Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C24H27NO2 |
| Molecular Weight | 361.4767 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)[C@@H]1CCCN(CCC=C2C3=CC=CC=C3CCC4=CC=CC=C24)C1
InChI
InChIKey=RXWDEUWOJGGNHU-HXUWFJFHSA-N
InChI=1S/C24H27NO2/c26-24(27)20-9-5-15-25(17-20)16-6-12-23-21-10-3-1-7-18(21)13-14-19-8-2-4-11-22(19)23/h1-4,7-8,10-12,20H,5-6,9,13-17H2,(H,26,27)/t20-/m1/s1
| Molecular Formula | C24H27NO2 |
| Molecular Weight | 361.4767 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Tue Apr 01 16:41:12 GMT 2025
by
admin
on
Tue Apr 01 16:41:12 GMT 2025
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| Record UNII |
BC73A8YT4A
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| Record Status |
Validated (UNII)
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| Record Version |
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REN 1869
Created by
admin on Tue Apr 01 16:41:12 GMT 2025 , Edited by admin on Tue Apr 01 16:41:12 GMT 2025
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PRIMARY | <b>ReN 1869</b>, a selective H1 receptor antagonist, was originated by Novo Nordisk and was being developed for analgesic purposes. However, the development of??... | ||
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170149-99-2
Created by
admin on Tue Apr 01 16:41:12 GMT 2025 , Edited by admin on Tue Apr 01 16:41:12 GMT 2025
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PRIMARY | |||
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9799039
Created by
admin on Tue Apr 01 16:41:12 GMT 2025 , Edited by admin on Tue Apr 01 16:41:12 GMT 2025
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BC73A8YT4A
Created by
admin on Tue Apr 01 16:41:12 GMT 2025 , Edited by admin on Tue Apr 01 16:41:12 GMT 2025
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PRIMARY |
| Related Record | Type | Details | ||
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TARGET -> INHIBITOR |
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SALT/SOLVATE -> PARENT |
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ACTIVE MOIETY |