NP-MRD: Showing NP-Card for hiiranlactone C (NP0040269)

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Record Information

Version

2.0

Created at

2021-06-20 22:28:40 UTC

Updated at

2021-06-30 00:14:04 UTC

NP-MRD ID

NP0040269

Secondary Accession Numbers

None

Natural Product Identification

Common Name

hiiranlactone C

Provided By

JEOL Database JEOL Logo

Description

Hiiranlactone C 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. hiiranlactone C is found in Neolitsea hiiranensis and Pseudopterogorgia sp.. hiiranlactone C was first documented in 2011 (Liou, B.-J., et al.). Based on a literature review very few articles have been published on hiiranlactone C.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306212100283D          

 38 39  0  0  0  0            999 V2000
   -2.8297   -2.2056   -2.0443 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5207   -1.9617   -1.8856 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5779   -1.1999   -2.8198 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2892   -0.6843   -4.0925 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4896   -2.1857   -3.2946 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7835   -1.8608   -3.3762 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7914   -2.7282   -3.7406 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9374   -1.9828   -3.6067 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0675   -2.3935   -3.8176 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6215   -0.6061   -3.1859 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6598    0.4271   -2.9963 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2978   -0.5711   -3.0818 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3619    0.5371   -2.7301 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0981   -0.0087   -2.0077 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8795    1.0923   -1.5933 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0798    2.2501   -2.2511 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5981    0.8581   -0.3016 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1445    0.1804    0.6084 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8133    1.4638   -0.3077 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5754    1.2400    0.8782 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3935   -1.8705   -2.9076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3766   -2.7627   -1.2883 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0564   -2.3466   -0.9744 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6039   -0.1332   -4.7463 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6959   -1.5115   -4.6884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1241   -0.0157   -3.8563 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1757   -3.1900   -3.5707 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2443    0.5574   -3.9126 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3421    0.1407   -2.1898 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2239    1.3971   -2.7388 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0878    1.0541   -3.6571 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8648    1.2701   -2.0875 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4957   -0.4434   -1.0757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7655    3.0093   -1.8832 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5790    2.4830   -3.1838 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7782    0.1722    1.0082 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0548    1.6457    1.7513 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5300    1.7624    0.7711 H   0  0  0  0  0  0  0  0  0  0  0  0
 14 33  1  1  0  0  0
  6 12  1  0  0  0  0
  3  5  1  0  0  0  0
  1  2  2  3  0  0  0
 16 15  2  3  0  0  0
 15 14  1  0  0  0  0
  3  2  1  1  0  0  0
 12 10  2  0  0  0  0
 10  8  1  0  0  0  0
  8  7  1  0  0  0  0
  7  6  1  0  0  0  0
  3 14  1  0  0  0  0
 15 17  1  0  0  0  0
 14 13  1  0  0  0  0
 17 19  1  0  0  0  0
 13 12  1  0  0  0  0
 19 20  1  0  0  0  0
 17 18  2  0  0  0  0
  3  4  1  0  0  0  0
 10 11  1  0  0  0  0
  5  6  2  0  0  0  0
  8  9  2  0  0  0  0
  1 21  1  0  0  0  0
  1 22  1  0  0  0  0
 16 34  1  0  0  0  0
 16 35  1  0  0  0  0
  2 23  1  0  0  0  0
 13 31  1  0  0  0  0
 13 32  1  0  0  0  0
  5 27  1  0  0  0  0
  4 24  1  0  0  0  0
  4 25  1  0  0  0  0
  4 26  1  0  0  0  0
 20 36  1  0  0  0  0
 20 37  1  0  0  0  0
 20 38  1  0  0  0  0
 11 28  1  0  0  0  0
 11 29  1  0  0  0  0
 11 30  1  0  0  0  0
M  END

