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stevioside

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chemical compound

Välised allikad

CAS Registry Number
57817-89-7[1][2]
Microsoft Academic ID
2778379570
LCCN
sh2013002015[3]
PubChem CID
442089[4]
MeSH descriptor ID
C012043[5]
UniChem compound ID
201337[6]
KEGG ID
C09189[7]
OpenAlex ID
C2778379570[8]
ChEMBL ID
CHEMBL444122[9]
CAB ID
168997[10]
InChIKey
UEDUENGHJMELGK-HYDKPPNVSA-N[4][11]
UNII
0YON5MXJ9P[1][12]
DrugBank ID
DB16882[12]
ChEBI ID
9271[9][13]

mapping relation type: täpne vaste

InChI
InChI=1S/C38H60O18/c1-16-11-37-9-5-20-35(2,7-4-8-36(20,3)34(50)55-32-29(49)26(46)23(43)18(13-40)52-32)21(37)6-10-38(16,15-37)56-33-30(27(47)24(44)19(14-41)53-33)54-31-28(48)25(45)22(42)17(12-39)51-31/h17-33,39-49H,1,4-15H2,2-3H3/t17-,18-,19-,20+,21+,22-,23-,24-,25+,26+,27+,28-,29-,30-,31+,32+,33+,35-,36-,37-,38+/m1/s1[4]
CosIng number
79199[14]
Open Food Facts food additive ID
e960-steviol-glycosides
SPLASH
splash10-0006-0000009000-8f33f594b1fb0b6d5894
splash10-002f-0002809000-588d2fa738c21ef3a427
Römpp online ID
RD-19-04072
SureChEMBL ID
SCHEMBL33428[15][12]
MassBank accession ID
MSBNK-Fukuyama_Univ-FU000316
MSBNK-Fukuyama_Univ-FU000317
MSBNK-Fukuyama_Univ-FU000318
DSSTOX compound identifier
DTXCID301281
Freebase
/m/010rbn2c
AICS Chemical ID (BEING DELETED)
20737
KNApSAcK ID
C00003485[7]
UMLS CUI
C0075246[16]
ECHA Substance Infocard ID
100.055.414[17]
LIPID MAPS ID
LMPR01040119[18]
ChemSpider ID
390625[19]
EC number
260-975-5[1]
DSSTox substance ID
DTXSID7021281[20][12]
Human Metabolome Database ID
HMDB0034945[15][12]
Encyclopædia Britannica Online ID
topic/stevioside

teema nimetus kujul: stevioside

RxNorm ID
37106[1]
Probes And Drugs ID
PD087252
National Library of Israel J9U ID
987007572887605171[21]

üksikjuht nähtusest

type of chemical entity

mille alamklass

kaurane diterpenoid
Steviooglükosiidid

kasutus

sweetener[22]

keemiline struktuur

mass/kaal

804,377965 aatommassiühik[23]

stereoisomer of

UEDUENGHJMELGK-YHFKYKSYSA-N[15][24]
UEDUENGHJMELGK-VESORUSYSA-N[15][24]
UEDUENGHJMELGK-PEKONUEISA-N[15][24]
UEDUENGHJMELGK-XNLJEJCTSA-N[24]

chemical formula

C₃₈H₆₀O₁₈[4]

canonical SMILES

CC12CCCC(C1CCC34C2CCC(C3)(C(=C)C4)OC5C(C(C(C(O5)CO)O)O)OC6C(C(C(C(O6)CO)O)O)O)(C)C(=O)OC7C(C(C(C(O7)CO)O)O)O[4]

isomeric SMILES

C[C@@]12CCC[C@@]([C@H]1CC[C@]34[C@H]2CC[C@](C3)(C(=C)C4)O[C@H]5[C@@H]([C@H]([C@@H]([C@H](O5)CO)O)O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O)(C)C(=O)O[C@H]7[C@@H]([C@H]([C@@H]([C@H](O7)CO)O)O)O[4]

found in taxon

korvõielised[25]
Paraguai suhkruleht[26][27][28][29][30][31][32][33][34][35][36][37][38][39][40][41][42][43][44][45][46][47][48][44][49][50][51][52][53][54][55][44]
Compositae[25]

physically interacts with

taste receptor type 2[56]

subjektil on roll: Agonist

on omadusega

kibedus[57]

