NP-MRD: Showing NP-Card for (1r,7e,9s,11e,13r,14s,16r,17s,18r,19s)-17-ethyl-21-hydroxy-19-[(1r)-1-(1h-indol-3-yl)ethyl]-7,9,16-trimethyl-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]henicosa-7,11,20-triene-2,5,6-trione (NP0235132)

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Record Information

Version

2.0

Created at

2022-09-06 17:35:26 UTC

Updated at

2022-09-06 17:35:26 UTC

NP-MRD ID

NP0235132

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,7e,9s,11e,13r,14s,16r,17s,18r,19s)-17-ethyl-21-hydroxy-19-[(1r)-1-(1h-indol-3-yl)ethyl]-7,9,16-trimethyl-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]henicosa-7,11,20-triene-2,5,6-trione

Description

(1R,7E,9S,11E,13R,14S,16R,17S,18R,19S)-17-ethyl-21-hydroxy-19-[(1R)-1-(1H-indol-3-yl)ethyl]-7,9,16-trimethyl-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]Henicosa-7,11,20-triene-2,5,6-trione belongs to the class of organic compounds known as 3-alkylindoles. 3-Alkylindoles are compounds containing an indole moiety that carries an alkyl chain at the 3-position. (1r,7e,9s,11e,13r,14s,16r,17s,18r,19s)-17-ethyl-21-hydroxy-19-[(1r)-1-(1h-indol-3-yl)ethyl]-7,9,16-trimethyl-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]henicosa-7,11,20-triene-2,5,6-trione is found in Stenocarpella macrospora. Based on a literature review very few articles have been published on (1R,7E,9S,11E,13R,14S,16R,17S,18R,19S)-17-ethyl-21-hydroxy-19-[(1R)-1-(1H-indol-3-yl)ethyl]-7,9,16-trimethyl-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]Henicosa-7,11,20-triene-2,5,6-trione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062219352D          

 41 46  0  0  1  0            999 V2000
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  1  2  1  0  0  0  0
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  3  4  1  0  0  0  0
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  5  6  1  6  0  0  0
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 20 37  1  0  0  0  0
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 38 39  1  6  0  0  0
 39 40  1  0  0  0  0
 38 40  1  0  0  0  0
  3 40  1  0  0  0  0
 40 41  1  1  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652309062219352D          

 41 46  0  0  1  0            999 V2000
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    1.0994   -3.6080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8947   -3.3890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4822   -3.9683    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5548   -2.3685    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5215   -1.6122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6824   -1.1852    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1525   -1.1749    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2934   -1.4522    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0938   -0.9718    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8489   -2.1472    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0505   -1.9393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0016   -1.1157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7602   -0.7913    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3869   -0.4545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4130   -0.6562    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5949    0.3439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0075    0.9231    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3903    0.5629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5982    1.3613    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0108    1.9406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3936    1.5804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9810    1.0011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7731    0.2027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3605   -0.3765    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1559   -0.1575    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9513    0.0616    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7433   -0.7368    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.5416   -0.9447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  1  0  0  0
  3  4  1  0  0  0  0
  4  5  1  1  0  0  0
  5  6  1  6  0  0  0
  6  7  1  6  0  0  0
  6  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
  5 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 20 18  1  6  0  0  0
  4 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  1  0  0  0
 32 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 37 36  1  1  0  0  0
 20 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  6  0  0  0
 39 40  1  0  0  0  0
 38 40  1  0  0  0  0
  3 40  1  0  0  0  0
 40 41  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0235132

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@H]1[C@H]2[C@@H](N=C(O)[C@]22[C@@H](\C=C\C[C@H](C)\C=C(C)\C(=O)C(=O)CCC2=O)[C@@H]2O[C@]12C)[C@H](C)C1=CNC2=CC=CC=C12

