NP-MRD: Showing NP-Card for 9-(2,4-dibromo-5-methoxyphenyl)-8-hydroxy-1,7-dimethyl-1,7-diazaspiro[4.4]nonan-6-one (NP0178536)

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Record Information

Version

2.0

Created at

2022-09-03 16:33:09 UTC

Updated at

2022-09-03 16:33:09 UTC

NP-MRD ID

NP0178536

Secondary Accession Numbers

None

Natural Product Identification

Common Name

9-(2,4-dibromo-5-methoxyphenyl)-8-hydroxy-1,7-dimethyl-1,7-diazaspiro[4.4]nonan-6-one

Description

NSC680527 belongs to the class of organic compounds known as phenylpyrrolidines. These are polycyclic aromatic compounds containing a benzene ring linked to a pyrrolidine ring through a CC or CN bond. Pyrrolidine is a five-membered saturated aliphatic heterocycle with one nitrogen atom and four carbon atoms. NSC680527 is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 43 45  0  0  0  0  0  0  0  0999 V2000
    4.3419    1.0465    2.4029 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9154    0.6699    1.2264 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2390    0.2959    0.1927 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8619    0.0955    0.2852 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1321   -0.2878   -0.7939 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2999   -0.4425   -0.9069 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8446   -1.8608   -0.6363 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3275   -2.7537   -1.5623 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2526   -1.5019   -0.9366 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1470   -2.3177   -1.6881 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5088   -0.2112   -0.3789 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5692    0.4317   -0.3556 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1363    0.2019    0.1901 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1109   -0.4824    1.5101 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3679    0.6686    2.4884 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7583    1.8263    1.6225 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0507    1.5849    0.3612 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6619    2.3490   -0.7132 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8163   -0.4761   -2.0261 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8649   -1.0263   -3.6115 Br  0  0  0  0  0  0  0  0  0  0  0  0
    3.1613   -0.2937   -2.1443 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8980    0.0919   -1.0425 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7644    0.3173   -1.1836 Br  0  0  0  0  0  0  0  0  0  0  0  0
    5.1035    0.4144    2.9446 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5295    1.2340    3.1946 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8776    2.0866    2.4081 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3624    0.2937    1.2423 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6835   -0.1336   -1.8738 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6776   -2.1331    0.3867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0385   -3.2176   -2.0591 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9938   -3.3852   -1.4853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0450   -2.1217   -2.8001 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1957   -2.0053   -1.4638 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9870   -1.2107    1.6702 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2477   -1.0646    1.8022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2057    0.4266    3.1852 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4643    0.9380    3.0477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8670    1.8574    1.4392 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4894    2.7988    2.0479 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6837    2.6360   -0.3413 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1154    3.3020   -0.8992 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8337    1.8019   -1.6358 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6956   -0.4429   -3.1101 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  2  0
 13 11  1  6
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
  5 19  2  0
 19 20  1  0
 19 21  1  0
 21 22  2  0
 22 23  1  0
 22  3  1  0
 13  6  1  0
 17 13  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  4 27  1  0
  6 28  1  6
  7 29  1  1
  8 30  1  0
 10 31  1  0
 10 32  1  0
 10 33  1  0
 14 34  1  0
 14 35  1  0
 15 36  1  0
 15 37  1  0
 16 38  1  0
 16 39  1  0
 18 40  1  0
 18 41  1  0
 18 42  1  0
 21 43  1  0
M  END


  Mrv1533004261501352D          

 23 25  0  0  0  0            999 V2000
    3.1634   -2.9519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9084   -2.1672    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1015   -1.9957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8465   -1.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0396   -1.0396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7846   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6674   -0.4849    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    0.8250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6674    1.3099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7846    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0396    1.8646    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2695    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7545    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5391    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5391   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7545   -0.2549    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2394   -0.9224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4875   -1.6527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3194   -1.4811    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    0.7425   -2.4373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5494   -2.6088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8044   -3.3934    0.0000 Br  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  2  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
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
  6 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
 16 17  1  0  0  0  0
 13 17  1  0  0  0  0
 17 18  1  0  0  0  0
  5 19  2  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
  3 22  1  0  0  0  0
 22 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0178536

