NP-MRD: Showing NP-Card for 8-hydroxy-13-methoxy-1,6-diazatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁵]hexadeca-5,7,9(16),10(15),11,13-hexaen-2-one (NP0320721)

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Record Information

Version

2.0

Created at

2022-09-11 22:32:28 UTC

Updated at

2022-09-11 22:32:29 UTC

NP-MRD ID

NP0320721

Secondary Accession Numbers

None

Natural Product Identification

Common Name

8-hydroxy-13-methoxy-1,6-diazatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁵]hexadeca-5,7,9(16),10(15),11,13-hexaen-2-one

Description

8-Hydroxy-13-methoxy-1,6-diazatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁵]Hexadeca-5(16),6,8,10(15),11,13-hexaen-2-one belongs to the class of organic compounds known as indolonaphthyridine alkaloids. These are a numerous and relatively straightforward subgroup of the b-carbolines, e.G. Canthin-6-one, in which an additional C3 unit is attached between C-1 and the indole nitrogen to form an additional ring. The group includes a few dimeric examples, such as Haplophytine. 8-hydroxy-13-methoxy-1,6-diazatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁵]hexadeca-5,7,9(16),10(15),11,13-hexaen-2-one is found in Eurycoma longifolia. It was first documented in 2002 (PMID: 31593387). Based on a literature review a significant number of articles have been published on 8-hydroxy-13-methoxy-1,6-diazatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁵]Hexadeca-5(16),6,8,10(15),11,13-hexaen-2-one (PMID: 27253005) (PMID: 27583328) (PMID: 36127157) (PMID: 36127156) (PMID: 36127155) (PMID: 36127154).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 32 35  0  0  0  0  0  0  0  0999 V2000
    4.7042   -1.2740    0.0141 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3532    0.0691   -0.1228 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0102    0.4620   -0.1215 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6643    1.7925   -0.2571 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3414    2.1871   -0.2566 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3504    1.2391   -0.1187 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0284    1.3560   -0.0853 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9463    2.3953   -0.1696 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4897    3.6781   -0.3271 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2847    2.0347   -0.0847 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7006    0.7412    0.0726 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7803   -0.2624    0.1529 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4574    0.0613    0.0726 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4463   -0.8065    0.1345 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7097   -0.1168    0.0193 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0318   -0.4916    0.0167 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7618   -2.1928    0.2984 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1627   -2.9923    0.6637 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1325   -2.6557    0.0433 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2191   -1.6496    0.3219 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7920   -1.3206    0.2358 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1923   -1.7909    0.8455 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4563   -1.7815   -0.9561 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4737    2.5154   -0.3641 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0620    3.2181   -0.3614 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0755    4.4912   -0.3975 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0294    2.8163   -0.1463 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2958   -1.5516    0.1251 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2091   -3.0652   -0.9792 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3242   -3.5185    0.7466 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6275   -1.7709    1.3525 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0870   -1.8163   -0.3675 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3 16  2  0
 16 15  1  0
 15  6  2  0
  6  5  1  0
  5  4  2  0
  6  7  1  0
  7 13  2  0
 13 14  1  0
 14 17  1  0
 17 18  2  0
 17 19  1  0
 19 20  1  0
 20 12  1  0
 12 11  2  0
 11 10  1  0
 10  8  2  0
  8  9  1  0
  4  3  1  0
  8  7  1  0
 14 15  1  0
 12 13  1  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
 16 28  1  0
  5 25  1  0
  4 24  1  0
 19 29  1  0
 19 30  1  0
 20 31  1  0
 20 32  1  0
 10 27  1  0
  9 26  1  0
M  END


  Mrv1652309122200322D          

 20 23  0  0  0  0            999 V2000
    3.5934    1.5402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3384    0.7556    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5314    0.5840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2765   -0.2006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4695   -0.3721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9175    0.2410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0925    0.2410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4595   -0.3721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2046   -1.1567    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2665   -0.2006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5214    0.5840    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9694    1.1971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1624    1.0256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5050    1.5105    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1724    1.0256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9794    1.1971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4188    2.3310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0862    2.8159    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3349    2.6666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0023    2.1816    0.0000 C   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  1  0  0  0  0
  4  5  2  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  1  0  0  0  0
  8 10  2  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
  7 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
  6 15  2  0  0  0  0
 15 16  1  0  0  0  0
  3 16  2  0  0  0  0
 14 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 12 20  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0320721

