NP-MRD: Showing NP-Card for Farnesylemefuranone D (NP0044640)

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Record Information

Version

2.0

Created at

2022-02-24 21:10:17 UTC

Updated at

2022-02-24 21:10:17 UTC

NP-MRD ID

NP0044640

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Farnesylemefuranone D

Description

Farnesylemefuranone D belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring. Based on a literature review very few articles have been published on Farnesylemefuranone D.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652302242222102D          

 29 30  0  0  0  0            999 V2000
    3.4990    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845    0.6979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435    2.1904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6284    1.5229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435    0.8555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3984    0.0709    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    3.1729    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845    2.3479    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2135    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9279    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9279    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6424    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3569    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0714    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7858    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7858    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5003    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2148    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9292    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6437    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3582    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6437    1.1104    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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  5  9  1  0  0  0  0
  9 10  2  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
  3 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  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
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
M  END

     RDKit          3D

 61 62  0  0  0  0  0  0  0  0999 V2000
   -3.9116    2.9514    2.0267 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3295    1.7085    1.7281 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1193    0.6508    1.3656 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4928    0.8526    1.3060 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3268   -0.1902    0.9528 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8087   -1.4229    0.6605 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4499   -1.5883    0.7277 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9039   -2.8326    0.4346 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5422   -0.5796    1.0767 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2281   -0.7819    1.1225 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1419   -1.0514    0.4525 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4268   -0.4725   -0.6231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6029    0.5674   -1.3539 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8167    1.4225   -1.0805 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2582    1.0533   -2.4349 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4932    0.4206   -2.8285 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5119    0.4050   -1.7397 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1947   -0.6348   -1.3916 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0297   -1.9314   -2.0535 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2062   -0.5102   -0.2581 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2455    0.8608    0.2844 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2073    1.0768    1.3521 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1438    0.3593    1.8624 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5285   -0.9935    1.4636 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9678    0.9426    3.0088 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9451   -2.3257    0.3214 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0934   -1.5252    0.4421 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7914   -0.2494    0.8145 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5994    0.7206    1.0111 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4247    3.3882    1.1427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0886    3.6219    2.3915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6651    2.8049    2.8428 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9057    1.8159    1.5338 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5295   -3.5800    0.1798 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3056   -2.1830    0.0716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2711   -1.2780    1.2642 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5023   -1.0456   -0.9334 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7521    0.8893   -1.1296 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6406    2.0729   -0.2064 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8846    2.1805   -1.9332 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4247    2.1584   -2.1988 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4408    1.1443   -3.3349 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9900    1.0594   -3.6283 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4158   -0.5632   -3.3357 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6479    1.3854   -1.2272 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9593   -2.5582   -1.8865 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9264   -1.8644   -3.1556 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1873   -2.5122   -1.6343 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8018   -1.2035    0.5484 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1333   -0.8730   -0.6943 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4907    1.6151   -0.5248 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2037    1.1221    0.6813 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1227    2.1143    1.8616 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0916   -0.9279    0.5008 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3394   -1.3904    2.1815 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7671   -1.7576    1.4243 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0179    0.6319    2.8461 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9387    2.0374    2.8870 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5531    0.6224    3.9672 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8673   -2.6424   -0.7406 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9947   -3.1872    1.0175 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  2  0
  6  7  1  0
  7  8  1  0
  7  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  2  3
 23 24  1  0
 23 25  1  0
  9  3  1  0
 28  5  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  4 33  1  0
 26 60  1  0
 26 61  1  0
  8 34  1  0
 11 35  1  0
 11 36  1  0
 12 37  1  0
 14 38  1  0
 14 39  1  0
 14 40  1  0
 15 41  1  0
 15 42  1  0
 16 43  1  0
 16 44  1  0
 17 45  1  0
 19 46  1  0
 19 47  1  0
 19 48  1  0
 20 49  1  0
 20 50  1  0
 21 51  1  0
 21 52  1  0
 22 53  1  0
 24 54  1  0
 24 55  1  0
 24 56  1  0
 25 57  1  0
 25 58  1  0
 25 59  1  0
M  END


  Mrv1652302242222102D          

 29 30  0  0  0  0            999 V2000
    3.4990    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845    0.6979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435    2.1904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6284    1.5229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435    0.8555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3984    0.0709    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    3.1729    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845    2.3479    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2135    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9279    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9279    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6424    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3569    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0714    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7858    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7858    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5003    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2148    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9292    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6437    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3582    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6437    1.1104    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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  5  9  1  0  0  0  0
  9 10  2  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
  3 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  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
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0044640

