Details
Stereochemistry | RACEMIC |
Molecular Formula | C20H23N3O2 |
Molecular Weight | 337.4155 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@]12N(C)CC[C@@]1(C)C3=C(C=CC(OC(=O)NC4=CC=CC=C4)=C3)N2C
InChI
InChIKey=PBHFNBQPZCRWQP-QUCCMNQESA-N
InChI=1S/C20H23N3O2/c1-20-11-12-22(2)18(20)23(3)17-10-9-15(13-16(17)20)25-19(24)21-14-7-5-4-6-8-14/h4-10,13,18H,11-12H2,1-3H3,(H,21,24)/t18-,20+/m1/s1
Molecular Formula | C20H23N3O2 |
Molecular Weight | 337.4155 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Phenserine (Axonyx/NIH). | 2000 Oct |
|
The integrated role of desferrioxamine and phenserine targeted to an iron-responsive element in the APP-mRNA 5'-untranslated region. | 2004 Dec |
|
The cholinesterase inhibitor, phenserine, improves Morris water maze performance of scopolamine-treated rats. | 2005 Jan 21 |
|
Anticholinesterase and pharmacokinetic profile of phenserine in healthy elderly human subjects. | 2005 Oct |
|
Phenserine. | 2007 Jul |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 09:46:11 GMT 2023
by
admin
on
Sat Dec 16 09:46:11 GMT 2023
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Record UNII |
N8142NV8UM
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Record Status |
Validated (UNII)
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Record Version |
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