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BML-275

Cat. No. M3946

All AbMole products are for research use only, cannot be used for human consumption.

BML-275 Structure
Synonym:

Dorsomorphin, Compound C

Size Price Availability Quantity
5mg USD 60  USD60 In stock
10mg USD 90  USD90 In stock
50mg USD 300  USD300 In stock
100mg USD 500  USD500 In stock
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Biological Activity

BML-275 inhibits BMP signals required for embryogenesis and promoted significant neural differentiation from human pluripotent stem cell (hPSC) lines. BML-275 acts as a potent, selective, reversible, and ATP-competitive inhibitor of AMPK (AMP-activated protein kinase); Ki = 109 nM in the presence of 5 μM ATP and the absence of AMP). BML-275 inhibited the cell proliferation of 4 human pancreatic cancer cell lines (MIA PaCa-2, Panc-1, Colo-357 and AsPC-1). In addition, BML-275 significantly increased the generation of intracellular reactive oxygen species (ROS), followed by induction of DNA damage signaling and apoptosis. Furthermore, BML-275 induced cell cycle arrest in the G2/M phase. BML-275 exerts its antitumor effects by inducing ROS generation, DNA damage and apoptosis via inhibition of the AMPK pathway and by inducing G2/M arrest via a pathway independent of AMPK, implicating its potential application as an antitumor agent for pancreatic cancer.

Product Citations
Chemical Information
Molecular Weight 399.49
Formula C24H25N5O
CAS Number 866405-64-3
Solubility (25°C) DMSO 3 mg/mL warming
Storage 2-8°C, protect from light
References

[1] Li X, et al. PLoS One. Acetic acid activates the AMP-activated protein kinase signaling pathway to regulate lipid metabolism in bovine hepatocytes.

[2] Duong HQ, et al. Int J Oncol. BML-275, an AMPK inhibitor, induces DNA damage, G2/M arrest and apoptosis in human pancreatic cancer cells.

[3] Vucicevic L, et al. Autophagy. Compound C induces protective autophagy in cancer cells through AMPK inhibition-independent blockade of Akt/mTOR pathway.

[4] Jin J, et al. J Lipid Res. AMPK inhibitor Compound C stimulates ceramide production and promotes Bax redistribution and apoptosis in MCF7 breast carcinoma cells.

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Keywords: BML-275, Dorsomorphin, Compound C supplier, AMPK, inhibitors, activators

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