SB408124
SB408124 Basic information
- Product Name:
- SB408124
- Synonyms:
-
- 1-(6,8-difluoro-2-methylquinolin-4-yl)-3-(4-(dimethylamino)phenyl)urea
- SB 4081241-(6,8-difluoro-2-methylquinolin-4-yl)-3-(4-(dimethylamino)phenyl)urea
- N-(6,8-DIFLUORO-2-METHYL-4-QUINOLINYL)-N'-[4-(DIMETHYLAMINO)PHENYL]UREA
- SB 408124
- SB-408124, CID4331799
- CS-1990
- SB 408124; SB408124
- Urea, N-(6,8-difluoro-2-methyl-4-quinolinyl)-N'-[4-(dimethylamino)phenyl]-
- CAS:
- 288150-92-5
- MF:
- C19H18F2N4O
- MW:
- 356.37
- EINECS:
- 604-604-1
- Product Categories:
-
- Inhibitors
- Orexin receptor
- Mol File:
- 288150-92-5.mol
SB408124 Chemical Properties
- Boiling point:
- 430.3±45.0 °C(Predicted)
- Density
- 1.371
- storage temp.
- Sealed in dry,2-8°C
- solubility
- DMSO: ~24 mg/mL
- form
- solid
- pka
- 12.12±0.43(Predicted)
- color
- olive-green
MSDS
- Language:English Provider:SigmaAldrich
SB408124 Usage And Synthesis
Uses
SB 408124 is a novel OX-1 antagonist.
Definition
ChEBI: 1-(6,8-difluoro-2-methyl-4-quinolinyl)-3-[4-(dimethylamino)phenyl]urea is a member of quinolines and an organohalogen compound.
Biological Activity
Selective non-peptide orexin OX 1 receptor antagonist (K b values are 21.7 and 1405 nM for human OX 1 and OX 2 receptors respectively). Blocks orexin-A induced grooming following oral administration in vivo .
storage
Store at RT
References
[1] langmead cj1, jerman jc, brough sj, scott c, porter ra, herdon hj.characterisation of the binding of [3h]-sb-674042, a novel nonpeptide antagonist, to the human orexin-1 receptor. br j pharmacol. 2004 jan;141(2):340-6.
[2] woldan-tambor a1, biegańska k, wiktorowska-owczarek a, zawilska jb. activation of orexin/hypocretin type 1 receptors stimulates camp synthesis in primary cultures of rat astrocytes. pharmacol rep. 2011;63(3):717-23.
[3] kis gk1, molnár ah, daruka l, gardi j, rákosi k, lászló f, lászló fa, varga c.the osmotically and histamine-induced enhancement of the plasma vasopressin level is diminished by intracerebroventricularly administered orexin in rats. pflugers arch. 2012 apr;463(4):531-6.
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