NP-MRD: Showing NP-Card for anthecularin (NP0025215)

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Record Information

Version

2.0

Created at

2021-06-19 17:23:55 UTC

Updated at

2021-06-29 23:50:00 UTC

NP-MRD ID

NP0025215

Secondary Accession Numbers

None

Natural Product Identification

Common Name

anthecularin

Provided By

JEOL Database JEOL Logo

Description

Anthecularin belongs to the class of organic compounds known as furofurans. These are organic compounds containing a two furan rings fused to each other. Furan is a five-membered aromatic ring with four carbon atoms and one oxygen atom. anthecularin is found in Anthemis auriculata. anthecularin was first documented in 2007 (Karioti, A., et al.). Based on a literature review very few articles have been published on Anthecularin.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306192119233D          

 36 39  0  0  0  0            999 V2000
   -2.8176   -0.7406    3.5711 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1309   -0.6138    2.2429 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9868    0.0781    2.0917 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2284    0.1737    0.8021 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2218   -0.2479    0.9807 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1970    0.2653    0.2061 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6332   -0.1411    0.3110 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8412    1.3131   -0.8239 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3181    1.5478   -0.9286 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1949    1.5794    0.4224 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5629    0.4668   -1.5652 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0156   -0.3910   -2.6556 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3568   -1.6408   -2.0643 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2396   -1.7761   -0.8443 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2339   -2.8207   -0.2114 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8967   -0.4877   -0.4185 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4123   -0.6780   -0.2661 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7947   -1.3031    1.0792 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9129   -1.7954    3.8483 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2658   -0.2342    4.3701 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8187   -0.3001    3.5255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5478    0.5940    2.9428 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4395   -1.0298    1.7050 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2564    0.7255    0.5535 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7891   -0.8949    1.0897 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9779   -0.5636   -0.6382 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3087    2.2518   -0.4984 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2688    1.0650   -1.7995 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1342    2.5191   -1.4008 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4602    0.9746   -1.9428 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7314   -0.5924   -3.4317 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8890    0.0421   -3.1484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9169    0.2952   -0.3416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8125   -1.2987   -1.0778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5381   -2.3684    1.0985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8848   -1.2373    1.1825 H   0  0  0  0  0  0  0  0  0  0  0  0
  9  8  1  0  0  0  0
  4  3  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18  2  1  0  0  0  0
  2  3  2  0  0  0  0
  6  8  1  0  0  0  0
 16 14  1  6  0  0  0
  4 16  1  0  0  0  0
 11 12  1  0  0  0  0
 16 11  1  0  0  0  0
 12 13  1  0  0  0  0
 14 13  1  0  0  0  0
 11  9  1  0  0  0  0
 14 15  2  0  0  0  0
  2  1  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  4  5  1  0  0  0  0
  4 10  1  0  0  0  0
  9 10  1  0  0  0  0
 11 30  1  6  0  0  0
  5 23  1  0  0  0  0
  9 29  1  6  0  0  0
  8 27  1  0  0  0  0
  8 28  1  0  0  0  0
 17 33  1  0  0  0  0
 17 34  1  0  0  0  0
 18 35  1  0  0  0  0
 18 36  1  0  0  0  0
  3 22  1  0  0  0  0
 12 31  1  0  0  0  0
 12 32  1  0  0  0  0
  1 19  1  0  0  0  0
  1 20  1  0  0  0  0
  1 21  1  0  0  0  0
  7 24  1  0  0  0  0
  7 25  1  0  0  0  0
  7 26  1  0  0  0  0
M  END

