NP-MRD: Showing NP-Card for pulcherrin D (NP0040619)

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Record Information

Version

2.0

Created at

2021-06-20 22:44:06 UTC

Updated at

2021-06-30 00:14:38 UTC

NP-MRD ID

NP0040619

Secondary Accession Numbers

None

Natural Product Identification

Common Name

pulcherrin D

Provided By

JEOL Database JEOL Logo

Description

Pulcherrin D belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. pulcherrin D is found in Caesalpinia pulcherrima. pulcherrin D was first documented in 2011 (Yodsaoue, O., et al.). Based on a literature review very few articles have been published on Pulcherrin D.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306212100443D          

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M  END

     RDKit          3D

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M  END


  Mrv1652306212100443D          

 58 61  0  0  0  0            999 V2000
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   -2.4777    0.3035    1.5289 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2143    1.9410    2.5823 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6108    1.2000    4.0761 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7525    2.9504    3.9369 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8258    2.8121    3.8806 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6291    3.1357    4.7594 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0177    1.4902    4.7102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1248    4.2874    2.5067 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8125    3.3273    1.2122 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2195    4.3574    0.4365 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1533    3.7393    1.7797 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1601    2.1426   -0.4716 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5566    2.4146   -0.2409 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1566    0.1083    2.5924 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0129    1.8504    2.6953 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8815    1.1586    1.3847 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1178   -0.2873   -0.4639 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9013    0.0753   -0.3181 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7708    0.4704   -1.6120 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9286   -3.3072   -3.4471 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2237   -4.8176   -1.8801 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9477   -3.8167    0.6350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6019   -4.0416   -1.3500 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4198   -3.5254    0.1146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0556   -2.3462   -1.1628 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6436   -1.7586    1.5429 H   0  0  0  0  0  0  0  0  0  0  0  0
 26 17  1  0  0  0  0
 23 24  1  0  0  0  0
 13 14  1  0  0  0  0
  7  8  1  6  0  0  0
 12  9  1  0  0  0  0
  5  4  1  0  0  0  0
 19 23  2  0  0  0  0
  7  6  1  0  0  0  0
  6  5  1  0  0  0  0
  5 26  1  0  0  0  0
  9  7  1  0  0  0  0
 15 14  1  0  0  0  0
 23 22  1  0  0  0  0
 22 21  2  0  0  0  0
 21 20  1  0  0  0  0
 20 19  1  0  0  0  0
 26 24  1  0  0  0  0
 24 25  1  0  0  0  0
 19 18  1  0  0  0  0
  9 10  1  1  0  0  0
 15  7  1  0  0  0  0
  9 11  1  0  0  0  0
 15 16  1  1  0  0  0
  4  2  1  0  0  0  0
  2  1  1  0  0  0  0
 13 12  1  0  0  0  0
  2  3  2  0  0  0  0
 18 17  1  0  0  0  0
 26 58  1  1  0  0  0
 15 17  1  0  0  0  0
 17 49  1  6  0  0  0
 13 42  1  0  0  0  0
 13 43  1  0  0  0  0
 12 40  1  0  0  0  0
 12 41  1  0  0  0  0
 14 44  1  0  0  0  0
 14 45  1  0  0  0  0
  6 31  1  0  0  0  0
  6 32  1  0  0  0  0
  5 30  1  6  0  0  0
 18 50  1  0  0  0  0
 18 51  1  0  0  0  0
 16 46  1  0  0  0  0
 16 47  1  0  0  0  0
 16 48  1  0  0  0  0
  8 33  1  0  0  0  0
 24 54  1  1  0  0  0
 22 53  1  0  0  0  0
 21 52  1  0  0  0  0
 25 55  1  0  0  0  0
 25 56  1  0  0  0  0
 25 57  1  0  0  0  0
 10 34  1  0  0  0  0
 10 35  1  0  0  0  0
 10 36  1  0  0  0  0
 11 37  1  0  0  0  0
 11 38  1  0  0  0  0
 11 39  1  0  0  0  0
  1 27  1  0  0  0  0
  1 28  1  0  0  0  0
  1 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0040619

