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coverage: cross-linking reagents, cross-linker related post-translational modifications, and derivatization reagents for GC-MS and LC-MS
creator: Alexander Leitner <leitner <-at-> imsb.biol.ethz.ch>
creator: Gerhard Mayer <mayerg97 <-at-> rub.de>
creator: Lutz Fischer <lfischer <-at-> staffmail.ed.ac.uk>
creator: Nils Hoffmann <nils.hoffmann <-at-> isas.de>
Indicates that the derivatization reagent can be detected by the specified chromophore.
Indicates that the cross-linking reagent has a linker that can be enabled by click chemistry.
Indicates that the derivatization reagent can be detected by the specified electrophore.
Indicates that the derivatization reagent can be detected by the specified fluorophore.
Indicates that the cross-linking reagent has a handle that can be used for detection/identification, enrichment or purification.
Indicates that the cross-linking reagent has a neutral loss reporter.
Indicates a property of a cross-linking or derivatization reagent.
Indicates that the cross-linking or derivatization reagent has the specified reactive group.
Indicates how the cross-linking reagent can be activated.
Indicates biochemical analogues of nucleobases, nucleosides or amino acids.
Indicates that the cross-linking reagent is cleavable.
Indicates that the cross-linking or derivatization reagent has an isotopic label.
Specifies the type of the cross-linker related chemical modification.
Indicates the chemical group that can react with the cross-linking or derivatization reagent.
Indicates the cross-linking reagent from which the chemical modification is derived.
The basic part of relationship indicating a top-level branch of this ontology.
Proteomics Standards Initiative cross-linking and derivatization controlled vocabulary.
Entity relevant to the domain of cross-linking in proteomics.
Dead-end modification resulting from a cross-linker reagent reacting only with one peptide.
cross-linker related chemical modification
A cross-linker acting as label transfer reagent.
Compound that can link two or more polymer chains.
A cross-linking reagent with identical reactive groups at each end of the spacer arm.
A cross-linking reagent with at least two different reactive groups.
OBSOLETE A cross-linking reagent that becomes reactive when exposed to ultraviolet or visible light.
This term was made obsolete because photo-reactivity is now encoded for the reactive groups of the cross-linkers, see (XLMOD:00108).
A cross-linking reagent causing direct conjugation without becoming part of the final cross-link between the target molecules.
Indicates that a cross-linker is deuterium labelled.
Indicates that a cross-linker is hydrolyzed, for example for NHS-type reagents -C(=O)-NHS was converted to -C(=O)-OH.
Indicates that a cross-linker is amidated.
Indicates that a cross-linker is membrane permeable.
Indicates that a cross-linker is hydrophilic.
Indicates that a cross-linker is fluorescent.
Indicates that a cross-linker is cleavable.
Indicates that a cross-linker is chemically cleavable.
Indicates that a cross-linker is mass-spectrometrically cleavable, i.e. contains a MS2 labile bond leading to fragments detected in MS3.
Indicates that a cross-linker facilitates enrichment.
Indicates that a cross-linker is iodinatable, e.g. for autoradiographic detection by radio-labelling with J-131.
Indicates a dead-end modification that was amidated by an ammonium salt, like e.g. bicarbonate, phosphate, chloride, for example for NHS-type reagents -C(=O)-NHS was converted to -C(=O)-NH2.
Indicates a dead-end modification that was amidated by Tris(hydroxymethyl)-aminomethane, for example for NHS-type reagents -C(=O)-NHS was converted to -C(=O)-NHC(CH2OH)3.
Indicates that a cross-linker contains a cleavable S-S bond, which is chemically cleavable by reducing agents like e.g. thiols, beta-mercaptoethanol, dithiothreitol (DTT), mercaptomethylamine or Tris(2-carboxyethyl)phosphin (TCEP).
Indicates that a cross-linker is chemically cleavable by the oxidizing agent periodate.
Indicates that a cross-linker is chemically cleavable by hydroxylamine.
An attribute describing a reactive group.
Indicates that a reactive group reacts with specific functional groups.
Indicates that a reactive group is reactive with primary amino (-NH2) groups.
Indicates that a reactive group is reactive with sulfhydryl (-SH) groups.
Indicates that a reactive group is reactive with carboxyl (-COOH) groups.
Indicates that a reactive group is reactive with aldehyde (-CHO) or carbonyl (-CO) groups.
Indicates that a reactive group is reactive with hydroxyl (-OH) groups.
Indicates that a reactive group is reactive with azide (-N3) groups.
Indicates that a cross-linker is cleavable by light.
Indicates that a cross-linker is mass-spectrometrically cleavable by collission induced dissociation.
Indicates that a cross-linker is labelled with carbon-13.
Indicates that a cross-linker is non-selective (i.e. can react with different amino acids, but also with DNA/RNA and carbohydrates (aldehyde reactive)).
Indicates that a cross-linker is chemically cleavable by the reducing agent DTT (dithiothreitol).
Indicates that a cross-linker is chemically cleavable by ammonium hydroxide.
Indicates that a cross-linker is mass-spectrometrically cleavable by in-source decay.
Indicates that a cross-linker is mass-spectrometrically cleavable (reducible) by thiols.
Indicates that a cross-linker is chemically cleavable by the reducing agent TCEP (Tris(2-carboxyethyl)phosphin).
Indicates that a cross-linker is chemically cleavable by the reducing agent mercaptoethanol.
Indicates that a cross-linker is mass defect labelled.
Indicates that a reactive group is reactive with thioether (R1-S-R2) groups.
Indicates that a reactive group is reactive with the heterocyclic imidazole groups.
Indicates that a cross-linker is thioesterized.
Indicates that a reactive group is reactive with RNA or DNA.
An amino acid derivative used in cross-linking experiments.
A handle attached to a cross-linker used for detection, affinity enrichment or purification.
A Biotin affinity handle, enrichable with avidin, streptavidin or neutravidin, attached to a cross-linker.
An alkyne (hadrocarbon with at least one C-C triple bond) tag, e.g. BARAC (biarylazacycloctynone) to enable enrichment of cross-linked peptides by either coupling of an affinity group with alkyne-azido click chemistry or by using immobilized azide linkers.
A dinitrobenzole affinity handle for enrichment with anti-DNB antibodies, attached to a cross-linker.
A photoreactive azide (-N3) tag to enable enrichment of cross-linked peptides with either immobilized alkyne linkers or by azide-alkyne click chemistry using biotin-alkyne respective biotin-phosphine.
An alpha-cyano-4-hydroxycinnamic acid UV-absorbing label for signal enhancement.
