304-20-1 Usage
Uses
Used in Pharmaceutical Industry:
Hydralazine hydrochloride is used as an antihypertensive agent for the treatment of high blood pressure and heart failure. It is also used as a vasodilator to study its effects on hypertension in T-cell frequencies in juvenile rats, myocardial ischemia-reperfusion (I/R) injury, and insulin secretion and glucose tolerance.
Used in Epigenetic Regulation:
Hydralazine hydrochloride is used as an inhibitor of DNA methyltransferase, modulating the epigenetic regulation of gene expression. It is a non-selective MAO-A/B inhibitor and a semicarbazide-sensitive amine oxidase inhibitor.
Used in Cancer Research:
Hydralazine is a non-nucleoside analog that inhibits DNA methylation and reactivates the expression of tumor suppressor genes. It is used in cancer research as a non-selective MAO-A/B inhibitor and a semicarbazide-sensitive amine oxidase inhibitor.
Chemical Properties:
Hydralazine hydrochloride is a white crystalline solid.
Brand Names:
Apresoline (Novartis) and Dralzine (Teva) are brand names for hydralazine hydrochloride.
Originator
Apresoline HCl,Ciba,US,1952
Manufacturing Process
30 parts by weight of phthalazone are converted to 1-chlorophthalazine by the
method described in Ber. d. deutsch. chem. Ges., vol 26, page 521 (1893).
The freshly obtained yet moist chloro compound is heated on the water bath
for two hours in a mixture of 100 parts by volume of ethyl alcohol and 90
parts by volume of hydrazine hydrate. Preferably after filtering, 1-hydrazinephthalazine crystallizes out in yellow needles on cooling.
It is filtered with suction and washed with cold ethyl alcohol. The compound is
crystallized from methyl alcohol, and melts, when rapidly heated, at 172° to
173°C. On warming in alcoholic or aqueous hydrochloric acid, the
hydrochloride of MP 273°C (with decomposition) is obtained.
Therapeutic Function
Antihypertensive
Contact allergens
Hydralazine is a hydrazine derivative used as a antihypertensive
drug. Skin rashes have been described during
treatment. Exposure occurs mainly in the pharmaceutical
industry. Cross-sensitivity is frequent with hydrazine,
which is considered to be a potent sensitizer.
Biochem/physiol Actions
Hydralazine hydrochloride has therapeutic effects against heart failure and high blood pressure.
Mechanism of action
The only drug in this group, hydralazine, does not fit neatly into the other mechanistic classes, in part because its
mechanism of action is not entirely clear. It appears to have multiple, direct effects on the VSM. Hydralazine, a
phthalazine-substituted hydrazine antihypertensive drug with a pKa of 7.3, is highly specific for arterial vessels,
producing its vasodilation by a couple of different mechanisms. First, it causes smooth muscle hyperpolarization, quite
likely through the opening of K+
channels. Activation therefore increases the efflux of potassium ions from the cells,
causing hyperpolarization of VSM cells and, thus, prolonging the opening of the potassium channel and sustaining a
greater vasodilation on arterioles than on veins. It also may inhibit the second messenger, IP3-induced release of
calcium from the smooth muscle sarcoplasmic reticulum (the PIP2 signal transduction pathway). Finally,
hydralazine stimulates the formation of NO by the vascular endothelium, leading to cGMP-mediated vasodilation. The arterial vasodilator action of hydralazine reduces systemic vascular resistance and arterial pressure.
Diastolic blood pressure usually is decreased more than systolic pressure is. The hydralazine-induced decrease in
blood pressure and peripheral resistance causes a reflex response, which is accompanied by increased heart rate,
cardiac output, stroke volume, and an increase in plasma renin activity. It has no direct effect on the heart. This
reflex response could offset the hypotensive effect of arteriolar dilation, limiting its antihypertensive effectiveness.
Hydralazine also causes sodium and water retention and expansion of plasma volume, which could develop tolerance
to its antihypertensive effect during prolonged therapy. Thus, coadministration of a diuretic improves the therapeutic
outcome.
Pharmacokinetics
Hydralazine is well absorbed from the GI tract and is metabolized in the GI mucosa (prehepatic systemic metabolism)
and in the liver by acetylation, hydroxylation, and conjugation with glucuronic acid. Little
of the hydralazine dose is excreted unchanged in urine but mainly as metabolites, which are without significant
therapeutic activity. A small amount of hydralazine is reportedly converted to a hydrazone, most likely with vitamin B6
(pyridoxine), which may be responsible for some its neurotoxic effects. Following the oral administration of hydralazine,
its antihypertensive effect begins in 20 to 30 minutes and lasts 2 to 4 hours. The plasma half-life of hydralazine
generally is 2 to 4 hours but, in some patients, may be up to 8 hours (i.e., slow acetylators). In slow acetylator patients
or those with impaired renal function, the plasma concentrations for hydralazine are increased and, possibly,
prolonged. Approximately 85% of hydralazine in the blood is bound to plasma proteins following administration of usual
doses.
First-pass acetylation in the GI mucosa and liver is related to genetic acetylator phenotype. Acetylation phenotype
is an important determinant of the plasma concentrations of hydralazine when the same dose of hydralazine is
administered orally. Slow acetylators have an autosomal recessive trait that results in a relative deficiency of the
hepatic enzyme N-acetyl transferase, thus prolonging the elimination half-life of hydralazine. This
population of hypertensive patients will require an adjustment in dose to reduce the increased overactive response.
