IκB IKK

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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IκB IKK

IκB IKK related products

Cat No.	Product Name	CAS No.	Product Description
V30592	ACHP Hydrochloride	406209-26-5	ACHP hydrochloride(also known as IKK-2 Inhibitor VIII), thehydrochloride salt of ACHP, is a novel, highly potent and selective IKK-β inhibitor with IC50 of 8.5 nM.
V0756	AZD3264	1609281-86-8	AZD3264 (AZD-3264; AZD 3264) is a novel and potent inhibitor of IKK2 (IkappaBKinase/(IκB) with potential anti-inflammatory and anticancer activity.
V0749	BAY 11-7082	19542-67-7	BAY 11-7082 (BAY-11-7082; BAY-117082) is a novel and potent NF-κB inhibitor with potential anti-inflammatory and anticancer activity.
V0760	Bay 11-7085	196309-76-9	BAY 11-7085 (BAY-11-7085; BAY 117085) is a novel, potent, soluble, irreversible inhibitor of TNFα-induced IκBα phosphorylation with potential anticancer activity.
V0755	BMS-345541	445430-58-0	BMS-345541 (BMS345541; BMS 345541) is a novel, highly potent andselectiveIKK-1/2inhibitorwith potential anticancer and anti-inflammatory activity.
V0750	IKK-16 (IKK Inhibitor VII; IKK 16)	873225-46-8	IKK-16 (also known as IKK Inhibitor VII; IKK-16; IKK16) is a novel, potent and selective IκBα kinase (IKK) inhibitor with potential anti-inflammatory activity.
V87868	IKKβ-IN-4	4815-35-4	IKKβ-IN-4 (compound 14) is an IkappaB kinase-β (ikkβ) inhibitor with IC50 of 1.9 μM.
V0752	IMD 0354	978-62-1	IMD-0354 (IMD0354; IMD-0354) is a novel, potent and selective IKKβ inhibitorwith potential anti-inflammatory activity.
V82225	Keap1-Nrf2-IN-8	2769963-54-2	Keap1-Nrf2-IN-8 (compound 12d) is a potent Keap1-Nrf2 PPI (Keap1-Nrf2 protein-protein interaction) inhibitor (antagonist) with IC50 of 64.5 nM and 14.2 nM in FP and TR-FRET assays, respectively.
V118451	LLVK TFA		LLVK TFA is a selective IκB phosphorylation inhibitor.
V0757	LY2409881 trihydrochloride	946518-60-1	LY2409881trihydrochloride (LY-2409881; LY 2409881), thetrihydrochloride salt of LY-2409881, is a novel, potent and selective IKK2 (IκB kinase β) inhibitor with potential anticancer and anti-inflammatory activity.
V0753	PS-1145	431898-65-6	PS-1145 (PS1145) is a novel, potent and specific IKK (IκB kinase) inhibitor with anticancer activity.
V0761	SC-514	354812-17-2	SC-514 (SC 514; SC514) is a novel, potent, orally bioactive, selective and reversible, and ATP-competitive IKK-2 inhibitor with potential anti-inflammatory activity.
V145643	TBK1 ligand 3	2115897-10-2	TBK1 ligand 3 is a TBK1 ligand that can be used as a target protein ligand for the synthesis of PROTAC UNC8209 and UNC8461.
V145644	TBK1-IN-2	3075572-35-6	TBK1-IN-2 is a potent TBK1 inhibitor (IC50: 775 pM).
V51259	TBK1/IKKε-IN-6	2306877-20-1	dual TBK1 and IKKε inhibitor
V0751	TPCA-1 (GW-683965; GW683965)	507475-17-4	TPCA-1 (also known as TPCA1; GW-683965; GW683965)is novel, potent, and selective inhibitor of IKK-2 with potential anti-inflammatory activity.
V0759	WS6	1421227-53-3	WS6 (WS6; WS 6) is a novel and potent small molecule modulator of β cell proliferation via modulation of Erb3 binding protein-1 (EBP1) and the IκB kinase pathway with important biological activity.
V0758	WS3	1421227-52-2	WS-3 (WS3; WS 3) is a novel and potent small molecule modulatior of Erb3 binding protein-1 (EBP1) and the IκB (IkappaB) kinase with important biological activity.
V11455	Amlexanox (AA673; CHX3673)	68302-57-8	Amlexanox (Amoxanox; AA-673; CHX-3673) is a potent and selective IKKε and TBK1 inhibitor which acts asanti-inflammatory antiallergic immunomodulator used to treat recurrent aphthous ulcers (canker sores), and (in Japan) several inflammatory conditions.