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 (60209):

Cat. No. Product Name CAS No. Purity Chemical Structure
  • HY-B1897A
    Menadione bisulfite sodium 130-37-0 99.87%
    Menadione bisulfite (sodium) is used as an agent to induce acute oxidative stress, and to function as a plant-defense activator against several pathogens.
    Menadione bisulfite sodium
  • HY-N0568
    Madecassoside 34540-22-2 ≥98.0%
    Madecassoside is a pentacyclic triterpene isolated from Centella asiatica and has anti-inflammatory properties. Antioxidant and anti-aging effects. Madecassoside is a pentacyclic triterpene isolated from Centella asiatica. Madecassoside is orally active and has inhibitory properties against inflammation, oxidation, apoptosis and autophagy. Madecassosid inhibits activities of p38 MAPK and NF-kB[5][6], exhibits an anti-apopototic property, activates Nrf2 expression to reduce the neurotoxicity. Madecassoside can be used in endocrine diseases, cardiovascular diseases, skin diseases and other diseases.
    Madecassoside
  • HY-W019711
    trans-Cinnamaldehyde 14371-10-9 ≥98.0%
    trans-Cinnamaldehyde can be used to prepare highly polyfunctionalized furan ring by reaction of alkyl isocyanides with dialkyl acetylenedicarboxylate. trans-Cinnamaldehyde can be used to synthesize trans-cinnamaldehyde -β-cyclodextrin complex, an antimicrobial edible coating that increases the shelf life of fresh-cut fruits.
    trans-Cinnamaldehyde
  • HY-D0719
    Fluorescein Diacetate 596-09-8 99.79%
    Fluorescein diacetate is a cell permeable esterase-substrate. Fluorescein diacetate can be used as a fluorogenic substrate for hGSTP1-1.
    Fluorescein Diacetate
  • HY-N0615
    Notoginsenoside R1 80418-24-2 ≥98.0%
    Notoginsenoside R1 (Sanchinoside R1), a saponin, is isolated from P. notoginseng. Notoginsenoside R1 exhibits anti-oxidation, anti-inflammatory, anti-angiogenic, and anti-apoptosis activities. Notoginsenoside R1 provides cardioprotection against ischemia/reperfusion (I/R) injury. Notoginsenoside R1 also provides neuroprotection in H2O2-induced oxidative damage in PC12 cells.
    Notoginsenoside R1
  • HY-41324
    7-keto-Deoxycholic acid 911-40-0 99.71%
    7-keto-Deoxycholic acid is a metabolite of bile acids in Clostridium absonum. 7-keto-Deoxycholic acid is also converted from Lactobacillus and Bifidobacterium with specific condition.
    7-keto-Deoxycholic acid
  • HY-P3208
    Endoproteinase Lys-C 72561-05-8
    Endoproteinase Lys-C is a protease that cleaves proteins on the C-terminal side of lysine residues and is commonly used for protein sequencing.
    Endoproteinase Lys-C
  • HY-113414
    Deoxycorticosterone 64-85-7 99.61%
    Deoxycorticosterone is a steroid hormone produced by the adrenal gland that possesses mineralocorticoid activity and acts as an aldosterone precursor. Deoxycorticosterone is an agonist for O. mykiss mineralocorticoid receptor (rtMR) transcription with EC50 of 0.16 nM. Deoxycorticosterone could acts as an immune stimulator in fish.
    Deoxycorticosterone
  • HY-W013046
    Phosphoribosyl pyrophosphate pentasodium 108321-05-7
    Phosphoribosyl pyrophosphate (PRPP) pentasodium is an important metabolite required in the biosynthesis of purine and pyrimidine nucleotides, the amino acids histidine and tryptophan, and the cofactors NAD and NADP.
    Phosphoribosyl pyrophosphate pentasodium
  • HY-W251428
    Phosphatidylglycerols (egg) sodium salt 383907-64-0 ≥98.0%
    Phosphatidylglycerols (PG) is a selective inhibitor targeting the TLR4 accessory protein CD14/MD-2 complex, inhibiting LPS or virus (such as RSV)-mediated inflammatory signaling pathways through competitive binding. Phosphatidylglycerols directly bind to viral particles to block infection, inhibit COX-2 expression to reduce the release of inflammatory factors (IL-6, IL-8), and improve oxidative stress by regulating mitochondrial membrane phospholipid remodeling. Phosphatidylglycerols can be taken orally or by inhalation and can be used in the study of chronic inflammatory diseases (such as atherosclerosis) and respiratory viral infections (such as RSV).
