NP-MRD: Showing NP-Card for 1-[(acetyloxy)methyl]-7-ethenyl-4a,8-dimethyl-2,3,4,4b,5,6,8a,9,10,10a-decahydrophenanthrene-1-carboxylic acid (NP0320719)

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Record Information

Version

2.0

Created at

2022-09-11 22:32:16 UTC

Updated at

2022-09-11 22:32:16 UTC

NP-MRD ID

NP0320719

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-[(acetyloxy)methyl]-7-ethenyl-4a,8-dimethyl-2,3,4,4b,5,6,8a,9,10,10a-decahydrophenanthrene-1-carboxylic acid

Description

1-[(Acetyloxy)methyl]-7-ethenyl-4a,8-dimethyl-1,2,3,4,4a,4b,5,6,8a,9,10,10a-dodecahydrophenanthrene-1-carboxylic acid belongs to the class of organic compounds known as isocopalane and spongiane diterpenoids. These are diterpenoids with a structure based on the isocopalane (Tetradecahydro-1,1,4a,7,8,8a-hexamethylphenanthrene) or the 15,16-epoxyisocopalane skeleton. 1-[(acetyloxy)methyl]-7-ethenyl-4a,8-dimethyl-2,3,4,4b,5,6,8a,9,10,10a-decahydrophenanthrene-1-carboxylic acid is found in Myrospermum frutescens. 1-[(Acetyloxy)methyl]-7-ethenyl-4a,8-dimethyl-1,2,3,4,4a,4b,5,6,8a,9,10,10a-dodecahydrophenanthrene-1-carboxylic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004231514482D          

 26 28  0  0  0  0            999 V2000
    2.1390   -4.9662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3637   -4.6841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7318   -5.2144    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2205   -3.8716    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4452   -3.5894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145   -3.4914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -3.4914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -3.4914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4733   -3.0591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1053   -2.5288    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6165   -3.8716    0.0000 O   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
  2  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
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 12 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
  6 21  1  0  0  0  0
 10 21  1  0  0  0  0
 15 22  1  0  0  0  0
 22 23  2  0  0  0  0
  6 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
M  END

     RDKit          3D

 58 60  0  0  0  0  0  0  0  0999 V2000
    6.2423    1.1691    0.7760 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5016    0.6639   -0.1614 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0430    0.5389   -0.1035 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3668    0.0119   -1.1072 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1097   -0.4537   -2.2973 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9038   -0.1196   -1.0651 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1889    1.1626   -1.4266 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2961    0.8660   -1.3924 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6883    0.3903   -0.0327 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1544    0.3167    0.1835 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9350   -0.2159   -0.9865 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3321   -0.0856   -0.7948 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2565   -0.4976   -1.7191 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7078   -0.3433   -1.4801 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8575   -1.0170   -2.7912 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6426    1.7312    0.3927 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8961    2.7203    0.3267 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9948    1.9806    0.6766 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5109   -0.4241    1.4335 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3265   -0.4489    2.4112 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2929   -1.3432    1.7246 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0691   -0.8503    0.3531 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1908   -2.0059   -0.6099 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5465   -0.6036    0.3252 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0749    0.2311    1.4196 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3139    1.0163    1.1093 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9273    1.5646    1.7132 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3300    1.2056    0.6090 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9754    0.2922   -1.0828 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7635    0.3362   -2.7231 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4327   -0.7637   -3.1203 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7200   -1.3705   -2.0587 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5209   -0.8890   -1.7687 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4996    1.4538   -2.4299 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3827    1.9827   -0.7271 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6215    0.2365   -2.2253 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8031    1.8573   -1.5483 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3054    1.1856    0.6795 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7476   -1.3176   -1.0917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6877    0.2369   -1.9393 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9453    0.6380   -0.9924 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2790   -0.4731   -2.4005 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0460   -1.1126   -0.7355 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6195    1.3128    1.0569 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7853   -1.4822    1.2678 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3461    0.0308    2.0039 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6724   -1.0145    3.3050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9469    0.5480    2.6268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7812   -2.3628    1.7044 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5782   -1.4687    2.3984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3802   -1.6942   -1.6308 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7282   -2.6631   -0.6457 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9822   -2.6664   -0.1857 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0304   -1.6238    0.4046 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3336   -0.4412    2.2930 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3465    0.9489    1.8517 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0151    1.0087    1.9866 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0871    2.1146    0.9702 H   0  0  0  0  0  0  0  0  0  0  0  0
 14 13  1  0
 13 15  2  0
 13 12  1  0
 12 11  1  0
 11 10  1  0
 10 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  6
 22 24  1  0
 24 25  1  0
 25 26  1  0
 26  3  1  0
  3  2  1  0
  2  1  2  3
  3  4  2  0
  4  5  1  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
 10 16  1  1
 16 18  1  0
 16 17  2  0
  9 10  1  0
  9 22  1  0
  6 24  1  0
 14 41  1  0
 14 42  1  0
 14 43  1  0
 11 39  1  0
 11 40  1  0
 19 45  1  0
 19 46  1  0
 20 47  1  0
 20 48  1  0
 21 49  1  0
 21 50  1  0
 23 51  1  0
 23 52  1  0
 23 53  1  0
 24 54  1  1
 25 55  1  0
 25 56  1  0
 26 57  1  0
 26 58  1  0
  2 29  1  0
  1 27  1  0
  1 28  1  0
  5 30  1  0
  5 31  1  0
  5 32  1  0
  6 33  1  6
  7 34  1  0
  7 35  1  0
  8 36  1  0
  8 37  1  0
  9 38  1  1
 18 44  1  0
M  END


