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 (73764):

Cat. No. Product Name CAS No. Purity Chemical Structure
  • HY-Y1213
    Carbon 7440-44-0 99.62%
    Carbon possesses unique physicochemical properties such as electrical and structural characteristics, making it a core material in the field of fuel cells. Carbon also serves as a pharmaceutical excipient and can be used in the synthesis of other compounds.
    Carbon
  • HY-Y1675
    Rivastigmine impurity 12 586-37-8 98%
    Rivastigmine impurity 12 (m-Methoxyacetophenone) is an impurity of Rivastigmine.
    Rivastigmine impurity 12
  • HY-100511
    Benzophenonetetracarboxylic acid 2479-49-4 99.55%
    Benzophenonetetracarboxylic acid (3,3',4,4'-Benzophenonetetracarboxylic acid) is particularly useful in the preparation of high performance polyimides and also useful as curing agents for epoxy resins.
    Benzophenonetetracarboxylic acid
  • HY-101108
    Tazarotenic acid 118292-41-4 98.67%
    Tazarotenic acid is the metabolite of Tazarotene. Tazarotenic acid binding to retinoic acid receptors (RARs) is the probable molecular target of retinoid action. Tazarotenic acid has the potential for the research of warty dyskeratoma.
    Tazarotenic acid
  • HY-101218
    N-Biotinyl-6-aminohexanoic acid 72040-64-3 99.84%
    N-Biotinyl-6-aminohexanoic acid (N-(+)-Biotinyl-6-aminohexanoic acid) can be used to perform biotinylation.
    N-Biotinyl-6-aminohexanoic acid
  • HY-103097
    ST271 106392-48-7 98.00%
    ST271 is a potent inhibitor of protein tyrosine kinase (PTK), inhibits phospholipase D activation stimulated by fMet-Leu-Phe and PAF, with IC50s of 6.7 and 9 μM, respectively.
    ST271
  • HY-103470
    K114 872201-12-2 ≥99.0%
    K114, a fluorescent Congo Red analogue, binds tightly to amyloid fibrils with an EC50 of 20-30 nM. K114 is an efficient detector of semen-derived enhancer of virus infection (SEVI).
    K114
  • HY-103694
    Nebularine 550-33-4 98.44%
    Nebularine 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.
    Nebularine
  • HY-105689
    AGN 192870 166977-57-7 98.49%
    AGN 192870 is a RAR neutral antagonist with Kds of 147, 33, and 42 nM for RARα, RARβ, and RARγ, respectively. AGN 192870 shows IC50s of 87 and 32 nM for RARαand RARγ, respectively. AGN 192870 shows RARβ partial agonism. AGN 192870 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
    AGN 192870
  • HY-109848
    3-(1H-Pyrazol-4-yl)benzoic acid 1002535-21-8 99.80%
    3-(1H-Pyrazol-4-yl)benzoic acid(3-Pyrazol-4-ylbenzoic acid) is a metal-organic framework (MOF).
    3-(1H-Pyrazol-4-yl)benzoic acid
  • HY-111173
    Diprotin B 90614-49-6 99.60%
    Diprotin B is a dipeptidyl aminopeptidase IV (DPP IV) inhibitor. The apparent competitive inhibition of DPP-IV by the diprotins is a kinetic artifact, derived from the substrate-like nature of tripeptides containing a penultimate proline residue.
    Diprotin B
  • HY-111535
    BoNT-IN-2 354784-03-5 98.0%
    BoNT-IN-2 (Compound 33) is a Botulinum Neurotoxin A Light Chain (BoNT/A LC) inhibitor with an IC50 of 4.5 μM.
    BoNT-IN-2
  • HY-111648
    6-O-Methyl Guanosine 7803-88-5 99.65%
    6-O-Methyl Guanosine is a Ribonucleoside. Replacement of the conserved G5, G8 or G12 residues in hammerhead ribozymes with 6-O-Methyl Guanosine reduces kcat without altering Km. 6-O-Methyl Guanosine exerts position-dependent regulatory effects on ribosomal velocity and fidelity. When 6-O-Methyl Guanosine is located at the first or third position of a codon, it decreases the accuracy of tRNA selection. When 6-O-Methyl Guanosine is located at the second position of a codon, it slows down the peptide bond formation rate of cognate aminoacyl-tRNA but does not change the reaction rate of near-cognate aminoacyl-tRNA.
    6-O-Methyl Guanosine
  • HY-113164
    Vitamin K1 2,3-epoxide 25486-55-9 99.99%
    Vitamin K1 2,3-epoxide is an inactive metabolite form of Vitamin K1 (HY-N0684), which is reduced to active vitamin by microsomal epoxide reductase in the vitamin K epoxide cycle. Vitamin K1 2,3-epoxide is involved in blood clotting.
    Vitamin K1 2,3-epoxide
  • HY-113242
    5-Nonadecylresorcinol 35176-46-6
    5-Nonadecylresorcinol is an alkylresorcinol and has inhibitory effects on the release of β-hexosaminidase in vitro.
    5-Nonadecylresorcinol
  • HY-114430
    Fmoc-Phe-Lys(Boc)-PAB-PNP 1646299-50-4 98.67%
    Fmoc-Phe-Lys(Boc)-PAB-PNP is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs).
    Fmoc-Phe-Lys(Boc)-PAB-PNP
  • HY-114907
    4',5'-Dibromofluorescein 596-03-2
    4',5'-Dibromofluorescein (Eosinic acid) is a fluorescein derivative that can used as a ligand for studying of protein properties by spectral analysis.
    4',5'-Dibromofluorescein
  • HY-114928
    Deiodoamiodarone 23551-25-9
    Deiodoamiodarone (L 3937; Dideiodo Amiodarone) is an intermediate of amiodarone. Amiodarone is a potent calmodulin antagonist.
    Deiodoamiodarone
  • HY-114991
    Leptospermone 567-75-9 98.46%
    Leptospermone is a competitive, reversible inhibitor for p-Hydroxyphenylpyruvate dioxygenase (HPPD), with an IC50 of 12.1 μM. Leptospermone exhibits herbicidal activity for its bleaching effect.
    Leptospermone
  • HY-116057
    Stemazole 317337-07-8 99.96%
    Stemazole is a protective agent that promotes stem cell survival. Stemazole has the protective effect of human embryonic stem cells (hESCs). Stemazole enhances clonal expansion of single cells and decreases apoptosis. Stemazole for the study of stem cell survival in starvation culture .
    Stemazole