     RDKit          3D

 36 39  0  0  0  0  0  0  0  0999 V2000
   -2.8176   -0.7406    3.5711 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1309   -0.6138    2.2429 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9868    0.0781    2.0917 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2284    0.1737    0.8021 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2218   -0.2479    0.9807 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1970    0.2653    0.2061 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6332   -0.1411    0.3110 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8412    1.3131   -0.8239 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3181    1.5478   -0.9286 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1949    1.5794    0.4224 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5629    0.4668   -1.5652 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0156   -0.3910   -2.6556 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3568   -1.6408   -2.0643 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2396   -1.7761   -0.8443 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2339   -2.8207   -0.2114 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8967   -0.4877   -0.4185 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4123   -0.6780   -0.2661 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7947   -1.3031    1.0792 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9129   -1.7954    3.8483 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2658   -0.2342    4.3701 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8187   -0.3001    3.5255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5478    0.5940    2.9428 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4395   -1.0298    1.7050 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2564    0.7255    0.5535 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7891   -0.8949    1.0897 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9779   -0.5636   -0.6382 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3087    2.2518   -0.4984 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2688    1.0650   -1.7995 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1342    2.5191   -1.4008 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4602    0.9746   -1.9428 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7314   -0.5924   -3.4317 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8890    0.0421   -3.1484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9169    0.2952   -0.3416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8125   -1.2987   -1.0778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5381   -2.3684    1.0985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8848   -1.2373    1.1825 H   0  0  0  0  0  0  0  0  0  0  0  0
  9  8  1  0
  4  3  1  1
 16 17  1  0
 17 18  1  0
 18  2  1  0
  2  3  2  0
  6  8  1  0
 16 14  1  6
  4 16  1  0
 11 12  1  0
 16 11  1  0
 12 13  1  0
 14 13  1  0
 11  9  1  0
 14 15  2  0
  2  1  1  0
  5  6  2  0
  6  7  1  0
  4  5  1  0
  4 10  1  0
  9 10  1  0
 11 30  1  6
  5 23  1  0
  9 29  1  6
  8 27  1  0
  8 28  1  0
 17 33  1  0
 17 34  1  0
 18 35  1  0
 18 36  1  0
  3 22  1  0
 12 31  1  0
 12 32  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  7 24  1  0
  7 25  1  0
  7 26  1  0
M  END


  Mrv1652306192119233D          

 36 39  0  0  0  0            999 V2000
   -2.8176   -0.7406    3.5711 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1309   -0.6138    2.2429 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9868    0.0781    2.0917 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2284    0.1737    0.8021 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2218   -0.2479    0.9807 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1970    0.2653    0.2061 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6332   -0.1411    0.3110 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8412    1.3131   -0.8239 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3181    1.5478   -0.9286 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1949    1.5794    0.4224 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5629    0.4668   -1.5652 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0156   -0.3910   -2.6556 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3568   -1.6408   -2.0643 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2396   -1.7761   -0.8443 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2339   -2.8207   -0.2114 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8967   -0.4877   -0.4185 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4123   -0.6780   -0.2661 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7947   -1.3031    1.0792 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9129   -1.7954    3.8483 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2658   -0.2342    4.3701 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8187   -0.3001    3.5255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5478    0.5940    2.9428 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4395   -1.0298    1.7050 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2564    0.7255    0.5535 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7891   -0.8949    1.0897 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9779   -0.5636   -0.6382 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3087    2.2518   -0.4984 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2688    1.0650   -1.7995 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1342    2.5191   -1.4008 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4602    0.9746   -1.9428 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7314   -0.5924   -3.4317 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8890    0.0421   -3.1484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9169    0.2952   -0.3416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8125   -1.2987   -1.0778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5381   -2.3684    1.0985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8848   -1.2373    1.1825 H   0  0  0  0  0  0  0  0  0  0  0  0
  9  8  1  0  0  0  0
  4  3  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18  2  1  0  0  0  0
  2  3  2  0  0  0  0
  6  8  1  0  0  0  0
 16 14  1  6  0  0  0
  4 16  1  0  0  0  0
 11 12  1  0  0  0  0
 16 11  1  0  0  0  0
 12 13  1  0  0  0  0
 14 13  1  0  0  0  0
 11  9  1  0  0  0  0
 14 15  2  0  0  0  0
  2  1  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  4  5  1  0  0  0  0
  4 10  1  0  0  0  0
  9 10  1  0  0  0  0
 11 30  1  6  0  0  0
  5 23  1  0  0  0  0
  9 29  1  6  0  0  0
  8 27  1  0  0  0  0
  8 28  1  0  0  0  0
 17 33  1  0  0  0  0
 17 34  1  0  0  0  0
 18 35  1  0  0  0  0
 18 36  1  0  0  0  0
  3 22  1  0  0  0  0
 12 31  1  0  0  0  0
 12 32  1  0  0  0  0
  1 19  1  0  0  0  0
  1 20  1  0  0  0  0
  1 21  1  0  0  0  0
  7 24  1  0  0  0  0
  7 25  1  0  0  0  0
  7 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0025215

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]C1=C(C([H])([H])[H])C([H])([H])C([H])([H])[C@@]23C(=O)OC([H])([H])[C@]2([H])[C@@]2([H])O[C@@]13C([H])=C(C([H])([H])[H])C2([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C15H18O3/c1-9-3-4-15-11(8-17-13(15)16)12-5-10(2)7-14(15,6-9)18-12/h6-7,11-12H,3-5,8H2,1-2H3/t11-,12+,14-,15+/m1/s1

