Products
| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 25085 | Umbralisib | 1532533-67-7 | 98% Min. |  |
| Umbralisib, also known as TGR1202 and RP5264 , is a highly specific, orally available | ||||
| 24098 | Ulodesine | 548486-59-5 | 98% Min. |  |
| Ulodesine, also known as BCX4208, is a purine nucleoside phosphorylase (PNP) inhibito | ||||
| 24094 | UNC5293 | 2226789-82-6 | 98% Min. |  |
| UNC5293 is a MERTK -selective and potent inhibitor ( Ki=190 pM). | ||||
| 20677 | UJN49930 ( UGT8-IN-1 ) | 2414349-93-0 | ≧98.0% | _2414349-93-0.png) |
| UJN49930 ( UGT8-IN-1 ) is an inhibitor of UDP-galactose ceramide galactosyltransferas | ||||
| 60634 | Ulodesine | 548486- 59-5 | 98% Min. | |
| 20629 | Usnoflast | 2455519-86-3 | 98% Min. |  |
| Usnoflast is a non-steroidal anti-inflammatory (NSAID). | ||||
| 20573 | URAT1 inhibitor 7 | 1632002-28-8 | 98% Min. |  |
| URAT1 inhibitor 7 (compound 10f) is a potent URAT1 inhibitor. | ||||
| 21249 | UAMC-1110 | 1448440-52-5 | 98% Min. |  |
| UAMC-1110, also known as SP-13786, is a novel potent and selective inhibitor of fibro | ||||
| 20110401 | U-18666A | 3039-71-2 | 98% Min. |  |
| U-18666A is an inhibitor of cholesterol synthesis. It acts by inhibiting desmosterol | ||||
| 2071516 | UCB9608 | 2244989-34-0 | 98% Min. |  |
| UCB9608 is a Potent, Orally Bioavailable PI4KIIIβ Inhibitor. UCB9608 showed the impr | ||||
| 2071515 | UCB9608 | 1616413-96-7 | 98% Min. |  |
| UCB9608 is a Potent, Orally Bioavailable PI4KIIIβ Inhibitor. UCB9608 showed the impr | ||||
| 112591 | U-73343 | 142878-12-4 | 98% Min. |  |
| U-73343 is a negative control (or inactive analogue) of U73122, which is a putative p | ||||
| 6111901 | UNC2541 | 1612782-86-1 | 98% Min. |  |
| UNC2541 is a potent and MerTK-specific inhibitor and exhibits sub-micro molar inhibit | ||||
| 193251 | UPGL00004 | 1890169-95-5 | >98% |  |
| UPGL00004 is a potent inhibitor of glutaminase C (GAC). | ||||
| 193223 | Umibecestat free base | 1387560-01-1 | >98% |  |
| Umibecestat, also known as CNP-520, is a beta-secretase inhibitor and is a drug candi | ||||
| 19343 | UVI3003 | 847239-17-2 | >98% |  |
| UVI3003 is a RXR antagonist. It displays high RXR binding affinity. UVI3003 does not | ||||
| 192142 | Upacicalcet | 1333218-50-0 | ≧98.0% |  |
| Upacicalcet (formerly SK-1403/AJT240) is a novel non-peptide calcimimetic agent that | ||||
| 1812292 | UC-1728 | 948304-40-3 | ≧98.0% |  |
| UC-1728, also known as t-TUCB, is a Soluble epoxide hydrolase inhibitor. | ||||
| 1810252 | URMC-099 | 1229582-33-5 | >98% |  |
| URMC-099 is an orally bioavailable, brain penetrant mixed lineage kinase (MLK) inhibi | ||||
| 186282 | UM-164 | 903564-48-7 | >98% |  |
| UM-164 is a anticancer inhibitor.CAS 903564-48-7. | ||||
| 18584 | UNC-926 free base | 1184136-10-4 | >98% |  |
| UNC-926 is a L3MBTL1 domain inhibitor. UNC-926 binds to the MBT domain of the L3MBTL1 | ||||
| 184105 | Upadacitinib | 1310726-60-3 | >98% |  |
| Upadacitinib, also known as ABT-494, is a potent and selective JAK inhibitors in deve | ||||
| 1791520 | UPF-1069 | 1048371-03-4 | 98.0% |  |
| UPF-1069 is a selective and potent PARP2 inhibitor. UPF-1069 induces apoptosis. UPF-1 | ||||
| 179153 | Ulixertinib HCl | 1956366-10-1 | 98.0% | |
| Ulixertinib, also known as BVD-523 and VRT752271, is an inhibitors of ERK protein kin | ||||
| 1791114 | UK-371804 | 256477-09-5 | 98.0% | |
| UK-371804 is a potent and selective uPA inhibitor with excellent enzyme potency (Ki 1 | ||||
| 178312 | UNC-669 | 314241-44-5 | 98.0% |  |
| UNC-669 is a L3MBTL domain inhibitor. UNC669 specifically targets lethal 3 malignant | ||||
| 17031008 | UK-371804 HCl | 256476-36-5 | 98% | |
| UK-371804 is a potent and selective urokinase-type plasmogen activator (uPA) inhibi | ||||
| 17030711 | URB602 | 565460-15-3 | 98% |  |
| URB602 is a selective inhibitor of monoglycerol lipase (MGL), exhibiting an IC50 of 2 | ||||
| 17030602 | Ubenimex | 58970-76-6 | 98% |  |
| Ubenimex, also known as NK 421 and Bestatin, is a CD13 inhibitor. Ubenimex attenuates | ||||
| 17011102 | UNC3866 | 1872382-47-2 | 98% | |
| UNC3866 is a potent antagonist of the methyllysine (Kme) reading function of the Poly | ||||