Indicates that a cross-linker is chemically cleavable by bases.
Indicates that a reactive group is reactive with hydrazines (N2H4).
Indicates that a reactive group is reactive with carbonyl (R1-CO-R2) groups.
Indicates that a cross-linker is oxidized, e.g. by oxidizing a carbonyl to a carboxyl functional group.
Indicates that a cross-linker is modified to it's alkene form (loss of two hydrogen atoms by forming a C=C double bond).
Indicates that a cross-linker is chemically cleavable by acids.
Indicates that a cross-linker contains a CID (Collision Induced Dissociation) cleavable C-S bond.
Indicates that a cross-linker is labelled with oxygen-18.
A Iminobiotin trifluoroacetamide affinity handle, enrichable with avidin, streptavidin or neutravidin, attached to a cross-linker.
Indicates that a reactive group is reactive with either of the glycoproteins avidin, streptavidin or neutravidin.
A nitrogeneous base occurring in nucleic acids.
A purine base occurring in nucleic acids.
A pyrimidine base occurring in nucleic acids.
A nucleobase derivative used in cross-linking experiments for protein-oligonucleotide cross-linking.
A combination of a nucleobase and a sugar (either ribose or deoxyribose).
A nucleoside derivative used in cross-linking experiments for protein-oligonucleotide cross-linking.
A biotin-alkyne affinity handle, which can be used for enrichment with click-chemistry.
A tetramethylrhodamine-alkyne affinity handle, which can be used for enrichment with click-chemistry.
A lipid analogue used in cross-linking experiments for lipid-protein cross-linking.
A sialic acid analogue used in cross-linking experiments for glycan-protein cross-linking.
Alkenization dead-end modification resulting from a cross-linker reagent reacting only with one peptide.
alkenized cross-linker related chemical modification
Ammonium amidation dead-end modification resulting from a cross-linker reagent reacting only with one peptide.
ammonium amidation cross-linker related chemical modification
Hydrolization dead-end modification resulting from a cross-linker reagent reacting only with one peptide.
hydrolization cross-linker related chemical modification
Oxidition dead-end modification resulting from a cross-linker reagent reacting only with one peptide.
oxidation cross-linker related chemical modification
Thio-esterization dead-end modification resulting from a cross-linker reagent reacting only with one peptide.
thioesterization cross-linker related chemical modification
Indicates that a cross-linker is chemically cleavable by formic acid.
Part of a cross-linker that reacts with the amino-acids of the protein.
A reactive group (N-hydroxysuccinimide) that reacts with lysines and N-termini but also serines, threonines and tyrosines.
A reactive group (N-hydroxysulfosuccinimide) that reacts with lysines and N-termini but also serines, threonines and tyrosines.
Photoreactive group (R1-CN2-R2) that inserts into any C-H or N-H bond.
A reactive group that reacts with amines.
A Carboxyl-to-amine (R1-N=C=N_R2) reactive chemical group.
(K,N,Q,R,Protein N-term)&(E,D,Protein C-term)
A reactive group that reacts with sulfhydryl groups.
A nitrophenyl azide photoreactive group.
Indicates that a reactive group is photoreactive.
A pyridinyldisulfide reactive group that reacts with sulfhydryl groups to form disulfide bonds.
A hydrazide reactive group (-CO-NH-NH2) that reacts with carbonyls to form hydrazone bonds.
An amine-reactive chemical group (R1-C(=NH)-OR2).
A reactive group (alpha-haloacetyl, halo-C2H5), mostly a iodoacetyl, bromoacetyl or chloroacetyl group, that reacts with sulfhydryl groups.
A reactive group (R-O-N-R2) that conjugates to carbonyls.
Photoreactive aryl(Ar)-substitited azide (N=N=N) group, that initiates addition reactions with double bonds or insertion into C-H and N-H bonds or reacts with primary amines.
An arginine-specific reactive group (H-CO-CO-H).
A reactive group (CH2=CH-CO-R) that reacts with sulfhydryl (-SH) groups.
Tetrafluorophenyl (TFP) azide (N=N=N) photoreactive group.
A reactive group (F5-Ph) that reacts with amines.
A reactive group (Ch3-SO2-S-R) that reacts with sulfhydryl (-SH) groups.
Photoreactive group that inserts into any C-H bond.
Indicates that a reactive group is thermoreactive.
An isocyanate (-N=C=O) that reacts with hydroxyl groups.
A hydroxyphenyl azid photoreactive group.
A iodoacetyl reactive group, that reacts with sulfhydryl groups.
A bromoacetyl reactive group, that reacts with sulfhydryl groups.
Platinum(II) coordinates with the side chains of methionine (Met), cysteine (Cys), and histidine(His), namely, thioether, sulfhydryl, and imidazole.
Reactive group (-NH2) that reacts with carboxyl (-COOH) groups.
A photoreactive group that reacts with pyrimidines, especially thymines of nucleic acids.
A photoreactive azido-methylcoumarin group.
A photoreactive perfluoroaryl azide group.
A photoreactive diazo (R1R2C=N=N) group.
A reactive group (-COOH) that reacts with primary amine (-NH2) groups.
A reactive group that reacts with amine groups.
A reactive group that reacts with hydroxyl groups.
A reactive group (C=O)that reacts with hydrazines (N2H4).
A hydrazone reactive group (C=NH-NHR) that reacts with carbonyls.
Used to incorporate sulfhydryl (-SH) groups into proteins as part of a two-step or heterobifunctional crosslinking strategy.
An aryl halide group (Ar-halogen) that reacts with primary amines.
A dimethylether (Ch3-O-CH3) reactive group that reacts with carboxyl groups.
Indicates that a reactive group is photocleavable.
Indicates that a reactive group is photoactivatable.
A pentylamine (CH3(CH2)4-NH2) reactive group that reacts with carboxyl groups.
A biotin reactive group that reacts with avidin, streptavidin or neutravidin.
A reactive group that reacts with guanin.
An imino (R1R2-C=N-R3) reactive group that reacts with primary amines.
An acyl chloride (R-CO-Cl) reactive group that reacts with alcohol, phenol, thiol and amines.
A sulfonyl chloride (R-SO2-Cl) reactive group.
A benzofurazan (2,1,3-benzoxadiazole) reactive group.
A halobenzofurazan (2,1,3-benzoxadiazole) reactive group with a halogen (-F, -Cl) modification.
A 4-substituted 1,2,4-triazoline-3,5-dione (TAD) reactive group.
An (alkyl- or aryl-substituted) boronic acid (R-B-(OH)2) reactive group.
An isothiocyanate (-N=C=S) reactive group.
