Receptor S1P
Os receptores de esfingosina-1-fosfato (S1P) são uma família de GPCRs que se ligam à molécula de sinalização lipídica esfingosina-1-fosfato. Esses receptores desempenham papéis críticos no tráfego de células imunológicas, desenvolvimento vascular e manutenção da integridade das barreiras endoteliais. Moduladores de receptores S1P estão sendo desenvolvidos para o tratamento de esclerose múltipla, câncer e doenças cardiovasculares devido à sua capacidade de influenciar respostas imunológicas e migração celular. Na CymitQuimica, oferecemos uma variedade de moduladores de receptores S1P de alta qualidade para apoiar sua pesquisa em imunologia, oncologia e biologia vascular.
Produtos da "Receptor S1P"
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41 produtos desta categoria.
TY-52156
CAS:TY-52156 is an effective and selective S1P3 receptor antagonist (Ki: 110 nM).Fórmula:C18H19Cl2N3OPureza:99.91%Cor e Forma:SolidPeso molecular:364.27Ref: TM-T17183
2mg40,00€5mg60,00€10mg87,00€25mg166,00€50mg298,00€100mg510,00€200mg683,00€1mL*10mM (DMSO)66,00€N,N-Dimethylsphingosine
CAS:N,N-Dimethylsphingosine,is a potent competitive SphK phosphorylation inhibitor.DMS is elevated in models of neuropathic pain by increasing IL-1β and MCP-1.Fórmula:C20H41NO2Pureza:98%Cor e Forma:Clear Colorless To Faint Yellow Liquid/White To Off-White PowderPeso molecular:327.55S1p receptor agonist 1
CAS:S1p receptor agonist 1 (S1p-receptor-agonist-1) is an S1P receptor agonist.Fórmula:C23H24FN3O3Pureza:99.07% - 99.90%Cor e Forma:SolidPeso molecular:409.45Ozanimod
CAS:Ozanimod (RPC-1063) (RPC1063) is a specific oral S1P Receptor 1 modulator.Fórmula:C23H24N4O3Pureza:98.68% - 99.58%Cor e Forma:SolidPeso molecular:404.46Ref: TM-T6923
1mg48,00€5mg96,00€10mg144,00€25mg283,00€50mg454,00€100mg655,00€200mg929,00€500mg1.378,00€1mL*10mM (DMSO)96,00€GSK2018682
CAS:GSK2018682 is an agonist of sphingosine-1-phosphate receptor (s1p1) and (s1p5) agonist(pEC50s of 7.7 and 7.2,respectively).Fórmula:C22H21ClN4O4Pureza:99.04%Cor e Forma:SolidPeso molecular:440.88W140 HBr
CAS:[(3S)-3-amino-4-(3-hexylanilino)-4-oxobutyl]phosphonic acid;hydrobromide is a S1P1 antagonist with Ki of 2.84 μM.Fórmula:C16H28BrN2O4PPureza:99.34%Cor e Forma:SoildPeso molecular:423.28Ref: TM-T60204
1mg115,00€2mg172,00€5mg255,00€10mg375,00€25mg562,00€50mg787,00€100mg1.074,00€1mL*10mM (DMSO)284,00€SK1-IN-1
CAS:SK1-IN-1 is a SPHK1 inhibitor (IC50: 58 nM), with potential anticancer activity, and can be used to study cancer and neurodegenerative diseases.Fórmula:C22H30N4O3Pureza:98.72%Cor e Forma:SolidPeso molecular:398.5BMS-960
