Page last updated: 2024-09-03

a 68930 and oxidopamine

a 68930 has been researched along with oxidopamine in 5 studies

Compound Research Comparison

Studies
(a 68930)
Trials
(a 68930)
Recent Studies (post-2010)
(a 68930)
Studies
(oxidopamine)
Trials
(oxidopamine)
Recent Studies (post-2010) (oxidopamine)
632198,63062,407

Protein Interaction Comparison

ProteinTaxonomya 68930 (IC50)oxidopamine (IC50)
Glyceraldehyde-3-phosphate dehydrogenaseHomo sapiens (human)8
DNA repair protein RAD52 homologHomo sapiens (human)0.779

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's5 (100.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Breese, GR; Criswell, HE; Jensen, KF; Johnson, KB; Mueller, RA; Simson, PE1
Ackerman, M; Artman, L; Asin, KE; Bednarz, L; Briggs, C; Britton, DR; DeNinno, MP; MacKenzie, R; Schoenleber, R; Trugman, JM1
Britton, DR; Curzon, P; Kebabian, JW1
Asin, KE; DeNinno, MP; Kebabian, JW; MacKenzie, R; Schoenleber, R1
Asin, K; Briggs, C; Britton, DR; DeNinno, M; Kebabian, JW; MacKenzie, RG; McKelvy, JF; Schoenleber, R1

Reviews

1 review(s) available for a 68930 and oxidopamine

ArticleYear
A68930: a potent and specific agonist for the D-1 dopamine receptor.
    American journal of hypertension, 1990, Volume: 3, Issue:6 Pt 2

    Topics: Animals; Benzopyrans; Chromans; Corpus Striatum; Denervation; Dopamine; Hydroxydopamines; Oxidopamine; Parkinson Disease; Rats; Receptors, Dopamine; Receptors, Dopamine D1; Stereoisomerism

1990

Other Studies

4 other study(ies) available for a 68930 and oxidopamine

ArticleYear
Comparison of the D1-dopamine agonists SKF-38393 and A-68930 in neonatal 6-hydroxydopamine-lesioned rats: behavioral effects and induction of c-fos-like immunoreactivity.
    The Journal of pharmacology and experimental therapeutics, 1992, Volume: 262, Issue:2

    Topics: 2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine; Animals; Animals, Newborn; Behavior, Animal; Benzazepines; Brain Chemistry; Chromans; Dopamine Agents; Dose-Response Relationship, Drug; Female; Motor Activity; Oxidopamine; Proto-Oncogene Proteins c-fos; Rats; Receptors, Dopamine; Receptors, Dopamine D1; Stereotyped Behavior

1992
A68930: a potent agonist selective for the dopamine D1 receptor.
    European journal of pharmacology, 1991, Jun-25, Volume: 199, Issue:2

    Topics: Adenylyl Cyclases; Animals; Benzazepines; Binding Sites; Carps; Chromans; Deoxyglucose; Dopamine Agents; Haloperidol; Male; Motor Activity; Oxidopamine; Rats; Rats, Inbred Strains; Receptors, Adrenergic, alpha; Receptors, Adrenergic, beta; Receptors, Dopamine; Receptors, Dopamine D1; Seizures; Substantia Nigra; Tumor Cells, Cultured

1991
Rapid reversal of denervation supersensitivity of dopamine D1 receptors by l-dopa or a novel dopamine D1 receptor agonist, A68930.
    European journal of pharmacology, 1991, Jul-23, Volume: 200, Issue:1

    Topics: 2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine; Analysis of Variance; Animals; Chromans; Denervation; Dopamine Agents; Levodopa; Male; Motor Activity; Oxidopamine; Rats; Rats, Inbred Strains; Receptors, Dopamine; Receptors, Dopamine D1

1991
(1R,3S)-1-(aminomethyl)-3,4-dihydro-5,6-dihydroxy-3-phenyl-1H-2-benzopyran: a potent and selective D1 agonist.
    Journal of medicinal chemistry, 1990, Volume: 33, Issue:11

    Topics: Animals; Benzazepines; Binding, Competitive; Chromans; Dopamine Agents; Hydroxydopamines; Molecular Structure; Oxidopamine; Rats; Receptors, Dopamine; Receptors, Dopamine D1; Stereoisomerism

1990