7
Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T13561 | AT6 | Others | |
AT6 is a PROTAC AT1 analog which is a highly selective bromodomain (Brd4) degrader. | |||
T75146 | KAT6-IN-1 | ||
KAT6-IN-1 is a potent KAT6 inhibitor. KAT6-IN-1 can be used in research of cancer [1] . | |||
T73129 | STAT6-IN-1 | ||
STAT6-IN-1, a STAT6 inhibitor, exhibits high affinity for the SH2 domain of STAT6 (IC 50 = 0.028 µM), making it suitable for research on allergic lung disease, allergic rhinitis, chronic obstructive pulmonary disease, or... | |||
T79185 | STAT6-IN-2 | STAT | |
STAT6-IN-2 (Comp R-84) serves as a STAT6 inhibitor, effectively reducing the secretion of the chemokine eotaxin-3, which is known to induce eosinophil infiltration. This compound is useful in the study of immune diseases... | |||
T15644 | KAT681 | T0681 | Thyroid hormone receptor(THR) |
KAT681 is a liver selective thyromimetic. | |||
T79186 | STAT6-IN-3 | STAT | |
STAT6-IN-3 (Compound 18a) serves as an inhibitor of STAT6 with an IC50 value of 44 nM, specifically targeting the Src Homology 2 (SH2) domain. It is utilized in research studies focused on inflammatory disorders, includi... | |||
T70919 | NAT6-297775 | ||
NAT6-297775 is a SHP2 inhibitor with IC50 =2.47uM. |