NP-MRD: Showing NP-Card for (1r,2r,4z,6s,7s,9s,13z)-6,7,10-trihydroxy-4,13-bis[(2e,4e)-1-hydroxyhexa-2,4-dien-1-ylidene]-2,6,9,11-tetramethyl-8-oxatricyclo[7.4.0.0²,⁷]tridec-10-ene-3,5,12-trione (NP0231012)

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Record Information

Version

2.0

Created at

2022-09-06 11:40:25 UTC

Updated at

2022-09-06 11:40:25 UTC

NP-MRD ID

NP0231012

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2r,4z,6s,7s,9s,13z)-6,7,10-trihydroxy-4,13-bis[(2e,4e)-1-hydroxyhexa-2,4-dien-1-ylidene]-2,6,9,11-tetramethyl-8-oxatricyclo[7.4.0.0²,⁷]tridec-10-ene-3,5,12-trione

Description

(1r,2r,4z,6s,7s,9s,13z)-6,7,10-trihydroxy-4,13-bis[(2e,4e)-1-hydroxyhexa-2,4-dien-1-ylidene]-2,6,9,11-tetramethyl-8-oxatricyclo[7.4.0.0²,⁷]tridec-10-ene-3,5,12-trione is found in Sarocladium strictum.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309062213402D          

 37 39  0  0  1  0            999 V2000
   -0.2218    2.8331    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4767    2.0485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0753    1.4354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1796    0.6508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3724    0.0377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1175   -0.7470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6895   -0.9185    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6695   -1.3601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4765   -1.1885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7314   -0.4039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0285   -1.8016    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3641   -1.0479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8535   -1.8016    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4056   -1.1885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1506   -0.4039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7027    0.2092    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3436   -0.2324    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0887    0.5522    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2817    0.7238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0268    1.5084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2198    1.6799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2125   -1.3601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7646   -0.7470    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4675   -2.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2744   -2.3162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9154   -2.7578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1704   -3.5424    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1085   -2.5862    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2800   -3.3932    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4410   -3.0712    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7736   -2.5862    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6021   -3.3932    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9666   -2.7578    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2757   -3.5227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2670   -3.1950    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4146   -2.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3924   -2.3162    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  6  0  0  0
 11 13  1  0  0  0  0
 13 14  1  1  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
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 14 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  2  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 13 28  1  0  0  0  0
 28 29  1  6  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 11 31  1  0  0  0  0
 31 32  1  1  0  0  0
 31 33  1  0  0  0  0
 33 34  1  6  0  0  0
 33 35  1  1  0  0  0
 33 36  1  0  0  0  0
  8 36  1  0  0  0  0
 36 37  2  0  0  0  0
M  END


  Mrv1652309062213402D          

 37 39  0  0  1  0            999 V2000
   -0.2218    2.8331    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4767    2.0485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0753    1.4354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1796    0.6508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3724    0.0377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1175   -0.7470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6895   -0.9185    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6695   -1.3601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4765   -1.1885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7314   -0.4039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0285   -1.8016    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3641   -1.0479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8535   -1.8016    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4056   -1.1885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1506   -0.4039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7027    0.2092    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3436   -0.2324    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0887    0.5522    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2817    0.7238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0268    1.5084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2198    1.6799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2125   -1.3601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7646   -0.7470    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4675   -2.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2744   -2.3162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9154   -2.7578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1704   -3.5424    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1085   -2.5862    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2800   -3.3932    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4410   -3.0712    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7736   -2.5862    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6021   -3.3932    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9666   -2.7578    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2757   -3.5227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2670   -3.1950    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4146   -2.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3924   -2.3162    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  6  0  0  0
 11 13  1  0  0  0  0
 13 14  1  1  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
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 14 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  2  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 13 28  1  0  0  0  0
 28 29  1  6  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 11 31  1  0  0  0  0
 31 32  1  1  0  0  0
 31 33  1  0  0  0  0
 33 34  1  6  0  0  0
 33 35  1  1  0  0  0
 33 36  1  0  0  0  0
  8 36  1  0  0  0  0
 36 37  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0231012

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C=C\C=C\C(\O)=C1/[C@H]2[C@](C)(O[C@@]3(O)[C@@]2(C)C(=O)\C(=C(\O)/C=C/C=C/C)C(=O)[C@]3(C)O)C(O)=C(C)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C28H32O9/c1-7-9-11-13-16(29)18-20(31)15(3)22(32)26(5)21(18)25(4)23(33)19(17(30)14-12-10-8-2)24(34)27(6,35)28(25,36)37-26/h7-14,21,29-30,32,35-36H,1-6H3/b9-7+,10-8+,13-11+,14-12+,18-16+,19-17-/t21-,25-,26+,27+,28+/m1/s1

