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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DCC3594 | ncx-2057 |
Novel NO-donor, suppressing inflammatory and nociceptive responses
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| DCC3593 | Nctu-alan-2026 |
Novel blocker of the interaction between FGF1 and FGFRD2 to inhibit cell proliferation, showing potent antiproliferent with less cytotoxicity.
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| DCC3592 | Ncs-8591 |
Beclin 1 mimetic, selectively binding to Bcl-xL and inducing autophagy, showing potent cytotoxicity in PC-3, PC-3a and DU145 prostate cancer cells
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| DCC3591 | Ncs-382 |
Analogue of γ-hydroxybutyric acid (GHB), acting as a substrate for both the monocarboxylate transporter subtype 1 (MCT1) and subtype 4 (MCT4)
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| DCC3590 | Ncrw0005-f05 |
Novel GPR139 receptor agonist
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| DCC3589 | Nco-04 |
Novel SIRT1 inhibitor, inducing cell death in adult T-cell leukaemia cells
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| DCC3588 | Ncgc2327 |
Novel potent inhibitor of IRAK1/4 and FLT3
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| DCC3587 | Ncgc00262654 |
Novel AMA1-RON2 Inhibitor
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| DCC3586 | Ncgc00249987 |
Novel allosteric Eya2 phosphatase inhibitor, specifically targeting migration, invadopodia formation, and invasion of lung cancer cells
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| DCC3585 | ncgc00242595 |
TSHR neutral antagonist, inhibiting stimulated signaling but not basal signaling
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| DCC3583 | Ncgc00120943 |
Novel Agonist for Human Resolvin D1 Receptor DRV1 with Pro-Resolving Functions
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| DCC3582 | Ncgc00117362 |
Novel inhibitor of ovarian cancer metastasis, adhesion, invasion and proliferation
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| DCC3581 | Ncdm-32 |
Potent pan KDM Inhibitor, inhibiting KDM2A, KDM7A, KDM7B, KDM4A, KDM4C, and KDM5A
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| DCC3580 | Ncb0970 |
Less active trans-isomer of NCB-0846, acting as the negative control for NCB-0846, showing 13-fold weaker TNIK enzyme-inhibitory activity
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| DCC3579 | Ncats-sm1441 |
First-in-class, potent, and selective Lactate dehydrogenase inhibitor
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| DCC3578 | Ncats-sm1440 |
First-in-class, potent, and selective Lactate dehydrogenase inhibitor
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| DCC3577 | Nc2213 |
Novel inhibitor of methionine aminopeptidase 2 (MetAP2)
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| DCC3576 | nc00094221 |
M. tuberculosis Dihydrofolate Reductase Inhibitor
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| DCC3575 | Nbti-5463 |
Novel bacterial type II topoisomerase inhibitor with activity against gram-negative bacteria and in vivo efficacy
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| DCC3574 | Nboh-2c-cn Hydrochloride |
Potent and selective 5-HT2A receptor agonist
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| DCC3573 | N-bn-thaz Fumarate |
Potent agonist of the human 5-HT2A and 5-HT2C receptors
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| DCC3572 | Nbd-14136 |
Novel CD4-mimetic HIV-1 entry inhibitor
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| DCC3571 | Nbd-10007 |
Novel HIV-1 entry inhibitor
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| DCC3570 | Nbd-09027 |
Novel HIV-1 entry inhibitor
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| DCC3569 | Nb-caged Tyrosine Hydrochloride |
L-Tyrosine caged with photosensitive ortho-nitrobenzyl side chain
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| DCC3568 | Nb-360 |
Biological Active Reagents
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| DCC3567 | Naxifylline |
Potent and selective A1 adenosine receptor antagonist
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| DCC3566 | Naveglitazar |
Dual peroxisome proliferator-activated receptor gamma and alpha (PPARgamma and PPARalpha) agonist
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| DCC3565 | Navarixin |
Novel CXC chemokine receptor 2 (CXCR2) antagonist
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| DCC3564 | Nav1.7 Blocker-801 |
Potent NaV1.7 blocker, being 5-10 fold more potent than NaV 1.2 and NaV 1.6
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