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 (190):

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) is a natural phenolic compound with diverse pharmacologic effects including anti-inflammatory, antioxidant, antiproliferative and antiangiogenic activities. Curcumin is an inhibitor of p300 histone acetylatransferase (HATs) and also shows inhibitory effects on NF-κB and MAPKs.
    Curcumin
  • HY-N0088
    Apocynin 498-02-2 99.97%
    Apocynin is a selective NADPH-oxidase inhibitor with an IC50 of 10 μM.
    Apocynin
  • HY-B0447B
    L-Epinephrine 51-43-4 >99.0%
    L-Epinephrine is a hormone secreted by the medulla of the adrenal glands. L-Epinephrine is an α-adrenergic and β-adrenergic receptor agonist.
    L-Epinephrine
  • 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-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-15194
    Dimethylcurcumin 52328-98-0 98.06%
    Dimethylcurcumin (ASC-J9) is an androgen receptor degradation enhancer that effectively suppresses castration resistant prostate cancer cell proliferation and invasion.
    Dimethylcurcumin
  • 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-13518
    Piceatannol 10083-24-6 98.10%
    Piceatannol is a selective inhibitor of protein tyrosine kinase Syk.
    Piceatannol
  • 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-12687
    Tizoxanide 173903-47-4 99.76%
    Tizoxanide is the active metabolite of Nitazoxanide, which is a thiazolide anti-infective compound against anaerobic bacteria, protozoa, and a range of viruses.
    Tizoxanide
  • 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-B0167
    Salicylic acid 69-72-7 >98.0%
    Salicylic 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 >98.0%
    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-N0020
    Echinacoside 82854-37-3 99.52%
    Echinacoside, one of the phenylethanoids isolated from the stems of Cistanche salsa, effectively inhibits Wnt/β-catenin signaling. Echinacoside elicits neuroprotection by activating Trk receptors and their downstream signal pathways. Antiosteoporotic activity.
    Echinacoside
  • HY-100583
    (-)-(S)-Equol 531-95-3 99.82%
    (-)-(S)-Equol is a high affinity ligand for estrogen receptor β with a Ki of 0.73 nM.
    (-)-(S)-Equol
  • HY-16558
    Butein 487-52-5 99.95%
    Butein, isolated from Dalbergia odorifera T. Chen, is a cAMP-specific PDE inhibitor with an IC50 of 10.4 μM for PDE4. Butein is a specific protein tyrosine kinase inhibitor with IC50s of 16 and 65 μM for EGFR and p60c-src in HepG2 cells. Butein sensitizes HeLa cells to Cisplatin through AKT and ERK/p38 MAPK pathways by targeting FoxO3a. Butein is a SIRT1 activator (STAC).
    Butein
  • HY-N0523
    Gallic acid 149-91-7 99.97%
    Gallic acid is an antioxidant which can inhibit both COX-2.
    Gallic acid
  • HY-14617
    Paradol 27113-22-0 99.88%
    Paradol is a pungent phenolic substance found in ginger and other Zingiberaceae plants. Paradol is an effective inhibitor of tumor promotion in mouse skin carcinogenesis, binds to cyclooxygenase (COX)-2 active site.
    Paradol