| Cat. No. |
Product Name |
Information |
| PC-61770 |
BTYNB
IMP1/c-Myc inhibitor
|
BTYNB is a potent and selective inhibitor of IMP1 binding to c-Myc mRNA with IC50 of 5 uM. |
| PC-61359 |
IRES-C11
c-Myc inhibitor
|
IRES-C11 is a spectfic c-Myc IRES (internal ribosome entry site) function inhibitor that prevents binding of hnRNP A1 to the Myc IRES and specifically inhibits Myc IRES activity in MM cells. |
| PC-61358 |
IRES-J007
IRES inhibitor
|
IRES-J007 is an improved IRES inhibitor that blocks IRES-hnRNP A1 binding, binds to a small pocket structure within the RRM-containing fragment of hnRNP A1 (UP1 fragment), inhibits cyclin D1 and c-MYC IRES activity to a greater extent compared with C11 (IRES-C11). |
| PC-70283 |
Stauprimide
NME2 inhibitor, Myc inhibitor
|
Stauprimide (N-Benzoyl-7-oxo Staurosporine) is a staurosporine analog that promotes embryonic stem cell (ESC) differentiation by inhibiting nuclear localization of the MYC transcription factor NME2, which in turn results in down-regulation of MYC transcription. |
| PC-60543 |
CBL0137
FACT inhibitor
|
CBL0137 (Curaxin CBL0137) is a histone chaperone FACT (facilitates chromatin transcription) and MYC signal inhibitor that markedly reduced tumor initiation and progression in vivo. |
| PC-60542 |
CMLD010509
|
CMLD010509 (SDS-1-021) is a rocaglate (flavagline) derivative that acts a highly specific inhibitor of the oncogenic translation program supporting MM, including key oncoproteins such as MYC, MDM2, CCND1, MAF, and MCL-1. |
| PC-60241 |
sAJM-589
c-Myc inhibitor
|
sAJM-589 (sAJM589) is a novel, potent small molecule Myc inhibitor that disrupts the Myc-Max leucine-zipper heterodimer with IC50 of 1.8 uM. |
| PC-45695 |
KJ-Pyr-9
c-Myc inhibitor
|
KJ-Pyr-9 is a novel small-molecule inhibitor of c-Myc (Kd=6.5 ± 1.0 nM). |
| PC-42299 |
10074-G5
c-Myc inhibitor
|
10074-G5 is a small molecules that disrupts c-Myc-Max heterodimerization, binds to and distorts the bHLH-ZIP domain of c-Myc. |
| PC-23437 |
NY2267
c-Myc inhibitor
|
NY2267 is a small molecule inhibitor of Myc-Max dimerization with IC50 of 36.5 uM in EMSA assays, inhibits Myc-induced oncogenic transformation in cell culture. |
| PC-23436 |
Mycro2
c-Myc inhibitor
|
Mycro2 is a selective small molecule inhibitor of c-Myc/Max dimerization with IC50 of 23 uM, inhibits c-Myc dependent transcription. |
| PC-23435 |
Mycro1
c-Myc inhibitor
|
Mycro1 is a selective small molecule inhibitor of c-Myc/Max dimerization with IC50 of 30 uM, inhibits c-Myc dependent transcription. |
