NP-MRD: Showing NP-Card for 7R-hydroxy-14-deoxyandrographolide (NP0033766)

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Record Information

Version

2.0

Created at

2021-06-20 17:41:31 UTC

Updated at

2021-06-30 00:03:45 UTC

NP-MRD ID

NP0033766

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7R-hydroxy-14-deoxyandrographolide

Provided By

JEOL Database JEOL Logo

Description

CHEMBL466745 belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety. 7R-hydroxy-14-deoxyandrographolide is found in Andrographis paniculata. 7R-hydroxy-14-deoxyandrographolide was first documented in 2008 (Chen, L., et al.). Based on a literature review very few articles have been published on CHEMBL466745.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306202119413D          

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     RDKit          3D

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    0.5234   -0.2991    0.3737 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9308    0.8561   -0.8897 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4128    1.0803    1.0392 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5512    2.5608    0.7588 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9221    0.4165    2.8312 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8169    1.7584    4.2076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9831    2.1027    4.3562 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3103    1.9815    4.8742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1229    0.5608    4.2208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6212    3.9414    2.6616 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1866    3.9469    1.6421 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0544    3.8140    3.5592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4635    0.2460    1.9414 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1183    2.7510    1.4019 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3373    1.6552    2.7358 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8418   -0.2248    1.2759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7475    0.6082    0.4680 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 16  1  0  0  0  0
  6 10  1  0  0  0  0
 10  9  1  0  0  0  0
 12  3  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24  2  1  0  0  0  0
  2  3  1  0  0  0  0
  9  8  1  0  0  0  0
 16 17  1  0  0  0  0
  8  7  1  0  0  0  0
 12 13  1  6  0  0  0
 15 14  1  0  0  0  0
 18 20  1  1  0  0  0
 16 18  1  0  0  0  0
 24 25  1  0  0  0  0
 18 22  1  0  0  0  0
 18 19  1  0  0  0  0
 12 14  1  0  0  0  0
 22 51  1  1  0  0  0
 12 22  1  0  0  0  0
 20 21  1  0  0  0  0
  7  6  2  0  0  0  0
  2  1  2  3  0  0  0
  3  4  1  0  0  0  0
 10 11  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  8 34  1  0  0  0  0
  8 35  1  0  0  0  0
  7 33  1  0  0  0  0
 15 41  1  0  0  0  0
 15 42  1  0  0  0  0
 16 43  1  1  0  0  0
 14 39  1  0  0  0  0
 14 40  1  0  0  0  0
 23 52  1  0  0  0  0
 23 53  1  0  0  0  0
 24 54  1  1  0  0  0
  3 28  1  1  0  0  0
 17 44  1  0  0  0  0
 13 36  1  0  0  0  0
 13 37  1  0  0  0  0
 13 38  1  0  0  0  0
 20 48  1  0  0  0  0
 20 49  1  0  0  0  0
 25 55  1  0  0  0  0
 19 45  1  0  0  0  0
 19 46  1  0  0  0  0
 19 47  1  0  0  0  0
 21 50  1  0  0  0  0
  1 26  1  0  0  0  0
  1 27  1  0  0  0  0
  4 29  1  0  0  0  0
  4 30  1  0  0  0  0
  5 31  1  0  0  0  0
  5 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0033766

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC([H])([H])[C@]1(C([H])([H])[H])[C@]([H])(O[H])C([H])([H])C([H])([H])[C@@]2(C([H])([H])[H])[C@@]([H])(C(=C([H])[H])[C@]([H])(O[H])C([H])([H])[C@]12[H])C([H])([H])C([H])([H])C1=C([H])C([H])([H])OC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H30O5/c1-12-14(5-4-13-7-9-25-18(13)24)19(2)8-6-17(23)20(3,11-21)16(19)10-15(12)22/h7,14-17,21-23H,1,4-6,8-11H2,2-3H3/t14-,15-,16+,17-,19+,20+/m1/s1

