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oxindole

" in MedChemExpress (MCE) Product Catalog:

26

Inhibitors & Agonists

1

Biochemical Assay Reagents

1

Peptides

11

Natural
Products

2

Isotope-Labeled Compounds

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-Y0061
    Oxindole
    3 Publications Verification

    2-Indolinone

    HIV Endogenous Metabolite Infection Neurological Disease Metabolic Disease Inflammation/Immunology Endocrinology Cancer
    Oxindole (Indolin-2-one) is an aromatic heterocyclic building block. 2-indolinone derivatives have become lead compounds in the research of kinase inhibitors.
    Oxindole
  • HY-59227

    6-Bromo-2-oxindole

    Biochemical Assay Reagents Others
    6-Bromo-2-oxindole is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
    6-Bromooxindole
  • HY-N0901
    Corynoxine
    3 Publications Verification

    Autophagy Neurological Disease Cancer
    Corynoxine, a tetracyclic oxindole alkaloid, is isolated from the hooks of Uncaria rhynchophylla. Corynoxine is a natural autophagy enhancer that promotes the clearance of alpha-synuclein via Akt/mTOR pathway .
    Corynoxine
  • HY-N4157

    mAChR 5-HT Receptor Bacterial Neurological Disease
    Isopteropodine is a positive modulator that selectively acts on muscarinic M1 and 5-HT2 receptors. Isopteropodine has an EC50 of 9.92 μM for acetylcholine and 14.5 μM for 5-HT. Isopteropodine also has antibacterial activity against Gram-positive bacteria, with MICs of 150 μg/mL and 250 μg/mL for Staphylococcus aureus and Bacillus subtilis, respectively. Isopteropodine enhances receptor function by increasing the affinity of agonists for receptors and can also inhibit the growth of specific Gram-positive bacteria, and can be used in cognitive impairment and antibacterial research .
    Isopteropodine
  • HY-W009666

    Dopamine Transporter Others
    6-Chloro-5-(2-chloroethyl)oxindole (Imp Z2) is an impurity of Ziprasidone (HY-14542), a substrate of the human dopamine transporter (hDAT) .
    6-Chloro-5-(2-chloroethyl)oxindole
  • HY-116959

    GHSR Metabolic Disease
    SM-130686 is an oxindole derivative and an active GH secretagogue (GHS). SM-130686 stimulates GH release with a Half-maximum stimulation of 6.3 nM. SM-130686 has an orally active .
    SM-130686
  • HY-N4156

    Others Others
    Pteropodine (compound 3) is a monoterpenoid oxindole alkaloid that can be isolated from Hamelia patens. Pteropodine modulates the functions of M1 muscarinic and 5-HT2 receptors. Pteropodine has antioxidant and antimutagenic properties .
    Pteropodine
  • HY-120720

    Others Cancer
    Isomitraphylline, an oxindole alkaloid, has potent anti-cancer activity .
    Isomitraphylline
  • HY-N9163

    Others Others
    Uncarine A is a oxindole alkaloid, which can be isolated from Ulzcaria berlzaysii F. Muell .
    Uncarine A
  • HY-N16467

    Speciofiline

    Others Cardiovascular Disease Neurological Disease Inflammation/Immunology Cancer
    Uncarine F (Speciofiline) is a pentacyclic oxindole alkaloid found in Uncaria tomentosa. Uncaria alkaloids have wide medicinal properties, including neuroprotective, anticancer, and antihypertensive activities. Uncaria alkaloids may stimulate the immune system, relax smooth muscles, dilate blood vessels, and act as a diuretic. Uncarine F can be used for the researches of cancer, immunology, cardiovascular and neurological disease .
    Uncarine F
  • HY-W746828

    Isotope-Labeled Compounds Others
    Oxindole-3-acetic acid- 13C6 is 13C labeled Oxindole-3-acetic acid .
    Oxindole-3-acetic acid-13C6
  • HY-108444

    VEGFR Cancer
    (Z)-FeCP-oxindole is a selective human vascular endothelial growth factor receptor 2 (VEGFR2) inhibitor with an IC50 value of 200 nM. (Z)-FeCP-oxindole can significantly inhibit VEGFR1 and PDGFRa or b at 10 μM. (Z)-FeCP-oxindole has some anticancer activity, acting on B16 murine melanoma lines with IC50 less than 1 μM .
    (Z)-FeCP-oxindole
  • HY-108444A

    VEGFR Cancer
    (Z)-FeCP-oxindole is a selective human vascular endothelial growth factor receptor 2 (VEGFR2) inhibitor with an IC50 value of 200 nM. (Z)-FeCP-oxindole can significantly inhibit VEGFR1 and PDGFRa or b at 10 μM. (Z)-FeCP-oxindole has some anticancer activity, acting on B16 murine melanoma lines with IC50 less than 1 μM .
    (E)-FeCP-oxindole
  • HY-Y0061R

    2-Indolinone (Standard)

