NP-MRD: Showing NP-Card for 5,12-dihydroxy-3,7,9,9-tetramethyl-7-(3-oxobutyl)-3,4-dihydro-2-oxatetraphene-1,6,8-trione (NP0322401)

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Record Information

Version

2.0

Created at

2022-09-12 01:09:05 UTC

Updated at

2022-09-12 01:09:06 UTC

NP-MRD ID

NP0322401

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5,12-dihydroxy-3,7,9,9-tetramethyl-7-(3-oxobutyl)-3,4-dihydro-2-oxatetraphene-1,6,8-trione

Description

5,12-Dihydroxy-3,7,9,9-tetramethyl-7-(3-oxobutyl)-3,4,6,7,8,9-hexahydro-1H-2-oxatetraphene-1,6,8-trione belongs to the class of organic compounds known as naphthopyrans. Naphthopyrans are compounds containing a pyran ring fused to a naphthalene moiety. Furan is a 6 membered-ring non-aromatic ring with five carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings. 5,12-dihydroxy-3,7,9,9-tetramethyl-7-(3-oxobutyl)-3,4-dihydro-2-oxatetraphene-1,6,8-trione is found in Garveia annulata. 5,12-Dihydroxy-3,7,9,9-tetramethyl-7-(3-oxobutyl)-3,4,6,7,8,9-hexahydro-1H-2-oxatetraphene-1,6,8-trione is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004231515362D          

 32 35  0  0  0  0            999 V2000
   -2.6835   -0.5034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4135   -1.2829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6033   -1.4389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3333   -2.2184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8734   -2.8421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6835   -2.6861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2236   -3.3098    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9535   -1.9066    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6033   -3.6216    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -4.2452    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7932   -3.7775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2531   -3.1539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5570   -3.3098    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0971   -2.6861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8271   -1.9066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3672   -1.2829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0971   -0.5034    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1773   -1.4389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1902   -0.6140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9919   -1.3083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2861   -0.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1007   -0.4070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3949    0.3638    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6211   -1.0471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4473   -2.2184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2575   -2.3743    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9073   -2.8421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5117   -3.4036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7797   -3.6571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0169   -1.7507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2531   -0.9711    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5231   -2.3743    0.0000 C   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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  2  8  1  0  0  0  0
  5  9  2  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
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 15 16  1  0  0  0  0
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 22 24  1  0  0  0  0
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 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
  4 32  2  0  0  0  0
 12 32  1  0  0  0  0
M  END

     RDKit          3D

 58 61  0  0  0  0  0  0  0  0999 V2000
    5.1924    1.9355   -2.3476 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7435    1.8166   -0.9108 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2123    2.7967   -0.4589 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9915    0.5635   -0.2344 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1522    0.1336    0.8783 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7656   -0.2858    0.7622 C   0  0  1  0  0  0  0  0  0  0  0  0
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    0.3413   -0.0830    0.2039 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.1408   -1.2544    0.0513 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3675   -1.9377   -0.0283 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5072   -1.1993    0.1340 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7590   -1.7891    0.0720 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4532    0.1784    0.3684 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2548    0.8511    0.4442 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0824    0.0994    0.2817 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8157    0.6913    0.3598 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7143    2.0092    0.5899 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1653    2.3248    0.6354 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5256    2.9776    0.4668 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.7521    3.4449   -0.9641 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6115    2.2400    0.8750 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6951    0.8975    0.5908 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8271    0.2973    0.5231 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3980   -2.2817   -0.1880 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2952   -3.5425    0.6512 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3579   -2.7745   -1.6441 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6926   -1.6181   -0.0186 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7439   -2.0243   -0.4442 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8500    2.8282   -2.4674 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7934    1.0668   -2.6574 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3178    2.0365   -3.0104 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1886   -0.2813   -0.9783 H   0  0  0  0  0  0  0  0  0  0  0  0
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    4.2221    0.9379    1.7146 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2318   -0.8412    2.1441 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5996   -0.0172    2.9318 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7387   -1.7697    2.3828 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0889   -3.1191   -0.2878 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4085   -3.0039   -0.2102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8242   -2.7988   -0.0994 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0671    2.7009    0.7061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5735    2.7932   -0.2018 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8186    2.6008    1.6307 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5448    3.9402    1.0695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0161    4.2199   -1.2265 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7794    3.8594   -0.9934 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7116    2.6115   -1.6787 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3172   -3.9708    0.6899 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6507   -4.2491    0.1310 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9820   -3.3098    1.6912 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7530   -1.9795   -2.2833 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9782   -3.6947   -1.6790 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3070   -3.0242   -1.8633 H   0  0  0  0  0  0  0  0  0  0  0  0
 24 23  1  0
 23 22  1  0
 22 18  1  0
 18 19  2  0
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  8  6  1  0
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 25 23  1  0
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  1 33  1  0
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  1 35  1  0
 29 53  1  0
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 29 55  1  0
 30 56  1  0
 30 57  1  0
 30 58  1  0
 12 43  1  0
 14 44  1  0
 16 45  1  0
M  END


