NP-MRD: Showing NP-Card for 2-{3-[(4e)-6-(2,6-dihydroxy-4-methylphenyl)-4-methylhex-4-en-1-yl]-5-(2-methylprop-1-en-1-yl)furan-2-yl}-5-hydroxy-3-methyl-6-[(2e,6e)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]cyclohexa-2,5-diene-1,4-dione (NP0308936)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-11 03:07:28 UTC

Updated at

2022-09-11 03:07:29 UTC

NP-MRD ID

NP0308936

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-{3-[(4e)-6-(2,6-dihydroxy-4-methylphenyl)-4-methylhex-4-en-1-yl]-5-(2-methylprop-1-en-1-yl)furan-2-yl}-5-hydroxy-3-methyl-6-[(2e,6e)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]cyclohexa-2,5-diene-1,4-dione

Description

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112205072D          

 50 52  0  0  0  0            999 V2000
   -2.7512    8.0652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7512    7.2402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0367    6.8277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4656    6.8277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4656    6.0027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1801    5.5902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1801    4.7652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4656    4.3527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8946    4.3527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8946    3.5277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6091    3.1152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6091    2.2902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3235    1.8777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8946    1.8777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8946    1.0527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1801    0.6402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4656    1.0527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4656    1.8777    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7512    0.6402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0367    1.0527    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7512   -0.1848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0367   -0.5973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4656   -0.5973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4656   -1.4223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7982   -1.9072    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0531   -2.6919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5682   -3.3593    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7477   -3.2731    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2628   -3.9405    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4122   -2.5194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8781   -2.6919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1331   -1.9072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9177   -1.6523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5308   -2.2043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3154   -1.9494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9285   -2.5014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7131   -2.2465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7570   -3.3084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3701   -3.8604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1986   -4.6674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4139   -4.9223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8008   -4.3703    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2424   -5.7293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8555   -6.2813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6840   -7.0883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6401   -6.0264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8117   -5.2194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5963   -4.9645    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1801   -0.1848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8946   -0.5973    0.0000 O   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
  2  4  2  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
  7  8  1  0  0  0  0
  7  9  2  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
 12 13  1  0  0  0  0
 12 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
 17 18  1  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  1  0  0  0  0
 21 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 26 31  2  0  0  0  0
 31 32  1  0  0  0  0
 24 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  2  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 41 42  1  0  0  0  0
 41 43  1  0  0  0  0
 43 44  2  0  0  0  0
 44 45  1  0  0  0  0
 44 46  1  0  0  0  0
 46 47  2  0  0  0  0
 40 47  1  0  0  0  0
 47 48  1  0  0  0  0
 23 49  1  0  0  0  0
 16 49  1  0  0  0  0
 49 50  2  0  0  0  0
M  END

