Budipine

Budipine

Clinical data
AHFS/Drugs.com	International Drug Names
ATC code	N04BX03 (WHO)
Identifiers
IUPAC name 1-tert-butyl-4,4-diphenylpiperidine
CAS Number	57982-78-2 Y
PubChem CID	68778
ChemSpider	62021 Y
UNII	L9026OPI2Z
KEGG	D07306 Y
ChEMBL	ChEMBL334491 Y
E number	{{#property:P628}}
ECHA InfoCard	{{#property:P2566}}
Chemical and physical data
Formula	C21H27N
Molar mass	293.446 g/mol
3D model (JSmol)	Interactive image
SMILES c1(ccccc1)C3(c2ccccc2)CCN(C(C)(C)C)CC3
InChI InChI=1S/C21H27N/c1-20(2,3)22-16-14-21(15-17-22,18-10-6-4-7-11-18)19-12-8-5-9-13-19/h4-13H,14-17H2,1-3H3 Y Key:QIHLUZAFSSMXHQ-UHFFFAOYSA-N Y
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WikiDoc Resources for Budipine
Articles
Most recent articles on Budipine Most cited articles on Budipine Review articles on Budipine Articles on Budipine in N Eng J Med, Lancet, BMJ
Media
Powerpoint slides on Budipine Images of Budipine Photos of Budipine Podcasts & MP3s on Budipine Videos on Budipine
Evidence Based Medicine
Cochrane Collaboration on Budipine Bandolier on Budipine TRIP on Budipine
Clinical Trials
Ongoing Trials on Budipine at Clinical Trials.gov Trial results on Budipine Clinical Trials on Budipine at Google
Guidelines / Policies / Govt
US National Guidelines Clearinghouse on Budipine NICE Guidance on Budipine NHS PRODIGY Guidance FDA on Budipine CDC on Budipine
Books
Books on Budipine
News
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Commentary
Blogs on Budipine
Definitions
Definitions of Budipine
Patient Resources / Community
Patient resources on Budipine Discussion groups on Budipine Patient Handouts on Budipine Directions to Hospitals Treating Budipine Risk calculators and risk factors for Budipine
Healthcare Provider Resources
Symptoms of Budipine Causes & Risk Factors for Budipine Diagnostic studies for Budipine Treatment of Budipine
Continuing Medical Education (CME)
CME Programs on Budipine
International
Budipine en Espanol Budipine en Francais
Business
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Experimental / Informatics
List of terms related to Budipine

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Budipine is an antiparkinson agent.

Its mechanism of action is not well characterized. It is believed to be an NMDA receptor antagonist, however, promoting the synthesis of dopamine.

Because it provides additional benefits relative to existing treatments, it probably does not precisely mimic the mechanism of an existing known treatment.

See also

• Piperidine