Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C34H31F3N2O2 |
| Molecular Weight | 556.6173 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC=CC=C1[C@H](C2=CC=CC3=CC=CC=C23)[C@@](C)(C#N)C(=O)N4CCC(CC4)C5=CC=CC(=C5)C(F)(F)F
InChI
InChIKey=JZPONCMNBSEYQW-CQTOTRCISA-N
InChI=1S/C34H31F3N2O2/c1-33(22-38,32(40)39-19-17-23(18-20-39)25-11-7-12-26(21-25)34(35,36)37)31(29-14-5-6-16-30(29)41-2)28-15-8-10-24-9-3-4-13-27(24)28/h3-16,21,23,31H,17-20H2,1-2H3/t31-,33+/m0/s1
| Molecular Formula | C34H31F3N2O2 |
| Molecular Weight | 556.6173 |
| 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
Fri Dec 15 15:35:43 UTC 2023
by
admin
on
Fri Dec 15 15:35:43 UTC 2023
|
| Record UNII |
QT9VF4MW6U
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
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Code | English | ||
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Code | English | ||
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Code | English | ||
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Systematic Name | English | ||
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Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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9829162
Created by
admin on Fri Dec 15 15:35:43 UTC 2023 , Edited by admin on Fri Dec 15 15:35:43 UTC 2023
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PRIMARY | |||
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WAY-204688
Created by
admin on Fri Dec 15 15:35:43 UTC 2023 , Edited by admin on Fri Dec 15 15:35:43 UTC 2023
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PRIMARY | |||
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QT9VF4MW6U
Created by
admin on Fri Dec 15 15:35:43 UTC 2023 , Edited by admin on Fri Dec 15 15:35:43 UTC 2023
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PRIMARY | |||
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DTXSID701336370
Created by
admin on Fri Dec 15 15:35:43 UTC 2023 , Edited by admin on Fri Dec 15 15:35:43 UTC 2023
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PRIMARY | |||
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796854-35-8
Created by
admin on Fri Dec 15 15:35:43 UTC 2023 , Edited by admin on Fri Dec 15 15:35:43 UTC 2023
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PRIMARY | |||
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SIM-688
Created by
admin on Fri Dec 15 15:35:43 UTC 2023 , Edited by admin on Fri Dec 15 15:35:43 UTC 2023
|
PRIMARY | HY-19498 CAS:796854-35-8 (Synonyms WAY 204688, WAY204688, SIM 688, SIM688, SIM-688) |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
ACTIVE MOIETY |
Class: Fluorobenzenes, Nitrile, Piperidine; Mechanism of Action: Estrogen receptor agonist, NF-kappa B inhibitor; Highest Development Phase: Discontinued for Rheumatoid arthritis; Most Recent Event: 11 Jan 2005 Phase-I clinical trials in Rheumatoid arthritis in USA (PO)
|