| Identification | Back Directory | [Name]
GUANABENZ ACETATE | [CAS]
23256-50-0 | [Synonyms]
br750
Wytens
Tenelid
WY-8678
FLA-137
Wytensin
Wy 8678 acetate
GUANABENZ ACETATE
GuanabenzAcetate>
GUANABENZACETATE,USP
guanabenz acetate salt
Guanabenz Acetate, ≥98%
Guanabenz Acetate (200 mg)
GUANABENZ ACETATE USP/EP/BP
[2,6-DICHLOROBENZYLIDENE)-AMINO]GUANIDINE
Guanabenz Acetate - CAS 23256-50-0 - Calbiochem
[(2,6-DICHLOROBENZYLIDENE)AMINO]GUANIDINE ACETATE
((2,6-dichlorobenzylidene)amino)-guanidinmonoacetate
1-(2,6-dichlorobenzylideneamino)guanidine acetate salt
[(2,6-dichlorobenzylidene)amino]-Guanidine monoacetate
3-[(2,6-dichlorophenyl)methylene]carbazamidine monoacetate
(E)-2-(2,6-dichlorobenzylidene)hydrazinecarboximidamide acetate
1-(2,6-Dichlorobenzylideneamino)guanidine acetate salt, WY-8678
2-((2,6-dichlorophenyl)methylene)-hydrazinecarboximidamidmonoacetate
HydrazinecarboxiMidaMide, 2-[(2,6-dichlorophenyl)Methylene]-, acetate
Hydrazinecarboximidamide, 2-[(2,6-dichlorophenyl)methylene]-, acetate (1:1)
Guanabenz acetate salt,1-(2,6-Dichlorobenzylideneamino)guanidine acetate salt, WY-8678 | [EINECS(EC#)]
245-534-7 | [Molecular Formula]
C10H12Cl2N4O2 | [MDL Number]
MFCD00153801 | [MOL File]
23256-50-0.mol | [Molecular Weight]
291.13 |
| Chemical Properties | Back Directory | [Melting point ]
227-229℃ (decomposition) | [storage temp. ]
Store at RT | [solubility ]
H2O: 11 mg/mL
| [form ]
solid
| [color ]
white
| [Water Solubility ]
water: 5mg/mL | [Merck ]
14,4558 | [Stability:]
Hygroscopic | [InChI]
InChI=1S/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)/b13-4+; | [InChIKey]
MCSPBPXATWBACD-GAYQJXMFSA-N | [SMILES]
C1(=C(Cl)C=CC=C1Cl)/C=N/NC(=N)N.C(=O)(O)C |
| Safety Data | Back Directory | [Hazard Codes ]
Xn | [Risk Statements ]
22 | [Safety Statements ]
22-36/37/39-45 | [RIDADR ]
UN 2811 6.1/PG 3
| [WGK Germany ]
3
| [RTECS ]
MF0382000
| [HazardClass ]
6.1(b) | [PackingGroup ]
III | [HS Code ]
2928002500 | [Storage Class]
6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects | [Hazard Classifications]
Acute Tox. 3 Oral | [Hazardous Substances Data]
23256-50-0(Hazardous Substances Data) |
| Hazard Information | Back Directory | [Uses]
antihypertensive | [Uses]
α2-adrenergic agonist and IGRS selective ligand | [Definition]
ChEBI: Guanabenz acetate is a dichlorobenzene. It has a role as a geroprotector. | [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. | [storage]
Store at RT |
|
| Company Name: |
J & K SCIENTIFIC LTD.
|
| Telephone: |
18210857532 18210857532 |
| Website: |
https://www.jkchemical.com |
| Company Name: |
Spectrum Chemical Manufacturing Corp.
|
| Telephone: |
021-021-021-67601398-809-809-809 15221380277 |
| Website: |
www.spectrumchemical.com/oa_html/index.jsp?minisite=10020&respid=22372&language=us |
| Company Name: |
LETOPHARM LIMITED
|
| Telephone: |
+86-21-5821 5861 |
| Website: |
www.letopharm.com |
| Company Name: |
Sigma-Aldrich
|
| Telephone: |
021-61415566 800-8193336 |
| Website: |
https://www.sigmaaldrich.cn |
|