NP-MRD: Showing NP-Card for Penicitrinol F (NP0011795)

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Record Information

Version

2.0

Created at

2021-01-05 21:22:28 UTC

Updated at

2021-07-15 17:09:57 UTC

NP-MRD ID

NP0011795

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Penicitrinol F

Provided By

NPAtlas

Description

Penicitrinol F is found in Unknown-fungus sp. SCSGAF0086. Based on a literature review very few articles have been published on (1R,3R,4S)-6,8-dihydroxy-1-(4-hydroxy-4-methyl-2-oxopentyl)-3,4,5-trimethyl-3,4-dihydro-1H-2-benzopyran-7-carboxylic acid.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242116593D          

 52 53  0  0  0  0            999 V2000
   -4.3041   -0.8483    0.5708 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2396    0.1557    0.2181 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4933    1.5024    0.5538 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6705    1.7517    1.1775 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5540    2.4951    0.2417 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8451    3.8651    0.6005 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0645    4.8059    0.3592 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0247    4.1894    1.2379 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3903    2.0975   -0.3988 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4285    3.0051   -0.7358 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1323    0.7628   -0.7349 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.4598   -1.8606   -1.2923 C   0  0  1  0  0  0  0  0  0  0  0  0
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    1.2956    0.2383   -0.5254 C   0  0  2  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
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 26 52  1  0  0  0  0
M  END

     RDKit          3D

 52 53  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1652306242116593D          

 52 53  0  0  0  0            999 V2000
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   -3.2396    0.1557    0.2181 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.7512   -0.2000    2.0027 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0487    0.0407    0.2628 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6746   -1.6114    0.8209 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5864    1.4940    1.9156 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8539    1.1697    1.8639 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7493    1.9389    0.4299 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7688   -2.0095    1.4364 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
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  5  9  2  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 23 26  1  1  0  0  0
 12  2  1  0  0  0  0
 18 11  1  0  0  0  0
  1 27  1  0  0  0  0
  1 28  1  0  0  0  0
  1 29  1  0  0  0  0
  4 30  1  0  0  0  0
  8 31  1  0  0  0  0
 10 32  1  0  0  0  0
 13 33  1  6  0  0  0
 14 34  1  0  0  0  0
 14 35  1  0  0  0  0
 14 36  1  0  0  0  0
 15 37  1  1  0  0  0
 16 38  1  0  0  0  0
 16 39  1  0  0  0  0
 16 40  1  0  0  0  0
 18 41  1  6  0  0  0
 19 42  1  0  0  0  0
 19 43  1  0  0  0  0
 22 44  1  0  0  0  0
 22 45  1  0  0  0  0
 24 46  1  0  0  0  0
 24 47  1  0  0  0  0
 24 48  1  0  0  0  0
 25 49  1  0  0  0  0
 25 50  1  0  0  0  0
 25 51  1  0  0  0  0
 26 52  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0011795

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC(=O)C1=C(O[H])C2=C(C(=C1O[H])C([H])([H])[H])[C@]([H])(C([H])([H])[H])[C@]([H])(O[C@]2([H])C([H])([H])C(=O)C([H])([H])C(O[H])(C([H])([H])[H])C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C19H26O7/c1-8-10(3)26-12(6-11(20)7-19(4,5)25)14-13(8)9(2)16(21)15(17(14)22)18(23)24/h8,10,12,21-22,25H,6-7H2,1-5H3,(H,23,24)/t8-,10-,12-/m1/s1

> <INCHI_KEY>
ALRKYRPHRIVAMM-HLUHBDAQSA-N

> <FORMULA>
C19H26O7

> <MOLECULAR_WEIGHT>
366.41

> <EXACT_MASS>
366.167853177

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
38.274898734557354

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,3R,4S)-6,8-dihydroxy-1-(4-hydroxy-4-methyl-2-oxopentyl)-3,4,5-trimethyl-3,4-dihydro-1H-2-benzopyran-7-carboxylic acid

