NP-MRD: Showing NP-Card for Bicycloalternarene F (NP0012178)

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Record Information

Version

2.0

Created at

2021-01-05 21:38:23 UTC

Updated at

2021-07-15 17:11:04 UTC

NP-MRD ID

NP0012178

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Bicycloalternarene F

Provided By

NPAtlas

Description

Bicycloalternarene F belongs to the class of organic compounds known as benzopyrans. These are organic compounds containing a benzene ring fused to a pyran ring. Pyran a six-membered heterocyclic, non-aromatic ring, made up of five carbon atoms and one oxygen atom and containing two double bonds. Bicycloalternarene F is found in Alternaria sp. JJY-32. Based on a literature review very few articles have been published on Bicycloalternarene F.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242117023D          

 57 58  0  0  0  0            999 V2000
    2.3023    1.7072   -1.0925 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2691    0.8465    0.0939 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1435    0.3872    0.6272 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1566    0.7270    0.0403 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8426   -0.5753   -0.3726 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1872   -0.1623   -0.9753 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9408    0.7367   -2.1685 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8176    0.6415    0.0222 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9688    0.2497    0.6794 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4980   -0.9527    0.5133 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6338   -1.9840   -0.1232 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0122   -1.3547   -1.3496 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1483   -2.2673   -1.9865 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8656   -1.2199    0.9449 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.6767    1.1702    1.6154 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.5300    0.7561    2.9380 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5392    0.4538    0.7505 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4016   -0.3088   -0.2473 C   0  0  2  0  0  0  0  0  0  0  0  0
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    7.7578   -1.1804    2.5474 H   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  1  0  0  0  0
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  9 10  2  0  0  0  0
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  2 20  1  0  0  0  0
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 18  9  1  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652306242117023D          

 57 58  0  0  0  0            999 V2000
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   -0.2357   -1.1602   -1.0648 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0774   -1.1109    0.5561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8406    1.7824   -1.8165 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0571    0.4114   -2.7555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8448    0.7008   -2.8357 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2153   -2.8795   -0.3997 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7743   -2.2678    0.5440 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7817   -1.0820   -2.0853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7745   -1.7768   -2.7565 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7425   -0.1609    1.1507 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6497   -0.2406    2.6376 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6959    2.0055    1.6840 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1464    1.3005    0.0875 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2089    2.1864    1.5412 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1803    1.3045    3.4685 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0365    1.3687    1.1204 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3875   -0.2335    1.6073 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5032    0.1959   -1.2052 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8274   -1.2593   -0.4550 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6958   -1.3590    1.2330 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5578    1.5939   -1.0418 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9685    0.6202   -1.6395 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3202    0.2014   -2.1301 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7578   -1.1804    2.5474 H   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  1  0  0  0  0
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 10 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
  2 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 12  6  1  0  0  0  0
 18  9  1  0  0  0  0
  1 28  1  0  0  0  0
  1 29  1  0  0  0  0
  1 30  1  0  0  0  0
  3 31  1  0  0  0  0
  4 32  1  0  0  0  0
  4 33  1  0  0  0  0
  5 34  1  0  0  0  0
  5 35  1  0  0  0  0
  7 36  1  0  0  0  0
  7 37  1  0  0  0  0
  7 38  1  0  0  0  0
 11 39  1  0  0  0  0
 11 40  1  0  0  0  0
 12 41  1  6  0  0  0
 13 42  1  0  0  0  0
 16 43  1  0  0  0  0
 16 44  1  0  0  0  0
 17 45  1  0  0  0  0
 17 46  1  0  0  0  0
 18 47  1  1  0  0  0
 19 48  1  0  0  0  0
 20 49  1  0  0  0  0
 20 50  1  0  0  0  0
 21 51  1  0  0  0  0
 21 52  1  0  0  0  0
 22 53  1  0  0  0  0
 24 54  1  0  0  0  0
 24 55  1  0  0  0  0
 24 56  1  0  0  0  0
 27 57  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0012178

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC(=O)C(=C(/[H])C([H])([H])C([H])([H])C(=C(/[H])C([H])([H])C([H])([H])[C@@]1(OC2=C(C(=O)C([H])([H])C([H])([H])[C@@]2([H])O[H])C([H])([H])[C@]1([H])O[H])C([H])([H])[H])\C([H])([H])[H])\C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C21H30O6/c1-13(6-4-8-14(2)20(25)26)7-5-11-21(3)18(24)12-15-16(22)9-10-17(23)19(15)27-21/h7-8,17-18,23-24H,4-6,9-12H2,1-3H3,(H,25,26)/b13-7+,14-8+/t17-,18+,21+/m1/s1

