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 (62101):

Cat. No. Product Name CAS No. Purity Chemical Structure
  • HY-W591379
    Amino-PEG19-amine 1260522-55-1 98%
    Amino-PEG19-amine is a PEG linker containing two amine functional groups. The hydrophilic PEG spacer increases solubility in aqueous media. The amino groups are reactive with carboxylic acids, activated NHS esters, carbonyls (ketone, aldehyde), etc.
    Amino-PEG19-amine
  • HY-W591390
    6-Azidohexanoic acid STP ester 2586197-38-6 98%
    6-Azidohexanoic Acid STP Ester is an amine-reactive, water-soluble labeling reagent with an azide group and a terminal 4-Sulfo-2,3,5,6-tetrafluorophenyl (STP) group. 6-Azidohexanoic Acid STP Ester is used to modify proteins, antibodies, and other amine-containing biopolymers in aqueous media. The azide group can react with alkyne, BCN, DBCO via Click Chemistry to yield a stable triazole linkage. STP esters can react with primary amines, forming covalent amide bonds, and typically display much better stability toward hydrolysis in aqueous media, resulting in more efficiency and better reproducible labeling of biopolymers.
    6-Azidohexanoic acid STP ester
  • HY-W591393
    Biotin Azide Plus 2669097-31-6 98%
    Biotin Azide Plus is a biotinylation reagent used for labeing glycoproteins, carbohydrate-containing compounds that have oxidizable sugars or aldehydes. Biotin Azide Plus is a complete copper-chelating system that acts simultaneously as both reactant and catalyst in CuAAC reactions. The azide group can react with alkyne, BCN, DBCO via Click Chemistry to yield a stable triazole linkage.
    Biotin Azide Plus
  • HY-W591439
    Fmoc-Lys(Boc)-PAB-PNP 870487-07-3 98%
    Fmoc-Lys(Boc)-PAB-PNP is a Boc-protected Lysine linked to 4-aminobenzoiate (PAB) with terminal Fmoc and PNP groups. The Fmoc group can be deprotected under basic conditions to release the free amine which can be used for further conjugations.
    Fmoc-Lys(Boc)-PAB-PNP
  • HY-W591440
    Fmoc-Cit-PAB-PNP 870487-05-1 98%
    Fmoc-Cit-PAB-PNP is a Citrulline linked to 4-aminobenzoiate (PAB) with terminal Fmoc and PNP groups. The Fmoc group can be deprotected under basic conditions to release the free amine which can be used for further conjugations. PNP group is a good leaving group when reacting with an amine-bearing payload.
    Fmoc-Cit-PAB-PNP
  • HY-W591441
    Fmoc-Ala-PAB-PNP 1491136-21-0 98%
    Fmoc-Ala-PAB-PNP is an Alanine linked to 4-aminobenzoiate (PAB) with terminal Fmoc and PNP groups. The Fmoc group can be deprotected under basic conditions to release the free amine which can be used for further conjugations. PNP is a good leaving group when reacting with an amine-bearing payload.
    Fmoc-Ala-PAB-PNP
  • HY-W591838
    Perfluoropentanesulfonic acid 2706-91-4 98%
    Perfluoropentanesulfonic acid (PFPeS) is a per- and polyfluoroalkyl substance, which can be found as contaminant in wastewater.
    Perfluoropentanesulfonic acid
  • HY-W591962
    5-Azidopentan-1-ol 170220-11-8 98%
    5-Azidopentan-1-ol (1-Pentanol, 5-azido-) is a linker containing an azide group and a terminal hydroxyl group. The azide group can react with alkyne, BCN, DBCO via Click Chemistry to yield a stable triazole linkage. The hydroxyl group enables further derivatization or replacement with other reactive functional groups.
    5-Azidopentan-1-ol
  • HY-W591963
    5-Azidopentyl 4-methylbenzenesulfonate 1407974-54-2 98%
    5-Azidopentyl 4-methylbenzenesulfonate (Tos-pentane-azide) is a linker containing an azide group and a tosyl group. The azide group can react with alkyne, BCN, DBCO via Click Chemistry to yield a stable triazole linkage. The tosyl group is a good leaving group for nucleophilic substitution reactions.