> <ALOGPS_LOGP>
1.92

> <JCHEM_LOGP>
3.755637584333333

> <ALOGPS_LOGS>
-2.89

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
13.28762785208919

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.5749909895207113

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7049074719545905

> <JCHEM_POLAR_SURFACE_AREA>
124.29

> <JCHEM_REFRACTIVITY>
95.5482

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.74e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,3R,4S)-6,8-dihydroxy-1-(4-hydroxy-4-methyl-2-oxopentyl)-3,4,5-trimethyl-3,4-dihydro-1H-2-benzopyran-7-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 52 53  0  0  0  0  0  0  0  0999 V2000
   -4.3041   -0.8483    0.5708 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2396    0.1557    0.2181 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4933    1.5024    0.5538 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6705    1.7517    1.1775 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5540    2.4951    0.2417 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8451    3.8651    0.6005 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0645    4.8059    0.3592 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0247    4.1894    1.2379 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3903    2.0975   -0.3988 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4285    3.0051   -0.7358 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1323    0.7628   -0.7349 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0654   -0.1886   -0.4182 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8372   -1.6191   -0.7387 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9381   -2.4845    0.5100 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4598   -1.8606   -1.2923 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4692   -3.1423   -2.1174 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0735   -0.8422   -2.1103 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0889    0.3721   -1.4287 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2956    0.2383   -0.5254 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4838   -0.1581   -1.2969 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3570   -0.3049   -2.5243 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8296   -0.4048   -0.7663 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9921   -0.2279    0.7069 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4678   -0.5462    1.0041 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7699    1.1701    1.2044 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2558   -1.1626    1.4430 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3955   -1.0005    1.6498 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2789   -0.3432    0.2776 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2681   -1.7443   -0.0533 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1959    2.4397    1.5455 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6951    4.8704    0.8947 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4204    3.9509   -0.5927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5814   -1.9626   -1.4814 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9342   -2.9306    0.7885 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1983   -1.8457    1.3549 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5830   -3.3641    0.3462 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2497   -2.0457   -0.4480 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3137   -3.0747   -2.8868 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3265   -4.0332   -1.4973 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4369   -3.2524   -2.6767 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3773    1.1150   -2.2262 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0953   -0.3818    0.3612 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5208    1.2681   -0.1149 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2210   -1.4162   -1.0231 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5530    0.3075   -1.2559 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7512   -0.2000    2.0027 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0487    0.0407    0.2628 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6746   -1.6114    0.8209 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5864    1.4940    1.9156 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8539    1.1697    1.8639 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7493    1.9389    0.4299 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7688   -2.0095    1.4364 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
  3  5  1  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  5  9  2  0
  9 10  1  0
  9 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
 22 23  1  0
 23 24  1  0
 23 25  1  0
 23 26  1  1
 12  2  1  0
 18 11  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  4 30  1  0
  8 31  1  0
 10 32  1  0
 13 33  1  6
 14 34  1  0
 14 35  1  0
 14 36  1  0
 15 37  1  1
 16 38  1  0
 16 39  1  0
 16 40  1  0
 18 41  1  6
 19 42  1  0
 19 43  1  0
 22 44  1  0
 22 45  1  0
 24 46  1  0
 24 47  1  0
 24 48  1  0
 25 49  1  0
 25 50  1  0
 25 51  1  0
 26 52  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      -4.304  -0.848   0.571  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.240   0.156   0.218  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.493   1.502   0.554  0.00  0.00           C+0
HETATM    4  O   UNK     0      -4.670   1.752   1.178  0.00  0.00           O+0
HETATM    5  C   UNK     0      -2.554   2.495   0.242  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.845   3.865   0.601  0.00  0.00           C+0
HETATM    7  O   UNK     0      -2.064   4.806   0.359  0.00  0.00           O+0
HETATM    8  O   UNK     0      -4.025   4.189   1.238  0.00  0.00           O+0
HETATM    9  C   UNK     0      -1.390   2.098  -0.399  0.00  0.00           C+0
HETATM   10  O   UNK     0      -0.429   3.005  -0.736  0.00  0.00           O+0
HETATM   11  C   UNK     0      -1.132   0.763  -0.735  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.065  -0.189  -0.418  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.837  -1.619  -0.739  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.938  -2.485   0.510  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.460  -1.861  -1.292  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.469  -3.142  -2.117  0.00  0.00           C+0
