NP-MRD: Showing NP-Card for (1's,2s,9r,9as,12's)-15'-hydroxy-2-methyl-2,9a-dihydro-1h-2',10',16'-triazaspiro[imidazo[1,2-a]indole-9,13'-tetracyclo[10.2.2.0²,¹¹.0⁴,⁹]hexadecane]-4',6',8',10',15'-pentaene-3,3'-dione (NP0221564)

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Record Information

Version

2.0

Created at

2022-09-05 23:10:49 UTC

Updated at

2022-09-05 23:10:50 UTC

NP-MRD ID

NP0221564

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1's,2s,9r,9as,12's)-15'-hydroxy-2-methyl-2,9a-dihydro-1h-2',10',16'-triazaspiro[imidazo[1,2-a]indole-9,13'-tetracyclo[10.2.2.0²,¹¹.0⁴,⁹]hexadecane]-4',6',8',10',15'-pentaene-3,3'-dione

Description

(1'S,2S,9R,9aS,12'S)-15'-hydroxy-2-methyl-1,2,3,9a-tetrahydro-2',10',16'-triazaspiro[imidazo[1,2-a]indole-9,13'-tetracyclo[10.2.2.0²,¹¹.0⁴,⁹]Hexadecane]-4',6',8',10',15'-pentaene-3,3'-dione belongs to the class of organic compounds known as pyridopyrimidines. Pyridopyrimidines are compounds containing a pyridopyrimidine, which consists of a pyridine fused to a pyrimidine. Pyridine is 6-membered ring consisting of five carbon atoms and a nitrogen atom. Pyrimidine is a 6-membered ring consisting of four carbon atoms and two nitrogen centers at the 1- and 3- ring positions. (1's,2s,9r,9as,12's)-15'-hydroxy-2-methyl-2,9a-dihydro-1h-2',10',16'-triazaspiro[imidazo[1,2-a]indole-9,13'-tetracyclo[10.2.2.0²,¹¹.0⁴,⁹]hexadecane]-4',6',8',10',15'-pentaene-3,3'-dione is found in Penicillium lapatayae. Based on a literature review very few articles have been published on (1'S,2S,9R,9aS,12'S)-15'-hydroxy-2-methyl-1,2,3,9a-tetrahydro-2',10',16'-triazaspiro[imidazo[1,2-a]indole-9,13'-tetracyclo[10.2.2.0²,¹¹.0⁴,⁹]Hexadecane]-4',6',8',10',15'-pentaene-3,3'-dione.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309062201102D          

 31 37  0  0  1  0            999 V2000
    7.1363    3.8463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3227    3.0426    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.7820    2.4194    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.2076    1.7127    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.0113    1.8990    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.0824    2.7210    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7891    3.1466    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4369    1.1923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2469    1.0357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5162    0.2559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9756   -0.3673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1656   -0.2107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8962    0.5691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1365    0.8907    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.1517    0.0659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4450   -0.3597    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.2973    0.1877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4847    0.3299    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2872    0.7376    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.4146    1.2900    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7078    0.8644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9859    1.2637    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2791    0.8381    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5572    1.2374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8504    0.8118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8656   -0.0131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5876   -0.4124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2943    0.0132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0163   -0.3860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0315   -1.2109    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7230    0.0396    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  4  3  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  2  6  1  0  0  0  0
  6  7  2  0  0  0  0
  5  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
  8 13  1  0  0  0  0
 14 13  1  6  0  0  0
  4 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 20 19  1  1  0  0  0
 14 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 23 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
 21 31  1  0  0  0  0
 16 31  1  6  0  0  0
M  END


