NP-MRD: Showing NP-Card for 16-Epikoumidine (NP0138166)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-05-31 17:00:52 UTC

Updated at

2022-05-31 17:00:52 UTC

NP-MRD ID

NP0138166

Secondary Accession Numbers

None

Natural Product Identification

Common Name

16-Epikoumidine

Description

{15-Ethylidene-3,17-diazapentacyclo[12.3.1.0²,¹⁰.0⁴,⁹.0¹²,¹⁷]Octadeca-2(10),4,6,8-tetraen-13-yl}methanol belongs to the class of organic compounds known as macroline alkaloids. These are alkaloids with a structure that is based on the tetracyclic macroline skeleton. The macroline skeleton arises by scission of the C-21 to N-4 bond of the akuammilan skeleton, and mostly occurs in bisindole alkaloids. 16-Epikoumidine is found in Alstonia angustifolia, Gelsemium sempervirens, Strychnos nux-vomica and Strychnos rubiginosa. {15-Ethylidene-3,17-diazapentacyclo[12.3.1.0²,¹⁰.0⁴,⁹.0¹²,¹⁷]Octadeca-2(10),4,6,8-tetraen-13-yl}methanol is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 44 48  0  0  0  0  0  0  0  0999 V2000
   -4.8675   -0.9790    0.9768 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9854   -1.1416   -0.2370 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8193   -0.5745   -0.3195 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9540   -0.7354   -1.5130 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6148   -0.5248   -1.0873 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3188    0.8323   -0.5841 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9067    1.0793   -1.3007 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8120    0.0642   -0.6398 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2397   -1.0229    0.0198 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2371   -1.7708    0.5437 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4168   -1.2348    0.2626 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7124   -1.5840    0.5486 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7807   -0.8267    0.1222 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5357    0.3041   -0.6064 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2397    0.6812   -0.9102 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1609   -0.0783   -0.4830 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2318   -1.2934    0.0895 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9981   -0.6309    1.1791 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    0.2906    0.6765 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5578    1.3991   -0.2777 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4677    2.6462    0.5929 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7302    3.1568    0.8587 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6540    0.0410    1.3782 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5916   -1.7002    1.7715 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9279   -1.1274    0.7399 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4150   -1.7658   -1.0148 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1889    0.0178   -2.2889 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0152   -1.7135   -1.9778 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1247    0.8529    0.4813 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2755    2.1003   -1.1564 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9039    0.8806   -2.3929 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1240   -2.6491    1.0950 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9265   -2.4879    1.1319 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7761   -1.1171    0.3559 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3608    0.9008   -0.9432 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0308    1.5713   -1.4837 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4497   -2.3700   -0.0331 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6202   -1.4695    1.6431 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4628   -0.2335    2.0276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7232    0.6932    1.4650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2906    1.6406   -1.0619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8128    3.3505    0.0558 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9768    2.4091    1.5629 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7465    4.1193    0.7330 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
  9 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 19  3  1  0
 17  5  1  0
 20  6  1  0
 16  8  1  0
 16 11  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  2 26  1  0
  4 27  1  0
  4 28  1  0
  6 29  1  1
  7 30  1  0
  7 31  1  0
 10 32  1  0
 12 33  1  0
 13 34  1  0
 14 35  1  0
 15 36  1  0
 17 37  1  6
 18 38  1  0
 18 39  1  0
 19 40  1  1
 20 41  1  6
 21 42  1  0
 21 43  1  0
 22 44  1  0
M  END


  Mrv1533004151514232D          

 22 26  0  0  0  0            999 V2000
   -1.4389   -0.5016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0850    0.2436    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2627    0.3098    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2871    0.9480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0821    0.6214    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4501   -0.3360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2834   -0.5597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0240   -0.1521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7490    0.6257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4038    1.1276    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.0834    0.6599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8857    0.8521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4533    0.2534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2186   -0.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4163   -0.7297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8487   -0.1310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8938    0.6568    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1650    0.1181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3854   -0.2352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8279   -0.9407    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7294   -1.7598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3895   -2.2547    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  0  0  0
  2  3  2  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
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
  8 16  1  0  0  0  0
 11 16  1  0  0  0  0
  9 17  1  0  0  0  0
  5 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
  3 19  1  0  0  0  0
 19 20  1  0  0  0  0
  6 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0138166

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC=C1CN2C3CC4=C(NC5=CC=CC=C45)C2CC1C3CO

> <INCHI_IDENTIFIER>
InChI=1S/C19H22N2O/c1-2-11-9-21-17-8-14-12-5-3-4-6-16(12)20-19(14)18(21)7-13(11)15(17)10-22/h2-6,13,15,17-18,20,22H,7-10H2,1H3

> <INCHI_KEY>
VXTDUGOBAOLMED-UHFFFAOYSA-N

> <FORMULA>
C19H22N2O

> <MOLECULAR_WEIGHT>
294.398

> <EXACT_MASS>
294.173213336

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
44

> <JCHEM_AVERAGE_POLARIZABILITY>
34.191277127456694

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
{15-ethylidene-3,17-diazapentacyclo[12.3.1.0²,¹⁰.0⁴,⁹.0¹²,¹⁷]octadeca-2(10),4,6,8-tetraen-13-yl}methanol

