NP-MRD: Showing NP-Card for debromomarinone (NP0264497)

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Record Information

Version

2.0

Created at

2022-09-08 08:02:56 UTC

Updated at

2022-09-08 08:02:56 UTC

NP-MRD ID

NP0264497

Secondary Accession Numbers

None

Natural Product Identification

Common Name

debromomarinone

Description

Debromomarinone belongs to the class of organic compounds known as naphthopyranones. Naphthopyranones are compounds containing a naphthopyran skeleton where a ring carbon bears a carboxylic acid group. Naphthtopyran is made up of the pyran ring fused to a naphthalene ring system. debromomarinone was first documented in 2015 (PMID: 26659564). Based on a literature review a small amount of articles have been published on Debromomarinone (PMID: 31549845) (PMID: 29534540).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082210022D          

 30 33  0  0  1  0            999 V2000
    2.6319    5.2935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6447    4.4686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3656    4.0673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9368    4.0450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9496    3.2201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2417    2.7965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2546    1.9716    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4400    2.1022    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0647    2.1275    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6048    1.5039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3347    0.7243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8748    0.1007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6048   -0.6789    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6850    0.2566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2251   -0.3671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0352   -0.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5753   -0.8348    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3052    0.5684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7651    1.1921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0352    1.9716    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9550    1.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4149    1.6598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6850    2.4393    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5246    0.5684    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2546   -0.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4444   -0.3671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1744   -1.1466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0957    0.2566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1744    1.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9845    1.1921    0.0000 C   0  0  1  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
  7  6  1  6  0  0  0
  7  8  1  1  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 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
 16 17  1  0  0  0  0
 16 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 14 21  1  0  0  0  0
 21 22  1  0  0  0  0
 10 22  1  0  0  0  0
 22 23  2  0  0  0  0
 24 11  1  1  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 30 29  1  1  0  0  0
 24 30  1  0  0  0  0
  7 30  1  0  0  0  0
M  END

     RDKit          3D

 58 61  0  0  0  0  0  0  0  0999 V2000
    5.3653   -2.5874   -0.7267 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5287   -1.3749   -0.5810 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2979   -0.5351   -1.7826 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9750   -0.9987    0.5603 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1363    0.2220    0.6939 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7517   -0.1680    1.1540 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8168    0.9980    1.3266 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4093    1.9320    2.3648 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3636    0.4517    1.9515 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2346   -0.2853    1.1742 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3584   -0.0220   -0.0896 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2874   -0.8226   -0.8885 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4413   -0.6121   -2.1012 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0477   -1.8977   -0.2220 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9240   -2.6437   -1.0034 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6477   -3.6522   -0.4144 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5290   -4.3942   -1.2260 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5084   -3.9176    0.9165 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6385   -3.1891    1.7301 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5379   -3.4967    3.0557 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9139   -2.1758    1.1297 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9853   -1.3578    1.8693 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8087   -1.5445    3.0879 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5961    1.0667   -0.7450 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5074    2.0446   -1.4086 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2748    3.3431   -1.5118 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2285    4.2400   -2.1847 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0003    3.8943   -0.9157 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1095    3.1573    0.4261 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4599    1.7080    0.0568 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2959   -3.2664    0.1450 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0071   -3.1678   -1.6083 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4432   -2.3243   -0.9053 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6383    0.4952   -1.6811 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7681   -0.9780   -2.6932 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1909   -0.5308   -1.9782 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1432   -1.6163    1.4478 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0395    0.6469   -0.3243 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6053    0.9704    1.3308 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3178   -0.9752    0.5388 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8758   -0.6111    2.1788 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7303    1.3205    3.2328 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6342    2.6405    2.7647 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3069    2.4544    1.9995 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0135   -2.4095   -2.0596 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1694   -5.2266   -1.6864 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0746   -4.7111    1.3918 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9953   -3.0979    3.7349 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0841    0.5492   -1.6220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4352    1.6937   -1.8457 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2618    4.1715   -1.7416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2717    4.1328   -3.2727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9268    5.3095   -1.9916 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8221    3.5629   -1.5845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0627    4.9737   -0.7927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8655    3.1963    0.9101 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9357    3.6167    0.9598 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3895    1.7987   -0.5440 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
  7  6  1  6
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  2  0
 11 24  1  0
 24 25  1  0
 25 26  2  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
 29 30  1  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 16 18  2  0
 18 19  1  0
 19 20  1  0
 19 21  2  0
 21 22  1  0
 22 23  2  0
 30  7  1  0
 21 14  1  0
 22 10  1  0
 30 24  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  3 34  1  0
  3 35  1  0
  3 36  1  0
  4 37  1  0
  5 38  1  0
  5 39  1  0
  6 40  1  0
  6 41  1  0
  8 42  1  0
  8 43  1  0
  8 44  1  0
 24 49  1  6
 25 50  1  0
 27 51  1  0
 27 52  1  0
 27 53  1  0
 28 54  1  0
 28 55  1  0
 29 56  1  0
 29 57  1  0
 30 58  1  6
 15 45  1  0
 17 46  1  0
 18 47  1  0
 20 48  1  0
M  END


