An anticancer agent
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Product Type

Nedaplatin

Item No. 29001

Technical Information
Formal Name
(SP-4-3)-diammine[2-(hydroxy-κO)acetato(2-)-κO]-platinum
CAS Number
95734-82-0
Synonyms
  • NSC 375101
Molecular Formula
C2H8N2O3Pt
Formula Weight
Purity
≥95%
A crystalline solid
Water: *soluble
SMILES
[NH3][Pt+2]([O-]C1=O)([O-]C1)[NH3]
InChi Code
InChI=1S/C2H3O3.2H3N.Pt/c3-1-2(4)5;;;/h1H2,(H,4,5);2*1H3;/q-1;;;+2/p-1
InChi Key
GYAVMUDJCHAASE-UHFFFAOYSA-M
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Nedaplatin is a derivative of cisplatin (Item No. 13119) with anticancer activity.1 Nedaplatin undergoes spontaneous hydrolysis to form platinum complexes that cross-link DNA resulting in apoptosis and cell death.2,3 It inhibits the growth of human NUGC-4 gastric and KSE-1 esophageal squamous carcinoma cells (IC50s = 4.6 and 3.4 μM, respectively) and inhibits S to G2 and G2/M to G1 cell cycle progression.4 Nedaplatin (44 mg/kg) decreases tumor volume and increases survival in a Lewis lung carcinoma syngeneic mouse model.1 Nedaplatin (40 mg/kg) also decreases tumor volume in an HNC-3 head and neck cancer mouse xenograft model.5 It exhibits reduced nephrotoxicity in rats compared with cisplatin.3

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Uchida, N., Takeda, Y., Hojo, K., et alSequence-dependent antitumour efficacy of combination chemotherapy of nedaplatin, a novel platinum complex, with 5-fluorouracil in an in vivo murine tumour model. Eur. J. Cancer 34(11), 1796-1801 (1998).

    2. Alberto, M.E., Lucas, M.F.A., Pavelka, M., et alThe second-generation anticancer drug Nedaplatin: A theoretical investigation on the hydrolysis mechanism. J. Phys. Chem. B 113(43), 14473-14479 (2009).

    3. Hanada, K., Suda, M., Kanai, N., et alPharmacokinetics and toxicodynamics of oxaliplatin in rats: Application of a toxicity factor to explain differences in the nephrotoxicity and myelosuppression induced by oxaliplatin and the other platinum antitumor derivatives. Pharm. Res. 27(9), 1893-1899 (2010).

    4. Tanaka, R., Takii, Y., Shibata, Y., et alIn vitro sequence-dependent interaction between nedaplatin and paclitaxel in human cancer cell lines. Cancer Chemother. Pharmacol. 56(3), 279-285 (2005).

    5. Yamada, H., Maki, H., Takeda, Y., et alEvaluation of combined nedaplatin and docetaxel therapy for human head and neck cancer in vivo. Anticancer Res. 26(2A), 989-994 (2006).