NP-MRD: Showing NP-Card for 5-[(acetyloxy)methyl]-5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-14-carboxylic acid (NP0288820)

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Record Information

Version

2.0

Created at

2022-09-09 18:42:16 UTC

Updated at

2022-09-09 18:42:17 UTC

NP-MRD ID

NP0288820

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-[(acetyloxy)methyl]-5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-14-carboxylic acid

Description

Annoglabasin B belongs to the class of organic compounds known as kaurane diterpenoids. These are diterpene alkaloids with a structure that is based on the kaurane skeleton. Kaurane is a tetracyclic compound that arises by cyclisation of a pimarane precursor followed by rearrangement. It possesses a [3,2,1]-bicyclic ring system with C15-C16 bridge connected to C13, forming the five-membered ring D. Annoglabasin B is an extremely weak basic (essentially neutral) compound (based on its pKa). Outside of the human body, annoglabasin b has been detected, but not quantified in, alcoholic beverages and fruits. 5-[(acetyloxy)methyl]-5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-14-carboxylic acid is found in Annona glabra and Ixora coccinea. This could make annoglabasin b a potential biomarker for the consumption of these foods.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv0541 05061307062D          

 26 29  0  0  0  0            999 V2000
    6.9371    2.2181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7828    2.9325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7366    0.4428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3550    0.7609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1623    0.0148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9942    0.2131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7314    2.6342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6222    1.5413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5456    0.6020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9121    2.4782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0998    1.1465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7383    2.0342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7862    2.5891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2148    2.6167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5599    0.6390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1409    1.3963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704    2.0040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1836    1.0613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6778    1.4980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0798    2.1630    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0032    1.2235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5715    1.6963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1988    3.4415    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1751    0.8399    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9989    2.2579    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5085    2.1905    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  1  0  0  0  0
  8  4  1  0  0  0  0
  9  4  1  0  0  0  0
 10  7  1  0  0  0  0
 14  1  1  0  0  0  0
 15  5  1  0  0  0  0
 15 11  1  0  0  0  0
 16 12  1  0  0  0  0
 16 15  1  0  0  0  0
 17  7  1  0  0  0  0
 18  6  1  0  0  0  0
 19 16  1  0  0  0  0
 20  2  1  0  0  0  0
 20  8  1  0  0  0  0
 20 13  1  0  0  0  0
 20 17  1  0  0  0  0
 21  3  1  0  0  0  0
 21  9  1  0  0  0  0
 21 17  1  0  0  0  0
 21 18  1  0  0  0  0
 22 10  1  0  0  0  0
 22 11  1  0  0  0  0
 22 12  1  0  0  0  0
 22 18  1  0  0  0  0
 23 14  2  0  0  0  0
 24 19  2  0  0  0  0
 25 19  1  0  0  0  0
 26 13  1  0  0  0  0
 26 14  1  0  0  0  0
M  END

     RDKit          3D

 60 63  0  0  0  0  0  0  0  0999 V2000
    6.2693    2.3248    0.4860 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8042    2.2393    0.3324 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1155    3.2783    0.3783 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1299    1.0386    0.1347 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7261    1.0144   -0.0062 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2774   -0.4081   -0.2060 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0042   -0.8509   -1.4953 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7573   -1.3440    0.8662 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7498   -2.4352    1.0440 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3902   -1.9969    1.4302 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0663   -0.7231    0.6988 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0466    0.3781    1.7188 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4688   -0.9375    0.2551 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5025   -0.6942    1.3543 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8404   -1.1734    0.7962 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1932   -0.5483   -0.5053 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1160   -0.9908   -1.5187 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9227   -0.2008   -0.9481 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9234   -0.0676   -2.0442 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3331    0.5094   -1.4210 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8337   -0.5751   -0.4728 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5542    1.1262   -0.6830 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0547    0.9220   -0.6126 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.6061    1.7392    0.4499 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2165    1.2436    1.4146 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4518    3.1142    0.3935 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6427    1.4746    1.1289 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5398    3.2996    0.9309 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8147    2.2284   -0.4818 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4834    1.5813   -0.9248 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2927    1.5344    0.8355 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5130   -1.7549   -1.8470 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0438   -1.1070   -1.2127 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0463   -0.0283   -2.2189 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0239   -0.8221    1.8196 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7225   -1.8606    0.5769 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1351   -3.1070    1.8523 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7771   -3.0612    0.1177 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3168   -2.8444    1.1844 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3210   -1.8828    2.5264 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9642    0.2651    2.3696 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0864    1.3821    1.3309 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7904    0.2048    2.4597 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5736   -2.0405    0.0212 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2672   -1.3568    2.2062 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6298    0.3524    1.6169 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7349   -2.2787    0.6016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6427   -0.9796    1.5277 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1718   -0.9393   -0.8181 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9703   -2.0735   -1.4030 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3629   -0.6581   -2.5244 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3319    0.5704   -2.8333 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6987   -1.0861   -2.4303 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0935    0.7454   -2.1825 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0598    1.3895   -0.7996 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7259   -1.5369   -1.0631 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1600    1.6849    0.1625 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3840    1.7964   -1.5772 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5480    1.2503   -1.5639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0506    3.6761    1.1255 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  6  5  1  1
  6  7  1  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  1
 11 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 22  1  1
 22 23  1  0
 23 24  1  0
 24 26  1  0
 24 25  2  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21  6  1  0
 21 11  1  0
 18 13  1  0
 23 16  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  5 30  1  0
  5 31  1  0
  7 32  1  0
  7 33  1  0
  7 34  1  0
  8 35  1  0
  8 36  1  0
  9 37  1  0
  9 38  1  0
 10 39  1  0
 10 40  1  0
 12 41  1  0
 12 42  1  0
 12 43  1  0
 13 44  1  6
 14 45  1  0
 14 46  1  0
 15 47  1  0
 15 48  1  0
 16 49  1  6
 17 50  1  0
 17 51  1  0
 22 57  1  0
 22 58  1  0
 23 59  1  6
 26 60  1  0
 19 52  1  0
 19 53  1  0
 20 54  1  0
 20 55  1  0
 21 56  1  6
M  END


