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Filtered Search Results
eMolecules 86123-10-6 | Fmoc-D-Phe-OH | Ambeed | MFCD00062955 | 387.435 | C24H21NO4 | 98.000 | OC(=O)[C@@H](Cc1ccccc1)NC(=O)OCC1c2ccccc2-c2ccccc12 | 10g | 552586695
Fmoc-D-Phe-OH | Ambeed | 86123-10-6 | MFCD00062955 | 387.435 | C24H21NO4 | 98.000 | OC(=O)[C@@H](Cc1ccccc1)NC(=O)OCC1c2ccccc2-c2ccccc12 | 10g | 552586695
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Medchemexpress LLC N-Formyl-Met-Leu-Phe | 59880-97-6 | 99.9% | 437.55 | 5 MG
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N-Formyl-Met-Leu-Phe (fMLP) is a chemotactic peptide and specific ligand for the N-formyl peptide receptor (FPR). It inhibits TNF-alpha secretion and is used in research on osteogenesis, inflammation, and immune responses.
- Specific ligand for N-formyl peptide receptor (FPR)
- Inhibits TNF-alpha secretion
- Promotes osteoblastic commitment and osteogenesis
- Suppresses adipogenic commitment
- Induces proinflammatory cytokine gene expression
- Synergistically induces inflammatory responses with LPS
- Promotes bone formation in zebrafish and rabbits
- Induces calprotectin release from polymorphonuclear cells (PMN)
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eMolecules 86123-10-6 | Fmoc-D-Phe-OH | Ambeed | MFCD00062955 | 387.435 | C24H21NO4 | 98.000 | OC(=O)[C@@H](Cc1ccccc1)NC(=O)OCC1c2ccccc2-c2ccccc12 | 5g | 552586694
Fmoc-D-Phe-OH | Ambeed | 86123-10-6 | MFCD00062955 | 387.435 | C24H21NO4 | 98.000 | OC(=O)[C@@H](Cc1ccccc1)NC(=O)OCC1c2ccccc2-c2ccccc12 | 5g | 552586694
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Medchemexpress LLC L-Phenylalanine-carboxy-13C, N-[(9H-fluoren-9-ylmethoxy)carbonyl]- | 916262-84-5 | 99.8% | C2313CH21NO4 | 5 MG
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This product is L-Phenylalanine-carboxy-13C, N-[(9H-fluoren-9-ylmethoxy)carbonyl]- (Fmoc-Phe-OH-13C), a highly pure chemical compound with a purity of 99.8%. It is supplied as a white to off-white solid.
- Supplied as a white to off-white solid
- Purity of 99.8% (HPLC)
- Isotopic enrichment of 99%
- Recommended for research use only
- Stable as powder at -20°C for 3 years or 4°C for 2 years
- Stable in solvent at -80°C for 6 months or -20°C for 1 month
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Medchemexpress LLC Suc-Ala-Ala-Phe-AMC | 71973-79-0 | MFCD00038448 | 99.9% | 564.59 | 100 MG
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Suc-Ala-Ala-Phe-AMC is a fluorogenic chymotrypsin substrate that can be hydrolyzed by endopeptidase. It has been utilized in both in vivo assays of the acrosome reaction and in vitro enzyme assays.
- Fluorogenic chymotrypsin substrate
- Hydrolyzable by endopeptidase
- Suitable for in vivo assays of acrosome reaction
- Suitable for in vitro enzyme assays
- Appears as a white to off-white solid
- High purity of 99.89%
- Soluble in DMSO at 250 mg/mL
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Medchemexpress LLC Fmoc-Gly-Gly-Phe-OH | 160036-44-2 | 99.5% | 501.53 g/mol | C28H27N3O6 | 5 G
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Fmoc-Gly-Gly-Phe-OH is an Fmoc-protected tripeptide used as a cleavable linker and intermediate in the synthesis of antibody-drug conjugates (ADCs). It is supplied for research use with supporting product data and safety documentation.
- Cleavable linker for ADC synthesis.
- High purity (99.5%).
- Molecular weight 501.53 g/mol.
- Molecular formula C28H27N3O6.
- Available in multiple pack sizes, including 5 g for synthesis scale-up.
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eMolecules 500770-78-5 | Boc-(S)-3-amino-3-(3-trifluoromethylphenyl)propionic acid | Chem-Impex | MFCD03003734 | 333.307 | C15H18F3NO4 | 98.000 | CC(C)(C)OC(=O)NC(CC(O)=O)c1cccc(c1)C(F)(F)F | 1g | 112747682
Boc-(S)-3-amino-3-(3-trifluoromethylphenyl)propionic acid | Chem-Impex | 500770-78-5 | MFCD03003734 | 333.307 | C15H18F3NO4 | 98.000 | CC(C)(C)OC(=O)NC(CC(O)=O)c1cccc(c1)C(F)(F)F | 1g | 112747682
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STA PHARMACEUTICAL US LLC N-Fmoc-2,5-difluoro-D-phenylalanine | 25 g | CAS 1253792-21-0 | MDL MFCD07372003
N-Fmoc-2,5-difluoro-D-phenylalanine is a Amino Acid reagent (Subcategory: Phe) sold by WuXi TIDES. Offered in 25 g. Store at 4 °C. SDS available for reference.
