Details
Stereochemistry | ACHIRAL |
Molecular Formula | C12H16ClN3O3S |
Molecular Weight | 317.792 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=C(NS(C)(=O)=O)C(Cl)=CC=C1OCC2=NCCN2
InChI
InChIKey=FOYWMEJSRSBQGB-UHFFFAOYSA-N
InChI=1S/C12H16ClN3O3S/c1-8-10(19-7-11-14-5-6-15-11)4-3-9(13)12(8)16-20(2,17)18/h3-4,16H,5-7H2,1-2H3,(H,14,15)
Dabuzalgron is an orally active and selective alpha1A/1L-adrenoreceptor partial agonist, developed by Roche. In anesthetized micropigs and rabbits, dabuzalgron produced non-selective, dose-dependent increases in intraurethral and arterial blood pressures. In conscious micropigs, both agents produced dose-dependent increases in urethral tension. Dabuzalgron was investigated in a clinical study in women with stress urinary incontinence (SUI). It was demonstrated that 1.5 mg of the drug administered twice daily lead to a significantly lower mean weekly number of SUI episodes with little or no cardiovascular effect. Despite positive results, no development of the drug was reported by Roche.
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
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Target ID: P35348|||B0ZBD9|||Q6RUJ8 Gene ID: 148.0 Gene Symbol: ADRA1A Target Organism: Homo sapiens (Human) Sources: https://www.ncbi.nlm.nih.gov/pubmed/28286875 |
21.0 nM [EC50] |
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NCI_THESAURUS |
C29709
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C481520
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C75036
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ACTIVE MOIETY
SALT/SOLVATE (PARENT)