  Mrv1652309062201102D          

 31 37  0  0  1  0            999 V2000
    7.1363    3.8463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3227    3.0426    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.7820    2.4194    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.2076    1.7127    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.0113    1.8990    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.0824    2.7210    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7891    3.1466    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4369    1.1923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2469    1.0357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5162    0.2559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9756   -0.3673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1656   -0.2107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8962    0.5691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1365    0.8907    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.1517    0.0659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4450   -0.3597    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.2973    0.1877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4847    0.3299    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2872    0.7376    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.4146    1.2900    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7078    0.8644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9859    1.2637    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2791    0.8381    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5572    1.2374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8504    0.8118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8656   -0.0131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5876   -0.4124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2943    0.0132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0163   -0.3860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0315   -1.2109    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7230    0.0396    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  4  3  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  2  6  1  0  0  0  0
  6  7  2  0  0  0  0
  5  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
  8 13  1  0  0  0  0
 14 13  1  6  0  0  0
  4 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 20 19  1  1  0  0  0
 14 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 23 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
 21 31  1  0  0  0  0
 16 31  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0221564

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1N[C@H]2N(C1=O)C1=CC=CC=C1[C@@]21C[C@@H]2N3C(=O)C4=CC=CC=C4N=C3[C@H]1N=C2O

> <INCHI_IDENTIFIER>
InChI=1S/C23H19N5O3/c1-11-20(30)28-15-9-5-3-7-13(15)23(22(28)24-11)10-16-19(29)26-17(23)18-25-14-8-4-2-6-12(14)21(31)27(16)18/h2-9,11,16-17,22,24H,10H2,1H3,(H,26,29)/t11-,16-,17+,22-,23+/m0/s1

> <INCHI_KEY>
WBCINSMUFGLFNX-PBSSQXKISA-N

> <FORMULA>
C23H19N5O3

> <MOLECULAR_WEIGHT>
413.437

> <EXACT_MASS>
413.148789492

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
50

> <JCHEM_AVERAGE_POLARIZABILITY>
42.23268695264261

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1'S,2S,9R,9aS,12'S)-15'-hydroxy-2-methyl-1,2,3,9a-tetrahydro-2',10',16'-triazaspiro[imidazo[1,2-a]indole-9,13'-tetracyclo[10.2.2.0^{2,11}.0^{4,9}]hexadecane]-4',6',8',10',15'-pentaene-3,3'-dione

> <JCHEM_LOGP>
0.06429678681166377

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
18.48308766519585

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.9458079140706492

> <JCHEM_PKA_STRONGEST_BASIC>
5.536012186179766

> <JCHEM_POLAR_SURFACE_AREA>
97.60000000000001

> <JCHEM_REFRACTIVITY>
111.9381

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1'S,2S,9R,9aS,12'S)-15'-hydroxy-2-methyl-2,9a-dihydro-1H-2',10',16'-triazaspiro[imidazo[1,2-a]indole-9,13'-tetracyclo[10.2.2.0^{2,11}.0^{4,9}]hexadecane]-4',6',8',10',15'-pentaene-3,3'-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0      13.321   7.180   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.669   5.679   0.000  0.00  0.00           C+0
HETATM    3  N   UNK     0      12.660   4.516   0.000  0.00  0.00           N+0
HETATM    4  C   UNK     0      13.454   3.197   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0      14.954   3.545   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0      15.087   5.079   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      16.406   5.874   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      15.749   2.226   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      17.261   1.933   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      17.764   0.478   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      16.754  -0.686   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      15.242  -0.393   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      14.740   1.062   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      13.321   1.663   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      13.350   0.123   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      12.031  -0.671   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      11.755   0.350   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      10.238   0.616   0.000  0.00  0.00           O+0
HETATM   19  N   UNK     0      11.736   1.377   0.000  0.00  0.00           N+0
HETATM   20  C   UNK     0      11.974   2.408   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      10.655   1.614   0.000  0.00  0.00           C+0
HETATM   22  N   UNK     0       9.307   2.359   0.000  0.00  0.00           N+0
HETATM   23  C   UNK     0       7.988   1.564   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.640   2.310   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.321   1.515   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.349  -0.024   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.697  -0.770   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       8.016   0.025   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       9.364  -0.721   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       9.392  -2.260   0.000  0.00  0.00           O+0
HETATM   31  N   UNK     0      10.683   0.074   0.000  0.00  0.00           N+0
CONECT    1    2                                                            
CONECT    2    1    3    6                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   14                                                  
CONECT    5    4    6    8                                                  
CONECT    6    5    2    7                                                  
CONECT    7    6                                                            
CONECT    8    5    9   13                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12    8   14                                                  
CONECT   14   13    4   15   20                                             
CONECT   15   14   16                                                       
CONECT   16   15   17   31                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   14   21                                                  
CONECT   21   20   22   31                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   28                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   23   29                                                  
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   21   16                                                  
MASTER        0    0    0    0    0    0    0    0   31    0   74    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₁₉N₅O₃

