NP-MRD: Showing NP-Card for Xerulin (NP0010911)

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Record Information

Version

2.0

Created at

2021-01-05 20:42:40 UTC

Updated at

2021-07-15 17:07:25 UTC

NP-MRD ID

NP0010911

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Xerulin

Provided By

NPAtlas

Description

5-(Tetradeca-2,4,6,12-tetraen-8,10-diyn-1-ylidene)-2,5-dihydrofuran-2-one belongs to the class of organic compounds known as butenolides. These are dihydrofurans with a carbonyl group at the C2 carbon atom. Xerulin is found in Xerula melanotricha and Xerula melanotricha sp. 80241. Xerulin was first documented in 1990 (PMID: 2272917). Based on a literature review very few articles have been published on 5-(tetradeca-2,4,6,12-tetraen-8,10-diyn-1-ylidene)-2,5-dihydrofuran-2-one.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242107423D          

 34 34  0  0  0  0            999 V2000
    8.0376    0.0891    0.5070 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1324   -0.8791    1.6099 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0903   -1.5948    1.9398 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8703   -1.4016    1.1934 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8415   -1.2256    0.5816 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6317   -1.0436   -0.1224 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5945   -0.9138   -0.7260 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3418   -0.7931   -1.4302 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2239   -0.4178   -0.7980 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9954   -0.3174   -1.5494 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1444    0.0218   -1.0853 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3311    0.3641    0.3540 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4814    0.6649    0.7791 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7314    0.9918    1.2414 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8488    1.0195    0.4840 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0201    0.7289   -0.9266 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3200    0.8920   -1.2357 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0534    1.2908   -0.0598 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2880    1.5437    0.0795 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1132    1.3576    0.9757 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4475   -0.3734   -0.4015 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5479    1.0672    0.7355 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9868    0.3637    0.2983 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0551   -0.9918    2.1300 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1695   -2.2940    2.7558 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3468   -1.0173   -2.4927 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2932   -0.2112    0.2411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9838   -0.5527   -2.6497 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9960    0.0577   -1.7390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4209    0.2304    0.9397 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9083    0.8856    2.0458 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9873    1.2791    2.3033 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2666    0.4372   -1.6122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7210    0.7422   -2.2066 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  3  0  0  0  0
  5  6  1  0  0  0  0
  6  7  3  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  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  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 15  1  0  0  0  0
  1 21  1  0  0  0  0
  1 22  1  0  0  0  0
  1 23  1  0  0  0  0
  2 24  1  0  0  0  0
  3 25  1  0  0  0  0
  8 26  1  0  0  0  0
  9 27  1  0  0  0  0
 10 28  1  0  0  0  0
 11 29  1  0  0  0  0
 12 30  1  0  0  0  0
 13 31  1  0  0  0  0
 14 32  1  0  0  0  0
 16 33  1  0  0  0  0
 17 34  1  0  0  0  0
M  END

     RDKit          3D

 34 34  0  0  0  0  0  0  0  0999 V2000
    8.0376    0.0891    0.5070 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1324   -0.8791    1.6099 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0903   -1.5948    1.9398 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8703   -1.4016    1.1934 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8415   -1.2256    0.5816 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6317   -1.0436   -0.1224 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5945   -0.9138   -0.7260 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3418   -0.7931   -1.4302 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2239   -0.4178   -0.7980 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9954   -0.3174   -1.5494 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1444    0.0218   -1.0853 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3311    0.3641    0.3540 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4814    0.6649    0.7791 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7314    0.9918    1.2414 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8488    1.0195    0.4840 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0201    0.7289   -0.9266 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3200    0.8920   -1.2357 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0534    1.2908   -0.0598 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2880    1.5437    0.0795 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1132    1.3576    0.9757 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4475   -0.3734   -0.4015 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5479    1.0672    0.7355 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9868    0.3637    0.2983 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0551   -0.9918    2.1300 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1695   -2.2940    2.7558 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3468   -1.0173   -2.4927 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2932   -0.2112    0.2411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9838   -0.5527   -2.6497 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9960    0.0577   -1.7390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4209    0.2304    0.9397 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9083    0.8856    2.0458 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9873    1.2791    2.3033 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2666    0.4372   -1.6122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7210    0.7422   -2.2066 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  3  0
  5  6  1  0
  6  7  3  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 15  1  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
  2 24  1  0
  3 25  1  0
  8 26  1  0
  9 27  1  0
 10 28  1  0
 11 29  1  0
 12 30  1  0
 13 31  1  0
 14 32  1  0
 16 33  1  0
 17 34  1  0
M  END


