NP-MRD: Showing NP-Card for (2e)-2-[(5s,7s,9s)-9-hydroxy-4,10-diazatetracyclo[8.6.1.0⁵,¹⁷.0¹¹,¹⁶]heptadeca-1(17),11,13,15-tetraen-7-yl]but-2-enal (NP0168556)

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Record Information

Version

2.0

Created at

2022-09-03 04:23:22 UTC

Updated at

2022-09-03 04:23:22 UTC

NP-MRD ID

NP0168556

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2e)-2-[(5s,7s,9s)-9-hydroxy-4,10-diazatetracyclo[8.6.1.0⁵,¹⁷.0¹¹,¹⁶]heptadeca-1(17),11,13,15-tetraen-7-yl]but-2-enal

Description

(2E)-2-[(5S,7S,9S)-9-hydroxy-4,10-diazatetracyclo[8.6.1.0⁵,¹⁷.0¹¹,¹⁶]Heptadeca-1(17),11,13,15-tetraen-7-yl]but-2-enal belongs to the class of organic compounds known as beta carbolines. Beta carbolines are compounds containing a 9H-pyrido[3,4-b]indole moiety. (2e)-2-[(5s,7s,9s)-9-hydroxy-4,10-diazatetracyclo[8.6.1.0⁵,¹⁷.0¹¹,¹⁶]heptadeca-1(17),11,13,15-tetraen-7-yl]but-2-enal is found in Strychnos johnsonii. Based on a literature review very few articles have been published on (2E)-2-[(5S,7S,9S)-9-hydroxy-4,10-diazatetracyclo[8.6.1.0⁵,¹⁷.0¹¹,¹⁶]Heptadeca-1(17),11,13,15-tetraen-7-yl]but-2-enal.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 45 48  0  0  0  0  0  0  0  0999 V2000
   -2.5455    0.3702    2.4048 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5342   -0.1999    1.4848 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1719   -0.5077    0.2546 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1724   -1.0713   -0.6364 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3575   -1.2703   -0.2701 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7682   -0.2638   -0.1538 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2000   -1.5839   -0.6143 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1508   -1.4447   -1.2729 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7969   -2.7399   -1.1866 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5243   -2.8698    0.0653 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7211   -1.9488   -0.0441 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1886   -0.5631   -0.0946 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9712   -0.3630   -0.6830 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6703    0.9255   -0.6316 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6727    1.5721   -0.0181 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8984    2.9124    0.3099 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0609    3.2683    0.9587 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0323    2.3537    1.3083 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8067    1.0318    0.9832 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6405    0.6577    0.3296 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5190    1.6446   -1.1236 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2345    2.3322   -2.2904 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6829    0.6986   -1.3183 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0094    0.5811    3.4012 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6770   -0.2750    2.6004 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2595    1.3765    2.0056 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5663   -0.3637    1.8326 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9480   -1.3503   -1.6663 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1457    0.1163    0.6579 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8961   -1.9898   -1.3779 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1378   -2.2830    0.2640 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0328   -1.2047   -2.3582 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1116   -3.5230   -1.2248 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8607   -2.5390    0.8958 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8177   -3.9255    0.1690 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2258   -2.1363   -1.0210 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4171   -2.0789    0.8107 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1357    3.6293    0.0353 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2461    4.3132    1.2191 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9398    2.6655    1.8201 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5513    0.2879    1.2444 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7930    2.3527   -0.3275 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6393    1.9371   -3.0932 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6168    0.1371   -2.2649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5985    1.3315   -1.3838 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  2  0
  3  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 21  1  0
 21 22  1  0
 21 23  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 23  6  1  0
 20 15  1  0
 13  8  1  0
 20 12  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  0
  4 28  1  0
  6 29  1  1
  7 30  1  0
  7 31  1  0
  8 32  1  6
  9 33  1  0
 10 34  1  0
 10 35  1  0
 11 36  1  0
 11 37  1  0
 21 42  1  1
 22 43  1  0
 23 44  1  0
 23 45  1  0
 16 38  1  0
 17 39  1  0
 18 40  1  0
 19 41  1  0
M  END


