NP-MRD: Showing NP-Card for 4-[(3e,7e)-4,8-dimethyl-10-(2,6,6-trimethyl-3-oxocyclohex-1-en-1-yl)deca-3,7-dien-1-yl]-5-hydroxy-5h-furan-2-one (NP0292787)

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Record Information

Version

2.0

Created at

2022-09-10 00:29:06 UTC

Updated at

2022-09-10 00:29:06 UTC

NP-MRD ID

NP0292787

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-[(3e,7e)-4,8-dimethyl-10-(2,6,6-trimethyl-3-oxocyclohex-1-en-1-yl)deca-3,7-dien-1-yl]-5-hydroxy-5h-furan-2-one

Description

Acantholide B belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety. 4-[(3e,7e)-4,8-dimethyl-10-(2,6,6-trimethyl-3-oxocyclohex-1-en-1-yl)deca-3,7-dien-1-yl]-5-hydroxy-5h-furan-2-one was first documented in 2004 (PMID: 15568767). Based on a literature review very few articles have been published on acantholide B.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102202292D          

 29 30  0  0  0  0            999 V2000
   -4.1801    5.7134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8946    6.1259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6091    5.7134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6091    4.8884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8946    4.4759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8946    3.6509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1801    3.2384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6091    3.2384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6091    2.4134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3235    2.0009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3235    1.1759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6091    0.7634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0380    0.7634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0380   -0.0616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7525   -0.4741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7525   -1.2991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0850   -1.7840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3400   -2.5687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8551   -3.2361    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1650   -2.5687    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4199   -1.7840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2045   -1.5291    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3235    6.1259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6057    5.3506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1360    6.2692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3235    6.9509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6091    7.3634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8946    6.9509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1801    7.3634    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  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
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 16 21  1  0  0  0  0
 21 22  1  0  0  0  0
  3 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 23 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
  2 28  1  0  0  0  0
 28 29  2  0  0  0  0
M  END

     RDKit          3D

 65 66  0  0  0  0  0  0  0  0999 V2000
   -3.6474   -2.0509    1.8935 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3074   -1.1074    0.9987 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8172    0.1239    0.8412 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6182    0.4624    1.5999 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3796    0.8636    0.9425 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7059   -0.0576    0.0248 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1840   -1.4159    0.3987 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.6907   -0.1929   -1.7965 C   0  0  0  0  0  0  0  0  0  0  0  0
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    8.3719   -0.8708    1.7852 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5953   -1.1698    1.9744 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5829   -0.0268    2.5276 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3114    0.0237    1.9855 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.0036    1.3434    1.6504 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5021    1.0763   -0.0569 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6907    1.3426   -1.3436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6253    2.4185    0.7001 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8591    0.7102   -0.5259 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5462   -0.4387    0.1473 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5383   -1.5178    0.3050 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7325   -2.6573   -0.1157 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7574   -1.6809    2.9377 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1602   -3.0584    1.9182 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6202   -2.2661    1.6058 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.8979   -1.4333    0.1291 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.8971   -0.6910   -3.5025 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2811    1.8933   -0.7601 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1319    0.7358    0.3401 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0227    2.0376   -0.5521 H   0  0  0  0  0  0  0  0  0  0  0  0
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    5.5364   -1.9578   -0.8722 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4220   -1.6431    0.4692 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8886   -2.0874   -0.0611 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5096   -0.2982    2.6997 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4461    1.7814    2.3365 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0111    2.1828   -1.1753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4030    1.7235   -2.1418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2840    0.4263   -1.7537 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.9735   -0.0824    1.1141 H   0  0  0  0  0  0  0  0  0  0  0  0
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 17 53  1  0
 21 54  1  1
 22 55  1  0
M  END


  Mrv1652309102202292D          

 29 30  0  0  0  0            999 V2000
   -4.1801    5.7134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8946    6.1259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6091    5.7134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6091    4.8884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8946    4.4759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8946    3.6509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1801    3.2384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6091    3.2384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6091    2.4134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3235    2.0009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3235    1.1759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6091    0.7634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.3400   -2.5687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8551   -3.2361    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1650   -2.5687    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4199   -1.7840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2045   -1.5291    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.6057    5.3506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.3235    6.9509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6091    7.3634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8946    6.9509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1801    7.3634    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  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
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 16 21  1  0  0  0  0
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  3 23  1  0  0  0  0
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  2 28  1  0  0  0  0
 28 29  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0292787