A chloroformate (Cl-CO-OR) reactive group.
A sulfonate (R1-SO2O-R2) reactive group.
An anhydride (R1-CO-O-CO-R2) reactive group.
Reactive group (-COOH) that reacts with amino (-NH2) groups.
A benzyl bromide (C6H5CH2Br) reactive group.
Indicates that a cross-linker is chemically cleavable by sodium dithionite.
A benzoyl bromide (C6H5COBr) reactive group.
Indicates a cross-linker facilitating IMAC (immobilized metal affinity chromatography) enrichment.
A phosphonic acid handle, which can be used for IMAC-enrichment.
Hydrolyzed bis(sulfosuccinimidyl)suberate.
Ammonium amidated bis(sulfosuccinimidyl)suberate.
Ammonium amidated disuccinimidyl suberate.
Deuterium labelled hydrolyzed disuccinimidyl 2,2,7,7-suberate.
Deuterium labelled ammonium amidated disuccinimidyl 2,2,7,7-suberate.
Deuterium labelled hydrolyzed disuccinimidyl 2,2,3,3,4,4,5,5,6,6,7,7-suberate.
Deuterium labelled ammonium amidated disuccinimidyl 2,2,3,3,4,4,5,5,6,6,7,7-suberate.
Deuterium labelled hydrolyzed bis(sulfosuccinimidyl) 2,2,7,7-suberate.
Deuterium labelled ammonium amidated bis(sulfosuccinimidyl) 2,2,7,7-suberate.
Hydrolyzed bis(sulfosuccinimidyl) glutarate.
Ammonium amidated bis(sulfosuccinimidyl) glutarate.
Ammonium amidated disuccinimidyl glutarate.
Deuterium labelled hydrolyzed disuccinimidyl 2,2,4,4-glutarate.
Deuterium labelled ammonium amidated disuccinimidyl 2,2,4,4-glutarate.
Deuterium labelled hydrolyzed bis(sulfosuccinimidyl) 2,2,4,4-glutarate.
Deuterium labelled ammonium amidated bis(sulfosuccinimidyl) 2,2,4,4-glutarate.
Biotin Aspartate Proline n-hydroxyphthalimide-stump.
Hydrolyzed dithiobis[succinimidyl propionate.
Ammonium amidated dithiobis[succinimidyl propionate.
Hydrolyzed ethylene glycolbis(succinimidylsuccinate).
Ammonium amidated ethylene glycolbis(succinimidylsuccinate).
Hydrolyzed bimane bisthiopropionic acid N-succinimidyl ester.
Ammonium amidated bimane bisthiopropionic acid N-succinimidyl ester.
Hydrolyzed cyanurbiotindipropionylsuccinimide.
Ammonium amidated cyanurbiotindipropionylsuccinimide.
Ammonium amidated disuccinimidyladipic acid.
Ammonium amidated TEABS cross-linking reagent.
Hydrolyzed deuterium labelled 3,3'-Dithiobis[sulfosuccinimidylpropionate].
Ammonium amidated deuterium labelled 3,3'-Dithiobis[sulfosuccinimidylpropionate].
Hydrolyzed deuterium-labelled dithiobis[succinimidyl propionate.
Ammonium amidated deuterium-labelled dithiobis[succinimidyl propionate.
Hydrolyzed ethylene glycolbis(sulfosuccinimidylsuccinate).
Ammonium amidated ethylene glycolbis(sulfosuccinimidylsuccinate).
Deuterium labelled hydrolyzed ethylene glycolbis(succinimidylsuccinate).
Deuterium labelled ammonium amidated ethylene glycolbis(succinimidylsuccinate).
Deuterium labelled hydrolyzed ethylene glycolbis(sulfosuccinimidylsuccinate).
Deuterium labelled ammonium amidated ethylene glycolbis(sulfosuccinimidylsuccinate).
Hydrolyzed 13C labelled disuccinimidyladipic acid.
Ammonium amidated 13C labelled disuccinimidyladipic acid.
Deuterium labelled hydrolyzed cyanurbiotindipropionylsuccinimide.
Deuterium labelled ammonium amidated cyanurbiotindipropionylsuccinimide.
Hydrolyzed cyanurbiotindimercaptopropionylsulfosuccinimide.
Ammonium amidated cyanurbiotindimercaptopropionylsulfosuccinimide.
Deuterium labelled hydrolyzed cyanurbiotindimercaptopropionylsulfosuccinimide.
Deuterium labelled ammonium amidated cyanurbiotindimercaptopropionylsulfosuccinimide.
Deuterium labelled hydrolyzed bis(sulfosuccinimidyl) 2,2,3,3,4,4,5,5,6,6,7,7-suberate.
Deuterium labelled ammonium amidated bis(sulfosuccinimidyl) 2,2,3,3,4,4,5,5,6,6,7,7-suberate.
Deuterium labelled hydrolyzed disuccinimidyl 2,2,3,3,4,4-glutarate.
Deuterium labelled ammonium amidated disuccinimidyl 2,2,3,3,4,4-glutarate.
Deuterium labelled hydrolyzed bis(sulfosuccinimidyl) 2,2,3,3,4,4-glutarate.
Deuterium labelled ammonium amidated bis(sulfosuccinimidyl) 2,2,3,3,4,4-glutarate.
Hydrolyzed Suberic acid 1,8-dihydrazide.
Deuterium labelled hydrolyzed suberic acid 1,8-dihydrazide.
Deuterium labelled hydrolyzed adipic acid 1,6-dihydrazide.
Hydrolyzed glutaric acid 1,5-dihydrazide.
Deuterium labelled hydrolyzed glutaric acid 1,5-dihydrazide.
Hydrolyzed bis-(N-hydroxysuccinimidyl) 3-amino-N-biotinoyl-1,5-pentanedioate.
Hydrolyzed bis-(N-hydroxysuccinimidyl) 5-amino-N-biotinoyl-1,9-nonanedioate.
Hydrolyzed dibenzoyloxysuccinimidylethyl phosphate.
Hydrolyzed bis(succinimidyl)-3-azidomethyl glutarate.
Hydrolyzed crosslinking reagent JMV 3378.
Hydrolyzed 4-[3-(2-{2-[(2,5-dioxo-pyrrolidin-1-yloxycarbonyl-methyl)-carbamoyl]-pyrrolidin-1-yl}-2-oxo-ethyl)-thioureido]-butyric acid 2,5-dioxo-pyrrolidin-1-yl ester.
Hydrolyzed NHS-amino butyric acid-urea-amino butyric acid-NHS.
Ammonium amidated diethylsuberthioimidate.
Hydrolyzed bis(sulfosuccinimidyl)suberate pentaethyleneglycol.
Ammonium amidated bis(sulfosuccinimidyl)suberate pentaethyleneglycol.
Hydrolyzed bis(2-[Succinimidooxycarbonyloxy]ethyl) sulfone.
Ammonium amidated bis(2-[Succinimidooxycarbonyloxy]ethyl) sulfone.
Ammonium amidated disuccinimidyl tartrate.
Hydrolyzed succinimidyl-ester diazirine.
Hydrolyzed L-2-amino-4,4-azi-pentanoic acid.
Oxidized L-2-amino-4,4-azi-pentanoic acid.
Alkenized L-2-amino-4,4-azi-pentanoic acid.
Hydrolyzed L-2-amino-5,5-azi-hexanoic acid.
Oxidized L-2-amino-5,5-azi-hexanoic acid.
Alkenized L-2-amino-5,5-azi-hexanoic acid.
Hydrolyzed N-(beta-Maleimidopropyloxy)succinimide ester.
Ammonium amidated N-(beta-Maleimidopropyloxy)succinimide ester.
Deuterium labelled hydrolyzed pimelic acid dihydrazide.
Hydrolyzed disuccinimidyl-succinamyl-aspartyl-proline.
Hydrolized Protein Interaction Reporter.
4'-hydroxymethyl-4,5'8-trimethylpsoralen reagent.
bis-[3-(2-ketobutyraldehyde)ether reagent.
4-[bis-(2-chloroethyl)amino]benzenebutanoic acid reagent.
4-[bis-(2-chloroethyl)amino]benzenebutanoic acid
The N-(4-azidosalicylamidyl)-1,2-dilauroyl-sn-glycero-3-phosphoethanolamine lipid analogue used for lipid-protein cross-linking.
The Ac5-5-SiaDAz sialic acid analogue used for glycan-protein cross-linking.
The Ac4-ManNDAz sialic acid analogue used for glycan-protein cross-linking.
The Ac4-ManNAc sialic acid analogue used for glycan-protein cross-linking.
The Ac4-GlcNDAz sialic acid analogue used for glycan-protein cross-linking.
The Ac5-methyl-SiaDAz sialic acid analogue used for glycan-protein cross-linking.
Sialylated LacNAc-biotin used for glycan-protein cross-linking.
Psoralen-PEG3-Biotin biotinylation reagent.
Photoactivatable Biotin biotinylation reagent.
Biotin 3-sulfo-N-hydroxysuccinimide ester sodium salt.
Sulfo-NHS-LC-Biotin biotinylation reagent.
NHS-SS-PEG4-Biotin biotinylation reagent.
Biotinamidohexanoyl-6-aminohexanoic acid N-hydroxysuccinimide ester.
Biotin disulfide N-hydroxysuccinimide ester.
NHS-Iminobiotin trifluoroacetamide biotinylation reagent.
Maleimide-PEG11-Biotin biotinylation reagent.
Iodoacetyl-PEG2-Biotin biotinylation reagent.
Iodoacetyl-LC-Biotin biotinylation reagent.
Amine-PEG3-Biotin biotinylation reagent.
Biocytine-Hydrazide biotinylation reagent.
Long chain Biocytine-Hydrazide biotinylation reagent.
Biotin-PEG4-Hydrazide biotinylation reagent.
3-Azidopyridine-adenine dinucleotide reagent.
A photoreactive amino acid analog of L-Leucine for incorporation during protein synthesis that can be used for in vivo labelling, cross-linking and protein-protein interaction studies in live cells.
A photoreactive amino acid analog of L-Methionine for incorporation during protein synthesis that can be used for in vivo labelling, cross-linking and protein-protein interaction studies in live cells.
A photoreactive amino acid analog of L-Isoleucine for incorporation during protein synthesis that can be used for in vivo labelling, cross-linking and protein-protein interaction studies in live cells.
A photoreactive amino acid analog of L-Phenylalanine for incorporation during protein synthesis that can be used for in vivo labelling, cross-linking and protein-protein interaction studies in live cells.
Deuterium labelled p-benzoyl-L-phenylalanine.
A photoreactive deuterium-labelled amino acid analog of L-Phenylalanine for incorporation during protein synthesis that can be used for in vivo labelling, cross-linking and protein-protein interaction studies in live cells.
Suberic acid bis(3-sulfo-N-hydroxysuccinimide ester)
Suberic acid bis(N-hydroxysuccinimide ester)
Deuterium labelled disuccinimidyl 2,2,7,7-suberate.
Deuterium labelled disuccinimidyl 2,2,3,3,4,4,5,5,6,6,7,7-suberate.
Deuterium labelled (bis(sulfosuccinimidyl) 2,2,7,7-suberate).
Glutaric acid bis(3-sulfo-N-hydroxysuccinimide ester)
Deuterium labelled disuccinimidyl 2,2,4,4-glutarate.
Deuterium labelled bis(sulfosuccinimidyl) 2,2,4,4-glutarate.
1-ethyl-3-(3-Dimethylaminopropyl)carbodiimide hydrochloride.
3-(3-Dimethylaminopropyl)-1-ethyl-carbodiimide hydrochloride
Used to conjugate carboxyl functional groups to primary amines from peptides and proteins and is ideal for covalently binding proteins or peptides to carboxyl containing beads, resins, or nanoparticles.
Biotin Aspartate Proline n-hydroxyphthalamide.
5-Azido-2-nitrobenzoic acid N-hydroxysuccinimide ester
N-(beta-Maleimidopropyloxy)succinimide ester.
3-Maleimidopropionic acid N-hydroxysuccinimide ester
6-Maleimidohexanoic acid N-hydroxysuccinimide ester.
N-(epsilon-Malaimidocaproyloxy) succinimide ester
N-[gamma-Maleimidobutyryloxy] succinimide.
4-Maleimdobutyric acid N-succinimidyl ester
N-Succinimidyl 3-[2-pyridyldithio]-propionate.
3-(2-Pyridyldithio)propionic acid N-hydroxysuccinimide ester
Succinimidyl 6-(3-[2-pyridyldithio]-propionamido)hexanoate.
Succinimidyl 6-(3-(2-Pyridyldithio)propionamido)hexanoate
Sulfosuccinimidyl 6-(3'-[2-pyridyldithio]-propionamido)hexanoate.
m-Maleimidobenzoyl-N-hydroxysuccinimide ester.
3-Maleimidobenzoic acid N-hydroxysuccinimide ester
meta-Maleimidobenzoyl-N-hydroxysuccinimide ester
m-Maleimidobenzoyl-N-hydroxysulfosuccinimide ester.
