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Results for "

g-108

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    7
    TargetMol | All_Pathways
  • Compound Libraries
    1
    TargetMol | Compound_Libraries
  • Inhibitory Antibodies
    1
    TargetMol | Inhibitory_Antibodies
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    2
    TargetMol | Recombinant_Protein
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    TargetMol | Antibody_Products
G108
G-108, G 108
T696632369750-66-1In house
G108 is an inhibitor of human cGAS and is used in the study of autoimmune diseases associated with human cGAS.
  • $490
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Inixaciclib
T696622370913-42-9
Inixaciclib is a potent CDK inhibitor, utilized in anticancer research.
  • $1,970
8-10 weeks
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SR 57227 hydrochloride
SR 57227A, SR 57227 hydrochloride
T2339477145-61-0
SR 57227 hydrochloride(SR 57227A ) is a potent, orally active and selective 5-HT3 receptor agonist. It with ability to cross the blood brain barrier. It has affinities (IC50) varying between 2.8 and 250 nM for 5-HT3 receptor binding sites in rat cortical membranes and on whole NG 108-15 cells or their membranes. Anti-depressant effects.
  • $30
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TargetMol | Inhibitor Sale
RG108
N-Phthalyl-L-tryptophan
T203848208-26-0
RG108 (N-Phthalyl-L-tryptophan) is a DNA methyltransferase inhibitor with an IC50 of 115 nM.
  • $39
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TargetMol | Citations Cited
(Rac)-RG108
(Rac)-N-Phthalyl-L-tryptophan
T20676132675-71-1
(Rac)-RG108 (NSC401077) is an inhibitor of DNMT1, effectively blocking DNA methyltransferases.
  • Inquiry Price
10-14 weeks
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Sarizotan
EMD 128130
T40439351862-32-3
Sarizotan (EMD 128130) is an orally active compound that acts as an agonist for serotonin 5-HT 1A receptors and dopamine receptors, with IC50 values of 6.5 nM for rat 5-HT 1A, 0.1 nM for human 5-HT 1A, 15.1 nM for rat D 2, 17 nM for human D 2, 6.8 nM for human D 3, and 2.4 nM for human D 4.2.
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    H-Arg-Gly-Asp-Cys-OH (trifluoroacetate salt)
    T35582
    H-Arg-Gly-Asp-Cys-OH is a tetrapeptide that contains the arginine-glycine-aspartate (RGD) motif, a sequence that acts as a recognition site for various adhesion proteins.1It inhibits the binding of fibrinogen to endothelial cells and ADP-stimulated platelets with IC50values of 320 and 35 μM, respectively.2Implantation of titanium rods coated with H-Arg-Gly-Asp-Cys-OH increases bone formation in rat femurs.3H-Arg-Gly-Asp-Cys-OH has been conjugated to polyethylenimine to improve gene transfection efficiency.4 1.Park, H.S., Kim, C., and Kang, Y.K.Preferred conformations of RGDX tetrapeptides to inhibit the binding of fibrinogen to plateletsBiopolymers63(5)298-313(2002) 2.Tranqui, L., Andrieux, A., Hudry-Clergeon, G., et al.Differential structural requirements for fibrinogen binding to platelets and to endothelial cellsJ. Cell Biol.108(6)2519-2527(1989) 3.Ferris, D.M., Moodie, G.D., Dimond, P.M., et al.RGD-coated titanium implants stimulate increased bone formation in vivoBiomaterials20(23-24)2323-2331(1999) 4.Kunath, K., Merdan, T., Hegener, O., et al.Integrin targeting using RGD-PEI conjugates for in vitro gene transferJ. Gene Med.5(7)588-599(2003)
    • $73
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