Chemical Structure : HIF inhibitor 3.2.16
Catalog No.: PC-26485Not For Human Use, Lab Use Only.
HIF inhibitor 3.2.16 is a potent, dual HIF-1/2 inhibitor with MST Kd of 47.4 nM for HIF-1α, inhibits the interaction of HIF-1α and HIF-2α with HIF-1β with IC50 of 110 nM and 62 nM in immunoblot assays.
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HIF inhibitor 3.2.16 is a potent, dual HIF-1/2 inhibitor with MST Kd of 47.4 nM for HIF-1α, inhibits the interaction of HIF-1α and HIF-2α with HIF-1β with IC50 of 110 nM and 62 nM in immunoblot assays.
3.2.16 enhances the antitumor activity of anti-CTLA-4 antibody in CRC.
3.2.16 enhances response to α-CTLA-4 in melanoma and prostate cancer models.
3.2.16 decreases mRNA expression of markers of angiogenesis (Angptl4, Vegf), T cell exhaustion (Lag-3, Pd-1, Tim-3), and other mediators of immunosuppression (Ca9, Cd47, Cd73, Glut1, Il-6, Pd-l1, Vegf) in E0771 tumors from mice.
| M.Wt | 327.43 | |
| Formula | C19H25N3O2 | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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1. Salman S, et al. J Exp Med. 2026 May 4;223(5):e20251009.

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