NP-MRD: Showing NP-Card for 10,21-dihydroxy-16,17-dimethoxy-6-(prop-1-en-2-yl)-2,7,20-trioxapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-3(11),4(8),9,14,16,18-hexaen-12-one (NP0320431)

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Record Information

Version

2.0

Created at

2022-09-11 22:04:31 UTC

Updated at

2022-09-11 22:04:31 UTC

NP-MRD ID

NP0320431

Secondary Accession Numbers

None

Natural Product Identification

Common Name

10,21-dihydroxy-16,17-dimethoxy-6-(prop-1-en-2-yl)-2,7,20-trioxapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-3(11),4(8),9,14,16,18-hexaen-12-one

Description

Villosin belongs to the class of organic compounds known as rotenones. These are rotenoids with a structure based on a 6a,12a-dihydrochromeno[3,4-b]chromen-12(6H)-one skeleton. Thus, villosin is considered to be a flavonoid. 10,21-dihydroxy-16,17-dimethoxy-6-(prop-1-en-2-yl)-2,7,20-trioxapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-3(11),4(8),9,14,16,18-hexaen-12-one is found in Hedychium gardnerianum, Tephrosia pentaphylla and Tephrosia villosa. 10,21-dihydroxy-16,17-dimethoxy-6-(prop-1-en-2-yl)-2,7,20-trioxapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-3(11),4(8),9,14,16,18-hexaen-12-one was first documented in 2014 (PMID: 25230490). Based on a literature review a small amount of articles have been published on Villosin (PMID: 32354114) (PMID: 29924604) (PMID: 28371315) (PMID: 26965832).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122200042D          

 31 35  0  0  0  0            999 V2000
    7.5691    0.0307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8484   -0.3709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8359   -1.1958    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1403    0.0524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3816   -0.2717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8390    0.3498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2623    1.0579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8607    1.7785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0358    1.7911    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6342    2.5118    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6125    1.0830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0141    0.3623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5908   -0.3458    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7659   -0.3333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3425   -1.0414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7441   -1.7620    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5176   -1.0288    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1161   -0.3082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2912   -0.2956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1104    0.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9353    0.4376    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3587   -0.2705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3129    1.1332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0887    1.8538    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3346    2.5619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1378    1.1206    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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 29 30  2  0  0  0  0
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M  END

     RDKit          3D

 53 57  0  0  0  0  0  0  0  0999 V2000
    4.3785    1.9269    0.3745 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3972    1.1148    0.2127 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6069    1.6103   -0.4921 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3817   -0.2752    0.6909 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1023   -0.6469    1.4465 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1872   -0.7814    0.2609 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9374   -1.0337   -0.8611 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2924   -1.1864   -2.0664 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8967   -1.0813   -2.1166 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3382   -1.2438   -3.3520 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.9583   -0.0672    2.6478 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -2.3007   -0.5134    2.5828 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9823   -0.2828    1.3744 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3610   -0.3315    1.3236 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0747   -0.1124    0.1625 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4740   -0.1698    0.1477 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2216   -0.4504    1.3006 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4234    0.1706   -1.0207 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1492    0.3894   -2.1829 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4693    0.6793   -3.3928 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0474    0.2215   -0.9808 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3243   -0.0010    0.1982 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8507    0.0724    0.1543 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2868   -0.7137   -0.9861 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.3931   -1.1885   -3.5666 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.4623   -0.5360    3.5064 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2166    1.6371    3.2694 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8737   -0.5568    2.2669 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.2703    0.4410    1.9453 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2315   -0.7963    0.9682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1615    0.7809   -4.2297 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7070   -0.1153   -3.5247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8917    1.6358   -3.3011 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5472    0.4459   -1.9204 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4783    1.1195    0.0610 H   0  0  0  0  0  0  0  0  0  0  0  0
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  2  1  2  3
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 31  7  1  0
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  1 32  1  0
  1 33  1  0
 15 43  1  1
 16 44  1  0
 19 45  1  0
M  END


  Mrv1652309122200042D          

 31 35  0  0  0  0            999 V2000
    7.5691    0.0307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8484   -0.3709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8359   -1.1958    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1403    0.0524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3816   -0.2717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8390    0.3498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2623    1.0579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8607    1.7785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0358    1.7911    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6342    2.5118    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6125    1.0830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0141    0.3623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5908   -0.3458    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7659   -0.3333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3425   -1.0414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7441   -1.7620    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5176   -1.0288    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1161   -0.3082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2912   -0.2956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1104    0.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9353    0.4376    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3587   -0.2705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3129    1.1332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0887    1.8538    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3346    2.5619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
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  9 10  1  0  0  0  0
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 29 30  2  0  0  0  0
  7 31  1  0  0  0  0
  4 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0320431