    5-Azidopentyl 4-methylbenzenesulfonate
  • HY-W591964
    t-Boc-aminooxy-pentane-azide 2496687-07-9 98%
    t-Boc-Aminooxy-pentane-azide is a linker containing an azide group and Boc-protected amino group. The azide group can react with alkyne, BCN, DBCO via Click Chemistry to yield a stable triazole linkage. The Boc group can be deprotected under mild acidic conditions to form the free amine.
    t-Boc-aminooxy-pentane-azide
  • HY-W591965
    t-Boc-aminooxy-pentane-amine 848349-01-9 98%
    t-Boc-Aminooxy-pentane-amine is a linker containing an aminooxy group and a primary amine. The aminooxy group can be used in bioconjugation. It reacts with an aldehyde to form an oxime bond. If a reductant is used, it will form a hydroxylamine linkage. The amino group is reactive with carboxylic acids, activated NHS esters, carbonyls (ketone, aldehyde) etc.
    t-Boc-aminooxy-pentane-amine
  • HY-W591969
    Benzyl (6-oxohexyl)carbamate 98648-05-6 98%
    Benzyl (6-oxohexyl)carbamate is a linker containing an aldehyde group and a benzyl (Cbz) protecting group. The aldehyde can react with hydrazine or hydrazide to form a hydrolytic acyl hydrozone linkage. The benzyl protecting group can be removed via hydrogenolysis to form a free amine.
    Benzyl (6-oxohexyl)carbamate
  • HY-W591970
    8-Bromooct-1-yne 81216-13-9 98%
    8-Bromooct-1-yne is a six carbon reagent containing an alkyne group and a bromide group. The alkyne group can react with azide-bearing compounds or biomolecules in Click Chemistry reactions under the catalyzation of copper.
    8-Bromooct-1-yne
  • HY-W591971
    5-((tert-Butoxycarbonyl)amino)pentyl 4-methylbenzenesulfonate 118811-34-0 98%
    5-((tert-Butoxycarbonyl)amino)pentyl 4-methylbenzenesulfonate is a PEG linker containing a Boc protected amine and a tosyl group. The protected amine can be deprotected under mild acidic conditions. The tosyl group is a very good leaving group for nucleophilic substitution reactions.
    5-((tert-Butoxycarbonyl)amino)pentyl 4-methylbenzenesulfonate
  • HY-W591972
    6-Hydroxyhexyl 4-methylbenzenesulfonate 75351-33-6 98%
    6-Hydroxyhexyl 4-methylbenzenesulfonate is a six carbon linker containing a hydroxyl group and a tosyl group. The hydroxyl group enables further derivatization or replacement with other reactive functional groups. The tosyl group is a very good leaving group for nucleophilic substitution reactions.
    6-Hydroxyhexyl 4-methylbenzenesulfonate
  • HY-W591973
    OTs-C6-NHBoc 86536-92-7 98%
    OTs-C6-NHBoc is a six carbon linker containing a tosyl group and Boc-protected amine group. 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.
    OTs-C6-NHBoc
  • HY-W591975
    Alkyne maleimide 2785323-77-3 98%
    Alkyne maleimide is a bifunctional linker reagent with a terminal malimide group and a propargyl group. The maleimide group will react with a thiol group to form a covalent bond, enabling the connection of biomolecule with a thiol. The propargyl group can be linked to azide-containing biomolecules via Click Chemistry.
    Alkyne maleimide
  • HY-W591977
    Boc-5-aminopentanoic NHS ester 82518-79-4 98%
    Boc-5-aminopentanoic NHS ester is a linker containing an NHS ester and a t-Boc protected amine group. The t-Boc group can be deprotected under mild acidic conditions to form a free amine. The NHS ester can be used to label the primary amines (-NH2) of proteins, amine-modified oligonucleotides, and other amine-containing molecules.
    Boc-5-aminopentanoic NHS ester
  • HY-W591982
    t-Boc-N-amido-PEG12-acid 187848-68-6 98%
    t-Boc-N-amido-PEG12-acid is a PEG linker containing a terminal carboxylic acid and Boc-protected amino group. The hydrophilic PEG spacer increases solubility in aqueous media. 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. The Boc group can be deprotected under mild acidic conditions to form the free amine.
    t-Boc-N-amido-PEG12-acid
  • HY-W591992
    PEG17 4669-05-0 98%
    PEG17 is a polymer consisiting of repeating ethylene glycol subunits and terminal hydroxyl groups. The ethylene glycol units increase the water solubility of hydrophobic compounds, allowing for them to be more compatible in aqueous settings. The terminal hydroxyl groups can react to further derivatize the compound.
    PEG17