NP-MRD: Showing NP-Card for 10-[(3z)-3-ethylidene-1h,2h,4h,6h,7h,12h,12bh-indolo[2,3-a]quinolizin-2-yl]-12-oxa-8,17-diazaheptacyclo[15.5.2.0¹,¹⁸.0²,⁷.0⁸,²².0¹¹,²¹.0¹⁵,²⁰]tetracosa-2,4,6,9,14-pentaene (NP0237855)

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Record Information

Version

2.0

Created at

2022-09-06 21:07:24 UTC

Updated at

2022-09-06 21:07:24 UTC

NP-MRD ID

NP0237855

Secondary Accession Numbers

None

Natural Product Identification

Common Name

10-[(3z)-3-ethylidene-1h,2h,4h,6h,7h,12h,12bh-indolo[2,3-a]quinolizin-2-yl]-12-oxa-8,17-diazaheptacyclo[15.5.2.0¹,¹⁸.0²,⁷.0⁸,²².0¹¹,²¹.0¹⁵,²⁰]tetracosa-2,4,6,9,14-pentaene

Description

Longicautadine belongs to the class of organic compounds known as strychnos alkaloids. These are alkaloids having a core structure based on the strychnan, stemmadenine (seco-curan), or the akuammicine (curan) skeleton. 10-[(3z)-3-ethylidene-1h,2h,4h,6h,7h,12h,12bh-indolo[2,3-a]quinolizin-2-yl]-12-oxa-8,17-diazaheptacyclo[15.5.2.0¹,¹⁸.0²,⁷.0⁸,²².0¹¹,²¹.0¹⁵,²⁰]tetracosa-2,4,6,9,14-pentaene is found in Strychnos chrysophylla, Strychnos matopensis, Strychnos ngouniensis and Strychnos nux-vomica. Based on a literature review very few articles have been published on Longicautadine.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062223072D          

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M  END

     RDKit          3D

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M  END


  Mrv1652309062223072D          

 43 53  0  0  0  0            999 V2000
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    7.1016   -4.5594    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.8276   -4.9512    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6046   -4.6739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2332   -5.2081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0849   -6.0196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3079   -6.2970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6792   -5.7628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6819   -5.0661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3249   -4.3223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5023   -4.2597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1452   -3.5159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3113   -3.4594    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9206   -2.6932    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1351   -2.3841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.8106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7064   -2.4122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6902   -1.5874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3964   -1.1609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1188   -1.5592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9035   -1.1906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5141   -0.3572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0586    0.3335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8877   -0.0036    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.8438   -0.0629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2092   -0.9031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8914   -1.4652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0470   -2.3060    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4698   -2.9206    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6262   -2.8249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1961   -2.0996    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5784   -1.3808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9948   -0.9226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4525   -0.6699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3620   -2.0130    0.0000 C   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
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  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
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
  8 16  1  0  0  0  0
 11 16  1  0  0  0  0
  9 17  1  0  0  0  0
  5 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
  3 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 23 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 20 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 34 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 32 42  1  0  0  0  0
 29 42  1  0  0  0  0
 39 43  1  0  0  0  0
 22 43  1  0  0  0  0
 29 43  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0237855

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C=C1/CN2CCC3=C(NC4=CC=CC=C34)C2CC1C1=CN2C3C4C5CC6N(CCC36C3=CC=CC=C23)CC5=CCOC14

> <INCHI_IDENTIFIER>
InChI=1S/C38H40N4O/c1-2-22-19-40-14-11-25-24-7-3-5-9-30(24)39-35(25)32(40)17-26(22)28-21-42-31-10-6-4-8-29(31)38-13-15-41-20-23-12-16-43-36(28)34(37(38)42)27(23)18-33(38)41/h2-10,12,21,26-27,32-34,36-37,39H,11,13-20H2,1H3/b22-2+

> <INCHI_KEY>
PTRWWFKHWVYDOM-QOABUSIESA-N

> <FORMULA>
C38H40N4O

> <MOLECULAR_WEIGHT>
568.765

> <EXACT_MASS>
568.320211924

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
83

> <JCHEM_AVERAGE_POLARIZABILITY>
66.08269440102717

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
10-[(3Z)-3-ethylidene-1H,2H,3H,4H,6H,7H,12H,12bH-indolo[2,3-a]quinolizin-2-yl]-12-oxa-8,17-diazaheptacyclo[15.5.2.0^{1,18}.0^{2,7}.0^{8,22}.0^{11,21}.0^{15,20}]tetracosa-2,4,6,9,14-pentaene

