P2 Receptor

ADC Related

ADC Antibody ADC Cytotoxin ADC Linker ADCs Drug-Linker Conjugates for ADC
Angiogenesis

5-alpha Reductase ALK Bcr-Abl BTK EGFR FAK FLT3 HER-2 HIF Src Syk VDA VEGFR
Anti-infection

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

Apoptosis ASK Bcl-2 Caspase c-Myc c-RET Cytohesin DAPK Ferroptosis FKBP IAP Mdm2 p53 PD-1 PD-L1 PERK PKD Ras RIP kinase ROS Survivin Thymidylate Synthase TNF Receptor TNFa TRADD
Autophagy

Autophagy LRRK2 Mitophagy OGA ULK
Cell Cycle

Antifolate APC Aurora Kinase BMI-1 CDK Chk c-Myc Eukaryotic Initiation Factor G-quadruplex HDAC HSP Kinesin LIMK Mad2 Microtubule(Tubulin) Mps1 Nucleoside Antimetabolite/Analog Nur77 p21 PAK PERK PFKFB PLK PPAR Ras Rho ROCK SRPK TOPK Topoisomerase Wee1
Cytoskeletal Signaling

Arp2 3 Complex Bcr-Abl Cardiac Myosin Dynamin Gap Junction Protein HSP Integrin Kinesin Microtubule Associated MLCK Myosin PAK TACC3 Wntbeta-catenin
DNA Damage

ATM(ATR) CRISPR(Cas9) DNA alkylator DNA Stain DNA(RNA) Synthesis GAK HDAC HSP Nucleoside Antimetabolite(Analog) OGG1 p97 PARG PARP RAD51 RNR Sirtuin SMN Telomerase Topoisomerase
Endocrinology & Hormones

5-alpha Reductase ACE Adrenergic Receptor Androgen Receptor Aromatase Estrogenprogestogen Receptor Glucocorticoid Receptor GPR Mineralocorticoid Receptor RAAS THR TSH Receptor
Epigenetics

AMPK Aurora Kinase DNA Methyltransferase Epigenetic Reader Domain EZH1 2 HDAC HIF Histone Acetyltransferase Histone Demethylase Histone Methyltransferase JAK MAT MicroRNA MLL Pim PKC Protein Arginine Deiminase Sirtuin Small Interfering RNA (siRNA) SMYD

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P2 Receptor

P2 Receptor related products

Cat No.	Product Name	CAS No.	Product Description
V0084	A-804598 (A804598)	1125758-85-1	A-804598(A 804598) is a structurally novel, CNS penetrant, potent, competitive, and selective antagonist of the purinergic P2X7 receptors (IC50 = 10 nM, 9 nM and 11 nM for rat, mouse and human P2X7 receptors respectively) with potential anti-inflammatory activity.
V1305	A-438079 HCl	899431-18-6	A-438079 HCl (A438079; A 438079),the hydrochloride salt of-438079,is a novel, potent, and selective P2X7 receptor antagonist with anti-Parkinsons disease effects.
V5171	AF-353 (Ro-4)	865305-30-2	AF-353 (Ro-4; AF353) is a novel, highly potent, selective and orally bioavailable P2X3/P2X2/3 receptor antagonist with a pIC50of 8.0 for both human and rat P2X3, and with a pIC50of 7.3 for human P2X2/3.
V17316	BX430	688309-70-8	BX430 is a novel, potent, selective allosteric/con-competitive antagonist of human P2X4 receptor channels with an IC50 of 0.54 μM.
V1302	MRS 2578	711019-86-2	MRS2578 (MRS-2578; MRS 2578) is a potent andselectiveP2Y6 receptor antagonist with potentially usefulness in controlling persistent storage symptoms in obstructed patients.
V1300	Prasugrel (PCR 4099; CS-747)	150322-43-3	Prasugrel (formerly CS-747,PCR-4099; LY-640315;trade name Effient; Prasita),a piperazine derivative,is an irreversible and thienopyridine-based ADP receptor (P2Y12) antagonist approvedas an antiplatelet and anticoagulantdrug used for the reduction of thrombotic cardiovascular events.
V1303	Ticagrelor (AZD6140)	274693-27-5	Ticagrelor (formerly AZD-6140; AR-C 126532XX; AZD6140;AR-C126532XX; Trade name: Brilinta; Brilique; Possia) is the first reversibly binding, potent and orally bioactiveP2Y12 receptor antagonist used as an antiplatelet and anticoagulant.
V1304	Ticlopidine HCl	53885-35-1	Ticlopidine HCl (Ticlodix; Ticlodone; 53-32C; 5332C; trade name Ticlid),the hydrochloride salt of ticlopidine, is a potentP2 receptor inhibitor against used as antiplatelet and anticoagulant.
V1301	Clopidogrel sulfate	120202-66-6	Clopidogrel sulfate (Plavix; Zyllt; Osvix; Plavitor, SR-25990C), the sulfate salt ofClopidogrel, is an orally bioavailable, thienopyridine class of antiplatelet agent acting as an irreversible inhibitor of ADP receptor (P2Y12).