NP-MRD: Showing NP-Card for 4-[(4e,6e,8s,11z)-14,15-dihydroxy-4,8,12-trimethyl-16-oxoheptadeca-4,6,11-trien-1-yl]-5-hydroxy-5h-furan-2-one (NP0292377)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-09 23:52:50 UTC

Updated at

2022-09-09 23:52:50 UTC

NP-MRD ID

NP0292377

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-[(4e,6e,8s,11z)-14,15-dihydroxy-4,8,12-trimethyl-16-oxoheptadeca-4,6,11-trien-1-yl]-5-hydroxy-5h-furan-2-one

Description

Sarcotin O belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety. Based on a literature review very few articles have been published on sarcotin O.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102201522D          

 30 30  0  0  1  0            999 V2000
    2.2022   -6.7034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9166   -7.1159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9166   -7.9409    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6311   -6.7034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6311   -5.8784    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3456   -7.1159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3456   -7.9409    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0600   -6.7034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7745   -7.1159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7745   -7.9409    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4890   -6.7034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4890   -5.8784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7745   -5.4659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7745   -4.6409    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.4890   -4.2284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0600   -4.2284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0600   -3.4034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3456   -2.9909    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3456   -2.1659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0600   -1.7534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6311   -1.7534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6311   -0.9284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9166   -0.5159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9166    0.3091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2492    0.7940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5041    1.5786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0192    2.2460    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3291    1.5786    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5841    0.7940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3687    0.5390    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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  1  0  0  0
 14 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
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  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
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 24 29  1  0  0  0  0
 29 30  1  0  0  0  0
M  END

     RDKit          3D

 66 66  0  0  0  0  0  0  0  0999 V2000
    8.8468    1.4640   -0.3393 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0544    1.6179   -1.5646 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0893    2.6750   -2.1649 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1989    0.5292   -2.1160 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.5709    0.9250   -3.2664 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3470   -0.1237   -1.1033 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7481   -1.2605   -1.6938 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4424    0.6833   -0.2694 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2563    1.2695   -0.8580 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3357    2.2950   -1.9303 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0462    0.9393   -0.4373 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6934   -0.0321    0.5956 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9267    0.5797    1.7505 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6093    1.2116    1.2953 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0789    1.7930    2.5066 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2794    0.1816    0.7108 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4845   -0.1295    1.1763 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3239   -1.1378    0.5841 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5128   -1.3898    1.1110 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9462   -0.6235    2.3005 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3080   -2.4703    0.5307 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5784   -2.0121   -0.0873 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5263   -1.3139    0.8242 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7563   -1.0123    0.0031 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2495    0.1637   -0.2416 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4312    0.0034   -1.0650 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2012    0.9078   -1.5218 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6159   -1.3403   -1.2980 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5830   -2.0393   -0.6480 C   0  0  2  0  0  0  0  0  0  0  0  0
   -9.1096   -2.9204    0.3117 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4691    0.6906    0.3518 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.8998    1.1436   -0.5941 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8802    2.4268    0.1989 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9488   -0.2592   -2.4422 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7988    0.3925   -4.0714 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0845   -0.6233   -0.3683 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1146   -1.6925   -1.0615 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2678    0.1007    0.6841 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0817    1.5496    0.1440 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2877    2.8735   -1.9174 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5594    3.1113   -1.7436 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0865    1.9293   -2.9314 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1819    1.4532   -0.9164 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5100   -0.6185    1.0353 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0124   -0.8211    0.1422 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6960   -0.2167    2.4874 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5317    1.3365    2.2900 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8170    2.0105    0.5553 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5354    2.5776    2.9969 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2610    1.0190    3.2549 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0140    2.3157    2.1872 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0674   -0.3566   -0.1547 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7916    0.4401    2.0421 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0091   -1.6817   -0.2725 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7940   -1.0698    2.8255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1053   -0.6779    3.0709 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1457    0.4353    2.0963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5356   -3.2200    1.3584 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6923   -3.0865   -0.1809 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4019   -1.3117   -0.9504 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1307   -2.8661   -0.5709 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8124   -1.8811    1.7227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0896   -0.3196    1.1216 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8963    1.1470    0.0789 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9632   -2.6235   -1.3649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3680   -3.0608    0.9642 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 14  1  0
 14 13  1  0
 13 12  1  0
 12 11  1  0
 11  9  2  0
  9 10  1  0
  9  8  1  0
  8  6  1  0
  6  7  1  0
  6  4  1  0
  4  5  1  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
 14 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  2  0
 26 28  1  0
 28 29  1  0
 29 30  1  0
 29 24  1  0
 15 49  1  0
 15 50  1  0
 15 51  1  0
 14 48  1  6
 13 46  1  0
 13 47  1  0
 12 44  1  0
 12 45  1  0
 11 43  1  0
 10 40  1  0
 10 41  1  0
 10 42  1  0
  8 38  1  0
  8 39  1  0
  6 36  1  1
  7 37  1  0
  4 34  1  6
  5 35  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
 16 52  1  0
 17 53  1  0
 18 54  1  0
 20 55  1  0
 20 56  1  0
 20 57  1  0
 21 58  1  0
 21 59  1  0
 22 60  1  0
 22 61  1  0
 23 62  1  0
 23 63  1  0
 25 64  1  0
 29 65  1  6
 30 66  1  0
M  END


