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Cat. No. Product Name Target Signaling Pathways
T4031 S1p receptor agonist 1

S1p-receptor-agonist-1

S1P Receptor; LPL Receptor GPCR/G Protein
S1p receptor agonist 1 (S1p-receptor-agonist-1) 是有口服活性的S1P 受体激动剂,具有诱导 S1P1 内化的活性,EC50为9.83 nM。它有潜力用于关节炎和实验性自身免疫性脑炎)的相关研究。
T6923 Ozanimod

奥扎莫德,RPC-1063

S1P Receptor; LPL Receptor GPCR/G Protein
Ozanimod (RPC-1063) 是一种选择性S1P1和S1P5受体激动剂,在[35S]-GTPγS 结合实验中,EC50分别为 410 pM 和 11 nM。它可研究治疗克罗恩病、溃疡性结肠炎、多发性硬化症和复发性多发性硬化症的试验。
T6403 Siponimod

辛波莫德,BAF-312

S1P Receptor; LPL Receptor GPCR/G Protein
Siponimod (BAF-312) 是有效,选择性的鞘氨醇-1-磷酸 (S1P)受体调节剂,对 S1P1 和 S1P5 受体具有特异性,EC50 分别为 0.39 nM 和 0.98 nM。 BAF312 对 S1P1 和 S1P5 受体的特异性比 S1P2、S1P3 和 S1P4 受体高 1000 倍以上。
T62517 S1p receptor agonist 2

S1p receptor agonist 2 (compound 1) 是一种 S1P5 受体的激动剂,选择性比 S1P1 和/或 S1P3 受体高。S1p receptor agonist 2 能够用于内源性 SIP 信号系统,以及减轻/预防中枢神经系统 (CNS) 疾病 (如神经退行性疾病) 的演技。
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。
T38826 Vibozilimod

Vibozilimod,SCD-044

S1P Receptor GPCR/G Protein
Vibozilimod (SCD-044) 是S1P 受体-1 (S1PR1)激动剂。
T22102 ML-178

CYM50179

Others Others
ML-178 是一种二氯苯,是鞘氨醇-1-磷酸受体4(S1PR4)的强效选择性激动剂,EC50 为 46 nM,在25 μM 的浓度下对其他 S1P 受体没有影响。
T62552 Ozanimod hydrochloride

Ozanimod (RPC-1063) hydrochloride 是一种鞘氨醇 1-磷酸 (S1P) 受体调节剂,能够高亲和力地选择性结合 S1P 受体亚型 1 (S1P1) 和 S1P5 (S1P5)。Ozanimod hydrochloride 能够调节 hS1P1 受体 (EC50: 1.03 nM) 和 hS1P5 受体 (EC50: 8.6 nM)。Ozanimod hydrochloride 能够用于研究复发性多发性硬化 (MS)。
T6673 SKI II

SphK-I2

Apoptosis; Wnt/beta-catenin; S1P Receptor Apoptosis; Cytoskeletal Signaling; GPCR/G Protein; Stem Cells
SKI II (SphK-I2) 是一种口服有效的合成鞘氨醇激酶 (SK)抑制剂,抑制 SK1 和 SK2,IC50值分别为 78 μM 和 45 μM。它通过诱导溶酶体/蛋白酶体降解,不可逆地抑制SK1。
T14930 Ceralifimod

ONO-4641

Others Others
Ceralifimod (ONO-4641) is a potent agonist for sphingosine 1-phosphate receptors 1 and 5 (EC50s: 27.3, 334 pM for human S1P receptor 1 and 5).
T15354 FTY720 (S)-Phosphate

(S)-FTY720 phosphate,(S)-FTY720P

Others Others
FTY720 (S)-Phosphate is an S1P receptor 1 (S1PR1) agonist. It is used in the research of acute inflammatory diseases such as acute lung injury.
T34402 RP-101075

RP101075

RP-101075 is a etabolite of Ozanimod. It exhibits a similar specificity profile as Ozanimod at the S1P receptor family in vitro, and pharmacodynamic profile in vivo.
T78091 (S)-FTY720-phosphonate

LPL Receptor GPCR/G Protein
FTY720 (S)-Phosphate,作为S1P受体1 (S1PR1) 激动剂,可用于研究急性肺损伤等急性炎症。
T41145 TASP 0277308

TASP 0277308 is a potent and selective sphingosine 1-phosphate 1 (S1P1) receptor antagonist (IC50 = 7.8 nM). TASP 0277308 inhibits S1P-induced chemotaxis (IC50 = 1.1-1.6 nM), HUVEC cell proliferation (IC50 = 3-3.6 nM) and suppresses angiogenesisin vivo. TASP 0277308 also blocks VEGF-induced tube-formation of HUVECsin vitroand reverses or impairs the development of arthritis or mechano-allodynia.
T38336 W140 (trifluoroacetate salt)

W140 (trifluoroacetate salt)

