编号 | 化学名称 | Cas号 | 纯度 | 化学结构 |
---|---|---|---|---|
20659 | XPW1 | 2700286-66-2 | 98% Min. | |
XPW1 is a potent and selective CDK9 inhibitor with excellent activity against clear c | ||||
20506 | XL092 | 2367004-54-2 | 98% Min. | |
XL092 is an ATP-competitive inhibitor of multiple RTKs including MET, VEGFR2, AXL and | ||||
2112067 | Xanomeline tartrate | 152854-19-8 (tartrate) | ≧98.0% | |
Xanomeline (LY-246,708) 是一种正构毒蕈碱乙酰胆碱受体 (mAChR) 激动剂, | ||||
2071549 | XP-59 | 890402-73-0 | 98% Min. | |
XP-59 is a potent inhibitor of the SARS-CoV Mpro | ||||
192143 | XP-23829 | 1208229-58-6 | >98% | |
XP-23829,又称福马酸替吡胺,是一种羟羧酸受体2配体,可用于银屑 | ||||
185282 | 希美加群 | 192939-46-1 | >98% | |
希美加群是一种抗凝剂,它被作为warfarin[1]的替代品进行了广泛的 | ||||
18579 | XMU-MP-1 | 2061980-01-4 | >98% | |
XMU-MP-1是一种有效且就有选择性的MST1/2抑制剂。 | ||||
17030608 | XMD8-92 | 1234480-50-2 | 98% | |
XMD8-92是一种BMK1抑制剂,是ERK5活性的高选择性抑制剂。 | ||||
17021312 | XMD16-5 | 1345098-78-3 | 98% | |
XMD16-5是一种新型的酪氨酸激酶非受体2(TNK2)抑制剂,对于D163E和R80 | ||||
17021311 | XMD8-87 | 1234480-46-6 | 98% | |
XMD8-87是一种新型的酪氨酸激酶非受体2(TNK2)抑制剂,ic50为38nmol / L | ||||
17033101 | XMU-MP-1 | 98% | ||
XMU-MP-1 is a reversible and selective MST1/2 inhibitor with IC50 values of 71.1 12. | ||||
611947 | 7-xylosyltaxol | 90332-66-4 | 98% | |
7-xylosyltaxol(Taxol-7-xyloside) is a taxol (Paclitaxel) derivative; Paclitaxel binds | ||||
161009016 | XL388 | 1251156-08-7 | 98% by HPLC | |
XL388 inhibited cellular phosphorylation of mTOR complex 1 (p-p70S6K, pS6, and p-4E-B | ||||
16071410 | XMD17-109 | 1435488-37-1 | 98% by HPLC | |
XMD17-109 is a novel, specific inhibitor of ERK-5 with an EC50 value of 4.2 M in HEK2 | ||||
16071016 | XCT790 | 725247-18-7 | 98% by HPLC | |
XCT790 is a potent and specific inverse agonist of ERR. XCT790 shows no significant a | ||||
021803 | XY1 | 1624117-53-8 | 98% | |
XY1 is a very close analogue of SGC707 (a potent, selective, and non-competitive inhi | ||||
011804 | X-396 | 1365267-27-1 | 98% | |
X-396 is an orally available small molecule inhibitor of the receptor tyrosine kinase | ||||
123011 | XL228 | 898280-07-4 | 98% | |
XL228 is a protein kinase inhibitor targeting IGF1R, the Aurora kinases, FGFR1-3, ABL | ||||
112006 | XEN907 | 912656-34-9 | 98% by HPLC | |
XEN907 is a spirooxindole blocker of NaV1.7 for the treatment of pain. | ||||
111910 | XL765 | 1123889-87-1 | 98% | |
XL765 is a PI3K/mTOR dual kinase inhibitor with IC50 values of 157 nM, 39 nM, 113 nM, | ||||
111301 | XL647 | 781613-23-8 | 98% | |
XL647 is an orally bioavailable small-molecule receptor tyrosine kinase inhibitor wit | ||||
51506 | XL147 | 956958-53-5 | 98% | |
XL147 (SAR245408) is a potent and highly selective inhibitor of class I PI3Ks (, , , | ||||
52632 | XAV-939 | 284028-89-3 | 98% | |
XAV939 is a small molecule and selective Wnt pathway -catenin-mediated transcription | ||||
52501 | XEN445 | 1515856-92-4 | 98% | |
XEN445 is a potent and selective EL inhibitor(IC50=0.237 uM), that showed good ADME a |