> <INCHI_KEY>
IJYNRXGMDZDCJS-IBHBTLNGSA-N

> <FORMULA>
C21H30O6

> <MOLECULAR_WEIGHT>
378.465

> <EXACT_MASS>
378.204238686

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
57

> <JCHEM_AVERAGE_POLARIZABILITY>
41.96867492270224

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2E,6E)-9-[(2S,3S,8R)-3,8-dihydroxy-2-methyl-5-oxo-3,4,5,6,7,8-hexahydro-2H-1-benzopyran-2-yl]-2,6-dimethylnona-2,6-dienoic acid

> <ALOGPS_LOGP>
2.43

> <JCHEM_LOGP>
2.275096414

> <ALOGPS_LOGS>
-4.06

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
13.573739786799681

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.01179715678666

> <JCHEM_PKA_STRONGEST_BASIC>
-3.2837114854636713

> <JCHEM_POLAR_SURFACE_AREA>
104.06000000000002

> <JCHEM_REFRACTIVITY>
104.39009999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.33e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2E,6E)-9-[(2S,3S,8R)-3,8-dihydroxy-2-methyl-5-oxo-4,6,7,8-tetrahydro-3H-1-benzopyran-2-yl]-2,6-dimethylnona-2,6-dienoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 57 58  0  0  0  0  0  0  0  0999 V2000
    2.3023    1.7072   -1.0925 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2691    0.8465    0.0939 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1435    0.3872    0.6272 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1566    0.7270    0.0403 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8426   -0.5753   -0.3726 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1872   -0.1623   -0.9753 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9408    0.7367   -2.1685 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8176    0.6415    0.0222 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9688    0.2497    0.6794 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4980   -0.9527    0.5133 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6338   -1.9840   -0.1232 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0122   -1.3547   -1.3496 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1483   -2.2673   -1.9865 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8656   -1.2199    0.9449 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3428   -2.3795    0.8170 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7150   -0.1576    1.5339 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1237    1.2118    1.1808 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6767    1.1702    1.6154 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.5300    0.7561    2.9380 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5392    0.4538    0.7505 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4016   -0.3088   -0.2473 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6714   -0.7157    0.3673 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8650   -0.3222   -0.0979 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9252    0.5521   -1.2700 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0878   -0.7527    0.5464 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1915   -0.3777    0.1012 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.0225   -1.5766    1.6508 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0890    1.0904   -2.0029 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3141    2.1213   -1.2314 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5754    2.5436   -1.0622 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1701   -0.2459    1.5047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1187    1.4473   -0.7753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8189    1.1707    0.8362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2357   -1.1602   -1.0648 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0774   -1.1109    0.5561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8406    1.7824   -1.8165 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0571    0.4114   -2.7555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8448    0.7008   -2.8357 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2153   -2.8795   -0.3997 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7743   -2.2678    0.5440 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7817   -1.0820   -2.0853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7745   -1.7768   -2.7565 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7425   -0.1609    1.1507 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6497   -0.2406    2.6376 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6959    2.0055    1.6840 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1464    1.3005    0.0875 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2089    2.1864    1.5412 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1803    1.3045    3.4685 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0365    1.3687    1.1204 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3875   -0.2335    1.6073 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5032    0.1959   -1.2052 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8274   -1.2593   -0.4550 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6958   -1.3590    1.2330 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5578    1.5939   -1.0418 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9685    0.6202   -1.6395 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3202    0.2014   -2.1301 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7578   -1.1804    2.5474 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  6  5  1  1
  6  7  1  0
  6  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 10 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
  2 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 23 25  1  0
 25 26  2  0
 25 27  1  0
 12  6  1  0
 18  9  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  3 31  1  0
  4 32  1  0
  4 33  1  0
  5 34  1  0
  5 35  1  0
  7 36  1  0
  7 37  1  0
  7 38  1  0
 11 39  1  0
 11 40  1  0
 12 41  1  6
 13 42  1  0
 16 43  1  0
 16 44  1  0
 17 45  1  0
 17 46  1  0
 18 47  1  1
 19 48  1  0
 20 49  1  0
 20 50  1  0
 21 51  1  0
 21 52  1  0
 22 53  1  0
 24 54  1  0
 24 55  1  0
 24 56  1  0
 27 57  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       2.302   1.707  -1.093  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.269   0.847   0.094  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.143   0.387   0.627  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.157   0.727   0.040  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.843  -0.575  -0.373  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.187  -0.162  -0.975  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.941   0.737  -2.168  0.00  0.00           C+0
HETATM    8  O   UNK     0      -2.818   0.642   0.022  0.00  0.00           O+0
HETATM    9  C   UNK     0      -3.969   0.250   0.679  0.00  0.00           C+0
HETATM   10  C   UNK     0      -4.498  -0.953   0.513  0.00  0.00           C+0
HETATM   11  C   UNK     0      -3.634  -1.984  -0.123  0.00  0.00           C+0
HETATM   12  C   UNK     0      -3.012  -1.355  -1.350  0.00  0.00           C+0
HETATM   13  O   UNK     0      -2.148  -2.267  -1.986  0.00  0.00           O+0
HETATM   14  C   UNK     0      -5.866  -1.220   0.945  0.00  0.00           C+0
HETATM   15  O   UNK     0      -6.343  -2.380   0.817  0.00  0.00           O+0
HETATM   16  C   UNK     0      -6.715  -0.158   1.534  0.00  0.00           C+0
