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Chemical compound
Cyclopropylamine is the organic compound with the formula C3H5NH2. It is a simple amine derivative of cyclopropane. As a precursor to pesticides and pharmaceuticals
Cyclopropylamine
Pharmaceutical compound
(TMT), also known as MCPA as well as trans-2-(3,4,5-trimethoxyphenyl)cyclopropylamine, is a possible psychedelic drug of the phenethylamine, scaline, and
3,4,5-Trimethoxytranylcypromine
3,4,5-Trimethoxytranylcypromine
Pharmaceutical compound
(1R,2R)-cyclopropylhistamine, or (1R,2R)-trans-2-(1H-imidazol-4-yl)cyclopropylamine, is a histamine H3 receptor agonist which was under development for
GT-2203
Class of compounds based upon the amphetamine structure
2010. The isopropylamine side chain of amphetamine is cyclized into a cyclopropylamine ring structure in tranylcypromine. Ghodse, Hamid (2002). Drugs and
Substituted_amphetamine
Chemical reaction
Chaplinski, V.; De Meijere, A. (1996). "A Versatile New Preparation of Cyclopropylamines from Acid Dialkylamides". Angew. Chem. Int. Ed. 35 (4): 413–14. doi:10
Kulinkovich_reaction
Chemical compound
Cyclopentylamine is a member of the aminocycloalkanes, which also includes cyclopropylamine, cyclobutylamine, and cyclohexylamine. Cyclopentylamine can be prepared
Cyclopentylamine
Chemical compound
"Small-Ring Compounds. VI. Cyclopropanol, Cyclopropyl Bromide and Cyclopropylamine". Journal of the American Chemical Society. 73 (7): 3176–3179. doi:10
Chlorocyclopropane
Chemical compound
"Small-Ring Compounds. VI. Cyclopropanol, Cyclopropyl Bromide and Cyclopropylamine". Journal of the American Chemical Society. 73 (7): 3176–3179. Bibcode:1951JAChS
Bromocyclopropane
Pharmaceutical compound
N-cyclopropyltryptamine, made from indole-3-oxalylchloride and benzyl cyclopropylamine with eventual hydrogenolysis of the benzyl group; mp 180–182. This
N-Cyclopropyltryptamine
Chemical compound
Cyclobutylamine is a member of the aminocycloalkanes, which also includes cyclopropylamine, cyclopentylamine, and cyclohexylamine. Oxidation with potassium permanganate
Cyclobutylamine
Chemical compound
prepared by a Pd-catalyzed cross coupling of 2,6-dibromotoluene and cyclopropylamine (Buchwald-Hartwig coupling). "Skin health". Health Canada. 9 May 2018
Ozenoxacin
Index of chemical compounds with the same molecular formula
(2-propen-1-amine) Aminocyclopropane Azetidine (trimethylenimine) Cyclopropylamine 2-Methylaziridine N-Methylaziridine This set index page lists chemical
C3H7N
Pharmaceutical compound
2006). Vangveravong S (1994). "Synthesis of trans-2-(indol-3-yl)cyclopropylamines: Rigid tryptamine analogues". ProQuest. ProQuest 304131663. Retrieved
1-Propyl-5-MeO-AMT
Canadian chemist
alkylamines) Ni/CyPAd-DalPhos (primary and secondary aliphatic alcohols, cyclopropylamine and variants) Ni/PAd-DalPhos (ammonia and primary alkylamines) Pd/Mor-DalPhos
Mark_Stradiotto
Chemical compound
PMID 24360800. Bertus P, Caillé J (March 2025). "Advances in the Synthesis of Cyclopropylamines". Chemical Reviews. 125 (6): 3242–3377. doi:10.1021/acs.chemrev.4c00674
Risdiplam
isopropyl mercuric iodide 38455-14-0 C3H7N azetidine 503-29-7 C3H7N cyclopropylamine 765-30-0 C3H7NO isoxazolidine 504-72-3 C3H7NO propanamide 79-05-0 C3H7NO2
List of compounds with carbon number 3
List_of_compounds_with_carbon_number_3
Chemical compound
"Small-Ring Compounds. VI. Cyclopropanol, Cyclopropyl Bromide and Cyclopropylamine". J. Am. Chem. Soc. 73 (7): 3176–3179. doi:10.1021/ja01151a053. Jongejan
Cyclopropanol
Chemical compound
2023-08-27. Vangveravong S (1994). "Synthesis of trans-2-(indol-3-yl)cyclopropylamines: Rigid tryptamine analogues". ProQuest. ProQuest 304131663. Retrieved
5-MeO-AMT
PMID 19284718. Bertus P, Caillé J (March 2025). "Advances in the Synthesis of Cyclopropylamines". Chem Rev. 125 (6): 3242–3377. doi:10.1021/acs.chemrev.4c00674. PMID 40048498
Phenylcyclopropylmethylamine
MAOI antidepressant
agents that were developed at that time. The condensation between cyclopropylamine [765-30-0] (1) and benzaldehyde [100-52-7] (2) gives N-benzylidenecyclopropylamine
Encyprate
Class of compounds
Vangveravong, Suwanna (1994). "Synthesis of trans-2-(indol-3-yl)cyclopropylamines: Rigid tryptamine analogues". ProQuest. Retrieved 22 March 2025. Although
Serotonin_releasing_agent
Drug class of antiplatelet agents
the optimization of pharmacokinetic properties. Addition of phenyl cyclopropylamine substituent in the 5 position gave high affinities. From this the first
Adenosine diphosphate receptor inhibitor
Adenosine_diphosphate_receptor_inhibitor
Pharmaceutical compound
receptors [88]. Vangveravong S (1994). Synthesis of trans-2-(indol-3-yl)cyclopropylamines: Rigid tryptamine analogues (Ph.D. thesis). Purdue University. ProQuest 304131663
LY-178210
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