Drug Information
| Drug General Information | Top | |||
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| Drug ID |
D05GPX
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| Drug Name |
Y-26763
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| Synonyms |
127408-31-5
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| Drug Type |
Small molecular drug
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| Indication | Discovery agent [ICD-11: N.A.] | Investigative | [1], [2] | |
| Structure |
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Download2D MOL |
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| Formula |
C14H16N2O4
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| Canonical SMILES |
CC(=O)N(C1C(C(OC2=C1C=C(C=C2)C#N)(C)C)O)O
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| InChI |
1S/C14H16N2O4/c1-8(17)16(19)12-10-6-9(7-15)4-5-11(10)20-14(2,3)13(12)18/h4-6,12-13,18-19H,1-3H3/t12-,13+/m1/s1
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| InChIKey |
IWTCFIIOUXJOOV-OLZOCXBDSA-N
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| CAS Number |
CAS 127408-31-5
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| PubChem Compound ID | ||||
| ChEBI ID |
CHEBI:92788
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| Target and Pathway | Top | |||
|---|---|---|---|---|
| Target(s) | Potassium channel unspecific (KC) | Target Info | Modulator | [1], [2] |
| References | Top | |||
|---|---|---|---|---|
| REF 1 | Y-26763: ATP-sensitive K+ channel activation and the inhibition of insulin release from human pancreatic beta-cells. Eur J Pharmacol. 2004 Feb 20;486(2):133-9. | |||
| REF 2 | Effects of a newly synthesized K+ channel opener, Y-26763, on noradrenaline-induced Ca2+ mobilization in smooth muscle of the rabbit mesenteric art... Br J Pharmacol. 1994 Jan;111(1):165-72. | |||
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