> <INCHI_IDENTIFIER>
InChI=1S/C34H40N2O5/c1-6-23-28-29(20(4)22-17-35-25-13-8-7-11-21(22)25)36-32(40)34(28)24(31-33(23,5)41-31)12-9-10-18(2)16-19(3)30(39)26(37)14-15-27(34)38/h7-9,11-13,16-18,20,23-24,28-29,31,35H,6,10,14-15H2,1-5H3,(H,36,40)/b12-9+,19-16+/t18-,20+,23-,24-,28-,29-,31-,33+,34-/m0/s1

> <INCHI_KEY>
LUGZLGYIMRDLBT-HIOWINIESA-N

> <FORMULA>
C34H40N2O5

> <MOLECULAR_WEIGHT>
556.703

> <EXACT_MASS>
556.293722396

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
81

> <JCHEM_AVERAGE_POLARIZABILITY>
60.332442702769384

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,7E,9S,11E,13R,14S,16R,17S,18R,19S)-17-ethyl-21-hydroxy-19-[(1R)-1-(1H-indol-3-yl)ethyl]-7,9,16-trimethyl-15-oxa-20-azatetracyclo[11.8.0.0^{1,18}.0^{14,16}]henicosa-7,11,20-triene-2,5,6-trione

> <JCHEM_LOGP>
5.607143155009957

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.844746594398433

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.7830683748934404

> <JCHEM_PKA_STRONGEST_BASIC>
5.378394387099131

> <JCHEM_POLAR_SURFACE_AREA>
112.11999999999998

> <JCHEM_REFRACTIVITY>
158.82769999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,7E,9S,11E,13R,14S,16R,17S,18R,19S)-17-ethyl-21-hydroxy-19-[(1R)-1-(1H-indol-3-yl)ethyl]-7,9,16-trimethyl-15-oxa-20-azatetracyclo[11.8.0.0^{1,18}.0^{14,16}]henicosa-7,11,20-triene-2,5,6-trione

> <JCHEM_VEBER_RULE>
0

$$$$

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      11.047  -3.538   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.562  -3.947   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.466  -2.866   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.981  -3.274   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.292  -4.651   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.000  -6.019   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.539  -6.089   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.171  -7.316   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.733  -8.750   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0       5.543  -9.727   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0       4.245  -8.898   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.760  -9.307   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.664  -8.225   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.052  -6.735   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.537  -6.326   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.633  -7.407   0.000  0.00  0.00           C+0
HETATM   17  N   UNK     0       4.769  -4.421   0.000  0.00  0.00           N+0
HETATM   18  C   UNK     0       4.707  -3.009   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       3.140  -2.212   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       5.885  -2.193   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.281  -2.711   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       3.908  -1.814   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       3.451  -4.008   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.961  -3.620   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.870  -2.083   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       3.286  -1.477   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       0.722  -0.848   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -0.771  -1.225   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       1.110   0.642   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       0.014   1.723   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       2.595   1.051   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       2.983   2.541   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       1.887   3.622   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       4.468   2.950   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       5.565   1.869   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       5.176   0.378   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       6.273  -0.703   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       7.758  -0.294   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       9.242   0.115   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       8.854  -1.375   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      10.344  -1.763   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   40                                                  
CONECT    4    3    5   20                                                  
CONECT    5    4    6   17                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   16                                                  
CONECT    9    8   10                                                       
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    5   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18    4   21   37                                             
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32                                                       
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   20   38                                                  
CONECT   38   37   39   40                                                  
CONECT   39   38   40                                                       
CONECT   40   39   38    3   41                                             
CONECT   41   40                                                            
MASTER        0    0    0    0    0    0    0    0   41    0   92    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₄H₄₀N₂O₅

Average Mass

556.7030 Da

Monoisotopic Mass

556.29372 Da

IUPAC Name

(1R,7E,9S,11E,13R,14S,16R,17S,18R,19S)-17-ethyl-21-hydroxy-19-[(1R)-1-(1H-indol-3-yl)ethyl]-7,9,16-trimethyl-15-oxa-20-azatetracyclo[11.8.0.0^{1,18}.0^{14,16}]henicosa-7,11,20-triene-2,5,6-trione