  Mrv1652309102201522D          

 30 30  0  0  1  0            999 V2000
    2.2022   -6.7034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9166   -7.1159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9166   -7.9409    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6311   -6.7034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6311   -5.8784    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3456   -7.1159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3456   -7.9409    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0600   -6.7034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7745   -7.1159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7745   -7.9409    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4890   -6.7034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4890   -5.8784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7745   -5.4659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7745   -4.6409    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.4890   -4.2284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0600   -4.2284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0600   -3.4034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3456   -2.9909    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3456   -2.1659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0600   -1.7534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6311   -1.7534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6311   -0.9284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9166   -0.5159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9166    0.3091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2492    0.7940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5041    1.5786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0192    2.2460    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3291    1.5786    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5841    0.7940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3687    0.5390    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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  1  0  0  0
 14 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
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  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
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 24 29  1  0  0  0  0
 29 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0292377

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H](CC\C=C(\C)CC(O)C(O)C(C)=O)\C=C\C=C(/C)CCCC1=CC(=O)OC1O

> <INCHI_IDENTIFIER>
InChI=1S/C24H36O6/c1-16(10-6-12-18(3)14-21(26)23(28)19(4)25)8-5-9-17(2)11-7-13-20-15-22(27)30-24(20)29/h5,8-9,12,15-16,21,23-24,26,28-29H,6-7,10-11,13-14H2,1-4H3/b8-5+,17-9+,18-12-/t16-,21?,23?,24?/m1/s1

> <INCHI_KEY>
QWSRTOLIHWJYKS-MYSNFVLMSA-N

> <FORMULA>
C24H36O6

> <MOLECULAR_WEIGHT>
420.546

> <EXACT_MASS>
420.251188879

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
66

> <JCHEM_AVERAGE_POLARIZABILITY>
47.6168311489014

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-[(4E,6E,8S,11Z)-14,15-dihydroxy-4,8,12-trimethyl-16-oxoheptadeca-4,6,11-trien-1-yl]-5-hydroxy-2,5-dihydrofuran-2-one

> <JCHEM_LOGP>
3.8356737933333322

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.700025597108853

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.287289071791524

> <JCHEM_PKA_STRONGEST_BASIC>
-3.2512887418168956

> <JCHEM_POLAR_SURFACE_AREA>
104.06

> <JCHEM_REFRACTIVITY>
120.10689999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
4-[(4E,6E,8S,11Z)-14,15-dihydroxy-4,8,12-trimethyl-16-oxoheptadeca-4,6,11-trien-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       4.111 -12.513   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.444 -13.283   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       5.444 -14.823   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       6.778 -12.513   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       6.778 -10.973   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       8.112 -13.283   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       8.112 -14.823   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       9.445 -12.513   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.779 -13.283   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.779 -14.823   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      12.113 -12.513   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      12.113 -10.973   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.779 -10.203   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.779  -8.663   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      12.113  -7.893   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.445  -7.893   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.445  -6.353   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.112  -5.583   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.112  -4.043   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.445  -3.273   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.778  -3.273   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.778  -1.733   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.444  -0.963   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.444   0.577   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.198   1.482   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.674   2.947   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       3.769   4.193   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       6.214   2.947   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       6.690   1.482   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       8.155   1.006   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   29                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   24   30                                                  
CONECT   30   29                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₃₆O₆

Average Mass

420.5460 Da

Monoisotopic Mass

420.25119 Da

IUPAC Name

4-[(4E,6E,8S,11Z)-14,15-dihydroxy-4,8,12-trimethyl-16-oxoheptadeca-4,6,11-trien-1-yl]-5-hydroxy-2,5-dihydrofuran-2-one