Average Mass

413.4370 Da

Monoisotopic Mass

413.14879 Da

IUPAC Name

(1'S,2S,9R,9aS,12'S)-15'-hydroxy-2-methyl-1,2,3,9a-tetrahydro-2',10',16'-triazaspiro[imidazo[1,2-a]indole-9,13'-tetracyclo[10.2.2.0^{2,11}.0^{4,9}]hexadecane]-4',6',8',10',15'-pentaene-3,3'-dione

Traditional Name

(1'S,2S,9R,9aS,12'S)-15'-hydroxy-2-methyl-2,9a-dihydro-1H-2',10',16'-triazaspiro[imidazo[1,2-a]indole-9,13'-tetracyclo[10.2.2.0^{2,11}.0^{4,9}]hexadecane]-4',6',8',10',15'-pentaene-3,3'-dione

CAS Registry Number

Not Available

SMILES

C[C@@H]1N[C@H]2N(C1=O)C1=CC=CC=C1[C@@]21C[C@@H]2N3C(=O)C4=CC=CC=C4N=C3[C@H]1N=C2O

InChI Identifier

InChI=1S/C23H19N5O3/c1-11-20(30)28-15-9-5-3-7-13(15)23(22(28)24-11)10-16-19(29)26-17(23)18-25-14-8-4-2-6-12(14)21(31)27(16)18/h2-9,11,16-17,22,24H,10H2,1H3,(H,26,29)/t11-,16-,17+,22-,23+/m0/s1

InChI Key

WBCINSMUFGLFNX-PBSSQXKISA-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
Penicillium lapatayae	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyridopyrimidines. Pyridopyrimidines are compounds containing a pyridopyrimidine, which consists of a pyridine fused to a pyrimidine. Pyridine is 6-membered ring consisting of five carbon atoms and a nitrogen atom. Pyrimidine is a 6-membered ring consisting of four carbon atoms and two nitrogen centers at the 1- and 3- ring positions.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Pyridopyrimidines

Sub Class

Not Available

Direct Parent

Pyridopyrimidines

Alternative Parents

Substituents

Alpha-amino acid or derivatives
Pyridopyrimidine
Quinazoline
Indole or derivatives
Delta-lactam
Piperidinone
Pyrimidone
Imidazolidinone
Piperidine
Benzenoid
Pyridine
Pyrimidine
Imidazolidine
Heteroaromatic compound
Tertiary carboxylic acid amide
Lactam
Carboxamide group
Secondary carboxylic acid amide
Carboxylic acid derivative
Azacycle
Amine
Organooxygen compound
Organonitrogen compound
Hydrocarbon derivative
Organic oxide
Organic nitrogen compound
Organic oxygen compound
Carbonyl group
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	0.064	ChemAxon
pKa (Strongest Acidic)	3.95	ChemAxon
pKa (Strongest Basic)	5.54	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	97.6 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	111.94 m³·mol⁻¹	ChemAxon
Polarizability	42.23 Å³	ChemAxon
Number of Rings	7	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

13082505

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

15939556

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1's,2s,9r,9as,12's)-15'-hydroxy-2-methyl-2,9a-dihydro-1h-2',10',16'-triazaspiro[imidazo[1,2-a]indole-9,13'-tetracyclo[10.2.2.0²,¹¹.0⁴,⁹]hexadecane]-4',6',8',10',15'-pentaene-3,3'-dione (NP0221564)

