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CP 31398 2HCl
Catalog No. A13522 -
Muscimol hydrobromide
Catalog No. A13459 GABA(A) receptor 激动剂Muscimol hydrobromide是抗抑郁药氟西汀的活性代谢产物，可抑制5-羟色胺的摄取，pKi值为7.35.1。诺氟西汀的S-对映体的5-羟色胺再摄取阻断效能比R-对映体高20倍（分别为pKis = 7.86与6.51）。 了解更多 -
5-R-Rivaroxaban
Catalog No. A14979 Factor Xa 抑制剂5-R-Rivaroxaban是利伐沙班的（R）对映异构体。利伐沙班是一种新型的口服直接Xa因子抑制剂，在晚期开发中用于预防和治疗血栓栓塞性疾病。 了解更多 -
9-Dihydro-13-acetylbaccatin III
Catalog No. A14982 9-Dihydro-13-acetylbaccatin III是紫杉醇类似物制剂的中间体。 了解更多 -
ABT-046
Catalog No. A14984 -
Choline Fenofibrate
Catalog No. A15044 -
Dabigatran etexilate mesylate
Catalog No. A15057 direct thrombin 抑制剂Dabigatran etexilate mesylate是达比加群的口服活性前药。达比加群是一种可逆的选择性直接凝血酶抑制剂（DTI），Ki值为4.5 nM。 了解更多 -
Dabigatran ethyl ester
Catalog No. A15058 -
Dabrafenib Mesylate
Catalog No. A15059 Raf 抑制剂Dabrafenib Mesylate是一种新颖，有效和选择性的Raf激酶抑制剂，能够抑制野生型B-Raf，B-RafV600E和c-Raf的激酶活性，IC50值分别为3.2、0.8和5.0 nM。 了解更多 -
Dasatinib hydrochloride
Catalog No. A15060 Src 抑制剂Dasatinib hydrochloride是一种有效的Abl/Src双重抑制剂，IC50分别<1 nM/0.8 nM。还可以抑制c-Kit（WT/c-Kit（D816V），IC50为79 nM/37 nM。有效，选择性Raf激酶抑制剂能够抑制野生型B-Raf，B-RafV600E和c -Raf的IC50值分别为3.2、0.8和5.0 nM。 了解更多 -
ABT 492 meglumine (Delafloxacin meglumine)
Catalog No. A15064 ABT 492 meglumine (Delafloxacin meglumine)对喹诺酮敏感和耐药的革兰氏阳性生物更有力，对环丙沙星家族肠杆菌科的某些成员具有类似于环丙沙星的活性，对喹诺酮敏感，非发酵性，革兰氏阴性生物具有类似的活性。 了解更多 -
Edoxaban tosylate
Catalog No. A15076 -
Etifoxine
Catalog No. A15083 -
Etifoxine hydrochloride
Catalog No. A15084 -
HOKU-81
Catalog No. A15117 -
Masitinib mesylate
Catalog No. A15152 KIT/PDGFR 抑制剂Masitinib mesylate是Kit和PDGFRα/β的新型抑制剂，IC50为200 nM和540 nM/800 nM，对ABL和c-Fms的抑制作用较弱。 了解更多 -
Nilotinib monohydrochloride monohydrate
Catalog No. A15186 -
NVP-BGJ398 phosphate
Catalog No. A15194 FGFR 抑制剂NVP-BGJ398 phosphate是一种新型的选择性泛特异性FGFR抑制剂，对FGFR1，FGFR2和FGFR3的IC50分别为0.9、1.4和1 nM。与FGFR4和VEGFR2相比，对FGFR具有40倍以上的选择性，并且对Abl，Fyn，Kit，Lck，Lyn和Yes的活性很小。 了解更多 -
Otenabant
Catalog No. A15200 -
Retigabine dihydrochloride
Catalog No. A15222 KCNQ channel openerRetigabine dihydrochloride是具有抗惊厥活性的Kv7.2-7.5（KCNQ2-5）神经元钾通道开放剂。 了解更多 -
Secalciferol
Catalog No. A15237 -
TBB
Catalog No. A15257 -
Vigabatrin
Catalog No. A15277 GABA-transaminase 抑制剂Vigabatrin是抑制性神经递质β-氨基丁酸（GABA）的结构类似物，它不可逆地抑制GABA转氨酶对GABA的分解代谢。 了解更多 -
CP 31398 dihydrochloride
Catalog No. A15346 p53 stabilizerCP 31398 dihydrochloride是p53稳定剂。在具有突变型或野生型p53的癌细胞系中稳定p53的活性构象并提高p53的活性。在体内抑制小的人类肿瘤异种移植物的生长。 了解更多 -
PhiKan 083
Catalog No. A15350 -
1,2,3,4,5,6-Hexabromocyclohexane
Catalog No. A15361 -
Cimigenol-3-O-alpha-L-arabinoside
Catalog No. A15407 Cimigenol-3-O-alpha-L-阿拉伯糖苷是从Cimicifuga foetida L.干燥的根茎中提取的。 了解更多 -
Amyloid b-Peptide (1-40) (human)
Catalog No. A15418 Amyloid b-Peptide (1-40) (human)是由淀粉样前体蛋白（APP）加工而成的肽。 了解更多 -
Atrasentan HCl
Catalog No. A15007 Endothelin 拮抗剂 receptorAtrasentan hydrochloride是一种开发用于治疗前列腺癌的内皮素拮抗剂受体（IC50 = 0.0551 nM，ETA）。 了解更多 -
Bikinin
Catalog No. A15526 -
Cannabichromene
Catalog No. A15497 TRPA1 activatior/TRPM8 blockerCannabichromene是一种主要的非精神植物大麻素，可抑制内源性大麻素失活并激活瞬时受体电位锚蛋白1（TRPA1）。内源性大麻素和TRPA1均可调节肠胃蠕动。 了解更多 -
Radotinib (IY-5511)
Catalog No. A13029 -
Mc-Val-Cit-PABC-PNP
Catalog No. A15766 -
ACP-196 (Acalabrutinib)
Catalog No. A15824 Btk 抑制剂ACP-196是Bruton酪氨酸激酶（BTK）抑制剂，具有潜在的抗肿瘤活性。它抑制BTK的活性并阻止B细胞抗原受体（BCR）信号传导途径的激活。 了解更多 -
Fiacitabine
Catalog No. A11422 HSV DNA replication 抑制剂Fiacitabine是单纯疱疹病毒(HSV)DNA复制的选择性抑制剂，HSV1和HSV2的IC50值分别为2.5 nM和12.6 nM。 了解更多 -
Napabucasin
Catalog No. A13474 -
NVP-BAW2881
Catalog No. A12693 VEGFR 抑制剂NVP-BAW2881是有效的选择性VEGFR抑制剂（血管内皮生长因子受体酪氨酸激酶抑制剂），IC50 为值9 nM，具有抑制慢性和急性皮肤炎症的作用。 了解更多
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