NP-MRD: Showing NP-Card for 13,14-dibromo-5-hydroxy-3-imino-2,4,9,15-tetraazatetracyclo[7.6.0.0¹,⁵.0¹¹,¹⁵]pentadeca-11,13-dien-10-one (NP0289413)

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Record Information

Version

2.0

Created at

2022-09-09 19:35:32 UTC

Updated at

2022-09-09 19:35:32 UTC

NP-MRD ID

NP0289413

Secondary Accession Numbers

None

Natural Product Identification

Common Name

13,14-dibromo-5-hydroxy-3-imino-2,4,9,15-tetraazatetracyclo[7.6.0.0¹,⁵.0¹¹,¹⁵]pentadeca-11,13-dien-10-one

Description

13,14-Dibromo-5-hydroxy-3-imino-2,4,9,15-tetraazatetracyclo[7.6.0.0¹,⁵.0¹¹,¹⁵]Pentadeca-11,13-dien-10-one belongs to the class of organic compounds known as imidazopyridines. These are organic polycyclic compounds containing an imidazole ring fused to a pyridine ring. Imidazole is 5-membered ring consisting of three carbon atoms, and two nitrogen centers at the 1- and 3-positions. Pyridine is a 6-membered ring consisting of five carbon atoms and one nitrogen center. 13,14-dibromo-5-hydroxy-3-imino-2,4,9,15-tetraazatetracyclo[7.6.0.0¹,⁵.0¹¹,¹⁵]pentadeca-11,13-dien-10-one is found in Agelas dispar. 13,14-Dibromo-5-hydroxy-3-imino-2,4,9,15-tetraazatetracyclo[7.6.0.0¹,⁵.0¹¹,¹⁵]Pentadeca-11,13-dien-10-one is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 31 34  0  0  0  0  0  0  0  0999 V2000
   -0.0843    3.5630   -0.0492 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4623    2.1946   -0.0248 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8618    1.5709    1.0730 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1471    0.2646    0.6757 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3564    0.4160   -0.1153 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2468   -0.9220    1.4822 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0805   -1.8979    0.5929 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6065   -1.8560   -0.8544 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3155   -1.2095   -0.9506 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9331   -1.6272   -1.4612 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1869   -2.5179   -2.3182 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9552   -0.7922   -0.7787 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3174   -0.6946   -0.5389 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4078    0.2433    0.4717 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0857    0.7834    1.2227 Br  0  0  0  0  0  0  0  0  0  0  0  0
    2.1501    0.6903    0.8180 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8615    1.9475    2.2023 Br  0  0  0  0  0  0  0  0  0  0  0  0
    1.2713    0.0377    0.0217 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0891    0.0334   -0.3778 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4366    1.2429   -1.1215 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0327    4.0929   -0.9303 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0889    4.0817    0.8334 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9238    1.0983    0.3022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2846   -1.4771    1.6351 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7473   -0.8334    2.4417 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1292   -2.8914    1.0219 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0943   -1.4606    0.5924 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5549   -2.9335   -1.1815 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3074   -1.3712   -1.5455 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0611   -1.2511   -1.0591 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6232    1.4754   -2.0801 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  6
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 14 16  2  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 19 20  1  6
 20  2  1  0
 19  4  1  0
 19  9  1  0
 18 12  1  0
  1 21  1  0
  1 22  1  0
  5 23  1  0
  6 24  1  0
  6 25  1  0
  7 26  1  0
  7 27  1  0
  8 28  1  0
  8 29  1  0
 13 30  1  0
 20 31  1  0
M  END


  Mrv1533004171503102D          

 20 23  0  0  0  0            999 V2000
    2.7645   -1.5079    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1624   -0.9439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3522   -1.0995    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9539   -0.3770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4559   -1.0347    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1505   -0.1896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0890    0.5999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4750    1.2020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2785    1.0146    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9554    1.4863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9716    2.3111    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6131    0.9883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4379    0.9720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6774    0.1825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4568   -0.0878    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    3.0005   -0.2892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9842   -1.1140    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    2.3427    0.2088    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5179    0.2251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2648   -0.1253    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 12 18  1  0  0  0  0
 18 19  1  0  0  0  0
  4 19  1  0  0  0  0
  9 19  1  0  0  0  0
 19 20  1  0  0  0  0
  2 20  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0289413