     RDKit          3D

 38 39  0  0  0  0  0  0  0  0999 V2000
   -2.8297   -2.2056   -2.0443 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5207   -1.9617   -1.8856 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5779   -1.1999   -2.8198 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2892   -0.6843   -4.0925 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4896   -2.1857   -3.2946 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7835   -1.8608   -3.3762 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7914   -2.7282   -3.7406 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9374   -1.9828   -3.6067 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0675   -2.3935   -3.8176 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6215   -0.6061   -3.1859 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6598    0.4271   -2.9963 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2978   -0.5711   -3.0818 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3619    0.5371   -2.7301 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0981   -0.0087   -2.0077 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8795    1.0923   -1.5933 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0798    2.2501   -2.2511 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5981    0.8581   -0.3016 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1445    0.1804    0.6084 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8133    1.4638   -0.3077 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5754    1.2400    0.8782 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3935   -1.8705   -2.9076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3766   -2.7627   -1.2883 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0564   -2.3466   -0.9744 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6039   -0.1332   -4.7463 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6959   -1.5115   -4.6884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1241   -0.0157   -3.8563 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1757   -3.1900   -3.5707 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2443    0.5574   -3.9126 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3421    0.1407   -2.1898 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2239    1.3971   -2.7388 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0878    1.0541   -3.6571 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8648    1.2701   -2.0875 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4957   -0.4434   -1.0757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7655    3.0093   -1.8832 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5790    2.4830   -3.1838 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7782    0.1722    1.0082 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0548    1.6457    1.7513 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5300    1.7624    0.7711 H   0  0  0  0  0  0  0  0  0  0  0  0
 14 33  1  1
  6 12  1  0
  3  5  1  0
  1  2  2  3
 16 15  2  3
 15 14  1  0
  3  2  1  1
 12 10  2  0
 10  8  1  0
  8  7  1  0
  7  6  1  0
  3 14  1  0
 15 17  1  0
 14 13  1  0
 17 19  1  0
 13 12  1  0
 19 20  1  0
 17 18  2  0
  3  4  1  0
 10 11  1  0
  5  6  2  0
  8  9  2  0
  1 21  1  0
  1 22  1  0
 16 34  1  0
 16 35  1  0
  2 23  1  0
 13 31  1  0
 13 32  1  0
  5 27  1  0
  4 24  1  0
  4 25  1  0
  4 26  1  0
 20 36  1  0
 20 37  1  0
 20 38  1  0
 11 28  1  0
 11 29  1  0
 11 30  1  0
M  END


  Mrv1652306212100283D          

 38 39  0  0  0  0            999 V2000
   -2.8297   -2.2056   -2.0443 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5207   -1.9617   -1.8856 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5779   -1.1999   -2.8198 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2892   -0.6843   -4.0925 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4896   -2.1857   -3.2946 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7835   -1.8608   -3.3762 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7914   -2.7282   -3.7406 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9374   -1.9828   -3.6067 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0675   -2.3935   -3.8176 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6215   -0.6061   -3.1859 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6598    0.4271   -2.9963 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2978   -0.5711   -3.0818 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3619    0.5371   -2.7301 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0981   -0.0087   -2.0077 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8795    1.0923   -1.5933 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0798    2.2501   -2.2511 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5981    0.8581   -0.3016 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1445    0.1804    0.6084 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8133    1.4638   -0.3077 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5754    1.2400    0.8782 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3935   -1.8705   -2.9076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3766   -2.7627   -1.2883 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0564   -2.3466   -0.9744 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6039   -0.1332   -4.7463 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6959   -1.5115   -4.6884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1241   -0.0157   -3.8563 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1757   -3.1900   -3.5707 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2443    0.5574   -3.9126 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3421    0.1407   -2.1898 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2239    1.3971   -2.7388 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0878    1.0541   -3.6571 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8648    1.2701   -2.0875 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4957   -0.4434   -1.0757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7655    3.0093   -1.8832 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5790    2.4830   -3.1838 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7782    0.1722    1.0082 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0548    1.6457    1.7513 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5300    1.7624    0.7711 H   0  0  0  0  0  0  0  0  0  0  0  0
 14 33  1  1  0  0  0
  6 12  1  0  0  0  0
  3  5  1  0  0  0  0
  1  2  2  3  0  0  0
 16 15  2  3  0  0  0
 15 14  1  0  0  0  0
  3  2  1  1  0  0  0
 12 10  2  0  0  0  0
 10  8  1  0  0  0  0
  8  7  1  0  0  0  0
  7  6  1  0  0  0  0
  3 14  1  0  0  0  0
 15 17  1  0  0  0  0
 14 13  1  0  0  0  0
 17 19  1  0  0  0  0
 13 12  1  0  0  0  0
 19 20  1  0  0  0  0
 17 18  2  0  0  0  0
  3  4  1  0  0  0  0
 10 11  1  0  0  0  0
  5  6  2  0  0  0  0
  8  9  2  0  0  0  0
  1 21  1  0  0  0  0
  1 22  1  0  0  0  0
 16 34  1  0  0  0  0
 16 35  1  0  0  0  0
  2 23  1  0  0  0  0
 13 31  1  0  0  0  0
 13 32  1  0  0  0  0
  5 27  1  0  0  0  0
  4 24  1  0  0  0  0
  4 25  1  0  0  0  0
  4 26  1  0  0  0  0
 20 36  1  0  0  0  0
 20 37  1  0  0  0  0
 20 38  1  0  0  0  0
 11 28  1  0  0  0  0
 11 29  1  0  0  0  0
 11 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0040269

