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
|
![]() |