Structure Database (LMSD)

Common Name
Heavenly blue anthocyanin
Systematic Name
Synonyms
LM ID
LMPK12010232
Formula
Exact Mass
Calculate m/z
1759.48325
Status
Curated

Classification

References

Taxonomy Information

Curated from
NCBI taxonomy class
Reference
Viridiplantae (#33090)
Flavonoid imported from http://metabolomics.jp/
Ipomoea nervosa (#139741)
Magnoliopsida (#3398)
Ergoline Alkaloids in Tropical Wood Roses.,
Science, 1965
Pubmed ID: 17842841

String Representations

InChiKey (Click to copy)
ISQXIVZPNCPLCO-JLYUAXMOSA-O
InChi (Click to copy)
InChI=1S/C79H90O45/c1-108-42-19-32(8-11-35(42)84)72-45(22-34-40(112-72)20-33(83)21-41(34)114-75-67(103)61(97)55(91)46(23-80)118-75)117-79-73(124-78-71(107)65(101)59(95)50(122-78)27-110-54(90)15-7-31-3-10-37(86)44(18-31)116-77-69(105)63(99)57(93)48(25-82)120-77)66(102)60(96)51(123-79)28-111-52(88)13-5-29-4-12-39(38(87)16-29)113-74-70(106)64(100)58(94)49(121-74)26-109-53(89)14-6-30-2-9-36(85)43(17-30)115-76-68(104)62(98)56(92)47(24-81)119-76/h2-22,46-51,55-71,73-82,91-107H,23-28H2,1H3,(H4-,83,84,85,86,87,89,90)/p+1/b13-5+/t46-,47-,48-,49-,50-,51-,55-,56-,57-,58-,59-,60-,61+,62+,63+,64+,65+,66+,67-,68-,69-,70-,71-,73-,74-,75-,76-,77-,78+,79-/m1/s1
SMILES (Click to copy)
C1(O[C@H]2[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O2)C=C(O)C=C2[O+]=C(C3C=C(OC)C(O)=CC=3)C(O[C@H]3[C@H](O[C@H]4[C@H](O)[C@@H](O)[C@H](O)[C@@H](COC(/C=C/C5C=C(O[C@H]6[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O6)C(O)=CC=5)=O)O4)[C@@H](O)[C@H](O)[C@@H](COC(/C=C/C4C=C(O)C(O[C@H]5[C@H](O)[C@@H](O)[C@H](O)[C@@H](COC(/C=C/C6C=CC(O)=C(O[C@H]7[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O7)C=6)=O)O5)=CC=4)=O)O3)=CC=12

Other Databases

METABOLOMICS ID
PubChem CID

Calculated Physicochemical Properties

Heavy Atoms 124
Rings 12
Aromatic Rings 6
Rotatable Bonds 32
Van der Waals Molecular Volume 1497.69
Topological Polar Surface Area 728.36
Hydrogen Bond Donors 25
Hydrogen Bond Acceptors 45
logP 3.73
Molar Refractivity 421.89

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Created at
-
Updated at
23rd Dec 2021