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TDBzcholine is able to bind to the nicotinic acetylcholine receptor. Once TDBzcholine is bound to the receptor, TDBzcholine can be activated by exposing the sample to
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radical that can react with amino acid residues in the receptor and become covalently bound to the receptor.
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InChI=1S/C14H17F3N3O2/c1-20(2,3)8-9-22-12(21)10-4-6-11(7-5-10)13(18-19-13)14(15,16)17/h4-7H,8-9H2,1-3H3/q+1
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Except where otherwise noted, data are given for materials in their
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316:light. This led to formation of a highly reactive
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201:C(C)(C)CCOC(C1=CC=C(C2(C(F)(F)F)N=N2)C=C1)=O
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354:Biochemical Pharmacology Lecture Notes
180:Key: IQGNIBHYFCIEEE-UHFFFAOYSA-N
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387:. You can help Knowledge (XXG) by
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454:Nicotinic acetylcholine receptors
350:"Pharmacology of cell excitation"
16:Diazirine analog of acetylcholine
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302:nicotinic acetylcholine receptor
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274:(at 25 °C , 100 kPa).
300:that can be used to label the
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383:-related article is a
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308:Mechanism of action
264: g·mol
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49:Identifiers
20:TDBzcholine
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210:Properties
66:496972-30-6
434:Diazirines
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336:References
296:analog of
257:Molar mass
155:NTU9QE4VZL
101:ChemSpider
77:3D model (
56:CAS Number
40:IUPAC name
294:diazirine
110:103875307
324:See also
135:90716102
318:carbene
262:316.304
122:PubChem
194:SMILES
34:Names
379:This
292:is a
169:InChI
79:JSmol
385:stub
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