> <JCHEM_LOGP>
4.666422588999998

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
11

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
16.374076090423806

> <JCHEM_PKA_STRONGEST_BASIC>
9.768700703632115

> <JCHEM_POLAR_SURFACE_AREA>
34.74000000000001

> <JCHEM_REFRACTIVITY>
174.05469999999994

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
10-[(3Z)-3-ethylidene-1H,2H,4H,6H,7H,12H,12bH-indolo[2,3-a]quinolizin-2-yl]-12-oxa-8,17-diazaheptacyclo[15.5.2.0^{1,18}.0^{2,7}.0^{8,22}.0^{11,21}.0^{15,20}]tetracosa-2,4,6,9,14-pentaene

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0       5.131 -10.377   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.000  -9.106   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.535  -9.223   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.202 -10.611   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0       9.737 -10.728   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0      10.404 -12.116   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      11.939 -12.233   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      12.808 -10.962   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      12.142  -9.574   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0      13.256  -8.511   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0      14.611  -9.242   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      16.062  -8.725   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      17.235  -9.722   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      16.958 -11.237   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      15.508 -11.754   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      14.335 -10.757   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.606  -9.457   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.940  -8.068   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.404  -7.951   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.738  -6.563   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.181  -6.458   0.000  0.00  0.00           C+0
HETATM   22  N   UNK     0       5.452  -5.027   0.000  0.00  0.00           N+0
HETATM   23  C   UNK     0       3.986  -4.450   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.667  -5.246   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.319  -4.503   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.288  -2.963   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.607  -2.167   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.955  -2.911   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.420  -2.223   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       4.693  -0.667   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       5.709   0.623   0.000  0.00  0.00           C+0
HETATM   32  N   UNK     0       7.257  -0.007   0.000  0.00  0.00           N+0
HETATM   33  C   UNK     0       9.042  -0.117   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       9.724  -1.686   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      10.997  -2.735   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      11.288  -4.305   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      10.210  -5.452   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       8.636  -5.273   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       7.833  -3.919   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       8.546  -2.577   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       7.457  -1.722   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       6.445  -1.250   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       6.276  -3.758   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   19                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   17                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   16                                                  
CONECT    9    8   10   17                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   16                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15    8   11                                                  
CONECT   17    9    5   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18    3   20                                                  
CONECT   20   19   21   38                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   43                                                  
CONECT   23   22   24   28                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   23   29                                                  
CONECT   29   28   30   42   43                                             
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33   42                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35   40                                                  
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   20   39                                                  
CONECT   39   38   40   43                                                  
CONECT   40   39   34   41                                                  
CONECT   41   40   42                                                       
CONECT   42   41   32   29                                                  
CONECT   43   39   22   29                                                  
MASTER        0    0    0    0    0    0    0    0   43    0  106    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₈H₄₀N₄O

Average Mass

568.7650 Da

Monoisotopic Mass

568.32021 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C\C=C1/CN2CCC3=C(NC4=CC=CC=C34)C2CC1C1=CN2C3C4C5CC6N(CCC36C3=CC=CC=C23)CC5=CCOC14

InChI Identifier

InChI=1S/C38H40N4O/c1-2-22-19-40-14-11-25-24-7-3-5-9-30(24)39-35(25)32(40)17-26(22)28-21-42-31-10-6-4-8-29(31)38-13-15-41-20-23-12-16-43-36(28)34(37(38)42)27(23)18-33(38)41/h2-10,12,21,26-27,32-34,36-37,39H,11,13-20H2,1H3/b22-2+

InChI Key

PTRWWFKHWVYDOM-QOABUSIESA-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
Strychnos chrysophylla	LOTUS Database	35616633
Strychnos matopensis	LOTUS Database	35616633
Strychnos ngouniensis	LOTUS Database	35616633
Strychnos nux-vomica	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as strychnos alkaloids. These are alkaloids having a core structure based on the strychnan, stemmadenine (seco-curan), or the akuammicine (curan) skeleton.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Strychnos alkaloids

Sub Class

Not Available

Direct Parent

Strychnos alkaloids

Alternative Parents

Substituents

Strychnan skeleton
Akuammicine-skeleton
Stemmadenine-skeleton
Beta-carboline
Carbazole
Pyridoindole
Quinolizine
3-alkylindole
Indole
Indole or derivatives
Indolizidine
Tertiary aliphatic/aromatic amine
Aralkylamine
Tetrahydropyridine
N-alkylpyrrolidine
Benzenoid
Piperidine
Heteroaromatic compound
Pyrrole
Pyrrolidine
Tertiary aliphatic amine
Tertiary amine
Azacycle
Organoheterocyclic compound
Oxacycle
Dialkyl ether
Enamine
Ether
Allylamine
Amine
Organic nitrogen compound
Organonitrogen compound
Organooxygen compound
Hydrocarbon derivative
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

