Chrysamine G - Moligand™, ≥95% , CAS No.6472-91-9

CAS: 6472-91-9 Cat. No.: C276464 Formula: C₂₆H₁₆N₄Na₂O₆ Peso molecolare: 526.41 PubChem CID: 135475357

QUALITÀ & PUREZZA Moligand™, ≥95%

Synonyms

Benzoic acid, 3,3'-((1,1'-biphenyl)-4,4'-diylbis(azo))bis(6-hydroxy-, disodium salt|Chrysamine|3,3'-((1,1'-Biphenyl)-4,4'-diylbis(azo))bis(6-hydroxybenzoic acid), disodium salt|direct yellow 1|disodium;2-carboxy-4-[[4-[4-[(3-carboxy-4-oxidophenyl)diazenyl]phenyl]phenyl]diazenyl]phenolate|Chrysamine G disodium salt|Chrysamine G|C.I. Direct Yellow 1|sodium 5,5'-(1E,1'E)-biphenyl-4,4'-diylbis(diazene-2,1-diyl)bis(2-hydroxybenzoate)|CHRYSAMINEG

Storage

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

Shipped In

Ice chest + Ice pads

Panoramica

Chrysamine G, a carboxylic acid analogue of Congo Red, can be used as a probe of amyloid deposition in Alzheimer's disease. Chrysamine G also can inhibit Aβ-induced toxicity in PC12 cells.

Specifiche

Sinonimi

Benzoic acid, 3,3'-((1,1'-biphenyl)-4,4'-diylbis(azo))bis(6-hydroxy-, disodium salt | Chrysamine | 3,3'-((1,1'-Biphenyl)-4,4'-diylbis(azo))bis(6-hydroxybenzoic acid), disodium salt | direct yellow 1 | disodium;2-carboxy-4-[[4-[4-[(3-carboxy-4-oxidophenyl)diazenyl]phenyl]phenyl]diazenyl]phenolate | Chrysamine G disodium salt | Chrysamine G Mostra altro

Specifiche e purezza

Moligand™, ≥95%

Meccanismi biochimici e fisiologici

Chrysamine G can penetrate the blood-brain barrier. It is useful in quantifying cerebral amyloid β (Aβ) deposition in Alzheimer′s disease (AD) pathological studies. New probe for β-amyloid aggregates.

Condizioni di conservazione di stoccaggio

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

Spedito in

Ice chest + Ice pads

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Grado

Moligand™

Nota

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.

Purezza

≥95%

Nomi e identificatori

Sorrisi canonici

C1=CC(=CC=C1C2=CC=C(C=C2)N=NC3=CC(=C(C=C3)[O-])C(=O)O)N=NC4=CC(=C(C=C4)[O-])C(=O)O.[Na+].[Na+]

IUPAC Name

disodium;2-carboxy-4-[[4-[4-[(3-carboxy-4-oxidophenyl)diazenyl]phenyl]phenyl]diazenyl]phenolate

InChIKey

AZOPGDOIOXKJRA-UHFFFAOYSA-L

INCHI

1S/C26H18N4O6.2Na/c31-23-11-9-19(13-21(23)25(33)34)29-27-17-5-1-15(2-6-17)16-3-7-18(8-4-16)28-30-20-10-12-24(32)22(14-20)26(35)36;;/h1-14,31-32H,(H,33,34)(H,35,36);;/q;2*+1/p-2

Isomeri SMILES

C1=CC(=CC=C1C2=CC=C(C=C2)N=NC3=CC(=C(C=C3)[O-])C(=O)O)N=NC4=CC(=C(C=C4)[O-])C(=O)O.[Na+].[Na+]

WGK Germania

3

PubChem CID

135475357

Peso molecolare

526.41

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Classe Benzene and substituted derivatives
      • Subclass Biphenyls and derivatives

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: Benzene and substituted derivatives
• Subclass: Biphenyls and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Benzidines
• Alternative Parents: Azobenzenes Salicylic acids Benzoic acids Benzoyl derivatives 1-hydroxy-2-unsubstituted benzenoids Vinylogous acids Carboxylic acid salts Azo compounds Propargyl-type 1,3-dipolar organic compounds Carboxylic acids Organooxygen compounds Organic zwitterions Organic sodium salts Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Azobenzene - Benzidine - Hydroxybenzoic acid - Salicylic acid or derivatives - Salicylic acid - Benzoic acid or derivatives - Benzoic acid - Benzoyl - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Vinylogous acid - Carboxylic acid salt - Azo compound - Organic 1,3-dipolar compound - Organic alkali metal salt - Carboxylic acid derivative - Propargyl-type 1,3-dipolar organic compound - Carboxylic acid - Organonitrogen compound - Organic zwitterion - Organic oxygen compound - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organic sodium salt - Organic nitrogen compound - Organic salt - Aromatic homomonocyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as benzidines. These are organic compounds containing the benzidine skeleton, made up of a biphenyl ring system substituted at the 4- and 4'-positions with a unsubstituted amine 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

Meccanismi d'azione

Proprietà chimiche e fisiche

• Solubilità: Soluble in DMSO
• Peso molecolare: 526.400 g/mol
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 10
• Rotatable Bond Count: 7
• Exact Mass: 526.087 Da
• Monoisotopic Mass: 526.087 Da
• Topological Polar Surface Area: 170.000 Ų
• Heavy Atom Count: 38
• Formal Charge: 0
• Complexity: 740.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 3

XLogP3