Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C17H23NO3 |
Molecular Weight | 289.3694 |
Optical Activity | ( - ) |
Defined Stereocenters | 4 / 4 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CN1[C@H]2CC[C@@H]1C[C@@H](C2)OC(=O)[C@H](CO)C3=CC=CC=C3
InChI
InChIKey=RKUNBYITZUJHSG-FXUDXRNXSA-N
InChI=1S/C17H23NO3/c1-18-13-7-8-14(18)10-15(9-13)21-17(20)16(11-19)12-5-3-2-4-6-12/h2-6,13-16,19H,7-11H2,1H3/t13-,14+,15+,16-/m1/s1
Molecular Formula | C17H23NO3 |
Molecular Weight | 289.3694 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 4 / 4 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:18:24 UTC 2023
by
admin
on
Fri Dec 15 15:18:24 UTC 2023
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Record UNII |
PX44XO846X
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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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WHO-VATC |
QA03CB31
Created by
admin on Fri Dec 15 15:18:25 UTC 2023 , Edited by admin on Fri Dec 15 15:18:25 UTC 2023
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WHO-ATC |
A03CB31
Created by
admin on Fri Dec 15 15:18:25 UTC 2023 , Edited by admin on Fri Dec 15 15:18:25 UTC 2023
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LIVERTOX |
NBK548870
Created by
admin on Fri Dec 15 15:18:25 UTC 2023 , Edited by admin on Fri Dec 15 15:18:25 UTC 2023
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WHO-ATC |
A03BA03
Created by
admin on Fri Dec 15 15:18:25 UTC 2023 , Edited by admin on Fri Dec 15 15:18:25 UTC 2023
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WHO-VATC |
QA03BA03
Created by
admin on Fri Dec 15 15:18:25 UTC 2023 , Edited by admin on Fri Dec 15 15:18:25 UTC 2023
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NCI_THESAURUS |
C29704
Created by
admin on Fri Dec 15 15:18:25 UTC 2023 , Edited by admin on Fri Dec 15 15:18:25 UTC 2023
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Code System | Code | Type | Description | ||
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PX44XO846X
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admin on Fri Dec 15 15:18:25 UTC 2023 , Edited by admin on Fri Dec 15 15:18:25 UTC 2023
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757064
Created by
admin on Fri Dec 15 15:18:25 UTC 2023 , Edited by admin on Fri Dec 15 15:18:25 UTC 2023
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58164
Created by
admin on Fri Dec 15 15:18:25 UTC 2023 , Edited by admin on Fri Dec 15 15:18:25 UTC 2023
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PX44XO846X
Created by
admin on Fri Dec 15 15:18:25 UTC 2023 , Edited by admin on Fri Dec 15 15:18:25 UTC 2023
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PRIMARY | |||
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1402
Created by
admin on Fri Dec 15 15:18:25 UTC 2023 , Edited by admin on Fri Dec 15 15:18:25 UTC 2023
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SUB14160MIG
Created by
admin on Fri Dec 15 15:18:25 UTC 2023 , Edited by admin on Fri Dec 15 15:18:25 UTC 2023
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PRIMARY | |||
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153970
Created by
admin on Fri Dec 15 15:18:25 UTC 2023 , Edited by admin on Fri Dec 15 15:18:25 UTC 2023
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PRIMARY | RxNorm | ||
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HYOSCYAMINE
Created by
admin on Fri Dec 15 15:18:25 UTC 2023 , Edited by admin on Fri Dec 15 15:18:25 UTC 2023
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100000077628
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DTXSID80889335
Created by
admin on Fri Dec 15 15:18:25 UTC 2023 , Edited by admin on Fri Dec 15 15:18:25 UTC 2023
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3552
Created by
admin on Fri Dec 15 15:18:25 UTC 2023 , Edited by admin on Fri Dec 15 15:18:25 UTC 2023
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C29104
Created by
admin on Fri Dec 15 15:18:25 UTC 2023 , Edited by admin on Fri Dec 15 15:18:25 UTC 2023
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CHEMBL1331216
Created by
admin on Fri Dec 15 15:18:25 UTC 2023 , Edited by admin on Fri Dec 15 15:18:25 UTC 2023
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DB00424
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101-31-5
Created by
admin on Fri Dec 15 15:18:25 UTC 2023 , Edited by admin on Fri Dec 15 15:18:25 UTC 2023
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202-933-0
Created by
admin on Fri Dec 15 15:18:25 UTC 2023 , Edited by admin on Fri Dec 15 15:18:25 UTC 2023
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17486
Created by
admin on Fri Dec 15 15:18:25 UTC 2023 , Edited by admin on Fri Dec 15 15:18:25 UTC 2023
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PRIMARY | |||
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m6167
Created by
admin on Fri Dec 15 15:18:25 UTC 2023 , Edited by admin on Fri Dec 15 15:18:25 UTC 2023
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PRIMARY | Merck Index |
Related Record | Type | Details | ||
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RACEMATE -> ENANTIOMER | |||
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SALT/SOLVATE -> PARENT |
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SALT/SOLVATE -> PARENT |
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SOLVATE->ANHYDROUS | |||
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BINDER->LIGAND |
BINDING
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SALT/SOLVATE -> PARENT |
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Related Record | Type | Details | ||
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PARENT -> IMPURITY |
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
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Related Record | Type | Details | ||
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ACTIVE MOIETY |
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Name | Property Type | Amount | Referenced Substance | Defining | Parameters | References |
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Biological Half-life | PHARMACOKINETIC |
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