NP-MRD: Showing NP-Card for (1r,2s,9r,10s,11s,12s,13s,16s)-9,12-dihydroxy-2,6,10,16-tetramethyl-14-oxatetracyclo[11.2.1.0²,¹¹.0⁵,¹⁰]hexadeca-4,6-diene-3,8,15-trione (NP0260376)

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Record Information

Version

2.0

Created at

2022-09-08 02:31:43 UTC

Updated at

2022-09-08 02:31:44 UTC

NP-MRD ID

NP0260376

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2s,9r,10s,11s,12s,13s,16s)-9,12-dihydroxy-2,6,10,16-tetramethyl-14-oxatetracyclo[11.2.1.0²,¹¹.0⁵,¹⁰]hexadeca-4,6-diene-3,8,15-trione

Description

(1R,2S,9R,10S,11S,12S,13S,16S)-9,12-dihydroxy-2,6,10,16-tetramethyl-14-oxatetracyclo[11.2.1.0²,¹¹.0⁵,¹⁰]Hexadeca-4,6-diene-3,8,15-trione belongs to the class of organic compounds known as steroid lactones. These are sterol lipids containing a lactone moiety linked to the steroid skeleton. (1r,2s,9r,10s,11s,12s,13s,16s)-9,12-dihydroxy-2,6,10,16-tetramethyl-14-oxatetracyclo[11.2.1.0²,¹¹.0⁵,¹⁰]hexadeca-4,6-diene-3,8,15-trione is found in Eurycoma longifolia. Based on a literature review very few articles have been published on (1R,2S,9R,10S,11S,12S,13S,16S)-9,12-dihydroxy-2,6,10,16-tetramethyl-14-oxatetracyclo[11.2.1.0²,¹¹.0⁵,¹⁰]Hexadeca-4,6-diene-3,8,15-trione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082204312D          

 25 28  0  0  1  0            999 V2000
    4.9606   -0.4836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5232    0.2160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9103    0.9445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4729    1.6440    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8600    2.3726    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6484    1.6150    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2110    2.3145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2613    0.8864    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8239    1.5859    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6987    0.1869    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3116   -0.5416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4871   -0.5707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1000   -1.2992    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0497    0.1289    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7182   -0.6266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4368    0.8574    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1086    1.6143    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6481    2.2384    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3122    1.8296    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6473    1.3411    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6146    0.5168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1423    0.1885    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2388   -0.0227    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0439    0.9126    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2196    0.9453    0.0000 C   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
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  1  0  0  0
  6  8  1  0  0  0  0
  8  9  1  1  0  0  0
  8 10  1  0  0  0  0
  2 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
 12 14  1  0  0  0  0
 14 15  1  1  0  0  0
 16 14  1  1  0  0  0
  8 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 19  1  0  0  0  0
 19 20  1  6  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 23 21  1  6  0  0  0
 14 23  1  0  0  0  0
 23 24  1  0  0  0  0
 19 24  1  0  0  0  0
 24 25  1  6  0  0  0
M  END

     RDKit          3D

 47 50  0  0  0  0  0  0  0  0999 V2000
   -3.8765   -2.1675   -1.1567 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2098   -0.9452   -0.6075 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9582   -0.0010   -0.0597 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3794    1.2168    0.4958 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1660    2.1716    0.7160 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9160    1.2881    0.7765 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5879    2.6617    0.6854 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1161    0.5544   -0.3090 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0652    1.4539   -1.4898 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7831   -0.7440   -0.6461 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0449   -1.8056   -1.0099 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3947   -1.7801   -1.1014 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0881   -2.7209   -1.5444 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1158   -0.5554   -0.6399 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6646    0.1368   -1.8126 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2230    0.1873    0.2686 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8877    1.3063    1.0221 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3870    2.3081    0.2464 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0519    0.6581    1.7803 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5462   -0.5551    2.3165 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7492   -1.6009    1.4607 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5160   -2.8139    1.6819 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3021   -1.0527    0.2018 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0472    0.1782    0.7365 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3031   -0.3473    1.3917 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9010   -2.9627   -0.3704 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4263   -2.5080   -2.0949 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9388   -1.9211   -1.3706 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0477   -0.1571   -0.0315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7013    0.8843    1.7808 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7584    3.0651    1.5684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2948    0.8275   -2.4011 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1648    2.0562   -1.5977 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9233    2.1907   -1.4666 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5303   -2.7576   -1.2573 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5499   -0.4699   -2.1780 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0523    1.1477   -1.6680 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9845    0.1530   -2.7137 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0432   -0.5553    1.0891 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1883    1.6517    1.8169 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2402    3.2203    0.5933 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4859    1.3225    2.5227 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9494   -1.7318   -0.3468 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2547    0.9128   -0.0394 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4333    0.1821    2.3446 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2159   -1.4296    1.6346 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2020   -0.1526    0.7823 H   0  0  0  0  0  0  0  0  0  0  0  0
 25 24  1  0
 24 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  2  0
 21 23  1  0
 23 14  1  0
 14 15  1  6
 14 16  1  0
 16 17  1  0
 17 18  1  0
 16  8  1  0
  8  9  1  6
  8  6  1  0
  6  7  1  0
  6  4  1  0
  4  5  2  0
  4  3  1  0
  3  2  2  0
  2  1  1  0
  2 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 23 24  1  0
 12 14  1  0
 17 19  1  0
 10  8  1  0
 25 45  1  0
 25 46  1  0
 25 47  1  0
 24 44  1  6
 19 42  1  1
 23 43  1  6
 15 36  1  0
 15 37  1  0
 15 38  1  0
 16 39  1  1
 17 40  1  1
 18 41  1  0
  9 32  1  0
  9 33  1  0
  9 34  1  0
  6 30  1  1
  7 31  1  0
  3 29  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
 11 35  1  0
M  END


