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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
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