NP-MRD: Showing NP-Card for Ornatipolide (NP0015553)

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Record Information

Version

2.0

Created at

2021-01-06 00:45:16 UTC

Updated at

2021-07-15 17:20:17 UTC

NP-MRD ID

NP0015553

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Ornatipolide

Provided By

NPAtlas

Description

Ornatipolide is found in Boletus and Retiboletus ornatipes. Ornatipolide was first documented in 1998 (PMID: 27397004). Based on a literature review very few articles have been published on 4-hydroxy-2,10-dioxatricyclo[12.2.2.1³,⁷]Nonadeca-1(16),3,5,7(19),14,17-hexaene-11,12-dione.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242117203D          

 36 38  0  0  0  0            999 V2000
    3.8693    2.4716   -0.6658 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0711    1.4432   -0.5336 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8652    0.2440    0.0316 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8398   -0.8180    0.4725 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2883   -0.6666    1.6933 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0426   -1.3116    2.0004 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4596   -2.0470    1.0580 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9777   -2.2597   -0.1498 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2324   -1.6201   -0.4825 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9378   -2.5629    1.4404 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8063   -1.4399    0.8470 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4531   -0.1197    1.0564 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1936    0.8678    0.4260 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2753    0.4286   -0.3550 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6496   -0.8848   -0.5500 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8520   -1.8640    0.0967 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2013   -3.2034   -0.0844 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8655    2.3079    0.2703 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4361    2.7391    0.0640 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4965    1.8005   -0.3309 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6846    1.5728   -0.9061 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5574    1.4215   -2.2258 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5444    0.6323    0.7597 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5580   -0.1770   -0.7162 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6466   -0.1193    2.6468 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7423   -1.1246    3.1028 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6689   -2.8861   -1.0156 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4646   -1.9509   -1.4904 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7251    0.2219    1.8740 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9187    1.1574   -0.8808 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4785   -1.1888   -1.1411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9758   -3.4508   -0.6435 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3521    2.6559   -0.7195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3487    2.9897    0.9855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1006    3.0158    1.1240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4393    3.7250   -0.4265 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  7 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 13 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21  2  1  0  0  0  0
  9  4  1  0  0  0  0
 16 11  2  0  0  0  0
  3 23  1  0  0  0  0
  3 24  1  0  0  0  0
  5 25  1  0  0  0  0
  6 26  1  0  0  0  0
  8 27  1  0  0  0  0
  9 28  1  0  0  0  0
 12 29  1  0  0  0  0
 14 30  1  0  0  0  0
 15 31  1  0  0  0  0
 17 32  1  0  0  0  0
 18 33  1  0  0  0  0
 18 34  1  0  0  0  0
 19 35  1  0  0  0  0
 19 36  1  0  0  0  0
M  END

     RDKit          3D

 36 38  0  0  0  0  0  0  0  0999 V2000
    3.8693    2.4716   -0.6658 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0711    1.4432   -0.5336 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8652    0.2440    0.0316 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8398   -0.8180    0.4725 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2883   -0.6666    1.6933 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0426   -1.3116    2.0004 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4596   -2.0470    1.0580 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9777   -2.2597   -0.1498 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2324   -1.6201   -0.4825 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9378   -2.5629    1.4404 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8063   -1.4399    0.8470 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4531   -0.1197    1.0564 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1936    0.8678    0.4260 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2753    0.4286   -0.3550 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6496   -0.8848   -0.5500 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8520   -1.8640    0.0967 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2013   -3.2034   -0.0844 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8655    2.3079    0.2703 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4361    2.7391    0.0640 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4965    1.8005   -0.3309 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6846    1.5728   -0.9061 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5574    1.4215   -2.2258 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5444    0.6323    0.7597 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5580   -0.1770   -0.7162 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6466   -0.1193    2.6468 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7423   -1.1246    3.1028 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6689   -2.8861   -1.0156 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4646   -1.9509   -1.4904 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7251    0.2219    1.8740 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9187    1.1574   -0.8808 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4785   -1.1888   -1.1411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9758   -3.4508   -0.6435 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3521    2.6559   -0.7195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3487    2.9897    0.9855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1006    3.0158    1.1240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4393    3.7250   -0.4265 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  7 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 13 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  2  0
 21  2  1  0
  9  4  1  0
 16 11  2  0
  3 23  1  0
  3 24  1  0
  5 25  1  0
  6 26  1  0
  8 27  1  0
  9 28  1  0
 12 29  1  0
 14 30  1  0
 15 31  1  0
 17 32  1  0
 18 33  1  0
 18 34  1  0
 19 35  1  0
 19 36  1  0
M  END