Commonsi kategooria

Stevioside

Viited

  1. ↑ 1,0 1,1 1,2 1,3 Global Substance Registration System, 20. november 2016, inglise keel, stevioside, 0YON5MXJ9P
  2. ↑ CAS Common Chemistry, 9. aprill 2021, UEDUENGHJMELGK-HYDKPPNVSA-N, https://commonchemistry.cas.org/detail?cas_rn=57817-89-7
  3. ↑ USA Kongressi raamatukogu, 16. jaanuar 2017
  4. ↑ 4,0 4,1 4,2 4,3 4,4 4,5 PubChem, 20. november 2016, inglise keel, 442089, Stevioside
  5. ↑ Medical Subject Headings, 14. märts 2018, C012043
  6. ↑ UniChem
  7. ↑ 7,0 7,1 ChEBI, 5. oktoober 2016, inglise keel, Stevioside, 9271
  8. ↑ OpenAlex, 26. jaanuar 2022, https://docs.openalex.org/download-snapshot/snapshot-data-format
  9. ↑ 9,0 9,1 ChEMBL, 20. november 2016, inglise keel, STEVIOSIDE, CHEMBL444122
  10. ↑ CAB Thesaurus, 6. aprill 2020
  11. ↑ ChEBI release 2020-09-01
  12. ↑ 12,0 12,1 12,2 12,3 12,4 UEDUENGHJMELGK-HYDKPPNVSA-N, InChIKey
  13. ↑ International Chemical Identifier, InChI=1S/C38H60O18/c1-16-11-37-9-5-20-35(2,7-4-8-36(20,3)34(50)55-32-29(49)26(46)23(43)18(13-40)52-32)21(37)6-10-38(16,15-37)56-33-30(27(47)24(44)19(14-41)53-33)54-31-28(48)25(45)22(42)17(12-39)51-31/h17-33,39-49H,1,4-15H2,2-3H3/t17-,18-,19-,20+,21+,22-,23-,24-,25+,26+,27+,28-,29-,30-,31+,32+,33+,35-,36-,37-,38+/m1/s1
  14. ↑ CosIng database, 28. detsember 2019, 79199, STEVIOSIDE, CAS no.: 57817-89-7
  15. ↑ 15,0 15,1 15,2 15,3 15,4 inferred from InChIKey
  16. ↑ UMLS 2023, 25. mai 2023, inferred by common MeSH mappings on source and on Wikidata
  17. ↑ ECHA Substance Infocard database, 27. detsember 2018, 100.055.414, (4α)-β-D-glucopyranosyl 13-[(2-O-β-D-glucopyranosyl-β-D-glucopyranosyl)oxy]kaur-16-en-18-oate, CAS no.: 57817-89-7
  18. ↑ LIPID MAPS, http://www.lipidmaps.org/rest/compound/lm_id/LM/all/download, 15. jaanuar 2022, UEDUENGHJMELGK-HYDKPPNVSA-N
  19. ↑ ChemSpider, 20. november 2016, inglise keel, 390625, Stevioside
  20. ↑ Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard
  21. ↑ National Library of Israel Names and Subjects Authority File
  22. ↑ Medical Subject Headings, 15. märts 2018, C012043
  23. ↑ PubChem, 5. oktoober 2016, inglise keel, 442089, Stevioside
  24. ↑ 24,0 24,1 24,2 24,3 inferred from InChI
  25. ↑ 25,0 25,1 Anti-inflammatory and immunomodulatory activities of stevioside and steviol on colonic epithelial cells
  26. ↑ Chemical constituents of flowers of Stevia rebaudiana BERTONI.
  27. ↑ Analysis of sweet diterpene glycosides from Stevia rebaudiana: improved HPLC method
  28. ↑ Contributions to the biotechnological production of sweeteners from stevia rebaudiana bertoni. I. A method for the serial analysis of diterpene glycosides by HPLC
  29. ↑ Contributions to the biotechnolgical production of sweeteners from stevia rebaudiana bertoni. III. Accumulation of secondary metabolites by means of a precursor and by elicitation of cell cultures
  30. ↑ Contributions to the biotechnological production of sweeteners from stevia rebaudiana bertoni. II. Induction of stevioside accumulation in cell cultures by variation of the nutrient medium and the analysis of small amounts of stevioside
  31. ↑ Determination of Stevioside in Plant Material and Fruit Teas
  32. ↑ Effects of Stevia rebaudiana natural products on rat liver mitochondria
  33. ↑ Effects of Stevioside and Its Relative Compounds on Growth of Rice and Lettuce Seedlings
  34. ↑ Examination of Steviol Glucosides Production by Hairy Root and Shoot Cultures of Stevia rebaudiana
  35. ↑ Features of development of Stevia rebaudiana shoots cultivated in the roller bioreactor and their production of steviol glycosides
  36. ↑ High-performance liquid chromatography of glycosides on a new type of hydroxyapatite column
  37. ↑ Inhibitory effect of steviol, a metabolite of stevioside, on glucose absorption in everted hamster intestine in vitro
  38. ↑ Natural high-intensity sweeteners
  39. ↑ Purification of Steviosides by Membrane and Ion Exchange Processes
  40. ↑ Rebaudioside F, a diterpene glycoside from Stevia rebaudiana
  41. ↑ Separation and quantitation of stevioside and rebaudioside a in plant extracts by normal-phase high performance liquid chromatography and thin-layer chromatography: A comparison
  42. ↑ Separation of natural product sweetening agents using overpressured layer chromatography
  43. ↑ Steviol quantification at the picomole level by high-performance liquid chromatography
  44. ↑ 44,0 44,1 44,2 Stevioside
  45. ↑ Subcritical Fluid Extraction of Stevia Sweeteners from Stevia rebaudiana
  46. ↑ Antiviral agents from natural sources
  47. ↑ A new diterpene glycoside from Stevia rebaudiana
  48. ↑ Glycosides from Stevia rebaudiana
  49. ↑ Mechanism of the hypoglycemic effect of stevioside, a glycoside of Stevia rebaudiana
  50. ↑ Recent Progress in Fourier Analysis
  51. ↑ Safety evaluation of Stevia and stevioside
  52. ↑ SWEET HERB OF PARAGUAY
  53. ↑ Naturally Occurring Phorbol Esters
  54. ↑ Quantitative analysis of stevioside (author's transl)
  55. ↑ Analysis of stevioside in Stevia rebaudiana
  56. ↑ Human psychometric and taste receptor responses to steviol glycosides
  57. ↑ BitterDB
Pärit leheküljelt "https://et.wikipedia.org/wiki/Eri:AboutTopic/Q415043"