> <INCHI_KEY>
KNCLIXUHDVRNQB-UQZPWQSVSA-N

> <FORMULA>
C20H30O5

> <MOLECULAR_WEIGHT>
350.455

> <EXACT_MASS>
350.209324066

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
37.617401009547535

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

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

> <ALOGPS_LOGP>
1.29

> <JCHEM_LOGP>
1.5064142126666662

> <ALOGPS_LOGS>
-2.85

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.513864107632102

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.36027954781673

> <JCHEM_PKA_STRONGEST_BASIC>
-1.2731319217924963

> <JCHEM_POLAR_SURFACE_AREA>
86.99000000000001

> <JCHEM_REFRACTIVITY>
95.0845

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.91e-01 g/l

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

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 55 57  0  0  0  0  0  0  0  0999 V2000
   -4.0895    1.1780   -1.6209 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3614    0.7438   -0.5750 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9132    0.2378   -0.6625 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4140   -0.1518   -2.0829 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1443   -1.3418   -2.7367 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1452   -2.5947   -1.9356 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1677   -3.2795   -1.4252 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6954   -4.4799   -0.7139 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2775   -4.4357   -0.8532 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9292   -3.3377   -1.5794 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2074   -3.0174   -1.8737 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9723    1.2634    0.1180 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0231    2.6372   -0.5980 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4973    0.7673    0.1133 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4084    1.5221    1.0765 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8951    1.4667    2.5096 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8266    2.1794    3.3279 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5518    2.0224    2.6719 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0193    1.6461    4.1097 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5959    3.5699    2.5765 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1515    4.1932    3.6195 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4818    1.3019    1.6213 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9722    1.7075    1.7045 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8583    0.7890    0.8569 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.1990    1.2520    0.9460 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7064    1.2035   -2.6346 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0893    1.5838   -1.4940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8822   -0.6967   -0.0837 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4751    0.7046   -2.7639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3532   -0.4169   -2.0401 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6652   -1.5482   -3.7025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1756   -1.0638   -2.9781 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2081   -3.0043   -1.5176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9556   -4.4548    0.3481 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0754   -5.4004   -1.1659 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8532    2.5276   -1.6741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2464    3.3224   -0.2599 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9825    3.1458   -0.4738 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5234   -0.2991    0.3737 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9308    0.8561   -0.8897 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4128    1.0803    1.0392 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5512    2.5608    0.7588 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9221    0.4165    2.8312 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8169    1.7584    4.2076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9831    2.1027    4.3562 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3103    1.9815    4.8742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1229    0.5608    4.2208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6212    3.9414    2.6616 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1866    3.9469    1.6421 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0544    3.8140    3.5592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4635    0.2460    1.9414 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1183    2.7510    1.4019 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3373    1.6552    2.7358 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8418   -0.2248    1.2759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7475    0.6082    0.4680 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 16  1  0
  6 10  1  0
 10  9  1  0
 12  3  1  0
 22 23  1  0
 23 24  1  0
 24  2  1  0
  2  3  1  0
  9  8  1  0
 16 17  1  0
  8  7  1  0
 12 13  1  6
 15 14  1  0
 18 20  1  1
 16 18  1  0
 24 25  1  0
 18 22  1  0
 18 19  1  0
 12 14  1  0
 22 51  1  1
 12 22  1  0
 20 21  1  0
  7  6  2  0
  2  1  2  3
  3  4  1  0
 10 11  2  0
  4  5  1  0
  5  6  1  0
  8 34  1  0
  8 35  1  0
  7 33  1  0
 15 41  1  0
 15 42  1  0
 16 43  1  1
 14 39  1  0
 14 40  1  0
 23 52  1  0
 23 53  1  0
 24 54  1  1
  3 28  1  1
 17 44  1  0
 13 36  1  0
 13 37  1  0
 13 38  1  0
 20 48  1  0
 20 49  1  0
 25 55  1  0
 19 45  1  0
 19 46  1  0
 19 47  1  0
 21 50  1  0
  1 26  1  0
  1 27  1  0
  4 29  1  0
  4 30  1  0
  5 31  1  0
  5 32  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      -4.090   1.178  -1.621  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.361   0.744  -0.575  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.913   0.238  -0.663  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.414  -0.152  -2.083  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.144  -1.342  -2.737  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.145  -2.595  -1.936  0.00  0.00           C+0
HETATM    7  C   UNK     0      -3.168  -3.280  -1.425  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.695  -4.480  -0.714  0.00  0.00           C+0
HETATM    9  O   UNK     0      -1.278  -4.436  -0.853  0.00  0.00           O+0
HETATM   10  C   UNK     0      -0.929  -3.338  -1.579  0.00  0.00           C+0
HETATM   11  O   UNK     0       0.207  -3.017  -1.874  0.00  0.00           O+0
HETATM   12  C   UNK     0      -0.972   1.263   0.118  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.023   2.637  -0.598  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.497   0.767   0.113  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.408   1.522   1.077  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.895   1.467   2.510  0.00  0.00           C+0
HETATM   17  O   UNK     0       1.827   2.179   3.328  0.00  0.00           O+0