  Mrv0541 05061307062D          

 26 29  0  0  0  0            999 V2000
    6.9371    2.2181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7828    2.9325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7366    0.4428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3550    0.7609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1623    0.0148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9942    0.2131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7314    2.6342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6222    1.5413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5456    0.6020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9121    2.4782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0998    1.1465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7383    2.0342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7862    2.5891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2148    2.6167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5599    0.6390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1409    1.3963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704    2.0040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1836    1.0613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6778    1.4980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0798    2.1630    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0032    1.2235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5715    1.6963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1988    3.4415    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1751    0.8399    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9989    2.2579    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5085    2.1905    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  1  0  0  0  0
  8  4  1  0  0  0  0
  9  4  1  0  0  0  0
 10  7  1  0  0  0  0
 14  1  1  0  0  0  0
 15  5  1  0  0  0  0
 15 11  1  0  0  0  0
 16 12  1  0  0  0  0
 16 15  1  0  0  0  0
 17  7  1  0  0  0  0
 18  6  1  0  0  0  0
 19 16  1  0  0  0  0
 20  2  1  0  0  0  0
 20  8  1  0  0  0  0
 20 13  1  0  0  0  0
 20 17  1  0  0  0  0
 21  3  1  0  0  0  0
 21  9  1  0  0  0  0
 21 17  1  0  0  0  0
 21 18  1  0  0  0  0
 22 10  1  0  0  0  0
 22 11  1  0  0  0  0
 22 12  1  0  0  0  0
 22 18  1  0  0  0  0
 23 14  2  0  0  0  0
 24 19  2  0  0  0  0
 25 19  1  0  0  0  0
 26 13  1  0  0  0  0
 26 14  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0288820

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OCC1(C)CCCC2(C)C3CCC4CC3(CC4C(O)=O)CCC12

> <INCHI_IDENTIFIER>
InChI=1S/C22H34O4/c1-14(23)26-13-20(2)8-4-9-21(3)17(20)7-10-22-11-15(5-6-18(21)22)16(12-22)19(24)25/h15-18H,4-13H2,1-3H3,(H,24,25)

> <INCHI_KEY>
ZKXLEDOCSSUHKY-UHFFFAOYSA-N

> <FORMULA>
C22H34O4

> <MOLECULAR_WEIGHT>
362.503

> <EXACT_MASS>
362.245709576

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_AVERAGE_POLARIZABILITY>
41.44073865153319

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5-[(acetyloxy)methyl]-5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-14-carboxylic acid