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]O[C@@]12C([H])([H])[C@]([H])(OC(=O)C([H])([H])[H])[C@@]3([H])[C@]([H])(C4=C(OC([H])=C4[H])C([H])([H])[C@]3([H])[C@@]1(C([H])([H])[H])C([H])([H])C([H])([H])C([H])([H])C2(C([H])([H])[H])C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C22H32O4/c1-13-15-7-10-25-17(15)11-16-19(13)18(26-14(2)23)12-22(24)20(3,4)8-6-9-21(16,22)5/h7,10,13,16,18-19,24H,6,8-9,11-12H2,1-5H3/t13-,16-,18-,19-,21+,22+/m0/s1

> <INCHI_KEY>
HOCAOPOBPZNWHL-AOBXKPQGSA-N

> <FORMULA>
C22H32O4

> <MOLECULAR_WEIGHT>
360.494

> <EXACT_MASS>
360.23005951

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
41.09164901057831

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2R,7R,9S,10S,11R)-7-hydroxy-2,6,6,11-tetramethyl-15-oxatetracyclo[8.7.0.0^{2,7}.0^{12,16}]heptadeca-12(16),13-dien-9-yl acetate

> <ALOGPS_LOGP>
4.28

> <JCHEM_LOGP>
3.5590451809999992

> <ALOGPS_LOGS>
-4.38

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.96412576641141

> <JCHEM_PKA_STRONGEST_BASIC>
-2.820497595985955

> <JCHEM_POLAR_SURFACE_AREA>
59.67

> <JCHEM_REFRACTIVITY>
99.201

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.52e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,7R,9S,10S,11R)-7-hydroxy-2,6,6,11-tetramethyl-15-oxatetracyclo[8.7.0.0^{2,7}.0^{12,16}]heptadeca-12(16),13-dien-9-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 58 61  0  0  0  0  0  0  0  0999 V2000
   -1.0290   -4.5923    4.2166 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3888   -3.3970    3.3891 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5255   -2.9696    3.2475 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2672   -2.8659    2.8289 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4587   -1.7099    1.9822 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5554   -0.4558    2.8635 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6217    0.8344    2.0239 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6950    0.6498    1.0643 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0181    2.1295    2.8547 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4800    2.0403    3.3879 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1527    2.3924    4.1072 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9751    3.3705    1.9218 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3137    3.5030    1.1180 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6155    2.2505    0.2979 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6960    0.9539    1.1506 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9921    1.0139    2.0042 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7746   -0.3083    0.1784 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9826   -0.2474   -0.8118 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2517   -1.5774   -1.3928 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1699   -1.7041   -2.3797 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2344   -3.0334   -2.6652 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3713   -3.7472   -1.8616 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7291   -2.7946   -1.0338 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6869   -2.9405    0.0259 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6745   -3.2213   -0.6261 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7083   -1.6709    0.9702 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9371   -5.0174    4.6534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5581   -5.3509    3.5863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3588   -4.2939    5.0266 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4020   -1.8140    1.4350 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2721   -0.4399    3.5805 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4579   -0.5554    3.4761 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4777    0.3035    1.5289 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2143    1.9410    2.5823 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6108    1.2000    4.0761 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7525    2.9504    3.9369 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8258    2.8121    3.8806 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6291    3.1357    4.7594 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0177    1.4902    4.7102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1248    4.2874    2.5067 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8125    3.3273    1.2122 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2195    4.3574    0.4365 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1533    3.7393    1.7797 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1601    2.1426   -0.4716 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5566    2.4146   -0.2409 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1566    0.1083    2.5924 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0129    1.8504    2.6953 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8815    1.1586    1.3847 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1178   -0.2873   -0.4639 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9013    0.0753   -0.3181 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7708    0.4704   -1.6120 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9286   -3.3072   -3.4471 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2237   -4.8176   -1.8801 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9477   -3.8167    0.6350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6019   -4.0416   -1.3500 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4198   -3.5254    0.1146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0556   -2.3462   -1.1628 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6436   -1.7586    1.5429 H   0  0  0  0  0  0  0  0  0  0  0  0
 26 17  1  0
 23 24  1  0
 13 14  1  0
  7  8  1  6
 12  9  1  0
  5  4  1  0
 19 23  2  0
  7  6  1  0
  6  5  1  0
  5 26  1  0
  9  7  1  0
 15 14  1  0
 23 22  1  0
 22 21  2  0
 21 20  1  0
 20 19  1  0
 26 24  1  0
 24 25  1  0
 19 18  1  0
  9 10  1  1
 15  7  1  0
  9 11  1  0
 15 16  1  1
  4  2  1  0
  2  1  1  0
 13 12  1  0
  2  3  2  0
 18 17  1  0
 26 58  1  1
 15 17  1  0
 17 49  1  6
 13 42  1  0
 13 43  1  0
 12 40  1  0
 12 41  1  0
 14 44  1  0
 14 45  1  0
  6 31  1  0
  6 32  1  0
  5 30  1  6
 18 50  1  0
 18 51  1  0
 16 46  1  0
 16 47  1  0
 16 48  1  0
  8 33  1  0
 24 54  1  1
 22 53  1  0
 21 52  1  0
 25 55  1  0
 25 56  1  0
 25 57  1  0
 10 34  1  0
 10 35  1  0
 10 36  1  0
 11 37  1  0
 11 38  1  0
 11 39  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
M  END

