Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
---|---|---|---|---|
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) is an orthosteric muscarinic acetylcholine receptor (mAChR) a | ||||
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, also known as tepilamide fumarate, is a hydroxycarboxylic acid receptor 2 l | ||||
185282 | Ximelagatran | 192939-46-1 | >98% | |
Ximelagatran is an anticoagulant that has been investigated extensively as a replacem | ||||
18579 | XMU-MP-1 | 2061980-01-4 | >98% | |
XMU-MP-1 is a potent and selective MST1/2 inhibitor. | ||||
17030608 | XMD8-92 | 1234480-50-2 | 98% | |
XMD8-92 is a BMK1 inhibitor and a highly selective inhibitor of ERK5 activity. XMD8-9 | ||||
17021312 | XMD16-5 | 1345098-78-3 | 98% | |
XMD16-5 is a novel tyrosine kinase nonreceptor 2(TNK2) inhibitor with IC50s of 16 n | ||||
17021311 | XMD8-87 | 1234480-46-6 | 98% | |
XMD8-87 is a novel tyrosine kinase nonreceptor 2(TNK2) inhibitor with IC50s of 38 n | ||||
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 |
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