NP-MRD: Showing NP-Card for ent-Kauran-17,19-dioic acid (NP0139144)

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Record Information

Version

1.0

Created at

2022-06-29 19:41:11 UTC

Updated at

2022-06-29 19:41:11 UTC

NP-MRD ID

NP0139144

Secondary Accession Numbers

None

Natural Product Identification

Common Name

ent-Kauran-17,19-dioic acid

Description

NSC83438 belongs to the class of organic compounds known as kaurane diterpenoids. These are diterpene alkaloids with a structure that is based on the kaurane skeleton. Kaurane is a tetracyclic compound that arises by cyclisation of a pimarane precursor followed by rearrangement. It possesses a [3,2,1]-bicyclic ring system with C15-C16 bridge connected to C13, forming the five-membered ring D. ent-Kauran-17,19-dioic acid is found in Annona glabra, Annona senegalensis, Annona squamosa, Mikania hirsutissima and Tripterygium wilfordii. NSC83438 is a weakly acidic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 54 57  0  0  0  0  0  0  0  0999 V2000
   -3.7398    0.7893   -1.5764 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9353    0.5867   -0.2813 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2064    1.8233    0.5427 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8764    2.7859    0.1007 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7131    1.9410    1.8460 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5037   -0.5527    0.4824 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5996   -1.6526    0.8803 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1288   -1.2471    0.9690 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7895   -0.7207   -0.4102 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3992   -1.7215   -1.4026 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4911    0.5819   -0.5773 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7314    1.6869    0.1727 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5970    1.8307   -0.5685 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3709    0.5711   -0.3042 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6571    0.6138   -1.1447 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4642   -0.4736   -0.4216 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8142   -1.8180   -0.5926 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4052   -1.8456   -0.0455 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6583   -0.6705   -0.6853 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3304    0.0284    1.0214 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3526    1.1240    1.1477 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0292    2.3057    1.4405 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7016    0.8753    0.9454 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9383    0.5608    1.0865 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0400    1.8363   -1.7126 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0943    0.5444   -2.4702 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6687    0.1820   -1.5659 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4046    2.1537    2.5715 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0710   -0.2277    1.4069 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3254   -1.0277   -0.1343 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8496   -2.0401    1.9023 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7011   -2.5675    0.2233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5765   -2.1810    1.2006 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0630   -0.4842    1.7468 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9131   -1.4918   -2.3959 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4651   -1.5781   -1.5446 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1901   -2.7553   -1.1332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3481    0.8727   -1.6621 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2951    2.6388    0.1317 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5248    1.4262    1.2077 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4134    1.9109   -1.6611 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1666    2.6809   -0.1568 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4933    0.2543   -2.1620 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1771    1.5676   -1.0510 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4979   -0.5179   -0.7560 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8042   -2.0638   -1.6559 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4197   -2.5535   -0.0417 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9521   -2.8112   -0.3409 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4226   -1.7896    1.0416 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8105   -0.8184   -1.7955 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5399   -0.7850    1.7436 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3197    0.4940    1.6377 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2924    0.0852    1.8351 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0162    1.6431    1.4010 H   0  0  0  0  0  0  0  0  0  0  0  0
  9 10  1  6
  9  8  1  0
  8  7  1  0
  7  6  1  0
  6  2  1  0
  2  1  1  0
  2 11  1  0
 11 12  1  0
 12 13  1  0
 14 13  1  1
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 16 20  1  0
 20 24  1  0
 20 21  1  0
 21 23  1  0
 21 22  2  0
  2  3  1  1
  3  5  1  0
  3  4  2  0
 11  9  1  0
 19 14  1  0
 19  9  1  0
 24 14  1  0
 10 35  1  0
 10 36  1  0
 10 37  1  0
  8 33  1  0
  8 34  1  0
  7 31  1  0
  7 32  1  0
  6 29  1  0
  6 30  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
 11 38  1  6
 12 39  1  0
 12 40  1  0
 13 41  1  0
 13 42  1  0
 15 43  1  0
 15 44  1  0
 16 45  1  6
 17 46  1  0
 17 47  1  0
 18 48  1  0
 18 49  1  0
 19 50  1  6
 20 51  1  1
 24 53  1  0
 24 54  1  0
 23 52  1  0
  5 28  1  0
M  END


  Mrv1533004171500112D          

 24 27  0  0  0  0            999 V2000
    1.8257    0.7777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0661   -0.0115    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6242    0.5960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4294    0.4164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6765   -0.3707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1184   -0.9782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8136   -1.4224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3132   -0.7987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7596   -1.4229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9506   -1.2543    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6469   -0.4671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1726    0.0666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4028    0.5335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1586    1.1914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0038    1.0309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2474    0.1857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7854   -0.2403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1637   -0.8483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5987   -0.3788    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1253    0.2563    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8854   -1.1523    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8017   -1.7400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3031   -2.3952    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9836   -1.8467    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
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  2  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  2 16  1  0  0  0  0
 11 16  1  0  0  0  0
 13 17  1  0  0  0  0
 17 18  1  0  0  0  0
 11 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
  6 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0139144

