NP-MRD: Showing NP-Card for phi,khi-Carotene (NP0065654)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-28 09:51:18 UTC

Updated at

2022-04-28 09:51:18 UTC

NP-MRD ID

NP0065654

Secondary Accession Numbers

None

Natural Product Identification

Common Name

phi,khi-Carotene

Description

Renieratene belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. phi,khi-Carotene is found in Reniera japonica and Tethya aurantium. phi,khi-Carotene was first documented in 2017 (PMID: 28412859). Based on a literature review very few articles have been published on Renieratene.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282211512D          

 40 41  0  0  0  0            999 V2000
    7.1447  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013  -16.0875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868  -16.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868  -17.3250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724  -17.7375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579  -19.8000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434  -20.2125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434  -21.0375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289  -21.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289  -22.2750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145  -22.6875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145  -23.5125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000  -23.9250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000  -24.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145  -25.1625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145  -25.9875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289  -26.4000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434  -25.9875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434  -25.1625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289  -24.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579  -26.4000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289  -27.2250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000  -26.4000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289  -23.9250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579  -21.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579  -17.3250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447  -11.5500    0.0000 C   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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  5  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  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
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 26 31  1  0  0  0  0
 29 32  1  0  0  0  0
 28 33  1  0  0  0  0
 27 34  1  0  0  0  0
 23 35  1  0  0  0  0
 19 36  1  0  0  0  0
 14 37  1  0  0  0  0
 10 38  1  0  0  0  0
  4 39  1  0  0  0  0
  1 40  1  0  0  0  0
M  END

     RDKit          3D

 88 89  0  0  0  0  0  0  0  0999 V2000
   -6.2443    3.3393    3.2648 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5614    2.3199    2.2585 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8021    1.8372    1.8806 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8760    1.4194    1.5536 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6153    0.5926    0.7090 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1065    0.0719   -0.4481 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6629    0.3070   -0.8312 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8727   -0.6507   -1.3415 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.1782   -0.8652   -1.0862 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.7664   -0.3633    0.0746 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.2053   -0.6044    0.3296 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.9814    0.3450    0.9362 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.6056    0.8549    2.1636 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4972    1.7904    1.6399 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1223    2.1297    1.8771 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2501    1.4608    1.1187 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8187    1.6552    1.2111 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1561    2.6285    2.1002 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0562    0.8954    0.4272 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3780    0.9065    0.3603 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8926    0.0259   -0.5785 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3149   -0.0823   -0.7384 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8324   -0.8611   -1.7123 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9196   -1.5794   -2.6212 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2298   -1.0811   -1.6655 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8959   -1.7582   -2.6505 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2110   -1.9273   -2.5101 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2390   -2.4223   -3.2593 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7724   -2.9220   -4.5655 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4884   -2.2509   -2.6998 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6445   -2.1402   -2.2675 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0495   -1.5154   -1.0100 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9604   -2.2665   -0.2234 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1331   -1.9529    1.1028 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4113   -0.9045    1.6486 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5311   -0.6185    3.0946 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5362   -0.1965    0.8357 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7576    0.9511    1.4157 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3447   -0.4747   -0.4707 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4678    0.4072   -1.2806 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4522    2.9117    3.9545 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0955    3.6811    3.8594 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7007    4.1799    2.7472 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4102    3.1216    1.9472 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5493    1.6679    2.5287 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5062    0.0650   -1.9083 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4388    1.3427   -0.5862 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0614   -0.3849   -0.2448 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3807   -1.0332   -2.2593 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.8118   -1.4187   -1.7759 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.6088   -1.1112   -0.5627 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.3889   -1.3028    1.1690 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.7709    0.3502    0.4525 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.6105    1.9720    2.1175 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.0901    0.5584    3.0906 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.6962    0.5815    2.2245 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7622    0.9989    0.9335 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8028    2.8297    2.5955 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6355    0.7707    0.3834 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1507    3.6256    1.5465 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7449    2.7870    3.0439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1146    2.3453    2.2656 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6141    0.1897   -0.2219 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0304    1.4696    0.9117 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1844   -0.5339   -1.1127 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0148    0.4312   -0.1080 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9205   -1.1328   -2.7276 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3165   -1.6527   -3.6668 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8165   -2.6470   -2.2728 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8453   -0.7086   -0.8595 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2807   -2.0807   -3.4510 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6821   -1.6701   -1.4734 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1814   -2.1285   -5.0841 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1437   -3.8416   -4.3859 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6018   -3.1986   -5.2353 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8456   -3.5671   -3.0812 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.4274   -2.3950   -2.9176 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.5183   -3.0682   -0.6465 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.8232   -2.5070    1.7408 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.4810   -0.6208    3.4986 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.1584   -1.3742    3.5656 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.9258    0.3957    3.2281 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8852    1.8774    0.8077 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1436    1.0836    2.4574 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6853    0.6945    1.5184 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9291    1.4343   -1.3040 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4319    0.4397   -0.9530 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4926    0.0719   -2.3365 H   0  0  0  0  0  0  0  0  0  0  0  0
 24 23  1  0
 23 25  1  0
 25 26  2  0
 26 27  1  0
 27 28  2  0
 28 29  1  0
 28 30  1  0
 30 31  2  0
 31 32  1  0
 32 39  2  0
 39 40  1  0
 39 37  1  0
 37 38  1  0
 37 35  2  0
 35 36  1  0
 35 34  1  0
 34 33  2  0
 23 22  2  0
 22 21  1  0
 21 20  2  0
 20 19  1  0
 19 17  2  0
 17 18  1  0
 17 16  1  0
 16 15  2  0
 15 14  1  0
 14  2  2  0
  2  1  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5 12  2  0
 12 13  1  0
 12 10  1  0
 10 11  1  0
 10  9  2  0
  9  8  1  0
  8  6  2  0
  6  7  1  0
 33 32  1  0
  6  5  1  0
 24 67  1  0
 24 68  1  0
 24 69  1  0
 25 70  1  0
 26 71  1  0
 27 72  1  0
 29 73  1  0
 29 74  1  0
 29 75  1  0
 30 76  1  0
 31 77  1  0
 40 86  1  0
 40 87  1  0
 40 88  1  0
 38 83  1  0
 38 84  1  0
 38 85  1  0
 36 80  1  0
 36 81  1  0
 36 82  1  0
 34 79  1  0
 33 78  1  0
 22 66  1  0
 21 65  1  0
 20 64  1  0
 19 63  1  0
 18 60  1  0
 18 61  1  0
 18 62  1  0
 16 59  1  0
 15 58  1  0
 14 57  1  0
  1 41  1  0
  1 42  1  0
  1 43  1  0
  3 44  1  0
  4 45  1  0
 13 54  1  0
 13 55  1  0
 13 56  1  0
 11 51  1  0
 11 52  1  0
 11 53  1  0
  9 50  1  0
  8 49  1  0
  7 46  1  0
  7 47  1  0
  7 48  1  0
M  END


