NP-MRD: Showing NP-Card for 1-O-acetyl hygrophorone E10 (NP0005255)

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Record Information

Version

2.0

Created at

2020-12-09 02:33:06 UTC

Updated at

2021-07-15 16:51:28 UTC

NP-MRD ID

NP0005255

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-O-acetyl hygrophorone E10

Provided By

NPAtlas

Description

(4R,5S)-4,5-dihydroxy-5-undecanoylcyclopent-2-en-1-yl acetate belongs to the class of organic compounds known as alpha-hydroxy ketones. These are organic compounds containing a carboxylic acid, and an amine group attached to the alpha carbon atom, relative to the C=O group. 1-O-acetyl hygrophorone E10 is found in Hygrophorus persoonii. Based on a literature review very few articles have been published on (4R,5S)-4,5-dihydroxy-5-undecanoylcyclopent-2-en-1-yl acetate.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242121113D          

 53 53  0  0  0  0            999 V2000
    7.3374    1.1754   -0.0655 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0203    0.4006   -0.3915 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7173    0.5428   -1.8427 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5715   -0.1418   -2.4277 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1869    0.0838   -2.0214 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7935   -0.2551   -0.6420 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2708    0.0378   -0.4828 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -0.4869   -0.1226    1.3175 C   0  0  2  0  0  0  0  0  0  0  0  0
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   -3.4466   -0.0443    1.7036 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6057    0.7033    2.4897 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4353    0.9058    1.0550 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.8144    0.4580   -0.2325 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6542    1.2013   -1.3679 C   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
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M  END

     RDKit          3D

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


  Mrv1652306242121113D          

 53 53  0  0  0  0            999 V2000
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   -1.1832   -0.5825   -0.6216 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9577   -2.0048    0.4224 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9251    0.8219    3.4279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0086    1.9228    0.9489 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0027    1.3869   -3.4837 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1654    0.3939   -2.5787 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4851   -0.2763   -2.9338 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3613    1.7753    1.8948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2617   -0.1805    3.6350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8847   -1.0281    3.6053 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1241   -2.7896    2.2493 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  1  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 15 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 13  1  0  0  0  0
  1 24  1  0  0  0  0
  1 25  1  0  0  0  0
  1 26  1  0  0  0  0
  2 27  1  0  0  0  0
  2 28  1  0  0  0  0
  3 29  1  0  0  0  0
  3 30  1  0  0  0  0
  4 31  1  0  0  0  0
  4 32  1  0  0  0  0
  5 33  1  0  0  0  0
  5 34  1  0  0  0  0
  6 35  1  0  0  0  0
  6 36  1  0  0  0  0
  7 37  1  0  0  0  0
  7 38  1  0  0  0  0
  8 39  1  0  0  0  0
  8 40  1  0  0  0  0
  9 41  1  0  0  0  0
  9 42  1  0  0  0  0
 10 43  1  0  0  0  0
 10 44  1  0  0  0  0
 14 45  1  0  0  0  0
 15 46  1  6  0  0  0
 18 47  1  0  0  0  0
 18 48  1  0  0  0  0
 18 49  1  0  0  0  0
 20 50  1  0  0  0  0
 21 51  1  0  0  0  0
 22 52  1  1  0  0  0
 23 53  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0005255

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]O[C@]1([H])C([H])=C([H])[C@]([H])(OC(=O)C([H])([H])[H])[C@]1(O[H])C(=O)C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C18H30O5/c1-3-4-5-6-7-8-9-10-11-15(20)18(22)16(21)12-13-17(18)23-14(2)19/h12-13,16-17,21-22H,3-11H2,1-2H3/t16-,17+,18+/m1/s1

> <INCHI_KEY>
CILVORWQHUXLRE-BLAYRMRBSA-N

> <FORMULA>
C18H30O5

> <MOLECULAR_WEIGHT>
326.433

> <EXACT_MASS>
326.209324066

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
37.22957964528517

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,4R,5S)-4,5-dihydroxy-5-undecanoylcyclopent-2-en-1-yl acetate

