Concanavalin A from Canavalia ensiformis (Jack bean), CAS No.11028-71-0

CAS: 11028-71-0 Cat. No.: C755215 EC Number: 234-258-2

GRADE & PURITY BioReagent, for Cell culture, Type IV-S, lyophilized powder, aseptically processed

Overview

Concanavalin A is a protein containing only β-sheets in its structure, and belongs to the legume lectins family.

Application:

Concanavalin A from Canavalia ensiformis (Jack bean) has been used:

• in in vitro cell proliferation assay and cell cycle assessment
• in lymphocyte proliferation
• in splenocyte culturing

Specifications

Product Name

Concanavalin A from Canavalia ensiformis (Jack bean), CAS No.11028-71-0

Grade

BioReagent, for Cell culture

Specifications & Purity

BioReagent, for cell culture, Type IV-S, lyophilized powder, aseptically processed

Biochemical and Physiological Mechanisms

Concanavalin A is known to stimulate acute hepatic inflammation and acts as a T‐cell mitogen. It has inhibitory effect on hepatocellular carcinoma by inducing autophagy.Con A is not blood group specific but has an affinity for terminal α-D-mannosyl and α-

CAS

11028-71-0

Molecule Type

Protein

Storage and Shipping

Concentration

Type IV-S, lyophilized powder, aseptically processed

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Nucleosides, nucleotides, and analogues
    • Class Pyrimidine nucleosides
      • Subclass Pyrimidine 2',3'-dideoxyribonucleosides

• Kingdom: Organic compounds
• Superclass: Nucleosides, nucleotides, and analogues
• Class: Pyrimidine nucleosides
• Subclass: Pyrimidine 2',3'-dideoxyribonucleosides
• Intermediate Tree Nodes: Not available
• Direct Parent: Pyrimidine 2',3'-dideoxyribonucleosides
• Alternative Parents: Benzenesulfonamides Benzoic acids Benzenesulfonyl compounds Benzoyl derivatives Pyrimidones Organosulfonamides Hydropyrimidines Vinylogous amides Tetrahydrofurans Heteroaromatic compounds Aminosulfonyl compounds Ureas Lactams Azo imides Azo compounds Oxacyclic compounds Monocarboxylic acids and derivatives Carboxylic acids Azacyclic compounds Primary alcohols Organopnictogen compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Not available
• Substituents: Pyrimidine 2',3'-dideoxyribonucleoside - Benzenesulfonamide - Benzenesulfonyl group - Benzoic acid - Benzoic acid or derivatives - Benzoyl - Pyrimidone - Benzenoid - Organosulfonic acid amide - Pyrimidine - Hydropyrimidine - Monocyclic benzene moiety - Heteroaromatic compound - Vinylogous amide - Aminosulfonyl compound - Tetrahydrofuran - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Urea - Lactam - Azo imide - Azo compound - Oxacycle - Azacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Primary alcohol - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Alcohol - Aromatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as pyrimidine 2',3'-dideoxyribonucleosides. These are compounds consisting of a pyrimidine linked to a ribose which lacks a hydroxyl group at positions 2 and 3.
• 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

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