110990-08-4
110990-08-4
Chemical Structure
(((9H-Fluoren-9-yl)methoxy)carbonyl)-D-lysine
- CAS No.: 110990-08-4
- Formula:C21H24N2O4
- Molecular Weight:368.43
IUPAC Name: (((9H-fluoren-9-yl)methoxy)carbonyl)-D-lysine
InChIKey: YRKFMPDOFHQWPI-LJQANCHMSA-N
SMILES: O=C(O)[C@H](NC(OCC1C2=C(C3=C1C=CC=C3)C=CC=C2)=O)CCCCN
Biological Activity: (((9H-Fluoren-9-yl)methoxy)carbonyl)-D-lysine is a lysine derivative[1].
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(((9H-Fluoren-9-yl)methoxy)carbonyl)-D-lysine | 99.51% | (((9H-Fluoren-9-yl)methoxy)carbonyl)-D-lysine is a lysine derivative. | ||||||||||||||||||||
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Fmoc-D-Lys(N3)-OH | 99.03% | Fmoc-D-Lys (N3)-OH is an Fmoc-protected azide-containing amino acid building block that is used in organic synthesis-related research. | ||||||||||||||||||||
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Fmoc-Lys(Me)2-OH hydrochloride | 99.36% | Fmoc-Lys(Me)2-OH HCl is a lysine derivative. | ||||||||||||||||||||
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Fmoc-Lys(Me)3-OH Chloride | 98.60% | Fmoc-Lys(Me)3-OH Chloride is a lysine derivative. | ||||||||||||||||||||
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Fmoc-Lys-OH | 99.93% | Fmoc-Lys-OH is a lysine derivative. | ||||||||||||||||||||
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Fmoc-D-Nle-OH | 99.11% | Fmoc-D-Nle-OH is a leucine derivative. | ||||||||||||||||||||
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Fmoc-L-Norleucine | 99.85% | Fmoc-L-Norleucine is a leucine derivative. | ||||||||||||||||||||
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Fmoc-Lys-OH hydrochloride | 99.84% | Fmoc-Lys-OH hydrochloride is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Fmoc-Lys-OH hydrochloride is also a alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs. | ||||||||||||||||||||
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Fmoc-D-Lys-OH.HCl | 99.66% | Fmoc-D-Lys-OH.HCl is a lysine derivative. | ||||||||||||||||||||
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Fmoc-Lys-OMe.HCl | 99.84% | Fmoc-Lys-OMe.HCl is a lysine derivative. | ||||||||||||||||||||
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N6-Diazo-L-Fmoc-lysine | 99.84% | N6-Diazo-L-Fmoc-lysine is an active compand and can be used in a variety of chemical studies. N6-Diazo-L-Fmoc-lysine is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups. | ||||||||||||||||||||
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