  Mrv1652304282211512D          

 40 41  0  0  0  0            999 V2000
    7.1447  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013  -16.0875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868  -16.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868  -17.3250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724  -17.7375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579  -19.8000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434  -20.2125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434  -21.0375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289  -21.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289  -22.2750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145  -22.6875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145  -23.5125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000  -23.9250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000  -24.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145  -25.1625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145  -25.9875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289  -26.4000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434  -25.9875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434  -25.1625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289  -24.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579  -26.4000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289  -27.2250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000  -26.4000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289  -23.9250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579  -21.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579  -17.3250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447  -11.5500    0.0000 C   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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  5  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  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
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 26 31  1  0  0  0  0
 29 32  1  0  0  0  0
 28 33  1  0  0  0  0
 27 34  1  0  0  0  0
 23 35  1  0  0  0  0
 19 36  1  0  0  0  0
 14 37  1  0  0  0  0
 10 38  1  0  0  0  0
  4 39  1  0  0  0  0
  1 40  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0065654

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C(\C=C\C=C(/C)\C=C\C1=C(C)C(C)=C(C)C=C1)=C/C=C/C=C(\C)/C=C/C=C(\C)/C=C/C1=C(C)C(C)=CC=C1C

> <INCHI_IDENTIFIER>
InChI=1S/C40H48/c1-29(17-13-19-31(3)21-26-39-27-25-33(5)36(8)38(39)10)15-11-12-16-30(2)18-14-20-32(4)22-28-40-35(7)24-23-34(6)37(40)9/h11-28H,1-10H3/b12-11+,17-13+,18-14+,26-21+,28-22+,29-15+,30-16+,31-19+,32-20+

> <INCHI_KEY>
JYXWNSQXDWWFEW-DPIQMXNXSA-N

> <FORMULA>
C40H48

> <MOLECULAR_WEIGHT>
528.824

> <EXACT_MASS>
528.375601546

> <JCHEM_ACCEPTOR_COUNT>
0

> <JCHEM_ATOM_COUNT>
88

> <JCHEM_AVERAGE_POLARIZABILITY>
70.43206309489734

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
1,2,4-trimethyl-3-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyl-18-(2,3,4-trimethylphenyl)octadeca-1,3,5,7,9,11,13,15,17-nonaen-1-yl]benzene

> <ALOGPS_LOGP>
9.16

> <JCHEM_LOGP>
12.584785660666668

> <ALOGPS_LOGS>
-7.50

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_POLAR_SURFACE_AREA>
0.0

> <JCHEM_REFRACTIVITY>
191.43680000000012

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.69e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1,2,4-trimethyl-3-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyl-18-(2,3,4-trimethylphenyl)octadeca-1,3,5,7,9,11,13,15,17-nonaen-1-yl]benzene

