Ceapin-A7 is a selective and highly potent inhibitor of the ATF6α, which can activate the response to ER stress, with IC50 of 0.59 μM.
research use only
Cat.No.E1099
| Related Targets | HSP JNK Antioxidant ROS eIF PERK IRE1 PKR ASK PDI |
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| Featured Inhibitors | Y-27632 Dihydrochloride SB431542 CHIR-99021 (Laduviglusib) RMC-7977 RMC-6236 (Daraxonrasib) MRTX1133 MG132 Z-VAD-FMK VT3989 IAG933 |
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In vitro |
DMSO
: 100 mg/mL
(212.62 mM)
Ethanol : 8 mg/mL Water : Insoluble |
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In vivo |
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| Molecular Weight | 470.32 | Formula | C20H12F6N4O3 |
Storage (From the date of receipt) | 3 years -20°C powder |
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| CAS No. | 2323027-38-7 | -- | Storage of Stock Solutions |
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| Synonyms | N/A | Smiles | FC(F)(F)C1=CC=C(C[N]2C=C(NC(=O)C3=NOC(=C3)C4=CC=CO4)C=N2)C(=C1)C(F)(F)F | ||
| Targets/IC50/Ki |
ATF6α
0.59 μM
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|---|---|
| In vitro |
Ceapin-A7 inhibits activation of ATF6α in response to ER stress without inhibiting ATF6β or SREBP activation. In U2-OS cells, this compound inhibits ER stress-induced upregulation of BiP. |
References |
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