914134
5-(Biotinamido)pentylamine TFA Salt
≥95%
別名:
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
実験式（ヒル表記法）:
C15H28N4O2S · xC2HF3O2
分子量:
328.47 (free base basis)
MDL番号:
UNSPSCコード:
12352116
NACRES:
NA.22
おすすめの製品
品質水準
アッセイ
≥95%
フォーム
powder
mp
116-121 °C
保管温度
2-8°C
SMILES記法
FC(F)(F)C(=O)O.S1[C@H]([C@H]2NC(=O)N[C@H]2C1)CCCCC(=O)NCCCCCN
InChI Key
QWKKJNXOPDNIEU-RGESYUBESA-N
アプリケーション
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)
Automate your Biotin tagging with Synple Automated Synthesis Platform (SYNPLE-SC002)
その他情報
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
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
関連製品
製品番号
詳細
価格
保管分類コード
11 - Combustible Solids
WGK
WGK 3
引火点(°F)
Not applicable
引火点(℃)
Not applicable
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
Jan Code
914134-VAR:
914134-BULK:
914134-250MG:
最新バージョンのいずれかを選択してください：
Suguru Yoshida et al.
Chemical communications (Cambridge, England), 54(30), 3705-3708 (2018-03-13)
A facile strategy for the synthesis of trifunctional molecules involving three sequential selective triazole-forming reactions is proposed. This method exploits three kinds of mechanistically different azido-type-selective cycloadditions. Three different azidophiles could be efficiently connected to a triazido platform molecule with
Renata Grzywa et al.
Chembiochem : a European journal of chemical biology, 15(17), 2605-2612 (2014-09-23)
Neutrophils are a type of granulocyte important in the "first line of defense" of the innate immune system. Upon activation, they facilitate the destruction of invading microorganisms by the production of superoxide radicals, as well as the release of the
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