HETATM   17  C   UNK     0      -6.124   1.212   1.181  0.00  0.00           C+0
HETATM   18  C   UNK     0      -4.677   1.170   1.615  0.00  0.00           C+0
HETATM   19  O   UNK     0      -4.530   0.756   2.938  0.00  0.00           O+0
HETATM   20  C   UNK     0       3.539   0.454   0.751  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.402  -0.309  -0.247  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.671  -0.716   0.367  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.865  -0.322  -0.098  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.925   0.552  -1.270  0.00  0.00           C+0
HETATM   25  C   UNK     0       8.088  -0.753   0.546  0.00  0.00           C+0
HETATM   26  O   UNK     0       9.191  -0.378   0.101  0.00  0.00           O+0
HETATM   27  O   UNK     0       8.023  -1.577   1.651  0.00  0.00           O+0
HETATM   28  H   UNK     0       2.089   1.090  -2.003  0.00  0.00           H+0
HETATM   29  H   UNK     0       3.314   2.121  -1.231  0.00  0.00           H+0
HETATM   30  H   UNK     0       1.575   2.544  -1.062  0.00  0.00           H+0
HETATM   31  H   UNK     0       1.170  -0.246   1.505  0.00  0.00           H+0
HETATM   32  H   UNK     0      -0.119   1.447  -0.775  0.00  0.00           H+0
HETATM   33  H   UNK     0      -0.819   1.171   0.836  0.00  0.00           H+0
HETATM   34  H   UNK     0      -0.236  -1.160  -1.065  0.00  0.00           H+0
HETATM   35  H   UNK     0      -1.077  -1.111   0.556  0.00  0.00           H+0
HETATM   36  H   UNK     0      -1.841   1.782  -1.817  0.00  0.00           H+0
HETATM   37  H   UNK     0      -1.057   0.411  -2.756  0.00  0.00           H+0
HETATM   38  H   UNK     0      -2.845   0.701  -2.836  0.00  0.00           H+0
HETATM   39  H   UNK     0      -4.215  -2.880  -0.400  0.00  0.00           H+0
HETATM   40  H   UNK     0      -2.774  -2.268   0.544  0.00  0.00           H+0
HETATM   41  H   UNK     0      -3.782  -1.082  -2.085  0.00  0.00           H+0
HETATM   42  H   UNK     0      -1.775  -1.777  -2.757  0.00  0.00           H+0
HETATM   43  H   UNK     0      -7.742  -0.161   1.151  0.00  0.00           H+0
HETATM   44  H   UNK     0      -6.650  -0.241   2.638  0.00  0.00           H+0
HETATM   45  H   UNK     0      -6.696   2.006   1.684  0.00  0.00           H+0
HETATM   46  H   UNK     0      -6.146   1.301   0.088  0.00  0.00           H+0
HETATM   47  H   UNK     0      -4.209   2.186   1.541  0.00  0.00           H+0
HETATM   48  H   UNK     0      -5.180   1.305   3.469  0.00  0.00           H+0
HETATM   49  H   UNK     0       4.037   1.369   1.120  0.00  0.00           H+0
HETATM   50  H   UNK     0       3.388  -0.234   1.607  0.00  0.00           H+0
HETATM   51  H   UNK     0       4.503   0.196  -1.205  0.00  0.00           H+0
HETATM   52  H   UNK     0       3.827  -1.259  -0.455  0.00  0.00           H+0
HETATM   53  H   UNK     0       5.696  -1.359   1.233  0.00  0.00           H+0
HETATM   54  H   UNK     0       6.558   1.594  -1.042  0.00  0.00           H+0
HETATM   55  H   UNK     0       7.968   0.620  -1.640  0.00  0.00           H+0
HETATM   56  H   UNK     0       6.320   0.201  -2.130  0.00  0.00           H+0
HETATM   57  H   UNK     0       7.758  -1.180   2.547  0.00  0.00           H+0
CONECT    1    2   28   29   30                                             
CONECT    2    1    3   20                                                  
CONECT    3    2    4   31                                                  
CONECT    4    3    5   32   33                                             
CONECT    5    4    6   34   35                                             
CONECT    6    5    7    8   12                                             
CONECT    7    6   36   37   38                                             
CONECT    8    6    9                                                       
CONECT    9    8   10   18                                                  
CONECT   10    9   11   14                                                  
CONECT   11   10   12   39   40                                             
CONECT   12   11   13    6   41                                             
CONECT   13   12   42                                                       
CONECT   14   10   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   43   44                                             
CONECT   17   16   18   45   46                                             
CONECT   18   17   19    9   47                                             
CONECT   19   18   48                                                       
CONECT   20    2   21   49   50                                             
CONECT   21   20   22   51   52                                             
CONECT   22   21   23   53                                                  
CONECT   23   22   24   25                                                  
CONECT   24   23   54   55   56                                             
CONECT   25   23   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   57                                                       
CONECT   28    1                                                            
CONECT   29    1                                                            
CONECT   30    1                                                            
CONECT   31    3                                                            
CONECT   32    4                                                            
CONECT   33    4                                                            
CONECT   34    5                                                            
CONECT   35    5                                                            
CONECT   36    7                                                            
CONECT   37    7                                                            
CONECT   38    7                                                            
CONECT   39   11                                                            
CONECT   40   11                                                            
CONECT   41   12                                                            
CONECT   42   13                                                            
CONECT   43   16                                                            
CONECT   44   16                                                            
CONECT   45   17                                                            
CONECT   46   17                                                            
CONECT   47   18                                                            
CONECT   48   19                                                            
CONECT   49   20                                                            
CONECT   50   20                                                            
CONECT   51   21                                                            
CONECT   52   21                                                            
CONECT   53   22                                                            
CONECT   54   24                                                            
CONECT   55   24                                                            
CONECT   56   24                                                            
CONECT   57   27                                                            
MASTER        0    0    0    0    0    0    0    0   57    0  116    0
END

