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Results for "

T3698

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    5
    TargetMol | All_Pathways
  • Natural Products
    1
    TargetMol | Natural_Products
  • Oligonucleotides
    1
    TargetMol | All_Pathways
alpha-Asarone
α-Asarone, trans-Asarone
T36982883-98-9
alpha-Asarone (trans-Asarone) is a psychoactive compound with antidepressant-like activity in mice.
  • $29
In Stock
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CCT369834
CCT-369834, CCT 369834
T202023
CCT369834 is a KIFC1 probe labeled with (TCO) and includes a butynyl linker.
  • Inquiry Price
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Cyclic-di-GMP disodium
cyclic diguanylate disodium, Cyclic di-GMP (sodium salt), c-di-GMP disodium, 5GP-5GP disodium, 3',5'-Cyclic diguanylic acid
T369832222132-40-1
Cyclic-di-GMP disodium (5GP-5GP disodium) is a STING agonist and a second messenger in bacteria. It is involved in a variety of processes in prokaryotes, including biofilm formation, motility, and cell cycle progression. Cyclic-di-GMP disodium (5GP-5GP disodium) exhibits antiproliferative activity against cancer cells, inducing increased CD4 receptor expression and cell cycle arrest, and is a novel therapeutic agent that can be developed to prevent or treat cancer.
  • $139
In Stock
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TargetMol | Inhibitor Hot
GSK 591 dihydrochloride
T369812320953-89-5
Potent and selective PRMT5 inhibitor (IC50 = 4 nM). Selective for PRMT5 over a panel of other PRMTs and lysine methyltransferases. Inhibits proliferation of mantle cell lymphoma (MCL) in vitro. To request the negative control for GSK 591, please fill out the SGC 2096 request form on the SGC website.
  • $1,330
35 days
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CXCR3 Antagonist 6c
T36982870998-13-3
CXCR3 antagonist 6c is an antagonist of chemokine (C-X-C motif) receptor 3 (CXCR3).1It inhibits calcium mobilization induced by chemokine (C-X-C motif) ligand 11 (CXCL11) in HEK293 cells expressing the human receptor (IC50= 0.06 μM). It is selective for CXCR3 over a panel of 14 human G protein-coupled receptors at 10 μM. CXCR3 antagonist 6c inhibits CXCR3-mediated migration of isolated human T cells (IC50= ~100 nM). 1.Cole, A.G., Stroke, I.L., Brescia, M.-R., et al.Identification and initial evaluation of 4-N-aryl-[1,4]diazepane ureas as potent CXCR3 antagonistsBioorg. Med. Chem. Lett.16(1)200-203(2006)
  • $178
35 days
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