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ITIC

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    64
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ITIC
T193861664293-06-4
ITIC, a non-fullerene acceptor, demonstrates exceptional thermal stability and exhibits a glass-crystal transition at a significantly lower temperature than its high glass transition temperature (Tg) of 180 °C. Furthermore, ITIC, which is an indacenodithienothiophene-based postfullerene electron acceptor, displays a distinct crystallization behavior, differing substantially from that of fullerenes.
  • $1,520
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ITIC-4F
T193852097998-59-7
ITIC-4F, an indacenodithienothiophene (IDTT)-based postfullerene electron acceptor, exhibits wide applicability in high-efficiency binary and ternary single-junction as well as tandem polymer solar cells (PSCs).
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Alkynyl Palmitic Acid
T1418599208-90-9
Alkynyl Palmitic Acid is an alkyl chain-based PROTAC linker that can be used in PROTAC synthesis.
  • $59
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TargetMol | Citations Cited
Citicoline
cytidine diphosphate-choline, cytidine 5'-diphosphocholine, Citicholine, CDP-Choline
T0136987-78-0
Citicoline (CDP-Choline) is an intermediate in the synthesis of phosphatidylcholine, a component of cell membranes. Citicoline exerts neuroprotective effects.
  • $30
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TargetMol | Citations Cited
Citicoline sodium
Citicoline sodium salt, CDP-choline
T120833818-15-4
Citicoline sodium (CDP-choline) is an endogenous intermediate in the synthesis of phosphatidylcholine. It also serves as a choline donor in the biosynthesis of the neurotransmitter acetylcholine. Citicoline sodium demonstrates protective effects in cerebral ischemia, traumatic brain injury, and memory disorders. Exogenous administration of citicoline to rodents (500 mg/kg i.p. immediately after ischemia and at 3-h reperfusion) has been shown to stimulate the synthesis of phosphatidylcholine, sphingomyelin, and cardiolipin and to attenuate the release of arachidonic acid and the accumulation of ceramide.
  • $30
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Aleuritic Acid
Aleuritolic acid, 9,10,16-trihydroxy-palmitic acid
T2886533-87-9
Aleuritic Acid (9,10,16-trihydroxy-palmitic acid), or α-aleuritic acid, is a major ingredient in shellac, constituting about 35% of it. It is used as a starting material in the perfume industry for the preparation of musk aroma.
  • $30
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Palmitic acid
Hexadecoic acid, hexadecanoic acid, Cetylic acid
T290857-10-3
Palmitic acid (Cetylic acid) is a natural product, a common saturated fatty acid found in animals, plants and microorganisms. Palmitic acid has antitumor activity.
  • $48
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TargetMol | Citations Cited
trans-Aconitic acid
T48614023-65-8
Trans-Aconitic acid is normally present in normal human urine, and it has been suggested that is present in larger amounts with Reye's syndrome and organic aciduria. trans-Aconitic acid is a substrate of enzyme trans-aconitate 2-methyltransferase (EC 2.1.
  • $30
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Palmitic acid sodium
Sodium palmitate, Palmitic acid sodium
T77788408-35-5
Palmitic acid sodium (Sodium palmitate) is a type of saturated fatty acid that is formed in fatty acid synthesis.Palmitic acid sodium promotes adipogenesis and cellular lipoatrophy in a variety of cell lines.
  • $30
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Anti-parasitic agent 3
T103282366983-10-8
Anti-parasitic agent 3 is effective against drug-resistant parasites.
  • $2,420
6-8 weeks
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2-Hydroxypalmitic acid
T124257764-67-0
2-Hydroxypalmitic acid is a saturated long-chain 2-hydroxy fatty acid with potential anti-inflammatory, antibacterial, anticancer, and neuroprotective activities, and it can also function as a surfactant.
  • $41
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Isopalmitic acid
T1248254669-02-7
Isopalmitic acid is a useful organic compound for research related to life sciences. The catalog number is T124825 and the CAS number is 4669-02-7.
  • $193
35 days
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Siraitic Acid A
T13885183374-15-4
Siraitic Acid A is a natural product(cucurbitane triterpenoid) isolated from the root of S. grosvenori .
  • $750
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Siraitic Acid B
T13886183374-16-5
Siraitic Acid B is a natural product(cucurbitane triterpenoid) isolated from the root of S. grosvenori .
  • $750
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RP-182-PEG3-K palmitic-acid
RP-182-PEG3-K(palmiTic acid)
T200692
RP-182-PEG3-K palmitic acid (Compound 1a) exhibits anti-tumor activity in a murine B16 melanoma allograft model and suppresses CD206highM2-like macrophages with an IC50 of 3.2 µM, promoting phagocytic action.
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RP-182-PEG3-K(palmitic acid)
T200819
RP-182-PEG3-K palmitic acid (Compound 1a) exhibits antitumor activity in mouse B16 melanoma syngeneic grafts and can inhibit CD206highM2-like macrophages (IC50 = 3.2 µM) while inducing phagocytosis.
