NP-MRD: Showing NP-Card for (-)-Kopsininic acid (NP0066811)

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Record Information

Version

2.0

Created at

2022-04-28 11:02:51 UTC

Updated at

2022-04-28 11:02:51 UTC

NP-MRD ID

NP0066811

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(-)-Kopsininic acid

Description

(1R,9R,16R,18S,21S)-2,12-diazahexacyclo[14.2.2.1⁹,¹².0¹,⁹.0³,⁸.0¹⁶,²¹]Henicosa-3,5,7-triene-18-carboxylic acid belongs to the class of organic compounds known as aspidofractine alkaloids. These are alkaloids with a structure that is based on the hexacyclic aspidofractine core. These compounds are related to the Aspidosperma group by formation of a C-2 to C-18 bond. (-)-Kopsininic acid is found in Kopsia hainanensis. Based on a literature review very few articles have been published on (1R,9R,16R,18S,21S)-2,12-diazahexacyclo[14.2.2.1⁹,¹².0¹,⁹.0³,⁸.0¹⁶,²¹]Henicosa-3,5,7-triene-18-carboxylic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 48 53  0  0  0  0  0  0  0  0999 V2000
    0.0796    3.9269   -0.4040 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7229    3.3460    0.3689 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7585    4.1200    0.8753 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5993    1.8979    0.7454 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8427    1.1156    0.3279 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5267    0.1017   -0.7551 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8034   -0.4894   -1.2400 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0836   -1.8711   -0.7320 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2791   -2.2572    0.4615 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8877   -2.0032    0.3599 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2601   -2.0148    1.6421 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2676   -0.5998    1.8173 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5760   -0.2241    0.4195 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9548   -0.6100    0.1154 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6059   -1.7894   -0.1949 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9702   -1.8394   -0.4264 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7346   -0.6948   -0.3533 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0920    0.4849   -0.0446 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7160    0.5555    0.1921 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8593    1.6452    0.5071 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5619    1.2406    0.1045 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4678    1.3086   -1.4304 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9240    0.9433   -1.8962 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4813   -0.8891   -0.3825 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6285    4.4630    1.8266 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4493    1.9102    1.8358 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5238    1.8668   -0.1732 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4149    0.7169    1.1610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7569   -0.5648   -2.3621 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6419    0.2310   -1.0270 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0022   -2.6521   -1.5308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1696   -1.8949   -0.4247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7024   -1.8218    1.4145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4096   -3.3676    0.5995 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9710   -2.2486    2.4688 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6018   -2.7330    1.6936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4874   -0.0448    2.3530 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1982   -0.6048    2.4525 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9993   -2.6835   -0.2511 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4089   -2.7911   -0.6626 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8103   -0.7099   -0.5314 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7168    1.3793    0.0079 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1477    2.5270    0.9355 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8437    2.2434   -1.8299 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1512    0.5014   -1.8115 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8667    0.3088   -2.8017 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5639    1.8113   -2.0774 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0064   -1.2462   -1.3428 H   0  0  0  0  0  0  0  0  0  0  0  0
  3  2  1  0
  2  1  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  6
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 13 12  1  1
 13 24  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 21 20  1  1
 21 22  1  0
 22 23  1  0
 21  4  1  0
 24  6  1  0
 19 14  1  0
 23  6  1  0
 24 10  1  0
 21 13  1  0
  3 25  1  0
  4 26  1  1
  5 27  1  0
  5 28  1  0
  7 29  1  0
  7 30  1  0
  8 31  1  0
  8 32  1  0
  9 33  1  0
  9 34  1  0
 11 35  1  0
 11 36  1  0
 12 37  1  0
 12 38  1  0
 24 48  1  6
 15 39  1  0
 16 40  1  0
 17 41  1  0
 18 42  1  0
 20 43  1  0
 22 44  1  0
 22 45  1  0
 23 46  1  0
 23 47  1  0
M  END


  Mrv1652304282213022D          

 24 29  0  0  1  0            999 V2000
    6.7143    0.0288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3060    0.6037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1040    1.4035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3102    1.6285    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7185    1.0536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9205    0.2538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8394    1.1527    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0933    2.0737    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.9080    2.3764    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.4505    1.6774    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8128    2.0860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1622    1.6652    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8765    1.0419    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6514    0.1748    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8187    0.0421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1996    0.6071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3151    1.4408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3212   -0.3372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8777    0.2921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4395    2.5557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3664    2.6425    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5986    3.4342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4003    3.6289    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0291    4.0311    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  7  5  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  4  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 12 11  1  6  0  0  0
 12 13  1  0  0  0  0
  7 13  1  0  0  0  0
 13 14  1  1  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 12 17  1  0  0  0  0
 14 18  1  0  0  0  0
 18 19  1  0  0  0  0
  7 19  1  0  0  0  0
 12 20  1  0  0  0  0
 20 21  1  0  0  0  0
  8 21  1  0  0  0  0
 21 22  1  6  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0066811

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC(=O)[C@H]1C[C@]23CCCN4CC[C@]5([C@H]24)C2=CC=CC=C2N[C@]15CC3

> <INCHI_IDENTIFIER>
InChI=1S/C20H24N2O2/c23-16(24)14-12-18-6-3-10-22-11-9-19(17(18)22)13-4-1-2-5-15(13)21-20(14,19)8-7-18/h1-2,4-5,14,17,21H,3,6-12H2,(H,23,24)/t14-,17+,18-,19-,20-/m1/s1

