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KCL-HO-1i is an orally active heme oxygenase-1 (HO-1) inhibitor with an IC50 of 123 nM for rat HO-1 and 128 nM for human HO-1. It targets immune-suppressive LYVE-1+ perivascular tumor-associated macrophages (PvTAMs) in the tumor microenvironment (TME) and reduces PvTAM-mediated immune evasion. In MMTV-PyMT mice with spontaneous breast cancer or C57Bl/6 mice with subcutaneous MN-MCA1 sarcoma, KCL-HO-1i demonstrates synergistic anti-tumor effects when combined with chemotherapy. It is applicable for cancer research.
| Pack Size | Price | USA Stock | Global Stock | Quantity |
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| 10 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
| Description | KCL-HO-1i is an orally active heme oxygenase-1 (HO-1) inhibitor with an IC50 of 123 nM for rat HO-1 and 128 nM for human HO-1. It targets immune-suppressive LYVE-1+ perivascular tumor-associated macrophages (PvTAMs) in the tumor microenvironment (TME) and reduces PvTAM-mediated immune evasion. In MMTV-PyMT mice with spontaneous breast cancer or C57Bl/6 mice with subcutaneous MN-MCA1 sarcoma, KCL-HO-1i demonstrates synergistic anti-tumor effects when combined with chemotherapy. It is applicable for cancer research. |
| Targets&IC50 | HO-1:123 nM (rat splenic microsomes) |
| In vitro | KCL-HO-1i exhibits inhibitory activity in rat spleen microsomes against rat heme oxygenase-1 (HO-1) with an IC50 of 123 nM and demonstrates similar effects in HEK293T cells with an IC50 of 128 nM. At a concentration of 25 μM over 16 hours, KCL-HO-1i enhances the transendothelial migration of CD8+ T cells, reversing migration limitations caused by IL-6-polarized bone marrow-derived macrophages in transwell assays. |
| In vivo | KCL-HO-1i administered alone at 27.8 mg/kg (25 μMol/kg) orally once daily for 21 days can slow tumor growth. It also works synergistically with chemotherapy (5-fluorouracil or Gemcitabine) to achieve sustained tumor growth control in MMTV-PyMT spontaneous mammary tumor mice and C57Bl/6 mice with subcutaneous MN-MCA1 sarcomas. |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. |
Dissolve 2 mg of the compound in 100 μL DMSO
to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
1) Add 100 μL of the DMSO
stock solution to 400 μL PEG300
and mix thoroughly until the solution becomes clear.
2) Add 50 μL Tween 80 and mix well until fully clarified.
3) Add 450 μL Saline,PBS or ddH2O
and mix thoroughly until a homogeneous solution is obtained.
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