| Catalog | name | Description | price |
|---|---|---|---|
| R-C-518 | HQL-79 cas:162641-16-9 | HQL-79 is a selective inhibitor of hematopoietic prostaglandin D (PGD) synthase, that structurally is a synthetic tetrazole compound originally prepared as a possible antihistamine. | price> |
| R-C-565 | ACY-1215 cas:1316214-52-4 | Ricolinostat (ACY-1215,Rocilinostat)is a selective HDAC6 inhibitor with IC50 of 5 nM in a cell-free assay.It is>10-fold more selective for HDAC6 than HDAC1/2/3(class I HDACs)with slight activity against HDAC8,minimal activity against HDAC4/5/7/9/11,Sirtuin1,and Sirtuin2.Ricolinostat (ACY-1215)suppresses cell proliferation and promotes apoptosis. | price> |
| R-C-587 | Amrubicin cas:110267-81-7 | Amrubicin is a synthetic anthracycline antibiotic.It inhibits DNA topoisomerase II. Antineoplastic. | price> |
| R-C-602 | CGK733 cas:905973-89-9 | CGK733,a thiourea-containing compound,was originally identified as a specific inhibitor of ATR and ATM kinases (IC50=~200 nM).In prematurely senescent breast, lung, and colon cancer cells CGK733 reportedly suppresses ATM-mediated p21 expression required for survival,resulting in cell death. | price> |
| R-C-627 | RI-1 (RAD51 inhibitor) cas:415713-60-9 | RI-1 is a small molecule that inhibits the central recombination protein RAD51. RI-1 specifically reduces gene conversion in human cells while stimulating single strand annealing.RI-1 binds covalently to the surface of RAD51 protein at cysteine 319 that likely destabilizes an interface used by RAD51 monomers to oligomerize into filaments on DNA. | price> |
| R-C-637 | PENTOSTATIN cas:53910-25-1 | Pentostatin is a potent inhibitor of adenosine deaminase.The drug is effective in the treatment of many lymphoproliferative malignancies,particularly hairy-cell leukemia.It is also synergistic with some other antineoplastic agents and has immunosuppressive activity. | price> |
| R-C-661 | SB1317 cas:937270-47-8 | SB1317 is a potent inhibitor of CDK2,JAK2,and FLT3 for the treatment of cancer, with IC50 of 13,73,and 56 nM for CDK2,JAK2 and FLT3,respectively. | price> |
| R-C-669 | BAY57-1293 cas:348086-71-5 | Pritelivir(AIC316),an inhibitor of the viral helicase-primase complex,exhibits antiviral activity in vitro and in animal models of herpes simplex virus (HSV) infection.Pritelivir is active against herpes simplex virus types 1 and 2 (HSV-1 and HSV-2)with the IC50 of 0.02 μM against HSV1-2. | price> |
| R-C-721 | Tenovin-3 CAS:1011301-27-1 | Tenovin-3 is a small molecule activator of p53 transcriptional activity. It increases p53 activity in MCF-7 cells when used at a concentration of 10 µM.It also increases the level of K40-acetylated alpha-tubulin in H1299 cells and inhibits SIRT2 protein deacetylase activity. | price> |
| R-C-730 | UPF-1069 CAS NO. 1048371-03-4 | UPF 1069 is a selective poly(ADP-ribose)polymerase (PARP)2 inhibitor(IC50 values are 0.3 and 8.0 μM for PARP-2 and PARP-1 respectively). | price> |

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