NP-MRD: Showing NP-Card for 16'-hydroxy-2,12'-dimethyl-2,9a-dihydro-1h-13'-oxa-2',10',17'-triazaspiro[imidazo[1,2-a]indole-9,14'-tetracyclo[10.3.2.0²,¹¹.0⁴,⁹]heptadecane]-4',6',8',10',16'-pentaene-3,3'-dione (NP0262545)

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Record Information

Version

2.0

Created at

2022-09-08 05:23:51 UTC

Updated at

2022-09-08 05:23:51 UTC

NP-MRD ID

NP0262545

Secondary Accession Numbers

None

Natural Product Identification

Common Name

16'-hydroxy-2,12'-dimethyl-2,9a-dihydro-1h-13'-oxa-2',10',17'-triazaspiro[imidazo[1,2-a]indole-9,14'-tetracyclo[10.3.2.0²,¹¹.0⁴,⁹]heptadecane]-4',6',8',10',16'-pentaene-3,3'-dione

Description

16'-Hydroxy-2,12'-dimethyl-1,2,3,9a-tetrahydro-13'-oxa-2',10',17'-triazaspiro[imidazo[1,2-a]indole-9,14'-tetracyclo[10.3.2.0²,¹¹.0⁴,⁹]Heptadecane]-4',6',8',10',16'-pentaene-3,3'-dione belongs to the class of organic compounds known as quinazolines. Quinazolines are compounds containing a quinazoline moiety, which is made up of two fused six-member aromatic rings, a benzene ring and a pyrimidine ring. 16'-hydroxy-2,12'-dimethyl-2,9a-dihydro-1h-13'-oxa-2',10',17'-triazaspiro[imidazo[1,2-a]indole-9,14'-tetracyclo[10.3.2.0²,¹¹.0⁴,⁹]heptadecane]-4',6',8',10',16'-pentaene-3,3'-dione is found in Aspergillus fumigatus and Penicillium lanosum. 16'-Hydroxy-2,12'-dimethyl-1,2,3,9a-tetrahydro-13'-oxa-2',10',17'-triazaspiro[imidazo[1,2-a]indole-9,14'-tetracyclo[10.3.2.0²,¹¹.0⁴,⁹]Heptadecane]-4',6',8',10',16'-pentaene-3,3'-dione is a strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004261504152D          

 33 39  0  0  0  0            999 V2000
    8.2871    5.4609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2235    4.6383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5207    4.2063    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.7144    3.4044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5369    3.3408    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.8516    4.1034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6535    4.2971    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.7306    2.5388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4562    2.1462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4789    1.3215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7761    0.8895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0505    1.2821    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0278    2.1068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3997    2.6417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2263    1.8352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4876    1.4679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7398    1.8164    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.1422    1.2477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3359    0.4458    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3508    1.4809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7532    0.9122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9618    1.1454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7681    1.9474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3658    2.5161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1571    2.2829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7547    2.8516    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.5461    2.6184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0523    3.2698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6850    4.0085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3476    2.7054    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.4926    2.1048    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3122    2.1990    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8772    3.2802    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
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 16 31  1  0  0  0  0
 31 32  2  0  0  0  0
 28 33  1  0  0  0  0
 14 33  1  0  0  0  0
M  END

     RDKit          3D

 54 60  0  0  0  0  0  0  0  0999 V2000
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   -1.7127   -1.5711   -0.0898 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0687   -0.2781    0.2855 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1770   -0.6640    1.4389 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8797    0.3057    1.8267 C   0  0  2  0  0  0  0  0  0  0  0  0
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   -0.8428   -0.9331    2.2818 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.5272    1.0959   -2.9716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1269    2.5883   -2.0982 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9480   -0.1971   -2.7213 H   0  0  0  0  0  0  0  0  0  0  0  0
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 19 47  1  0
M  END


  Mrv1533004261504152D          

 33 39  0  0  0  0            999 V2000
    8.2871    5.4609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2235    4.6383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5207    4.2063    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.7144    3.4044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5369    3.3408    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.8516    4.1034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6535    4.2971    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.7306    2.5388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4562    2.1462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4789    1.3215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7761    0.8895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0505    1.2821    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0278    2.1068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3997    2.6417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2263    1.8352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4876    1.4679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7398    1.8164    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.1422    1.2477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3359    0.4458    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3508    1.4809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7532    0.9122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9618    1.1454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7681    1.9474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3658    2.5161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1571    2.2829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7547    2.8516    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
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    6.3476    2.7054    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
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M  END
> <DATABASE_ID>
NP0262545

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1NC2N(C1=O)C1=CC=CC=C1C21CC2N3C(=O)C4=CC=CC=C4N=C3C(C)(NC2=O)O1

> <INCHI_IDENTIFIER>
InChI=1S/C24H21N5O4/c1-12-19(31)28-16-10-6-4-8-14(16)24(22(28)25-12)11-17-18(30)27-23(2,33-24)21-26-15-9-5-3-7-13(15)20(32)29(17)21/h3-10,12,17,22,25H,11H2,1-2H3,(H,27,30)

