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 (62017):

Cat. No. Product Name CAS No. Purity Chemical Structure
  • HY-W800703
    Alexa Fluor 594 azide 1872449-19-8 98%
    Alexa Fluor 594 azide is a bright red fluorescent azide-activated probe that reacts with terminal alkynes via a copper-catalyzed click reaction (CuAAC) for single-molecule imaging.
    Alexa Fluor 594 azide
  • HY-W800704
    BP Fluor 594 alkyne 1962073-89-7 98%
    BP Fluor 594 alkyne is a bright, red-fluorescent alkyne-activated probe routinely used for imaging of azide-containing biomolecules. BP Fluor 594 alkyne reacts with azides via a copper-catalyzed click reaction (CuAAC) to form a stable triazole linker.
    BP Fluor 594 alkyne
  • HY-W800706
    Azidobutanamide-tri-(carboxyethoxymethyl)-methane 2644752-90-7 98%
    Azidobutanamide-tri-(carboxyethoxymethyl)-methane is a aqueous soluble PEG linker with an azide group with three terminal carboxylic acids. The azide group can react with alkyne, BCN, DBCO via Click Chemistry to yield a stable triazole linkage. The terminal carboxylic acids can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond.
    Azidobutanamide-tri-(carboxyethoxymethyl)-methane
  • HY-W800708
    N-(TCO)-N-bis(PEG4-acid) 2644769-96-8 98%
    N-(TCO)-N-bis(PEG4-acid) is a branched click chemistry reagent with a terminal TCO group and two terminal carboxylic acids. This reagent can react with tetrazine-containing molecule to form a stable covalent bond . The inverse-electron demand Diels-Alder cycloaddition reaction of TCO with tetrazines is the fastest bioorthogonal reaction with exceptional selectivity. The terminal carboxylic acids can react with primary amino groups in the presence of activators (e.g. EDC, HATU ).
    N-(TCO)-N-bis(PEG4-acid)
  • HY-W800709
    N-(acid-PEG10)-N-bis(PEG10-azide) 2803119-06-2 98%
    N-(acid-PEG10)-N-bis(PEG10-azide) is a very popular PEG reagent containing a terminal carboxylic acid and two azide groups. The hydrophilic PEG spacer increases solubility in aqueous media. The azide groups can react with alkyne, BCN, DBCO via Click Chemistry to yield a stable triazole linkage. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond.
    N-(acid-PEG10)-N-bis(PEG10-azide)
  • HY-W800711
    SPDP-Gly-Pro-NHS ester 2655501-79-2 98%
    SPDP-Gly-Pro-NHS ester is a linker with SPDP and NHS ester moieties. The SPDP is an amine and thiol reactive crosslinker. It is also membrane permeable, allowing it to participate in intracellular crosslinking reactions. The NHS ester is amine reactive and forms stable amide bonds.
    SPDP-Gly-Pro-NHS ester
  • HY-W800712
    t-Boc-N-Amido-PEG11-Tos 1556847-56-3 98%
    t-Boc-N-Amido-PEG11-Tos is a PEG linker containing a tosyl group and Boc-protected amine group. The hydrophilic PEG spacer increases the water solubility of a compound in aqueous media. The tosyl group is a very good leaving group for nucleophilic substitution reactions. The Boc group can be deprotected under mild acidic conditions to form a free amine.
    t-Boc-N-Amido-PEG11-Tos
  • HY-W800713
    SPDP-Gly-Pro-acid 2655501-78-1 98%
    SPDP-Gly-Pro-acid is a linker with SPDP and carboxylic acid moieties. The SPDP is an amine and thiol reactive crosslinker. It is also membrane permeable, allowing it to participate in intracellular crosslinking reactions. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond.
    SPDP-Gly-Pro-acid
  • HY-W800714
    SPDP-Gly-Gly-methoxy 2655474-48-7 98%
    SPDP-Gly-Gly-methoxy is a linker with SPDP and methyl ester moiety. The SPDP is an amine and thiol reactive crosslinker. It is also membrane permeable, allowing it to participate in intracellular crosslinking reactions.
    SPDP-Gly-Gly-methoxy
  • HY-W800715
    (Acid-PEG10)-Tri-(Azide-PEG10-ethoxymethyl)-methane 2803119-05-1 98%
    (Acid-PEG10)-Tri-(Azide-PEG10-ethoxymethyl)-methane can undergo Click Chemistry with Propargyl, BCN or DBCO reagents. Carboxylic acid (CO2H) group is reactive with primary amino groups in the presence of EDCor HATU.
    (Acid-PEG10)-Tri-(Azide-PEG10-ethoxymethyl)-methane
  • HY-W800716
    Tri(Azide-PEG10-NHCO-ethyloxyethyl)amine 2375600-60-3 98%
    Tri(Azide-PEG10-NHCO-ethyloxyethyl)amine is a branched PEG linker with three terminal azide groups. The azide groups enable PEGylation via Click Chemistry.
