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| 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. |