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(OC)C=C2C3C(OC4=C(C(O)=CC5=C4CC(O5)C(C)=C)C3=O)C(O)OC2=C1

> <INCHI_IDENTIFIER>
InChI=1S/C23H22O8/c1-9(2)13-6-11-14(29-13)7-12(24)19-20(25)18-10-5-16(27-3)17(28-4)8-15(10)30-23(26)22(18)31-21(11)19/h5,7-8,13,18,22-24,26H,1,6H2,2-4H3

> <INCHI_KEY>
RMAYNNFCPNGTQW-UHFFFAOYSA-N

> <FORMULA>
C23H22O8

> <MOLECULAR_WEIGHT>
426.421

> <EXACT_MASS>
426.131467668

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
43.43849302573797

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
10,21-dihydroxy-16,17-dimethoxy-6-(prop-1-en-2-yl)-2,7,20-trioxapentacyclo[11.8.0.0^{3,11}.0^{4,8}.0^{14,19}]henicosa-3(11),4(8),9,14,16,18-hexaen-12-one

> <JCHEM_LOGP>
3.3023885510000004

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.543975563901633

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.771907251670426

> <JCHEM_PKA_STRONGEST_BASIC>
-4.232656856741373

> <JCHEM_POLAR_SURFACE_AREA>
103.68000000000002

> <JCHEM_REFRACTIVITY>
108.7231

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
10,21-dihydroxy-16,17-dimethoxy-6-(prop-1-en-2-yl)-2,7,20-trioxapentacyclo[11.8.0.0^{3,11}.0^{4,8}.0^{14,19}]henicosa-3(11),4(8),9,14,16,18-hexaen-12-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0      14.129   0.057   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.784  -0.692   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      12.760  -2.232   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.462   0.098   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.046  -0.507   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.033   0.653   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.823   1.975   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.073   3.320   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.534   3.343   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       6.784   4.689   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       6.743   2.022   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.493   0.676   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       6.703  -0.645   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       5.163  -0.622   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.373  -1.944   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       5.122  -3.289   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       2.833  -1.920   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       2.083  -0.575   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.543  -0.552   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.206   0.793   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -1.746   0.817   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -2.536  -0.505   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.584   2.115   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -0.166   3.460   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       0.625   4.782   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.124   2.092   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.874   0.747   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.413   0.723   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.204   2.045   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       4.454   3.390   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0      11.324   1.632   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   31                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   12                                                  
CONECT    7    6    8   31                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   29                                                  
CONECT   12   11    6   13                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   28                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19   27                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   23                                                  
CONECT   21   20   22                                                       
CONECT   22   21                                                            
CONECT   23   20   24   26                                                  
CONECT   24   23   25                                                       
CONECT   25   24                                                            
CONECT   26   23   27                                                       
CONECT   27   26   18   28                                                  
CONECT   28   27   14   29                                                  
CONECT   29   28   11   30                                                  
CONECT   30   29                                                            
CONECT   31    7    4                                                       
MASTER        0    0    0    0    0    0    0    0   31    0   70    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₂₂O₈

Average Mass

426.4210 Da

Monoisotopic Mass

426.13147 Da

IUPAC Name

10,21-dihydroxy-16,17-dimethoxy-6-(prop-1-en-2-yl)-2,7,20-trioxapentacyclo[11.8.0.0^{3,11}.0^{4,8}.0^{14,19}]henicosa-3(11),4(8),9,14,16,18-hexaen-12-one

Traditional Name

10,21-dihydroxy-16,17-dimethoxy-6-(prop-1-en-2-yl)-2,7,20-trioxapentacyclo[11.8.0.0^{3,11}.0^{4,8}.0^{14,19}]henicosa-3(11),4(8),9,14,16,18-hexaen-12-one

CAS Registry Number

Not Available

SMILES

COC1=C(OC)C=C2C3C(OC4=C(C(O)=CC5=C4CC(O5)C(C)=C)C3=O)C(O)OC2=C1

InChI Identifier

InChI=1S/C23H22O8/c1-9(2)13-6-11-14(29-13)7-12(24)19-20(25)18-10-5-16(27-3)17(28-4)8-15(10)30-23(26)22(18)31-21(11)19/h5,7-8,13,18,22-24,26H,1,6H2,2-4H3

InChI Key

RMAYNNFCPNGTQW-UHFFFAOYSA-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, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, 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
Hedychium gardnerianum	LOTUS Database	35616633
Tephrosia pentaphylla	LOTUS Database	35616633
Tephrosia villosa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as rotenones. These are rotenoids with a structure based on a 6a,12a-dihydrochromeno[3,4-b]chromen-12(6H)-one skeleton.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Isoflavonoids

