NP-MRD: Showing NP-Card for Lophirone D (NP0054853)

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Record Information

Version

2.0

Created at

2022-04-28 01:04:28 UTC

Updated at

2022-04-28 01:04:28 UTC

NP-MRD ID

NP0054853

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Lophirone D

Description

Lophirone d belongs to the class of organic compounds known as 2-arylbenzofuran flavonoids. These are phenylpropanoids containing the 2-phenylbenzofuran moiety. Thus, lophirone D is considered to be a flavonoid. Lophirone D is found in Lophira alata and Lophira lanceolata . Lophirone D was first documented in 2019 (PMID: 31585261). Based on a literature review a small amount of articles have been published on Lophirone d.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282203042D          

 30 33  0  0  0  0            999 V2000
    3.3523    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    2.1904    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    0.8555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8838    0.0709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4358   -0.5422    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1712    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5837    0.8085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4087    0.8085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8212    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4087    2.2374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5837    2.2374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6462    1.5229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668   -0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -0.5396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957   -0.1271    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -1.3646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957   -1.7771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957   -2.6021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -3.0146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668   -2.6021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668   -1.7771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.3646    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -3.8396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  4  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
  8 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 12 17  1  0  0  0  0
 15 18  1  0  0  0  0
  2 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 23 28  1  0  0  0  0
 28 29  1  0  0  0  0
 26 30  1  0  0  0  0
M  END

     RDKit          3D

 46 49  0  0  0  0  0  0  0  0999 V2000
   -2.8449    2.6805   -0.4066 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8634    1.7398    0.4170 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7828    0.3831   -0.0385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8182   -0.4528   -0.3664 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2686   -0.2285   -0.3400 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8501    0.9317    0.0822 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2486    1.0723    0.0712 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0835    0.0675   -0.3569 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4697    0.2022   -0.3697 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5008   -1.1006   -0.7819 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1304   -1.2445   -0.7736 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2392   -1.5935   -0.7432 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9536   -1.5369   -0.6773 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9129   -2.4297   -0.9508 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4030   -2.0565   -0.7734 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7640   -0.8018   -0.3233 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1762   -0.4737   -0.1582 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5667    0.6786    0.2573 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8785    1.1667    0.4745 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8422    2.4269    0.9122 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1886    0.6035    0.3255 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5285   -0.6501   -0.0988 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8656   -1.0715   -0.1975 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8948   -0.2509    0.1254 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1971   -0.6800    0.0228 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5880    1.0130    0.5546 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2821    1.4323    0.6536 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0064    2.7279    1.0949 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2329    0.0815   -0.0515 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5719   -0.3005   -0.2328 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9396    1.9558    1.4612 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2449    1.7499    0.4324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6802    1.9850    0.4044 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9094    0.5755   -1.2178 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1002   -1.9318   -1.1317 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6583   -2.1720   -1.1107 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1854   -3.4237   -1.3069 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1628   -2.8108   -1.0088 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8491   -1.2723   -0.4121 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7137    1.3957    0.4763 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7729   -1.3438   -0.3677 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0668   -2.0897   -0.5449 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7199   -1.1310    0.7531 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4040    1.7004    0.8234 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7106    3.3828    1.3484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0922    1.0942    0.3064 H   0  0  0  0  0  0  0  0  0  0  0  0
  9  8  1  0
  8  7  2  0
  7  6  1  0
  6  5  2  0
  5 11  1  0
 11 10  2  0
  5  4  1  0
  4  3  2  0
  3  2  1  0
  2  1  2  0
  3 30  1  0
 30 29  2  0
 29 16  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 19 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  2  0
 24 25  1  0
 24 26  1  0
 26 27  2  0
 27 28  1  0
 16 15  2  0
 15 14  1  0
 14 13  2  0
 13 12  1  0
 10  8  1  0
 12  4  1  0
 13 30  1  0
 27 21  1  0
  9 34  1  0
  7 33  1  0
  6 32  1  0
 11 36  1  0
 10 35  1  0
  2 31  1  0
 29 46  1  0
 17 39  1  0
 18 40  1  0
 22 41  1  0
 23 42  1  0
 25 43  1  0
 26 44  1  0
 28 45  1  0
 15 38  1  0
 14 37  1  0
M  END


  Mrv1652304282203042D          

 30 33  0  0  0  0            999 V2000
    3.3523    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    2.1904    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    0.8555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8838    0.0709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4358   -0.5422    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1712    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5837    0.8085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4087    0.8085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8212    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4087    2.2374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5837    2.2374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6462    1.5229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668   -0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -0.5396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957   -0.1271    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -1.3646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957   -1.7771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957   -2.6021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -3.0146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668   -2.6021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668   -1.7771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.3646    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -3.8396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  4  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
  8 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 12 17  1  0  0  0  0
 15 18  1  0  0  0  0
  2 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 23 28  1  0  0  0  0
 28 29  1  0  0  0  0
 26 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0054853

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC1=CC=C(C=C1)C1=C(C=O)C2=CC(\C=C\C(=O)C3=CC=C(O)C=C3O)=CC=C2O1

> <INCHI_IDENTIFIER>
InChI=1S/C24H16O6/c25-13-20-19-11-14(1-9-21(28)18-8-7-17(27)12-22(18)29)2-10-23(19)30-24(20)15-3-5-16(26)6-4-15/h1-13,26-27,29H/b9-1+