  Mrv1652306242117203D          

 36 38  0  0  0  0            999 V2000
    3.8693    2.4716   -0.6658 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0711    1.4432   -0.5336 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8652    0.2440    0.0316 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8398   -0.8180    0.4725 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2883   -0.6666    1.6933 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0426   -1.3116    2.0004 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4596   -2.0470    1.0580 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9777   -2.2597   -0.1498 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2324   -1.6201   -0.4825 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9378   -2.5629    1.4404 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8063   -1.4399    0.8470 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4531   -0.1197    1.0564 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1936    0.8678    0.4260 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2753    0.4286   -0.3550 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6496   -0.8848   -0.5500 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8520   -1.8640    0.0967 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2013   -3.2034   -0.0844 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8655    2.3079    0.2703 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4361    2.7391    0.0640 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4965    1.8005   -0.3309 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6846    1.5728   -0.9061 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5574    1.4215   -2.2258 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5444    0.6323    0.7597 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5580   -0.1770   -0.7162 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6466   -0.1193    2.6468 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7423   -1.1246    3.1028 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6689   -2.8861   -1.0156 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4646   -1.9509   -1.4904 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7251    0.2219    1.8740 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9187    1.1574   -0.8808 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4785   -1.1888   -1.1411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9758   -3.4508   -0.6435 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3521    2.6559   -0.7195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3487    2.9897    0.9855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1006    3.0158    1.1240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4393    3.7250   -0.4265 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  7 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 13 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21  2  1  0  0  0  0
  9  4  1  0  0  0  0
 16 11  2  0  0  0  0
  3 23  1  0  0  0  0
  3 24  1  0  0  0  0
  5 25  1  0  0  0  0
  6 26  1  0  0  0  0
  8 27  1  0  0  0  0
  9 28  1  0  0  0  0
 12 29  1  0  0  0  0
 14 30  1  0  0  0  0
 15 31  1  0  0  0  0
 17 32  1  0  0  0  0
 18 33  1  0  0  0  0
 18 34  1  0  0  0  0
 19 35  1  0  0  0  0
 19 36  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0015553

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C2OC3=C([H])C([H])=C(C([H])=C3[H])C([H])([H])C(=O)C(=O)OC([H])([H])C([H])([H])C(C([H])=C1[H])=C2[H]

> <INCHI_IDENTIFIER>
InChI=1S/C17H14O5/c18-14-6-3-12-7-8-21-17(20)15(19)9-11-1-4-13(5-2-11)22-16(14)10-12/h1-6,10,18H,7-9H2

> <INCHI_KEY>
MTLMXGMZDJWCOI-UHFFFAOYSA-N

> <FORMULA>
C17H14O5

> <MOLECULAR_WEIGHT>
298.294

> <EXACT_MASS>
298.084123551

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
36

> <JCHEM_AVERAGE_POLARIZABILITY>
29.594730943977897

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-hydroxy-2,10-dioxatricyclo[12.2.2.1^{3,7}]nonadeca-1(16),3,5,7(19),14,17-hexaene-11,12-dione

> <ALOGPS_LOGP>
3.00

> <JCHEM_LOGP>
3.516051529999999

> <ALOGPS_LOGS>
-3.76

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.42120028202605

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.426607837092314

> <JCHEM_PKA_STRONGEST_BASIC>
-3.7300080306325127

> <JCHEM_POLAR_SURFACE_AREA>
72.83000000000001

> <JCHEM_REFRACTIVITY>
79.012

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.16e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-hydroxy-2,10-dioxatricyclo[12.2.2.1^{3,7}]nonadeca-1(16),3,5,7(19),14,17-hexaene-11,12-dione

