Structure Database (LMSD)
Systematic Name
3-O-(4-O-β-D-glucopyranosyl-β-D-glucopyranosyl)-3β,14β,16β-trihydroxy-19-oxo-5α-bufa-20,22-dienolide
Synonyms
No other lipid differing only in stereochemistry/bond geometry found
3D model of
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)
SREVWSOCPHTQPW-VLOFFNASSA-N
InChi (Click to copy)
InChI=1S/C36H52O16/c1-34-8-7-19-20(36(34,47)11-21(40)25(34)16-2-5-24(41)48-14-16)4-3-17-10-18(6-9-35(17,19)15-39)49-32-30(46)28(44)31(23(13-38)51-32)52-33-29(45)27(43)26(42)22(12-37)50-33/h2,5,14-15,17-23,25-33,37-38,40,42-47H,3-4,6-13H2,1H3/t17-,18-,19-,20+,21-,22+,23+,25-,26+,27-,28+,29+,30+,31+,32+,33-,34+,35+,36-/m0/s1
SMILES (Click to copy)
C1[C@]2(C=O)[C@@]3([H])CC[C@]4(C)[C@@]([H])(C5=COC(=O)C=C5)[C@@H](O)C[C@]4(O)[C@]3([H])CC[C@@]2([H])C[C@@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](O[C@H]3[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O3)[C@@H](CO)O2)C1
Other Databases
PubChem CID
Calculated Physicochemical Properties
Heavy Atoms
52
Rings
7
Aromatic Rings
1
Rotatable Bonds
8
Van der Waals Molecular Volume
664.02
Topological Polar Surface Area
270.41
Hydrogen Bond Donors
9
Hydrogen Bond Acceptors
16
logP
3.23
Molar Refractivity
181.70
Admin
Created at
5th Jun 2020
Updated at
5th Jun 2020