NP-MRD: Showing NP-Card for Ligulacephalin C (NP0072207)

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Record Information

Version

2.0

Created at

2022-04-28 17:34:38 UTC

Updated at

2022-04-28 17:34:38 UTC

NP-MRD ID

NP0072207

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Ligulacephalin C

Description

(13S)-13-(5,6-dimethoxy-1-benzofuran-2-yl)-4,5-dimethoxy-13-methyl-10-methylidene-8-oxatricyclo[7.4.0.0²,⁷]Trideca-1(9),2,4,6-tetraene belongs to the class of organic compounds known as benzofurans. These are organic compounds containing a benzene ring fused to a furan. Furan is a five-membered aromatic ring with four carbon atoms and one oxygen atom. Ligulacephalin C is found in Ligularia stenocephala MATSUM.ET KOIDZ and Pojarkovia pojarkovae. Based on a literature review very few articles have been published on (13S)-13-(5,6-dimethoxy-1-benzofuran-2-yl)-4,5-dimethoxy-13-methyl-10-methylidene-8-oxatricyclo[7.4.0.0²,⁷]Trideca-1(9),2,4,6-tetraene.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282219342D          

 32 36  0  0  1  0            999 V2000
    3.2075   -1.1370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7703   -1.8367    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3006   -2.4687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0656   -2.1596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0080   -1.3366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7157   -2.6675    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6009   -3.4845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8359   -3.7936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1858   -3.2856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7211   -4.6105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3712   -5.1185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2510   -3.9924    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1362   -4.8094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8985   -0.3721    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3464    0.2410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6014    1.0256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9339    1.5105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2665    1.0256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5214    0.2410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9694   -0.3721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1624   -0.2006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0925    0.5840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4595    1.1971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8995    0.7556    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4515    0.1425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3896   -0.8137    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1966   -0.6422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4084    1.1971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6633    1.9817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9604    0.5840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7054   -0.2006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1988   -0.8093    0.0000 C   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
  1  5  2  0  0  0  0
  4  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  3  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  0  0  0  0
 14  1  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 15 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 18 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 21 26  1  0  0  0  0
 26 27  1  0  0  0  0
 16 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 14 31  1  0  0  0  0
 14 32  1  1  0  0  0
M  END

     RDKit          3D

 58 62  0  0  0  0  0  0  0  0999 V2000
    0.8120   -3.1287   -2.6964 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1878   -2.8708   -1.4719 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9117   -3.8234   -0.3972 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8827   -3.2024    0.9673 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8539   -1.7179    1.0127 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1000   -1.2972    2.4430 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5376   -1.2493    0.7044 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6345   -1.9793    0.3136 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6884   -1.0983    0.1507 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0043   -1.2501   -0.2209 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8214   -0.1386   -0.2896 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1566   -0.2331   -0.6585 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7551   -1.4727   -0.9845 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3294    1.1161    0.0104 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1569    2.2142   -0.0628 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7406    3.5284    0.2254 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0064    1.2385    0.3798 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1628    0.1470    0.4583 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9115    0.0209    0.7753 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7310   -1.0324    0.0475 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8857   -1.6235   -1.1962 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6949   -0.8453   -1.8797 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0755    0.1978   -1.1824 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8930    1.2855   -1.4197 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1305    2.2742   -0.4760 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9691    3.3671   -0.7534 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5585    3.4109   -2.0358 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5281    2.1830    0.7672 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7845    3.1851    1.6870 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1507    3.0633    2.9565 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7077    1.0920    1.0057 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4842    0.1229    0.0601 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9891   -2.4598   -3.5360 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2957   -4.0546   -2.8996 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0483   -4.4645   -0.6370 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7899   -4.5389   -0.3879 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7089   -3.5486    1.6293 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0543   -3.5677    1.4770 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1742   -1.2543    2.6870 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6848   -2.1221    3.0866 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5134   -0.4091    2.7442 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6776   -3.0270    0.1621 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3863   -2.2318   -0.4546 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8643   -1.3024   -0.9670 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4533   -2.1993   -0.1986 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4444   -1.7994   -1.9872 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5909    4.1995    0.4578 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1458    3.9595   -0.6065 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1460    3.4592    1.1772 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6242    2.2277    0.6145 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3588    1.3402   -2.4054 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0969    2.4697   -2.2753 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3270    4.2169   -2.1049 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8355    3.5794   -2.8505 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5216    3.8002    3.6784 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3013    2.0597    3.4048 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0593    3.1610    2.7567 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2460    1.0225    1.9578 H   0  0  0  0  0  0  0  0  0  0  0  0
 16 15  1  0
 15 14  1  0
 14 11  2  0
 11 12  1  0
 12 13  1  0
 11 10  1  0
 10  9  2  0
  9  8  1  0
  8  7  2  0
  7 19  1  0
 19 18  1  0
 18 17  2  0
  7  5  1  0
  5  6  1  1
  5  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  2  3
  2 21  1  0
 21 20  2  0
 20 32  1  0
 32 31  2  0
 31 28  1  0
 28 29  1  0
 29 30  1  0
 28 25  2  0
 25 26  1  0
 26 27  1  0
 25 24  1  0
 24 23  2  0
 23 22  1  0
 17 14  1  0
 20  5  1  0
 23 32  1  0
 18  9  1  0
 22 21  1  0
 16 47  1  0
 16 48  1  0
 16 49  1  0
 13 44  1  0
 13 45  1  0
 13 46  1  0
 10 43  1  0
  8 42  1  0
 17 50  1  0
  6 39  1  0
  6 40  1  0
  6 41  1  0
  4 37  1  0
  4 38  1  0
  3 35  1  0
  3 36  1  0
  1 33  1  0
  1 34  1  0
 31 58  1  0
 30 55  1  0
 30 56  1  0
 30 57  1  0
 27 52  1  0
 27 53  1  0
 27 54  1  0
 24 51  1  0
M  END


