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102767-28-2

102767-28-2 structure
102767-28-2 structure
  • Name: Levetiracetam
  • Chemical Name: levetiracetam
  • CAS Number: 102767-28-2
  • Molecular Formula: C8H14N2O2
  • Molecular Weight: 170.209
  • Catalog: API Nervous system medication Antiepileptic and anticonvulsant
  • Create Date: 2018-08-03 08:47:19
  • Modify Date: 2024-01-02 12:27:12
  • Levetiracetam(UCB L059) is a novel anticonvulsant with antihyperalgesic efficacy in inflammatory pain.Target: Calcium ChannelLevetiracetam is used to control some types of seizures in patients with epilepsy. This medicine cannot cure epilepsy and will only work to control seizures for as long as you continue to use it. The exact mechanism for levetiracetam is unknown. However, the drug binds to a synaptic vesicle protein, SV2A, which is believed to impede nerve conduction across synapses [1].Levetiracetam (10-200 mg/kg), ibuprofen (12.5-100 mg/kg), celecoxib (3.75-30 mg/kg), paracetamol (50-200 mg/kg), caffeine (15-100 mg/kg), and 2-drug combinations of levetiracetam with analgesics/caffeine produced a significant, dose-dependent reduction of inflammatory hyperalgesia. Isobolographic analysis revealed that levetiracetam exerts a synergistic interaction with analgesics, with approximately 7-, 9-, and 11-fold reduction of doses of both drugs in combination of levetiracetam with paracetamol, celecoxib, and ibuprofen, respectively. Analysis of the log dose-response curves for levetiracetam (1-50 mg/kg) in the presence of caffeine (10 mg/kg) and levetiracetam applied alone also revealed a synergistic interaction. Levetiracetam's ED50 in the presence of caffeine was reduced approximately 11-fold [2].Clinical indications: Epilepsy; Social phobiaFDA Approved Date: November 2008Toxicity: depression; hallucinations; suicidal thoughts

Name levetiracetam
Synonyms (2S)-2-(2-Oxopyrrolidin-1-yl)butanamide
levetiracetamum
2(S)-(2-oxopyrrolidin-1-yl)butyramide
KEPPRA
(2S)-2-(2-Oxo-1-pyrrolidinyl)butanamide
(S)-Etiracetam
Etiracetam levo-isomer
EINECS 200-659-6
ucb L059
(aS)-a-Ethyl-2-oxo-1-pyrrolidineacetamide
1-pyrrolidineacetamide, a-ethyl-2-oxo-, (aS)-
1-Pyrrolidineacetamide, α-ethyl-2-oxo-, (αS)-
(S)-2-(2-Oxopyrrolidin-1-yl)Butanamide
SIB S1
(S)-2-(2-Oxo-1-pyrrolidinyl)butyramide
MFCD03265610
SIB-S1
(-)-(S)-α-Ethyl-2-oxo-1-pyrrolidineacetamide
Keppra XR
Levetiracetam
Description Levetiracetam(UCB L059) is a novel anticonvulsant with antihyperalgesic efficacy in inflammatory pain.Target: Calcium ChannelLevetiracetam is used to control some types of seizures in patients with epilepsy. This medicine cannot cure epilepsy and will only work to control seizures for as long as you continue to use it. The exact mechanism for levetiracetam is unknown. However, the drug binds to a synaptic vesicle protein, SV2A, which is believed to impede nerve conduction across synapses [1].Levetiracetam (10-200 mg/kg), ibuprofen (12.5-100 mg/kg), celecoxib (3.75-30 mg/kg), paracetamol (50-200 mg/kg), caffeine (15-100 mg/kg), and 2-drug combinations of levetiracetam with analgesics/caffeine produced a significant, dose-dependent reduction of inflammatory hyperalgesia. Isobolographic analysis revealed that levetiracetam exerts a synergistic interaction with analgesics, with approximately 7-, 9-, and 11-fold reduction of doses of both drugs in combination of levetiracetam with paracetamol, celecoxib, and ibuprofen, respectively. Analysis of the log dose-response curves for levetiracetam (1-50 mg/kg) in the presence of caffeine (10 mg/kg) and levetiracetam applied alone also revealed a synergistic interaction. Levetiracetam's ED50 in the presence of caffeine was reduced approximately 11-fold [2].Clinical indications: Epilepsy; Social phobiaFDA Approved Date: November 2008Toxicity: depression; hallucinations; suicidal thoughts
Related Catalog
References

[1]. Meehan AL, et al. A new mechanism for antiepileptic drug action: vesicular entry may mediate the effects of levetiracetam. J Neurophysiol. 2011 Sep;106(3):1227-39.

[2]. Tomi MA, et al. Levetiracetam interacts synergistically with nonsteroidal analgesics and caffeine to produce antihyperalgesia in rats. J Pain. 2013 Nov;14(11):1371-82.

Density 1.2±0.1 g/cm3
Boiling Point 395.9±25.0 °C at 760 mmHg
Melting Point 118-119°C
Molecular Formula C8H14N2O2
Molecular Weight 170.209
Flash Point 193.2±23.2 °C
Exact Mass 170.105530
PSA 63.40000
LogP -0.67
Vapour Pressure 0.0±0.9 mmHg at 25°C
Index of Refraction 1.519
Symbol GHS07
GHS07
Signal Word Warning
Hazard Statements H302-H319
Precautionary Statements P305 + P351 + P338
Personal Protective Equipment dust mask type N95 (US);Eyeshields;Gloves
Hazard Codes Xn: Harmful;
Risk Phrases R22
Safety Phrases S26
RIDADR NONH for all modes of transport
RTECS UX9656166
HS Code 2933990090
HS Code 2933790090
Summary 2933790090. other lactams. VAT:17.0%. Tax rebate rate:9.0%. . MFN tariff:9.0%. General tariff:20.0%