> <INCHI_KEY>
AZPTZMIACWMVSO-PBOLBBRVSA-N

> <FORMULA>
C20H24N2O2

> <MOLECULAR_WEIGHT>
324.424

> <EXACT_MASS>
324.183778021

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
48

> <JCHEM_AVERAGE_POLARIZABILITY>
35.536410872711826

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,9R,16R,18S,21S)-2,12-diazahexacyclo[14.2.2.1^{9,12}.0^{1,9}.0^{3,8}.0^{16,21}]henicosa-3,5,7-triene-18-carboxylic acid

> <ALOGPS_LOGP>
2.82

> <JCHEM_LOGP>
-0.5906658379503543

> <ALOGPS_LOGS>
-2.96

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
17.774592212175243

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.162463615829481

> <JCHEM_PKA_STRONGEST_BASIC>
10.374685874247644

> <JCHEM_POLAR_SURFACE_AREA>
52.57000000000001

> <JCHEM_REFRACTIVITY>
92.2674

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.52e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,9R,16R,18S,21S)-2,12-diazahexacyclo[14.2.2.1^{9,12}.0^{1,9}.0^{3,8}.0^{16,21}]henicosa-3,5,7-triene-18-carboxylic acid

> <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      12.533   0.054   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.638   1.127   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      13.261   2.620   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.779   3.040   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.675   1.967   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      11.052   0.474   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.033   2.152   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.507   3.871   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0      11.028   4.436   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0       8.308   3.131   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.117   3.894   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.903   3.108   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.236   1.945   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0       6.816   0.326   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0       5.261   0.079   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.106   1.133   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.321   2.689   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.066  -0.629   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.105   0.545   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.420   4.771   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.151   4.933   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.584   6.411   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      10.080   6.774   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       7.521   7.525   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    9                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8   13   19                                             
CONECT    8    7    9   10   21                                             
CONECT    9    8    4                                                       
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   17   20                                             
CONECT   13   12    7   14                                                  
CONECT   14   13   15   18                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   12                                                       
CONECT   18   14   19                                                       
CONECT   19   18    7                                                       
CONECT   20   12   21                                                       
CONECT   21   20    8   22                                                  
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   58    0
END

View in JSmol

Synonyms

Value	Source
(1R,9R,16R,18S,21S)-2,12-Diazahexacyclo[14.2.2.1,.0,.0,.0,]henicosa-3,5,7-triene-18-carboxylate	Generator

Chemical Formula

C₂₀H₂₄N₂O₂

Average Mass

324.4240 Da

Monoisotopic Mass

324.18378 Da

IUPAC Name

(1R,9R,16R,18S,21S)-2,12-diazahexacyclo[14.2.2.1^{9,12}.0^{1,9}.0^{3,8}.0^{16,21}]henicosa-3,5,7-triene-18-carboxylic acid

Traditional Name

(1R,9R,16R,18S,21S)-2,12-diazahexacyclo[14.2.2.1^{9,12}.0^{1,9}.0^{3,8}.0^{16,21}]henicosa-3,5,7-triene-18-carboxylic acid

CAS Registry Number

Not Available

SMILES

OC(=O)[C@H]1C[C@]23CCCN4CC[C@]5([C@H]24)C2=CC=CC=C2N[C@]15CC3

InChI Identifier

InChI=1S/C20H24N2O2/c23-16(24)14-12-18-6-3-10-22-11-9-19(17(18)22)13-4-1-2-5-15(13)21-20(14,19)8-7-18/h1-2,4-5,14,17,21H,3,6-12H2,(H,23,24)/t14-,17+,18-,19-,20-/m1/s1

InChI Key

AZPTZMIACWMVSO-PBOLBBRVSA-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
Kopsia hainanensis	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as aspidofractine alkaloids. These are alkaloids with a structure that is based on the hexacyclic aspidofractine core. These compounds are related to the Aspidosperma group by formation of a C-2 to C-18 bond.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Aspidofractine alkaloids

Sub Class

Not Available

Direct Parent

Aspidofractine alkaloids

Alternative Parents

Substituents

Aspidofractine skeleton
Aspidosperma alkaloid
Carbazole
Quinoline-6-carboxylic acid
Azaspirodecane
Quinolidine
Indole or derivatives
Dihydroindole
Indolizidine
Aralkylamine
Secondary aliphatic/aromatic amine
Benzenoid
N-alkylpyrrolidine
Piperidine
Pyrrolidine
Amino acid
Amino acid or derivatives
Tertiary aliphatic amine
Tertiary amine
Azacycle
Carboxylic acid derivative
Carboxylic acid
Organoheterocyclic compound
Secondary amine
Monocarboxylic acid or derivatives
Organic nitrogen compound
Hydrocarbon derivative
Carbonyl group
Organic oxide
Amine
Organic oxygen compound
Organonitrogen compound
Organooxygen compound
Organopnictogen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	2.82	ALOGPS
logP	-0.59	ChemAxon
logS	-3	ALOGPS
pKa (Strongest Acidic)	4.16	ChemAxon
pKa (Strongest Basic)	10.37	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	52.57 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	92.27 m³·mol⁻¹	ChemAxon
Polarizability	35.54 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	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

162924422

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (-)-Kopsininic acid (NP0066811)

MOL for NP0066811 ((-)-Kopsininic acid)

3D MOL for NP0066811 ((-)-Kopsininic acid)

3D SDF for NP0066811 ((-)-Kopsininic acid)

3D-SDF for NP0066811 ((-)-Kopsininic acid)

PDB for NP0066811 ((-)-Kopsininic acid)

3D PDB for NP0066811 ((-)-Kopsininic acid)

SMILES for NP0066811 ((-)-Kopsininic acid)

INCHI for NP0066811 ((-)-Kopsininic acid)

Structure for NP0066811 ((-)-Kopsininic acid)

3D Structure for NP0066811 ((-)-Kopsininic acid)