2,4-Diamino-6,7-dimethoxyquinoline derivatives as alpha 1-adrenoceptor antagonists and antihypertensive agents.
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Synthesis of Substituted Quinolines by the Electrophilic Cyclization of N-(2-Alkynyl)anilines.6-Chloro-2-methyl-4-phenyl-3-[1-phenyl-5-(2-thien-yl)-4,5-dihydro-1H-pyrazol-3-yl]quinoline6-Chloro-3-[5-(3-meth-oxy-8-methyl-4-quinol-yl)-1-phenyl-4,5-dihydro-1H-pyrazol-3-yl]-2-methyl-4-phenyl-quinoline.1-(6-Chloro-2-methyl-4-phenyl-3-quinol-yl)ethanone.7-Chloro-3,3-dimethyl-9-phenyl-1,2,3,4-tetra-hydro-acridin-1-one.3-Acetyl-6-chloro-2-methyl-4-phenyl-quinolinium hydrogen sulfate.3-Acetyl-6-chloro-2-methyl-4-phenyl-quinolinium perchlorate.(2E,4E)-1-(6-Chloro-2-methyl-4-phenyl-3-quinol-yl)-5-phenyl-penta-2,4-dien-1-one.2-Cyano-quinolin-1-ium hydrogen sulfate.8-Hy-droxy-quinolin-1-ium nitrate.2-Cyano-quinolin-1-ium nitrate.4-Meth-oxy-quinolinium-2-carboxyl-ate dihydrate.(E)-1-(2-Methyl-4-phenyl-quinolin-3-yl)-3-phenyl-prop-2-en-1-oneRecent advances in the design and synthesis of prazosin derivatives.Identification of 2,4-diamino-6,7-dimethoxyquinoline derivatives as G9a inhibitors†Electronic supplementary information (ESI) available. See DOI: 10.1039/c4md00274a.(2E)-1-(6-Chloro-2-methyl-4-phenyl-quinolin-3-yl)-3-phenyl-prop-2-en-1-one.4-Chloro-3-methyl-phenyl quinoline-2-carboxyl-ate.3,4-Di-methyl-phenyl quinoline-2-carboxyl-ate.Tandem Cu-catalyzed ketenimine formation and intramolecular nucleophile capture: Synthesis of 1,2-dihydro-2-iminoquinolines from 1-(o-acetamidophenyl)propargyl alcohols2-Isopropyl-5-methyl-cyclo-hexyl quinoline-2-carboxyl-ate.(E)-1-(2,4-Dimethyl-quinolin-3-yl)-3-(4-methyl-phen-yl)prop-2-en-1-one.N-[(2-Chloro-3-quinol-yl)meth-yl]-4-fluoro-aniline.(2E)-3-(4-Bromo-phen-yl)-1-(2-methyl-4-phenyl-3-quinol-yl)prop-2-en-1-one.4-Methyl-phenyl quinoline-2-carboxyl-ate.3-(4-Chloro-phen-yl)-1-(2-methyl-4-phenyl-quinolin-3-yl)prop-2-en-1-one.(2E)-3-(4-Chloro-phen-yl)-1-(2,4-dimethyl-quinolin-3-yl)prop-2-en-1-oneHistone lysine methyltransferase structure activity relationships that allow for segregation of G9a inhibition and anti-Plasmodium activity† †The authors declare no competing interests. ‡ ‡Electronic supplementary information (ESI) available: SuppleHistone lysine methyltransferase structure activity relationships that allow for segregation of G9a inhibition and anti-Plasmodium activity.Facile Synthesis and Photophysical Characterization of New Quinoline Dyes.
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P2860
2,4-Diamino-6,7-dimethoxyquinoline derivatives as alpha 1-adrenoceptor antagonists and antihypertensive agents.
description
1988 nî lūn-bûn
@nan
1988年の論文
@ja
1988年論文
@yue
1988年論文
@zh-hant
1988年論文
@zh-hk
1988年論文
@zh-mo
1988年論文
@zh-tw
1988年论文
@wuu
1988年论文
@zh
1988年论文
@zh-cn
name
2,4-Diamino-6,7-dimethoxyquino ...... s and antihypertensive agents.
@en
2,4-Diamino-6,7-dimethoxyquino ...... s and antihypertensive agents.
@nl
type
label
2,4-Diamino-6,7-dimethoxyquino ...... s and antihypertensive agents.
@en
2,4-Diamino-6,7-dimethoxyquino ...... s and antihypertensive agents.
@nl
prefLabel
2,4-Diamino-6,7-dimethoxyquino ...... s and antihypertensive agents.
@en
2,4-Diamino-6,7-dimethoxyquino ...... s and antihypertensive agents.
@nl
P2093
P356
P1476
2,4-Diamino-6,7-dimethoxyquino ...... s and antihypertensive agents.
@en
P2093
Campbell SF
Hardstone JD
P304
P356
10.1021/JM00400A025
P407
P577
1988-05-01T00:00:00Z