Products
| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| S-204149 | Methyl 4-(2-Aminoethyl)benzoate Hydrochloride | 56161-89-8 | 96% Min. | benzoate_Hydrochloride_56161-89-8.png) |
| 523192 | 3-methoxy-1-methyl-4-nitro-1H-pyrazole | 1201935-85-4 | 95% Min. |  |
| Sun-shine Chemical provides 3-methoxy-1-methyl-4-nitro-1H-pyrazole(CAS 1201935-85-4) | ||||
| 523191 | 3-methoxy-1H-pyrazole | 215610-30-3 | 95% Min. |  |
| Sun-shine Chemical provides 3-methoxy-1H-pyrazole (CAS 215610-30-3) with high quality | ||||
| 5141901 | 3-methoxy-4-nitro-1H-pyrazole | 400755-41-1 | 95% Min. |  |
| 4281905 | methyl 2-bromo-5-fluoro-3-(4-methylphenylsulfonamido)benzoate | 2086689-91-8 | >98% |  |
| methyl 2-bromo-5-fluoro-3-(4-methylphenylsulfonamido)benzoate | ||||
| 193264 | MDK1846 | 2102501-84-6 | >98% |  |
| MDK1846 is a potent ketohexokinase (KHK) inhibitor. | ||||
| 1932010 | MMG-11 | 313254-94-3 | >98% |  |
| MMG-11 is a potent and selective dual inhibitor of TLR2/1 and TLR2/6 signaling with l | ||||
| 19311 | ML221 | 877636-42-5 | >98% |  |
| ML221 is an antagonist of the apelin (APJ) receptor. | ||||
| 192279 | Melphalan flufenamide | 380449-51-4 | >98% |  |
| Melphalan flufenamide, also known as Melflufen, J-1, or Prodrug J-1, is a melphalan p | ||||
| 192214 | ML184 | 794572-10-4 | >98% |  |
| CID2440433, also known as ML-184, is a potent synthetic agonist of GPR55 (EC50 = 0.26 | ||||
| 192191 | Mitapivat | 1260075-17-9 | >98% |  |
| Mitapivat, also known as PKM2 activator 1020 is a PKM2 activator (pyruvate kinase act | ||||
| 192183 | MK-3903 | 1219737-12-8 | >98% |  |
| MK-3903 is a potent and selective AMPK activator (EC50 = 8 nM). | ||||
| 191283 | Myriocin | 35891-70-4 | >98% |  |
| Myriocin, also known as antibiotic ISP-1 and thermozymocidin, is an atypical amino ac | ||||
| 191256 | MA242 TFA | 1049704-18-8 | >98% |  |
| MA242 is a Dual Inhibitors of MDM2 and NFAT1 for Pancreatic Cancer Therapy. MA242 dec | ||||
| 191252 | MIK665 | 1799631-75-6 | >98% |  |
| MIK665, also known as S 64315, is an inhibitor of induced myeloid leukemia cell diffe | ||||
| 191211 | MY 5445 | 78351-75-4 | >98% |  |
| MY 5445 is a potential platelet aggregation inhibitor. | ||||
| 19131 | MRS1706 | 264622-53-9 | >98% |  |
| MRS1706 is a selective adenosine A2B receptor inverse agonist with Ki values of 1.39, | ||||
| 1812296 | MRS1177 | 183721-13-3 | >98% |  |
| MRS1177 is a bioactive chemical. | ||||
| 1812295 | MLN-4760 | 305335-31-3 | >98% |  |
| MLN-4760 is an angiotensin-converting (ACE2) inhibitor. In huMNCs, MLN-4760-B detecte | ||||
| 1812254 | MDK-8384 | 761438-38-4 | >98% |  |
| MDK-8384, also known as ALK inhibitor 2, is a potent and selective ALK inhibitor. | ||||
| 181255 | Mavacamten | 1642288-47-8 | >98% |  |
| Mavacamten, also known as SAR-439152 and MYK-461, is a myosin inhibitor potentially f | ||||
| 181251 | MK-2048 | 869901-69-9 | >98% |  |
| MK-2048 is a a second-generation HIV-1 integrase inhibitor. | ||||
| 1811282 | ML 351 | 847163-28-4 | >98% |  |
| ML 351 is a selective 12/15 LOX inhibitor that is active in vivo. | ||||
| 1811261 | Maropitant | 147116-67-4 | >98% |  |
| Maropitan, also known as CJ 11972, is a neurokinin (NK1) receptor antagonist. | ||||
| 181152 | MBQ-167 | 2097938-73-1 | >98% |  |
| MBQ-167 is a potent, dual Rac/Cdc42 inhibitor with IC50 of 103/78 nM, respectively, i | ||||
| 1810301 | MDK4882 | 94164-88-2 | >98% |  |
| MDK4882 also known as PKM2 inhibitor or compound 3k, is a PKM2 inhibitor. | ||||
| 181022 | MU-380 | 2109805-78-7 | >98% |  |
| MU-380 is a potent and selective CHK1 inhibitor. | ||||
| 1810228 | MRS1220 | 183721-15-5 | >98% |  |
| MRS1220 is a potent and highly selective antagonist at the human A3 adenosine recepto | ||||
| 1810174 | ME0328 | 1445251-22-8 | >98% |  |
| ME0328 is an inhibitor of PARP-3 (IC50 = 0.89 μM). | ||||
| 18962 | MDK-4823 | 1908414-82-3 | >98% |  |
| MDK-4823, also known as LMPTP inhibitor1; is a potent inhibitor of the low-molecular- | ||||