Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C14H18N2O3 |
| Molecular Weight | 262.3043 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CNC(=O)OC1=CC2=C(C=C1)N(C)[C@H]3OCC[C@@]23C
InChI
InChIKey=LXTKNVLLWOLCOV-JSGCOSHPSA-N
InChI=1S/C14H18N2O3/c1-14-6-7-18-12(14)16(3)11-5-4-9(8-10(11)14)19-13(17)15-2/h4-5,8,12H,6-7H2,1-3H3,(H,15,17)/t12-,14-/m0/s1
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| An interrupted Fischer indolization approach toward fused indoline-containing natural products. | 2009-08-06 |
|
| Accommodation of physostigmine and its analogues by acetylcholinesterase is dominated by hydrophobic interactions. | 2009-01-01 |
|
| Novel anticholinesterases based on the molecular skeletons of furobenzofuran and methanobenzodioxepine. | 2005-02-24 |
|
| Efficient formal total synthesis of physostigmine and physovenine: conformational analysis of key intermediates. | 2002-02 |
Patents
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Preferred Name | English | ||
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| Code System | Code | Type | Description | ||
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442113
Created by
admin on Mon Mar 31 21:50:38 GMT 2025 , Edited by admin on Mon Mar 31 21:50:38 GMT 2025
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H67Q5553UW
Created by
admin on Mon Mar 31 21:50:38 GMT 2025 , Edited by admin on Mon Mar 31 21:50:38 GMT 2025
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DTXSID90877566
Created by
admin on Mon Mar 31 21:50:38 GMT 2025 , Edited by admin on Mon Mar 31 21:50:38 GMT 2025
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m8767
Created by
admin on Mon Mar 31 21:50:38 GMT 2025 , Edited by admin on Mon Mar 31 21:50:38 GMT 2025
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PRIMARY | Merck Index | ||
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6091-05-0
Created by
admin on Mon Mar 31 21:50:38 GMT 2025 , Edited by admin on Mon Mar 31 21:50:38 GMT 2025
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PRIMARY |
SUBSTANCE RECORD
