Details
Stereochemistry | ACHIRAL |
Molecular Formula | C17H17NO3 |
Molecular Weight | 283.3218 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 1 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OC1=CC=C(CCNC(=O)\C=C\C2=CC=CC=C2)C=C1O
InChI
InChIKey=OICMBMJTQCLGNP-VQHVLOKHSA-N
InChI=1S/C17H17NO3/c19-15-8-6-14(12-16(15)20)10-11-18-17(21)9-7-13-4-2-1-3-5-13/h1-9,12,19-20H,10-11H2,(H,18,21)/b9-7+
Molecular Formula | C17H17NO3 |
Molecular Weight | 283.3218 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 1 |
Optical Activity | NONE |
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 07:58:24 UTC 2023
by
admin
on
Sat Dec 16 07:58:24 UTC 2023
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Record UNII |
3FD7ZX4Y88
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Record Status |
Validated (UNII)
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Record Version |
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DTXSID20762133
Created by
admin on Sat Dec 16 07:58:24 UTC 2023 , Edited by admin on Sat Dec 16 07:58:24 UTC 2023
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24285615
Created by
admin on Sat Dec 16 07:58:24 UTC 2023 , Edited by admin on Sat Dec 16 07:58:24 UTC 2023
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103188-45-0
Created by
admin on Sat Dec 16 07:58:24 UTC 2023 , Edited by admin on Sat Dec 16 07:58:24 UTC 2023
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105954-99-2
Created by
admin on Sat Dec 16 07:58:24 UTC 2023 , Edited by admin on Sat Dec 16 07:58:24 UTC 2023
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NON-SPECIFIC STEREOCHEMISTRY | |||
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3FD7ZX4Y88
Created by
admin on Sat Dec 16 07:58:24 UTC 2023 , Edited by admin on Sat Dec 16 07:58:24 UTC 2023
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Related Record | Type | Details | ||
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Among the compounds tested in this study, N-coumaroyldopamine and N-caffeoyldopamine were the two most potent compounds, able to increase cAMP at the concentrations < 0.05 uM in U937 cells. The decreasing order of potency was N-coumaroyldopamine > N- affeoyldopamine > N-feruloyldopamine > N-sinapoyldopamine > N-cinnamoyldopamine.
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PARENT -> CONSTITUENT ALWAYS PRESENT |
90 uM IC50 vs in vitro prostaglandin synthesis
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