Pregabalin CAS 148553-50-8
Introduction:Basic information about Pregabalin CAS 148553-50-8, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Pregabalin Basic informationDescription Generic formulation Indications Dose titration Plasma levels monitoring Antiepileptic drus and therapeutic drugs for neuropathic pain Cautions Adverse effects Interactions Special populations Behavioural and cognitive effects in patients with epilepsy Psychiatric use
| Product Name: | Pregabalin |
| Synonyms: | 3(S)-(AMINOMETHYL)-5-METHYLHEXANOIC ACID;(3S)-3-(AMINOMETHYL)-5-METHYLHEXANOIC ACID;PREGABALIN;Pregablin;3-(Aminomethyl)-5-methyl-hexanoic acid;PREDNISOLONESODIUMPHOSPHATE;(R)-Pregabalin;(S)-Pregabalin |
| CAS: | 148553-50-8 |
| MF: | C8H17NO2 |
| MW: | 159.23 |
| EINECS: | 604-639-1 |
| Product Categories: | Miscellaneous Biochemicals;APIs;Intermediates & Fine Chemicals;Neurochemicals;Pharmaceuticals;API;Pfizer compounds;pharmaceutical;148553-50-8;john's |
| Mol File: | 148553-50-8.mol |
Pregabalin Chemical Properties
| Melting point | 194-196°C |
| alpha | D23 +10.52° (c = 1.06 in water) |
| Boiling point | 274.0±23.0 °C(Predicted) |
| density | 0.997±0.06 g/cm3(Predicted) |
| Fp | 9℃ |
| storage temp. | 2-8°C |
| solubility | deionized water: ≥10mg/mL |
| form | white powder |
| pka | 4.23±0.10(Predicted) |
| color | white to beige |
| Water Solubility | Soluble to 100 mM in water |
| BCS Class | 1 |
| InChI | InChI=1S/C8H17NO2/c1-6(2)3-7(5-9)4-8(10)11/h6-7H,3-5,9H2,1-2H3,(H,10,11)/t7-/m0/s1 |
| InChIKey | AYXYPKUFHZROOJ-ZETCQYMHSA-N |
| SMILES | C(O)(=O)C[C@@H](CN)CC(C)C |
| CAS DataBase Reference | 148553-50-8(CAS DataBase Reference) |
Safety Information
| Hazard Codes | Xn,T,F |
| Risk Statements | 63-48/22-39/23/24/25-23/24/25-11 |
| Safety Statements | 22-36/37-45-16-7 |
| RIDADR | UN1230 - class 3 - PG 2 - Methanol, solution |
| WGK Germany | 3 |
| HS Code | 29224999 |
| Storage Class | 11 - Combustible Solids |
| Hazard Classifications | Repr. 2 STOT SE 3 |
| Hazardous Substances Data | 148553-50-8(Hazardous Substances Data) |
| Description | Pregabalin is a second- generation antiepileptic drug (AED) known with the proprietary brand name of Lyrica® (Pfizer, Tadworth) in the UK and USA (Pfizer, New York, NY). |
| Generic formulation | MHRA/ CHM advice to minimize risk when switching patients with epilepsy between different manufacturers’ products (including generic products):
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| Indications | Epilepsy Adjunctive therapy of focal seizures with and without secondary generalization. Recommendations summarized from NICE (2012)
Psychiatry Generalized anxiety disorder. Neurology Peripheral and central neuropathic pain. |
| Dose titration |
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| Plasma levels monitoring | Pregabalin pharmacokinetics are linear over the recommended daily dose range; inter- subject pharmacokinetic variability for pregabalin is low (<20%) and multiple dose pharmacokinetics are predictable from single- dose data. Therefore, there is no need for routine monitoring of plasma concentrations of pregabalin. |
| Antiepileptic drus and therapeutic drugs for neuropathic pain | Pregabalin is a new antiepileptic drug, having a γ-amino butyric acid structure on its molecular structure, which has anticonvulsant effects, and is successfully developed by the company Pfizer for the treatment of peripheral neuropathic pain, or adjuvant treatment of partial seizures. In December 2008, the US Food and Drug Administration (FDA) approved pregabalin (trade name "Lyrica") for the treatment of diabetic peripheral neuropathic pain (DPN) and postherpetic neuralgia (PHN)which are Both the most common neuropathic pains. Neuropathic pain is one of the most difficult chronic pain syndromes to treat , dull pain, burning, tingling as the main feature, there are a lot of incentives of neuralgia, diabetes, infections (such as herpes zoster), cancer and AIDS, etc. can cause neurological pain, in Europe about 3% of the population suffer from neuralgia torture. The above information is edited by the chemicalbook of Tian Ye. |
| Cautions |
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| Adverse effects | Pregabalin can be associated with adverse effects at the level of the nervous system and other systems. |
| Interactions |
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| Special populations | Hepatic impairment No dose adjustment is required for patients with hepatic impairment. Renal impairment Reduce maintenance dose according to degree of reduction in creatinine clearance. Pregnancy
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| Behavioural and cognitive effects in patients with epilepsy | Pregalin is characterized by a good behavioural profile. This AED does not appear to have significant negative effects on mood or behaviour in patients with epilepsy, although depression has been reported in some patients (dose- dependent effects of mild- to- moderate intensity). A potential abuse or misuse of pregabalin has also been reported, with implications in terms of dependence and withdrawal. pregabalin is also associated with limited negative cognitive effects, mainly related to sedation, decreased arousal, decreased attention and concentration (dose- dependent effects of mild- to- moderate intensity). |