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 36 38  0  0  0  0  0  0  0  0999 V2000
    3.8693    2.4716   -0.6658 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0711    1.4432   -0.5336 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8652    0.2440    0.0316 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8398   -0.8180    0.4725 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2883   -0.6666    1.6933 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0426   -1.3116    2.0004 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4596   -2.0470    1.0580 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9777   -2.2597   -0.1498 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2324   -1.6201   -0.4825 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9378   -2.5629    1.4404 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8063   -1.4399    0.8470 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4531   -0.1197    1.0564 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1936    0.8678    0.4260 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2753    0.4286   -0.3550 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6496   -0.8848   -0.5500 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8520   -1.8640    0.0967 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2013   -3.2034   -0.0844 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8655    2.3079    0.2703 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4361    2.7391    0.0640 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4965    1.8005   -0.3309 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6846    1.5728   -0.9061 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5574    1.4215   -2.2258 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5444    0.6323    0.7597 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5580   -0.1770   -0.7162 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6466   -0.1193    2.6468 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7423   -1.1246    3.1028 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6689   -2.8861   -1.0156 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4646   -1.9509   -1.4904 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7251    0.2219    1.8740 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9187    1.1574   -0.8808 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4785   -1.1888   -1.1411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9758   -3.4508   -0.6435 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3521    2.6559   -0.7195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3487    2.9897    0.9855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1006    3.0158    1.1240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4393    3.7250   -0.4265 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  7 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 13 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  2  0
 21  2  1  0
  9  4  1  0
 16 11  2  0
  3 23  1  0
  3 24  1  0
  5 25  1  0
  6 26  1  0
  8 27  1  0
  9 28  1  0
 12 29  1  0
 14 30  1  0
 15 31  1  0
 17 32  1  0
 18 33  1  0
 18 34  1  0
 19 35  1  0
 19 36  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  O   UNK     0       3.869   2.472  -0.666  0.00  0.00           O+0
HETATM    2  C   UNK     0       3.071   1.443  -0.534  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.865   0.244   0.032  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.840  -0.818   0.473  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.288  -0.667   1.693  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.043  -1.312   2.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.460  -2.047   1.058  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.978  -2.260  -0.150  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.232  -1.620  -0.483  0.00  0.00           C+0
HETATM   10  O   UNK     0      -0.938  -2.563   1.440  0.00  0.00           O+0
HETATM   11  C   UNK     0      -1.806  -1.440   0.847  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.453  -0.120   1.056  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.194   0.868   0.426  0.00  0.00           C+0
HETATM   14  C   UNK     0      -3.275   0.429  -0.355  0.00  0.00           C+0
HETATM   15  C   UNK     0      -3.650  -0.885  -0.550  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.852  -1.864   0.097  0.00  0.00           C+0
HETATM   17  O   UNK     0      -3.201  -3.203  -0.084  0.00  0.00           O+0
HETATM   18  C   UNK     0      -1.865   2.308   0.270  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.436   2.739   0.064  0.00  0.00           C+0
HETATM   20  O   UNK     0       0.497   1.801  -0.331  0.00  0.00           O+0
HETATM   21  C   UNK     0       1.685   1.573  -0.906  0.00  0.00           C+0
HETATM   22  O   UNK     0       1.557   1.422  -2.226  0.00  0.00           O+0
HETATM   23  H   UNK     0       4.544   0.632   0.760  0.00  0.00           H+0
HETATM   24  H   UNK     0       4.558  -0.177  -0.716  0.00  0.00           H+0
HETATM   25  H   UNK     0       2.647  -0.119   2.647  0.00  0.00           H+0
HETATM   26  H   UNK     0       0.742  -1.125   3.103  0.00  0.00           H+0
HETATM   27  H   UNK     0       0.669  -2.886  -1.016  0.00  0.00           H+0
HETATM   28  H   UNK     0       2.465  -1.951  -1.490  0.00  0.00           H+0
HETATM   29  H   UNK     0      -0.725   0.222   1.874  0.00  0.00           H+0
HETATM   30  H   UNK     0      -3.919   1.157  -0.881  0.00  0.00           H+0
HETATM   31  H   UNK     0      -4.479  -1.189  -1.141  0.00  0.00           H+0
HETATM   32  H   UNK     0      -3.976  -3.451  -0.644  0.00  0.00           H+0
HETATM   33  H   UNK     0      -2.352   2.656  -0.720  0.00  0.00           H+0
HETATM   34  H   UNK     0      -2.349   2.990   0.986  0.00  0.00           H+0
HETATM   35  H   UNK     0      -0.101   3.016   1.124  0.00  0.00           H+0
HETATM   36  H   UNK     0      -0.439   3.725  -0.427  0.00  0.00           H+0
CONECT    1    2                                                            
CONECT    2    1    3   21                                                  
CONECT    3    2    4   23   24                                             
CONECT    4    3    5    9                                                  
CONECT    5    4    6   25                                                  
CONECT    6    5    7   26                                                  
CONECT    7    6    8   10                                                  
CONECT    8    7    9   27                                                  
CONECT    9    8    4   28                                                  
CONECT   10    7   11                                                       
CONECT   11   10   12   16                                                  
CONECT   12   11   13   29                                                  
CONECT   13   12   14   18                                                  
CONECT   14   13   15   30                                                  
CONECT   15   14   16   31                                                  
CONECT   16   15   17   11                                                  
CONECT   17   16   32                                                       
CONECT   18   13   19   33   34                                             
CONECT   19   18   20   35   36                                             
CONECT   20   19   21                                                       
CONECT   21   20   22    2                                                  
CONECT   22   21                                                            
CONECT   23    3                                                            
CONECT   24    3                                                            
CONECT   25    5                                                            
CONECT   26    6                                                            
CONECT   27    8                                                            
CONECT   28    9                                                            
CONECT   29   12                                                            
CONECT   30   14                                                            
CONECT   31   15                                                            
CONECT   32   17                                                            
CONECT   33   18                                                            
CONECT   34   18                                                            
CONECT   35   19                                                            
CONECT   36   19                                                            
MASTER        0    0    0    0    0    0    0    0   36    0   76    0
END

