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Results for "

4′ hydroxy 2′ methylacetophenone

" in TargetMol Product Catalog
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4′-Hydroxy-2′-methylacetophenone
T36738875-59-2
4′-Hydroxy-2′-methylacetophenone, a red wine aroma compound isolated from the cv. Bobal grape variety, exhibits ciliate toxicity and inhibits T. pyriformis growth with an IC50 of 0.65 mM[1][2].
    7-10 days
    Inquiry
    2'-Hydroxy-4'-methylacetophenone
    Fr142986921-64-8
    2'-Hydroxy-4'-methylacetophenone, a phenolic compound isolated from Angelicae koreana roots, possesses acaricidal properties and can be used in the preparation of 4'-methyl-2'-[(p-tolylsulfonyl)oxy]acetophenone.
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    Staurosporine
    CGP 41251, Antibiotic AM-2282, AM-2282
    T668062996-74-1
    Staurosporine (AM-2282) is a protein kinase inhibitor with ATP-competitive and non-selective inhibitory activity (IC50=6 15 2 3 3000 nM) against PKC, PKA, c-Fgr, phosphorylase kinase and TAOK2. Staurosporine also induces apoptosis.
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    TargetMol | Inhibitor Hot
    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
    Paclitaxel
    Taxol, NSC 125973
    T096833069-62-4
    Paclitaxel (Taxol) is a natural product and a microtubule polymer stabilizer. Paclitaxel has anti-tumor activity and causes cell death by inducing mitotic arrest, apoptosis, and cell autophagy.
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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.
    • Inquiry Price
    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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    TargetMol | Inhibitor Hot
    PCO371
    2,4-Imidazolidinedione, 1-(3,5-dimethyl-4-(2-((4-oxo-2-(4-(trifluoromethoxy)phenyl)-1,3,8-triazaspiro(4.5)dec-1-en-8-yl)sulfonyl)ethyl)phenyl)-5,5-dimethyl-
    T164421613373-33-3
    PCO371 (2,4-Imidazolidinedione, 1-(3,5-dimethyl-4-(2-((4-oxo-2-(4-(trifluoromethoxy)phenyl)-1,3,8-triazaspiro(4.5)dec-1-en-8-yl)sulfonyl)ethyl)phenyl)-5,5-dimethyl-) is an orally active full agonist of parathyroid hormone receptor 1. It has no effect on PTH type 2 receptor.
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    TargetMol | Inhibitor Hot
    3-Methyladenine
    NSC 66389, 3-MA
    T18795142-23-4
    3-Methyladenine (3-MA) is a PI3K inhibitor that selectively inhibits class IB PI3Kγ (IC50 = 60 μM) and class III VPS34 (IC50 = 25 μM). 3-Methyladenine inhibits autophagy.
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    TargetMol | Inhibitor Hot
    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
    Orellanine
    2-(1,3-dihydroxy-4-oxopyridin-2-yl)-1,3-dihydroxypyridin-4-one
    T3381737338-80-0
    Orellanine is a nephrotoxic compound extracted from the mushroom Cortinarius orellanus. Orellanine strongly inhibits the synthesis of macromolecules (Proteins, RNA and DNA) in Madin-Darby canine kidney cells and in rat liver mitochondria.
    • Inquiry Price
    6-8 weeks
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    TargetMol | Inhibitor Hot
    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
    Bleomycin Sulfate
    NSC125066, Blenoxane
    T61169041-93-4
    Bleomycin Sulfate (Blenoxane) is a glycopeptide antibiotic, an inhibitor of DNA synthesis. Bleomycin Sulfate causes DNA strand breaks but not RNA strand breaks. Bleomycin Sulfate has antitumor activity.
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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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    TargetMol | Inhibitor Hot
    Taurocholic acid
    N-Choloyltaurine
    TN225981-24-3
    Taurocholic acid (N-Choloyltaurine) is a bile acid involved in the emulsification of fats.Taurocholic acid is cytoprotective, preventing tumor necrosis factor-alpha-induced cholangiocyte damage via a PI3K-mediated pathway.
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    TargetMol | Inhibitor Hot
    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.
    • Inquiry Price
    8-10 weeks
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    7-Chlorokynurenic acid
    7-CKA, 7-chloro-4-hydroxy-2-carboxyquinoline
    T10191L18000-24-3In house
    7-Chlorokynurenic acid (7-chloro-4-hydroxy-2-carboxyquinoline) is an effecitve and selective antagonist of NMDA receptor with IC50 of 0.56 μM for the glycine B coagonist site. 7-Chlorokynurenic acid inhibits the reuptake of glutamate into synaptic vesicles with a Ki of 0.59 μM and shows antinociceptive actions after neuraxial delivery.
    • Inquiry Price
    4-6 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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    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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    Ro 09-0680
    Ro-09-0680, Ro 09 0680
    T2855187112-49-0In house
    Ro 09-0680, a compound derived from Salvia miltiorrhiza, is a potent inhibitor of collagen-induced platelet aggregation in rabbits with potential anti-inflammatory activity for the study of cardiovascular disease.
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    7-10 days
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