Oseltamivir EP Impurity E HCl
Oseltamivir EP Impurity E HCl Basic information
- Product Name:
- Oseltamivir EP Impurity E HCl
- Synonyms:
-
- Oseltamivir Methyl Ester HCl
- methyl (3R,4R,5S)-4-acetamido-5-amino-3-(pentan-3-yloxy)cyclohex-1-ene-1-carboxylate
- Oseltamivir EP Impurity E HCl
- methyl(3R,4R,5S)-4-acetamido-5-amino-3-(1-ethyl-propxy)cyclohex-1-ene-1-carboxlate
- (3R,4R,5S)-methyl 4-acetamido-5-amino
- Oseltamivir EP Impurity E:Oseltamivir Impurity E
- Oseltamivir Impurity(Oseltamivir EP Impurity E)
- Oseltamivir EP Impuruty E
- CAS:
- 208720-78-9
- MF:
- C15H27ClN2O4
- MW:
- 334.84
- Mol File:
- 208720-78-9.mol
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Oseltamivir EP Impurity E HCl Chemical Properties
- InChI
- InChI=1/C15H26N2O4.ClH/c1-5-11(6-2)21-13-8-10(15(19)20-4)7-12(16)14(13)17-9(3)18;/h8,11-14H,5-7,16H2,1-4H3,(H,17,18);1H/t12-,13+,14+;/s3
- InChIKey
- VXUUEBWFJPUQGY-XGEKKEJANA-N
- SMILES
- O([C@@H]1C=C(C(=O)OC)C[C@H](N)[C@H]1NC(=O)C)C(CC)CC.Cl |&1:1,9,11,r|
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Oseltamivir EP Impurity E HCl Usage And Synthesis
Uses
Oseltamivir acid methyl ester hydrochloride is a precursor form of the neuraminidase inhibitor and antiviral oseltamivir acid. Oseltamivir acid methyl ester hydrochloride is converted to oseltamivir acid by carboxylesterase 1 (CES1)[1].
References
[1] Mai Shimizu, et al. Systematic Approach for Screening of Prodrugs: Evaluation Using Oseltamivir Analogues as Models. J Pharm Sci. 2021 Feb;110(2):925-934. DOI:10.1016/j.xphs.2020.10.018
Oseltamivir EP Impurity E HClSupplier
Tianjin shijia biomedical technology co., LTD Gold
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- 15022261580 15022261580;
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S.Z. PhyStandard Bio-Tech. Co., Ltd.
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- 021-64609169 18901607656
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BOC Sciences
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- 16314854226
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Shenzhen SUNGENING Bio-Medical Co., Ltd.
- Tel
- 0755-0755-28967200-8062 13631290199
- wxf@sungening.com
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- (3R,4R,5R)-3-(1-Ethylpropoxy)-4-hydroxy-5-[(Methylsulfonyl)oxy]-1-cyclohexene-1-carboxylic Acid Ethyl Ester
- OseltaMivir Acid Hydrochloride
- (3R,4R,5R)-4-(1-Ethylpropoxy)-3-hydroxy-5-[(Methylsulfonyl)oxy]-1-cyclohexene-1-carboxylic Acid Ethyl Ester