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Others

 
Cat. No. Product Name Effect Purity Chemical Structure
  • HY-122057
    Bisdionin F
    Bisdionin F is a compound with the ability to restore the antibacterial function of macrophages, which can block the arginase activity induced by Candida albicans and restore the nitric oxide production and antibacterial function of macrophages.
    Bisdionin F
  • HY-N14744
    Lanopylin B2
    Lanopylin B2 can inhibit recombinant human lanosterol synthase (EC 5.4.99.7) with an IC50 of 41 μM.
    Lanopylin B2
  • HY-W026038
    (Z)-Non-2-en-1-ol
    (Z)-Non-2-en-1-ol (Cis-2-Nonen-1-ol) is a natural compound that can be found in passion fruit and prickly pear. (Z)-Non-2-en-1-ol can be used to enhance food taste.
    (Z)-Non-2-en-1-ol
  • HY-165040
    1-Palmitoyl-2-stearoyl-rac-glycerol
    1-Palmitoyl-2-stearoyl-rac-glycerol (DG(16:0/18:0/0:0)) is a compound mentioned in the study of the activation of ADP-ribosylation factor 1 GTPase activating protein by phosphatidylcholine-derived diacylglycerol, and related studies have shown that it may be involved in certain feedback mechanisms within cells.
    1-Palmitoyl-2-stearoyl-rac-glycerol
  • HY-N14593
    Roridin D
    Roridin D is a natural compound foun in Myrothecium roridum S-1135 (NRRL 3005).
    Roridin D
  • HY-N14624
    Pelagiomicin B
    Pelagiomicin B is a natural compound found in the strain of Pelagiobacter variabilis.
    Pelagiomicin B
  • HY-106300
    AA 193
    AA 193 is a uricosuric agent. AA 193 increases urate excretion in hyperuricemic rats.
    AA 193
  • HY-N14440
    Furaquinocin C
    Furaquinocin CA can kill HeLa S3 and B16 melanoma cells, but has no antibacterial activity.
    Furaquinocin C
  • HY-156407
    Adam-20-S
    Inhibitor
    Adam-20-S is a potent glucosinolate sulfatase inhibitor with an IC50 value of 9.04 μg/mL. Adam-20-S impaires glucosinolate metabolism to produce more toxic isothiocyanates in P. xylostella.
    Adam-20-S
  • HY-160453
    MC-Gly-Gly-Phe-Gly-NH-CH2-O-cyclopropane-CH2COOH
    MC-Gly-Gly-Phe-Gly-NH-CH2-O-cyclopropane-CH2COOH is a camptothecin derivative. MC-Gly-Gly-Phe-Gly-NH-CH2-O-cyclopropane-CH2COOH can be used for antibody drug conjugate (ADC).
    MC-Gly-Gly-Phe-Gly-NH-CH2-O-cyclopropane-CH2COOH
  • HY-N13976
    Belactosin C
    Belactosin C is found in the strain of Streptomyces sp. that inhibits HeLa S3 cells with the IC50 of 200 μM.
    Belactosin C
  • HY-N15381
    Taxine A
    Taxine A (Taxin A) is a crystalline alkaloid that can be isolated from the needles of Taxus baccata L (yew).
    Taxine A
  • HY-135137
    Leptosin I
    Leptosin I is found in the strain of Leptosphaeria sp. OUPS-4. Leptosin I inhibits Leukemia lymphocyte P388 in culture with an ED50 of 1.13 μg/mL.
    Leptosin I
  • HY-118311
    (Z)-W 3699
    (Z)-W 3699 is a potential choleretic. (Z)-W 3699 can increase the solubility of cholesterol in the gallbladder by altering the secretion of micellar bile acids. (Z)-W 3699 can prevent the formation of cholesterol-containing gallstones in dogs.
    (Z)-W 3699
  • HY-159093
    Antitumor agent-178
    GSCs-IN-1 (compound 4 h) is a potent and selective GSCs inhibitor. GSCs-IN-1 has the potential for the research of cancer.
    Antitumor agent-178
  • HY-N15377
    2,6-Dimethoxy-4-hydroxyacetophenone
    2,6-Dimethoxy-4-hydroxyacetophenone is an acetophenone compound found in the bulbs of Pancratium maritimum.
    2,6-Dimethoxy-4-hydroxyacetophenone
  • HY-165164
    Methotrexate-alpha-alanine
    Methotrexate-alpha-alanine is a prodrug for activation by enzyme-monoclonal antibody conjugates. Methotrexate-alpha-alanine shows cytotoxicity.
    Methotrexate-alpha-alanine
  • HY-N13202
    Black Currant Extract
    Black Currant Extract is a black currant extract, and its components include: Anthocyanidins. Black Currant Extract is an anti-inflammatory agent that can neutralize the cytotoxic effects of nicotine on epithelial cells and fibroblasts in a dose-dependent manner. Black Currant Extract can also inhibit LPS-induced IL-6 secretion by human macrophages..
    Black Currant Extract
  • HY-137055
    PF-3774076
    PF-3774076 is a highly central nervous system (CNS) penetrant, potent, and selective human α1A-adrenoceptor partial agonist. It exhibits good potency and selectivity in multiple binding and functional assays. PF-3774076 increases peak urethral pressure in anesthetized female dogs in a dose-dependent manner via a central mechanism. PF-3774076 affects both the proximal and distal portions of the urethra in vivo. These properties suggest that PF-3774076 may have significant benefit in the treatment of stress urinary incontinence (SUI) as a CNS-penetrant α1A receptor partial agonist. However, despite its partial agonism and selectivity for α1A receptors, PF-3774076 failed to provide adequate safety differences in in vivo models of cardiovascular function. This may be due to the simultaneous activation of both peripheral and central α1A receptors. These data suggest that while central α1A partial agonists may have significant benefit in the treatment of SUI, this class of agents may have difficulty achieving the desired urethral selectivity without affecting cardiovascular function.
    PF-3774076
  • HY-W854727
    N-Methylfulleropyrrolidine
    N-Methylfulleropyrrolidine serves as an electron acceptor molecule characterized by its fullerene core and a nitrogen-free lone pair associated with the pyrrolidine ring. This compound can act as an intermediate in the synthesis of various functionalized fullerenes and plays a significant role in the development of opto-electronic devices. Comprehensive studies have been conducted on the photoinduced energy and electron transfer processes between oligothienylenevinylenes and N-Methylfulleropyrrolidine (MP-C60).
    N-Methylfulleropyrrolidine
Cat. No. Product Name / Synonyms Application Reactivity