> <ALOGPS_LOGP>
3.88

> <JCHEM_LOGP>
4.059863647

> <ALOGPS_LOGS>
-5.25

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.731142640894326

> <JCHEM_PKA_STRONGEST_BASIC>
-6.995029951282697

> <JCHEM_POLAR_SURFACE_AREA>
63.60000000000001

> <JCHEM_REFRACTIVITY>
98.48639999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.06e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-[(acetyloxy)methyl]-5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-14-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0      12.949   4.140   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.061   5.474   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.108   0.827   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.129   1.420   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.170   0.028   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.722   0.398   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.099   4.917   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.628   2.877   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.618   1.124   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.569   4.626   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.053   2.140   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.378   3.797   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.934   4.833   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      11.601   4.885   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.045   1.193   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.263   2.606   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.105   3.741   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.076   1.981   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.265   2.796   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.616   4.038   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.606   2.284   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.933   3.166   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      11.571   6.424   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0      -2.194   1.568   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0      -1.865   4.215   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0      10.282   4.089   0.000  0.00  0.00           O+0
CONECT    1   14                                                            
CONECT    2   20                                                            
CONECT    3   21                                                            
CONECT    4    8    9                                                       
CONECT    5    6   15                                                       
CONECT    6    5   18                                                       
CONECT    7   10   17                                                       
CONECT    8    4   20                                                       
CONECT    9    4   21                                                       
CONECT   10    7   22                                                       
CONECT   11   15   22                                                       
CONECT   12   16   22                                                       
CONECT   13   20   26                                                       
CONECT   14    1   23   26                                                  
CONECT   15    5   11   16                                                  
CONECT   16   12   15   19                                                  
CONECT   17    7   20   21                                                  
CONECT   18    6   21   22                                                  
CONECT   19   16   24   25                                                  
CONECT   20    2    8   13   17                                             
CONECT   21    3    9   17   18                                             
CONECT   22   10   11   12   18                                             
CONECT   23   14                                                            
CONECT   24   19                                                            
CONECT   25   19                                                            
CONECT   26   13   14                                                       
MASTER        0    0    0    0    0    0    0    0   26    0   58    0
END

View in JSmol

Synonyms

Value	Source
ent-19-Acetoxy-16a-kauran-17-carboxylic acid	HMDB
5-[(Acetyloxy)methyl]-5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-14-carboxylate	Generator

Chemical Formula

C₂₂H₃₄O₄

Average Mass

362.5030 Da

Monoisotopic Mass

362.24571 Da

IUPAC Name

5-[(acetyloxy)methyl]-5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-14-carboxylic acid

Traditional Name

5-[(acetyloxy)methyl]-5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-14-carboxylic acid

CAS Registry Number

Not Available

SMILES

CC(=O)OCC1(C)CCCC2(C)C3CCC4CC3(CC4C(O)=O)CCC12

InChI Identifier

InChI=1S/C22H34O4/c1-14(23)26-13-20(2)8-4-9-21(3)17(20)7-10-22-11-15(5-6-18(21)22)16(12-22)19(24)25/h15-18H,4-13H2,1-3H3,(H,24,25)

InChI Key

ZKXLEDOCSSUHKY-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

Species Name	Source	Reference
Annona glabra	LOTUS Database	35616633
Ixora coccinea	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as kaurane diterpenoids. These are diterpene alkaloids with a structure that is based on the kaurane skeleton. Kaurane is a tetracyclic compound that arises by cyclisation of a pimarane precursor followed by rearrangement. It possesses a [3,2,1]-bicyclic ring system with C15-C16 bridge connected to C13, forming the five-membered ring D.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Kaurane diterpenoids

Alternative Parents

Not Available

Substituents

Not Available

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
logP	3.88	ALOGPS
logP	4.06	ChemAxon
logS	-5.2	ALOGPS
pKa (Strongest Acidic)	4.73	ChemAxon
pKa (Strongest Basic)	-7	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	63.6 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	98.49 m³·mol⁻¹	ChemAxon
Polarizability	41.44 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

HMDB0033398

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB011432

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

73657054

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 5-[(acetyloxy)methyl]-5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-14-carboxylic acid (NP0288820)

MOL for NP0288820 (5-[(acetyloxy)methyl]-5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-14-carboxylic acid)

3D MOL for NP0288820 (5-[(acetyloxy)methyl]-5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-14-carboxylic acid)

3D SDF for NP0288820 (5-[(acetyloxy)methyl]-5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-14-carboxylic acid)

3D-SDF for NP0288820 (5-[(acetyloxy)methyl]-5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-14-carboxylic acid)

PDB for NP0288820 (5-[(acetyloxy)methyl]-5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-14-carboxylic acid)

3D PDB for NP0288820 (5-[(acetyloxy)methyl]-5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-14-carboxylic acid)

SMILES for NP0288820 (5-[(acetyloxy)methyl]-5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-14-carboxylic acid)

INCHI for NP0288820 (5-[(acetyloxy)methyl]-5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-14-carboxylic acid)

Structure for NP0288820 (5-[(acetyloxy)methyl]-5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-14-carboxylic acid)

3D Structure for NP0288820 (5-[(acetyloxy)methyl]-5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-14-carboxylic acid)