NP-MRD: Showing NP-Card for 11,12-epoxyaigialomycin D (NP0032444)

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Record Information

Version

2.0

Created at

2021-06-19 23:14:48 UTC

Updated at

2021-06-30 00:01:37 UTC

NP-MRD ID

NP0032444

Secondary Accession Numbers

None

Natural Product Identification

Common Name

11,12-epoxyaigialomycin D

Provided By

JEOL Database JEOL Logo

Description

11,12-epoxyaigialomycin D is found in Hypomyces subiculosus. 11,12-epoxyaigialomycin D was first documented in 2006 (Wee, J. L., et al.). Based on a literature review very few articles have been published on (2R,4R,7S,8R,9E,12S)-7,8,16,18-tetrahydroxy-12-methyl-3,13-dioxatricyclo[13.4.0.0²,⁴]Nonadeca-1(15),9,16,18-tetraen-14-one.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306202101143D          

 47 49  0  0  0  0            999 V2000
    2.5278    3.4013    2.5049 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0143    2.0051    2.1524 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2743    1.4043    3.3612 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8189   -0.0095    3.1309 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6384   -1.0748    3.1081 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2285   -2.4931    2.8136 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1805   -2.6567    2.9777 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6517   -2.9664    1.3962 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0467   -4.2470    1.1566 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3058   -2.0123    0.2380 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1895   -1.8113   -0.0235 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4135   -0.6926   -0.9942 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7834   -0.3124   -1.1390 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9148    0.6625   -0.5237 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5643    1.8943   -1.3266 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4781    2.3944   -2.2794 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1596    3.4831   -3.0895 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0418    3.9602   -4.0128 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0759    4.1034   -2.9927 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9953    3.6384   -2.0608 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2098    4.2751   -2.0369 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6698    2.5712   -1.2039 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6699    2.1993   -0.1843 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8638    2.1440   -0.4421 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0971    2.1136    1.0404 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.7392   -3.1134    1.3981 H   0  0  0  0  0  0  0  0  0  0  0  0
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  1 26  1  0  0  0  0
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  9 37  1  0  0  0  0
 11 40  1  0  0  0  0
 11 41  1  0  0  0  0
 12 42  1  6  0  0  0
M  END

     RDKit          3D

 47 49  0  0  0  0  0  0  0  0999 V2000
    2.5278    3.4013    2.5049 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0143    2.0051    2.1524 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2743    1.4043    3.3612 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8189   -0.0095    3.1309 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.6699    2.1993   -0.1843 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8638    2.1440   -0.4421 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0971    2.1136    1.0404 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0685    3.8462    1.6633 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2027    3.3696    3.3658 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6958    4.0763    2.7343 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8585    1.3569    1.8841 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.2465   -0.1500    2.9550 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652306202101143D          

 47 49  0  0  0  0            999 V2000
    2.5278    3.4013    2.5049 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0143    2.0051    2.1524 C   0  0  1  0  0  0  0  0  0  0  0  0
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 10 38  1  0  0  0  0
 10 39  1  0  0  0  0
  8 36  1  1  0  0  0
  6 34  1  1  0  0  0
  5 33  1  0  0  0  0
 21 47  1  0  0  0  0
 18 45  1  0  0  0  0
  1 26  1  0  0  0  0
  1 27  1  0  0  0  0
  1 28  1  0  0  0  0
  7 35  1  0  0  0  0
  9 37  1  0  0  0  0
 11 40  1  0  0  0  0
 11 41  1  0  0  0  0
 12 42  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0032444

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C([H])C(O[H])=C2C(=C1[H])[C@@]1([H])O[C@]1([H])C([H])([H])C([H])([H])[C@]([H])(O[H])[C@]([H])(O[H])\C([H])=C([H])\C([H])([H])[C@@]([H])(OC2=O)C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C18H22O7/c1-9-3-2-4-12(20)13(21)5-6-15-17(25-15)11-7-10(19)8-14(22)16(11)18(23)24-9/h2,4,7-9,12-13,15,17,19-22H,3,5-6H2,1H3/b4-2+/t9-,12+,13-,15+,17+/m0/s1