Traditional Name

4-[(4E,6E,8S,11Z)-14,15-dihydroxy-4,8,12-trimethyl-16-oxoheptadeca-4,6,11-trien-1-yl]-5-hydroxy-5H-furan-2-one

CAS Registry Number

Not Available

SMILES

C[C@@H](CC\C=C(\C)CC(O)C(O)C(C)=O)\C=C\C=C(/C)CCCC1=CC(=O)OC1O

InChI Identifier

InChI=1S/C24H36O6/c1-16(10-6-12-18(3)14-21(26)23(28)19(4)25)8-5-9-17(2)11-7-13-20-15-22(27)30-24(20)29/h5,8-9,12,15-16,21,23-24,26,28-29H,6-7,10-11,13-14H2,1-4H3/b8-5+,17-9+,18-12-/t16-,21?,23?,24?/m1/s1

InChI Key

QWSRTOLIHWJYKS-MYSNFVLMSA-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
Long chain fatty alcohol
Fatty alcohol
Acyloin
Beta-hydroxy ketone
2-furanone
Fatty acyl
Monosaccharide
Alpha-hydroxy ketone
Dihydrofuran
Alpha,beta-unsaturated carboxylic ester
Enoate ester
1,2-diol
Carboxylic acid ester
Secondary alcohol
Hemiacetal
Ketone
Lactone
Organoheterocyclic compound
Carboxylic acid derivative
Oxacycle
Monocarboxylic acid or derivatives
Organic oxygen compound
Carbonyl group
Alcohol
Organooxygen compound
Organic oxide
Hydrocarbon derivative
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	3.84	ChemAxon
pKa (Strongest Acidic)	7.29	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	104.06 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	120.11 m³·mol⁻¹	ChemAxon
Polarizability	47.62 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

8652646

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10477236

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4-[(4e,6e,8s,11z)-14,15-dihydroxy-4,8,12-trimethyl-16-oxoheptadeca-4,6,11-trien-1-yl]-5-hydroxy-5h-furan-2-one (NP0292377)

MOL for NP0292377 (4-[(4e,6e,8s,11z)-14,15-dihydroxy-4,8,12-trimethyl-16-oxoheptadeca-4,6,11-trien-1-yl]-5-hydroxy-5h-furan-2-one)

3D MOL for NP0292377 (4-[(4e,6e,8s,11z)-14,15-dihydroxy-4,8,12-trimethyl-16-oxoheptadeca-4,6,11-trien-1-yl]-5-hydroxy-5h-furan-2-one)

3D SDF for NP0292377 (4-[(4e,6e,8s,11z)-14,15-dihydroxy-4,8,12-trimethyl-16-oxoheptadeca-4,6,11-trien-1-yl]-5-hydroxy-5h-furan-2-one)

3D-SDF for NP0292377 (4-[(4e,6e,8s,11z)-14,15-dihydroxy-4,8,12-trimethyl-16-oxoheptadeca-4,6,11-trien-1-yl]-5-hydroxy-5h-furan-2-one)

PDB for NP0292377 (4-[(4e,6e,8s,11z)-14,15-dihydroxy-4,8,12-trimethyl-16-oxoheptadeca-4,6,11-trien-1-yl]-5-hydroxy-5h-furan-2-one)

3D PDB for NP0292377 (4-[(4e,6e,8s,11z)-14,15-dihydroxy-4,8,12-trimethyl-16-oxoheptadeca-4,6,11-trien-1-yl]-5-hydroxy-5h-furan-2-one)

SMILES for NP0292377 (4-[(4e,6e,8s,11z)-14,15-dihydroxy-4,8,12-trimethyl-16-oxoheptadeca-4,6,11-trien-1-yl]-5-hydroxy-5h-furan-2-one)

INCHI for NP0292377 (4-[(4e,6e,8s,11z)-14,15-dihydroxy-4,8,12-trimethyl-16-oxoheptadeca-4,6,11-trien-1-yl]-5-hydroxy-5h-furan-2-one)

Structure for NP0292377 (4-[(4e,6e,8s,11z)-14,15-dihydroxy-4,8,12-trimethyl-16-oxoheptadeca-4,6,11-trien-1-yl]-5-hydroxy-5h-furan-2-one)

3D Structure for NP0292377 (4-[(4e,6e,8s,11z)-14,15-dihydroxy-4,8,12-trimethyl-16-oxoheptadeca-4,6,11-trien-1-yl]-5-hydroxy-5h-furan-2-one)