HEADER    PROTEIN                                 21-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   21-JUN-21         0                                  
HETATM    1  C   UNK     0      -1.029  -4.592   4.217  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.389  -3.397   3.389  0.00  0.00           C+0
HETATM    3  O   UNK     0      -2.526  -2.970   3.248  0.00  0.00           O+0
HETATM    4  O   UNK     0      -0.267  -2.866   2.829  0.00  0.00           O+0
HETATM    5  C   UNK     0      -0.459  -1.710   1.982  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.555  -0.456   2.864  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.622   0.834   2.024  0.00  0.00           C+0
HETATM    8  O   UNK     0      -1.695   0.650   1.064  0.00  0.00           O+0
HETATM    9  C   UNK     0      -1.018   2.130   2.855  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.480   2.040   3.388  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.153   2.392   4.107  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.975   3.370   1.922  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.314   3.503   1.118  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.616   2.251   0.298  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.696   0.954   1.151  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.992   1.014   2.004  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.775  -0.308   0.178  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.983  -0.247  -0.812  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.252  -1.577  -1.393  0.00  0.00           C+0
HETATM   20  O   UNK     0       3.170  -1.704  -2.380  0.00  0.00           O+0
HETATM   21  C   UNK     0       3.234  -3.033  -2.665  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.371  -3.747  -1.862  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.729  -2.795  -1.034  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.687  -2.941   0.026  0.00  0.00           C+0
HETATM   25  C   UNK     0      -0.675  -3.221  -0.626  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.708  -1.671   0.970  0.00  0.00           C+0
HETATM   27  H   UNK     0      -1.937  -5.017   4.653  0.00  0.00           H+0
HETATM   28  H   UNK     0      -0.558  -5.351   3.586  0.00  0.00           H+0
HETATM   29  H   UNK     0      -0.359  -4.294   5.027  0.00  0.00           H+0
HETATM   30  H   UNK     0      -1.402  -1.814   1.435  0.00  0.00           H+0
HETATM   31  H   UNK     0       0.272  -0.440   3.580  0.00  0.00           H+0
HETATM   32  H   UNK     0      -1.458  -0.555   3.476  0.00  0.00           H+0
HETATM   33  H   UNK     0      -2.478   0.304   1.529  0.00  0.00           H+0
HETATM   34  H   UNK     0      -3.214   1.941   2.582  0.00  0.00           H+0
HETATM   35  H   UNK     0      -2.611   1.200   4.076  0.00  0.00           H+0
HETATM   36  H   UNK     0      -2.753   2.950   3.937  0.00  0.00           H+0
HETATM   37  H   UNK     0       0.826   2.812   3.881  0.00  0.00           H+0
HETATM   38  H   UNK     0      -0.629   3.136   4.759  0.00  0.00           H+0
HETATM   39  H   UNK     0      -0.018   1.490   4.710  0.00  0.00           H+0
HETATM   40  H   UNK     0      -1.125   4.287   2.507  0.00  0.00           H+0
HETATM   41  H   UNK     0      -1.813   3.327   1.212  0.00  0.00           H+0
HETATM   42  H   UNK     0       0.220   4.357   0.437  0.00  0.00           H+0
HETATM   43  H   UNK     0       1.153   3.739   1.780  0.00  0.00           H+0
HETATM   44  H   UNK     0      -0.160   2.143  -0.472  0.00  0.00           H+0
HETATM   45  H   UNK     0       1.557   2.415  -0.241  0.00  0.00           H+0
HETATM   46  H   UNK     0       2.157   0.108   2.592  0.00  0.00           H+0
HETATM   47  H   UNK     0       2.013   1.850   2.695  0.00  0.00           H+0
HETATM   48  H   UNK     0       2.882   1.159   1.385  0.00  0.00           H+0
HETATM   49  H   UNK     0      -0.118  -0.287  -0.464  0.00  0.00           H+0
HETATM   50  H   UNK     0       2.901   0.075  -0.318  0.00  0.00           H+0
HETATM   51  H   UNK     0       1.771   0.470  -1.612  0.00  0.00           H+0
HETATM   52  H   UNK     0       3.929  -3.307  -3.447  0.00  0.00           H+0
HETATM   53  H   UNK     0       2.224  -4.818  -1.880  0.00  0.00           H+0
HETATM   54  H   UNK     0       0.948  -3.817   0.635  0.00  0.00           H+0
HETATM   55  H   UNK     0      -0.602  -4.042  -1.350  0.00  0.00           H+0
HETATM   56  H   UNK     0      -1.420  -3.525   0.115  0.00  0.00           H+0
HETATM   57  H   UNK     0      -1.056  -2.346  -1.163  0.00  0.00           H+0