MOL for NP0221564 ((1's,2s,9r,9as,12's)-15'-hydroxy-2-methyl-2,9a-dihydro-1h-2',10',16'-triazaspiro[imidazo[1,2-a]indole-9,13'-tetracyclo[10.2.2.0²,¹¹.0⁴,⁹]hexadecane]-4',6',8',10',15'-pentaene-3,3'-dione)

3D MOL for NP0221564 ((1's,2s,9r,9as,12's)-15'-hydroxy-2-methyl-2,9a-dihydro-1h-2',10',16'-triazaspiro[imidazo[1,2-a]indole-9,13'-tetracyclo[10.2.2.0²,¹¹.0⁴,⁹]hexadecane]-4',6',8',10',15'-pentaene-3,3'-dione)

3D SDF for NP0221564 ((1's,2s,9r,9as,12's)-15'-hydroxy-2-methyl-2,9a-dihydro-1h-2',10',16'-triazaspiro[imidazo[1,2-a]indole-9,13'-tetracyclo[10.2.2.0²,¹¹.0⁴,⁹]hexadecane]-4',6',8',10',15'-pentaene-3,3'-dione)

3D-SDF for NP0221564 ((1's,2s,9r,9as,12's)-15'-hydroxy-2-methyl-2,9a-dihydro-1h-2',10',16'-triazaspiro[imidazo[1,2-a]indole-9,13'-tetracyclo[10.2.2.0²,¹¹.0⁴,⁹]hexadecane]-4',6',8',10',15'-pentaene-3,3'-dione)

PDB for NP0221564 ((1's,2s,9r,9as,12's)-15'-hydroxy-2-methyl-2,9a-dihydro-1h-2',10',16'-triazaspiro[imidazo[1,2-a]indole-9,13'-tetracyclo[10.2.2.0²,¹¹.0⁴,⁹]hexadecane]-4',6',8',10',15'-pentaene-3,3'-dione)

3D PDB for NP0221564 ((1's,2s,9r,9as,12's)-15'-hydroxy-2-methyl-2,9a-dihydro-1h-2',10',16'-triazaspiro[imidazo[1,2-a]indole-9,13'-tetracyclo[10.2.2.0²,¹¹.0⁴,⁹]hexadecane]-4',6',8',10',15'-pentaene-3,3'-dione)

SMILES for NP0221564 ((1's,2s,9r,9as,12's)-15'-hydroxy-2-methyl-2,9a-dihydro-1h-2',10',16'-triazaspiro[imidazo[1,2-a]indole-9,13'-tetracyclo[10.2.2.0²,¹¹.0⁴,⁹]hexadecane]-4',6',8',10',15'-pentaene-3,3'-dione)

INCHI for NP0221564 ((1's,2s,9r,9as,12's)-15'-hydroxy-2-methyl-2,9a-dihydro-1h-2',10',16'-triazaspiro[imidazo[1,2-a]indole-9,13'-tetracyclo[10.2.2.0²,¹¹.0⁴,⁹]hexadecane]-4',6',8',10',15'-pentaene-3,3'-dione)

Structure for NP0221564 ((1's,2s,9r,9as,12's)-15'-hydroxy-2-methyl-2,9a-dihydro-1h-2',10',16'-triazaspiro[imidazo[1,2-a]indole-9,13'-tetracyclo[10.2.2.0²,¹¹.0⁴,⁹]hexadecane]-4',6',8',10',15'-pentaene-3,3'-dione)

3D Structure for NP0221564 ((1's,2s,9r,9as,12's)-15'-hydroxy-2-methyl-2,9a-dihydro-1h-2',10',16'-triazaspiro[imidazo[1,2-a]indole-9,13'-tetracyclo[10.2.2.0²,¹¹.0⁴,⁹]hexadecane]-4',6',8',10',15'-pentaene-3,3'-dione)