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Cat. No. Product Name Field of Application Chemical Structure
DC23942 CX-4945 sodium salt(Silmitasertib) Featured CX-4945 Sodium Salt is a water soluble CX-4945 (GLXC-04060), First-in-class Casein kinase 2 (CK2) inhibitor, sequentially attenuating the proteins in PI3K/Akt and MAPK pathways.
DC24074 CX-546 Featured CX546 is an AMPA receptor potentiator and GluR activator, binds specifically to the agonist bound non-desensitized receptor.
DC7810 CX-5461 Featured CX-5461 is an inhibitor of rRNA synthesis, selectively inhibits Pol I-driven transcription of rRNA, has no effect on Pol II, and possesses 250-to 300-fold selectivity for inhibition of rRNA transcription versus DNA replication and protein translation.
DC7153 CX6258 Featured CX-6258 is a potent, orally efficacious Pim 1/2/3 kinase(IC50=5 nM/25 nM/16 nM) inhibitor with excellent biochemical potency and kinase selectivity.
DC9925 CXD101(AZD-9468) Featured CXD101(AZD-9468) is a novel histone deacetylase (HDAC) inhibitor with potential antineoplastic activity.
DC10620 CY-09 Featured CY-09 is an NLRP3 inhibitor.
DC10576 Cyantraniliprole Featured Cyantraniliprole(HGW-86) is an insecticide of the ryanoid class; has activity against pests such as Diaphorina citri that have developed resistance to other classes insecticides.
DC10442 Cyazofamid Featured Cyazofamid is a foliar fungicide approved for use in the EU.
DC10775 Fadraciclib (CYC065) Featured CYC065 is an orally bioavailable inhibitor of cyclin dependent kinases 2, 5 and 9 (CDK2/5/9) with potential antineoplastic and chemoprotective activities.
DC7325 CYC116 Featured CYC116 is a potent inhibitor of Aurora A/B with Ki of 8.0 nM/9.2 nM.
DC10541 Cyclo(RGDfC) Featured Cyclo (RGDfC), avb3 Integrin Binding Cyclic RGD Peptide,This is a cyclic RGDfC sequence, an integrin avb3-affine peptide.
DC26050 Cyclo(L-Pro-L-Val) Featured Cyclo(L-Pro-L-Val) is a diketopiperazine that has been found in the marine sponge T. ignis, the bacterium B. pumilus, and the fungus A. fumigatus, among others.
DC8055 Cyclo(-RGDfK) Featured cyclo(-RGDfK,-Arg-Gly-Asp-D-Phe-Lys)) is a selective αvβ3-integrin antagonist.
DC8399 Cyclo(RGDyK) Featured Cyclo(RGDyK) is a potent and selective αVβ3 integrin inhibitor with IC50 of 20 nM.
DC11446 Cycloastragenol Featured Cycloastragenol, the aglycone derivative of astragaloside A, can be found in various species of Astragalus and is reported to activate telomerase.
DC9058 Cyclobenzaprine HCl Featured Cyclobenzaprine Hcl is a skeletal muscle relaxant and a central nervous system (CNS) depressant.
DCAPI1537 Flunixin Meglumine Featured Cyclooxigenase inhibitor. Anti-inflammatory, analgesic and antipyretic.
DC9910 CYCLOPAMINE Featured Cyclopamine(11-Deoxojervine) is a specific Hedgehog (Hh) signaling pathway antagonist of Smoothened (Smo) with IC50 of 46 nM.
DC9013 Cyclophosphamide Featured Cyclophosphamide is a synthetic alkylating agent chemically related to the nitrogen mustards with antineoplastic and immunosuppressive activities.
DC4115 Cyclosporin A Featured Cyclosporin A (Cyclosporine A) is a potent immunosuppressive agent commonly administered after allogeneic organ transplants to suppress immune system activity and prevent rejection.
DCAPI1374 Cyclovirobuxin D(Bebuxine) Featured Cyclovirobuxin D(Bebuxine)
DC10610 CycLuc1(Luciferase substrate) Featured CycLuc1 is a luciferase substrate which offers brighter bioluminescence and improved imaging in mouse models at lower doses than the standard D-luciferin.
DC12469 CYH33 Featured CYH33 (CYH-33) is a novel potent, PI3Kα-selective inhibitor with IC50 of 5.9 nM/598 nM/ 78.7 nM/225 nM aginst class I PI3K isoform α/β/δ/γ, respectively.
DC8088 CYM5442 Featured CYM-5442 is a highly-selective S1P1 (Spingosine 1-Phosphate Receptor 1) agonist.
DC3107 Momelotinib (CYT387,CYT-387) Featured CYT387 is an ATP-competitive inhibitor of JAK1 and JAK2 with IC50 of 11 nM and 18 nM, respectively.
DC9835 Cytochalasin H Featured Cytochalasin H is a potent inhibitor of actin incorporation into filaments,a cell-permeable fungal toxin used in actin polymerization studies and cytological research.
DCAPI1566 Cytarabine hydrochloride Featured Cytosine β-D-arabinofuranoside hydrochloride is an anti-leukemic agent which binds to topoisomerase I resulting in DNA fragmentation and inhibition of replication. In addition this compound does not have any effects on RNA synthesis. Cytosine β-D-arabinof
DC10125 CZ415 Featured CZ415 is a potent and highly selective mTOR inhibitor.
DC7734 CZC24832 Featured CZC24832 is the first selective PI3Kγinhibitor with IC50 of 27 nM, with 10-fold selectivity over PI3Kβ and >100-fold selectivity over PI3Kα and PI3Kδ.
DC7113 CZC-25146 Featured CZC-25146 is a potent, selective and metabolically stable LRRK2 inhibitor with IC50 of 4.76 nM/6.87 nM for wild type LRRK2 and G2019S LRRK2 respectively.

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