Compounds > pinacidil
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pinacidil and 7-chloro-3-isopropylamino-4h-1,2,4-benzothiadiazine 1,1-dioxide

pinacidil has been researched along with 7-chloro-3-isopropylamino-4h-1,2,4-benzothiadiazine 1,1-dioxide in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (66.67)29.6817
2010's1 (33.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Antoine, MH; Becker, B; Boverie, S; Dabrowski, M; de Tullio, P; Hansen, JB; Lebrun, P; Ouedraogo, R; Pirotte, B; Sebille, S; Somers, F; Wahl, P1
Antoine, MH; Becker, B; de Tullio, P; Florence, X; Lebrun, P; Michaux, C; Pirotte, B; Sebille, S; Wouters, J1
Boverie, S; de Tullio, P; Lebrun, P; Michaux, C; Pirotte, B1

Other Studies

3 other study(ies) available for pinacidil and 7-chloro-3-isopropylamino-4h-1,2,4-benzothiadiazine 1,1-dioxide

ArticleYear
Toward tissue-selective pancreatic B-cells KATP channel openers belonging to 3-alkylamino-7-halo-4H-1,2,4-benzothiadiazine 1,1-dioxides.
    Journal of medicinal chemistry, 2003, Jul-17, Volume: 46, Issue:15

    Topics: Adenosine Triphosphate; Animals; Aorta; Benzothiadiazines; Diazoxide; Female; Glucose; In Vitro Techniques; Insulin; Insulin Secretion; Ion Channel Gating; Islets of Langerhans; Isomerism; Molecular Conformation; Muscle Relaxation; Muscle, Smooth, Vascular; Oocytes; Organ Specificity; Patch-Clamp Techniques; Potassium Channels; Rats; Rats, Wistar; Structure-Activity Relationship; Xenopus laevis

2003
New R/S-3,4-dihydro-2,2-dimethyl-6-halo-4-(phenylaminothiocarbonylamino)-2H-1-benzopyrans structurally related to (+/-)-cromakalim as tissue-selective pancreatic beta-cell K(ATP) channel openers.
    Bioorganic & medicinal chemistry, 2008, May-15, Volume: 16, Issue:10

    Topics: Animals; Aorta; ATP-Binding Cassette Transporters; Benzopyrans; Cromakalim; Diazoxide; Drug Evaluation, Preclinical; Insulin-Secreting Cells; Molecular Structure; Pinacidil; Potassium Channels; Quantum Theory; Rats; Rats, Wistar; Stereoisomerism; Structure-Activity Relationship; Temperature; Time Factors

2008
Impact of the nature of the substituent at the 3-position of 4H-1,2,4-benzothiadiazine 1,1-dioxides on their opening activity toward ATP-sensitive potassium channels.
    Journal of medicinal chemistry, 2011, May-12, Volume: 54, Issue:9

    Topics: Animals; Aorta; Benzothiadiazines; Diazoxide; Female; Hydrogen Bonding; Hydrogen-Ion Concentration; In Vitro Techniques; Insulin; Insulin Secretion; Insulin-Secreting Cells; Ion Channel Gating; KATP Channels; Models, Molecular; Molecular Conformation; Muscle Contraction; Muscle Relaxation; Muscle, Smooth; Rats; Rats, Wistar; Stereoisomerism; Structure-Activity Relationship; Uterus

2011