Cat.No. | Name | Information |
---|---|---|
M3209 | Oxfendazole | Oxfendazole is the sulfoxide form of fenbendazole which is a broad spectrum benzimidazole anthelmintic. |
M41231 | Sutidiazine | Sutidiazine (ZY-19489) is an orally active and antimalarial agent. |
M41230 | 8CN | 8CN, a 2-amino-thiophene derivative, has anti-leishmanial activity. |
M41229 | Propamidine | Propamidine is a covalent inhibitor of TMPRSS2 and has some antibacterial activity.. |
M41228 | Calarene | Calarene is an insecticide that can be obtained from the stem of Kadsura heteroclite. |
M41227 | Sporogen AO-1 | Sporogen AO-1 is a fungal metabolite originally isolated from the fungusAspergillus oryzae. |
M41226 | NPD-2975 | NPD-2975 is an orally active antitrypanosomal agent, against Human African Trypanosomiasis (HAT). |
M41225 | AcrB-IN-2 | AcrB-IN-2 is an AcrB efflux pump inhibitor, with ability to potentiate the effect of antibiotics. |
M41224 | Phylloflavan | Phylloflavan is an antileishmanial agent with an intracellular EC50 of 3.2 nM in RAW 264.7 cells. |
M41223 | TbPTR1 inhibitor 2 | TbPTR1 inhibitor 2 is a PTR1 enzyme inhibitor, with IC50s of 34.2 and 32.9 μM for TbPTR1 and LmPTR1. |
M41222 | DCN-83 | DCN-83, an anti-leishmania agent, is most potent against the amastigote form with an IC50 of 0.71 μM. |
M41221 | CpCDPK1/TgCDPK1-IN-2 | CpCDPK1/TgCDPK1-IN-2 is a CpCDPK1 and TgCDPK1 inhibitor with IC50 values of 12 and 5 nM, respectively. |
M41220 | CpCDPK1/TgCDPK1-IN-1 | CpCDPK1/TgCDPK1-IN-1 is a potent CpCDPK1/TgCDPK1 dual inhibitor (IC50: 10 nM and 5.0 nM respectively). |
M41219 | AcrB-IN-4 | Efflux pump-IN-4 is an AcrB efflux pump inhibitor, with ability to potentiate the effect of antibiotics. |
M41218 | AcrB-IN-3 | Efflux pump-IN-3 is an AcrB efflux pump inhibitor, with ability to potentiate the effect of antibiotics. |
M41217 | Lunasin | Lunasin is a bioactive peptide with antioxidant, anti-inflammatory, anticancer and anti-aging properties. |
M41216 | trans-Clopenthixol dihydrochloride | trans-Clopenthixol ((E)-Clopenthixol) dihydrochloride is an antibiotic agent, without neuroleptic effect. |
M41215 | CpCDPK1/TgCDPK1-IN-3 | CpCDPK1/TgCDPK1-IN-3 is a CpCDPK1 and TgCDPK1 inhibitor with IC50 values of 0.003 and 0.0036 µM, respectively. |
M41214 | HSP90-IN-21 | HSP90-IN-21 (5e) is an antiplasmodial agent, with IC50 values of 0.04, 0.17 and 2.91 μM against erythrocytic stage of P. |
M41213 | TSC26 | TSC26, a thiosemicarbazone, is a potent cruzipain (CZP) inhibitor with an IC50 of 175 nM, a pIC50 of 6.76 and a pKa of 6.6. |
M41212 | TSC24 | TSC24, a thiosemicarbazone, is a potent cruzipain (CZP) inhibitor with an IC50 of 2.86 nM, a pIC50 of 8.54 and a pKa of 8.6. |
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