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产品目录

编号化学名称Cas号纯度化学结构
20659XPW12700286-66-298% Min.
XPW1 is a potent and selective CDK9 inhibitor with excellent activity against clear c
20506 XL0922367004-54-298% Min.
XL092 is an ATP-competitive inhibitor of multiple RTKs including MET, VEGFR2, AXL and
2112067 Xanomeline tartrate152854-19-8 (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-59890402-73-098% Min.
XP-59 is a potent inhibitor of the SARS-CoV Mpro
192143XP-238291208229-58-6>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
18579XMU-MP-12061980-01-4>98%
XMU-MP-1是一种有效且就有选择性的MST1/2抑制剂。
17030608XMD8-921234480-50-298% 
XMD8-92是一种BMK1抑制剂,是ERK5活性的高选择性抑制剂。
17021312XMD16-51345098-78-398% 
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
17021311XMD8-871234480-46-698% 
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
17033101XMU-MP-198% 
XMU-MP-1 is a reversible and selective MST1/2 inhibitor with IC50 values of 71.1 12.
6119477-xylosyltaxol90332-66-498% 
7-xylosyltaxol(Taxol-7-xyloside) is a taxol (Paclitaxel) derivative; Paclitaxel binds
161009016XL3881251156-08-798% by HPLC 
XL388 inhibited cellular phosphorylation of mTOR complex 1 (p-p70S6K, pS6, and p-4E-B
16071410XMD17-1091435488-37-198% by HPLC 
XMD17-109 is a novel, specific inhibitor of ERK-5 with an EC50 value of 4.2 M in HEK2
16071016XCT790725247-18-798% by HPLC 
XCT790 is a potent and specific inverse agonist of ERR. XCT790 shows no significant a
021803XY11624117-53-898% 
XY1 is a very close analogue of SGC707 (a potent, selective, and non-competitive inhi
011804X-3961365267-27-198% 
X-396 is an orally available small molecule inhibitor of the receptor tyrosine kinase
123011XL228898280-07-498% 
XL228 is a protein kinase inhibitor targeting IGF1R, the Aurora kinases, FGFR1-3, ABL
112006XEN907912656-34-998% by HPLC 
XEN907 is a spirooxindole blocker of NaV1.7 for the treatment of pain.
111910XL7651123889-87-198% 
XL765 is a PI3K/mTOR dual kinase inhibitor with IC50 values of 157 nM, 39 nM, 113 nM,
111301XL647781613-23-898% 
XL647 is an orally bioavailable small-molecule receptor tyrosine kinase inhibitor wit
51506XL147956958-53-598% 
XL147 (SAR245408) is a potent and highly selective inhibitor of class I PI3Ks (, , ,
52632XAV-939284028-89-398% 
XAV939 is a small molecule and selective Wnt pathway -catenin-mediated transcription
52501XEN4451515856-92-498% 
XEN445 is a potent and selective EL inhibitor(IC50=0.237 uM), that showed good ADME a