NP-MRD: Showing NP-Card for methyl 2-[5-(acetyloxy)-4-methylpent-3-en-1-yl]-9-(furan-3-yl)-6-methylnona-2,6-dienoate (NP0184751)

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Record Information

Version

2.0

Created at

2022-09-03 23:57:20 UTC

Updated at

2022-09-03 23:57:20 UTC

NP-MRD ID

NP0184751

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 2-[5-(acetyloxy)-4-methylpent-3-en-1-yl]-9-(furan-3-yl)-6-methylnona-2,6-dienoate

Description

Methyl 2-[5-(acetyloxy)-4-methylpent-3-en-1-yl]-9-(furan-3-yl)-6-methylnona-2,6-dienoate belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. Methyl 2-[5-(acetyloxy)-4-methylpent-3-en-1-yl]-9-(furan-3-yl)-6-methylnona-2,6-dienoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004151517092D          

 28 28  0  0  0  0            999 V2000
    5.5691    5.6518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8546    6.0643    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1401    5.6518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1401    4.8268    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4256    6.0643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7112    5.6518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7112    4.8268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9967    4.4143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9967    3.5893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2822    3.1768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2822    2.3518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5678    1.9393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5678    1.1143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2352    0.6294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9803   -0.1553    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1553   -0.1553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0997    0.6294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7112    3.1768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4256    6.8893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1401    7.3018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1401    8.1268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8546    8.5393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5691    8.1268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8546    9.3643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1401    9.7768    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1401   10.6018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4256   11.0143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8546   11.0143    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
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  4  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  4  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  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
 13 17  1  0  0  0  0
  9 18  1  0  0  0  0
  5 19  1  0  0  0  0
 19 20  1  0  0  0  0
 21 20  1  4  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
 26 28  1  0  0  0  0
M  END

     RDKit          3D

 60 60  0  0  0  0  0  0  0  0999 V2000
   -0.1837   -3.8106    1.7338 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2492   -2.9801    0.6043 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6857   -2.0354    0.2617 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6808   -1.9340    1.0603 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5579   -1.2139   -0.9143 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4060   -1.2113   -1.7956 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6043   -2.0587   -1.7943 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8501   -1.1849   -1.7232 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8777   -0.3564   -0.5084 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8679   -0.9778    0.8388 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9119    0.9565   -0.6092 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9394    1.7753    0.6310 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1985    2.6143    0.6520 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3814    1.7233    0.6191 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0428    1.2557   -0.4865 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0848    0.4575   -0.0373 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0218    0.4685    1.2561 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0399    1.1962    1.7042 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6805   -0.2187   -1.1359 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9484   -0.9646   -1.3335 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0835   -0.0085   -1.5607 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0900   -0.0233   -0.7200 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0983   -0.9644    0.4238 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2351    0.9026   -0.9026 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3742    1.7427    0.2262 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3150    2.5675    0.5612 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3967    3.4784    1.7406 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2846    2.5263   -0.1558 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8464   -3.7664    2.1425 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5486   -4.8294    1.5740 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8576   -3.3479    2.5131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3402   -0.4957   -2.6587 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6786   -2.6361   -2.7715 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6768   -2.7929   -1.0091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9000   -0.5308   -2.6132 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7279   -1.8701   -1.6845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9415   -0.6662    1.3550 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7230   -0.6657    1.4626 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9346   -2.0945    0.7795 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9193    1.4141   -1.5726 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8242    1.1609    1.5393 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0532    2.4707    0.6163 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1621    3.3033   -0.2168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1906    3.2608    1.5545 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8235    1.4505   -1.5290 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8130   -0.0743   -0.6520 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8107    1.3394    2.7542 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7568    0.4529   -0.2483 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4684    0.3863   -2.0197 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8812   -1.5676   -2.2735 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2192   -1.6479   -0.5361 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0954    0.6835   -2.3872 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9829   -0.7798    1.0836 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2125   -0.8603    1.0736 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1326   -2.0136    0.0694 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0899    1.5806   -1.7753 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1773    0.3459   -1.1210 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6830    4.5062    1.4166 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1768    3.0600    2.4083 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4318    3.5016    2.2534 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
  3  5  1  0
  5 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 26 28  2  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  9 11  2  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 18  2  0
 18 17  1  0
 17 16  1  0
 16 15  2  0
 15 14  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
 19 48  1  0
 19 49  1  0
 20 50  1  0
 20 51  1  0
 21 52  1  0
 23 53  1  0
 23 54  1  0
 23 55  1  0
 24 56  1  0
 24 57  1  0
 27 58  1  0
 27 59  1  0
 27 60  1  0
  6 32  1  0
  7 33  1  0
  7 34  1  0
  8 35  1  0
  8 36  1  0
 10 37  1  0
 10 38  1  0
 10 39  1  0
 11 40  1  0
 12 41  1  0
 12 42  1  0
 13 43  1  0
 13 44  1  0
 18 47  1  0
 16 46  1  0
 15 45  1  0
M  END


