NP-MRD: Showing NP-Card for 3-{[(1r,2s,4as,8as)-1,2,4a-trimethyl-5-methylidene-hexahydro-2h-naphthalen-1-yl]methyl}-5-methoxycyclohex-5-ene-1,2,4-trione (NP0195598)

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Record Information

Version

2.0

Created at

2022-09-04 13:29:16 UTC

Updated at

2022-09-04 13:29:16 UTC

NP-MRD ID

NP0195598

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-{[(1r,2s,4as,8as)-1,2,4a-trimethyl-5-methylidene-hexahydro-2h-naphthalen-1-yl]methyl}-5-methoxycyclohex-5-ene-1,2,4-trione

Description

(-)-Ilimaquinone belongs to the class of organic compounds known as prenylquinones. These are quinones with a structure characterized by the quinone ring substituted by an prenyl side-chain. 3-{[(1r,2s,4as,8as)-1,2,4a-trimethyl-5-methylidene-hexahydro-2h-naphthalen-1-yl]methyl}-5-methoxycyclohex-5-ene-1,2,4-trione is found in Dactylospongia elegans. Based on a literature review very few articles have been published on (-)-ilimaquinone.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042215292D          

 26 28  0  0  1  0            999 V2000
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8163   -2.3784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0416   -2.3784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4788   -3.0781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3033   -3.0493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6906   -2.3208    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7405   -3.7489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5650   -3.7201    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3532   -4.4774    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5287   -4.5061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1414   -5.2346    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5785   -5.9342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0915   -3.8065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2670   -3.8353    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  2  7  1  0  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 11 13  1  0  0  0  0
  6 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 22 25  1  0  0  0  0
 16 25  1  0  0  0  0
 25 26  2  0  0  0  0
M  END

     RDKit          3D

 56 58  0  0  0  0  0  0  0  0999 V2000
   -3.9806   -0.8952    2.3723 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1089   -1.2757    1.4778 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6304   -2.6672    1.4344 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3341   -2.8512    0.7279 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4496   -1.6608    0.7012 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1220   -0.3284    0.5936 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5742   -0.3290    0.4740 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2058   -0.6802   -0.8283 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0429    1.0745    0.8155 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3887    2.1361    0.0006 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0499    1.8990   -0.5360 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0277    2.4268   -1.9823 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3504    0.6170   -0.3470 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1351   -0.0847   -1.6680 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9875    0.7228    0.3345 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1065    1.4369   -0.2751 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6535    0.9961   -1.5480 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4087    1.4693   -2.6849 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6111   -0.1310   -1.5606 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7790   -0.7959   -2.6176 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3778   -0.5064   -0.3810 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1719    0.2171    0.7069 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9021   -0.1271    1.8617 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1932   -0.6789    1.7801 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2309    1.3270    0.7204 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4250    2.1891    1.6255 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3547   -1.6421    3.1076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3953    0.1146    2.4754 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4033   -3.2406    0.8402 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6570   -3.1595    2.4375 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4645   -3.2634   -0.3172 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7984   -3.6961    1.2582 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2513   -1.7385    1.5824 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2408   -1.8010   -0.1830 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9281    0.1697    1.6013 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0451   -1.6885   -1.1937 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0493    0.1391   -1.5577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3265   -0.6328   -0.6389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8222    1.2109    1.8922 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1455    1.0594    0.7205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1255    2.3564   -0.8349 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4616    3.0897    0.6104 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3701    2.6692   -0.0368 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7273    1.8303   -2.5869 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5050    3.4587   -1.9680 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0395    2.5895   -2.3812 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9041   -0.8728   -1.8472 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8257   -0.6324   -1.7125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1570    0.5681   -2.5491 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3615   -0.3142    0.5978 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8714    1.1728    1.3742 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9417    2.5791   -0.2790 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0685   -1.3378   -0.4306 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2206   -1.6326    1.2269 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9414    0.0560    1.3788 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5102   -0.9113    2.8195 H   0  0  0  0  0  0  0  0  0  0  0  0
 24 23  1  0
 23 22  1  0
 22 21  2  0
 21 19  1  0
 19 20  2  0
 19 17  1  0
 17 18  2  0
 17 16  1  0
 16 15  1  0
 13 15  1  1
 13 14  1  0
 13 11  1  0
 11 12  1  0
 11 10  1  0
 10  9  1  0
  9  7  1  0
  7  8  1  6
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  2  3
 16 25  1  0
 25 26  2  0
 25 22  1  0
  6 13  1  0
  2  7  1  0
 24 54  1  0
 24 55  1  0
 24 56  1  0
 21 53  1  0
 16 52  1  6
 15 50  1  0
 15 51  1  0
 14 47  1  0
 14 48  1  0
 14 49  1  0
 11 43  1  1
 12 44  1  0
 12 45  1  0
 12 46  1  0
 10 41  1  0
 10 42  1  0
  9 39  1  0
  9 40  1  0
  8 36  1  0
  8 37  1  0
  8 38  1  0
  6 35  1  1
  5 33  1  0
  5 34  1  0
  4 31  1  0
  4 32  1  0
  3 29  1  0
  3 30  1  0
  1 27  1  0
  1 28  1  0
M  END


