Structure Database (LMSD)

Common Name
Trillfurostanoside E
Systematic Name
26-O-β-D-glucopyranosyl-(25R)-furost-5,16(17),20(22)-trien-3β,26-diol-3-O-α-l-rhamnopyranosyl-(1-4)-[α-l-rhamnopyranosyl-(1-2)]-β-D-glucopyranoside
Synonyms
  • 3-O-(Rhaa1-4(Rhaa1-2)Glcb)-26-O-(Glcb)-furosta-5,16(17),20(22)-trien-3beta,26-diol
LM ID
LMST01070015
Formula
Exact Mass
Calculate m/z
1028.519215
Status
Active

Classification

References

Taxonomy Information

Curated from
NCBI taxonomy class
Reference
Trillium tschonoskii (#82502)
Magnoliopsida (#3398)
Furostanol Saponins from Trillium tschonoskii Promote the Expansion of Human Cord Blood Hematopoietic Stem and Progenitor Cells.,
J Nat Prod, 2020
Pubmed ID: 32870000

String Representations

InChiKey (Click to copy)
JEHNFGITDKMNCQ-KNPFTWAPSA-N
InChi (Click to copy)
InChI=1S/C51H80O21/c1-20(19-64-46-40(60)39(59)36(56)31(17-52)69-46)7-10-29-21(2)33-30(68-29)16-28-26-9-8-24-15-25(11-13-50(24,5)27(26)12-14-51(28,33)6)67-49-45(72-48-42(62)38(58)35(55)23(4)66-48)43(63)44(32(18-53)70-49)71-47-41(61)37(57)34(54)22(3)65-47/h8,20,22-23,25-28,31-32,34-49,52-63H,7,9-19H2,1-6H3/t20-,22+,23+,25+,26-,27+,28+,31-,32-,34+,35+,36-,37-,38-,39+,40-,41-,42-,43+,44-,45-,46-,47+,48+,49-,50+,51+/m1/s1
SMILES (Click to copy)
[C@]12(CC=C3C[C@@H](O[C@H]4[C@H](O[C@H]5[C@H](O)[C@H](O)[C@@H](O)[C@H](C)O5)[C@@H](O)[C@H](O[C@H]5[C@H](O)[C@H](O)[C@@H](O)[C@H](C)O5)[C@@H](CO)O4)CC[C@]3(C)[C@@]1([H])CC[C@]1(C)C3C(=C(CC[C@H](CO[C@H]4[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O4)C)OC=3C[C@@]21[H])C)[H]

Other Databases

PubChem CID

Calculated Physicochemical Properties

Heavy Atoms 72
Rings 9
Aromatic Rings 1
Rotatable Bonds 14
Van der Waals Molecular Volume 945.39
Topological Polar Surface Area 338.02
Hydrogen Bond Donors 12
Hydrogen Bond Acceptors 21
logP 5.71
Molar Refractivity 259.37

Admin

Created at
7th Sep 2020
Updated at
7th Sep 2020