3-Maleimidobenzoic acid N-hydroxysulfosuccinimide ester
meta-Maleimidobenzoyl-N-hydroxysulfosuccinimide ester
S-(2-thiopyridyl)-3-mercaptopropionic acid hydrazide
Bromoacetic acid N-hydroxysuccinimide ester
Iodoacetic acid N-hydroxysuccinimide ester
4-(N-Maleimidomethyl)cyclohexanecarboxylic acid N-hydroxysuccinimide ester
N-Succinimidyl 4-(maleimidomethyl)cyclohexanecarboxylate
Succinimidyl trans-4-(N-maleimidylmethyl)cyclohexane-1-carboxylate
4-(N-Maleimidomethyl)cyclohexane-1-carboxylic acid 3-sulfo-N-hydroxysuccinimide ester
N-Succinimidyl 4-[4-maleimidophenyl]butyrate.
4-(4-Maleimidophenyl)butyric acid N-hydroxysuccinimide ester
Succinimidyl 6-[(3-maleimido)propionamido]-hexanoate
N-Sulfosuccinimidyl-6-[4'-azido-2'-nitrophenylamino] hexanoate.
1-[6-[(4-azido-2-nitro-phenyl)amino]hexanoyloxy]-2,5-Dioxo-pyrrolidine-3-sulfonic acid
Sulfosuccinimidyl 6-((4'-azido-2'-nitrophenyl)amino)hexanoate
Sulfosuccinimidyl 6-((4-azido-2-nitrophenyl)amino)hexanoate
3,3'-Dithiodipropionic acid di(N-hydroxysuccinimide ester)
Di(N-succinimidyl) 3,3'-Dithiodipropionate
Deuterium labelled Dithiobis[1,1,2,2,2,2,3,3-succinimidyl propionate.
Sebacic acid bis[N-hydroxysuccinimide ester].
Sebacic acid bis(N-hydroxysuccinimide ester)
3,3'-Dithiobispropionic Acid Bis-sulfosuccinimidyl Ester
Ethylene glycolbis(succinimidylsuccinate).
Ethylene Glycol-Bis (Succinic Acid N-Hydroxysuccinimide Ester)
Ethylene glycol bis (succinimidylsuccinate)
Ethylene glycolbis(sulfosuccinimidylsuccinate).
Bis(sulfo-N-succinimidyl) ethylene glycol disuccinate
Ethylene Glycol-Bis (Succinic Acid N-Hydroxysulfosuccinimide Ester)
Ethylene glycol bis(sulfosuccinimidylsuccinate)
Ethylene glycol disuccinate bis(sulfo-N-succinimidyl) ester
Used to convert alcohols and amines into carbamates, esters, and ureas.
Cyclohexaamine, N,N'-methanetetraylbis-(9CI)
Used for coupling amines and carboxylates without the insertion of spacer atoms.
Used in conjunction with EDC-HCl (EDAC-HCl) to convert carboxyl groups to NHS esters which react with primary amines.
Used in conjunction with EDC-HCl (EDAC-HCl) to convert carboxyl groups to Sulfo-NHS esters which react with primary amines.
Bimane bisthiopropionic acid N-succinimidyl ester.
An isotopically-coded cleavable crosslinker affinity-purifyable with antibodies.
Click-enabled linker for interacting proteins.
Biotin-aspartate-Rink-glycine cross-linker composed of a biotin affinity handle (B), a pentafluorophenyl (PFP) ester modified aspartate reside (D), a Rink group (R), and a PFP ester modified glycine reside (G).
Deuterium labelled 3,3'-Dithiobis[sulfosuccinimidylpropionate].
Deuterium labelled ethylene glycolbis(succinimidylsuccinate).
Deuterium labelled ethylene glycolbis(sulfosuccinimidylsuccinate).
Deuterium labelled cyanurbiotindipropionylsuccinimide.
Deuterium labelled cyanurbiotindimercaptopropionylsulfosuccinimide.
Deuterium labelled suberic acid 1,8-dihydrazide.
Deuterium labelled adipic acid 1,6-dihydrazide.
Deuterium labelled glutaric acid 1,5-dihydrazide.
Deuterium labelled (bis(sulfosuccinimidyl) 2,2,3,3,4,4,5,5,6,6,7,7-suberate).
Deuterium labelled disuccinimidyl 2,2,3,3,4,4-glutarate.
Deuterium labelled bis(sulfosuccinimidyl) 2,2,3,3,4,4-glutarate.
Succinimidyl 4-(N-maleimidomethyl)cyclohexane-1-carboxy-(6-amidocaproate).
3,6,9,12-Tetraoxatetradecane-1,14-diyl dimethanethiosulfonate cross-linker.
3,6,9,12-Tetraoxatetradecane-1,14-diyl dimethanethiosulfonate
3,6,9-Trioxaundecane-1,11-diyl dimethanethiosulfonate cross-linker.
3,6,9-Trioxaundecane-1,11-diyl dimethanethiosulfonate
1,1-Methanediyl Bismethanethiosulfonate.
N-Succinimidyloxycarbonylpentyl methanethiosulfonate.
6-[(Methanethisulfonyl)thio]hexanoic acid, N-succinimidyl ester
3,6-dioxaoctane-1,8-diyl dimethanethiosulfonate.
3,6-Dioxaoctane-1,8-diyl Bismethanethiosulfonate
Bis(2-[Succinimidooxycarbonyloxy]ethyl) sulfone.
1,4-Di-(3'-[2'pyridyldithio]-propionamido) butane.
N-gamma-Maleimidobutyryloxysulfosuccinimide ester.
N-(epsilon-Maleimidocaproic acid) hydrazide.
N-(epsilon-Maleimidocaproic acid)hydrazide, TriFluoroacetic Acid.
2,5-Dihydro-2,5-dioxo-1H-pyrrole-1-hexanoic Acid Hydrazide 2,2,2-Trifluoroacetate
N-(epsilon-Maleimidocaproyloxy) sulfo succinimide ester.
6-Maleimidocaproic Acid Sulfo-N-Succinimidyl Ester
4-[(2-Iodoacetyl)amino]benzoic Acid 2,5-dioxo-1-pyrrolidinyl Ester
Sulfo succinimidyl 4-(maleimidophenyl) butyrate.
Succinimidyl-[(N-maleimidopropionamido)-tetraethyleneglycol] ester.
O-[N-(3-Maleimidopropionyl)aminoethyl]-O'-[3-(N-succinimidyloxy)-3-oxopropyl]triethylene glycol
Succinimidyl-[(N-maleimidopropionamido)-dodecaethyleneglycol] ester
Bis(beta-[4-azidosalicylamido]-ethyl) disulfide.
Bis(2-(4-azidosalicylamido)ethyl) disulfide
N, N'-(Dithiobis-ethylene)bis(4-azido-2-hydroxy-benzamide)
N-Hydroxysuccinimidyl-4-azidosalicyclic acid.
Sulfosuccinimidyl 2-(7-amino-4-methylcoumarin-3-acetamido)ethyl-1,3-dithiopropionate.
Sulfosuccinimidyl 2-(m-azido-o-nitrobenzamido)-ethyl-1,3'-dithiopropionate.
N-Succinimidyl 6-(4-azido-2-nitroanilino)hexanoate.
6-(4-Azido-2-nitrophenylamino)hexanoic acid N-hydroxysuccinimide ester
Sulfosuccinimidyl (4-azidophenyl)-1,3'-dithiopropionate.
Bis(2,5-dioxopyrrolidin-1-yl) 2,2'-(2,4-dibromophenylsulfonylazanediyl)diacetate.
Bis-(N-hydroxysuccinimidyl) 3-amino-N-biotinoyl-1,5-pentanedioate.
Bis-(N-hydroxysuccinimidyl) 5-amino-N-biotinoyl-1,9-nonanedioate.
N-succinimidyl p-benzoyldihydrocinnamate.
Deuterium labelled N-succinimidyl p-benzoyldihydrocinnamate.
S-Methyl 5,5'-thiodipentanoylhydroxysuccinimidemethylsulfate cross-linker.
S-Methyl 5,5'-thiodipentanoylhydroxysuccinimidemethylsulfate
Dibenzoyloxysuccinimidylethyl phosphate.
Bis(succinimidyl)-3-azidomethyl glutarate.
4-[3-(2-{2-[(2,5-dioxo-pyrrolidin-1-yloxycarbonyl-methyl)-carbamoyl]-pyrrolidin-1-yl}-2-oxo-ethyl)-thioureido]-butyric acid 2,5-dioxo-pyrrolidin-1-yl ester.
NHS-butyric acid-thiourea-glycine-proline-glycine-NHS
NHS-amino butyric acid-urea-amino butyric acid-NHS.
Succinimidyl 2-([4,4'-azipentanamido]ethyl)-1,3'-dithiopropionate.
Sulfosuccinimidyl 2-([4,4'-azipentanamido]ethyl)-1,3'-dithiopropionate.
DC4 cross-linker containing a DABCO (1,4-diazabicyclo[2.2.2]octane) moiety.
Sulfosuccinimidyl(4-azido-salicylamido) hexanoate.
Succinimidyl 6-(4,4'-azipentanamido)hexanoate
Sulfosuccinimidyl 6-(4,4'-azipentanamido)hexanoate
Dimethyl pimelinediimidate dihydrochloride
1,8-Dimethoxyoctane-1,8-diyldiammonium dichloride
Dimethyl ester octanediimidic acid dihydrochloride
Dimethyl 3,3'-dithiobispropionimidate dihydrochloride.
Bis(2-[Sulfosuccinimidooxycarbonyloxy]ethyl) sulfone.
2,5-dioxopyrrolidin-1-yl) 4-azidobenzoate
N-Succinimidyl (4-azidophenyl) 1,3´-dithiopropionate.
Succinimidyl-[(N-maleimidopropionamido)-diethyleneglycol] ester.
Succinimidyl-[(N-maleimidopropionamido)-hexaethyleneglycol] ester.
Succinimidyl-[(N-maleimidopropionamido)-octaethyleneglycol] ester.
Succinimidyl-[(N-maleimidopropionamido)-tetracosaethyleneglycol] ester.
11-Maleimidoundecanoic Acid Sulfo-N-Succinimidyl Ester cross-linker.
11-Maleimidoundecanoic Acid Sulfo-N-Succinimidyl Ester
3-N-Maleimidobenzoic Acid N-Succinimidyl Ester cross-linker.
3-N-Maleimidobenzoic Acid N-Succinimidyl Ester
N-Succinimidyl 3-(Bromoacetamido)propionate cross-linker.
N-Succinimidyl 3-(Bromoacetamido)propionate
1,3-Propanediyl bismethanethiosulfonate.
1,5-Pentanediyl bismethanethiosulfonate.
Succinimidyl(4-azido-salicylamido) hexanoate.
3-([2-Aminoethyl] dithio)-propionic acid hydrochloride.
N-(alpha-Maleimidoacetoxy)-succinimide ester.
N-(beta-Maleimidopropionic acid)hydrazide.
C6-Succinimidyl 4-hydrazinonicotinate acetone hydrazone.
Succinimdyl 3-(bromoacetamido)propionate.
Succinimidyl 4-hydrazidoterephthalate hydrochloride.
N-(kappa-maleimidoundecanoyloxy)sulfosuccinimide ester.
beta-(tris[hydroxymethyl]phosphine)propionic acid.
N-(kappa-Maleimidoundecanoic acid)hydrazide.
4-(4-N-Maleimidophenyl)butyric acid hydrazide-HCl.
Succinimidyl-2-(m-azido-o-nitrobenzamido)ethyl 1,3'-dithiopropionate.
Sulfosuccinimidyl-2-(m-azido-o-nitrobenzamido)ethyl 1,3'-dithiopropionate.
Sulfosuccinimidyl 2-(4-azidosalicylamido) ethyl-1,3-dithioproprioonate.
Succinimidyl 2-(4-azidosalicylamido) ethyl-1,3-dithioproprioonate.
Bis(sulfosuccinimidyl)suberate pentaethyleneglycol.
Bis(sulfosuccinimidyl)suberate nonaethyleneglycol.
N-hydroxysuccinimide ester ethane azide.
N-hydroxysuccinimide ester tetraoxapentadecane azide.
N-hydroxysuccinimide ester dodecaoxanonatriacontane azide.
4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride.
Deuterium labelled pimelic acid dihydrazide.
13C labelled azidobenzoic acid succinimide.
13C labelled carboxy-benzophenone-succinimide.
13C labelled succinimidyl-ester diazirine.
Deuterium labelled dimethyl disuccinimidyl sulfoxide.
Succinic acid succinimidyl ester 5-thioyloxy-2-nitrobenzyl ester.
Di 6-(3-succinimidyl carbonyloxymethyl-4-nitro-phenoxy)-hexanoic acid disulfide diethanol ester.
Azide-tagged acid-cleavable disuccinimidyl-bissulfoxide.
