NP-MRD: Showing NP-Card for Atrovenetinone methyl acetal (NP0005809)

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Record Information

Version

2.0

Created at

2020-12-09 02:57:49 UTC

Updated at

2021-07-15 16:53:02 UTC

NP-MRD ID

NP0005809

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Atrovenetinone methyl acetal

Provided By

NPAtlas

Description

Atrovenetinone methyl acetal is found in Penicillium. Atrovenetinone methyl acetal was first documented in 2005 (PMID: 15813183). Based on a literature review very few articles have been published on 3,6,15-trihydroxy-3-methoxy-8,12,13,13-tetramethyl-11-oxatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁴]Hexadeca-1(15),5,7,9(16),10(14)-pentaene-2,4-dione.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242118233D          

 47 50  0  0  0  0            999 V2000
    5.5771    1.2708    1.6737 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2919    1.7437    1.6050 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3590    0.8943    1.0806 C   0  0  2  0  0  0  0  0  0  0  0  0
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    2.3591   -0.0967   -1.0067 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5890   -0.8983   -2.1038 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8995   -1.0454   -2.5801 O   0  0  0  0  0  0  0  0  0  0  0  0
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    1.0820    0.1034   -0.4688 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0222    1.5727    1.2366 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

 47 50  0  0  0  0  0  0  0  0999 V2000
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    4.2919    1.7437    1.6050 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3590    0.8943    1.0806 C   0  0  2  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652306242118233D          

 47 50  0  0  0  0            999 V2000
    5.5771    1.2708    1.6737 C   0  0  0  0  0  0  0  0  0  0  0  0
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  1 30  1  0  0  0  0
  4 31  1  0  0  0  0
  9 32  1  0  0  0  0
 10 33  1  0  0  0  0
 12 34  1  0  0  0  0
 12 35  1  0  0  0  0
 12 36  1  0  0  0  0
 17 37  1  0  0  0  0
 23 38  1  0  0  0  0
 23 39  1  0  0  0  0
 23 40  1  0  0  0  0
 24 41  1  0  0  0  0
 24 42  1  0  0  0  0
 24 43  1  0  0  0  0
 25 44  1  6  0  0  0
 26 45  1  0  0  0  0
 26 46  1  0  0  0  0
 26 47  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0005809

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C([H])C(=C2C3=C(C(O[H])=C4C(=O)[C@](O[H])(OC([H])([H])[H])C(=O)C1=C24)C(C([H])([H])[H])(C([H])([H])[H])[C@@]([H])(O3)C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C20H20O7/c1-7-6-9(21)11-12-10(7)16-14(19(3,4)8(2)27-16)15(22)13(12)18(24)20(25,26-5)17(11)23/h6,8,21-22,25H,1-5H3/t8-,20+/m0/s1

> <INCHI_KEY>
NOAOQFJXKUUYHO-UHFFFAOYSA-N

> <FORMULA>
C20H20O7

> <MOLECULAR_WEIGHT>
372.373

> <EXACT_MASS>
372.120902984

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
38.199566184317575

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3R,12S)-3,6,15-trihydroxy-3-methoxy-8,12,13,13-tetramethyl-11-oxatetracyclo[7.6.1.0^{5,16}.0^{10,14}]hexadeca-1(15),5(16),6,8,10(14)-pentaene-2,4-dione

> <ALOGPS_LOGP>
2.78

> <JCHEM_LOGP>
4.332121677

> <ALOGPS_LOGS>
-3.14

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.234204587218091

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.642270151478457

> <JCHEM_PKA_STRONGEST_BASIC>
-4.282636381915539

> <JCHEM_POLAR_SURFACE_AREA>
113.29

> <JCHEM_REFRACTIVITY>
96.71029999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.68e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3R,12S)-3,6,15-trihydroxy-3-methoxy-8,12,13,13-tetramethyl-11-oxatetracyclo[7.6.1.0^{5,16}.0^{10,14}]hexadeca-1(15),5(16),6,8,10(14)-pentaene-2,4-dione

