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pirenzepine dihydrochloride

CAS: 29868-97-1

Molecular Formula: C19H23Cl2N5O2

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Tabe - Names and Identifiers

Name pirenzepine dihydrochloride
Synonyms Tabe
Leblon
Maghen
Ulcosan
Renzepin
Gasteril
Ulcuforton
Pirenzepine HCL
PIRENZEPINE HCL HYDRATE
pirenzepine hydrochloride
pirenzepine dihydrochloride
11-[2-(4-methylpiperazin-1-yl)acetyl]-5H-pyrido[2,3-b][1,4]benzodiazepin-6-one hydrate hydrochloride
11-[(4-methylpiperazin-1-yl)acetyl]-5,11-dihydro-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one dihydrochloride
5,11-Dihydro-11-((4-methylpiperazin-1-yl)acetyl)-6H-pyrido(2,3-b)-(1,4)benzodiazepin-6-one dihydrochloride
5,11-dihydro-11-[2-(4-methyl-1-piperazinyl)acetyl]-6H-pyrido[2,3-β][1,4]benzo- diazepin-6-one Dihydrochloride
CAS 29868-97-1
EINECS 249-907-5
InChI InChI=1/C19H21N5O2.ClH.H2O/c1-22-9-11-23(12-10-22)13-17(25)24-16-7-3-2-5-14(16)19(26)21-15-6-4-8-20-18(15)24;;/h2-8H,9-13H2,1H3,(H,21,26);1H;1H2

Tabe - Physico-chemical Properties

Molecular FormulaC19H23Cl2N5O2
Molar Mass424.32
Melting Point248-250°C
Solubility H2O: 50mg/mL
Appearancepowder
Colorwhite
Storage ConditionInert atmosphere,2-8°C
SensitiveHygroscopic
MDLMFCD00055214
UseFor the treatment of gastric and duodenal ulcer, acute gastric mucosal bleeding and other diseases
In vitro study The antisecretory properties of pirenzepine on gastric acid and pepsin secretion may be attributed to the antagonistic activity of the drug on muscarinic M1 receptors of gastric intramural plexuses, whereas the effect on parietal muscarinic M2 receptors seems of less importance. Additional inhibitory mechanisms on gastric secretion may be represented by pirenzepine-induced increase in somatostatin release from gastrointestinal system. Significant cytoprotective properties of pirenzepinehave been observed on a variety of experimentally induced peptic ulcerations. Pirenzepine (5-500 μg/mL) inhibits agonist-(acetylcholine-, carbachol- or nicotine-) induced contractions of the toad isolated rectus abdominis muscle, and depresses electrically provoked twitches of the rat phrenic nerve-hemidiaphragm muscle preparation.
In vivo study Pirenzepine is potent in impairing learning of an avoidance; much higher doses are required to antagonize other central muscarinic effects. Pirenzepine is found to impair passive avoidance learning when given i.c.v. 20 min pre-training. The median latencies in pirenzepine-treated animals are 79.5, 11, 27 and 25.5 seconds with doses of 0.03, 0.1, 0.3 and 1 μg per mouse respectively. Acid and pepsin secretion stimulated by either bethanechol or the vagus are inhibited in a dose-responsive manner by pirenzepine. Pirenzepine (5-25 mg/kg i.v.) depresses indirect electrical stimulation-evoked twitches of the cat tibialis anterior and soleus muscle preparations.

Tabe - Risk and Safety

WGK Germany2
RTECSUU7883000

Tabe - Preparation solution concentration reference

 1mg5mg10mg
1 mM2.357 ml11.784 ml23.567 ml
5 mM0.471 ml2.357 ml4.713 ml
10 mM0.236 ml1.178 ml2.357 ml
5 mM0.047 ml0.236 ml0.471 ml
Last Update:2024-01-02 23:10:35
Tabe
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Product Name: 11-(2-(4-Methylpiperazin-1-yl)acetyl)-5,11-dihydro-6H-benzo[e]pyrido[3,2-b][1,4]diazepin-6-one dihydrochloride Visit Supplier Webpage Request for quotation
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Tabe
NSC9205
SODIUM TELLURATE
C.I. Pigment Violet 5
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