> <INCHI_KEY>
DZSIQVIZFPZAMV-TZCGFCPBSA-N

> <FORMULA>
C28H32O9

> <MOLECULAR_WEIGHT>
512.555

> <EXACT_MASS>
512.20463261

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
69

> <JCHEM_AVERAGE_POLARIZABILITY>
52.09792309852669

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2R,4Z,6S,7S,9S,13Z)-6,7,10-trihydroxy-4,13-bis[(2E,4E)-1-hydroxyhexa-2,4-dien-1-ylidene]-2,6,9,11-tetramethyl-8-oxatricyclo[7.4.0.0^{2,7}]tridec-10-ene-3,5,12-trione

> <JCHEM_LOGP>
3.250285555666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
3.9396719492708514

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.235039815319984

> <JCHEM_PKA_STRONGEST_BASIC>
-4.389491855754167

> <JCHEM_POLAR_SURFACE_AREA>
161.59

> <JCHEM_REFRACTIVITY>
143.75930000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,4Z,6S,7S,9S,13Z)-6,7,10-trihydroxy-4,13-bis[(2E,4E)-1-hydroxyhexa-2,4-dien-1-ylidene]-2,6,9,11-tetramethyl-8-oxatricyclo[7.4.0.0^{2,7}]tridec-10-ene-3,5,12-trione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0      -0.414   5.288   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.890   3.824   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.141   2.679   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.335   1.215   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.695   0.070   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.219  -1.394   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -1.287  -1.715   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       1.250  -2.539   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.756  -2.219   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       3.232  -0.754   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       3.787  -3.363   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.413  -1.956   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.327  -3.363   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.357  -2.219   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.881  -0.754   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       6.912   0.390   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       4.375  -0.434   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.899   1.031   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.393   1.351   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.917   2.816   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.410   3.136   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.863  -2.539   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       8.894  -1.394   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       8.339  -4.003   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       9.846  -4.324   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       7.309  -5.148   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       7.785  -6.612   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       5.802  -4.828   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.123  -6.334   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       4.557  -5.733   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       3.311  -4.828   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       2.991  -6.334   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       1.804  -5.148   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       2.381  -6.576   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       0.498  -5.964   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       0.774  -4.003   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -0.732  -4.324   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   36                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   13   31                                             
CONECT   12   11                                                            
CONECT   13   11   14   28                                                  
CONECT   14   13   15   22                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20                                                            
CONECT   22   14   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   13   29   30                                             
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   11   32   33                                             
CONECT   32   31                                                            
CONECT   33   31   34   35   36                                             
CONECT   34   33                                                            
CONECT   35   33                                                            
CONECT   36   33    8   37                                                  
CONECT   37   36                                                            
MASTER        0    0    0    0    0    0    0    0   37    0   78    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₈H₃₂O₉

Average Mass

512.5550 Da

Monoisotopic Mass

512.20463 Da

IUPAC Name

(1R,2R,4Z,6S,7S,9S,13Z)-6,7,10-trihydroxy-4,13-bis[(2E,4E)-1-hydroxyhexa-2,4-dien-1-ylidene]-2,6,9,11-tetramethyl-8-oxatricyclo[7.4.0.0^{2,7}]tridec-10-ene-3,5,12-trione

Traditional Name

(1R,2R,4Z,6S,7S,9S,13Z)-6,7,10-trihydroxy-4,13-bis[(2E,4E)-1-hydroxyhexa-2,4-dien-1-ylidene]-2,6,9,11-tetramethyl-8-oxatricyclo[7.4.0.0^{2,7}]tridec-10-ene-3,5,12-trione

CAS Registry Number

Not Available

SMILES

C\C=C\C=C\C(\O)=C1/[C@H]2[C@](C)(O[C@@]3(O)[C@@]2(C)C(=O)\C(=C(\O)/C=C/C=C/C)C(=O)[C@]3(C)O)C(O)=C(C)C1=O

InChI Identifier

InChI=1S/C28H32O9/c1-7-9-11-13-16(29)18-20(31)15(3)22(32)26(5)21(18)25(4)23(33)19(17(30)14-12-10-8-2)24(34)27(6,35)28(25,36)37-26/h7-14,21,29-30,32,35-36H,1-6H3/b9-7+,10-8+,13-11+,14-12+,18-16+,19-17-/t21-,25-,26+,27+,28+/m1/s1