  Mrv1652309082210022D          

 30 33  0  0  1  0            999 V2000
    2.6319    5.2935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6447    4.4686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3656    4.0673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9368    4.0450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9496    3.2201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2417    2.7965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2546    1.9716    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4400    2.1022    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0647    2.1275    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6048    1.5039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3347    0.7243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8748    0.1007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6048   -0.6789    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6850    0.2566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2251   -0.3671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0352   -0.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5753   -0.8348    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3052    0.5684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7651    1.1921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0352    1.9716    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9550    1.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4149    1.6598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6850    2.4393    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5246    0.5684    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2546   -0.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4444   -0.3671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1744   -1.1466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0957    0.2566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1744    1.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9845    1.1921    0.0000 C   0  0  1  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
  7  6  1  6  0  0  0
  7  8  1  1  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 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
 16 17  1  0  0  0  0
 16 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 14 21  1  0  0  0  0
 21 22  1  0  0  0  0
 10 22  1  0  0  0  0
 22 23  2  0  0  0  0
 24 11  1  1  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 30 29  1  1  0  0  0
 24 30  1  0  0  0  0
  7 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0264497

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCC[C@]1(C)OC2=C([C@H]3C=C(C)CC[C@@H]13)C(=O)C1=CC(O)=CC(O)=C1C2=O

> <INCHI_IDENTIFIER>
InChI=1S/C25H28O5/c1-13(2)6-5-9-25(4)18-8-7-14(3)10-16(18)21-22(28)17-11-15(26)12-19(27)20(17)23(29)24(21)30-25/h6,10-12,16,18,26-27H,5,7-9H2,1-4H3/t16-,18+,25-/m0/s1

> <INCHI_KEY>
DPALYVVGGATILJ-UVNWJPITSA-N

> <FORMULA>
C25H28O5

> <MOLECULAR_WEIGHT>
408.494

> <EXACT_MASS>
408.193674002

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
45.330546583877506

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(4aR,5S,12bS)-8,10-dihydroxy-2,5-dimethyl-5-(4-methylpent-3-en-1-yl)-4,4a,5,7,12,12b-hexahydro-3H-6-oxatetraphene-7,12-dione

> <JCHEM_LOGP>
4.891605949666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.814015183363324

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.216675086686458

> <JCHEM_PKA_STRONGEST_BASIC>
-5.00418209573455

> <JCHEM_POLAR_SURFACE_AREA>
83.83

> <JCHEM_REFRACTIVITY>
118.69129999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(4aR,5S,12bS)-8,10-dihydroxy-2,5-dimethyl-5-(4-methylpent-3-en-1-yl)-3,4,4a,12b-tetrahydro-6-oxatetraphene-7,12-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0       4.913   9.881   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.937   8.341   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.282   7.592   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.615   7.551   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.639   6.011   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.318   5.220   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.342   3.680   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.821   3.924   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       3.854   3.971   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       4.862   2.807   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.358   1.352   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.366   0.188   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       4.862  -1.267   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       6.879   0.479   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.887  -0.685   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.399  -0.394   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      10.407  -1.558   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       9.903   1.061   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.895   2.225   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       9.399   3.680   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       7.383   1.934   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.375   3.098   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       6.879   4.553   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       2.846   1.061   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.342  -0.394   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.830  -0.685   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.326  -2.140   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -0.179   0.479   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       0.326   1.934   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       1.838   2.225   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9   30                                             
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11   22                                                  
CONECT   11   10   12   24                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   21                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   14   22                                                  
CONECT   22   21   10   23                                                  
CONECT   23   22                                                            
CONECT   24   11   25   30                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   24    7                                                  
MASTER        0    0    0    0    0    0    0    0   30    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₂₈O₅

