NP-MRD: Showing NP-Card for 14-deoxy-17-hydroxyandrographolide (NP0031899)

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Record Information

Version

2.0

Created at

2021-06-19 22:51:13 UTC

Updated at

2021-06-30 00:00:46 UTC

NP-MRD ID

NP0031899

Secondary Accession Numbers

None

Natural Product Identification

Common Name

14-deoxy-17-hydroxyandrographolide

Provided By

JEOL Database JEOL Logo

Description

14-Deoxy-17-hydroxyandrographolide belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety. 14-deoxy-17-hydroxyandrographolide is found in Andrographis paniculata. 14-deoxy-17-hydroxyandrographolide was first documented in 2006 (PMID: 16562826). Based on a literature review very few articles have been published on 14-deoxy-17-hydroxyandrographolide.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306202100513D          

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M  END

     RDKit          3D

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M  END


  Mrv1652306202100513D          

 57 59  0  0  0  0            999 V2000
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    1.0787    0.1924    0.4497 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1049   -1.7639   -1.8951 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0466   -0.7700   -1.4041 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0583   -4.8646    0.0651 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7511   -4.1849   -1.5410 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3345   -4.0094   -0.7908 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9623   -3.3645    2.1398 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2740   -1.6406    1.9562 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1701   -2.3259    0.7330 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0512   -2.8551   -0.9921 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0112   -4.6975    0.6787 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3098   -3.5503    1.9653 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3871   -4.5804    1.2438 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0623   -4.1926   -0.4386 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6785   -2.2232    1.8171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7884   -1.8416    0.6167 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5823   -3.5598    0.9590 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2401   -3.2773   -1.1423 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0311   -1.6492   -1.1191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1107    0.8294    0.2625 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4608   -0.0320    0.9274 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3164   -0.4519   -1.4121 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9025    0.3488   -2.0741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3545    1.1966   -0.8865 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4137    3.7145   -1.7736 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2083    3.7187    0.0034 H   0  0  0  0  0  0  0  0  0  0  0  0
 22 21  1  0  0  0  0
  2 17  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 17  1  0  0  0  0
 21 20  2  0  0  0  0
  2  1  1  1  0  0  0
  4  3  1  0  0  0  0
 17 18  1  0  0  0  0
  5  7  1  0  0  0  0
  7  9  1  1  0  0  0
  7 11  1  0  0  0  0
 14 15  1  0  0  0  0
  2  3  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
  2 11  1  0  0  0  0
 24 25  2  0  0  0  0
 20 24  1  0  0  0  0
  7  8  1  0  0  0  0
 23 22  1  0  0  0  0
 11 41  1  6  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
 24 23  1  0  0  0  0
  9 10  1  0  0  0  0
 15 16  1  0  0  0  0
 22 56  1  0  0  0  0
 22 57  1  0  0  0  0
 21 55  1  0  0  0  0
  4 31  1  0  0  0  0
  4 32  1  0  0  0  0
  5 33  1  6  0  0  0
  3 29  1  0  0  0  0
  3 30  1  0  0  0  0
 12 42  1  0  0  0  0
 12 43  1  0  0  0  0
 13 44  1  0  0  0  0
 13 45  1  0  0  0  0
 14 46  1  1  0  0  0
 17 50  1  6  0  0  0
  1 26  1  0  0  0  0
  1 27  1  0  0  0  0
  1 28  1  0  0  0  0
 18 51  1  0  0  0  0
 18 52  1  0  0  0  0
  9 38  1  0  0  0  0
  9 39  1  0  0  0  0
 15 47  1  0  0  0  0
 15 48  1  0  0  0  0
 19 53  1  0  0  0  0
 19 54  1  0  0  0  0
  8 35  1  0  0  0  0
  8 36  1  0  0  0  0
  8 37  1  0  0  0  0
  6 34  1  0  0  0  0
 10 40  1  0  0  0  0
 16 49  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0031899

