Structure Database (LMSD)
Common Name
Echinasteroside C
Systematic Name
(25S)-3-O-(2-O-methyl-β-D-xylopyranosyl)-cholest-4-ene-3β,6β,8,15α,16β,26-hexaol
Synonyms
3D model of Echinasteroside C
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)
NHMQTYHFQPGJFK-KGFVJONFSA-N
InChi (Click to copy)
InChI=1S/C33H56O10/c1-17(15-34)7-6-8-18(2)24-26(38)27(39)29-32(24,4)12-10-23-31(3)11-9-19(13-20(31)21(35)14-33(23,29)40)43-30-28(41-5)25(37)22(36)16-42-30/h13,17-19,21-30,34-40H,6-12,14-16H2,1-5H3/t17-,18+,19-,21+,22+,23+,24-,25-,26+,27-,28+,29+,30-,31-,32+,33-/m0/s1
SMILES (Click to copy)
C1[C@]2(C)[C@@]3([H])CC[C@]4(C)[C@@]([H])([C@]([H])(C)CCC[C@@H](CO)C)[C@@H](O)[C@H](O)[C@@]4([H])[C@]3(O)C[C@@H](O)C2=C[C@@H](O[C@@H]2OC[C@@H](O)[C@H](O)[C@H]2OC)C1
Other Databases
PubChem CID
Calculated Physicochemical Properties
Heavy Atoms
43
Rings
5
Aromatic Rings
0
Rotatable Bonds
9
Van der Waals Molecular Volume
602.92
Topological Polar Surface Area
171.37
Hydrogen Bond Donors
7
Hydrogen Bond Acceptors
10
logP
4.65
Molar Refractivity
163.10
Admin
Created at
21st Dec 2020
Updated at
19th Feb 2024