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Cancer

货号 产品名 CAS号 信息
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.
CSN22492 PROTAC Linker 1 1835705-53-7 PROTAC Linker 1 is a linker used to link the warhead and the E3 ligase ligand.
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.
CSN22451 LY 222306 154446-98-7 LY 222306 is a glycinamide ribonucleotide formyltransferase (GARFT) inhibitor with a Ki of 0.77 nM.
CSN22476 OSW-1 145075-81-6 OSW-1, isolated from Ornithogalum caudatum, is a specific antagonist of osterol-binding protein (OSBP) and OSBP-related protein 4 (ORP4) with GI50s in the nanomolar range in human cancer lines.
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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