Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C22H19N3O4 |
Molecular Weight | 389.404 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@@]12CC3=C(NC4=C3C=CC=C4)[C@@H](N1C(=O)CN(C)C2=O)C5=CC6=C(OCO6)C=C5
InChI
InChIKey=WOXKDUGGOYFFRN-KKSFZXQISA-N
InChI=1S/C22H19N3O4/c1-24-10-19(26)25-16(22(24)27)9-14-13-4-2-3-5-15(13)23-20(14)21(25)12-6-7-17-18(8-12)29-11-28-17/h2-8,16,21,23H,9-11H2,1H3/t16-,21-/m0/s1
Molecular Formula | C22H19N3O4 |
Molecular Weight | 389.404 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
(6S ,12AS)-Tadalafil is an inactive enantiomer of "Tadalafil" which is the active ingredient in Cialis which is used to treat erectile dysfunction. Tadalafil has 4 isomers [(RR), (SS), (RS), and (SR)], of which (RR) is the name-sake isomer and potent inhibitor of phosphodiesterase-5. The (RS) diastereomer is the only other isomer with some PDE-5 inhibitory activity.
Originator
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
The identification of (-)-trans-tadalafil, tadalafil, and sildenafil in counterfeit Cialis and the optical purity of tadalafil stereoisomers. | 2010 Feb 5 |
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Stereochemistry of the tadalafil diastereoisomers: a critical assessment of vibrational circular dichroism, electronic circular dichroism, and optical rotatory dispersion. | 2013 Nov 14 |
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Nickel(II)-assisted enantiomeric differentiation and quantitation of tadalafil by direct electrospray ionization mass spectrometry. | 2017 Jul |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 08:39:53 GMT 2023
by
admin
on
Sat Dec 16 08:39:53 GMT 2023
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Record UNII |
HZ6QJN0D4Z
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Record Status |
Validated (UNII)
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9908373
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DTXSID40212165
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Related Record | Type | Details | ||
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PARENT -> IMPURITY |
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
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