HETATM   58  H   UNK     0       1.644  -1.759   1.543  0.00  0.00           H+0
CONECT    1    2   27   28   29                                             
CONECT    2    4    1    3                                                  
CONECT    3    2                                                            
CONECT    4    5    2                                                       
CONECT    5    4    6   26   30                                             
CONECT    6    7    5   31   32                                             
CONECT    7    8    6    9   15                                             
CONECT    8    7   33                                                       
CONECT    9   12    7   10   11                                             
CONECT   10    9   34   35   36                                             
CONECT   11    9   37   38   39                                             
CONECT   12    9   13   40   41                                             
CONECT   13   14   12   42   43                                             
CONECT   14   13   15   44   45                                             
CONECT   15   14    7   16   17                                             
CONECT   16   15   46   47   48                                             
CONECT   17   26   18   15   49                                             
CONECT   18   19   17   50   51                                             
CONECT   19   23   20   18                                                  
CONECT   20   21   19                                                       
CONECT   21   22   20   52                                                  
CONECT   22   23   21   53                                                  
CONECT   23   24   19   22                                                  
CONECT   24   23   26   25   54                                             
CONECT   25   24   55   56   57                                             
CONECT   26   17    5   24   58                                             
CONECT   27    1                                                            
CONECT   28    1                                                            
CONECT   29    1                                                            
CONECT   30    5                                                            
CONECT   31    6                                                            
CONECT   32    6                                                            
CONECT   33    8                                                            
CONECT   34   10                                                            
CONECT   35   10                                                            
CONECT   36   10                                                            
CONECT   37   11                                                            
CONECT   38   11                                                            
CONECT   39   11                                                            
CONECT   40   12                                                            
CONECT   41   12                                                            
CONECT   42   13                                                            
CONECT   43   13                                                            
CONECT   44   14                                                            
CONECT   45   14                                                            
CONECT   46   16                                                            
CONECT   47   16                                                            
CONECT   48   16                                                            
CONECT   49   17                                                            
CONECT   50   18                                                            
CONECT   51   18                                                            
CONECT   52   21                                                            
CONECT   53   22                                                            
CONECT   54   24                                                            
CONECT   55   25                                                            
CONECT   56   25                                                            
CONECT   57   25                                                            
CONECT   58   26                                                            
MASTER        0    0    0    0    0    0    0    0   58    0  122    0
END

