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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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Fludrocortisone acetate is an orally active synthetic mineralocorticoid. It effectively controls sodium retention and is used in studies of cardiac injury, adrenal insufficiency, and orthostatic hypotension. Research indicates its role in managing conditions related to sodium balance and cardiovascular health.
Effectively controls sodium retention
Supports research into cardiac injury
Supports research into adrenal insufficiency
Supports research into orthostatic hypotension
Demonstrates efficacy in reducing specific enzyme activities related to cardiac injury
Shown to decrease UACR in healthy cats
Contributes to restoring quiescent morphology in choroidal endothelial cells
Assists in reducing membrane permeability in stimulated choroidal endothelial cells
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Sitafloxacin hydrate is an orally active fluoroquinolone antibiotic with in vitro activity against a broad spectrum of Gram-positive and -negative bacteria, including anaerobic bacteria and atypical pathogens. It is utilized in the study of respiratory and urinary tract infections, and exhibits good activity against Mycobacterium avium in vivo.
Orally active fluoroquinolone antibiotic
Active against a broad spectrum of Gram-positive and -negative bacteria
Effective against anaerobic bacteria and atypical pathogens
Used in respiratory tract infection studies
Used in urinary tract infection studies
Shows good activity against Mycobacterium avium in mice
Eliminates bacteria in the spleen and lungs
Demonstrates strong activity against mycobacteria in macrophages
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Azido-PEG5-alcohol is an azide-terminated polyethylene glycol (PEG) linker containing five ethylene glycol units that is used as a click-chemistry reagent and as a linker in bioconjugation workflows. It participates in copper-catalyzed and strain-promoted azide-alkyne cycloaddition reactions and is supplied for research use only.
Azide functional group for click chemistry
Five-unit PEG spacer adds hydrophilicity and flexibility
Suitable for antibody-drug conjugate and PROTAC linker synthesis
Characterized by NMR and LC-MS, purity >97.0%
Available in multiple package sizes, including 25 G
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Phenyl 2-bromoacetate is a biochemical reagent that can be used as a biological material or organic compound for life science-related research. It is intended for research use only and is not sold to patients.
Biochemical reagent
Can be used as a biological material
Can be used as an organic compound
Suitable for life science related research
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N3-PEG3-CH2CH2-Boc is a Boc-protected, azide-terminated PEG3 linker used in conjugation chemistry for synthesizing PROTACs and antibody-drug conjugates. It contains a three-unit polyethylene glycol spacer with an azide functional group that enables click chemistry reactions such as copper-catalyzed azide-alkyne cycloaddition (CuAAC) and strain-promoted azide-alkyne cycloaddition (SPAAC).
Boc-protected azide terminus for selective conjugation.
Three-unit PEG spacer provides flexibility and improves solubility.
Compatible with CuAAC and SPAAC click reaction methodologies.
High purity suitable for synthetic applications (≥98.0%).
Available in multiple pack sizes, including 250 MG.
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BCN-PEG3-OH is a BCN-functionalized, 4-unit polyethylene glycol (PEG) linker and click-chemistry reagent used as a non-cleavable linker in antibody-drug conjugate (ADC) synthesis. It contains a bicyclo[6.1.0]non-4-yne (BCN) group that reacts via strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-functionalized molecules, enabling efficient bioconjugation.
Non-cleavable 4-unit PEG linker for ADC synthesis.
BCN group enables SPAAC click chemistry with azides.
High purity (99.6% by LCMS).
Light yellow oil appearance.
Stored at -20°C under nitrogen; in solvent: -80°C for 6 months, -20°C for 1 month.
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