HETATM   17  O   UNK     0      -0.074  -0.842  -2.110  0.00  0.00           O+0
HETATM   18  C   UNK     0       0.089   0.372  -1.429  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.296   0.238  -0.525  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.484  -0.158  -1.297  0.00  0.00           C+0
HETATM   21  O   UNK     0       2.357  -0.305  -2.524  0.00  0.00           O+0
HETATM   22  C   UNK     0       3.830  -0.405  -0.766  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.992  -0.228   0.707  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.468  -0.546   1.004  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.770   1.170   1.204  0.00  0.00           C+0
HETATM   26  O   UNK     0       3.256  -1.163   1.443  0.00  0.00           O+0
HETATM   27  H   UNK     0      -4.396  -1.000   1.650  0.00  0.00           H+0
HETATM   28  H   UNK     0      -5.279  -0.343   0.278  0.00  0.00           H+0
HETATM   29  H   UNK     0      -4.268  -1.744  -0.053  0.00  0.00           H+0
HETATM   30  H   UNK     0      -5.196   2.440   1.546  0.00  0.00           H+0
HETATM   31  H   UNK     0      -4.695   4.870   0.895  0.00  0.00           H+0
HETATM   32  H   UNK     0      -0.420   3.951  -0.593  0.00  0.00           H+0
HETATM   33  H   UNK     0      -2.581  -1.963  -1.481  0.00  0.00           H+0
HETATM   34  H   UNK     0      -0.934  -2.931   0.789  0.00  0.00           H+0
HETATM   35  H   UNK     0      -2.198  -1.846   1.355  0.00  0.00           H+0
HETATM   36  H   UNK     0      -2.583  -3.364   0.346  0.00  0.00           H+0
HETATM   37  H   UNK     0       0.250  -2.046  -0.448  0.00  0.00           H+0
HETATM   38  H   UNK     0       0.314  -3.075  -2.887  0.00  0.00           H+0
HETATM   39  H   UNK     0      -0.327  -4.033  -1.497  0.00  0.00           H+0
HETATM   40  H   UNK     0      -1.437  -3.252  -2.677  0.00  0.00           H+0
HETATM   41  H   UNK     0       0.377   1.115  -2.226  0.00  0.00           H+0
HETATM   42  H   UNK     0       1.095  -0.382   0.361  0.00  0.00           H+0
HETATM   43  H   UNK     0       1.521   1.268  -0.115  0.00  0.00           H+0
HETATM   44  H   UNK     0       4.221  -1.416  -1.023  0.00  0.00           H+0
HETATM   45  H   UNK     0       4.553   0.308  -1.256  0.00  0.00           H+0
HETATM   46  H   UNK     0       5.751  -0.200   2.003  0.00  0.00           H+0
HETATM   47  H   UNK     0       6.049   0.041   0.263  0.00  0.00           H+0
HETATM   48  H   UNK     0       5.675  -1.611   0.821  0.00  0.00           H+0
HETATM   49  H   UNK     0       4.586   1.494   1.916  0.00  0.00           H+0
HETATM   50  H   UNK     0       2.854   1.170   1.864  0.00  0.00           H+0
HETATM   51  H   UNK     0       3.749   1.939   0.430  0.00  0.00           H+0
HETATM   52  H   UNK     0       3.769  -2.010   1.436  0.00  0.00           H+0
CONECT    1    2   27   28   29                                             
CONECT    2    1    3   12                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3   30                                                       
CONECT    5    3    6    9                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6   31                                                       
CONECT    9    5   10   11                                                  
CONECT   10    9   32                                                       
CONECT   11    9   12   18                                                  
CONECT   12   11   13    2                                                  
CONECT   13   12   14   15   33                                             
CONECT   14   13   34   35   36                                             
CONECT   15   13   16   17   37                                             
CONECT   16   15   38   39   40                                             
CONECT   17   15   18                                                       
CONECT   18   17   19   11   41                                             
CONECT   19   18   20   42   43                                             
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   44   45                                             
CONECT   23   22   24   25   26                                             
CONECT   24   23   46   47   48                                             
CONECT   25   23   49   50   51                                             
CONECT   26   23   52                                                       
CONECT   27    1                                                            
CONECT   28    1                                                            
CONECT   29    1                                                            
CONECT   30    4                                                            
CONECT   31    8                                                            
CONECT   32   10                                                            
CONECT   33   13                                                            
CONECT   34   14                                                            
CONECT   35   14                                                            
CONECT   36   14                                                            
CONECT   37   15                                                            
CONECT   38   16                                                            
CONECT   39   16                                                            
CONECT   40   16                                                            
CONECT   41   18                                                            
CONECT   42   19                                                            
CONECT   43   19                                                            
CONECT   44   22                                                            
CONECT   45   22                                                            
CONECT   46   24                                                            
CONECT   47   24                                                            
CONECT   48   24                                                            
CONECT   49   25                                                            
CONECT   50   25                                                            
CONECT   51   25                                                            
CONECT   52   26                                                            
MASTER        0    0    0    0    0    0    0    0   52    0  106    0
END

