Structure Database (LMSD)
Common Name
Trillfurostanoside G
Systematic Name
26-O-β-D-glucopyranosyl-(25R)-furostan-3β,5α,6β,17α,22α,26-hexahydroxy-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)-furosta-3beta,5alpha,6beta,17alpha,22alpha,26-hexol
No other lipid differing only in stereochemistry/bond geometry found
3D model of Trillfurostanoside G
Please note: Where there are chiral atoms but the stereochemistry is undefined, the 3D model takes an arbitrary conformation
Classification
Category
Main Class
Sub Class
References
String Representations
InChiKey (Click to copy)
UGOIXOPVIZAGKG-WQZKAANRSA-N
InChi (Click to copy)
InChI=1S/C57H96O29/c1-20(19-76-48-40(68)38(66)35(63)29(17-58)81-48)8-13-56(74)24(5)57(75)32(86-56)15-28-26-14-31(60)55(73)16-25(9-11-53(55,6)27(26)10-12-54(28,57)7)80-52-47(85-50-42(70)37(65)34(62)22(3)78-50)44(72)46(30(18-59)82-52)84-51-43(71)39(67)45(23(4)79-51)83-49-41(69)36(64)33(61)21(2)77-49/h20-52,58-75H,8-19H2,1-7H3/t20-,21+,22+,23+,24-,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+,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@@]3(O)[C@@H]([C@@](O)(CC[C@H](CO[C@H]4[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O4)C)O[C@H]3C[C@@]21[H])C)[H]
Other Databases
PubChem CID
Calculated Physicochemical Properties
Heavy Atoms
86
Rings
10
Aromatic Rings
0
Rotatable Bonds
16
Van der Waals Molecular Volume
1125.97
Topological Polar Surface Area
478.09
Hydrogen Bond Donors
18
Hydrogen Bond Acceptors
29
logP
3.89
Molar Refractivity
301.66
Admin
Created at
7th Sep 2020
Updated at
7th Sep 2020