> <DATABASE_NAME>
NP-MRD

> <SMILES>
NC1=NC2(O)CCCN3C(=O)C4=CC(Br)=C(Br)N4C23N1

> <INCHI_IDENTIFIER>
InChI=1S/C11H11Br2N5O2/c12-5-4-6-8(19)17-3-1-2-10(20)11(17,16-9(14)15-10)18(6)7(5)13/h4,20H,1-3H2,(H3,14,15,16)

> <INCHI_KEY>
LERJEFMIFQBNIN-UHFFFAOYSA-N

> <FORMULA>
C11H11Br2N5O2

> <MOLECULAR_WEIGHT>
405.05

> <EXACT_MASS>
402.927951

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
31

> <JCHEM_AVERAGE_POLARIZABILITY>
30.8035682461488

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-amino-13,14-dibromo-5-hydroxy-2,4,9,15-tetraazatetracyclo[7.6.0.0¹,⁵.0¹¹,¹⁵]pentadeca-3,11,13-trien-10-one

> <ALOGPS_LOGP>
0.79

> <JCHEM_LOGP>
1.163934554

> <ALOGPS_LOGS>
-2.21

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.721867404368956

> <JCHEM_PKA_STRONGEST_BASIC>
6.810808284642895

> <JCHEM_POLAR_SURFACE_AREA>
95.88

> <JCHEM_REFRACTIVITY>
78.28259999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.47e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-amino-13,14-dibromo-5-hydroxy-2,4,9,15-tetraazatetracyclo[7.6.0.0¹,⁵.0¹¹,¹⁵]pentadeca-3,11,13-trien-10-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  N   UNK     0       5.160  -2.815   0.000  0.00  0.00           N+0
HETATM    2  C   UNK     0       4.037  -1.762   0.000  0.00  0.00           C+0
HETATM    3  N   UNK     0       2.524  -2.052   0.000  0.00  0.00           N+0
HETATM    4  C   UNK     0       1.781  -0.704   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       0.851  -1.932   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       0.281  -0.354   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.166   1.120   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.887   2.244   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0       2.387   1.894   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0       3.650   2.774   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       3.680   4.314   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       4.878   1.845   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.417   1.814   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.864   0.341   0.000  0.00  0.00           C+0
HETATM   15 Br   UNK     0       8.319  -0.164   0.000  0.00  0.00          Br+0
HETATM   16  C   UNK     0       5.601  -0.540   0.000  0.00  0.00           C+0
HETATM   17 Br   UNK     0       5.571  -2.079   0.000  0.00  0.00          Br+0
HETATM   18  N   UNK     0       4.373   0.390   0.000  0.00  0.00           N+0
HETATM   19  C   UNK     0       2.833   0.420   0.000  0.00  0.00           C+0
HETATM   20  N   UNK     0       4.228  -0.234   0.000  0.00  0.00           N+0
CONECT    1    2                                                            
CONECT    2    1    3   20                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6   19                                             
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   19                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   18                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   12   19                                                  
CONECT   19   18    4    9   20                                             
CONECT   20   19    2                                                       
MASTER        0    0    0    0    0    0    0    0   20    0   46    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₁H₁₁Br₂N₅O₂

Average Mass

405.0500 Da

Monoisotopic Mass

402.92795 Da

IUPAC Name

3-amino-13,14-dibromo-5-hydroxy-2,4,9,15-tetraazatetracyclo[7.6.0.0¹,⁵.0¹¹,¹⁵]pentadeca-3,11,13-trien-10-one

Traditional Name

3-amino-13,14-dibromo-5-hydroxy-2,4,9,15-tetraazatetracyclo[7.6.0.0¹,⁵.0¹¹,¹⁵]pentadeca-3,11,13-trien-10-one

CAS Registry Number

Not Available

SMILES

NC1=NC2(O)CCCN3C(=O)C4=CC(Br)=C(Br)N4C23N1

InChI Identifier

InChI=1S/C11H11Br2N5O2/c12-5-4-6-8(19)17-3-1-2-10(20)11(17,16-9(14)15-10)18(6)7(5)13/h4,20H,1-3H2,(H3,14,15,16)

