1. Others

Others

There are a number of inhibitors, agonists, and antagonists which we cannot make precise classification because the research area is still unknown.

Others Related Products (73764):

Cat. No. Product Name CAS No. Purity Chemical Structure
  • HY-119825
    Sarracine 2492-09-3 98%
    Sarracine is a Alkaloids product that can be isolated from the herbs of Senecio scandens..
    Sarracine
  • HY-119845
    Agamanone 143381-59-3 98%
    Agamanone is an active compound.
    Agamanone
  • HY-119863
    Barthrin 70-43-9 98%
    Barthrin is a pyrethroid insecticide. The toxicity of Barthrin to housefly (Musca domestica L.) at the 50% mortality level is 14 % of that of Barthrin (HY-B1559).
    Barthrin
  • HY-119955
    Amflutizole 82114-19-0 98%
    Amflutizole (LY-141894) is an inhibitor of xanthine oxidase. Amflutizole abolishes free radical formation and release in cerebral ischemia/reperfusion mice.
    Amflutizole
  • HY-119984
    DNP-INT 69311-70-2 98%
    DNP-INT is a potent photosynthetic electron transport chain (PETC) inhibitor. DNP-INT competently inhibits the oxidation of plastid quinoline by binding to the Q0 site of Cyt-b6f (Kd=1.4 nM), thereby inhibiting electron transfer in plants.
    DNP-INT
  • HY-119987
    Sudan orange G 2051-85-6 98%
    Sudan orange G is an azo dye. Sudan orange G, after enzymatic oxidation, generates oligomers and even polymers through free radical coupling reactions.
    Sudan orange G
  • HY-120021
    tert-Butyl 4-(1H-indol-4-yl)piperazine-1-carboxylate 252978-89-5 98%
    tert-Butyl 4-(1H-indol-4-yl)piperazine-1-carboxylate is a synthetic intermediate useful for pharmaceutical synthesis..
    tert-Butyl 4-(1H-indol-4-yl)piperazine-1-carboxylate
  • HY-120042
    Heptenophos 23560-59-0 98%
    Heptenophos is an inhibitor of AChE and plasma carboxylesterase (CES). By inhibiting AChE activity, Heptenophos causes the accumulation of acetylcholine at cholinergic synapses, thereby triggering typical symptoms of organophosphate poisoning. Heptenophos exhibits rapid lethal toxicity in male albino mice, but its toxic effects are effectively antagonized by obidoxime, and Memantine (HY-B0591) further enhances the detoxification efficacy of obidoxime. Therefore, Heptenophos is commonly used in studies related to the mechanism of organophosphate poisoning and detoxification strategies.
    Heptenophos
  • HY-120047
    Rutamarin 13164-05-1 98%
    Rutamarin ((+)-Rutamarin) is a natural product.
    Rutamarin
  • HY-12008Y
    Erlotinib impurity 45 183321-83-7 98.71%
    Erlotinib impurity 45 is an impurity of Erlotinib (HY-50896).
    Erlotinib impurity 45
  • HY-12008Z
    Erlotinib impurity 44 183321-85-9 98.60%
    Erlotinib impurity 44 is an impurity of Erlotinib (HY-50896).
    Erlotinib impurity 44
  • HY-120106
    BG14 1628784-50-8 98%
    BG14 is a chemical optical modulation of epigenetic regulation of transcription (COMET) probe. BG14 enables high-resolution optical control of epigenetic mechanisms using visible light and can photochromically inhibit human histone deacetylases (HDACs). BG14 can be used to study the dynamic regulation of the human genome.
    BG14
  • HY-120187
    DDCPPB-Glu 149325-95-1 98%
    DDCPPB-Glu (compound 3a) is a compound with anti-tumor activity, which has the activity of inhibiting tumor cell growth and prolonging survival. DDCPPB-Glu has growth inhibition effect on various tumor cell lines, can increase the survival time of leukemia mice, and has inhibitory effect on tumors such as colon cancer and lung cancer.
    DDCPPB-Glu
  • HY-120188
    CC618 1680204-90-3 99.94%
    CC618 is a selective PPARβ/δ antagonist. CC618 covalently modifies conserved Cys249 in the PPARβ/δ ligand-binding pocket via nucleophilic aromatic substitution, converting its thiol moiety to a 5-trifluoromethyl-2-pyridylthioether.
    CC618
  • HY-120201
    7-Hydroxy coumarin glucuronide sodium 168286-98-4 98%
    7-Hydroxy coumarin glucuronide sodium is a benzopyrone and a metabolite of 7-hydroxy coumarin.
    7-Hydroxy coumarin glucuronide sodium
  • HY-120209
    Pigment Yellow 13 5102-83-0 98%
    Pigment Yellow 13 is an active compound.
    Pigment Yellow 13
  • HY-120240
    AND-302 1380201-88-6 98%
    AND-302 is a small molecule anticonvulsant with activity in preventing glutamate- or hydrogen peroxide-induced cell death and decreased neuronal viability in in vitro hippocampal cultures.
    AND-302
  • HY-120247
    TASP0434299 1520893-08-6 98%
    TASP0434299 (Compound 10) is a labeled ligand for the vasopressin V1b receptor. TASP0434299 exhibits high binding affinity for human and murine V1B receptors, with IC50 values of 0.526 nM and 0.641 nM, respectively, and shows potent antagonistic activity against the human V1B receptor with an IC50 of 0.639 nM. TASP0434299 is a substrate for human and rhesus monkey P-glycoprotein, resulting in low brain uptake in rhesus monkeys. TASP0434299 binds to V1B receptors in rat and monkey pituitary tissues in a saturable and specific manner both in vitro and in vivo. When radiolabeled with tritium or 11C, TASP0434299 serves as a prototype V1B receptor radiotracer to visualize V1B receptor in the pituitary gland of anesthetized monkeys via positron emission tomography.
    TASP0434299
  • HY-120278
    4-Ethoxyquinazoline 16347-96-9 98%
    4-Ethoxyquinazoline is a selective small molecule activator of bacterial glycoside hydrolases (AC50=3.5 mM).
    4-Ethoxyquinazoline
  • HY-120336
    Ranolazine impurity 9 172430-46-5 98%
    Ranolazine impurity 9 is an impurity of Ranolazine.
    Ranolazine impurity 9