Picrinine - ≥99% , CAS No.4684-32-6

CAS: 4684-32-6 Cat. No.: P650084 Peso molecular: 338.40 PubChem CID: 6738085

GRADE & PURITY ≥99%

Synonyms

Picrinine | FT-0698441 | B2703-092765 | Methyl 14-ethylidene-18-oxa-2,12-diazahexacyclo[9.6.1.19,15.01,9.03,8.012,17]nonadeca-3,5,7-triene-19-carboxylate | DTXSID30425161

Storage

Protected from light,Store at -20°C,Desiccated

Shipped In

Ice chest + Ice pads

Descripción general

Picrinine, an akuammiline alkaloid, is isolated from the leaves of Alstonia scholaris . Picrinine exhibits anti-inflammatory activity through inhibition of the 5-lipoxygenase enzyme

Form:Solid

IC50& Target:5-Lipoxygenase

Specifications

Sinónimos

Picrinine | FT-0698441 | B2703-092765 | Methyl 14-ethylidene-18-oxa-2, 12-diazahexacyclo[9.6.1.19, 15.01, 9.03, 8.012, 17]nonadeca-3, 5, 7-triene-19-carboxylate | DTXSID30425161

Especificaciones y pureza

≥99%

Mecanismos bioquímicos y fisiológicos

Picrinine, an akuammiline alkaloid, is isolated from the leaves of Alstonia scholaris . Picrinine exhibits anti-inflammatory activity through inhibition of the 5-lipoxygenase enzyme.

Condiciones de almacenamiento de almacenamiento

Protected from light, Store at -20°C, Desiccated

Enviado en

Ice chest + Ice pads

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Tipo de acción

INHIBITOR

Pureza

≥99%

Nombres e identificadores

• Sonrisas canónicas: CC=C1CN2C3CC1C(C45C3(NC6=CC=CC=C64)OC2C5)C(=O)OC
• IUPAC Name: methyl 14-ethylidene-18-oxa-2,12-diazahexacyclo[9.6.1.19,15.01,9.03,8.012,17]nonadeca-3,5,7-triene-19-carboxylate
• InChIKey: BDXYPHKGNUGUFG-UHFFFAOYSA-N
• INCHI: 1S/C20H22N2O3/c1-3-11-10-22-15-8-12(11)17(18(23)24-2)19-9-16(22)25-20(15,19)21-14-7-5-4-6-13(14)19/h3-7,12,15-17,21H,8-10H2,1-2H3
• Isómeros SMILES: CC=C1CN2C3CC1C(C45C3(NC6=CC=CC=C64)OC2C5)C(=O)OC
• CAS alternativo: 4684-32-6
• PubChem CID: 6738085
• Términos de entrada MeSH: picrinine
• Peso molecular: 338.40

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Clase Indoles and derivatives
      • Subclass Pyridoindoles

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Clase: Indoles and derivatives
• Subclass: Pyridoindoles
• Intermediate Tree Nodes: Not available
• Direct Parent: Beta carbolines
• Alternative Parents: Carbazoles Quinolizidines Indolines Piperidines Benzenoids Oxolanes Oxazolidines Methyl esters Hemiaminals Oxacyclic compounds Monocarboxylic acids and derivatives Azacyclic compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Beta-carboline - Carbazole - Quinolizidine - Dihydroindole - Piperidine - Benzenoid - Oxazolidine - Oxolane - Methyl ester - Carboxylic acid ester - Hemiaminal - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Oxacycle - Azacycle - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organic oxide - Amine - Carbonyl group - Organic oxygen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound
• Descripción: This compound belongs to the class of organic compounds known as beta carbolines. These are compounds containing a 9H-pyrido[3,4-b]indole 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

Propiedades químicas y físicas

• Solubilidad: DMSO : 33.33 mg/mL (98.49 mM; ultrasonic and warming and heat to 60°C)