Details
Stereochemistry | ACHIRAL |
Molecular Formula | C23H25FN2O |
Molecular Weight | 364.4558 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CN[C@]1(CC[C@@]2(CC1)OCCC3=C2NC4=C3C=C(F)C=C4)C5=CC=CC=C5
InChI
InChIKey=AMXGKMSRYLZAEO-YHBQERECSA-N
InChI=1S/C23H25FN2O/c1-25-22(16-5-3-2-4-6-16)10-12-23(13-11-22)21-18(9-14-27-23)19-15-17(24)7-8-20(19)26-21/h2-8,15,25-26H,9-14H2,1H3/t22-,23-
Molecular Formula | C23H25FN2O |
Molecular Weight | 364.4558 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Lexanopadol is a potent ORL-1 agonist (opioid receptor like -1), nociceptin receptor agonists and opioid mu receptor agonists. Preliminary evidence suggests that targeting ORL-1 receptors may have synergistic effects with mu receptors hence enhancing the therapeutic profile of Lexanopadol in the treatment of pain. Lexanopadol is particularly suited for the management of moderate to severe chronic pain, including neuropathic pain. Lexanopadol hemicitrate is in phase II clinical trials for the treatment of pain. However there is no recent development reported.
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 09:02:52 GMT 2023
by
admin
on
Sat Dec 16 09:02:52 GMT 2023
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Record UNII |
DZ4NDW1LZX
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Record Status |
Validated (UNII)
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Record Version |
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C170119
Created by
admin on Sat Dec 16 09:02:52 GMT 2023 , Edited by admin on Sat Dec 16 09:02:52 GMT 2023
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1357348-09-4
Created by
admin on Sat Dec 16 09:02:52 GMT 2023 , Edited by admin on Sat Dec 16 09:02:52 GMT 2023
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DZ4NDW1LZX
Created by
admin on Sat Dec 16 09:02:52 GMT 2023 , Edited by admin on Sat Dec 16 09:02:52 GMT 2023
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300000034332
Created by
admin on Sat Dec 16 09:02:52 GMT 2023 , Edited by admin on Sat Dec 16 09:02:52 GMT 2023
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CHEMBL3301613
Created by
admin on Sat Dec 16 09:02:52 GMT 2023 , Edited by admin on Sat Dec 16 09:02:52 GMT 2023
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24798598
Created by
admin on Sat Dec 16 09:02:52 GMT 2023 , Edited by admin on Sat Dec 16 09:02:52 GMT 2023
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9765
Created by
admin on Sat Dec 16 09:02:52 GMT 2023 , Edited by admin on Sat Dec 16 09:02:52 GMT 2023
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BC-23
Created by
admin on Sat Dec 16 09:02:52 GMT 2023 , Edited by admin on Sat Dec 16 09:02:52 GMT 2023
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Related Record | Type | Details | ||
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TARGET -> AGONIST |
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ACTIVE MOIETY |
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