CAS:BMS-960 is an S1P agonist with potential anti-tumour activity for cancer research.Fórmula:C26H23F3N4O5Pureza:97.74% - 99.28%Cor e Forma:SolidPeso molecular:528.48CYM-5541
CAS:CYM-5541 (ML249) is a selective and allosteric S1P3 receptor agonist.Fórmula:C19H28N2O2Pureza:97.34% - 98.39%Cor e Forma:SolidPeso molecular:316.44Ref: TM-T3961
2mg38,00€5mg57,00€10mg92,00€25mg160,00€50mg254,00€100mg373,00€500mg873,00€1mL*10mM (DMSO)64,00€ASP-4058
CAS:ASP-4058: Safe, oral S1P1/S1P5 agonist; improves autoimmune encephalomyelitis in mice.Fórmula:C19H12F6N4O2Pureza:99.5% - 99.51%Cor e Forma:SolidPeso molecular:442.31Siponimod
CAS:Siponimod (BAF312) modulates S1P1/S1P5 with EC50s of 0.39/0.98 nM; >1000x selectivity over S1P2-4.Fórmula:C29H35F3N2O3Pureza:97.08% - 99.40%Cor e Forma:SolidPeso molecular:516.59Cenerimod
CAS:Cenerimod (ACT-334441) is an S1P1 agonist used in the study of murine experimental autoimmune encephalomyelitis (EAE) and murine scleroderma.Fórmula:C25H31N3O5Pureza:97.43% - 99.97%Cor e Forma:SolidPeso molecular:453.53SphK1&2-IN-1
CAS:SphK1&2-IN-1 is a sphingosine kinase inhibitor with anti-inflammatory, antitumor and hemostatic effects.Fórmula:C14H14N2O3SPureza:99.27%Cor e Forma:SolidPeso molecular:290.34GLPG2938
CAS:GLPG2938 (1-(2-Ethoxy-6-(trifluoromethyl)pyridin-4-yl)-3-((5-methyl-6-(1-methyl-3-(trifluoromethyl)-1H-pyrazol-4-yl)pyridazin-3-yl)methyl)urea) is a potent andFórmula:C20H19F6N7O2Pureza:98.25%Cor e Forma:SolidPeso molecular:503.4Ref: TM-T9199
1mg84,00€5mg153,00€10mg264,00€25mg550,00€50mg792,00€100mg1.093,00€200mg1.454,00€1mL*10mM (DMSO)166,00€Vibozilimod
CAS:Vibozilimod (SCD-044) is S1P receptor-1 (S1PR1) agonist .Fórmula:C29H36ClN3O5Pureza:99.47%Cor e Forma:SolidPeso molecular:542.07SAR-114137
CAS:SAR-114137 is a histone sphingomyelin kinase inhibitor used in the study of molluscum arteriosum and peripheral neuropathic pain.Fórmula:C25H34N4O7SPureza:100% - 99.57%Cor e Forma:SolidPeso molecular:534.63MHP
CAS:MHP (Methyl caprooyl tyrosinate) is an activator of sphingosine kinase (SPHK1), and significantly stimulates CAMP mRNA and protein production in KC.Fórmula:C16H23NO4Pureza:98.58%Cor e Forma:SolidPeso molecular:293.36Ref: TM-T4658
1mg47,00€2mg64,00€5mg111,00€10mg188,00€25mg376,00€50mg563,00€100mg800,00€1mL*10mM (DMSO)127,00€CS 2100
CAS:CS 2100 (1-[[4-Ethyl-5-[5-(4-phenoxyphenyl)-1,2,4-oxadiazol-3-yl]-2-thienyl]methyl]-3-azetidinecarboxylic acid) is an S1P1 agonist.Fórmula:C25H23N3O4SPureza:98.13%Cor e Forma:SolidPeso molecular:461.53VPC 23019
CAS:VPC 23019 is a competitive antagonist at the S1P1 and S1P3 receptors (pKi= 7.86 and 5.93, respectively).Fórmula:C17H29N2O5PPureza:98%Cor e Forma:SolidPeso molecular:372.4AMG-369
