NP-MRD: Showing NP-Card for (12s)-11-methyl-3,5-dioxa-11,13-diazapentacyclo[10.8.1.0²,⁶.0⁸,²¹.0¹⁵,²⁰]henicosa-1(21),2(6),7,13,15,17,19-heptaene (NP0244157)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-07 04:52:46 UTC

Updated at

2022-09-07 04:52:46 UTC

NP-MRD ID

NP0244157

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(12s)-11-methyl-3,5-dioxa-11,13-diazapentacyclo[10.8.1.0²,⁶.0⁸,²¹.0¹⁵,²⁰]henicosa-1(21),2(6),7,13,15,17,19-heptaene

Description

(12S)-11-methyl-3,5-dioxa-11,13-diazapentacyclo[10.8.1.0²,⁶.0⁸,²¹.0¹⁵,²⁰]Henicosa-1(21),2(6),7,13,15,17,19-heptaene belongs to the class of organic compounds known as azahomoaporphines. These are analogues of homoaporphines where a nitrogen atom replaces one carbon atom of the cyclopheptane ring. Based on a literature review very few articles have been published on (12S)-11-methyl-3,5-dioxa-11,13-diazapentacyclo[10.8.1.0²,⁶.0⁸,²¹.0¹⁵,²⁰]Henicosa-1(21),2(6),7,13,15,17,19-heptaene.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 38 42  0  0  0  0  0  0  0  0999 V2000
   -3.2473    1.9354    0.5908 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4715    0.7351    0.5532 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2973   -0.4723    0.6837 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7815   -1.6568   -0.0823 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2776   -1.7351   -0.0837 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5769   -2.8907    0.1144 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7991   -2.8122    0.1473 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4804   -1.5929   -0.0116 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7277   -0.4682   -0.2015 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6712   -0.5040   -0.2510 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6543    0.5585   -0.5813 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1638    1.6402   -1.3225 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0915    2.2735   -1.5385 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1751    1.9101   -0.8871 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0569    2.9692   -0.8744 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2751    2.8567   -0.2238 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6041    1.6802    0.4145 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7242    0.5826    0.4181 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5404    0.7355   -0.2376 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8109   -1.8584    0.0595 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9981   -3.1244    0.6495 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7833   -3.7702    0.3214 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8689    2.7391   -0.0622 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2034    2.3583    1.6357 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3214    1.7635    0.3842 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3186   -0.2414    0.2704 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3269   -0.7289    1.7512 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1829   -1.7600   -1.1057 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1428   -2.5857    0.4522 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1135   -3.8407    0.2411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3813    0.0531   -1.3533 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0168    3.1128   -2.2016 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7784    3.8861   -1.3813 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9513    3.6936   -0.2256 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5312    1.5347    0.9353 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9469   -0.2949    0.9614 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8848   -3.6534    0.2677 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0417   -3.0281    1.7734 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8 20  1  0
 20 21  1  0
 21 22  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 11  2  1  0
 19 14  1  0
 10  5  1  0
 22  7  1  0
 19  9  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  3 26  1  0
  3 27  1  0
  4 28  1  0
  4 29  1  0
  6 30  1  0
 21 37  1  0
 21 38  1  0
 11 31  1  6
 13 32  1  0
 15 33  1  0
 16 34  1  0
 17 35  1  0
 18 36  1  0
M  END


  Mrv1652309072206522D          

 22 26  0  0  1  0            999 V2000
    1.2932   -2.4890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3457   -1.6657    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6816   -1.1762    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7734   -0.3563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5294   -0.0259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6212    0.7940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3772    1.1244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0413    0.6349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9495   -0.1850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1935   -0.5154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9805   -1.3124    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4708   -1.9759    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.2953   -2.0062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8330   -1.3805    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6119   -1.6525    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2369   -1.1140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0830   -0.3034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3041   -0.0315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6791   -0.5700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7120    1.1152    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4625    1.9016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6375    1.9072    0.0000 O   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
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  5 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11  2  1  6  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  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 14 19  1  0  0  0  0
  9 19  1  0  0  0  0
  8 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
  7 22  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0244157

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CN1CCC2=CC3=C(OCO3)C3=C2[C@@H]1N=CC1=CC=CC=C31

> <INCHI_IDENTIFIER>
InChI=1S/C18H16N2O2/c1-20-7-6-11-8-14-17(22-10-21-14)16-13-5-3-2-4-12(13)9-19-18(20)15(11)16/h2-5,8-9,18H,6-7,10H2,1H3/t18-/m1/s1

> <INCHI_KEY>
IYXPLTSTKGDBLL-GOSISDBHSA-N

> <FORMULA>
C18H16N2O2

> <MOLECULAR_WEIGHT>
292.338

> <EXACT_MASS>
292.121177763

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
38

> <JCHEM_AVERAGE_POLARIZABILITY>
31.825082566764962

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(12S)-11-methyl-3,5-dioxa-11,13-diazapentacyclo[10.8.1.0^{2,6}.0^{8,21}.0^{15,20}]henicosa-1(21),2(6),7,13,15,17,19-heptaene

> <JCHEM_LOGP>
3.328182969666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
3.2749428196678125

> <JCHEM_POLAR_SURFACE_AREA>
34.06

> <JCHEM_REFRACTIVITY>
85.11980000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(12S)-11-methyl-3,5-dioxa-11,13-diazapentacyclo[10.8.1.0^{2,6}.0^{8,21}.0^{15,20}]henicosa-1(21),2(6),7,13,15,17,19-heptaene