Alkyne-tagged acid-cleavable disuccinimidyl-bissulfoxide.
Polyethylene glycol photo-cleavable Leiker.
Biotinylated azo-Leiker 1 with an azobenzene-based chemical cleavage site.
Biotinylated azo-Leiker 2 with an azobenzene-based chemical cleavage site.
Deuterium labelled biotinylated azo-Leiker 2 with an azobenzene-based chemical cleavage site.
18O labelled (bis(sulfosuccinimidyl) 2,2,7,7-suberate).
Photo-cleavable Protein Interaction Reporter.
PEG5-Biotin-Dimer for crosslinking avidin molecules.
S-Methyl 5,5'-thiodipentanoylhydroxysuccinimide cross-linker.
S-Methyl 5,5'-thiodipentanoylhydroxysuccinimide
Sulfo-N-hydroxysuccinimidyl-2-(6-[biotinamido]-2-(p-azido benzamido)-hexanoamido) ethyl-1,3'-dithioproprionate
N-hydroxysuccinimidyl-2-(6-[biotinamido]-2-(p-azido benzamido)-hexanoamido) ethyl-1,3'-dithioproprionate
13C labelled 2,4,6-triazido-1,3,5-triazine.
Linker containing a dialkoxydiphenylsilane group.
Entity relevant to the domain of derivatization in chromatography.
Chemical reagent, which transforms a polar group in a molecule into a non-polar group in order to make the molecule volatile and analyzable by GC-MS.
Derivatization reagent replacing an active hydrogen by an aliphatic or aliphatic-aromatic group.
Silylation reagent replacing an active hydrogen by a silyl group.
Acylation reagent replacing an active hydrogen by a acyl (R-C=O-) group.
Fluorinated anhydride derivatization reagent.
Fluoracylimidazole derivatization reagent.
Halogenation reagent which can produce both silylated and halogenated derivatives.
Chiral derivatization reagent with an enatiomerically pure chiral derivatizing agent to form two diastereomeric derivatives that can be separated by gas chromatography.
Chemical reagent, which transforms an analyte so that its stability, separation, extraction, ionization efficiency and MS2 detectability are improved in LC-MS analysis.
Trimethylsilyl (TMS) reagent replacing an active hydrogen by a silyl group.
Dimethylsilyl (DMS) reagent replacing an active hydrogen by a silyl group.
Trifluoroacetyl (TFA) reagent replacing an active hydrogen by a silyl group.
Derivatization reagent replacing an active hydrogen by an aliphatic-aromatic group, e.g. a -phenyl, -tolyl, -xylyl, -naphthy, -benzyl group.
A chromophore group attached to a derivatization reagent for enhanced UB- or VIS-detectability.
A fluorophore group attached to a derivatization reagent for enhanced fluorescence or chemiluminescence detectability.
An electrophore group attached to a derivatization reagent for enhanced electrochemical detectability.
Indicates that a reactive group is reactive with secondary amino (=NH) groups.
Indicates that a derivatization reagent is reactive with active hydrogens like e.g. from -SH, -OH, -NH, -COOH groups.
Indicates that a derivatization reagent is reactive with amides.
Indicates that a derivatization reagent is reactive with amino acids.
Indicates that a derivatization reagent is reactive with nitrosamines.
Indicates that a derivatization reagent is reactive with sulfonamides.
Indicates that a derivatization reagent is reactive with carbohydrates and sugars.
Indicates that a derivatization reagent is reactive with catecholamines.
Indicates that a derivatization reagent is reactive with sulfides.
Indicates that a derivatization reagent is reactive with phenols.
Indicates that a derivatization reagent is reactive with ketones.
Indicates that a derivatization reagent is reactive with biphosphonate drugs.
Indicates that a derivatization reagent is reactive with steroids.
Indicates that a derivatization reagent is reactive with thiols.
Indicates that a derivatization reagent is reactive with vitamin D metabolites.
Indicates that a derivatization reagent is reactive with nucleosides.
Indicates that a derivatization reagent is reactive with cholesterols.
Indicates that a derivatization reagent is reactive with histamines.
Indicates that a derivatization reagent is reactive with glycans.
Indicates that a derivatization reagent is reactive with alpha-keto-acids.
Indicates that a derivatization reagent is reactive with citric acid.
Indicates that a derivatization reagent is reactive with phosphate.
Indicates that a derivatization reagent is reactive with perfluorinated carboxylic acids.
Indicates that a derivatization reagent is reactive with sialic acid.
Indicates that a derivatization reagent is reactive with bile acids.
Boron trifluoride derivatization reagent.
(-)-alpha-Methoxy-alpha-trifluoromethylphenylacetic acid.
Oximation reagent replacing an aldehyde keto group with an O-methyloxime group.
Deuterium labelled N-methyl-trimethylsilyltrifluoroacetamide.
Deuterium labelled N-methyl-N-t-butyldimethylsilyltrifluoroacetamide.
Deuterium labelled methyl chloroformate.
Triisopropylsilyl trifluoromethanesulfonate.
Triethylsilyl trifluoromethanesulfonate.
Tert-Butyldimethylsilyl methallylsulfinate.
3,3,3-Trifluoro-2-methoxy-2-phenylpropanoic acid.
4-Bromophenacyl trifluoro-methanesulfonate.
2,3,5,6-Tetrafluoro-4-ethanol(trifluoromethyl)benzyl bromide.
O-(2,3,4,5,6-Pentafluorobenzyl)hydroxylamine hydrochloride.
N,N-Dimethylformamidediisopropyl acetal.
N,N-Dimethylformamidedineopentyl acetal.
N,N-Dimethylformamidedi-tert-butyl acetal.
5-dimethylamino-1-naphthalenesulfonyl chloride
N-hydroxysuccinimide esters of N-alkyl(C1-C4)nicotinic acids.
2-fluoro-1-methylpyridinium p-toluenesulfonate.
5-dimethylaminonaphthalene-1-sulfonyl hydrazine
1-(2-hydrazino-2-oxoethyl)pyridinium chloride
1-(carboxymethyl)pyridium chloride hydrazide
1-(carboxymethyl)trimethylammonium chloride hydrazide
4-[2-(Trimethylammonio)ethoxy]anilinium dibromide.
4-(2-((4-bromophenethyl)dimethylammonio)ethoxy)benzenaminium dibromide.
6-aminoquinolyl-N-hydroxysuccinimidyl carbamate.
(2-[4-aminophenoxy]ethyl)trimethylammonium bromide.
Pentafluorophenacyl trifluoromethanesulfonate.
4-substituted 1,2,4-triazoline-3,5-dione (TAD).