CAS:AMG-369 (AMG 247) is an S1P1/S1P5 dual agonist that delays the development of experimental autoimmune encephalomyelitis in rats.Fórmula:C26H22FN3O2SPureza:98.39% - 98.92%Cor e Forma:SolidPeso molecular:459.54Amgen-23
CAS:Amgen-23 is a selective and highly potent sphingosine kinase 1 (SPHK1) inhibitor that inhibits SPHK2 and can be used in anticancer research.Fórmula:C23H25Cl2N3O2SPureza:97.31%Cor e Forma:SolidPeso molecular:478.44Opaganib
CAS:Opaganib (ABC294640) is an orally active and specific sphingosine kinase-2 (SphK2) inhibitor (IC50: 60 μM).Fórmula:C23H25ClN2OPureza:98.86% - 99.85%Cor e Forma:SolidPeso molecular:380.91Ref: TM-T6750
1mg40,00€2mg52,00€5mg85,00€10mg124,00€25mg240,00€50mg415,00€100mg615,00€1mL*10mM (DMSO)87,00€Ponesimod
CAS:Ponesimod (ACT-128800) is an orally available sphingosine-1-phosphate receptor 1 (S1PR1, S1P1) agonist with potential immunomodulating activity.Fórmula:C23H25ClN2O4SPureza:98.22% - 99.42%Cor e Forma:SolidPeso molecular:460.97Ref: TM-T3258
1mg46,00€2mg59,00€5mg93,00€10mg131,00€25mg234,00€50mg404,00€100mg597,00€500mg1.283,00€1mL*10mM (DMSO)97,00€CYM-5520
CAS:CYM-5520 is a noncompetitive allosteric agonist of S1P2Fórmula:C21H19N3O2Pureza:99.47%Cor e Forma:SolidPeso molecular:345.39Ref: TM-T22703
1mg48,00€2mg64,00€5mg94,00€10mg142,00€25mg250,00€50mg374,00€100mg557,00€1mL*10mM (DMSO)103,00€PF429242 dihydrochloride
CAS:PF429242 dihydrochloride can reversibly inhibit S1P (IC50 of 175 nM).Fórmula:C25H37Cl2N3O2Pureza:98.67%Cor e Forma:SolidPeso molecular:482.49MP-A08
CAS:MP-A08 selectively inhibits SPHK1; targets SphK1 & SphK2 with Ki of 6.9 μM & 27 μM, respectively.Fórmula:C27H25N3O4S2Pureza:98.04%Cor e Forma:SolidPeso molecular:519.64CYM5442
CAS:CYM5442 is an S1P agonist, targeting to Sphingosine.Fórmula:C23H27N3O4Pureza:96.65% - 97.57%Cor e Forma:SolidPeso molecular:409.48SLM6031434 HCl
CAS:SLM6031434 HCl (SLM-6031434 HCl) is a SphK2 inhibitor that reduces LPS-induced TNF伪 and IL-1尾 production.Fórmula:C22H31ClF3N5O2Pureza:98%Cor e Forma:SolidPeso molecular:489.96Etrasimod
CAS:Etrasimod (APD334) is a specific and orally available antagonist of the sphingosine-1-phosphate-1 (S1P1) receptor (IC50: 1.88 nM in CHO cells).Fórmula:C26H26F3NO3Pureza:99.17% - 99.77%Cor e Forma:SolidPeso molecular:457.48Ref: TM-TQ0227
1mg52,00€5mg111,00€10mg180,00€25mg243,00€50mg305,00€100mg424,00€1mL*10mM (DMSO)113,00€K6PC-5
CAS: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.Fórmula:C19H37NO4Pureza:98.55%Cor e Forma:SolidPeso molecular:343.5SK1-I hydrochloride
CAS:SK1-I hydrochloride is a selective and competitive SphK1 inhibitor and sphingosine analog ,anti-leukemic to inhibit tumor cell growth and promote apoptosis.Fórmula:C17H28ClNO2Pureza:99.80%Cor e Forma:SolidPeso molecular:313.86TASP 0277308