  Mrv1652309032206232D          

 23 26  0  0  1  0            999 V2000
   -2.1362    2.2987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7397    1.7363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5545    0.9323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1581    0.3699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9728   -0.4340    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7656    0.6908    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6410   -0.1247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9256   -0.5357    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9784   -1.4029    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3027   -1.8764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4451   -1.5280    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5173   -0.7062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1583   -0.2327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0832    0.5562    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9081    0.5702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4496    1.1927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2594    1.0349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5277    0.2548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9862   -0.3677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1764   -0.2099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3829    1.2368    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0281    1.9522    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2058    1.2968    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  2  0  0  0  0
  6  3  1  6  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  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
  8 13  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  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
 19 20  2  0  0  0  0
 12 20  1  0  0  0  0
 15 20  1  0  0  0  0
 14 21  1  0  0  0  0
 21 22  1  6  0  0  0
 21 23  1  0  0  0  0
  6 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0168556

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C=C(\C=O)[C@H]1C[C@@H]2NCCC3=C2N([C@@H](O)C1)C1=CC=CC=C31

> <INCHI_IDENTIFIER>
InChI=1S/C19H22N2O2/c1-2-12(11-22)13-9-16-19-15(7-8-20-16)14-5-3-4-6-17(14)21(19)18(23)10-13/h2-6,11,13,16,18,20,23H,7-10H2,1H3/b12-2-/t13-,16-,18-/m0/s1

> <INCHI_KEY>
YQIYGKCKHVXNPT-JQPPFCHESA-N

> <FORMULA>
C19H22N2O2

> <MOLECULAR_WEIGHT>
310.397

> <EXACT_MASS>
310.168127956

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
35.171701215355576

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2E)-2-[(5S,7S,9S)-9-hydroxy-4,10-diazatetracyclo[8.6.1.0^{5,17}.0^{11,16}]heptadeca-1(17),11,13,15-tetraen-7-yl]but-2-enal

> <ALOGPS_LOGP>
1.99

> <JCHEM_LOGP>
2.221802516333333

> <ALOGPS_LOGS>
-3.51

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.325998258397085

> <JCHEM_PKA_STRONGEST_BASIC>
8.927165749744436

> <JCHEM_POLAR_SURFACE_AREA>
54.260000000000005

> <JCHEM_REFRACTIVITY>
91.3698

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.65e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2E)-2-[(5S,7S,9S)-9-hydroxy-4,10-diazatetracyclo[8.6.1.0^{5,17}.0^{11,16}]heptadeca-1(17),11,13,15-tetraen-7-yl]but-2-enal

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0      -3.987   4.291   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.114   3.241   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.768   1.740   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -5.895   0.691   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -5.549  -0.810   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -3.296   1.290   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -3.063  -0.233   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.728  -1.000   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0      -1.826  -2.619   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0      -0.565  -3.503   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.831  -2.852   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.966  -1.318   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.295  -0.434   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0       0.155   1.038   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0       1.695   1.064   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.706   2.226   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.218   1.932   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.718   0.476   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.708  -0.686   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.196  -0.392   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -0.715   2.309   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       0.052   3.644   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -2.251   2.421   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    6                                                  
CONECT    4    3    5                                                       
CONECT    5    4                                                            
CONECT    6    3    7   23                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   13                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   20                                                  
CONECT   13   12    8   14                                                  
CONECT   14   13   15   21                                                  
CONECT   15   14   16   20                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   12   15                                                  
CONECT   21   14   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21    6                                                       
MASTER        0    0    0    0    0    0    0    0   23    0   52    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₂₂N₂O₂

Average Mass

310.3970 Da

Monoisotopic Mass

310.16813 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C\C=C(\C=O)[C@H]1C[C@@H]2NCCC3=C2N([C@@H](O)C1)C1=CC=CC=C31

InChI Identifier

InChI=1S/C19H22N2O2/c1-2-12(11-22)13-9-16-19-15(7-8-20-16)14-5-3-4-6-17(14)21(19)18(23)10-13/h2-6,11,13,16,18,20,23H,7-10H2,1H3/b12-2-/t13-,16-,18-/m0/s1

InChI Key

YQIYGKCKHVXNPT-JQPPFCHESA-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 johnsonii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as beta carbolines. Beta carbolines are compounds containing a 9H-pyrido[3,4-b]indole moiety.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Pyridoindoles

