NP-MRD: Showing NP-Card for 14-Deoxy-11-oxoandrographolide (NP0065147)

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Record Information

Version

2.0

Created at

2022-04-28 09:24:40 UTC

Updated at

2022-04-28 09:24:40 UTC

NP-MRD ID

NP0065147

Secondary Accession Numbers

None

Natural Product Identification

Common Name

14-Deoxy-11-oxoandrographolide

Description

14-Deoxy-11-oxoandrographolide belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety. 14-Deoxy-11-oxoandrographolide is found in Andrographis paniculata . 14-Deoxy-11-oxoandrographolide was first documented in 2003 (PMID: 22900306). Based on a literature review a small amount of articles have been published on 14-Deoxy-11-oxoandrographolide (PMID: 34997448) (PMID: 25491534).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 53 55  0  0  0  0  0  0  0  0999 V2000
    1.0904   -2.8234   -0.4724 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5134   -1.6527   -0.7635 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3284   -1.4798   -1.9870 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6770   -0.8641   -1.6353 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6404   -0.5305   -0.1563 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9284   -0.0972    0.4301 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1383   -0.7794    1.7926 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0844   -0.6023   -0.4466 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3154   -0.2591    0.0901 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1284    1.3608    0.6397 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7745    2.0155   -0.4082 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8781    2.0871    1.0816 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7289    1.1432    1.3694 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4584    0.3726    0.1034 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2247    1.3698   -0.9838 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7434   -0.5369    0.2007 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0387    0.1292    0.0883 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0730    1.3264   -0.0194 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2472   -0.6943    0.1136 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5356   -0.0209   -0.0086 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7863    1.2545   -0.1424 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2824    1.4707   -0.2298 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8066    0.1869   -0.1306 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8325   -0.7562    0.0038 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9164   -2.0109    0.1206 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6977   -2.9859    0.3920 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8954   -3.6343   -1.2001 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1892   -0.9551   -2.8114 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4744   -2.5217   -2.4089 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4505   -1.6703   -1.8073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9705   -0.0449   -2.2855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3950   -1.5248    0.3296 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2487   -0.0291    2.6089 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0239   -1.4437    1.7987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2657   -1.4497    1.9853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0362   -0.2285   -1.4703 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0574   -1.7336   -0.4103 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2749    0.0274    1.0242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8539    1.4808    1.5040 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5393    1.7253   -1.2974 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6561    2.8413    0.3220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0292    2.6661    2.0393 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1660    1.8002    1.5328 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9477    0.5381    2.2406 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1704    1.6493   -1.5190 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5681    1.1030   -1.7085 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1092    2.3664   -0.5634 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6821   -0.9476    1.2667 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2880   -1.3460    1.0257 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1203   -1.4459   -0.7290 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1039    2.0945   -0.1929 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5434    2.0884    0.6542 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4697    1.9714   -1.1818 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  7  1  1
  6  8  1  0
  8  9  1  0
  6 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  6
 14  5  1  0
  5  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  2  3
  2 16  1  0
 16 17  1  0
 17 18  2  0
 17 19  1  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  2  0
  5  6  1  0
 24 20  1  0
 16 14  1  0
  7 33  1  0
  7 34  1  0
  7 35  1  0
  8 36  1  0
  8 37  1  0
  9 38  1  0
 10 39  1  1
 11 40  1  0
 12 41  1  0
 12 42  1  0
 13 43  1  0
 13 44  1  0
 15 45  1  0
 15 46  1  0
 15 47  1  0
  5 32  1  1
  4 30  1  0
  4 31  1  0
  3 28  1  0
  3 29  1  0
  1 26  1  0
  1 27  1  0
 16 48  1  1
 19 49  1  0
 19 50  1  0
 21 51  1  0
 22 52  1  0
 22 53  1  0
M  END


  Mrv1652304282211242D          

 25 27  0  0  1  0            999 V2000
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4760    2.5474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7309    3.3320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5559    3.3320    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8109    2.5474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5955    2.2925    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3873   -2.3784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3873   -2.3784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2118   -2.4072    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
  4 11  1  6  0  0  0
  7 12  1  6  0  0  0
 12 13  2  0  0  0  0
 12 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
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 15 19  1  0  0  0  0
 19 20  2  0  0  0  0
  5 21  1  6  0  0  0
  3 22  1  1  0  0  0
  3 23  1  6  0  0  0
 23 24  1  0  0  0  0
  2 25  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0065147

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@]1(CO)[C@H](O)CC[C@]2(C)[C@@H]1CCC(=C)[C@H]2C(=O)CC1=CCOC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H28O5/c1-12-4-5-15-19(2,8-6-16(23)20(15,3)11-21)17(12)14(22)10-13-7-9-25-18(13)24/h7,15-17,21,23H,1,4-6,8-11H2,2-3H3/t15-,16+,17-,19+,20-/m0/s1