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C(CC\C=C(/C)CCC1=C(C)C(=O)CCC1(C)C)=C/CCC1=CC(=O)OC1O

> <INCHI_IDENTIFIER>
InChI=1S/C25H36O4/c1-17(10-7-11-20-16-23(27)29-24(20)28)8-6-9-18(2)12-13-21-19(3)22(26)14-15-25(21,4)5/h9-10,16,24,28H,6-8,11-15H2,1-5H3/b17-10+,18-9+

> <INCHI_KEY>
XPWNPMMYRFJXQW-SCNFBCNRSA-N

> <FORMULA>
C25H36O4

> <MOLECULAR_WEIGHT>
400.559

> <EXACT_MASS>
400.261359639

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
65

> <JCHEM_AVERAGE_POLARIZABILITY>
47.00179945722779

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4-[(3E,7E)-4,8-dimethyl-10-(2,6,6-trimethyl-3-oxocyclohex-1-en-1-yl)deca-3,7-dien-1-yl]-5-hydroxy-2,5-dihydrofuran-2-one

> <JCHEM_LOGP>
5.983451297666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.79016877746944

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.244709966756547

> <JCHEM_PKA_STRONGEST_BASIC>
-4.27173086790421

> <JCHEM_POLAR_SURFACE_AREA>
63.6

> <JCHEM_REFRACTIVITY>
119.36579999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
4-[(3E,7E)-4,8-dimethyl-10-(2,6,6-trimethyl-3-oxocyclohex-1-en-1-yl)deca-3,7-dien-1-yl]-5-hydroxy-5H-furan-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0      -7.803  10.665   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -9.137  11.435   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -10.470  10.665   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0     -10.470   9.125   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -9.137   8.355   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -9.137   6.815   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -7.803   6.045   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0     -10.470   6.045   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0     -10.470   4.505   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0     -11.804   3.735   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0     -11.804   2.195   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0     -10.470   1.425   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0     -13.138   1.425   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0     -13.138  -0.115   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0     -14.471  -0.885   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0     -14.471  -2.425   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0     -13.225  -3.330   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0     -13.701  -4.795   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0     -12.796  -6.041   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0     -15.241  -4.795   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0     -15.717  -3.330   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0     -17.182  -2.854   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0     -11.804  11.435   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0     -12.331   9.988   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0     -13.321  11.702   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0     -11.804  12.975   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0     -10.470  13.745   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -9.137  12.975   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -7.803  13.745   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   28                                                  
CONECT    3    2    4   23                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   21                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   16   22                                                  
CONECT   22   21                                                            
CONECT   23    3   24   25   26                                             
CONECT   24   23                                                            
CONECT   25   23                                                            
CONECT   26   23   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27    2   29                                                  
CONECT   29   28                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₃₆O₄

Average Mass

400.5590 Da

Monoisotopic Mass

400.26136 Da

IUPAC Name

4-[(3E,7E)-4,8-dimethyl-10-(2,6,6-trimethyl-3-oxocyclohex-1-en-1-yl)deca-3,7-dien-1-yl]-5-hydroxy-2,5-dihydrofuran-2-one

Traditional Name

4-[(3E,7E)-4,8-dimethyl-10-(2,6,6-trimethyl-3-oxocyclohex-1-en-1-yl)deca-3,7-dien-1-yl]-5-hydroxy-5H-furan-2-one

CAS Registry Number

Not Available

SMILES

C\C(CC\C=C(/C)CCC1=C(C)C(=O)CCC1(C)C)=C/CCC1=CC(=O)OC1O

InChI Identifier

InChI=1S/C25H36O4/c1-17(10-7-11-20-16-23(27)29-24(20)28)8-6-9-18(2)12-13-21-19(3)22(26)14-15-25(21,4)5/h9-10,16,24,28H,6-8,11-15H2,1-5H3/b17-10+,18-9+

