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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DCC2955 | Kras4b-pdeδ Stabilizer C19 |
Novel stabilizer of the KRAS4b-PDEδ complex, decreasing the proliferation of colorectal cancer cells, and increasing apoptosis via decreased activation of oncogenic KRAS4b signaling
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| DCC2954 | Kras4b-in-d14 |
Novel specific inhibitor of oncogenic KRAS4b signaling, stabilizing the KRAS4b-PDEδ complex and remarkably decreasing tumor size and triggered apoptosis of tumor cells
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| DCC2953 | Kras(g12c)-in-1 |
Novel irreversible inhibitor of KRAS(G12C)
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| DCC2952 | Kr-31762 |
Novel KATP channel opener, exerting cardioprotective effects by opening SarcKATP channels in rat models of ischemia/reperfusion-induced heart injury
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| DCC2951 | Kr-25210 |
Novel enteroviral replication inhibitor through a non-capsid binding mode with EC 50 values of 2.5, 2.2, and 3.7 μM against hRV B14, A21, and A71, respectively, targeting the replication stages in the virus
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| DCC2950 | Kr-12-a4 |
Potent antimicrobial peptide against gram-positive and gram-negative bacteria and relatively high LPS-neutralization activity
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| DCC2949 | Kpu-300 |
Novel potent antimicrotubule agent, exhibiting potent cytotoxicity against HT-29 cells by strongly binding to tubulin and inducing microtubule depolymn.
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| DCC2948 | Kpt-6604 |
Novel selective, orally bioavailable, PAK4 allosteric modulator against triple negative breast cancer
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| DCC2947 | kp1212 |
Novel non-chain terminating nucleoside analog anti-HIV inhibitor
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| DCC2946 | Kongensin D |
Natural anti-TNBC agent, significantly suppressing the triple-negative breast cancer (TNBC) tumor growth without causing side effects
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| DCC2945 | Kmup-4 |
Novel enhancer of cGMP activity; Aortic smooth muscle relaxant
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| DCC2944 | Kmup-3 |
Novel enhancer of cGMP activity; Aortic smooth muscle relaxant
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| DCC2943 | Kms88009 |
Novel inhibitor of amyloid-β aggregation, ameliorating the neurodegenerative disorder
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| DCC2942 | kms80013 |
Novel inhibitor of amyloid-
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| DCC2941 | Kmn-80 |
Novel Potent and Selective EP4 Agonist
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| DCC2940 | Kmn-010034 |
Novel Potent Hematopoietic Prostaglandin D2 Synthase (H-PGDS) Inhibitor
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| DCC2939 | kmi-1764 |
Novel BACE1 inhibitor with a non-acidic heterocycle at the P1' position
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| DCC2938 | Km-5-66 |
Novel inhibitor of the BfrB-Bfd complex, binding BfrB in the P. aeruginosa cytosol, blocking the BfrB-Bfd interaction and inhibiting iron mobilization from BfrB, resulting in cytosolic iron limitation that is manifested in a pyoverdine hyperproduction phe
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| DCC2937 | Km-5-25 |
Novel inhibitor of the BfrB-Bfd complex, binding BfrB in the P. aeruginosa cytosol, blocking the BfrB-Bfd interaction and inhibiting iron mobilization from BfrB, resulting in cytosolic iron limitation that is manifested in a pyoverdine hyperproduction phe
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| DCC2936 | km10340 |
Selective S1P3 agonist
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| DCC2935 | Km05382 |
CDK9 inhibitor, inhibiting transcription of GAPDH
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| DCC2934 | Boc-phe-leu-glup(oph) |
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| DCC2933 | Kl-l9p |
Novel antibiotic sensitizer, promoting the rearrangement of the bacterial membrane that enables hydrophobic antibiotics to permeate, strongly sensitizing Gram-negative bacteria to linezolid (Lzd), rifampicin (Rif), or clarithromycin (Clr)
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| DCC2932 | Klk6-in-42 |
First-in-class inhibitor of Kallikrein-related peptidase 6 (KLK6), promoting the differentiation of OPCs into mature oligodendrocytes in vitro
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| DCC2931 | Klk6-in-32 |
First-in-class inhibitor of Kallikrein-related peptidase 6 (KLK6), promoting the differentiation of OPCs into mature oligodendrocytes in vitro
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| DCC2930 | Klebsazolicin |
Novel inhibitor of 70S ribosome by obstructing the peptide exit tunnel
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| DCC2929 | Kld-12 |
Self-assembling peptide, forming a hydrogel matrix to support growth of cells in the presence of an ionic solution, enhancing chondrogenic differentiation of bone marrow stromal cells (BMSCs)
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| DCC2928 | Kl-1156 |
Novel NF-κB inhibitor and lipopolysaccharide (LPS)-induced nitric oxide production inhibitor
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| DCC2927 | Kkha-761 |
Potent D3 receptor antagonist with high 5-HT1A receptor affinity
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| DCC2926 | Kj-pyr-10 |
Novel specific inhibitor of MYC
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