CAS:NH2-UAMC1110 TFA is an aminobutoxy derivative of UAMC1110 used in the synthesis of FAPI-QS. UAMC1110 is a fibroblast activating protein (fap) inhibitor.Fórmula:C23H28Cl2N6O3SCor e Forma:SolidPeso molecular:539.48LX-2931
CAS:LX-2931(LX-3305) is a sphingosine-1-phosphate cleavage enzyme (S1P) inhibitor for the treatment of rheumatoid arthritis.Fórmula:C9H15N3O5Pureza:100% - 99.83%Cor e Forma:SolidPeso molecular:245.23SEW2871
CAS:SEW 2871 is an orally available, highly selective S1P1 agonist. It activates ERK, Akt and Rac signaling pathways and induces S1P1 internalization and recycling.Fórmula:C20H10F6N2OSPureza:99.62%Cor e Forma:White SolidPeso molecular:440.36CYM50374
CAS:CYM50374 inhibits Sphingosine-1-phosphate receptor 4 (S1P4 ) with an IC50 of µM.Fórmula:C19H19NO3SPureza:98.4% - 98.49%Cor e Forma:SolidPeso molecular:341.42Ref: TM-T27106
1mg333,00€5mg787,00€10mg1.074,00€25mg1.510,00€50mg1.882,00€100mg2.375,00€500mg4.655,00€ML-031
CAS:ML-031 activated S1P2 with an EC50 value of 1 μM in an S1P reporter assay.Fórmula:C19H20N2O3Pureza:99.21%Cor e Forma:SolidPeso molecular:324.374-Deoxypyridoxine hydrochloride
CAS:4-Deoxypyridoxine HCl halts S1P breakdown by blocking SPL, reducing apoptosis in insulinoma cells like S1P.Fórmula:C8H12ClNO2Pureza:99.86%Cor e Forma:White To Off White Crystalline PowderPeso molecular:189.64Amiselimod hydrochloride
CAS:Amiselimod hydrochloride (MT-1303 hydrochloride) is a sphingosine 1-phosphate receptor-1 (S1P1) modulator.Fórmula:C19H31ClF3NO3Pureza:99.55%Cor e Forma:SolidPeso molecular:413.9Ref: TM-T10305
1mg38,00€2mg49,00€5mg80,00€10mg120,00€25mg215,00€50mg354,00€100mg512,00€200mg738,00€1mL*10mM (DMSO)88,00€Ozanimod hydrochloride
CAS:Ozanimod (RPC-1063) HCl is a selective S1P1/S1P5 modulator with high affinity, used in relapsing MS research.Fórmula:C23H25ClN4O3Pureza:99.81%Cor e Forma:SolidPeso molecular:440.92Ref: TM-T62552
1mg66,00€5mg139,00€10mg202,00€25mg416,00€50mg652,00€100mg938,00€500mg1.872,00€1mL*10mM (DMSO)154,00€CYM50308
CAS:CYM50308 is a high affinity agonist of sphingosine-1-phosphate receptor 4 (S1P4-R) (EC50: 56 nM).Fórmula:C20H21F2N3O2SPureza:99.43% - 99.63%Cor e Forma:SolidPeso molecular:405.46Ref: TM-T15032
1mg62,00€5mg140,00€10mg202,00€25mg324,00€50mg455,00€100mg597,00€200mg842,00€500mg1.225,00€SLP9101555
SLP9101555 is a potent and selective sphingosine kinase 2 (SphK2) inhibitor with a Ki of 90 nM.SLP9101555 has a high affinity for SphK2, which is 200-foldFórmula:C16H22BrClN2Pureza:99%Cor e Forma:SolidPeso molecular:357.72Ref: TM-T63047
1mg333,00€5mg787,00€10mg1.074,00€25mg1.510,00€50mg1.882,00€100mg2.375,00€500mg4.655,00€1mL*10mM (DMSO)663,00€