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      13.337 -23.100   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      14.670 -23.870   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      14.670 -25.410   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      13.337 -26.180   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      12.003 -25.410   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      12.003 -23.870   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.669 -23.100   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      10.669 -26.180   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.669 -27.720   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.336 -28.490   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.336 -30.030   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.002 -30.800   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.002 -32.340   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.668 -33.110   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.668 -34.650   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.335 -35.420   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.335 -36.960   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.001 -37.730   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.001 -39.270   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.667 -40.040   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.667 -41.580   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.334 -42.350   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.334 -43.890   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.000 -44.660   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.000 -46.200   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -1.334 -46.970   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -1.334 -48.510   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -2.667 -49.280   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -4.001 -48.510   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -4.001 -46.970   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -2.667 -46.200   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -5.335 -49.280   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -2.667 -50.820   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       0.000 -49.280   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       2.667 -44.660   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       5.335 -40.040   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       5.335 -32.340   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       8.002 -27.720   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      13.337 -27.720   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      13.337 -21.560   0.000  0.00  0.00           C+0
CONECT    1    2    6   40                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   39                                                  
CONECT    5    4    6    8                                                  
CONECT    6    5    1    7                                                  
CONECT    7    6                                                            
CONECT    8    5    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   38                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   37                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   36                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   35                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   31                                                  
CONECT   27   26   28   34                                                  
CONECT   28   27   29   33                                                  
CONECT   29   28   30   32                                                  
CONECT   30   29   31                                                       
CONECT   31   30   26                                                       
CONECT   32   29                                                            
CONECT   33   28                                                            
CONECT   34   27                                                            
CONECT   35   23                                                            
CONECT   36   19                                                            
CONECT   37   14                                                            
CONECT   38   10                                                            
CONECT   39    4                                                            
CONECT   40    1                                                            
MASTER        0    0    0    0    0    0    0    0   40    0   82    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₀H₄₈

Average Mass

528.8240 Da

Monoisotopic Mass

528.37560 Da

IUPAC Name

1,2,4-trimethyl-3-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyl-18-(2,3,4-trimethylphenyl)octadeca-1,3,5,7,9,11,13,15,17-nonaen-1-yl]benzene

Traditional Name

1,2,4-trimethyl-3-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyl-18-(2,3,4-trimethylphenyl)octadeca-1,3,5,7,9,11,13,15,17-nonaen-1-yl]benzene

CAS Registry Number

Not Available

SMILES

C\C(\C=C\C=C(/C)\C=C\C1=C(C)C(C)=C(C)C=C1)=C/C=C/C=C(\C)/C=C/C=C(\C)/C=C/C1=C(C)C(C)=CC=C1C

InChI Identifier

InChI=1S/C40H48/c1-29(17-13-19-31(3)21-26-39-27-25-33(5)36(8)38(39)10)15-11-12-16-30(2)18-14-20-32(4)22-28-40-35(7)24-23-34(6)37(40)9/h11-28H,1-10H3/b12-11+,17-13+,18-14+,26-21+,28-22+,29-15+,30-16+,31-19+,32-20+

InChI Key

JYXWNSQXDWWFEW-DPIQMXNXSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Reniera japonica	-	KNApSAcK
Tethya aurantium	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Diterpenoids

Alternative Parents

Substituents

Diterpenoid
Styrene
Benzenoid
Monocyclic benzene moiety
Aromatic hydrocarbon
Branched unsaturated hydrocarbon
Cyclic olefin
Unsaturated hydrocarbon
Olefin
Hydrocarbon
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic 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	9.16	ALOGPS
logP	12.58	ChemAxon
logS	-7.5	ALOGPS
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	0	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	0 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	191.44 m³·mol⁻¹	ChemAxon
Polarizability	70.43 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	Yes	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

C00022818

Chemspider ID

59700439

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

12442707

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Salvo A, Giuffrida D, Rotondo A, Pasquale P, La Torre GL, Dugo G: Determination and quantification of carotenoids in sea sponges Raspaciona aculeata and Dictyonella marsilii present in the Ganzirri Lake (Messina), Italy. Nat Prod Res. 2017 Oct;31(20):2397-2404. doi: 10.1080/14786419.2017.1309537. Epub 2017 Apr 17. [PubMed:28412859 ]

Showing NP-Card for phi,khi-Carotene (NP0065654)

MOL for NP0065654 (phi,khi-Carotene)

3D MOL for NP0065654 (phi,khi-Carotene)

3D SDF for NP0065654 (phi,khi-Carotene)

3D-SDF for NP0065654 (phi,khi-Carotene)

PDB for NP0065654 (phi,khi-Carotene)

3D PDB for NP0065654 (phi,khi-Carotene)

SMILES for NP0065654 (phi,khi-Carotene)

INCHI for NP0065654 (phi,khi-Carotene)

Structure for NP0065654 (phi,khi-Carotene)

3D Structure for NP0065654 (phi,khi-Carotene)