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC([H])([H])[C@@]1([H])C([H])([H])C([H])([H])[C@]2([H])[C@](C([H])([H])[H])(C([H])([H])O[H])[C@]([H])(O[H])C([H])([H])C([H])([H])[C@@]2(C([H])([H])[H])[C@]1([H])C([H])([H])C([H])([H])C1=C([H])C([H])([H])OC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H32O5/c1-19-9-7-17(23)20(2,12-22)16(19)6-4-14(11-21)15(19)5-3-13-8-10-25-18(13)24/h8,14-17,21-23H,3-7,9-12H2,1-2H3/t14-,15-,16+,17-,19+,20+/m1/s1

> <INCHI_KEY>
LMOGEODVJJLYGW-UQZPWQSVSA-N

> <FORMULA>
C20H32O5

> <MOLECULAR_WEIGHT>
352.471

> <EXACT_MASS>
352.22497413

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
57

> <JCHEM_AVERAGE_POLARIZABILITY>
39.14297785899566

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-{2-[(1R,2S,4aS,5R,6R,8aS)-6-hydroxy-2,5-bis(hydroxymethyl)-5,8a-dimethyl-decahydronaphthalen-1-yl]ethyl}-2,5-dihydrofuran-2-one

> <ALOGPS_LOGP>
1.36

> <JCHEM_LOGP>
1.7261462039999997

> <ALOGPS_LOGS>
-3.52

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.51402992581314

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.360371683153588

> <JCHEM_PKA_STRONGEST_BASIC>
-1.4885020507732798

> <JCHEM_POLAR_SURFACE_AREA>
86.99000000000001

> <JCHEM_REFRACTIVITY>
95.64319999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.07e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-{2-[(1R,2S,4aS,5R,6R,8aS)-6-hydroxy-2,5-bis(hydroxymethyl)-5,8a-dimethyl-octahydronaphthalen-1-yl]ethyl}-5H-furan-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 57 59  0  0  0  0  0  0  0  0999 V2000
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   -0.7872   -2.6170    0.0523 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -4.5778    0.3300   -1.2098 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2686    1.6422   -1.1066 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5625    1.9260   -0.9677 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7806    3.3831   -0.9456 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4763    3.9380   -1.0984 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5672    2.9297   -1.2059 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3679    3.0717   -1.3593 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6413   -1.4961    2.5106 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9568    0.1443    1.9802 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3238   -0.4293    2.0471 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0758   -0.3680   -1.6520 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.1261    0.5786   -1.2423 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0787    0.1924    0.4497 H   0  0  0  0  0  0  0  0  0  0  0  0
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    2.3345   -4.0094   -0.7908 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9623   -3.3645    2.1398 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2740   -1.6406    1.9562 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1701   -2.3259    0.7330 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0512   -2.8551   -0.9921 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0112   -4.6975    0.6787 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3098   -3.5503    1.9653 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3871   -4.5804    1.2438 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0623   -4.1926   -0.4386 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6785   -2.2232    1.8171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7884   -1.8416    0.6167 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5823   -3.5598    0.9590 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2401   -3.2773   -1.1423 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0311   -1.6492   -1.1191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1107    0.8294    0.2625 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4608   -0.0320    0.9274 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3164   -0.4519   -1.4121 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9025    0.3488   -2.0741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3545    1.1966   -0.8865 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4137    3.7145   -1.7736 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2083    3.7187    0.0034 H   0  0  0  0  0  0  0  0  0  0  0  0
 22 21  1  0
  2 17  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 17  1  0
 21 20  2  0
  2  1  1  1
  4  3  1  0
 17 18  1  0
  5  7  1  0
  7  9  1  1
  7 11  1  0
 14 15  1  0
  2  3  1  0
 18 19  1  0
 19 20  1  0
  2 11  1  0
 24 25  2  0
 20 24  1  0
  7  8  1  0
 23 22  1  0
 11 41  1  6
  4  5  1  0
  5  6  1  0
 24 23  1  0
  9 10  1  0
 15 16  1  0
 22 56  1  0
 22 57  1  0
 21 55  1  0
  4 31  1  0
  4 32  1  0
  5 33  1  6
  3 29  1  0
  3 30  1  0
 12 42  1  0
 12 43  1  0
 13 44  1  0
 13 45  1  0
 14 46  1  1
 17 50  1  6
  1 26  1  0
  1 27  1  0
  1 28  1  0
 18 51  1  0
 18 52  1  0
  9 38  1  0
  9 39  1  0
 15 47  1  0
 15 48  1  0
 19 53  1  0
 19 54  1  0
  8 35  1  0
  8 36  1  0
  8 37  1  0
  6 34  1  0
 10 40  1  0
 16 49  1  0
M  END

