Cellulose diéthylaminoéthyle - 40-160μm , CAS No.9013-34-7

CAS: 9013-34-7 Cat. No.: D301700 Numéro CE: 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

A conserver entre 2 et 8°C

Shipped In

Glace humide

Vue d’ensemble

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

Synonymes

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

Spécifications et pureté

40-160μm

Conditions de stockage de stockage

A conserver entre 2 et 8°C

Expédié en

Glace humide

Noms et identifiants

• Pubchem Sid: 508812064
• Sourires canoniques: 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)
• Isomères SMILES: C1=CN=C(C2=C1N(C=N2)C3C(C(C(O3)CO)O)O)N
• WGK Allemagne: 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
    • Classe Imidazole[4,5-c]pyridine ribonucleosides and ribonucleotides

• Kingdom: Organic compounds
• Superclass: Nucleosides, nucleotides, and analogues
• Classe: 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
• Description: 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

Cibles associées (humaines)

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

Mécanismes d'action

Propriétés chimiques et physiques

• Sensibilité: Moisture sensitive.;Heat Sensitive
• Poids moléculaire: 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

Références

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]

2. Chunqing Ai, Lu Wang, Xingchen Ye, Xiaomeng Ren, Shuang Song, Xuelu Li.  (2026)  Fucoidan from giant kelp alleviates postmenopausal osteoporosis by regulating the betaine-OPG/RANKL/RANK signaling axis.  FOOD RESEARCH INTERNATIONAL,      [PMID:] [10.1016/j.foodres.2026.120150]