NP-MRD: Showing NP-Card for Pestalrone B (NP0010977)

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Record Information

Version

2.0

Created at

2021-01-05 20:45:42 UTC

Updated at

2021-07-15 17:07:37 UTC

NP-MRD ID

NP0010977

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Pestalrone B

Provided By

NPAtlas

Description

Pestalrone B belongs to the class of organic compounds known as 1,4-dioxepanes. These are dioxepanes with the two ring oxygen atoms at position 1 and 4, respectively. Pestalrone B is found in Monochaetia karstenii and Pestalotiopsis karstenii. Pestalrone B was first documented in 2012 (PMID: 22805506). Based on a literature review very few articles have been published on Pestalrone B.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242107433D          

 33 34  0  0  0  0            999 V2000
   -3.9221    0.6002    0.0619 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5793   -0.8564   -0.2172 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3039   -1.1703    0.5375 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2332   -0.2359    0.0164 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0488   -0.5636    0.7866 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1048    0.4038    0.2281 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6125    1.6739    0.4902 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3596    2.6813   -0.0843 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3938    0.0988    0.8962 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4191   -0.5764    0.0715 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1625   -2.0376   -0.0480 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1458   -1.1908   -1.1237 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7992   -0.8974   -1.6934 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3412   -1.6390   -2.6219 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1159    0.1771   -1.1744 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0149    0.7823   -0.0978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3177    1.2869   -0.5372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7278    0.8118    1.1510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4167   -0.9377   -1.2993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3784   -1.4904    0.1805 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4111   -0.9723    1.6109 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9535   -2.2036    0.3054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4750    0.8290    0.2250 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0964   -0.3375   -1.0589 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3476   -1.6044    0.6810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0621   -0.2936    1.8473 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8781    3.6432    0.1890 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4174    2.6799    0.1684 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2719    2.6228   -1.2064 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2351   -0.5308    1.8220 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8565    1.0453    1.3067 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4688   -0.4798    0.4738 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9135   -1.3188   -1.9161 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  6  0  0  0
  7  8  1  0  0  0  0
  6  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15  6  1  0  0  0  0
 12 10  1  0  0  0  0
  1 16  1  0  0  0  0
  1 17  1  0  0  0  0
  1 18  1  0  0  0  0
  2 19  1  0  0  0  0
  2 20  1  0  0  0  0
  3 21  1  0  0  0  0
  3 22  1  0  0  0  0
  4 23  1  0  0  0  0
  4 24  1  0  0  0  0
  5 25  1  0  0  0  0
  5 26  1  0  0  0  0
  8 27  1  0  0  0  0
  8 28  1  0  0  0  0
  8 29  1  0  0  0  0
  9 30  1  0  0  0  0
  9 31  1  0  0  0  0
 10 32  1  6  0  0  0
 12 33  1  6  0  0  0
M  END

     RDKit          3D

 33 34  0  0  0  0  0  0  0  0999 V2000
   -3.9221    0.6002    0.0619 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5793   -0.8564   -0.2172 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3039   -1.1703    0.5375 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2332   -0.2359    0.0164 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0488   -0.5636    0.7866 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1048    0.4038    0.2281 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6125    1.6739    0.4902 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3596    2.6813   -0.0843 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3938    0.0988    0.8962 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4191   -0.5764    0.0715 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1625   -2.0376   -0.0480 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1458   -1.1908   -1.1237 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7992   -0.8974   -1.6934 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3412   -1.6390   -2.6219 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1159    0.1771   -1.1744 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0149    0.7823   -0.0978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3177    1.2869   -0.5372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7278    0.8118    1.1510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4167   -0.9377   -1.2993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3784   -1.4904    0.1805 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4111   -0.9723    1.6109 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9535   -2.2036    0.3054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4750    0.8290    0.2250 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0964   -0.3375   -1.0589 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3476   -1.6044    0.6810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0621   -0.2936    1.8473 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8781    3.6432    0.1890 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4174    2.6799    0.1684 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2719    2.6228   -1.2064 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2351   -0.5308    1.8220 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8565    1.0453    1.3067 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4688   -0.4798    0.4738 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9135   -1.3188   -1.9161 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  6
  7  8  1  0
  6  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 13 15  1  0
 15  6  1  0
 12 10  1  0
  1 16  1  0
  1 17  1  0
  1 18  1  0
  2 19  1  0
  2 20  1  0
  3 21  1  0
  3 22  1  0
  4 23  1  0
  4 24  1  0
  5 25  1  0
  5 26  1  0
  8 27  1  0
  8 28  1  0
  8 29  1  0
  9 30  1  0
  9 31  1  0
 10 32  1  6
 12 33  1  6
M  END


