Kipukasin D - Moligand™, ≥95% , CAS No.948574-00-3

CAS: 948574-00-3 Cat. No.: K463246 Formule: C₁₉H₂₂N₂O₉ Poids moléculaire: 422.39

GRADE & PURITY Moligand™, ≥95%

Storage

Protected from light,Store at -20°C

Shipped In

Ice chest + Ice pads

Vue d’ensemble

Kipukasin D is a natural nucleoside derived from Aspergillus versicolor, exhibiting potent antibacterial activity. It operates primarily as a bacterial inhibitor, making it valuable for research involving bacterial infections and microbial resistance mechanisms. This compound is useful for studies in pharmacology, microbiology, and drug development focused on identifying new antimicrobial agents.

Specifications

Spécifications et pureté

Moligand™, ≥95%

Conditions de stockage de stockage

Protected from light,Store at -20°C

Expédié en

Ice chest + Ice pads

Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.

Grade

Moligand™

Type d'action

INHIBITOR

Pureté

≥95%

Noms et identifiants

• Sourires canoniques: O=C(C1=C(C=C(C=C1C)OC)OC)O[C@@H]2[C@H](O[C@H]([C@@H]2O)N(C(N3)=O)C=CC3=O)CO
• InChIKey: LQYPUZKOEZWGBX-BASLNEPJSA-N
• INCHI: 1S/C19H22N2O9/c1-9-6-10(27-2)7-11(28-3)14(9)18(25)30-16-12(8-22)29-17(15(16)24)21-5-4-13(23)20-19(21)26/h4-7,12,15-17,22,24H,8H2,1-3H3,(H,20,23,26)/t12-,15-,16-,17-/m1/s1
• Poids moléculaire: 422.39
• Reaxy-Rn: 11289468
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=11289468&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Nucleosides, nucleotides, and analogues
    • Classe Pyrimidine nucleosides

• Kingdom: Organic compounds
• Superclass: Nucleosides, nucleotides, and analogues
• Classe: Pyrimidine nucleosides
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Pyrimidine nucleosides
• Alternative Parents: Glycosylamines O-methoxybenzoic acids and derivatives P-methoxybenzoic acids and derivatives Benzoic acid esters Dimethoxybenzenes Pentoses Anisoles Benzoyl derivatives Phenoxy compounds Pyrimidones Alkyl aryl ethers Toluenes Hydropyrimidines Oxolanes Vinylogous amides Heteroaromatic compounds Ureas Carboxylic acid esters Lactams Secondary alcohols Azacyclic compounds Oxacyclic compounds Hydrocarbon derivatives Organonitrogen compounds Primary alcohols Organic oxides
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Pyrimidine nucleoside - Glycosyl compound - N-glycosyl compound - O-methoxybenzoic acid or derivatives - P-methoxybenzoic acid or derivatives - Benzoate ester - Pentose monosaccharide - Dimethoxybenzene - M-dimethoxybenzene - Benzoic acid or derivatives - Anisole - Methoxybenzene - Phenoxy compound - Benzoyl - Phenol ether - Toluene - Pyrimidone - Alkyl aryl ether - Monosaccharide - Hydropyrimidine - Benzenoid - Pyrimidine - Monocyclic benzene moiety - Heteroaromatic compound - Vinylogous amide - Oxolane - Urea - Carboxylic acid ester - Lactam - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Ether - Organic oxide - Alcohol - Primary alcohol - Organooxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Organonitrogen compound - Organic oxygen compound - Aromatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as pyrimidine nucleosides. These are compounds comprising a pyrimidine base attached to a ribosyl or deoxyribosyl 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

Propriétés chimiques et physiques

• Solubilité: DMSO: 1mg/mL
• Sensibilité: Light sensitive
• Point d'éclair (°F): Not applicable
• Point d'éclair (°C): Not applicable