24
2
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T9992 |
SphK1&2-IN-1
|
S1P Receptor | GPCR/G Protein |
SphK1&2-IN-1 是一种鞘氨醇激酶抑制剂,具有抗炎、抗肿瘤和止血作用。 | |||
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。 | |||
T61965 | SphK1-IN-1 | ||
SphK1-IN-1 是SphK1的抑制剂,显示出抗肿瘤活性。SphK1-IN-1 抑制 SphK1 的 ATP 酶,IC50= 2.48 μM。SphK1-IN-1 具有癌症研究的价值。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
T4658 |
MHP
Methyl caprooyl tyrosinate |
S1P Receptor | GPCR/G Protein |
MHP (Methyl caprooyl tyrosinate) 是一种鞘氨醇激酶 (SPHK1) 激活剂,可显著增加 CAMP mRNA 和蛋白水平,还可增强抗微生物防御能力和先天免疫力。 | |||
T27710 |
K6PC-5
K6PC5,K6PC 5 |
S1P Receptor | GPCR/G Protein |
K6PC-5 is a ceramide derivative that acts as an activator of sphingosine kinase 1 (SPHK1), inducing a swift and temporary rise in intracellular calcium levels. With its potential applications in skin diseases associated with abnormal keratinocyte function, as well as in studies on neurodegeneration and virus infection, K6PC-5 presents a promising compound for research purposes. | |||
T0640 |
Benzyl butyl phthalate
BBP,邻苯二甲酸丁苄酯,1,2-benzenedicarboxylic acid,butyl phenylmethyl ester,Butyl benzyl phthalate |
Others; Aryl Hydrocarbon Receptor | Immunology/Inflammation; Others |
Benzyl butyl phthalate (1,2-benzenedicarboxylic acid) 是邻苯二甲酸酯的一员,可激活乳腺癌细胞中的芳香烃受体,刺激 SPHK1/S1P/S1PR3 信号传导,促进转移性乳腺癌干细胞的形成。它通过上调 Zeb1 的表达,可引起血管瘤细胞的迁移和侵袭。 | |||
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。 | |||
T12927 | SK1-IN-1 | S1P Receptor | GPCR/G Protein |
SK1-IN-1 is a potent inhibitor of sphingosine kinase 1 (SPHK1)(IC50 of 58 nM). | |||
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 ). | |||
T28803 |
SLC5111312 HCl
SLC5111312 hydrochloride,SLC 5111312,SLC-5111312,SLC5111312 |
||
SLC5111312 is an inhibitor of SphK1 and SphK2. | |||
T34658 |
SLP7111228
SLP-7111228,SLP 7111228 |
||
SLP7111228 is an effective and selective SphK1 inhibitor (Ki = 48 nM). | |||
T28801 |
SLC4011540
SLC-4011540,SLC 4011540 |
||
SLC4011540 is a potent and selective SphK1/2 dual inhibitor with Ki value of 120 nM and 90 nM respectively. | |||
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。 | |||
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. | |||
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... | |||
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。 | |||
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)。 | |||
T70614 |
SLR080811 HCl
|
||
SLR080811 is a SphK inhibitor. Sphingosine-1-phosphate (S1P) is a ubiquitous, endogenous small molecule that is synthesized by two isoforms of sphingosine kinase (SphK1 and 2). Intervention of the S1P signaling pathway has attracted significant attention because alteration of S1P levels is linked to several disease states including cancer, fibrosis, and sickle cell disease. | |||
T70613 |
SLP120701 HCl
|
||
SLP120701 is a potent and selective sphingosine kinase 2 inhibitor. Sphingosine-1-phosphate (S1P) is a ubiquitous, endogenous small molecule that is synthesized by two isoforms of sphingosine kinase (SphK1 and 2). Intervention of the S1P signaling pathway has attracted significant attention because alteration of S1P levels is linked to several disease states including cancer, fibrosis, and sickle cell disease. | |||
T30485 |
SK1-I
BML 258,BML-258,BML258,BML-258 HCl |
||
BML-258 HCl was removed and discontinued. |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPY-04432 |
Sphingosine Kinase 1/SPHK1 Protein, Human, Recombinant
SPHK,SPHK1,sphingosine kinase |
Human | Baculovirus Insect Cells |
Sphingosine Kinase 1/SPHK1 Protein, Human, Recombinant is expressed in Baculovirus insect cells. The predicted molecular weight is 42.7 kDa and the accession number is Q9NYA1-1. | |||
TMPY-04431 |
Sphingosine Kinase 1/SPHK1 Protein, Human, Recombinant (His & GST)
SPHK,SPHK1,SPK,sphingosine kinase... |
Human | Baculovirus Insect Cells |
Sphingosine Kinase 1/SPHK1 Protein, Human, Recombinant (His & GST) is expressed in Baculovirus insect cells with His and GST tag. The predicted molecular weight is 70.3 kDa and the accession number is Q9NYA1-1. |