NP-MRD: Showing NP-Card for 4,5,10-trihydroxy-7-methyl-1,1-bis(3-methylbut-2-en-1-yl)anthracen-2-one (NP0277301)

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Record Information

Version

2.0

Created at

2022-09-09 01:53:01 UTC

Updated at

2022-09-09 01:53:02 UTC

NP-MRD ID

NP0277301

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4,5,10-trihydroxy-7-methyl-1,1-bis(3-methylbut-2-en-1-yl)anthracen-2-one

Description

Vismin belongs to the class of organic compounds known as anthracenes. These are organic compounds containing a system of three linearly fused benzene rings. 4,5,10-trihydroxy-7-methyl-1,1-bis(3-methylbut-2-en-1-yl)anthracen-2-one is found in Vismia macrophylla. 4,5,10-trihydroxy-7-methyl-1,1-bis(3-methylbut-2-en-1-yl)anthracen-2-one was first documented in 2003 (PMID: 12828475). Based on a literature review very few articles have been published on Vismin (PMID: 23472469).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092203532D          

 29 31  0  0  0  0            999 V2000
    6.2579   -1.3900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4454   -1.5332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1633   -2.3085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9151   -0.9012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1027   -1.0445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0421   -1.0445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2296   -0.9012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6993   -1.5332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8868   -1.3900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9815   -2.3085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
  6 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
  6 18  1  0  0  0  0
 18 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
 22 23  1  0  0  0  0
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 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 20 27  1  0  0  0  0
 27 28  2  0  0  0  0
 17 28  1  0  0  0  0
 28 29  1  0  0  0  0
M  END

     RDKit          3D

 57 59  0  0  0  0  0  0  0  0999 V2000
   -1.1806    3.7324    1.8164 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7881    2.7973    0.7724 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2676    2.8579    0.6211 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9839    2.0309    0.0831 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4005    1.0964   -0.9332 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9776   -0.3598   -0.7010 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5533   -0.9245    0.5808 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0436   -0.9335    0.5408 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7425   -2.0637    0.6987 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0854   -3.3766    0.9232 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2236   -1.9790    0.6442 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5357   -1.0860   -1.8503 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7526   -1.5437   -1.7857 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7670   -1.3009   -3.0424 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.1914   -0.0715    0.4688 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5631    0.0021    0.4703 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2318    0.3273    1.6679 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6032    0.4055    1.6864 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3393    0.7516    2.9554 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3411    0.1738    0.5627 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6786   -0.1545   -0.6494 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5192   -0.3596   -1.6853 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3075   -0.2288   -0.6518 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6534   -0.5541   -1.8462 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4071   -0.7769   -2.9423 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0938    3.7709    1.6920 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5198    3.3534    2.7832 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5964    4.7268    1.6452 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6451    3.8928    0.8205 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.0998    2.1193    0.2924 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9661    1.3393   -1.9473 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5044    1.0582   -1.0065 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1143   -1.9085    0.7802 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.6103   -3.7703   -0.0047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7892   -4.1253    1.2852 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7085   -2.6069    1.4249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5864   -0.9448    0.6528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5182   -2.4090   -0.3561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2632   -1.6365   -3.9635 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1138   -0.8202   -5.0564 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6397    0.1101    1.3778 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6477    0.5061    2.5386 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8397    0.3584    3.8410 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4953    1.8440    2.9508 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3555    0.2942    2.9161 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4188    0.2433    0.6103 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4267   -0.5842   -2.5941 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2458   -0.9995   -3.8462 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  3
  9 10  1  0
  9 11  1  0
  6 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  2  0
 15 16  1  0
 15 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 22 24  1  0
 24 25  2  0
 25 26  1  0
 25 27  1  0
 27 28  2  0
 28 29  1  0
 18  6  1  0
 27 20  1  0
 28 17  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  3 33  1  0
  3 34  1  0
  3 35  1  0
  4 36  1  0
  5 37  1  0
  5 38  1  0
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 10 42  1  0
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 19 50  1  0
 21 51  1  0
 23 52  1  0
 23 53  1  0
 23 54  1  0
 24 55  1  0
 26 56  1  0
 29 57  1  0
M  END


  Mrv1652309092203532D          

 29 31  0  0  0  0            999 V2000
    6.2579   -1.3900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4454   -1.5332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1633   -2.3085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9151   -0.9012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1027   -1.0445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0421   -1.0445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2296   -0.9012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6993   -1.5332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8868   -1.3900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9815   -2.3085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.1434    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
  6 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
  6 18  1  0  0  0  0
 18 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
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
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 20 27  1  0  0  0  0
 27 28  2  0  0  0  0
 17 28  1  0  0  0  0
 28 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0277301

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCC1(CC=C(C)C)C(=O)C=C(O)C2=C1C=C1C=C(C)C=C(O)C1=C2O

> <INCHI_IDENTIFIER>
InChI=1S/C25H28O4/c1-14(2)6-8-25(9-7-15(3)4)18-12-17-10-16(5)11-19(26)22(17)24(29)23(18)20(27)13-21(25)28/h6-7,10-13,26-27,29H,8-9H2,1-5H3

