Cat.No. | Product Name | Target | |
---|---|---|---|
M6166 | Bevacizumab | VEGFR/PDGFR | |
bevacizumab | |||
Humanized vascular endothelial growth factor (VEGF) antibody (bevacizumab; Avastin) is a highly effective monoclonal antibody against metastatic colorectal cancer and several other advanced late stage cancers. | |||
M6223 | Tocilizumab | Immunology/Inflammation | |
MRA; atlizumab | |||
Tocilizumab is a humanized monoclonal antibody that binds to the interleukin-6 receptor, MW: 148 KD. | |||
M6222 | Adalimumab | TNF-alpha | |
LU200134, D2E7 | |||
Adalimumab is the first fully human, recombinant IgG1 monoclonal antibody that specifically targets human TNF-alpha, MW: 144.19 KD. | |||
M3864 | Remdesivir | Anti-infection | |
GS-5734 | |||
Remdesivir, also known as GS-5734, is a nucleoside analogue with in vitro activity against multiple RNA viruses, including Ebola and CoV. | |||
M2510 | Chloroquine diphosphate | Autophagy | |
Chloroquine Phosphate | |||
Chloroquine diphosphate is a 4-aminoquinoline anti-malarial and anti-rheumatoid agent. | |||
M5159 | Hydroxychloroquine Sulfate | Autophagy | |
HCQ sulfate | |||
Hydroxychloroquine Sulfate is an inhibitor of autophagy and toll-like receptor (TLR) 7/9. | |||
M5438 | Azithromycin | Anti-infection | |
CP 62993 | |||
Azithromycin is an antibiotic by inhibiting protein synthesis, used for the treatment of bacterial infections. | |||
M6094 | Darunavir | HIV Protease | |
TMC114; TMC-114; TMC 114 | |||
Darunavir is a nonpeptidic HIV protease inhibitor, used to treat HIV infection. | |||
M1959 | Oseltamivir | Anti-infection | |
Tamiflu | |||
Oseltamivir is a potent and selective inhibitor of influenza virus neuraminidase enzyme. | |||
M3334 | Ribavirin | Anti-infection | |
Ribavirin (Copegus) is an anti-viral agent indicated for severe RSV infection (individually), hepatitis C infection and other viral infections. | |||
M5053 | Arbidol hydrochloride | Anti-infection | |
Umifenovir hydrochloride | |||
Arbidol hydrochloride is an broad-spectrum antiviral chemical agent which can inhibit cell entry of enveloped viruses by blocking viral fusion with host cell membrane. | |||
M2487 | Camostat Mesilate | Others | |
FOY-305; Camostat mesylate | |||
Camostat is a trypsin-like protease inhibitor, inhibits airway epithelial sodium channel (ENaC) function with IC50 of 50 nM, less potent to trpsin, prostasin and matriptase. | |||
M5803 | Nafamostat Mesylate | Others | |
FUT-175 | |||
Nafamostat mesilate is a synthetic serine protease inhibitor, used as an anticoagulant during hemodialysis. | |||
M6264 | Favipiravir | DNA/RNA Synthesis | |
T-705 | |||
Favipiravir (T-705) is a potent and selective RNA-dependent RNA polymerase inhibitor, used to treat influenza virus infections. | |||
M2159 | Ritonavir | HIV Protease | |
ABT-538 | |||
Ritonavir (ABT-538) is an HIV protease inhibitor used frequently as a booster of other protease inhbitors. | |||
M9113 | Bictegravir | Integrase | |
GS-9883 | |||
Bictegravir (GS-9883) is a novel, potent inhibitor of HIV-1 integrase with an IC50 of 7.5 nM. | |||
M2158 | Lopinavir | HIV Protease | |
ABT-378 | |||
Lopinavir is a potent HIV protease inhibitor with Ki of 1.3 pM. | |||
