Structure Database (LMSD)
Common Name
Dioscoreside E
Systematic Name
3-O-(Glcb1-3(Rhaa1-2)Glcb)-26-O-(Glcb)-23S-methoxy-(25R)-furosta-5,20(22)-dien-3β,26-diol
Synonyms
- 26-O-beta-D-glucopyranosyl-3beta,26-dihydroxy-23(S)-methoxy-25(R)-furosta-5,20(22)-dien-3-O-alpha-L-rhamnopyranosyl(1-2)-[beta-D-glucopyranosyl(1-3)]-beta-D-glucopyranoside
No other lipid differing only in stereochemistry/bond geometry found
3D model of Dioscoreside E
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)
WSWNKHNNDHPGMZ-OXNGKDHZSA-N
InChi (Click to copy)
InChI=1S/C52H84O23/c1-20(19-67-47-41(63)39(61)35(57)30(16-53)71-47)13-29(66-6)44-21(2)33-28(70-44)15-27-25-8-7-23-14-24(9-11-51(23,4)26(25)10-12-52(27,33)5)69-50-46(75-48-42(64)38(60)34(56)22(3)68-48)45(37(59)32(18-55)73-50)74-49-43(65)40(62)36(58)31(17-54)72-49/h7,20,22,24-43,45-50,53-65H,8-19H2,1-6H3/t20-,22+,24+,25-,26+,27+,28+,29+,30-,31-,32-,33+,34+,35-,36-,37-,38-,39+,40+,41-,42-,43-,45+,46-,47-,48+,49+,50-,51+,52+/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]5[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O5)[C@H](O)[C@@H](CO)O4)CC[C@]3(C)[C@@]1([H])CC[C@]1(C)[C@H]3C(=C([C@@H](OC)C[C@@H](C)CO[C@H]4[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O4)O[C@H]3C[C@@]21[H])C)[H]
Other Databases
PubChem CID
Calculated Physicochemical Properties
Heavy Atoms
75
Rings
9
Aromatic Rings
0
Rotatable Bonds
16
Van der Waals Molecular Volume
993.81
Topological Polar Surface Area
365.64
Hydrogen Bond Donors
13
Hydrogen Bond Acceptors
23
logP
5.29
Molar Refractivity
268.68
Admin
Created at
-
Updated at
13th Sep 2021