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Tiagabine hydrochloride

CAS No.
145821-59-6
Chemical Name:
Tiagabine hydrochloride
Synonyms
GABITRIL;CS-1356;TIAGABINE HCL;TGB hydrochloride;NO328 hydrochloride;Tiagabine, NO 050328;Tiagabine ethyl ester;iagabinehydrochloride;NO050328 hydrochloride;Gabitril hydrochloride
CBNumber:
CB5162581
Molecular Formula:
C20H26ClNO2S2
Molecular Weight:
412.01
MDL Number:
MFCD07369025
MOL File:
145821-59-6.mol
MSDS File:
SDS
Last updated:2023-06-30 15:45:59

Tiagabine hydrochloride Properties

Melting point >192oC dec.
alpha D20 -11°
Flash point 9℃
storage temp. 2-8°C
solubility H2O: soluble10mg/mL, clear
pka pKa1 3.3; pKa2 9.4(at 25℃)
form powder
color white to beige
optical activity [α]/D -9 to -12°, c = 1 in H2O
Merck 14,9417
Stability Stable for 1 year from date of purchase as supplied. Solutions in DMSO, ethanol, or distilled water may be stored at -20° for up to 3 months.
InChIKey YUKARLAABCGMCN-PKLMIRHRSA-N
CAS DataBase Reference 145821-59-6(CAS DataBase Reference)
FDA UNII DQH6T6D8OY

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms
GHS02,GHS06,GHS08
Signal word  Danger
Hazard statements  H225-H301+H311+H331-H370
Precautionary statements  P210-P260-P280-P301+P310-P311
Hazard Codes  Xn,T,F
Risk Statements  20/21/22-39/23/24/25-23/24/25-11
Safety Statements  36/37-45-16-7
RIDADR  UN1230 - class 3 - PG 2 - Methanol, solution
WGK Germany  3
RTECS  TM6128245
HS Code  2934.99.3000

Tiagabine hydrochloride price More Price(41)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich SML0035 Tiagabine hydrochloride ≥98% (HPLC) 145821-59-6 10mg $76.7 2024-03-01 Buy
Sigma-Aldrich T-081 Tiagabine hydrochloride solution 1.0?mg/mL in methanol (as free base), ampule of 1?mL, certified reference material, Cerilliant? 145821-59-6 1mL $146 2024-03-01 Buy
TCI Chemical T3165 Tiagabine Hydrochloride >99.0%(HPLC) 145821-59-6 50mg $93 2021-12-16 Buy
TCI Chemical T3165 Tiagabine Hydrochloride >99.0%(HPLC) 145821-59-6 250mg $300 2024-03-01 Buy
Cayman Chemical 22926 Tiagabine (hydrochloride) ≥98% 145821-59-6 5mg $32 2024-03-01 Buy
Product number Packaging Price Buy
SML0035 10mg $76.7 Buy
T-081 1mL $146 Buy
T3165 50mg $93 Buy
T3165 250mg $300 Buy
22926 5mg $32 Buy

Tiagabine hydrochloride Chemical Properties,Uses,Production

Chemical Properties

Tiagabine hydrochloride is a whitish, odorless, crystalline powder with a molecular formula of C20H25NO2S2HCl and a molecular weight of 412.0. Tiagabine hydrochloride was originally synthesized by Novo Nordisk Pharmaceuticals in Denmark.
It was licensed in Europe in 1996 and in the United States in 1997, under the brand name Gabitril1. Gabitril1 is available in the form of 2, 4, 12, and 16 mg tablets. It is marketed by Cephalon.
The antiepileptic drug tiagabine is a lipophilic derivative of nipecotic acid. Nipecotic acid inhibits GABA reuptake, but does not cross the blood brain barrier and is effective against seizures in animal models only when injected in the cerebral ventricles (Croucher et al. 1983). Tiagabine’s lipophilic anchor permits the passage of nipecotic acid from the systemic circulation across the blood brain barrier to the central nervous system (Krogsgaard-Larsen et al. 2000).

Indications

Tiagabine is licensed by the United States Food and Drug Administration (FDA) for adjunctive therapy in adults, and children of 12 years and older in the treatment of partial seizures with or without secondary generalization. There is no evidence to support a broader spectrum of action in epilepsy (Ben-Menachem 1995; Bialer et al. 2007). Tiagabine is also licensed in Europe by the European Medicines Agency (EMEA) for the same indications.