> <ALOGPS_LOGP>
3.18

> <JCHEM_LOGP>
3.3701774046666664

> <ALOGPS_LOGS>
-3.85

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.143674990150263

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.105801205021896

> <JCHEM_PKA_STRONGEST_BASIC>
-3.5199564296592456

> <JCHEM_POLAR_SURFACE_AREA>
83.83

> <JCHEM_REFRACTIVITY>
88.468

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.66e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,4R,5S)-4,5-dihydroxy-5-undecanoylcyclopent-2-en-1-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 53 53  0  0  0  0  0  0  0  0999 V2000
    7.3374    1.1754   -0.0655 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0203    0.4006   -0.3915 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7173    0.5428   -1.8427 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5715   -0.1418   -2.4277 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1869    0.0838   -2.0214 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7935   -0.2551   -0.6420 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2708    0.0378   -0.4828 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9625   -0.3332    0.9382 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4869   -0.1226    1.3175 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3369   -0.9670    0.4292 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7823   -0.8652    0.6878 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5127   -1.5486   -0.0331 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4466   -0.0443    1.7036 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6057    0.7033    2.4897 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4353    0.9058    1.0550 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.8144    0.4580   -0.2325 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6542    1.2013   -1.3679 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0874    0.6365   -2.6784 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1421    2.3469   -1.2680 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5961    0.9851    1.9762 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5435    0.0123    2.8394 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3523   -0.8396    2.6138 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.7587   -2.0310    2.0617 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1346    0.8127   -0.7286 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1578    2.2482   -0.1250 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5468    0.9005    0.9880 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2221   -0.6287   -0.0563 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2923    0.9536    0.2690 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7892    1.6396   -2.1597 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6466    0.1254   -2.3722 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6121    0.0608   -3.5560 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8153   -1.2589   -2.4194 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8064    1.1156   -2.2903 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5408   -0.5796   -2.6965 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8385   -1.3771   -0.5102 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2335    0.2755    0.1866 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1377    1.1155   -0.6881 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7540   -0.5756   -1.2374 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1383   -1.4427    1.0205 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6515    0.2322    1.5914 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6999    0.9577    1.1674 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5633   -0.4248    2.3924 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1832   -0.5825   -0.6216 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9577   -2.0048    0.4224 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9251    0.8219    3.4279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0086    1.9228    0.9489 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0027    1.3869   -3.4837 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1654    0.3939   -2.5787 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4851   -0.2763   -2.9338 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3613    1.7753    1.8948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2617   -0.1805    3.6350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8847   -1.0281    3.6053 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1241   -2.7896    2.2493 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 13 14  1  1
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 17 19  2  0
 15 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  1  0
 22 13  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  0
  2 28  1  0
  3 29  1  0
  3 30  1  0
  4 31  1  0
  4 32  1  0
  5 33  1  0
  5 34  1  0
  6 35  1  0
  6 36  1  0
  7 37  1  0
  7 38  1  0
  8 39  1  0
  8 40  1  0
  9 41  1  0
  9 42  1  0
 10 43  1  0
 10 44  1  0
 14 45  1  0
 15 46  1  6
 18 47  1  0
 18 48  1  0
 18 49  1  0
 20 50  1  0
 21 51  1  0
 22 52  1  1
 23 53  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       7.337   1.175  -0.066  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.020   0.401  -0.392  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.717   0.543  -1.843  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.572  -0.142  -2.428  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.187   0.084  -2.021  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.793  -0.255  -0.642  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.271   0.038  -0.483  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.963  -0.333   0.938  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.487  -0.123   1.317  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.337  -0.967   0.429  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.782  -0.865   0.688  0.00  0.00           C+0
HETATM   12  O   UNK     0      -3.513  -1.549  -0.033  0.00  0.00           O+0
HETATM   13  C   UNK     0      -3.447  -0.044   1.704  0.00  0.00           C+0
HETATM   14  O   UNK     0      -2.606   0.703   2.490  0.00  0.00           O+0
HETATM   15  C   UNK     0      -4.435   0.906   1.055  0.00  0.00           C+0
HETATM   16  O   UNK     0      -4.814   0.458  -0.233  0.00  0.00           O+0
HETATM   17  C   UNK     0      -4.654   1.201  -1.368  0.00  0.00           C+0
HETATM   18  C   UNK     0      -5.087   0.637  -2.678  0.00  0.00           C+0
