Structure Database (LMSD)

Common Name
Isovitexin 7-O-xyloside-2''-O-glucoside
Systematic Name
Synonyms
LM ID
LMPK12110296
Formula
Exact Mass
Calculate m/z
726.200735
Status
Active

Classification

References

Taxonomy Information

Curated from
NCBI taxonomy class
Reference
Viridiplantae (#33090)
Flavonoid imported from http://metabolomics.jp/

String Representations

InChiKey (Click to copy)
BICGASJNMVSQHP-ZSVNUCJESA-N
InChi (Click to copy)
InChI=1S/C32H38O19/c33-7-17-23(40)26(43)30(51-32-28(45)25(42)22(39)18(8-34)50-32)29(48-17)20-16(49-31-27(44)21(38)13(37)9-46-31)6-15-19(24(20)41)12(36)5-14(47-15)10-1-3-11(35)4-2-10/h1-6,13,17-18,21-23,25-35,37-45H,7-9H2/t13-,17-,18-,21+,22-,23-,25+,26+,27-,28-,29+,30-,31+,32+/m1/s1
SMILES (Click to copy)
C1(C2C=CC(O)=CC=2)=CC(=O)C2C(O)=C([C@H]3[C@H](O[C@H]4[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O4)[C@@H](O)[C@H](O)[C@@H](CO)O3)C(O[C@H]3[C@H](O)[C@@H](O)[C@H](O)CO3)=CC=2O1

Other Databases

METABOLOMICS ID
PubChem CID

Calculated Physicochemical Properties

Heavy Atoms 51
Rings 6
Aromatic Rings 3
Rotatable Bonds 8
Van der Waals Molecular Volume 601.19
Topological Polar Surface Area 325.33
Hydrogen Bond Donors 12
Hydrogen Bond Acceptors 19
logP 1.51
Molar Refractivity 173.23

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Created at
-
Updated at
7th Oct 2021