| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| 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. |
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| DC10442 | Cyazofamid Featured | Cyazofamid is a foliar fungicide approved for use in the EU. |
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| 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. |
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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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| DC26110 | Cyclapolin 1 | Cyclapolin 1 is a potent and selective PLK1 inhibitor that promotes loss of centrosome integrity and microtubule nucleating ability apparently through increased accessibility of protein phosphatases. |
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| DC26115 | Cyclapolin 9 | Cyclapolin 9 is a potent, selective, and ATP-competitive polo-like kinase PLK1 inhibitor with IC50 of 500 nM.. |
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| DC10541 | Cyclo(RGDfC) Featured | Cyclo (RGDfC), avb3 Integrin Binding Cyclic RGD Peptide,This is a cyclic RGDfC sequence, an integrin avb3-affine peptide. |
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| DC10368 | Cyclo(his-pro) | Cyclo(His-Pro) is a cyclic dipeptide structurally related to tyreotropin-releasing hormone. |
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| 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. |
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| DC8055 | Cyclo(-RGDfK) Featured | cyclo(-RGDfK,-Arg-Gly-Asp-D-Phe-Lys)) is a selective αvβ3-integrin antagonist. |
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| DC8399 | Cyclo(RGDyK) Featured | Cyclo(RGDyK) is a potent and selective αVβ3 integrin inhibitor with IC50 of 20 nM. |
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| DC11446 | Cycloastragenol Featured | Cycloastragenol, the aglycone derivative of astragaloside A, can be found in various species of Astragalus and is reported to activate telomerase. |
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| DC9058 | Cyclobenzaprine HCl Featured | Cyclobenzaprine Hcl is a skeletal muscle relaxant and a central nervous system (CNS) depressant. |
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| DC20657 | Cyclocreatine Phosphate | Cyclocreatine Phosphate (AM 285) is an analog of the creatine kinase CKMT1 substrate creatine and inhibitor of the creatine biosynthesis pathway. |
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| DCAPI1537 | Flunixin Meglumine Featured | Cyclooxigenase inhibitor. Anti-inflammatory, analgesic and antipyretic. |
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| DC20350 | Cyclopamine tartrate | Cyclopamine tartrate is a natural steroidal alkaloid that inhibits hedgehog (Hh) signaling with IC50 of 46 nM. |
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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. |
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| DC11214 | Cyclophilin inhibitor C31 | Cyclophilin inhibitor C31 (SMCypI C31) is a small-molecule cyclophilin (CypA) inhibitor (SMCypI) with PPIase inhibition IC50 of 0.1 uM, displays anti-HCV activity (HCV Gt1b replicon EC50=0.4 uM) and disrupts the CypA-NS5A interaction. |
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| DC9013 | Cyclophosphamide Featured | Cyclophosphamide is a synthetic alkylating agent chemically related to the nitrogen mustards with antineoplastic and immunosuppressive activities. |
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| DC4115 | Cyclosporin A Featured | Cyclosporin A (Cyclosporine A) is an immunosuppressant agent widely used in post-allogeneic organ transplant to reduce the activity of the immune system. |
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| DC20101 | Cyclosporin A-Derivative 1 Free base | Cyclosporin A-Derivative 1 (Free base) is a crystalline intermediate derived from the opening of cyclosporin A extracted from patent WO 2013167703 A1. Cyclosporin A is an immunosuppressive agent which can bind to the cyclophilin and inhibit calcineurin. |
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| DCAPI1346 | Cyclosporine (Neoral) | Cyclosporine (Neoral) |
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| DC23630 | Cyclothiazide | Cyclothiazide (Doburil) is a positive allosteric modulator of the AMPA and kainate receptors that potentiates AMPA-mediated glutamate currents. |
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| DCAPI1374 | Cyclovirobuxin D(Bebuxine) Featured | Cyclovirobuxin D(Bebuxine) |
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| 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. |
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| DC20351 | CYD-1-79 | CYD-1-79 is a potent, selective 5-HT2C receptor positive allosteric modulator (PAM), potentiates 5-HT-evoked intracellular calcium release in cells stably expressing the human 5-HT2CR but not the 5-HT2AR cells.. |
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| DC23283 | CYD-2-11 | CYD-2-11 is a novel potent, selective Bax agonist that targets the structural pocket proximal to S184 in the C-terminal region of Bax (Ki=34.1 nM). |
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| 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. |
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| DC12470 | CYH33 methanesulfonate | 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. |
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| DC8088 | CYM5442 Featured | CYM-5442 is a highly-selective S1P1 (Spingosine 1-Phosphate Receptor 1) agonist. |
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