Average Mass

408.4940 Da

Monoisotopic Mass

408.19367 Da

IUPAC Name

(4aR,5S,12bS)-8,10-dihydroxy-2,5-dimethyl-5-(4-methylpent-3-en-1-yl)-4,4a,5,7,12,12b-hexahydro-3H-6-oxatetraphene-7,12-dione

Traditional Name

(4aR,5S,12bS)-8,10-dihydroxy-2,5-dimethyl-5-(4-methylpent-3-en-1-yl)-3,4,4a,12b-tetrahydro-6-oxatetraphene-7,12-dione

CAS Registry Number

Not Available

SMILES

CC(C)=CCC[C@]1(C)OC2=C([C@H]3C=C(C)CC[C@@H]13)C(=O)C1=CC(O)=CC(O)=C1C2=O

InChI Identifier

InChI=1S/C25H28O5/c1-13(2)6-5-9-25(4)18-8-7-14(3)10-16(18)21-22(28)17-11-15(26)12-19(27)20(17)23(29)24(21)30-25/h6,10-12,16,18,26-27H,5,7-9H2,1-4H3/t16-,18+,25-/m0/s1

InChI Key

DPALYVVGGATILJ-UVNWJPITSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthopyranones. Naphthopyranones are compounds containing a naphthopyran skeleton where a ring carbon bears a carboxylic acid group. Naphthtopyran is made up of the pyran ring fused to a naphthalene ring system.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Naphthopyrans

Sub Class

Naphthopyranones

Direct Parent

Naphthopyranones

Alternative Parents

Substituents

Naphthopyranone
Naphthoquinone
Naphthalene
Aryl ketone
Quinone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Pyranone
Phenol
Benzenoid
Pyran
Vinylogous ester
Vinylogous acid
Ketone
Oxacycle
Organic oxygen compound
Organooxygen compound
Hydrocarbon derivative
Organic oxide
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	4.89	ChemAxon
pKa (Strongest Acidic)	7.22	ChemAxon
pKa (Strongest Basic)	-5	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	83.83 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	118.69 m³·mol⁻¹	ChemAxon
Polarizability	45.33 Å³	ChemAxon
Number of Rings	4	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

Not Available

Chemspider ID

8584615

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Debromomarinone

METLIN ID

Not Available

PubChem Compound

10409178

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Murray LAM, Fallon T, Sumby CJ, George JH: Total Synthesis of Naphterpin and Marinone Natural Products. Org Lett. 2019 Oct 18;21(20):8312-8315. doi: 10.1021/acs.orglett.9b03095. Epub 2019 Sep 24. [PubMed:31549845 ]
Park JS, Kwon HC: New Naphthoquinone Terpenoids from Marine Actinobacterium, Streptomyces sp. CNQ-509. Mar Drugs. 2018 Mar 12;16(3). pii: md16030090. doi: 10.3390/md16030090. [PubMed:29534540 ]
Leipoldt F, Zeyhle P, Kulik A, Kalinowski J, Heide L, Kaysser L: Diversity of ABBA Prenyltransferases in Marine Streptomyces sp. CNQ-509: Promiscuous Enzymes for the Biosynthesis of Mixed Terpenoid Compounds. PLoS One. 2015 Dec 14;10(12):e0143237. doi: 10.1371/journal.pone.0143237. eCollection 2015. [PubMed:26659564 ]
LOTUS database [Link]

Showing NP-Card for debromomarinone (NP0264497)

MOL for NP0264497 (debromomarinone)

3D MOL for NP0264497 (debromomarinone)

3D SDF for NP0264497 (debromomarinone)

3D-SDF for NP0264497 (debromomarinone)

PDB for NP0264497 (debromomarinone)

3D PDB for NP0264497 (debromomarinone)

SMILES for NP0264497 (debromomarinone)

INCHI for NP0264497 (debromomarinone)

Structure for NP0264497 (debromomarinone)

3D Structure for NP0264497 (debromomarinone)