Details
Stereochemistry | RACEMIC |
Molecular Formula | C16H21NO3 |
Molecular Weight | 275.3428 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC=C(C=C1OC2CCCC2)C3CNC(=O)C3
InChI
InChIKey=HJORMJIFDVBMOB-UHFFFAOYSA-N
InChI=1S/C16H21NO3/c1-19-14-7-6-11(12-9-16(18)17-10-12)8-15(14)20-13-4-2-3-5-13/h6-8,12-13H,2-5,9-10H2,1H3,(H,17,18)
Molecular Formula | C16H21NO3 |
Molecular Weight | 275.3428 |
Charge | 0 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Optical Activity | ( + / - ) |
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:32:19 UTC 2023
by
admin
on
Fri Dec 15 15:32:19 UTC 2023
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Record UNII |
K676NL63N7
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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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NCI_THESAURUS |
C257
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NCI_THESAURUS |
C744
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admin on Fri Dec 15 15:32:19 UTC 2023 , Edited by admin on Fri Dec 15 15:32:19 UTC 2023
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Code System | Code | Type | Description | ||
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SUB10367MIG
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4362
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K676NL63N7
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CHEMBL63
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262-771-1
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DTXSID3044124
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D020889
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m9650
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PRIMARY | Merck Index | ||
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5092
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760125
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85416-74-6
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DB01954
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61413-54-5
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104872
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100000084332
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ROLIPRAM
Created by
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40133
Created by
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C72842
Created by
admin on Fri Dec 15 15:32:19 UTC 2023 , Edited by admin on Fri Dec 15 15:32:19 UTC 2023
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Related Record | Type | Details | ||
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TARGET -> INHIBITOR |
IC50
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ENANTIOMER -> RACEMATE |
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TARGET -> INHIBITOR |
Rolipram has good brain penetration, or an ability to pass the blood−brain barrier.
IC50
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ENANTIOMER -> RACEMATE |
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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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BRAIN/PLASMA RATIO | PHARMACOKINETIC |
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Species BIOLOGICAL PHARMACOKINETIC |
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