  Mrv1652309082204312D          

 25 28  0  0  1  0            999 V2000
    4.9606   -0.4836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5232    0.2160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9103    0.9445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4729    1.6440    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8600    2.3726    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6484    1.6150    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2110    2.3145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2613    0.8864    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8239    1.5859    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6987    0.1869    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3116   -0.5416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4871   -0.5707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1000   -1.2992    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0497    0.1289    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7182   -0.6266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4368    0.8574    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1086    1.6143    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6481    2.2384    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3122    1.8296    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6473    1.3411    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6146    0.5168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1423    0.1885    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2388   -0.0227    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0439    0.9126    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2196    0.9453    0.0000 C   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
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  1  0  0  0
  6  8  1  0  0  0  0
  8  9  1  1  0  0  0
  8 10  1  0  0  0  0
  2 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
 12 14  1  0  0  0  0
 14 15  1  1  0  0  0
 16 14  1  1  0  0  0
  8 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 19  1  0  0  0  0
 19 20  1  6  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 23 21  1  6  0  0  0
 14 23  1  0  0  0  0
 23 24  1  0  0  0  0
 19 24  1  0  0  0  0
 24 25  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0260376

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1[C@@H]2OC(=O)[C@H]1[C@]1(C)[C@@H]([C@@H]2O)[C@]2(C)[C@@H](O)C(=O)C=C(C)C2=CC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C19H22O6/c1-7-5-10(20)16(23)18(3)9(7)6-11(21)19(4)12-8(2)14(25-17(12)24)13(22)15(18)19/h5-6,8,12-16,22-23H,1-4H3/t8-,12-,13+,14-,15-,16-,18+,19+/m0/s1

> <INCHI_KEY>
PKCDREAJEQQORV-MUWLIOEWSA-N

> <FORMULA>
C19H22O6

> <MOLECULAR_WEIGHT>
346.379

> <EXACT_MASS>
346.141638428

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
34.74029808552408

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,2S,9R,10S,11S,12S,13S,16S)-9,12-dihydroxy-2,6,10,16-tetramethyl-14-oxatetracyclo[11.2.1.0^{2,11}.0^{5,10}]hexadeca-4,6-diene-3,8,15-trione

> <JCHEM_LOGP>
0.768616409333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.903083853183706

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.836477302062779

> <JCHEM_PKA_STRONGEST_BASIC>
-3.300530017523175

> <JCHEM_POLAR_SURFACE_AREA>
100.9

> <JCHEM_REFRACTIVITY>
88.59830000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,9R,10S,11S,12S,13S,16S)-9,12-dihydroxy-2,6,10,16-tetramethyl-14-oxatetracyclo[11.2.1.0^{2,11}.0^{5,10}]hexadeca-4,6-diene-3,8,15-trione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0       9.260  -0.903   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.443   0.403   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.166   1.763   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.349   3.069   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       9.072   4.429   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       6.810   3.015   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       5.994   4.320   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       6.088   1.655   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.271   2.960   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.904   0.349   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.182  -1.011   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.643  -1.065   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       3.920  -2.425   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       3.826   0.241   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.207  -1.170   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.549   1.600   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.936   3.013   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       4.943   4.178   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       2.449   3.415   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       1.208   2.503   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       1.147   0.965   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -0.266   0.352   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       2.312  -0.042   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.949   1.704   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.410   1.764   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   10                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   10   16                                             
CONECT    9    8                                                            
CONECT   10    8    2   11                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16   23                                             
CONECT   15   14                                                            
CONECT   16   14    8   17                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   24                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   14   24                                                  
CONECT   24   23   19   25                                                  
CONECT   25   24                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₂₂O₆

Average Mass

346.3790 Da

Monoisotopic Mass

346.14164 Da

IUPAC Name

(1R,2S,9R,10S,11S,12S,13S,16S)-9,12-dihydroxy-2,6,10,16-tetramethyl-14-oxatetracyclo[11.2.1.0^{2,11}.0^{5,10}]hexadeca-4,6-diene-3,8,15-trione

Traditional Name

(1R,2S,9R,10S,11S,12S,13S,16S)-9,12-dihydroxy-2,6,10,16-tetramethyl-14-oxatetracyclo[11.2.1.0^{2,11}.0^{5,10}]hexadeca-4,6-diene-3,8,15-trione