> <INCHI_KEY>
NIYNEOZUYHJSJS-VWRXRXDESA-N

> <FORMULA>
C18H22O7

> <MOLECULAR_WEIGHT>
350.367

> <EXACT_MASS>
350.136553048

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
35.68405369828221

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R,4R,7S,8R,9E,12S)-7,8,16,18-tetrahydroxy-12-methyl-3,13-dioxatricyclo[13.4.0.0^{2,4}]nonadeca-1(15),9,16,18-tetraen-14-one

> <ALOGPS_LOGP>
0.66

> <JCHEM_LOGP>
2.0209575553333337

> <ALOGPS_LOGS>
-2.31

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.27370279603373

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.428838772397992

> <JCHEM_PKA_STRONGEST_BASIC>
-3.1718025720144523

> <JCHEM_POLAR_SURFACE_AREA>
119.75000000000001

> <JCHEM_REFRACTIVITY>
89.942

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.73e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,4R,7S,8R,9E,12S)-7,8,16,18-tetrahydroxy-12-methyl-3,13-dioxatricyclo[13.4.0.0^{2,4}]nonadeca-1(15),9,16,18-tetraen-14-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 47 49  0  0  0  0  0  0  0  0999 V2000
    2.5278    3.4013    2.5049 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0143    2.0051    2.1524 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2743    1.4043    3.3612 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8189   -0.0095    3.1309 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6384   -1.0748    3.1081 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2285   -2.4931    2.8136 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1805   -2.6567    2.9777 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6517   -2.9664    1.3962 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0467   -4.2470    1.1566 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3058   -2.0123    0.2380 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1895   -1.8113   -0.0235 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4135   -0.6926   -0.9942 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7834   -0.3124   -1.1390 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9148    0.6625   -0.5237 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5643    1.8943   -1.3266 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4781    2.3944   -2.2794 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1596    3.4831   -3.0895 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0418    3.9602   -4.0128 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0759    4.1034   -2.9927 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9953    3.6384   -2.0608 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2098    4.2751   -2.0369 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6698    2.5712   -1.2039 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6699    2.1993   -0.1843 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8638    2.1440   -0.4421 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0971    2.1136    1.0404 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0685    3.8462    1.6633 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2027    3.3696    3.3658 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6958    4.0763    2.7343 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8585    1.3569    1.8841 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9161    1.4330    4.2505 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3864    2.0071    3.5905 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2465   -0.1500    2.9550 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7028   -0.9272    3.2787 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6881   -3.1538    3.5582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3718   -3.5215    2.5625 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7392   -3.1134    1.3981 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3858   -4.5723    0.3035 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7466   -2.4192   -0.6824 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7949   -1.0437    0.3953 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7296   -1.5920    0.8998 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6178   -2.7329   -0.4341 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1704   -0.7763   -1.9013 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0725    0.8087    0.5411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4421    1.9006   -2.3864 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8566    3.4320   -3.9750 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3240    4.9381   -3.6417 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8557    3.7107   -1.5615 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 16  2  0
 17 19  2  0
 22 23  1  0
  4  5  2  0
 10  8  1  0
  8  6  1  0
  6  5  1  0
 15 14  1  0
 20 21  1  0
 25 23  1  0
 17 18  1  0
 19 20  1  0
 23 24  2  0
 20 22  2  0
  2  1  1  0
 22 15  1  0
  6  7  1  0
 25  2  1  0
  8  9  1  0
  4  3  1  0
 10 11  1  0
  3  2  1  0
 14 12  1  0
 12 11  1  0
 16 17  1  0
 14 13  1  0
 12 13  1  0
 16 44  1  0
 19 46  1  0
 14 43  1  1
  3 30  1  0
  3 31  1  0
  2 29  1  6
  4 32  1  0
 10 38  1  0
 10 39  1  0
  8 36  1  1
  6 34  1  1
  5 33  1  0
 21 47  1  0
 18 45  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  7 35  1  0
  9 37  1  0
 11 40  1  0
 11 41  1  0
 12 42  1  6
M  END