> <INCHI_KEY>
YXZRMZMSHRWRLO-OSRDXIQISA-N

> <FORMULA>
C15H18O3

> <MOLECULAR_WEIGHT>
246.306

> <EXACT_MASS>
246.12559444

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
36

> <JCHEM_AVERAGE_POLARIZABILITY>
26.20082742554455

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,6R,10R,11S)-3,13-dimethyl-8,15-dioxatetracyclo[9.3.1.0^{1,6}.0^{6,10}]pentadeca-2,13-dien-7-one

> <ALOGPS_LOGP>
2.10

> <JCHEM_LOGP>
1.9278714856666668

> <ALOGPS_LOGS>
-2.67

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.255833825382506

> <JCHEM_POLAR_SURFACE_AREA>
35.53

> <JCHEM_REFRACTIVITY>
67.88230000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.29e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,6R,10R,11S)-3,13-dimethyl-8,15-dioxatetracyclo[9.3.1.0^{1,6}.0^{6,10}]pentadeca-2,13-dien-7-one

> <JCHEM_VEBER_RULE>
1

$$$$

     RDKit          3D

 36 39  0  0  0  0  0  0  0  0999 V2000
   -2.8176   -0.7406    3.5711 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1309   -0.6138    2.2429 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9868    0.0781    2.0917 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2284    0.1737    0.8021 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2218   -0.2479    0.9807 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1970    0.2653    0.2061 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6332   -0.1411    0.3110 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8412    1.3131   -0.8239 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3181    1.5478   -0.9286 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1949    1.5794    0.4224 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5629    0.4668   -1.5652 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0156   -0.3910   -2.6556 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3568   -1.6408   -2.0643 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2396   -1.7761   -0.8443 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2339   -2.8207   -0.2114 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8967   -0.4877   -0.4185 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4123   -0.6780   -0.2661 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7947   -1.3031    1.0792 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9129   -1.7954    3.8483 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2658   -0.2342    4.3701 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8187   -0.3001    3.5255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5478    0.5940    2.9428 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4395   -1.0298    1.7050 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2564    0.7255    0.5535 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7891   -0.8949    1.0897 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9779   -0.5636   -0.6382 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3087    2.2518   -0.4984 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2688    1.0650   -1.7995 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1342    2.5191   -1.4008 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4602    0.9746   -1.9428 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7314   -0.5924   -3.4317 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8890    0.0421   -3.1484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9169    0.2952   -0.3416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8125   -1.2987   -1.0778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5381   -2.3684    1.0985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8848   -1.2373    1.1825 H   0  0  0  0  0  0  0  0  0  0  0  0
  9  8  1  0
  4  3  1  1
 16 17  1  0
 17 18  1  0
 18  2  1  0
  2  3  2  0
  6  8  1  0
 16 14  1  6
  4 16  1  0
 11 12  1  0
 16 11  1  0
 12 13  1  0
 14 13  1  0
 11  9  1  0
 14 15  2  0
  2  1  1  0
  5  6  2  0
  6  7  1  0
  4  5  1  0
  4 10  1  0
  9 10  1  0
 11 30  1  6
  5 23  1  0
  9 29  1  6
  8 27  1  0
  8 28  1  0
 17 33  1  0
 17 34  1  0
 18 35  1  0
 18 36  1  0
  3 22  1  0
 12 31  1  0
 12 32  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  7 24  1  0
  7 25  1  0
  7 26  1  0
M  END