Clinical Applications

Tiagabine is currently used as adjunctive treatment in adults and children 12 years and older, suffering from partial-onset seizures, which cannot be satisfactorily controlled with other antiepileptic drugs. This indication was based on the results of five multi-center, double-blind, placebo-controlled clinical trials (two cross over and three parallel group studies) that proved its efficacy in patients with refractory partial seizures. These studies included a total of 951 adult and adolescent patients treated with add-on tiagabine at doses ranging from 16 to 56 mg compared to placebo (Ben-Menachem 1995; Richens et al. 1995; Sachdeo et al. 1997; Kalviainen et al. 1998; Uthman et al. 1998; Crawford et al. 2001). An integrated analysis of these studies demonstrated a significant 50% reduction in all seizure types in 23% of the tiagabine-treated group compared to 9% of the placebotreated group during a 7–12 week period (Ben-Menachem 1995). Doses between 32 and 56 mg in three or four divided doses were more effective than placebo (Sachdeo et al. 1997; Uthman et al. 1998). There was a dose–response relationship with greater efficacy at 56 mg/day (Uthman et al. 1998).

Drug Interactions

Tiagabine has minimal potential interaction with other drugs (Leppik et al. 1999). Tiagabine is not known to cause either induction or inhibition of hepatic microsomal enzyme systems. Consequently tiagabine does not alter the plasma concentrations of other drugs including antiepileptic drugs that undergo hepatic metabolism (Gustavson et al. 1998a, b). However, enzyme-inducing drugs accelerate the hepatic metabolism of tiagabine (So et al. 1995). There is no clinically relevant interaction between tiagabine and digoxin (Snel et al. 1998).

Description

Tiagabine (145821-59-6) is a clinically useful anticonvulsant.1?It is also used to treat anxiety/panic disorder2?and neuropathic pain3. Tiagabine inhibits GABA-reuptake (IC50?[3H]GABA uptake = 67 nM)?via?inhibiting GABA transporter 1(GAT1) blocking both neuronal and glial GABA re-uptake.4,5

Chemical Properties

White to Off-White Solid

Originator

Gabitril,Cephalon, Inc.,USA

Uses

A GABA uptake inhibitor. Anticonvulsant.

Uses

Tiagabine Hydrochloride is a GABA uptake inhibitor and an anticonvulsant (1,2,3). It is used to treat epilepsy, anxiety disorders, and panic disorder. Neuroprotective & Neuroresearch Product.

Uses

Tiagabine hydrochloride was used to study serotoninergic transmission in G1 cells. It has also been used to study its anti-aging effects on the sensory neurons of C. elegans.

Definition

ChEBI: A hydrochloride resulting from the reaction of equimolar amounts of tiagabine and hydrogen chloride. A GABA reuptake inhibitor, it is used for the treatment of epilepsy.

Manufacturing Process

A solution of 34 ml of n-butyl lithium in 30 ml of anhydrous ether was cooled to -65°C under nitrogen and 5.3 ml of 3-methyl-2-bromothiophene in 10 ml anhydrous ether was added dropwise over a period of 10 min. The reaction mixture was stirred at -65°C for 1 h and 2.7 ml of ethyl 4-bromo-butyrate in 10 ml of anhydrous ether was added slowly. The reaction was stirred for 4 h while the temperature raised to -20°C, 20 ml water was added, and the mixture was stirred for 5 min after which the aqueous layer was removed. The ether layer was washed with 20 ml of water, and the combined aqueous phases were extracted with 50 ml of ether. The combined organic phases were dried over anhydrous sodium sulfate, which after evaporation yielded 9 g of 1- bromo-4,4-bis(3-methylthien-2-yl)but-3-ene as an oil. This compound was without further purification used for coupling with ethyl nipecotate.
A suspension of 5.0 g of 1-bromo-4,4-bis(3-methylthien-2-yl)but-3-ene, 3.4 g of nipecotic acid ethyl ester and 3.3 g of potassium carbonate in 150 ml of dry acetone was kept under reflux for 15 h. The reaction mixture was evaporated and, after addition of 30 ml of water, the resulting solution was extracted twice with 50 ml of ethyl acetate. The ethyl acetate extracts were dried and evaporated leaving 7.3 g of an oil. By column chromatography on silica gel using methanol as eluent, N-(4,4-bis(3-methylthien-2-yl)but-3-enyl)nipecotic acid ethyl ester was isolated.
5.3 g of N-(4,4-bis(3-methylthien-2-yl)but-3-enyl)nipecotic acid ethyl ester was dissolved in 100 ml of ethanol and 200 ml of an 8 N sodium hydroxide solution was added. The mixture was heated at reflux for 1 h, cooled and acidified by adding 10% hydrochloric acid. The resulting solution was evaporated and 100 ml of water was added to the residue. The resulting acid solution was extracted with ethyl acetate and the dried extract was evaporated to give (R)-N-(4,4-bis(3-methylthien-2-yl)but-3-enyl)nipecotic acid hydrochloride, melting point 187°-189°C.

