116821-47-7
116821-47-7
Chemical Structure
Fmoc-GABA-OH
- CAS No.: 116821-47-7
- Formula:C19H19NO4
- Molecular Weight:325.36
IUPAC Name: 4-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)butanoic acid
InChIKey: ACUIFAAXWDLLTR-UHFFFAOYSA-N
SMILES: O=C(O)CCCNC(OCC1C2=C(C3=C1C=CC=C3)C=CC=C2)=O
Biological Activity: Fmoc-4-aminobutanoic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
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Fmoc-GABA-OH | 99.49% | Fmoc-4-aminobutanoic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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Fmoc-β-Ala-OH | 99.93% | Fmoc-β-Ala-OH is an alanine derivative. | ||||||||||||||||||||
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Fmoc-ε-Acp-OH | 99.45% | Fmoc-ε-Acp-OH is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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Fmoc-7-amino-heptanoic acid | Fmoc-7-amino-heptanoic acid is an alkane chain with terminal Fmoc-protected amine and carboxylic acid groups. Fmoc-7-amino-heptanoic acid can be used as a PROTAC linker in the synthesis of PROTACs. The Fmoc group can be deprotected under basic condition to obtain the free amine which can be used for further conjugations. 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. | |||||||||||||||||||||
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Fmoc-5-Ava-OH | 99.44% | Fmoc-5-Ava-OH is an amino acid derivative with an Fmoc protecting group, which can be used to synthesize fatty acid-based dimeric peptides with PSD-95 inhibitory activity. | ||||||||||||||||||||
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(9H-Fluoren-9-yl)methyl (3-aminopropyl)carbamate hydrochloride | 99.88% | (9H-Fluoren-9-yl)methyl (3-aminopropyl)carbamate hydrochloride is a PROTAC linker that can be used in the synthesis of PROTACs. | ||||||||||||||||||||
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(9H-Fluoren-9-yl)methyl (4-aminobutyl)carbamate hydrochloride | (9H-Fluoren-9-yl)methyl (4-aminobutyl)carbamate hydrochloride is a PROTAC linker that can be used in the synthesis of PROTACs. | |||||||||||||||||||||
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(9H-Fluoren-9-yl)methyl (4-aminobutyl)carbamate | (9H-Fluoren-9-yl)methyl (4-aminobutyl)carbamate is a PROTAC linker that can be used in the synthesis of PROTACs. | |||||||||||||||||||||
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Fmoc-Gly-OH-15N | 99.67% | Fmoc-Gly-OH-15N (Fmoc-glycine-15N) is the 15N labeled Fmoc-Gly-OH (HY-Y1250). Fmoc-Gly-OH (Fmoc glycine) is a Fmoc-protected glycine derivative, can be used for the synthesis of compounds. | ||||||||||||||||||||
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Fmoc-Gly-OH-2-13C,15N | 99.55% | Fmoc-Gly-OH-2-13C,15N (Fmoc-glycine-2-13C,15N) is the 13C,15N labeled Fmoc-Gly-OH (HY-Y1250). Fmoc-Gly-OH (Fmoc glycine) is a Fmoc-protected glycine derivative, can be used for the synthesis of compounds. | ||||||||||||||||||||
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Fmoc-Gly-OH-13C | Fmoc-Gly-OH-13C (Fmoc-glycine-13C) is a 13C-labeled Fmoc-Gly-OH (HY-Y1250). Fmoc-Gly-OH (Fmoc glycine) is a Fmoc-protected glycine derivative, can be used for the synthesis of compounds. | |||||||||||||||||||||
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