HEADER    PROTEIN                                 19-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-JUN-21         0                                  
HETATM    1  C   UNK     0      -2.818  -0.741   3.571  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.131  -0.614   2.243  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.987   0.078   2.092  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.228   0.174   0.802  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.222  -0.248   0.981  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.197   0.265   0.206  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.633  -0.141   0.311  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.841   1.313  -0.824  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.318   1.548  -0.929  0.00  0.00           C+0
HETATM   10  O   UNK     0      -0.195   1.579   0.422  0.00  0.00           O+0
HETATM   11  C   UNK     0      -0.563   0.467  -1.565  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.016  -0.391  -2.656  0.00  0.00           C+0
HETATM   13  O   UNK     0       0.357  -1.641  -2.064  0.00  0.00           O+0
HETATM   14  C   UNK     0      -0.240  -1.776  -0.844  0.00  0.00           C+0
HETATM   15  O   UNK     0      -0.234  -2.821  -0.211  0.00  0.00           O+0
HETATM   16  C   UNK     0      -0.897  -0.488  -0.419  0.00  0.00           C+0
HETATM   17  C   UNK     0      -2.412  -0.678  -0.266  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.795  -1.303   1.079  0.00  0.00           C+0
HETATM   19  H   UNK     0      -2.913  -1.795   3.848  0.00  0.00           H+0
HETATM   20  H   UNK     0      -2.266  -0.234   4.370  0.00  0.00           H+0
HETATM   21  H   UNK     0      -3.819  -0.300   3.526  0.00  0.00           H+0
HETATM   22  H   UNK     0      -0.548   0.594   2.943  0.00  0.00           H+0
HETATM   23  H   UNK     0       1.440  -1.030   1.705  0.00  0.00           H+0
HETATM   24  H   UNK     0       4.256   0.726   0.554  0.00  0.00           H+0
HETATM   25  H   UNK     0       3.789  -0.895   1.090  0.00  0.00           H+0
HETATM   26  H   UNK     0       3.978  -0.564  -0.638  0.00  0.00           H+0
HETATM   27  H   UNK     0       2.309   2.252  -0.498  0.00  0.00           H+0
HETATM   28  H   UNK     0       2.269   1.065  -1.800  0.00  0.00           H+0
HETATM   29  H   UNK     0       0.134   2.519  -1.401  0.00  0.00           H+0
HETATM   30  H   UNK     0      -1.460   0.975  -1.943  0.00  0.00           H+0
HETATM   31  H   UNK     0      -0.731  -0.592  -3.432  0.00  0.00           H+0
HETATM   32  H   UNK     0       0.889   0.042  -3.148  0.00  0.00           H+0
HETATM   33  H   UNK     0      -2.917   0.295  -0.342  0.00  0.00           H+0
HETATM   34  H   UNK     0      -2.813  -1.299  -1.078  0.00  0.00           H+0
HETATM   35  H   UNK     0      -2.538  -2.368   1.099  0.00  0.00           H+0
HETATM   36  H   UNK     0      -3.885  -1.237   1.183  0.00  0.00           H+0
CONECT    1    2   19   20   21                                             
CONECT    2   18    3    1                                                  
CONECT    3    4    2   22                                                  
CONECT    4    3   16    5   10                                             
CONECT    5    6    4   23                                                  
CONECT    6    8    5    7                                                  
CONECT    7    6   24   25   26                                             
CONECT    8    9    6   27   28                                             
CONECT    9    8   11   10   29                                             
CONECT   10    4    9                                                       
CONECT   11   12   16    9   30                                             
CONECT   12   11   13   31   32                                             
CONECT   13   12   14                                                       
CONECT   14   16   13   15                                                  
CONECT   15   14                                                            
CONECT   16   17   14    4   11                                             
CONECT   17   16   18   33   34                                             
CONECT   18   17    2   35   36                                             
CONECT   19    1                                                            
CONECT   20    1                                                            
CONECT   21    1                                                            
CONECT   22    3                                                            
CONECT   23    5                                                            
CONECT   24    7                                                            
CONECT   25    7                                                            
CONECT   26    7                                                            
CONECT   27    8                                                            
CONECT   28    8                                                            
CONECT   29    9                                                            
CONECT   30   11                                                            
CONECT   31   12                                                            
CONECT   32   12                                                            
CONECT   33   17                                                            
CONECT   34   17                                                            
CONECT   35   18                                                            
CONECT   36   18                                                            
MASTER        0    0    0    0    0    0    0    0   36    0   78    0
END

