(4aR,9bS)-2,8-dimethyl-1,3,4,4a,5,9b-hexahydropyrido[4,3-b]indole;dihydrochloride
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(4aR,9bS)-2,8-dimethyl-1,3,4,4a,5,9b-hexahydropyrido[4,3-b]indole;dihydrochloride
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CAS No:
85248-60-8
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Formula:
C13H20Cl2N2
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Chemical Name:
(4aR,9bS)-2,8-dimethyl-1,3,4,4a,5,9b-hexahydropyrido[4,3-b]indole;dihydrochloride
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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;95751-51-2;UNII-3203ZPX474;cis-(-)-2,3,4,4a,5,9b-Hexahydro-2,8-dimethyl-1H-pyrido(4,3-b)indole dihydrochloride;3203ZPX474;85248-60-8;C13H20Cl2N2;Stobadin dihydrochloride;(+)-Stobadine dihydrochloride;(-)-Stobadine dihydrochloride;DH 1011;DH 1111;1H-Pyrido(4,3-b)indole, 2,3,4,4a,5,9b-hexahydro-2,8-dimethyl-, dihydrochloride, cis-(+)-;1H-Pyrido(4,3-b)indole, 2,3,4,4a,5,9b-hexahydro-2,8-dimethyl-, dihydrochloride, cis-(-)-;SCHEMBL2140086;DTXSID70914822;AKOS030489732;1H-Pyrido(4,3-b)indole, 2,3,4,4a,5,9b-hexahydro-2,8-dimethyl-, dihydrochloride, (4aR,9bS)-;(4aR,9bS)-2,8-dimethyl-1,3,4,4a,5,9b-hexahydropyrido[4,3-b]indole;dihydrochloride;2,8-Dimethyl-2,3,4,4a,5,9b-hexahydro-1H-pyrido[4,3-b]indole--hydrogen chloride (1/2);Rac-(4aR,9bS)-2,8-dimethyl-1H,2H,3H,4H,4aH,5H,9bH-pyrido[4,3-b]indole dihydrochloride;94452-31-0
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CAS No:
(4aR,9bS)-2,8-dimethyl-1,3,4,4a,5,9b-hexahydropyrido[4,3-b]indole;dihydrochloride Basic Attributes
275.21 g/mol
274.1003540 g/mol
3203ZPX474
Drug Information
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.)|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 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.)|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.)
(-)-stobadin
Computed Properties
Molecular Weight:275.21
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:2
Exact Mass:274.1003540
Monoisotopic Mass:274.1003540
Topological Polar Surface Area:15.3
Heavy Atom Count:17
Complexity:241
Defined Atom Stereocenter Count:2
Covalently-Bonded Unit Count:3
Compound Is Canonicalized:Yes
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