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Organic compounds with acidic properties, organic acids are generally weak acids incapable of complete dissociation in water. Available in a range of chemical compositions and acid strengths, they can be used for various industrial and everyday applications.
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MS9427 TFA is a potent PROTAC EGFR degrader that selectively targets and degrades mutant EGFR through both the ubiquitin/proteasome system (UPS) and autophagy/lysosome pathways. This compound effectively inhibits the proliferation of NSCLC cells and shows antiproliferative activity against HCC-827 cells.
Potent PROTAC EGFR degrader
Selectively degrades mutant EGFR
Utilizes ubiquitin/proteoteasome system and autophagy/lysosome pathways
Inhibits proliferation of non-small cell lung cancer (NSCLC) cells
Exhibits antiproliferative activity against HCC-827 cells
Induces EGFRDel19 degradation
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MTvkPABC-P5 TFA is the trifluoroacetic acid (TFA) salt of a synthetic Toll-like receptor 7 (TLR7) agonist. It functions as an immune stimulant used in research applications, including the synthesis of immune-stimulating antibody conjugates (ISACs).
Acts as a TLR7 agonist and immune stimulant.
Suitable for synthesis of immune-stimulating antibody conjugates (ISACs).
Provided as a solid TFA salt.
High purity, 98.8%.
Molecular weight 1190.22, formula C54H74F3N11O16.
Available as 25 MG quantity.
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Cilengitide is a potent and selective integrin inhibitor for αvβ3 and αvβ5 receptor, with IC50 values of 4 nM and 79 nM, respectively. It inhibits integrin-mediated binding to vitronectin.
Potent and selective integrin inhibitor
Targets αvβ3 receptor with IC50 of 4 nM
Targets αvβ5 receptor with IC50 of 79 nM
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Thanatin TFA is an inducible cationic antimicrobial peptide (AMP) with a single-disulfide-bond-containing β-hairpin structure. It exhibits broad-spectrum activity against Gram-negative and Gram-positive bacteria, as well as various fungal species. This peptide functions by competitively replacing divalent cations from the bacterial outer membrane, leading to its disruption.
Exhibits broad-spectrum activity against Gram-negative and Gram-positive bacteria.
Effective against various species of fungi.
Disrupts bacterial outer membrane.
Potent inhibitory effect on NDM-1-producing E. coli and K. pneumoniae strains.
Increases survival rates and decreases bacterial titers in infected mice.
Rescues pathological damages in a dose-dependent manner in vivo.
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CCZ01048 TFA is an α-MSH analogue that exhibits high binding affinity to melanocortin 1 receptor (MC1R) with a Ki of 0.31 nM. It shows rapid internalization into B16F10 melanoma cells and demonstrates high in vivo stability, making it a promising candidate for PET imaging of malignant melanoma.
α-MSH analogue
High binding affinity to melanocortin 1 receptor (MC1R) with a Ki of 0.31 nM
Rapid internalization into B16F10 melanoma cells
High in vivo stability
Promising candidate for PET imaging of malignant melanoma
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BRP (BRINP2-related peptide) TFA is a peptide that exhibits anti-obesity activity by activating FOS. It functions independently of leptin, GLP-1 receptor, and melanocortin 4 receptor.
Exhibits anti-obesity activity
Activates FOS in the central nervous system
Functions independently of leptin, GLP-1 receptor, and melanocortin 4 receptor
Classified as a peptide and therapeutic peptide
Related to metabolic disease research
Acts as an AP-1 activator
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MPSD TFA is the TFA salt form of MPSD, a 25-amino acid peptide derived from the effector domain sequence of the intracellular membrane protein myristoylated alanine-rich C-kinase substrate (MARCKS). It functions as a biological probe to study membrane curvature and lipid composition, specifically recognizing phosphatidylserine.
TFA salt form of MPSD
25-amino acid peptide
Derived from MARCKS protein
Detects membrane curvature
Identifies phosphatidylserine
Useful as a biological probe
White to off-white solid appearance
Soluble in DMSO and H2O
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FTI-276 trifluoroacetate is the trifluoroacetate salt of a small-molecule inhibitor of protein farnesyl transferase. It is provided as a solid for research use and exhibits sub-nanomolar activity against both Plasmodium falciparum and human PFT, making it suitable for biochemical and antiparasitic research applications.
Potent protein farnesyl transferase inhibition at sub-nanomolar concentrations.
Provided as the trifluoroacetate (TFA) salt to aid handling and formulation.
High reported purity, approximately 98%.
Supplied in small, research-ready quantities suitable for assay development.
Characterized by published chemical identifiers for unambiguous compound identification.
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PHF6 TFA is a self-assembly sequence capable of initiating the full-length tau protein aggregation, mapped to the third microtubule-binding repeat region of the tau protein. Aggregated PHF6 TFA potentiates NLRP3 inflammasome expression and autophagy in human microglial cells.
Purity: 99.45%
Molecular weight: 748.91 (free base)
Chemical formula: C36H60N8O9.xC2HF3O2
Appearance: Solid
Color: White to off-white
Sequence: Val-Gln-Ile-Val-Tyr-Lys
Solubility in H2O: ≥ 50 mg/mL
Store sealed and away from moisture
Powder storage: -80°C for 2 years, -20°C for 1 year
In-solvent storage: -80°C for 6 months, -20°C for 1 month
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G7-18NATE TFA is a peptide inhibitor of Grb7. It binds to the Grb7-SH2 domain with micromolar affinity (Kd = 18.1 μM). G7-18NATE TFA inhibits cell proliferation, motility, cell invasion, and 3D culture formation in several cancer cell lines.
Peptide inhibitor of Grb7
Binds to the Grb7-SH2 domain with micromolar affinity (Kd = 18.1 μM)
Inhibits cell proliferation, motility, cell invasion, and 3D culture formation in several cancer cell lines
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