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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC5668 | Zwittermicin A |
Natural antibiotic, having diverse biological activities including broad-spectrum antibiosis against Bacteria and lower Eukarya, plant disease suppression, and enhancement of the insecticidal activity of Bacillus thuringiensis toxin against lepidopteran l
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| DCC5667 | Z-wehd-fmk |
Potent, cell-permeable and irreversible caspase-1/5 inhibitor
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| DCC5666 | Zuclopenthixol Dihydrochloride |
Antagonist of D1 and D2 dopamine receptors.
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| DCC5665 | Zu-4280011 |
Novel COX-2 inhibitor
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| DCC5664 | Ztz240 |
Novel potentiator of KCNQ2 potassium channels
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| DCC5663 | Ztb23(r) |
The first potent and selective Mycobacterium tuberculosis Zmp1 inhibitor
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| DCC5662 | Zp1-12cl |
Novel zinc sensor with a chloroalkane linker, reacting specifically with the engineered protein HaloTag, binding zinc ions with a threefold fluorescence enhancement
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| DCC5661 | Zolimidine |
Gastroprotective agent for the treatment of peptic ulcer
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| DCC5660 | Zoledronate Disodium |
Inhibitor of osteoclastogenesis and macrophage recruitment, decreasing bone turnover and stabilizing the bone matrix, exhibiting diverse anti-tumor effects in osteosarcoma
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| DCC5659 | Zolantidine Dimaleate |
Potent, selective, and brain penetrating H2 receptor antagonist
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| DCC5658 | Zofenoprilat |
Inducer of functional angiogenesis through increased H 2 S availability
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| DCC5657 | Zn-htsm |
Novel antidiabetic agent for the treatment of type 2 diabetes mellitus (DM)
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| DCC5656 | Zm39923 Hydrochloride |
Potent, selective inhibitor of Janus tyrosine kinase 3 (JAK3)
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| DCC5655 | Zm-260384 |
Potassium channel opener
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| DCC5654 | zm-253270 |
Selective nonpeptide, NK-2 receptor (NK-2R) antagonist
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| DCC5653 | Zm-244085 |
K-Channel opener (PCO) activating predominantly KATP channels in vitro to relax bladder detrusors
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| DCC5652 | zm-230487 |
5-Lipoxygenase (5-LO) inhibitor
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| DCC5651 | zm-189154 |
Non-steroidal pure antioestrogen
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| DCC5650 | Zm-181037 |
ATP-sensitive potassium channel-blocker; Eukalemic diuretic
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| DCC5649 | Zld10a |
Novel potent and highly selective inhibitor of wild-type and mutant versions of EZH2
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| DCC5648 | Zl3138 |
Novel β-catenin/B-cell lymphoma 9 (BCL9) inhibitor, disrupting the β-catenin/BCL9 protein-protein interaction (PPI) with a Ki of 0.96 μM and without affecting the β-catenin/E-cadherin interaction in living cells, displaying good selectivity for β-catenin/
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| DCC5647 | Zl0516 |
Novel potent and selective BRD4 bromodomain 1 (BD1) inhibitor
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| DCC5646 | Zl0513 |
Novel potent and selective BRD4 bromodomain 1 (BD1) inhibitor
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| DCC5645 | Zl006-05 |
Novel dual mordulator of nNOS-PSD-95 interaction and GABA A receptor
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| DCC5644 | Zk-806450 |
Novel potent inhibitor of factor Xa (FXa)
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| DCC5643 | Zk-304709 |
Novel oral multitarget tumour growth inhibitor
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| DCC5642 | Zk230211 |
Type III progesterone receptor antagonist with enhanced antiproliferative properties
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| DCC5641 | Zk187638 |
Non-competitive AMPA receptor antagonist
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| DCC5640 | Zinpyr-1 |
Cell-permeable fluorometric zinc sensor
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| DCC5639 | Zinc69811181 |
Novel ASCT2 inhibitor
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