Sphingosine-1-phosphate (S1P) is a bioactive lipid that exhibits a broad spectrum of biological activities including cell proliferation, survival, migration, cytoskeletal organization, and morphogenesis. It exerts its activity by binding to five distinct G protein-coupled receptors, S1P1/EDG-1, S1P2/EDG-5, S1P3/EDG-3, S1P4/EDG-6, and S1P5/EDG-8. W140 is an inactive enantiomer of W146, a selective S1P1 antagonist (Ki = 77 nM), that binds to the S1P1 receptor with a Ki of 4.6 μM (2a = W146; 2b = W...
T83910 S1PL-IN-31

Sphingosine-1-Phosphate Lyase Inhibitor 31,S1PL Inhibitor 31,S1P Lyase Inhibitor 31

S1PL-IN-31是一种鞘氨醇-1-磷酸(S1P)裂解酶的抑制剂(IC50 = 210 nM),同时也是Smoothened(Smo)受体的对抗剂(IC50 = 440 nM)。在体内,S1PL-IN-31 (每天2 mg/kg)能够防止实验性自身免疫性脑炎(EAE)模型大鼠中,由髓鞘少突胶质细胞糖蛋白(MOG)肽段MOG29-152诱发的颈部及胸部淋巴细胞渗透和神经肌肉虚弱。该化合物降低了大鼠的淋巴细胞总数及CD4+ T细胞、CD8+ T细胞和B细胞的水平。S1PL-IN-31 (每天3及10 mg/kg剂量)在雄性和雌性大鼠心脏和淋巴结中增加了S1P水平,并且在雌性大鼠中降低了心率。
T37548 azido-FTY720

azido-FTY720

FTY720 is a derivative of ISP-1 (myriocin), a fungal metabolite of the Chinese herb Iscaria sinclarii as well as a structural analog of sphingosine. It is a novel immune modulator that prolongs allograft transplant survival in numerous models by inhibiting lymphocyte emigration from lymphoid organs. FTY720 is phosphorylated by sphingosine kinase, which then acts as a potent agonist at four of the sphingosine-1-phosphate (S1P) receptors (S1P1, S1P3, S1P4, and S1P5). Down-regulation of S1P1 recept...
T37187 D-erythro/L-threo Lysosphingomyelin (d18:1)

D-erythro/L-threo Lysosphingomyelin (d18:1)

Lysosphingomyelin is an endogenous bioactive sphingolipid and a constituent of lipoproteins.1,2It is produced by the removal of the acyl group from sphingomyelin by a deacylase and acts as a precursor in the biosynthesis of sphingosine-1-phosphate . D-erythroLysosphingomyelin is an agonist of the S1P receptors S1P1, S1P2, and S1P3(EC50s = 167.7, 368.1, and 482.6 nM, respectively, for the human receptors).3It is also an agonist of the orphan receptor ovarian cancer G protein-coupled receptor 1 (O...

化合物

S1p receptor agonist 1
Cat.No: T4031
Synonym: S1p-receptor-agonist-1
Target: S1P Receptor, LPL Receptor
Ozanimod
Cat.No: T6923
Synonym: 奥扎莫德,RPC-1063
Target: S1P Receptor, LPL Receptor
Siponimod
Cat.No: T6403
Synonym: 辛波莫德,BAF-312
Target: S1P Receptor, LPL Receptor
S1p receptor agonist 2
Cat.No: T62517
Synonym:
Target:
PF-543 hydrochloride
Cat.No: T8840
Synonym: PF-543
Target: Apoptosis, S1P Receptor, Autophagy, LPL Receptor
PF-543
Cat.No: T6085
Synonym: Sphingosine Kinase 1 Inhibitor II,PF 543
Target: Apoptosis, S1P Receptor, Autophagy, LPL Receptor
Vibozilimod
Cat.No: T38826
Synonym: Vibozilimod,SCD-044
Target: S1P Receptor
ML-178
Cat.No: T22102
Synonym: CYM50179
Target: Others
Ozanimod hydrochloride
Cat.No: T62552
Synonym:
Target:
SKI II
Cat.No: T6673
Synonym: SphK-I2
Target: Apoptosis, Wnt/beta-catenin, S1P Receptor
Ceralifimod
Cat.No: T14930
Synonym: ONO-4641
Target: Others
FTY720 (S)-Phosphate
Cat.No: T15354
Synonym: (S)-FTY720 phosphate,(S)-FTY720P
Target: Others
RP-101075
Cat.No: T34402
Synonym: RP101075
Target:
(S)-FTY720-phosphonate
Cat.No: T78091
Synonym:
Target: LPL Receptor
TASP 0277308
Cat.No: T41145
Synonym:
Target:
W140 (trifluoroacetate salt)
Cat.No: T38336
Synonym: W140 (trifluoroacetate salt)
Target:
S1PL-IN-31
Cat.No: T83910
Synonym: Sphingosine-1-Phosphate Lyase Inhibitor 31,S1PL Inhibitor 31,S1P Lyase Inhibitor 31
Target:
azido-FTY720
Cat.No: T37548
Synonym: azido-FTY720
Target:
D-erythro/L-threo Lysosphingomyelin (d18:1)
Cat.No: T37187
Synonym: D-erythro/L-threo Lysosphingomyelin (d18:1)
Target:
TargetMol Loading
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