CAS 60142-95-2|Gabapentin HCl
| Common Name | Gabapentin HCl | ||
|---|---|---|---|
| CAS Number | 60142-95-2 | Molecular Weight | 207.69800 |
| Density | / | Boiling Point | 314.4ºC at 760mmHg |
| Molecular Formula | C9H18ClNO2 | Melting Point | 148-151℃ (ethanol ) |
| MSDS | / | Flash Point | 144ºC |
Names
| Name | 2-[1-(aminomethyl)cyclohexyl]acetic acid,hydrochloride |
|---|---|
| Synonym | More Synonyms |
Gabapentin HCl BiologicalActivity
| Description | Gabapentin (Neurontin) is a pharmaceutical drug, specifically a GABA analog. It was originally developed to treat epilepsy, and currently is also used to relieve neuropathic pain.IC50 Value: 140 nM (α2δ subunit of calcium channel) [1]Target: Calcium Channelin vitro: Gabapentin, baclofen and CGP 44532 all reduced the electrically stimulated release of [3H]glutamic acid (IC50=20 microM, 0.8 microM and 2 microM, respectively). Gabapentin was without effect on the release of [3H]GABA, whilst baclofen (IC50=8 microM) and CGP 44532 (IC50=1 microM) inhibited [3H]GABA release [2]. A large inhibition of calcium currents by gabapentin was observed in pyramidal neocortical cells (up to 34%). Significantly, the gabapentin-mediated inhibition of calcium currents saturated at particularly low concentrations (around 10 microM), at least in neocortical neurons (IC50 about 4 microM) [3].in vivo: Gabapentin produced an anti-allodynic effect over the 7-day period, reducing the expression of pro-inflammatory cytokines but increasing the expression of IL-10 (TNF-α, 316.0 ± 69.7 pg/mL vs 88.8 ± 24.4 pg/mL; IL-1β, 1,212.9 ± 104.5 vs 577.4 ± 97.1 pg/mL; IL-6, 254.0 ± 64.8 pg/mL vs 125.5 ± 44.1 pg/mL; IL-10, 532.1 ± 78.7 pg/mL vs 918.9 ± 63.1 pg/mL). The suppressive effect of gabapentin on pro-inflammatory cytokine expression was partially blocked by the anti-IL-10 antibody [4].Toxicity: No new safety signals or adverse event trends relating to GEn exposure were identified [5].Clinical trial: / |
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| Related Catalog | Signaling Pathways >>Membrane Transporter/Ion Channel >>Calcium ChannelResearch Areas >>Neurological Disease |
| References | [1]. Receveur JM, et al. Synthesis and biological evaluation of conformationally restricted Gabapentin analogues. Bioorg Med Chem Lett. 1999 Aug 16;9(16):2329-34. [2]. Parker DA, et al. Gabapentin activates presynaptic GABAB heteroreceptors in rat cortical slices. Eur J Pharmacol. 2004 Jul 14;495(2-3):137-43. [3]. Stefani A, et al. Gabapentin inhibits calcium currents in isolated rat brain neurons. Neuropharmacology. 1998;37(1):83-91. [4]. Lee BS, et al. Intrathecal gabapentin increases interleukin-10 expression and inhibits pro-inflammatory cytokine in a rat model of neuropathic pain. J Korean Med Sci. 2013 Feb;28(2):308-14. [5]. Harden RN, et al. A Phase 2a, Randomized, Crossover Trial of Gabapentin Enacarbil for the Treatment of Postherpetic Neuralgia inGabapentin Inadequate Responders. Pain Med. 2013 Sep 18. |
Chemical & Physical Properties
| Boiling Point | 314.4ºC at 760mmHg |
|---|---|
| Melting Point | 148-151℃ (ethanol ) |
| Molecular Formula | C9H18ClNO2 |
| Molecular Weight | 207.69800 |
| Flash Point | 144ºC |
| Exact Mass | 207.10300 |
| PSA | 63.32000 |
| LogP | 2.87260 |
| InChIKey | XBUDZAQEMFGLEU-UHFFFAOYSA-N |
| SMILES | Cl.NCC1(CC(=O)O)CCCCC1 |
| Storage condition | -20°C |
Synonyms
| 1-(Aminomethyl)cyclohexaneacetic acid hydrochloride |
| Gabarone,Neurontin,Gabapentin Hydrochloride |
| Gabapentin (hydrochloride) |
| Gabapentin HCl |
| S1338_Selleck |
| 2-[1-(aminomethyl)cyclohexyl]acetic acid hydrochloride |
| Gabarone |
| UNII-N0PY5N5AFW |
| Neurontin |
