Cyprodenate: Difference between revisions
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{{Short description|Chemical compound}} |
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{{Drugbox |
{{Drugbox |
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| Watchedfields = changed |
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| verifiedrevid = |
| verifiedrevid = 444141768 |
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| IUPAC_name = 2-dimethylaminoethyl 3-cyclohexylpropanoate |
| IUPAC_name = 2-dimethylaminoethyl 3-cyclohexylpropanoate |
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| image = Cyprodenate.svg |
| image = Cyprodenate.svg |
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| tradename = |
| tradename = |
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| Drugs.com = {{drugs.com|international|cyprodenate}} |
| Drugs.com = {{drugs.com|international|cyprodenate}} |
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| routes_of_administration = |
| routes_of_administration = |
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<!--Identifiers--> |
<!--Identifiers--> |
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| CAS_number_Ref = {{cascite|correct|??}} |
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| CAS_number = 15585-86-1 |
| CAS_number = 15585-86-1 |
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| ATC_prefix = |
| ATC_prefix = N06BX04 |
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| PubChem = 71875 |
| PubChem = 71875 |
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| DrugBank_Ref = {{drugbankcite|correct|drugbank}} |
| DrugBank_Ref = {{drugbankcite|correct|drugbank}} |
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| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
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| ChemSpiderID = 64892 |
| ChemSpiderID = 64892 |
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| ChEMBL = 2106590 |
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| UNII_Ref = {{fdacite|correct|FDA}} |
| UNII_Ref = {{fdacite|correct|FDA}} |
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| UNII = I44VIC13P8 |
| UNII = I44VIC13P8 |
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<!--Chemical data--> |
<!--Chemical data--> |
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| C=13 | H=25 | N=1 | O=2 |
| C=13 | H=25 | N=1 | O=2 |
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| molecular_weight = 227.34 |
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| InChI = 1/C13H25NO2/c1-14(2)10-11-16-13(15)9-8-12-6-4-3-5-7-12/h12H,3-11H2,1-2H3 |
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| InChIKey = MPOYJPINNSIHAK-UHFFFAOYAN |
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| StdInChI_Ref = {{stdinchicite|correct|chemspider}} |
| StdInChI_Ref = {{stdinchicite|correct|chemspider}} |
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| StdInChI = 1S/C13H25NO2/c1-14(2)10-11-16-13(15)9-8-12-6-4-3-5-7-12/h12H,3-11H2,1-2H3 |
| StdInChI = 1S/C13H25NO2/c1-14(2)10-11-16-13(15)9-8-12-6-4-3-5-7-12/h12H,3-11H2,1-2H3 |
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'''Cyprodenate''' ('''Actebral''') is a [[stimulant]] drug.<ref>{{ |
'''Cyprodenate''' ('''Actebral''') is a [[stimulant]] drug.<ref>{{cite journal | vauthors = Dormard Y, Levron JC, Le Fur JM | title = Pharmacokinetic study of maleate acid of 2-(N,N-dimethylaminoethanol-14C1)-cyclohexylpropionate (cyprodenate) and of N,N-dimethylaminoethanol-14C1 in animals | journal = Arzneimittel-Forschung | volume = 25 | issue = 2 | pages = 201–7 | date = February 1975 | pmid = 1173033 }}</ref> It was used for counteracting the effects of [[benzodiazepine]] tranquillizer drugs before the development of newer [[antidotes]] such as [[flumazenil]].<ref>{{cite journal | vauthors = Bobkov I, Morozov IS | title = [Correction of psychodepressive effects of benzodiazepine tranquilizers by administration of psychostimulants] | language = English | journal = Biulleten' Eksperimental'noi Biologii I Meditsiny | volume = 94 | issue = 10 | pages = 48–51 | date = October 1982 | pmid = 6129008 | doi = 10.1007/BF00827201 | s2cid = 19153614 }}</ref> It produces [[dimethylethanolamine]] as a [[metabolite]].{{citation needed|date=September 2018}} |
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== See also == |
== See also == |
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{{Stimulants}} |
{{Stimulants}} |
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{{Nootropics}} |
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{{Psychostimulants, agents used for ADHD and nootropics}} |
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{{Acetylcholine receptor modulators}} |
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{{Monoamine releasing agents}} |
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[[Category:Nootropics]] |
[[Category:Nootropics]] |
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[[Category:Stimulants]] |
[[Category:Stimulants]] |
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[[Category: |
[[Category:Propionate esters]] |
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[[Category: |
[[Category:Dimethylamino compounds]] |
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[[Category:Prodrugs]] |
[[Category:Prodrugs]] |
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[[Category:Cyclohexyl compounds]] |
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Latest revision as of 07:57, 25 March 2024
Clinical data | |
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AHFS/Drugs.com | International Drug Names |
ATC code | |
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CAS Number | |
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CompTox Dashboard (EPA) | |
ECHA InfoCard | 100.036.025 |
Chemical and physical data | |
Formula | C13H25NO2 |
Molar mass | 227.348 g·mol−1 |
3D model (JSmol) | |
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(verify) |
Cyprodenate (Actebral) is a stimulant drug.[1] It was used for counteracting the effects of benzodiazepine tranquillizer drugs before the development of newer antidotes such as flumazenil.[2] It produces dimethylethanolamine as a metabolite.[citation needed]
See also[edit]
References[edit]
- ^ Dormard Y, Levron JC, Le Fur JM (February 1975). "Pharmacokinetic study of maleate acid of 2-(N,N-dimethylaminoethanol-14C1)-cyclohexylpropionate (cyprodenate) and of N,N-dimethylaminoethanol-14C1 in animals". Arzneimittel-Forschung. 25 (2): 201–7. PMID 1173033.
- ^ Bobkov I, Morozov IS (October 1982). "[Correction of psychodepressive effects of benzodiazepine tranquilizers by administration of psychostimulants]". Biulleten' Eksperimental'noi Biologii I Meditsiny. 94 (10): 48–51. doi:10.1007/BF00827201. PMID 6129008. S2CID 19153614.