HEADER    PROTEIN                                 20-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-JUN-21         0                                  
HETATM    1  C   UNK     0      -1.336  -0.737   1.788  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.462  -1.216   0.319  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.787  -0.169  -0.611  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.735  -0.159  -0.529  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.332  -1.524  -0.848  0.00  0.00           C+0
HETATM    6  O   UNK     0       2.757  -1.429  -0.746  0.00  0.00           O+0
HETATM    7  C   UNK     0       0.790  -2.668   0.061  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.258  -4.008  -0.586  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.407  -2.611   1.483  0.00  0.00           C+0
HETATM   10  O   UNK     0       2.812  -2.859   1.477  0.00  0.00           O+0
HETATM   11  C   UNK     0      -0.787  -2.617   0.052  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.454  -3.720   0.894  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.943  -3.821   0.588  0.00  0.00           C+0
HETATM   14  C   UNK     0      -3.698  -2.490   0.753  0.00  0.00           C+0
HETATM   15  C   UNK     0      -5.177  -2.718   0.386  0.00  0.00           C+0
HETATM   16  O   UNK     0      -5.315  -3.013  -0.997  0.00  0.00           O+0
HETATM   17  C   UNK     0      -3.004  -1.348  -0.061  0.00  0.00           C+0
HETATM   18  C   UNK     0      -3.786  -0.006   0.063  0.00  0.00           C+0
HETATM   19  C   UNK     0      -4.578   0.330  -1.210  0.00  0.00           C+0
HETATM   20  C   UNK     0      -5.269   1.642  -1.107  0.00  0.00           C+0
HETATM   21  C   UNK     0      -6.563   1.926  -0.968  0.00  0.00           C+0
HETATM   22  C   UNK     0      -6.781   3.383  -0.946  0.00  0.00           C+0
HETATM   23  O   UNK     0      -5.476   3.938  -1.098  0.00  0.00           O+0
HETATM   24  C   UNK     0      -4.567   2.930  -1.206  0.00  0.00           C+0
HETATM   25  O   UNK     0      -3.368   3.072  -1.359  0.00  0.00           O+0
HETATM   26  H   UNK     0      -1.641  -1.496   2.511  0.00  0.00           H+0
HETATM   27  H   UNK     0      -1.957   0.144   1.980  0.00  0.00           H+0
HETATM   28  H   UNK     0      -0.324  -0.429   2.047  0.00  0.00           H+0
HETATM   29  H   UNK     0      -1.076  -0.368  -1.652  0.00  0.00           H+0
HETATM   30  H   UNK     0      -1.135   0.844  -0.385  0.00  0.00           H+0
HETATM   31  H   UNK     0       1.126   0.579  -1.242  0.00  0.00           H+0
HETATM   32  H   UNK     0       1.079   0.192   0.450  0.00  0.00           H+0
HETATM   33  H   UNK     0       1.105  -1.764  -1.895  0.00  0.00           H+0
HETATM   34  H   UNK     0       3.047  -0.770  -1.404  0.00  0.00           H+0
HETATM   35  H   UNK     0       1.058  -4.865   0.065  0.00  0.00           H+0
HETATM   36  H   UNK     0       0.751  -4.185  -1.541  0.00  0.00           H+0
HETATM   37  H   UNK     0       2.334  -4.009  -0.791  0.00  0.00           H+0
HETATM   38  H   UNK     0       0.962  -3.365   2.140  0.00  0.00           H+0
HETATM   39  H   UNK     0       1.274  -1.641   1.956  0.00  0.00           H+0
HETATM   40  H   UNK     0       3.170  -2.326   0.733  0.00  0.00           H+0
HETATM   41  H   UNK     0      -1.051  -2.855  -0.992  0.00  0.00           H+0
HETATM   42  H   UNK     0      -1.011  -4.697   0.679  0.00  0.00           H+0
HETATM   43  H   UNK     0      -1.310  -3.550   1.965  0.00  0.00           H+0
HETATM   44  H   UNK     0      -3.387  -4.580   1.244  0.00  0.00           H+0
HETATM   45  H   UNK     0      -3.062  -4.193  -0.439  0.00  0.00           H+0
HETATM   46  H   UNK     0      -3.679  -2.223   1.817  0.00  0.00           H+0
HETATM   47  H   UNK     0      -5.788  -1.842   0.617  0.00  0.00           H+0
HETATM   48  H   UNK     0      -5.582  -3.560   0.959  0.00  0.00           H+0
HETATM   49  H   UNK     0      -6.240  -3.277  -1.142  0.00  0.00           H+0
HETATM   50  H   UNK     0      -3.031  -1.649  -1.119  0.00  0.00           H+0
HETATM   51  H   UNK     0      -3.111   0.829   0.263  0.00  0.00           H+0
HETATM   52  H   UNK     0      -4.461  -0.032   0.927  0.00  0.00           H+0
HETATM   53  H   UNK     0      -5.316  -0.452  -1.412  0.00  0.00           H+0
HETATM   54  H   UNK     0      -3.902   0.349  -2.074  0.00  0.00           H+0
HETATM   55  H   UNK     0      -7.354   1.197  -0.887  0.00  0.00           H+0
