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Cat. No. Product Name Field of Application Chemical Structure
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)
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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