Others 4

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
GPCR & G Protein

5-HT Receptor Adenosine Receptor Adenylate Cyclase Adrenergic Receptor Angiotensin Receptor APJ Bombesin Receptor Bradykinin Receptor cAMP Cannabinoid Receptor CaSR CCK receptor CCR CGRP Receptor CRFR CXCR Dopamine Receptor EBI2 Endothelin Receptor Formyl Peptide Receptor Free Fatty Acid Receptor G protein-coupled Bile Acid Receptor GCGR GHSR GLP Receptor Glucagon Receptor GnRH Receptor GPCR19 GPR GPR109A Guanylate Cyclase Hedgehog(Smoothened) ROCK Histamine Receptor ICMT Leukotriene Receptor LPA Receptor LPL Receptor LTR mAChR Melanocortin Receptor Melatonin Receptor mGluR Motilin Receptor MRGPR MT Receptor Neurokinin Receptor Neuropeptide Y Receptor Neurotensin Receptor NPY receptor Opioid Receptor OX Receptor Oxytocin Receptor P2Y Receptor PAFR PAR PKD PKG Prostaglandin Receptor Ras RGS Protein S1P Receptor SGLT Sigma Receptor Somatostatin Receptor TAAR TSH Receptor Urotensin Receptor Vasopressin Receptor

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Others 4

Others 4 related products

Cat No.	Product Name	CAS No.	Product Description
V4205	Amicarbazone	129909-90-6	Amicarbazone (also known as BAY-MKH3586 and BAY314666) is a novel, potent inhibitor of photosynthetic electron transport via binding to the Qb domain of photosystem II (PSII); Amicarbazone is a new triazolinone herbicide with a broad spectrum of weed control.
V4243	AZD6482 S-isomer	1173900-37-2	AZD6482 S-isomer, is an isomer of AZD6482 which is a novel, potent, selective and ATP competitive PI3Kβ inhibitor with IC50 of 10 nM, 8-, 87- and is 109-fold more selective to PI3Kβ than PI3Kδ, PI3Kα and PI3Kγ in cell-free assays.
V4171	BAY-524	1445830-39-6	BAY-524is a novel and potent Bub1 inhibitor with anIC50of 450 nM for human Bub1 in the presence of 2 mM ATP.
V4168	BAY-598 R-isomer	1906920-28-2	BAY-598 R-isomer (R-BAY598) is the R-enantiomer of BAY589 which is a peptide-competitive SMYD2 inhibitor with antineoplastic activity.
V4164	BAY-677	2117404-84-7	BAY-677 is an inactive and negative control for BAY-678.
V4129	BLU-782	2141955-96-4	BLU-782 has been discontinued.
V4273	Bucladesine (Dibutyryl-cAMP)	362-74-3	Bucladesine (DC2797; DC-2797; Dibutyryl-cAMP) is a potent and cell-permeable PKA activator and a cAMP analog that mimics the action of endogenous cAMP.
V4136	Dioctyl decanedioate	2432-87-3	Dioctyl decanedioate (decadioic acid, dioctyl ester; Decanedioic acid, dioctyl ester; decanedioicaciddioctylester; Dioctyl-1,10-decanedioate) is a biochemical.
V4161	Diroximel fumarate	1577222-14-0	Diroximel fumarate (also known as ALKS 8700) is a novel compound that is taken orally and rapidly converted into monomethyl fumarate (MMF).
V4210	Emiglitate	80879-63-6	Emiglitate (also known as BAY o 1248) is a novel, potent, selective and competitive inhibitor ofα-glucoside hydrolase.
V4148	Fenebrutinib (GDC-0853) HCl	2128304-54-9	Fenebrutinib HCl (formerly known RG-7845; GDC-0853 hydrochloride) is an orally bioavailable, and noncovalent (reversible) brutons tyrosine kinase (BTK) inhibitor (Ki = 0.91 nM) with anticancer and anti-inflammatory activity.
V4137	GSK-2336805	1256390-53-0	GSK-2336805 (also known as GSK-805; GSK2336805; JNJ-56914845) is a novel and potent inhibitor of HCV NS5A.
V4046	Irosustat	288628-05-7	Irosustat (formerlyknown as STX64, BN83495 or 667 coumate) is a novel potent and irreversibleinhibitor of steroid sulfatasewith anIC50of 8 nM and has the potential for treating breast cancer.
V4075	LGD-4033	1165910-22-4	LGD-4033 (also known as VK-5211 and Ligandrol) isa novel, potent and selective androgen receptor modulator (SARM) and is being investigated by Ligand Pharmaceuticals for treatment of conditions such as muscle wasting and osteoporosis.
V4291	MK-6240	1841078-87-2	MK-6240 is a novel positron emission tomography (PET) tracer fordetecting neurofibrillary tangles (NFTs).
V4015	ML-290	1482500-76-4	ML-290, a 2-acetamido-N-phenylbenzamide analog, is a novel potent, selective and orally bioactive agonist of the relaxin/insulin-like family peptide receptor (RXFP1)and an activator of anti-fibrotic genes with anEC50of 94 nM.
V4010	ML-7	109376-83-2	ML-7 (ML7) is a potent Myosin light chain kinase (MLCK) inhibitor with IC50of 300 nM and IC50>10 μM for MLCK and TRPC6 channel respectively.
V4023	ML132	1230628-71-3	ML132 (also known as NCGC 00185682) is a potent and selectivecaspase 1inhibitor with anIC50of 0.316 nM.
V4225	NSC 77674	737-86-0	NSC77674 (also known as PIH or Pyridoxal isonicotinoyl hydrazone) is is a novel, potent, lipophilic, nontoxic, iron-chelating agent that shows high iron chelation efficacy both in vitro in cell culture models and in vivo in rats and mice.
V4132	PROTAC-VHL-ligand	1448297-52-6	PROTAC-VHL-ligand or Protein degrader 1 is a novel and potent small molecule ligand forVHL (Von Hippel-Lindau), anE3 ligasewhich has been targeted by many PROTACs (proteolysis-targeting chimeras) degarders.