Chemical Structure : Kukoamine A
CAS No.: 75288-96-9
Catalog No.: PC-26771Not For Human Use, Lab Use Only.
Kukoamine A (KuA) is a potent and selective inhibitor of Crithidia fasciculata trypanothione reductase (TR) with Ki of 1.8 uM, with no significant inhibition on human glutathione reductase, possesses antioxidant, anti-inflammatory activities.
| Packing | Price | Stock | Quantity |
|---|---|---|---|
| 5 mg | $128 | In stock | |
| 10 mg | $198 | In stock | |
| 25 mg | $348 | In stock | |
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| 100 mg | Get quote |
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Kukoamine A (KuA) is a potent and selective inhibitor of Crithidia fasciculata trypanothione reductase (TR) with Ki of 1.8 uM, with no significant inhibition on human glutathione reductase, possesses antioxidant, anti-inflammatory activities.
Kukoamine A inhibits human glioblastoma cell growth and migration in vitro and in vivo through apoptosis induction and epithelial-mesenchymal transition attenuation by downregulating expressions of 5-LOX and C/EBPβ.
Kukoamine A disrupts AARS2-AP-2γ interaction and, demonstrates improved liver targeting, potent antitumour activity and synergy with PD-1 blockade in hepatocellular carcinoma (HCC).
| M.Wt | ||
| Formula | C28H42N4O6 | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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| Chemical Name/SMILES |
Benzenepropanamide, N,N'-[1,4-butanediylbis(imino-3,1-propanediyl)]bis[3,4-dihydroxy- |
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1. Ponasik JA, et al. Biochem J. 1995 Oct 15;311 ( Pt 2)(Pt 2):371-5.
2. Chitkul B, et al. Bioorg Med Chem Lett. 2000 Oct 16;10(20):2367-9.
3. Wang Q, et al. Sci Rep. 2016 Nov 8;6:36543.
4. Li Q, et al. Gut. 2026 May 11:gutjnl-2025-337330.

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