RDKit          3D

36 39  0  0  0  0  0  0  0  0999 V2000
   -2.8176   -0.7406    3.5711 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1309   -0.6138    2.2429 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9868    0.0781    2.0917 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2284    0.1737    0.8021 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2218   -0.2479    0.9807 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1970    0.2653    0.2061 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6332   -0.1411    0.3110 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8412    1.3131   -0.8239 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3181    1.5478   -0.9286 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1949    1.5794    0.4224 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5629    0.4668   -1.5652 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0156   -0.3910   -2.6556 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3568   -1.6408   -2.0643 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2396   -1.7761   -0.8443 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2339   -2.8207   -0.2114 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8967   -0.4877   -0.4185 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4123   -0.6780   -0.2661 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7947   -1.3031    1.0792 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9129   -1.7954    3.8483 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2658   -0.2342    4.3701 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8187   -0.3001    3.5255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5478    0.5940    2.9428 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4395   -1.0298    1.7050 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2564    0.7255    0.5535 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7891   -0.8949    1.0897 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9779   -0.5636   -0.6382 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3087    2.2518   -0.4984 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2688    1.0650   -1.7995 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1342    2.5191   -1.4008 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4602    0.9746   -1.9428 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7314   -0.5924   -3.4317 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8890    0.0421   -3.1484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9169    0.2952   -0.3416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8125   -1.2987   -1.0778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5381   -2.3684    1.0985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8848   -1.2373    1.1825 H   0  0  0  0  0  0  0  0  0  0  0  0
  9  8  1  0
  4  3  1  1
 16 17  1  0
 17 18  1  0
 18  2  1  0
  2  3  2  0
  6  8  1  0
 16 14  1  6
  4 16  1  0
 11 12  1  0
 16 11  1  0
 12 13  1  0
 14 13  1  0
 11  9  1  0
 14 15  2  0
  2  1  1  0
  5  6  2  0
  6  7  1  0
  4  5  1  0
  4 10  1  0
  9 10  1  0
 11 30  1  6
  5 23  1  0
  9 29  1  6
  8 27  1  0
  8 28  1  0
 17 33  1  0
 17 34  1  0
 18 35  1  0
 18 36  1  0
  3 22  1  0
 12 31  1  0
 12 32  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  7 24  1  0
  7 25  1  0
  7 26  1  0
M  END

View in JSmol View DFT Assignments 3D Conformers

Synonyms

Not Available

Chemical Formula

C₁₅H₁₈O₃

Average Mass

246.3060 Da

Monoisotopic Mass

246.12559 Da

IUPAC Name

(1R,6R,10R,11S)-3,13-dimethyl-8,15-dioxatetracyclo[9.3.1.0^{1,6}.0^{6,10}]pentadeca-2,13-dien-7-one

Traditional Name

(1R,6R,10R,11S)-3,13-dimethyl-8,15-dioxatetracyclo[9.3.1.0^{1,6}.0^{6,10}]pentadeca-2,13-dien-7-one

CAS Registry Number

Not Available

SMILES

[H]C1=C(C([H])([H])[H])C([H])([H])C([H])([H])[C@@]23C(=O)OC([H])([H])[C@]2([H])[C@@]2([H])O[C@@]13C([H])=C(C([H])([H])[H])C2([H])[H]

InChI Identifier

InChI=1S/C15H18O3/c1-9-3-4-15-11(8-17-13(15)16)12-5-10(2)7-14(15,6-9)18-12/h6-7,11-12H,3-5,8H2,1-2H3/t11-,12+,14-,15+/m1/s1

InChI Key

YXZRMZMSHRWRLO-OSRDXIQISA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 125 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 150 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 175 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 225 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 250 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, chcl3, 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
Anthemis auriculata	JEOL database	Karioti, A., et al, J. Org. Chem. 72, 8103 (2007)

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as furofurans. These are organic compounds containing a two furan rings fused to each other. Furan is a five-membered aromatic ring with four carbon atoms and one oxygen atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Furofurans

Sub Class

Not Available

Direct Parent

Furofurans

Alternative Parents

Substituents

Furofuran
Gamma butyrolactone
Pyran
Oxolane
Carboxylic acid ester
Lactone
Monocarboxylic acid or derivatives
Ether
Dialkyl ether
Carboxylic acid derivative
Oxacycle
Organooxygen compound
Carbonyl group
Organic oxide
Organic oxygen compound
Hydrocarbon derivative
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	2.1	ALOGPS
logP	1.93	ChemAxon
logS	-2.7	ALOGPS
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	35.53 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	67.88 m³·mol⁻¹	ChemAxon
Polarizability	26.2 Å³	ChemAxon
Number of Rings	4	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

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

21430012

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

23651215

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Karioti, A., et al. (2007). Karioti, A., et al, J. Org. Chem. 72, 8103 (2007). J. Org. Chem..

Showing NP-Card for anthecularin (NP0025215)

MOL for NP0025215 (anthecularin)

3D MOL for NP0025215 (anthecularin)

3D SDF for NP0025215 (anthecularin)

3D-SDF for NP0025215 (anthecularin)

PDB for NP0025215 (anthecularin)

3D PDB for NP0025215 (anthecularin)

SMILES for NP0025215 (anthecularin)

INCHI for NP0025215 (anthecularin)

Structure for NP0025215 (anthecularin)

3D Structure for NP0025215 (anthecularin)