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]C([H])=C([H])[C@@]1(C([H])=C2OC(=O)C(=C2C([H])([H])[C@@]1([H])C(=C([H])[H])C(=O)OC([H])([H])[H])C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C16H18O4/c1-6-16(4)8-13-11(9(2)15(18)20-13)7-12(16)10(3)14(17)19-5/h6,8,12H,1,3,7H2,2,4-5H3/t12-,16+/m0/s1

> <INCHI_KEY>
JVYKKRDPTBBMIB-BLLLJJGKSA-N

> <FORMULA>
C16H18O4

> <MOLECULAR_WEIGHT>
274.316

> <EXACT_MASS>
274.12050906

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
38

> <JCHEM_AVERAGE_POLARIZABILITY>
29.571952181054048

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl 2-[(5R,6S)-6-ethenyl-3,6-dimethyl-2-oxo-2,4,5,6-tetrahydro-1-benzofuran-5-yl]prop-2-enoate

> <ALOGPS_LOGP>
3.11

> <JCHEM_LOGP>
2.7327388586666665

> <ALOGPS_LOGS>
-3.47

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-6.619331892533639

> <JCHEM_POLAR_SURFACE_AREA>
52.60000000000001

> <JCHEM_REFRACTIVITY>
76.75229999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.31e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl 2-[(5R,6S)-6-ethenyl-3,6-dimethyl-2-oxo-4,5-dihydro-1-benzofuran-5-yl]prop-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 38 39  0  0  0  0  0  0  0  0999 V2000
   -2.8297   -2.2056   -2.0443 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5207   -1.9617   -1.8856 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5779   -1.1999   -2.8198 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2892   -0.6843   -4.0925 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4896   -2.1857   -3.2946 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7835   -1.8608   -3.3762 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7914   -2.7282   -3.7406 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9374   -1.9828   -3.6067 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0675   -2.3935   -3.8176 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6215   -0.6061   -3.1859 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6598    0.4271   -2.9963 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2978   -0.5711   -3.0818 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3619    0.5371   -2.7301 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0981   -0.0087   -2.0077 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8795    1.0923   -1.5933 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0798    2.2501   -2.2511 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5981    0.8581   -0.3016 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1445    0.1804    0.6084 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8133    1.4638   -0.3077 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5754    1.2400    0.8782 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3935   -1.8705   -2.9076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3766   -2.7627   -1.2883 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0564   -2.3466   -0.9744 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6039   -0.1332   -4.7463 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6959   -1.5115   -4.6884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1241   -0.0157   -3.8563 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1757   -3.1900   -3.5707 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2443    0.5574   -3.9126 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3421    0.1407   -2.1898 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2239    1.3971   -2.7388 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0878    1.0541   -3.6571 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8648    1.2701   -2.0875 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4957   -0.4434   -1.0757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7655    3.0093   -1.8832 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5790    2.4830   -3.1838 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7782    0.1722    1.0082 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0548    1.6457    1.7513 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5300    1.7624    0.7711 H   0  0  0  0  0  0  0  0  0  0  0  0
 14 33  1  1
  6 12  1  0
  3  5  1  0
  1  2  2  3
 16 15  2  3
 15 14  1  0
  3  2  1  1
 12 10  2  0
 10  8  1  0
  8  7  1  0
  7  6  1  0
  3 14  1  0
 15 17  1  0
 14 13  1  0
 17 19  1  0
 13 12  1  0
 19 20  1  0
 17 18  2  0
  3  4  1  0
 10 11  1  0
  5  6  2  0
  8  9  2  0
  1 21  1  0
  1 22  1  0
 16 34  1  0
 16 35  1  0
  2 23  1  0
 13 31  1  0
 13 32  1  0
  5 27  1  0
  4 24  1  0
  4 25  1  0
  4 26  1  0
 20 36  1  0
 20 37  1  0
 20 38  1  0
 11 28  1  0
 11 29  1  0
 11 30  1  0
M  END

