Structure Database (LMSD)

Common Name
Trillfurostanoside A
Systematic Name
26-O-β-D-glucopyranosyl-(25R)-furost-17-en-16,22-dione-3β,5α,6β,26-tetrahydroxy-3-O-α-l-rhamnopyranosyl-(1-4)-α-l-rhamnopyranosyl-(1-4)-[α-l-rhamnopyranosyl-(1-2)]-β-D-glucopyranoside
Synonyms
  • 3-O-(Rhaa1-4Rhaa1-4(Rhaa1-2)Glcb)-(25R)-furost-5en,26,22-dione-3beta,5alpha,6beta,26-tetrol
LM ID
LMST01070020
Formula
Exact Mass
Calculate m/z
1224.57752
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)
ANSRILXVZQLJPD-SYAAVTRTSA-N
InChi (Click to copy)
InChI=1S/C57H92O28/c1-20(19-76-50-42(70)40(68)37(65)31(17-58)81-50)8-9-29(60)21(2)34-30(61)15-28-26-14-33(62)57(75)16-25(10-13-56(57,7)27(26)11-12-55(28,34)6)80-54-49(85-52-44(72)39(67)36(64)23(4)78-52)46(74)48(32(18-59)82-54)84-53-45(73)41(69)47(24(5)79-53)83-51-43(71)38(66)35(63)22(3)77-51/h20,22-28,31-33,35-54,58-59,62-75H,8-19H2,1-7H3/b34-21+/t20-,22+,23+,24+,25+,26-,27+,28+,31-,32-,33-,35+,36+,37-,38-,39-,40+,41+,42-,43-,44-,45-,46+,47+,48-,49-,50-,51+,52+,53+,54-,55+,56-,57+/m1/s1
SMILES (Click to copy)
[C@]12(C[C@@H](O)[C@@]3(O)C[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]6[C@H](O)[C@H](O)[C@@H](O)[C@H](C)O6)[C@H](C)O5)[C@@H](CO)O4)CC[C@]3(C)[C@@]1([H])CC[C@]1(C)/C(=C(/C(CC[C@H](CO[C@H]3[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O3)C)=O)\C)/C(=O)C[C@@]21[H])[H]

Other Databases

PubChem CID

Calculated Physicochemical Properties

Heavy Atoms 85
Rings 9
Aromatic Rings 0
Rotatable Bonds 17
Van der Waals Molecular Volume 1121.62
Topological Polar Surface Area 460.47
Hydrogen Bond Donors 16
Hydrogen Bond Acceptors 28
logP 4.03
Molar Refractivity 298.90

Admin

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