NP-MRD: Showing NP-Card for 2-hydroxy-6-methyl-6,11-diazatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),3,9,12,14-pentaene-4-carboximidic acid (NP0208760)

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Record Information

Version

2.0

Created at

2022-09-05 05:53:22 UTC

Updated at

2022-09-05 05:53:22 UTC

NP-MRD ID

NP0208760

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-hydroxy-6-methyl-6,11-diazatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),3,9,12,14-pentaene-4-carboximidic acid

Description

2-Hydroxy-6-methyl-6,11-diazatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]Hexadeca-1(16),3,9,12,14-pentaene-4-carboximidic acid belongs to the class of organic compounds known as lysergamides. These are amides of Lysergic acids. Based on a literature review very few articles have been published on 2-hydroxy-6-methyl-6,11-diazatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]Hexadeca-1(16),3,9,12,14-pentaene-4-carboximidic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 38 41  0  0  0  0  0  0  0  0999 V2000
    2.6517    3.0609   -0.1795 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5157    2.5468    0.0253 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5607    1.2895    0.0518 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7827    0.6816    0.3399 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4298    0.4443   -0.1966 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2501    0.9661   -0.4737 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1666   -0.0609   -0.7098 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3930   -0.8278   -1.8258 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1124    0.6609   -0.8187 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2513    1.9140   -1.4278 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5073    2.4711   -1.4493 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6229    1.8382   -0.8948 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4648    0.6044   -0.3005 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3080   -0.2779    0.3162 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5624   -1.3492    0.7005 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2295   -1.1550    0.3284 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2172    0.0627   -0.2851 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9642   -1.9171    0.4431 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1959   -0.9551    0.5300 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4625   -1.6314    0.6216 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9246   -1.8221    1.9670 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5056   -1.0492   -0.1604 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2073    0.9668    1.2325 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0442    2.0117   -0.5275 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4153   -0.2881   -2.6405 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3733    2.3567   -1.8462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6184    3.4504   -1.9243 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6044    2.3039   -0.9267 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3211   -0.1083    0.4397 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9365   -2.2153    1.2124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8104   -2.5665   -0.4603 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0425   -2.5693    1.3260 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0940   -0.3268    1.4407 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1816   -2.3036    2.6330 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7786   -2.5553    1.9075 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3500   -0.8884    2.4145 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4947   -1.3396    0.3036 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5423   -1.4231   -1.1862 H   0  0  0  0  0  0  0  0  0  0  0  0
 21 20  1  0
 20 22  1  0
 22  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  6
  7 19  1  0
 19 18  1  0
 18 16  1  0
 16 15  2  0
 15 14  1  0
 14 13  1  0
 13 12  2  0
 12 11  1  0
 11 10  2  0
 10  9  1  0
  9 17  2  0
  5  3  1  0
  3  4  1  0
  3  2  2  0
 19 20  1  0
 17 16  1  0
  9  7  1  0
 17 13  1  0
 21 34  1  0
 21 35  1  0
 21 36  1  0
 22 37  1  0
 22 38  1  0
  6 24  1  0
  8 25  1  0
 19 33  1  1
 18 31  1  0
 18 32  1  0
 15 30  1  0
 14 29  1  0
 12 28  1  0
 11 27  1  0
 10 26  1  0
  4 23  1  0
  2  1  1  0
M  END


  Mrv1652309052207532D          

 21 24  0  0  0  0            999 V2000
    3.2789    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    1.2375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4223    0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8500   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5771   -1.3590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7925   -1.6139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1794   -1.0619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3509   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1340    0.4125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.3509    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1355    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1355   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8500    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.8250    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  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  4  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 11 19  2  0  0  0  0
 15 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
  2 21  1  0  0  0  0
  9 21  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0208760

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CN1CC(=CC2(O)C1CC1=CNC3=CC=CC2=C13)C(O)=N

> <INCHI_IDENTIFIER>
InChI=1S/C16H17N3O2/c1-19-8-10(15(17)20)6-16(21)11-3-2-4-12-14(11)9(7-18-12)5-13(16)19/h2-4,6-7,13,18,21H,5,8H2,1H3,(H2,17,20)

> <INCHI_KEY>
MVQSONRXBDJXNB-UHFFFAOYSA-N

> <FORMULA>
C16H17N3O2

> <MOLECULAR_WEIGHT>
283.331

> <EXACT_MASS>
283.132076799

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
38

> <JCHEM_AVERAGE_POLARIZABILITY>
30.01106963681025

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-hydroxy-6-methyl-6,11-diazatetracyclo[7.6.1.0^{2,7}.0^{12,16}]hexadeca-1(16),3,9,12,14-pentaene-4-carboximidic acid