  Mrv1652309042215292D          

 26 28  0  0  1  0            999 V2000
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8163   -2.3784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0416   -2.3784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4788   -3.0781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3033   -3.0493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6906   -2.3208    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7405   -3.7489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5650   -3.7201    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3532   -4.4774    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5287   -4.5061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1414   -5.2346    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5785   -5.9342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0915   -3.8065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2670   -3.8353    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  2  7  1  0  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 11 13  1  0  0  0  0
  6 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 22 25  1  0  0  0  0
 16 25  1  0  0  0  0
 25 26  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0195598

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(=O)C(=O)C(C[C@]2(C)[C@@H](C)CC[C@@]3(C)[C@H]2CCCC3=C)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C22H30O4/c1-13-7-6-8-18-21(13,3)10-9-14(2)22(18,4)12-15-19(24)16(23)11-17(26-5)20(15)25/h11,14-15,18H,1,6-10,12H2,2-5H3/t14-,15?,18+,21+,22+/m0/s1

> <INCHI_KEY>
CDRGHPRWMQCYME-LZGFSABTSA-N

> <FORMULA>
C22H30O4

> <MOLECULAR_WEIGHT>
358.478

> <EXACT_MASS>
358.214409446

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
38.64071326120039

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-{[(1R,2S,4aS,8aS)-1,2,4a-trimethyl-5-methylidene-decahydronaphthalen-1-yl]methyl}-5-methoxycyclohex-5-ene-1,2,4-trione

> <JCHEM_LOGP>
5.032359288666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.499515967671336

> <JCHEM_PKA_STRONGEST_BASIC>
-4.937742551145429

> <JCHEM_POLAR_SURFACE_AREA>
60.440000000000005

> <JCHEM_REFRACTIVITY>
102.12199999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
3-{[(1R,2S,4aS,8aS)-1,2,4a-trimethyl-5-methylidene-hexahydro-2H-naphthalen-1-yl]methyl}-5-methoxycyclohex-5-ene-1,2,4-trione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.334   0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.390  -4.440   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.944  -4.440   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.760  -5.746   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.300  -5.692   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       5.022  -4.332   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       5.116  -6.998   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       6.655  -6.944   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       4.393  -8.358   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.854  -8.411   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       2.131  -9.771   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       2.947 -11.077   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.037  -7.105   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       0.498  -7.159   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   13                                                  
CONECT    7    6    2    8    9                                             
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11    6   14   15                                             
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17   25                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23   25                                                  
CONECT   23   22   24                                                       
CONECT   24   23                                                            
CONECT   25   22   16   26                                                  
CONECT   26   25                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₃₀O₄