HEADER    PROTEIN                                 20-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-JUN-21         0                                  
HETATM    1  C   UNK     0       2.528   3.401   2.505  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.014   2.005   2.152  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.274   1.404   3.361  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.819  -0.010   3.131  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.638  -1.075   3.108  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.228  -2.493   2.814  0.00  0.00           C+0
HETATM    7  O   UNK     0      -0.181  -2.657   2.978  0.00  0.00           O+0
HETATM    8  C   UNK     0       1.652  -2.966   1.396  0.00  0.00           C+0
HETATM    9  O   UNK     0       1.047  -4.247   1.157  0.00  0.00           O+0
HETATM   10  C   UNK     0       1.306  -2.012   0.238  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.190  -1.811  -0.024  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.414  -0.693  -0.994  0.00  0.00           C+0
HETATM   13  O   UNK     0      -1.783  -0.312  -1.139  0.00  0.00           O+0
HETATM   14  C   UNK     0      -0.915   0.663  -0.524  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.564   1.894  -1.327  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.478   2.394  -2.279  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.160   3.483  -3.090  0.00  0.00           C+0
HETATM   18  O   UNK     0      -2.042   3.960  -4.013  0.00  0.00           O+0
HETATM   19  C   UNK     0       0.076   4.103  -2.993  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.995   3.638  -2.061  0.00  0.00           C+0
HETATM   21  O   UNK     0       2.210   4.275  -2.037  0.00  0.00           O+0
HETATM   22  C   UNK     0       0.670   2.571  -1.204  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.670   2.199  -0.184  0.00  0.00           C+0
HETATM   24  O   UNK     0       2.864   2.144  -0.442  0.00  0.00           O+0
HETATM   25  O   UNK     0       1.097   2.114   1.040  0.00  0.00           O+0
HETATM   26  H   UNK     0       3.068   3.846   1.663  0.00  0.00           H+0
HETATM   27  H   UNK     0       3.203   3.370   3.366  0.00  0.00           H+0
HETATM   28  H   UNK     0       1.696   4.076   2.734  0.00  0.00           H+0
HETATM   29  H   UNK     0       2.858   1.357   1.884  0.00  0.00           H+0
HETATM   30  H   UNK     0       1.916   1.433   4.250  0.00  0.00           H+0
HETATM   31  H   UNK     0       0.386   2.007   3.591  0.00  0.00           H+0
HETATM   32  H   UNK     0      -0.247  -0.150   2.955  0.00  0.00           H+0
HETATM   33  H   UNK     0       2.703  -0.927   3.279  0.00  0.00           H+0
HETATM   34  H   UNK     0       1.688  -3.154   3.558  0.00  0.00           H+0
HETATM   35  H   UNK     0      -0.372  -3.522   2.563  0.00  0.00           H+0
HETATM   36  H   UNK     0       2.739  -3.113   1.398  0.00  0.00           H+0
HETATM   37  H   UNK     0       1.386  -4.572   0.304  0.00  0.00           H+0
HETATM   38  H   UNK     0       1.747  -2.419  -0.682  0.00  0.00           H+0
HETATM   39  H   UNK     0       1.795  -1.044   0.395  0.00  0.00           H+0
HETATM   40  H   UNK     0      -0.730  -1.592   0.900  0.00  0.00           H+0
HETATM   41  H   UNK     0      -0.618  -2.733  -0.434  0.00  0.00           H+0
HETATM   42  H   UNK     0       0.170  -0.776  -1.901  0.00  0.00           H+0
HETATM   43  H   UNK     0      -1.073   0.809   0.541  0.00  0.00           H+0
HETATM   44  H   UNK     0      -2.442   1.901  -2.386  0.00  0.00           H+0
HETATM   45  H   UNK     0      -2.857   3.432  -3.975  0.00  0.00           H+0
HETATM   46  H   UNK     0       0.324   4.938  -3.642  0.00  0.00           H+0
HETATM   47  H   UNK     0       2.856   3.711  -1.562  0.00  0.00           H+0
CONECT    1    2   26   27   28                                             
CONECT    2    1   25    3   29                                             
CONECT    3    4    2   30   31                                             
CONECT    4    5    3   32                                                  
CONECT    5    4    6   33                                                  
CONECT    6    8    5    7   34                                             
CONECT    7    6   35                                                       
CONECT    8   10    6    9   36                                             
CONECT    9    8   37                                                       
CONECT   10    8   11   38   39                                             
CONECT   11   10   12   40   41                                             
CONECT   12   14   11   13   42                                             
CONECT   13   14   12                                                       
CONECT   14   15   12   13   43                                             
CONECT   15   16   14   22                                                  
CONECT   16   15   17   44                                                  
CONECT   17   19   18   16                                                  
CONECT   18   17   45                                                       
CONECT   19   17   20   46                                                  
CONECT   20   21   19   22                                                  
CONECT   21   20   47                                                       
CONECT   22   23   20   15                                                  
CONECT   23   22   25   24                                                  
CONECT   24   23                                                            
CONECT   25   23    2                                                       
CONECT   26    1                                                            
CONECT   27    1                                                            
CONECT   28    1                                                            
CONECT   29    2                                                            
CONECT   30    3                                                            
CONECT   31    3                                                            
CONECT   32    4                                                            
CONECT   33    5                                                            
CONECT   34    6                                                            
CONECT   35    7                                                            
CONECT   36    8                                                            
CONECT   37    9                                                            
CONECT   38   10                                                            
CONECT   39   10                                                            
CONECT   40   11                                                            
CONECT   41   11                                                            
CONECT   42   12                                                            
CONECT   43   14                                                            
CONECT   44   16                                                            
CONECT   45   18                                                            
CONECT   46   19                                                            
CONECT   47   21                                                            
MASTER        0    0    0    0    0    0    0    0   47    0   98    0
END