RDKit          3D

36 38  0  0  0  0  0  0  0  0999 V2000
    3.8693    2.4716   -0.6658 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0711    1.4432   -0.5336 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8652    0.2440    0.0316 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8398   -0.8180    0.4725 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2883   -0.6666    1.6933 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0426   -1.3116    2.0004 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4596   -2.0470    1.0580 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9777   -2.2597   -0.1498 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2324   -1.6201   -0.4825 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9378   -2.5629    1.4404 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8063   -1.4399    0.8470 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4531   -0.1197    1.0564 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1936    0.8678    0.4260 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2753    0.4286   -0.3550 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6496   -0.8848   -0.5500 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8520   -1.8640    0.0967 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2013   -3.2034   -0.0844 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8655    2.3079    0.2703 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4361    2.7391    0.0640 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4965    1.8005   -0.3309 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6846    1.5728   -0.9061 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5574    1.4215   -2.2258 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5444    0.6323    0.7597 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5580   -0.1770   -0.7162 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6466   -0.1193    2.6468 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7423   -1.1246    3.1028 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6689   -2.8861   -1.0156 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4646   -1.9509   -1.4904 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7251    0.2219    1.8740 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9187    1.1574   -0.8808 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4785   -1.1888   -1.1411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9758   -3.4508   -0.6435 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3521    2.6559   -0.7195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3487    2.9897    0.9855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1006    3.0158    1.1240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4393    3.7250   -0.4265 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  7 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 13 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  2  0
 21  2  1  0
  9  4  1  0
 16 11  2  0
  3 23  1  0
  3 24  1  0
  5 25  1  0
  6 26  1  0
  8 27  1  0
  9 28  1  0
 12 29  1  0
 14 30  1  0
 15 31  1  0
 17 32  1  0
 18 33  1  0
 18 34  1  0
 19 35  1  0
 19 36  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₁₇H₁₄O₅

Average Mass

298.2940 Da

Monoisotopic Mass

298.08412 Da

IUPAC Name

4-hydroxy-2,10-dioxatricyclo[12.2.2.1^{3,7}]nonadeca-1(16),3,5,7(19),14,17-hexaene-11,12-dione

Traditional Name

4-hydroxy-2,10-dioxatricyclo[12.2.2.1^{3,7}]nonadeca-1(16),3,5,7(19),14,17-hexaene-11,12-dione

CAS Registry Number

Not Available

SMILES

OC1=CC=C2CCOC(=O)C(=O)CC3=CC=C(OC1=C2)C=C3

InChI Identifier

InChI=1S/C17H14O5/c18-14-6-3-12-7-8-21-17(20)15(19)9-11-1-4-13(5-2-11)22-16(14)10-12/h1-6,10,18H,7-9H2

InChI Key

MTLMXGMZDJWCOI-UHFFFAOYSA-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
Melittangium boletus	NPAtlas	27397004
Retiboletus ornatipes	LOTUS Database	35616633

Chemical Taxonomy

Description

This compound belongs to the class of organic compounds known as diarylethers. These are organic compounds containing the dialkyl ether functional group, with the formula ROR', where R and R' are aryl groups.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Ethers

Direct Parent

Diarylethers

Alternative Parents

Substituents

Diaryl ether
1-hydroxy-2-unsubstituted benzenoid
Phenol
Benzenoid
Cyclic ketone
Lactone
Ketone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Carbonyl group
Hydrocarbon derivative
Organic oxide
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	3	ALOGPS
logP	3.52	ChemAxon
logS	-3.8	ALOGPS
pKa (Strongest Acidic)	8.43	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	72.83 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	79.01 m³·mol⁻¹	ChemAxon
Polarizability	29.59 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

NPAtlas ID

NPA005772

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

78434738

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

102120370

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Shibata H, Fukuda T, Wada T, Morita Y, Hashimoto T, Asakawa Y: Ornatipolide, a Novel Phenolic Metabolite from the Basidiomycete, Boletus ornatipes. Biosci Biotechnol Biochem. 1998;62(7):1432-4. doi: 10.1271/bbb.62.1432. [PubMed:27397004 ]

Showing NP-Card for Ornatipolide (NP0015553)

MOL for NP0015553 (Ornatipolide)

3D MOL for NP0015553 (Ornatipolide)

3D SDF for NP0015553 (Ornatipolide)

3D-SDF for NP0015553 (Ornatipolide)

PDB for NP0015553 (Ornatipolide)

3D PDB for NP0015553 (Ornatipolide)

SMILES for NP0015553 (Ornatipolide)

INCHI for NP0015553 (Ornatipolide)

Structure for NP0015553 (Ornatipolide)

3D Structure for NP0015553 (Ornatipolide)