ALK

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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ALK

ALK related products

Cat No.	Product Name	CAS No.	Product Description
V111536	(E)-Belizatinib	1388225-72-6	(E)-Belitazartinib ((E)-TSR-011) (compound 36) is the (E)-isomer of belitazartinib, a potent, selective, and orally effective anaplastic lymphoma kinase (ALK) inhibitor with an enzymatic IC50 of 0.005 μM and a cellular IC50 of 0.048 μM.
V110318	ALK/HDAC-IN-2		ALK/HDAC-IN-2 (compound 19b) is an ALK/HDAC inhibitor with IC₅₀ values of 8 nM for wild-type ALK and 1.18 μM for all HDACs.
V128534	ALK5-IN-86		ALK5-IN-86 is a selective ALK5 inhibitor with an IC50 value of 0.267 μM.
V131234	CDD-1115	3034215-86-3	CDD-1115 is a potent and selective BMPR2 inhibitor with an IC50 of 1.8 nM and 6.2 nM for Kiapp.
V138720	LDN-193688	1062368-51-7	LDN-193688 is an ALK2 inhibitor with IC₅₀ values of 104, 18, 235, 1530, and 1080 nM for ALK1, ALK2, ALK3, ALK4, and ALK5, respectively.
V108935	PROTAC EML4-ALK Degrader-2	2417174-28-6	PROTAC EML4-ALK Degrader-2 is an EML4-ALK PROTAC degrader.
V18838	X-376	1365267-27-1	X-376 (an analog ofEnsartinib or X-396) is a novel, potent and highly selectiveALK inhibitor with IC50of 0.61 nM and the potential to be used for treating non-small cell lung cancer.