RDKit          3D

58 61  0  0  0  0  0  0  0  0999 V2000
   -1.0290   -4.5923    4.2166 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3888   -3.3970    3.3891 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5255   -2.9696    3.2475 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2672   -2.8659    2.8289 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4587   -1.7099    1.9822 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5554   -0.4558    2.8635 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6217    0.8344    2.0239 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6950    0.6498    1.0643 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0181    2.1295    2.8547 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4800    2.0403    3.3879 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1527    2.3924    4.1072 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9751    3.3705    1.9218 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3137    3.5030    1.1180 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6155    2.2505    0.2979 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6960    0.9539    1.1506 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9921    1.0139    2.0042 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7746   -0.3083    0.1784 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9826   -0.2474   -0.8118 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2517   -1.5774   -1.3928 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1699   -1.7041   -2.3797 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2344   -3.0334   -2.6652 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3713   -3.7472   -1.8616 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7291   -2.7946   -1.0338 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6869   -2.9405    0.0259 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6745   -3.2213   -0.6261 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7083   -1.6709    0.9702 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9371   -5.0174    4.6534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5581   -5.3509    3.5863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3588   -4.2939    5.0266 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4020   -1.8140    1.4350 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2721   -0.4399    3.5805 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4579   -0.5554    3.4761 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4777    0.3035    1.5289 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2143    1.9410    2.5823 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6108    1.2000    4.0761 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7525    2.9504    3.9369 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8258    2.8121    3.8806 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6291    3.1357    4.7594 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0177    1.4902    4.7102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1248    4.2874    2.5067 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8125    3.3273    1.2122 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2195    4.3574    0.4365 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1533    3.7393    1.7797 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1601    2.1426   -0.4716 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5566    2.4146   -0.2409 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1566    0.1083    2.5924 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0129    1.8504    2.6953 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8815    1.1586    1.3847 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1178   -0.2873   -0.4639 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9013    0.0753   -0.3181 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7708    0.4704   -1.6120 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9286   -3.3072   -3.4471 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2237   -4.8176   -1.8801 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9477   -3.8167    0.6350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6019   -4.0416   -1.3500 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4198   -3.5254    0.1146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0556   -2.3462   -1.1628 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6436   -1.7586    1.5429 H   0  0  0  0  0  0  0  0  0  0  0  0
 26 17  1  0
 23 24  1  0
 13 14  1  0
  7  8  1  6
 12  9  1  0
  5  4  1  0
 19 23  2  0
  7  6  1  0
  6  5  1  0
  5 26  1  0
  9  7  1  0
 15 14  1  0
 23 22  1  0
 22 21  2  0
 21 20  1  0
 20 19  1  0
 26 24  1  0
 24 25  1  0
 19 18  1  0
  9 10  1  1
 15  7  1  0
  9 11  1  0
 15 16  1  1
  4  2  1  0
  2  1  1  0
 13 12  1  0
  2  3  2  0
 18 17  1  0
 26 58  1  1
 15 17  1  0
 17 49  1  6
 13 42  1  0
 13 43  1  0
 12 40  1  0
 12 41  1  0
 14 44  1  0
 14 45  1  0
  6 31  1  0
  6 32  1  0
  5 30  1  6
 18 50  1  0
 18 51  1  0
 16 46  1  0
 16 47  1  0
 16 48  1  0
  8 33  1  0
 24 54  1  1
 22 53  1  0
 21 52  1  0
 25 55  1  0
 25 56  1  0
 25 57  1  0
 10 34  1  0
 10 35  1  0
 10 36  1  0
 11 37  1  0
 11 38  1  0
 11 39  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
M  END

