2-Nitrofenil β-D-glucopiranósido - ≥99% , CAS No.2816-24-2

CAS: 2816-24-2 Cat. No.: N107920 Peso molecular: 301.25 Beilstein Registry Number: 92206 Número EC: 220-568-5

GRADE & PURITY ≥99%

Synonyms

2-Nitrophenyl-I(2)-D-glucopyranoside | ortho-nitrophenyl beta-D-glucopyranoside | EN300-7375394 | N-[5-[(9,10-dioxo-1-anthryl)amino]-9,10-dioxo-1-anthryl]benzamide | EINECS 220-568-5 | 2-Nitrophenyl b-D-glucopyranoside | A819354 | A-D-glucopyranoside | be

Storage

Conservar a 2-8°C

Shipped In

Hielo húmedo

Descripción general

el 2-Nitrofenil beta-D-glucopiranósido se utiliza como sustrato para la ß -glucosidasa.

Specifications

Sinónimos

2-Nitrophenyl-I(2)-D-glucopyranoside | ortho-nitrophenyl beta-D-glucopyranoside | EN300-7375394 | N-[5-[(9, 10-dioxo-1-anthryl)amino]-9, 10-dioxo-1-anthryl]benzamide | EINECS 220-568-5 | 2-Nitrophenyl b-D-glucopyranoside | A819354 | A-D-glucopyranoside | be

Especificaciones y pureza

≥99%

Condiciones de almacenamiento de almacenamiento

Conservar a 2-8°C

Enviado en

Hielo húmedo

Pureza

≥99%

Nombres e identificadores

• Pubchem Sid: 488186747
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488186747
• Sonrisas canónicas: C1=CC=C(C(=C1)[N+](=O)[O-])OC2C(C(C(C(O2)CO)O)O)O
• IUPAC Name: (2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-(2-nitrophenoxy)oxane-3,4,5-triol
• InChIKey: KUWPCJHYPSUOFW-RMPHRYRLSA-N
• INCHI: 1S/C12H15NO8/c14-5-8-9(15)10(16)11(17)12(21-8)20-7-4-2-1-3-6(7)13(18)19/h1-4,8-12,14-17H,5H2/t8-,9-,10+,11-,12-/m1/s1
• Isómeros SMILES: C1=CC=C(C(=C1)[N+](=O)[O-])O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O
• WGK Alemania: 3
• Peso molecular: 301.25
• Beilstein: 92206
• Reaxy-Rn: 15247465
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=15247465&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Clase Organooxygen compounds
      • Subclass Carbohydrates and carbohydrate conjugates
        • Level5 Glycosyl compounds
          • Level6 Phenolic glycosides

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Clase: Organooxygen compounds
• Subclass: Carbohydrates and carbohydrate conjugates
• Intermediate Tree Nodes: Glycosyl compounds
• Direct Parent: Phenolic glycosides
• Alternative Parents: Hexoses O-glycosyl compounds Nitrobenzenes Nitroaromatic compounds Phenol ethers Phenoxy compounds Oxanes Secondary alcohols Oxacyclic compounds Organic oxoazanium compounds Propargyl-type 1,3-dipolar organic compounds Acetals Polyols Organopnictogen compounds Organonitrogen compounds Organic zwitterions Organic oxides Primary alcohols Hydrocarbon derivatives
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Phenolic glycoside - Hexose monosaccharide - O-glycosyl compound - Nitrobenzene - Phenoxy compound - Nitroaromatic compound - Phenol ether - Monocyclic benzene moiety - Monosaccharide - Oxane - Benzenoid - C-nitro compound - Organic nitro compound - Secondary alcohol - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Acetal - Oxacycle - Organic oxoazanium - Organoheterocyclic compound - Polyol - Organopnictogen compound - Organic oxide - Organonitrogen compound - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Primary alcohol - Organic zwitterion - Aromatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose.
• 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)

Homo sapiens (32628 Activities)

Explore this target

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

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Soluble in water
• Punto de fusión (°C): 141-142℃
• Peso molecular: 301.250 g/mol
• XLogP3: -1.200
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 8
• Rotatable Bond Count: 3
• Exact Mass: 301.08 Da
• Monoisotopic Mass: 301.08 Da
• Topological Polar Surface Area: 145.000 Ų
• Heavy Atom Count: 21
• Formal Charge: 0
• Complexity: 362.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 5
• 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: 1

Referencias

1. Wu Zongzhan, Dou Wenyu, Yang Xiaolin, Niu Tengfei, Han Zhuzhen, Yang Li, Wang Rufeng, Wang Zhengtao.  (2024)  Novel glycosidase from Paenibacillus lactis 154 hydrolyzing the 28-O-β-d-glucopyranosyl ester bond of oleanane-type saponins.  APPLIED MICROBIOLOGY AND BIOTECHNOLOGY,  108  (1): (1-13).  [PMID:38573330] [10.1007/s00253-024-13109-2]

2. Chen Li, Han Yan, Wei Feng, Manni Yue, Hua Cao, Xiaojuan Ji, Zeng Tu, Zengtao Yang.  (2025)  Sterilization effect of power airborn ultrasound combined with ultraviolet radiation on bacteria.  ULTRASONICS SONOCHEMISTRY,      [PMID:41067059] [10.1016/j.ultsonch.2025.107594]