  Mrv1652306242107433D          

 33 34  0  0  0  0            999 V2000
   -3.9221    0.6002    0.0619 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5793   -0.8564   -0.2172 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3039   -1.1703    0.5375 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2332   -0.2359    0.0164 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0488   -0.5636    0.7866 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1048    0.4038    0.2281 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6125    1.6739    0.4902 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3596    2.6813   -0.0843 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3938    0.0988    0.8962 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4191   -0.5764    0.0715 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1625   -2.0376   -0.0480 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1458   -1.1908   -1.1237 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7992   -0.8974   -1.6934 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3412   -1.6390   -2.6219 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1159    0.1771   -1.1744 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0149    0.7823   -0.0978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3177    1.2869   -0.5372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7278    0.8118    1.1510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4167   -0.9377   -1.2993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3784   -1.4904    0.1805 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4111   -0.9723    1.6109 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9535   -2.2036    0.3054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4750    0.8290    0.2250 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0964   -0.3375   -1.0589 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3476   -1.6044    0.6810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0621   -0.2936    1.8473 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8781    3.6432    0.1890 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4174    2.6799    0.1684 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2719    2.6228   -1.2064 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2351   -0.5308    1.8220 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8565    1.0453    1.3067 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4688   -0.4798    0.4738 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9135   -1.3188   -1.9161 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  6  0  0  0
  7  8  1  0  0  0  0
  6  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15  6  1  0  0  0  0
 12 10  1  0  0  0  0
  1 16  1  0  0  0  0
  1 17  1  0  0  0  0
  1 18  1  0  0  0  0
  2 19  1  0  0  0  0
  2 20  1  0  0  0  0
  3 21  1  0  0  0  0
  3 22  1  0  0  0  0
  4 23  1  0  0  0  0
  4 24  1  0  0  0  0
  5 25  1  0  0  0  0
  5 26  1  0  0  0  0
  8 27  1  0  0  0  0
  8 28  1  0  0  0  0
  8 29  1  0  0  0  0
  9 30  1  0  0  0  0
  9 31  1  0  0  0  0
 10 32  1  6  0  0  0
 12 33  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0010977

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]C([H])([H])O[C@]1(OC(=O)[C@]2([H])O[C@]2([H])C1([H])[H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C11H18O4/c1-3-4-5-6-11(13-2)7-8-9(14-8)10(12)15-11/h8-9H,3-7H2,1-2H3/t8-,9-,11+/m1/s1

> <INCHI_KEY>
NINCXQRSQVSCLG-KKZNHRDASA-N

> <FORMULA>
C11H18O4

> <MOLECULAR_WEIGHT>
214.261

> <EXACT_MASS>
214.12050906

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
33

> <JCHEM_AVERAGE_POLARIZABILITY>
22.49981463347531

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,4S,6R)-4-methoxy-4-pentyl-3,7-dioxabicyclo[4.1.0]heptan-2-one

