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Results for "

1,3-bis(4-chloro-3-(trifluoromethyl)phenyl)urea

" in TargetMol Product Catalog
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1,3-Bis(4-chloro-3-(trifluoromethyl)phenyl)urea
T64474370-50-3
1,3-Bis(4-chloro-3-(trifluoromethyl)phenyl)urea is a useful organic compound for research related to life sciences. The catalog number is T64474 and the CAS number is 370-50-3.
    7-10 days
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    Corticosterone
    Kendall's compound B, Corticosterone (From plants), 17-Deoxycortisol, 11β,21-Dihydroxyprogesterone
    T0948L50-22-6
    Corticosterone (Kendall's compound B) is an adrenocortical steroid with salocorticoid and glucocorticoid activity that is orally active. Corticosterone is involved in the regulation of energy, immune responses, and stress responses in the body.
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    TargetMol | Inhibitor Hot
    deoxynivalenol
    Vomitoxin, 4-Deoxynivalenol
    T1509751481-10-8
    Deoxynivalenol (Vomitoxin) is a mycotoxin produced by Fusarium spp. of the single trichothecene family and is commonly found in contaminated food and feed.Deoxynivalenol crosses the intestinal mucosa via a cellular bypass at the tight junctions.Deoxynivalenol transporters are unaffected by inhibitors of P-glycoprotein (PgP) or multidrug resistance-associated protein (MRP). Deoxynivalenol commonly causes diarrhea, vomiting, and gastrointestinal inflammation in humans and animals.
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    7-10 days
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    TargetMol | Inhibitor Hot
    Resveratrol
    trans-Resveratrol, SRT 501
    T1558501-36-0
    Resveratrol (SRT 501) is a polyphenolic natural product, a plant antitoxin with antioxidant and chemopreventive activities. Resveratrol has a wide range of targets including COX, SIRT, LOC, etc. Resveratrol induces autophagy and apoptosis.
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    Dinaciclib
    SCH 727965, PS-095760
    T1912779353-01-4
    Dinaciclib (SCH 727965) is a selective CDK inhibitor targeting CDK1, CDK2, CDK5, and CDK9 (IC50 = 3 1 1 4 nM). It exhibits potential antitumor activity by inhibiting the incorporation of thoracic glycan (dThd) DNA.
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    Puromycin dihydrochloride
    Puromycin 2HCl, CL13900 dihydrochloride
    T221958-58-2
    Puromycin dihydrochloride (CL13900 dihydrochloride) is a cinnamamide adenosine antibiotic and an inhibitor of protein synthesis. Puromycin dihydrochloride inhibits protein synthesis by binding to RNA and has antitumor and antitrypanosomal activity.
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    TargetMol | Inhibitor Hot
    (E)-Daporinad
    FK866, Daporinad, APO866, (E)-N-[4-(1-BENZOYL-PIPERIDIN-4-YL)-BUTYL]-3-PYRIDIN-3-YL-ACRYLAMIDE
    T2644658084-64-1
    (E)-Daporinad (FK866) is a highly specific, non-competitive small molecule inhibitor of nicotinamide phosphoribosyltransferase (NAMPT) with potential anti-tumor and anti-angiogenic activities with an IC50 value of 0.09 nM.
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    Palmatine chloride
    T271810605-02-4
    Palmatine chloride an isoquinoline alkaloid, is an important medicinal herbal extract with diverse pharmacological and biological properties.
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    TargetMol | Inhibitor Hot
    Citronellol
    dihydrogeraniol
    T3240106-22-9
    Citronellol ((±)-β-Citronellol) is used in insect repellents and perfumes and as a mite attractant.
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    TargetMol | Inhibitor Hot
    Arachidonic acid
    Vevodar, Immunocytophyte, Immunocytophyt, arachidonate
    T4129506-32-1
    Arachidonic acid (Immunocytophyte) is an unsaturated, essential fatty acid. It is found in animal and human fat as well as in the liver, brain, and glandular organs, and is a constituent of animal phosphatides. It is formed by the synthesis from dietary linoleic acid and is a precursor in the biosynthesis of prostaglandins, thromboxanes, and leukotrienes.
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    Dehydrocorydaline
    Dehydrocorydalin, 13-Methylpalmatine
    T5S235830045-16-0
    1. Dehydrocorydaline (13-Methylpalmatine) exerts anti-metastatic potential via suppression of MMPs and Bcl-2 signaling in NSC-LC cells. 2. Dehydrocorydaline stimulates p38 MAPK activation, which can enhance heterodimerization of MyoD and E proteins, thus resulting in MyoD activation and myoblast differentiation. 3. Dehydrocorydaline shows antiplatelet effects, it inhibits thrombin-induced platelet aggregation in a low dose ( IC50= 34.914 ug mL). 4. Dehydrocorydaline has anti-inflammatory and antinociceptive effects. 5. Dehydrocorydaline inhibits MCF-7 cell proliferation by inducing apoptosis mediated by regulating Bax Bcl-2, activating caspases as well as cleaving PARP.