RDKit          3D

47 49  0  0  0  0  0  0  0  0999 V2000
    2.5278    3.4013    2.5049 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0143    2.0051    2.1524 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2743    1.4043    3.3612 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8189   -0.0095    3.1309 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6384   -1.0748    3.1081 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2285   -2.4931    2.8136 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1805   -2.6567    2.9777 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6517   -2.9664    1.3962 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0467   -4.2470    1.1566 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3058   -2.0123    0.2380 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1895   -1.8113   -0.0235 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4135   -0.6926   -0.9942 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7834   -0.3124   -1.1390 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9148    0.6625   -0.5237 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5643    1.8943   -1.3266 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4781    2.3944   -2.2794 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1596    3.4831   -3.0895 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0418    3.9602   -4.0128 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0759    4.1034   -2.9927 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9953    3.6384   -2.0608 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2098    4.2751   -2.0369 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6698    2.5712   -1.2039 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6699    2.1993   -0.1843 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8638    2.1440   -0.4421 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0971    2.1136    1.0404 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0685    3.8462    1.6633 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2027    3.3696    3.3658 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6958    4.0763    2.7343 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8585    1.3569    1.8841 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9161    1.4330    4.2505 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3864    2.0071    3.5905 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2465   -0.1500    2.9550 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7028   -0.9272    3.2787 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6881   -3.1538    3.5582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3718   -3.5215    2.5625 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7392   -3.1134    1.3981 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3858   -4.5723    0.3035 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7466   -2.4192   -0.6824 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7949   -1.0437    0.3953 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7296   -1.5920    0.8998 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6178   -2.7329   -0.4341 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1704   -0.7763   -1.9013 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0725    0.8087    0.5411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4421    1.9006   -2.3864 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8566    3.4320   -3.9750 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3240    4.9381   -3.6417 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8557    3.7107   -1.5615 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 16  2  0
 17 19  2  0
 22 23  1  0
  4  5  2  0
 10  8  1  0
  8  6  1  0
  6  5  1  0
 15 14  1  0
 20 21  1  0
 25 23  1  0
 17 18  1  0
 19 20  1  0
 23 24  2  0
 20 22  2  0
  2  1  1  0
 22 15  1  0
  6  7  1  0
 25  2  1  0
  8  9  1  0
  4  3  1  0
 10 11  1  0
  3  2  1  0
 14 12  1  0
 12 11  1  0
 16 17  1  0
 14 13  1  0
 12 13  1  0
 16 44  1  0
 19 46  1  0
 14 43  1  1
  3 30  1  0
  3 31  1  0
  2 29  1  6
  4 32  1  0
 10 38  1  0
 10 39  1  0
  8 36  1  1
  6 34  1  1
  5 33  1  0
 21 47  1  0
 18 45  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  7 35  1  0
  9 37  1  0
 11 40  1  0
 11 41  1  0
 12 42  1  6
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₂₂O₇

