Products
| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 6111413 | Roquinimex | 84088-42-6 | 98% |  |
| Roquinimex (Linomide; PNU212616; ABR212616) is a quinoline derivative immunostimulant | ||||
| 6111024 | RHPS4 | 390362-78-4 | 98% |  |
| RHPS4 is a potent inhibitor of Telomerase at submicromolar. | ||||
| 611924 | RGB-286638 | 784210-87-3 | 98% |  |
| RGB-286638 is a novel CDK inhibitor with IC50s of 1 nM/2 nM/3 nM/4 nM/5 nM for cyclin | ||||
| 611909 | RK-33 | 1070773-09-9 | 98% | |
| RK-33 is an RNA helicase inhibitor against DDX3, and inhibit its helicase activity.RK | ||||
| 1673101 | RO8994 | 1309684-94-3 | 98% |  |
| RO8994 is a potent and selective spiroindolinone MDM2 inhibitor for cancer therapy. | ||||
| 16071112 | RO5045337 | 939981-39-2 | 98% by HPLC |  |
| RO5045337, also known as R7112, RG7112, is a MDM2 antagonist with potential antineopl | ||||
| 16070103 | RSL 3 | 1219810-16-8 | 98% by HPLC | |
| RSL 3 | ||||
| 16062107 | (R) QuinoxP(R) | 866081-62-1 | 97% by HPLC | QuinoxP(R)-cas-866081-62-1.png) |
| (R) QuinoxP(R) | ||||
| 166154 | Ro41-1049(HCl) | 127500-84-9 | 98% by HPLC | -cas-127500-84-9.png) |
| Ro 41-1049 is an inhibitor of the enzyme monoamine oxidase type A(MAO-A). | ||||
| 16061501 | RS-1 | 312756-74-4 | 98% by HPLC |  |
| 4-BroMo-N-(4-broMophenyl)-3-[[(phenylMethyl)aMino]sulfonyl]benzaMide;RAD51-stimulator | ||||
| 16060701 | Relugolix | 737789-87-6 | 98% by HPLC |  |
| Relugolix, also known as TAK-385, is a luteinizing hormone-releasing hormone (LH-RH) | ||||
| 16060303 | RO31-8220 mesylate | 138489-18-6 | 98% by HPLC |  |
| Ro 31-8220 is a PKC-inhibitor, which inhibits stimulated fluid pinocytosis of human P | ||||
| 031003 | R112 | 575474-82-7 | 98% |  |
| R112 is an ATP-competitive inhibitor of Syk kinase with a Ki of 96 nM. R112 inhibits | ||||
| 031001 | Ro 46-2005 | 150725-87-4 | 98% |  |
| Ro 46-2005 is a novel synthetic non-peptide endothelin receptor antagonist, inhibits | ||||
| 030909 | RAD140 | 1182367-47-0 | 98% |  |
| Coming soon! | ||||
| 011907 | Robalzotan tartrate hydrate | 169758-66-1 | 98% |  |
| Coming soon! | ||||
| 011307 | Radotinib | 926037-48-1 | 98% |  |
| Radotinib is an orally available, a second-generation tyrosine kinase inhibitor of Bc | ||||
| 01118 | Ruxolitinib | 941678-49-5 | 98% |  |
| Ruxolitinib is the first potent, selective, JAK1/2 inhibitor to enter the clinic with | ||||
| 010812 | Ro 5126766 | 946128-88-7 | 98% |  |
| Ro 5126766 is a potent and selective dual RAF/MEK inhibitor. For SK-MEL-28, SK-MEL-2, | ||||
| 010810 | Refametinib | 923032-37-5 | 98% |  |
| Refametinib is an orally bioavailable selective MEK inhibitor with potential antineop | ||||
| 010412 | Raltegravir | 518048-05-0 | 98% |  |
| Raltegravir is a pyrrolidinone derivative and HIV INTEGRASE INHIBITOR that is used in | ||||
| 123018 | Ridaforolimus | 572924-54-0 | 98% |  |
| Ridaforolimus is a selective mTOR inhibitor with IC50 of 0.2 nM; while not classified | ||||
| 123010 | R428 | 1037624-75-1 | 98% |  |
| R428 is a potent and selective small-molecule inhibitor(IC50=14 nM), blocks the activ | ||||
| 123005 | Rucaparib | 283173-50-2 | 98% |  |
| Rucaparib is an inhibitor of PARP with Ki of 1.4 nM for PARP1, also showing binding a | ||||
| 123001 | RO4929097 | 847925-91-1 | 98% |  |
| RO4929097 is a secretase inhibitor with IC50 of 4 nM, inhibiting cellular processing | ||||
| 122928 | R788 | 901119-35-5 | 98% |  |
| Fostamatinib is a small molecule Syk kinase inhibitor with potential anti-inflammator | ||||
| 122927 | R406 free base | 841290-80-0 | 98% |  |
| R406 is a potent inhibitor of immunoglobulin E (IgE)- and IgG-mediated activation of | ||||
| 122917 | RGB-286638 free base | 784210-88-4 | 98% |  |
| RGB-286638 is a novel CDK inhibitor with IC50s of 1 nM/2 nM/3 nM/4 nM/5 nM for cyclin | ||||
| 122904 | Ravidasvir hydrochloride | 1303533-81-4 | 98% |  |
| Ravidasvir is a second-generation, orally active, potent and selective HCV NS5A prote | ||||
| 122837 | Rofecoxib | 162011-90-7 | 98% |  |
| Rofecoxib is a synthetic, nonsteroidal derivative of phenyl-furanone with antiinflamm | ||||