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Gabapentin

HCID 6919078
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Grundinformationen

CAS
60142-96-3
Standard-SMILES
[NH3+]CC1(CC(=O)[O-])CCCCC1
InChIKey
UGJMXCAKCUNAIE-UHFFFAOYSA-N
Summenformel
C9H17NO2
Durchschnittliche Molmasse
171,24 g/mol

Namen und Bezeichner

Bevorzugter Name
Gabapentin
Lokaler Name
Gabapentin
Englischer Name
Gabapentin
Summenformel
C9H17NO2
Molmasse
171.24

Namen und Synonyme

GABAPENTINENEURONTINGABAPENTIN HYDROCHLORIDE1-(Aminomethyl)-cyclohexaneacetic acid, NeurontinGOE-3450Gabapentin API1-(AMINOMETHYL)CYCLOHEXANEACETIC ACID2-[1-(aminomethyl)cyclohexyl]acetic acidci945go3450

Datenbank-Bezeichner

CAS
60142-96-3
PubChem CID
6919078

Eigenschaften

Physikochemische Eigenschaften

Schmelzpunkt
162 °C · 162°C
Siedepunkt
314.4 · 314.4±15.0 °C(Predicted)
Dichte
1.058 · 1.058±0.06 g/cm3(Predicted)
Flammpunkt
9 ℃ · 9℃
storage temp.
2 · 2-8°C
Löslichkeit
2 O: · H2O: 10 mg/mL
Aggregatzustand
solid
pka
1 · pKa1 (25°) 3.68; pKa2 10.70
Farbe
off-white
Wasserlöslichkeit
100 mM · water: 100mM
Merck
14 · 14,4319
BRN
2359739 · 2359739
BCS Class
3 · 3
Stabilität
1 year · Stable for 1 year from date of purchase as supplied. Solutions in distilled water may be stored at -20°C for up to 3 months.
Major Application
pharmaceutical (small molecule)
InChI
1S/C9H17NO2/c10-7-9(6-8(11)12)4-2-1-3-5-9/h1-7,10H2,(H,11,12)
InChIKey
UGJMXCAKCUNAIE-UHFFFAOYSA-N
SMILES
NCC1(CCCCC1)CC(O)=O
CAS Datenbank
60142 · 60142-96-3(CAS DataBase Reference)
EPA chemische Informationen
1 · Cyclohexaneacetic acid, 1-(aminomethyl)- (60142-96-3)

Sicherheit und Regulatorisches

Sicherheitsangaben dienen nur zur Orientierung und ersetzen weder das Sicherheitsdatenblatt (SDB) des Lieferanten noch geltende Vorschriften oder eine fachliche Bewertung.

Sicherheitsdaten

wgk
3
ridadr
UN3259
hs_code
29224999
RTECS-Nr.
GU6496000
risk_code
61-36/37/38-39/23/24/25-23/24/25-11
hazard_code
T,Xi,F
safety_code
53-26-36/37/39-45-36-36/37-16
hazard_class
IRRITANT
Speicherklasse
3 - Flammable liquids
Giftige Stoffe Daten
60142-96-3(Hazardous Substances Data)
Hazard Classifications
Acute Tox. 3 DermalAcute Tox. 3 InhalationAcute Tox. 3 OralFlam. Liq. 2STOT SE 1

Chemie und Industrie

Anwendungen · 3 Einträge

BeschreibungGabapentin was introduced in 1993 in the UK and early 1994 in the USA as an adjunctive therapy in the treatment of refractory partial seizures and secondarily generalized tonic-clonic seizures. Although being a lipophilic analog of the neurotransmitter GABA, gabapentin appears to exert its anticonvulsive function by a GABA receptor independent mechanism, possibly involving the L-system amino acid transporter protein. Gabapentin easily crosses the blood brain barrier and exhibits a favorable pharmacokinetic profile with high tolerability. It does not interfere with the metabolism of other concomitant administered antiepileptic drugs, thus having a low potential for drug interactions. Studies are currently underway for the use of gabapentin as mono-therapy for the treatment of various seizures.

HistoryGabapentin is a pharmacologically active amino acid, discovered by the pharmaceutical company Parke-Davis, now owned by Warner-Lambert, a division of Pfizer in 1974. Although it was first approved as a treatment for partial seizures in 1993, Pfizer pleaded guilty to illegally marketing gabapentin for unapproved uses in 2004 and was heavily fined by the US Department of Justice for defrauding public health care programs. When this adjunctive use was approved by the US Food and Drug Administration (FDA) in late 1993, Warner-Lambert released gabapentin under the brand name Neurontin, expecting it to make no more than $500,000. But the 2001 sales of Neurontin raked in $1.2 billion.

VerwendenGabapentin is an Amino acid structurally related to γ-Aminobutyric Acid (GABA), designed to cross the blood brain barrier. Used as an anticonvulsant.

Vor- und nachgelagerte Produkte

Vorgelagerte Rohstoffe

NatriumazidCyclohexanEthyl-chlorformiatMethanolN,N-Diethylethanamin

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Ergänzende Hinweise · 1 Eintrag

DefinitionChEBI: Gabapentin is a gamma-amino acid that is cyclohexane substituted at position 1 by aminomethyl and carboxymethyl groups. Used for treatment of neuropathic pain and restless legs syndrome. It has a role as an anticonvulsant, a calcium channel blocker, an environmental contaminant and a xenobiotic. It is functionally related to a gamma-aminobutyric acid.