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Cat. No. Product Name CAS No. Information
CSN24085 Smurf1-IN-A01  1007647-73-5 Smurf1-IN-A01 is an inhibitor of negatively regulatory factor Smurf1 for promoting bone formation.
CSN24138 V-9302 HCl  N/A V-9302 HCl is a competitive and selective antagonist of transmembrane glutamine flux that selectively and potently targets the amino acid transporter
CSN24154 Defensamide  1104874-94-3 Defensamide is an activator of SPHK1, and significantly stimulates CAMP mRNA and protein production in KC.
CSN24152 AGI 1067  216167-82-7 is phenolic antioxidant with anti-inflammatory and antiplatelet effects and is potentially useful for the treatment of atherosclerosis and type 2 diab
CSN24156 E260  1241537-79-0 E260 is an inhibitor of the Fer/FerT kinase with Kd of 0.85 μM, selectively evokes metabolic stress and necrotic death in cancer cells.
CSN24168 IKE  1801530-11-9 IKE is a potent, metabolically stable inhibitor of system Xc- and inducer of ferroptosis potentially suitable for in vivo applic
CSN24177 Baloxavir marboxil  1985606-14-1 Baloxavir marboxil is an inhibitor of cap-dependent endonuclease of influenza A and B viruses.
CSN24164 BAY-218  2162982-11-6 BAY-218 is an AHR antagonist.
CSN24170 D3-βArr   662164-09-2 D3-βArr is a positive allosteric TSH Receptor modulator.
CSN24162 ST271  106392-48-7 ST271 is a potent inhibitor of protein tyrosine kinase (PTK), inhibits phospholipase D activation stimulated by fMet-Leu-Phe and PAF, with IC50s of 6.
CSN24161 GSK369796 2HCl  1010411-21-8 GSK369796 2HCl is an affordable and effective antimalarial and inhibits hERG potassium ion channel repolarization with an IC50 of 7.5 μM.
CSN24198 NACM-OPT HCl  N/A NAcM-OPT is an orally bioavailable cullin neddylation 1 (DCN1) inhibitor, which specific and reversible inhibits the interaction of N-Acetyl-UBE2M and
CSN24205 1A-116  1430208-73-3 1A-116 is a specific Rac1 inhibitor.
CSN24206 Calcein  1461-15-0 Calcein is a compound used for fluorometric determination of calcium and EDTA titration.
CSN24208 ML-18  1422269-30-4 ML-18 is a nonpeptide BRS-3 antagonist with IC50 value of 4.8μM.
CSN24255 (±)-Fargesin  31008-19-2 Fargesin is a lignan from Magnolia fargesii, an oriental medicine used in the treatment of nasal congestion and sinusitis.
CSN24266 Anle138b  882697-00-9 Anle138b is an oligomeric aggregation inhibitor which can block the formation of pathological aggregates of prion protein (PrP(Sc)) and of α-synuclein
CSN24257 BMS-986195  1912445-55-6 BMS-986195 is a potent, covalent, irreversible BTK inhibitor with IC50 value of 0.1nM.
CSN24273 SB-423562  351490-27-2 SB-423562 is a short-acting calcium-sensing receptor (CaR) antagonist.
CSN24275 LY-3200882  1898283-02-7 LY3200882 is a novel and highly selective inhibitor of TGF-β receptor type 1 (TGFβRI).
CSN24287 Traxoprodil mesylate  189894-57-3 Traxoprodil a selective antagonist of the NR2B subunit of the NMDA receptor.
CSN24301 BQR695  1513879-21-4 BQR695 is a PI4K specific inhibitor with IC50 value of 80nM.
CSN24302 MK-7246  1218918-62-7 MK-7246 is a potent and selective CRTH2 antagonist with Ki value of 2.5nM.
CSN24317 GI 530159  69563-88-8 GI 530159 is a selective and mechano-sensitive K2P channel opener, exhibits selectivity for TREK1/2 over TRAAK, TASK3 and a range of other potassium c
CSN24469 FDI-6  313380-27-7 FDI-6 is an inhibitor of FOXM1 that block DNA binding. It act by specifically downregulating FOXM1-activated genes.
CSN24470 GSK3179106  1627856-64-7 GSK3179106 is a potent, selective and gut-restricted RET kinase inhibitor with IC50 value of 0.4nM.
CSN24481 GArdiquimod trifluoroacetate  1159840-61-5 Gardiquimod trifluoroacetate is a specific TLR7 agonist.
