NP-MRD: Showing NP-Card for 2-{1,5,12-trimethyl-11-oxo-10-oxatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadec-7-en-5-yl}ethoxysulfonic acid (NP0155055)

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Record Information

Version

2.0

Created at

2022-09-02 12:03:24 UTC

Updated at

2022-09-02 12:03:25 UTC

NP-MRD ID

NP0155055

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-{1,5,12-trimethyl-11-oxo-10-oxatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadec-7-en-5-yl}ethoxysulfonic acid

Description

(2-{1,5,12-Trimethyl-11-oxo-10-oxatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]Hexadec-7-en-5-yl}ethoxy)sulfonic acid 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 (2-{1,5,12-trimethyl-11-oxo-10-oxatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]Hexadec-7-en-5-yl}ethoxy)sulfonic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022214032D          

 27 30  0  0  0  0            999 V2000
    4.8059    0.1433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2756   -0.7752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7453   -1.4072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0274   -2.1825    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4971   -2.8145    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    2.9668   -3.4465    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1291   -3.3448    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8651   -2.2842    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8500   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1355   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3509   -0.2549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1340    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9590    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3509    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4561    1.2515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1794    1.8869    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7925    2.4389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5771    2.1840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8500    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4997    1.7459    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1355    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -0.4125    0.0000 C   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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  2  0  0  0  0
  6  9  1  0  0  0  0
  2 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
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  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
 12 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 15 26  1  0  0  0  0
 19 26  1  0  0  0  0
 13 27  1  0  0  0  0
  2 27  1  0  0  0  0
M  END

     RDKit          3D

 57 60  0  0  0  0  0  0  0  0999 V2000
    2.4747   -1.4208   -1.2929 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1886   -0.1431   -0.4921 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4940    0.5979   -0.3393 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5368   -0.1925    0.4012 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6828    0.5912    0.4759 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9328   -0.1547    1.2734 S   0  0  0  0  0  6  0  0  0  0  0  0
    6.8505    0.1494    2.7625 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9585   -1.6258    1.1285 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4241    0.4625    0.7674 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5971   -0.5728    0.8068 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2486   -1.2347    0.4746 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7090   -0.1082    0.2912 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0909    0.8813   -0.6324 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8469    1.9589   -0.8994 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1604    2.0266   -0.2602 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0254    2.4190    1.1028 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9264    1.7540    1.9025 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1088    1.8329    3.1485 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7194    0.8552    1.0149 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.0331    1.5561    0.6372 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0719   -0.4026    1.7107 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1009   -1.5156    0.6618 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6249   -1.7201    0.2939 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0370   -0.4869   -0.2978 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8220   -0.7803   -1.7908 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9184    0.7235   -0.2280 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2417    0.7501   -1.2428 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6775   -1.5456   -2.0350 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5687   -2.2945   -0.6118 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4722   -1.3375   -1.7996 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8802    0.8210   -1.3454 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3435    1.5665    0.1812 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8179   -1.1117   -0.1522 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2294   -0.4323    1.4366 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2623    0.8934   -0.1287 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1868   -1.3275    1.3305 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3682    0.2754    1.4868 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0522   -1.9267    1.3102 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3864   -1.8573   -0.4343 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9056    0.3373    1.2899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4737    2.7169   -1.5561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7695    2.8062   -0.7575 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8043    2.6152    0.4888 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3732    1.0721   -0.3007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8066    1.3754    1.4144 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0246   -0.2914    2.2286 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2439   -0.6430    2.4296 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5243   -2.4426    1.0426 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6405   -1.0958   -0.2114 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6351   -2.5960   -0.4134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1299   -2.0797    1.2040 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7903   -1.2075   -2.1440 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6606    0.1467   -2.3622 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0538   -1.5512   -1.9466 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5892    0.7371   -1.1353 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2011    0.3770   -2.2884 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6482    1.7993   -1.3379 H   0  0  0  0  0  0  0  0  0  0  0  0
 19 20  1  6
 19 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  6
 24 26  1  0
 26 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 15 14  1  0
 14 13  2  0
 13 27  1  0
 27  2  1  0
  2  1  1  6
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  9  1  0
  6  7  2  0
  6  8  2  0
  2 10  1  0
 10 11  1  0
 11 12  1  0
 26 19  1  0
 12 13  1  0
 17 19  1  0
 12 24  1  0
 20 43  1  0
 20 44  1  0
 20 45  1  0
 21 46  1  0
 21 47  1  0
 22 48  1  0
 22 49  1  0
 23 50  1  0
 23 51  1  0
 25 52  1  0
 25 53  1  0
 25 54  1  0
 26 55  1  6
 15 42  1  6
 14 41  1  0
 27 56  1  0
 27 57  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  3 31  1  0
  3 32  1  0
  4 33  1  0
  4 34  1  0
  9 35  1  0
 10 36  1  0
 10 37  1  0
 11 38  1  0
 11 39  1  0
 12 40  1  1
M  END


