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Targets Recommended: S1P Receptor

24

抑制剂 & 化合物

2

重组蛋白

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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-1SphK1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.

化合物

SphK1&2-IN-1
Cat.No: T9992
Synonym:
Target: S1P Receptor
SphK1-IN-2
Cat.No: T63835
Synonym:
Target:
SphK1-IN-1
Cat.No: T61965
Synonym:
Target:
PF-543 hydrochloride
Cat.No: T8840
Synonym: PF-543
Target: Apoptosis, S1P Receptor, Autophagy, LPL Receptor
MP-A08
Cat.No: T16128
Synonym:
Target: S1P Receptor
SKI-178
Cat.No: T9014
Synonym:
Target: Apoptosis, S1P Receptor
SLP9101555
Cat.No: T63047
Synonym:
Target: S1P Receptor, LPL Receptor
MHP
Cat.No: T4658
Synonym: Methyl caprooyl tyrosinate
Target: S1P Receptor
K6PC-5
Cat.No: T27710
Synonym: K6PC5,K6PC 5
Target: S1P Receptor
Benzyl butyl phthalate
Cat.No: T0640
Synonym: BBP,邻苯二甲酸丁苄酯,1,2-benzenedicarboxylic acid,butyl phenylmethyl ester,Butyl benzyl phthalate
Target: Others, Aryl Hydrocarbon Receptor
PF-543
Cat.No: T6085
Synonym: Sphingosine Kinase 1 Inhibitor II,PF 543
Target: Apoptosis, S1P Receptor, Autophagy, LPL Receptor
SK1-IN-1
Cat.No: T12927
Synonym:
Target: S1P Receptor
PF-543 Citrate
Cat.No: T12436
Synonym: Sphingosine Kinase 1 Inhibitor II Citrate
Target: S1P Receptor
SLC5111312 HCl
Cat.No: T28803
Synonym: SLC5111312 hydrochloride,SLC 5111312,SLC-5111312,SLC5111312
Target:
SLP7111228
Cat.No: T34658
Synonym: SLP-7111228,SLP 7111228
Target:
SLC4011540
Cat.No: T28801
Synonym: SLC-4011540,SLC 4011540
Target:
Biotin Sphingosine
Cat.No: T83883
Synonym: Biotinyl Sphingosine
Target:
K145
Cat.No: T11739
Synonym:
Target: Others
VT-ME6
Cat.No: T70900
Synonym:
Target:
Amgen-23
Cat.No: T63132
Synonym:
Target:
SK1- I hydrochloride
Cat.No: T60798
Synonym:
Target:
SLR080811 HCl
Cat.No: T70614
Synonym:
Target:
SLP120701 HCl
Cat.No: T70613
Synonym:
Target:
SK1-I
Cat.No: T30485
Synonym: BML 258,BML-258,BML258,BML-258 HCl
Target:
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.

重组蛋白

Sphingosine Kinase 1/SPHK1 Protein, Human, Recombinant
Cat.No: TMPY-04432
Species: Human
Expression System: Baculovirus Insect Cells
Sphingosine Kinase 1/SPHK1 Protein, Human, Recombinant (His & GST)
Cat.No: TMPY-04431
Species: Human
Expression System: Baculovirus Insect Cells
TargetMol Loading
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