HETATM   56  H   UNK     0      -7.414   3.715  -1.774  0.00  0.00           H+0
HETATM   57  H   UNK     0      -7.208   3.719   0.003  0.00  0.00           H+0
CONECT    1    2   26   27   28                                             
CONECT    2   17    1    3   11                                             
CONECT    3    4    2   29   30                                             
CONECT    4    3    5   31   32                                             
CONECT    5    7    4    6   33                                             
CONECT    6    5   34                                                       
CONECT    7    5    9   11    8                                             
CONECT    8    7   35   36   37                                             
CONECT    9    7   10   38   39                                             
CONECT   10    9   40                                                       
CONECT   11   12    7    2   41                                             
CONECT   12   11   13   42   43                                             
CONECT   13   12   14   44   45                                             
CONECT   14   13   17   15   46                                             
CONECT   15   14   16   47   48                                             
CONECT   16   15   49                                                       
CONECT   17    2   14   18   50                                             
CONECT   18   17   19   51   52                                             
CONECT   19   18   20   53   54                                             
CONECT   20   21   19   24                                                  
CONECT   21   22   20   55                                                  
CONECT   22   21   23   56   57                                             
CONECT   23   22   24                                                       
CONECT   24   25   20   23                                                  
CONECT   25   24                                                            
CONECT   26    1                                                            
CONECT   27    1                                                            
CONECT   28    1                                                            
CONECT   29    3                                                            
CONECT   30    3                                                            
CONECT   31    4                                                            
CONECT   32    4                                                            
CONECT   33    5                                                            
CONECT   34    6                                                            
CONECT   35    8                                                            
CONECT   36    8                                                            
CONECT   37    8                                                            
CONECT   38    9                                                            
CONECT   39    9                                                            
CONECT   40   10                                                            
CONECT   41   11                                                            
CONECT   42   12                                                            
CONECT   43   12                                                            
CONECT   44   13                                                            
CONECT   45   13                                                            
CONECT   46   14                                                            
CONECT   47   15                                                            
CONECT   48   15                                                            
CONECT   49   16                                                            
CONECT   50   17                                                            
CONECT   51   18                                                            
CONECT   52   18                                                            
CONECT   53   19                                                            
CONECT   54   19                                                            
CONECT   55   21                                                            
CONECT   56   22                                                            
CONECT   57   22                                                            
MASTER        0    0    0    0    0    0    0    0   57    0  118    0
END

