T78091 |
(S)-FTY720-phosphonate
|
1142015-10-8
|
98%
|
|
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 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%
|
|
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%
|
|
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 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 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) is an S1P receptor agonist.
|
T8840 |
PF-543 hydrochloride
|
1706522-79-3
|
99.92%
|
|
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) 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 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 (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 (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 is an effective and selective S1P3 receptor antagonist (Ki: 110 nM).
|
T10305 |
Amiselimod hydrochloride
|
942398-84-7
|
99.68%
|
|
Amiselimod hydrochloride (MT-1303 hydrochloride) is a sphingosine 1-phosphate receptor-1 (S1P1) modulator.
|
T2171 |
SEW2871
|
256414-75-2
|
99.62%
|
|
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 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, 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 is a lysophosphatidic acid receptors antagonist
|
T7832 |
Ibrolipim
|
133208-93-2
|
99.47%
|
|
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 is a selective inhibitor of S1PR1 with a pIC50 of 7.6.
|