P2Y Receptor
P2Y Receptor(P2Y受体)
P2Y Receptor is a family of purinergic G protein-coupled receptors, stimulated by nucleotides.
P2Y Receptor 相关产品(60)
- GC17476MRS 2500 tetraammonium saltCAS: 779323-43-2
Highly potent and selective antagonist of the platelet P2Y1 receptor
- GC35710ClopidogrelCAS: 113665-84-2纯度: >99.00%
Clopidogrel Bisulfate (SR-25990C, Clopidogrel hydrogen sulfate, Iscover, Plavix) is an oral, thienopyridine class antiplatelet agent.
- GC35711Clopidogrel thiolactoneCAS: 1147350-75-1纯度: >98.00%
Clopidogrel thiolactone是一种P2Y12受体抑制剂, 是一种有效的抗血小板药物。
- GC36680N6-(4-Hydroxybenzyl)adenosineCAS: 110505-75-4纯度: >99.00%
N6-(4-Hydroxybenzyl)adenosine抑制由胶原诱导的血小板聚集, IC50范围为6.77-141 μM。
- GC39759MRS2500 tetraammoniumCAS: 630103-23-0
MRS2500 tetraammonium 是一种高效、选择性和稳定的 P2Y1 受体拮抗剂 (Ki=0.78 nM)。MRS2500 tetraammonium 抑制 ADP 诱导的人血小板聚集，IC50 值为 0.95 nM。具有抗血栓活性。
- GC41668(±)-Clopidogrel (hydrochloride)CAS: 130209-90-4纯度: >98.00%
A prodrug of the platelet purinergic P2Y12 receptor antagonist
- GC45111UDP-α-D-Glucose (sodium salt)CAS: 28053-08-9纯度: >99.50% / >98.00%
A stereoisomer of UDP-α-D-glucose
- GC600162-Methylthioadenosine diphosphate trisodiumCAS: 475193-31-8纯度: >98.00%
An agonist of P2Y receptors
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC17320 | NF 157 | 104869-26-3 | >90.00% | |
NF 157 是一种高度选择性的纳摩尔 P2Y11 拮抗剂，pKi 为 7.35。 | ||||
| GC17464 | Prasugrel | 150322-43-3 | >98.00% | |
A prodrug form of R-99224 | ||||
| GC17476 | MRS 2500 tetraammonium salt | 779323-43-2 | - | |
Highly potent and selective antagonist of the platelet P2Y1 receptor | ||||
| GC17742 | NF 340 | 202982-98-7 | - | |
NF 340 是一种有效的选择性 P2Y11 受体拮抗剂。 | ||||
| GC18472 | Elinogrel | 936500-94-6 | - | |
A reversible P2Y 12 antagonist | ||||
| GC19081 | BPTU | 870544-59-5 | >99.00% | |
A P2Y 1 receptor antagonist | ||||
| GC31664 | Diquafosol tetrasodium (INS365) | 211427-08-6 | >98.00% | |
A P2Y 2 and P2Y 4 receptor agonist | ||||
| GC32594 | TAK-024 | 186971-69-7 | - | |
TAK-024是一种血小板抑制剂，在人，猴和豚鼠中的IC50值分别为31,79和51nM。 | ||||
| GC35710 | Clopidogrel | 113665-84-2 | >99.00% | |
Clopidogrel Bisulfate (SR-25990C, Clopidogrel hydrogen sulfate, Iscover, Plavix) is an oral, thienopyridine class antiplatelet agent. | ||||
| GC35711 | Clopidogrel thiolactone | 1147350-75-1 | >98.00% | |
Clopidogrel thiolactone是一种P2Y12受体抑制剂, 是一种有效的抗血小板药物。 | ||||
| GC36680 | N6-(4-Hydroxybenzyl)adenosine | 110505-75-4 | >99.00% | |
N6-(4-Hydroxybenzyl)adenosine抑制由胶原诱导的血小板聚集, IC50范围为6.77-141 μM。 | ||||
| GC36957 | Prasugrel Maleic acid | 389574-20-3 | - | |
Prasugrel (PCR 4099) 马来酸盐是是血小板抑制剂，IC50为1.8 μM。 | ||||
| GC37705 | Suramin | 145-63-1 | >98.00% | |
A polysulfonated naphthylurea with antiviral, antiparasitic, and anticancer activities | ||||
| GC37901 | Vicagrel | 1314081-53-2 | >98.50% | |
Vicagrel 氯吡格雷的醋酸衍生物，是一种 P2Y12 血小板抑制剂，可用于治疗血栓形成，羧酸酯酶 2 (CES2) 的底物。Vicagrel 具有良好的安全性和优异的抗血小板活性，可作为抗血小板药物。 | ||||
| GC39759 | MRS2500 tetraammonium | 630103-23-0 | - | |
MRS2500 tetraammonium 是一种高效、选择性和稳定的 P2Y1 受体拮抗剂 (Ki=0.78 nM)。MRS2500 tetraammonium 抑制 ADP 诱导的人血小板聚集，IC50 值为 0.95 nM。具有抗血栓活性。 | ||||
| GC41668 | (±)-Clopidogrel (hydrochloride) | 130209-90-4 | >98.00% | |
A prodrug of the platelet purinergic P2Y12 receptor antagonist | ||||
| GC43137 | Cangrelor (sodium salt) | 163706-36-3 | >98.00% | |
An ATP analog with antithrombic properties | ||||
| GC45111 | UDP-α-D-Glucose (sodium salt) | 28053-08-9 | >99.50% / >98.00% | |
A stereoisomer of UDP-α-D-glucose | ||||
| GC46239 | YM-254890 | 568580-02-9 | >95.00% | |
A cyclic depsipeptide Gα q/11 inhibitor | ||||
| GC50080 | PPTN hydrochloride | 1992047-65-0 | >99.50% | |
A P2Y 14 receptor antagonist | ||||
| GC50081 | AR-C 118925XX | 216657-60-2 | >97.00% | |
选择性和竞争性 P2Y2 拮抗剂 | ||||
| GC50222 | MRS 2905 | - | - | |
Potent and selective P2Y14 receptor agonist | ||||
| GC50224 | SAR 216471 hydrochloride | 1279829-64-9 | - | |
Potent P2Y12 antagonist; orally available | ||||
| GC60016 | 2-Methylthioadenosine diphosphate trisodium | 475193-31-8 | >98.00% | |
An agonist of P2Y receptors | ||||