RDKit          3D

57 59  0  0  0  0  0  0  0  0999 V2000
   -1.3361   -0.7365    1.7876 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4619   -1.2162    0.3191 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7869   -0.1694   -0.6113 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7351   -0.1591   -0.5294 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3316   -1.5242   -0.8476 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7565   -1.4288   -0.7463 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7898   -2.6682    0.0605 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2581   -4.0075   -0.5857 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4069   -2.6115    1.4833 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8123   -2.8590    1.4767 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7872   -2.6170    0.0523 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4542   -3.7203    0.8941 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9435   -3.8211    0.5876 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6977   -2.4905    0.7529 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.1767   -2.7182    0.3860 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3154   -3.0130   -0.9967 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0043   -1.3484   -0.0613 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.7861   -0.0062    0.0627 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5778    0.3300   -1.2098 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2686    1.6422   -1.1066 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5625    1.9260   -0.9677 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7806    3.3831   -0.9456 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4763    3.9380   -1.0984 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5672    2.9297   -1.2059 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3679    3.0717   -1.3593 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6413   -1.4961    2.5106 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9568    0.1443    1.9802 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3238   -0.4293    2.0471 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0758   -0.3680   -1.6520 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1350    0.8440   -0.3851 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1261    0.5786   -1.2423 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0787    0.1924    0.4497 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1049   -1.7639   -1.8951 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0466   -0.7700   -1.4041 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0583   -4.8646    0.0651 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7511   -4.1849   -1.5410 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3345   -4.0094   -0.7908 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9623   -3.3645    2.1398 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2740   -1.6406    1.9562 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1701   -2.3259    0.7330 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0512   -2.8551   -0.9921 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0112   -4.6975    0.6787 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3098   -3.5503    1.9653 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3871   -4.5804    1.2438 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0623   -4.1926   -0.4386 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6785   -2.2232    1.8171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7884   -1.8416    0.6167 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5823   -3.5598    0.9590 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2401   -3.2773   -1.1423 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0311   -1.6492   -1.1191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1107    0.8294    0.2625 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4608   -0.0320    0.9274 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3164   -0.4519   -1.4121 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9025    0.3488   -2.0741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3545    1.1966   -0.8865 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4137    3.7145   -1.7736 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2083    3.7187    0.0034 H   0  0  0  0  0  0  0  0  0  0  0  0
 22 21  1  0
  2 17  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 17  1  0
 21 20  2  0
  2  1  1  1
  4  3  1  0
 17 18  1  0
  5  7  1  0
  7  9  1  1
  7 11  1  0
 14 15  1  0
  2  3  1  0
 18 19  1  0
 19 20  1  0
  2 11  1  0
 24 25  2  0
 20 24  1  0
  7  8  1  0
 23 22  1  0
 11 41  1  6
  4  5  1  0
  5  6  1  0
 24 23  1  0
  9 10  1  0
 15 16  1  0
 22 56  1  0
 22 57  1  0
 21 55  1  0
  4 31  1  0
  4 32  1  0
  5 33  1  6
  3 29  1  0
  3 30  1  0
 12 42  1  0
 12 43  1  0
 13 44  1  0
 13 45  1  0
 14 46  1  1
 17 50  1  6
  1 26  1  0
  1 27  1  0
  1 28  1  0
 18 51  1  0
 18 52  1  0
  9 38  1  0
  9 39  1  0
 15 47  1  0
 15 48  1  0
 19 53  1  0
 19 54  1  0
  8 35  1  0
  8 36  1  0
  8 37  1  0
  6 34  1  0
 10 40  1  0
 16 49  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₃₂O₅