HEADER    PROTEIN                                 21-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   21-JUN-21         0                                  
HETATM    1  C   UNK     0      -2.830  -2.206  -2.044  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.521  -1.962  -1.886  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.578  -1.200  -2.820  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.289  -0.684  -4.093  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.490  -2.186  -3.295  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.784  -1.861  -3.376  0.00  0.00           C+0
HETATM    7  O   UNK     0       2.791  -2.728  -3.741  0.00  0.00           O+0
HETATM    8  C   UNK     0       3.937  -1.983  -3.607  0.00  0.00           C+0
HETATM    9  O   UNK     0       5.067  -2.393  -3.818  0.00  0.00           O+0
HETATM   10  C   UNK     0       3.622  -0.606  -3.186  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.660   0.427  -2.996  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.298  -0.571  -3.082  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.362   0.537  -2.730  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.098  -0.009  -2.008  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.880   1.092  -1.593  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.080   2.250  -2.251  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.598   0.858  -0.302  0.00  0.00           C+0
HETATM   18  O   UNK     0      -1.145   0.180   0.608  0.00  0.00           O+0
HETATM   19  O   UNK     0      -2.813   1.464  -0.308  0.00  0.00           O+0
HETATM   20  C   UNK     0      -3.575   1.240   0.878  0.00  0.00           C+0
HETATM   21  H   UNK     0      -3.393  -1.871  -2.908  0.00  0.00           H+0
HETATM   22  H   UNK     0      -3.377  -2.763  -1.288  0.00  0.00           H+0
HETATM   23  H   UNK     0      -1.056  -2.347  -0.974  0.00  0.00           H+0
HETATM   24  H   UNK     0      -0.604  -0.133  -4.746  0.00  0.00           H+0
HETATM   25  H   UNK     0      -1.696  -1.512  -4.688  0.00  0.00           H+0
HETATM   26  H   UNK     0      -2.124  -0.016  -3.856  0.00  0.00           H+0
HETATM   27  H   UNK     0       0.176  -3.190  -3.571  0.00  0.00           H+0
HETATM   28  H   UNK     0       5.244   0.557  -3.913  0.00  0.00           H+0
HETATM   29  H   UNK     0       5.342   0.141  -2.190  0.00  0.00           H+0
HETATM   30  H   UNK     0       4.224   1.397  -2.739  0.00  0.00           H+0
HETATM   31  H   UNK     0       1.088   1.054  -3.657  0.00  0.00           H+0
HETATM   32  H   UNK     0       1.865   1.270  -2.087  0.00  0.00           H+0
HETATM   33  H   UNK     0       0.496  -0.443  -1.076  0.00  0.00           H+0
HETATM   34  H   UNK     0      -1.766   3.009  -1.883  0.00  0.00           H+0
HETATM   35  H   UNK     0      -0.579   2.483  -3.184  0.00  0.00           H+0
HETATM   36  H   UNK     0      -3.778   0.172   1.008  0.00  0.00           H+0
HETATM   37  H   UNK     0      -3.055   1.646   1.751  0.00  0.00           H+0
HETATM   38  H   UNK     0      -4.530   1.762   0.771  0.00  0.00           H+0
CONECT    1    2   21   22                                                  
CONECT    2    1    3   23                                                  
CONECT    3    5    2   14    4                                             
CONECT    4    3   24   25   26                                             
CONECT    5    3    6   27                                                  
CONECT    6   12    7    5                                                  
CONECT    7    8    6                                                       
CONECT    8   10    7    9                                                  
CONECT    9    8                                                            
CONECT   10   12    8   11                                                  
CONECT   11   10   28   29   30                                             
CONECT   12    6   10   13                                                  
CONECT   13   14   12   31   32                                             
CONECT   14   33   15    3   13                                             
CONECT   15   16   14   17                                                  
CONECT   16   15   34   35                                                  
CONECT   17   15   19   18                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   36   37   38                                             
CONECT   21    1                                                            
CONECT   22    1                                                            
CONECT   23    2                                                            
CONECT   24    4                                                            
CONECT   25    4                                                            
CONECT   26    4                                                            
CONECT   27    5                                                            
CONECT   28   11                                                            
CONECT   29   11                                                            
CONECT   30   11                                                            
CONECT   31   13                                                            
CONECT   32   13                                                            
CONECT   33   14                                                            
CONECT   34   16                                                            
CONECT   35   16                                                            
CONECT   36   20                                                            
CONECT   37   20                                                            
CONECT   38   20                                                            
MASTER        0    0    0    0    0    0    0    0   38    0   78    0
END