Average Mass

350.3670 Da

Monoisotopic Mass

350.13655 Da

IUPAC Name

(2R,4R,7S,8R,9E,12S)-7,8,16,18-tetrahydroxy-12-methyl-3,13-dioxatricyclo[13.4.0.0^{2,4}]nonadeca-1(15),9,16,18-tetraen-14-one

Traditional Name

(2R,4R,7S,8R,9E,12S)-7,8,16,18-tetrahydroxy-12-methyl-3,13-dioxatricyclo[13.4.0.0^{2,4}]nonadeca-1(15),9,16,18-tetraen-14-one

CAS Registry Number

Not Available

SMILES

[H]OC1=C([H])C(O[H])=C2C(=C1[H])[C@@]1([H])O[C@]1([H])C([H])([H])C([H])([H])[C@]([H])(O[H])[C@]([H])(O[H])\C([H])=C([H])\C([H])([H])[C@@]([H])(OC2=O)C([H])([H])[H]

InChI Identifier

InChI=1S/C18H22O7/c1-9-3-2-4-12(20)13(21)5-6-15-17(25-15)11-7-10(19)8-14(22)16(11)18(23)24-9/h2,4,7-9,12-13,15,17,19-22H,3,5-6H2,1H3/b4-2+/t9-,12+,13-,15+,17+/m0/s1

InChI Key

NIYNEOZUYHJSJS-VWRXRXDESA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Hypomyces subiculosus	JEOL database	Wee, J. L., et al, J. Nat. Prod. 69, 1456 (2006)

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	0.66	ALOGPS
logP	2.02	ChemAxon
logS	-2.3	ALOGPS
pKa (Strongest Acidic)	8.43	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	119.75 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	89.94 m³·mol⁻¹	ChemAxon
Polarizability	35.68 Å³	ChemAxon
Number of Rings	3	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

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

17250181

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

16091603

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Wee, J. L., et al. (2006). Wee, J. L., et al, J. Nat. Prod. 69, 1456 (2006) . J. Nat. Prod..

Showing NP-Card for 11,12-epoxyaigialomycin D (NP0032444)

MOL for NP0032444 (11,12-epoxyaigialomycin D)

3D MOL for NP0032444 (11,12-epoxyaigialomycin D)

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3D PDB for NP0032444 (11,12-epoxyaigialomycin D)

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INCHI for NP0032444 (11,12-epoxyaigialomycin D)

Structure for NP0032444 (11,12-epoxyaigialomycin D)

3D Structure for NP0032444 (11,12-epoxyaigialomycin D)