Chetomin
Chemical Name: (3S,5aR,10bS,11aS)-2,3,5a,6,10b,11-hexahydro-3-(hydroxymethyl)-10b-(3-[(1S,4S)-3-[[4-(hydroxymethyl)-5,7-dimethyl-6,8-dioxo-2,3-dithia-5,7-diazabicyclo[2.2.2]oct-1-yl)methyl]-1H-indol-1-yl]-2-methyl-3,11a-epidithio-11aH-pyrazino[1',2':1,5]pyrrolo[2,3-b]indole-1,4-dione
Purity: ≥98%
Biological Activity
Targets the CH1 domain of CBP/p300; inhibits interaction of HIF-1α, HIF-2α and STAT2 with CBP/p300. Attenuates hypoxia-induced gene expression in vitro and in vivo; radiosensitizes human HT 1080 fibrosarcoma cells in vitro.Technical Data
The technical data provided above is for guidance only.
For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
Background References
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Transcriptional switches: chemical approaches to gene regulation.
Lee and Mapp
J.Biol.Chem., 2010;285:11033 -
Small molecule blockade of transcriptional coactivation of the hypoxia-inducible factor pathway.
Kung et al.
Cancer Cell, 2004;6:33 -
Effects of HIF-1 inhibition by chetomin on hypoxia-related transcription and radiosensitivity in HT 1080 human fibrosarcoma cells.
Staab et al.
BMC Cancer, 2007;13:213
Product Datasheets
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Citation for Chetomin
The citations listed below are publications that use Tocris products. Selected citations for Chetomin include:
1 Citation: Showing 1 - 1
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Angiopoietin-like 4 promotes angiogenesis in the tendon and is increased in cyclically loaded tendon fibroblasts.
Authors: Mousavizadeh Et al.
J Physiol 2016;594:2971
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