Tris(trimethoxyphenyl)phosphonium compound.
1S-pentafluorophenyl tris(2,4,6-trimethoxyphenyl)phosphonium acetate bromide.
(4-hydrazino-4-oxobutyl) [tris(2,4,6-trimethoxyphenyl)phosphonium bromide.
Tris(2,4,6,-trimethoxyphenyl)phosphonium acetic acid.
Tris(2,4,6,-trimethoxyphenyl)phosphonium ethanoic acid bromide.
Tris(2,4,6,-trimethoxyphenyl)phosphonium propionic acid bromide.
Tris(2,4,6,-trimethoxyphenyl)phosphonium propylamine bromide.
Sulfur trioxide N,N-dimethyl-formamide complex.
2-acrylamino-2-methyl-propanesulfonic acid.
2-Acrylamido-2-methyl-1-propanesulfonic acid
4-Nitro-7-(1-piperazinyl)-2,1,3-benzoxadiazole hydrochloride
3-(2,5-dioxopyrrolidin-1-yl-oxycarbonyl)propyl]trimethylammonium chloride.
N-methylnicotinic acid N-hydroxysuccinimide ester.
Deuterium labelled N-methylnicotinic acid N-hydroxysuccinimide ester.
N-propylnicotinic acid N-hydroxysuccinimide ester.
Deuterium labelled N-propylnicotinic acid N-hydroxysuccinimide ester.
N-butylnicotinic acid N-hydroxysuccinimide ester.
Deuterium labelled N-butylnicotinic acid N-hydroxysuccinimide ester.
4-N,N,N-trimethylammonioanilylN'-hydroxysuccinimidyl carbamate iodide.
p-N,N,N-trimethylammonioanilylN'-hydroxysuccinimidyl carbamate iodide
Deuterium labelled p-N,N,N-trimethylammonioanilylN'-hydroxysuccinimidyl carbamate iodide.
Deuterium labelled 4-methylpiperazine acetyl succinimide.
Deuterium labelled 4-methylpiperadinebutyryl succinimide.
Deuterium labelled dimethylaminobutyryl succinimide.
Pentafluorophenyl-activated ester of polyethyleneglycol.
13C labelled pentafluorophenyl-activated ester of polyethyleneglycol.
Deuterium labelled 2-bromo-1-methylpyridinium iodide.
Deuterium labelled 3-carbinol-1-methylpyridinium iodide.
13C labelled p-dimethylaminophenacyl bromide.
Deuterium labelled 7-(N,N-dimethylaminosulfonyl)-4-(aminoethyl)piperadino-2,1-3-benzoxadiazole.
Deuterium labelled 7-(N,N-dimethylaminosulfonyl)-4-piperadino-2,1-3-benzoxadiazole.
Deuterium labelled pyridinioacetohydrazide chloride.
Deuterium labelled 2,4-dinitrophenylhydrazine.
1-(4-lsopropyl) phenyl-3-methyl-5-pyrazolone.
(5-N-succinimidoxy-5-oxopentyl)triphenylphosphonium bromide.
Triplex 5-diethylaminonaphthalene-1-sulfonyl chloride.
5-N-succinimidoxy-5-oxopentyl)triphenylphosphonium bromide.
2,5-dioxopyrrolidin-1-yl N-tri(pyrrolidino)phosphoranylideneamino carbamate.
Butyl 1-(pyridin-4-yl) piperidine 4-carboxylate.
O-2,3,4,5,6-(pentafluorobenzyl) hydroxylamine hydrochloride.
N-hydroxy-benzotriazolyl-(S)-naproxen ester.
4-(4-methyl-1-piperazyl)-3-nitrobenzoyl azide.
2-(2-[7H-dibenzo (a,g)carbazol-7-yl]-ethoxy)ethyl chloroformate.
N-methyl pyridinium-3-sulfonyl chloride.
2,4-dimethoxy-6-piperazin-1-yl pyrimidine.
1-(3-Aminopropyl)-3-bromoquinolinium bromide.
(S)-2,5-dioxopyrrolidin-1-yl-1-(4,6-dimethoxy-1,3,5-triazin-2-yl) pyrrolidine-2-carboxylate.
(R)-2,5-dioxopyrrolidin-1-yl-1-(4,6-dimethoxy-1,3,5-triazin-2-yl) pyrrolidine-2-carboxylate.
Deuterium labelled 4-(4-dimethylaminophenyl)-1,2,4-triazole-3,5-dione.
N-methyl-nicotinic acid N-hydroxysuccinimide ester.
A LC-MS derivatization reagent containing a fluoro-dinitrobenzene structure.
A LC-MS derivatization reagent containing a fluoro-dinitrophenyl structure.
1-Fluoro-2,4-dinitrophenyl-5-L-alanine amide
1-Fluoro-2,4-dinitrophenyl-5-D-alanine amide
1,2-Benzo-3,4-dihydrocarbazole-9-ethyl chloroformate.
(-)-1-(9-fluorenyl)-ethyl chloroformate.
(+)-1-(9-fluorenyl)-ethyl chloroformate.
2-(2,3-Naphthalimino)ethyl trifluoromethanesulfonate.
2-(2,3-Naphthalimino)ethyl trifluoromethanesulphonate
4-[2-(N,N-dimethylamino) ethylaminosulfonyl]-7-(2-aminobutylamino)-2,1,3-benzoxadiazole.
2-Amino-N,N,N-trimethylethanaminium chloride.
2,3,4,6-Tetra-O-acetyl-beta-D-glucopyranosyl isothiocyanate.
3-bromoactonyltrimethylammonium bromide.
1,2-dimethylimidazole-4-sulfonyl chloride.
Ferrocenecarboxylic acid-(2-maleimidoyl)ethylamide.
4-hydrazino-N,N,N-trimethyl-4-oxobutanaminium iodide.
3,4-dihydro-3,4-dioxonaphthalene-1-sulphonic acid
7-chloro-2,1,3-benzoxadiazole-4-sulfonylaminoethyltrimethylammonium chloride.
4- bromomethyl-6,7-methylenedioxycoumarin.
N-(1-naphthyl)ethylene diamine dihydrochloride.
Succinimidyloxycarbonylmethyl tris(2,4,6-trimethoxyphenyl)phosphonium bromide.
5-dimethylamino-1-naphthalenesulfonyl aminoethanol.
Urea crosslinker – C2-arm, NHS ester (DSAU)
Indicates that a cross-linker is generated through an enzymatic reaction.
protein-glutamine gamma-glutamyltransferase.Indicates that a cross-linker is generated by a transglutaminase enzymatic reaction.