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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 TD-198946, a thienoindazole derivative, is a potent chondrogenic agent.
CSN26189 Afimoxifene  68392-35-8 Afimoxifene is the active metabolite of tamoxifen and a selective estrogen receptor (ER) modulator that is widely used in the therapeutic and chemopre
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
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.
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
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.
CSN27848 GW604714X  853953-65-8 GW604714X is a highly specific MPC (mitochondrial pyruvate carrier) inhibitor with Ki value<0.1nM.
CSN27868 16-(S)-ML188  1417700-12-9 16-(S)-ML188 is a non-covalent SARS-CoV 3CLpro inhibitor with good enzyme and antiviral inhibitory activity.
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
CSN26245 TAO Kinase inhibitor 1  850467-66-2 TAO Kinase inhibitor 1 is a selective, ATP-competitive thousand-and-one amino acid kinases (TAOK) inhibitor with IC50s of 11 to 15 nM for TAOK1 and 2,
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.
CSN28771 8-Azaadenosine  10299-44-2 8-Azaadenosine is an ADAR1inhibitor.
CSN28783 NSC 617145  203115-63-3 NSC 617145 is a WRN helicase inhibitor with IC50 value of 250nM.
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
CSN29557 CLT-003  100823-03-8 TC11 is a potent inhibitor of tumor cell proliferation and an inducer of apoptosis via activation of caspase-3, 8 and 9.
CSN29564 DUN99845  727699-84-5 DUN99845 was reported as a STING inhbiitor, which inhibited the activation of the STING signal pathway and to prevent or treat a STING-​mediated disea
CSN29561 VU0071063  333415-38-6 VU0071063 can activate native Kir6.2/SUR1 channels, thereby inhibiting glucose-stimulated calcium entry in isolated mouse pancreatic β cells.
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