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 47 50  0  0  0  0  0  0  0  0999 V2000
    5.5771    1.2708    1.6737 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2919    1.7437    1.6050 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3590    0.8943    1.0806 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2454   -0.2992    1.8030 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4884    0.5955   -0.3509 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4755    0.8747   -1.0770 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3591   -0.0967   -1.0067 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5890   -0.8983   -2.1038 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8995   -1.0454   -2.5801 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5346   -1.5394   -2.7130 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2488   -1.3548   -2.1935 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9044   -2.0353   -2.8327 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0169   -0.5556   -1.0992 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2595   -0.3863   -0.6052 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4731    0.4102    0.4783 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4038    1.0723    1.1117 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6873    1.8497    2.1869 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8716    0.9058    0.6208 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0820    0.1034   -0.4688 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0222    1.5727    1.2366 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8560    2.6363    1.8423 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9302    0.3952    0.7709 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1316   -0.3678    2.0480 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4790    1.7907    0.8682 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5065   -0.2814   -0.4293 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.5931   -1.2589   -0.1315 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4512   -0.9440   -1.0767 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2511    2.0556    2.1260 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6325    0.3295    2.2849 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9808    1.1158    0.6548 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0894   -1.0707    1.1873 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0476   -1.6400   -3.3891 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6610   -2.1696   -3.5635 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6709   -1.3430   -3.2259 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3932   -2.7281   -2.1195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5543   -2.6765   -3.6920 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0966    2.3752    2.7637 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6142    0.2131    2.8545 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6010   -1.3225    1.9702 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1877   -0.4502    2.3591 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0069    2.4413    0.1201 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3902    2.2213    1.8756 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5716    1.7434    0.6084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9197    0.4589   -1.1735 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6028   -0.7691   -0.2205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5256   -1.7603    0.8324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6252   -2.0764   -0.9100 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  3  2  1  1
  3  4  1  0
  3  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  2  0
 10 11  1  0
 11 12  1  0
 11 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 16 18  2  0
 18 19  1  0
 18 20  1  0
 20 21  2  0
 15 22  1  0
 22 23  1  1
 22 24  1  0
 22 25  1  0
 25 26  1  0
 25 27  1  0
 20  3  1  0
 19  7  2  0
 19 13  1  0
 27 14  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  4 31  1  0
  9 32  1  0
 10 33  1  0
 12 34  1  0
 12 35  1  0
 12 36  1  0
 17 37  1  0
 23 38  1  0
 23 39  1  0
 23 40  1  0
 24 41  1  0
 24 42  1  0
 24 43  1  0
 25 44  1  6
 26 45  1  0
 26 46  1  0
 26 47  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0       5.577   1.271   1.674  0.00  0.00           C+0
HETATM    2  O   UNK     0       4.292   1.744   1.605  0.00  0.00           O+0
HETATM    3  C   UNK     0       3.359   0.894   1.081  0.00  0.00           C+0
HETATM    4  O   UNK     0       3.245  -0.299   1.803  0.00  0.00           O+0
HETATM    5  C   UNK     0       3.488   0.596  -0.351  0.00  0.00           C+0
HETATM    6  O   UNK     0       4.476   0.875  -1.077  0.00  0.00           O+0
HETATM    7  C   UNK     0       2.359  -0.097  -1.007  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.589  -0.898  -2.104  0.00  0.00           C+0
HETATM    9  O   UNK     0       3.900  -1.045  -2.580  0.00  0.00           O+0
HETATM   10  C   UNK     0       1.535  -1.539  -2.713  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.249  -1.355  -2.193  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.904  -2.035  -2.833  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.017  -0.556  -1.099  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.260  -0.386  -0.605  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.473   0.410   0.478  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.404   1.072   1.112  0.00  0.00           C+0
HETATM   17  O   UNK     0      -0.687   1.850   2.187  0.00  0.00           O+0
