2,8-dimethyl-1,3,4,4a,5,9b-hexahydropyrido[4,3-b]indole
-
![2,8-dimethyl-1,3,4,4a,5,9b-hexahydropyrido[4,3-b]indole structure](https://file.echemi.com/fileManage/upload/canonicalSmiles/20220812/c8fa913cc689458a9d5099935258cd22.png "2,8-dimethyl-1,3,4,4a,5,9b-hexahydropyrido[4,3-b]indole")
2,8-dimethyl-1,3,4,4a,5,9b-hexahydropyrido[4,3-b]indole
structure -
-
CAS No:
17411-19-7
-
Formula:
C13H18N2
-
Chemical Name:
2,8-dimethyl-1,3,4,4a,5,9b-hexahydropyrido[4,3-b]indole
-
Synonyms:
(-)-stobadin;(-)-stobadin dihydrochloride;(-)-stobadine;(-)-stobadine dihydrochloride;2,3,4,4a,5,9b-hexahydro-2,8-dimethyl-1H-pyrido(4,3-b)indole;carbidine;DH 1011;DH-1011;dicarbine;dicarbine dihydrochloride;dicarbine dihydrochloride, (+)-isomer;dicarbine dihydrochloride, (cis)-(+)-isomer;dicarbine dihydrochloride, (cis)-(-)-isomer;dicarbine dihydrochloride, (trans)-isomer;dicarbine fumarate (1:1);dicarbine hydrochloride;dicarbine oxalate (1:1), (cis)-(+)-isomer;dicarbine, (cis)-(+)-isomer;dicarbine, (cis)-(+-)-isomer;dicarbine, (cis)-(-)-isomer;DP 10131;DP-1031;stobadin;stobadin dihydrochloride;stobadin dipalmitate;stobadine;stobadine dihydrochloride;stobadine dipalmitate;Dicarbine;17411-19-7;Carbidine;2,8-Dimethyl-2,3,4,4a,5,9b-hexahydro-1H-pyrido[4,3-b]indole;UNII-Y0EA50IJ3V;2,8-dimethyl-1,3,4,4a,5,9b-hexahydropyrido[4,3-b]indole;Y0EA50IJ3V;2,3,4,4a,5,9b-Hexahydro-2,8-dimethyl-1H-pyrido(4,3-b)indole;DSSTox_CID_26193;DSSTox_RID_81424;Dicarbine [INN];DSSTox_GSID_46193;Dicarbinum;Dicarbina;Dicarbinum [INN-Latin];Dicarbina [INN-Spanish];2,8-dimethylpiperidino[4,3-b]indoline;CAS-17411-19-7;85202-17-1;2,3,4,4a,5,9b-Hexahydro-2,8-dimethyl-1H-pyrido[4,3-b]indole;F1176-0001;NCGC00160499-01;Oprea1_207813;Oprea1_821882;CBDivE_013399;SCHEMBL169837;CHEMBL2106105;DTXSID0046193;HMS1675B02;Tox21_111858;1H-Pyrido(4,3-b)indole, 2,3,4,4a,5,9b-hexahydro-2,8-dimethyl-;BBL039601;SBB001648;STK348971;AKOS000115493;AKOS016345002;Tox21_111858_1;MCULE-1151227089;NCGC00263512-01;HY-127086;ST4048446;CS-0062539;FT-0603834;AB00276532-02;Boc-(S)-3-Amino-3-(2-naphthyl)-propionicacid;Q4161450;2,8-dimethyl-2,3,4,4a,5,9b-hexahydro-1 h-pyrido[4,3-b]indole;2,8-Dimethyl-2,3,4,4a,5,9b-hexahydro-1H-pyrido[4,3-b]indole #;5H-Pyrido[4,3-b]indole, 1,2,3,4,4a,9b-hexahydro-2,8-dimethyl-;Pyrido[3,4-b]indole, 1,2,3,4,4a,9b-hexahydro-2,8-dimethyl-;2,8-DIMETHYL-1H,2H,3H,4H,4AH,5H,9BH-PYRIDO[4,3-B]INDOLE
-
CAS No:
2,8-dimethyl-1,3,4,4a,5,9b-hexahydropyrido[4,3-b]indole Basic Attributes
202.30 g/mol
202.146998583 g/mol
Y0EA50IJ3V
DTXSID0046193
Drug Information
Agents that reduce the frequency or rate of spontaneous or induced mutations independently of the mechanism involved. (See all compounds classified as Antimutagenic Agents.)|Agents used for the treatment or prevention of cardiac arrhythmias. They may affect the polarization-repolarization phase of the action potential, its excitability or refractoriness, or impulse conduction or membrane responsiveness within cardiac fibers. Anti-arrhythmia agents are often classed into four main groups according to their mechanism of action: sodium channel blockade, beta-adrenergic blockade, repolarization prolongation, or calcium channel blockade. (See all compounds classified as Anti-Arrhythmia Agents.)|Agents that control agitated psychotic behavior, alleviate acute psychotic states, reduce psychotic symptoms, and exert a quieting effect. They are used in SCHIZOPHRENIA; senile dementia; transient psychosis following surgery; or MYOCARDIAL INFARCTION; etc. These drugs are often referred to as neuroleptics alluding to the tendency to produce neurological side effects, but not all antipsychotics are likely to produce such effects. Many of these drugs may also be effective against nausea, emesis, and pruritus. (See all compounds classified as Antipsychotic Agents.)|An agent that causes the production of physical defects in the developing embryo. (See all compounds classified as Teratogens.)|Naturally occurring or synthetic substances that inhibit or retard oxidation reactions. They counteract the damaging effects of oxidation in animal tissues. (See all compounds classified as Antioxidants.)
(-)-stobadin
Computed Properties
Molecular Weight:202.30
XLogP3:2.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Exact Mass:202.146998583
Monoisotopic Mass:202.146998583
Topological Polar Surface Area:15.3
Heavy Atom Count:15
Complexity:241
Undefined Atom Stereocenter Count:2
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
Request for Quotation