  Mrv1652304282219342D          

 32 36  0  0  1  0            999 V2000
    3.2075   -1.1370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7703   -1.8367    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3006   -2.4687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0656   -2.1596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0080   -1.3366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7157   -2.6675    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6009   -3.4845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8359   -3.7936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1858   -3.2856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7211   -4.6105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3712   -5.1185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2510   -3.9924    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1362   -4.8094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8985   -0.3721    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3464    0.2410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6014    1.0256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9339    1.5105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2665    1.0256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5214    0.2410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9694   -0.3721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1624   -0.2006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0925    0.5840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4595    1.1971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8995    0.7556    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4515    0.1425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3896   -0.8137    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1966   -0.6422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4084    1.1971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6633    1.9817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9604    0.5840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7054   -0.2006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1988   -0.8093    0.0000 C   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
  1  5  2  0  0  0  0
  4  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  3  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  0  0  0  0
 14  1  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 15 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 18 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 21 26  1  0  0  0  0
 26 27  1  0  0  0  0
 16 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 14 31  1  0  0  0  0
 14 32  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0072207

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(OC)C=C2C=C(OC2=C1)[C@@]1(C)CCC(=C)C2=C1C1=CC(OC)=C(OC)C=C1O2

> <INCHI_IDENTIFIER>
InChI=1S/C26H26O6/c1-14-7-8-26(2,23-10-15-9-19(27-3)21(29-5)12-17(15)31-23)24-16-11-20(28-4)22(30-6)13-18(16)32-25(14)24/h9-13H,1,7-8H2,2-6H3/t26-/m1/s1

> <INCHI_KEY>
UYFWZQOVYGPJFE-AREMUKBSSA-N

> <FORMULA>
C26H26O6

> <MOLECULAR_WEIGHT>
434.488

> <EXACT_MASS>
434.172938557

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
47.80079036387847

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(13S)-13-(5,6-dimethoxy-1-benzofuran-2-yl)-4,5-dimethoxy-13-methyl-10-methylidene-8-oxatricyclo[7.4.0.0^{2,7}]trideca-1(9),2,4,6-tetraene

> <ALOGPS_LOGP>
5.66

> <JCHEM_LOGP>
4.752040815666668

> <ALOGPS_LOGS>
-4.88

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-2.5192460724935666

> <JCHEM_POLAR_SURFACE_AREA>
63.2

> <JCHEM_REFRACTIVITY>
130.7694

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.75e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(13S)-13-(5,6-dimethoxy-1-benzofuran-2-yl)-4,5-dimethoxy-13-methyl-10-methylidene-8-oxatricyclo[7.4.0.0^{2,7}]trideca-1(9),2,4,6-tetraene