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC2=C(COC2=O)C(O)=C1OC\C=C(/C)CC\C=C(/C)CCC=C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C24H32O5/c1-16(2)8-6-9-17(3)10-7-11-18(4)12-13-28-23-21(27-5)14-19-20(22(23)25)15-29-24(19)26/h8,10,12,14,25H,6-7,9,11,13,15H2,1-5H3/b17-10+,18-12+

> <INCHI_KEY>
KBPHWZWKDRMLNM-VZRGJMDUSA-N

> <FORMULA>
C24H32O5

> <MOLECULAR_WEIGHT>
400.515

> <EXACT_MASS>
400.22497413

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
61

> <JCHEM_AVERAGE_POLARIZABILITY>
46.25186007605987

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-hydroxy-6-methoxy-5-{[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]oxy}-1,3-dihydro-2-benzofuran-1-one

> <ALOGPS_LOGP>
5.63

> <JCHEM_LOGP>
5.589716868

> <ALOGPS_LOGS>
-5.14

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.937774760479758

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.725714375252657

> <JCHEM_PKA_STRONGEST_BASIC>
-4.660377081075986

> <JCHEM_POLAR_SURFACE_AREA>
64.99000000000001

> <JCHEM_REFRACTIVITY>
118.2686

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.90e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-hydroxy-6-methoxy-5-{[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]oxy}-3H-2-benzofuran-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-FEB-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-22         0                                  
HETATM    1  C   UNK     0       6.531   2.073   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       5.198   1.303   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       3.864   2.073   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.530   1.303   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.197   2.073   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.197   3.613   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.268   4.089   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -1.173   2.843   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -0.268   1.597   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -0.744   0.132   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       2.530   4.383   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       2.530   5.923   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       3.864   3.613   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       5.198   4.383   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       6.531   3.613   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.865   4.383   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.199   3.613   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.199   2.073   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      10.533   4.383   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      11.866   3.613   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      13.200   4.383   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      14.534   3.613   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      14.534   2.073   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      15.867   4.383   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      17.201   3.613   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      18.535   4.383   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      19.868   3.613   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      21.202   4.383   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      19.868   2.073   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   13                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    9                                                  
CONECT    6    5    7   11                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8    5   10                                                  
CONECT   10    9                                                            
CONECT   11    6   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11    3   14                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₃₂O₅

Average Mass

400.5150 Da

Monoisotopic Mass

400.22497 Da

IUPAC Name

4-hydroxy-6-methoxy-5-{[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]oxy}-1,3-dihydro-2-benzofuran-1-one

Traditional Name

4-hydroxy-6-methoxy-5-{[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]oxy}-3H-2-benzofuran-1-one

CAS Registry Number

Not Available

SMILES

COC1=CC2=C(COC2=O)C(O)=C1OC\C=C(/C)CC\C=C(/C)CCC=C(C)C

InChI Identifier

InChI=1S/C24H32O5/c1-16(2)8-6-9-17(3)10-7-11-18(4)12-13-28-23-21(27-5)14-19-20(22(23)25)15-29-24(19)26/h8,10,12,14,25H,6-7,9,11,13,15H2,1-5H3/b17-10+,18-12+

InChI Key

KBPHWZWKDRMLNM-VZRGJMDUSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 125 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 150 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 175 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 225 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 250 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, Chloroform-d, 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, 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
Aspergillus	Linington's dataset npmrd_submissions_20220207	33322904

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Terpene lactones

Alternative Parents

Substituents

Terpene lactone
Farsesane sesquiterpenoid
Sesquiterpenoid
Gallic acid or derivatives
Isobenzofuranone
Phthalide
Isocoumaran
Anisole
1-hydroxy-4-unsubstituted benzenoid
Alkyl aryl ether
Benzenoid
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Ether
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
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	5.63	ALOGPS
logP	5.59	ChemAxon
logS	-5.1	ALOGPS
pKa (Strongest Acidic)	8.73	ChemAxon
pKa (Strongest Basic)	-4.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	64.99 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	118.27 m³·mol⁻¹	ChemAxon
Polarizability	46.25 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	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

99740768

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

156580997

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Farnesylemefuranone D (NP0044640)

MOL for NP0044640 (Farnesylemefuranone D)

3D MOL for NP0044640 (Farnesylemefuranone D)

3D SDF for NP0044640 (Farnesylemefuranone D)

3D-SDF for NP0044640 (Farnesylemefuranone D)

PDB for NP0044640 (Farnesylemefuranone D)

3D PDB for NP0044640 (Farnesylemefuranone D)

SMILES for NP0044640 (Farnesylemefuranone D)

INCHI for NP0044640 (Farnesylemefuranone D)

Structure for NP0044640 (Farnesylemefuranone D)

3D Structure for NP0044640 (Farnesylemefuranone D)