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Results for "

Bioassay

" in MedChemExpress (MCE) Product Catalog:

11

Inhibitors & Agonists

2

Natural
Products

1

Isotope-Labeled Compounds

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-W015343

    m-Methoxyphenylacetic acid

    Endogenous Metabolite Others
    3-Methoxyphenylacetic acid (m-Methoxyphenylacetic acid), a m-hydroxyphenylacetic acid (m-OHPAA) derivative, is a phytotoxin in Rhizoctonia solani. 3-Methoxyphenylacetic acid is used to develop a toxin-mediated bioassay for resistance to rhizoctonia root rot .
    3-Methoxyphenylacetic acid
  • HY-W004599
    Bicinchoninic acid
    5+ Cited Publications

    Herbicide Others
    Bicinchoninic acid (compound 8) is an AHAS inhibitor, in an in vivo bioassay targeting the root growth inhibition of rapeseed, at a concentration of 100 μg/mL, it exhibited very low activity, with only a 1.4% root length inhibition rate .
    Bicinchoninic acid
  • HY-112102

    SSHB

    Akt PI3K Endogenous Metabolite Metabolic Disease
    (22S,23S)-Homobrassinolide is one of the most active brassinosteroids in inducing plant growth in various plant bioassay systems. (22S,23S)-Homobrassinolide shows Akt-dependent anabolic activity in rat skeletal muscle cells. Orally active .
    (22S,23S)-Homobrassinolide
  • HY-B0226S

    Nitrofural-13C,15N2

    Isotope-Labeled Compounds Infection
    Nitrofurazone- 13C, 15N2 (Nitrofural- 13C, 15N2) is the 13C and 15N labled Nitrofurazone (HY-B0226) . Nitrofurazone is a potential antibiotic that can be used topically to treat wounds, burns, ulcers and skin infections to combat various microorganisms and to prepare surfactants . Nitrofurazone may affect the ecosystem function in Marine environment and affect the functional processes of epiphytic fauna .
    Nitrofurazone-13C,15N2
  • HY-N7374

    Endogenous Metabolite Infection
    Cyperine is a phytotoxic fungal metabolite that has been found in A. cypericola. It inhibits A. thaliana enoyl-acyl carrier protein reductase (ENR; IC50=89 μM). Cyperine induces necrosis in a panel of nine plant species in a leaf bioassay and inhibits root growth in A. thaliana seedlings (IC50=38.4 μM).
    Cyperin
  • HY-127119

    Endogenous Metabolite Neurological Disease
    Benanserin hydrochloride is a serotonin antagonist with psychopharmacological activity. Benanserin hydrochloride can be used to study specific behavioral manifestations in monitoring systems for drug effects. The effects of Benanserin hydrochloride can be sensitively and effectively assessed, for example, by measuring muscle movement capacity and reaction time. Benanserin hydrochloride is suitable for monitoring specific muscle physiological changes. The biological activity of Benanserin hydrochloride can provide reproducible bioassay parameters for experiments .
    Benanserin hydrochloride
  • HY-167688

    Endogenous Metabolite Cardiovascular Disease
    GSK-1562590 is a uropeptide-II receptor antagonist with high affinity and selectivity. GSK-1562590 exhibits significant antagonistic activity in multiple bioassays and, in contrast, displays relatively sustained receptor binding times. GSK-1562590 can inhibit human urinary peptide-II-induced aortic contraction in rats in experiments, and its effect can last for at least 24 hours .
    GSK-1562590
  • HY-W015343R

    Endogenous Metabolite Others
    3-Methoxyphenylacetic acid (Standard)
  • HY-161818

    PD-1/PD-L1 Inflammation/Immunology
    LLW-018 is a potent PD-1/PD-L1 inhibitor with an IC50 value of 2.61 nM. LLW-018 can interrupt PD-1/PD-L1 interaction with an IC50 value of 0.88 μM by cell-based PD-1/PD-L1 blockade bioassays. LLW-018 has the potential for immunotherapy research .
    LLW-018
  • HY-163559

    HPPD Others
    HPPD-IN-4 (Compound III-29) is a selective inhibitor of HPPD with anIC50 of 0.19 μM. HPPD-IN-4 is primarily used in the study of high-efficiency herbicides .
    HPPD-IN-4
  • HY-130349

    L-656,748

    GABA Receptor Infection
    Emamectin B1a (L-656,748) is a semisynthetic derivative of avermectin B1a that binds to GABA receptors (Ki=17.6 nM in rat brain membranes) and enhances GABA responses. Emamectin B1a acitivates GABAA receptors α1β1γ2, α1β2γ2, and α1β3γ2 with IC50s of 57, 210, and 49.8 nM, respectively. Emamectin B1a also binds to glycine receptors, inhibiting glycine receptors with an IC50=218 nM in rat spinal cord. Emamectin B1a (1.067 ng/mL) caused 90% mortality of S. exigua larvae in foliar spray bioassays and topical application, making it more toxic than avermectin B1.
    Emamectin B1a

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