Chloroprocaine drug data and news

Chloroprocaine drug data, resources, and news articles (when available). Onconews.org provides news on cancer research. This section, which includes profiles on medicines that may or not be cancer-related is in beta form. If things run smoothly we will be releasing a new format late in the summer of 2006.

Generic name Chloroprocaine
Brand Names/Synonyms Astracaine 4%; Astracaine 4% Forte; CHLOROPROCAINE; Carbocaine; Carbocaine with Neo-Cobefrin; Chirocaine; Chlor-Procaine; Chloroprocain; Chloroprocaine; Chloroprocaine Hcl; Chloroprocainum [Inn-Latin]; Chlorprocaine; Chlorprocainum; Citanest Forte; Citanest Plain; Cloroprocaina [Inn-Spanish]; Dalcaine; Dilocaine; Duranest; Duranest-Mpf; HSDB 3301; Halestyn; Isocaine; Isocaine 2%; Isocaine 3%; L-Caine; Lidoject-1; Lidoject-2; Marcaine; Marcaine Spinal; Nesacaine; Nesacaine-Ce; Nesacaine-Mpf; Novocain; Octocaine; Octocaine-100; Octocaine-50; Piocaine; Polocaine; Polocaine-Mpf; Pontocaine; Sensorcaine; Sensorcaine Forte; Sensorcaine-Mpf; Sensorcaine-Mpf Spinal; Septocaine; Ultracaine D-S; Ultracaine D-S Forte; Xylocaine; Xylocaine 5% Spinal; Xylocaine Test Dose; Xylocaine-Mpf; Xylocaine-Mpf with Glucose
Indication For the production of local anesthesia by infiltration and peripheral nerve block. They are not to be used for lumbar or caudal epidural anesthesia.
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Description Not Available
Pharmacology Chloroprocaine is an anesthetic agent indicated for production of local or regional anesthesia, particularly for oral surgery. Chloroprocaine (like cocaine) has the advantage of constricting blood vessels which reduces bleeding, unlike other local anesthetics like lidocaine. Chloroprocaine is an ester anesthetic.
Mechanism Of Action Chloroprocaine acts mainly by inhibiting sodium influx through voltage gated sodium channels in the neuronal cell membrane of peripheral nerves. When the influx of sodium is interrupted, an action potential cannot arise and signal conduction is thus inhibited. The receptor site is thought to be located at the cytoplasmic (inner) portion of the sodium channel. Chloroprocaine has also been shown to bind or antagonize the function of N-methyl-D-aspartate (NMDA) receptors as well as nicotinic acetylcholine receptors and the serotonin receptor-ion channel complex.
Chloroprocaine News
(When available)

Abraxis BioScience Announces Co-Promotion Agreement with ...  Apr 26, 2006
...including EMLA(R) (Eutectic Mixture of Lidocaineand Prilocaine), Xylocaine(R) (lidocaine), Polocaine(R) (mepivacaine),Nesacaine(R) (chloroprocaine HCl Injection ... - Finanzen.net,

Abraxis BioScience Announces Co-Promotion Agreement with ...  Apr 27, 2006
EMLA(R) (Eutectic Mixture of Lidocaine and Prilocaine), Xylocaine(R) (lidocaine), Polocaine(R) (mepivacaine), Nesacaine(R) (chloroprocaine HCl Injection, USP ... - PharmaLive.com (press release),

Dosage Forms LIQUID
Drug_Category Anesthetics; Local Anesthetics; ATC:N01BA04
Absorption Not Available
Interactions Interactions for Chloroprocaine:

The administration of local anesthetic solutions containing epinephrine or norepinephrine to patients receiving monoamine oxidase inhibitors, tricyclic antidepressants or phenothiazines may produce severe, prolonged hypotension or hypertension. Concurrent use of these agents should generally be avoided. In situations when concurrent therapy is necessary, careful patient monitoring is essential.

Concurrent administration of vasopressor drugs (for the treatment of hypotension related to obstetric blocks) and ergot-type oxytocic drugs may cause severe, persistent hypertension or cerebrovascular accidents.

The para-aminobenzoic acid metabolite of chloroprocaine inhibits the action of sulfonamides. Therefore, chloroprocaine should not be used in any condition in which a sulfonamide drug is being employed.

Toxicity Not Available
Organisms Affected Humans and other mammals
Chemical IUPAC Name 2-diethylaminoethyl4-amino-2-chloro-benzoate
Chemical Formula C13H19ClN2O2
Molecular Weight 270.755 g/mol
Smiles String CCN(CC)CCOC(=O)C1=C(C=C(C=C1)N)Cl
Melting Point Not Available
Water Solubility 665 mg/L
State Solid
LogP/Hphobicity 2.464
Isoelectric Point Not Available
Biotransformation Not Available
Half Life 21 +/- 2 seconds
Protein Binding [%] Not Available
RxList Link RXlist
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Drug Reference http://www.drugs.com/cons/Chloroprocaine.html
http://www.rxlist.com/cgi/generic3/chloroprocaine.htm
Drug Type Approved Drug
Accession No APRD00404
CAS Registry Number 133-16-4
KEGG Compound ID C07877
PubChem ID SID:10079
PharmGKB ID PA448946
SwissProt ID Not Available
GenBank ID Not Available
Drug ID Number [DIN] 613304

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