Mag-Fura-2 AM (Magnesium Ion Fluorescent Probe) - BioReagent, Biological Stain, for fluorescence analysis, for microscopy, ≥96% , CAS No.130100-20-8

CAS: 130100-20-8 Cat. No.: M1453637 Molecular Weight: 722.56

GRADE & PURITY BioReagent, Biological Stain, for Fluorescence analysis, for Microscopy, ≥96%

Synonyms

Mag-Fura-2 AM | Mag-fura-2,am

Storage

Protected from light,Store at -20°C,Avoid repeated freezing and thawing

Shipped In

Ice chest + Ice pads

Application

Cell Staining‌, Fluorescence Analysis

Overview

Mag-Fura-2 AM (Magnesium Ion Fluorescent Probe) is a fluorescent dye which is useful for measuring changes in cytosolic Mg²⁺ with Ex/Em=336/503 nm. Mag-Fura-2 AM can be used to study the characteristics of Mg²⁺ transport in the brush border membrane vesicles of the ileum of animals. Mag-Fura-2 AM is used as a Ca²⁺-sensitive fluorescent indicator to detect the calcium signal transduction in the sarcoplasmic reticulum, cytoplasm and mitochondria during the activation process of rabbit aortic smooth muscle cells.

Specifications

Synonyms

Mag-Fura-2 AM | Mag-fura-2, am

Specifications & Purity

BioReagent, Biological Stain, for fluorescence analysis, for microscopy, ≥96%

Stability And Storage

Store at -20℃ long term (12 months). Store in the dark. Avoid freeze/thaw cycle.

Storage

Protected from light, Store at -20°C, Avoid repeated freezing and thawing

Shipped In

Ice chest + Ice pads

This product requires cold chain shipping. Ground and other economy services are not available.

Grade

Biological Stain, BioReagent, for Fluorescence analysis, for Microscopy

Purity

≥96%

Names and Identifiers

• Canonical Smiles: CC(=O)OCOC(=O)CN(CC(=O)OCOC(=O)C)C1=C(C=C2C=C(OC2=C1)C3=NC=C(O3)C(=O)OCOC(=O)C)OCC(=O)OCOC(=O)C
• IUPAC Name: acetyloxymethyl 2-[5-[2-(acetyloxymethoxy)-2-oxoethoxy]-6-[bis[2-(acetyloxymethoxy)-2-oxoethyl]amino]-1-benzofuran-2-yl]-1,3-oxazole-5-carboxylate
• InChIKey: PCDUVTXECKTHBH-UHFFFAOYSA-N
• INCHI: 1S/C30H30N2O19/c1-16(33)42-12-46-26(37)9-32(10-27(38)47-13-43-17(2)34)21-7-22-20(5-23(21)41-11-28(39)48-14-44-18(3)35)6-24(50-22)29-31-8-25(51-29)30(40)49-15-45-19(4)36/h5-8H,9-15H2,1-4H3
• Isomeric SMILES: CC(=O)OCOC(=O)CN(CC(=O)OCOC(=O)C)C1=C(C=C2C=C(OC2=C1)C3=NC=C(O3)C(=O)OCOC(=O)C)OCC(=O)OCOC(=O)C
• Molecular Weight: 722.56

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Class Carboxylic acids and derivatives
      • Subclass Amino acids, peptides, and analogues
        • Level5 Amino acids and derivatives
          • Level6 Alpha amino acids and derivatives
            • Level7 Alpha amino acid esters

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Class: Carboxylic acids and derivatives
• Subclass: Amino acids, peptides, and analogues
• Intermediate Tree Nodes: Amino acids and derivatives - Alpha amino acids and derivatives
• Direct Parent: Alpha amino acid esters
• Alternative Parents: Phenoxyacetic acid derivatives Benzofurans Dialkylarylamines Alkyl aryl ethers Acylals 2,5-disubstituted oxazoles Heteroaromatic compounds Furans Oxacyclic compounds Azacyclic compounds Acetals Organopnictogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Alpha-amino acid ester - Phenoxyacetate - Benzofuran - Dialkylarylamine - Tertiary aliphatic/aromatic amine - Alkyl aryl ether - 2,5-disubstituted 1,3-oxazole - Acylal - Benzenoid - Azole - Heteroaromatic compound - Furan - Oxazole - Carboxylic acid ester - Tertiary amine - Acetal - Oxacycle - Azacycle - Ether - Organoheterocyclic compound - Organic oxide - Carbonyl group - Organopnictogen compound - Hydrocarbon derivative - Organic nitrogen compound - Amine - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Aromatic heteropolycyclic compound
• Description: This compound belongs to the class of organic compounds known as alpha amino acid esters. These are ester derivatives of alpha amino acids.
• 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

Chemical and Physical Properties

• Solubility: Soluble in DMSO
• Sensitivity: Light-sensitive