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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DCC3490 | Mrs7469 |
Novel highly selective A1 adenosine receptor (A1AR) agonist
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| DCC3489 | Mrs7396 |
Bitopic fluorescent antagonist of the A2A adenosine receptor
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| DCC3488 | Mrs4654 |
Novel potent P2Y14 Receptor Antagonist (IC 50 , 15 nM)
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| DCC3487 | Mrs4608 |
Novel potent antagonist of P2Y 14 receptor (P2Y 14 R) (IC 50 ~20 nM at hP2Y 14 R/mP2Y 14 R)
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| DCC3486 | Mrs4598 |
Novel highly potent human CD73 inhibitor (K i = 0.673 nM)
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| DCC3485 | Mrs2964 |
Potent and selective P2Y6 receptor agonist
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| DCC3484 | mrs2957 |
Potent P2Y6 agonist
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| DCC3483 | mrs2768 |
Selective P2Y2 agonist
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| DCC3482 | mrs2693 Trisodium |
Selective P2Y6 agonist
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| DCC3481 | mrs2690 |
Potent P2Y14 receptor agonist
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| DCC3480 | Mrs2220 |
Selective enhancer of the ATP effects at fast desensitizing P2X (P2X1 and P2X3) receptors
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| DCC3479 | Mrl-770 |
Novel selective and reproducible inhibitor of DNA synthesis in E. coli JL553
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| DCC3478 | Mrl-367 |
Novel potent and selective RORγT inhibitor, showing no appreciable activity against a panel of related nuclear hormone receptors
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| DCC3477 | Mrl-299 |
Novel potent RORγT inhibitor
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| DCC3476 | Mrl-248 |
Novel potent and selective RORγT inhibitor, showing no appreciable activity against a panel of related nuclear hormone receptors
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| DCC3475 | Mri-1891 |
Novel peripheral CB1R antagonist, being highly biased toward inhibiting CB1R-induced β-arrestin-2 (βArr2) recruitment over G-protein activation
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| DCC3474 | Mrgx1-activator-1 |
Activator of MrgX1 receptor signaling
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| DCC3473 | Mrgprx1 Pam 1t |
Novel positive allosteric modulator (PAM) of mas-related G protein-coupled receptor X1 (MRGPRX1), reducing behavioral heat hypersensitivity in humanized MRGPRX1 mice, demonstrating the therapeutic potential in treating neuropathic pain
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| DCC3472 | Mr6-31-2 |
Novel inhibitor of the main protease (Mpro) of SARS-CoV-2
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| DCC3471 | Mr22388 |
Novel, potent inducer of apoptosis via the MAP kinase pathways. Inhibitor of several kinases including the tyrosine kinase FLT3-ITD
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| DCC3470 | Mq02-439 |
Novel highly potent and selective 5-HT2C agonist
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| DCC3469 | Mpx-007 |
Novel potent and selective antagonist of GluN2A-containing NMDA receptors
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| DCC3468 | Mptp-in-22 |
Novel mitochondrial permeability transition pore (mPTP) inhibitor
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| DCC3467 | Mpt0b451 |
Novel Dual HDAC6 and Tubulin Inhibitor, Displaying Anti-tumor Ability in Human Cancer Cells
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| DCC3466 | Mpt0b206 |
Novel tubulin polymerization inhibitor
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| DCC3465 | Mps-bay2b |
Novel inhibitor of MPS1
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| DCC3464 | mps1 Inhibitor I |
Novel Mps1 Kinase Inhibitor
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| DCC3463 | Mpro-in-n3 |
Novel main protease (Mpro) inhibitor, inhibiting MHV-A29, HCoV-229E, FOPV replication, and SARS-CoV-2 viral cell entry
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| DCC3462 | Mpp Dihydrochloride |
Specific estrogen receptor α (ERα) antagonist
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| DCC3461 | Mpo-0029 |
Potent and selective COX-2 inhibitor
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