Details
Stereochemistry | ACHIRAL |
Molecular Formula | C8H14N2O.ClH |
Molecular Weight | 190.671 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 1 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CO\N=C\C1=CCCN(C)C1
InChI
InChIKey=WEBMRZODPLSRKR-MLBSPLJJSA-N
InChI=1S/C8H14N2O.ClH/c1-10-5-3-4-8(7-10)6-9-11-2;/h4,6H,3,5,7H2,1-2H3;1H/b9-6+;
Molecular Formula | C8H14N2O |
Molecular Weight | 154.2096 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 1 |
Optical Activity | NONE |
Molecular Formula | ClH |
Molecular Weight | 36.461 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Milameline (previously known as RU 35926/CI-979), a partial muscarinic agonist that was developed as a cognition-enhancing agent for the treatment of patients with Alzheimer's disease. In spite of this drug has achieved phase III clinical trials, further studies were apparently discontinued.
Originator
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/10188788
CI-979/RU35926 (milameline) was well tolerated at doses of 0.002-1.0 mg with cholinergic symptoms such as hypersalivation and sweating, observed at 2-4 mg.
Route of Administration:
Oral
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 05:09:16 GMT 2023
by
admin
on
Sat Dec 16 05:09:16 GMT 2023
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Record UNII |
W867E71LPD
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Record Status |
Validated (UNII)
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Record Version |
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-
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Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C47796
Created by
admin on Sat Dec 16 05:09:16 GMT 2023 , Edited by admin on Sat Dec 16 05:09:16 GMT 2023
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9571001
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C91040
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admin on Sat Dec 16 05:09:16 GMT 2023 , Edited by admin on Sat Dec 16 05:09:16 GMT 2023
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GG-92
Created by
admin on Sat Dec 16 05:09:16 GMT 2023 , Edited by admin on Sat Dec 16 05:09:16 GMT 2023
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PRIMARY | |||
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139886-04-7
Created by
admin on Sat Dec 16 05:09:16 GMT 2023 , Edited by admin on Sat Dec 16 05:09:16 GMT 2023
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PRIMARY | |||
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W867E71LPD
Created by
admin on Sat Dec 16 05:09:16 GMT 2023 , Edited by admin on Sat Dec 16 05:09:16 GMT 2023
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PRIMARY | |||
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CHEMBL151938
Created by
admin on Sat Dec 16 05:09:16 GMT 2023 , Edited by admin on Sat Dec 16 05:09:16 GMT 2023
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PRIMARY |
Related Record | Type | Details | ||
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PARENT -> SALT/SOLVATE |
Related Record | Type | Details | ||
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ACTIVE MOIETY |