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IMM-H007

Cat. No. M11462

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

IMM-H007 Structure
Size Price Availability Quantity
1mg USD 70 In stock
5mg USD 165 In stock
10mg USD 270 In stock
25mg USD 440 In stock
50mg USD 640 In stock
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Quality Control & Documentation
Biological Activity

Imm-h007 is an adenosine derivative that is an activator of the AMP-Activated Protein Kinase (AMPK). Imm-h007 is a potential drug for the treatment of cardiac insufficiency. Imm-h007 negatively regulates endothelial inflammation by inactivating NF-κB and JNK/AP1 signaling. Imm-h007 can inhibit the degradation of ABCA1 (ATP binding cassette subfamily a member 1) and promote its cell surface localization in macrophages, thus promoting cholesterol efflux.

Chemical Information
Molecular Weight 485.45
Formula C22H23N5O8
CAS Number 1221412-23-2
Solubility (25°C) DMSO ≥ 60 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Shuai-Xing Wang, et al. Acta Pharmacol Sin. IMM-H007 attenuates isoprenaline-induced cardiac fibrosis through targeting TGFβ1 signaling pathway

[2] Z-L Zhang, et al. Eur Rev Med Pharmacol Sci. Preclinical pharmacokinetic study of a novel lipid-lowering agent, IMM-H007

[3] Jinjin Yu, et al. Toxicol Appl Pharmacol. IMM-H007, a novel small molecule inhibitor for atherosclerosis, represses endothelium inflammation by regulating the activity of NF-κB and JNK/AP1 signaling

[4] Weipeng Ge, et al. Eur J Pharmacol. IMM-H007 improves heart function via reducing cardiac fibrosis

[5] Min-Jie Wang, et al. Eur J Pharmacol. The cordycepin derivative IMM-H007 improves endothelial dysfunction by suppressing vascular inflammation and promoting AMPK-dependent eNOS activation in high-fat diet-fed ApoE knockout mice

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Keywords: IMM-H007 supplier, AMPK, inhibitors, activators

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