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NEW
Item number: TGM-T89778-10mg
Description: DBCO-PEG24-NHS ester is a click chemistry reagent featuring an NHS ester functionality, allowing for specific and efficient covalent bonding with primary amines (such as lysine residue side chains or aminosilane-coated surfaces) under neutral or slightly basic conditions. The hydrophilic polyethylene...
| MW: | 1530.74 D |
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NEW
Item number: TGM-T89781-10mg
Description: (2S)-N3-IsoSer is a click chemistry reagent characterized as a chiral alpha-hydroxy acid with an azide group. Target: ADC Linker. Smiles: [C@@H](C(O)=O)(CN=[N+]=[N-])O
| MW: | 131.09 D |
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NEW
Item number: TGM-T89783-10mg
Description: N3-Gly-Gly-OH is a click chemistry reagent that holds significant potential for applications in the binding of nucleic acids, lipids, proteins, and other molecules. Click chemistry is employed across various research domains due to its high yield, specificity, and simplicity, contributing to its broad...
| MW: | 158.12 D |
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NEW
Item number: TGM-T89784-10mg
Description: Z-L-Aha-OH (DCHA) is a click chemistry reagent that contains an azido group. Target: ADC Linker. Smiles: N(C1CCCCC1)C2CCCCC2.[C@H](NC(OCC1=CC=CC=C1)=O)(CCN=[N+]=[N-])C(O)=O
| MW: | 459.58 D |
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NEW
Item number: TGM-T89789-10mg
Description: H-D-Tyr(Propargyl)-OH is a click chemistry reagent that contains an Alkyne group, allowing it to undergo a copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules that possess an Azide group. This compound is specifically designed for applications involving azide-containing...
| Keywords: | O-Propargyl-D-tyrosine |
| MW: | 219.24 D |
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NEW
Item number: TGM-T89800-10mg
Description: H-L-Tyr(3-N3)-OH is a click chemistry reagent containing an azide group. This compound enables copper-catalyzed azide-alkyne cycloaddition reactions (CuAAc) with molecules that have an alkyne group. It can also undergo strain-promoted alkyne-azide cycloaddition reactions (SPAAC) with molecules...
| MW: | 222.2 D |
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NEW
Item number: TGM-T89802-10mg
Description: DecarboxyBiotin-Alkyne is a click chemistry reagent featuring an alkyne group. Click chemistry is extensively applied in the coupling of nucleic acids, lipids, proteins, and other molecules due to its beneficial properties such as high yield, high specificity, and simplicity, making it invaluable across...
| MW: | 238.35 D |
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NEW
Item number: TGM-T89805-10mg
Description: Boc-L-Phe(4-NH-Poc)-OH is a chemical reagent with an azido group used in peptide synthesis as a protected orthogonal building block. The propargyl group, commonly abbreviated as Poc or Pryoc, serves as a standard alkyne component for click conjugation and can be combined with tetrazine connectors in...
| MW: | 362.38 D |
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NEW
Item number: TGM-T89808-10mg
Description: N3-TOTA-Suc is a click chemistry reagent that features an azide group. Click chemistry is known for its excellent bioorthogonality, characterized by biocompatibility, rapid action, and high specificity within biological environments. This compound is capable of undergoing copper-catalyzed azide-alkyne...
| MW: | 346.38 D |
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NEW
Item number: TGM-T89809-10mg
Description: (2S,3R)-H-Abu(3-N3)-OH (hydrochloride) is a click chemistry reagent containing an azide group. This compound can undergo a copper-catalyzed azide-alkyne cycloaddition reaction (CuAAC) with molecules that possess an alkyne group. Additionally, it is capable of engaging in strain-promoted alkyne-azide...
| MW: | 180.59 D |
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NEW
Item number: TGM-T89813-10mg
Description: Boc-D-Lys(N3)-OH is a Boc-protected amino acid derivative that serves as a click chemistry reagent and as an intermediate for synthesizing linkers. Target: ADC Linker. Smiles: [C@@H](NC(OC(C)(C)C)=O)(CCCCN=[N+]=[N-])C(O)=O
| MW: | 272.3 D |
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NEW
Item number: TGM-T89817-10mg
Description: N3-L-Lys(Boc)-OH is a click chemistry reagent featuring an azide group that can undergo a copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing an alkyne group. Additionally, it can participate in strain-promoted azide-alkyne cycloaddition reactions (SPAAC) with...
| MW: | 272.3 D |
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