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Organic compounds that contain one or more carbonyl (a carbon atom with a double bond to an oxygen atom) functional groups. Includes compounds with functional groups that contain a carbonyl in their structure such as ketones, aldehydes, and others.
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6A-azido-6A-deoxy-β-cyclodextrin is an azide-functionalized β-cyclodextrin derivative used as a reagent for click chemistry and bioconjugation. It contains a single azido substituent at the 6A position, is water-soluble, and enables efficient labeling and conjugation under aqueous conditions.
Enables copper-catalyzed azide-alkyne cycloaddition (CuAAC) for bioconjugation.
Single azido handle for site-selective modification.
Water-soluble scaffold compatible with aqueous reactions.
Applicable to host-guest chemistry and carrier modification.
Supplied with high reported chemical purity for reproducible results.
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Antitumor agent-127 (compound 1) is a parent macrocyclic peptide that displays nanomolar cell-based binding to ROR1 and relatively good internalization in 786-O and MDA-MB-231 tumor cell lines. It does not induce apoptosis in Mia PaCa-2 cells, a model pancreatic tumor cell line with low cell surface expression of ROR1.
Displays nanomolar cell-based binding to ROR1.
Demonstrates good internalization in 786-O and MDA-MB-231 tumor cell lines.
Does not induce apoptosis in Mia PaCa-2 cells.
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Small and Specialty Supplier Partner Small and/or specialty supplier based on Federal laws and SBA requirements. Learn More
6A-azido-6A-deoxy-β-cyclodextrin is an azide-functionalized derivative of β-cyclodextrin used as a water-soluble click-chemistry reagent and bioconjugation building block. The azido group enables copper-catalyzed and strain-promoted azide-alkyne cycloaddition reactions for conjugation to alkyne-bearing molecules in chemical biology and drug-delivery research.
Azide-functionalized for copper-catalyzed and strain-promoted azide-alkyne cycloaddition.
Water-soluble β-cyclodextrin derivative for aqueous reactions.
Suitable for bioconjugation and drug delivery research.
Enables site-specific conjugation to alkyne-containing partners.
Solid form, suitable for standard handling and storage.
Compatible with common analytical methods such as HPLC and NMR.
Encompass Procurement Services Non-distribution item offered as a customer accommodation; additional freight charges may apply. Learn More