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产品目录

编号化学名称Cas号纯度化学结构
20494YW20652131223-85-198% Min.
YW2065 has excellent anti-colorectal cancer effects in vitro and in vivo. YW2065 achi
21241YKL-05-0991936529-65-598% Min.
YKL-05-099 is a selective inhibitor of Salt-Inducible Kinase (SIK).
2073105YCN47284181147-28-498% Min.
YCN47284 is an aromatic guanylhydrazone compounds with antimalarial activity.
2071610 YUN27078879127-07-898% Min.
YUN27078, also known as EGFR inhibitor, is an EGFR inhibitor. It directly depolymeriz
193193Y06137 2226534-49-0>98%
Y06137是一种有效的选择性BET抑制剂,它与Kd为81 nM的BRD4(1)溴域结合
193151YF-2盐酸盐1312005-62-1>98%
YF-2盐酸盐是一个具有高度选择性,血脑屏障渗透组蛋白乙酰转移酶
192213YH239-EE 1364488-67-4>98%
YH239-EE是一种高效的p53-MDM2拮抗剂。
185172Y-39983游离199433-58-4>98%
Y-39983 (游离),也被称为Y-33075,是一种有效的、选择性的ROCK家族抑
18578YL-09191339058-04-6>98%
YL-0919是一种日常5-HT1A受体拮抗剂,具有选择性的 5 -羟色胺再摄取
1710139YU-2382591943733-16-1>98%
YU238259表现出有效的合成致死性设置中的DNA损伤反应和DNA修复缺陷
1791521Y-29794 甲苯磺酸酯143984-17-298.0%
Y-29794甲苯磺酸酯是一种口服有效的,强有力的和特定的非肽脯氨
17030112Y15盐酸4506-66-598% 
Y15盐酸,也称为FAK抑制剂14,是一种直接FAK自身磷酸化抑制剂,阻塞
17021305Y-39983盐酸盐173897-44-498% 
Y-39983是一种选择性的与之相关的蛋白激酶(ROCK)抑制剂,其IC50为3.
17021302740 Y-P (PDGFR 740Y-P)1236188-16-198% 
740 Y-P是PI3K的细胞渗透磷肽激活剂。
17109009YM-58483 (BTP2)223499-30-798% 
YM-58483/BTP2是一种能调节非兴奋细胞(如淋巴细胞)活化的贮藏操作C
16122849YM-90709163769-88-898% 
YM-90709 is an interleukin-5 receptor antagonist. YM-90709 inhibits the binding of IL
16122848Y-29794 Tosylate129184-48-198% 
Y-29794 Tosylate is an orally active, potent and specific non-peptide prolyl endopept
6111512YHO-133511346753-00-198% 
YHO-13351 is the water-soluble prodrug of YHO-13177, which is a potent and specific i
6111511YHO-13177912287-56-098% 
YHO-13177 is a potent and specific inhibitor of BCRP; potentiated the cytotoxicity of
6111414YM-155 hydrochloride355406-09-698% 
YM155 is a potent survivin suppressant by inhibiting Survivin promoter activity with
611813YLF-466D1273323-67-398% 
YLF-466D is an allosteric AMPK activator.YLF466D activated recombinant human 111, 211
16070918Y27632(free base)146986-50-798% by HPLC 
Y27632 is a selective ROCK inhibitor, which inhibits ET-1-induced increases in natriu
030910YK111370003-76-198% 
Coming soon!
010421Y-27632 dihydrochloride129830-38-297% 
Y-27632 2Hcl is a selective ROCK1 (p160ROCK) inhibitor with Ki of 140 nM, exhibits &g
121426YM-201636371942-69-798% 
YM201636 is a selective PIKfyve inhibitor with IC50 of 33 nM, less potent to p110.
110219YL-10936341-25-098% 
YL-109 has ability to inhibit breast cancer cell growth and invasiveness in vitro and
52516Y-320288250-47-598% 
Y-320 is a new phenylpyrazoleanilide immunomodulator; inhibits IL-17 production by CD