MK 996
- Product Name
- MK 996
- CAS No.
- 157263-00-8
- Chemical Name
- MK 996
- Synonyms
- MK 996;L-159282;3-((2'-(Benzoylaminosulfonyl)biphenyl-4-yl)methyl)-2-ethyl-5,7-dimethyl-3H-imidazo(4,5-B)pyridine;Benzamide, N-[[4'-[(2-ethyl-5,7-dimethyl-3H-imidazo[4,5-b]pyridin-3-yl)methyl][1,1'-biphenyl]-2-yl]sulfonyl]-
- CBNumber
- CB21389124
- Molecular Formula
- C30H28N4O3S
- Formula Weight
- 524.63
- MOL File
- 157263-00-8.mol
MK 996 Property
- Density
- 1.27±0.1 g/cm3(Predicted)
- storage temp.
- Store at -20°C
- solubility
- Soluble in DMSO
- pka
- 4.70±0.10(Predicted)
N-Bromosuccinimide Price
- Product number
- CSN22035
- Product name
- L-159282
- Packaging
- 5mg
- Price
- $2346
- Updated
- 2021/12/16
- Product number
- CSN22035
- Product name
- L-159282
- Packaging
- 25mg
- Price
- $7130
- Updated
- 2021/12/16
MK 996 Chemical Properties,Usage,Production
Uses
L-159282 is a highly potent, orally active, nonpeptide angiotensin II receptor antagonist, with anti-hypertensive activity.
in vivo
In the anesthetized chimpanzee, L-159282 (1 mg/kg, iv) produces 100% inhibition of the AII pressor response and is still active (52%) at 24 h. In aortic coarcted (high renin) rats, L-159282 (3 mg/kg, p.o.) reduces blood pressure to normotensive (< 120 mm Hg) levels without reflex tachycardia. This dose of L-159282 reduces blood pressure to approximately the same level as both losartan (3 mg/kg, p.o.) and enalapril (3 mg/kg, p.o.) in this model[1].
References
[1] Kivlighn SD, et al. In vivo pharmacology of a novel AT1 selective angiotensin II receptor antagonist, MK-996. Am J Hypertens. 1995 Jan;8(1):58-66. DOI:10.1016/0895-7061(94)00169-c
MK 996 Preparation Products And Raw materials
Raw materials
Preparation Products
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