Average Mass

352.4710 Da

Monoisotopic Mass

352.22497 Da

IUPAC Name

3-{2-[(1R,2S,4aS,5R,6R,8aS)-6-hydroxy-2,5-bis(hydroxymethyl)-5,8a-dimethyl-decahydronaphthalen-1-yl]ethyl}-2,5-dihydrofuran-2-one

Traditional Name

3-{2-[(1R,2S,4aS,5R,6R,8aS)-6-hydroxy-2,5-bis(hydroxymethyl)-5,8a-dimethyl-octahydronaphthalen-1-yl]ethyl}-5H-furan-2-one

CAS Registry Number

Not Available

SMILES

[H]OC([H])([H])[C@@]1([H])C([H])([H])C([H])([H])[C@]2([H])[C@](C([H])([H])[H])(C([H])([H])O[H])[C@]([H])(O[H])C([H])([H])C([H])([H])[C@@]2(C([H])([H])[H])[C@]1([H])C([H])([H])C([H])([H])C1=C([H])C([H])([H])OC1=O

InChI Identifier

InChI=1S/C20H32O5/c1-19-9-7-17(23)20(2,12-22)16(19)6-4-14(11-21)15(19)5-3-13-8-10-25-18(13)24/h8,14-17,21-23H,3-7,9-12H2,1-2H3/t14-,15-,16+,17-,19+,20+/m1/s1

InChI Key

LMOGEODVJJLYGW-UQZPWQSVSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Andrographis paniculata	JEOL database	Shen, Y. -H., et al, J. Nat. Prod. 69, 319 (2006)

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Diterpene lactones

Alternative Parents

Substituents

Diterpene lactone
Diterpenoid
Clerodane diterpenoid
2-furanone
Cyclic alcohol
Dihydrofuran
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Carboxylic acid ester
Lactone
Secondary alcohol
Monocarboxylic acid or derivatives
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxide
Alcohol
Carbonyl group
Organooxygen compound
Primary alcohol
Organic oxygen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	1.36	ALOGPS
logP	1.73	ChemAxon
logS	-3.5	ALOGPS
pKa (Strongest Acidic)	13.36	ChemAxon
pKa (Strongest Basic)	-1.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	86.99 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	95.64 m³·mol⁻¹	ChemAxon
Polarizability	39.14 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

9806438

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11631693

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Shen YH, Li RT, Xiao WL, Xu G, Lin ZW, Zhao QS, Sun HD: ent-Labdane diterpenoids from Andrographis paniculata. J Nat Prod. 2006 Mar;69(3):319-22. doi: 10.1021/np050160u. [PubMed:16562826 ]
Shen, Y. -H., et al. (2006). Shen, Y. -H., et al, J. Nat. Prod. 69, 319 (2006). J. Nat. Prod..

Showing NP-Card for 14-deoxy-17-hydroxyandrographolide (NP0031899)

MOL for NP0031899 (14-deoxy-17-hydroxyandrographolide)

3D MOL for NP0031899 (14-deoxy-17-hydroxyandrographolide)

3D SDF for NP0031899 (14-deoxy-17-hydroxyandrographolide)

3D-SDF for NP0031899 (14-deoxy-17-hydroxyandrographolide)

PDB for NP0031899 (14-deoxy-17-hydroxyandrographolide)

3D PDB for NP0031899 (14-deoxy-17-hydroxyandrographolide)

SMILES for NP0031899 (14-deoxy-17-hydroxyandrographolide)

INCHI for NP0031899 (14-deoxy-17-hydroxyandrographolide)

Structure for NP0031899 (14-deoxy-17-hydroxyandrographolide)

3D Structure for NP0031899 (14-deoxy-17-hydroxyandrographolide)