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Anti-infection

Antibiotic Arenavirus Bacterial CMV Enterovirus Filovirus Fungal HBV HCV HCV Protease HIV HIV Integrase HIV Protease HSV Influenza Virus Orthopoxvirus Parasite TMV Reverse Transcriptase RSV SARS-CoV Virus Protease
Apoptosis

Apoptosis Bcl-2 Family Caspase c-Myc Ferroptosis FKBP IAP Family MDM-2/p53 PKD Necroptosis Pyroptosis RIP kinase Thymidylate Synthase TNF Receptor TRADD Cuproptosis
Autophagy

Autophagy FKBP LRRK2 Mitophagy OGA ULK
Cell Cycle/DNA Damage

Antifolate APC ATM/ATR Aurora Kinase BMI-1 Casein Kinase CDK Checkpoint Kinase (Chk) CRISPR/Cas9 Deubiquitinase DNA Alkylator/Crosslinker DNA/RNA Synthesis DNA-PK Early 2 Factor (E2F) Eukaryotic Initiation Factor (eIF) GAK G-quadruplex HDAC HSP IRE1 Kinesin LIM Kinase (LIMK) Microtubule/Tubulin Mps1 DNA Stain Nucleoside Antimetabolite/Analog Nur77 p97 PAK PARP PERK Polo-like Kinase (PLK) PPAR RAD51 Cyclin G-associated Kinase (GAK) ROCK ATF6 Haspin Kinase Sirtuin SRPK PDI Telomerase TOPK Topoisomerase Wee1
Cytoskeletal Signaling

Arp2/3 Complex Dynamin Gap Junction Protein Integrin Kinesin Microtubule/Tubulin Mps1 Myosin PAK ROCK
Endocrinology/Hormones

Adrenergic Receptor Androgen Receptor Angiotensin-converting Enzyme (ACE) Aromatase Cholecystokinin Receptor TSH Receptor Estrogen Receptor/ERR GHSR Glucocorticoid Receptor GNRH Receptor Mineralocorticoid Receptor Opioid Receptor PGD synthase PGE synthase Progesterone Receptor Thyroid Hormone Receptor
Epigenetics

AMPK Aurora Kinase DNA Methyltransferase Epigenetic Reader Domain HDAC Histone Acetyltransferase Histone Demethylase Histone Methyltransferase MicroRNA PARP PKC Protein Arginine Deiminase Methionine Adenosyltransferase (MAT) Sirtuin JAK
GPCR/G Protein

5-HT Receptor Adenosine Receptor Adenylate Cyclase (AC) Adiponectin Receptor Adrenergic Receptor Angiotensin Receptor Bombesin Receptor Bradykinin Receptor Cannabinoid Receptor CaSR CCR CGRP Receptor Cholecystokinin Receptor CRFR CXCR TSH Receptor Neuropeptide Y Receptor Dopamine Receptor EBI2/GPR183 Endothelin Receptor Formyl peptide receptor (FPR) GHSR Glucagon Receptor Glucocorticoid Receptor GNRH Receptor GPR109A GPR119 GPR139 GPR27 GPR55 GPR84 Guanylate Cyclase Histamine Receptor Imidazoline Receptor Leukotriene Receptor LPL Receptor mAChR Melanocortin Receptor Melatonin Receptor mGluR Neurokinin Receptor Neurotensin Receptor Opioid Receptor Orexin Receptor (OX Receptor) Oxytocin Receptor P2Y Receptor PKG Prostaglandin Receptor Protease-Activated Receptor (PAR) Apelin Receptor (APJ) Ras GPR88 Free Fatty Acid Receptor E3 Ligase Ligand-Linker Conjugates RGS GPR4 Secretin Receptor Mas-related G-protein-coupled Receptor (MRGPR) GPR35 GPR52 MCHR1 (GPR24) Leukotriene Receptor GLP Receptor Somatostatin Receptor Arrestin Platelet-activating Factor Receptor (PAFR) Mas-related G-protein-coupled Receptor (MRGPR) Kisspeptin Receptor G Protein-coupled Receptor Kinase (GRK) G protein-coupled Bile Acid Receptor 1 Succinate Receptor 1 Protease Activated Receptor (PAR) Vasopressin Receptor

