| R2101062 |
FIT-039 |
FIT-039 是一种选择性,ATP 竞争性且具有口服活性的 CDK9 抑制剂,对 CKD9/cyclin T1 的 IC50 为 5.8 μM。FIT-039
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| R2101063 |
SR8278 |
SR8278 是一种竞争性核血红素受体 REV-ERB 合成拮抗剂。SR8278 抑制 REV-ERBα 转录活性,EC50 为 0.47 μM。SR8278
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| R2101064 |
VPC23019 |
VPC23019,一种含芳基酰胺的鞘氨醇 1-磷酸 (S1P) receptor 调节剂,S1P1 和 S1P3 受体的竞争性拮抗剂 (pKis=7.86 和
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| R2101065 |
HS-1793 |
HS-1793 is a stable resveratrol analog that protects cardiac against mitochondri
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| R2101066 |
Mycro3 |
Mycro 3 是一种有效的选择性 c-Myc 抑制剂。
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| R2101067 |
RBC10 |
RBC10 is an inhibitor of Ral binding to RALBP1 (the effector).
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| R2101068 |
PD089828 |
PD-089828 是 ATP 竞争性 FGFR-1、PDGFR-β 和 EGFR (IC50 分别为 0.15, 1.76, 5.47 µM) 抑制剂和 c-
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| R2101069 |
CRANAD-28 |
CRANAD-28, a blood brain barrier (BBB) penetrable two-photon imaging probe, acts
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| R2101070 |
BPU-11 |
BPU-11 is a HCN4 CLP ligand. It acts by modulating channel function and complete
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| R2101071 |
CE3F4 |
CE3F4 是一种选择性的 Epac1 拮抗剂,对 Epac1 和 Epac2(B) 的 IC50 值分别为 10.7 μM 和 66 μM。
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| R2101072 |
NIBR-0213 |
A potent, selective, orally active S1P1 antagonist with IC50 of 2.5 nM Ca2+ mobi
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| R2101073 |
BDP5290 |
BDP5290 是 ROCK 和 MRCK 的有效抑制剂,对于 ROCK1,ROCK2,MRCKα 和 MRCKβ 的 IC50 值分别为 5 nM,50 nM
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| R2101074 |
PH-064 |
PH-064 (BIM-46187) 是摘自专利FR 2879460 A1中的钠离子通道抑制剂。
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| R2101075 |
ry785;Kv2-IN-A1 |
Kv2-IN-A1 is a Kv2.1 and Kv2.2 inhibitor.
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| R2101076 |
DD1 |
DD1 is a proteasome inhibitor that induces human myeloid tumor-selective apoptos
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| R2101077 |
AEM1 |
NRF2抑制剂AEM1是癌细胞中NRF2转录活性的特异性小分子抑制剂,对一组>100种激酶(包括PI3K,AKT和PKC的同种型)没有活性;广泛降低NRF
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| R2101078 |
SAR405 R enantiomer |
SAR405 R enantiomer 是活性低于 SAR405 的一个对映体。 SAR405 是一个 PIK3C3/Vps34 抑制剂。
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| R2101079 |
(S)-3,4-DCPG |
mGlu8a agonist
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| R2101080 |
JCP174 |
JCP174 is an inhibitor of a depalmitoylase that enhances Toxoplasma host-cell in
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| R2101081 |
SGA360 |
SGA360 is a selective modulator of aryl hydrocarbon (Ah) receptor that exhibits
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| R2101082 |
WAY-169916 |
WAY-169916 is a pathway-selective inhibitor of estrogen receptor (ER) that acts
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| R2101083 |
Creatine riboside |
Creatine riboside 是一种尿代谢产物,也是一种肺癌的诊断和预后的生物标志物。
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| R2101084 |
BRD6688 |
BRD6688 is a selective HDAC2 inhibitor. It acts by enhancing the learning and me
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| R2101085 |
RH01687 |
RH01687 is a small molecule that protect pancreatic β cells against endoplasmic
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| R2101086 |
PS210 |
PS 210是PDK1的有效特异性激活剂,其靶向PDK1的PIF结合口袋,不改变121种激酶(S6K,PKB/Akt或GSK3)中的任何一种的活性。
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