Y0001498
Lopinavir
European Pharmacopoeia (EP) Reference Standard
About This Item
Recommended Products
biological source
synthetic
grade
pharmaceutical primary standard
Agency
EP
API family
lopinavir
packaging
pkg of 170 mg
manufacturer/tradename
EDQM
storage condition
protect from light
application(s)
pharmaceutical (small molecule)
format
neat
shipped in
ambient
storage temp.
2-8°C
InChI
1S/C37H48N4O5/c1-25(2)34(41-20-12-19-38-37(41)45)36(44)39-30(21-28-15-7-5-8-16-28)23-32(42)31(22-29-17-9-6-10-18-29)40-33(43)24-46-35-26(3)13-11-14-27(35)4/h5-11,13-18,25,30-32,34,42H,12,19-24H2,1-4H3,(H,38,45)(H,39,44)(H,40,43)/t30-,31-,32-,34-/m0/s1
InChI key
KJHKTHWMRKYKJE-SUGCFTRWSA-N
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General description
Lopinavir is an antiretroviral agent and a protease inhibitor indicated for the management of human immunodeficiency virus (HIV) infection. It is a key component of Kaletra, the co-formulation of lopinavir and ritonavir.
Application
Packaging
Other Notes
related product
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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Protocols
Lopinavir assay setup saves time and improves efficiency with shorter columns, meeting European pharmacopoeia guidelines.
Lopinavir assay setup saves time and improves efficiency with shorter columns, meeting European pharmacopoeia guidelines.
Lopinavir assay setup saves time and improves efficiency with shorter columns, meeting European pharmacopoeia guidelines.
Lopinavir assay setup saves time and improves efficiency with shorter columns, meeting European pharmacopoeia guidelines.
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