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• 157716-52-4 | Perifosine (Catalog# : 52613)Perifosine (KRX-0401; D-21266; NSC 639966) is a novel Akt inhibitor with IC50 of 4.7
• 1191951-57-1 | PHT-427 (Catalog# : 52583)PHT-427 is a dual Akt and PDPK1 inhibitor (high affinity binding for the PH domains o
• 1349796-36-6 | PI3K-IN-1 (Catalog# : 52560)PI3K-IN-1 is a potent inhibitor of PI3K, more information can be found in patent WO20
• 152121-53-4 | PD 169316 (Catalog# : 52513)PD 169316 is a potent, cell-permeable and selective p38 MAP kinase inhibitor (IC50 =
• 153436-54-5 | PD153035 (Catalog# : 52223)PD153035(ZM 252868; AG 1517) is a potent and specific inhibitor of EGFR with Ki and I
• 1627676-59-8 | PFI-2 (Catalog# : 52113)PFI-2 is a potent, selective, and cell-activelysine methyltransferase SETD7inhibitor
• 1454846-35-5 | PF-06463922 (Catalog# : 51701)PF-06463922 is an orally available, ATP-competitive inhibitor of the receptor tyrosin
• 150323-78-7 | Quipazine dimaleate (Catalog# : 20462)Quipazine dimaleate is a selective 5-HT3 receptor agonist that also displays antagoni
• 1893397-65-3 | QUN97653 (Catalog# : 204507)QUN97653, also known as TBK1/IKKε-IN-5, is a dual TBK1 and IKKε inhibitor, with IC5
• 1334719-95-7 | Q-203 (Catalog# : 17106003)Q-203是一种有效的、具有选择性的新药。
• 1135695-98-5 | Q-VD-OPH (Catalog# : 16071010)Q-VD-OPH is a selective, brain and cell permeable, highly potent and irreversible inh
• 144875-48-9 | Qesiquimod (Catalog# : 120814)Qesiquimod is a potent synthetic agonist of TLR7/TLR8 that possesses antiviral and an
• 1443361-20-3 | 3-Quinolinecarboxylic acid, 1,4-dihydro-8- methoxy-1-[(4-methoxyphenyl)methyl]-4-oxo-, ethyl ester (Catalog# : 102902)Coming soon!
• 1237744-13-6 | QNZ46 (Catalog# : 91006)QNZ46 is a noncompetitive and voltage-independent antagonist selective for NR2C/D con
• 1494684-33-1 | Risovalisib mesylate (Catalog# : 24078)CYH33 (CYH-33) is a novel potent, PI3Kα-selective inhibitor with IC50 of 5.9 nM/598
• 1423719-27-0 | (R,S)-BI 1015550 (Catalog# : 230403)BI 1015550 is a novel PDE4 inhibitor showing a preferential enzymatic inhibition of P
• 139339-45-0 | Ro 24-7429 (Catalog# : 2320201)Ro24-7429是一种有效的口服活性HIV-1 反式激活蛋白Tat 拮抗剂和一种
• 1239729-06-6 | 布瑞拉沙秦（Brilaroxazine） (Catalog# : 822224)RP-5063（Brilaroxazine） 是一种多模式的血清素和多巴胺受体调节剂，
• 1859053-21-6 | Rucaparib Camsylate (Catalog# : 20316)Rucaparib camsylate is a potent, orally available inhibitor of poly ADP-ribose polyme
• 1281870-42-5 | Rhosin hydrochloride (Catalog# : 21235)
• 1831116-75-6 | (R,Z)-1-(4-((3-chloro-4-((3-fluorobenzyl)oxy)phenyl)amino) quinazolin-6-yl)but-2-yn-1-one O-morpholin-3-ylmethyl oxime (Catalog# : 20123102)
• 1809275-69-1 | Razuprotafib sodium (Catalog# : 201221)Razuprotafib，也称为AKB-9778，是血管内皮蛋白酪氨酸磷酸酶（VE-PTP）
• 1008510-37-9 | Razuprotafib (Catalog# : 20102901)Razuprotafib，也称为AKB-9778，是血管内皮蛋白酪氨酸磷酸酶（VE-PTP）
• 1787294-07-8 | Remibrutinib ( LOU064 ) (Catalog# : 2073103)Remibrutinib ( LOU064 ) is a Potent and Highly Selective Covalent Inhibitor of Bruton
• 1809249-37-3 | Remdesivir (Catalog# : 2071545)Remdesivir, also known as GS-5734, is a prodrug form of the antiviral nucleoside anal
• 171230-81-2 | (R)-methyl 2-(tert-butyldimethylsilyloxy)propanoate (Catalog# : 202329)
• 1221443-23-7 | 3-[(2RS)-tetrahydro-2H-pyran-2-yloxy]propanoic acid (Catalog# : 2062017)
• 1369768-29-5 | [(1R,2S)-2-(3-fluorophenyl)-2-(hydroxymethyl)cyclopropyl]-methyl acetate (Catalog# : 2062004)
• 1443530-05-9 | Rogaratinib (Catalog# : 192277)Rogaratinib, 也称为BAY-1163877, 是一种异常的成纤维细胞生长因子受体
• 1342276-76-9 | RKI-1313 (Catalog# : 19183)RKI-1313是RKI-1447 (GLXC-05200)的阴性对照，是Rho-相关ROCK激酶的有效抑