NP-MRD: Showing NP-Card for 6alpha,16,18-Trihydroxycleroda-3,13-dien-15,16-olide (NP0140924)

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Record Information

Version

2.0

Created at

2022-06-29 21:58:46 UTC

Updated at

2022-06-29 21:58:46 UTC

NP-MRD ID

NP0140924

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6alpha,16,18-Trihydroxycleroda-3,13-dien-15,16-olide

Description

1017233-48-5 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 1017233-48-5.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652306292223582D          

 25 27  0  0  1  0            999 V2000
   -1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3873    0.7284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3873    0.7284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0499    1.4281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3374    2.1565    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1544    2.2713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2977    3.0838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0392    3.4454    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5692    3.4711    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0242    2.8980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8367    3.0413    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  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  1  0  0  0  0
  2  7  1  0  0  0  0
  7  8  1  1  0  0  0
  7  9  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 11 16  1  0  0  0  0
 16 17  1  0  0  0  0
  6 18  1  1  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
  5 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
  5 24  1  1  0  0  0
  4 25  1  1  0  0  0
M  END

     RDKit          3D

 55 57  0  0  0  0  0  0  0  0999 V2000
   -0.3923   -3.0845   -1.2699 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0355   -2.3181   -0.0240 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9965   -2.4043    1.0911 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7821   -1.1682    1.4020 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0767   -1.5592    1.7566 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9006   -0.2259    0.2430 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0321   -0.6955   -0.6339 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4245    1.1150    0.7045 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0059    1.3909    2.0070 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3892    2.7258    2.1145 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2978    2.0543   -0.2305 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7330    1.8989   -1.5695 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9155    0.6370   -1.7866 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6174    0.0945   -0.4193 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4910   -0.9066   -0.3188 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2004   -1.0179   -1.6178 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4141   -0.6140    0.8208 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1390    0.6091    0.9910 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2882    1.0361    0.1820 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0105    0.5221   -0.7672 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0687    1.4313   -1.2278 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9337    1.2546   -2.1187 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9214    2.5535   -0.4654 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8884    2.4238    0.4300 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4228    2.4472    1.7319 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5209   -3.3998   -1.8344 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9781   -3.9821   -0.9450 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0259   -2.5538   -1.9863 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8961   -2.8801    0.3209 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7014   -3.2602    0.8636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5071   -2.7129    2.0460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3869   -0.5971    2.2646 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3699   -2.3147    1.1560 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2473   -0.0266   -1.4896 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9656   -1.7171   -1.0027 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9613   -0.5706    0.0194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2161    1.2411    2.7973 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8978    0.7853    2.2541 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6307    3.3262    2.3395 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6568    3.0507    0.0369 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0314    2.7751   -1.7112 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4894    2.0539   -2.3883 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0181    0.9116   -2.3812 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4818   -0.0505   -2.4417 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1832    1.0077    0.1165 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5164   -1.3918   -2.4401 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0263   -1.7658   -1.4826 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6649   -0.0831   -1.9759 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2109   -1.4600    0.7319 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9295   -0.9430    1.8050 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4651    1.5255    1.1306 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5878    0.5721    2.0668 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8847   -0.4729   -1.1754 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0737    3.1730    0.3253 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7935    1.5601    1.9554 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  4  6  1  0
  6  7  1  6
  6 14  1  0
 14 13  1  0
 13 12  1  0
 12 11  1  0
 11  8  2  0
  8  9  1  0
  9 10  1  0
 14 15  1  0
 15 16  1  6
 15 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 21 23  1  0
 23 24  1  0
 24 25  1  0
 15  2  1  0
 24 19  1  0
  8  6  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  2 29  1  1
  3 30  1  0
  3 31  1  0
  4 32  1  1
  5 33  1  0
  7 34  1  0
  7 35  1  0
  7 36  1  0
 14 45  1  1
 13 43  1  0
 13 44  1  0
 12 41  1  0
 12 42  1  0
 11 40  1  0
  9 37  1  0
  9 38  1  0
 10 39  1  0
 16 46  1  0
 16 47  1  0
 16 48  1  0
 17 49  1  0
 17 50  1  0
 18 51  1  0
 18 52  1  0
 20 53  1  0
 24 54  1  1
 25 55  1  0
M  END