HETATM   18  C   UNK     0       0.872   0.906   0.621  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.082   0.103  -0.469  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.022   1.573   1.237  0.00  0.00           C+0
HETATM   21  O   UNK     0       1.856   2.636   1.842  0.00  0.00           O+0
HETATM   22  C   UNK     0      -2.930   0.395   0.771  0.00  0.00           C+0
HETATM   23  C   UNK     0      -3.132  -0.368   2.048  0.00  0.00           C+0
HETATM   24  C   UNK     0      -3.479   1.791   0.868  0.00  0.00           C+0
HETATM   25  C   UNK     0      -3.506  -0.281  -0.429  0.00  0.00           C+0
HETATM   26  C   UNK     0      -4.593  -1.259  -0.132  0.00  0.00           C+0
HETATM   27  O   UNK     0      -2.451  -0.944  -1.077  0.00  0.00           O+0
HETATM   28  H   UNK     0       6.251   2.056   2.126  0.00  0.00           H+0
HETATM   29  H   UNK     0       5.633   0.330   2.285  0.00  0.00           H+0
HETATM   30  H   UNK     0       5.981   1.116   0.655  0.00  0.00           H+0
HETATM   31  H   UNK     0       3.089  -1.071   1.187  0.00  0.00           H+0
HETATM   32  H   UNK     0       4.048  -1.640  -3.389  0.00  0.00           H+0
HETATM   33  H   UNK     0       1.661  -2.170  -3.563  0.00  0.00           H+0
HETATM   34  H   UNK     0      -1.671  -1.343  -3.226  0.00  0.00           H+0
HETATM   35  H   UNK     0      -1.393  -2.728  -2.119  0.00  0.00           H+0
HETATM   36  H   UNK     0      -0.554  -2.676  -3.692  0.00  0.00           H+0
HETATM   37  H   UNK     0      -0.097   2.375   2.764  0.00  0.00           H+0
HETATM   38  H   UNK     0      -2.614   0.213   2.854  0.00  0.00           H+0
HETATM   39  H   UNK     0      -2.601  -1.323   1.970  0.00  0.00           H+0
HETATM   40  H   UNK     0      -4.188  -0.450   2.359  0.00  0.00           H+0
HETATM   41  H   UNK     0      -3.007   2.441   0.120  0.00  0.00           H+0
HETATM   42  H   UNK     0      -3.390   2.221   1.876  0.00  0.00           H+0
HETATM   43  H   UNK     0      -4.572   1.743   0.608  0.00  0.00           H+0
HETATM   44  H   UNK     0      -3.920   0.459  -1.174  0.00  0.00           H+0
HETATM   45  H   UNK     0      -5.603  -0.769  -0.221  0.00  0.00           H+0
HETATM   46  H   UNK     0      -4.526  -1.760   0.832  0.00  0.00           H+0
HETATM   47  H   UNK     0      -4.625  -2.076  -0.910  0.00  0.00           H+0
CONECT    1    2   28   29   30                                             
CONECT    2    1    3                                                       
CONECT    3    2    4    5   20                                             
CONECT    4    3   31                                                       
CONECT    5    3    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   19                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8   32                                                       
CONECT   10    8   11   33                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11   34   35   36                                             
CONECT   13   11   14   19                                                  
CONECT   14   13   15   27                                                  
CONECT   15   14   16   22                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16   37                                                       
CONECT   18   16   19   20                                                  
CONECT   19   18    7   13                                                  
CONECT   20   18   21    3                                                  
CONECT   21   20                                                            
CONECT   22   15   23   24   25                                             
CONECT   23   22   38   39   40                                             
CONECT   24   22   41   42   43                                             
CONECT   25   22   26   27   44                                             
CONECT   26   25   45   46   47                                             
CONECT   27   25   14                                                       
CONECT   28    1                                                            
CONECT   29    1                                                            
CONECT   30    1                                                            
CONECT   31    4                                                            
CONECT   32    9                                                            
CONECT   33   10                                                            
CONECT   34   12                                                            
CONECT   35   12                                                            
CONECT   36   12                                                            
CONECT   37   17                                                            
CONECT   38   23                                                            
CONECT   39   23                                                            
CONECT   40   23                                                            
CONECT   41   24                                                            
CONECT   42   24                                                            
CONECT   43   24                                                            
CONECT   44   25                                                            
CONECT   45   26                                                            
CONECT   46   26                                                            
CONECT   47   26                                                            
MASTER        0    0    0    0    0    0    0    0   47    0  100    0
END

