Misplaced Pages

Platycodin D

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
Platycodin D
Names
IUPAC name 3-C-(Hydroxymethyl)-β-D-erythrofuranosyl-(1→3)-β-D-xylopyranosyl-(1→4)-α-L-rhamnopyranosyl-(1→2)-α-L-arabinopyranosyl 3β-(β-D-glucopyranosyloxy)-2β,16α,23,24-hydroxyolean-12-en-28-oate
Systematic IUPAC name (1S,1R,1S,1S,3S,3R,3S,3R,3S,5S,5R,5S,5R,7S,7R,7R)-1,1,3,3,5,5,7,7-Octahydroxy-7-(hydroxymethyl)-3-methyl-2,4,6-trioxa-1(3),3(2,5),5(2,4)-tris(oxana)-7(2)-oxolanaheptaphan-1-yl (4aR,5R,6aS,6bR,8aR,10R,11S,12aR,12bR,14bS)-5,11-dihydroxy-9,9-bis(hydroxymethyl)-2,2,6a,6b,12a-pentamethyl-10-{oxy}-1,3,4,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-octadecahydropicene-4a(2H)-carboxylate
Identifiers
CAS Number
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.208.719 Edit this at Wikidata
EC Number
  • 683-210-0
KEGG
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C57H92O28/c1-23-40(81-45-39(72)41(28(64)18-76-45)82-49-43(73)56(75,21-61)22-78-49)36(69)38(71)46(79-23)83-42-33(66)27(63)17-77-48(42)85-50(74)57-12-11-51(2,3)13-25(57)24-7-8-30-52(4)14-26(62)44(84-47-37(70)35(68)34(67)29(16-58)80-47)55(19-59,20-60)31(52)9-10-53(30,5)54(24,6)15-32(57)65/h7,23,25-49,58-73,75H,8-22H2,1-6H3/t23-,25-,26-,27-,28+,29+,30+,31+,32+,33-,34+,35-,36-,37+,38+,39+,40-,41-,42+,43-,44-,45-,46-,47-,48-,49-,52+,53+,54+,56+,57+/m0/s1Key: CYBWUNOAQPMRBA-NDTOZIJESA-N
SMILES
  • C1((((O1)O2((CO2OC(=O)34CCC(C3C5=CC6(5(C4O)C)(CC76(C((C7(CO)CO)O8((((O8)CO)O)O)O)O)C)C)(C)C)O)O)O)O)O9(((CO9)O)O1((CO1)(CO)O)O)O
Properties
Chemical formula C57H92O28
Molar mass 1225.335 g·mol
Hazards
GHS labelling:
Pictograms GHS07: Exclamation mark
Signal word Warning
Hazard statements H302
Precautionary statements P264, P270, P301+P312, P330, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references
Chemical compound

Platycodin D is a chemical compound extracted from the roots of Platycodon grandiflorus. It has been studied in vitro for potential spermicidal and antiinflammatory effects.

References

  1. Zongliang, Lu (2013). "Evaluation of the Spermicidal and Contraceptive Activity of Platycodin D, a Saponin from Platycodon grandiflorum". PLOS ONE. 8 (11): e82068. Bibcode:2013PLoSO...882068L. doi:10.1371/journal.pone.0082068. PMC 3841115. PMID 24303079.
  2. Hong, J.; Shin, K. H.; Lim, S. S.; Kwak, J. H.; Zee, O.; Ishihara, K.; Hirasawa, N.; Seyama, T.; Ohuchi, K. (2008). "Lead compounds for anti-inflammatory drugs isolated from the plants of the traditional oriental medicine in Korea". Inflammation & Allergy - Drug Targets. 7 (3): 195–202. doi:10.2174/187152808785748100. PMID 18782027.


Stub icon

This article about an organic compound is a stub. You can help Misplaced Pages by expanding it.

Categories: