ATPase

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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ATPase

ATPase related products

Cat No.	Product Name	CAS No.	Product Description
V2325	BRITE-338733	503105-88-2	BRITE-338733 is a RecA ATPase inhibitor (antagonist) with IC50 of 4.7 µM.
V0191	BTB06584	219793-45-0	BTB06584 (BTB-06584; BTB 06584) is a novel, potent and IF1-dependent inhibitor of the mitochondrial F1 Fo-ATPase, acting by selectively inhibiting mitochondrial F1 Fo-ATPase activity without compromising ATP synthesis and to limit ischaemia-induced injury caused by reversal of the mitochondrial F1 Fo-ATPsynthase.
V8748	Bufalin	465-21-4	Bufalin is a novel and potent inhibitor of steroid receptor coactivator 3 (SRC-3) with anticancer,anti-inflammatory and antinociceptive activity.
V17787	CDN-1163	892711-75-0	CDN-1163 is a small molecule activator of sarco/endoplasmic reticulum Ca2+-ATPase (SERCA).
V2377	KM 91104	304481-60-5	KM91104 is a cell-penetrating/penetrable V-ATPase inhibitor that specifically targets the a3-b2 subunit of V-ATPase.
V25685	ML367	381168-77-0	ML367 is a novel andpotent inhibitor of ATPase family AAA domain-containing protein 5 (ATAD5) stabilization, it acts as a probe molecule that has low micromolar inhibitory activity.
V0180	(-)-Blebbistatin (S-Blebbistatin)	856925-71-8	Blebbistatin is a potent, selective, reversible and cell-permeable small molecule inhibitor for non muscle myosin II ATPase with IC50 of around 2 μM in cell-free assays.
V6322	Oxytetracycline	79-57-2	Oxytetracycline (Lenocycline; Oxyterracine; Oxyterracyne; Tarosin; Oxymykoin) is a naturally occurring tetracycline class of antibiotic extracted from the actinomycete STREPTOMYCES rimosus with a broad-spectrum of antibacterial effects.
V26869	Oleandrin	465-16-7	Oleandrin (PBI-05204) inhibits Na+, K+-ATPase activity with IC50 of 620 nM.
V9143	Thapsigargin	67526-95-8	Thapsigargin is a novel and potent non-competitive inhibitor of the sarco/endoplasmic reticulum Ca2+ ATPase (SERCA) and an Endoplasmic Reticulum (ER) stress inducing agent.
V26870	Oleic acid	112-80-1	Oleic acid(also known as 9-cis-Octadecenoic acid; 9Z-Octadecenoic acid) is the most common and abundantmonounsaturatedfatty acid (FA), acting asaNa+/K+ATPaseactivator.
V16014	Tegoprazan	942195-55-3	Tegoprazan, a novel and potent P-CAB (potassium-competitive acid blocker),is a next-generation therapeutics developed for the treatment of acid-related gastrointestinal diseases such as gastroesophageal reflux disease (GERD) and peptic ulcers, acting bycontroling gastric acid secretion and motility.
V6079	Rhodamine 123 (RH-123; R-22420)	62669-70-9	Rhodamine dyes are membrane-permeable/penetrable cationic fluorescent probes that can specifically identify mitochondrial membrane potential, thereby attaching to mitochondria and producing bright fluorescence.