InChI Key

XPWNPMMYRFJXQW-SCNFBCNRSA-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 diterpene lactones. These are diterpenoids containing a lactone moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Diterpene lactones

Alternative Parents

Substituents

Diterpene lactone
Diterpenoid
Cyclohexenone
2-furanone
Dihydrofuran
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Carboxylic acid ester
Hemiacetal
Ketone
Lactone
Cyclic ketone
Oxacycle
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organoheterocyclic compound
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Aldehyde
Carbonyl group
Organooxygen compound
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic 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	5.98	ChemAxon
pKa (Strongest Acidic)	7.24	ChemAxon
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	63.6 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	119.37 m³·mol⁻¹	ChemAxon
Polarizability	47 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	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

C00043230

Chemspider ID

9398377

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11223324

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Elkhayat E, Edrada R, Ebel R, Wray V, van Soest R, Wiryowidagdo S, Mohamed MH, Muller WE, Proksch P: New luffariellolide derivatives from the Indonesian sponge Acanthodendrilla sp. J Nat Prod. 2004 Nov;67(11):1809-17. doi: 10.1021/np040118j. [PubMed:15568767 ]
LOTUS database [Link]

Showing NP-Card for 4-[(3e,7e)-4,8-dimethyl-10-(2,6,6-trimethyl-3-oxocyclohex-1-en-1-yl)deca-3,7-dien-1-yl]-5-hydroxy-5h-furan-2-one (NP0292787)

MOL for NP0292787 (4-[(3e,7e)-4,8-dimethyl-10-(2,6,6-trimethyl-3-oxocyclohex-1-en-1-yl)deca-3,7-dien-1-yl]-5-hydroxy-5h-furan-2-one)

3D MOL for NP0292787 (4-[(3e,7e)-4,8-dimethyl-10-(2,6,6-trimethyl-3-oxocyclohex-1-en-1-yl)deca-3,7-dien-1-yl]-5-hydroxy-5h-furan-2-one)

3D SDF for NP0292787 (4-[(3e,7e)-4,8-dimethyl-10-(2,6,6-trimethyl-3-oxocyclohex-1-en-1-yl)deca-3,7-dien-1-yl]-5-hydroxy-5h-furan-2-one)

3D-SDF for NP0292787 (4-[(3e,7e)-4,8-dimethyl-10-(2,6,6-trimethyl-3-oxocyclohex-1-en-1-yl)deca-3,7-dien-1-yl]-5-hydroxy-5h-furan-2-one)

PDB for NP0292787 (4-[(3e,7e)-4,8-dimethyl-10-(2,6,6-trimethyl-3-oxocyclohex-1-en-1-yl)deca-3,7-dien-1-yl]-5-hydroxy-5h-furan-2-one)

3D PDB for NP0292787 (4-[(3e,7e)-4,8-dimethyl-10-(2,6,6-trimethyl-3-oxocyclohex-1-en-1-yl)deca-3,7-dien-1-yl]-5-hydroxy-5h-furan-2-one)

SMILES for NP0292787 (4-[(3e,7e)-4,8-dimethyl-10-(2,6,6-trimethyl-3-oxocyclohex-1-en-1-yl)deca-3,7-dien-1-yl]-5-hydroxy-5h-furan-2-one)

INCHI for NP0292787 (4-[(3e,7e)-4,8-dimethyl-10-(2,6,6-trimethyl-3-oxocyclohex-1-en-1-yl)deca-3,7-dien-1-yl]-5-hydroxy-5h-furan-2-one)

Structure for NP0292787 (4-[(3e,7e)-4,8-dimethyl-10-(2,6,6-trimethyl-3-oxocyclohex-1-en-1-yl)deca-3,7-dien-1-yl]-5-hydroxy-5h-furan-2-one)

3D Structure for NP0292787 (4-[(3e,7e)-4,8-dimethyl-10-(2,6,6-trimethyl-3-oxocyclohex-1-en-1-yl)deca-3,7-dien-1-yl]-5-hydroxy-5h-furan-2-one)