  Mrv1652306242107423D          

 34 34  0  0  0  0            999 V2000
    8.0376    0.0891    0.5070 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1324   -0.8791    1.6099 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0903   -1.5948    1.9398 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8703   -1.4016    1.1934 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8415   -1.2256    0.5816 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6317   -1.0436   -0.1224 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5945   -0.9138   -0.7260 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3418   -0.7931   -1.4302 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2239   -0.4178   -0.7980 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9954   -0.3174   -1.5494 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1444    0.0218   -1.0853 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3311    0.3641    0.3540 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4814    0.6649    0.7791 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7314    0.9918    1.2414 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8488    1.0195    0.4840 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0201    0.7289   -0.9266 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3200    0.8920   -1.2357 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0534    1.2908   -0.0598 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2880    1.5437    0.0795 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1132    1.3576    0.9757 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4475   -0.3734   -0.4015 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5479    1.0672    0.7355 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9868    0.3637    0.2983 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0551   -0.9918    2.1300 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1695   -2.2940    2.7558 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3468   -1.0173   -2.4927 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2932   -0.2112    0.2411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9838   -0.5527   -2.6497 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9960    0.0577   -1.7390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4209    0.2304    0.9397 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9083    0.8856    2.0458 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9873    1.2791    2.3033 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2666    0.4372   -1.6122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7210    0.7422   -2.2066 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  3  0  0  0  0
  5  6  1  0  0  0  0
  6  7  3  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  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  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 15  1  0  0  0  0
  1 21  1  0  0  0  0
  1 22  1  0  0  0  0
  1 23  1  0  0  0  0
  2 24  1  0  0  0  0
  3 25  1  0  0  0  0
  8 26  1  0  0  0  0
  9 27  1  0  0  0  0
 10 28  1  0  0  0  0
 11 29  1  0  0  0  0
 12 30  1  0  0  0  0
 13 31  1  0  0  0  0
 14 32  1  0  0  0  0
 16 33  1  0  0  0  0
 17 34  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0010911

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]\C(C#CC#C\C([H])=C(\[H])C([H])([H])[H])=C(\[H])/C(/[H])=C(/[H])C([H])=C([H])C(\[H])=C1\OC(=O)C([H])=C1[H]

> <INCHI_IDENTIFIER>
InChI=1S/C18H14O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-17-15-16-18(19)20-17/h2-3,8-16H,1H3/b3-2-,9-8+,11-10-,13-12-,17-14+

> <INCHI_KEY>
NVTZKVXKAGVWNW-UHFFFAOYSA-N

> <FORMULA>
C18H14O2

> <MOLECULAR_WEIGHT>
262.308

> <EXACT_MASS>
262.099379691

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
34

> <JCHEM_AVERAGE_POLARIZABILITY>
31.269337834333985

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(5E)-5-[(4Z,6E,12Z)-tetradeca-2,4,6,12-tetraen-8,10-diyn-1-ylidene]-2,5-dihydrofuran-2-one

> <ALOGPS_LOGP>
4.99

> <JCHEM_LOGP>
4.2000070879999996

> <ALOGPS_LOGS>
-4.69

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-6.9465919333233055

> <JCHEM_POLAR_SURFACE_AREA>
26.3

> <JCHEM_REFRACTIVITY>
90.08479999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.30e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(5E)-5-[(4Z,6E,12Z)-tetradeca-2,4,6,12-tetraen-8,10-diyn-1-ylidene]furan-2-one

