GABAPENTIN-D6 HYDROCHLORIDE
GABAPENTIN-D6 HYDROCHLORIDE Basic information
- Product Name:
- GABAPENTIN-D6 HYDROCHLORIDE
- Synonyms:
-
- GABAPENTIN-D6 HYDROCHLORIDE
- 1-(aminomethyl)cyclohexaneacetic acid hydrochloride
- Neurontin hydrochloride
- 2-(1-(aminomethyl)cyclohexyl)acetic acid hydrochloride
- Cyclohexaneacetic acid, 1-(aminomethyl)-, hydrochloride (1:1)
- Neurontin HCl
- 1-(Amino Methyl) Cyclohexane Acetic Acid Hydrochloride Hemihydrate Salt
- 1-AMINOMETHYL CYCLOHEXANACTIC ACID HYDROCHLORIDE
- CAS:
- 60142-95-2
- MF:
- C9H12ClD6NO2
- MW:
- 213.73
- EINECS:
- 262-075-8
- Product Categories:
-
- Inhibitors
- Mol File:
- Mol File
GABAPENTIN-D6 HYDROCHLORIDE Chemical Properties
- Melting point:
- 148-151℃ (ethanol )
- Density
- 0.001g/cm3 at 20℃
- storage temp.
- Refrigerator
- solubility
- DMSO (Slightly), Methanol (Slightly)
- form
- Solid
- color
- White to Off-White
- LogP
- -1.33--1.17 at pH4-9
- Surface tension
- 63.69mN/m at 1g/L and 20℃
GABAPENTIN-D6 HYDROCHLORIDE Usage And Synthesis
Uses
Gabapentin Hydrochloride is a salt analogue of Gabapentin-d6 (G117253), a labelled amino acid structurally related to γ-Aminobutyric Acid (GABA), designed to cross the blood brain barrier. Used as an anticonvulsant.
Biological Activity
gabapentin (neurontin) is a pharmaceutical drug, specifically a gaba analog. it was originally developed to treatepilepsy, and currently is also used to relieve neuropathic pain.
in vivo
Gabapentin (5 and 10 mg/kg; i.p.; once; male BALB/c mice) hydrochloride has improving effects on spatial and emotional cognitive performance of naive mice in Morris water maze (MWM), passive avoidance (PA) and modified elevated plus maze (mEPM) tasks[2].
Gabapentin (1-100 mg/kg; i.p.; once; male mice) hydrochloride has analgesic effect and reduces writhing in a dose-dependent manner[3].
| Animal Model: | Male BALB/c mice (35-45 g)[2] |
| Dosage: | 5 and 10 mg/kg |
| Administration: | Intraperitoneal injection; once |
| Result: | Increased the time spent in target quadrant and decreased the distance to platform in MWM test . Decreased the transfer latency on second day in mEPM test . Prolonged retention latency in PA test . |
| Animal Model: | Male mice (26-30 g)[3] |
| Dosage: | 1, 5, 10, 50 and 100 mg/kg |
| Administration: | Intraperitoneal injection; once |
| Result: | Produced 45-70% inhibition of writhing. |
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