NP-MRD: Showing NP-Card for Agathadiol diacetate (NP0140450)

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Record Information

Version

2.0

Created at

2022-06-29 21:34:58 UTC

Updated at

2022-06-29 21:34:58 UTC

NP-MRD ID

NP0140450

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Agathadiol diacetate

Description

Agathadiol diacetate belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. Agathadiol diacetate is found in Cryptomeria japonica. Based on a literature review very few articles have been published on Agathadiol diacetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652306292223342D          

 28 29  0  0  1  0            999 V2000
   -1.4289    2.4750    0.0000 C   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 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    4.9500    0.0000 C   0  0  0  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    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   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
   -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  0  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  2  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  1  0  0  0  0  0  0  0  0  0
    1.8163   -2.3784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0416   -2.3784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4788   -3.0781    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0915   -3.8065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5287   -4.5061    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2670   -3.8353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    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  2  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  1  0  0  0  0
  2  9  1  0  0  0  0
  9 10  1  0  0  0  0
 11 10  1  6  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  0  0  0  0
 16 15  1  6  0  0  0
 16 17  1  0  0  0  0
 11 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 16 21  1  0  0  0  0
 21 22  1  1  0  0  0
 21 23  1  6  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 17 28  1  6  0  0  0
M  END

     RDKit          3D

 66 67  0  0  0  0  0  0  0  0999 V2000
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    0.0538    1.6210    1.0461 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6107    2.6326    0.1622 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9004    2.0477   -0.4323 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0907    0.7241    0.2488 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4971    0.1875    0.1967 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.3133    1.1616    1.0130 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0362    0.0071   -1.1585 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3015   -0.4954   -1.2356 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5460   -0.0705   -0.9507 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7717   -0.9230   -1.1431 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6861    1.0920   -0.5040 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5494   -1.1263    0.9359 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2382   -1.7967    1.1372 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2590   -1.6382    0.0245 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0018   -0.1737   -0.2009 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5270    0.0100   -1.6070 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2133    0.2067    0.6795 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5017   -0.1515    0.0063 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6315    0.1890    0.9480 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9814   -0.1544    0.3840 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1397    0.1681    1.2447 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1293   -0.6967   -0.7937 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3218   -1.0911   -1.5305 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5842   -0.9078   -1.0572 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2337    0.3006   -0.9559 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6012    0.3545   -0.4113 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6700    1.3479   -1.3226 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4174    3.0752    2.5520 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9914    1.3713    2.9348 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0633    3.0413   -0.6139 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9345    3.5060    0.7708 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7627    2.6957   -0.2512 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8110    1.9622   -1.5431 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9416    0.9620    1.3543 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6336    1.4828    1.8975 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1312    0.6570    1.5416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5288    2.1110    0.5308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8960    0.9264   -1.8087 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3842   -0.7629   -1.7113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6078   -1.6803   -1.9255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6003   -0.2306   -1.3785 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0441   -1.4573   -0.2131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2362   -1.8330    0.3837 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0261   -1.0314    1.9425 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4440   -2.9039    1.2326 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7880   -1.5192    2.1181 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3286   -2.1781    0.3260 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6114   -2.1365   -0.8895 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2830   -0.7652   -1.7572 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0472    0.9865   -1.8168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2413   -0.1658   -2.4006 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1207   -0.4397    1.5802 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6784    0.4443   -0.9188 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4738   -1.2458   -0.1726 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5667    1.2862    1.1429 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5011   -0.3233    1.9056 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7960    0.1595    2.3453 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9281   -0.6091    1.2628 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5037    1.1940    1.0959 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1243   -0.8820   -1.3019 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1373   -2.1850   -1.8219 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2632   -0.5887   -2.5664 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0973    1.3226   -0.5399 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2059   -0.4204   -0.9247 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6067    0.1054    0.6899 H   0  0  0  0  0  0  0  0  0  0  0  0
 27 26  1  0
 26 28  2  0
 26 25  1  0
 25 24  1  0
 24 23  1  0
 23 21  2  0
 21 22  1  0
 21 20  1  0
 20 19  1  0
 19 18  1  0
 18  2  1  0
  2  1  2  3
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  1
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 10 12  2  0
  6 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  6
 16 18  1  0
 16  5  1  0
 27 64  1  0
 27 65  1  0
 27 66  1  0
 24 62  1  0
 24 63  1  0
 23 61  1  0
 22 58  1  0
 22 59  1  0
 22 60  1  0
 20 56  1  0
 20 57  1  0
 19 54  1  0
 19 55  1  0
 18 53  1  1
  1 29  1  0
  1 30  1  0
  3 31  1  0
  3 32  1  0
  4 33  1  0
  4 34  1  0
  5 35  1  1
  7 36  1  0
  7 37  1  0
  7 38  1  0
  8 39  1  0
  8 40  1  0
 11 41  1  0
 11 42  1  0
 11 43  1  0
 13 44  1  0
 13 45  1  0
 14 46  1  0
 14 47  1  0
 15 48  1  0
 15 49  1  0
 17 50  1  0
 17 51  1  0
 17 52  1  0
M  END