> <JCHEM_VEBER_RULE>
1

$$$$

     RDKit          3D

 34 34  0  0  0  0  0  0  0  0999 V2000
    8.0376    0.0891    0.5070 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1324   -0.8791    1.6099 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0903   -1.5948    1.9398 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8703   -1.4016    1.1934 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8415   -1.2256    0.5816 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6317   -1.0436   -0.1224 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5945   -0.9138   -0.7260 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3418   -0.7931   -1.4302 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2239   -0.4178   -0.7980 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9954   -0.3174   -1.5494 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1444    0.0218   -1.0853 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3311    0.3641    0.3540 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4814    0.6649    0.7791 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7314    0.9918    1.2414 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8488    1.0195    0.4840 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0201    0.7289   -0.9266 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3200    0.8920   -1.2357 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0534    1.2908   -0.0598 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2880    1.5437    0.0795 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1132    1.3576    0.9757 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4475   -0.3734   -0.4015 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5479    1.0672    0.7355 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9868    0.3637    0.2983 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0551   -0.9918    2.1300 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1695   -2.2940    2.7558 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3468   -1.0173   -2.4927 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2932   -0.2112    0.2411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9838   -0.5527   -2.6497 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9960    0.0577   -1.7390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4209    0.2304    0.9397 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9083    0.8856    2.0458 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9873    1.2791    2.3033 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2666    0.4372   -1.6122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7210    0.7422   -2.2066 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  3  0
  5  6  1  0
  6  7  3  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 15  1  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
  2 24  1  0
  3 25  1  0
  8 26  1  0
  9 27  1  0
 10 28  1  0
 11 29  1  0
 12 30  1  0
 13 31  1  0
 14 32  1  0
 16 33  1  0
 17 34  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       8.038   0.089   0.507  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.132  -0.879   1.610  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.090  -1.595   1.940  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.870  -1.402   1.193  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.841  -1.226   0.582  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.632  -1.044  -0.122  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.595  -0.914  -0.726  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.342  -0.793  -1.430  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.224  -0.418  -0.798  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.995  -0.317  -1.549  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.144   0.022  -1.085  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.331   0.364   0.354  0.00  0.00           C+0
HETATM   13  C   UNK     0      -3.481   0.665   0.779  0.00  0.00           C+0
HETATM   14  C   UNK     0      -4.731   0.992   1.241  0.00  0.00           C+0
HETATM   15  C   UNK     0      -5.849   1.020   0.484  0.00  0.00           C+0
HETATM   16  C   UNK     0      -6.020   0.729  -0.927  0.00  0.00           C+0
HETATM   17  C   UNK     0      -7.320   0.892  -1.236  0.00  0.00           C+0
HETATM   18  C   UNK     0      -8.053   1.291  -0.060  0.00  0.00           C+0
HETATM   19  O   UNK     0      -9.288   1.544   0.080  0.00  0.00           O+0
HETATM   20  O   UNK     0      -7.113   1.358   0.976  0.00  0.00           O+0
HETATM   21  H   UNK     0       8.447  -0.373  -0.402  0.00  0.00           H+0
HETATM   22  H   UNK     0       8.548   1.067   0.736  0.00  0.00           H+0
HETATM   23  H   UNK     0       6.987   0.364   0.298  0.00  0.00           H+0
HETATM   24  H   UNK     0       9.055  -0.992   2.130  0.00  0.00           H+0
HETATM   25  H   UNK     0       7.170  -2.294   2.756  0.00  0.00           H+0
HETATM   26  H   UNK     0       1.347  -1.017  -2.493  0.00  0.00           H+0
HETATM   27  H   UNK     0       0.293  -0.211   0.241  0.00  0.00           H+0
HETATM   28  H   UNK     0      -0.984  -0.553  -2.650  0.00  0.00           H+0
HETATM   29  H   UNK     0      -2.996   0.058  -1.739  0.00  0.00           H+0
HETATM   30  H   UNK     0      -1.421   0.230   0.940  0.00  0.00           H+0
HETATM   31  H   UNK     0      -2.908   0.886   2.046  0.00  0.00           H+0
HETATM   32  H   UNK     0      -4.987   1.279   2.303  0.00  0.00           H+0
HETATM   33  H   UNK     0      -5.267   0.437  -1.612  0.00  0.00           H+0
HETATM   34  H   UNK     0      -7.721   0.742  -2.207  0.00  0.00           H+0
CONECT    1    2   21   22   23                                             
CONECT    2    1    3   24                                                  
CONECT    3    2    4   25                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   26                                                  
CONECT    9    8   10   27                                                  
CONECT   10    9   11   28                                                  
CONECT   11   10   12   29                                                  
CONECT   12   11   13   30                                                  
CONECT   13   12   14   31                                                  
CONECT   14   13   15   32                                                  
CONECT   15   14   16   20                                                  
CONECT   16   15   17   33                                                  
CONECT   17   16   18   34                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   15                                                       
CONECT   21    1                                                            
CONECT   22    1                                                            
CONECT   23    1                                                            
CONECT   24    2                                                            
CONECT   25    3                                                            
CONECT   26    8                                                            
CONECT   27    9                                                            
CONECT   28   10                                                            
CONECT   29   11                                                            
CONECT   30   12                                                            
CONECT   31   13                                                            
CONECT   32   14                                                            
CONECT   33   16                                                            
CONECT   34   17                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   68    0
END

