| CSN23793 |
SGC-GAK-1
|
2226517-76-4 |
SGC GAK 1 is an inhibitor of cyclin G associated kinase (GAK) with Kd of 1.9 nM. |
| CSN23766 |
BIBF0775
|
334951-90-5 |
BIBF0775 is an inhibitor of transforming growth factor β receptor I (TGFβRI) by soaking into the kinase domain of TGFβRI. |
| CSN22468 |
MOZ-IN-2
|
2055397-88-9 |
MOZ-IN-2 is an inhibitor of protein MOZ, a member of histone acetyltransferases, with an IC50 of 125 μM. |
| CSN22506 |
SJ000291942
|
425613-09-8 |
SJ000291942 is an activator of the canonical bone morphogenetic proteins (BMP) signaling pathway. BMPs are members of the transforming growth factor beta (TGFβ) family of secreted signaling molecules. |
| CSN22494 |
QX77
|
1798331-92-6 |
QX77 is a chaperone-mediated autophagy (CMA) activator. |
| CSN22467 |
WM-1119
|
2055397-28-7 |
MOZ-IN-1 is an inhibitor of MOZ which is a member of histone acetyltransferases with IC50 of 0.051 μM. |
| CSN22428 |
Hesperin
|
4430-35-7 |
Hesperin is a bioactive ingredient present in Japanese horseradish (wasabi) and has been shown to be an Nrf2 activator. |
| CSN22525 |
Troxacitabine
|
145918-75-8 |
Troxacitabine is nucleoside analog with potent anticancer activity. |
| CSN22470 |
NAV-2729
|
419547-11-8 |
NAV-2729 is a selective ARF6 inhibitor with IC50 of 1 μM. |
| CSN22514 |
TAK-778
|
180185-61-9 |
TAK-778 is a derivative of ipriflavone and has been shown to induce bone growth in in vitro and in vivo models. |
| CSN22432 |
IP3K Inhibitor
|
519178-28-0 |
IP3K Inhibitor is a IP3K inhibitor with an IC50 of 10.2 μM. |
| CSN22453 |
LY309887
|
127228-54-0 |
LY309887 is a potent inhibitor of glycinamide ribonucleotide formyltransferase (GARFT), with a Ki of 6.5 nM, and has antitumor activity. |
| CSN22499 |
Ropidoxuridine
|
93265-81-7 |
Ropidoxuridine is an orally available, halogenated thymidine analog and is a potential radiosensitizer for use in human tumors. |
| CSN23752 |
Elemicin
|
487-11-6 |
Elemicin is a phenylpropene with anticancer and antifungal activities, it exhibits anticholinergic-like effects in humans. |
| CSN23772 |
E3 Ligase Ligand-Linker Conjugates 20
|
1950635-15-0 |
Thalidomide-O-amido-C8-Amine is a PROTAC block consist of Thalidomide linked to alkyl with Amine functional group for conjugation reactions. |
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