PI3K / Akt / mTOR
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KU 59403
Catalog No. A20928 -
CP-466722
Catalog No. A11086 -
Schisandrin B
Catalog No. A11991 Schisandrin B是从五味子五味子或五味子的果实中分离出的最丰富的二苯并环辛二烯,它是一种安全的ATR和P-gp抑制剂。 了解更多 -
CGK 733
Catalog No. A13191 -
Mirin
Catalog No. A15842 -
AZD6738 (Ceralasertib)
Catalog No. A15794 ATR 抑制剂AZD6738是一种有效的ATR激酶抑制剂,对分离的酶的IC50为1 nM,对细胞中ATR激酶依赖性CHK1磷酸化的IC50为74 nM。 了解更多 -
AZD0156
Catalog No. A16419 -
Chloroquine Phosphate
Catalog No. A16445 Chloroquine Phosphate是一种4-氨基喹啉抗疟和抗类风湿药,也可作为ATM活化剂。 了解更多 -
KU-60019
Catalog No. A10507 -
JNJ-47117096 hydrochloride
Catalog No. A21542 MELK inhibitorJNJ-47117096 hydrochloride is potent and selective MELK inhibitor, with an IC50 of 23 nM, also effectively inhibits Flt3, with an IC50 of 18 nM. 了解更多 -
MELK-8a hydrochloride
Catalog No. A21751 MELK inhibitorMELK-8a hydrochloride is a novel maternal embryonic leucine zipper kinase (MELK) inhibitor with an IC50 of 2 nM. 了解更多 -
Phenformin hydrochloride
Catalog No. A10717 Phenformin hydrochloride是双胍类药物中苯乙双胍的盐酸盐,具有抗糖尿病活性。 了解更多 -
WZ4003
Catalog No. A14312 -
HTH-01-015
Catalog No. A16281 NUAK1 抑制剂HTH-01-015是NUAK1的有效和选择性抑制剂(IC50 = 100 nM),并且不影响包括其他AMPK家族成员在内的139种其他激酶的活性。 了解更多 -
PF-06409577
Catalog No. A16801 AMPK 激活剂PF-06409577是口服生物可利用的AMPK激活剂,在TR-FRET试验中,对AMPK α1β1γ1的EC50为7 nM。在膜片钳试验(100 uM)中没有检测到对hERG的抑制作用,也不是人类主要细胞色素P450亚型微粒体活性的抑制剂(IC50>100 uM)。 了解更多 -
MK8722
Catalog No. A13392 -
ZLN024
Catalog No. A21963 -
Dorsomorphin 2HCl
Catalog No. A13720 BMP 抑制剂Dorsomorphin 2HCl (BML-275)是BMP信号传导的选择性小分子抑制剂,可促进胚胎干细胞的心肌发生。Dorsomorphin通过抑制骨形态发生蛋白信号转导逆转乳腺癌起始细胞的间质表型。 了解更多 -
ex229 (compound 991)
Catalog No. A16795 AMPK 激活剂ex229 (compound 991)是一种有效的AMPK活化剂,在活化AMPK方面比A769662的效力高5-10倍。 了解更多 -
BML-275 (Dorsomorphin)
Catalog No. A11970 AMPK 抑制剂BML-275 (Dorsomorphin)是一种可渗透细胞的吡唑并嘧啶化合物,显示为AMP激活的蛋白激酶(AMPK)和脂肪酸合酶抑制剂。 了解更多 -
Acadesine (Aicar,NSC 105823)
Catalog No. A10028 AMPK 激活剂Acadesine (Aicar,NSC 105823)是肝细胞和脂肪细胞中AMPK的选择性激活剂。 了解更多 -
A-769662
Catalog No. A11071 -
CHIR-98014
Catalog No. A11085 -
TWS119
Catalog No. A11223 -
Tideglusib
Catalog No. A11592 GSK-3 抑制剂Tideglusib是一种不可逆的,非ATP竞争性的GSK-3β抑制剂,无细胞试验中IC50为60 nM。用于治疗阿尔茨海默氏病和进行性核上性麻痹。 了解更多 -
AZD2858
Catalog No. A13060 -
1-Azakenpaullone
Catalog No. A14303 GSK-3β 抑制剂1-Azakenpaullone是一种有效的选择性GSK-3β抑制剂,IC50为18 nM,选择性比CDK1/cyclin B和CDK5/p25高100倍。 了解更多 -
IM-12
Catalog No. A14196 -
Bikinin
Catalog No. A15526 -
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最新产品
BIO
Catalog No. A17129 -
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VP3.15
Catalog No. A18538 dual PDE7/GSK-3 inhibitorVP3.15 is a potent, orally bioavailable and CNS-penetrant dual phosphodiesterase (PDE)7- glycogen synthase kinase (GSK)3 inhibitor, with IC50s of 1.59 μM and 0.88 μM for PDE7 and GSK-3, respectively. VP3.15 has neuroprotective and neuroreparative activities, thus as potential combined anti-inflammatory and pro-remyelinating therapies for multiple sclerosis (MS). 了解更多 -
CHIR-99021 monohydrochloride
Catalog No. A21430 GSK-3α/β inhibitorCHIR-99021 monohydrochloride (CT99021 monohydrochloride) is a GSK-3α/β inhibitor with IC50 of 10 nM/6.7 nM; > 500-fold selectivity for GSK-3 versus its closest homologs CDC2 and ERK2, as well as other protein kinases. 了解更多 -
CHIR-99021 trihydrochloride
Catalog No. A21436 GSK-3α/β inhibitorCHIR-99021 trihydrochloride (CT99021 trihydrochloride) is a GSK-3α/β inhibitor with IC50 of 10 nM/6.7 nM. 了解更多