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0       2.414  -4.646   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0       2.512  -3.109   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0       1.272  -2.196   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.444  -0.665   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.855  -0.048   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.026   1.482   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.437   2.099   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.677   1.185   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.506  -0.345   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.095  -0.962   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.697  -2.450   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0       4.612  -3.688   0.000  0.00  0.00           N+0
HETATM   13  C   UNK     0       6.151  -3.745   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.155  -2.577   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.609  -3.085   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.775  -2.079   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.488  -0.566   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.034  -0.059   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.868  -1.064   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       6.929   2.082   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       6.463   3.550   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       4.923   3.560   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   11                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   10                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   22                                                  
CONECT    8    7    9   20                                                  
CONECT    9    8   10   19                                                  
CONECT   10    9    5   11                                                  
CONECT   11   10    2   12                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   19                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   14    9                                                  
CONECT   20    8   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21    7                                                       
MASTER        0    0    0    0    0    0    0    0   22    0   52    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₁₆N₂O₂

Average Mass

292.3380 Da

Monoisotopic Mass

292.12118 Da

IUPAC Name

(12S)-11-methyl-3,5-dioxa-11,13-diazapentacyclo[10.8.1.0^{2,6}.0^{8,21}.0^{15,20}]henicosa-1(21),2(6),7,13,15,17,19-heptaene

Traditional Name

(12S)-11-methyl-3,5-dioxa-11,13-diazapentacyclo[10.8.1.0^{2,6}.0^{8,21}.0^{15,20}]henicosa-1(21),2(6),7,13,15,17,19-heptaene

CAS Registry Number

Not Available

SMILES

CN1CCC2=CC3=C(OCO3)C3=C2[C@@H]1N=CC1=CC=CC=C31

InChI Identifier

InChI=1S/C18H16N2O2/c1-20-7-6-11-8-14-17(22-10-21-14)16-13-5-3-2-4-12(13)9-19-18(20)15(11)16/h2-5,8-9,18H,6-7,10H2,1H3/t18-/m1/s1

InChI Key

IYXPLTSTKGDBLL-GOSISDBHSA-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 azahomoaporphines. These are analogues of homoaporphines where a nitrogen atom replaces one carbon atom of the cyclopheptane ring.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Azahomoaporphines

Sub Class

Not Available

Direct Parent

Azahomoaporphines

Alternative Parents

Substituents

Azahomoaporphine
Benzazepine
Tetrahydroisoquinoline
Benzodioxole
Azepine
Benzenoid
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Acetal
Oxacycle
Azacycle
Organooxygen compound
Organonitrogen compound
Imine
Hydrocarbon derivative
Organopnictogen compound
Organic oxygen compound
Organic nitrogen 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	3.33	ChemAxon
pKa (Strongest Basic)	3.27	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	34.06 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	85.12 m³·mol⁻¹	ChemAxon
Polarizability	31.83 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	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

163073108

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (12s)-11-methyl-3,5-dioxa-11,13-diazapentacyclo[10.8.1.0²,⁶.0⁸,²¹.0¹⁵,²⁰]henicosa-1(21),2(6),7,13,15,17,19-heptaene (NP0244157)

MOL for NP0244157 ((12s)-11-methyl-3,5-dioxa-11,13-diazapentacyclo[10.8.1.0²,⁶.0⁸,²¹.0¹⁵,²⁰]henicosa-1(21),2(6),7,13,15,17,19-heptaene)

3D MOL for NP0244157 ((12s)-11-methyl-3,5-dioxa-11,13-diazapentacyclo[10.8.1.0²,⁶.0⁸,²¹.0¹⁵,²⁰]henicosa-1(21),2(6),7,13,15,17,19-heptaene)

3D SDF for NP0244157 ((12s)-11-methyl-3,5-dioxa-11,13-diazapentacyclo[10.8.1.0²,⁶.0⁸,²¹.0¹⁵,²⁰]henicosa-1(21),2(6),7,13,15,17,19-heptaene)

3D-SDF for NP0244157 ((12s)-11-methyl-3,5-dioxa-11,13-diazapentacyclo[10.8.1.0²,⁶.0⁸,²¹.0¹⁵,²⁰]henicosa-1(21),2(6),7,13,15,17,19-heptaene)

PDB for NP0244157 ((12s)-11-methyl-3,5-dioxa-11,13-diazapentacyclo[10.8.1.0²,⁶.0⁸,²¹.0¹⁵,²⁰]henicosa-1(21),2(6),7,13,15,17,19-heptaene)

3D PDB for NP0244157 ((12s)-11-methyl-3,5-dioxa-11,13-diazapentacyclo[10.8.1.0²,⁶.0⁸,²¹.0¹⁵,²⁰]henicosa-1(21),2(6),7,13,15,17,19-heptaene)

SMILES for NP0244157 ((12s)-11-methyl-3,5-dioxa-11,13-diazapentacyclo[10.8.1.0²,⁶.0⁸,²¹.0¹⁵,²⁰]henicosa-1(21),2(6),7,13,15,17,19-heptaene)

INCHI for NP0244157 ((12s)-11-methyl-3,5-dioxa-11,13-diazapentacyclo[10.8.1.0²,⁶.0⁸,²¹.0¹⁵,²⁰]henicosa-1(21),2(6),7,13,15,17,19-heptaene)

Structure for NP0244157 ((12s)-11-methyl-3,5-dioxa-11,13-diazapentacyclo[10.8.1.0²,⁶.0⁸,²¹.0¹⁵,²⁰]henicosa-1(21),2(6),7,13,15,17,19-heptaene)

3D Structure for NP0244157 ((12s)-11-methyl-3,5-dioxa-11,13-diazapentacyclo[10.8.1.0²,⁶.0⁸,²¹.0¹⁵,²⁰]henicosa-1(21),2(6),7,13,15,17,19-heptaene)