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(C2C(O)N(C)C(=O)C22CCCN2C)=C(Br)C=C1Br

> <INCHI_IDENTIFIER>
InChI=1S/C16H20Br2N2O3/c1-19-6-4-5-16(19)13(14(21)20(2)15(16)22)9-7-12(23-3)11(18)8-10(9)17/h7-8,13-14,21H,4-6H2,1-3H3

> <INCHI_KEY>
XPXNSHHFRHGAHC-UHFFFAOYSA-N

> <FORMULA>
C16H20Br2N2O3

> <MOLECULAR_WEIGHT>
448.155

> <EXACT_MASS>
445.984069

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
43

> <JCHEM_AVERAGE_POLARIZABILITY>
37.66926602226783

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
9-(2,4-dibromo-5-methoxyphenyl)-8-hydroxy-1,7-dimethyl-1,7-diazaspiro[4.4]nonan-6-one

> <ALOGPS_LOGP>
2.56

> <JCHEM_LOGP>
2.6246180393333325

> <ALOGPS_LOGS>
-3.23

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.0312136597605

> <JCHEM_PKA_STRONGEST_BASIC>
6.260590182971933

> <JCHEM_POLAR_SURFACE_AREA>
53.010000000000005

> <JCHEM_REFRACTIVITY>
94.87900000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.67e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
9-(2,4-dibromo-5-methoxyphenyl)-8-hydroxy-1,7-dimethyl-1,7-diazaspiro[4.4]nonan-6-one

> <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       5.905  -5.510   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       5.429  -4.046   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       3.923  -3.725   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.447  -2.261   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.941  -1.941   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.465  -0.476   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -1.246  -0.905   0.000  0.00  0.00           O+0
HETATM    9  N   UNK     0      -0.000   1.540   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0      -1.246   2.445   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.465   2.016   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       1.941   3.481   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       2.370   0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.275   2.016   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.740   1.540   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.740  -0.000   0.000  0.00  0.00           C+0
HETATM   17  N   UNK     0       3.275  -0.476   0.000  0.00  0.00           N+0
HETATM   18  C   UNK     0       4.180  -1.722   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.910  -3.085   0.000  0.00  0.00           C+0
HETATM   20 Br   UNK     0      -0.596  -2.765   0.000  0.00  0.00          Br+0
HETATM   21  C   UNK     0       1.386  -4.550   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.892  -4.870   0.000  0.00  0.00           C+0
HETATM   23 Br   UNK     0       3.368  -6.334   0.000  0.00  0.00          Br+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   22                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   19                                                  
CONECT    6    5    7   13                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11    6   14   17                                             
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   13   18                                                  
CONECT   18   17                                                            
CONECT   19    5   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21    3   23                                                  
CONECT   23   22                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   50    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₆H₂₀Br₂N₂O₃

Average Mass

448.1550 Da

Monoisotopic Mass

445.98407 Da

IUPAC Name

9-(2,4-dibromo-5-methoxyphenyl)-8-hydroxy-1,7-dimethyl-1,7-diazaspiro[4.4]nonan-6-one

Traditional Name

9-(2,4-dibromo-5-methoxyphenyl)-8-hydroxy-1,7-dimethyl-1,7-diazaspiro[4.4]nonan-6-one

CAS Registry Number

Not Available

SMILES

COC1=CC(C2C(O)N(C)C(=O)C22CCCN2C)=C(Br)C=C1Br

InChI Identifier

InChI=1S/C16H20Br2N2O3/c1-19-6-4-5-16(19)13(14(21)20(2)15(16)22)9-7-12(23-3)11(18)8-10(9)17/h7-8,13-14,21H,4-6H2,1-3H3

