Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T63618 | SphK2-IN-1 | ||
SphK2-IN-1 是 SphK2 抑制剂,其 IC50 值为 0.359 μM。SphK2-IN-1 能够用于研究癌症,炎症,神经和心血管疾病。 | |||
T63017 |
SphK2-IN-2
|
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SphK2-IN-2 (21g) 是一种有效的、选择性的 SphK2 抑制剂 (IC50: 0.23 μM)。 | |||
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。 | |||
T63047 |
SLP9101555
|
S1P Receptor; LPL Receptor | GPCR/G Protein |
SLP9101555 是一种有效且具有选择性的鞘氨醇激酶 2(SphK2)抑制剂,Ki 为90 nM。SLP9101555对SphK2具有很高的亲和力,是 SphK1 的 200 倍。SLP9101555 显著降低细胞外 S1P 鞘氨醇 1- 磷酸(S1P)水平。 | |||
T6750 |
Opaganib
ABC294640 |
S1P Receptor | GPCR/G Protein |
Opaganib (ABC294640) 是选择性和竞争性的鞘氨醇激酶 2 (SK2) 抑制剂,Ki 为 9.8 μM。 | |||
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。 | |||
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。 | |||
T9014 |
SKI-178
|
Apoptosis; S1P Receptor | Apoptosis; GPCR/G Protein |
SKI-178 是一种鞘氨醇激酶-1(SphK1)和 SphK2抑制剂,以 CDK1 依赖性方式诱导人急性髓性白血病细胞凋亡。 | |||
T11739 |
K145
|
Others | Others |
K145 is inactive against SphK1 and other protein kinases. K145 induces cell apoptosis and has potently antitumor activity. K145 is a selective, substrate-competitive and orally active SphK2 inhibitor with an IC50 of 4.3 µM and a Ki of 6.4 µM. | |||
T28802 |
SLC4101431
SLC-4101431,SLC 4101431 |
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SLC4101431 is a potent SphK2 inhibitor with Ki value of 90 nM. | |||
T28806 |
SLM6031434 HCl
SLM 6031434,SLM6031434,SLM-6031434 |
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SLM6031434 is selective inhibitor of SphK2. | |||
T63835 | SphK1-IN-2 | ||
SphK1-IN-2 是一种有效的、选择性的 SphK1 抑制剂,能够作用于 SphK1 (IC50: 19.81 nM) 和 SphK2 (IC50>10 nM)。SphK1-IN-2 能够诱导细胞周期阻滞和凋亡 (apoptosis),表现出抗增殖作用,能够用于研究癌症。 | |||
T28803 |
SLC5111312 HCl
SLC5111312 hydrochloride,SLC 5111312,SLC-5111312,SLC5111312 |
||
SLC5111312 is an inhibitor of SphK1 and SphK2. | |||
T70071 |
SLM6031434 (free base)
|
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SLM6031434 (free base) is an inhibitor of sphingosine kinase type 2 (SphK2). It consists of pedant 1-guanidino-2-phenyloxadiazolylpyrrolidine group. | |||
T83883 |
Biotin Sphingosine
Biotinyl Sphingosine |
||
Biotin sphingosine(d18:1)是一种衍生自sphingosine的生物素化合物。它被用于检测细胞裂解物中sphingosine kinase 1 (SPHK1)和SPHK2的磷酸化活性的实验中。 | |||
T63132 | Amgen-23 | ||
Amgen-23 (compound 23) 是一种鞘氨醇激酶 (SPHK) 的有效抑制剂,作用于 SPHK1 (IC50: 20 μM) 和 SPHK2 (IC50: 1.6 μM)。Amgen-23 能够用于抗癌的研究。 | |||
T70900 | VT-ME6 | ||
VT-ME6 is a potent and selective sphingosine kinase 2 inhibitor. VT-ME6, contained a quaternary ammonium group as a warhead and established that a positively charged moiety is necessary for engaging key amino acid residues in the enzyme binding pocket.13,14 This compound is moderately potent (Ki = 8 lM) and displays three-fold selectivity for SphK2 over SphK1. Sphingosine-1-phosphate (S1P) is a ubiquitous, endogenous small molecule that is synthesized by two isoforms of sphingosine kinase (SphK... | |||
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。 |