> <INCHI_KEY>
QTLOYOSKGRNTNQ-XLUWADSXSA-N

> <FORMULA>
C24H16O6

> <MOLECULAR_WEIGHT>
400.386

> <EXACT_MASS>
400.094688235

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
42.42823868006889

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5-[(1E)-3-(2,4-dihydroxyphenyl)-3-oxoprop-1-en-1-yl]-2-(4-hydroxyphenyl)-1-benzofuran-3-carbaldehyde

> <ALOGPS_LOGP>
4.65

> <JCHEM_LOGP>
5.068481575

> <ALOGPS_LOGS>
-4.27

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.501669964213134

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.108134514592594

> <JCHEM_PKA_STRONGEST_BASIC>
-3.022559997464973

> <JCHEM_POLAR_SURFACE_AREA>
107.97

> <JCHEM_REFRACTIVITY>
113.25849999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.17e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
lophirone D

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       6.258   3.613   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.258   2.073   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.924   1.303   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.590   2.073   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.590   3.613   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.924   4.383   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       2.126   4.089   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       1.220   2.843   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.126   1.597   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.650   0.132   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       2.680  -1.012   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -0.320   2.843   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.090   1.509   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.630   1.509   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -3.400   2.843   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.630   4.177   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.090   4.177   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -4.940   2.843   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       7.591   1.303   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.591  -0.237   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.925  -1.007   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      10.259  -0.237   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       8.925  -2.547   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      10.259  -3.317   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      10.259  -4.857   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.925  -5.627   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       7.591  -4.857   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       7.591  -3.317   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       6.258  -2.547   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       8.925  -7.167   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3   19                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    9                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8                                                       
CONECT    8    7    9   12                                                  
CONECT    9    8    4   10                                                  
CONECT   10    9   11                                                       
CONECT   11   10                                                            
CONECT   12    8   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   18                                                  
CONECT   16   15   17                                                       
CONECT   17   16   12                                                       
CONECT   18   15                                                            
CONECT   19    2   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   28                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   30                                                  
CONECT   27   26   28                                                       
CONECT   28   27   23   29                                                  
CONECT   29   28                                                            
CONECT   30   26                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₁₆O₆

Average Mass

400.3860 Da

Monoisotopic Mass

400.09469 Da

IUPAC Name

5-[(1E)-3-(2,4-dihydroxyphenyl)-3-oxoprop-1-en-1-yl]-2-(4-hydroxyphenyl)-1-benzofuran-3-carbaldehyde

Traditional Name

lophirone D

CAS Registry Number

Not Available

SMILES

OC1=CC=C(C=C1)C1=C(C=O)C2=CC(\C=C\C(=O)C3=CC=C(O)C=C3O)=CC=C2O1

InChI Identifier

InChI=1S/C24H16O6/c25-13-20-19-11-14(1-9-21(28)18-8-7-17(27)12-22(18)29)2-10-23(19)30-24(20)15-3-5-16(26)6-4-15/h1-13,26-27,29H/b9-1+

InChI Key

QTLOYOSKGRNTNQ-XLUWADSXSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Lophira alata	LOTUS Database	35616633
Lophira lanceolata	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 2-arylbenzofuran flavonoids. These are phenylpropanoids containing the 2-phenylbenzofuran moiety.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

2-arylbenzofuran flavonoids

Sub Class

Not Available

Direct Parent

2-arylbenzofuran flavonoids

Alternative Parents

Substituents

2-arylbenzofuran flavonoid
Furanochalcone
2'-hydroxychalcone
Neolignan skeleton
2-phenylbenzofuran
Phenylbenzofuran
Cinnamic acid or derivatives
Benzofuran
Resorcinol
Aryl ketone
Styrene
Benzoyl
Phenol
1-hydroxy-2-unsubstituted benzenoid
1-hydroxy-4-unsubstituted benzenoid
Aryl-aldehyde
Benzenoid
Monocyclic benzene moiety
Acryloyl-group
Heteroaromatic compound
Enone
Furan
Vinylogous acid
Alpha,beta-unsaturated ketone
Ketone
Oxacycle
Organoheterocyclic compound
Aldehyde
Organic oxygen compound
Organooxygen compound
Organic oxide
Hydrocarbon derivative
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Chalcones and dihydrochalcones (LMPK12120074 )

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	4.65	ALOGPS
logP	5.07	ChemAxon
logS	-4.3	ALOGPS
pKa (Strongest Acidic)	7.11	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	107.97 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	113.26 m³·mol⁻¹	ChemAxon
Polarizability	42.43 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00007165

Chemspider ID

24845881

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

14376455

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Lopatriello A, Sore H, Habluetzel A, Parapini S, D'Alessandro S, Taramelli D, Taglialatela-Scafati O: Identification of a potent and selective gametocytocidal antimalarial agent from the stem barks of Lophira lanceolata. Bioorg Chem. 2019 Dec;93:103321. doi: 10.1016/j.bioorg.2019.103321. Epub 2019 Sep 26. [PubMed:31585261 ]

Showing NP-Card for Lophirone D (NP0054853)

MOL for NP0054853 (Lophirone D)

3D MOL for NP0054853 (Lophirone D)

3D SDF for NP0054853 (Lophirone D)

3D-SDF for NP0054853 (Lophirone D)

PDB for NP0054853 (Lophirone D)

3D PDB for NP0054853 (Lophirone D)

SMILES for NP0054853 (Lophirone D)

INCHI for NP0054853 (Lophirone D)

Structure for NP0054853 (Lophirone D)

3D Structure for NP0054853 (Lophirone D)