Details
Stereochemistry | ACHIRAL |
Molecular Formula | C18H14F3N5O3S2 |
Molecular Weight | 469.461 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1(C)N(C(=S)N(C1=O)C2=CC=C(C#N)C(=C2)C(F)(F)F)C3=CC=CC(=N3)S(N)(=O)=O
InChI
InChIKey=JIIHFLNYGVNTFP-UHFFFAOYSA-N
InChI=1S/C18H14F3N5O3S2/c1-17(2)15(27)25(11-7-6-10(9-22)12(8-11)18(19,20)21)16(30)26(17)13-4-3-5-14(24-13)31(23,28)29/h3-8H,1-2H3,(H2,23,28,29)
Molecular Formula | C18H14F3N5O3S2 |
Molecular Weight | 469.461 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Design and synthesis of an androgen receptor pure antagonist (CH5137291) for the treatment of castration-resistant prostate cancer. | 2010 Dec 1 |
|
Biological properties of androgen receptor pure antagonist for treatment of castration-resistant prostate cancer: optimization from lead compound to CH5137291. | 2011 Sep |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 08:03:24 GMT 2023
by
admin
on
Sat Dec 16 08:03:24 GMT 2023
|
Record UNII |
A5ZX7J376H
|
Record Status |
Validated (UNII)
|
Record Version |
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-
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1043446-39-4
Created by
admin on Sat Dec 16 08:03:24 GMT 2023 , Edited by admin on Sat Dec 16 08:03:24 GMT 2023
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44462785
Created by
admin on Sat Dec 16 08:03:24 GMT 2023 , Edited by admin on Sat Dec 16 08:03:24 GMT 2023
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PRIMARY | |||
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A5ZX7J376H
Created by
admin on Sat Dec 16 08:03:24 GMT 2023 , Edited by admin on Sat Dec 16 08:03:24 GMT 2023
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PRIMARY |
Related Record | Type | Details | ||
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ACTIVE MOIETY |