CSN24499 SAR-20347  1450881-55-6 SAR-20347 is a TYK2 and JAK inhibitor with IC50 values of 0.6, 23, 26 and 41nM for TYK2, JAK1, JAK2 and JAK3, respectively.
CSN24505 JMS-17-2  1380392-05-1 JMS-17-2 is a potent and selective CX3CR1 antagonist with an IC50 of 0.32 nM.
CSN24507 EN6  1808714-73-9 EN6 covalently targets cysteine 277 in the ATP6V1A subunit of the lysosomal the vacuolar H+ ATPase (v-ATPase). It is a small-molecule in vivo activato
CSN24508 Acid Red 52  3520-42-1 Sulforhodamine B is a dye used for cell density determination, based on the measurement of cellular protein content.
CSN24614 N,N'-(Octane-1,8-diyl)bis(2,2-dichloroacetamide)  1477-57-2 WIN 18446 is an inhibitor of aldehyde dehydrogenase 1a2 (ALDH1a2) with IC50 of 0.3 μM.
CSN24625 Losartan carboxylic acid  124750-92-1 EXP 3174 is a selective and noncompetitive antagonist of AT1 receptor with IC50 of 37 nM.
CSN24747 KKL-35  865285-29-6 KKL-35, a potent member of the oxadiazole family, against the human pathogen Legionella pneumophila and other related species that can also cause Legi
CSN24780 2-HBA  131359-24-5 2-HBA is a potent inducer of NAD(P)H:quinone acceptor oxidoreductase 1 (NQO1) which can also activate caspase-3 and caspase-10.
CSN24782 Lotamilast  947620-48-6 Lotamilast (RVT-501; E6005) is a selective phosphodiesterase 4 (PDE4) inhibitor with an IC50 of 2.8 nM.
CSN24801 TP353  1253799-29-9 TP353 is a CDK7 inhibitor.
CSN25213 MRTX1257  2206736-04-9 MRTX1257 is a selective, covalent K-Ras G12C inhibitor with oral activity in animal models of cancer.
CSN25255 Emodepside  155030-63-0 Emodepside is an antiparasitic that is effective against a number of gastrointestinal nematodes, used in cat.
CSN25258 Spermidine 3HCl  334-50-9 Spermidine, a precursor of spermine, is a polyamine derived from putrescine and could help stabilize some membranes and nucleic acid structures.
CSN25272 RG-13022  136831-48-6 RG-13022 significantly inhibited EGF-stimulated autophosphorylation of its receptor in two breast cancer cell lines that have abundant, although not a
CSN25307 Rg3039  1005504-62-0 RG3039 is an orally bioavailable and brain-penetrant DcpS inhibitor with IC50 of 0.069 nM.
CSN25551 EIDD-2801  2349386-89-4 EIDD-2801 is an orally bioavailable prodrug of EIDD-1931, which has a broad-spectrum antiviral activity against 39 multiple coronaviruses, including S
CSN25566 Danicopan  1903768-17-1 Danicopan is selective and orally active small-molecule factor D inhibitor, shows high binding affinity to human Factor D with Kd value of 0.54 nM. It
CSN25632 CADD522  199735-88-1 CADD522 is a small molecule that inhibits the DNA binding of RUNX2. It negatively regulated transcription of RUNX2 target genes such as matrix metallo
CSN25635 OGG1 Inhibitor O8  350997-39-6 O8 OGG1 Inhibitor is an inhibitor of OGG1 with IC50 value of 0.35μM in fluorescence-based OGG1 assays. It can inhibit Schiff base formation during OGG
CSN25655 Mycro-3  944547-46-0 Mycro3 is a small-molecule inhibitor of Myc-Max dimerization. The average residual tumor of Pdx1-cre/KRAS* mice after Mycro3 treatment (100mg/kg, oral
CSN25872 MAC-545496  838810-96-1 MAC-545496 is a nanomolar inhibitor of GraR. It reverses β-lactam resistance in the community-acquired MRSA USA300 strain.
CSN25874 VLX600  327031-55-0 VLX600 is preferentially active against quiescent cells in colon cancer 3-D microtissues. VLX600 shows enhanced cytotoxic activity under conditions of
CSN26106 JCN037  2305154-31-6 JCN037 is a potent EGFR inhibitor with IC50 values of 2.49 nM, 3.95 nM and 4.48 nM for EGFR, p-wtEGFR and pEGFRvⅢ, respectively. It displayed potent a
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