HETATM   19  O   UNK     0      -4.142   2.347  -1.268  0.00  0.00           O+0
HETATM   20  C   UNK     0      -5.596   0.985   1.976  0.00  0.00           C+0
HETATM   21  C   UNK     0      -5.543   0.012   2.839  0.00  0.00           C+0
HETATM   22  C   UNK     0      -4.352  -0.840   2.614  0.00  0.00           C+0
HETATM   23  O   UNK     0      -4.759  -2.031   2.062  0.00  0.00           O+0
HETATM   24  H   UNK     0       8.135   0.813  -0.729  0.00  0.00           H+0
HETATM   25  H   UNK     0       7.158   2.248  -0.125  0.00  0.00           H+0
HETATM   26  H   UNK     0       7.547   0.901   0.988  0.00  0.00           H+0
HETATM   27  H   UNK     0       6.222  -0.629  -0.056  0.00  0.00           H+0
HETATM   28  H   UNK     0       5.292   0.954   0.269  0.00  0.00           H+0
HETATM   29  H   UNK     0       5.789   1.640  -2.160  0.00  0.00           H+0
HETATM   30  H   UNK     0       6.647   0.125  -2.372  0.00  0.00           H+0
HETATM   31  H   UNK     0       4.612   0.061  -3.556  0.00  0.00           H+0
HETATM   32  H   UNK     0       4.815  -1.259  -2.419  0.00  0.00           H+0
HETATM   33  H   UNK     0       2.806   1.116  -2.290  0.00  0.00           H+0
HETATM   34  H   UNK     0       2.541  -0.580  -2.696  0.00  0.00           H+0
HETATM   35  H   UNK     0       2.838  -1.377  -0.510  0.00  0.00           H+0
HETATM   36  H   UNK     0       3.233   0.276   0.187  0.00  0.00           H+0
HETATM   37  H   UNK     0       1.138   1.115  -0.688  0.00  0.00           H+0
HETATM   38  H   UNK     0       0.754  -0.576  -1.237  0.00  0.00           H+0
HETATM   39  H   UNK     0       1.138  -1.443   1.020  0.00  0.00           H+0
HETATM   40  H   UNK     0       1.652   0.232   1.591  0.00  0.00           H+0
HETATM   41  H   UNK     0      -0.700   0.958   1.167  0.00  0.00           H+0
HETATM   42  H   UNK     0      -0.563  -0.425   2.392  0.00  0.00           H+0
HETATM   43  H   UNK     0      -1.183  -0.583  -0.622  0.00  0.00           H+0
HETATM   44  H   UNK     0      -0.958  -2.005   0.422  0.00  0.00           H+0
HETATM   45  H   UNK     0      -2.925   0.822   3.428  0.00  0.00           H+0
HETATM   46  H   UNK     0      -4.009   1.923   0.949  0.00  0.00           H+0
HETATM   47  H   UNK     0      -5.003   1.387  -3.484  0.00  0.00           H+0
HETATM   48  H   UNK     0      -6.165   0.394  -2.579  0.00  0.00           H+0
HETATM   49  H   UNK     0      -4.485  -0.276  -2.934  0.00  0.00           H+0
HETATM   50  H   UNK     0      -6.361   1.775   1.895  0.00  0.00           H+0
HETATM   51  H   UNK     0      -6.262  -0.181   3.635  0.00  0.00           H+0
HETATM   52  H   UNK     0      -3.885  -1.028   3.605  0.00  0.00           H+0
HETATM   53  H   UNK     0      -4.124  -2.790   2.249  0.00  0.00           H+0
CONECT    1    2   24   25   26                                             
CONECT    2    1    3   27   28                                             
CONECT    3    2    4   29   30                                             
CONECT    4    3    5   31   32                                             
CONECT    5    4    6   33   34                                             
CONECT    6    5    7   35   36                                             
CONECT    7    6    8   37   38                                             
CONECT    8    7    9   39   40                                             
CONECT    9    8   10   41   42                                             
CONECT   10    9   11   43   44                                             
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   15   22                                             
CONECT   14   13   45                                                       
CONECT   15   13   16   20   46                                             
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17   47   48   49                                             
CONECT   19   17                                                            
CONECT   20   15   21   50                                                  
CONECT   21   20   22   51                                                  
CONECT   22   21   23   13   52                                             
CONECT   23   22   53                                                       
CONECT   24    1                                                            
CONECT   25    1                                                            
CONECT   26    1                                                            
CONECT   27    2                                                            
CONECT   28    2                                                            
CONECT   29    3                                                            
CONECT   30    3                                                            
CONECT   31    4                                                            
CONECT   32    4                                                            
CONECT   33    5                                                            
CONECT   34    5                                                            
CONECT   35    6                                                            
CONECT   36    6                                                            
CONECT   37    7                                                            
CONECT   38    7                                                            
CONECT   39    8                                                            
CONECT   40    8                                                            
CONECT   41    9                                                            
CONECT   42    9                                                            
CONECT   43   10                                                            
CONECT   44   10                                                            
CONECT   45   14                                                            
CONECT   46   15                                                            
CONECT   47   18                                                            
CONECT   48   18                                                            
CONECT   49   18                                                            
CONECT   50   20                                                            
CONECT   51   21                                                            
CONECT   52   22                                                            
CONECT   53   23                                                            
MASTER        0    0    0    0    0    0    0    0   53    0  106    0
END

