| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DC25089 | Esomeprazole agnesium trihydrate | A proton pump inhibitor that reduces stomach acid secretion by inhibition of the H+/K+-ATPase in the parietal cells. |
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| DC24176 | Esomeprazole potassium salt | A proton pump inhibitor that reduces stomach acid secretion by inhibition of the H+/K+-ATPase in the parietal cells. |
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| DC23938 | Esomeprazole sodium Featured | A proton pump inhibitor that reduces stomach acid secretion by inhibition of the H+/K+-ATPase in the parietal cells. |
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| DC11545 | IPAG Featured | IPAG is a prototypic selective inhibitor of sigma1 receptor that engages the unfolded protein response and induces autophagy in cancer cells. |
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| DC23004 | PSMA-ligand-1 Featured | A PSMA (prostate-specific membrane antigen) ligand-tubulysin compound.. |
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| DC20605 | Enexasogaol | A pungent agent isolated from Zingiber officinale Roscoe, has been known to have anti-tumor and anti-inflammatory effects. |
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| DC11949 | SR-653234 | A purine scaffold casein kinase 1δ/1ε (CK1δ/ε) inhibitor with IC50 of 160/540 nM, respectively.. |
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| DC22348 | Zalcitabine Featured | A pyrimidine analog reverse transcriptase inhibitor (NRTI) for the treatment of HIV/AIDS. |
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| DC22388 | Mefloquine hydrochloride | A quinoline antimalarial drug that is structurally related to the antiarrhythmic agent quinidine. |
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| DC21407 | AG-1295 | A quinoxaline-type tyrphostin that acts as a potent and selective inhibitor of PDGFR kinase in vitro and in Swiss 3T3 cells with IC50 of 0.3-1 uM. |
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| DC23472 | TASP0434299 | A radioligand candidate for arginine vasopressin 1B (V1B) receptor that exhibits high binding affinities for human and rat V1B receptors with IC50 of 0.526 and 0.641 nM, respectively. |
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| DC26104 | UVI 2008 | A RARβ/γ agonist originated from TTNPB, is also a selective inhibitor of aldo-keto reductase family member 1B10 (AKR1B10) with IC50 of 6.1 uM. |
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| DC22985 | BMS-948 | A RARβ-selective agonist that exhibits a full transcriptional agonistic activity and activating RARβ as efficiently as the reference agonist TTNPB. |
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| DC7350 | 9-methyladenine | A receptor adenine derivative binding membrane brain animal cell line.For the detailed information of 9-methyladenine, the solubility of 9-methyladenine in water, the solubility of 9-methyladenine in DMSO, the solubility of 9-methyladenine in PBS buffer, the animal experiment (test) of 9-methyladenine, the cell expriment (test) of 9-methyladenine, the in vivo, in vitro and clinical trial test of 9-methyladenine, the EC50, IC50,and Affinity of 9-methyladenine, Please contact DC Chemicals.. |
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| DC23842 | L-783277 | A resorcylic lactone type covalent kinase inhibitor that inhibits ALK1 with IC50 of 125 nM, also inhibits FLT3, VEGFR2, VEGFR3, MEK2 with IC50 of 1-10 nM.. |
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| DC7054 | AM580 Featured | A retinoic acid analog and selective RARα agonist |
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| DC24096 | Dabigatran ethyl ester | A reversible and selective, direct thrombin inhibitor (DTI) with Ki value of 4.5 nM. |
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| DC11918 | CMLD010509 | A rocaglate (flavagline) derivative that acts a highly specific inhibitor of the oncogenic translation program supporting MM, including key oncoproteins such as MYC, MDM2, CCND1, MAF, and MCL-1. |
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| DC22367 | Bromethalin | A rodenticide that poisons the central nervous system by uncoupling mitochondrial oxidative phosphorylation, which causes a decrease in adenosine triphosphate (ATP) synthesis.. |
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| DC21011 | KP-1019 sodium salt | A ruthenium complex anticancer agent that is useful for metastatic tumors and cis-platin resistant tumors. |
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| DC20822 | BMT-052 | A second generation, orally biovailable pan-genotypic HCV NS5B polymerase inhibitor with EC50 of 1-10 nM. |
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| DC24180 | Cetirizine | A second-generation antihistamine that acts as a selective H1 receptor antagonist. |
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| DC22589 | Eltanexor | A second-generation SINE, orally bioavailable Exportin 1 (XPO1,CRM1) inhibitor with markedly reduced brain penetration compared to selinexor (30-fold less). |
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| DC23944 | K-7174 Featured | A selctive small molecule inhibitor of the transcription factor GATA-binding protein 2 (GATA2). |
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| DC23943 | K-7174 dihydrochloride Featured | K-7174 dihydrochloride is a selctive small molecule inhibitor of the transcription factor GATA-binding protein 2 (GATA2). |
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| DC20568 | Tec Kinase-IN-6 | A selecitve small molecule toward Tec kinase-mediated tyrosine phosphorylation of FGF2 with IC50 of 8.9 uM. |
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| DC23996 | Capadenoson Featured | Capadenoson is a selective agonist of adenosine-A1 receptor. |
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| DC22954 | MG-624 Featured | MG624 is a potent and selective neuronal α7 nAChR antagonist with a Ki of 106 nM. |
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| DC21853 | Ogerin Featured | A selective GPR68 positive allosteric modulator (pEC50=6.83) with minimal PAM activity at the related proton-sensing GPCRs GPR4 and GPR65. |
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| DC20596 | O-phenanthroline | A selective inhibitor of 26S proteasome subunit Rpn11 with IC50 of 10±2 uM. |
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