 2

XLogP3