  Mrv1533004231515362D          

 32 35  0  0  0  0            999 V2000
   -2.6835   -0.5034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4135   -1.2829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6033   -1.4389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3333   -2.2184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8734   -2.8421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6835   -2.6861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2236   -3.3098    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9535   -1.9066    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6033   -3.6216    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -4.2452    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7932   -3.7775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2531   -3.1539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5570   -3.3098    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0971   -2.6861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8271   -1.9066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3672   -1.2829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0971   -0.5034    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1773   -1.4389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1902   -0.6140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9919   -1.3083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2861   -0.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1007   -0.4070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3949    0.3638    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6211   -1.0471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4473   -2.2184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2575   -2.3743    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.5117   -3.4036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7797   -3.6571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0169   -1.7507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2531   -0.9711    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5231   -2.3743    0.0000 C   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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  2  8  1  0  0  0  0
  5  9  2  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
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 16 17  2  0  0  0  0
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 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
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 15 30  2  0  0  0  0
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 12 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0322401

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1CC2=C3C(O)=C4C(=O)C(C)(CCC(C)=O)C(=O)C(C)(C)C4=CC3=CC(O)=C2C(=O)O1

> <INCHI_IDENTIFIER>
InChI=1S/C25H26O7/c1-11(26)6-7-25(5)21(29)19-15(24(3,4)23(25)31)9-13-10-16(27)18-14(17(13)20(19)28)8-12(2)32-22(18)30/h9-10,12,27-28H,6-8H2,1-5H3

> <INCHI_KEY>
QLSJVXODKOKHPU-UHFFFAOYSA-N

> <FORMULA>
C25H26O7

> <MOLECULAR_WEIGHT>
438.476

> <EXACT_MASS>
438.167853177

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
46.34491110828077

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
5,12-dihydroxy-3,7,9,9-tetramethyl-7-(3-oxobutyl)-3,4,6,7,8,9-hexahydro-1H-2-oxatetraphene-1,6,8-trione

> <ALOGPS_LOGP>
3.70

> <JCHEM_LOGP>
5.6526501636666655

> <ALOGPS_LOGS>
-4.55

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.246869207421858

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.105224901764215

> <JCHEM_PKA_STRONGEST_BASIC>
-4.719654417689822

> <JCHEM_POLAR_SURFACE_AREA>
117.97000000000001

> <JCHEM_REFRACTIVITY>
117.75509999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.23e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5,12-dihydroxy-3,7,9,9-tetramethyl-7-(3-oxobutyl)-3,4-dihydro-2-oxatetraphene-1,6,8-trione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 23-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-APR-15         0                                  
HETATM    1  C   UNK     0      -5.009  -0.940   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.505  -2.395   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.993  -2.686   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.489  -4.141   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -3.497  -5.305   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -5.009  -5.014   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -6.017  -6.178   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0      -5.513  -3.559   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -2.993  -6.760   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -4.001  -7.924   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -1.481  -7.051   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.472  -5.887   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.040  -6.178   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.048  -5.014   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.544  -3.559   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.552  -2.395   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       2.048  -0.940   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       4.064  -2.686   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.088  -1.146   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.585  -2.442   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.134  -1.003   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.655  -0.760   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       8.204   0.679   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       8.626  -1.955   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.568  -4.141   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       6.081  -4.432   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       3.560  -5.305   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.688  -6.353   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.322  -6.827   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       0.032  -3.268   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      -0.472  -1.813   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      -0.977  -4.432   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    8                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   32                                                  
CONECT    5    4    6    9                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    2                                                       
CONECT    9    5   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   32                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   27                                                  
CONECT   15   14   16   30                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20   25                                             
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   18   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   14   28   29                                             
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30   15   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30    4   12                                                  
MASTER        0    0    0    0    0    0    0    0   32    0   70    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₂₆O₇

