MK-3903
- Product Name
- MK-3903
- CAS No.
- 1219737-12-8
- Chemical Name
- MK-3903
- Synonyms
- MK-3903;MK-3903 ,S8803;MK-3903, 10 mM in DMSO;MK-3903; MK 3903; MK3903;1219737-12-8;AMPK,MK3903,AMP-activated protein kinase,inhibit,Inhibitor,MK-3903;Benzoic acid, 5-[(5-[1,1'-biphenyl]-4-yl-6-chloro-1H-benzimidazol-2-yl)oxy]-2-methyl-;5-((6-([1,1'-Biphenyl]-4-yl)-5-chloro-1H-benzo[d]imidazol-2-yl)oxy)-2-methylbenzoic acid
- CBNumber
- CB52516050
- Molecular Formula
- C27H19ClN2O3
- Formula Weight
- 454.9
- MOL File
- 1219737-12-8.mol
MK-3903 Property
- Boiling point:
- 712.6±70.0 °C(Predicted)
- Density
- 1.349±0.06 g/cm3(Predicted)
- storage temp.
- Store at -20°C
- solubility
- DMSO:100.0(Max Conc. mg/mL);219.83(Max Conc. mM)
- form
- A solid
- pka
- 3.40±0.25(Predicted)
- color
- White to off-white
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P280Wear protective gloves/protective clothing/eye protection/face protection.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- 29661
- Product name
- MK-3903
- Packaging
- 1mg
- Price
- $49
- Updated
- 2024/03/01
- Product number
- 29661
- Product name
- MK-3903
- Packaging
- 25mg
- Price
- $534
- Updated
- 2024/03/01
- Product number
- 29661
- Product name
- MK-3903
- Packaging
- 5mg
- Price
- $168
- Updated
- 2024/03/01
- Product number
- 29661
- Product name
- MK-3903
- Packaging
- 10mg
- Price
- $310
- Updated
- 2024/03/01
- Product number
- M424850
- Product name
- MK-3903
- Packaging
- 1mg
- Price
- $85
- Updated
- 2021/12/16
MK-3903 Chemical Properties,Usage,Production
Uses
MK-3903 is a potent and selective AMP-activated protein kinase (AMPK) activator with an EC50 of 8 nM.
in vivo
The pharmacokinetics of MK-3903 (compound 42) in C57BL/6 mice, Sprague to Dawley rats, and beagle dogs are characterized by moderate systemic plasma clearance (5.0 to13 mL/min/kg), a volume of distribution at steady state of 0.6 to 1.1 L/kg, and a terminal halflife of ~2h. Acute oral administration of MK-3903 (3, 10, and 30 mg/kg) to high-fructose fed db/+ mice results in significant inhibition of hepatic fatty acid synthesis (FAS) for all three doses[1].
IC 50
AMPK: 8 nM (EC50)
MK-3903 Preparation Products And Raw materials
Raw materials
Preparation Products
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