Name | N-(3-methoxy-5-methylpyrazin-2-yl)-2-[4-(1,3,4-oxadiazol-2-yl)phenyl]pyridine-3-sulfonamide |
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Synonyms |
N-(3-Methoxy-5-methyl-2-pyrazinyl)-2-[4-(1,3,4-oxadiazol-2-yl)phenyl]-3-pyridinesulfonamide
Zd 4054 S1456_Selleck ZD4054 Zibotentan |
Description | Zibotentan (ZD4054) is an orally administered, potent and specific ETA-receptor (endothelin A receptor) antagonist (IC50 = 21 nM). IC50 value: 21 nM Target: ETA receptorZibotentan is capable of inhibiting or reducing the multitude of effects that are evoked by ET-1 activation of the ETA receptor and which promote tumor survival, growth and progression. Zibotentan (ZD4054) treatment produced significant inhibition of tumor growth in ovarian and breast xenografts. |
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Related Catalog | |
References |
[1]. Zibotentan James, N.D., Growcott, J.W. Drugs Fut 2009, 34(8): 624. |
Density | 1.4±0.1 g/cm3 |
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Boiling Point | 637.0±65.0 °C at 760 mmHg |
Molecular Formula | C19H16N6O4S |
Molecular Weight | 424.433 |
Flash Point | 339.0±34.3 °C |
Exact Mass | 424.095367 |
PSA | 141.37000 |
LogP | 2.38 |
Vapour Pressure | 0.0±1.9 mmHg at 25°C |
Index of Refraction | 1.628 |
Storage condition | -20°C |
Symbol |
GHS07 |
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Signal Word | Warning |
Hazard Statements | H302 |
Precautionary Statements | P301 + P312 + P330 |
RIDADR | NONH for all modes of transport |
RTECS | UT7937700 |