Specifications
- CAS: 1253792-21-0
- MDL: MFCD07372003
- InChIKey: VLGUITFILRLIFL-JOCHJYFZSA-N
- Molecular Weight: 423.416
- Molecular Formula: C24H19F2NO4
- Purity: ≥95%
- Container Type: 125 mL HDPE
- Pack Size: 25 g
- Net Weight: 25 g
- Gross Weight: 54.3 g
- Commodity Code: 29242970
- Country Of Origin: China
- IUPAC: (R)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(2,5-difluorophenyl)propanoic acid
- SMILES: FC1=CC=C(C=C1C[C@@H](NC(OCC2C3=CC=CC=C3C4=CC=CC=C42)=O)C(O)=O)F
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Medchemexpress LLC Fmoc-Phe(4-Br)-OH | 198561-04-5 | 99.83% | 466.32 | 5 G
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Fmoc-Phe(4-Br)-OH is a widely used amino acid derivative. It can be utilized in the synthesis of compounds, for studying protein-protein interactions, and in the development of biomaterials. Additionally, it can be incorporated into peptide chains during peptide synthesis.
- Used in the synthesis of compounds.
- Applicable for the study of protein-protein interactions.
- Aids in the development of biomaterials.
- Can be incorporated into peptide chains during peptide synthesis.
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Medchemexpress LLC Carbamic acid, N-[2-[2-(2-propyn-1-yloxy)ethoxy]ethyl]-, 1,1-dimethylethyl ester | 869310-84-9 | MFCD22418469 | 97.0% | 243.30 g/mol | C12H21NO4 | 1 G
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Propargyl-PEG2-NHBoc is a PEG-based propargyl linker containing a Boc-protected amine and a terminal alkyne, designed for bioconjugation and linker synthesis in research applications. It is compatible with click chemistry and is supplied at research-scale quantities with high purity.
- Contains terminal alkyne for copper-catalyzed azide-alkyne cycloaddition (CuAAC).
- Boc-protected primary amine for controlled deprotection and further functionalization.
- PEG2 spacer improves aqueous solubility and flexibility for conjugation.
- Suitable as a cleavable linker for ADC and PROTAC synthesis and general bioconjugation.
- Supplied at high purity (≥97%) and available in small research quantities such as 1 G.
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Medchemexpress LLC L-Phenylalanine,Indole-15N | 84344-22-9 | 205.22 | 50 MG
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L-Phenylalanine,Indole-15N is the 15N labeled L-Tryptophan. L-Tryptophan (Tryptophan) is an essential amino acid that is the precursor of serotonin, melatonin, and vitamin B3. This compound is for research use only. We do not sell to patients.
- Can be used as a tracer
- Can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS
- Stable heavy isotopes have been incorporated into drug molecules for quantitation during the drug development process
- Deuteration has gained attention for its potential to affect the pharmacokinetic and metabolic profiles of drugs
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eMolecules 169243-86-1 | Fmoc-Phe(4-F)-OH | ChemScene | MFCD00191197 | 405.425 | C24H20FNO4 | 98.000 | OC(=O)[C@H](Cc1ccc(F)cc1)NC(=O)OCC1c2ccccc2-c2ccccc12 | 1g | 662676339
Fmoc-Phe(4-F)-OH | ChemScene | 169243-86-1 | MFCD00191197 | 405.425 | C24H20FNO4 | 98.000 | OC(=O)[C@H](Cc1ccc(F)cc1)NC(=O)OCC1c2ccccc2-c2ccccc12 | 1g | 662676339
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eMolecules 169243-86-1 | Fmoc-Phe(4-F)-OH | ChemScene | MFCD00191197 | 405.425 | C24H20FNO4 | 98.000 | OC(=O)[C@H](Cc1ccc(F)cc1)NC(=O)OCC1c2ccccc2-c2ccccc12 | 5g | 536854525
Fmoc-Phe(4-F)-OH | ChemScene | 169243-86-1 | MFCD00191197 | 405.425 | C24H20FNO4 | 98.000 | OC(=O)[C@H](Cc1ccc(F)cc1)NC(=O)OCC1c2ccccc2-c2ccccc12 | 5g | 536854525
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Medchemexpress LLC Z-VAD(OMe)-FMK (Z-Val-Ala-Asp(OMe)-FMK) | 187389-52-2 | 467.49 | 1 ML
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Z-VAD(OMe)-FMK (Z-Val-Ala-Asp(OMe)-FMK) is a cell-permeable and irreversible pan-caspase inhibitor. It also acts as an ubiquitin carboxy-terminal hydrolase L1 (UCHL1) inhibitor, modifying UCHL1 by targeting its active site. This broad-spectrum caspase inhibitor has been shown to inhibit the intracellular activation of caspase-like proteases, offering neurovascular protection and improving neurological outcomes in various studies.
- Cell-permeable and irreversible pan-caspase inhibitor
- Inhibits ubiquitin carboxy-terminal hydrolase L1 (UCHL1)
- Suppresses caspase-3 activity in lung tissues
- Decreases caspase-3 activation and reduces blood-brain barrier permeability
- Relieves vasospasm and abolishes brain edema
- Blocks cell death induced by SMN deficiency
- Significantly prolongs survival rate in mice after LPS injection
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Medchemexpress LLC L-Cycloserine | 339-72-0 | 98.84% | 5 MG
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L-Cycloserine is an oral inhibitor of the enzyme gamma-aminobutyric acid (GABA) transaminase (GABA-t) and branched-chain transaminases in Mycobacterium tuberculosis. It has anticonvulsant properties and inhibits the synthesis of neurotensin in mouse brains.
- Oral inhibitor of GABA transaminase and branched-chain transaminases in Mycobacterium tuberculosis.
- Possesses anticonvulsant properties.
- Inhibits the synthesis of neurotensin in mouse brains.
- Inhibits the growth of M. tuberculosis with an MIC of 0.3 μg/mL.
- Has anticonvulsant effects in mice.
- Enhances the inhibitory effect on GABA-T activity and boosts anticonvulsant effects in mice.
- Reduces brain content of gangliosides.
- Affects the level of inhibition of 3-keto-dihydrosphingosine synthase.
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