2. Others

Others

Others

Related Products

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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 (63441):

Cat. No. Product Name CAS No. Purity Chemical Structure
  • HY-D1157
    HKPerox-2 2245230-79-7 99.79%
    HKPerox-2 is a highly sensitive green fluorescent probe for the specific detection of H2O2 in living cells with a maximum excitation wavelength and emission wavelength of 520 nm and 543 nm, respectively.
    HKPerox-2
  • HY-D1537
    Dibenzocyclooctyne-Cy5.5 2643308-61-4 99.21%
    Dibenzocyclooctyne-Cy5.5 (DBCO-Cy5.5) is a fluorescent dye. Dibenzocyclooctyne-Cy5.5 can be used to syntheses calcium-binding near-infrared fluorescent nanoprobe for bone tissue imaging.
    Dibenzocyclooctyne-Cy5.5
  • HY-N2176
    S-(+)-Marmesin 13849-08-6 99.73%
    S-(+)-Marmesin is a natural coumarin, exhibiting COX-2/5-LOX dual inhibitory activity.
    S-(+)-Marmesin
  • HY-N2325
    D-(+)-Cellobiose 528-50-7 99.94%
    D-(+)-Cellobiose is a water-soluble disaccharide and an important intermediate product in the degradation process of cellulose and hemicellulose. D-(+)-cellobiose is used as a carbon source by microorganisms in fermentation processes, where it is converted into ethanol or other metabolic products. D-(+)-Cellobiose has significant application value in biofuel production, such as bioethanol.
    D-(+)-Cellobiose
  • HY-N7404
    Nε,Nε,Nε-Trimethyllysine chloride 55528-53-5 ≥99.0%
    Nε,Nε,Nε-Trimethyllysine chloride serves as a precursor for gut flora-dependent formation of N,N,N-trimethyl-5-aminovaleric acid (TMAVA).
    Nε,Nε,Nε-Trimethyllysine chloride
  • HY-N7948
    Isomaltotetraose 35997-20-7
    Isomaltotetraose is one of isomalto-oligosaccharide (IMO), the main hydrolysis end products of DexKQ. Isomaltotetraose can induce dextranase synthesis.
    Isomaltotetraose
  • HY-P2861
    Sarcosine oxidase, Bacillus 9029-22-5
    Sarcosine oxidase, Bacillus (SAO) can catalyze the oxidative demethylation of sarcosine to generate glycine, H2O2, 5,10-CH2-tetrahydrofolate, which are often used in biochemical reactions.
    Sarcosine oxidase, Bacillus
  • HY-P2963
    Nuclease P1 54576-84-0
    Nuclease P1 is a single-stranded specific endonuclease, it hydrolyzes nucleic acids into 5'-mononucleotides and cleaves the single-stranded region of a double-stranded nucleic acid. Nuclease P1 is one of the most well-known single stranded specific nucleases in the field of molecular biology, it is widely used in the pharmaceutical and food industries. Nuclease P1 can be obtained by fermentation of Penicillium citrinum: through extraction process, ultrafiltration concentration, drying and purification, etc.
    Nuclease P1
  • HY-100551
    meso-Erythritol 149-32-6 ≥98.0%
    meso-Erythritol is a sugar alcohol that found in a variety of foods (e.g., pear, watermelon), is 60-80% as sweet as sucrose, and can be used as low-calorie sweetener food additives.
    meso-Erythritol
  • HY-103601
    (S,R,S)-AHPC-PEG4-N3 1797406-81-5 99.93%
    (S,R,S)-AHPC-PEG4-N3 is a synthesized E3 ligase ligand-linker conjugate that incorporates the (S,R,S)-AHPC based VHL ligand and 4-unit PEG linker used in PROTAC technology. (S,R,S)-AHPC-PEG4-N3 is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
    (S,R,S)-AHPC-PEG4-N3
  • HY-107819
    5α-Cholestan-3β-ol 80-97-7 ≥98.0%
    5α-Cholestan-3β-ol is a derivitized steroid compound.
    5α-Cholestan-3β-ol
  • HY-112103
    6-(γ,γ-Dimethylallylamino)purine 2365-40-4 99.94%
    6-(γ,γ-Dimethylallylamino)purine is a plant growth substance.
    6-(γ,γ-Dimethylallylamino)purine
  • HY-112634
    SIRT5 inhibitor 1 2166487-21-2 99.65%
    SIRT5 inhibitor 1 is a potent Human Sirtuin 5 deacylase inhibitor, with an IC50 of 0.11 μM.
    SIRT5 inhibitor 1
  • HY-112729
    HC-056456 7733-96-2 ≥98.0%
    HC-056456 is an effective but not perfectly-selective blocker of CatSper channels. The [Na+]i rise is slowed by HC-056456 (IC50~3 µM).
    HC-056456
  • HY-117678
    TG-2-IN-1 135273-74-4 ≥98.0%
    TG-2-IN-1 (Compound D003) is a transglutaminase-2 (TGM-2) inhibitor. TG-2-IN-1 can be used for the research of myopia.
    TG-2-IN-1
  • HY-124717
    YC-001 748778-73-6 99.43%
    YC-001 is an inverse agonist and antagonist of rod opsin. YC-001 reversibly binds rod opsin and stabilizes the rod opsin structure. YC-001 protects mice from bright light-induced retinal degeneration. YC-001 has the potential for the research of retinal degeneration.
    YC-001
  • HY-126726
    KOdiA-PC 439904-33-3 ≥99.0%
    Oxidized low-density lipoprotein (oxLDL) particles contain low molecular weight species that are cytotoxic and proatherogenic. Many of these species were recently isolated and purified from oxLDL and identified as phosphatidylcholine species containing fragmented oxidized short-chain fatty acid residues at the sn-2 position. 1-(Palmitoyl)-2-(5-keto-6-octene-dioyl)phosphatidylcholine or KOdiA-PC is one of the most potent CD36 ligands of the oxLDL species. KOdiA-PC confers CD36 scavenger receptor binding affinity to LDL at a frequency of only 2 to 3 KOdiA-PC molecules/LDL particle and may be one of the more important structural determinants of oxLDL.
    KOdiA-PC
  • HY-134978
    (Rac)-SHIN2 2204289-53-0 99.09%
    (Rac)-SHIN2 is a pyrazolopyran derivative and a serine hydroxymethyltransferase (SHMT) inhibitor. (Rac)-SHIN2 has antibacterial activity and low cytotoxicity against Hep2 cells. (Rac)-SHIN2 exerts potent antibacterial activity against both vancomycin-susceptible and vanA-type vancomycin-resistant Enterococcus.
    (Rac)-SHIN2
  • HY-147369
    NFATc1-IN-1 1912422-56-0 99.97%
    NFATc1-IN-1 (compound A04) is a potent inhibitor of RANKL-induced osteoclast formation, with an IC50 of 1.57 μM. NFATc1-IN-1 shows anti-osteoclastogenic effects through reducing the RANKL-induced nuclear translocation of NFATc1. NFATc1-IN-1 can be used for osteoclastic diseases research.
    NFATc1-IN-1
  • HY-148949
    Kallikrein 5-IN-2 2361160-57-6 98.96%
    Kallikrein 5-IN-2 (compound 21) is a selective Kallikrein KLK5 inhibitor (pIC50=7.1). KLK5 inhibition may normalise epidermal shedding and reduce the associated inflammation and itching.
    Kallikrein 5-IN-2