  Mrv1652306292223342D          

 28 29  0  0  1  0            999 V2000
   -1.4289    2.4750    0.0000 C   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 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    4.9500    0.0000 C   0  0  0  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    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   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
   -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  0  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  2  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  1  0  0  0  0  0  0  0  0  0
    1.8163   -2.3784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0416   -2.3784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4788   -3.0781    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0915   -3.8065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5287   -4.5061    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2670   -3.8353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    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  2  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  1  0  0  0  0
  2  9  1  0  0  0  0
  9 10  1  0  0  0  0
 11 10  1  6  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  0  0  0  0
 16 15  1  6  0  0  0
 16 17  1  0  0  0  0
 11 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 16 21  1  0  0  0  0
 21 22  1  1  0  0  0
 21 23  1  6  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 17 28  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0140450

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC\C=C(/C)CC[C@H]1C(=C)CC[C@H]2[C@@](C)(COC(C)=O)CCC[C@]12C

> <INCHI_IDENTIFIER>
InChI=1S/C24H38O4/c1-17(12-15-27-19(3)25)8-10-21-18(2)9-11-22-23(5,16-28-20(4)26)13-7-14-24(21,22)6/h12,21-22H,2,7-11,13-16H2,1,3-6H3/b17-12+/t21-,22-,23+,24+/m0/s1

> <INCHI_KEY>
LBHXIQMBWNFUCB-AOYOYUNPSA-N

> <FORMULA>
C24H38O4

> <MOLECULAR_WEIGHT>
390.564

> <EXACT_MASS>
390.277009704

$$$$

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   4.620   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.000   6.160   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       1.334   6.930   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       1.334   8.470   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       2.667   9.240   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       0.000   9.240   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+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       3.390  -4.440   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.944  -4.440   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       2.760  -5.746   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       2.037  -7.105   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       2.854  -8.411   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       0.498  -7.159   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       1.334   0.770   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    9                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6                                                            
CONECT    9    2   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   17                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   21                                                  
CONECT   17   16   11   18   28                                             
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   16   22   23                                             
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   17                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   58    0
END

View in JSmol

Synonyms

Value	Source
Agathadiol diacetic acid	Generator

Chemical Formula

C₂₄H₃₈O₄

Average Mass

390.5640 Da

Monoisotopic Mass

390.27701 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(=O)OC\C=C(/C)CC[C@H]1C(=C)CC[C@H]2[C@@](C)(COC(C)=O)CCC[C@]12C

InChI Identifier

InChI=1S/C24H38O4/c1-17(12-15-27-19(3)25)8-10-21-18(2)9-11-22-23(5,16-28-20(4)26)13-7-14-24(21,22)6/h12,21-22H,2,7-11,13-16H2,1,3-6H3/b17-12+/t21-,22-,23+,24+/m0/s1

InChI Key

LBHXIQMBWNFUCB-AOYOYUNPSA-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
Cryptomeria japonica	LOTUS Database	35616633

Chemical Taxonomy

Description

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

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Diterpenoids

Alternative Parents

Substituents

Diterpenoid
Labdane diterpenoid
Dicarboxylic acid or derivatives
Carboxylic acid ester
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic 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

28424372

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

91884742

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Agathadiol diacetate (NP0140450)

MOL for NP0140450 (Agathadiol diacetate)

3D MOL for NP0140450 (Agathadiol diacetate)

3D SDF for NP0140450 (Agathadiol diacetate)

3D-SDF for NP0140450 (Agathadiol diacetate)

PDB for NP0140450 (Agathadiol diacetate)

3D PDB for NP0140450 (Agathadiol diacetate)

SMILES for NP0140450 (Agathadiol diacetate)

INCHI for NP0140450 (Agathadiol diacetate)

Structure for NP0140450 (Agathadiol diacetate)

3D Structure for NP0140450 (Agathadiol diacetate)