Approximately 50% of African Americans and Caucasians, and the majority of American Indians, Eskimos, and Orientals
are rapid acetylators of hydralazine. This population of patients will have subtherapeutic plasma concentrations of
hydralazine because of its rapid metabolism to inactive metabolites and shorter elimination times. Patients with
hydralazine-induced systemic lupus erythematosus frequently are slow acetylators.
Clinical Use
Hydralazine hydrochloride is useful in the treatment ofmoderate-to-severe hypertension. It is often used in conjunctionwith less potent antihypertensive agents, becauseside effects occur frequently when it is used alone in adequatedoses. In combinations, it can be used in lower andsafer doses. Its action appears to be centered on the smoothmuscle of the vascular walls, with a decrease in peripheralresistance to blood flow. This results in increased bloodflow through the peripheral blood vessels. It also has theunique property of increasing renal blood flow, an importantconsideration in patients with renal insufficiency.Hydralazine hydrochloride acts on vascular smooth muscleto cause relaxation. Its mechanism of action is unclear. Itinterferes with Ca2+ entry andCa2+release from intracellularstores and reportedly causes activation of guanylate cyclase,resulting in increased levels of cGMP. All of thesebiochemical events can cause vasodilation.
Drug interactions
The coadministration of diuretics and other hypotensive drugs may have a synergistic effect, resulting in a marked
decrease in blood pressure.
Metabolism
Hydralazine undergoes considerable first-pass
metabolism by acetylation in the gastrointestinal
mucosa and liver. The rate of metabolism is genetically
determined and depends upon the acetylator status of
the individual. Systemic metabolism in the liver is by
hydroxylation of the ring system and conjugation with
glucuronic acid; most sources suggest that N-acetylation
is not of major importance in systemic clearance and that
therefore acetylator status does not affect elimination.
Hydralazine is excreted mainly in urine as metabolites.
Purification Methods
It crystallises from MeOH and has m 172-173o(dec). [Druey et al. Helv Chim Acta 34 195 1951, Beilstein 25 III/IV 4552.] It is an antihypertensive.
Check Digit Verification of cas no
The CAS Registry Mumber 304-20-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,0 and 4 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 304-20:
(5*3)+(4*0)+(3*4)+(2*2)+(1*0)=31
31 % 10 = 1
So 304-20-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H8N4.ClH/c9-11-8-7-4-2-1-3-6(7)5-10-12-8;/h1-5H,9H2,(H,11,12);1H/p-1
304-20-1Relevant articles and documents
Synthesis and characterization of various alkyl, aryl and hetero aryl substituted hydrazines and study of their biological activity
Gupta, Anil,Goklani, Poonam
, p. 1041 - 1044 (2017)
Due to the presence of N-N linkage hydrazines are well-known for their diverse biological activity.N-N linkage has been used as a key structural motif in various bioactive agents. A series of aryl, alkyl and hetero aryl substituted hydrazine derivatives has been synthesized, for this diazotization of alkyl, aryl amines has been done, followed by reduction with stannous chloride or sodium sulfite. All synthesized compounds were characterized by elemental analysis, IR, 1H-NMR, Mass spectra and their biological activity has been studied.
Access to phthalazinones via palladium-catalyzed three-component cycloamino-carbonylation of 2-formylaryl tosylates, hydrazines and CO
Liu, Bin,Zhang, Chunlei,Zhou, Xigeng
, p. 8282 - 8286 (2016/12/02)
The palladium-catalyzed three-component cycloaminocarbonylation of 2-formylaryl tosylates with hydrazines and carbon monoxide has been established, which provides an efficient method for synthesis of substituted phthalazinones. In addition, by applying this protocol as the key step, Hydralazine can easily be synthesized in 65% yield.
Manufacture of pure hydralazine salts
-
Page/Page column 4; 6, (2008/06/13)
The present invention provides an improved process of preparing hydralazine hydrochloride, which involves the preparation of 1-chlorophthalazine salt and further reacting with hydrazine followed by purification of hydralazine hydrochloride, which is free of phosphate, does not contain any individual impurities more than 0.05%, total impurities less than 0.5%, and a hydrazine content of not more than 0.001%, and preferably less than 0.0003%. One benefit of improved purity is enhanced storage stability.
Synthesis of hydrazine derivatives of pyridazine
-
Page/Page column 7, (2008/06/13)
The present invention relates to both a novel method of preparing hydralazine hydrochloride and to a novel method of preparing hydrazine derivatives of compounds containing a pyridazine ring, including, for example, pyridazines, phthalazines and other compounds containing the pyridazine ring.
Stable hydrazalazine pharmaceutical compositions
-
Page/Page column 6-7, (2008/06/13)
The present invention relates to stable and highly purified stable hydralazine hydrochloride compositions and stable hydralazine-containing pharmaceutical compositions. A sterile aqueous injectable pharmaceutical composition suitable for parenteral administration is described comprising a therapeutically effective dose of hydralazine hydrochloride in a pharmaceutically acceptable carrier or diluent wherein said hydralazine hydrochloride is essentially free of phthalazines, hydrazine and metal ions. In addition, a stable sterile aqueous pharmaceutical composition comprising hydralazine hydrochloride in a pharmaceutically acceptable salt or diluent is described that is colorless and has no visible particulate matter.
Naphthalenone phthalazinylhydrazones
-
, (2008/06/13)
Naphthalenone phthalazinylhydrazones of the formula: STR1 are disclosed. In the above formula R1 is hydrogen or alkyl, R2 is alkyl, preferably branched alkyl, or N, R1 and R2 taken together forming a heterocyclic ring. These compounds are useful as antihypertensive agents.
