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| 货号 | 产品名称 | CAS号 | 简介 |
|---|---|---|---|
| CSN20392 | MDL28170 | 88191-84-8 | MDL28170 is a potent, selective inhibitor of calpain and cathepsin B (Ki values are 10 and 25 nM respectively) that does not inhibit trypsin-like seri |
| CSN26140 | TRULI | 1424635-83-5 | TRULI is an ATP-competitive inhibitor of Lats kinases. It is a potent, non-toxic, and reversible inhibitor of Hippo signaling which causes Yap-depende |
| CSN26180 | PU-02 | 313984-77-9 | PU-02 is an antagonist of serotonin (5-HT) receptor subtype 5-HT3. |
| CSN27205 | ILK-IN-3 | 6975-75-3 | ILK-IN-3 is an integrin linked kinase inhibitor. |
| CSN27206 | CIL62 | 117593-36-9 | CIL56 is a inducer of regulated, non-apoptotic cell death. It is a lead compound of FIN56, |
| CSN27211 | JX06 | 729-46-4 | JX06 is a selective covalent PDK1 inhibitor with IC50 values of 49, 101 and 313nM for PDK-1, PDK-2 and PDK-3, respectively. |
| CSN27238 | Nafenopin | 3771-19-5 | Nafenopin is a peroxisome proliferator that is used to promote liver tumors. It has been used as an antihyperlipoproteinemic agent. |
| CSN27244 | 2′,5′-Dideoxyadenosine | 6698-26-6 | 2',5'-Dideoxyadenosine is a potent and non-competitive adenylyl cyclase inhibitor via binding the P-site with an IC50 of 3 µM . 2',5'-Dideoxyadenosine |
| CSN27600 | TD-198946 | 364762-86-7 | |
| CSN26189 | Afimoxifene | 68392-35-8 | |
| CSN27710 | SKF-34288 HCl | 320386-54-7 | SKF-34288 HCl is a PEPCK inhibitor which could inhibit glucose synthesis through inhibition of PEPCK in the gluconeogenesis pathway. |
| CSN27722 | AZ9482 | 1825345-33-2 | AZ9482 is a PARP inhibitor with IC50 values of 1, 1, 46, 640, 9, and 160nM for PARP1, -2, -3, -6, TNKS1/PARP5a, and TNKS2, respectively. |
| CSN27724 | MitoBloCK-10 | 394694-98-5 | MitoBloCK-10 is the first small molecule modulator to attenuate PAM (protein-associated motor) complex activity. It binds to a specific pocket in the |
| CSN27725 | COH-SR4 | 73439-19-7 | COH-SR4 is an AMPK activator with anticancer properties. It significantly inhibited adipocyte differentiation in a dose-dependent manner in 3T3-L1 cel |
| CSN-BF1001 | NP-40 Cell Lysis Buffer | N/A | |
| CSN27723 | MID-1 | 312608-54-1 | MID-1 is a MG53-IRS-1 interaction disruptor. It abolished MG53-mediated IRS-1 ubiquitination and degradation, as well as sensitized insulin signaling |
| CSN27735 | MALAT1-IN-1 | 827327-28-6 | |
| CSN27743 | GW806742X | 579515-63-2 | GW806742X is an ATP mimetic MLKL inhibitor with Kd value of 9.3μM, and a VEGFR2 inhibitor with IC50 value of 2nM. |
| CSN27766 | Lavendustin B | 125697-91-8 | Lavendustin B is a competitive Glut1 inhibitor with Ki value of 15µM. |
| CSN27767 | ICCB280 | 2041072-41-5 | ICCB280 is a potent inducer of C/EBPα and myeloid differentiation. |
| CSN27773 | mTOR inhibitor-1 | 468747-17-3 | mTOR inhibitor-1 is an ATP-competitive inhibitor of mTOR. It suppressed A549 cell proliferation and induced autophagy. |
| CSN27768 | AT-56 | 162640-98-4 | AT 56 is an orally active L-PGDS inhibitor with IC50 value of 95μM. It inhibits the production of PGD2 from PGH2 in vitro, with no effect on PG |
| CSN27779 | CEBPα inducer 1 | 2374285-52-4 | CEBPα inducer 1 is a potent inducer of C/EBPα and myeloid differentiation. |
| CSN27841 | PFM01 | 1558598-41-6 | PFM 01 is a MRE11 endonuclease inhibitor which can prevent double-stranded break resection. It enhances NHEJ and reduces homologous recombination. |
