商品介绍
Lopinavir (ABT-378), designed in response to Val82 mutant strains of HIV [1], is a potent inhibitor of HIV protease with Ki of 1.3-3.6 pM. Lopinavir inhibits replication of HIV-1 with an EC50 of 6-17 nM. [2]Ritonavir was found to inhibit the metabolism of lopinavir with no other antagonistic effects; therefore lopinavir"s drug exposure can be enhanced by co-formulation with ritonavir. In the presence of 50% human serum, the mean EC50 of lopinavir for five laboratory HIV-1 isolates ranged from 65 to 289 nM. [3]
Technical information:
Chemical Formula: | | C37H48N4O5 |
CAS #: | | 192725-17-0 |
Molecular Weight: | | 628.8 |
Purity: | | > 98% |
Appearance: | | White |
Chemical Name: | | (S)-N-((2S,4S,5S)-5-(2-(2,6-dimethylphenoxy)acetamido)-4-hydroxy-1,6-diphenylhexan-2-yl)-3-methyl-2-(2-oxo-tetrahydropyrimidin-1(2H)-yl)butanamide |
Solubility: | | Up to 100 mM in DMSO |
Synonyms: | | ABT-378, ABT378, Lopinavir |
Shipping Condition: The product is shipped in a glass vial at ambient temperature.Storage condition: For longer shelf life, store solid powder at 4oC desiccated, or store DMSO solution at -20oC.
Reference:
1. | Stoll et al., X-ray Crystallographic Structure of ABT-378 (Lopinavir) Boudn to HIV-1 Protease. Bioorg. Med. Chem. 2002, 10, 2803-2806. Pubmed ID:12057670 |
2. | Sham et al., ABT-378, a Highly Potent Inhibitor of the Human Immunodeficiency Virus Protease. Antimicrob. Agents Chemother. 1998, 42(12), 3218-3224. Pubmed ID:9835517 |
3. | Qazi et al., Lopinavir/ritonavir (ABT-378/r). Expert Opin. Pharmacother. 2002, 3(2), 315-327. |
Other Information:
Product Specification (pdf) MSDS (pdf) Certificate of Analysis is available upon request.
品牌介绍
Cellagen Technology 公司位于美国加州San Diego,该公司致力于干细胞相关产品的研发和生产。基于多年为世界*的生物公司提供OEM产品的经验,目前Cellagen Technology公司利用自身优势,拓展了原有产品线,推出了以StemRegenin 1(SR1)为代表的多种自有品牌产品。 NamePriceCat # (Powder)Cat # (10 mM in DMSO)Pathway/Target7,8-Dihydroxyflavone1173C7181-10N/ATrkBA7696622023C2769-10N/AAMPKA83-011513C2831-2C2831-2sTGF-β/ALK4,5,7Abiraterone1853C2247-2C2247-2sP450-CYP17BEZ235833C2392-2C2392-2sPI3K, mTORBIX-012941513C2491-5C2491-5sEpigenetics/G9a HMTCHIR990213553C2447-2C2447-2sGSK3β CP-6905501343C2716-2C2716-2sJAK1,2,3Cyclopamine2193C2925-2C2925-2sHedgehog/SmoDAPT1853C3178-5C3178-5sNotch/γ-secretaseForskolin1853C3677-10N/AAdenylate cyclaseFTY7201173C3897-5C3897-5sS1P receptorsGDC-09411513C4321-5C4321-5sPI3KHh-Ag1.53043C4412-2C4412-2sHedgehog/SmoINCB0184241853C4622-2C4622-2sJAK1/2IWP-31853BackorderBackorderWntKHS1011853C5471-5C5471-5sNeural differentiationLDE2252363C5332-2C5332-2sHedgehog/SmoLDN-1931893723C5361-2C5361-2sBMP/ALK2,3Leukadherin-1#VALUE!C5385-2C5385-2sCD11b, CD18LY2940022193C5929-5C5929-5sPI3KP7C32363C7723-10N/Aneurogenic, neuroprotectivePD03259013723C7303-2C7303-2sMEK1, MEK2PD03329912193C7306-2C7306-2sCdk4, Cdk6PS481343C7748-5C7748-5sPDK1Pyrintegrin3383C7974-1C7974-1sES cell survivalR4062193C7406-2C7406-2sSykR7883723C7788-5C7788-5sSykRapamycin2193C7272-5C7272-5smTORReversine1173C7383-2C7383-2sA3 Adenosine ReceptorRO49290972703C7649-2C7649-2sNotch/γ-secretaseSB4315421513C7243-5C7243-5sTGF-β/ALK4,5,7SF16703723C7316-2C7316-2spTENSitagliptin1513C7482-5C7482-5sDPP-4SRT17202363C7781-2C7781-2sSIRT1StemRegenin1 (SR1)3723C7710-1C7710-1sAryl hydrocarbon receptorSU54022703C7854-1C7854-1sFGFRThiazovivin3553C8442-1C8442-1sROCKUrsolic Acid1853C8776-10N/ASTAT3VX-6801173C8916-10N/AAurora kinaseWnt-C592703C7641-2C7641-2sWntXAV9392703C9289-2C9289-2sWntY-276321853C9127-2C9127-2sROCKhuman Activin A5423P4228-1031910 µg37383P4228-1002199100 µghuman BMP-4 3723P4267-1021910 µg25483P4267-1001499100 µghuman bFGF 3383P4234-5019950 µg23783P4234-5001399500 µgmouse LIF 3383P6543-1019910 µg23783P6543-1001399100 µghuman Wnt-3a 3723P4968-1021910 µg