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
200MG Get Quote Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

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.
molnova catalog
related products
  • Kinetin riboside

    A cytokinin analog that displays potent antiproliferative activity against various human cancer cell lines.

  • Alexidine dihydrochl...

    Alexidine dihydrochloride has antifungal and antibiofilm activity against a diverse range of fungal pathogens.

  • ASK1-IN-2

    ASK1-IN-2 is a potent and orally active inhibitor of apoptosis signal-regulating kinase 1 (ASK1), with an IC50 of 32.8 nM. ASK1-IN-2 can potentially be used as a therapeutic strategy for ulcerative colitis.