> <ALOGPS_LOGP>
1.69

> <JCHEM_LOGP>
2.4449478019999997

> <ALOGPS_LOGS>
-1.68

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-3.9968401906624096

> <JCHEM_POLAR_SURFACE_AREA>
48.06

> <JCHEM_REFRACTIVITY>
52.87020000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.44e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,4S,6R)-4-methoxy-4-pentyl-3,7-dioxabicyclo[4.1.0]heptan-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 33 34  0  0  0  0  0  0  0  0999 V2000
   -3.9221    0.6002    0.0619 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5793   -0.8564   -0.2172 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3039   -1.1703    0.5375 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2332   -0.2359    0.0164 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0488   -0.5636    0.7866 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1048    0.4038    0.2281 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6125    1.6739    0.4902 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3596    2.6813   -0.0843 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3938    0.0988    0.8962 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4191   -0.5764    0.0715 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1625   -2.0376   -0.0480 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1458   -1.1908   -1.1237 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7992   -0.8974   -1.6934 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3412   -1.6390   -2.6219 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1159    0.1771   -1.1744 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0149    0.7823   -0.0978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3177    1.2869   -0.5372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7278    0.8118    1.1510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4167   -0.9377   -1.2993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3784   -1.4904    0.1805 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4111   -0.9723    1.6109 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9535   -2.2036    0.3054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4750    0.8290    0.2250 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0964   -0.3375   -1.0589 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3476   -1.6044    0.6810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0621   -0.2936    1.8473 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8781    3.6432    0.1890 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4174    2.6799    0.1684 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2719    2.6228   -1.2064 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2351   -0.5308    1.8220 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8565    1.0453    1.3067 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4688   -0.4798    0.4738 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9135   -1.3188   -1.9161 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  6
  7  8  1  0
  6  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 13 15  1  0
 15  6  1  0
 12 10  1  0
  1 16  1  0
  1 17  1  0
  1 18  1  0
  2 19  1  0
  2 20  1  0
  3 21  1  0
  3 22  1  0
  4 23  1  0
  4 24  1  0
  5 25  1  0
  5 26  1  0
  8 27  1  0
  8 28  1  0
  8 29  1  0
  9 30  1  0
  9 31  1  0
 10 32  1  6
 12 33  1  6
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      -3.922   0.600   0.062  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.579  -0.856  -0.217  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.304  -1.170   0.538  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.233  -0.236   0.016  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.049  -0.564   0.787  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.105   0.404   0.228  0.00  0.00           C+0
HETATM    7  O   UNK     0       0.613   1.674   0.490  0.00  0.00           O+0
HETATM    8  C   UNK     0       1.360   2.681  -0.084  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.394   0.099   0.896  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.419  -0.576   0.072  0.00  0.00           C+0
HETATM   11  O   UNK     0       3.163  -2.038  -0.048  0.00  0.00           O+0
HETATM   12  C   UNK     0       3.146  -1.191  -1.124  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.799  -0.897  -1.693  0.00  0.00           C+0
HETATM   14  O   UNK     0       1.341  -1.639  -2.622  0.00  0.00           O+0
HETATM   15  O   UNK     0       1.116   0.177  -1.174  0.00  0.00           O+0
HETATM   16  H   UNK     0      -5.015   0.782  -0.098  0.00  0.00           H+0
HETATM   17  H   UNK     0      -3.318   1.287  -0.537  0.00  0.00           H+0
HETATM   18  H   UNK     0      -3.728   0.812   1.151  0.00  0.00           H+0
HETATM   19  H   UNK     0      -3.417  -0.938  -1.299  0.00  0.00           H+0
HETATM   20  H   UNK     0      -4.378  -1.490   0.181  0.00  0.00           H+0
HETATM   21  H   UNK     0      -2.411  -0.972   1.611  0.00  0.00           H+0
HETATM   22  H   UNK     0      -1.954  -2.204   0.305  0.00  0.00           H+0
HETATM   23  H   UNK     0      -1.475   0.829   0.225  0.00  0.00           H+0
HETATM   24  H   UNK     0      -1.096  -0.338  -1.059  0.00  0.00           H+0
HETATM   25  H   UNK     0       0.348  -1.604   0.681  0.00  0.00           H+0
HETATM   26  H   UNK     0      -0.062  -0.294   1.847  0.00  0.00           H+0
HETATM   27  H   UNK     0       0.878   3.643   0.189  0.00  0.00           H+0
HETATM   28  H   UNK     0       2.417   2.680   0.168  0.00  0.00           H+0
HETATM   29  H   UNK     0       1.272   2.623  -1.206  0.00  0.00           H+0
HETATM   30  H   UNK     0       2.235  -0.531   1.822  0.00  0.00           H+0
HETATM   31  H   UNK     0       2.857   1.045   1.307  0.00  0.00           H+0
HETATM   32  H   UNK     0       4.469  -0.480   0.474  0.00  0.00           H+0
HETATM   33  H   UNK     0       3.914  -1.319  -1.916  0.00  0.00           H+0
CONECT    1    2   16   17   18                                             
CONECT    2    1    3   19   20                                             
CONECT    3    2    4   21   22                                             
CONECT    4    3    5   23   24                                             
CONECT    5    4    6   25   26                                             
CONECT    6    5    7    9   15                                             
CONECT    7    6    8                                                       
CONECT    8    7   27   28   29                                             
CONECT    9    6   10   30   31                                             
CONECT   10    9   11   12   32                                             
CONECT   11   10   12                                                       
CONECT   12   11   13   10   33                                             
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13    6                                                       
CONECT   16    1                                                            
CONECT   17    1                                                            
CONECT   18    1                                                            
CONECT   19    2                                                            
CONECT   20    2                                                            
CONECT   21    3                                                            
CONECT   22    3                                                            
CONECT   23    4                                                            
CONECT   24    4                                                            
CONECT   25    5                                                            
CONECT   26    5                                                            
CONECT   27    8                                                            
CONECT   28    8                                                            
CONECT   29    8                                                            
CONECT   30    9                                                            
CONECT   31    9                                                            
CONECT   32   10                                                            
CONECT   33   12                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   68    0
END

