23256-50-0 Usage
Uses
Different sources of media describe the Uses of 23256-50-0 differently. You can refer to the following data:
1. antihypertensive
2. α2-adrenergic agonist and IGRS selective ligand
Brand name
Wytensin (Wyeth).
General Description
Guanabenz acetate, [(2,6-dichlorobenzylidene)amino]guanidine monoacetate (Wytensin), is acentral 2-adrenergic agonist that reduces the release of norepinephrinefrom the neuron when stimulated. The effect ofthe drug results in decreased sympathetic tone in the heart,kidneys, and peripheral blood vessels. The drug does not produceorthostatic hypotension.
Biological Activity
α 2 -adrenergic agonist and IGRS (imidazoline I 2 binding site) selective ligand.
Biochem/physiol Actions
Centrally acting α2 adrenoceptor agonist; I2 imidazoline binding site ligand; antihypertensive.
Pharmacokinetics
The oral bioavailability of guanabenz is 70 to 80%. Following an oral dose, the hypotensive effect of guanabenz begins
within 1 hour, peaks within 2 to 7 hours, and is diminished within 6 to 8 hours. It has an elimination half-life averaging
4 to 14 hours. The blood pressure response can persist for at least 12 hours. Following IV dosing, guanabenz is
distributed into the CNS, with brain concentrations 3 to 70 times higher than concurrent plasma concentrations.
Guanabenz is approximately 90% bound to plasma proteins. In patients with hepatic or renal impairment, its elimination
half-life may be prolonged.
Guanabenz is metabolized principally by hydroxylation to its inactive metabolite, 4-hydroxyguanabenz, which is
eliminated in the urine as its glucuronide (major) and sulfate conjugates. Guanabenz and its inactive
metabolites are excreted principally in urine, with approximately 70 to 80% of its oral dose excreted in urine within 24
hours and approximately 10–30% in feces via enterohepatic cycling. Approximately 40% of an oral dose of guanabenz
is excreted in urine as 4-hydroxyguanabenz and its glucuronide, and less than 5% is excreted unchanged. The
remainder is excreted as unidentified metabolites and their conjugates.
Clinical Use
Overall, the therapeutic applications for guanabenz are similar to those of clonidine and other α2-adrenergic agonists.
One advantage for guanabenz is its once-a-day dosing schedule. Guanabenz has been used in diabetic patients with
hypertension without adverse effect on the control of or therapy for diabetes, and it has been effective in hypertensive
patients with chronic obstructive pulmonary disease, including asthma, chronic bronchitis, or emphysema. Guanabenz
has been used alone or in combination with naltrexone in the management of opiate withdrawal in patients physically
dependent on opiates and undergoing detoxification. Guanabenz also has been used as an analgesic in a limited
number of patients with chronic pain
Side effects
Overall, the frequency of adverse effects produced by guanabenz is similar to that produced by clonidine and the other
α2-adrenergic agonists, but the incidence is lower. As with the other centrally active sympatholytics (e.g., clonidine),
abrupt withdrawal of guanabenz may result in rebound hypertension, but the withdrawal syndrome symptoms appear to
be less severe.
Check Digit Verification of cas no
The CAS Registry Mumber 23256-50-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,2,5 and 6 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 23256-50:
(7*2)+(6*3)+(5*2)+(4*5)+(3*6)+(2*5)+(1*0)=90
90 % 10 = 0
So 23256-50-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H8Cl2N4.C2H4O2/c9-6-2-1-3-7(10)5(6)4-13-14-8(11)12;1-2(3)4/h1-4H,(H4,11,12,14);1H3,(H,3,4)