Sub Class

Rotenoids

Direct Parent

Rotenones

Alternative Parents

Substituents

Rotenone or derivatives
8-prenylated isoflavanone
Isoflavanone
Isoflavan
Chromone
1-benzopyran
Chromane
Benzopyran
Coumaran
Aryl alkyl ketone
Aryl ketone
Anisole
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Benzenoid
Vinylogous acid
Hemiacetal
Ketone
Oxacycle
Organoheterocyclic compound
Ether
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Rotenoid flavonoids (LMPK12060026 )

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	3.3	ChemAxon
pKa (Strongest Acidic)	8.77	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	103.68 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	108.72 m³·mol⁻¹	ChemAxon
Polarizability	43.44 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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

C00009578

Chemspider ID

22370034

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

14427376

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Tavares WR, Barreto MDC, Seca AML: Uncharted Source of Medicinal Products: The Case of the Hedychium Genus. Medicines (Basel). 2020 Apr 28;7(5). pii: medicines7050023. doi: 10.3390/medicines7050023. [PubMed:32354114 ]
Hu HJ, Zhou Y, Han ZZ, Shi YH, Zhang SS, Wang ZT, Yang L: Abietane Diterpenoids from the Roots of Clerodendrum trichotomum and Their Nitric Oxide Inhibitory Activities. J Nat Prod. 2018 Jul 27;81(7):1508-1516. doi: 10.1021/acs.jnatprod.7b00814. Epub 2018 Jun 20. [PubMed:29924604 ]
Su SY, Xue JJ, Yang GY, Lei C, Hou AJ: New Cytotoxic Alkylated Chalcones from Fatoua villosa. Chem Biodivers. 2017 Jun;14(6). doi: 10.1002/cbdv.201700076. Epub 2017 May 10. [PubMed:28371315 ]
Li YP, Zhao SM, Xu JJ, Zeng GZ, Li Y, Tan NH, Yang Y: New Labdane diterpenes from Hedychium yunnanense with cytotoxicity and inhibitory effects on nitric oxide production. Nat Prod Res. 2016 Dec;30(23):2669-2674. doi: 10.1080/14786419.2016.1143829. Epub 2016 Mar 11. [PubMed:26965832 ]
Li L, Wu L, Wang M, Sun J, Liang J: Abietane diterpenoids from Clerodendrum trichotomum and correction of NMR data of Villosin C and B. Nat Prod Commun. 2014 Jul;9(7):907-10. [PubMed:25230490 ]
LOTUS database [Link]

Showing NP-Card for 10,21-dihydroxy-16,17-dimethoxy-6-(prop-1-en-2-yl)-2,7,20-trioxapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-3(11),4(8),9,14,16,18-hexaen-12-one (NP0320431)

MOL for NP0320431 (10,21-dihydroxy-16,17-dimethoxy-6-(prop-1-en-2-yl)-2,7,20-trioxapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-3(11),4(8),9,14,16,18-hexaen-12-one)

3D MOL for NP0320431 (10,21-dihydroxy-16,17-dimethoxy-6-(prop-1-en-2-yl)-2,7,20-trioxapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-3(11),4(8),9,14,16,18-hexaen-12-one)

3D SDF for NP0320431 (10,21-dihydroxy-16,17-dimethoxy-6-(prop-1-en-2-yl)-2,7,20-trioxapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-3(11),4(8),9,14,16,18-hexaen-12-one)

3D-SDF for NP0320431 (10,21-dihydroxy-16,17-dimethoxy-6-(prop-1-en-2-yl)-2,7,20-trioxapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-3(11),4(8),9,14,16,18-hexaen-12-one)

PDB for NP0320431 (10,21-dihydroxy-16,17-dimethoxy-6-(prop-1-en-2-yl)-2,7,20-trioxapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-3(11),4(8),9,14,16,18-hexaen-12-one)

3D PDB for NP0320431 (10,21-dihydroxy-16,17-dimethoxy-6-(prop-1-en-2-yl)-2,7,20-trioxapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-3(11),4(8),9,14,16,18-hexaen-12-one)

SMILES for NP0320431 (10,21-dihydroxy-16,17-dimethoxy-6-(prop-1-en-2-yl)-2,7,20-trioxapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-3(11),4(8),9,14,16,18-hexaen-12-one)

INCHI for NP0320431 (10,21-dihydroxy-16,17-dimethoxy-6-(prop-1-en-2-yl)-2,7,20-trioxapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-3(11),4(8),9,14,16,18-hexaen-12-one)

Structure for NP0320431 (10,21-dihydroxy-16,17-dimethoxy-6-(prop-1-en-2-yl)-2,7,20-trioxapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-3(11),4(8),9,14,16,18-hexaen-12-one)

3D Structure for NP0320431 (10,21-dihydroxy-16,17-dimethoxy-6-(prop-1-en-2-yl)-2,7,20-trioxapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-3(11),4(8),9,14,16,18-hexaen-12-one)