  Mrv1533004151517092D          

 28 28  0  0  0  0            999 V2000
    5.5691    5.6518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8546    6.0643    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1401    5.6518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1401    4.8268    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4256    6.0643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7112    5.6518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7112    4.8268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9967    4.4143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9967    3.5893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2822    3.1768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2822    2.3518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5678    1.9393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5678    1.1143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2352    0.6294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9803   -0.1553    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1553   -0.1553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0997    0.6294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7112    3.1768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4256    6.8893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1401    7.3018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1401    8.1268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8546    8.5393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5691    8.1268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8546    9.3643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1401    9.7768    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1401   10.6018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4256   11.0143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8546   11.0143    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
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  4  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  4  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  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
 13 17  1  0  0  0  0
  9 18  1  0  0  0  0
  5 19  1  0  0  0  0
 19 20  1  0  0  0  0
 21 20  1  4  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
 26 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0184751

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C(CCC=C(C)COC(C)=O)=CCCC(C)=CCCC1=COC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C23H32O5/c1-18(8-5-11-21-14-15-27-17-21)9-6-12-22(23(25)26-4)13-7-10-19(2)16-28-20(3)24/h8,10,12,14-15,17H,5-7,9,11,13,16H2,1-4H3

> <INCHI_KEY>
PNCVSYIHSUKALM-UHFFFAOYSA-N

> <FORMULA>
C23H32O5

> <MOLECULAR_WEIGHT>
388.504

> <EXACT_MASS>
388.22497413

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
44.36204111443338

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl 2-[5-(acetyloxy)-4-methylpent-3-en-1-yl]-9-(furan-3-yl)-6-methylnona-2,6-dienoate

> <ALOGPS_LOGP>
5.95

> <JCHEM_LOGP>
5.337329792666667

> <ALOGPS_LOGS>
-4.63

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7865724565078076

> <JCHEM_POLAR_SURFACE_AREA>
65.74000000000001

> <JCHEM_REFRACTIVITY>
112.43289999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
9.05e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl 2-[5-(acetyloxy)-4-methylpent-3-en-1-yl]-9-(furan-3-yl)-6-methylnona-2,6-dienoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 15-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   15-APR-15         0                                  
HETATM    1  C   UNK     0      10.396  10.550   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       9.062  11.320   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       7.728  10.550   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       7.728   9.010   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       6.395  11.320   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.061  10.550   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.061   9.010   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.727   8.240   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.727   6.700   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.393   5.930   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.393   4.390   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.060   3.620   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.060   2.080   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.306   1.175   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       1.830  -0.290   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       0.290  -0.290   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.186   1.175   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.061   5.930   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.395  12.860   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.728  13.630   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.728  15.170   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       9.062  15.940   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      10.396  15.170   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.062  17.480   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       7.728  18.250   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       7.728  19.790   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       6.395  20.560   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       9.062  20.560   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   19                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   18                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   17                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   13                                                       
CONECT   18    9                                                            
CONECT   19    5   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   28                                                  
CONECT   27   26                                                            
CONECT   28   26                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   56    0
END

