Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C24H42O21 |
Molecular Weight | 666.5777 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 19 / 19 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@@](O[C@H]1O[C@H](CO)[C@@]([H])(O[C@H]2O[C@H](CO)[C@@H](O[C@@]3([H])O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@H]1O)([C@H](O)CO)[C@H](O)[C@@H](O)C=O
InChI
InChIKey=UYQJCPNSAVWAFU-KVXMBEGHSA-N
InChI=1S/C24H42O21/c25-1-6(30)11(32)19(7(31)2-26)43-23-17(38)14(35)21(9(4-28)41-23)45-24-18(39)15(36)20(10(5-29)42-24)44-22-16(37)13(34)12(33)8(3-27)40-22/h1,6-24,26-39H,2-5H2/t6-,7+,8+,9+,10+,11+,12+,13-,14+,15+,16+,17+,18+,19+,20+,21+,22+,23+,24+/m0/s1
Molecular Formula | C24H42O21 |
Molecular Weight | 666.5777 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 19 / 19 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Generation of furosine and color in infant/enteral formula-resembling systems. | 2004 Aug 25 |
|
DFT conformation and energies of amylose fragments at atomic resolution. Part 2: 'Band-flip' and 'kink' forms of alpha-maltotetraose. | 2009 Feb 17 |
|
DFT conformation and energies of amylose fragments at atomic resolution. Part 1: Syn forms of alpha-maltotetraose. | 2009 Feb 17 |
|
Characterization of nimbidiol as a potent intestinal disaccharidase and glucoamylase inhibitor present in Azadirachta indica (neem) useful for the treatment of diabetes. | 2013 Oct |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 17:50:29 GMT 2023
by
admin
on
Fri Dec 15 17:50:29 GMT 2023
|
Record UNII |
BO88JLT87R
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English |
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
DTXSID50865722
Created by
admin on Fri Dec 15 17:50:29 GMT 2023 , Edited by admin on Fri Dec 15 17:50:29 GMT 2023
|
PRIMARY | |||
|
34612-38-9
Created by
admin on Fri Dec 15 17:50:29 GMT 2023 , Edited by admin on Fri Dec 15 17:50:29 GMT 2023
|
PRIMARY | |||
|
143180
Created by
admin on Fri Dec 15 17:50:29 GMT 2023 , Edited by admin on Fri Dec 15 17:50:29 GMT 2023
|
PRIMARY | |||
|
28460
Created by
admin on Fri Dec 15 17:50:29 GMT 2023 , Edited by admin on Fri Dec 15 17:50:29 GMT 2023
|
PRIMARY | |||
|
DB02237
Created by
admin on Fri Dec 15 17:50:29 GMT 2023 , Edited by admin on Fri Dec 15 17:50:29 GMT 2023
|
PRIMARY | |||
|
61988
Created by
admin on Fri Dec 15 17:50:29 GMT 2023 , Edited by admin on Fri Dec 15 17:50:29 GMT 2023
|
PRIMARY | |||
|
BO88JLT87R
Created by
admin on Fri Dec 15 17:50:29 GMT 2023 , Edited by admin on Fri Dec 15 17:50:29 GMT 2023
|
PRIMARY | |||
|
123966
Created by
admin on Fri Dec 15 17:50:29 GMT 2023 , Edited by admin on Fri Dec 15 17:50:29 GMT 2023
|
PRIMARY | |||
|
252-111-0
Created by
admin on Fri Dec 15 17:50:29 GMT 2023 , Edited by admin on Fri Dec 15 17:50:29 GMT 2023
|
PRIMARY |
Related Record | Type | Details | ||
---|---|---|---|---|
|
PARENT -> METABOLITE |
Icodextrin is metabolized by alpha-amylase into oligosaccharides with a lower degree of polymerization (DP), including maltose (DP2), maltotriose (DP3), maltotetraose (DP4), and higher molecular weight species.
|