Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
---|---|---|---|---|
20459 | Methyl 3-methyl-1,2,4-thiadiazole-5-carboxylate | 352356-71-9 | 98% Min. | ![]() |
20457 | Mitiperstat | 1933460-19-5 | 98% Min. | ![]() |
Mitiperstat is a myeloperoxidase inhibitor. | ||||
171462 | MRTX0902 | 2654743-22-1 | ≧98.0% | ![]() |
MRTX0902is a potent SOS1 inhibitor which can be used for the therapeutic intervention | ||||
20414 | Methanone, (3,5-dibromophenyl)(2-methoxy-4-pyridinyl)- | 915412-80-5 | 98% Min. | ![]() |
20407 | methyl 4-(2-aminoethoxy)benzoate hydrochloride | 210113-85-2 | 98% Min. | ![]() |
20398 | 3-METHOXY-4-[(4-METHOXYBENZYL)OXY]BENZENECARBALDEHYDE | 129047-38-7 | 98% Min. | ![]() |
20395 | methyl (3-chloropyrazin-2-yl)acetate | 235748-94-4 | 98% Min. | ![]() |
20394 | 7-methoxy-8-[3-(4-morpholinyl)propoxy]-Imidazo[1,2-c]quinazolin-5-amine | 1032570-74-3 | 98% Min. | ![]() |
20364 | methyl 3-bromo-4-ethoxy-5-formylbenzoate | 2385682-18-6 | 98% Min. | ![]() |
20363 | methyl 3-bromo-5-formyl-4-hydroxybenzoate | 706820-79-3 | 98% Min. | ![]() |
20362 | Methyl 3-formyl-4-hydroxybenzoate | 24589-99-9 | 98% Min. | ![]() |
L20346 | Mycro3 | 944547-46-0 | 98% Min. | ![]() |
Mycro3 is an inhibitor of Myc-Max dimerization. | ||||
L20331 | MELK-8a | 1922153-17-0 | 98% Min. | ![]() |
MELK-8a Dihydrochloride is a novel inhibitor of maternal embryonic leucine zipper kin | ||||
L20329 | MTI-31 | 1567915-38-1 | 98% Min. | ![]() |
MTI-31 is a bioactive chemical. | ||||
20325 | MKC-8866 | 1338934-59-0 | 98% Min. | ![]() |
MKC-8866, also known as IRE1-IN-8866, is an inhibitor of IRE1 RNase activity. MKC8866 | ||||
20320 | MDK-7553 | 1700637-55-3 | 98% Min. | ![]() |
MDK-7553, also known as CD38 inhibitor 78c and Compound-78c, is a potent CD38 inhibit | ||||
204122 | Mitochonic Acid 5 | 1354707-41-7 | 98% Min. | ![]() |
Mitochonic Acid 5 is a derivative of the plant hormone indole-3-acetic acid. It has b | ||||
20293 | MK-8722 | 1394371-71-1 | 98% Min. | ![]() |
MK-8722 is a potent pan-AMPK activator. MK-8722 improves glucose homeostasis but indu | ||||
20291 | MRTX1133 | 2621928-55-8 | 98% Min. | ![]() |
MRTX1133 is a potent and selective KRAS G12D inhibitor. MRTX1133 targets the KRAS G12 | ||||
20287 | ML-SI3 | 891016-02-7 | 98% Min. | ![]() |
ML-SI3 is a chemical compound which acts as an "antagonist" (i.e. channel b | ||||
20261 | MYF-01-37 | 2416417-65-5 | 98% Min. | ![]() |
MYF-01-37 is a novel covalent inhibitor of TEAD targeting Cys380 when incubated with | ||||
21256 | 3-Methyl-1,2,4-thiadiazole-5-carbohydrazide | 1375066-73-1 | 98% Min. | ![]() |
21245 | MUN91789 | 2144491-78-9 | 98% Min. | ![]() |
MUN91789, also known as CPD77, is a potent inhibitor of SARS-CoV-2 main protease. MUN | ||||
21243 | MVN38807 | 2379438-80-7 | 98% Min. | ![]() |
MVN38807, also known as Y-1, is neuraminidase (NA) inhibitor used in preparation of d | ||||
20112602 | ML008 | 442898-34-2 | 98% Min. | ![]() |
ML008, also known as NCGC00092410, is a potent and selective inhibitor of glucocerebr | ||||
20111803 | Mobocertinib free base | 1847461-43-1 | 98% Min. | ![]() |
Mobocertinib, also known as TAK-788 and AP32788, is an investigational TKI with poten | ||||
20103003 | ML380 | 1627138-52-6 | ≧98.0% | ![]() |
ML380 is a highly potent and the first CNS penetrant M5 positive allosteric modulator | ||||
2071634 | METHYL 2,6-DICHLOROBENZOATE | 14920-87-7 | 98% Min. | |
2071611 | MAC-545496 | 838810-96-1 | 98% Min. | ![]() |
MAC-545496 is potent GraR inhibitor (glycopeptide-resistance-associated protein R). M | ||||
2071518 | MA-0204 | 2095128-17-7 | 98% Min. | ![]() |
MA-0204 is a highly potent and selective PPARd modulator (PPARδ EC50 = 0.4 nM; PPARa |
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