1,2,3,4,4a,9a-Hexahydro-3,6-dimethyl-9H-pyrido[4,3-b]indole, dihydrochloride

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1,2,3,4,4a,9a-Hexahydro-3,6-dimethyl-9H-pyrido[4,3-b]indole, dihydrochloride Basic information
Product Name:1,2,3,4,4a,9a-Hexahydro-3,6-dimethyl-9H-pyrido[4,3-b]indole, dihydrochloride
Synonyms:ART-CHEM-BB B006591;AKOS B006591;2,8-DIMETHYL-2,3,4,4A,5,9B-HEXAHYDRO-1 H-PYRIDO[4,3-B ]INDOLE;TIMTEC-BB SBB001648;(-)-Stobadine;(-)-Stopadin;Stobadin;2,8-Dimethyl-2,3,4,4aR,5,9bS-hexahydro-1H-pyrido(4,3-b)indole
CAS:85202-17-1
MF:C13H18N2
MW:202.3
EINECS:
Product Categories:
Mol File:85202-17-1.mol
1,2,3,4,4a,9a-Hexahydro-3,6-dimethyl-9H-pyrido[4,3-b]indole, dihydrochloride Structure
1,2,3,4,4a,9a-Hexahydro-3,6-dimethyl-9H-pyrido[4,3-b]indole, dihydrochloride Chemical Properties
Boiling point 305.733±42.00 °C(Press: 760.00 Torr)(predicted)
density 1.044±0.06 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted)
storage temp. -20°C
solubility DMSO: >100mM
form A solid
pka8.5 (pKa2)
color White to off-white
Safety Information
MSDS Information
1,2,3,4,4a,9a-Hexahydro-3,6-dimethyl-9H-pyrido[4,3-b]indole, dihydrochloride Usage And Synthesis
UsesStobadine is a potent antioxidant and prevents free radical induced alterations in ER membrane fluidity. Stobadine can be used for effective cardio- and neuroprotectants development based on antioxidant or free radical scavenging mechanisms of action[1].
References[1] L Horáková, et al. Antioxidant and pharmacodynamic effects of pyridoindole stobadine. Gen Pharmacol. 1998 May;30(5):627-38. DOI:10.1016/s0306-3623(97)00300-5
1,2,3,4,4a,9a-Hexahydro-3,6-dimethyl-9H-pyrido[4,3-b]indole, dihydrochloride Preparation Products And Raw materials
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