> <ALOGPS_LOGP>
3.09

> <JCHEM_LOGP>
2.208447367666666

> <ALOGPS_LOGS>
-2.98

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
16.383949956496217

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.354320520552662

> <JCHEM_PKA_STRONGEST_BASIC>
6.483224008275117

> <JCHEM_POLAR_SURFACE_AREA>
39.260000000000005

> <JCHEM_REFRACTIVITY>
89.32079999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.10e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
{15-ethylidene-3,17-diazapentacyclo[12.3.1.0²,¹⁰.0⁴,⁹.0¹²,¹⁷]octadeca-2(10),4,6,8-tetraen-13-yl}methanol

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 15-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   15-APR-15         0                                  
HETATM    1  C   UNK     0      -2.686  -0.936   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.025   0.455   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.490   0.578   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.536   1.770   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0       2.020   1.160   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0       2.707  -0.627   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.262  -1.045   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.645  -0.284   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.131   1.168   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0       6.354   2.105   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0       7.622   1.232   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.120   1.591   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.180   0.473   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.741  -1.003   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.244  -1.362   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.184  -0.244   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.535   1.226   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.175   0.220   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.719  -0.439   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.545  -1.756   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.362  -3.285   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       2.594  -4.209   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   19                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   17                                                  
CONECT    6    5    7   20                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   16                                                  
CONECT    9    8   10   17                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   16                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15    8   11                                                  
CONECT   17    9    5   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18    3   20                                                  
CONECT   20   19    6   21                                                  
CONECT   21   20   22                                                       
CONECT   22   21                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   52    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₂₂N₂O

Average Mass

294.3980 Da

Monoisotopic Mass

294.17321 Da

IUPAC Name

{15-ethylidene-3,17-diazapentacyclo[12.3.1.0²,¹⁰.0⁴,⁹.0¹²,¹⁷]octadeca-2(10),4,6,8-tetraen-13-yl}methanol

Traditional Name

{15-ethylidene-3,17-diazapentacyclo[12.3.1.0²,¹⁰.0⁴,⁹.0¹²,¹⁷]octadeca-2(10),4,6,8-tetraen-13-yl}methanol

CAS Registry Number

124096-81-7

SMILES

CC=C1CN2C3CC4=C(NC5=CC=CC=C45)C2CC1C3CO

InChI Identifier

InChI=1S/C19H22N2O/c1-2-11-9-21-17-8-14-12-5-3-4-6-16(12)20-19(14)18(21)7-13(11)15(17)10-22/h2-6,13,15,17-18,20,22H,7-10H2,1H3

InChI Key

VXTDUGOBAOLMED-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
Alstonia angustifolia	LOTUS Database	35616633
Gelsemium sempervirens	LOTUS Database	35616633
Strychnos nux-vomica	LOTUS Database	35616633
Strychnos rubiginosa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as macroline alkaloids. These are alkaloids with a structure that is based on the tetracyclic macroline skeleton. The macroline skeleton arises by scission of the C-21 to N-4 bond of the akuammilan skeleton, and mostly occurs in bisindole alkaloids.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Macroline alkaloids

Sub Class

Not Available

Direct Parent

Macroline alkaloids

Alternative Parents

Substituents

Macroline skeleton
Sarpagine-skeleton
Vobasan skeleton
Beta-carboline
Pyridoindole
3-alkylindole
Indole
Indole or derivatives
Quinuclidine
Aralkylamine
Benzenoid
Piperidine
1,3-aminoalcohol
Pyrrole
Heteroaromatic compound
Tertiary aliphatic amine
Tertiary amine
Organoheterocyclic compound
Azacycle
Primary alcohol
Organonitrogen compound
Organooxygen compound
Hydrocarbon derivative
Organic oxygen compound
Amine
Alcohol
Organic nitrogen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

a small molecule (10-DEOXYSARPAGINE )

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	3.09	ALOGPS
logP	2.21	ChemAxon
logS	-3	ALOGPS
pKa (Strongest Acidic)	15.35	ChemAxon
pKa (Strongest Basic)	6.48	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	39.26 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	89.32 m³·mol⁻¹	ChemAxon
Polarizability	34.19 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	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

626363

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 16-Epikoumidine (NP0138166)

MOL for NP0138166 (16-Epikoumidine)

3D MOL for NP0138166 (16-Epikoumidine)

3D SDF for NP0138166 (16-Epikoumidine)

3D-SDF for NP0138166 (16-Epikoumidine)

PDB for NP0138166 (16-Epikoumidine)

3D PDB for NP0138166 (16-Epikoumidine)

SMILES for NP0138166 (16-Epikoumidine)

INCHI for NP0138166 (16-Epikoumidine)

Structure for NP0138166 (16-Epikoumidine)

3D Structure for NP0138166 (16-Epikoumidine)