ALB-127158
ALB-127158 Basic information
- Product Name:
- ALB-127158
- Synonyms:
-
- ALB-127158
- ALB-127158A
- ALB-127158A; ALB 127158A; ALB127158A; ALB-127158(A); ALB127158(A); ALB 127158(A); ALB-127158; ALB 127158; ALB127158;1173154-32-9
- 2(1H)-Pyridinone, 4-[(5-fluoro-2-pyridinyl)methoxy]-1-(2,3,4,5-tetrahydro-5-methyl-1H-pyrido[4,3-b]indol-7-yl)-
- 4-((5-fluoropyridin-2-yl)methoxy)-1-(5-methyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indol-7-yl)pyridin-2(1H)-one
- CAS:
- 1173154-32-9
- MF:
- C23H21FN4O2
- MW:
- 404.44
- Mol File:
- 1173154-32-9.mol
ALB-127158 Chemical Properties
- Boiling point:
- 660.3±55.0 °C(Predicted)
- Density
- 1.36±0.1 g/cm3(Predicted)
- storage temp.
- Store at -20°C
- solubility
- Ethanol : 2 mg/mL (4.95 mM)
- form
- Solid
- pka
- 10.33±0.20(Predicted)
- color
- White to off-white
ALB-127158 Usage And Synthesis
Uses
ALB 127158(a), is a potent and selective melanin concentrating hormone 1 (MCH1) receptor antagonist.
in vivo
In a mouse diet induced obesity (DIO) model, ALB-127158(a) produces a significant sustained decrease in body weight and food intake in the range of 5-15 mg/kg bid. The weight reduction is predominantly due to a decrease in fat content. In high fat diet (HFD) rats, ALB-127158(a) produces significant weight loss and food reduction at doses as low as 1.25 mg/kg po. Doses > 1.25 mg/kg po produces weight loss > 6%, maximal weight loss of about 10% in rats is observed at 10 mg/kg. Following single and multiple oral administration of ALB-127158(a), ALB-127158(a) is rapidly absorbed (median tmax attains between 1 and 3 h post dose in lean and overweight/obese subjects) with a trend to decrease over dose suggesting a slower absorption rate of ALB-127158(a) at lower doses. After single doses, ALB-127158(a) has a mean half-life (t1/2) of 18 to 21 h. Slightly longer mean t1/2 estimates of approximately 26 h are obtained following multiple dosing in overweight/obese subjects; steady-state plasma ALB-127158(a) is attained within 6 to 8 days of dosing[1].
ALB-127158Supplier
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