> <JCHEM_LOGP>
-1.439972794916516

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
13.233105947523857

> <JCHEM_PKA_STRONGEST_ACIDIC>
0.11905886843735658

> <JCHEM_PKA_STRONGEST_BASIC>
12.367999997430472

> <JCHEM_POLAR_SURFACE_AREA>
83.34

> <JCHEM_REFRACTIVITY>
91.6267

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
2-hydroxy-6-methyl-6,11-diazatetracyclo[7.6.1.0^{2,7}.0^{12,16}]hexadeca-1(16),3,9,12,14-pentaene-4-carboximidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0       6.121   3.850   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0       6.121   2.310   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0       7.454   1.540   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.454   0.000   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.788  -0.770   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0      10.122   0.000   0.000  0.00  0.00           N+0
HETATM    7  O   UNK     0       8.788  -2.310   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       6.121  -0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.787   0.000   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       4.787  -1.540   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       3.453  -0.770   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.944  -2.537   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.479  -3.013   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.335  -1.982   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.655  -0.476   0.000  0.00  0.00           C+0
HETATM   16  N   UNK     0      -0.250   0.770   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0       0.655   2.016   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.120   1.540   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.120  -0.000   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.453   2.310   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.787   1.540   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   21                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    8                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5                                                            
CONECT    8    4    9                                                       
CONECT    9    8   10   11   21                                             
CONECT   10    9                                                            
CONECT   11    9   12   19                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   19                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18   11   15                                                  
CONECT   20   18   21                                                       
CONECT   21   20    2    9                                                  
MASTER        0    0    0    0    0    0    0    0   21    0   48    0
END

View in JSmol

Synonyms

Value	Source
2-Hydroxy-6-methyl-6,11-diazatetracyclo[7.6.1.0,.0,]hexadeca-1(16),3,9,12,14-pentaene-4-carboximidate	Generator

Chemical Formula

C₁₆H₁₇N₃O₂

Average Mass

283.3310 Da

Monoisotopic Mass

283.13208 Da

IUPAC Name

2-hydroxy-6-methyl-6,11-diazatetracyclo[7.6.1.0^{2,7}.0^{12,16}]hexadeca-1(16),3,9,12,14-pentaene-4-carboximidic acid

Traditional Name

2-hydroxy-6-methyl-6,11-diazatetracyclo[7.6.1.0^{2,7}.0^{12,16}]hexadeca-1(16),3,9,12,14-pentaene-4-carboximidic acid

CAS Registry Number

Not Available

SMILES

CN1CC(=CC2(O)C1CC1=CNC3=CC=CC2=C13)C(O)=N

InChI Identifier

InChI=1S/C16H17N3O2/c1-19-8-10(15(17)20)6-16(21)11-3-2-4-12-14(11)9(7-18-12)5-13(16)19/h2-4,6-7,13,18,21H,5,8H2,1H3,(H2,17,20)

InChI Key

MVQSONRXBDJXNB-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 lysergamides. These are amides of Lysergic acids.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Ergoline and derivatives

Sub Class

Lysergic acids and derivatives

Direct Parent

Lysergamides

Alternative Parents

Substituents

Lysergic acid amide
Benzoquinoline
Pyrroloquinoline
Quinoline
3-alkylindole
Indole
Indole or derivatives
Isoindole or derivatives
Aralkylamine
Benzenoid
Heteroaromatic compound
Tertiary alcohol
Pyrrole
Tertiary aliphatic amine
Tertiary amine
Azacycle
Organoheterocyclic compound
Carboximidic acid
Carboximidic acid derivative
Amine
Alcohol
Organic nitrogen compound
Hydrocarbon derivative
Organic oxygen compound
Organonitrogen compound
Organooxygen compound
Organopnictogen 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	-1.4	ChemAxon
pKa (Strongest Acidic)	0.12	ChemAxon
pKa (Strongest Basic)	12.37	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	83.34 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	91.63 m³·mol⁻¹	ChemAxon
Polarizability	30.01 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	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

85697758

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-hydroxy-6-methyl-6,11-diazatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),3,9,12,14-pentaene-4-carboximidic acid (NP0208760)

MOL for NP0208760 (2-hydroxy-6-methyl-6,11-diazatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),3,9,12,14-pentaene-4-carboximidic acid)

3D MOL for NP0208760 (2-hydroxy-6-methyl-6,11-diazatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),3,9,12,14-pentaene-4-carboximidic acid)

3D SDF for NP0208760 (2-hydroxy-6-methyl-6,11-diazatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),3,9,12,14-pentaene-4-carboximidic acid)

3D-SDF for NP0208760 (2-hydroxy-6-methyl-6,11-diazatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),3,9,12,14-pentaene-4-carboximidic acid)

PDB for NP0208760 (2-hydroxy-6-methyl-6,11-diazatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),3,9,12,14-pentaene-4-carboximidic acid)

3D PDB for NP0208760 (2-hydroxy-6-methyl-6,11-diazatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),3,9,12,14-pentaene-4-carboximidic acid)

SMILES for NP0208760 (2-hydroxy-6-methyl-6,11-diazatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),3,9,12,14-pentaene-4-carboximidic acid)

INCHI for NP0208760 (2-hydroxy-6-methyl-6,11-diazatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),3,9,12,14-pentaene-4-carboximidic acid)

Structure for NP0208760 (2-hydroxy-6-methyl-6,11-diazatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),3,9,12,14-pentaene-4-carboximidic acid)

3D Structure for NP0208760 (2-hydroxy-6-methyl-6,11-diazatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),3,9,12,14-pentaene-4-carboximidic acid)