Therapeutic Function

Antiepileptic

Biochem/physiol Actions

Tiagabine increases the synaptic GABA and enhances the neuronal inhibition. It is effective as adjunctive treatment of epilepsy and anxiety disorders.

storage

Room temperature (desiccate)

References

1) Schacter (1999)?A Review of the Antiepileptic Drug Tiagabine, Clin. Neuropharmacol.?22?312 2) Schwartz and Nihalani (2006)?Tiagabine in anxiety disorders, Expert Opin. Pharmacother.?7?1977 3) Novak?et al.?(2001)?Treatment of Painful Sensory Neuropathy With Tiagabine: A Pilot Study, Clin. Auton. Res.?11?357 4) Braestrup?et al.?(1990)?(R)-N-[4,4-bis(3-methyl-2-thienyl)but-3-en-1-yl)nipecotic Acid Binds With High Affinity to the Brain Gamma-Aminobutyric Acid Uptake Carrier, J. Neurochem. 54 639 5) Nielsen?et al.?(1991)?Characterization of Tiagabine (NO-328), a New Potent and Selective GABA Uptake Inhibitor, Eur. J. Pharmacol.?196?257

Tiagabine hydrochloride Preparation Products And Raw materials

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View Lastest Price from Tiagabine hydrochloride manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Tiagabine hydrochloride pictures 2021-07-13 Tiagabine hydrochloride
145821-59-6
US $15.00-10.00 / KG 1KG 99%+ HPLC Monthly supply of 1 ton Zhuozhou Wenxi import and Export Co., Ltd
Tiagabine hydrochloride pictures 2021-07-09 Tiagabine hydrochloride
145821-59-6
US $15.00-10.00 / KG 1KG 99%+ HPLC Monthly supply of 1 ton Zhuozhou Wenxi import and Export Co., Ltd
Tiagabine hydrochloride pictures 2019-12-23 Tiagabine hydrochloride
145821-59-6
US $1.00 / g 100g 98%min G/KG/T Career Henan Chemical Co

Tiagabine hydrochloride Spectrum

TIAGABINE HYDROCHLORIDE THYMOL IODIDE - PURIFIED GRADE (3R)-1-[4,4-Bis(3-methylthiophen-2-yl)but-3-enyl]piperidine-3-carboxylic acid hydrochloride (3R)-1-[4,4-bis(3-methyl-2-thienyl)but-3-enyl]nipecotic acid hydrochloride Tiagabine Hydrochloride (300 mg) Tiagabine-d6 hydrochloride (3R)-1-[4,4-Bis(3-Methyl-2-thienyl)-3-butenyl]-3-piperidinecarboxylic Acid Hydrochloride TIAGABINE HClHYDROCHLORIDE Tiagabine ethyl ester 3-Piperidinecarboxylicacid, 1-[4,4-bis(3-Methyl-2-thienyl)-3-buten-1-yl]-, hydrochloride (1:1), (3R)- (-)-(R)-1-[4,4-bis(3-methyl-2-thienyl)-3-butenyl]nipecotic acid hydrochloride (3R)-1-[4,4-Bis(3-methyl-2-thienyl)-3-buten-1-yl]-3-piperidinecarboxylic acid hydrochloride Tiagabine hydrochloride solution (R)-1-(4,4-Bis(3-methylthiophen-2-yl)but-3-en-1-yl)piperidine-3-carboxylic acid hydrochloride TIAGABINE HCL NO050328 hydrochloride NO328 hydrochloride TGB hydrochloride CS-1356 Tiagabine, NO 050328 Gabitril hydrochloride Tiagabine Hydrochloride (1667280) 23-Dihydrostigmasterol GABITRIL iagabinehydrochloride 145821-59-6 C20H25NO2S2ClH C20H25NO2S2HCl API Heterocycles Intermediates & Fine Chemicals Neurochemicals Pharmaceuticals Sulfur & Selenium Compounds Tiagabine 145821-59-6