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Martin Ernst; Johann-Peter Melder; Franz Ingo Berger; Christian Koch (2022). "Ethanolamines and
Propanolamines".
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contain both alcohols and amino groups. Two amino acids are alkanolamines, formally speaking:
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Organic compounds with hydroxyl and amino groups on an alkane backbone
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is yet another medicinally useful derivative of ethanolamine.
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gives the corresponding 2-aminoalcohols. Examples include
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that are often generated by the reaction of amines with
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127:2-amino-2-methyl-1-propanol is a precursor to
80:backbone. Most alkanolamines are colorless.
193:2-Aminoalcohols are an important class of
478:at the U.S. National Library of Medicine
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245:Hydrogenation or hydride reduction of
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480:Medical Subject Headings
185:is the simplest member.
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163:is a component of some
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38:(amino alcohols) are
293:Aminomethyl propanol
282:dimethylethanolamine
407:Smith, Michael B.;
289:-methylethanolamine
42:that contain both
424:978-0-471-72091-1
385:(adrenaline) and
380:neurotransmitters
367:Tropane alkaloids
195:organic compounds
74:functional groups
40:organic compounds
32:organic chemistry
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114:Ethanolamine
100:formaldehyde
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383:epinephrine
358:Veratridine
301:propranolol
247:amino acids
179:hemiaminals
161:Sphingosine
490:Categories
394:References
321:Heptaminol
309:Isoetarine
129:oxazolines
362:veratrine
267:tyrosinol
496:Alcohols
411:(2007),
376:hormones
371:atropine
369:such as
343:peptides
339:proteins
305:pindolol
271:tyrosine
251:prolinol
233:solvents
214:O + R−NH
199:epoxides
44:hydroxyl
259:valinol
255:proline
218:→ RNHC
143:valinol
501:Amines
482:(MeSH)
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347:serine
269:(from
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261:(from
253:(from
147:valine
78:alkane
76:on an
65:, and
50:) and
337:Most
240:bases
52:amino
453:ISBN
419:ISBN
378:and
360:and
349:and
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63:−NHR
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307:.
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67:−NR
56:−NH
48:−OH
30:In
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226:OH
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181:.
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287:N
224:4
222:H
220:2
216:2
212:4
210:H
208:2
206:C
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