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

4585652

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5478042

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 10-[(3z)-3-ethylidene-1h,2h,4h,6h,7h,12h,12bh-indolo[2,3-a]quinolizin-2-yl]-12-oxa-8,17-diazaheptacyclo[15.5.2.0¹,¹⁸.0²,⁷.0⁸,²².0¹¹,²¹.0¹⁵,²⁰]tetracosa-2,4,6,9,14-pentaene (NP0237855)

MOL for NP0237855 (10-[(3z)-3-ethylidene-1h,2h,4h,6h,7h,12h,12bh-indolo[2,3-a]quinolizin-2-yl]-12-oxa-8,17-diazaheptacyclo[15.5.2.0¹,¹⁸.0²,⁷.0⁸,²².0¹¹,²¹.0¹⁵,²⁰]tetracosa-2,4,6,9,14-pentaene)

3D MOL for NP0237855 (10-[(3z)-3-ethylidene-1h,2h,4h,6h,7h,12h,12bh-indolo[2,3-a]quinolizin-2-yl]-12-oxa-8,17-diazaheptacyclo[15.5.2.0¹,¹⁸.0²,⁷.0⁸,²².0¹¹,²¹.0¹⁵,²⁰]tetracosa-2,4,6,9,14-pentaene)

3D SDF for NP0237855 (10-[(3z)-3-ethylidene-1h,2h,4h,6h,7h,12h,12bh-indolo[2,3-a]quinolizin-2-yl]-12-oxa-8,17-diazaheptacyclo[15.5.2.0¹,¹⁸.0²,⁷.0⁸,²².0¹¹,²¹.0¹⁵,²⁰]tetracosa-2,4,6,9,14-pentaene)

3D-SDF for NP0237855 (10-[(3z)-3-ethylidene-1h,2h,4h,6h,7h,12h,12bh-indolo[2,3-a]quinolizin-2-yl]-12-oxa-8,17-diazaheptacyclo[15.5.2.0¹,¹⁸.0²,⁷.0⁸,²².0¹¹,²¹.0¹⁵,²⁰]tetracosa-2,4,6,9,14-pentaene)

PDB for NP0237855 (10-[(3z)-3-ethylidene-1h,2h,4h,6h,7h,12h,12bh-indolo[2,3-a]quinolizin-2-yl]-12-oxa-8,17-diazaheptacyclo[15.5.2.0¹,¹⁸.0²,⁷.0⁸,²².0¹¹,²¹.0¹⁵,²⁰]tetracosa-2,4,6,9,14-pentaene)

3D PDB for NP0237855 (10-[(3z)-3-ethylidene-1h,2h,4h,6h,7h,12h,12bh-indolo[2,3-a]quinolizin-2-yl]-12-oxa-8,17-diazaheptacyclo[15.5.2.0¹,¹⁸.0²,⁷.0⁸,²².0¹¹,²¹.0¹⁵,²⁰]tetracosa-2,4,6,9,14-pentaene)

SMILES for NP0237855 (10-[(3z)-3-ethylidene-1h,2h,4h,6h,7h,12h,12bh-indolo[2,3-a]quinolizin-2-yl]-12-oxa-8,17-diazaheptacyclo[15.5.2.0¹,¹⁸.0²,⁷.0⁸,²².0¹¹,²¹.0¹⁵,²⁰]tetracosa-2,4,6,9,14-pentaene)

INCHI for NP0237855 (10-[(3z)-3-ethylidene-1h,2h,4h,6h,7h,12h,12bh-indolo[2,3-a]quinolizin-2-yl]-12-oxa-8,17-diazaheptacyclo[15.5.2.0¹,¹⁸.0²,⁷.0⁸,²².0¹¹,²¹.0¹⁵,²⁰]tetracosa-2,4,6,9,14-pentaene)

Structure for NP0237855 (10-[(3z)-3-ethylidene-1h,2h,4h,6h,7h,12h,12bh-indolo[2,3-a]quinolizin-2-yl]-12-oxa-8,17-diazaheptacyclo[15.5.2.0¹,¹⁸.0²,⁷.0⁸,²².0¹¹,²¹.0¹⁵,²⁰]tetracosa-2,4,6,9,14-pentaene)

3D Structure for NP0237855 (10-[(3z)-3-ethylidene-1h,2h,4h,6h,7h,12h,12bh-indolo[2,3-a]quinolizin-2-yl]-12-oxa-8,17-diazaheptacyclo[15.5.2.0¹,¹⁸.0²,⁷.0⁸,²².0¹¹,²¹.0¹⁵,²⁰]tetracosa-2,4,6,9,14-pentaene)