Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C44H70O23 |
| Molecular Weight | 967.0128 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 26 / 26 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@@]8(O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC(=O)[C@]2(C)CCC[C@@]3(C)[C@]4([H])CC[C@@]5(C[C@]4(CC5=C)CC[C@]23[H])O[C@]6([H])O[C@H](CO)[C@@H](O)[C@H](O)[C@H]6O[C@]7([H])O[C@H](CO)[C@@H](O)[C@H](O)[C@H]7O)O[C@H](CO)[C@@H](O)[C@H](O)[C@H]8O
InChI
InChIKey=RLLCWNUIHGPAJY-SFUUMPFESA-N
InChI=1S/C44H70O23/c1-17-11-43-9-5-22-41(2,7-4-8-42(22,3)40(59)66-38-34(30(55)26(51)20(14-47)62-38)64-36-32(57)28(53)24(49)18(12-45)60-36)23(43)6-10-44(17,16-43)67-39-35(31(56)27(52)21(15-48)63-39)65-37-33(58)29(54)25(50)19(13-46)61-37/h18-39,45-58H,1,4-16H2,2-3H3/t18-,19-,20-,21-,22+,23+,24-,25-,26-,27-,28+,29+,30+,31+,32-,33-,34-,35-,36+,37+,38+,39+,41-,42-,43-,44+/m1/s1
| Molecular Formula | C44H70O23 |
| Molecular Weight | 967.0128 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 26 / 26 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Rebaudioside E is one of the associated glycosides found in the stevia plant. It is generally present in preparations of Steviol glycosides at levels lower than stevioside or Rebaudioside A. Food sweetener. Rebaudioside E is minor component of S.
rebaudiana and tastes about 150-200 times sweeter than
sucrose and is non-caloric.
Approval Year
Sample Use Guides
Steviol, steviolbioside, Reb A and Reb E (Rebaudioside E), were each dissolved in appropriate solvents to provide a set of 200 mg/mL spiking solutions. These solutions were further diluted 10 with their corresponding vehicle to provide another set of dosing solutions at a target concentration of 20 mg/mL. When spiked to the incubation samples (ie. a 100 dilution) it was anticipated that these solutions would result in the target testing concentrations of 2 mg/mL and 0.2 mg/mL, respectively. Reb E incubated at 0.2 mg/mL was also rapidly metabolized to steviol, with almost all converted to steviol after 16 h of incubation.
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 08:31:54 UTC 2023
by
admin
on
Sat Dec 16 08:31:54 UTC 2023
|
| Record UNII |
693TGS3OHR
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Common Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
m9513
Created by
admin on Sat Dec 16 08:31:54 UTC 2023 , Edited by admin on Sat Dec 16 08:31:54 UTC 2023
|
PRIMARY | Merck Index | ||
|
DTXSID301019861
Created by
admin on Sat Dec 16 08:31:54 UTC 2023 , Edited by admin on Sat Dec 16 08:31:54 UTC 2023
|
PRIMARY | |||
|
72710721
Created by
admin on Sat Dec 16 08:31:54 UTC 2023 , Edited by admin on Sat Dec 16 08:31:54 UTC 2023
|
PRIMARY | |||
|
63279-14-1
Created by
admin on Sat Dec 16 08:31:54 UTC 2023 , Edited by admin on Sat Dec 16 08:31:54 UTC 2023
|
PRIMARY | |||
|
145018
Created by
admin on Sat Dec 16 08:31:54 UTC 2023 , Edited by admin on Sat Dec 16 08:31:54 UTC 2023
|
PRIMARY | |||
|
100000182012
Created by
admin on Sat Dec 16 08:31:54 UTC 2023 , Edited by admin on Sat Dec 16 08:31:54 UTC 2023
|
PRIMARY | |||
|
823
Created by
admin on Sat Dec 16 08:31:54 UTC 2023 , Edited by admin on Sat Dec 16 08:31:54 UTC 2023
|
PRIMARY | |||
|
693TGS3OHR
Created by
admin on Sat Dec 16 08:31:54 UTC 2023 , Edited by admin on Sat Dec 16 08:31:54 UTC 2023
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
PARENT -> CONSTITUENT ALWAYS PRESENT |
