[CAS NO. 136609-26-2] RP 70676
PRODUCTS SPECIFICATIONS [136609-26-2]
DESCRIPTION [136609-26-2]
Overview
| MDL | - |
|---|---|
| Molecular Weight | 416.58 |
| Molecular Formula | C25H28N4S |
| SMILES | CC1=CC(C)=NN1CCCCCSC2=NC(C3=CC=CC=C3)=C(C4=CC=CC=C4)N2 |
Summary
IC50 & Target
IC50: 25 nM (Rat ACAT), 44 nM (Rabbit ACAT) [1]
In Vitro
RP 70676 is a potent inhibitor of rabbit arterial ACAT (IC 50 = 40 nM) and has been shown to be an effective inhibitor of ACAT derived from a number of tissues and species including man. The IC 50 values range from 21 nM for hamster liver ACAT to 108 nM for enzyme from the intestine of cholesterol fed rabbits; in human hepatic tissues the mean IC 50 is 44 nM. In whole cell P388D, murine macrophages the compound has an IC 50 of 540 nM.
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
In Vivo
RP 70676 (10 mg/kg, p.o.) is well absorbed with plasma levels in NZW rabbits [1] .
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Appearance
Solid
Shipping
Room temperature in continental US; may vary elsewhere.
Storage
| Powder | -20°C | 3 years |
|---|---|---|
| 4°C | 2 years | |
| In solvent | -80°C | 6 months |
| -20°C | 1 month |
Solvent & Solubility
DMSO : 125 mg/mL ( 300.06 mM ; Need ultrasonic)
Stock Solutions
| Concentration Solvent Mass | 1 mg | 5 mg | 10 mg |
|---|
| 1 mM | 2.4005 mL | 12.0025 mL | 24.0050 mL |
| 5 mM | 0.4801 mL | 2.4005 mL | 4.8010 mL |
| 10 mM | 0.2400 mL | 1.2002 mL | 2.4005 mL |
