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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC1078 | Bms-986104 |
Novel S1P1 receptor modulator
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| DCC1077 | Bms-986034 |
Novel GPR119 agonist
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| DCC1076 | Bms-961 |
Selective RARγ agonist
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| DCC1075 | Bms-960 |
Novel Agonist of Sphingosine-1-Phosphate (S1P1)
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| DCC1074 | Bms-903452 |
Potent and selective GPR119 agonist
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| DCC1073 | Bms-902483 |
Potent alpha7 Nicotinic receptor partial agonist, improving cognition in preclinical rodent model
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| DCC1072 | Bms-883559 |
Novel inhibitor of the influenza nucleoprotein (INF-NP)
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| DCC1071 | Bms-870145 |
Novel potent and selective P2Y1 purinergic receptor antagonist.
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| DCC1070 | Bms-821095 |
Potent, Orally Bioavailable, Metabolically Stable Thumb Site 1 Inhibitor of the Hepatitis C Virus NS5B RNA-Dependent, RNA Polymerase
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| DCC1069 | Bms-764459 |
Novel potent antagonist of corticotropin-releasing factor/hormone receptor 1 (CRHR-1)
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| DCC1068 | Bms-763534 |
Novel potent antagonist of corticotropin-releasing factor/hormone receptor 1 (CRHR-1)
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| DCC1067 | Bms-698861 |
Novel Novel γ-secretase modulator, decreasing Aß1-40 and Aß1-42 and increasing Aß1-37 and Aß1-38 in rat brain modulator, decreasing Aß1-40 and Aß1-42 and increasing Aß1-37 and Aß1-38 in rat brain
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| DCC1066 | Bms-665053 |
Novel potent antagonist of corticotropin-releasing factor/hormone receptor 1 (CRHR-1)
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| DCC1065 | Bms-585248 |
Novel Inhibitor of human immunodeficiency virus type 1 (HIV-1) attachment
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| DCC1064 | Bms-566394 |
Novel, potent, exceptionally selective inhibitor of TNF-α Converting Enzyme (TACE)
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| DCC1063 | Bms-538305 Tartrate |
Potent and selective dipeptidyl peptidase IV (DPP-IV) inhibitor
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| DCC1062 | Bms-488043 |
Novel Inhibitor of human immunodeficiency virus type 1 (HIV-1) attachment
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| DCC1061 | Bms-422461 |
Prodrug of the novel fluoro-substituted camptothecin analog, BMS-286309
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| DCC1060 | Bms-351 |
Novel Selective CYP17A1 Lyase Inhibitor
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| DCC1059 | Bms-341 |
Novel dissociated glucocorticoid receptor modulator
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| DCC1058 | Bms-286309 |
Novel fluoro-substituted camptothecin, inducing topoisomerase I-mediated DNA breaks
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| DCC1057 | Bms-281384 |
Highly potent and selective phosphodiesterase 5 (PDE 5) inhibitor
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| DCC1056 | Bms-262084 |
Potent and selective beta-lactam tryptase inhibitor, inhibiting factor XIa and producing antithrombotic efficacy with minimal bleeding time prolongation
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| DCC1055 | Bms-250685 |
Selective ATP hydrolase inhibitor
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| DCC1054 | Bms-243117 |
Potent and selective p56(lck) inhibitor
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| DCC1053 | Bms-201620 |
Potent and selective β3 full agonist
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| DCC1052 | Bms-199264 Hydrochloride |
Novel potent inhibitor of the ATP hydrolase activity of mitochondrial F1F0 ATP synthase
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| DCC1051 | Bms-193885 |
Novel and selective neuropeptide Y1 receptor antagonist
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| DCC1050 | bms-189532 |
Retinoic acid receptor (RAR) pan-antagonist
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| DCC1049 | Bms-187745 |
Squalene synthase inhibitor
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