Page last updated: 2024-12-06
bornaprine
Description
Research Excerpts
Clinical Trials
Roles
Classes
Pathways
Study Profile
Bioassays
Related Drugs
Related Conditions
Protein Interactions
Research Growth
Market Indicators
Description
bornaprine: beneficial effect in Parkinsonism due to inhibition of muscarinic or nicotinic transmission [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]
Cross-References
ID Source | ID |
---|---|
PubMed CID | 30160 |
CHEMBL ID | 4297087 |
CHEBI ID | 135406 |
SCHEMBL ID | 924755 |
MeSH ID | M0048189 |
Synonyms (12)
Synonym |
---|
bornaprine |
3-(diethylamino)propyl 2-phenyl-2-norbornanecarboxylate |
bornaprine (inn) |
20448-86-6 |
D07302 |
CHEBI:135406 |
SCHEMBL924755 |
BDNMABJZSXTKAQ-UHFFFAOYSA-N |
Q4946040 |
3-(diethylamino)propyl 2-phenylbicyclo[2.2.1]heptane-2-carboxylate |
CHEMBL4297087 |
DTXSID20864944 |
Research Excerpts
Treatment
Excerpt | Reference | Relevance |
---|---|---|
"The bornaprine treatment, at 2 or 4 mg day(-1) dosage, has been effective and safe to contrast hyperhidrosis, in the acute phase of spinal cord-injured patients. " | ( Hyperhidrosis treatment with bornaprine in the acute phase of spinal cord-injured patients. Bertolotto, F; Losio, L; Massone, A; Moretto, S; Oggerino, C; Ottonello, M; Sergi, R, 2008) | 1.2 |
Pharmacokinetics
Excerpt | Reference | Relevance |
---|---|---|
" The curves showed no obvious differences in their pharmacokinetic properties." | ( [The disposition of bornaprine hydrochloride in the rat. 1. Pharmacokinetics: synthesis, plasma level and elimination]. Hege, G; Neidlein, R; Pichler, B; Weymann, J, 1989) | 0.6 |
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]
Drug Classes (1)
Class | Description |
---|---|
monoterpenoid | Any terpenoid derived from a monoterpene. The term includes compounds in which the C10 skeleton of the parent monoterpene has been rearranged or modified by the removal of one or more skeletal atoms (generally methyl groups). |
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res] |
Research
Studies (16)
Timeframe | Studies, This Drug (%) | All Drugs % |
---|---|---|
pre-1990 | 12 (75.00) | 18.7374 |
1990's | 2 (12.50) | 18.2507 |
2000's | 1 (6.25) | 29.6817 |
2010's | 1 (6.25) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
Market Indicators
Research Demand Index: 24.33
According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be moderate demand-to-supply ratio for research on this compound.
| This Compound (24.33) All Compounds (24.57) |
Study Types
Publication Type | This drug (%) | All Drugs (%) |
---|---|---|
Trials | 7 (38.89%) | 5.53% |
Reviews | 0 (0.00%) | 6.00% |
Case Studies | 1 (5.56%) | 4.05% |
Observational | 0 (0.00%) | 0.25% |
Other | 10 (55.56%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |