| | Purinergics
- 2-Methylthio-ADP trisodium salt
A potent purinergic agonist for the receptors P2Y1, P2Y12 and P2Y13 and a platelet aggregating agent. In addition, studies show that 2-Methylthio-ADP trisodium salt functions better as a human platelet adenylate cyclase inhibitor than a platelet aggregator.| カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-203464 | 34983-48-7 | C11H14N5Na3O10P2S | 10 mg |
- 2-Methylthioadenosine 5'-monophosphate triethylammonium salt hydrate
The only known preferential antagonist for the P2Y(AC) receptor. The platelet ADP receptor that is coupled to adenyl cyclase and is also referred to as the P2Y ADP receptor.| カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-213854 | 22140-20-1 (non-salt) | C11H16N5O7PS ·xC6H15N ·yH2O | 5 mg |
- 2-Methylthioadenosine Triphosphate Tetrasodium Salt
An ATP analog that induces aortic smooth muscle relaxation in rat (EC50 = 240 nM).| カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-202910 | 43170-89-4 | C11H14N5O13P3S ·4Na | 10 mg |
- 2-ThioUTP tetrasodium salt
Potent and selective P2Y2 agonist (EC50 values are 0.035, 0.35 and 1.5 μM for hP2Y2, hP2Y4 and hP2Y6 receptors respectively).| カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-203773 | 35763-29-2 | C9H11N2Na4O14P3S | 1 mg |
- 5-BDBD
Potent P2X4 receptor antagonist. Has been shown to block P2X4-mediated currents in Chinese hamster ovary cells .| カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-290784 | 768404-03-1 | C17H11BrN2O2 | 10 mg/50 mg |
- α,β-Methyleneadenosine 5'-triphosphate lithium salt
P2 purinoceptor agonist which is more potent than ATP at the P2X subtype.| カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-257039 | 104809-20-3 | C11H18N5O12P3•xLi+ | 5 mg/10 mg |
- 7-(2,3-Dihydroxypropyl)theophylline
| カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-357961 | 479-18-5 | C10H14N4O4 | 100 g/500 g |
- 9-Methyluric acid
| カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-362184 | 55441-71-9 | C6H6N4O3 | 50 mg |
- α,β-Methyleneadenosine 5'-triphosphate trisodium salt
P2-purinoceptor agonist. Also shown to inhibit adenylate cyclase (Ki = 0.5 μM).| カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-204428 | 7292-42-4 | C11H15N5Na3O12P3 | 10 mg |
- A 438079 hydrochloride
A competitive P2X7 receptor antagonist that does not substantially affect the activity of other P2 receptors.| カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-203788 | 899507-36-9 | C13H9Cl2N5•HCl | 10 mg/50 mg |
- A 740003
A competitive antagonist of P2X7 receptors that has been shown to potently block proinflammatory cytokine IL-1β.| カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-291774 | 861393-28-4 | C26H30N6O3 | 10 mg/50 mg |
- AR-C 66096 tetrasodium salt
| カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-361107 | 145783-24-0 | C14H18F2N5Na4O12P3S | 1 mg |
- AZ 10606120 dihydrochloride
| カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-361113 | N/A | C25H34N4O2.2HCl | 10 mg/50 mg |
- BzATP triethylammonium salt
Prototypic P2X7 receptor agonist that exhibits 5 - 10 fold greater potency than ATP (EC50 = 0.7 μM in HEK 293 cells). Exhibits partial agonist activity at P2X1 (pEC50 = 8.7) and P2Y1 receptors and can be used as a photoaffinity label for ATPase.| カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-203862 | 112898-15-4 | C24H24N5O15P3 ·C18H45N3 | 1 mg |
- Chloro-IB-MECA
A3 adenosine receptor agonist.| カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-257229 | 163042-96-4 | N/A | 5 mg |
- (±)-Clopidogrel hydrochloride
A thienopyridine adenosine diphosphate (ADP)-receptor antagonist, which functions as a selective irreversible P2Y12 receptor antagonist.| カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-203553 | 90055-48-4 | C16H16NO2SCl.HCl | 10 mg/50 mg |
- Cytidine 5'-triphosphate disodium salt
A P2X purinergic receptor agonist. | カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-217995 | 36051-68-0 | C9H14N3Na2O14P3 | 500 mg/1 g |
- GW 791343 hydrochloride
P2X7 allosteric modulator. Exhibits species-specific activity and acts as a negative allosteric modulator of human P2X7 (pIC50 = 6.9 - 7.2). A positive allosteric modulator of rat P2X7.| カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-203992 | 1019779-04-4 | C20H24F2N4O ·3HCl | 10 mg/50 mg |
- iso-PPADS tetrasodium salt
P2X-purinoceptor antagonist (pKi = 6.5) displaying similar activity to PPADS (sc-202770).| カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-204019 | N/A | C14H10N3Na4O12PS2 | 10 mg/50 mg |
- MRS 2179 tetrasodium salt
| カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-361263 | 101204-49-3 | C11H13N5O9P2Na4 | 10 mg/50 mg |
- MRS 2211
A selective and competitive P2Y13 receptor antagonist.| カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-204101 | N/A | C14H10N4O8Na2PCl•xNaCl•xNaOH•xH2O | 10 mg/50 mg |
- MRS 2219
Cyclic pyridoxine-alpha4, 5-monophosphate, compound. Selective potentiator of ATP-evoked responses at rat P2X1 receptors (EC500 = 5.9 µM).| カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-204102 | 14141-47-0 | C8H10NO5P | 10 mg/50 mg |
- MRS 2279
| カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-361264 | 367909-40-8 | C13H18ClN5O8P2.2NH3 | 1 mg |
- MRS 2365
| カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-361265 | 436847-09-5 | C13H16N5O9P2SNa3 | 1 mg |
- MRS 2500 tetraammonium salt
| カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-361266 | 779323-43-2 | C13H18N5O8P2I.4NH3 | 1 mg |
- MRS 2578
A symmetric aryl diisothiocyanate derivative that is shown to inhibit P2Y receptors. P2Y receptors are G-coupled receptors that are ATP activated and initiate an intracellular chain of reactions.| カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-204103 | 711019-86-2 | C20H20N6S4•2C2H6OS | 10 mg/50 mg |
- MRS 2690
Potent P2Y14 receptor agonist (EC50 = 49 nM) that displays 7-fold higher potency than UDP-glucose.
| カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-204104 | N/A | C15H22N2Na2O16P2S | 1 mg |
- MRS 2693 trisodium salt
MRS2693 trisodium salt is a selective P2Y6 agonist which is reported to display no activity at other P2Y subtypes.| カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-358788 | 911391-37-2 | C9H10IN2Na3O12P2 | 1 mg |
- MRS 2768 tetrasodium salt
A selective P2Y2 agonist. | カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-311440 | 1047980-83-5 | C15H16N2O18P4Na4 | 1 mg |
- NF 023
A subtype selective, competitive and reversible P2X1 receptor antagonist. Displays IC50 values of 0.21, 28.9, > 50 and > 100 μM for human P2X1, P2X3, P2X2, and P2X4-mediated responses respectively. Selective over adrenoceptors, histamine and P2Y receptors. Also selectively inhibits the α-subunit of Go/i (EC50 ~ 300 nM).
| カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-204124 | 104869-31-0 | C35H20Na6N4O21S6 | 10 mg/50 mg |
- NF 023 hydrate
This is a potent, selective P2X1 purinoceptor antagonist.| カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-257898 | 104869-31-0 (anhydrous) | C35H20N4O21S6 ·6Na ·xH2O | 10 mg |
- NF 110
Potent P2X3 receptor antagonist. Also exhibits anti-tumor activity in several tumor types.| カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-203642 | 111150-22-2 | C41H28N6Na4O17S4•xH2O | 10 mg/50 mg |
- NF 157
| カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-204125 | 104869-26-3 | C49H28F2N6Na6O23S6 | 10 mg/50 mg |
- NF 279
Suramin analog that is a highly selective, competitive, and reversible ATP-antagonist of P2X receptor. Effectively discriminates between P2Y and P2X receptors.| カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-202730 | 202983-32-2 | C49H30N6O23S6 ·6Na | 5 mg |
- NF 546
| カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-361275 | N/A | C47H44N6Na4O17P4 | 10 mg/50 mg |
- PIT
Purinergic P2Y receptor ligand. Displays mixed antagonism at P2Y receptors in some smooth muscles but potentiates responses to ATP in other systems (chick brain recombinant P2Y1 receptor and sympathetic/purinergic nerve stimulation).| カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-203665 | 56583-49-4 | C13H8N2O2.C7H8O3S | 10 mg/50 mg |
- PPADS tetrasodium salt
Non-selective P2 purinergic antagonist. Blocks recombinant P2X1, P2X2, P2X3, P2X5, native P2Y2-like, and recombinant P2Y4 receptors.| カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-202770 | 149017-66-3 | C14H10N3Na4O12PS2 | 10 mg/50 mg |
- PPNDS
Potent and selective P2X1 receptor antagonist (pKB = 7.43 in rat vas deferens). Up to 52-fold selective over P2Y1 receptors, and selective over α1A-adrenoceptors, A1, A2B, ecto-nucleotidase, H1, M3 receptors.| カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-204211 | N/A | C18H11N4Na4O14PS2 | 10 mg/50 mg |
- PSB 0474
Potent and selective P2Y6 receptor agonist (EC50 values are 7, > 1000 and > 10000 nM for P2Y6, P2Y2 and P2Y4 receptors respectively).| カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-203668 | 917567-60-3 | C17H18N2Na2O13P2 | 1 mg |
- Ro 0437626
Selective P2X1 purinergic receptor antagonist (IC50 = 3 μM) that displays > 30-fold selectivity over P2X2, P2X3 and P2X2/3 receptors (IC50 > 100 μM).| カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-204239 | 134362-79-1 | C27H35N5O4S | 1 mg/10 mg |
- RO-3
Selective homomeric P2X3 and heteromeric P2X2/3 receptor antagonist (pIC50 values are 7.0 and 5.9 respectively) that exhibits no activity at P2X1, P2X2, P2X4, P2X5 and P2X7 receptors (IC50 > 10 μM). Attenuates nociceptive sensitivity in animal models of pain. Orally active and brain penetrant.
| カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-204242 | N/A | C16H22N4O2 | 10 mg |
- TNP-ATP triethylammonium salt
A selective P2X receptor antagonist which inhibits ATP-induced currents in cells, specifically P2X1, P2X3 and heteromeric P2X2/3 receptors.| カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-204348 | 61368-63-6 | C16H13N8O19P3•C24H64N4 | 5 mg |
- UDP disodium salt
An endogenous P2Y receptor agonist, which specifically activates P2Y6 receptors.| カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-204372 | 27821-45-0 | C9H12N2Na2O12P2•xH2O | 50 mg |
- Uridine 5'-diphosphate sodium salt from Saccharomyces cerevisiae
A P2Y receptor agonist. | カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-222401 | 21931-53-3 | C9H14N2O12P2•xNa | 25 mg/100 mg |
- Uridine 5'-triphosphate tris salt
An agonist to the P2Y receptor.| カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-213136 | 108321-53-5 | C9H15N2O15P3 | 100 mg/500mg |
- Uridine 5'-triphosphate trisodium salt dihydrate
An agonist of the P2Y receptor.| カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-213137 | 116295-90-0 | C9H16N2Na3O17P3 | 250 mg |
- UTPγS trisodium salt
Enzymatically stable, selective P2Y2 and P2Y4 receptor agonist.| カタログ # | CAS Number | Molecular Formula | Unit |
|---|
| sc-204376 | N/A | C9H12N2Na3O14P3S | 1 mg |
|