> <INCHI_KEY>
UACVIOSHILFFIH-UHFFFAOYSA-N

> <FORMULA>
C25H28O4

> <MOLECULAR_WEIGHT>
392.495

> <EXACT_MASS>
392.198759382

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
57

> <JCHEM_AVERAGE_POLARIZABILITY>
43.96176219922249

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4,5,10-trihydroxy-7-methyl-1,1-bis(3-methylbut-2-en-1-yl)-1,2-dihydroanthracen-2-one

> <JCHEM_LOGP>
5.998318190333333

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.633843001604944

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.277979071504281

> <JCHEM_PKA_STRONGEST_BASIC>
-5.919972970665012

> <JCHEM_POLAR_SURFACE_AREA>
77.76

> <JCHEM_REFRACTIVITY>
120.09909999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
4,5,10-trihydroxy-7-methyl-1,1-bis(3-methylbut-2-en-1-yl)anthracen-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0      11.681  -2.595   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.165  -2.862   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.638  -4.309   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.175  -1.682   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.658  -1.950   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.679  -1.950   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.162  -1.682   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.172  -2.862   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.655  -2.595   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.699  -4.309   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.002   0.000   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       9.336  -0.770   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       6.668   3.850   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.335  -0.000   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.000   0.000   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       1.334   3.850   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       4.001   3.850   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   12   18                                             
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    6   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   28                                                  
CONECT   18   17    6   19                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   27                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   20   28                                                  
CONECT   28   27   17   29                                                  
CONECT   29   28                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₂₈O₄

Average Mass

392.4950 Da

Monoisotopic Mass

392.19876 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(C)=CCC1(CC=C(C)C)C(=O)C=C(O)C2=C1C=C1C=C(C)C=C(O)C1=C2O

InChI Identifier

InChI=1S/C25H28O4/c1-14(2)6-8-25(9-7-15(3)4)18-12-17-10-16(5)11-19(26)22(17)24(29)23(18)20(27)13-21(25)28/h6-7,10-13,26-27,29H,8-9H2,1-5H3

InChI Key

UACVIOSHILFFIH-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
Vismia macrophylla	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as anthracenes. These are organic compounds containing a system of three linearly fused benzene rings.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Anthracenes

Sub Class

Not Available

Direct Parent

Anthracenes

Alternative Parents

Substituents

Anthracene
1-naphthol
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Vinylogous acid
Cyclic ketone
Ketone
Polyol
Enol
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic compounds

External Descriptors

Not Available

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

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00045135

Chemspider ID

137214

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Visible minority

METLIN ID

Not Available

PubChem Compound

155775

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Tiani GM, Ahmed I, Krohn K, Green IR, Nkengfack AE: Kenganthranol F, a new anthranol from Psorospermum aurantiacum. Nat Prod Commun. 2013 Jan;8(1):103-4. [PubMed:23472469 ]
Hussein AA, Bozzi B, Correa M, Capson TL, Kursar TA, Coley PD, Solis PN, Gupta MP: Bioactive constituents from three Vismia species. J Nat Prod. 2003 Jun;66(6):858-60. doi: 10.1021/np020566w. [PubMed:12828475 ]
LOTUS database [Link]

Showing NP-Card for 4,5,10-trihydroxy-7-methyl-1,1-bis(3-methylbut-2-en-1-yl)anthracen-2-one (NP0277301)

MOL for NP0277301 (4,5,10-trihydroxy-7-methyl-1,1-bis(3-methylbut-2-en-1-yl)anthracen-2-one)

3D MOL for NP0277301 (4,5,10-trihydroxy-7-methyl-1,1-bis(3-methylbut-2-en-1-yl)anthracen-2-one)

3D SDF for NP0277301 (4,5,10-trihydroxy-7-methyl-1,1-bis(3-methylbut-2-en-1-yl)anthracen-2-one)

3D-SDF for NP0277301 (4,5,10-trihydroxy-7-methyl-1,1-bis(3-methylbut-2-en-1-yl)anthracen-2-one)

PDB for NP0277301 (4,5,10-trihydroxy-7-methyl-1,1-bis(3-methylbut-2-en-1-yl)anthracen-2-one)

3D PDB for NP0277301 (4,5,10-trihydroxy-7-methyl-1,1-bis(3-methylbut-2-en-1-yl)anthracen-2-one)

SMILES for NP0277301 (4,5,10-trihydroxy-7-methyl-1,1-bis(3-methylbut-2-en-1-yl)anthracen-2-one)

INCHI for NP0277301 (4,5,10-trihydroxy-7-methyl-1,1-bis(3-methylbut-2-en-1-yl)anthracen-2-one)

Structure for NP0277301 (4,5,10-trihydroxy-7-methyl-1,1-bis(3-methylbut-2-en-1-yl)anthracen-2-one)

3D Structure for NP0277301 (4,5,10-trihydroxy-7-methyl-1,1-bis(3-methylbut-2-en-1-yl)anthracen-2-one)