  Mrv1533004231514482D          

 26 28  0  0  0  0            999 V2000
    2.1390   -4.9662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3637   -4.6841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7318   -5.2144    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2205   -3.8716    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4452   -3.5894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145   -3.4914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -3.4914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -3.4914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4733   -3.0591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1053   -2.5288    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6165   -3.8716    0.0000 O   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
  2  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
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 12 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
  6 21  1  0  0  0  0
 10 21  1  0  0  0  0
 15 22  1  0  0  0  0
 22 23  2  0  0  0  0
  6 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0320719

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OCC1(CCCC2(C)C3CCC(C=C)=C(C)C3CCC12)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C22H32O4/c1-5-16-7-9-18-17(14(16)2)8-10-19-21(18,4)11-6-12-22(19,20(24)25)13-26-15(3)23/h5,17-19H,1,6-13H2,2-4H3,(H,24,25)

> <INCHI_KEY>
MMAYUYRWDRFNKQ-UHFFFAOYSA-N

> <FORMULA>
C22H32O4

> <MOLECULAR_WEIGHT>
360.494

> <EXACT_MASS>
360.23005951

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
41.258115727252715

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1-[(acetyloxy)methyl]-7-ethenyl-4a,8-dimethyl-1,2,3,4,4a,4b,5,6,8a,9,10,10a-dodecahydrophenanthrene-1-carboxylic acid

> <ALOGPS_LOGP>
4.17

> <JCHEM_LOGP>
4.170852984333334

> <ALOGPS_LOGS>
-4.98

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.510089443352802

> <JCHEM_PKA_STRONGEST_BASIC>
-6.996177251081641

> <JCHEM_POLAR_SURFACE_AREA>
63.60000000000001

> <JCHEM_REFRACTIVITY>
101.06789999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.75e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-[(acetyloxy)methyl]-7-ethenyl-4a,8-dimethyl-2,3,4,4b,5,6,8a,9,10,10a-decahydrophenanthrene-1-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 23-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-APR-15         0                                  
HETATM    1  C   UNK     0       3.993  -9.270   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.546  -8.744   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       1.366  -9.733   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       2.278  -7.227   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       0.831  -6.700   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.564  -5.184   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.206  -3.850   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.564  -2.516   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.104  -2.516   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.874  -3.850   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.644  -2.516   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.414  -3.850   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.184  -2.516   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.724  -2.516   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.494  -3.850   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.724  -5.184   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.494  -6.517   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.184  -5.184   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.414  -6.517   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.874  -6.517   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.104  -5.184   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       9.034  -3.850   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.804  -2.516   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.883  -5.710   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -2.063  -4.720   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0      -1.151  -7.227   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   21   24                                             
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12   21                                             
CONECT   11   10                                                            
CONECT   12   10   13   18                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   22                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   12   19                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20    6   10                                                  
CONECT   22   15   23                                                       
CONECT   23   22                                                            
CONECT   24    6   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   56    0
END

View in JSmol

Synonyms

Value	Source
1-[(Acetyloxy)methyl]-7-ethenyl-4a,8-dimethyl-1,2,3,4,4a,4b,5,6,8a,9,10,10a-dodecahydrophenanthrene-1-carboxylate	Generator