> <INCHI_KEY>
POEYRUBMWIOMTB-UHFFFAOYSA-N

> <FORMULA>
C24H21N5O4

> <MOLECULAR_WEIGHT>
443.463

> <EXACT_MASS>
443.159354176

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
45.18961477002842

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2,12'-dimethyl-1,2,3,9a-tetrahydro-13'-oxa-2',10',17'-triazaspiro[imidazolidino[1,2-a]indole-9,14'-tetracyclo[10.3.2.0²,¹¹.0⁴,⁹]heptadecane]-4',6',8',10'-tetraene-3,3',16'-trione

> <ALOGPS_LOGP>
0.64

> <JCHEM_LOGP>
1.394725470333333

> <ALOGPS_LOGS>
-3.13

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
18.45808954109751

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.829431135549106

> <JCHEM_PKA_STRONGEST_BASIC>
4.625219791485515

> <JCHEM_POLAR_SURFACE_AREA>
103.34000000000002

> <JCHEM_REFRACTIVITY>
117.7049

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.30e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2,12'-dimethyl-2,9a-dihydro-1H-13'-oxa-2',10',17'-triazaspiro[imidazolidino[1,2-a]indole-9,14'-tetracyclo[10.3.2.0²,¹¹.0⁴,⁹]heptadecane]-4',6',8',10'-tetraene-3,3',16'-trione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 26-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   26-APR-15         0                                  
HETATM    1  C   UNK     0      15.469  10.194   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      15.351   8.658   0.000  0.00  0.00           C+0
HETATM    3  N   UNK     0      14.039   7.852   0.000  0.00  0.00           N+0
HETATM    4  C   UNK     0      14.400   6.355   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0      15.936   6.236   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0      16.523   7.660   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      18.020   8.021   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      16.297   4.739   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      17.652   4.006   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      17.694   2.467   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      16.382   1.660   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      15.028   2.393   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      14.985   3.933   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      13.813   4.931   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      13.489   3.426   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      12.110   2.740   0.000  0.00  0.00           C+0
HETATM   17  N   UNK     0      10.714   3.391   0.000  0.00  0.00           N+0
HETATM   18  C   UNK     0       9.599   2.329   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       9.960   0.832   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       8.121   2.764   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.006   1.703   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.529   2.138   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.167   3.635   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.283   4.697   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       7.760   4.261   0.000  0.00  0.00           C+0
HETATM   26  N   UNK     0       8.876   5.323   0.000  0.00  0.00           N+0
HETATM   27  C   UNK     0      10.353   4.888   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      11.298   6.104   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      10.612   7.483   0.000  0.00  0.00           C+0
HETATM   30  N   UNK     0      11.849   5.050   0.000  0.00  0.00           N+0
HETATM   31  C   UNK     0      12.120   3.929   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      13.649   4.105   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0      12.838   6.123   0.000  0.00  0.00           O+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   33                                             
CONECT   15   14   16                                                       
CONECT   16   15   17   31                                                  
CONECT   17   16   18   27                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   25                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   20   26                                                  
CONECT   26   25   27                                                       
CONECT   27   26   17   28                                                  
CONECT   28   27   29   30   33                                             
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   16   32                                                  
CONECT   32   31                                                            
CONECT   33   28   14                                                       
MASTER        0    0    0    0    0    0    0    0   33    0   78    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₂₁N₅O₄

Average Mass

443.4630 Da

Monoisotopic Mass

443.15935 Da

IUPAC Name

2,12'-dimethyl-1,2,3,9a-tetrahydro-13'-oxa-2',10',17'-triazaspiro[imidazolidino[1,2-a]indole-9,14'-tetracyclo[10.3.2.0²,¹¹.0⁴,⁹]heptadecane]-4',6',8',10'-tetraene-3,3',16'-trione

Traditional Name

2,12'-dimethyl-2,9a-dihydro-1H-13'-oxa-2',10',17'-triazaspiro[imidazolidino[1,2-a]indole-9,14'-tetracyclo[10.3.2.0²,¹¹.0⁴,⁹]heptadecane]-4',6',8',10'-tetraene-3,3',16'-trione

CAS Registry Number

Not Available

SMILES

CC1NC2N(C1=O)C1=CC=CC=C1C21CC2N3C(=O)C4=CC=CC=C4N=C3C(C)(NC2=O)O1

InChI Identifier

InChI=1S/C24H21N5O4/c1-12-19(31)28-16-10-6-4-8-14(16)24(22(28)25-12)11-17-18(30)27-23(2,33-24)21-26-15-9-5-3-7-13(15)20(32)29(17)21/h3-10,12,17,22,25H,11H2,1-2H3,(H,27,30)

InChI Key

POEYRUBMWIOMTB-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
Aspergillus fumigatus	LOTUS Database	35616633
Penicillium lanosum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as quinazolines. Quinazolines are compounds containing a quinazoline moiety, which is made up of two fused six-member aromatic rings, a benzene ring and a pyrimidine ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Diazanaphthalenes

