3,6-DIBROMO-ALPHA-(1-PIPERAZINYLMETHYL)-9H-CARBAZOLE-9-ETHANOL DIHYDROCHLORIDE
3,6-DIBROMO-ALPHA-(1-PIPERAZINYLMETHYL)-9H-CARBAZOLE-9-ETHANOL DIHYDROCHLORIDE Basic information
- Product Name:
- 3,6-DIBROMO-ALPHA-(1-PIPERAZINYLMETHYL)-9H-CARBAZOLE-9-ETHANOL DIHYDROCHLORIDE
- Synonyms:
-
- BAX CHANNEL BLOCKER
- Baxchannelblocker2HCl
- 3,6-DIBROMO-ALPHA-(1-PIPERAZINYLMETHYL)-9H-CARBAZOLE-9-ETHANOL DIHYDROCHLORIDE
- 3,6-Dibromo-α-(1-piperazinylmethyl)-9H-carbazole-9-ethanoldihydrochloride
- Bax channel blocke
- Bax channel blocker(BAI-1)
- 1-(3,6-Dibromo-9H-carbazoL
- 9H-Carbazole-9-ethanol, 3,6-dibromo-α-(1-piperazinylmethyl)-
- CAS:
- 335165-68-9
- MF:
- C19H21Br2N3O
- MW:
- 467.2
- Product Categories:
-
- Caspases/Apoptosis
- Apoptosis Inhibitors
- Mol File:
- 335165-68-9.mol
3,6-DIBROMO-ALPHA-(1-PIPERAZINYLMETHYL)-9H-CARBAZOLE-9-ETHANOL DIHYDROCHLORIDE Chemical Properties
- Boiling point:
- 388.1±42.0 °C(Predicted)
- Density
- 1.71±0.1 g/cm3(Predicted)
- storage temp.
- Keep in dark place,Inert atmosphere,Room temperature
- solubility
- ≥28.2 mg/mL in DMSO with ultrasonic; insoluble in EtOH; insoluble in H2O
- form
- solid
- pka
- 14.48±0.20(Predicted)
- color
- White
3,6-DIBROMO-ALPHA-(1-PIPERAZINYLMETHYL)-9H-CARBAZOLE-9-ETHANOL DIHYDROCHLORIDE Usage And Synthesis
Uses
Bax channel blocker is a potent inhibitor of Bax-mediated mitochondrial cytochrome c release.
Biological Activity
Potent inhibitor of Bax-mediated mitochondrial cytochrome c release (IC 50 = 0.52 μ M). Suggested to inhibit Bax channel formation/activity.
in vitro
bax channel blocker, a 3,6-dibromocarbazole derivative, was observed to inhibit cytochrome c releasing from mitochondria by bax channel modulation. the monohydroxy analogue bax channel blocker remained the unprecedented inhibition of bax-induced cytochrome c release at 10 μm. the ic50 value of bax channel blocker was determined to be 0.52 μm, indicating that bax channel blocker was a bax channel inhibitor as hypothesized. moreover, in the liposome assay, bax channel blocker showing significant inhibition (>65%) of cytochrome c release at 10 μm also demonstrated sub-micromolar ic50 value [1].
IC 50
0.52 μm in bax assay
References
[1] bombrun a,gerber p,casi g,terradillos o,antonsson b,halazy s. 3,6-dibromocarbazole piperazine derivatives of 2-propanol as first inhibitors of cytochrome c release via bax channel modulation. j med chem.2003 oct 9;46(21):4365-8.
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3,6-DIBROMO-ALPHA-(1-PIPERAZINYLMETHYL)-9H-CARBAZOLE-9-ETHANOL DIHYDROCHLORIDE(335165-68-9)Related Product Information
- Carbazole-9-ethanol
- 3,6-DIBROMO-ALPHA-(1-PIPERAZINYLMETHYL)-9H-CARBAZOLE-9-ETHANOL DIHYDROCHLORIDE
- 5-Bromo-1-methyl-1H-indole
- 1-(4-[2-HYDROXY-3-(1,3,6-TRIBROMO-9H-CARBAZOL-9-YL)PROPYL]PIPERAZINO)-3-(1,3,6-TRIBROMO-9H-CARBAZOL-9-YL)PROPAN-2-OL DIHYDROCHLORIDE
- 3,6-Dibromo-9-ethylcarbazole
- 3-Bromo-9H-carbazole
- 3-(1H-INDOL-1-YL)PROPAN-1-AMINE HYDROCHLORIDE
- 5-BROMO-1-ETHYL-1H-INDOLE
- 1-PROPYL-PIPERAZINE MONOHYDROBROMIDE
- 1-(3,6-DIBROMO-9H-CARBAZOL-9-YL)-3-(DIMETHYLAMINO)PROPAN-2-OL
- 1-N-PROPYLPIPERAZINE DIHYDROBROMIDE
- 3,6-Dibromocarbazole