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 (73744):

Cat. No. Product Name CAS No. Purity Chemical Structure
  • HY-173193
    S-cEt-U phosphoramidite 945628-51-3 98%
    S-cEt-U phosphoramidite is a modified phosphoramidite monomer that can be used for the oligonucleotide synthesis.
    S-cEt-U phosphoramidite
  • HY-173289
    LNP Lipid-26 2089251-49-8 98%
    LNP Lipid-26 can be applied in the generation of lipid nanoparticles (LNPs).
    LNP Lipid-26
  • HY-173308
    QSY-21 1200894-41-2 98.77%
    QSY-21 is a fluorescence quencher. QSY-21 possesses broad absorption in far red and NIR range, and can quench fluorescence of dyes that emit in this region. This is a carboxylic acid derivative. QSY-21 has intense absorption maximum at 661 nm, making it useful as an acceptor in fluorescence resonance energy transfer (FRET) applications. It is a common quencher for Cyanine5, Cyanine5.5, AF 647, or other spectrally similar fluorescent dyes.
    QSY-21
  • HY-173569
    DBCO-propargyl-PEG5-TFP ester 2764923-68-2
    DBCO-propargyl-PEG5-TFP ester is an amine-reactive labeling reagent. DBCO-propargyl-PEG5-TFP ester contains a DBCO group, which can undergo a strain-promoted alkyne-azide cycloaddition (SPAAC) reaction with molecules containing an azide group[1].
    DBCO-propargyl-PEG5-TFP ester
  • HY-17412B
    4-Epiminocycline 43168-51-0 98%
    4-Epiminocycline is a Minocycline (HY-17412A) degradation product. Minocycline (HY-17412A) is an antibiotic that has anti-inflammatory, anticancer, antibacterial, immunomodulatory and neuroprotective effects.
    4-Epiminocycline
  • HY-17479S
    Amfenac-d5 2749329-56-2 98%
    Amfenac-d5 is the deuterium labeled Amfenac. Amfenac is an orally active and potent anti-inflammatory compound possessing antipyretic and analgesic properties. Amfenac can be used for the research of acute and chronic inflammation.
    Amfenac-d5
  • HY-175994
    Fmoc-β-Ala-Trp(Boc)-OH 99.36%
    Fmoc-β-Ala-Trp(Boc)-OH is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs).
    Fmoc-β-Ala-Trp(Boc)-OH
  • HY-176513
    Cy-OH-LP 99.0%
    Cy-OH-LP is a turn-on fluorescent and photoacoustic probe that can detect lipid-associated hydroxyl radicals. Cy-OH-LP can be oxidized to Cy7 in the presence of hydroxyl radicals, which displays weak fluorescent and photoacoustic signals in water-soluble environments and strong fluorescent and photoacoustic signals in lipid-rich environments due to its lipid solubility. Cy-OH-LP can be used for in vivo photoacoustic imaging of hydroxyl radicals.
    Cy-OH-LP
  • HY-176998
    LP238-p 2764963-41-7 98%
    LP238-p is a type of lipid molecule.
    LP238-p
  • HY-177164
    3'-NH2-TTP 99614-94-5
    3'-NH2-TTP is a nucleotide analogue with an amino group modified at the 3' end of TTP.
    3'-NH2-TTP
  • HY-177165
    3'-NH2-CTP 85708-23-2 98%
    3'-NH2-CTP is a nucleotide analog with an amino group modified at the 3' end of CTP.
    3'-NH2-CTP
  • HY-177493
    SSTR3 Agonist-1 3086695-73-7
    SSTR3 Agonist-1 (Compound EX 38) is an orally active SSTR3 agonist, with an EC50 of 0.14 nM. SSTR3 Agonist-1 reduces the kidney cystic index. SSTR3 Agonist-1 can be used in the research of autosomal dominant polycystic kidney disease.
    SSTR3 Agonist-1
  • HY-177590
    14-3-3-IN-2 919751-10-3 98.41%
    14-3-3-IN-2 is a 14-3-3 protein inhibitor with an IC50 of 15 nM. 14-3-3-IN-2 can disrupt the interaction of 14-3-3α with aminopeptidase N and down-regulate 14-3-3α increased MMP-1 mRNA levels.
    14-3-3-IN-2
  • HY-177764
    Tet-v2.0-ethyl 2036323-77-8
    Tet-v2.0-ethyl is a tetrazine non-canonical amino acid. Tet-v2.0-ethyl can stably exist within living cells without being degraded, enabling in situ labeling of intracellular biomolecules. Tet-v2.0-ethyl is mainly used as a bioorthogonal labeling tool compound.
    Tet-v2.0-ethyl
  • HY-177894
    Fmoc-Asp(OMpe)-Cbz 180675-10-9 99.40%
    Fmoc-Asp(OMpe)-Cbz is a drug intermediate that can be used for the synthesis of Fmoc-Asp(OMpe)-OH.
    Fmoc-Asp(OMpe)-Cbz
  • HY-182338
    2’-Thiouridine 31281-28-4 98%
    2'-Thiouridine is a key modified nucleoside at the wobble position of tRNA anticodons. 2'-Thiouridine mainly exists in tRNAs for glutamic acid, glutamine, lysine, etc., and participates in precise decoding regulation.
    2’-Thiouridine
  • HY-185464
    DBCO-Headpiece
    DBCO-Headpiece is a conjugate of DBCO-PEG4-NHS ester (HY-140272) and Headpiece (HY-185129).
    DBCO-Headpiece
  • HY-18599A
    Chitinase-IN-2 hydrochloride 2070014-83-2 99.78%
    Chitinase-IN-2 hydrochloride is an inhibitor of insect chitinase and N-acetylhexosaminidase.
    Chitinase-IN-2 hydrochloride
  • HY-186175
    DMG-PEG2000-Mal-Cys-penetratin
    DMG-PEG2000-Mal-Cys-penetratin is a conjugate composed of dimyristoylglycerol (DMG), a PEG chain, and terminal maleimide (Mal). DMG-PEG2000-Mal-Cys-penetratin combines the membrane compatibility of lipids, the specific Michael addition reaction with thiol-containing (-SH) biomolecules (such as peptides, antibodies, and aptamers) by maleimide, and cell-penetrating peptides, making it suitable for research on biomaterial construction and drug delivery to cells.
    DMG-PEG2000-Mal-Cys-penetratin
  • HY-186176
    DSPE-PEG2000-Mal-Cys-penetratin
    DSPE-PEG2000-Mal-Cys-penetratin is a conjugate composed of DSPE, a PEG chain, and terminal maleimide (Mal). DSPE-PEG2000-Mal-Cys-penetratin combines the membrane compatibility of lipids, the ability to undergo specific Michael addition reactions with thiol-containing (-SH) biomolecules (such as peptides, antibodies, and aptamers), and the ability to penetrate cell membranes, making it suitable for research on biomaterial construction and drug delivery to cells.
    DSPE-PEG2000-Mal-Cys-penetratin