All Products

or product name starting with: A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

VU 0650786 is a mGlu3 negative allosteric modulator. VU 0650786 has an mGlu2 IC50 ...

VU 0650991 is a non-competitive GLP-1 antagonist that is orally bioavailable and a...

VU0652925 is a PAR4 antagonist. VU0652925 had a PAC1 IC50 of 43.0 pM (-pIC50±SEM:...

VU0661013 is a novel highly potent and specific inhibitor of myeloid cell leukemia...

VU 1545 is a positive allosteric modulator of metabotropic glutamate receptor type...

VU590 is a small molecule inhibitor of KCNJ1 (IC50 = 294 nM).

VU591 is the first reported selective, small-molecule ROMK inhibitor. It inhibits ...

VU6001192 is a mGlu2 negative allosteric modulator

VU6001376 is a potent and selective mGlu4 PAMs. It has EC50 = 50.1 nM, 50.5% GluMa...

VU6001966 is a potent and selective mGlu2 inhibitor and Negative allosteric modula...

VU6004256 is a novel selective muscarinic receptor M1 positive allosteric modulato...

VU6004909 is a mGlu1 PAM.

VU6005649 is a potent and CNS Penetrant mGlu7/8 Receptor PAM with in vivo efficacy...

VU6007477 is a novel M1 PAM. VU6007477 resulted in good rat M1 PAM potency (EC50 =...

VU6007678 is a muscarinic acetylcholine receptor positive allosteric modulator (PAM).

VU6007705 is a muscarinic acetylcholine receptor positive allosteric modulator (PAM).

VU6008555 is a muscarinic acetylcholine receptor positive allosteric modulator (PAM).

VU6009453 is a novel M4 positive allosteric modulator (PAM). VU6009453 showed good...

VU 6010572 is a negative allosteric modulator (NAM) for mGlu. VU 6010572 has an IC...

VU6010608 is a potent mGlu7 NAM. VU6010608 showed excellent CNS penetration (Kp 1....

VU6012962 is an orally bioavailable and CNS-penetrant metabotropic glutamate recep...

VU6013429 is a mGlu1 PAM.

VU6015929 is a selective discoidin domain receptor inhibitor. VU6015929 potently b...

VU6015929 HCl

VU6015929 is a novel selective discoidin domain receptor 1/2 (DDR1/2) inhibitor, p...

VU6017587 is a novel selective mGlu3 NAM, showing efficacy in tail suspension, ele...

VU625 is a potent and selective inhibitor of aedes aegypti inward rectifier potass...

VU661013 is a MCL-1 Inhibitor Combined with Venetoclax Rescues Venetoclax Resistan...

VU714 Oxalate

VU714 Oxalate is a novel Kir7.1 channel inhibitor. The inward rectifier potassium ...

VU717 is a inhibitor of native Kir4.1 channels in astrocytes.

VU-922 is a bioactive chemical.

VU937 is a negative control for VU041 (GLXC-11938), an inwardly rectifying potassi...

VUF10132 is a full inverse agonist at CXCR3 N3.35A.

VUF 10166 is an antagonist of the serotonin receptor subtype 5-HT3A. It is selecti...

VUF-10214 is a H4 receptor-ligand. In vivo studies in the rat reveal that VUF-1021...

VUF-10214 is a H4 receptor-ligand. In vivo studies in the rat reveal that VUF-1021...

VUF10460 is a histamine H4 receptor agonist.

VUF-10497 is a histamine H4 receptor inverse agonist (pKi = 7.57). VUF-10497 also ...

VUF11211 is a potent CXCR3 antagonist. It acts by extending from the minor pocket ...

VUF-11222 is a high affinity non-peptide CXCR3 agonist (pKi = 7.2).

VUF14480 is a covalent partial agonist that interacts with cysteine 98(3.36) of th...

VUF14481 is a H4 receptor ligand.

VUF14738 is a robust and fatigue-resistant photoswitchable GPCR antagonist.

VUF14862 is a robust and fatigue-resistant photoswitchable GPCR antagonist.

VUF15888 is a novel photoswitchable modulator of the CXCR3 chemokine receptor.

VUF16216 is a CXCR3 ligand which photoswitches from antagonism to agonism.

VUF16620 is a novel photoswitchable modulator of the CXCR3 chemokine receptor.

VUF16839 is a high-affinity non-imidazole histamine H3 receptor agonist.

VUF16839 HCl

VUF16839 is a novel potent non-imidazole histamine H3 receptor agonist with in viv...

VUF 4904 is a bioactive chemical.

VUF 5207 is a bioactive chemical.