     RDKit          3D

106108  0  0  0  0  0  0  0  0999 V2000
   12.2664    1.6033   -0.8839 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1427    0.7384    0.3454 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.7769    1.1639    1.6264 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4834   -0.3906    0.2863 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3163   -1.2871    1.4316 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8420   -1.4880    1.6967 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1369   -2.0772    0.5493 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5080   -3.3872    0.0001 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1273   -1.4111   -0.0074 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3932   -1.9438   -1.1492 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9645   -2.2750   -0.9777 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0535   -1.1986   -0.5747 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2076   -0.5018    0.7285 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0518   -0.8254   -1.3631 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0875    0.2390   -1.0440 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6825   -0.2106   -1.0024 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3270   -1.4611   -1.1831 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2570   -2.4522   -1.4226 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0776   -1.8719   -1.1434 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3917   -3.0823   -1.3202 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1311   -0.8759   -0.8965 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5470   -1.3117   -0.9534 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8220    0.3506   -0.7120 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7052    1.4837   -0.4497 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7223    2.5298   -1.3134 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5627    3.4356   -0.9027 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8569    4.7204   -1.5773 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0526    5.2455   -1.6677 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2412    6.5397   -2.3647 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2288    4.5612   -1.0888 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1448    3.0326    0.2538 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5795    1.7482    0.5484 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0219    1.0033    1.7399 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2458    0.1660    1.6279 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3854    1.1039    1.2339 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6826    0.3660    1.0668 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7922   -0.6987    0.0315 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7021    0.6702    1.8201 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0590    0.1558    1.9031 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5679   -0.8852    1.0569 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9425   -0.5511   -0.2541 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7537    0.7817   -0.6567 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4701   -1.4897   -1.1031 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.6628   -2.8002   -0.7268 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.2343   -3.8084   -1.6610 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2964   -3.1246    0.5547 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7578   -2.2156    1.4536 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4044   -2.5996    2.7292 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6304    0.7573   -0.7570 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9668    1.9542   -0.5814 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.7137    2.5759   -0.5639 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.9259    1.0444   -1.5758 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.2881    1.7425   -1.3860 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.4499    2.0255    1.3948 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.0226    1.5742    2.3275 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.3632    0.3774    2.1183 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.0314   -0.6913   -0.6530 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.7428   -0.8117    2.3460 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.8432   -2.2497    1.2551 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7367   -2.0757    2.6272 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.4335   -0.4700    1.9526 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.3387   -3.8037    0.6079 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6778   -4.1471    0.1320 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.8610   -3.3773   -1.0450 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8749   -0.4494    0.4148 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4653   -1.2497   -2.0392 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9126   -2.8813   -1.5199 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6159   -2.6990   -1.9695 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7894   -3.1276   -0.2704 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7204    0.4657    0.5719 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8221   -1.0807    1.4530 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2191   -0.3577    1.2336 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9851   -1.3582   -2.3168 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2017    0.9985   -1.8859 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3826    0.8323   -0.1431 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7466   -2.9411   -0.6925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7917   -2.0520   -0.1802 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2072   -0.4498   -1.0134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6143   -1.9080   -1.9241 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9662    5.1992   -2.0038 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5409    7.3299   -1.9909 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1128    6.3401   -3.4493 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2710    6.9420   -2.2193 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1291    4.7989   -1.7365 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5142    4.9631   -0.0941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1425    3.4673   -1.1392 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8858    3.5208    0.8856 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1827    0.3115    2.0400 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1782    1.6822    2.6175 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5323   -0.1245    2.7000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2458   -0.7247    1.0461 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1379    1.5175    0.2542 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4889    1.8102    2.0541 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2677   -0.3718   -0.8978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7576   -1.0390   -0.2708 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3131   -1.5540    0.4503 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4660    1.5164    2.5604 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2081   -0.1834    2.9834 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8063    1.0619    1.9084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3758    1.4667   -0.0485 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7504   -1.2059   -2.1031 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.3916   -4.1517   -2.2866 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.0147   -3.3037   -2.2558 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.6124   -4.6547   -1.0473 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4299   -4.1462    0.9008 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0084   -2.0491    3.4488 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  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  1  0
 12 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 17 19  1  0
 19 20  2  0
 19 21  1  0
 21 22  1  0
 21 23  2  0
 23 24  1  0
 24 32  2  0
 32 33  1  0
 33 34  1  0
 34 35  1  0
 35 36  1  0
 36 37  1  0
 36 38  2  0
 38 39  1  0
 39 40  1  0
 40 41  2  0
 41 42  1  0
 41 43  1  0
 43 44  2  0
 44 45  1  0
 44 46  1  0
 46 47  2  0
 47 48  1  0
 32 31  1  0
 31 26  2  0
 26 25  1  0
 26 27  1  0
 27 28  2  3
 28 29  1  0
 28 30  1  0
 23 49  1  0
 49 50  2  0
 49 16  1  0
 25 24  1  0
 47 40  1  0
  1 51  1  0
  1 52  1  0
  1 53  1  0
  3 54  1  0
  3 55  1  0
  3 56  1  0
  4 57  1  0
  5 58  1  0
  5 59  1  0
  6 60  1  0
  6 61  1  0
  8 62  1  0
  8 63  1  0
  8 64  1  0
  9 65  1  0
 10 66  1  0
 10 67  1  0
 11 68  1  0
 11 69  1  0
 13 70  1  0
 13 71  1  0
 13 72  1  0
 14 73  1  0
 15 74  1  0
 15 75  1  0
 18 76  1  0
 22 77  1  0
 22 78  1  0
 22 79  1  0
 33 88  1  0
 33 89  1  0
 34 90  1  0
 34 91  1  0
 35 92  1  0
 35 93  1  0
 37 94  1  0
 37 95  1  0
 37 96  1  0
 38 97  1  0
 39 98  1  0
 39 99  1  0
 42100  1  0
 43101  1  0
 45102  1  0
 45103  1  0
 45104  1  0
 46105  1  0
 48106  1  0
 31 87  1  0
 27 80  1  0
 29 81  1  0
 29 82  1  0
 29 83  1  0
 30 84  1  0
 30 85  1  0
 30 86  1  0
M  END