HETATM   18  C   UNK     0      -0.552   2.022   2.672  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.019   1.646   4.110  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.596   3.570   2.576  0.00  0.00           C+0
HETATM   21  O   UNK     0       0.152   4.193   3.619  0.00  0.00           O+0
HETATM   22  C   UNK     0      -1.482   1.302   1.621  0.00  0.00           C+0
HETATM   23  C   UNK     0      -2.972   1.708   1.704  0.00  0.00           C+0
HETATM   24  C   UNK     0      -3.858   0.789   0.857  0.00  0.00           C+0
HETATM   25  O   UNK     0      -5.199   1.252   0.946  0.00  0.00           O+0
HETATM   26  H   UNK     0      -3.706   1.204  -2.635  0.00  0.00           H+0
HETATM   27  H   UNK     0      -5.089   1.584  -1.494  0.00  0.00           H+0
HETATM   28  H   UNK     0      -1.882  -0.697  -0.084  0.00  0.00           H+0
HETATM   29  H   UNK     0      -1.475   0.705  -2.764  0.00  0.00           H+0
HETATM   30  H   UNK     0      -0.353  -0.417  -2.040  0.00  0.00           H+0
HETATM   31  H   UNK     0      -1.665  -1.548  -3.703  0.00  0.00           H+0
HETATM   32  H   UNK     0      -3.176  -1.064  -2.978  0.00  0.00           H+0
HETATM   33  H   UNK     0      -4.208  -3.004  -1.518  0.00  0.00           H+0
HETATM   34  H   UNK     0      -2.956  -4.455   0.348  0.00  0.00           H+0
HETATM   35  H   UNK     0      -3.075  -5.400  -1.166  0.00  0.00           H+0
HETATM   36  H   UNK     0      -0.853   2.528  -1.674  0.00  0.00           H+0
HETATM   37  H   UNK     0      -0.246   3.322  -0.260  0.00  0.00           H+0
HETATM   38  H   UNK     0      -1.982   3.146  -0.474  0.00  0.00           H+0
HETATM   39  H   UNK     0       0.523  -0.299   0.374  0.00  0.00           H+0
HETATM   40  H   UNK     0       0.931   0.856  -0.890  0.00  0.00           H+0
HETATM   41  H   UNK     0       2.413   1.080   1.039  0.00  0.00           H+0
HETATM   42  H   UNK     0       1.551   2.561   0.759  0.00  0.00           H+0
HETATM   43  H   UNK     0       0.922   0.417   2.831  0.00  0.00           H+0
HETATM   44  H   UNK     0       1.817   1.758   4.208  0.00  0.00           H+0
HETATM   45  H   UNK     0      -1.983   2.103   4.356  0.00  0.00           H+0
HETATM   46  H   UNK     0      -0.310   1.982   4.874  0.00  0.00           H+0
HETATM   47  H   UNK     0      -1.123   0.561   4.221  0.00  0.00           H+0
HETATM   48  H   UNK     0      -1.621   3.941   2.662  0.00  0.00           H+0
HETATM   49  H   UNK     0      -0.187   3.947   1.642  0.00  0.00           H+0
HETATM   50  H   UNK     0       1.054   3.814   3.559  0.00  0.00           H+0
HETATM   51  H   UNK     0      -1.464   0.246   1.941  0.00  0.00           H+0
HETATM   52  H   UNK     0      -3.118   2.751   1.402  0.00  0.00           H+0
HETATM   53  H   UNK     0      -3.337   1.655   2.736  0.00  0.00           H+0
HETATM   54  H   UNK     0      -3.842  -0.225   1.276  0.00  0.00           H+0
HETATM   55  H   UNK     0      -5.747   0.608   0.468  0.00  0.00           H+0
CONECT    1    2   26   27                                                  
CONECT    2   24    3    1                                                  
CONECT    3   12    2    4   28                                             
CONECT    4    3    5   29   30                                             
CONECT    5    4    6   31   32                                             
CONECT    6   10    7    5                                                  
CONECT    7    8    6   33                                                  
CONECT    8    9    7   34   35                                             
CONECT    9   10    8                                                       
CONECT   10    6    9   11                                                  
CONECT   11   10                                                            
CONECT   12    3   13   14   22                                             
CONECT   13   12   36   37   38                                             
CONECT   14   15   12   39   40                                             
CONECT   15   16   14   41   42                                             
CONECT   16   15   17   18   43                                             
CONECT   17   16   44                                                       
CONECT   18   20   16   22   19                                             
CONECT   19   18   45   46   47                                             
CONECT   20   18   21   48   49                                             
CONECT   21   20   50                                                       
CONECT   22   23   18   51   12                                             
CONECT   23   22   24   52   53                                             
CONECT   24   23    2   25   54                                             
CONECT   25   24   55                                                       
CONECT   26    1                                                            
CONECT   27    1                                                            
CONECT   28    3                                                            
CONECT   29    4                                                            
CONECT   30    4                                                            
CONECT   31    5                                                            
CONECT   32    5                                                            
CONECT   33    7                                                            
CONECT   34    8                                                            
CONECT   35    8                                                            
CONECT   36   13                                                            
CONECT   37   13                                                            
CONECT   38   13                                                            
CONECT   39   14                                                            
CONECT   40   14                                                            
CONECT   41   15                                                            
CONECT   42   15                                                            
CONECT   43   16                                                            
CONECT   44   17                                                            
CONECT   45   19                                                            
CONECT   46   19                                                            
CONECT   47   19                                                            
CONECT   48   20                                                            
CONECT   49   20                                                            
CONECT   50   21                                                            
CONECT   51   22                                                            
CONECT   52   23                                                            
CONECT   53   23                                                            
CONECT   54   24                                                            
CONECT   55   25                                                            
MASTER        0    0    0    0    0    0    0    0   55    0  114    0
END