  Mrv1652309022214032D          

 27 30  0  0  0  0            999 V2000
    4.8059    0.1433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2756   -0.7752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7453   -1.4072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0274   -2.1825    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4971   -2.8145    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    2.9668   -3.4465    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1291   -3.3448    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8651   -2.2842    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8500   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1355   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3509   -0.2549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1340    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9590    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3509    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4561    1.2515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1794    1.8869    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7925    2.4389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5771    2.1840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8500    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4997    1.7459    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1355    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -0.4125    0.0000 C   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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  2  0  0  0  0
  6  9  1  0  0  0  0
  2 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
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  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
 12 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 15 26  1  0  0  0  0
 19 26  1  0  0  0  0
 13 27  1  0  0  0  0
  2 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0155055

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC12CCCC3(C)C1C(OC2=O)C=C1CC(C)(CCOS(O)(=O)=O)CCC31

> <INCHI_IDENTIFIER>
InChI=1S/C20H30O6S/c1-18(9-10-25-27(22,23)24)8-5-14-13(12-18)11-15-16-19(14,2)6-4-7-20(16,3)17(21)26-15/h11,14-16H,4-10,12H2,1-3H3,(H,22,23,24)

> <INCHI_KEY>
ZRFMKYKOLFQQPF-UHFFFAOYSA-N

> <FORMULA>
C20H30O6S

> <MOLECULAR_WEIGHT>
398.51

> <EXACT_MASS>
398.17630986

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
57

> <JCHEM_AVERAGE_POLARIZABILITY>
41.42473138455239

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2-{1,5,12-trimethyl-11-oxo-10-oxatetracyclo[7.6.1.0^{2,7}.0^{12,16}]hexadec-7-en-5-yl}ethoxy)sulfonic acid

> <ALOGPS_LOGP>
0.45

> <JCHEM_LOGP>
3.501093504333332

> <ALOGPS_LOGS>
-5.02

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
-1.5826306207140597

> <JCHEM_PKA_STRONGEST_BASIC>
-7.132180604536536

> <JCHEM_POLAR_SURFACE_AREA>
89.9

> <JCHEM_REFRACTIVITY>
100.15750000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.81e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-{1,5,12-trimethyl-11-oxo-10-oxatetracyclo[7.6.1.0^{2,7}.0^{12,16}]hexadec-7-en-5-yl}ethoxysulfonic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       8.971   0.267   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.454  -0.000   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.981  -1.447   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.991  -2.627   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       7.518  -4.074   0.000  0.00  0.00           O+0
HETATM    6  S   UNK     0       6.528  -5.254   0.000  0.00  0.00           S+0
HETATM    7  O   UNK     0       5.538  -6.433   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0       7.708  -6.244   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0       5.348  -4.264   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       7.454   1.540   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.121   2.310   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.787   1.540   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.787   0.000   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.453  -0.770   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.120  -0.000   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       0.655  -0.476   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -0.250   0.770   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -1.790   0.770   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       0.655   2.016   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.851   2.336   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.335   3.522   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.479   4.553   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.944   4.077   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.453   2.310   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.666   3.259   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.120   1.540   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.121  -0.770   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   10   27                                             
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8    9                                             
CONECT    7    6                                                            
CONECT    8    6                                                            
CONECT    9    6                                                            
CONECT   10    2   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   24                                                  
CONECT   13   12   14   27                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   26                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21   26                                             
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   12   25   26                                             
CONECT   25   24                                                            
CONECT   26   24   15   19                                                  
CONECT   27   13    2                                                       
MASTER        0    0    0    0    0    0    0    0   27    0   60    0
END