InChI Key

XPXNSHHFRHGAHC-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenylpyrrolidines. These are polycyclic aromatic compounds containing a benzene ring linked to a pyrrolidine ring through a CC or CN bond. Pyrrolidine is a five-membered saturated aliphatic heterocycle with one nitrogen atom and four carbon atoms.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Pyrrolidines

Sub Class

Phenylpyrrolidines

Direct Parent

Phenylpyrrolidines

Alternative Parents

Substituents

3-phenylpyrrolidine
Alpha-amino acid or derivatives
Diazaspirononane
Phenoxy compound
Anisole
Methoxybenzene
Phenol ether
Alkyl aryl ether
Bromobenzene
Halobenzene
Aralkylamine
Aryl bromide
Aryl halide
Monocyclic benzene moiety
Benzenoid
N-alkylpyrrolidine
Pyrrolidone
2-pyrrolidone
Tertiary carboxylic acid amide
Pyrrole
Tertiary aliphatic amine
Tertiary amine
Amino acid or derivatives
Lactam
Carboxamide group
Alkanolamine
Azacycle
Carboxylic acid derivative
Ether
Carbonyl group
Organic oxide
Organic oxygen compound
Organic nitrogen compound
Amine
Organohalogen compound
Organobromide
Organopnictogen compound
Organooxygen compound
Organonitrogen compound
Hydrocarbon derivative
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	2.56	ALOGPS
logP	2.62	ChemAxon
logS	-3.2	ALOGPS
pKa (Strongest Acidic)	13.03	ChemAxon
pKa (Strongest Basic)	6.26	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	53.01 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	94.88 m³·mol⁻¹	ChemAxon
Polarizability	37.67 Å³	ChemAxon
Number of Rings	3	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

387125

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 9-(2,4-dibromo-5-methoxyphenyl)-8-hydroxy-1,7-dimethyl-1,7-diazaspiro[4.4]nonan-6-one (NP0178536)

MOL for NP0178536 (9-(2,4-dibromo-5-methoxyphenyl)-8-hydroxy-1,7-dimethyl-1,7-diazaspiro[4.4]nonan-6-one)

3D MOL for NP0178536 (9-(2,4-dibromo-5-methoxyphenyl)-8-hydroxy-1,7-dimethyl-1,7-diazaspiro[4.4]nonan-6-one)

3D SDF for NP0178536 (9-(2,4-dibromo-5-methoxyphenyl)-8-hydroxy-1,7-dimethyl-1,7-diazaspiro[4.4]nonan-6-one)

3D-SDF for NP0178536 (9-(2,4-dibromo-5-methoxyphenyl)-8-hydroxy-1,7-dimethyl-1,7-diazaspiro[4.4]nonan-6-one)

PDB for NP0178536 (9-(2,4-dibromo-5-methoxyphenyl)-8-hydroxy-1,7-dimethyl-1,7-diazaspiro[4.4]nonan-6-one)

3D PDB for NP0178536 (9-(2,4-dibromo-5-methoxyphenyl)-8-hydroxy-1,7-dimethyl-1,7-diazaspiro[4.4]nonan-6-one)

SMILES for NP0178536 (9-(2,4-dibromo-5-methoxyphenyl)-8-hydroxy-1,7-dimethyl-1,7-diazaspiro[4.4]nonan-6-one)

INCHI for NP0178536 (9-(2,4-dibromo-5-methoxyphenyl)-8-hydroxy-1,7-dimethyl-1,7-diazaspiro[4.4]nonan-6-one)

Structure for NP0178536 (9-(2,4-dibromo-5-methoxyphenyl)-8-hydroxy-1,7-dimethyl-1,7-diazaspiro[4.4]nonan-6-one)

3D Structure for NP0178536 (9-(2,4-dibromo-5-methoxyphenyl)-8-hydroxy-1,7-dimethyl-1,7-diazaspiro[4.4]nonan-6-one)