Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T11234 | ESI-08 | cAMP | GPCR/G Protein |
ESI-08 是 EPAC2 的有效拮抗剂,IC50 为 8.4 μM。 ESI-08 特异性阻断 cAMP 诱导的 EPAC 活化,但不阻断 cAMP 介导的 PKA 活化。 | |||
T12616L |
CE3F4
|
cAMP | GPCR/G Protein |
CE3F4 是选择性的Epac1拮抗剂,能够作用于 Epac1 (IC50:10.7 μM)和 Epac2(B) (IC50:66 μM)。 | |||
T2244 |
ESI-09
|
cAMP; Virus Protease | GPCR/G Protein; Microbiology/Virology |
ESI-09是一种新型非环状核苷酸EPAC 的拮抗剂,对EPAC1和EPAC2的IC50值分别为3.2和1.4 μM。 | |||
T24154 |
I942
I 942,I-942 |
cAMP | GPCR/G Protein |
I942 是一种新型且具有选择性的非环核苷酸 (NCN) EPAC1 激动剂,可激活交换蛋白调节人脐血管中的炎症基因表达,可抑制与心血管疾病相关的促炎细胞因子信号传导。 | |||
T11212 |
EPAC 5376753
5-{[5-(2,4-dichlorophenyl)furan-2-yl]methylidene}-2-thioxodihydropyrimidine-4,6(1H,5H)-dione |
cAMP | GPCR/G Protein |
EPAC 5376753 是 EPAC1 的变构抑制剂,在瑞士 3T3 细胞中的 IC50 为 4 µM。 | |||
T6536 |
HJC0350
|
cAMP | GPCR/G Protein |
HJC0350 是一种有效地、选择性的EPAC2拮抗剂(IC50:0.3 µM)。 | |||
T15485 |
HJC0197
|
cAMP; Ras | GPCR/G Protein; MAPK |
HJC0197 是Epac1(cAMP 1 直接激活的交换蛋白) 和Epac2 拮抗剂,其对Epac2 的IC50值为5.9 μM。它在等浓度 cAMP 存在下能够降低 Epac1 介导的 Rap1-GDP 交换活性。它能够选择性阻断 cAMP 诱导的 Epac 活化。 | |||
T12616 |
(R)-CE3F4
|
Others | Others |
(R)-CE3F4 is a selective inhibitor of exchange protein directly activated by cAMP isoform 1 (Epac1)(IC50 of 4.2 μM), | |||
T22014 |
8-CPT-2Me-cAMP, sodium salt
|
||
8-CPT-2Me-cAMP sodium is a sodium salt compound that selectively activates exchange proteins activated by cAMP (Epac). These Epac proteins are cAMP-sensitive guanine nucleotide exchange factors (GEFs) responsible for activating small GTPases Rap1 and Rap2. 8-CPT-2Me-cAMP sodium specifically activates Epac1 with an EC50 value of 2.2 μM, while showing no activation of PKA with an EC50 value greater than 10 μM [1]. Additionally, 8-CPT-2Me-cAMP sodium stimulates the Epac-mediated release of calcium ... |