RDKit          3D

55 57  0  0  0  0  0  0  0  0999 V2000
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  7  6  2  0
  2  1  2  3
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  3 28  1  1
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 19 45  1  0
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  1 26  1  0
  1 27  1  0
  4 29  1  0
  4 30  1  0
  5 31  1  0
  5 32  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₃₀O₅

Average Mass

350.4550 Da

Monoisotopic Mass

350.20932 Da

IUPAC Name

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

Traditional Name

3-{2-[(1S,3R,4aS,5R,6R,8aS)-3,6-dihydroxy-5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-hexahydro-1H-naphthalen-1-yl]ethyl}-5H-furan-2-one

CAS Registry Number

Not Available

SMILES

[H]OC([H])([H])[C@]1(C([H])([H])[H])[C@]([H])(O[H])C([H])([H])C([H])([H])[C@@]2(C([H])([H])[H])[C@@]([H])(C(=C([H])[H])[C@]([H])(O[H])C([H])([H])[C@]12[H])C([H])([H])C([H])([H])C1=C([H])C([H])([H])OC1=O

InChI Identifier

InChI=1S/C20H30O5/c1-12-14(5-4-13-7-9-25-18(13)24)19(2)8-6-17(23)20(3,11-21)16(19)10-15(12)22/h7,14-17,21-23H,1,4-6,8-11H2,2-3H3/t14-,15-,16+,17-,19+,20+/m1/s1

InChI Key

KNCLIXUHDVRNQB-UQZPWQSVSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
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, 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, 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, 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	Chen, L., et al, J. Nat. Prod. 71, 852 (2008)

Chemical Taxonomy

Classification

Not classified

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	1.29	ALOGPS
logP	1.51	ChemAxon
logS	-2.8	ALOGPS
pKa (Strongest Acidic)	13.36	ChemAxon
pKa (Strongest Basic)	-1.3	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	4	ChemAxon
Refractivity	95.08 m³·mol⁻¹	ChemAxon
Polarizability	37.62 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

24692916

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

24879275

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Chen, L., et al. (2008). Chen, L., et al, J. Nat. Prod. 71, 852 (2008) . J. Nat. Prod..

Showing NP-Card for 7R-hydroxy-14-deoxyandrographolide (NP0033766)

MOL for NP0033766 (7R-hydroxy-14-deoxyandrographolide)

3D MOL for NP0033766 (7R-hydroxy-14-deoxyandrographolide)

3D SDF for NP0033766 (7R-hydroxy-14-deoxyandrographolide)

3D-SDF for NP0033766 (7R-hydroxy-14-deoxyandrographolide)

PDB for NP0033766 (7R-hydroxy-14-deoxyandrographolide)

3D PDB for NP0033766 (7R-hydroxy-14-deoxyandrographolide)

SMILES for NP0033766 (7R-hydroxy-14-deoxyandrographolide)

INCHI for NP0033766 (7R-hydroxy-14-deoxyandrographolide)

Structure for NP0033766 (7R-hydroxy-14-deoxyandrographolide)

3D Structure for NP0033766 (7R-hydroxy-14-deoxyandrographolide)