View in JSmol

Synonyms

Value	Source
Methyl 2-[5-(acetyloxy)-4-methylpent-3-en-1-yl]-9-(furan-3-yl)-6-methylnona-2,6-dienoic acid	Generator

Chemical Formula

C₂₃H₃₂O₅

Average Mass

388.5040 Da

Monoisotopic Mass

388.22497 Da

IUPAC Name

methyl 2-[5-(acetyloxy)-4-methylpent-3-en-1-yl]-9-(furan-3-yl)-6-methylnona-2,6-dienoate

Traditional Name

methyl 2-[5-(acetyloxy)-4-methylpent-3-en-1-yl]-9-(furan-3-yl)-6-methylnona-2,6-dienoate

CAS Registry Number

Not Available

SMILES

COC(=O)C(CCC=C(C)COC(C)=O)=CCCC(C)=CCCC1=COC=C1

InChI Identifier

InChI=1S/C23H32O5/c1-18(8-5-11-21-14-15-27-17-21)9-6-12-22(23(25)26-4)13-7-10-19(2)16-28-20(3)24/h8,10,12,14-15,17H,5-7,9,11,13,16H2,1-4H3

InChI Key

PNCVSYIHSUKALM-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Sesquiterpenoids

Alternative Parents

Substituents

Sesquiterpenoid
Farsesane sesquiterpenoid
Fatty alcohol ester
Fatty acid ester
Dicarboxylic acid or derivatives
Fatty acyl
Heteroaromatic compound
Furan
Methyl ester
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Carboxylic acid ester
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Organic oxide
Organooxygen compound
Carbonyl group
Organic oxygen compound
Hydrocarbon derivative
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	5.95	ALOGPS
logP	5.34	ChemAxon
logS	-4.6	ALOGPS
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	65.74 Å²	ChemAxon
Rotatable Bond Count	14	ChemAxon
Refractivity	112.43 m³·mol⁻¹	ChemAxon
Polarizability	44.36 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	No	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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 2-[5-(acetyloxy)-4-methylpent-3-en-1-yl]-9-(furan-3-yl)-6-methylnona-2,6-dienoate (NP0184751)

MOL for NP0184751 (methyl 2-[5-(acetyloxy)-4-methylpent-3-en-1-yl]-9-(furan-3-yl)-6-methylnona-2,6-dienoate)

3D MOL for NP0184751 (methyl 2-[5-(acetyloxy)-4-methylpent-3-en-1-yl]-9-(furan-3-yl)-6-methylnona-2,6-dienoate)

3D SDF for NP0184751 (methyl 2-[5-(acetyloxy)-4-methylpent-3-en-1-yl]-9-(furan-3-yl)-6-methylnona-2,6-dienoate)

3D-SDF for NP0184751 (methyl 2-[5-(acetyloxy)-4-methylpent-3-en-1-yl]-9-(furan-3-yl)-6-methylnona-2,6-dienoate)

PDB for NP0184751 (methyl 2-[5-(acetyloxy)-4-methylpent-3-en-1-yl]-9-(furan-3-yl)-6-methylnona-2,6-dienoate)

3D PDB for NP0184751 (methyl 2-[5-(acetyloxy)-4-methylpent-3-en-1-yl]-9-(furan-3-yl)-6-methylnona-2,6-dienoate)

SMILES for NP0184751 (methyl 2-[5-(acetyloxy)-4-methylpent-3-en-1-yl]-9-(furan-3-yl)-6-methylnona-2,6-dienoate)

INCHI for NP0184751 (methyl 2-[5-(acetyloxy)-4-methylpent-3-en-1-yl]-9-(furan-3-yl)-6-methylnona-2,6-dienoate)

Structure for NP0184751 (methyl 2-[5-(acetyloxy)-4-methylpent-3-en-1-yl]-9-(furan-3-yl)-6-methylnona-2,6-dienoate)

3D Structure for NP0184751 (methyl 2-[5-(acetyloxy)-4-methylpent-3-en-1-yl]-9-(furan-3-yl)-6-methylnona-2,6-dienoate)