View in JSmol

Synonyms

Value	Source
(2-{1,5,12-trimethyl-11-oxo-10-oxatetracyclo[7.6.1.0,.0,]hexadec-7-en-5-yl}ethoxy)sulfonate	Generator
(2-{1,5,12-trimethyl-11-oxo-10-oxatetracyclo[7.6.1.0,.0,]hexadec-7-en-5-yl}ethoxy)sulphonate	Generator
(2-{1,5,12-trimethyl-11-oxo-10-oxatetracyclo[7.6.1.0,.0,]hexadec-7-en-5-yl}ethoxy)sulphonic acid	Generator

Chemical Formula

C₂₀H₃₀O₆S

Average Mass

398.5100 Da

Monoisotopic Mass

398.17631 Da

IUPAC Name

(2-{1,5,12-trimethyl-11-oxo-10-oxatetracyclo[7.6.1.0^{2,7}.0^{12,16}]hexadec-7-en-5-yl}ethoxy)sulfonic acid

Traditional Name

2-{1,5,12-trimethyl-11-oxo-10-oxatetracyclo[7.6.1.0^{2,7}.0^{12,16}]hexadec-7-en-5-yl}ethoxysulfonic acid

CAS Registry Number

Not Available

SMILES

CC12CCCC3(C)C1C(OC2=O)C=C1CC(C)(CCOS(O)(=O)=O)CCC31

InChI Identifier

InChI=1S/C20H30O6S/c1-18(9-10-25-27(22,23)24)8-5-14-13(12-18)11-15-16-19(14,2)6-4-7-20(16,3)17(21)26-15/h11,14-16H,4-10,12H2,1-3H3,(H,22,23,24)

InChI Key

ZRFMKYKOLFQQPF-UHFFFAOYSA-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

Pimarane diterpenoid
Diterpenoid
Diterpene lactone
Naphthofuran
Sulfuric acid ester
Alkyl sulfate
Sulfate-ester
Sulfuric acid monoester
Gamma butyrolactone
Tetrahydrofuran
Organic sulfuric acid or derivatives
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic 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	0.45	ALOGPS
logP	3.5	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Acidic)	-1.6	ChemAxon
pKa (Strongest Basic)	-7.1	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	89.9 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	100.16 m³·mol⁻¹	ChemAxon
Polarizability	41.42 Å³	ChemAxon
Number of Rings	4	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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

162928913

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-{1,5,12-trimethyl-11-oxo-10-oxatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadec-7-en-5-yl}ethoxysulfonic acid (NP0155055)

MOL for NP0155055 (2-{1,5,12-trimethyl-11-oxo-10-oxatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadec-7-en-5-yl}ethoxysulfonic acid)

3D MOL for NP0155055 (2-{1,5,12-trimethyl-11-oxo-10-oxatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadec-7-en-5-yl}ethoxysulfonic acid)

3D SDF for NP0155055 (2-{1,5,12-trimethyl-11-oxo-10-oxatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadec-7-en-5-yl}ethoxysulfonic acid)

3D-SDF for NP0155055 (2-{1,5,12-trimethyl-11-oxo-10-oxatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadec-7-en-5-yl}ethoxysulfonic acid)

PDB for NP0155055 (2-{1,5,12-trimethyl-11-oxo-10-oxatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadec-7-en-5-yl}ethoxysulfonic acid)

3D PDB for NP0155055 (2-{1,5,12-trimethyl-11-oxo-10-oxatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadec-7-en-5-yl}ethoxysulfonic acid)

SMILES for NP0155055 (2-{1,5,12-trimethyl-11-oxo-10-oxatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadec-7-en-5-yl}ethoxysulfonic acid)

INCHI for NP0155055 (2-{1,5,12-trimethyl-11-oxo-10-oxatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadec-7-en-5-yl}ethoxysulfonic acid)

Structure for NP0155055 (2-{1,5,12-trimethyl-11-oxo-10-oxatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadec-7-en-5-yl}ethoxysulfonic acid)

3D Structure for NP0155055 (2-{1,5,12-trimethyl-11-oxo-10-oxatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadec-7-en-5-yl}ethoxysulfonic acid)