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522:"Synthesis of Some Disaccharides Containing an L-Rhamnopyranosyl or L-Mannopyranosyl Residue, and the Substrate-specificity of α-L-Rhamnosidase from
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InChI=1S/C12H22O10/c1-3-5(13)7(15)10(18)12(21-3)20-2-4-6(14)8(16)9(17)11(19)22-4/h3-19H,2H2,1H3/t3-,4+,5-,6+,7+,8-,9+,10+,11+,12+/m0/s1
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InChI=1/C12H22O10/c1-3-5(13)7(15)10(18)12(21-3)20-2-4-6(14)8(16)9(17)11(19)22-4/h3-19H,2H2,1H3/t3-,4+,5-,6+,7+,8-,9+,10+,11+,12+/m0/s1
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Except where otherwise noted, data are given for materials in their
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Kamiya, Shintaro; Sachiko Esaki; Reiko Tanaka (1985).
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285:DTXSID401226338 DTXSID70896972, DTXSID401226338
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87:6-O-(6-Deoxy-alpha-L-mannopyranosyl)-D-glucose
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85:6-O-(α-L-Rhamnopyranosyl)-D-glucopyranose,
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530:Agricultural and Biological Chemistry
315:Key: OVVGHDNPYGTYIT-BNXXONSGSA-N
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325:Key: OVVGHDNPYGTYIT-BNXXONSGBT
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74:)-6-oxymethyl]oxane-2,3,4,5-tetrol
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414:(at 25 °C , 100 kPa).
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346:O(C1O(O)(O)(O)1O)2O((O)(O)2O)C
83:6-O-(α-L-Rhamnosyl)-D-glucose,
1:
581:. You can help Knowledge by
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491:) that is present in some
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55:-Rhamnopyranosyl-(1→6)-β-
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638:Organic compound stubs
573:This article about an
498:. It is prepared from
543:10.1271/bbb1961.49.55
66:Systematic IUPAC name
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441:Infobox references
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524:Aspergillus niger
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268:CompTox Dashboard
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93:Identifiers
81:Other names
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404:1.662 g/mL
355:Properties
192:100.001.832
154:CHEBI:27522
72:2R,3S,4S,5S
622:Categories
514:References
504:hydrolysis
496:glycosides
390:Molar mass
256:0C4U3505G3
165:ChemSpider
121:3D model (
100:CAS Number
48:IUPAC name
18:Rutinoside
493:flavonoid
469:rhamnosyl
213:202-014-4
205:EC Number
28:Rutinose
453:Rutinose
477:glucose
455:is the
434:what is
432: (
400:Density
223:PubChem
110:90-74-4
549:26 May
429:verify
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339:SMILES
236:441429
174:390162
42:Names
577:is a
500:rutin
304:InChI
145:ChEBI
123:JSmol
579:stub
551:2009
247:UNII
538:doi
502:by
463:-α-
273:EPA
226:CID
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487:O
483:H
475:-
473:D
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465:L
461:O
424:N
380:O
374:H
368:C
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57:D
53:L
20:)
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