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LPL Receptor

The lysophospholipid receptor (LPL-R) group are members of the G protein-coupled receptor family of integral membrane proteins that are important for lipid signaling. In humans, there are eight LPL receptors, each encoded by a separate gene. These LPL receptor genes are also sometimes referred to as "Edg" (an acronym for endothelial differentiation gene).
Signaling Pathways | Target | TargetMol
Cat. No. Product name CAS No. Purity Chemical Structure
T78091 (S)-FTY720-phosphonate 1142015-10-8 98%
(S)-FTY720-phosphonate
FTY720 (S)-Phosphate, an S1P receptor 1 (S1PR1) agonist, is utilized in studying acute inflammatory diseases, including acute lung injury.
T78160 SLB1122168 formic 98%
SLB1122168 formic
SLB1122168 is a potent inhibitor of Spns2-mediated sphingosine-1-phosphate (S1P) release, exhibiting an IC50 value of 94 nM [1].
T79816 S1P1 agonist 6 2433782-42-2 98%
S1P1 agonist 6
Compound I (S1P1 agonist 6) is an S1P1 agonist that mitigates autoimmune activity by inhibiting lymphocyte trafficking and has potential as an immunosuppressive ...
T79817 S1P1 agonist 6 hemicalcium 2941310-03-6 98%
S1P1 agonist 6 hemicalcium
Compound I (S1P1 agonist 6 hemicalcium) is an S1P1 agonist that diminishes autoimmune activity by inhibiting lymphocyte trafficking, and serves as an immunosuppr...
T81114 Spns2-IN-1 98%
Spns2-IN-1
Spns2-IN-1 is a potent Spns2 inhibitor, effectively impeding Spns2-dependent S1P transport with an IC50 value of 1.4±0.3 μM, crucial for modulating the immune re...
T17237 VPC 23019 449173-19-7 98%
VPC 23019
VPC 23019 is a competitive antagonist at the S1P1 and S1P3 receptors (pKi= 7.86 and 5.93, respectively). It is also an agonist at the S1P4 and S1P5 receptors (pE...
T4031 S1p receptor agonist 1 1514888-56-2 99.94%
S1p receptor agonist 1
S1p receptor agonist 1 (S1p-receptor-agonist-1) is an S1P receptor agonist.
T8840 PF-543 hydrochloride 1706522-79-3 99.92%
PF-543 hydrochloride
PF-543 hydrochloride (PF-543) inhibits SphK1 with a K(i) of 3.6 nM, is sphingosine-competitive and is more than 100-fold selective for SphK1 over the SphK2 isofo...
T10293 AM095 free acid 1228690-36-5 99.9%
AM095 free acid
AM095 (free acid) is a potent LPA1 receptor antagonist (IC50s: 0.98 and 0.73 μM for recombinant human or mouse LPA1).
T15031 CYM50260 1355026-60-6 99.88%
CYM50260
CYM50260 is a potent and exquisitely selective agonist of sphingosine-1-phosphate 4 receptor (S1P4-R, EC50= nM) with no activity against S1P1-R, S1P2-R, S1P3-R a...
T7939 Fingolimod 162359-55-9 99.76%
Fingolimod
Fingolimod (FTY-720A) is an antagonist of sphingosine 1-phosphate (S1P) (IC50 of 0.033 nM in K562 and NK cells).
T6923 Ozanimod 1306760-87-1 99.74%
Ozanimod
Ozanimod (RPC-1063) (RPC1063) is a specific oral S1P Receptor 1 modulator. Ozanimod has been used in trials studying the treatment of Crohn's Disease, Ulcerative...
T17183 TY-52156 934369-14-9 99.73%
TY-52156
TY-52156 is an effective and selective S1P3 receptor antagonist (Ki: 110 nM).
T10305 Amiselimod hydrochloride 942398-84-7 99.68%
Amiselimod hydrochloride
Amiselimod hydrochloride (MT-1303 hydrochloride) is a sphingosine 1-phosphate receptor-1 (S1P1) modulator.
T2171 SEW​2871 256414-75-2 99.62%
SEW​2871
SEW 2871 is an orally available, highly selective S1P1 agonist with an EC50 of 13.8 nM.It reduces the number of lymphocytes in the blood and is used in studies r...
T10385 ASP-4058 952565-91-2 99.51%
ASP-4058
ASP-4058 is a selective, safe, and orally active second-generation agonist of sphingosine phosphate receptors 1 and 5 (S1P1 and S1P5).ASP-4058 ameliorates experi...
