Product Details
Place of Origin: China
Brand Name: Sunshine
Certification: ISO,COA
Model Number: 192725-17-0
Payment & Shipping Terms
Minimum Order Quantity: Negotiation
Price: Negotiation
Packaging Details: Aluminum Foil Bag, Drum
Delivery Time: 7-15 days
Payment Terms: T/T, L/C, D/A, Western Union
Supply Ability: TON
CAS NO:: |
192725-17-0 |
Appearance :: |
White To Off-white Crystalline Solid |
Molecular Formula:: |
C37H48N4O5 |
Molecular Weight:: |
628.80 |
EINECS NO:: |
813-811-7 |
MDL NO:: |
MFCD22373646/MFCD04973616 |
CAS NO:: |
192725-17-0 |
Appearance :: |
White To Off-white Crystalline Solid |
Molecular Formula:: |
C37H48N4O5 |
Molecular Weight:: |
628.80 |
EINECS NO:: |
813-811-7 |
MDL NO:: |
MFCD22373646/MFCD04973616 |
Product Description
Product Name: Lopinavir CAS NO: 192725-17-0
Synonyms:
Koletr;
ABT 378;
Lopinavir;
Aluviran;
Koletra;;
1(2H)-Pyrimidineacetamide, N-[(1S,3S,4S)-4-[[2-(2,6-dimethylphenoxy)acetyl]amino]-3-hydroxy-5-phenyl-1-(phenylmethyl)pent yl]tetrahydro-α-(1-methylethyl)-2-oxo-, (αS)-;
(2S)-N-[(2S,4S,5S)-5-{[(2,6-Dimethylphenoxy)acetyl]amino}-4-hydroxy-1,6-diphenyl-2-hexanyl]-3-methyl-2-(2-oxotetrahydro-1(2H)-pyrimidinyl)butanamide;
Chemical & Physical Properties
Appearance : White to off-white Crystalline Solid
Assay : ≥99%
Density: 1.163±0.1 g/cm3
Boiling Point: 924.1°C at 760 mmHg
Flash Point: 512.7℃
Melting point:124-127℃
Solubility:DMSO: soluble20mg/mL, clear
Lopinavir, the sixth HIV protease inhibitor in the “navir” class, was launched in coformulation with ritonavir, another HIV protease inhibitor already marketed (Abbott, 1996); this original formulation was introduced as Kaletra for use in combination with either nucleoside or non-nucleoside reverse transcriptase inhibitors for the treatment of AIDS in adults and children. Lopinavir is a peptidomimetic compound with a structural core identical to that of ritonavir, on which terminal groups, particularly a modified valine, were introduced by peptide coupling procedures. Lopinavir is a potent competitive inhibitor of HIV-I protease exhibiting high potential against ritonavir-resistant mutations. In several animal species, pharmacokinetic studies with the lopinavirlritonavir association showed that the modest properties of lopinavir were significantly improved in presence of ritonavir, in terms of Cmax and duration of action. Ritonavir inhibits the P450 isoenzyme CYP3A4 and the human liver microsomal metabolism of lopinavir, so strongly amplifying plasma levels of this latter component. In AIDS patients, the plasma HIV RNA level was considerably reduced and the CD4+ T-cell counts increased after administration of lopinavir combined with relatively small doses of ritonavir. Kaletra is intended to be used jointly with other antiretroviral agents.
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