  Mrv1652309112205072D          

 50 52  0  0  0  0            999 V2000
   -2.7512    8.0652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7512    7.2402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0367    6.8277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4656    6.8277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4656    6.0027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1801    5.5902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1801    4.7652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4656    4.3527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8946    4.3527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8946    3.5277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6091    3.1152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6091    2.2902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3235    1.8777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8946    1.8777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8946    1.0527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1801    0.6402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4656    1.0527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4656    1.8777    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7512    0.6402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0367    1.0527    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7512   -0.1848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0367   -0.5973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4656   -0.5973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4656   -1.4223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7982   -1.9072    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0531   -2.6919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5682   -3.3593    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7477   -3.2731    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2628   -3.9405    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4122   -2.5194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8781   -2.6919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1331   -1.9072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9177   -1.6523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5308   -2.2043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3154   -1.9494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9285   -2.5014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7131   -2.2465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7570   -3.3084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3701   -3.8604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1986   -4.6674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4139   -4.9223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8008   -4.3703    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2424   -5.7293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8555   -6.2813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6840   -7.0883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6401   -6.0264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8117   -5.2194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5963   -4.9645    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1801   -0.1848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8946   -0.5973    0.0000 O   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
  2  4  2  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
  7  8  1  0  0  0  0
  7  9  2  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
 12 13  1  0  0  0  0
 12 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
 17 18  1  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  1  0  0  0  0
 21 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 26 31  2  0  0  0  0
 31 32  1  0  0  0  0
 24 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  2  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 41 42  1  0  0  0  0
 41 43  1  0  0  0  0
 43 44  2  0  0  0  0
 44 45  1  0  0  0  0
 44 46  1  0  0  0  0
 46 47  2  0  0  0  0
 40 47  1  0  0  0  0
 47 48  1  0  0  0  0
 23 49  1  0  0  0  0
 16 49  1  0  0  0  0
 49 50  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0308936

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCC\C(C)=C\CC\C(C)=C\CC1=C(O)C(=O)C(C)=C(C2=C(CCC\C(C)=C\CC3=C(O)C=C(C)C=C3O)C=C(O2)C=C(C)C)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C44H56O6/c1-27(2)13-10-14-29(5)15-11-16-30(6)20-22-37-42(48)40(33(9)41(47)43(37)49)44-34(26-35(50-44)23-28(3)4)18-12-17-31(7)19-21-36-38(45)24-32(8)25-39(36)46/h13,15,19-20,23-26,45-46,49H,10-12,14,16-18,21-22H2,1-9H3/b29-15+,30-20+,31-19+

> <INCHI_KEY>
JUPSTCZUZHJAGO-FGESODLRSA-N

> <FORMULA>
C44H56O6

> <MOLECULAR_WEIGHT>
680.926

> <EXACT_MASS>
680.407689523

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
106

> <JCHEM_AVERAGE_POLARIZABILITY>
80.54026182469026

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-{3-[(4E)-6-(2,6-dihydroxy-4-methylphenyl)-4-methylhex-4-en-1-yl]-5-(2-methylprop-1-en-1-yl)furan-2-yl}-5-hydroxy-3-methyl-6-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]cyclohexa-2,5-diene-1,4-dione