InChI Key

LERJEFMIFQBNIN-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
Agelas dispar	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as imidazopyridines. These are organic polycyclic compounds containing an imidazole ring fused to a pyridine ring. Imidazole is 5-membered ring consisting of three carbon atoms, and two nitrogen centers at the 1- and 3-positions. Pyridine is a 6-membered ring consisting of five carbon atoms and one nitrogen center.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Imidazopyridines

Sub Class

Not Available

Direct Parent

Imidazopyridines

Alternative Parents

Substituents

Imidazopyridine
2-heteroaryl carboxamide
Aryl bromide
Aryl halide
Piperidine
Substituted pyrrole
2-imidazoline
Heteroaromatic compound
Pyrrole
Tertiary carboxylic acid amide
Carboxamide group
Guanidine
Lactam
Ortho amide
Carboxylic acid derivative
Alkanolamine
Azacycle
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Carboximidamide
Organic nitrogen compound
Organooxygen compound
Organonitrogen compound
Organobromide
Organohalogen compound
Hydrocarbon derivative
Organic oxide
Amine
Organic oxygen 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	0.79	ALOGPS
logP	1.16	ChemAxon
logS	-2.2	ALOGPS
pKa (Strongest Acidic)	10.72	ChemAxon
pKa (Strongest Basic)	6.81	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	95.88 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	78.28 m³·mol⁻¹	ChemAxon
Polarizability	30.8 Å³	ChemAxon
Number of Rings	4	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

14351174

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 13,14-dibromo-5-hydroxy-3-imino-2,4,9,15-tetraazatetracyclo[7.6.0.0¹,⁵.0¹¹,¹⁵]pentadeca-11,13-dien-10-one (NP0289413)

MOL for NP0289413 (13,14-dibromo-5-hydroxy-3-imino-2,4,9,15-tetraazatetracyclo[7.6.0.0¹,⁵.0¹¹,¹⁵]pentadeca-11,13-dien-10-one)

3D MOL for NP0289413 (13,14-dibromo-5-hydroxy-3-imino-2,4,9,15-tetraazatetracyclo[7.6.0.0¹,⁵.0¹¹,¹⁵]pentadeca-11,13-dien-10-one)

3D SDF for NP0289413 (13,14-dibromo-5-hydroxy-3-imino-2,4,9,15-tetraazatetracyclo[7.6.0.0¹,⁵.0¹¹,¹⁵]pentadeca-11,13-dien-10-one)

3D-SDF for NP0289413 (13,14-dibromo-5-hydroxy-3-imino-2,4,9,15-tetraazatetracyclo[7.6.0.0¹,⁵.0¹¹,¹⁵]pentadeca-11,13-dien-10-one)

PDB for NP0289413 (13,14-dibromo-5-hydroxy-3-imino-2,4,9,15-tetraazatetracyclo[7.6.0.0¹,⁵.0¹¹,¹⁵]pentadeca-11,13-dien-10-one)

3D PDB for NP0289413 (13,14-dibromo-5-hydroxy-3-imino-2,4,9,15-tetraazatetracyclo[7.6.0.0¹,⁵.0¹¹,¹⁵]pentadeca-11,13-dien-10-one)

SMILES for NP0289413 (13,14-dibromo-5-hydroxy-3-imino-2,4,9,15-tetraazatetracyclo[7.6.0.0¹,⁵.0¹¹,¹⁵]pentadeca-11,13-dien-10-one)

INCHI for NP0289413 (13,14-dibromo-5-hydroxy-3-imino-2,4,9,15-tetraazatetracyclo[7.6.0.0¹,⁵.0¹¹,¹⁵]pentadeca-11,13-dien-10-one)

Structure for NP0289413 (13,14-dibromo-5-hydroxy-3-imino-2,4,9,15-tetraazatetracyclo[7.6.0.0¹,⁵.0¹¹,¹⁵]pentadeca-11,13-dien-10-one)

3D Structure for NP0289413 (13,14-dibromo-5-hydroxy-3-imino-2,4,9,15-tetraazatetracyclo[7.6.0.0¹,⁵.0¹¹,¹⁵]pentadeca-11,13-dien-10-one)