Lobaplatin (D-19466)

CAS No. 135558-11-1

Lobaplatin (D-19466)( D-19466 )

Catalog No. M21767 CAS No. 135558-11-1

Lobaplatin (D-19466) is a diastereometric mixture of platinum(II) complexes. Lobaplatin (D-19466) shows activity for a variety of tumour types and is a promising antitumour chemotherapeutic agent.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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Biological Information

  • Product Name
    Lobaplatin (D-19466)
  • Note
    Research use only, not for human use.
  • Brief Description
    Lobaplatin (D-19466) is a diastereometric mixture of platinum(II) complexes. Lobaplatin (D-19466) shows activity for a variety of tumour types and is a promising antitumour chemotherapeutic agent.
  • Description
    Lobaplatin (D-19466) is a diastereometric mixture of platinum(II) complexes. Lobaplatin (D-19466) shows activity for a variety of tumour types and is a promising antitumour chemotherapeutic agent.
  • In Vitro
    Lobaplatin (D-19466, 0.25-32 μg/mL; 24-72 h) exhibits anti-proliferative activities against esophageal squamous cell carcinoma (ESCC) cell lines.Lobaplatin (0-16 μg/mL; 48 h) induces esophageal squamous cell carcinoma (ESCC) apoptosis and modulates expression of apoptosis-related proteins.Lobaplatin (1.45 μg/mL; 0-48 h; SMMC-7721 cells) arrests cell cycle progression at G1 and G2/M phases in a time-dependent manner.Lobaplatin (1.45 μg/mL; 0-48 h; SMMC-7721 cells) inhibits the mRNA levels of cyclin B, CDK1, and CDC25C phosphatase, down-regulates Rb/E2F complexes and up-regulates of CDK inhibitors. TCell Viability Assay Cell Line:KYSE-410 cells and EC-109 cells Concentration:0.25, 0.5, 1, 2, 4, 8, 16 and 32 μg/mL Incubation Time:24, 48 and 72 hours Result:Inhibited the growth of KYSE-410 and EC-109 cells in a dose- and time-dependent manner.Inhibited the clone formation activity of KYSE-410 and EC-109 cells in a dosedependent manner.Apoptosis Analysis Cell Line:KYSE-410 cells and EC-109 cells Concentration:0.25, 1, 4 and 16 μg/mL Incubation Time:48 hours Result: Increased the percentage of apoptotic cells in a dose-dependent manner.Western Blot Analysis Cell Line:KYSE-410 cells and EC-109 cells Concentration:0, 1, 4 and 16 μg/mLIncubation Time:48 hours Result: Increased expressions of cleaved-caspase-3, cleaved-caspase-8, cleaved-caspase-9 and Bax, while decreased expression of Bcl-2.Cell Cycle Analysis Cell Line:SMMC-7721 cells Concentration:1.45 μg/mL Incubation Time:0, 24, 36 and 48 hours Result:Arrested the proportions of G1, S, and G2/M phases in cells were 45.31, 22.88, and 31.81% at 0 h, 59.91, 11.92, and 28.17% at 24 h, 56.89, 2.83, and 40.28% at 36 h, and 53.80, 2.07, and 44.13% at 48 h, respectively.Western Blot Analysis Cell Line:SMMC-7721 cells Concentration:1.45 μg/mL Incubation Time:0, 24, 36 and 48 hours Result:Down-regulated cyclin B, CDK1, CDC25C, phosphorylated CDK1 (pCDK1), pCDK4, Rb, E2F, and pRb, and up-regulated p53, p21, and p27.
  • In Vivo
    Lobaplatin (5 and 10 mg/kg; i.p.; once a week, for 3 weeks) suppresses tumor growth of esophageal squamous cell carcinoma (ESCC) xenograft. Animal Model:Male BALB/c nude mice (4-6 weeks) with ESCC xenograft Dosage:Intraperitoneal injection; once a week, for 3 weeks Administration:5 and 10 mg/kg Result:Suppressed tumor volumes in a dose-dependent manner.Increased expressions of Bax and decreased expressions of Bcl-2.
  • Synonyms
    D-19466
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    ——
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    135558-11-1
  • Formula Weight
    397.33
  • Molecular Formula
    C?H??N?O?Pt
  • Purity
    >98% (HPLC)
  • Solubility
    H2O : ≥ 50 mg/mL (125.84 mM; DMSO can inactivate Lobaplatin's activity)
  • SMILES
    CC1[O-][Pt+2]2([NH2]CC3C(CC3)C[NH2]2)[O-]C1=O
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Cao H, et al. Lobaplatin Inhibits Prostate Cancer Proliferation and Migration Through Regulation of BCL2 and BAX. Dose Response. 2019 Jun 5;17(2):1559325819850981. 2. McKeage MJ, et al. Lobaplatin: a new antitumour platinum drug. Expert Opin Investig Drugs. 2001 Jan;10(1):119-28.
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