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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. |
| CSN22537 | α-2,3-sialyltransferase-IN-1 | 881179-06-2 | α-2,3-sialyltransferase-IN-1 is a noncompetitive α-2,3-sialyltransferase inhibitor with an IC50 of 6 μM. |
| CSN22492 | PROTAC Linker 1 | 1835705-53-7 | PROTAC Linker 1 is a linker used to link the warhead and the E3 ligase ligand. |
| 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. |
| 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. |
| CSN22462 | Mcl1-IN-4 | 1580484-04-3 | Mcl1-IN-4 is an inhibitor of Mcl1 with an IC50 of 0.2 μM. |
| CSN22496 | RH1 | 221635-42-3 | RH1 is a potent bioreductive agent with profound anti-cancer activity in vitro and in vivo. |
| CSN22509 | SNT-207707 | 1064662-40-3 | SNT-207707 is a selective, potent and orally active melanocortin MC-4 receptor antagonist with an IC50 of 8 nM (binding) and 5 nM (function) on the MC-4 receptor. |
| 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. |
| CSN22534 | WIT 002 | 240427-90-1 | WIT 002 is an antagonist of 20-hydroxyeicosatetraenoic acid (20-HETE). |
| CSN22515 | Target Protein-binding Moiety 13 | 1092369-24-8 | PROTAC FKBP12-binding moiety 1 is a synthetic ligand for FKBP, used as a warhead ligand for conjugation reactions of PROTAC targeting on FKBP12. |
| CSN22517 | Target Protein-binding Moiety 8 | 910297-51-7 | PROTAC Bcr-Abl-binding moiety 1 is a Dasatinib-based warhead ligand for conjugation reactions of PROTAC targeting on Bcr-Abl. |
| CSN23752 | Elemicin | 487-11-6 | Elemicin is a phenylpropene with anticancer and antifungal activities, it exhibits anticholinergic-like effects in humans. |