Direct Parent

Beta carbolines

Alternative Parents

Substituents

Beta-carboline
Pyrroloazepine
3-alkylindole
Indole
Azepine
Aralkylamine
Benzenoid
Alpha,beta-unsaturated aldehyde
Enal
Pyrrole
Heteroaromatic compound
Alkanolamine
Secondary aliphatic amine
Secondary amine
Azacycle
Organic oxide
Aldehyde
Organooxygen compound
Organonitrogen compound
Organopnictogen compound
Carbonyl group
Organic oxygen compound
Organic nitrogen compound
Hydrocarbon derivative
Amine
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	1.99	ALOGPS
logP	2.22	ChemAxon
logS	-3.5	ALOGPS
pKa (Strongest Acidic)	13.33	ChemAxon
pKa (Strongest Basic)	8.93	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	54.26 Å²	ChemAxon
Rotatable Bond Count	2	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

163187206

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2e)-2-[(5s,7s,9s)-9-hydroxy-4,10-diazatetracyclo[8.6.1.0⁵,¹⁷.0¹¹,¹⁶]heptadeca-1(17),11,13,15-tetraen-7-yl]but-2-enal (NP0168556)

MOL for NP0168556 ((2e)-2-[(5s,7s,9s)-9-hydroxy-4,10-diazatetracyclo[8.6.1.0⁵,¹⁷.0¹¹,¹⁶]heptadeca-1(17),11,13,15-tetraen-7-yl]but-2-enal)

3D MOL for NP0168556 ((2e)-2-[(5s,7s,9s)-9-hydroxy-4,10-diazatetracyclo[8.6.1.0⁵,¹⁷.0¹¹,¹⁶]heptadeca-1(17),11,13,15-tetraen-7-yl]but-2-enal)

3D SDF for NP0168556 ((2e)-2-[(5s,7s,9s)-9-hydroxy-4,10-diazatetracyclo[8.6.1.0⁵,¹⁷.0¹¹,¹⁶]heptadeca-1(17),11,13,15-tetraen-7-yl]but-2-enal)

3D-SDF for NP0168556 ((2e)-2-[(5s,7s,9s)-9-hydroxy-4,10-diazatetracyclo[8.6.1.0⁵,¹⁷.0¹¹,¹⁶]heptadeca-1(17),11,13,15-tetraen-7-yl]but-2-enal)

PDB for NP0168556 ((2e)-2-[(5s,7s,9s)-9-hydroxy-4,10-diazatetracyclo[8.6.1.0⁵,¹⁷.0¹¹,¹⁶]heptadeca-1(17),11,13,15-tetraen-7-yl]but-2-enal)

3D PDB for NP0168556 ((2e)-2-[(5s,7s,9s)-9-hydroxy-4,10-diazatetracyclo[8.6.1.0⁵,¹⁷.0¹¹,¹⁶]heptadeca-1(17),11,13,15-tetraen-7-yl]but-2-enal)

SMILES for NP0168556 ((2e)-2-[(5s,7s,9s)-9-hydroxy-4,10-diazatetracyclo[8.6.1.0⁵,¹⁷.0¹¹,¹⁶]heptadeca-1(17),11,13,15-tetraen-7-yl]but-2-enal)

INCHI for NP0168556 ((2e)-2-[(5s,7s,9s)-9-hydroxy-4,10-diazatetracyclo[8.6.1.0⁵,¹⁷.0¹¹,¹⁶]heptadeca-1(17),11,13,15-tetraen-7-yl]but-2-enal)

Structure for NP0168556 ((2e)-2-[(5s,7s,9s)-9-hydroxy-4,10-diazatetracyclo[8.6.1.0⁵,¹⁷.0¹¹,¹⁶]heptadeca-1(17),11,13,15-tetraen-7-yl]but-2-enal)

3D Structure for NP0168556 ((2e)-2-[(5s,7s,9s)-9-hydroxy-4,10-diazatetracyclo[8.6.1.0⁵,¹⁷.0¹¹,¹⁶]heptadeca-1(17),11,13,15-tetraen-7-yl]but-2-enal)