Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C25H30F3N3O4 |
Molecular Weight | 493.5186 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
C[C@H](CC1=CC(C(N)=O)=C2N(CCCO)C=CC2=C1)NCCOC3=CC=CC=C3OCC(F)(F)F
InChI
InChIKey=VICSLOHTZDWOFF-QGZVFWFLSA-N
InChI=1S/C25H30F3N3O4/c1-17(30-8-12-34-21-5-2-3-6-22(21)35-16-25(26,27)28)13-18-14-19-7-10-31(9-4-11-32)23(19)20(15-18)24(29)33/h2-3,5-7,10,14-15,17,30,32H,4,8-9,11-13,16H2,1H3,(H2,29,33)/t17-/m1/s1
Molecular Formula | C25H30F3N3O4 |
Molecular Weight | 493.5186 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
KMD-3241 (Dehydro Silodosin) is a silodosin metabolite (also known as an impurity of Silodosin). Silodosin is a selective antagonsit of alpha-1a adrenergic receptor which was developed by Kissei Pharmaceutical and approved by FDA under the name Rapaflo for the treatment of signs and symptoms associated with benign prostatic hyperplasia. The affnities of silodosin metabolites, KMD-3241, KMD-3289 and
KMD-3295, for alpha1A-AR subtype receptor were equal to or lower than that of silodosin.
Originator
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Thu Jul 06 16:23:01 UTC 2023
by
admin
on
Thu Jul 06 16:23:01 UTC 2023
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Record UNII |
6787MV7QU0
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Record Status |
Validated (UNII)
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Record Version |
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-
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9891871
Created by
admin on Thu Jul 06 16:23:01 UTC 2023 , Edited by admin on Thu Jul 06 16:23:01 UTC 2023
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6787MV7QU0
Created by
admin on Thu Jul 06 16:23:01 UTC 2023 , Edited by admin on Thu Jul 06 16:23:01 UTC 2023
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DTXSID20432445
Created by
admin on Thu Jul 06 16:23:01 UTC 2023 , Edited by admin on Thu Jul 06 16:23:01 UTC 2023
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175870-21-0
Created by
admin on Thu Jul 06 16:23:01 UTC 2023 , Edited by admin on Thu Jul 06 16:23:01 UTC 2023
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Related Record | Type | Details | ||
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PARENT -> METABOLITE |
MINOR
FECAL; PLASMA; URINE
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