Millepachine

CAS No. 1393922-01-4

Millepachine( —— )

Catalog No. M28201 CAS No. 1393922-01-4

Millepachine is a natural product found in the Chinese herbal medicine with strong antitumor effects against numerous human cancer cells.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 177 Get Quote
10MG 295 Get Quote
25MG 502 Get Quote
50MG 709 Get Quote
100MG 1008 Get Quote
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Biological Information

  • Product Name
    Millepachine
  • Note
    Research use only, not for human use.
  • Brief Description
    Millepachine is a natural product found in the Chinese herbal medicine with strong antitumor effects against numerous human cancer cells.
  • Description
    Millepachine is a natural product found in the Chinese herbal medicine with strong antitumor effects against numerous human cancer cells.(In Vitro):Millepachine (2-8 μM; 24 h) inhibits ATP-binding cassette transporter activity in A2780CP cells. Millepachine (2-8 μM; 24 or 48 h) induces significant G2/M arrest and apoptosis of cisplatin-sensitive A2780S and cisplatin-resistant A2780CP cells. The percentage of cells in the G2/M fraction increased from 15.99% in vehicle cells to 24.93%, 60.67%, and 77.31% at dose of 2, 4, and 8 μM in A2780S cells, respectively. Millepachine (2-8 μM; 24 h) decreases topoisomerase II levels in A2780S and A2780CP cells. Millepachine (1.25-20 μM; 48 h) remarkably inhibits the proliferation of cisplatin-resistant A2780CP cells with an IC50 of 4 μM.(In Vivo):Millepachine (20 mg/kg; i.v.) reduced tumor volume and tumor weight with the inhibitory rate of 73.21% and 65.58% in A2780S and A2780CP xenograft models, respectively. Millepachine does not induce acquired drug resistance in an excised A2780S xenograft model.
  • In Vitro
    Millepachine (1.25-20 μM; 48 h) remarkably inhibits the proliferation of cisplatin-resistant A2780CP cells.Millepachine (2-8 μM; 24 or 48 h) induces G2/M arrest and apoptosis cisplatin-sensitive A2780S and cisplatin-resistant A2780CP cells.Millepachine (2-8 μM; 24 h) decreases topoisomerase II levels in A2780S and A2780CP cells.Millepachine (2-8 μM; 24 h) inhibits ATP-binding cassette transporter activity in A2780CP cells.Cell Proliferation Assay Cell Line:A2780CP cells Concentration:0, 1.25, 2.5, 5, 10, 20 μM Incubation Time:48 hours Result:Inhibited the cells proliferation with an IC50 of 4 μM.Cell Cycle Analysis Cell Line:A2780S and A2780CP cells Concentration:2, 4, 8 μM Incubation Time:24 or 48 hours Result:Induced significant G2/M arrest both in both cells.The percentage of cells in the G2/M fraction increased from 15.99% in vehicle cells to 24.93%, 60.67%, and 77.31% at dose of 2, 4, and 8 μM in A2780S cells, respectively.Apoptosis Analysis Cell Line:A2780S and A2780CP cells Concentration:2, 4, 8 μM Incubation Time:24 or 48 hours Result:The percentage of apoptotic cells increased from 1.49% in vehicle cells to 10.98%, 20.60%, and 39.43% at dose of 2, 4, and 8 μM in A2780S cells, respectively.The percentage of apoptotic cells increased from 0.87% to 10.97%, 25.28%, and 37.59% in A2780CP cells, respectively.Western Blot Analysis Cell Line:A2780S and A2780CP cells Concentration:0, 2, 4, 8 μM Incubation Time:24 hours Result:Decreased the levels of topoisomerase II (TOPO II) in both cells.
  • In Vivo
    Millepachine (20 mg/kg; i.v. every two days for 14 day) inhibits tumor growth in mice.Millepachine (20 mg/kg; i.v. every two days for 14 day) does not induce acquired drug resistance in an excised A2780S xenograft model. Animal Model:Female BALB/c nude mice (6 weeks) are injected A2780S or A2780CP cells Dosage:20 mg/kg Administration:I.v. every two days for 2-14 days Result:Reduced tumor volume and tumor weight with the inhibitory rate of 73.21% and 65.58% in A2780S (after seven times injection) and A2780CP (after six times injection) xenograft model, respectively.
  • Synonyms
    ——
  • Pathway
    Apoptosis
  • Target
    Apoptosis
  • Recptor
    NO
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    1393922-01-4
  • Formula Weight
    350.41
  • Molecular Formula
    C22H22O4
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 100 mg/mL (285.38 mM)
  • SMILES
    CC(C)(C=Cc1c(cc2)OC)Oc1c2C(/C=C/c(cc1)ccc1OC)=O
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.KUBO, MICHINORI, et al. Scutellariae radix. X. Inhibitory effects of various flavonoids on histamine release from rat peritoneal mast cells in vitro. Chem. Pharm. Bull., 1984, 32(12):5051-4.
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