Elslager, Edward F.’s team published research in Journal of Heterocyclic Chemistry in 1973 | CAS: 50292-25-6

Journal of Heterocyclic Chemistry published new progress about Antimalarials. 50292-25-6 belongs to class chlorides-buliding-blocks, name is 3,4-Dichlorobenzene-1-carboximidamide hydrochloride, and the molecular formula is C7H7Cl3N2, Related Products of chlorides-buliding-blocks.

Elslager, Edward F. published the artcileAntimalarial drugs. 34. Synthesis of 5,5′-[[3-(dimethylamino)propyl]imino]bis[3-(trichloromethyl)-1,2,4-thiadiazole] and related thiadiazoles as antimalarial agents, Related Products of chlorides-buliding-blocks, the main research area is antimalarial thiadiazole derivative.

The condensation of 5-chloro-3-(trichloromethyl)-1,2,4-thiadiazole with N,N-dimethyl-1,3-propanediamine gave 5-[[3-(dimethylamino)propyl]-amino]-3-(trichloromethyl)-1,2,4-thiadiazole and 5,5′-[[3-(dimethylamino)propyl]imino]bis[3-(trichloromethyl)-1,2,-4-thiadiazole] (I), together with 5,5′-[(3-methyl[3-(trichloromethyl)-1,2,4-thiadiazole-5-yl]amino]propyl)imino]bis[3-(trichloromethyl)-1,2,4-thiadiazole] which was formed by a displacement of the distal methyl group of I. The antimalarial activity of I prompted the preparation of 5-amino-3-(trichloromethyl, methyl, and 3,4-dichlorophenyl)-1,2,-4-thiadiazoles and 5,5′-[[(dialkylamino)alkyl]imino]bis[3-(trichloromethyl, methyl, and 3,4-dichlorophenyl)-1,2,4-thiadiazoles] from an amine and the requisite 5-chloro-3-substituted-1,2,4-thiadiazoles, which were prepared from the appropriate amidine and trichloromethylsulfenyl chloride. 5-[3-[(Diethylamino)methyl]-p-anisidino]-3-(trichloromethyl)-1,2,-4-thiadiazole was active against a chloroquine-resistant line of Plasmodium berghei in the mouse. Structure-activity relations against P. berghei in mice and P. gallinaceum in chicks are discussed.

Journal of Heterocyclic Chemistry published new progress about Antimalarials. 50292-25-6 belongs to class chlorides-buliding-blocks, name is 3,4-Dichlorobenzene-1-carboximidamide hydrochloride, and the molecular formula is C7H7Cl3N2, Related Products of chlorides-buliding-blocks.

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Fuller, Ray W.’s team published research in Journal of Medicinal Chemistry in 1975 | CAS: 50292-25-6

Journal of Medicinal Chemistry published new progress about Structure-activity relationship. 50292-25-6 belongs to class chlorides-buliding-blocks, name is 3,4-Dichlorobenzene-1-carboximidamide hydrochloride, and the molecular formula is C7H7Cl3N2, HPLC of Formula: 50292-25-6.

Fuller, Ray W. published the artcileNorepinephrine N-methyltransferase inhibition by benzamidines, phenylacetamidines, benzylguanidines, and phenylethylguanidines, HPLC of Formula: 50292-25-6, the main research area is norepinephrine methyltransferase inhibitor amidine; guanidine aryl methyltransferase inhibitor.

Mono- and dichloro derivatives of 21 title compounds and 18 benzylamines, α-methylbenzylamines, and amphetamines were studied as inhibitors of norepinephrine N-methyltransferase (EC 2.1.1.28) [9037-68-7]. The 2 most effective inhibitors in vitro were 2,3-dichlorobenzamidine-HCl (I-HCl) [55154-87-5] and 3,4-dichlorophenylacetamidine (II) [55154-91-1] with pI50 values of 5.55 and 5.36, resp. I and II are reversible inhibitors and competitive with norepinephrine in vitro, but are not effective in blocking enzyme activity in vivo in rats.

Journal of Medicinal Chemistry published new progress about Structure-activity relationship. 50292-25-6 belongs to class chlorides-buliding-blocks, name is 3,4-Dichlorobenzene-1-carboximidamide hydrochloride, and the molecular formula is C7H7Cl3N2, HPLC of Formula: 50292-25-6.

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics