Details
Stereochemistry | ACHIRAL |
Molecular Formula | 2C8H10N6.5H2O.2H2O4S |
Molecular Weight | 666.644 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
O.O.O.O.O.OS(O)(=O)=O.OS(O)(=O)=O.NNC1=C2C=CC=CC2=C(NN)N=N1.NNC3=C4C=CC=CC4=C(NN)N=N3
InChI
InChIKey=JOPVPUGEMVRMOY-UHFFFAOYSA-N
InChI=1S/2C8H10N6.2H2O4S.5H2O/c2*9-11-7-5-3-1-2-4-6(5)8(12-10)14-13-7;2*1-5(2,3)4;;;;;/h2*1-4H,9-10H2,(H,11,13)(H,12,14);2*(H2,1,2,3,4);5*1H2
Molecular Formula | C8H10N6 |
Molecular Weight | 190.2052 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Molecular Formula | H2O4S |
Molecular Weight | 98.078 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Molecular Formula | H2O |
Molecular Weight | 18.0153 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
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 |
---|---|---|
Effects of acute hypotension and hypertension on serum TSH concentrations in male rats. | 1979 Oct |
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[Rare liver damage caused by an antihypertensive and anti-arrhythmic agents]. | 1980 Apr 1 |
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Side-effects with long-term labetalol: an open study of 251 patients in a single centre. | 1983 |
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Action of vasodilating drugs on small and large arteries of hypertensive patients. | 1983 Jul-Aug |
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Mode of antihypertensive action of nitrendipine. | 1984 |
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Additive effects of dihydralazine during enflurane or isoflurane hypotensive anaesthesia for spinal fusion. | 1988 May |
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Human cytochrome P450 2E1 is a major autoantigen associated with halothane hepatitis. | 1996 Oct-Nov |
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[Hypertensive disorders in pregnancy]. | 2001 Feb 15 |
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Plasma volume and blood pressure regulation in hypertensive pregnancy. | 2004 Jul |
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Protein adduct-trapping by hydrazinophthalazine drugs: mechanisms of cytoprotection against acrolein-mediated toxicity. | 2004 Mar |
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Flow-injection chemiluminescence determination of dihydralazine sulfate based on hexacyanoferrate(III) oxidation sensitized by eosin Y. | 2004 Oct 8 |
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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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Mechanism-based inhibition of cytochrome P450 3A4 by therapeutic drugs. | 2005 |
|
Isolated sarcoid granulomatous interstitial nephritis responding to infliximab therapy. | 2005 Feb |
|
Antihypertensive therapy in patients with pre-eclampsia: A prospective randomised multicentre study comparing dihydralazine with urapidil. | 2006 Aug |
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[Hypertension in pregnancy]. | 2006 Mar |
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Progress curve analysis of CYP1A2 inhibition: a more informative approach to the assessment of mechanism-based inactivation? | 2007 Dec |
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Method development for dihydralazine with HPLC-MS/MS--an old but tricky substance in human plasma. | 2007 Jan 17 |
|
Nitric oxide-deficiency regulates hepatic heme oxygenase-1. | 2008 Feb |
|
Maternal and fetal hemodynamic effects induced by nitric oxide donors and plasma volume expansion in pregnancies with gestational hypertension complicated by intrauterine growth restriction with absent end-diastolic flow in the umbilical artery. | 2008 Jan |
|
Synthetic and natural compounds that interact with human cytochrome P450 1A2 and implications in drug development. | 2009 |
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Hemodynamic, morphometric and autonomic patterns in hypertensive rats - Renin-Angiotensin system modulation. | 2010 |
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[Drugs during preeclampsia. Fetal risks and pharmacology]. | 2010 Apr |
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Flow-injection chemiluminescence determination of dihydralazine sulfate in serum using luminol and diperiodatocuprate (III) system. | 2010 Jan |
|
Autoimmune hepatitis triggered by nitrofurantoin: a case series. | 2010 Sep 23 |
|
A correlation between the in vitro drug toxicity of drugs to cell lines that express human P450s and their propensity to cause liver injury in humans. | 2014 Jan |
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.
Unknown
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 18:37:19 GMT 2023
by
admin
on
Fri Dec 15 18:37:19 GMT 2023
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Record UNII |
3RYP614N6L
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Record Status |
Validated (UNII)
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Record Version |
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3RYP614N6L
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71587248
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70175-06-3
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100000076099
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ANHYDROUS->SOLVATE | |||
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PARENT -> SALT/SOLVATE |
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IMPURITY -> PARENT |
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ACTIVE MOIETY |