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Results for "

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  • Inhibitors & Agonists
    50
    TargetMol | Inhibitors_Agonists
  • Peptide Products
    1
    TargetMol | Peptide_Products
  • Natural Products
    15
    TargetMol | Natural_Products
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    1
    TargetMol | Recombinant_Protein
Omaveloxolone
RTA-408
T69191474034-05-3
Omaveloxolone (RTA-408) (RTA-408) is a synthetic triterpenoid that activates the cytoprotective transcription factor Nrf2 and inhibits NF-κB signaling. Phase 2.
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Vadimezan
NSC 640488, DMXAA, ASA-404, 5,6-Dimethylxanthenone-4-acetic Acid
T6273117570-53-3
Vadimezan (DMXAA) is a vascular disrupting agent, a murine STING agonist, and an inducer of cytokines such as type I IFN. Vadimezan has antitumor activity and induces a rapid cessation of blood flow in tumors without affecting blood flow in normal tissues.
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MSA-2
T8798129425-81-6
MSA-2 is an orally available non-nucleotide STING agonist. The non-covalent dimer of MSA-2 binds to STING with nanomolar affinity. It shows anti-tumor activity in syngeneic mouse tumor models, synergizes with anti-PD-1, stimulates tumor secretion of interferon-β, induces tumor regression, and has long-lasting anti-tumor immunity. [3]
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SR-717
T86552375421-09-1
SR-717 is a cGAMP analog, a non-nucleoside STING agonist that induces a closed activation conformation of STING. SR-717 has antitumor activity and promotes activation of immune cells and cross-presentation of antigens.
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C-176
STING inhibitor 1, C176
T5154314054-00-7
C-176 (STING inhibitor 1) is a STING inhibitor with selectivity and blood-brain barrier permeability. C-176 inhibits STING-mediated IFNβ production and possesses anti-inflammatory activity.
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H-151
T5674941987-60-6
H-151 is a highly potent and selective STING antagonist. H-151 covalently binds to Cys91 of STING and inhibits palmitoylation of Cys91, thereby inhibiting STING activity. H-151 can be used in the study of autoinflammatory diseases in vivo and ex vivo.
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TargetMol
diABZI STING agonist-1 trihydrochloride
T55162138299-34-8In house
diABZI STING agonist-1 (trihydrochloride) is a stimulator of interferon genes (STING) receptor agonist.
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CCCP
Carbonyl Cyanide m-Chlorophenylhydrazone, Carbonyl cyanide 3-chlorophenylhydrazone
T7081555-60-2
CCCP (Carbonyl Cyanide m-Chlorophenylhydrazone) is an oxidative phosphorylation (OXPHOS) inhibitor and mitochondrial proton carrier uncoupler. CCCP inhibits the activation of STING and its downstream signaling molecules TBK1 and IRF3.
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ADU-S100 ammonium salt
ML RR-S2 CDA ammonium salt, MIW815 ammonium salt
T10252L21638750-96-5
ADU-S100 ammonium salt is an activator of stimulator of interferon genes (STING). ADU-S100 ammonium salt leads to potent and systemic tumor regression and immunity.
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6-8 weeks
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diABZI STING agonist-1 (Tautomerism)
diABZI STING agonist (Compound 3)
T110352138498-18-5
diABZI STING agonist-1 (Tautomerism) (diABZI STING agonist (Compound 3)) is a selective stimulator of interferon genes (STING) receptor agonist, with EC50s of 130, 186 nM for human and mouse, respectively.
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Nerisopam
EGIS-6775, GYKI 52322, GYKI52322, EGIS6775, GYKI-52322
T28159102771-12-0In house
Nerisopam is an agonist of gamma-aminobutyric acid (GABA) receptor.
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6-8weeks
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Enerisant HCl
T704891152749-07-9In house
Enerisant HCl is a novel potent and selective histamine H3 receptor antagonist, a substrate for P-gp, mediated by cytochrome P450 (CYP) and transporter proteins.
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6-8 weeks
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Inaperisone
T6808799323-21-4In house
Inaperisone is a novel centrally acting muscle relaxant that inhibits the voiding reflex. Inaperisone may inhibit the voiding reflex by acting indirectly on GABAB receptors in the brainstem.
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Silperisone HCl
RGH5002, SILA336, RGH-5002, Silperisone hydrochloride, SILA-336
T28778140944-30-5In house
Silperisone HCl (RGH-5002) blocks sodium and calcium channels in cells, decreases excitability and contractility of muscle cells, reduces peripheral tone, and acts as a muscle relaxant and peripheral vasodilator. Silperisone HCl is used to treat recurrent painful myoclonus due to spinal cord injury, abnormal hypertonia due to cerebrovascular disease, dystonia symptoms, cone tension syndrome, multiple sclerosis myospasm and myelitis. silperisone is a sodium channel protein type 2 alpha channel blocker. silperisone is an organosilicon similar to tolperisone, an organosilicon compound with centrally acting muscle relaxant properties.
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6-8weeks
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Lanperisone HCl
NK 433
T71356116287-13-9In house
Lanperisone HCl (NK 433) is a novel orally available centrally acting muscle relaxant with anticancer activity and inhibits mono- and polysynaptic reflex potentials.Lanperisone HCl acts by inducing non-apoptotic cell death in the cell cycle and translational independence.
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6-8 weeks
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Tolperisone hydrochloride
Tolperisone HCl, Muscalm, Midocalm
T05113644-61-9
Tolperisone hydrochloride (Muscalm), a centrally acting muscle relaxant, is used in the therapy of pathologically increased tone of the cross-striated muscle resulted by neurological diseases (damage of the encephalomyelitis, myelopathy, multiple sclerosis, pyramidal tract) and of spastic paralysis and other encephalopathies manifested with muscular dystonia.
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Eperisone hydrochloride
T500556839-43-1
Eperisone is a skeletal muscle relaxant and a spasmolytic agent related structurally to Tolperisone.
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Pterisolic acid B
T125924
Pterisolic acid B is a useful organic compound for research related to life sciences and the catalog number is T125924.
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Asteriscunolide A
T124126
Asteriscunolide A is a useful organic compound for research related to life sciences and the catalog number is T124126.
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Perisesaccharide C
TN20571311473-28-5
Perisesaccharide C is a natural product
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Lerisetron
T8441143257-98-1
Lerisetron is an antagonist of serotonin type 3 (5-HT3) receptor, with antiemetic activity.
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Perisesaccharide B
TN20561095261-93-0
Perisesaccharide B is a natural product
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Monnieriside A
T125921
Monnieriside A is a useful organic compound for research related to life sciences and the catalog number is T125921.
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Lanperisone
T32561116287-14-0
Lanperisone is a muscle relaxant.
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1-2 weeks
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