Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C12H14ClNO2 |
Molecular Weight | 239.698 |
Optical Activity | ( - ) |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
N[C@]1(CCC[C@@H](O)C1=O)C2=C(Cl)C=CC=C2
InChI
InChIKey=CFBVGSWSOJBYGC-ZYHUDNBSSA-N
InChI=1S/C12H14ClNO2/c13-9-5-2-1-4-8(9)12(14)7-3-6-10(15)11(12)16/h1-2,4-5,10,15H,3,6-7,14H2/t10-,12-/m1/s1
Molecular Formula | C12H14ClNO2 |
Molecular Weight | 239.698 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 16:09:35 GMT 2023
by
admin
on
Sat Dec 16 16:09:35 GMT 2023
|
Record UNII |
HB1X671CEU
|
Record Status |
Validated (UNII)
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Record Version |
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-
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Code System | Code | Type | Description | ||
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89504167
Created by
admin on Sat Dec 16 16:09:35 GMT 2023 , Edited by admin on Sat Dec 16 16:09:35 GMT 2023
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PRIMARY | |||
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Hydroxynorketamine
Created by
admin on Sat Dec 16 16:09:35 GMT 2023 , Edited by admin on Sat Dec 16 16:09:35 GMT 2023
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PRIMARY | |||
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120199-64-6
Created by
admin on Sat Dec 16 16:09:35 GMT 2023 , Edited by admin on Sat Dec 16 16:09:35 GMT 2023
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PRIMARY | |||
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HB1X671CEU
Created by
admin on Sat Dec 16 16:09:35 GMT 2023 , Edited by admin on Sat Dec 16 16:09:35 GMT 2023
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PRIMARY |
Related Record | Type | Details | ||
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RACEMATE -> ENANTIOMER |
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TARGET -> ACTIVATOR |
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SALT/SOLVATE -> PARENT |
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TARGET -> ACTIVATOR |
PROVIDES SUSTAIN ACTIVATION OF RECEPTOR
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Related Record | Type | Details | ||
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PARENT -> METABOLITE ACTIVE |
MAJOR METABOLITE IN PLASMA
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Related Record | Type | Details | ||
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ACTIVE MOIETY |
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