RDKit          3D

34 34  0  0  0  0  0  0  0  0999 V2000
    8.0376    0.0891    0.5070 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1324   -0.8791    1.6099 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0903   -1.5948    1.9398 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8703   -1.4016    1.1934 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8415   -1.2256    0.5816 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6317   -1.0436   -0.1224 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5945   -0.9138   -0.7260 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3418   -0.7931   -1.4302 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2239   -0.4178   -0.7980 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9954   -0.3174   -1.5494 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1444    0.0218   -1.0853 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3311    0.3641    0.3540 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4814    0.6649    0.7791 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7314    0.9918    1.2414 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8488    1.0195    0.4840 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0201    0.7289   -0.9266 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3200    0.8920   -1.2357 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0534    1.2908   -0.0598 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2880    1.5437    0.0795 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1132    1.3576    0.9757 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4475   -0.3734   -0.4015 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5479    1.0672    0.7355 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9868    0.3637    0.2983 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0551   -0.9918    2.1300 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1695   -2.2940    2.7558 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3468   -1.0173   -2.4927 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2932   -0.2112    0.2411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9838   -0.5527   -2.6497 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9960    0.0577   -1.7390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4209    0.2304    0.9397 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9083    0.8856    2.0458 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9873    1.2791    2.3033 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2666    0.4372   -1.6122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7210    0.7422   -2.2066 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  3  0
  5  6  1  0
  6  7  3  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 15  1  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
  2 24  1  0
  3 25  1  0
  8 26  1  0
  9 27  1  0
 10 28  1  0
 11 29  1  0
 12 30  1  0
 13 31  1  0
 14 32  1  0
 16 33  1  0
 17 34  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₁₈H₁₄O₂

Average Mass

262.3080 Da

Monoisotopic Mass

262.09938 Da

IUPAC Name

(5E)-5-[(4Z,6E,12Z)-tetradeca-2,4,6,12-tetraen-8,10-diyn-1-ylidene]-2,5-dihydrofuran-2-one

Traditional Name

(5E)-5-[(4Z,6E,12Z)-tetradeca-2,4,6,12-tetraen-8,10-diyn-1-ylidene]furan-2-one

CAS Registry Number

Not Available

SMILES

CC=CC#CC#CC=CC=CC=CC=C1OC(=O)C=C1

InChI Identifier

InChI=1S/C18H14O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-17-15-16-18(19)20-17/h2-3,8-16H,1H3

InChI Key

NVTZKVXKAGVWNW-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
Xerula melanotricha	NPAtlas	2272917
Xerula melanotricha sp. 80241	Fungi	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as butenolides. These are dihydrofurans with a carbonyl group at the C2 carbon atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Dihydrofurans

Sub Class

Furanones

Direct Parent

Butenolides

Alternative Parents

Substituents

2-furanone
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Enol ester
Lactone
Carboxylic acid ester
Oxacycle
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic 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	4.99	ALOGPS
logP	4.2	ChemAxon
logS	-4.7	ALOGPS
pKa (Strongest Basic)	-6.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	26.3 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	90.08 m³·mol⁻¹	ChemAxon
Polarizability	31.27 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

NPAtlas ID

NPA004033

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

131570

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Kuhnt D, Anke T, Besl H, Bross M, Herrmann R, Mocek U, Steffan B, Steglich W: Antibiotics from basidiomycetes. XXXVII. New inhibitors of cholesterol biosynthesis from cultures of Xerula melanotricha Dorfelt. J Antibiot (Tokyo). 1990 Nov;43(11):1413-20. doi: 10.7164/antibiotics.43.1413. [PubMed:2272917 ]

Showing NP-Card for Xerulin (NP0010911)

MOL for NP0010911 (Xerulin)

3D MOL for NP0010911 (Xerulin)

3D SDF for NP0010911 (Xerulin)

3D-SDF for NP0010911 (Xerulin)

PDB for NP0010911 (Xerulin)

3D PDB for NP0010911 (Xerulin)

SMILES for NP0010911 (Xerulin)

INCHI for NP0010911 (Xerulin)

Structure for NP0010911 (Xerulin)

3D Structure for NP0010911 (Xerulin)