View in JSmol View DFT Assignments 3D Conformers

Synonyms

Not Available

Chemical Formula

C₂₂H₃₂O₄

Average Mass

360.4940 Da

Monoisotopic Mass

360.23006 Da

IUPAC Name

(1S,2R,7R,9S,10S,11R)-7-hydroxy-2,6,6,11-tetramethyl-15-oxatetracyclo[8.7.0.0^{2,7}.0^{12,16}]heptadeca-12(16),13-dien-9-yl acetate

Traditional Name

(1S,2R,7R,9S,10S,11R)-7-hydroxy-2,6,6,11-tetramethyl-15-oxatetracyclo[8.7.0.0^{2,7}.0^{12,16}]heptadeca-12(16),13-dien-9-yl acetate

CAS Registry Number

Not Available

SMILES

[H]O[C@@]12C([H])([H])[C@]([H])(OC(=O)C([H])([H])[H])[C@@]3([H])[C@]([H])(C4=C(OC([H])=C4[H])C([H])([H])[C@]3([H])[C@@]1(C([H])([H])[H])C([H])([H])C([H])([H])C([H])([H])C2(C([H])([H])[H])C([H])([H])[H])C([H])([H])[H]

InChI Identifier

InChI=1S/C22H32O4/c1-13-15-7-10-25-17(15)11-16-19(13)18(26-14(2)23)12-22(24)20(3,4)8-6-9-21(16,22)5/h7,10,13,16,18-19,24H,6,8-9,11-12H2,1-5H3/t13-,16-,18-,19-,21+,22+/m0/s1

InChI Key

HOCAOPOBPZNWHL-AOBXKPQGSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 125 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 150 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 175 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 225 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 250 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, chcl3, 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
Caesalpinia pulcherrima	JEOL database	Yodsaoue, O., et al, Tetrahedron, 67, 6838 (2011)

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
Naphthofuran
Benzofuran
Cyclic alcohol
Heteroaromatic compound
Furan
Tertiary alcohol
Carboxylic acid ester
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Hydrocarbon derivative
Organic oxide
Alcohol
Organic oxygen compound
Carbonyl group
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	4.28	ALOGPS
logP	3.56	ChemAxon
logS	-4.4	ALOGPS
pKa (Strongest Acidic)	13.96	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	59.67 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	99.2 m³·mol⁻¹	ChemAxon
Polarizability	41.09 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

28288934

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

54597502

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Yodsaoue, O., et al. (2011). Yodsaoue, O., et al, Tetrahedron, 67, 6838 (2011). Tetrahedron.

Showing NP-Card for pulcherrin D (NP0040619)

MOL for NP0040619 (pulcherrin D)

3D MOL for NP0040619 (pulcherrin D)

3D SDF for NP0040619 (pulcherrin D)

3D-SDF for NP0040619 (pulcherrin D)

PDB for NP0040619 (pulcherrin D)

3D PDB for NP0040619 (pulcherrin D)

SMILES for NP0040619 (pulcherrin D)

INCHI for NP0040619 (pulcherrin D)

Structure for NP0040619 (pulcherrin D)

3D Structure for NP0040619 (pulcherrin D)