| CSN27839 | NSD2-PWWP1 antagonist 3f | 1210906-48-1 | NSD2-PWWP1 antagonist 3f can bind to the NSD2-PWWP1 domain with Kd value of 3.4μM and abrogates histone H3K36me2 binding to the PWWP1 domain in cells. |
| CSN27842 | IT-603 | 292168-90-2 | IT-603 is a c-Rel inhibitor with IC50 value of 3μM. |
| CSN27837 | Rhodamine 123 | 62669-70-9 | |
| CSN27843 | Sulforhodamine 101 | 60311-02-6 | Sulforhodamine 101, a fluorescent dye (Ex ~586nm, Em ~606nm), is a selective astrocyte marker. |
| CSN27847 | EMAC10101d | 2561476-24-0 | EMAC10101d is a potent and selective Carbonic Anhydrase II inhibitor. |
| CSN27848 | GW604714X | 853953-65-8 | GW604714X is a highly specific MPC (mitochondrial pyruvate carrier) inhibitor with Ki value<0.1nM. |
| CSN27850 | YUM70 | 423145-35-1 | YUM70 is a GRP78 inhibitor with IC50 value of 1.5μM and resulted in ER stress-mediated apoptosis. It inhibited pancreatic cancer cell growth in vit |
| CSN27849 | Seralutinib | 1619931-27-9 | Seralutinib is a potent and novel inhaled PDGFR inhibitor, used in the study for pulmonary arterial hypertension. |
| CSN27868 | 16-(S)-ML188 | 1417700-12-9 | |
| CSN27872 | Melatonin Biotin | 2193462-87-0 | Melatonin Biotin is compound conjuncted melatonin with biotin. |
| CSN27873 | ChX710 | 2438721-44-7 | ChX710 can boost cellular response to cytosolic DNA via STING. It efficiently primed cellular response to transfected plasmid DNA as assessed by poten |
| CSN28337 | Pseudouridine | 1445-07-4 | Pseudouridine is a modified nucleoside. |
| CSN27986 | 1,2-DOPC | 4235-95-4 | 1,2-DOPC is a phospholipid utilized for liposome production. |
| CSN28422 | MK2-IN-3 | 724711-21-1 | MK2 Inhibitor III is a potent and selective MK-2 inhibitor with IC50 value of 8.5nM. |
| CSN28421 | MDK6620 | 304456-62-0 | MDK6620 is a potent and selective IMP1 inhibitor by inhibiting IMP1 binding to c-Myc mRNA with IC50 value of 5μM. It downregulates several mRNA transc |
| CSN28430 | GSK2837808A | 1445879-21-9 | GSK2837808A is a potent and selective LDHA and LDHB inhibitor with IC50 values of 2.6nM and 43nM for LDHA and LDHB, respectively. It reduces glucose u |
| CSN28431 | YKL-05-099 | 1936529-65-5 | YKL-05-099 is a selective SIK inhibitor with IC50 values of 10 nM, 40 nM and 30 nM for SIK1, SIK2 and SIK3, respectively. |
| CSN26245 | TAO Kinase inhibitor 1 | 850467-66-2 | |
| CSN28747 | ALC-0315 | 2036272-55-4 | ALC-0315, a cationic lipid, is a potent siRNA delivery vehicle. It can be used to form LNPs. |
| CSN28763 | LY293111 | 161172-51-6 | LY293111 is a potent LTB4 receptor antagonist with IC50 values of 17.6nM and 6.3nM for inhibition of the specific binding of radiolabeled-LTB4 to isol |
| CSN28765 | MYLS22 | 306959-01-3 | MYLS22 is a first-in-class small molecule-specific OPA1 inhibitor which inhibits tumor angiogenesis, impacts tumor growth and metastatization dependen |
| CSN28769 | TKN87180 | 756487-18-0 | TKN8718 is a hydrolyzable ADC linker. |
| CSN28768 | Fmoc-Phe-Lys(Boc)-PAB | 206133-42-8 | Fmoc-Phe-Lys(Boc)-PAB is a hydrolyzable ADC linker. |
| CSN28782 | CA-4948 | 1801344-14-8 | CA-4948 is a selective and orally bioavailable IRAK4 Inhibitor. It exhibited desirable ADME and PK profiles including good oral bioavailability in mic |
| CSN28781 | BOS172722 | 1578245-44-9 | BOS172722 is clinical candidate Mps1 inhibitor with IC50 value of 11nM. |
| CSN28785 | EGFR-IN-5 | 2225887-26-1 | EGFR-IN-5 is an inhibitor of EGFR with IC50 values of 10.4 nM, 1.1 nM, 34 nM and 7.2 nM for EGFR, EGFRL858R, EGFRL858R/T790M, and EGFRL858R/T790M/C797 |