Sub Class

Benzodiazines

Direct Parent

Quinazolines

Alternative Parents

Substituents

Alpha-amino acid or derivatives
Quinazoline
Indole or derivatives
Meta-oxazepine
Pyrimidone
Imidazolidinone
Pyrimidine
Benzenoid
Imidazolidine
Heteroaromatic compound
Tertiary carboxylic acid amide
Cyclic carboximidic acid
Lactam
Carboxamide group
Azacycle
Oxacycle
Carboxylic acid derivative
Propargyl-type 1,3-dipolar organic compound
Organic 1,3-dipolar compound
Organic oxygen compound
Organooxygen compound
Organonitrogen compound
Hydrocarbon derivative
Organic oxide
Organic nitrogen compound
Carbonyl group
Amine
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	0.64	ALOGPS
logP	1.39	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Acidic)	9.83	ChemAxon
pKa (Strongest Basic)	4.63	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	103.34 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	117.7 m³·mol⁻¹	ChemAxon
Polarizability	45.19 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

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

72807707

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 16'-hydroxy-2,12'-dimethyl-2,9a-dihydro-1h-13'-oxa-2',10',17'-triazaspiro[imidazo[1,2-a]indole-9,14'-tetracyclo[10.3.2.0²,¹¹.0⁴,⁹]heptadecane]-4',6',8',10',16'-pentaene-3,3'-dione (NP0262545)

MOL for NP0262545 (16'-hydroxy-2,12'-dimethyl-2,9a-dihydro-1h-13'-oxa-2',10',17'-triazaspiro[imidazo[1,2-a]indole-9,14'-tetracyclo[10.3.2.0²,¹¹.0⁴,⁹]heptadecane]-4',6',8',10',16'-pentaene-3,3'-dione)

3D MOL for NP0262545 (16'-hydroxy-2,12'-dimethyl-2,9a-dihydro-1h-13'-oxa-2',10',17'-triazaspiro[imidazo[1,2-a]indole-9,14'-tetracyclo[10.3.2.0²,¹¹.0⁴,⁹]heptadecane]-4',6',8',10',16'-pentaene-3,3'-dione)

3D SDF for NP0262545 (16'-hydroxy-2,12'-dimethyl-2,9a-dihydro-1h-13'-oxa-2',10',17'-triazaspiro[imidazo[1,2-a]indole-9,14'-tetracyclo[10.3.2.0²,¹¹.0⁴,⁹]heptadecane]-4',6',8',10',16'-pentaene-3,3'-dione)

3D-SDF for NP0262545 (16'-hydroxy-2,12'-dimethyl-2,9a-dihydro-1h-13'-oxa-2',10',17'-triazaspiro[imidazo[1,2-a]indole-9,14'-tetracyclo[10.3.2.0²,¹¹.0⁴,⁹]heptadecane]-4',6',8',10',16'-pentaene-3,3'-dione)

PDB for NP0262545 (16'-hydroxy-2,12'-dimethyl-2,9a-dihydro-1h-13'-oxa-2',10',17'-triazaspiro[imidazo[1,2-a]indole-9,14'-tetracyclo[10.3.2.0²,¹¹.0⁴,⁹]heptadecane]-4',6',8',10',16'-pentaene-3,3'-dione)

3D PDB for NP0262545 (16'-hydroxy-2,12'-dimethyl-2,9a-dihydro-1h-13'-oxa-2',10',17'-triazaspiro[imidazo[1,2-a]indole-9,14'-tetracyclo[10.3.2.0²,¹¹.0⁴,⁹]heptadecane]-4',6',8',10',16'-pentaene-3,3'-dione)

SMILES for NP0262545 (16'-hydroxy-2,12'-dimethyl-2,9a-dihydro-1h-13'-oxa-2',10',17'-triazaspiro[imidazo[1,2-a]indole-9,14'-tetracyclo[10.3.2.0²,¹¹.0⁴,⁹]heptadecane]-4',6',8',10',16'-pentaene-3,3'-dione)

INCHI for NP0262545 (16'-hydroxy-2,12'-dimethyl-2,9a-dihydro-1h-13'-oxa-2',10',17'-triazaspiro[imidazo[1,2-a]indole-9,14'-tetracyclo[10.3.2.0²,¹¹.0⁴,⁹]heptadecane]-4',6',8',10',16'-pentaene-3,3'-dione)

Structure for NP0262545 (16'-hydroxy-2,12'-dimethyl-2,9a-dihydro-1h-13'-oxa-2',10',17'-triazaspiro[imidazo[1,2-a]indole-9,14'-tetracyclo[10.3.2.0²,¹¹.0⁴,⁹]heptadecane]-4',6',8',10',16'-pentaene-3,3'-dione)

3D Structure for NP0262545 (16'-hydroxy-2,12'-dimethyl-2,9a-dihydro-1h-13'-oxa-2',10',17'-triazaspiro[imidazo[1,2-a]indole-9,14'-tetracyclo[10.3.2.0²,¹¹.0⁴,⁹]heptadecane]-4',6',8',10',16'-pentaene-3,3'-dione)