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC2=C(C=C1)C1=C3N2C(=O)CCC3=NC=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C15H12N2O3/c1-20-8-2-3-9-11(6-8)17-13(19)5-4-10-15(17)14(9)12(18)7-16-10/h2-3,6-7,18H,4-5H2,1H3

> <INCHI_KEY>
SIUWQFWHIAGMLE-UHFFFAOYSA-N

> <FORMULA>
C15H12N2O3

> <MOLECULAR_WEIGHT>
268.272

> <EXACT_MASS>
268.084792254

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
32

> <JCHEM_AVERAGE_POLARIZABILITY>
27.569449202689874

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
8-hydroxy-13-methoxy-1,6-diazatetracyclo[7.6.1.0^{5,16}.0^{10,15}]hexadeca-5,7,9(16),10(15),11,13-hexaen-2-one

> <JCHEM_LOGP>
0.9113644146666665

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.18026011237662

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.499876945377158

> <JCHEM_PKA_STRONGEST_BASIC>
3.8425182613093902

> <JCHEM_POLAR_SURFACE_AREA>
64.35

> <JCHEM_REFRACTIVITY>
71.8708

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
8-hydroxy-13-methoxy-1,6-diazatetracyclo[7.6.1.0^{5,16}.0^{10,15}]hexadeca-5,7,9(16),10(15),11,13-hexaen-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0       6.708   2.875   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       6.232   1.410   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       4.725   1.090   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.249  -0.374   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.743  -0.695   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.713   0.450   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.173   0.450   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.858  -0.695   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -0.382  -2.159   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -2.364  -0.374   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0      -2.840   1.090   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0      -1.810   2.235   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.303   1.914   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0       0.943   2.820   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0       2.189   1.914   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.695   2.235   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.782   4.351   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       2.028   5.256   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -0.625   4.978   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.871   4.072   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   16                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   15                                                  
CONECT    7    6    8   13                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   20                                                  
CONECT   13   12    7   14                                                  
CONECT   14   13   15   17                                                  
CONECT   15   14    6   16                                                  
CONECT   16   15    3                                                       
CONECT   17   14   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   12                                                       
MASTER        0    0    0    0    0    0    0    0   20    0   46    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₁₂N₂O₃

Average Mass

268.2720 Da

Monoisotopic Mass

268.08479 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

COC1=CC2=C(C=C1)C1=C3N2C(=O)CCC3=NC=C1O

InChI Identifier

InChI=1S/C15H12N2O3/c1-20-8-2-3-9-11(6-8)17-13(19)5-4-10-15(17)14(9)12(18)7-16-10/h2-3,6-7,18H,4-5H2,1H3

InChI Key

SIUWQFWHIAGMLE-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
Eurycoma longifolia	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as indolonaphthyridine alkaloids. These are a numerous and relatively straightforward subgroup of the b-carbolines, e.G. Canthin-6-one, in which an additional C3 unit is attached between C-1 and the indole nitrogen to form an additional ring. The group includes a few dimeric examples, such as Haplophytine.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Indolonaphthyridine alkaloids

Sub Class

Not Available

Direct Parent

Indolonaphthyridine alkaloids

Alternative Parents

Substituents

Indolo[3,2-1de][1,5]naphthyridine
Beta-carboline
Pyridoindole
Diazanaphthalene
Naphthyridine
Indole
Indole or derivatives
Anisole
Alkyl aryl ether
Hydroxypyridine
Pyridine
Benzenoid
Heteroaromatic compound
Pyrrole
Lactam
Azacycle
Ether
Organoheterocyclic compound
Organooxygen compound
Organonitrogen compound
Organic nitrogen compound
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
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	0.91	ChemAxon
pKa (Strongest Acidic)	8.5	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

