Structure Database (LMSD)
Common Name
Tarenninoside E
Systematic Name
Synonyms
- 6'-O-(E)-cinnamoylixoside
3D model of Tarenninoside 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
Level 4 Class
References
Taxonomy Information
Curated from
NCBI taxonomy class
Reference
Tarenna attenuata
(#1547788)
Magnoliopsida
(#3398)
Iridoid constituents of Tarenna attenuata.,
J Nat Prod, 2006
J Nat Prod, 2006
Pubmed ID:
16792422
String Representations
InChiKey (Click to copy)
FCWMFHCKWKKWPV-VAYBDKCBSA-N
InChi (Click to copy)
InChI=1S/C25H26O13/c26-17(9-6-12-4-2-1-3-5-12)35-11-16-18(27)19(28)20(29)23(37-16)38-24-25(34)14(7-8-15(25)22(32)33)13(10-36-24)21(30)31/h1-6,8-10,14,16,18-20,23-24,27-29,34H,7,11H2,(H,30,31)(H,32,33)/b9-6+/t14-,16-,18+,19+,20-,23+,24+,25-/m1/s1
SMILES (Click to copy)
C1(C(=O)O)[C@@]2([H])CC=C(C(O)=O)[C@@]2(O)[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@@H](O)[C@@H](COC(/C=C/C3=CC=CC=C3)=O)O2)OC=1
Other Databases
PubChem CID
Calculated Physicochemical Properties
Heavy Atoms
38
Rings
4
Aromatic Rings
1
Rotatable Bonds
9
Van der Waals Molecular Volume
471.23
Topological Polar Surface Area
213.65
Hydrogen Bond Donors
6
Hydrogen Bond Acceptors
13
logP
1.44
Molar Refractivity
127.64
Admin
Created at
24th Jul 2020
Updated at
24th Jul 2020