CAS Registry Number

Not Available

SMILES

C[C@@H]1[C@@H]2OC(=O)[C@H]1[C@]1(C)[C@@H]([C@@H]2O)[C@]2(C)[C@@H](O)C(=O)C=C(C)C2=CC1=O

InChI Identifier

InChI=1S/C19H22O6/c1-7-5-10(20)16(23)18(3)9(7)6-11(21)19(4)12-8(2)14(25-17(12)24)13(22)15(18)19/h5-6,8,12-16,22-23H,1-4H3/t8-,12-,13+,14-,15-,16-,18+,19+/m0/s1

InChI Key

PKCDREAJEQQORV-MUWLIOEWSA-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
Eurycoma longifolia	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as steroid lactones. These are sterol lipids containing a lactone moiety linked to the steroid skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroid lactones

Direct Parent

Steroid lactones

Alternative Parents

Substituents

Steroid lactone
C-19 quassinoid skeleton
Diterpene lactone
Diterpenoid
Spongiane diterpenoid
Hydroxysteroid
11-alpha-hydroxysteroid
11-hydroxysteroid
Caprolactone
Cyclohexenone
Oxepane
Gamma butyrolactone
Tetrahydrofuran
Cyclic alcohol
Secondary alcohol
Carboxylic acid ester
Cyclic ketone
Ketone
Lactone
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Alcohol
Organic oxide
Organic oxygen compound
Hydrocarbon derivative
Carbonyl group
Organooxygen compound
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	0.77	ChemAxon
pKa (Strongest Acidic)	12.84	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	100.9 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	88.6 m³·mol⁻¹	ChemAxon
Polarizability	34.74 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

162939829

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,2s,9r,10s,11s,12s,13s,16s)-9,12-dihydroxy-2,6,10,16-tetramethyl-14-oxatetracyclo[11.2.1.0²,¹¹.0⁵,¹⁰]hexadeca-4,6-diene-3,8,15-trione (NP0260376)

MOL for NP0260376 ((1r,2s,9r,10s,11s,12s,13s,16s)-9,12-dihydroxy-2,6,10,16-tetramethyl-14-oxatetracyclo[11.2.1.0²,¹¹.0⁵,¹⁰]hexadeca-4,6-diene-3,8,15-trione)

3D MOL for NP0260376 ((1r,2s,9r,10s,11s,12s,13s,16s)-9,12-dihydroxy-2,6,10,16-tetramethyl-14-oxatetracyclo[11.2.1.0²,¹¹.0⁵,¹⁰]hexadeca-4,6-diene-3,8,15-trione)

3D SDF for NP0260376 ((1r,2s,9r,10s,11s,12s,13s,16s)-9,12-dihydroxy-2,6,10,16-tetramethyl-14-oxatetracyclo[11.2.1.0²,¹¹.0⁵,¹⁰]hexadeca-4,6-diene-3,8,15-trione)

3D-SDF for NP0260376 ((1r,2s,9r,10s,11s,12s,13s,16s)-9,12-dihydroxy-2,6,10,16-tetramethyl-14-oxatetracyclo[11.2.1.0²,¹¹.0⁵,¹⁰]hexadeca-4,6-diene-3,8,15-trione)

PDB for NP0260376 ((1r,2s,9r,10s,11s,12s,13s,16s)-9,12-dihydroxy-2,6,10,16-tetramethyl-14-oxatetracyclo[11.2.1.0²,¹¹.0⁵,¹⁰]hexadeca-4,6-diene-3,8,15-trione)

3D PDB for NP0260376 ((1r,2s,9r,10s,11s,12s,13s,16s)-9,12-dihydroxy-2,6,10,16-tetramethyl-14-oxatetracyclo[11.2.1.0²,¹¹.0⁵,¹⁰]hexadeca-4,6-diene-3,8,15-trione)

SMILES for NP0260376 ((1r,2s,9r,10s,11s,12s,13s,16s)-9,12-dihydroxy-2,6,10,16-tetramethyl-14-oxatetracyclo[11.2.1.0²,¹¹.0⁵,¹⁰]hexadeca-4,6-diene-3,8,15-trione)

INCHI for NP0260376 ((1r,2s,9r,10s,11s,12s,13s,16s)-9,12-dihydroxy-2,6,10,16-tetramethyl-14-oxatetracyclo[11.2.1.0²,¹¹.0⁵,¹⁰]hexadeca-4,6-diene-3,8,15-trione)

Structure for NP0260376 ((1r,2s,9r,10s,11s,12s,13s,16s)-9,12-dihydroxy-2,6,10,16-tetramethyl-14-oxatetracyclo[11.2.1.0²,¹¹.0⁵,¹⁰]hexadeca-4,6-diene-3,8,15-trione)

3D Structure for NP0260376 ((1r,2s,9r,10s,11s,12s,13s,16s)-9,12-dihydroxy-2,6,10,16-tetramethyl-14-oxatetracyclo[11.2.1.0²,¹¹.0⁵,¹⁰]hexadeca-4,6-diene-3,8,15-trione)