> <JCHEM_LOGP>
11.948532879

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
9.19310454362765

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.542522099233431

> <JCHEM_PKA_STRONGEST_BASIC>
-2.847327117420458

> <JCHEM_POLAR_SURFACE_AREA>
107.97

> <JCHEM_REFRACTIVITY>
212.02330000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
16

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
2-{3-[(4E)-6-(2,6-dihydroxy-4-methylphenyl)-4-methylhex-4-en-1-yl]-5-(2-methylprop-1-en-1-yl)furan-2-yl}-5-hydroxy-3-methyl-6-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]cyclohexa-2,5-diene-1,4-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0      -5.136  15.055   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.136  13.515   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.802  12.745   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -6.469  12.745   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -6.469  11.205   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -7.803  10.435   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -7.803   8.895   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -6.469   8.125   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -9.137   8.125   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -9.137   6.585   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0     -10.470   5.815   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0     -10.470   4.275   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0     -11.804   3.505   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -9.137   3.505   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -9.137   1.965   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -7.803   1.195   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -6.469   1.965   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -6.469   3.505   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -5.136   1.195   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -3.802   1.965   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -5.136  -0.345   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -3.802  -1.115   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -6.469  -1.115   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -6.469  -2.655   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -5.223  -3.560   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -5.699  -5.025   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -4.794  -6.271   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -3.262  -6.110   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -2.357  -7.356   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -2.636  -4.703   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -7.239  -5.025   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -7.715  -3.560   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -9.180  -3.084   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0     -10.324  -4.115   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0     -11.789  -3.639   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0     -12.933  -4.669   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0     -14.398  -4.193   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0     -12.613  -6.176   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0     -13.757  -7.206   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0     -13.437  -8.712   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0     -11.973  -9.188   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0     -10.828  -8.158   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0     -11.653 -10.695   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0     -12.797 -11.725   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0     -12.477 -13.232   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0     -14.262 -11.249   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0     -14.582  -9.743   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0     -16.046  -9.267   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0      -7.803  -0.345   0.000  0.00  0.00           C+0
HETATM   50  O   UNK     0      -9.137  -1.115   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   49                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   49                                                  
CONECT   24   23   25   32                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   31                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28                                                            
CONECT   31   26   32                                                       
CONECT   32   31   24   33                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   41   47                                                  
CONECT   41   40   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41   44                                                       
CONECT   44   43   45   46                                                  
CONECT   45   44                                                            
CONECT   46   44   47                                                       
CONECT   47   46   40   48                                                  
CONECT   48   47                                                            
CONECT   49   23   16   50                                                  
CONECT   50   49                                                            
MASTER        0    0    0    0    0    0    0    0   50    0  104    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₄H₅₆O₆

Average Mass

680.9260 Da

Monoisotopic Mass

680.40769 Da

IUPAC Name

2-{3-[(4E)-6-(2,6-dihydroxy-4-methylphenyl)-4-methylhex-4-en-1-yl]-5-(2-methylprop-1-en-1-yl)furan-2-yl}-5-hydroxy-3-methyl-6-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]cyclohexa-2,5-diene-1,4-dione

Traditional Name

CAS Registry Number

Not Available

SMILES

CC(C)=CCC\C(C)=C\CC\C(C)=C\CC1=C(O)C(=O)C(C)=C(C2=C(CCC\C(C)=C\CC3=C(O)C=C(C)C=C3O)C=C(O2)C=C(C)C)C1=O

InChI Identifier

InChI=1S/C44H56O6/c1-27(2)13-10-14-29(5)15-11-16-30(6)20-22-37-42(48)40(33(9)41(47)43(37)49)44-34(26-35(50-44)23-28(3)4)18-12-17-31(7)19-21-36-38(45)24-32(8)25-39(36)46/h13,15,19-20,23-26,45-46,49H,10-12,14,16-18,21-22H2,1-9H3/b29-15+,30-20+,31-19+

InChI Key

JUPSTCZUZHJAGO-FGESODLRSA-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
Albatrellopsis flettii	LOTUS Database	35616633
Albatrellus cristatus	LOTUS Database	35616633