> <INCHI_KEY>
WZHWNAKOQGIEEB-NDLGOLERSA-N

> <FORMULA>
C20H28O5

> <MOLECULAR_WEIGHT>
348.439

> <EXACT_MASS>
348.193674002

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
37.80480529591282

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

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

> <ALOGPS_LOGP>
1.65

> <JCHEM_LOGP>
1.8139747363333338

> <ALOGPS_LOGS>
-3.11

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.467552723157876

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.907476971283046

> <JCHEM_PKA_STRONGEST_BASIC>
-2.785463160023589

> <JCHEM_POLAR_SURFACE_AREA>
83.83000000000001

> <JCHEM_REFRACTIVITY>
94.23629999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.72e-01 g/l

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

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.335  -0.000   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       1.334   2.310   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.755   4.755   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.231   6.220   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       4.771   6.220   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       5.247   4.755   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       6.712   4.279   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       1.334   0.770   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.723  -4.440   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.723  -4.440   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       2.262  -4.493   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0      -2.667  -3.080   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3   25                                                  
CONECT    3    2    4   22   23                                             
CONECT    4    3    5   11                                                  
CONECT    5    4    6    7   21                                             
CONECT    6    5    1                                                       
CONECT    7    5    8   12                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10    4                                                       
CONECT   12    7   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16   19                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   15   20                                                  
CONECT   20   19                                                            
CONECT   21    5                                                            
CONECT   22    3                                                            
CONECT   23    3   24                                                       
CONECT   24   23                                                            
CONECT   25    2                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   54    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₈O₅

Average Mass

348.4390 Da

Monoisotopic Mass

348.19367 Da

IUPAC Name

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

Traditional Name

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

CAS Registry Number

Not Available

SMILES

C[C@@]1(CO)[C@H](O)CC[C@]2(C)[C@@H]1CCC(=C)[C@H]2C(=O)CC1=CCOC1=O

InChI Identifier

InChI=1S/C20H28O5/c1-12-4-5-15-19(2,8-6-16(23)20(15,3)11-21)17(12)14(22)10-13-7-9-25-18(13)24/h7,15-17,21,23H,1,4-6,8-11H2,2-3H3/t15-,16+,17-,19+,20-/m0/s1

InChI Key

WZHWNAKOQGIEEB-NDLGOLERSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Andrographis paniculata	Plant	KNApSAcK

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
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Secondary alcohol
Lactone
Ketone
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Primary alcohol
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Alcohol
Organic oxygen compound
Carbonyl group
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	1.65	ALOGPS
logP	1.81	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Acidic)	11.91	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	83.83 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	94.24 m³·mol⁻¹	ChemAxon
Polarizability	37.8 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

C00022255

Chemspider ID

8150644

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

9975052

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Shivashankar S, Sangeetha MK: The Natural Ligand for Metalloproteinase-A Multifaceted Drug Target. Appl Biochem Biotechnol. 2022 Apr;194(4):1716-1739. doi: 10.1007/s12010-021-03778-4. Epub 2022 Jan 8. [PubMed:34997448 ]
Koushik Kumar G, Prasanna G, Marimuthu T, Saraswathi NT: Structural basis for complementary and alternative medicine: Phytochemical interaction with non-structural protein 2 protease-a reverse engineering strategy. Chin J Integr Med. 2015 Jun;21(6):445-52. doi: 10.1007/s11655-014-1764-z. Epub 2014 Dec 9. [PubMed:25491534 ]
Lala S, Nandy AK, Mahato SB, Basu MK: Delivery in vivo of 14-deoxy-11-oxoandrographolide, an antileishmanial agent, by different drug carriers. Indian J Biochem Biophys. 2003 Jun;40(3):169-74. [PubMed:22900306 ]

Showing NP-Card for 14-Deoxy-11-oxoandrographolide (NP0065147)

MOL for NP0065147 (14-Deoxy-11-oxoandrographolide)

3D MOL for NP0065147 (14-Deoxy-11-oxoandrographolide)

3D SDF for NP0065147 (14-Deoxy-11-oxoandrographolide)

3D-SDF for NP0065147 (14-Deoxy-11-oxoandrographolide)

PDB for NP0065147 (14-Deoxy-11-oxoandrographolide)

3D PDB for NP0065147 (14-Deoxy-11-oxoandrographolide)

SMILES for NP0065147 (14-Deoxy-11-oxoandrographolide)

INCHI for NP0065147 (14-Deoxy-11-oxoandrographolide)

Structure for NP0065147 (14-Deoxy-11-oxoandrographolide)

3D Structure for NP0065147 (14-Deoxy-11-oxoandrographolide)