RDKit          3D

38 39  0  0  0  0  0  0  0  0999 V2000
   -2.8297   -2.2056   -2.0443 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5207   -1.9617   -1.8856 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5779   -1.1999   -2.8198 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2892   -0.6843   -4.0925 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4896   -2.1857   -3.2946 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7835   -1.8608   -3.3762 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7914   -2.7282   -3.7406 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9374   -1.9828   -3.6067 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0675   -2.3935   -3.8176 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6215   -0.6061   -3.1859 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6598    0.4271   -2.9963 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2978   -0.5711   -3.0818 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3619    0.5371   -2.7301 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0981   -0.0087   -2.0077 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8795    1.0923   -1.5933 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0798    2.2501   -2.2511 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5981    0.8581   -0.3016 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1445    0.1804    0.6084 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8133    1.4638   -0.3077 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5754    1.2400    0.8782 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3935   -1.8705   -2.9076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3766   -2.7627   -1.2883 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0564   -2.3466   -0.9744 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6039   -0.1332   -4.7463 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6959   -1.5115   -4.6884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1241   -0.0157   -3.8563 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1757   -3.1900   -3.5707 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2443    0.5574   -3.9126 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3421    0.1407   -2.1898 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2239    1.3971   -2.7388 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0878    1.0541   -3.6571 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8648    1.2701   -2.0875 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4957   -0.4434   -1.0757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7655    3.0093   -1.8832 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5790    2.4830   -3.1838 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7782    0.1722    1.0082 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0548    1.6457    1.7513 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5300    1.7624    0.7711 H   0  0  0  0  0  0  0  0  0  0  0  0
 14 33  1  1
  6 12  1  0
  3  5  1  0
  1  2  2  3
 16 15  2  3
 15 14  1  0
  3  2  1  1
 12 10  2  0
 10  8  1  0
  8  7  1  0
  7  6  1  0
  3 14  1  0
 15 17  1  0
 14 13  1  0
 17 19  1  0
 13 12  1  0
 19 20  1  0
 17 18  2  0
  3  4  1  0
 10 11  1  0
  5  6  2  0
  8  9  2  0
  1 21  1  0
  1 22  1  0
 16 34  1  0
 16 35  1  0
  2 23  1  0
 13 31  1  0
 13 32  1  0
  5 27  1  0
  4 24  1  0
  4 25  1  0
  4 26  1  0
 20 36  1  0
 20 37  1  0
 20 38  1  0
 11 28  1  0
 11 29  1  0
 11 30  1  0
M  END

View in JSmol View DFT Assignments 3D Conformers

Synonyms

Not Available

Chemical Formula

C₁₆H₁₈O₄

Average Mass

274.3160 Da

Monoisotopic Mass

274.12051 Da

IUPAC Name

methyl 2-[(5R,6S)-6-ethenyl-3,6-dimethyl-2-oxo-2,4,5,6-tetrahydro-1-benzofuran-5-yl]prop-2-enoate

Traditional Name

methyl 2-[(5R,6S)-6-ethenyl-3,6-dimethyl-2-oxo-4,5-dihydro-1-benzofuran-5-yl]prop-2-enoate

CAS Registry Number

Not Available

SMILES

[H]C([H])=C([H])[C@@]1(C([H])=C2OC(=O)C(=C2C([H])([H])[C@@]1([H])C(=C([H])[H])C(=O)OC([H])([H])[H])C([H])([H])[H])C([H])([H])[H]

InChI Identifier

InChI=1S/C16H18O4/c1-6-16(4)8-13-11(9(2)15(18)20-13)7-12(16)10(3)14(17)19-5/h6,8,12H,1,3,7H2,2,4-5H3/t12-,16+/m0/s1

InChI Key

JVYKKRDPTBBMIB-BLLLJJGKSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
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, 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, 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, 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, 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
Neolitsea hiiranensis	JEOL database	Liou, B.-J., et al, Phytochem. 72, 415 (2011)
Pseudopterogorgia sp.	-	KNApSAcK

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

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

benzofurans (CHEBI:69078 )

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	3.11	ALOGPS
logP	2.73	ChemAxon
logS	-3.5	ALOGPS
pKa (Strongest Basic)	-6.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	52.6 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	76.75 m³·mol⁻¹	ChemAxon
Polarizability	29.57 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

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

35518220

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

52912460

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Liou, B.-J., et al. (2011). Liou, B.-J., et al, Phytochem. 72, 415 (2011). Phytochem..

Showing NP-Card for hiiranlactone C (NP0040269)

MOL for NP0040269 (hiiranlactone C)

3D MOL for NP0040269 (hiiranlactone C)

3D SDF for NP0040269 (hiiranlactone C)

3D-SDF for NP0040269 (hiiranlactone C)

PDB for NP0040269 (hiiranlactone C)

3D PDB for NP0040269 (hiiranlactone C)

SMILES for NP0040269 (hiiranlactone C)

INCHI for NP0040269 (hiiranlactone C)

Structure for NP0040269 (hiiranlactone C)

3D Structure for NP0040269 (hiiranlactone C)