  Mrv1652306292223582D          

 25 27  0  0  1  0            999 V2000
   -1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3873    0.7284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3873    0.7284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0499    1.4281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3374    2.1565    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1544    2.2713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2977    3.0838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0392    3.4454    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5692    3.4711    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0242    2.8980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8367    3.0413    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  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  1  0  0  0  0
  2  7  1  0  0  0  0
  7  8  1  1  0  0  0
  7  9  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 11 16  1  0  0  0  0
 16 17  1  0  0  0  0
  6 18  1  1  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
  5 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
  5 24  1  1  0  0  0
  4 25  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0140924

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1C[C@H](O)[C@]2(C)[C@H](CCC=C2CO)[C@@]1(C)CCC1=CC(=O)OC1O

> <INCHI_IDENTIFIER>
InChI=1S/C20H30O5/c1-12-9-16(22)20(3)14(11-21)5-4-6-15(20)19(12,2)8-7-13-10-17(23)25-18(13)24/h5,10,12,15-16,18,21-22,24H,4,6-9,11H2,1-3H3/t12-,15-,16+,18?,19+,20+/m1/s1

> <INCHI_KEY>
ANOAUERKWIARIN-HKQZTGDUSA-N

> <FORMULA>
C20H30O5

> <MOLECULAR_WEIGHT>
350.455

> <EXACT_MASS>
350.209324066

$$$$

HEADER    PROTEIN                                 29-JUN-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-JUN-22         0                                  
HETATM    1  C   UNK     0      -2.667   0.000   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.723   1.360   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.723   1.360   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.093   2.666   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.630   4.025   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.155   4.240   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.422   5.756   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -3.806   6.431   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0      -1.063   6.479   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       0.045   5.410   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       1.562   5.677   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       4.001  -5.390   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       1.334  -3.850   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       0.000  -4.620   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   25                                                  
CONECT    5    4    6   21   24                                             
CONECT    6    5    7   18                                                  
CONECT    7    6    2    8    9                                             
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   16                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   11   17                                                  
CONECT   17   16                                                            
CONECT   18    6   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20    5   22                                                  
CONECT   22   21   23                                                       
CONECT   23   22                                                            
CONECT   24    5                                                            
CONECT   25    4                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   54    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₃₀O₅

Average Mass

350.4550 Da

Monoisotopic Mass

350.20932 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@@H]1C[C@H](O)[C@]2(C)[C@H](CCC=C2CO)[C@@]1(C)CCC1=CC(=O)OC1O

InChI Identifier

InChI=1S/C20H30O5/c1-12-9-16(22)20(3)14(11-21)5-4-6-15(20)19(12,2)8-7-13-10-17(23)25-18(13)24/h5,10,12,15-16,18,21-22,24H,4,6-9,11H2,1-3H3/t12-,15-,16+,18?,19+,20+/m1/s1

InChI Key

ANOAUERKWIARIN-HKQZTGDUSA-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
Clerodane diterpenoid
2-furanone
Cyclic alcohol
Dihydrofuran
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Secondary alcohol
Lactone
Hemiacetal
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Primary alcohol
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Alcohol
Organic oxygen 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

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

33823568

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

24796275

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 6alpha,16,18-Trihydroxycleroda-3,13-dien-15,16-olide (NP0140924)

MOL for NP0140924 (6alpha,16,18-Trihydroxycleroda-3,13-dien-15,16-olide)

3D MOL for NP0140924 (6alpha,16,18-Trihydroxycleroda-3,13-dien-15,16-olide)

3D SDF for NP0140924 (6alpha,16,18-Trihydroxycleroda-3,13-dien-15,16-olide)

3D-SDF for NP0140924 (6alpha,16,18-Trihydroxycleroda-3,13-dien-15,16-olide)

PDB for NP0140924 (6alpha,16,18-Trihydroxycleroda-3,13-dien-15,16-olide)

3D PDB for NP0140924 (6alpha,16,18-Trihydroxycleroda-3,13-dien-15,16-olide)

SMILES for NP0140924 (6alpha,16,18-Trihydroxycleroda-3,13-dien-15,16-olide)

INCHI for NP0140924 (6alpha,16,18-Trihydroxycleroda-3,13-dien-15,16-olide)

Structure for NP0140924 (6alpha,16,18-Trihydroxycleroda-3,13-dien-15,16-olide)

3D Structure for NP0140924 (6alpha,16,18-Trihydroxycleroda-3,13-dien-15,16-olide)