(RS)-Butyryltimolol - ≥98% , CAS No.2320274-78-8

CAS: 2320274-78-8 Cat. No.: B649262 Formula: C₁₇H₃₀N₄O₄S Peso molecolare: 386.51 PubChem CID: 23276806

GRADE & PURITY ≥98%

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Panoramica

(RS)-Butyryltimolol is the racemate of Butyryltimolol. Butyryltimolol, an effective proagent of Timolol, improves the corneal penetration of Timolol Butyryltimolol is a β-adrenergic blocker .

In Vitro

Butyryltimolol, a prodrug of Timolol, is equally effective as 240-min nasolacrimal blockade in enhancing ocular drug absorption. MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Form:Oil

IC50& Target:β adrenergic receptor

Specifications

Specifiche e purezza

≥98%

Meccanismi biochimici e fisiologici

(RS)-Butyryltimolol is the racemate of Butyryltimolol. Butyryltimolol, an effective proagent of Timolol, improves the corneal penetration of Timolol. Butyryltimolol is a β-adrenergic blocker.

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.

Tipo di azione

INHIBITOR

Purezza

≥98%

Nomi e identificatori

• Sorrisi canonici: CCCC(=O)OC(CNC(C)(C)C)COC1=NSN=C1N2CCOCC2
• IUPAC Name: [1-(tert-butylamino)-3-[(4-morpholin-4-yl-1,2,5-thiadiazol-3-yl)oxy]propan-2-yl] butanoate
• InChIKey: IGJCFKQCZRWRRM-UHFFFAOYSA-N
• INCHI: 1S/C17H30N4O4S/c1-5-6-14(22)25-13(11-18-17(2,3)4)12-24-16-15(19-26-20-16)21-7-9-23-10-8-21/h13,18H,5-12H2,1-4H3
• Isomeri SMILES: CCCC(=O)OC(CNC(C)(C)C)COC1=NSN=C1N2CCOCC2
• PubChem CID: 23276806
• Peso molecolare: 386.51

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Classe Organonitrogen compounds
      • Subclass Amines
        • Level5 Tertiary amines
          • Level6 Tertiary alkylarylamines
            • Level7 Dialkylarylamines

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Classe: Organonitrogen compounds
• Subclass: Amines
• Intermediate Tree Nodes: Tertiary amines - Tertiary alkylarylamines
• Direct Parent: Dialkylarylamines
• Alternative Parents: Alkyl aryl ethers Fatty acid esters Imidolactams Morpholines Thiadiazoles Heteroaromatic compounds Amino acids and derivatives Carboxylic acid esters Oxacyclic compounds Dialkylamines Dialkyl ethers Azacyclic compounds Monocarboxylic acids and derivatives Hydrocarbon derivatives Carbonyl compounds Organic oxides
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Dialkylarylamine - Alkyl aryl ether - Fatty acid ester - Morpholine - Oxazinane - Fatty acyl - Imidolactam - Azole - Heteroaromatic compound - Thiadiazole - Amino acid or derivatives - Carboxylic acid ester - Azacycle - Oxacycle - Monocarboxylic acid or derivatives - Ether - Secondary aliphatic amine - Dialkyl ether - Carboxylic acid derivative - Secondary amine - Organoheterocyclic compound - Organooxygen compound - Hydrocarbon derivative - Organic oxygen compound - Carbonyl group - Organic oxide - Aromatic heteromonocyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as dialkylarylamines. These are aliphatic aromatic amines in which the amino group is linked to two aliphatic chains and one aromatic group.
• 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

Proprietà chimiche e fisiche

• Solubilità: DMSO : 100 mg/mL (258.73 mM; Need ultrasonic)