T4278 AM966 1228690-19-4 99.49%
AM966
AM966, a excellent affinity, specific, oral LPA1(IC50=17 nM) antagonist, suppresses LPA-stimulated intracellular calcium release.
T22834 H2L 5765834 420841-84-5 99.47%
H2L 5765834
H2L 5765834 is a lysophosphatidic acid receptors antagonist
T7832 Ibrolipim 133208-93-2 99.47%
Ibrolipim
Ibrolipim (NO-1886) attenuates high glucose-induced endothelial dysfunction in cultured human umbilical vein endothelial cells via PI3K/Akt pathway.
T12821 S1PR1 modulator 1 2328109-05-1 99.44%
S1PR1 modulator 1
S1PR1 modulator 1 is a selective inhibitor of S1PR1 with a pIC50 of 7.6.
(S)-FTY720-phosphonate
T78091
FTY720 (S)-Phosphate, an S1P receptor 1 (S1PR1) agonist, is utilized in studying acute inflammatory diseases, including acute lung injury.
SLB1122168 formic
T78160
SLB1122168 is a potent inhibitor of Spns2-mediated sphingosine-1-phosphate (S1P) release, exhibiting an IC50 value of 94 nM [1].
S1P1 agonist 6
T79816
Compound I (S1P1 agonist 6) is an S1P1 agonist that mitigates autoimmune activity by inhibiting lymphocyte trafficking and has potential as an immunosuppressive ...
S1P1 agonist 6 hemicalcium
T79817
Compound I (S1P1 agonist 6 hemicalcium) is an S1P1 agonist that diminishes autoimmune activity by inhibiting lymphocyte trafficking, and serves as an immunosuppr...
Spns2-IN-1
T81114
Spns2-IN-1 is a potent Spns2 inhibitor, effectively impeding Spns2-dependent S1P transport with an IC50 value of 1.4±0.3 μM, crucial for modulating the immune re...
VPC 23019
T17237
VPC 23019 is a competitive antagonist at the S1P1 and S1P3 receptors (pKi= 7.86 and 5.93, respectively). It is also an agonist at the S1P4 and S1P5 receptors (pE...
S1p receptor agonist 1
T4031
S1p receptor agonist 1 (S1p-receptor-agonist-1) is an S1P receptor agonist.
PF-543 hydrochloride
T8840
PF-543 hydrochloride (PF-543) inhibits SphK1 with a K(i) of 3.6 nM, is sphingosine-competitive and is more than 100-fold selective for SphK1 over the SphK2 isofo...
AM095 free acid
T10293
AM095 (free acid) is a potent LPA1 receptor antagonist (IC50s: 0.98 and 0.73 μM for recombinant human or mouse LPA1).
CYM50260
T15031
CYM50260 is a potent and exquisitely selective agonist of sphingosine-1-phosphate 4 receptor (S1P4-R, EC50= nM) with no activity against S1P1-R, S1P2-R, S1P3-R a...
Fingolimod
T7939
Fingolimod (FTY-720A) is an antagonist of sphingosine 1-phosphate (S1P) (IC50 of 0.033 nM in K562 and NK cells).
Ozanimod
T6923
Ozanimod (RPC-1063) (RPC1063) is a specific oral S1P Receptor 1 modulator. Ozanimod has been used in trials studying the treatment of Crohn's Disease, Ulcerative...
TY-52156
T17183
TY-52156 is an effective and selective S1P3 receptor antagonist (Ki: 110 nM).
Amiselimod hydrochloride
T10305
Amiselimod hydrochloride (MT-1303 hydrochloride) is a sphingosine 1-phosphate receptor-1 (S1P1) modulator.
SEW​2871
T2171
SEW 2871 is an orally available, highly selective S1P1 agonist with an EC50 of 13.8 nM.It reduces the number of lymphocytes in the blood and is used in studies r...
ASP-4058
T10385
ASP-4058 is a selective, safe, and orally active second-generation agonist of sphingosine phosphate receptors 1 and 5 (S1P1 and S1P5).ASP-4058 ameliorates experi...
AM966
T4278
AM966, a excellent affinity, specific, oral LPA1(IC50=17 nM) antagonist, suppresses LPA-stimulated intracellular calcium release.
H2L 5765834
T22834
H2L 5765834 is a lysophosphatidic acid receptors antagonist
Ibrolipim
T7832
Ibrolipim (NO-1886) attenuates high glucose-induced endothelial dysfunction in cultured human umbilical vein endothelial cells via PI3K/Akt pathway.
S1PR1 modulator 1
T12821
S1PR1 modulator 1 is a selective inhibitor of S1PR1 with a pIC50 of 7.6.
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TargetMol