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Chemical Structure : Trequinsin hydrochloride
CAS No.: 78416-81-6
Catalog No.: PC-62884Not For Human Use, Lab Use Only.
Trequinsin hydrochloride (HL 725) is a potent, cell-permeable, orally active inhibitor of cGMP-inhibited phosphodiesterase (PDE3 IC50=250 pM), inhibits arachidonic acid-induced aggregation of human platelets with IC50 of 50 pM.
| Packing | Price | Stock | Quantity |
|---|---|---|---|
| 5 mg | $138 | In stock | |
| 10 mg | $218 | In stock | |
| 25 mg | $378 | In stock | |
| 50 mg | Get quote | ||
| 100 mg | Get quote |
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Trequinsin hydrochloride (HL 725) is a potent, cell-permeable, orally active inhibitor of cGMP-inhibited phosphodiesterase (PDE3 IC50=250 pM), inhibits arachidonic acid-induced aggregation of human platelets with IC50 of 50 pM.
Trequinsin reduces systemic blood pressure in both normotensive and hypertensive animal models.
| M.Wt | 441.956 | |
| Formula | C24H28ClN3O3 | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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| Chemical Name/SMILES |
2,3,6,7-Tetrahydro-9,10-dimethoxy-3-methyl-2-[(2,4,6-trimethylphenyl)imino]-4H-pyrimido[6,1-a]isoquinolin-4-one hydrochloride |
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1. Lal B, et al. J Med Chem. 1984 Nov;27(11):1470-80.
2. Ruppert D, et al. Life Sci. 1982 Nov 8;31(19):2037-43.
3. Darius H, et al. Br J Pharmacol. 1985 Mar;84(3):735-41.
4. Blaskó G, et al. Thromb Res. 1986 Jul 15;43(2):249-50.
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