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Organometallic compounds contain direct bonds between carbon atoms and metal atoms/ions and play roles as homogeneous catalysts and stoichiometric reagents in reactions; available in various chemical compositions, quantities, purities, and reagent grades.
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TBDMS-PEG3-OH is a tert-butyldimethylsilyl (TBDMS)-protected PEG3 alcohol used as a linker or spacer in organic synthesis, PROTAC construction, and drug-delivery conjugation. It provides a protected terminal alcohol for selective deprotection and coupling reactions.
Provides a TBDMS-protected terminal alcohol for selective deprotection and coupling.
Suitable as a PEG3 linker or spacer in medicinal chemistry and PROTAC synthesis.
High purity (≥98%) and molecular weight 264.43 g/mol.
Liquid, colorless to light yellow, convenient for solution-phase reactions.
Recommended storage: pure form -20°C (long term) or 4°C (short term); in solvent store at -80°C.
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N-Fmoc-4-(tert-butoxycarbonylmethoxy)-L-phenylalanine is an Fmoc-protected derivative of L-phenylalanine used as a building block in peptide synthesis and related peptide chemistry applications. It features an N-Fmoc protecting group on the amine and a tert-butoxycarbonylmethoxy protecting group at the 4-position of the phenyl ring, supplied as a solid powder with reported high purity for synthetic use.
Fmoc-protected amino acid for solid-phase peptide synthesis.
Tert-butoxycarbonylmethoxy group at the 4-position provides orthogonal protection.
Molecular formula: C30H31NO7.
Molecular weight approximately 517.6 daltons.
Purity by NMR: ≥98.0%.
Solid powder form; store at -20°C for long-term stability.
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N-Fmoc-4-(tert-butoxycarbonylmethoxy)-L-phenylalanine is an Fmoc-protected phenylalanine derivative used as a protected amino acid building block for peptide synthesis and chemical research. It features a tert-butoxycarbonyl-protected methoxy substituent at the 4-position of the aromatic ring and is supplied as a solid with formula C30H31NO7 and molecular weight 517.57 g/mol. Typical purity is ≥98.0% and recommended storage is powder: -20°C (up to 3 years) or 4°C (up to 2 years); in solvent: -80°C (up to 6 months) or -20°C (up to 1 month).
Fmoc-protected amino acid suitable for solid-phase peptide synthesis.
Boc-protected methoxy group at the 4-position of the aromatic ring.
Chemical formula C30H31NO7 and molecular weight 517.57 g/mol.
Purity ≥98.0% by 1H NMR.
Supplied as a solid; follow recommended powder and solvent storage conditions.
Intended for research use only.
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3-(Trimethoxysilyl)propyl methacrylate is a reactive monomer and silane coupling agent 3-(Trimethoxysilyl)propyl methacrylate can be used to prepare nanoparticles[1][2]
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NHPI-PEG3-C2-Pfp ester is a noncleavable, trifunctional 3-unit polyethylene glycol (PEG) linker bearing an N-hydroxyphthalimide (NHPI) group and a perfluorophenyl (Pfp) activated ester. It is used for bioconjugation and in the synthesis of antibody-drug conjugates (ADCs). Intended for research use only.
Noncleavable 3-unit PEG linker
NHPI functional group for site-specific conjugation
Perfluorophenyl activated ester for amine coupling
Molecular weight about 533.4 g/mol; formula C23H20F5NO8
Purity greater than 96%
Intended for research use only, not for human or animal use
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Biotin-PEG3-SS-azide is a cleavable three-unit polyethylene glycol linker bearing a biotin group and a terminal azide, designed for conjugation chemistry in research applications. It is suitable for click chemistry reactions and as a cleavable linker in the synthesis of antibody-drug conjugates.
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Tolterodine tartrate is an mAChR inhibitor and a substrate for cytochrome P450 enzymes. It competitively binds acetylcholine, reducing sympathetic excitation and inhibiting involuntary bladder muscle contraction. It also restores the Nrf2/NF-κB signaling pathway, protecting against inflammatory response and ferroptosis. It is used for research on urinary tract infections and overactive bladder.
mAChR inhibitor
Substrate for cytochrome P450 enzymes
Competitively binds acetylcholine
Reduces sympathetic excitation
Inhibits involuntary bladder muscle contraction
Restores Nrf2/NF-κB signaling pathway
Protects against inflammatory response and ferroptosis
Ameliorates LPS-induced oxidative stress
Research use for urinary tract infections and overactive bladder
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N-(Azido-PEG3)-N-(PEG2-amine)-PEG3-acid is a PEG-based PROTAC linker primarily used in the synthesis of PROTACs. It acts as a versatile click chemistry reagent, facilitating selective degradation of target proteins via the intracellular ubiquitin-proteasome system.
Contains an Azide group
Participates in copper-catalyzed azide-alkyne cycloaddition reactions (CuAAc) with molecules possessing Alkyne groups
Undergoes strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups
Functions as a PROTAC linker
Utilized in PROTAC synthesis
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