RDKit          3D

52 53  0  0  0  0  0  0  0  0999 V2000
   -4.3041   -0.8483    0.5708 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2396    0.1557    0.2181 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4933    1.5024    0.5538 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6705    1.7517    1.1775 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5540    2.4951    0.2417 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8451    3.8651    0.6005 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0645    4.8059    0.3592 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0247    4.1894    1.2379 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3903    2.0975   -0.3988 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4285    3.0051   -0.7358 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1323    0.7628   -0.7349 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0654   -0.1886   -0.4182 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8372   -1.6191   -0.7387 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9381   -2.4845    0.5100 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4598   -1.8606   -1.2923 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4692   -3.1423   -2.1174 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0735   -0.8422   -2.1103 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0889    0.3721   -1.4287 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2956    0.2383   -0.5254 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4838   -0.1581   -1.2969 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3570   -0.3049   -2.5243 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8296   -0.4048   -0.7663 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9921   -0.2279    0.7069 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4678   -0.5462    1.0041 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7699    1.1701    1.2044 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2558   -1.1626    1.4430 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3955   -1.0005    1.6498 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2789   -0.3432    0.2776 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2681   -1.7443   -0.0533 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1959    2.4397    1.5455 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6951    4.8704    0.8947 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4204    3.9509   -0.5927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5814   -1.9626   -1.4814 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9342   -2.9306    0.7885 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1983   -1.8457    1.3549 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5830   -3.3641    0.3462 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2497   -2.0457   -0.4480 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3137   -3.0747   -2.8868 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3265   -4.0332   -1.4973 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4369   -3.2524   -2.6767 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3773    1.1150   -2.2262 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0953   -0.3818    0.3612 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5208    1.2681   -0.1149 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2210   -1.4162   -1.0231 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5530    0.3075   -1.2559 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7512   -0.2000    2.0027 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0487    0.0407    0.2628 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6746   -1.6114    0.8209 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5864    1.4940    1.9156 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8539    1.1697    1.8639 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7493    1.9389    0.4299 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7688   -2.0095    1.4364 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
  3  5  1  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  5  9  2  0
  9 10  1  0
  9 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
 22 23  1  0
 23 24  1  0
 23 25  1  0
 23 26  1  1
 12  2  1  0
 18 11  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  4 30  1  0
  8 31  1  0
 10 32  1  0
 13 33  1  6
 14 34  1  0
 14 35  1  0
 14 36  1  0
 15 37  1  1
 16 38  1  0
 16 39  1  0
 16 40  1  0
 18 41  1  6
 19 42  1  0
 19 43  1  0
 22 44  1  0
 22 45  1  0
 24 46  1  0
 24 47  1  0
 24 48  1  0
 25 49  1  0
 25 50  1  0
 25 51  1  0
 26 52  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
(1R,3R,4S)-6,8-Dihydroxy-1-(4-hydroxy-4-methyl-2-oxopentyl)-3,4,5-trimethyl-3,4-dihydro-1H-2-benzopyran-7-carboxylate	Generator

Chemical Formula

C₁₉H₂₆O₇

Average Mass

366.4100 Da

Monoisotopic Mass

366.16785 Da

IUPAC Name

(1R,3R,4S)-6,8-dihydroxy-1-(4-hydroxy-4-methyl-2-oxopentyl)-3,4,5-trimethyl-3,4-dihydro-1H-2-benzopyran-7-carboxylic acid

Traditional Name

(1R,3R,4S)-6,8-dihydroxy-1-(4-hydroxy-4-methyl-2-oxopentyl)-3,4,5-trimethyl-3,4-dihydro-1H-2-benzopyran-7-carboxylic acid

CAS Registry Number

Not Available

SMILES

C[C@H]1O[C@H](CC(=O)CC(C)(C)O)C2=C([C@@H]1C)C(C)=C(O)C(C(O)=O)=C2O

InChI Identifier

InChI=1S/C19H26O7/c1-8-10(3)26-12(6-11(20)7-19(4,5)25)14-13(8)9(2)16(21)15(17(14)22)18(23)24/h8,10,12,21-22,25H,6-7H2,1-5H3,(H,23,24)/t8-,10-,12-/m1/s1

InChI Key

ALRKYRPHRIVAMM-HLUHBDAQSA-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
Unknown-fungus sp. SCSGAF0086	NPAtlas	23697953

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	1.92	ALOGPS
logP	3.76	ChemAxon
logS	-2.9	ALOGPS
pKa (Strongest Acidic)	1.57	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	124.29 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	95.55 m³·mol⁻¹	ChemAxon
Polarizability	38.27 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

NPA011105

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

30770799

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

102368377

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Penicitrinol F (NP0011795)

MOL for NP0011795 (Penicitrinol F)

3D MOL for NP0011795 (Penicitrinol F)

3D SDF for NP0011795 (Penicitrinol F)

3D-SDF for NP0011795 (Penicitrinol F)

PDB for NP0011795 (Penicitrinol F)

3D PDB for NP0011795 (Penicitrinol F)

SMILES for NP0011795 (Penicitrinol F)

INCHI for NP0011795 (Penicitrinol F)

Structure for NP0011795 (Penicitrinol F)

3D Structure for NP0011795 (Penicitrinol F)