1. Natural Products
  2. Phenols

Phenols

Phenolic compounds are a class of chemical compounds consisting of a hydroxyl group (-OH) bonded directly to an aromatic hydrocarbon group, produced by plants and microorganisms, with variation between and within species. As they are present in food consumed in human diets and in plants used in traditional medicine of several cultures, their role in human health and disease is a subject of research. Some phenols are germicidal and are used in formulating disinfectants. Others possess antioxidative, estrogenic or endocrine disrupting activity.

Phenols (289):

Cat. No. Product Name CAS No. Purity Chemical Structure
  • HY-16561
    Resveratrol 501-36-0 99.70%
    Resveratrol (trans-Resveratrol; SRT501), a natural polyphenolic phytoalexin that possesses anti-oxidant, anti-inflammatory, cardioprotective, and anti-cancer properties. Resveratrol (SRT 501) has a wide spectrum of targets including mTOR, JAK, β-amyloid, Adenylyl cyclase, IKKβ, DNA polymerase. Resveratrol also is a specific SIRT1 activator. Resveratrol is a potent pregnane X receptor (PXR) inhibitor.
    Resveratrol
  • HY-N0005
    Curcumin 458-37-7
    Curcumin (Diferuloylmethane), a natural phenolic compound, is a p300/CREB-binding protein-specific inhibitor of acetyltransferase, represses the acetylation of histone/nonhistone proteins and histone acetyltransferase-dependent chromatin transcription. Curcumin shows inhibitory effects on NF-κB and MAPKs, and has diverse pharmacologic effects including anti-inflammatory, antioxidant, antiproliferative and antiangiogenic activities.
    Curcumin
  • HY-17362
    Vancomycin hydrochloride 1404-93-9 99.66%
    Vancomycin hydrochloride is an antibiotic for the treatment of bacterial infections. It acts by inhibiting the second stage of cell wall synthesis of susceptible bacteria. Vancomycin also alters the permeability of the cell membrane and selectively inhibits ribonucleic acid synthesis.
    Vancomycin hydrochloride
  • HY-A0070A
    Liothyronine 6893-02-3 99.28%
    Liothyronine is an active form of thyroid hormone, which binds to β1 thyroid hormone receptor (TRβ1), and activates its activity.
    Liothyronine
  • HY-N0088
    Apocynin 498-02-2 99.97%
    Apocynin is a selective NADPH-oxidase inhibitor with an IC50 of 10 μM.
    Apocynin
  • HY-100599
    Urolithin A 1143-70-0 98.05%
    Urolithin A, a gut-microbial metabolite of ellagic acid, exerts anti-inflammatory, antiproliferative, and antioxidant properties. Urolithin A induces autophagy and apoptosis, suppresses cell cycle progression, and inhibits DNA synthesis.
    Urolithin A
  • HY-13715
    Norepinephrine 51-41-2 98.08%
    Norepinephrine (Levarterenol; L-Noradrenaline) is a β1-selective adrenergic receptor agonist with EC50 of 5.37 μM.
    Norepinephrine
  • HY-N0077
    Ginkgolic Acid 22910-60-7 99.59%
    Ginkgolic Acid is a natural compound that inhibits SUMOylation with an IC50 of 3.0 μM in in vitro assay.
    Ginkgolic Acid
  • HY-N1362
    Salvianolic acid B 121521-90-2 99.93%
    Salvianolic acid B is an active ingredient of Salvia miltiorrhiza, which has been widely applied in China for the management of various microcirculation-related disorders, such as cardiovascular disease, cerebrovascular disease, and diabetic vascular complication.
    Salvianolic acid B
  • HY-B0447A
    L-Epinephrine Bitartrate 51-42-3 >99.0%
    L-Epinephrine bitartrate is an α-adrenergic and β-adrenergic receptor agonist. L-Epinephrine is a hormone secreted by the medulla of the adrenal glands.
    L-Epinephrine Bitartrate
  • HY-15194
    Dimethylcurcumin 52328-98-0 98.19%
    Dimethylcurcumin (ASC-J9) is an androgen receptor degradation enhancer that effectively suppresses castration resistant prostate cancer cell proliferation and invasion.
    Dimethylcurcumin
  • HY-N0523
    Gallic acid 149-91-7 99.85%
    Gallic acid is an antioxidant which can inhibit both COX-2.
    Gallic acid
  • HY-B0183
    Ellagic acid 476-66-4 99.92%
    Ellagic acid is a natural antioxidant, and acts as a potent and ATP-competitive CK2 inhibitor, with an IC50 of 40 nM and a Ki of 20 nM.
    Ellagic acid
  • HY-N0294
    Protocatechuic acid 99-50-3 99.95%
    Protocatechuic acid is a phenolic compound which exhibits neuroprotective effect.
    Protocatechuic acid
  • HY-N0120A
    Polydatin 27208-80-6 98.95%
    Polydatin (Piceid), extracted from the roots of Polygonum cuspidatum Sieb, a widely used traditional Chinese remedies, possesses anti-inflammatory activity in several experimental models. Polydatin (Piceid) inhibits G6PD and induces oxidative and ER stresses.
    Polydatin
  • HY-13518
    Piceatannol 10083-24-6 98.10%
    Piceatannol is a selective inhibitor of protein tyrosine kinase Syk.
    Piceatannol
  • HY-B0167
    Salicylic acid 69-72-7 >98.0%
    Salicylic acid (2-Hydroxybenzoic acid) inhibits cyclo-oxygenase-2 (COX-2) activity independently of transcription factor (NF-κB) activation.
    Salicylic acid
  • HY-B2136
    Tannic acid 1401-55-4
    Tannic acid is a novel hERG channel blocker with IC50 of 3.4 μM.
    Tannic acid
  • HY-B0388
    Probucol 23288-49-5 99.97%
    Probucol (DH-581) is an anti-hyperlipidemic drug by lowering the level of cholesterol in the bloodstream by increasing the rate of LDL catabolism.
    Probucol
  • HY-N0643
    Carnosol 5957-80-2 99.90%
    Carnosol is a potent Ribosomal S6 Kinase (RSK2) inhibitor that could be useful for treating gastric cancer, with an IC50 of ~5.5 μM.
    Carnosol