Average Mass

358.4780 Da

Monoisotopic Mass

358.21441 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

COC1=CC(=O)C(=O)C(C[C@]2(C)[C@@H](C)CC[C@@]3(C)[C@H]2CCCC3=C)C1=O

InChI Identifier

InChI=1S/C22H30O4/c1-13-7-6-8-18-21(13,3)10-9-14(2)22(18,4)12-15-19(24)16(23)11-17(26-5)20(15)25/h11,14-15,18H,1,6-10,12H2,2-5H3/t14-,15?,18+,21+,22+/m0/s1

InChI Key

CDRGHPRWMQCYME-LZGFSABTSA-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

Species Name	Source	Reference
Dactylospongia elegans	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as prenylquinones. These are quinones with a structure characterized by the quinone ring substituted by an prenyl side-chain.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Quinone and hydroquinone lipids

Direct Parent

Prenylquinones

Alternative Parents

Substituents

Prenylbenzoquinone
Quinone
M-benzoquinone
Cyclohexenone
1,3-diketone
1,3-dicarbonyl compound
Vinylogous ester
Cyclic ketone
Ketone
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic 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

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00030510

Chemspider ID

34890385

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

91935541

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-{[(1r,2s,4as,8as)-1,2,4a-trimethyl-5-methylidene-hexahydro-2h-naphthalen-1-yl]methyl}-5-methoxycyclohex-5-ene-1,2,4-trione (NP0195598)

MOL for NP0195598 (3-{[(1r,2s,4as,8as)-1,2,4a-trimethyl-5-methylidene-hexahydro-2h-naphthalen-1-yl]methyl}-5-methoxycyclohex-5-ene-1,2,4-trione)

3D MOL for NP0195598 (3-{[(1r,2s,4as,8as)-1,2,4a-trimethyl-5-methylidene-hexahydro-2h-naphthalen-1-yl]methyl}-5-methoxycyclohex-5-ene-1,2,4-trione)

3D SDF for NP0195598 (3-{[(1r,2s,4as,8as)-1,2,4a-trimethyl-5-methylidene-hexahydro-2h-naphthalen-1-yl]methyl}-5-methoxycyclohex-5-ene-1,2,4-trione)

3D-SDF for NP0195598 (3-{[(1r,2s,4as,8as)-1,2,4a-trimethyl-5-methylidene-hexahydro-2h-naphthalen-1-yl]methyl}-5-methoxycyclohex-5-ene-1,2,4-trione)

PDB for NP0195598 (3-{[(1r,2s,4as,8as)-1,2,4a-trimethyl-5-methylidene-hexahydro-2h-naphthalen-1-yl]methyl}-5-methoxycyclohex-5-ene-1,2,4-trione)

3D PDB for NP0195598 (3-{[(1r,2s,4as,8as)-1,2,4a-trimethyl-5-methylidene-hexahydro-2h-naphthalen-1-yl]methyl}-5-methoxycyclohex-5-ene-1,2,4-trione)

SMILES for NP0195598 (3-{[(1r,2s,4as,8as)-1,2,4a-trimethyl-5-methylidene-hexahydro-2h-naphthalen-1-yl]methyl}-5-methoxycyclohex-5-ene-1,2,4-trione)

INCHI for NP0195598 (3-{[(1r,2s,4as,8as)-1,2,4a-trimethyl-5-methylidene-hexahydro-2h-naphthalen-1-yl]methyl}-5-methoxycyclohex-5-ene-1,2,4-trione)

Structure for NP0195598 (3-{[(1r,2s,4as,8as)-1,2,4a-trimethyl-5-methylidene-hexahydro-2h-naphthalen-1-yl]methyl}-5-methoxycyclohex-5-ene-1,2,4-trione)

3D Structure for NP0195598 (3-{[(1r,2s,4as,8as)-1,2,4a-trimethyl-5-methylidene-hexahydro-2h-naphthalen-1-yl]methyl}-5-methoxycyclohex-5-ene-1,2,4-trione)