1658416-54-6
Chemical Structure
Sulfo-cyanine3 azide
- CAS No.: 1658416-54-6
- Formula:C33H42N6O7S2
- Molecular Weight:698.85
IUPAC Name: 2-((E)-3-((E)-1-(6-((3-azidopropyl)amino)-6-oxohexyl)-3,3-dimethyl-5-sulfoindolin-2-ylidene)prop-1-en-1-yl)-1,3,3-trimethyl-3H-indol-1-ium-5-sulfonate
InChIKey: NBJWKWQEUZHLOH-UHFFFAOYSA-N
SMILES: [N-]=[N+]=NCCCNC(CCCCCN1C2=CC=C(S(=O)(O)=O)C=C2C(C)(C)/C1=C\C=C\C3=[N+](C)C4=C(C3(C)C)C=C(S(=O)([O-])=O)C=C4)=O
Biological Activity: Sulfo-cyanine3 azide is an azide cyanine dye and fluorescent probe (Ex/Em=548/563 nm). Sulfo-cyanine3 azide can be involved in synthesis of fused tricyclic heterocycles, produces immunostimulatory agents[1][2]. It contains an azide group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing alkyne groups. It can also undergo ring strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing DBCO or BCN groups.
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Sulfo-cyanine3 azide | Sulfo-cyanine3 azide is an azide cyanine dye and fluorescent probe (Ex/Em=548/563 nm). Sulfo-cyanine3 azide can be involved in synthesis of fused tricyclic heterocycles, produces immunostimulatory agents. It contains an azide group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing alkyne groups. It can also undergo ring strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing DBCO or BCN groups. | |||||||||||||||||||||
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References
- [1]. Hsieh PY, et al. Harnessing Fluorescent Moenomycin A Antibiotics for Bacterial Cell Wall Imaging Studies. Chembiochem. 2021 Dec 10;22(24):3462-3468. [Content Brief]
- [2]. David, Sunil A, et al. Preparation of fused tricyclic heterocycles as therapeutic compounds and methods of use thereof: World Intellectual Property Organization, WO2020009946[P]. 2020-01-09.
