DC23942 |
CX-4945 sodium salt(Silmitasertib)
Featured
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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. |
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DC24074 |
CX-546
Featured
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CX546 is an AMPA receptor potentiator and GluR activator, binds specifically to the agonist bound non-desensitized receptor. |
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DC7810 |
CX-5461
Featured
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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. |
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DC7153 |
CX6258
Featured
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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. |
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DC9925 |
CXD101(AZD-9468)
Featured
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CXD101(AZD-9468) is a novel histone deacetylase (HDAC) inhibitor with potential antineoplastic activity. |
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DC10620 |
CY-09
Featured
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CY-09 is an NLRP3 inhibitor. |
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DC10576 |
Cyantraniliprole
Featured
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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. |
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DC10442 |
Cyazofamid
Featured
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Cyazofamid is a foliar fungicide approved for use in the EU. |
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DC10775 |
Fadraciclib (CYC065)
Featured
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CYC065 is an orally bioavailable inhibitor of cyclin dependent kinases 2, 5 and 9 (CDK2/5/9) with potential antineoplastic and chemoprotective activities. |
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DC7325 |
CYC116
Featured
|
CYC116 is a potent inhibitor of Aurora A/B with Ki of 8.0 nM/9.2 nM. |
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DC10541 |
Cyclo(RGDfC)
Featured
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Cyclo (RGDfC), avb3 Integrin Binding Cyclic RGD Peptide,This is a cyclic RGDfC sequence, an integrin avb3-affine peptide. |
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DC26050 |
Cyclo(L-Pro-L-Val)
Featured
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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. |
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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. |
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DCAPI1537 |
Flunixin Meglumine
Featured
|
Cyclooxigenase inhibitor. Anti-inflammatory, analgesic and antipyretic. |
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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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