    Phosphatidylglycerols (egg) sodium salt
  • HY-D1416
    HMBR 1287651-36-8 98.43%
    HMBR is an analogue with an additional methyl group on the aromatic ring and is non-fluorescent. HMBR conjugated with Y-FAST emits yellow fluorescence under blue light excitation (Ex= 419 nm; Em= 525–539 nm). HMBR is non-toxic to zebrafish embryos. HMBR has high cell permeability.
    HMBR
  • HY-D1498
    Mag-Fluo-4 AM 1097709-31-3
    Mag-Fluo-4 AM is a fluorecent Ca2+ chelator, with high affinity for calcium. Mag-Fluo-4 AM can specifically identify intracellular calcium ions, with high sensitivity, low cytotoxicity, increased AM acetylmethyl ester can enter the cell well, after being sheared by the intracellular esterase stay in the cell to bind to calcium ions, produce strong fluorescence.
    Mag-Fluo-4 AM
  • HY-160769
    NIBR-LTSi 99.97%
    NIBR-LTSi is an orally active and selective LATS kinase inhibitor. NIBR-LTSi can activate YAP signaling. NIBR-LTSi promotes stem cell proliferation, maintains stemness and blocks differentiation. NIBR-LTSi accelerates liver regeneration following extended hepatectomy in mice.
    NIBR-LTSi
  • HY-W004563
    Neocuproine 484-11-7 ≥98.0%
    Neocuproine is an organic compound commonly used as a complexing reagent and copper ion detector. It can form stable complexes with copper ions, and can play a catalytic role in certain chemical reactions and analytical methods. In addition, this compound is also widely used in some biomedical fields, such as in the study of copper metabolism disorders and neurodegenerative diseases
    Neocuproine
  • HY-101897
    Fura-2 AM 108964-32-5 ≥99.0%
    Fura-2 AM is a high affinity, intracellular, UV light-excitable and ratiometric fluorescent Ca2+ (calcium ion) indicator.
    Fura-2 AM
  • HY-103447
    Zearalenone 17924-92-4 98.50%
    Zearalenone is a mycotoxin produced mainly by fungi belonging to the genus Fusarium in foods and feeds. Possess oestrogenic activity in pigs, cattle and sheep, with low acute toxicity. Causes precocious development of mammae and other estrogenic effects in young gilts.
    Zearalenone
  • HY-111915
    1,2-Dioleoyl-sn-glycero-3-phosphate, sodium salt 108392-02-5 ≥98.0%
    1,2-Dioleoyl-sn-glycero-3-phosphate sodium salt (18:1 PA) is an anionic lipid that can be used to prepare liposomes, micelles and artificial membranes.
    1,2-Dioleoyl-sn-glycero-3-phosphate, sodium salt
  • HY-W007408
    tert-Butyl 2-aminoacetate 6456-74-2 99.64%
    tert-Butyl 2-aminoacetate is a Glycine (HY-Y0966) derivative.
    tert-Butyl 2-aminoacetate
  • HY-D0974
    Sulforhodamine B sodium salt 3520-42-1 99.43%
    Sulforhodamine B sodium salt is a fluorescent dye with uses spanning from laser-induced fluorescence (LIF) to the quantification of cellular proteins of cultured cells.
    Sulforhodamine B sodium salt
  • HY-P1036
    Compstatin 206645-99-0 98.84%
    Compstatin, a 13-residue cyclic peptide, is a potent inhibitor of the complement system C3 with species specificity. Compstatin binds to baboon C3 and is resistant to proteolytic cleavage in baboon blood (similar to humans). Compstatin inhibits only the activation of primates’ complement system. Compstatin exhibits IC50 values of 63 μM and 12 μM for classical and alterative complement pathway, respectively.
    Compstatin