Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C20H21NOS2 |
Molecular Weight | 355.517 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
C[C@H](NCC=C(C1=CSC=C1)C2=CSC=C2)[C@H](O)C3=CC=CC=C3
InChI
InChIKey=JQSHEDRVRBSFCZ-YWZLYKJASA-N
InChI=1S/C20H21NOS2/c1-15(20(22)16-5-3-2-4-6-16)21-10-7-19(17-8-11-23-13-17)18-9-12-24-14-18/h2-9,11-15,20-22H,10H2,1H3/t15-,20-/m0/s1
Tinofedrine is a dithienylamine derivative patented by Deutsche Gold- und Silber-Scheideanstalt vorm. Roessler for improvement of cerebral and peripheral blood flow. In anesthetized dogs, Tinofedrine causes a remarkable increase of cardiac output by positive inotropic and chronotropic stimulation of the heart and simultaneous reduction of peripheral vascular resistance. In comparison with typical beta-agonists Tinofedrine at isotropically equieffective doses, has a much weaker effect on the heart rate. In coronary circulation, Tinofedrine causes vasodilation so that in a therapeutic dose range increased workload is equalized by sufficient myocardial supply.
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/7222859
0.12 to 0.17 mg/kg
Route of Administration:
Intravenous
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NCI_THESAURUS |
C87053
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C018159
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m498
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3666
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C90634
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SUB11076MIG
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3033341
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ACTIVE MOIETY
SALT/SOLVATE (PARENT)