RDKit          3D

53 53  0  0  0  0  0  0  0  0999 V2000
    7.3374    1.1754   -0.0655 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0203    0.4006   -0.3915 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7173    0.5428   -1.8427 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5715   -0.1418   -2.4277 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1869    0.0838   -2.0214 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7935   -0.2551   -0.6420 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2708    0.0378   -0.4828 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9625   -0.3332    0.9382 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4869   -0.1226    1.3175 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3369   -0.9670    0.4292 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7823   -0.8652    0.6878 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5127   -1.5486   -0.0331 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4466   -0.0443    1.7036 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6057    0.7033    2.4897 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4353    0.9058    1.0550 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.8144    0.4580   -0.2325 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6542    1.2013   -1.3679 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0874    0.6365   -2.6784 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1421    2.3469   -1.2680 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5961    0.9851    1.9762 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5435    0.0123    2.8394 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3523   -0.8396    2.6138 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.7587   -2.0310    2.0617 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1346    0.8127   -0.7286 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1578    2.2482   -0.1250 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5468    0.9005    0.9880 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2221   -0.6287   -0.0563 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2923    0.9536    0.2690 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7892    1.6396   -2.1597 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6466    0.1254   -2.3722 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6121    0.0608   -3.5560 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8153   -1.2589   -2.4194 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8064    1.1156   -2.2903 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5408   -0.5796   -2.6965 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8385   -1.3771   -0.5102 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2335    0.2755    0.1866 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1377    1.1155   -0.6881 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7540   -0.5756   -1.2374 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1383   -1.4427    1.0205 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6515    0.2322    1.5914 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6999    0.9577    1.1674 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5633   -0.4248    2.3924 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1832   -0.5825   -0.6216 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9577   -2.0048    0.4224 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9251    0.8219    3.4279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0086    1.9228    0.9489 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0027    1.3869   -3.4837 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1654    0.3939   -2.5787 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4851   -0.2763   -2.9338 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3613    1.7753    1.8948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2617   -0.1805    3.6350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8847   -1.0281    3.6053 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1241   -2.7896    2.2493 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 13 14  1  1
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 17 19  2  0
 15 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  1  0
 22 13  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  0
  2 28  1  0
  3 29  1  0
  3 30  1  0
  4 31  1  0
  4 32  1  0
  5 33  1  0
  5 34  1  0
  6 35  1  0
  6 36  1  0
  7 37  1  0
  7 38  1  0
  8 39  1  0
  8 40  1  0
  9 41  1  0
  9 42  1  0
 10 43  1  0
 10 44  1  0
 14 45  1  0
 15 46  1  6
 18 47  1  0
 18 48  1  0
 18 49  1  0
 20 50  1  0
 21 51  1  0
 22 52  1  1
 23 53  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
(4R,5S)-4,5-Dihydroxy-5-undecanoylcyclopent-2-en-1-yl acetic acid	Generator

