Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
---|---|---|---|---|
25017 | M3554 | 2763252-25-9 | ≧95.0% | |
M3554, a novel anti-GD2 antibody drug conjugate. | ||||
25016 | MD-43 | ≧98.0% | ||
MD-43 is a potent and selective degrader of MCT4. | ||||
24158 | ML-202 | 1221186-52-2 | 98% Min. | |
ML-202 is an activator of pyruvate kinase M2 (PKM2). | ||||
24151 | ML353 | 2990506-75-5 | 98% Min. | |
ML353 is a selective ligand of mGlu5 silent allosteric modulator (SAM). | ||||
24150 | MIF098 | 1208448-95-6 | 98% Min. | |
MIF098 is a macrophage migration inhibitory factor (MIF) antagonist. | ||||
24129 | 2-MNG | 2101538-28-5 | 98% Min. | |
2-MNG is an inhibitor for melanogenesis with an average IC50 of 49.5μM. 2-MNG alone | ||||
24124 | Mevrometostatum | 1844849-10-0 | 98% Min. | |
Mevrometostatum is an enhancer of zeste homolog 2 (EZH2) inhibitor. | ||||
24044 | 3-(methylsulfonyl)propanenitrile | 54863-37-5 | 98% Min. | |
Dapansutrile is a potent, orally active and selectiveNLRP3inflammasome inhibitor. Dap | ||||
20675 | Mavoglurant | 543906-09-8 | 98% Min. | |
262401 | MRTX1719 | 2630904-45-7 | ≧96.0% | |
MRTX1719 is a potent and selective binder to the PRMT5•MTA complex and selectively | ||||
20615 | Mavodelpar | 942594-93-6 | 98% Min. | |
Mavodelpar is a peroxisome proliferator activated receptor (PPAR) delta agonist. | ||||
20611 | MRTX849 | 2326521-71-3 | 98% Min. | |
Adagrasib, also known as MRTX849, is a potent, highly selective, oral available KRAS | ||||
20592 | Migoprotafib | 2377352-49-1 | 98% Min. | |
Migoprotafib, also known as GDC-1971 and RLY-1971, is a SHP2 allosteric inhibitor. GD | ||||
20572 | Mtb-IN-2 | 2861190-30-7 | 98% Min. | |
Mtb-IN-2 (compound 10c) is an antimicrobial agent against Mycobacterium tuberculosis | ||||
20542 | MBX-8025 lysine anhydrous | 928821-41-4 | 98% Min. | |
MBX-8025 lysine anhydrous is a selective PPAR-delta agonist. | ||||
20529 | Milademetan free base | 1398568-47-2 | 98% Min. | |
Milademetan, also known as DS-3032b or DS-3032, is a potent and selective MDM2 inhibi | ||||
20528 | muvalaplin | 2565656-70-2 | 98% Min. | |
20503 | MK-8189 | 1424371-93-6 | 98% Min. | |
MK-8189 is a Highly Potent and Selective PDE10A Inhibitor for the Treatment of Schizo | ||||
20470 | MCUF-651 | 2747162-85-0 | 98% Min. | |
MCUF-651 is a small molecule guanylyl cyclase A receptor positive allosteric modulato | ||||
20466 | Moracin C | 69120-06-5 | 98% Min. | |
Moracin C is a phenolic compound isolated from Artocarpus heterophyllus. Moracin C su | ||||
20464 | ML192 | 460331-61-7 | 98% Min. | |
ML192, also known as MLS000526305 and CID1434953, is a selective ligands for GPR55. T | ||||
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. | |
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