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Antiparasitic agent-24
T205381
Antiparasitic agent-24 (Compound 14a) is an antiparasitic compound with EC50 values of 0.005 μM for L. maj, 0.069 μM for L. don, 0.82 μM for T. brucei, and 4.1 μM for T. cruzi.
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Antiparasitic agent-26
T206195
Antiparasitic agent-26 (Compound 8) is an antiparasitic compound that effectively inhibits the growth of Naegleria fowleri, with an IC50 of 22.87 μM (trophozoite stage) and 25.16 μM (cyst stage). It exerts its antiparasitic effects by inducing programmed cell death, which includes cytosolic calcium accumulation, mitochondrial membrane potential collapse, ATP synthesis inhibition, ROS accumulation, and chromatin condensation. Antiparasitic agent-26 can be utilized in research on primary amoebic meningoencephalitis (PAM).
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Antiparasitic agent-25
T206419
Antiparasitic agent-25 (Compounds 11) is an orally active antiparasitic compound. It inhibits the invasion and replication capabilities of parasites and has an irreversible effect on Toxoplasma gondii. The agent significantly reduces the replication rate of Toxoplasma gondii, with an IC50 value of 6.33 μM, and exhibits low cytotoxicity, having a CC50 value of 285 μM.
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Antiparasitic agent-21
T209007
Antiparasitic agent-21 (compound 28) exhibits selective antiparasitic activity against Naegleria fowleri, with an EC50 of 0.92 μM. Additionally, Antiparasitic agent-21 demonstrates excellent blood-brain barrier permeability.
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Antiparasitic agent-22
T209857
Antiparasitic agent-22 (Compound 24) is a broad-spectrum antiparasitic compound that inhibits the procyclic form of T. brucei, L. infantum, and L. tropica with IC50 values of 2.41, 5.95, and 8.98 μM, respectively, and the amastigote form of L. infantum with an IC50 of 8.18 μM. It also shows inhibitory activity against the P. falciparum W2 strain with an IC50 of 0.155 μM. Additionally, Antiparasitic agent-22 exhibits low cytotoxicity in THP1 cells, with a CC50 of 64.16 μM.
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Antiparasitic agent-27
T2125253048504-54-4
Antiparasitic agent-27 (Compound 2) is a potent antiparasitic compound targeting Leishmania infantum with an IC50 of 3.1 μM. It induces cell cycle arrest in the G0/G1 phase and enhances reactive oxygen species (ROS) production to trigger programmed cell death, showing promise for visceral leishmaniasis (VL) research.
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10-14 weeks
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2-Fluoropalmitic acid
2-Fluorohexadecanoic acid
T2184216518-94-8
2-Fluoropalmitic acid (2-Fluorohexadecanoic acid), a fatty acid containing fluorine atoms, serves as a potential therapeutic agent for glioblastoma (GBM) by inhibiting the viability, proliferation, and stem-like phenotype of glioma stem cells (GSCs), suppressing the expression of phosphorylated erk, CD133, and SOX-2, and leading to decreased MMP-2 activity and increased methylation of the MGMT promoter.
  • $626
6-8 weeks
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Palmitic acid-1-13C
T3578957677-53-9
Palmitic acid-13C is intended for use as an internal standard for the quantification of palmitic acid by GC- or LC-MS. Palmitic acid is a 16-carbon saturated fatty acid. It comprises approximately 25% of human total plasma lipids.1 It increases protein levels of COX-2 in RAW 264.7 cells when used at a concentration of 75 μM.2 Palmitic acid is involved in the acylation of proteins to anchor membrane-bound proteins to the lipid bilayer.2,3,4,5,6 |1. Santos, M.J., López-Jurado, M., Llopis, J., et al. Influence of dietary supplementation with fish oil on plasma fatty acid composition in coronary heart disease patients. Ann. Nutr. Metab. 39(1), 52-62 (1995).|2. Lee, J.Y., Sohn, K.H., Rhee, S.H., et al. Saturated fatty acids, but not unsaturated fatty acids, induced the expression of cyclooxygenase-2 mediated through toll-like receptor 4. J. Biol. Chem. 276(20), 16683-16689 (2001).|3. Dietzen, D.J., Hastings, W.R., and Lublin, D.M. Caveolin is palmitoylated on multiple cysteine residues. Palmitoylation is not necessary for localization of caveolin to caveolae. J. Biol. Chem. 270(12), 6838-6842 (1995).|4. Robinson, L.J., and Michel, T. Mutagenesis of palmitoylation sites in endothelial nitric oxide synthase identifies a novel motif for dual acylation and subcellular targeting. Proc. Nat. Acad. Sci. USA 92(25), 11776-11780 (1995).|5. Topinka, J.R., and Bredt, D.S. N-terminal palmitoylation of PSD-95 regulates association with cell membranes and interaction with K+ channel Kv1.4. Neuron 20(1), 125-134 (1998).|6. Miggin, S.M., Lawler, O.A., and Kinsella, B.T. Palmitoylation of the human prostacyclin receptor. Functional implications of palmitoylation and isoprenylation. J. Biol. Chem. 278(9), 6947-6958 (2003).
  • $36
7-10 days
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