Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C14H16N2O3 |
| Molecular Weight | 260.2884 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
ONC(=N)CC(O)COC1=C2C=CC=CC2=CC=C1
InChI
InChIKey=UPZVYDSBLFNMLK-UHFFFAOYSA-N
InChI=1S/C14H16N2O3/c15-14(16-18)8-11(17)9-19-13-7-3-5-10-4-1-2-6-12(10)13/h1-7,11,17-18H,8-9H2,(H2,15,16)
| Molecular Formula | C14H16N2O3 |
| Molecular Weight | 260.2884 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Kinetic resolution of 1-chloro-3-(1-naphthyloxy)-2-propanol, an intermediate in the synthesis of beta-adrenergic receptor blockers. | 2003-06 |
|
| [Acute nadoxolol poisoning. A multicentric study of 35 cases]. | 1982-05 |
|
| [Clinical study of a new anti-arrhythmia agent: nadoxolol]. | 1976-04 |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.drugfuture.com/chemdata/nadoxolol.html
LD50 in mice (mg/kg): 180 i.v.; 1000 orally
Route of Administration:
Other
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:13:34 GMT 2025
by
admin
on
Mon Mar 31 18:13:34 GMT 2025
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| Record UNII |
SK43HU1689
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| Record Status |
Validated (UNII)
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| Record Version |
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Preferred Name | English | ||
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| Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C29576
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1866
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SK43HU1689
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Nadoxolol
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SUB09112MIG
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m1212
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PRIMARY | Merck Index | ||
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C006154
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31462
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CHEMBL357513
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DTXSID90968903
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3322
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100000084409
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54063-51-3
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37333
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C90798
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| Related Record | Type | Details | ||
|---|---|---|---|---|
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ENANTIOMER -> RACEMATE | |||
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ENANTIOMER -> RACEMATE | |||
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SALT/SOLVATE -> PARENT |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |