Alternate TextTo enhance service speed and avoid tariff delays, we've opened a US warehouse. All US orders ship directly from our US facility.
Home > Products

Products

You can also try the following methods, and our professionals will serve you Customized Consultation
Cat. No. Product Name Field of Application Chemical Structure
DCC5557 Xl-418
Novel Akt1/2 inhibitor
More description
DCC5556 Xl-147
Novel Potent Pan-Filovirus Inhibitor, showing potent inhibition against infectious EBOV Zaire (0.09 μM) and MARV (0.64 μM)
More description
DCC5555 Xl-13n
Novel dual inhibitor of AF9 and ENL YEATS domains
More description
DCC5554 Xist Ligand X1
Novel non-coding RNA prototype Xist ligand, specifically binding the RepA motif of Xist, reducing the conformational space of RepA, displacing cognate interacting protein factors (PRC2 and SPEN), suppressing histone H3K27 trimethylation, and blocking init
More description
DCC5553 Xie18-6
Novel INK4C inhibitor, specifically blocking the bioactivity of p18 protein and promoting human and murine hematopoietic stem cell ex vivo expansion
More description
DCC5552 Xen103
Potent and Selective Stearoyl-CoA Desaturase-1 Inhibitor
More description
DCC5551 xc-409
Novel PKM2 activator
More description
DCC5550 XAX-162
Quantity (mg or Unit) Unit Price ($/mg or $/Unit) Final Price 100 $26.55 Total: $2,655.00 50 $30.68 Total: $1,534.00 25 $35.99 Total: $899.75 10 $42.48 Total: $424.80 5 $50.15 Total: $250.75
More description
DCC5549 Xantholipin B
Novel antibiotic, showing 3- to 10-fold greater cytotoxicity than Xantholipin against a select panel of human cancer cell lines, demonstrating powerful antimicrobial activity against both Gram-positive bacteria and fungi
More description
DCC5548 Xantholipin
Antibiotic, exhibiting strong antibacterial activities and showing potent cytotoxicity, inhibiting HSP47 gene expression produced by Streptomyces sp
More description
DCC5547 Xanthoangelol
Natural antibacterial agent against Gram-positive bacterial pathogens such as methicillin-resistant Staphylococcus aureus (MRSA), Enterococcus faecium and Enterococcus faecalis
More description
DCC5546 Wyk431
Potent inhibitor of proliferation activity against a broad spectrum of human cancer cell lines, induces G2/M phase arrest and apoptosis through the PI3K/Akt pathway
More description
DCC5545 Wye-687 Dihydrochloride
Potent, ATP-competitive inhibitor of mammalian target of rapamycin (mTOR)
More description
DCC5544 Wx-671
Novel urokinase inhibitor
More description
DCC5543 Wwl123
Novel α/ß-hydrolase domain 6 (ABHD6) inhibitor
More description
DCC5542 Wu-07047
Simplified analog of the selective Gαq/11 inhibitor YM-25489
More description
DCC5541 Wsj-557
Novel xanthine oxidase inhibitor
More description
DCC5540 Ws-691
Novel highly potent and orally active ABCB1 modulator capable of overcoming MDR, stabilizing ABCB1 by directly binding to ABCB1, stimulating the activity of ABCB1 ATPase without inhibitory activity against CYP3A4, increasing the sensitivity of SW620/Ad300
More description
DCC5539 Ws-47-js03
Novel potent RET kinase inhibitor with >500-fold selectivity against KDR (Kinase insert Domain Receptor) in cellular assays
More description
DCC5538 wrr-483
Analog of K11777; Irriversible effective cysteine protease inhibitor with trypanocidal activity in cell culture and animal model with comparable efficacy to K11777.
More description
DCC5537 Wrr-391
Novel potent inhibitor of Schistosoma mansoni cathepsin B1 (SmCB1) with IC50 ~0.2 nM
More description
DCC5536 Wrr-286
Novel potent inhibitor of Schistosoma mansoni cathepsin B1 (SmCB1) with IC50 ~0.6 nM
More description
DCC5535 Wr99210
Potent inhibitor of Plasmodium falciparum dihydrofolate reductase (DHFR)
More description
DCC5534 Wqe-134
Novel Dual Inhibitor of Nitric Oxide and Prostaglandin E2 Production
More description
DCC5533 Wp-871 Monohydrate
Main active metabolite of tazanolast, inhibiting dose-dependently compound 48/80-induced histamine release from rat peritoneal mast cells
More description
DCC5532 Wp1193
Novel inhibitor of the JAK2/STAT3 pathway
More description
DCC5531 Wo-459
Novel GPR52 agonist, dose-dependently inducing elevation of intracellular cAMP in HEK293/GPR52 cells
More description
DCC5530 Wny0824
Novel dual BRD4 and PLK1 inhibitor (IC 50 values of 109 and 22 nM, respectively), showing strong antiproliferative activity against cancer cells
More description
DCC5529 Wnt/hh-in-1
Novel potent dual inhibitor of Wnt and hedgehog signalings, blocking porcupine and smoothened
More description
DCC5528 Wnk-in-3
Novel Allosteric WNK Kinase Inhibitor
More description

Customized Consultation X

Your information is safe with us. * Required Fields.

Your name
Company
Email
Procuct Name
Cat. No.
Remark
Verification code
Please fill out the characters in the picture
X