RDKit          3D

33 34  0  0  0  0  0  0  0  0999 V2000
   -3.9221    0.6002    0.0619 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5793   -0.8564   -0.2172 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3039   -1.1703    0.5375 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2332   -0.2359    0.0164 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0488   -0.5636    0.7866 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1048    0.4038    0.2281 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6125    1.6739    0.4902 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3596    2.6813   -0.0843 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3938    0.0988    0.8962 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4191   -0.5764    0.0715 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1625   -2.0376   -0.0480 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1458   -1.1908   -1.1237 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7992   -0.8974   -1.6934 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3412   -1.6390   -2.6219 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1159    0.1771   -1.1744 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0149    0.7823   -0.0978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3177    1.2869   -0.5372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7278    0.8118    1.1510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4167   -0.9377   -1.2993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3784   -1.4904    0.1805 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4111   -0.9723    1.6109 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9535   -2.2036    0.3054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4750    0.8290    0.2250 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0964   -0.3375   -1.0589 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3476   -1.6044    0.6810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0621   -0.2936    1.8473 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8781    3.6432    0.1890 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4174    2.6799    0.1684 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2719    2.6228   -1.2064 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2351   -0.5308    1.8220 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8565    1.0453    1.3067 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4688   -0.4798    0.4738 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9135   -1.3188   -1.9161 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  6
  7  8  1  0
  6  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 13 15  1  0
 15  6  1  0
 12 10  1  0
  1 16  1  0
  1 17  1  0
  1 18  1  0
  2 19  1  0
  2 20  1  0
  3 21  1  0
  3 22  1  0
  4 23  1  0
  4 24  1  0
  5 25  1  0
  5 26  1  0
  8 27  1  0
  8 28  1  0
  8 29  1  0
  9 30  1  0
  9 31  1  0
 10 32  1  6
 12 33  1  6
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₁₁H₁₈O₄

Average Mass

214.2610 Da

Monoisotopic Mass

214.12051 Da

IUPAC Name

(1R,4S,6R)-4-methoxy-4-pentyl-3,7-dioxabicyclo[4.1.0]heptan-2-one

Traditional Name

(1R,4S,6R)-4-methoxy-4-pentyl-3,7-dioxabicyclo[4.1.0]heptan-2-one

CAS Registry Number

Not Available

SMILES

CCCCC[C@]1(C[C@H]2O[C@H]2C(=O)O1)OC

InChI Identifier

InChI=1S/C11H18O4/c1-3-4-5-6-11(13-2)7-8-9(14-8)10(12)15-11/h8-9H,3-7H2,1-2H3/t8-,9-,11+/m1/s1

InChI Key

NINCXQRSQVSCLG-KKZNHRDASA-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
Monochaetia karstenii	LOTUS Database	35616633
Pestalotiopsis karstenii	NPAtlas	22805506

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 1,4-dioxepanes. These are dioxepanes with the two ring oxygen atoms at position 1 and 4, respectively.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Dioxepanes

Sub Class

1,4-dioxepanes

Direct Parent

1,4-dioxepanes

Alternative Parents

Substituents

Ketal
Delta_valerolactone
Delta valerolactone
1,4-dioxepane
Oxane
Lactone
Carboxylic acid ester
Oxacycle
Monocarboxylic acid or derivatives
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	1.69	ALOGPS
logP	2.44	ChemAxon
logS	-1.7	ALOGPS
pKa (Strongest Basic)	-4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	48.06 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	52.87 m³·mol⁻¹	ChemAxon
Polarizability	22.5 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

NPA002303

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

78439605

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139583738

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Luo du Q, Zhang L, Shi BZ, Song XM: Two new oxysporone derivatives from the fermentation broth of the endophytic plant fungus Pestalotiopsis karstenii isolated from stems of Camellia sasanqua. Molecules. 2012 Jul 17;17(7):8554-60. doi: 10.3390/molecules17078554. [PubMed:22805506 ]

Showing NP-Card for Pestalrone B (NP0010977)

MOL for NP0010977 (Pestalrone B)

3D MOL for NP0010977 (Pestalrone B)

3D SDF for NP0010977 (Pestalrone B)

3D-SDF for NP0010977 (Pestalrone B)

PDB for NP0010977 (Pestalrone B)

3D PDB for NP0010977 (Pestalrone B)

SMILES for NP0010977 (Pestalrone B)

INCHI for NP0010977 (Pestalrone B)

Structure for NP0010977 (Pestalrone B)

3D Structure for NP0010977 (Pestalrone B)