    Tri(Azide-PEG10-NHCO-ethyloxyethyl)amine
  • HY-W800717
    Tetra-(amido-PEG10-azide) 2375600-75-0 98%
    Tetra-(amido-PEG10-azide) is a branched PEG linker with four terminal azide groups. The azide groups enable PEGylation via Click Chemistry.
    Tetra-(amido-PEG10-azide)
  • HY-W800718
    Methyltetrazine-amido-Tri-(acid-PEG1-ethoxymethyl)-methane 2665664-66-2 98%
    Methyltetrazine-amido-Tri-(acid-PEG1-ethoxymethyl)-methane is a click chemistry PEG reagent which contains three carboxylic acid groups and a methyltetrazine group. This reagent can react with TCO-containing compounds to form a stable covalent bond without the catalysis of Cu or elevated temperatures. The inverse-electron demand Diels-Alder cycloaddition reaction of TCO with tetrazines is the fastest bioorthogonal reaction with exceptional selectivity. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond.
    Methyltetrazine-amido-Tri-(acid-PEG1-ethoxymethyl)-methane
  • HY-W800719
    N-Boc-N'-(PEG1-t-butyl ester)-L-Lysine-amido-Mal 2665661-79-8 98%
    N-Boc-N'-(PEG1-t-butyl ester)-L-Lysine-amido-Mal is the amino acid, lysine, with a maleimide at its C-terminus, a Boc-protecting group on its α-amine, and an amido-PEG1-t-butyl ester on its ε-amine. Maleimide is a thiol-reactive covalent group used to conjugate cysteine residues, while the Boc and the t-butyl ester can be later deprotected to perform further reactions.
    N-Boc-N'-(PEG1-t-butyl ester)-L-Lysine-amido-Mal
  • HY-W800720
    S-(Pyridin-2-ylthio)-L-homocysteine 2668173-78-0 98%
    (S)-2-amino-4-(2-(pyridin-2-yl)disulfanyl)butanoic acid is a small molecule reagent with a 2-thiopyridine linked to a short amino acid. SPDP is a thiol-specific labeling reagent, commonly used in reversibly binding cysteine residues on proteins. The disulfide bond it forms with the cysteine is selectively cleaved in the reducing environment of the cell cytoplasm.
    S-(Pyridin-2-ylthio)-L-homocysteine
  • HY-W800721
    Methyltetrazine-amido-bis-(carboxyethoxymethyl)-methane 2698339-32-9 98%
    Methyltetrazine-amido-bis-(carboxyethoxymethyl)-methane is a click chemistry PEG reagent which contains three carboxylic acid groups and a methyltetrazine group. This reagent can react with TCO-containing compounds to form a stable covalent bond without the catalysis of Cu or elevated temperatures. The inverse-electron demand Diels-Alder cycloaddition reaction of TCO with tetrazines is the fastest bioorthogonal reaction with exceptional selectivity. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond.
    Methyltetrazine-amido-bis-(carboxyethoxymethyl)-methane
  • HY-W800722
    N-(PEG1-acid)-L-Lysine-amido-Mal 2698339-21-6 98%
    N-(PEG1-acid)-L-Lysine-amido-Mal is a PEG based linker with terminal malimide and carboxylic acid groups. The hydrophilic PEG spacer increases solubility in aqueous media. The maleimide group will react with a thiol group to form a covalent bond, enabling the connection of biomolecule with a thiol. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond.
    N-(PEG1-acid)-L-Lysine-amido-Mal
  • HY-W800723
    Methyltetrazine-PEG2-DBCO 2698340-95-1 98%
    Methyltetrazine-PEG2-DBCO is a TCO reactive reagent with a DBCO group and water-soluble PEG spacer. This reagent can be used to convert azido-containing peptides or proteins into tetrazine-modified peptides or protein without catalyst or axillary reagents. DBCO is commonly used for copper-free Click Chemistry reactions.
    Methyltetrazine-PEG2-DBCO
  • HY-W800724
    Methyltetrazine-PEG4-DBCO 2698339-24-9 98%
    Methyltetrazine-PEG4-DBCO is a PEG linker with a terminal TCO reactive reagent and a DBCO group. DBCO is commonly used for copper-free Click Chemistry reactions. Methyltetrazine can be used to convert azido-containing peptides or proteins into tetrazine-modified peptides or protein without catalyst or axillary reagents.
    Methyltetrazine-PEG4-DBCO
  • HY-W800725
    m-PEG2-DBCO 2698341-01-2 98%
    m-PEG2-DBCO is a monodisperse PEG reagents which can enable copper-free Click Chemistry through the reaction of DBCO with azide.
    m-PEG2-DBCO