Chemical Taxonomy

Classification

Not classified

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	11.95	ChemAxon
pKa (Strongest Acidic)	5.54	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	107.97 Å²	ChemAxon
Rotatable Bond Count	16	ChemAxon
Refractivity	212.02 m³·mol⁻¹	ChemAxon
Polarizability	80.54 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-{3-[(4e)-6-(2,6-dihydroxy-4-methylphenyl)-4-methylhex-4-en-1-yl]-5-(2-methylprop-1-en-1-yl)furan-2-yl}-5-hydroxy-3-methyl-6-[(2e,6e)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]cyclohexa-2,5-diene-1,4-dione (NP0308936)

MOL for NP0308936 (2-{3-[(4e)-6-(2,6-dihydroxy-4-methylphenyl)-4-methylhex-4-en-1-yl]-5-(2-methylprop-1-en-1-yl)furan-2-yl}-5-hydroxy-3-methyl-6-[(2e,6e)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]cyclohexa-2,5-diene-1,4-dione)

3D MOL for NP0308936 (2-{3-[(4e)-6-(2,6-dihydroxy-4-methylphenyl)-4-methylhex-4-en-1-yl]-5-(2-methylprop-1-en-1-yl)furan-2-yl}-5-hydroxy-3-methyl-6-[(2e,6e)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]cyclohexa-2,5-diene-1,4-dione)

3D SDF for NP0308936 (2-{3-[(4e)-6-(2,6-dihydroxy-4-methylphenyl)-4-methylhex-4-en-1-yl]-5-(2-methylprop-1-en-1-yl)furan-2-yl}-5-hydroxy-3-methyl-6-[(2e,6e)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]cyclohexa-2,5-diene-1,4-dione)

3D-SDF for NP0308936 (2-{3-[(4e)-6-(2,6-dihydroxy-4-methylphenyl)-4-methylhex-4-en-1-yl]-5-(2-methylprop-1-en-1-yl)furan-2-yl}-5-hydroxy-3-methyl-6-[(2e,6e)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]cyclohexa-2,5-diene-1,4-dione)

PDB for NP0308936 (2-{3-[(4e)-6-(2,6-dihydroxy-4-methylphenyl)-4-methylhex-4-en-1-yl]-5-(2-methylprop-1-en-1-yl)furan-2-yl}-5-hydroxy-3-methyl-6-[(2e,6e)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]cyclohexa-2,5-diene-1,4-dione)

3D PDB for NP0308936 (2-{3-[(4e)-6-(2,6-dihydroxy-4-methylphenyl)-4-methylhex-4-en-1-yl]-5-(2-methylprop-1-en-1-yl)furan-2-yl}-5-hydroxy-3-methyl-6-[(2e,6e)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]cyclohexa-2,5-diene-1,4-dione)

SMILES for NP0308936 (2-{3-[(4e)-6-(2,6-dihydroxy-4-methylphenyl)-4-methylhex-4-en-1-yl]-5-(2-methylprop-1-en-1-yl)furan-2-yl}-5-hydroxy-3-methyl-6-[(2e,6e)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]cyclohexa-2,5-diene-1,4-dione)

INCHI for NP0308936 (2-{3-[(4e)-6-(2,6-dihydroxy-4-methylphenyl)-4-methylhex-4-en-1-yl]-5-(2-methylprop-1-en-1-yl)furan-2-yl}-5-hydroxy-3-methyl-6-[(2e,6e)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]cyclohexa-2,5-diene-1,4-dione)

Structure for NP0308936 (2-{3-[(4e)-6-(2,6-dihydroxy-4-methylphenyl)-4-methylhex-4-en-1-yl]-5-(2-methylprop-1-en-1-yl)furan-2-yl}-5-hydroxy-3-methyl-6-[(2e,6e)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]cyclohexa-2,5-diene-1,4-dione)

3D Structure for NP0308936 (2-{3-[(4e)-6-(2,6-dihydroxy-4-methylphenyl)-4-methylhex-4-en-1-yl]-5-(2-methylprop-1-en-1-yl)furan-2-yl}-5-hydroxy-3-methyl-6-[(2e,6e)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]cyclohexa-2,5-diene-1,4-dione)