OHM1 is an analog of the HIF1α C-terminal transactivation domain (CTAD) that selectively inhibits the interaction between HIF1α and the coactivators p300/CBP. With an affinity of 0.53 μM for the CH1 domain, OHM1 effectively disrupts HIF1α-mediated transcriptional activity. This compound is valuable for research applications focused on hypoxia signaling, cancer biology, and the regulation of cellular responses to oxygen levels.
OHM1 is an analog of the HIF1α C-terminal transactivation domain (CTAD) that selectively inhibits the interaction between HIF1α and the coactivators p300/CBP. With an affinity of 0.53 μM for the CH1 domain, OHM1 effectively disrupts HIF1α-mediated transcriptional activity. This compound is valuable for research applications focused on hypoxia signaling, cancer biology, and the regulation of cellular responses to oxygen levels.
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