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ChemicalBook > Product Catalogue >Biochemical Engineering >Inhibitors >DNA damage >DNA / RNA Synthesis inhibitors >Nedaplatin

Nedaplatin

Nedaplatin Structure
  • ₹0
  • Product name: Nedaplatin
  • CAS: 95734-82-0
  • MF: C2H6N2O3Pt
  • MW: 301.17
  • EINECS:
  • MDL Number:MFCD00866374
  • Synonyms:(glycolato-o,o')diammineplatinum(ii);cis-diammine(glycolato)platinum(ii);NEDAPLATIN;254-s ;o(sup2))-diammine(hydroxyacetato(2-)-o(sup1(sp-4-3)-platinu ;Nedaplait;o(sup 2))- diammine(hydroxyacetato(2-)-o(sup 1 (sp-4-3)-platinu (glycolato-o,o')diammineplatinum(ii) 254-s cis-diammine(glycolato)platinum(ii) nedaplatin nsc 375101d;2,2-diaMino-1,3-dioxa-2-platinacyclopentan-4-one
Manufacturer Product number Product description Packaging Price Updated Buy

Properties

storage temp. :Inert atmosphere,Store in freezer, under -20°C
solubility :H2O : 13.6 mg/mL (44.86 mM; Need ultrasonic and warming; DMSO can inactivate Nedaplatin's activity)DMF : < 1 mg/mL (insoluble; DMSO can inactivate Nedaplatin's activity)
form :Powder
color :Light yellow to yellow

Safety Information

Symbol(GHS): GHS hazard pictograms
Signal word: Warning
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
H302 Harmful if swallowed Acute toxicity,oral Category 4 Warning GHS hazard pictograms P264, P270, P301+P312, P330, P501
Precautionary statements:
P280 Wear protective gloves/protective clothing/eye protection/face protection.
P305+P351+P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

Description

Nedaplatin, a novel second generation platinum complex, was marketed in Japan for the treatment of a variety of cancers including: head and neck, small-cell and non-small cell lung, oesophageal, prostatic, testicular, ovarian, cervical, bladder, and uterine cancers. Platinum anticancer agents, prototyped by cisplatin, have been reported to be hydrolyzed to the mono- or diaquated species of diamine platinum which react with nucleophilic sites on DNA to cause intrastrand and interstrand crosslinks and DNA-protein crosslinks, which result in cytotoxicity. Nedaplatin was reportedly more active than cisplatin against several solid tumors while sharing less nephro- and gastrointestinal toxicity to cisplatin in viva The minimal renal toxicity displayed by nedaplatin allows its use in patients with deteriorated renal function.

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