M3568 | Darunavir Ethanolate | HIV Protease | |
TMC114 | |||
Darunavir Ethanolate is an HIV protease inhibitor. | |||
M4824 | Dolutegravir sodium | HIV Protease | |
GSK-1349572A, DTG | |||
Dolutegravir sodium is a potent, second generation HIV integrase inhibitor (IC₅₀ = 2.7 nM) that displays potent antiviral activity. | |||
M3468 | Methylprednisolone | Immunology/Inflammation | |
U 7532 | |||
Methylprednisolone is a synthetic corticosteroid with anti-inflammatory and immunomodulating properties. | |||
M2225 | Thalidomide | TNF-alpha | |
Thalomid | |||
Thalidomide is a selective inhibitor of tumor necrosis factor α (TNF-α) synthesis. | |||
M2328 | Pirfenidone | TGF-beta/Smad | |
AMR69 | |||
Pirfenidone inhibits TGF-β bioactivity by affecting TGF-β2 mRNA expression and processing of pro-TGF-β in CCL-64 cells. | |||
M1831 | Cyclosporine A | Immunology/Inflammation | |
Cyclosporine | |||
Cyclosporine A is a powerful immunosuppressive agent that inhibits the T-cell receptor signal transduction pathway. | |||
M1787 | INCB18424 | JAK | |
Ruxolitinib | |||
INCB18424 is a potent inhibitor of both JAK1 and JAK2 with selectivity versus JAK3 and TYK2 (IC50 values of 2.7, 4.5, 332, and 19 nM, respectively, in biochemical assays). | |||
M2152 | Carfilzomib | Proteasome | |
PR-171 | |||
Carfilzomib (PR-171) is a novel and selective, irreversible proteasome inhibitor with IC50 of <5 nM. | |||
M1712 | FTY720 | Src-bcr-Abl | |
Fingolimod | |||
FTY720 (Fingolimod) is a sphingosine-1-phosphate receptor 1 receptor. | |||
M1701 | Dasatinib | Src-bcr-Abl | |
BMS-354825 | |||
Dasatinib (BMS-354825) is a small molecule inhibitor of both the SRC and BCR/ABL tyrosine kinases, with IC50's for the isolated kinases of 0.55 and 3.0 nM, respectively. | |||
M3380 | Pitavastatin Calcium | Autophagy | |
Pitavastatin hemicalcium; NK-104 | |||
Pitavastatin calcium is a novel member of the medication class of statins. | |||
M3241 | Imatinib | c-Kit | |
STI571 | |||
Imatinib is a multi-target inhibitor of v-Abl, c-Kit and PDGFR with IC50 of 0.6 μM, 0.1 μM and 0.1 μM, respectively. | |||
M3493 | Mitoxantrone | Topoisomerase | |
Mitozantrone | |||
Mitoxantrone is a type II topoisomerase inhibitor with IC50 of 2.0 μM, 0.42 mM for HepG2 and MCF-7/wt cells, respectively. | |||
M2283 | Rosuvastatin calcium | Autophagy | |
Crestor | |||
Rosuvastatin (Crestor) is a member of statins and used to treat high cholesterol and related conditions. | |||
M3624 | Boceprevir | HCV Protease | |
EBP-520, SCH503034 | |||
Boceprevir (EBP-520, SCH503034) is an HCV protease inhibitor (Ki=14 nM) for the treatment of hepatitis C virus infection. | |||
M3433 | Nitazoxanide | Others | |
NTZ; NSC 697855 | |||
Nitazoxanide is a synthetic nitrothiazolyl-salicylamide derivative and an antiprotozoal agent (IC50 for canine influenza virus ranges from 0.17 to 0.21 μM). | |||
M2256 | Ivermectin | Autophagy | |
Stromectol | |||
Ivermectin is a positive allosteric modulator of the α7 neuronal nicotinic acetylcholine receptor and the purinergic P2X4 receptor. | |||
M3121 | Vitamin C | Vitamin | |
Ascorbic acid | |||
Vitamin C is a water-soluble vitamin indicated for the prevention and treatment of scurvy. |
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