RDKit          3D

57 58  0  0  0  0  0  0  0  0999 V2000
    2.3023    1.7072   -1.0925 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2691    0.8465    0.0939 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1435    0.3872    0.6272 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1566    0.7270    0.0403 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8426   -0.5753   -0.3726 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1872   -0.1623   -0.9753 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9408    0.7367   -2.1685 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8176    0.6415    0.0222 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9688    0.2497    0.6794 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4980   -0.9527    0.5133 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6338   -1.9840   -0.1232 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0122   -1.3547   -1.3496 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1483   -2.2673   -1.9865 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8656   -1.2199    0.9449 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3428   -2.3795    0.8170 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7150   -0.1576    1.5339 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1237    1.2118    1.1808 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6767    1.1702    1.6154 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.5300    0.7561    2.9380 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5392    0.4538    0.7505 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4016   -0.3088   -0.2473 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6714   -0.7157    0.3673 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8650   -0.3222   -0.0979 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9252    0.5521   -1.2700 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0878   -0.7527    0.5464 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1915   -0.3777    0.1012 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.0225   -1.5766    1.6508 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0890    1.0904   -2.0029 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3141    2.1213   -1.2314 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5754    2.5436   -1.0622 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1701   -0.2459    1.5047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1187    1.4473   -0.7753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8189    1.1707    0.8362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2357   -1.1602   -1.0648 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0774   -1.1109    0.5561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8406    1.7824   -1.8165 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0571    0.4114   -2.7555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8448    0.7008   -2.8357 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2153   -2.8795   -0.3997 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7743   -2.2678    0.5440 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7817   -1.0820   -2.0853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7745   -1.7768   -2.7565 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7425   -0.1609    1.1507 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6497   -0.2406    2.6376 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6959    2.0055    1.6840 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1464    1.3005    0.0875 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2089    2.1864    1.5412 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1803    1.3045    3.4685 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0365    1.3687    1.1204 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3875   -0.2335    1.6073 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5032    0.1959   -1.2052 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8274   -1.2593   -0.4550 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6958   -1.3590    1.2330 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5578    1.5939   -1.0418 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9685    0.6202   -1.6395 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3202    0.2014   -2.1301 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7578   -1.1804    2.5474 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  6  5  1  1
  6  7  1  0
  6  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 10 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
  2 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 23 25  1  0
 25 26  2  0
 25 27  1  0
 12  6  1  0
 18  9  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  3 31  1  0
  4 32  1  0
  4 33  1  0
  5 34  1  0
  5 35  1  0
  7 36  1  0
  7 37  1  0
  7 38  1  0
 11 39  1  0
 11 40  1  0
 12 41  1  6
 13 42  1  0
 16 43  1  0
 16 44  1  0
 17 45  1  0
 17 46  1  0
 18 47  1  1
 19 48  1  0
 20 49  1  0
 20 50  1  0
 21 51  1  0
 21 52  1  0
 22 53  1  0
 24 54  1  0
 24 55  1  0
 24 56  1  0
 27 57  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₂₁H₃₀O₆

