Saquinavir EP Impurity E
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| Catalogue No.: | VE0022057 |
|---|---|
| CAS No.: | N/A |
| Mol. Formula: | C38H49N5O6 |
| Mol. Weight: | 671.8 g/mol |
Additional information on Saquinavir EP Impurity E
Parent drug
SaquinavirIUPAC Name
(3S)-4-[[(1S, 2R)-1-Benzyl-3-[(3S, 4aS, 8aS)-3-[(1, 1-dimethylethyl)carbamoyl]octahydroisoquinolin-2(1H)-yl]-2-hydroxypropyl]amino]-4-oxo-3-[(quinolin-2-ylcarbonyl)amino]butanoic acidPharmacopoeial Synonyms
N/AOther Synonyms
N/ASmiles
O=C(N[C@@H](CC(O)=O)C(N[C@H]([C@H](O)CN1C[C@](CCCC2)([H])[C@]2([H])C[C@H]1C(NC(C)(C)C)=O)CC3=CC=CC=C3)=O)C4=NC5=CC=CC=C5C=C4InChI
InChI=1S/C38H49N5O6/c1-38(2, 3)42-37(49)32-20-26-14-7-8-15-27(26)22-43(32)23-33(44)30(19-24-11-5-4-6-12-24)40-36(48)31(21-34(45)46)41-35(47)29-18-17-25-13-9-10-16-28(25)39-29/h4-6, 9-13, 16-18, 26-27, 30-33, 44H, 7-8, 14-15, 19-23H2, 1-3H3, (H, 40, 48)(H, 41, 47)(H, 42, 49)(H, 45, 46)/t26-, 27+, 30-, 31-, 32-, 33+/m0/s1Description
The compound Saquinavir EP Impurity E is a well-documented reference standard that adheres to strict regulatory requirements set by USP EMA JP and BP. It?s highly suited for use in various applications like analytical method development method validation (AMV) and quality control (QC) especially when manufacturing Saquinavir. Whether you’re preparing for ANDA or NDA submissions | this product provides the accuracy you need. Plus | it comes with a comprehensive Structure Elucidation Report (SER) | which ensures its reliability for precise analytical work.
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