Others 12

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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Others 12

Others 12 related products

Cat No.	Product Name	CAS No.	Product Description
V62306	WH-10417-099	2769753-42-4	WH-10417-099 is a degrader that collectively induces degradation of the largest number of unique kinases (over 125 unique kinases).
V61868	Windaus ketone	55812-80-1	Windaus ketone is a VD formation blocker.
V60560	Wnt pathway inhibitor 4	663214-57-1	Wnt pathway inhibitor 4 (compound 16D) is an anti-cancer compound with anti-cancer/tumor cell growth/proliferation activity.
V57744	WRN inhibitor 3	2923009-48-5	WRN inhibitor 3 (example 110), a cyclic vinyl sulfone compound, is an inhibitor (blocker/antagonist) of Wemer syndrome ATP-dependent helicase (WRN).
V61764	WRN inhibitor 4	2923009-45-2	WRN inhibitor 4 (example 107), a cyclic vinyl sulfone compound, is an inhibitor (blocker/antagonist) of Wemer syndrome ATP-dependent helicase (WRN).
V58593	WRN inhibitor 5	2923009-95-2	WRN inhibitor 5 (example 157), a cyclic vinyl sulfone compound, is an inhibitor (blocker/antagonist) of Wemer syndrome ATP-dependent helicase (WRN).
V64341	WRR139	2138924-36-2	WRR139 is a bioactive peptide vinyl sulfone involved in disease processes such as inflammation and cancer.
V62579	WSF1-IN-1	2379577-82-7	WSF1-IN-1 (compound 136) is an orally bioactive WSF1 inhibitor that may be utilized in tumor research related to the Wolfram syndrome gene WSF1.
V61929	WYC-210	2131803-93-3	WYC-210, an analogue of Tazarotene, is a retinoid with low anti-cancer activity.
V62415	WZ4141R	2319589-98-3	WZ4141R is an intermediate in compound synthesis.
V64246	X5050	2404756-81-4	X5050 is an inhibitor (blocker/antagonist) of REST with EC50 of 2.1 μM.
V58567	XF056-132	2694057-55-9	XF056-132 is the salt form of trifluoroacetic acid (TFA).
V61652	XIAP antagonist 1	375835-04-4	XIAP antagonist 1 is a XIAP-specific antagonist.
V60352	XIAP BIR2/BIR2-3 inhibitor-2	1609384-83-9	XIAP BIR2/BIR2-2 inhibitor-3 is a dual (bifunctional) inhibitor of BIR2 and BIR2-3 with IC 50s less than 1 nM.
V61690	XL388-C2-NH2	2250061-94-8	XL388-C2-NH2 is a monomer compound.
V60419	XM462	1045857-53-1	XM462 is a dihydroceramide desaturase inhibitor.
V64385	XMD-17-51 TFA	2436579-93-8	XMD-17-51 TFA is a pyrimidine-valium compound that regulates proteases.
V60318	XN methylpyrazole (XP)	2820169-36-4	XN methyl pyrazole ameliorates diet-induced obesity and induces energy expenditure in high-fat diet mice.
V58579	Y08262	2450965-18-9	Y08262 is a potent and specific CBP bromodomain inhibitor.
V64349	yGsy2p-IN-H23	1269190-98-8	yGsy2p-IN-H23 is a potent inhibitor of yeast glycogen synthase 2 (yGsy2p) with IC50 of 875 µM for human glycogen synthase 1 (hGYS1).