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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T77549 | Nurr1 agonist 2 | Others | |
Nurr1 agonist 2 is a Nurr1 agonist with an EC50 value of 0.07 μM. Nurr1 agonist 2 increases the mRNA expression of the Nurr1-regulated genes tyrosine hydroxylase (TH) and vesicular amino acid transporter 2 (VMAT2). Nurr1... | |||
T78088 | Nurr1 agonist 4 | Others | |
Nurr1 agonist 4 (compound 8) serves as a potent Nurr1 agonist, exhibiting an EC50 value of 2.1 μM [1]. | |||
T81634 | Nurr1 agonist 6 | ||
Compound 13, a Nurr1 agonist, exhibits a dissociation constant (Kd) of 1.5 μM and an effective concentration for 50% response (EC50) of 3 μM [1]. | |||
T81632 | Nurr1 agonist 8 | ||
Compound 111 (Nurr1 agonist 8) is a Nurr1 agonist exhibiting an EC50 value of 0.09 μM [1]. | |||
T81633 | Nurr1 agonist 7 | ||
Nurr1 agonist 7 (compound 110) is an agonist targeting the Nurr1 receptor and exhibits an EC50 of 0.12 μM [1]. | |||
T60443 | Nurr1 agonist 1 | ||
Nurr1 agonist 1 is an inverse agonist tool for the neuroprotective transcription factor Nurr1 which is an appealing target to treat neurodegenerative diseases. | |||
T81635 | Nurr1 agonist 5 | ||
Compound 5o, a Nurr1 agonist, exhibits neuroprotective properties as a transcription factor Nurr1 agonist, possessing a dissociation constant (Kd) of 0.5 μM and a half-maximal effective concentration (EC50) of 3 μM [1]. | |||
T83894 | 4A7C-301-Nurr1 Agonist | 4A7C-301-Nuclear Receptor-Related 1 | |
The compound 4A7C-301-Nurr1 agonist is a specific agonist for the nuclear receptor-related 1 (Nurr1). By binding to the Nurr1 ligand-binding domain with an IC50 value of 48.22 nM, it enhances the transcriptional activity... | |||
T78049 | Nurr1 inverse agonist-1 | Others | |
Nurr1 Inverse Agonist-1 is an inverse agonist for the neuroprotective transcription factor Nurr1, serving as a research tool. | |||
T8381 | Amodiaquine | Others , Histone Methyltransferase , Parasite | |
Amodiaquine is a synthetic aminoquinoline, used to treat malaria. | |||
T27620 | IP7e | IP 7e,IP-7e,isoxazolo-pyridinone 7e | Others |
IP7e (isoxazolo-pyridinone 7e) is a Nurr1 activator with an EC50 value of 3.9 nM. | |||
T0381 | Amodiaquine dihydrochloride dihydrate | Amodiaquine hydrochloride,Amodiaquin dihydrochloride dihydrate | Histone Methyltransferase , Parasite , Histamine Receptor |
Amodiaquine dihydrochloride dihydrate (Amodiaquine hydrochloride) is the hydrochloride salt of amodiaquine, an orally active 4-aminoquinoline derivative with antimalarial and anti-inflammatory properties. | |||
T3106 | C-DIM12 | Apoptosis , Others | |
C-DIM12 induced expression of Nurr1-regulated genes. C-DIM12 increased expression of transfected human Nurr1, induced Nurr1 protein expression in primary dopaminergic neurons and enhanced neuronal survival from exposure ... | |||
T35159 | XCT0135908 | XCT 0135908,XCT-0135908 | |
XCT0135908 is a selectivity agonist of RXR -Nurr1 over a broad range of other RXR dimerization partners but with a rather low potency. | |||
T70237 | HX-600 | ||
HX-600 is a synthetic agonist for the RXR-Nurr1 heterodimer complex. HX-600 prevents ischemia-induced neuronal damage. | |||
T22242 | Amodiaquine hydrochloride | ||
Amodiaquine dihydrochloride (Amodiaquin dihydrochloride), a member of the 4-aminoquinoline class, serves as an antimalarial agent and exhibits potent oral activity as a histamine N-methyltransferase inhibitor, displaying... | |||
T69921 | BRF110 | ||
BRF110 is a brain penetrant, potent and selective agonist of nuclear receptor-related 1 (Nurr1):Retinoid X receptor α (RXRα) heterodimer. BRF110 is a neuroprotective agent that prevents dopaminergic neuron demise and str... | |||
T83328 | 4A7C-301 | ||
4A7C-301, a Nurr1 agonist, exhibits potent neuroprotective effects in vitro and markedly mitigates neuropathological abnormalities while enhancing motor and olfactory functions in male mouse models with AAV2-mediated α-s... |