Average Mass

438.4760 Da

Monoisotopic Mass

438.16785 Da

IUPAC Name

5,12-dihydroxy-3,7,9,9-tetramethyl-7-(3-oxobutyl)-3,4,6,7,8,9-hexahydro-1H-2-oxatetraphene-1,6,8-trione

Traditional Name

5,12-dihydroxy-3,7,9,9-tetramethyl-7-(3-oxobutyl)-3,4-dihydro-2-oxatetraphene-1,6,8-trione

CAS Registry Number

Not Available

SMILES

CC1CC2=C3C(O)=C4C(=O)C(C)(CCC(C)=O)C(=O)C(C)(C)C4=CC3=CC(O)=C2C(=O)O1

InChI Identifier

InChI=1S/C25H26O7/c1-11(26)6-7-25(5)21(29)19-15(24(3,4)23(25)31)9-13-10-16(27)18-14(17(13)20(19)28)8-12(2)32-22(18)30/h9-10,12,27-28H,6-8H2,1-5H3

InChI Key

QLSJVXODKOKHPU-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
Garveia annulata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthopyrans. Naphthopyrans are compounds containing a pyran ring fused to a naphthalene moiety. Furan is a 6 membered-ring non-aromatic ring with five carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Naphthopyrans

Sub Class

Not Available

Direct Parent

Naphthopyrans

Alternative Parents

Substituents

Naphthopyran
Naphthoquinone
2-naphthol
1-naphthol
Benzopyran
Isochromane
Naphthalene
2-benzopyran
Tetralin
Aryl alkyl ketone
Aryl ketone
Quinone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Benzenoid
Pyran
Vinylogous acid
Cyclic ketone
Lactone
Ketone
Carboxylic acid ester
Oxacycle
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Hydrocarbon derivative
Carbonyl group
Organic oxide
Organooxygen compound
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic 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
logP	3.7	ALOGPS
logP	5.65	ChemAxon
logS	-4.6	ALOGPS
pKa (Strongest Acidic)	8.11	ChemAxon
pKa (Strongest Basic)	-4.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	117.97 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	117.76 m³·mol⁻¹	ChemAxon
Polarizability	46.34 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 5,12-dihydroxy-3,7,9,9-tetramethyl-7-(3-oxobutyl)-3,4-dihydro-2-oxatetraphene-1,6,8-trione (NP0322401)

MOL for NP0322401 (5,12-dihydroxy-3,7,9,9-tetramethyl-7-(3-oxobutyl)-3,4-dihydro-2-oxatetraphene-1,6,8-trione)

3D MOL for NP0322401 (5,12-dihydroxy-3,7,9,9-tetramethyl-7-(3-oxobutyl)-3,4-dihydro-2-oxatetraphene-1,6,8-trione)

3D SDF for NP0322401 (5,12-dihydroxy-3,7,9,9-tetramethyl-7-(3-oxobutyl)-3,4-dihydro-2-oxatetraphene-1,6,8-trione)

3D-SDF for NP0322401 (5,12-dihydroxy-3,7,9,9-tetramethyl-7-(3-oxobutyl)-3,4-dihydro-2-oxatetraphene-1,6,8-trione)

PDB for NP0322401 (5,12-dihydroxy-3,7,9,9-tetramethyl-7-(3-oxobutyl)-3,4-dihydro-2-oxatetraphene-1,6,8-trione)

3D PDB for NP0322401 (5,12-dihydroxy-3,7,9,9-tetramethyl-7-(3-oxobutyl)-3,4-dihydro-2-oxatetraphene-1,6,8-trione)

SMILES for NP0322401 (5,12-dihydroxy-3,7,9,9-tetramethyl-7-(3-oxobutyl)-3,4-dihydro-2-oxatetraphene-1,6,8-trione)

INCHI for NP0322401 (5,12-dihydroxy-3,7,9,9-tetramethyl-7-(3-oxobutyl)-3,4-dihydro-2-oxatetraphene-1,6,8-trione)

Structure for NP0322401 (5,12-dihydroxy-3,7,9,9-tetramethyl-7-(3-oxobutyl)-3,4-dihydro-2-oxatetraphene-1,6,8-trione)

3D Structure for NP0322401 (5,12-dihydroxy-3,7,9,9-tetramethyl-7-(3-oxobutyl)-3,4-dihydro-2-oxatetraphene-1,6,8-trione)