2. Others

Others

Others

Related Products

PDF 58.49 MB

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 (73784):

Cat. No. Product Name CAS No. Purity Chemical Structure
  • HY-139351
    Gibberellins A4/A7 8030-53-3
    Gibberellins A4/A7 induces stimulation of tracheid production in the terminal shoot of intact plants is mediated through an increase in the IAA level in the cambial region.
    Gibberellins A4/A7
  • HY-139988
    2-O-DMT-Sulfonyldiethanol phosphoramidite 108783-02-4
    2-O-DMT-Sulfonyldiethanol phosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
    2-O-DMT-Sulfonyldiethanol phosphoramidite
  • HY-141667
    MBD 33984-50-8 ≥98.0%
    MBD (7-(p-Methoxybenzylamino)-4-nitrobenz-2,1,3-oxadiazole), a new fluorescent probe for protein and nucleoprotein conformation, is applied to bacterial ribosomes and to bovine trypsinogen and trypsin. MBD is strongly fluorescent upon binding to a hydrophobic area of a macromolecule.
    MBD
  • HY-148665
    FABP-IN-2 1426533-99-4 99.78%
    FABP-IN-2 is a novel FABP3 ligand. FABP-IN-2 inhibits FABP3/FABP4 with an IC50 of 1.16 μM and 4.27 μM respectively.
    FABP-IN-2
  • HY-151698
    TCO-NHS Ester (axial) 1610931-22-0 99.84%
    TCO-NHS Ester axial is a click chemistry reagent that can be used as a building block in amine reactions. TCO-NHS Ester axial contains TCO groups, which can undergo inverse electron demand Diels-Alder reaction (iEDDA) with molecules containing Tetrazine groups.
    TCO-NHS Ester (axial)
  • HY-152720
    3’-Azido-3’-deoxyuridine 70580-88-0 99.97%
    3’-Azido-3’-deoxyuridine is a purine nucleoside analogue. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc. 3’-Azido-3’-deoxyuridine 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.
    3’-Azido-3’-deoxyuridine
  • HY-153737
    113-N16B 98.0%
    113-N16B is an ionizable cationic lipid used for the generation of lipid nanoparticles (LNPs). 113-N16B delivers mRNA preferentially to pulmonary endothelial cells.
    113-N16B
  • HY-154639
    Polyoxyl 20 Cetostearyl Ether 68439-49-6
    Polyoxyl 20 Cetostearyl Ether can be used as an excipient, such as Emulsifier and solubilizer for emulsions and creams, etc. Pharmaceutical excipients, or pharmaceutical auxiliaries, refer to other chemical substances used in the pharmaceutical process other than pharmaceutical ingredients. Pharmaceutical excipients generally refer to inactive ingredients in pharmaceutical preparations, which can improve the stability, solubility and processability of pharmaceutical preparations. Pharmaceutical excipients also affect the absorption, distribution, metabolism, and elimination (ADME) processes of co-administered drugs.
    Polyoxyl 20 Cetostearyl Ether
  • HY-154830
    Lysophosphatidylcholine C19:0 108273-88-7 99.0%
    Lysophosphatidylcholine C19:0 (1-Nonadecanoyl-2-hydroxy-sn-glycero-3-phosphocholine) is an acyl chain lipid. Lysophosphatidylcholine C19:0 increases IL-1beta secretion.
    Lysophosphatidylcholine C19:0
  • HY-155788
    DSPE-PEG-DBCO ammonium 2052955-83-4 99.90%
    DSPE-PEG-DBCO ammonium is the ammonium salt form of DSPE-PEG-DBCO. DSPE-PEG-DBCO ammonium is utilized in copper-free click chemistry through SPAAC conjugation with an azido-functionalized peptide ligand. DSPE-PEG-DBCO ammonium is applied in drug-delivery and nanoparticle research.
    DSPE-PEG-DBCO ammonium
  • HY-155902
    Mal-PEG5000-OH 88504-24-9 99.97%
    Mal-PEG5000-OH can be used as a macroinitiator to obtain amphiphilic diblock copolymers by ring-opening polymerization of LA. Nanoparticles prepared using amphiphilic block copolymers can form active drug delivery systems. Nanoparticles encapsulate Triptolide (HY-32735), which can avoid the disadvantage of Triptolide’s poor water solubility and reduce its toxicity.
    Mal-PEG5000-OH
  • HY-157034
    LU-002i 1838705-22-8 99.76%
    LU-002i is a subunit-selective human proteasome β2c and β2i inhibitor with an IC50 value of 220 nM for β2i.
    LU-002i
  • HY-157423
    16:1 (DELTA 9-Cis) PC 56815-99-7 99.0%
    16:1 (DELTA 9-Cis) PC is a phospholipid metabolite .
    16:1 (DELTA 9-Cis) PC
  • HY-158664
    2-Amino-ATP sodium solution (100 mM) 99.92%
    2-Amino-ATP sodium solution (100 mM) is a labeled modified deoxyoligonucleotide (dNTP) that can release pyrophosphate to produce fluorescence and has special applications in gene synthesis and sequencing.
    2-Amino-ATP sodium solution (100 mM)
  • HY-158772
    m7G(5')ppp(5')(2'OMeA)pU ammonium solution (100 mM) 99.6%
    m7G(5')ppp(5')(2'OMeA)pU ammonium is a cap analog that can be used for in vitro transcription of mRNA.
    m7G(5')ppp(5')(2'OMeA)pU ammonium solution (100 mM)
  • HY-159180
    p-NCS-Bz-NODA-GA 1660127-21-8 99.46%
    p-NCS-Bz-NODA-GA is a bifunctional chelator.
    p-NCS-Bz-NODA-GA
  • HY-164862
    N-(NHS ester-PEG2)-N-bis(PEG3-azide) 99.90%
    N-(NHS ester-PEG2)-N-bis(PEG3-azide) is a PEG linker with an NHS ester group and two terminal azide groups. N-(NHS ester-PEG2)-N-bis(PEG3-azide) can be utilized in Click Chemistry.
    N-(NHS ester-PEG2)-N-bis(PEG3-azide)
  • HY-168324
    UP158 489402-33-7
    UP158 enhances the activity of ATPase, and activates valosin-containing protein (VCP) with an EC50 of 2.57 μM.
    UP158
  • HY-171702
    8PPD-Q 99.88%
    8PPD-Q, a para-phenylenediamine quinonec, is a rubber antioxidant. 8PPD-Q has superior antioxidant and anti-ozone activities but is toxic to the aquatic species, especially salmonids. 8PPD-Q can be used for environmental pollution research.
    8PPD-Q
  • HY-176886
    LATS-IN-2 2248728-49-4 99.45%
    LATS-IN-2 is an efficiently acting LATS (large tumor suppressor kinase) inhibitor. LATS-IN-2 shows potent inhibitory activity against LATS1 with an IC50 value of 1.3 nM. LATS-IN-2 suppresses the phosphorylation of YAP by inhibiting LATS kinase activity. LATS-IN-2 increases the thickness of the epidermis in mice. LATS-IN-2 can be used for the study of ocular diseases such as limbal stem cell deficiency and corneal endothelial dysfunction.
    LATS-IN-2