InChI Key

DZSIQVIZFPZAMV-TZCGFCPBSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Acremonium strictum	LOTUS Database	35616633

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	3.25	ChemAxon
pKa (Strongest Acidic)	3.24	ChemAxon
pKa (Strongest Basic)	-4.4	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	161.59 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	143.76 m³·mol⁻¹	ChemAxon
Polarizability	52.1 Å³	ChemAxon
Number of Rings	3	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

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,2r,4z,6s,7s,9s,13z)-6,7,10-trihydroxy-4,13-bis[(2e,4e)-1-hydroxyhexa-2,4-dien-1-ylidene]-2,6,9,11-tetramethyl-8-oxatricyclo[7.4.0.0²,⁷]tridec-10-ene-3,5,12-trione (NP0231012)

MOL for NP0231012 ((1r,2r,4z,6s,7s,9s,13z)-6,7,10-trihydroxy-4,13-bis[(2e,4e)-1-hydroxyhexa-2,4-dien-1-ylidene]-2,6,9,11-tetramethyl-8-oxatricyclo[7.4.0.0²,⁷]tridec-10-ene-3,5,12-trione)

3D MOL for NP0231012 ((1r,2r,4z,6s,7s,9s,13z)-6,7,10-trihydroxy-4,13-bis[(2e,4e)-1-hydroxyhexa-2,4-dien-1-ylidene]-2,6,9,11-tetramethyl-8-oxatricyclo[7.4.0.0²,⁷]tridec-10-ene-3,5,12-trione)

3D SDF for NP0231012 ((1r,2r,4z,6s,7s,9s,13z)-6,7,10-trihydroxy-4,13-bis[(2e,4e)-1-hydroxyhexa-2,4-dien-1-ylidene]-2,6,9,11-tetramethyl-8-oxatricyclo[7.4.0.0²,⁷]tridec-10-ene-3,5,12-trione)

3D-SDF for NP0231012 ((1r,2r,4z,6s,7s,9s,13z)-6,7,10-trihydroxy-4,13-bis[(2e,4e)-1-hydroxyhexa-2,4-dien-1-ylidene]-2,6,9,11-tetramethyl-8-oxatricyclo[7.4.0.0²,⁷]tridec-10-ene-3,5,12-trione)

PDB for NP0231012 ((1r,2r,4z,6s,7s,9s,13z)-6,7,10-trihydroxy-4,13-bis[(2e,4e)-1-hydroxyhexa-2,4-dien-1-ylidene]-2,6,9,11-tetramethyl-8-oxatricyclo[7.4.0.0²,⁷]tridec-10-ene-3,5,12-trione)

3D PDB for NP0231012 ((1r,2r,4z,6s,7s,9s,13z)-6,7,10-trihydroxy-4,13-bis[(2e,4e)-1-hydroxyhexa-2,4-dien-1-ylidene]-2,6,9,11-tetramethyl-8-oxatricyclo[7.4.0.0²,⁷]tridec-10-ene-3,5,12-trione)

SMILES for NP0231012 ((1r,2r,4z,6s,7s,9s,13z)-6,7,10-trihydroxy-4,13-bis[(2e,4e)-1-hydroxyhexa-2,4-dien-1-ylidene]-2,6,9,11-tetramethyl-8-oxatricyclo[7.4.0.0²,⁷]tridec-10-ene-3,5,12-trione)

INCHI for NP0231012 ((1r,2r,4z,6s,7s,9s,13z)-6,7,10-trihydroxy-4,13-bis[(2e,4e)-1-hydroxyhexa-2,4-dien-1-ylidene]-2,6,9,11-tetramethyl-8-oxatricyclo[7.4.0.0²,⁷]tridec-10-ene-3,5,12-trione)

Structure for NP0231012 ((1r,2r,4z,6s,7s,9s,13z)-6,7,10-trihydroxy-4,13-bis[(2e,4e)-1-hydroxyhexa-2,4-dien-1-ylidene]-2,6,9,11-tetramethyl-8-oxatricyclo[7.4.0.0²,⁷]tridec-10-ene-3,5,12-trione)

3D Structure for NP0231012 ((1r,2r,4z,6s,7s,9s,13z)-6,7,10-trihydroxy-4,13-bis[(2e,4e)-1-hydroxyhexa-2,4-dien-1-ylidene]-2,6,9,11-tetramethyl-8-oxatricyclo[7.4.0.0²,⁷]tridec-10-ene-3,5,12-trione)