Chemical Formula

C₁₈H₃₀O₅

Average Mass

326.4330 Da

Monoisotopic Mass

326.20932 Da

IUPAC Name

(1S,4R,5S)-4,5-dihydroxy-5-undecanoylcyclopent-2-en-1-yl acetate

Traditional Name

(1S,4R,5S)-4,5-dihydroxy-5-undecanoylcyclopent-2-en-1-yl acetate

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCC(=O)[C@]1(O)[C@H](O)C=CC1OC(C)=O

InChI Identifier

InChI=1S/C18H30O5/c1-3-4-5-6-7-8-9-10-11-15(20)18(22)16(21)12-13-17(18)23-14(2)19/h12-13,16-17,21-22H,3-11H2,1-2H3/t16-,17?,18+/m1/s1

InChI Key

CILVORWQHUXLRE-BLAYRMRBSA-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
Hygrophorus persoonii	NPAtlas	15110686

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as alpha-hydroxy ketones. These are organic compounds containing a carboxylic acid, and an amine group attached to the alpha carbon atom, relative to the C=O group.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbonyl compounds

Direct Parent

Alpha-hydroxy ketones

Alternative Parents

Substituents

Tertiary alcohol
Alpha-hydroxy ketone
Secondary alcohol
Carboxylic acid ester
1,2-diol
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxide
Hydrocarbon derivative
Alcohol
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic homomonocyclic 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	3.18	ALOGPS
logP	3.37	ChemAxon
logS	-3.8	ALOGPS
pKa (Strongest Acidic)	11.11	ChemAxon
pKa (Strongest Basic)	-3.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	83.83 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	88.47 m³·mol⁻¹	ChemAxon
Polarizability	37.23 Å³	ChemAxon
Number of Rings	1	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

NPA007152

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

9488367

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11313400

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for 1-O-acetyl hygrophorone E10 (NP0005255)

MOL for NP0005255 (1-O-acetyl hygrophorone E10)

3D MOL for NP0005255 (1-O-acetyl hygrophorone E10)

3D SDF for NP0005255 (1-O-acetyl hygrophorone E10)

3D-SDF for NP0005255 (1-O-acetyl hygrophorone E10)

PDB for NP0005255 (1-O-acetyl hygrophorone E10)

3D PDB for NP0005255 (1-O-acetyl hygrophorone E10)

SMILES for NP0005255 (1-O-acetyl hygrophorone E10)

INCHI for NP0005255 (1-O-acetyl hygrophorone E10)

Structure for NP0005255 (1-O-acetyl hygrophorone E10)

3D Structure for NP0005255 (1-O-acetyl hygrophorone E10)