| Psychiatric use | Pregabalin has an approved indication and is widely used for the treatment of generalized anxiety disorder. Several randomized, double- blind, placebocontrolled trials found that pregabalin is an effective treatment for patients with generalized anxiety disorder and social anxiety disorder. Possible implications in the treatment of mood disorders and benzodiazepines dependence are emerging. Moreover, pregabalin may be a therapeutic agent for the treatment of alcohol abuse, in both withdrawal phase and relapse prevention. |
| Description | Pregabalin (Lyrica), a derivative of GABA that is closely related to gabapentin, has undergone extensive research for its efficacy in treating conditions such as generalized anxiety disorder (GAD), fibromyalgia, neuropathic pain, and partial complex seizures. It seems to have a more targeted effect on the a2-δ subunit of calcium channels in the brain compared to gabapentin. Pregabalin was granted FDA approval at the end of 2004 for the treatment of neuropathic pain and epilepsy. In 2008, it became the first medication approved for the management of fibromyalgia. Although pregabalin was approved for GAD treatment in the European Union in 2006, it has not yet received FDA approval for GAD in the United States as of the time of writing. |
| Chemical Properties | Off-White Solid |
| Originator | Warner-Lambert (US) |
| Uses | S-Enantiomer of Pregabalin. A GABA analogue used as an anticonvulsant. Anxiolytic analgesic used to treat peripheral neuropathic pain and fibromyalgia. |
| Uses | Pregabalin is an anticonvulsant drug used for neuropathic pain, as an adjunct therapy for partial seizures, and in generalized anxiety disorder. It was designed as a more potent successor to gabapentin. Pregabalin is marketed by Pfizer under the trade nam |
| Definition | ChEBI: Pregabalin is a gamma-amino acid that is gamma-aminobutyric acid (GABA) carrying an isobutyl substitutent at the beta-position (the S-enantiomer). Binds with high affinity to the alpha2-delta site (an auxiliary subunit of voltage-gated calcium channels) in central nervous system tissues. It has a role as an anticonvulsant and a calcium channel blocker. It is functionally related to a gamma-aminobutyric acid. |
| Brand name | Lyrica (CP). |
| General Description | Pregabalin, marketed as the anticonvulsant drug Lyrica, is used in the treatment of epilepsy and generalized anxiety disorder. Along with other anticonvulsants such as gabapentin and levetiracetam, pregabalin is also used to treat neuropathic pain. This certified reference standard is suitable for pregabalin GC/MS or LC/MS applications from forensic analysis, clinical toxicology and pain prescription monitoring to urine drug testing. |
| Biochem/physiol Actions | Pregabalin is a lipophilic GABA analog/ligand at α2δ subunit of voltage-dependent Ca2+ channels. Pregabalin is an anticonvulsant, anxiolytic analgesic used to treat peripheral neuropathic pain and fibromyalgia. |
| Clinical Use | Antiepileptic Neuropathic pain Generalised anxiety disorder |
| Synthesis | Several syntheses of pregabalin (X) have been disclosed in the literature, including process scale-up comparison ofseveral different routes. The most cost efficient routeas described in the publication is shown in the Scheme.Condensation of diethyl malonate 69 in the presense ofdiisopropyl amine in acetic acid gave a,b-unsaturated diester70 in high yield. Reaction of the enone diester withpotassium cyanide gave cyano diester 71 in 95% yield. In aremarkable three step, one pot process, the nitrile in 71 washydrolyzed followed by decarboxylation of one of the estersto provide 72 in 73% yield. Resolution of the twoenantiomers was achieved using (S)-(+)-mandellic acid, oneof the best acid found after many salt screening, to give, aftertwo recrystallization, a 99:1 ratio of the desired diastereomer.Removal of the acid was done with wet THF instead of baseseparation, to avoid salt impurities, and one recrystallizationin ethanol gave 100% ee diastereomer in 25 ¨C 29% overallyield. It?ˉs worth noting that the Pfizer group have come upwith a new process of preparing pregabalin (X) viaenantioselective reduction, that promises to further reducecost and waste associated with the manufacture of this drug. |
| target | Estrogen receptor | Calcium Channel | GABA Receptor | Antifection | 5-HT Receptor | Progestogen receptor |
| Drug interactions | Potentially hazardous interactions with other drugs Antidepressants: anticonvulsant effect antagonised. Antimalarials: anticonvulsant effect antagonised by mefloquine. Antipsychotics: anticonvulsant effect antagonised. Orlistat: possible increased risk of convulsions. |
| Metabolism | Pregabalin undergoes negligible metabolism, and about 98% of a dose is excreted in the urine as unchanged drug. |
Pregabalin Preparation Products And Raw materials
| Raw materials | 157422-27-0-->Hexanoic acid, 5-methyl-3-(nitromethyl)-, (3S)--->Pregabalin Impurity 99 |
