Page last updated: 2024-08-23

flutroline and butaclamol

flutroline has been researched along with butaclamol in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	2 (100.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Harbert, CA; Koe, BK; Weissman, A; Welch, WM	1
Ewing, FE; Harbert, CA; Koe, BK; Weissman, A; Welch, WM	1

Other Studies

2 other study(ies) available for flutroline and butaclamol

Article	Year
Neuroleptics from the 4a,9b-cis- and 4a,9b-trans-2,3,4,4a,5,9b-hexahydro-1H-pyrido[4,3-b]indole series. 2. Journal of medicinal chemistry, 1986, Volume: 29, Issue:10 Topics: Animals; Antipsychotic Agents; Carbolines; Hydrogen Bonding; Molecular Conformation; Rats; Receptors, Dopamine; Structure-Activity Relationship	1986
4a,9b-trans-8-Fluoro-5-(4-fluorophenyl)-2-[4-(4-fluorophenyl)-4-hydroxybutyl]-2,3,4,4a,5,9b-hexahydro-1H-pyrido[4,3-b]indole hydrochloride, a new potent neuroleptic. Journal of medicinal chemistry, 1980, Volume: 23, Issue:8 Topics: Animals; Antipsychotic Agents; Carbolines; Dextroamphetamine; Humans; In Vitro Techniques; Indoles; Models, Molecular; Rats; Receptors, Dopamine; Stereoisomerism; Stereotyped Behavior	1980

Article

Year

Neuroleptics from the 4a,9b-cis- and 4a,9b-trans-2,3,4,4a,5,9b-hexahydro-1H-pyrido[4,3-b]indole series. 2.

Journal of medicinal chemistry, 1986, Volume: 29, Issue:10

Topics: Animals; Antipsychotic Agents; Carbolines; Hydrogen Bonding; Molecular Conformation; Rats; Receptors, Dopamine; Structure-Activity Relationship

1986

4a,9b-trans-8-Fluoro-5-(4-fluorophenyl)-2-[4-(4-fluorophenyl)-4-hydroxybutyl]-2,3,4,4a,5,9b-hexahydro-1H-pyrido[4,3-b]indole hydrochloride, a new potent neuroleptic.

Journal of medicinal chemistry, 1980, Volume: 23, Issue:8

Topics: Animals; Antipsychotic Agents; Carbolines; Dextroamphetamine; Humans; In Vitro Techniques; Indoles; Models, Molecular; Rats; Receptors, Dopamine; Stereoisomerism; Stereotyped Behavior

1980