Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TQ0138 |
K145 hydrochloride
K145盐酸盐 |
Apoptosis; S1P Receptor | Apoptosis; GPCR/G Protein |
K145 hydrochloride 是选择性的,底物竞争性的和口服有效的SphK2抑制剂,IC50为 4.3 µM,Ki 为 6.4 µM。它可诱导细胞凋亡,显示出强大的抗肿瘤活性。 | |||
T8840 |
PF-543 hydrochloride
PF-543 |
Apoptosis; S1P Receptor; Autophagy; LPL Receptor | Apoptosis; Autophagy; GPCR/G Protein |
PF-543 hydrochloride (PF-543) 是一种选择性可逆和鞘氨醇竞争性SPHK1抑制剂,对SPHK1的选择性是 SPHK2 的 100 倍以上。它还是全血中 1-磷酸鞘氨醇形成的有效抑制剂,诱导细胞凋亡、坏死和自噬。 | |||
T6085 |
PF-543
Sphingosine Kinase 1 Inhibitor II,PF 543 |
Apoptosis; S1P Receptor; Autophagy; LPL Receptor | Apoptosis; Autophagy; GPCR/G Protein |
PF-543 (Sphingosine Kinase 1 Inhibitor II) 是一种选择性可逆和鞘氨醇竞争性 SPHK1抑制剂,可诱导细胞凋亡、坏死和自噬。它对 SPHK1的选择性是 SPHK2 的 100 倍以上。它还抑制全血中 1-磷酸鞘氨醇形成,IC50为 26.7 nM。 | |||
T16128 |
MP-A08
|
S1P Receptor | GPCR/G Protein |
MP-A08 是高度选择性和 ATP 竞争性的 SPHK1 抑制剂。 | |||
T12436 |
PF-543 Citrate
Sphingosine Kinase 1 Inhibitor II Citrate |
S1P Receptor | GPCR/G Protein |
PF-543 Citrate is an inhibitor of sphingosine-competitive SPHK1(IC50 of 2 nM ). | |||
T70816 |
(R)-FTY720-OMe
|
||
(R)-FTY720-OMe is a structural analogue of FTY720 which acts as a specific competitive inhibitor of sphingosine kinase 2 (SK2). Furthermore, (R)-FTY720-OMe does not inhibit sphingosine kinase 1 (SK1) activity. | |||
T60798 |
SK1- I hydrochloride
|
||
SK1-I hydrochloride (BML-258 hydrochloride) 是鞘氨醇类似物,能够增强细胞自噬并显示抗癌活性。SK1-I hydrochloride 是同工酶特异性SPHK1竞争抑制剂 (Ki = 10 μM)。 |