Average Mass

378.4650 Da

Monoisotopic Mass

378.20424 Da

IUPAC Name

(2E,6E)-9-[(2S,3S,8R)-3,8-dihydroxy-2-methyl-5-oxo-3,4,5,6,7,8-hexahydro-2H-1-benzopyran-2-yl]-2,6-dimethylnona-2,6-dienoic acid

Traditional Name

(2E,6E)-9-[(2S,3S,8R)-3,8-dihydroxy-2-methyl-5-oxo-4,6,7,8-tetrahydro-3H-1-benzopyran-2-yl]-2,6-dimethylnona-2,6-dienoic acid

CAS Registry Number

Not Available

SMILES

C\C(CC\C=C(/C)C(O)=O)=C/CC[C@]1(C)OC2=C(C[C@@H]1O)C(=O)CC[C@H]2O

InChI Identifier

InChI=1S/C21H30O6/c1-13(6-4-8-14(2)20(25)26)7-5-11-21(3)18(24)12-15-16(22)9-10-17(23)19(15)27-21/h7-8,17-18,23-24H,4-6,9-12H2,1-3H3,(H,25,26)/b13-7+,14-8+/t17-,18+,21+/m1/s1

InChI Key

IJYNRXGMDZDCJS-IBHBTLNGSA-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
Alternaria sp. JJY-32	NPAtlas	24128115

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzopyrans. These are organic compounds containing a benzene ring fused to a pyran ring. Pyran a six-membered heterocyclic, non-aromatic ring, made up of five carbon atoms and one oxygen atom and containing two double bonds.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

Not Available

Direct Parent

Benzopyrans

Alternative Parents

Substituents

Benzopyran
Bicyclic monoterpenoid
Monoterpenoid
Medium-chain fatty acid
Cyclohexenone
Branched fatty acid
Heterocyclic fatty acid
Methyl-branched fatty acid
Hydroxy fatty acid
Fatty acyl
Fatty acid
Unsaturated fatty acid
Vinylogous ester
Secondary alcohol
Ketone
Carboxylic acid derivative
Carboxylic acid
Oxacycle
Monocarboxylic acid or derivatives
Alcohol
Carbonyl group
Hydrocarbon derivative
Organic oxygen compound
Organooxygen compound
Organic oxide
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	2.43	ALOGPS
logP	2.28	ChemAxon
logS	-4.1	ALOGPS
pKa (Strongest Acidic)	5.01	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	104.06 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	104.39 m³·mol⁻¹	ChemAxon
Polarizability	41.97 Å³	ChemAxon
Number of Rings	2	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

NPA011947

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

30771205

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

72704671

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Bicycloalternarene F (NP0012178)

MOL for NP0012178 (Bicycloalternarene F)

3D MOL for NP0012178 (Bicycloalternarene F)

3D SDF for NP0012178 (Bicycloalternarene F)

3D-SDF for NP0012178 (Bicycloalternarene F)

PDB for NP0012178 (Bicycloalternarene F)

3D PDB for NP0012178 (Bicycloalternarene F)

SMILES for NP0012178 (Bicycloalternarene F)

INCHI for NP0012178 (Bicycloalternarene F)

Structure for NP0012178 (Bicycloalternarene F)

3D Structure for NP0012178 (Bicycloalternarene F)