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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
121 Results for "
EDC
" in MedChemExpress (MCE) Product Catalog:
Products (121)
121 Results for "EDC" in MCE Product Catalog:
18
18
6
Research Areas:
Oxybenzone (Benzophenone 3) is a commonly used UV filter in sun tans and skin protectants. Oxybenzone act as endocrine disrupting chemicals (EDCs) and can pass through the placental and blood-brain barriers. Benzophenone-3 impairs autophagy, alters epigenetic status, and disrupts retinoid X receptor signaling in apoptotic neuronal cells .
3
3 Cited Publications
Cat. No.: HY-K0225
MCE Carboxyl Magnetic beads (200 nm, 10 mg/mL) are characterized by superparamagnetism, fast magnetic response, abundant carboxyl functional groups, monodispersity, and submicron scale particle size. Biological ligands (proteins, peptides, oligonucleotides, drug molecules, etc.) can be covalently coupled to the surface of microspheres under the action of special chemical reagents (such as EDC).
2
Target:
Etidocaine (hydrochloride) is a long aminoamide local agent that can suppress or relieve pain .
Cat. No.: HY-18260S2
CAS No.: 263261-65-0
Cat. No.: HY-18260S
CAS No.: 96210-87-6
Cat. No.: HY-W012001
CAS No.: 60142-89-4
Target:
Research Areas:
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-W654077
Synonyms: BPAF-d4; 4,4'-(Perfluoropropane-2,2-diyl)diphenol-d4
Cat. No.: HY-18260S1
CAS No.: 86588-58-1
Cat. No.: HY-18260S6
CAS No.: 120155-79-5
Cat. No.: HY-D2751
CAS No.: 1178534-61-6
Cat. No.: HY-W441002
CAS No.: 248253-94-3
Cat. No.: HY-W097128
CAS No.: 128917-74-8
Target:
Research Areas:
Fmoc-12-aminododecanoic acid is an alkane chain with terminal Fmoc-protected amine and carboxylic acid groups. The compound can be used as a PROTAC linker in the synthesis of PROTACs. The Fmoc group can be deprotected under basic condition to obtain the free amine which can be used for further conjugations. 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.
Cat. No.: HY-B2080
CAS No.: 36637-18-0
Synonyms: EDC
Target:
Etidocaine (EDC) is a long aminoamide local anesthetic .
Cat. No.: HY-W008213
CAS No.: 6342-60-5
Cat. No.: HY-A0067S
CAS No.: 1219798-54-5
Cat. No.: HY-W005828
CAS No.: 173435-78-4
Target:
Research Areas:
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-W009030
CAS No.: 126631-93-4
Target:
Research Areas:
N-Fmoc-8-aminooctanoic acid can be used as a PROTAC linker in the synthesis of PROTACs. N-Fmoc-8-aminooctanoic acid is an alkane chain with terminal Fmoc-protected amine and carboxylic acid groups. The Fmoc group can be deprotected under basic condition to obtain the free amine which can be used for further conjugations. 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.
Cat. No.: HY-W009056
CAS No.: 127582-76-7
Target:
Research Areas:
Fmoc-7-amino-heptanoic acid is an alkane chain with terminal Fmoc-protected amine and carboxylic acid groups. Fmoc-7-amino-heptanoic acid can be used as a PROTAC linker in the synthesis of PROTACs. The Fmoc group can be deprotected under basic condition to obtain the free amine which can be used for further conjugations. 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.
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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
