| Identification | Back Directory | [Name]
FMOC-HIS-OH | [CAS]
116611-64-4 | [Synonyms]
Fmoc-His
FMOC-HIS-OH
Fmoc-L-His-OH
FMOC-HISTIDINE
FMOC-L-HISTIDINE
Nα-Fmoc-L-histidine
N-α-Fmoc-L-histidine
N-a-Fmoc-L-histidine
FMOC-HIS-OH USP/EP/BP
Nα-Fmoc-L-histidine99%
N^a-Fmoc-L-histidine,98%
N-.ALPHA.-FMOC -L-HISTIDINE
(9H-Fluoren-9-yl)MethOxy]Carbonyl His-OH
N-[(9H-Fluoren-9-ylMethoxy)carbonyl]-L-histidine
N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-L-HISTIDINE
(((9H-Fluoren-9-yl)methoxy)carbonyl)-L-histidine
Nα-(9H-Fluorene-9-ylmethoxycarbonyl)-L-histidine
(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-(1H-imidazol-5-yl)propanoicaci
(S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-(1H-imidazol-4-yl)propanoic acid
(2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-(1H-imidazol-5-yl)propanoic acid | [Molecular Formula]
C21H19N3O4 | [MDL Number]
MFCD00190885 | [MOL File]
116611-64-4.mol | [Molecular Weight]
377.39 |
| Chemical Properties | Back Directory | [Melting point ]
171-174 °C(Solv: methanol (67-56-1); water (7732-18-5)) | [Boiling point ]
706.7±60.0 °C(Predicted) | [density ]
1.372±0.06 g/cm3(Predicted) | [storage temp. ]
2-8°C | [solubility ]
DMSO (Slightly), DMF (Slightly, Sonicated), Methanol (Very Slightly, Heated) | [form ]
Solid | [pka]
3.26±0.10(Predicted) | [color ]
White | [InChIKey]
SIRPVCUJLVXZPW-IBGZPJMESA-N | [SMILES]
C(O)(=O)[C@H](CC1N=CNC=1)NC(OCC1C2=C(C=CC=C2)C2=C1C=CC=C2)=O |
| Hazard Information | Back Directory | [Description]
Nα-Fmoc-L-histidine (FMOC-HIS-OH) holds great significance as a synthetic amino acid extensively employed in peptide synthesis. Its versatility makes it a highly sought-after reagent, widely used in various synthetic processes to create peptides, proteins, and even small molecules. Moreover, it catalyzes peptide and protein synthesis, further enhancing its utility. It is pivotal in unravelling biological processes such as enzymatic catalysis, protein structure, and drug design. Notably, this remarkable amino acid aids in understanding cell signalling pathways, which bear paramount importance in comprehending the mechanisms underlying diseases. The mechanism of action for Nα-Fmoc-L-histidine revolves around its ability to form essential peptide bonds. These bonds arise through a reaction with specific reagents, like DCC, leading to the creation of peptides. Subsequently, deprotection of the peptide bond occurs with the addition of a base, such as sodium hydroxide, followed by an acid, like trifluoroacetic acid. | [Uses]
Nα-Fmoc-L-histidine is an N-Fmoc-protected form of L-Histidine (H456010). L-Histidine is an essential amino acid that plays an important role in mitochondrial glutamine transport and has potential of abolishing oxidative stress caused by brain edema.L-Histidine promotes zinc uptake in human erythrocyes and also has potential as an antioxidant therapy for acute mammary inflammation in cattle. |
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