163048154

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Authors unspecified: Childhood Vascular Tumors Treatment (PDQ(R)): Patient Version. 2002. [PubMed:27253005 ]
Authors unspecified: Childhood Esophageal Cancer Treatment (PDQ(R)): Health Professional Version. 2002. [PubMed:31593387 ]
Authors unspecified: Financial Toxicity and Cancer Treatment (PDQ(R)): Health Professional Version. 2002. [PubMed:27583328 ]
Gadot R, Najera R, Hirani S, Anand A, Storch E, Goodman WK, Shofty B, Sheth SA: Efficacy of deep brain stimulation for treatment-resistant obsessive-compulsive disorder: systematic review and meta-analysis. J Neurol Neurosurg Psychiatry. 2022 Sep 20. pii: jnnp-2021-328738. doi: 10.1136/jnnp-2021-328738. [PubMed:36127157 ]
Koggel LM, Lantinga MA, Buchner FL, Drenth JPH, Frankema JS, Heeregrave EJ, Heringa M, Numans ME, Siersema PD: Predictors for inappropriate proton pump inhibitor use: observational study in primary care. Br J Gen Pract. 2022 Jun 24. pii: BJGP.2022.0178. doi: 10.3399/BJGP.2022.0178. [PubMed:36127156 ]
Lynch C, Harrison S, Emery JD, Clelland C, Dorman L, Collins C, Johansen ML, Lawrenson R, Surgey A, Weller D, Jarbol DE, Balasubramaniam K, Nicholson BD: Variation in suspected cancer referral pathways in primary care: comparative analysis across the International Benchmarking Cancer Partnership. Br J Gen Pract. 2022 Jun 22. pii: BJGP.2022.0110. doi: 10.3399/BJGP.2022.0110. [PubMed:36127155 ]
Barends H, Botman F, Walstock E, Dessel NC, van der Wouden JC, Olde Hartman T, Dekker J, van der Horst HE: Lost in fragmentation - care coordination when somatic symptoms persist: a qualitative study of patients' experiences. Br J Gen Pract. 2022 Oct 27;72(724):e790-e798. doi: 10.3399/BJGP.2021.0566. Print 2022 Nov. [PubMed:36127154 ]
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LOTUS database [Link]

Showing NP-Card for 8-hydroxy-13-methoxy-1,6-diazatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁵]hexadeca-5,7,9(16),10(15),11,13-hexaen-2-one (NP0320721)

MOL for NP0320721 (8-hydroxy-13-methoxy-1,6-diazatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁵]hexadeca-5,7,9(16),10(15),11,13-hexaen-2-one)

3D MOL for NP0320721 (8-hydroxy-13-methoxy-1,6-diazatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁵]hexadeca-5,7,9(16),10(15),11,13-hexaen-2-one)

3D SDF for NP0320721 (8-hydroxy-13-methoxy-1,6-diazatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁵]hexadeca-5,7,9(16),10(15),11,13-hexaen-2-one)

3D-SDF for NP0320721 (8-hydroxy-13-methoxy-1,6-diazatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁵]hexadeca-5,7,9(16),10(15),11,13-hexaen-2-one)

PDB for NP0320721 (8-hydroxy-13-methoxy-1,6-diazatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁵]hexadeca-5,7,9(16),10(15),11,13-hexaen-2-one)

3D PDB for NP0320721 (8-hydroxy-13-methoxy-1,6-diazatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁵]hexadeca-5,7,9(16),10(15),11,13-hexaen-2-one)

SMILES for NP0320721 (8-hydroxy-13-methoxy-1,6-diazatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁵]hexadeca-5,7,9(16),10(15),11,13-hexaen-2-one)

INCHI for NP0320721 (8-hydroxy-13-methoxy-1,6-diazatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁵]hexadeca-5,7,9(16),10(15),11,13-hexaen-2-one)

Structure for NP0320721 (8-hydroxy-13-methoxy-1,6-diazatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁵]hexadeca-5,7,9(16),10(15),11,13-hexaen-2-one)

3D Structure for NP0320721 (8-hydroxy-13-methoxy-1,6-diazatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁵]hexadeca-5,7,9(16),10(15),11,13-hexaen-2-one)