LIMK

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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LIMK

LIMK related products

Cat No.	Product Name	CAS No.	Product Description
V75994	8β,9α-Dihydroxylindan-4(5),7(11)-dien-8alpha,12-olide	956707-04-3	8β,9α-Dihydroxylindan-4(5),7(11)-dien-8alpha,12-olide (compound 3) is a sesquiterpene with anti-LIMK1 activity.
V2986	BMS-3	1338247-30-5	BMS-3 is a potent inhibitor of the LIM kinase (LIMK)with IC50 of 5nM and 6 nM for LIMK1 and LIMK2 respectively.
V2987	BMS-5	1338247-35-0	BMS-5, also known as LIMKI-3, isan analog of BMS-3and potent inhibitor of the LIM kinase (LIMK) with IC50 values of 7 and 8 nM for LIMK1 and LIMK2 respectively.
V106777	LIMK1 inhibitor 2	67795-42-0	LIMK1 inhibitor 2 (Compound 41) is a LIMK1 inhibitor with IC50 of 9 μM.
V31728	R-10015	2097938-51-5	R-10015 is a broad-spectrum antiviral compound that treats HIV infection. It binds to the ATP-binding pocket and inhibits LIM domain kinase (LIMK) with a potent and selective manner, with an IC50 of 38 nM for human LIMK1.
V144474	S3 Fragment		S3 Fragment is a bioactive peptide.
V81344	S3 Fragments		S3 Fragment is a biologically active peptide.
V145038	SM311		SM311 is a chemical probe that is a potent and selective irreversible inhibitor of LIMK1 (EC50 = 0.045 μM, with more than 30 times higher selectivity for LIMK2).