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914134

Sigma-Aldrich

5-(Biotinamido)pentylamine TFA Salt

≥95%

Sinónimos:

N-(5-Aminopentyl)-5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pent, Biotin cadaverine TFA, Biotin-DAPe TFA

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About This Item

Fórmula empírica (notación de Hill):
C15H28N4O2S · xC2HF3O2
Peso molecular:
328.47 (free base basis)
Número MDL:
MFCD03452814
Código UNSPSC:
12352116
NACRES:
NA.22

Nivel de calidad

100

Ensayo

≥95%

Formulario

powder

mp

116-121 °C

temp. de almacenamiento

2-8°C

cadena SMILES

FC(F)(F)C(=O)O.S1[C@H]([C@H]2NC(=O)N[C@H]2C1)CCCCC(=O)NCCCCCN

Clave InChI

QWKKJNXOPDNIEU-RGESYUBESA-N

Aplicación

5-(Biotinamido)pentylamine TFA Salt is a versatile biotinylated linker that can be incorporated into chemical tools via its terminal amino group. Labeling materials or proteins with biotin provides a means to enrich and capture targets from biological systems.

Automate your Biotin tagging with Synple Automated Synthesis Platform (SYNPLE-SC002)

Otras notas

Site-selective conversion of azido groups at carbonyl α-positions into oxime groups leading triazide to a triple click conjugation scaffold

Convergent synthesis of trifunctional molecules by three sequential azido-type-selective cycloadditions

Locked by Design: A Conformationally Constrained Transglutaminase Tag Enables Efficient Site-Specific Conjugation

Synthesis of Novel Phosphonic-Type Activity-Based Probes for Neutrophil Serine Proteases and Their Application in Spleen Lysates of Different Organisms

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Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

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Sung Kook Chun et al.
ACS chemical biology, 9(3), 703-710 (2014-01-07)
Circadian rhythms, biological oscillations with a period of about 24 h, are maintained by a genetically determined innate time-keeping system called the molecular circadian clockwork. Despite the physiological and clinical importance of the circadian clock, the development of small molecule
Marianne van Wyk et al.
Chemical communications (Cambridge, England), (4), 398-400 (2007-01-16)
Coenzyme A analogues are synthesized in a one-pot preparation by biotransformation of pantothenate thioesters through the simultaneous use of three CoA biosynthetic enzymes, followed by aminolysis.
Taiki Yokoi et al.
Chemical communications (Cambridge, England), 55(13), 1891-1894 (2018-12-21)
This paper reports the selective conversion of alkyl azido groups at the carbonyl α-position into oximes through β-elimination of dinitrogen, followed by transoximation. With this method and diazo conversion, a triazido molecule was transformed into a triple click conjugation scaffold
Collette S Guy et al.
Organic & biomolecular chemistry, 17(43), 9524-9528 (2019-10-30)
Dimeric benzoboroxoles that are covalently linked by a short scaffold enhance selective anti-tubercular activity. These multimeric benzoboroxole compounds are capable of engaging the specific extracellular Mycobacterium tuberculosis glycans, do not lead to the evolution of resistance and bypass the need
Aoi Teraoka et al.
Chemical communications (Cambridge, England), 50(6), 664-666 (2013-11-28)
A facile and useful method for preparing caged DNAs was developed. The method includes a caging reaction of a linear dsDNA having a minimal sequence of protein expression with Bio-Bhc-diazo and affinity separation of the caged DNA. Effective suppression and
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