Malonoben
Chemical compound
From Wikipedia, the free encyclopedia
Malonoben (also known as tyrphostin A9, SF-6847, GCP5126, and AG-17) is an uncoupling agent/protonophore.[1][2] As of 1974 when it was discovered, it was considered the most powerful agent of this type, with a potency over 1800 times that of 2,4-dinitrophenol - the prototypical uncoupling agent - and about 3 times the effectiveness of 5-chloro-3-tert-butyl-2'-chloro-4'-nitrosalicylanilide.[3]
| Names | |
|---|---|
| Preferred IUPAC name
[(3,5-di-tert-Butyl-4-hydroxyphenyl)methylidene]propanedinitrile | |
| Other names
Tyrphostin A9; SF-6847; GCP5126; and AG-17 | |
| Identifiers | |
3D model (JSmol) |
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| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.162.608 |
| EC Number |
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| KEGG | |
PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C18H22N2O | |
| Molar mass | 282.387 g·mol−1 |
| Melting point | 142 °C (288 °F; 415 K) ±1° |
| Hazards | |
| GHS labelling: | |
| Danger | |
| H301, H311, H331 | |
| P261, P264, P270, P271, P280, P301+P310, P302+P352, P304+P340, P311, P312, P321, P322, P330, P361, P363, P403+P233, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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