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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
131 Results for "
Boc protecting groups
" in MedChemExpress (MCE) Product Catalog:
Products (131)
131 Results for "Boc protecting groups" in MCE Product Catalog:
Cat. No.: HY-W012001
CAS No.: 60142-89-4
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Boc-7-Aminoheptanoic acid can be used as a PROTAC linker in the synthesis of PROTACs and other conjugation applications. Boc-7-Aminoheptanoic acid is an alkane chain with terminal carboxlic acid and Boc-protected amino groups. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond. The Boc group can be deprotected under mild acidic conditions to form the free amine.
Cat. No.: HY-W010922
CAS No.: 162558-25-0
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Cat. No.: HY-W007056
CAS No.: 197632-75-0
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Cat. No.: HY-W047788
CAS No.: 10270-94-7
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Cat. No.: HY-42773
CAS No.: 88829-82-7
Synonyms: 1-Boc-1,8-diaminooctane
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tert-Butyl (8-aminooctyl)carbamate (1-Boc-1,8-diaminooctane) can be used as a PROTAC linker in the synthesis of PROTACs. tert-butyl (8-aminooctyl)carbamate is an alkane chain with terminal amine and Boc-protected amino groups. Amine group is reactive with carboxylic acids, activated NHS esters, carbonyls (ketone, aldehyde) etc. The Boc group can be deprotected under mild acidic conditions to form the free amine.
Cat. No.: HY-W041856
CAS No.: 30100-16-4
Synonyms: Boc-8-aminooctanoic acid
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N-Boc-8-amino-octanoic acid (Boc-8-aminooctanoic acid) can be used as a PROTAC linker in the synthesis of PROTACs. N-Boc-8-amino-octanoic acid is an alkane chain with terminal carboxlic acid and Boc-protected amino groups. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond. The Boc group can be deprotected under mild acidic conditions to form the free amine.
Cat. No.: HY-W047688
CAS No.: 216961-61-4
Synonyms: 1-Boc-1,10-diaminodecane
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tert-Butyl (10-aminodecyl) carbamate (1-Boc-1,10-diaminodecane) is a synthetic intermediate that serves as a PROTAC linker in PROTAC synthesis and other conjugation applications. tert-Butyl (10-aminodecyl) carbamate is an alkane chain with a terminal amine and a Boc-protected amino group. The amine group can react with carboxylic acids, active NHS esters, carbonyl groups (ketones, aldehydes), etc. The Boc group can be deprotected under mild acidic conditions to form a free amine .
Cat. No.: HY-34738
CAS No.: 58885-58-8
Synonyms: 3-(Boc-amino)-1-propanol
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Cat. No.: HY-W009229
CAS No.: 13726-84-6
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Boc-Glu (OtBu)-OH is a glutamic acid-derived protected amino acid with its N-terminal amino group protected by tert-butyloxycarbonyl (Boc) and side-chain carboxyl group protected by tert-butyl ester (OtBu), serving as an orthogonally protected building block for polypeptide synthesis. Boc-Glu (OtBu)-OH is applicable to research on the synthesis of peptide compounds .
Cat. No.: HY-W077219
CAS No.: 102185-38-6
Synonyms: Boc-Arg(Mtr)-OH
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Cat. No.: HY-W039729
CAS No.: 75178-90-4
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5-(Boc-amino)-1-pentanol is a linker containing a hydroxyl group and Boc-protected amino group. The hydroxyl group enables further derivatization or replacement with other reactive functional groups. The Boc group can be deprotected under mild acidic conditions to form the free amine.
Cat. No.: HY-W101935
CAS No.: 113712-06-4
Synonyms: N-Boc-D-arginine hydrochloride
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Cat. No.: HY-W575291
CAS No.: 1451262-84-2
Synonyms: N-Boc-oct-7-yn-1-amine
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tert-Butyl oct-7-yn-1-ylcarbamate (N-Boc-oct-7-yn-1-amine) is crosslinker consisting of a propargyl group and a t-Boc protected amine group. The propargyl group reacts with azide-bearing compounds or biomolecules via copper catalyzed Click Chemistry reactions. The t-Boc protected amine can be deprotected under mild acidic conditions.
Cat. No.: HY-W1049061
Cat. No.: HY-W005828
CAS No.: 173435-78-4
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9-(Boc-amino)nonanoic Acid is an alkane chain with terminal carboxlic acid and Boc-protected amino groups. 9-(Boc-amino)nonanoic acid can be used as a PROTAC linker in the synthesis of PROTACs. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond. The Boc group can be deprotected under mild acidic conditions to form the free amine.
Cat. No.: HY-140232B
Cat. No.: HY-W259542
CAS No.: 634926-63-9
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O-Proparagyl-N-Boc-ethanolamine is crosslinker consisting of a propargyl group and a t-Boc protected amine group. The propargyl group reacts with azide-bearing compounds or biomolecules via copper catalyzed Click Chemistry reactions. The t-Boc protected amine can be deprotected under mild acidic conditions.
Cat. No.: HY-W089230
CAS No.: 20866-46-0
Synonyms: N,N'-Di-tert-butoxycarbonyl-L-histidine
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Cat. No.: HY-W005561
CAS No.: 3350-15-0
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Cat. No.: HY-W101495
CAS No.: 200936-87-4
Synonyms: N-Boc-L-leucine monohydrate
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Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