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       5.987  -2.122   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       5.171  -3.428   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       6.161  -4.608   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.589  -4.031   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.482  -2.495   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.803  -4.979   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.588  -6.504   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.160  -7.081   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.947  -6.133   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       6.946  -8.606   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       8.160  -9.554   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       9.802  -7.453   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       9.587  -8.978   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.410  -0.695   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.380   0.450   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.856   1.914   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       3.610   2.820   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       2.364   1.914   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.840   0.450   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.810  -0.695   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.303  -0.374   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.173   1.090   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.858   2.235   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -1.679   1.410   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -2.709   0.266   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -0.727  -1.519   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -2.234  -1.199   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.362   2.235   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.838   3.699   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       7.393   1.090   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       6.917  -0.374   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       4.104  -1.511   0.000  0.00  0.00           C+0
CONECT    1    2    5   14                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4    9                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4    1                                                       
CONECT    6    4    7                                                       
CONECT    7    6    8   12                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8    3                                                       
CONECT   10    8   11                                                       
CONECT   11   10                                                            
CONECT   12    7   13                                                       
CONECT   13   12                                                            
CONECT   14    1   15   31   32                                             
CONECT   15   14   16   19                                                  
CONECT   16   15   17   28                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   23                                                  
CONECT   19   18   15   20                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   26                                                  
CONECT   22   21   23   24                                                  
CONECT   23   22   18                                                       
CONECT   24   22   25                                                       
CONECT   25   24                                                            
CONECT   26   21   27                                                       
CONECT   27   26                                                            
CONECT   28   16   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   14                                                       
CONECT   32   14                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   72    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₆H₂₆O₆

Average Mass

434.4880 Da

Monoisotopic Mass

434.17294 Da

IUPAC Name

(13S)-13-(5,6-dimethoxy-1-benzofuran-2-yl)-4,5-dimethoxy-13-methyl-10-methylidene-8-oxatricyclo[7.4.0.0^{2,7}]trideca-1(9),2,4,6-tetraene

Traditional Name

(13S)-13-(5,6-dimethoxy-1-benzofuran-2-yl)-4,5-dimethoxy-13-methyl-10-methylidene-8-oxatricyclo[7.4.0.0^{2,7}]trideca-1(9),2,4,6-tetraene

CAS Registry Number

Not Available

SMILES

COC1=C(OC)C=C2C=C(OC2=C1)[C@@]1(C)CCC(=C)C2=C1C1=CC(OC)=C(OC)C=C1O2

InChI Identifier

InChI=1S/C26H26O6/c1-14-7-8-26(2,23-10-15-9-19(27-3)21(29-5)12-17(15)31-23)24-16-11-20(28-4)22(30-6)13-18(16)32-25(14)24/h9-13H,1,7-8H2,2-6H3/t26-/m1/s1

InChI Key

UYFWZQOVYGPJFE-AREMUKBSSA-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
Ligularia stenocephala MATSUM.ET KOIDZ	Plant	KNApSAcK
Pojarkovia pojarkovae	LOTUS Database	35616633

Chemical Taxonomy

Description

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

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzofurans

Sub Class

Not Available

Direct Parent

Benzofurans

Alternative Parents

Substituents

Benzofuran
Anisole
Alkyl aryl ether
Benzenoid
Heteroaromatic compound
Furan
Oxacycle
Ether
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
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	5.66	ALOGPS
logP	4.75	ChemAxon
logS	-4.9	ALOGPS
pKa (Strongest Basic)	-2.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	63.2 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	130.77 m³·mol⁻¹	ChemAxon
Polarizability	47.8 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

9843960

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11669228

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Ligulacephalin C (NP0072207)

MOL for NP0072207 (Ligulacephalin C)

3D MOL for NP0072207 (Ligulacephalin C)

3D SDF for NP0072207 (Ligulacephalin C)

3D-SDF for NP0072207 (Ligulacephalin C)

PDB for NP0072207 (Ligulacephalin C)

3D PDB for NP0072207 (Ligulacephalin C)

SMILES for NP0072207 (Ligulacephalin C)

INCHI for NP0072207 (Ligulacephalin C)

Structure for NP0072207 (Ligulacephalin C)

3D Structure for NP0072207 (Ligulacephalin C)