Diethylaminoethyl cellulose - 40-160μm , CAS No.9013-34-7

CAS: 9013-34-7 Cat. No.: D301700 Número EC: 618-482-1

GRADE & PURITY 40-160μm

Synonyms

Adenosine, 3-deaza- | MLS003106659 | 1-.beta.-d-Arabinofuranosyl-1H-imidazo[4,5-c]pyridin-4-amine | NSC167897 | NSC-167897 | 1H-Imidazo[4, 4-amino-1-.beta.-D-ribofuranosyl- | 2-(4-aminoimidazo[4,5-c]pyridin-1-yl)-5-(hydroxymethyl)oxolane-3,4-diol | SMR001

Storage

Store at 2-8°C

Shipped In

Wet ice

Descripción general

A strong anion exchange medium for column chromatography. Insoluble in water, acids, alkalis, and ethanol.

Applications

Diethylaminoethyl dextran cellulose can be used in protein chromatography, ion exchange chromatography, and as anion exchange media. Diethylaminoethyl dextran cellulose has been used to study sperm motility, sperm capacitation, and sperm-oocyte interactions. It has also been used in studies of patients with IgA nephropathy.

Specifications

Sinónimos

Adenosine, 3-deaza- | MLS003106659 | 1-.beta.-d-Arabinofuranosyl-1H-imidazo[4, 5-c]pyridin-4-amine | NSC167897 | NSC-167897 | 1H-Imidazo[4, 4-amino-1-.beta.-D-ribofuranosyl- | 2-(4-aminoimidazo[4, 5-c]pyridin-1-yl)-5-(hydroxymethyl)oxolane-3, 4-diol | SMR001

Especificaciones y pureza

40-160μm

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C

Enviado en

Wet ice

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

Nombres e identificadores

• Sonrisas canónicas: C1=CN=C(C2=C1N(C=N2)C3C(C(C(O3)CO)O)O)N
• IUPAC Name: 2-(4-aminoimidazo[4,5-c]pyridin-1-yl)-5-(hydroxymethyl)oxolane-3,4-diol
• InChIKey: DBZQFUNLCALWDY-UHFFFAOYSA-N
• INCHI: 1S/C11H14N4O4/c12-10-7-5(1-2-13-10)15(4-14-7)11-9(18)8(17)6(3-16)19-11/h1-2,4,6,8-9,11,16-18H,3H2,(H2,12,13)
• Isómeros SMILES: C1=CN=C(C2=C1N(C=N2)C3C(C(C(O3)CO)O)O)N
• WGK Alemania: 3
• Reaxy-Rn: 24730589
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=24730589&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Nucleosides, nucleotides, and analogues
    • Clase Imidazole[4,5-c]pyridine ribonucleosides and ribonucleotides

• Kingdom: Organic compounds
• Superclass: Nucleosides, nucleotides, and analogues
• Clase: Imidazole[4,5-c]pyridine ribonucleosides and ribonucleotides
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Imidazole[4,5-c]pyridine ribonucleosides and ribonucleotides
• Alternative Parents: Glycosylamines Pentoses Imidazo-[4,5-c]pyridines Aminopyridines and derivatives N-substituted imidazoles Imidolactams Tetrahydrofurans Heteroaromatic compounds Secondary alcohols Oxacyclic compounds Azacyclic compounds Primary amines Primary alcohols Organopnictogen compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Imidazole[4,5-c]pyridine ribonucleoside,ribonucleotide or analogue - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Imidazopyridine - Imidazo-[4,5-c]pyridine - Aminopyridine - Monosaccharide - Imidolactam - Pyridine - N-substituted imidazole - Azole - Heteroaromatic compound - Imidazole - Tetrahydrofuran - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Primary amine - Organic nitrogen compound - Amine - Alcohol - Hydrocarbon derivative - Organopnictogen compound - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Primary alcohol - Aromatic heteropolycyclic compound
• Descripción: This compound belongs to the class of organic compounds known as imidazole[4,5-c]pyridine ribonucleosides and ribonucleotides. These are organic compounds in which the C-1 of a ribosyl moiety is N-linked to an imidazole[4,5-c]pyridine ring system. Nucleotides have a phosphate group linked to the C5 carbon of the ribose (or deoxyribose) 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

Objetivos asociados (humanos)

TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)

Discover Target: TDP1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mecanismos de acción

Propiedades químicas y físicas

• Sensibilidad: Moisture sensitive.;Heat Sensitive
• Peso molecular: 266.250 g/mol
• XLogP3: -1.600
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 7
• Rotatable Bond Count: 2
• Exact Mass: 266.102 Da
• Monoisotopic Mass: 266.102 Da
• Topological Polar Surface Area: 127.000 Ų
• Heavy Atom Count: 19
• Formal Charge: 0
• Complexity: 334.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 4
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Referencias

1. Fang Long, Zuomin Hu, Huanzhao Luo, Zhongxing Chu, Shuqin Li, Yaping Zhou, Anping Li, Feijun Luo.  (2026)  Remodeling of Bamboo (Phyllostachys edulis) Shoot Polysaccharides by Monascus purpureus Fermentation Enhances Antioxidant Protection in Caco-2 Cells.  Foods,  15  (4): (704).  [PMID:41750896] [10.3390/foods15040704]