S1P receptor inhibitor
Products Related to S1P receptor inhibitor(22)
- GC14350CYM 50358 hydrochloridePurity: >97.00%
CYM 50358 hydrochloride is a potent and selective sphingosine-1-phosphate receptor 4 (S1P4) antagonist, functioning by blocking the S1P₄ receptor.
- GC16873N,N-DimethylsphingosineCAS: 119567-63-4Purity: >98.00%
N,N-Dimethylsphingosine is a potent inhbitor of SphK (sphingosine kinase) as an endogenous metabolite of sphingosine produced in various tissues and tumor cell lines.
- GC17004Sphingosine-1-phosphateCAS: 26993-30-6Purity: >98.00%
Sphingosine-1-phosphate, a lipid mediator formed by the metabolism of sphingomyelin, is an agonist of S1P receptors.
- GC172182-fluoro Palmitic AcidCAS: 16518-94-8Purity: >98.00%
inhibits sphingosine biosynthesis and long-chain acyl-CoA synthetase
- GC13712FTY720 PhosphateCAS: 402615-91-2Purity: >99.00%
sphingosine-1-phosphate (S1P) receptors agonist
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC10728 | CYM 50260 | 1355026-60-6 | >99.00% | |
S1P4 agonist | ||||
| GC12947 | JTE 013 | 383150-41-2 | >99.50% | |
JTE 013 is a potent, orally available, and targeted S1P2 antagonist, with an IC 50 value of 22±9nM for rat S1P2. | ||||
| GC13966 | CS 2100 | 913827-99-3 | >98% | |
S1P1 agonist | ||||
| GC14350 | CYM 50358 hydrochloride | - | >97.00% | |
CYM 50358 hydrochloride is a potent and selective sphingosine-1-phosphate receptor 4 (S1P4) antagonist, functioning by blocking the S1P₄ receptor. | ||||
| GC14532 | TC-G 1006 | 1324003-64-6 | >99.50% | |
S1P1 Agonist III is a potent and orally active S1P1 agonist with EC50 of 18 nM; no activity on S1P3. | ||||
| GC14672 | RP 001 hydrochloride | 1781880-34-9 | >98.00% | |
S1P1 receptor agonist | ||||
| GC15694 | VPC 23019 | 449173-19-7 | >99.50% | |
S1P1/S1P3 receptor antagonist | ||||
| GC15903 | CYM 50308 | 1345858-76-5 | >98.00% | |
S1P4 agonist | ||||
| GC16567 | CYM 5442 hydrochloride | 1783987-80-3 | >98.50% | |
S1P1 agonist, potent and selective | ||||
| GC16621 | W146 | 909725-61-7 | >98.00% | |
W146 is a selective antagonist of Sphingosine 1-phosphate receptors 1 (S1PR1) with an EC 50 value of 398nM. | ||||
| GC16873 | N,N-Dimethylsphingosine | 119567-63-4 | >98.00% | |
N,N-Dimethylsphingosine is a potent inhbitor of SphK (sphingosine kinase) as an endogenous metabolite of sphingosine produced in various tissues and tumor cell lines. | ||||
| GC16946 | CYM 5541 | 945128-26-7 | >98.00% | |
sphingosine-1-phosphate receptor 3 (S1P3) allosteric agonist | ||||
| GC17004 | Sphingosine-1-phosphate | 26993-30-6 | >98.00% | |
Sphingosine-1-phosphate, a lipid mediator formed by the metabolism of sphingomyelin, is an agonist of S1P receptors. | ||||
| GC17019 | TC-SP 14 | 1257093-40-5 | >98% | |
agonist of Sphingosine-1-Phosphate Receptor 1 (S1P1) | ||||
| GC17218 | 2-fluoro Palmitic Acid | 16518-94-8 | >98.00% | |
inhibits sphingosine biosynthesis and long-chain acyl-CoA synthetase | ||||
| GC18116 | SEW 2871 | 256414-75-2 | >98.00% | |
sphingosine-1-phosphate 1 (S1P1) receptor agonist | ||||
| GC10433 | ML-178 | 1355026-47-9 | >98% | |
ML-178 (compound 22n) is a potent and selective S1P4-R (Sphingosine-1-phosphate4 receptor) agonist with an EC50 of 46 nM. | ||||
| GC11668 | ML-031 | 852230-33-2 | >98% | |
ML-031 is a potent and selective agonist Sphingosine 1-phosphate receptor 2 (S1PR2) with an IC50 and EC50 of 1.0 and 1.03 μM. ML-031 has the potential for the research of cancer diseases. | ||||
| GC13712 | FTY720 Phosphate | 402615-91-2 | >99.00% | |
sphingosine-1-phosphate (S1P) receptors agonist | ||||
| GC13720 | TY 52156 | 934369-14-9 | >99.50% | |
sphingosine-1-phosphate receptor 3 (SIP3) antagonist | ||||
| GC15765 | CYM 5520 | 1449747-00-5 | >99.50% | |
CYM 5520 is a selective and allosteric sphingosine 1-phosphate receptor 2 (S1PR2) agonist with an EC 50 of 480nM. | ||||
| GC17720 | W123 | 1345982-24-2 | >98.00% | |
S1P1 antagonist | ||||
