Details
Stereochemistry | ACHIRAL |
Molecular Formula | C8H10N6 |
Molecular Weight | 190.2052 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
NNC1=C2C=CC=CC2=C(NN)N=N1
InChI
InChIKey=VQKLRVZQQYVIJW-UHFFFAOYSA-N
InChI=1S/C8H10N6/c9-11-7-5-3-1-2-4-6(5)8(12-10)14-13-7/h1-4H,9-10H2,(H,11,13)(H,12,14)
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/6477782
Sources: https://www.ncbi.nlm.nih.gov/pubmed/6477782
Dihydralazine is a compound with antihypertensive properties and is in clinical trials, where is studied its effect on kidney function and hormones in healthy individuals.
Approval Year
PubMed
Title | Date | PubMed |
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Ketanserin for the treatment of preeclampsia. | 2001 |
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[Reversible loss of vision in severe preeclampsia: case report and review of the literature]. | 2003 Nov-Dec |
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3,6-Bis(2-pyridyl)di-1,2,4-triazolo[3,4-a:4',3'-c]phthalazine. | 2004 Sep |
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Morbidity and development in childhood of infants born after temporising treatment of early onset pre-eclampsia. | 2005 Jul |
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Evaluation of a strict protocol approach in managing women with severe disease due to hypertension in pregnancy: a before and after study. | 2005 Sep 30 |
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Changes in metabolism and blood flow following catecholamine stimulation in the synovial membrane measured with microdialysis. | 2006 Feb |
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Nitric oxide-deficiency regulates hepatic heme oxygenase-1. | 2008 Feb |
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Regression of glomerulosclerosis in subtotally nephrectomized rats: effects of monotherapy with losartan, spironolactone, and their combination. | 2008 Jul |
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Effects of dihydralazine on renal water and aquaporin-2 excretion in humans. | 2009 |
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[Drugs during preeclampsia. Fetal risks and pharmacology]. | 2010 Apr |
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Autoimmune hepatitis triggered by nitrofurantoin: a case series. | 2010 Sep 23 |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/6477782
The influence of a pure afterload reduction on systolic time intervals and various echocardiographic indices was assessed in six healthy volunteers, who underwent a single blind placebo controlled trial of three regimens of intravenous dihydralazine (6.25, 12.5, and 25.0 mg).
Route of Administration:
Intravenous
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/7140679
Curator's Comment: In mice bone marrow cells, dihydralazine induced a modest but statistically significant increase over controls in the frequency of sister chromatid exchanges, the rank of potencies being in this case dihydralazine greater than endralazine greater than hydralazine. In the Ames reversion test all three drugs behaved as direct-acting mutagens of low potency, whose activity was not influenced by rat liver nor by mouse liver or lung S-9 fractions. Hydralazine and dihydralazine elicited mixed genetic mechanisms of mutations, while endralazine exclusively induced frameshift errors in Salmonella DNA.
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C270
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Dihydralazine
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ACTIVE MOIETY
SALT/SOLVATE (PARENT)
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