RDKit          3D

47 50  0  0  0  0  0  0  0  0999 V2000
    5.5771    1.2708    1.6737 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2919    1.7437    1.6050 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3590    0.8943    1.0806 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2454   -0.2992    1.8030 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4884    0.5955   -0.3509 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4755    0.8747   -1.0770 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3591   -0.0967   -1.0067 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5890   -0.8983   -2.1038 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8995   -1.0454   -2.5801 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5346   -1.5394   -2.7130 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2488   -1.3548   -2.1935 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9044   -2.0353   -2.8327 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0169   -0.5556   -1.0992 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2595   -0.3863   -0.6052 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4731    0.4102    0.4783 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4038    1.0723    1.1117 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6873    1.8497    2.1869 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8716    0.9058    0.6208 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0820    0.1034   -0.4688 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0222    1.5727    1.2366 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8560    2.6363    1.8423 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9302    0.3952    0.7709 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1316   -0.3678    2.0480 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4790    1.7907    0.8682 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5065   -0.2814   -0.4293 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.5931   -1.2589   -0.1315 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4512   -0.9440   -1.0767 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2511    2.0556    2.1260 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6325    0.3295    2.2849 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9808    1.1158    0.6548 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0894   -1.0707    1.1873 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0476   -1.6400   -3.3891 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6610   -2.1696   -3.5635 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6709   -1.3430   -3.2259 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3932   -2.7281   -2.1195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5543   -2.6765   -3.6920 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0966    2.3752    2.7637 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6142    0.2131    2.8545 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6010   -1.3225    1.9702 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1877   -0.4502    2.3591 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0069    2.4413    0.1201 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3902    2.2213    1.8756 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5716    1.7434    0.6084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9197    0.4589   -1.1735 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6028   -0.7691   -0.2205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5256   -1.7603    0.8324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6252   -2.0764   -0.9100 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  3  2  1  1
  3  4  1  0
  3  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  2  0
 10 11  1  0
 11 12  1  0
 11 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 16 18  2  0
 18 19  1  0
 18 20  1  0
 20 21  2  0
 15 22  1  0
 22 23  1  1
 22 24  1  0
 22 25  1  0
 25 26  1  0
 25 27  1  0
 20  3  1  0
 19  7  2  0
 19 13  1  0
 27 14  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  4 31  1  0
  9 32  1  0
 10 33  1  0
 12 34  1  0
 12 35  1  0
 12 36  1  0
 17 37  1  0
 23 38  1  0
 23 39  1  0
 23 40  1  0
 24 41  1  0
 24 42  1  0
 24 43  1  0
 25 44  1  6
 26 45  1  0
 26 46  1  0
 26 47  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
Atrovenetinone methyl acetic acid	Generator

Chemical Formula

C₂₀H₂₀O₇

Average Mass

372.3730 Da

Monoisotopic Mass

372.12090 Da

IUPAC Name

(3R,12S)-3,6,15-trihydroxy-3-methoxy-8,12,13,13-tetramethyl-11-oxatetracyclo[7.6.1.0^{5,16}.0^{10,14}]hexadeca-1(15),5(16),6,8,10(14)-pentaene-2,4-dione

Traditional Name

(3R,12S)-3,6,15-trihydroxy-3-methoxy-8,12,13,13-tetramethyl-11-oxatetracyclo[7.6.1.0^{5,16}.0^{10,14}]hexadeca-1(15),5(16),6,8,10(14)-pentaene-2,4-dione

CAS Registry Number

Not Available

SMILES

COC1(O)C(=O)C2=C(O)C=C(C)C3=C2C(=C(O)C2=C3OC(C)C2(C)C)C1=O

InChI Identifier

InChI=1S/C20H20O7/c1-7-6-9(21)11-12-10(7)16-14(19(3,4)8(2)27-16)15(22)13(12)18(24)20(25,26-5)17(11)23/h6,8,21-22,25H,1-5H3

InChI Key

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

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Penicillium	NPAtlas	15813183

Chemical Taxonomy

Classification

Not classified

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	2.78	ALOGPS
logP	4.33	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Acidic)	7.64	ChemAxon
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	113.29 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	96.71 m³·mol⁻¹	ChemAxon
Polarizability	38.2 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

NPAtlas ID

NPA019234

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

28282510

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

49767936

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Shiomi K, Matsui R, Isozaki M, Chiba H, Sugai T, Yamaguchi Y, Masuma R, Tomoda H, Chiba T, Yan H, Kitamura Y, Sugiura W, Omura S, Tanaka H: Fungal phenalenones inhibit HIV-1 integrase. J Antibiot (Tokyo). 2005 Jan;58(1):65-8. doi: 10.1038/ja.2005.8. [PubMed:15813183 ]

Showing NP-Card for Atrovenetinone methyl acetal (NP0005809)

MOL for NP0005809 (Atrovenetinone methyl acetal)

3D MOL for NP0005809 (Atrovenetinone methyl acetal)

3D SDF for NP0005809 (Atrovenetinone methyl acetal)

3D-SDF for NP0005809 (Atrovenetinone methyl acetal)

PDB for NP0005809 (Atrovenetinone methyl acetal)

3D PDB for NP0005809 (Atrovenetinone methyl acetal)

SMILES for NP0005809 (Atrovenetinone methyl acetal)

INCHI for NP0005809 (Atrovenetinone methyl acetal)

Structure for NP0005809 (Atrovenetinone methyl acetal)

3D Structure for NP0005809 (Atrovenetinone methyl acetal)