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436:"Biosynthesis of the C(7)-cyclitol moiety of acarbose in Actinoplanes species SE50/110. 7-O-phosphorylation of the initial cyclitol precursor leads to proposal of a new biosynthetic pathway"
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Laube, Heiner (March 2002). "Acarbose An Update of Its
Therapeutic Use in Diabetes Treatment".
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InChI=1S/C7H13NO4/c8-4-1-3(2-9)5(10)7(12)6(4)11/h1,4-7,9-12H,2,8H2/t4-,5+,6-,7-/m0/s1
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InChI=1/C7H13NO4/c8-4-1-3(2-9)5(10)7(12)6(4)11/h1,4-7,9-12H,2,8H2/t4-,5+,6-,7-/m0/s1
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found as a substructure of pseudooligosaccharides such as the antidiabetic drug
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Except where otherwise noted, data are given for materials in their
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Zhang CS, Stratmann A, Block O, et al. (June 2002).
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It is an intermediate formed by microbial degradation of
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324:(at 25 °C , 100 kPa).
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522:. You can help Knowledge by
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373:and the antibiotic
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260:O1\C(=C/(N)(O)1O)CO
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64:Identifiers
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17:Valienamine
584:Amine stubs
375:validamycin
363:Valienamine
269:Properties
563:Categories
475:CID 193758
394:References
307:Molar mass
136:ChemSpider
92:3D model (
81:38231-86-6
71:CAS Number
569:Cyclitols
383:species.
365:is a C-7
462:11937512
371:acarbose
479:PubChem
344:what is
342: (
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157:PubChem
579:Amines
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339:verify
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253:SMILES
170:193758
145:168149
116:ChEMBL
31:Names
518:is a
516:amine
477:from
218:InChI
94:JSmol
520:stub
458:PMID
448:doi
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187:EPA
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300:4
297:O
294:N
288:H
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55:S
51:R
47:S
43:S
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