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P2Y Receptor

P2Y Receptor相关产品（15）

货号	产品名	中文名称	产品描述
SJ-MX3739	BPTU		BPTU (BMS-646786) is an allosteric P2Y1 antagonist. Prevents inhibition of spontaneous contraction of rat and mouse colon induced by electrical field stimulation, nicotine and P2Y agonists. Acts as n antithrombotic agent and reduces platelet aggregation.
SJ-MX2713	Prasugrel hydrochloride	盐酸普拉格雷	Prasugrel hydrochloride，一种噻吩吡啶和前药，抑制血小板功能。Prasugrel hydrochloride 是一种有效的 P2Y12 受体拮抗剂，抑制 ADP 诱导的血小板聚集。
SJ-MX3277	Prasugrel	普拉格雷	Prasugrel is novel thienopyridine antiplatelet prodrug that is metabolized to the thiol-containing active metabolite R-138727,which binds to and irreversibly inhibits the platelet P2Y12ADP receptor. Prasugrel is metabolized by the liver- and intestinal-dominant carboxylesterases CE1 and CE2 to give a mixture of four enantiomers that inhibit platelet aggregation.
SJ-MX3948	Uridine-5'-diphosphate disodium salt	尿苷-5'-二磷酸二钠盐	Uridine-5'-diphosphate disodium salt 是一种有效的选择性 P2Y6 受体激动剂 (EC50=300 nM; 对人 P2Y6 受体 pEC50=6.52)。Uridine-5'-diphosphate disodium salt 是一种内源性代谢产物 (endogenous metabolite)，催化多种底物的葡糖醛酸糖化反应，可用于核酸生物合成 (RNA biosynthesis)。
SJ-MX4369	N6-(4-Hydroxybenzyl) adenosine	N6-羟苄腺苷	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。
SJ-MX4720	PIT		PIT (2,2'-Pyridylisatogen tosylate) 是 P2Y1 受体的选择性和非竞争性拮抗剂，对人 P2Y1 受体的 IC50 值为 0.14 μM。PIT 在不影响核苷酸结合的情况下拮抗 P2Y1 受体信号。PIT 是一些平滑肌中代谢性嘌呤受体 (P2Y 家族) 对 ATP 反应的不可逆拮抗剂。
SJ-MX5829	AZD1283		AZD1283 是 P2Y12 受体拮抗剂，EC50为 3.0 ug/kg/min，结合的 IC50 为11 nM。
SJ-MN1722	Uridine 5′-diphosphoglucose disodium salt
SJ-MX4855	Uridine 5'-diphosphate sodium salt	尿苷-5'-二磷酸钠盐
SJ-MX2143	Ticagrelor (AZD6140)	替卡格雷	Ticagrelor (AZD6140) 是可逆的，具有口服活性的 P2Y12 受体拮抗剂，可用来研究血小板聚集。
SJ-MX1834	MRS 2578		MRS 2578 是一种选择性强的 P2Y6 受体拮抗剂，IC50 为 37 nM (人) 和 98 nM (大鼠)。MRS 2578在 P2Y1、P2Y2、P2Y4 和 P2Y11 受体上活性不明显。
SJ-MX0852	Cangrelor Tetrasodium	坎格雷洛四钠盐	Cangrelor tetrasodium 是一种三磷酸腺苷类似物，是一种可逆的、选择性的血小板 P2Y12 拮抗剂，具有迅速有效的抗血小板作用。Cangrelor tetrasodium 直接阻断腺苷二磷酸 (ADP) 诱导的血小板活化和聚集。Cangrelor tetrasodium 也是一种非特异性的 GPR17 拮抗剂。
SJ-MX2965	Clopidogrel hydrogen sulfate	硫酸氢氯吡格雷	Clopidogrel hydrogen sulfate 是一种抗血小板活性分子，可防止血栓形成。Clopidogrel hydrogen sulfate 抑制 CYP2B6和 CYP2C19， IC,sub>50 分别为 18.2 nM 和 524 nM。 Clopidogrel hydrogen sulfate 是一种有效的抗血栓剂，可抑制 ADP 诱导的血小板聚集。Clopidogrel hydrogen sulfate 也是一种具有口服活性 P2Y(12) 抑制剂。
SJ-MX2965A	Clopidogrel	氯吡格雷	Clopidogrel 是一种以 P2Y12 受体为靶点的、具有口服活性的血小板抑制剂。Clopidogrel 可用于抑制冠状动脉疾病、周围血管疾病和脑血管疾病中的血凝块。
SJ-MX4827	Diquafosol tetrasodium