Chemical Formula

C₂₂H₃₂O₄

Average Mass

360.4940 Da

Monoisotopic Mass

360.23006 Da

IUPAC Name

1-[(acetyloxy)methyl]-7-ethenyl-4a,8-dimethyl-1,2,3,4,4a,4b,5,6,8a,9,10,10a-dodecahydrophenanthrene-1-carboxylic acid

Traditional Name

1-[(acetyloxy)methyl]-7-ethenyl-4a,8-dimethyl-2,3,4,4b,5,6,8a,9,10,10a-decahydrophenanthrene-1-carboxylic acid

CAS Registry Number

Not Available

SMILES

CC(=O)OCC1(CCCC2(C)C3CCC(C=C)=C(C)C3CCC12)C(O)=O

InChI Identifier

InChI=1S/C22H32O4/c1-5-16-7-9-18-17(14(16)2)8-10-19-21(18,4)11-6-12-22(19,20(24)25)13-26-15(3)23/h5,17-19H,1,6-13H2,2-4H3,(H,24,25)

InChI Key

MMAYUYRWDRFNKQ-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
Myrospermum frutescens	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as isocopalane and spongiane diterpenoids. These are diterpenoids with a structure based on the isocopalane (Tetradecahydro-1,1,4a,7,8,8a-hexamethylphenanthrene) or the 15,16-epoxyisocopalane skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Isocopalane and spongiane diterpenoids

Alternative Parents

Substituents

Isocopalane diterpenoid
Phenanthrene
Hydrophenanthrene
Dicarboxylic acid or derivatives
Carboxylic acid ester
Carboxylic acid
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
logP	4.17	ALOGPS
logP	4.17	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Acidic)	4.51	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	5	ChemAxon
Refractivity	101.07 m³·mol⁻¹	ChemAxon
Polarizability	41.26 Å³	ChemAxon
Number of Rings	3	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

73821803

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1-[(acetyloxy)methyl]-7-ethenyl-4a,8-dimethyl-2,3,4,4b,5,6,8a,9,10,10a-decahydrophenanthrene-1-carboxylic acid (NP0320719)

MOL for NP0320719 (1-[(acetyloxy)methyl]-7-ethenyl-4a,8-dimethyl-2,3,4,4b,5,6,8a,9,10,10a-decahydrophenanthrene-1-carboxylic acid)

3D MOL for NP0320719 (1-[(acetyloxy)methyl]-7-ethenyl-4a,8-dimethyl-2,3,4,4b,5,6,8a,9,10,10a-decahydrophenanthrene-1-carboxylic acid)

3D SDF for NP0320719 (1-[(acetyloxy)methyl]-7-ethenyl-4a,8-dimethyl-2,3,4,4b,5,6,8a,9,10,10a-decahydrophenanthrene-1-carboxylic acid)

3D-SDF for NP0320719 (1-[(acetyloxy)methyl]-7-ethenyl-4a,8-dimethyl-2,3,4,4b,5,6,8a,9,10,10a-decahydrophenanthrene-1-carboxylic acid)

PDB for NP0320719 (1-[(acetyloxy)methyl]-7-ethenyl-4a,8-dimethyl-2,3,4,4b,5,6,8a,9,10,10a-decahydrophenanthrene-1-carboxylic acid)

3D PDB for NP0320719 (1-[(acetyloxy)methyl]-7-ethenyl-4a,8-dimethyl-2,3,4,4b,5,6,8a,9,10,10a-decahydrophenanthrene-1-carboxylic acid)

SMILES for NP0320719 (1-[(acetyloxy)methyl]-7-ethenyl-4a,8-dimethyl-2,3,4,4b,5,6,8a,9,10,10a-decahydrophenanthrene-1-carboxylic acid)

INCHI for NP0320719 (1-[(acetyloxy)methyl]-7-ethenyl-4a,8-dimethyl-2,3,4,4b,5,6,8a,9,10,10a-decahydrophenanthrene-1-carboxylic acid)

Structure for NP0320719 (1-[(acetyloxy)methyl]-7-ethenyl-4a,8-dimethyl-2,3,4,4b,5,6,8a,9,10,10a-decahydrophenanthrene-1-carboxylic acid)

3D Structure for NP0320719 (1-[(acetyloxy)methyl]-7-ethenyl-4a,8-dimethyl-2,3,4,4b,5,6,8a,9,10,10a-decahydrophenanthrene-1-carboxylic acid)