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    TargetMol | Inhibitor Hot
    Valproic Acid
    VPA, Sodium valproate, Depakine, 2-Propylvaleric Acid, 2-Propylpentanoic Acid
    T706499-66-1
    Valproic Acid (2-Propylpentanoic Acid) is an HDAC inhibitor that inhibits HDAC1 activity, induces HDAC2 degradation, and is orally active. Valproic Acid can be used in epilepsy and bipolar disorder research.
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    GPR34 receptor antagonist 2
    Tyrosine, N-[(2E)-3-(4'-chloro[1,1'-biphenyl]-4-yl)-1-oxo-2-propen-1-yl]-O-(phenylmethyl)-, gpr34-receptor-antagonist-2
    T8848907952-06-1
    GPR34 receptor antagonist 2 (Tyrosine, N-[(2E)-3-(4'-chloro[1,1'-biphenyl]-4-yl)-1-oxo-2-propen-1-yl]-O-(phenylmethyl)-) is an anti-inflammatory agent.
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    Gardenin A
    TN411421187-73-5
    Gardenin A shows neurotrophic effects via activating MAPK ERK, PKC, and PKA. Gardenin A exhibits antidepressant, anticonvulsant and anxiolytic effects.
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    TargetMol | Inhibitor Hot
    Wighteone
    Erythrinin B, 6-Isopentenylgenistein
    TN525451225-30-0
    Wighteone (Erythrinin B) is a small molecule compound derived from Genista ephedroides with potential antifungal and anticancer activity against EGFR L858R T790M mutant non-small cell lung cancer.
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    7-10 days
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    TargetMol | Inhibitor Hot
    Phorbol 12-myristate 13-acetate
    PMA
    TQ019816561-29-8
    Phorbol 12-myristate 13-acetate (PMA), a member of the phorbol ester group of natural products, activates PKC, SphK, and NF-κB, and induces THP1 cell differentiation.
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    TargetMol | Inhibitor Hot
    1-PeCSO
    S-1-Propenyl-L-cysteine sulfoxide
    T100253836-24-6In house
    1-PeCSO is isolated from onion or garlic bulbs. It acts as a key compound in garlic greening and reacts with lachrymatory factor synthase.
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    8-10 weeks
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    Asperphenamate
    T1039063631-36-7In house
    Asperphenamate is a fungal metabolite of Aspergillus flatiipes. The IC50s for T47D cells, MDA-MB-231 cells, and HL-60 cells are 92.3 μM, 96.5 μM, and 97.9 μM. Asperphenamate shows an anticancer effect.
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    6-8 weeks
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    Xanthine oxidase-IN-1
    4-(3-Cyano-5,6-difluoroindol-1-yl)-2-hydroxybenzoic acid
    T105091071970-13-2In house
    Xanthine oxidase-IN-1 is an effective inhibitor of xanthine oxidase with an IC50 value of 6.5 nM. It plays a central role in purine catabolism through the degradation of bioactive nucleotides facilitated by nucleic acid and nucleotide intermediates.
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    8-10weeks
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    gamma-secretase modulator 1
    N-[3-methoxy-4-(4-methylimidazol-1-yl)phenyl]-4-phenyl-4,5,6,7-tetrahydro-1,3-benzothiazol-2-amine
    T113581172637-87-4In house
    gamma-secretase modulator 1 is a modulator of γ secretase and can be used in studies about the treatment of Alzheimer's disease.
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    6-8 weeks
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    (4R)-RO5263397
    T12745L1357266-80-8In house
    (4R)-4-(3-Fluoro-2-methylphenyl)-4,5-dihydro-2-oxazolamin was active against TRACE AMINE ASSOCIATED RECEPTOR (TAAR 1) with an EC50 of 0.017 μM and could be used to study neurological disorders.
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    Apricitabine
    AVX754, SPD754
    T14313160707-69-7In house
    Apricitabine (SPD754) is a highly selective and orally active HIV-1 reverse transcriptase inhibitor (Ki=0.08 μM), the (-) enantiomer of 2′-deoxy-3′-oxy-4′-thiocytidine (dOTC) . Apricitabine inhibits DNA polymerase α, β and γ with Ki values of 300 μM, 12 μM and 112.25 μM, respectively. Apricitabine has shown good antiretroviral therapeutic efficacy in antiretroviral HIV-infected patients, with good tolerability and low selective resistance.
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    6-8weeks
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    Rutin hydrate
    Rutoside, Sophorin, Quercetin-3-O-rutinoside
    T22417190836-14-7In house
    Rutin hydrate (Sophorin), a kind of glycoside, widely exists in many plants including citrus fruit.
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    (Iso)-Rilmakalim
    T26086L184653-89-2In house
    1-((3R,4S)-3-hydroxy-2,2-dimethyl-6-(phenylsulfonyl)chroman-4-yl)pyrrolidin-2-one is an isomer of Rilmakalim, a potassium channel opener (PCO), which can activate ATP-sensitive K+ channels in the heart or other tissues
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