    Reference Standards HIV Endogenous Metabolite Infection Neurological Disease Metabolic Disease Inflammation/Immunology Endocrinology Cancer
    Oxindole (Standard) is the analytical standard of Oxindole. This product is intended for research and analytical applications. Oxindole (Indolin-2-one) is an aromatic heterocyclic building block. 2-indolinone derivatives have become lead compounds in the research of kinase inhibitors.
    Oxindole (Standard)
  • HY-117034

    Others Others
    Rankinidine is an oxindole alkaloid that is isolated from the MeOH extract of the stem of Gelsemium rankinii .
    Rankinidine
  • HY-N0901B

    Autophagy Neurological Disease Cancer
    Corynoxine hydrochloride, a tetracyclic oxindole alkaloid, is isolated from the hooks of Uncaria macrophylla. Corynoxine hydrochloride is a natural autophagy enhancer that promotes the clearance of alpha-synuclein via Akt/mTOR pathway .
    Corynoxine hydrochloride
  • HY-115943

    CDK Cancer
    Anticancer agent 30 (compound 6f-Z), a 3-arylidene-2-oxindole derivative, is a selective CDK2 inhibitor with potent anticancer activity .
    Anticancer agent 30
  • HY-169359

    Ligands for E3 Ligase Others
    4-Methylphenoxyacetic acid-Oxindole-CF3 is the E3 ligase ligand part of L134 (HY-169358). 4-Methylphenoxyacetic acid-Oxindole-CF3 can be utilized in PROTAC synthesis .
    L321
  • HY-114023

    Phosphodiesterase (PDE) Neurological Disease
    BML-288 (compound Oxindole 1) is a potent PDE2 inhibitor with an IC50 value of 40 nM. BML-288 has the potential for the research of osteoarthritis pain .
    BML-288
  • HY-N4157R

    Reference Standards mAChR 5-HT Receptor Bacterial Neurological Disease
    Isopteropodine (Standard) is the analytical standard of Isopteropodine (HY-N4157). This product is intended for research and analytical applications. Isopteropodine is a positive modulator that selectively acts on muscarinic M1 and 5-HT2 receptors. Isopteropodine has an EC50 of 9.92 μM for acetylcholine and 14.5 μM for 5-HT. Isopteropodine also has antibacterial activity against Gram-positive bacteria, with MICs of 150 μg/mL and 250 μg/mL for Staphylococcus aureus and Bacillus subtilis, respectively. Isopteropodine enhances receptor function by increasing the affinity of agonists for receptors and can also inhibit the growth of specific Gram-positive bacteria, and can be used in cognitive impairment and antibacterial research .
    Isopteropodine (Standard)
  • HY-153556

    CDK VEGFR Src Others
    GW297361 is an oxindole CDK inhibitor that elicits a Pho85-selective response in cells. GW297361 inhibits yeast Cdk1 and Pho85 with IC50s of 20 nM and 400 nM in vitro, respectively .
    GW297361
  • HY-Z0036R

    Reference Standards
    N-Acetyl-2-oxindole (Standard) is the analytical standard of N-Acetyl-2-oxindole. This product is intended for research and analytical applications.
    N-Acetyl-2-oxindole (Standard)
  • HY-108444R

    Reference Standards VEGFR Cancer
    (Z)-FeCP-oxindole (Standard) is the analytical standard of (Z)-FeCP-oxindole (HY-108444). This product is intended for research and analytical applications. (Z)-FeCP-oxindole is a selective human vascular endothelial growth factor receptor 2 (VEGFR2) inhibitor with an IC50 value of 200 nM. (Z)-FeCP-oxindole can significantly inhibit VEGFR1 and PDGFRa or b at 10 μM. (Z)-FeCP-oxindole has some anticancer activity, acting on B16 murine melanoma lines with IC50 less than 1 μM .
    (Z)-FeCP-oxindole (Standard)
  • HY-Y0061S

    2-Indolinone-d4

    Isotope-Labeled Compounds Others
    Oxindole-d4 (2-Indolinone-d4) is the deuterium labeled Oxindole (HY-Y0061). Oxindole (Indolin-2-one) is an aromatic heterocyclic building block. 2-indolinone derivatives have become lead compounds in the research of kinase inhibitors.
    Oxindole-d4
  • HY-186155

    AMPK Metabolic Disease
    AMPK activator 19 (Compound 57), alkene oxindole derivative, is an AMPK activator. AMPK activator 19 can be used for the research of diseases that are related to AMPK regulation, such as obesity, dyslipidemia, hyperglycemia, type 1 or type 2 diabetes .
    AMPK activator 19
  • HY-P4948

    Biochemical Assay Reagents Others
    Coumarin-phalloidin is a kind of phalloidin labeled with Coumarin (HY-N0709). Coumarin-phalloidin is a new type of actin probe that can be used for triple immunofluorescence microscopic observation of the cell skeleton .
    Coumarin-Phalloidin

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