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC12CCCC(C)(C1CCC13CC(CCC21)C(C3)C(O)=O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H30O4/c1-18-7-3-8-19(2,17(23)24)14(18)6-9-20-10-12(4-5-15(18)20)13(11-20)16(21)22/h12-15H,3-11H2,1-2H3,(H,21,22)(H,23,24)

> <INCHI_KEY>
HITLMPHPGUZLGI-UHFFFAOYSA-N

> <FORMULA>
C20H30O4

> <MOLECULAR_WEIGHT>
334.456

> <EXACT_MASS>
334.214409446

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
37.25977515082826

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-5,14-dicarboxylic acid

> <ALOGPS_LOGP>
3.66

> <JCHEM_LOGP>
4.091201992333334

> <ALOGPS_LOGS>
-4.08

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
4.931310214942394

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.205005558397894

> <JCHEM_POLAR_SURFACE_AREA>
74.6

> <JCHEM_REFRACTIVITY>
89.27739999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.76e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-5,14-dicarboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0       3.408   1.452   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.857  -0.022   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.899   1.113   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.402   0.777   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.863  -0.692   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.821  -1.826   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.119  -2.655   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.318  -1.491   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.285  -2.656   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.774  -2.341   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.208  -0.872   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.322   0.124   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.752   0.996   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.296   2.224   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.874   1.924   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.328   0.347   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.466  -0.449   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.306  -1.583   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -2.984  -0.707   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -3.967   0.478   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      -3.519  -2.151   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       5.230  -3.248   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       6.166  -4.471   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       3.703  -3.447   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    8   16                                             
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8   22                                             
CONECT    7    6                                                            
CONECT    8    6    2    9                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   16   18                                             
CONECT   12   11   13                                                       
CONECT   13   12   14   17                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15    2   11                                                  
CONECT   17   13   18   19                                                  
CONECT   18   17   11                                                       
CONECT   19   17   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22    6   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   54    0
END

View in JSmol

Synonyms

Value	Source
5,9-Dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-5,14-dicarboxylate	Generator
5,9-Dimethyltetracyclo[11.2.1.0,.0,]hexadecane-5,14-dicarboxylate	Generator

Chemical Formula

C₂₀H₃₀O₄

Average Mass

334.4560 Da

Monoisotopic Mass

334.21441 Da

IUPAC Name

5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-5,14-dicarboxylic acid

Traditional Name

5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-5,14-dicarboxylic acid

CAS Registry Number

Not Available

SMILES

CC12CCCC(C)(C1CCC13CC(CCC21)C(C3)C(O)=O)C(O)=O

InChI Identifier

InChI=1S/C20H30O4/c1-18-7-3-8-19(2,17(23)24)14(18)6-9-20-10-12(4-5-15(18)20)13(11-20)16(21)22/h12-15H,3-11H2,1-2H3,(H,21,22)(H,23,24)

InChI Key

HITLMPHPGUZLGI-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Annona glabra	LOTUS Database	35616633
Annona senegalensis	LOTUS Database	35616633
Annona squamosa	LOTUS Database	35616633
Mikania hirsutissima	LOTUS Database	35616633
Tripterygium wilfordii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as kaurane diterpenoids. These are diterpene alkaloids with a structure that is based on the kaurane skeleton. Kaurane is a tetracyclic compound that arises by cyclisation of a pimarane precursor followed by rearrangement. It possesses a [3,2,1]-bicyclic ring system with C15-C16 bridge connected to C13, forming the five-membered ring D.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Kaurane diterpenoids

Alternative Parents

Substituents

Kaurane diterpenoid
Dicarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	3.66	ALOGPS
logP	4.09	ChemAxon
logS	-4.1	ALOGPS
pKa (Strongest Acidic)	4.21	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	74.6 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	89.28 m³·mol⁻¹	ChemAxon
Polarizability	37.26 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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

494049

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for ent-Kauran-17,19-dioic acid (NP0139144)

MOL for NP0139144 (ent-Kauran-17,19-dioic acid)

3D MOL for NP0139144 (ent-Kauran-17,19-dioic acid)

3D SDF for NP0139144 (ent-Kauran-17,19-dioic acid)

3D-SDF for NP0139144 (ent-Kauran-17,19-dioic acid)

PDB for NP0139144 (ent-Kauran-17,19-dioic acid)

3D PDB for NP0139144 (ent-Kauran-17,19-dioic acid)

SMILES for NP0139144 (ent-Kauran-17,19-dioic acid)

INCHI for NP0139144 (ent-Kauran-17,19-dioic acid)

Structure for NP0139144 (ent-Kauran-17,19-dioic acid)

3D Structure for NP0139144 (ent-Kauran-17,19-dioic acid)