Traditional Name

(1R,7E,9S,11E,13R,14S,16R,17S,18R,19S)-17-ethyl-21-hydroxy-19-[(1R)-1-(1H-indol-3-yl)ethyl]-7,9,16-trimethyl-15-oxa-20-azatetracyclo[11.8.0.0^{1,18}.0^{14,16}]henicosa-7,11,20-triene-2,5,6-trione

CAS Registry Number

Not Available

SMILES

CC[C@H]1[C@H]2[C@@H](N=C(O)[C@]22[C@@H](\C=C\C[C@H](C)\C=C(C)\C(=O)C(=O)CCC2=O)[C@@H]2O[C@]12C)[C@H](C)C1=CNC2=CC=CC=C12

InChI Identifier

InChI=1S/C34H40N2O5/c1-6-23-28-29(20(4)22-17-35-25-13-8-7-11-21(22)25)36-32(40)34(28)24(31-33(23,5)41-31)12-9-10-18(2)16-19(3)30(39)26(37)14-15-27(34)38/h7-9,11-13,16-18,20,23-24,28-29,31,35H,6,10,14-15H2,1-5H3,(H,36,40)/b12-9+,19-16+/t18-,20+,23-,24-,28-,29-,31-,33+,34-/m0/s1

InChI Key

LUGZLGYIMRDLBT-HIOWINIESA-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
Stenocarpella macrospora	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 3-alkylindoles. 3-Alkylindoles are compounds containing an indole moiety that carries an alkyl chain at the 3-position.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Indoles

Direct Parent

3-alkylindoles

Alternative Parents

Substituents

3-alkylindole
Isoindole or derivatives
Oxepane
Benzenoid
Substituted pyrrole
Heteroaromatic compound
Cyclic carboximidic acid
Pyrroline
Pyrrole
Cyclic ketone
Ketone
Oxacycle
Azacycle
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Ether
Oxirane
Dialkyl ether
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
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	5.61	ChemAxon
pKa (Strongest Acidic)	2.78	ChemAxon
pKa (Strongest Basic)	5.38	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	112.12 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	158.83 m³·mol⁻¹	ChemAxon
Polarizability	60.33 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	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

163054132

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,7e,9s,11e,13r,14s,16r,17s,18r,19s)-17-ethyl-21-hydroxy-19-[(1r)-1-(1h-indol-3-yl)ethyl]-7,9,16-trimethyl-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]henicosa-7,11,20-triene-2,5,6-trione (NP0235132)

MOL for NP0235132 ((1r,7e,9s,11e,13r,14s,16r,17s,18r,19s)-17-ethyl-21-hydroxy-19-[(1r)-1-(1h-indol-3-yl)ethyl]-7,9,16-trimethyl-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]henicosa-7,11,20-triene-2,5,6-trione)

3D MOL for NP0235132 ((1r,7e,9s,11e,13r,14s,16r,17s,18r,19s)-17-ethyl-21-hydroxy-19-[(1r)-1-(1h-indol-3-yl)ethyl]-7,9,16-trimethyl-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]henicosa-7,11,20-triene-2,5,6-trione)

3D SDF for NP0235132 ((1r,7e,9s,11e,13r,14s,16r,17s,18r,19s)-17-ethyl-21-hydroxy-19-[(1r)-1-(1h-indol-3-yl)ethyl]-7,9,16-trimethyl-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]henicosa-7,11,20-triene-2,5,6-trione)

3D-SDF for NP0235132 ((1r,7e,9s,11e,13r,14s,16r,17s,18r,19s)-17-ethyl-21-hydroxy-19-[(1r)-1-(1h-indol-3-yl)ethyl]-7,9,16-trimethyl-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]henicosa-7,11,20-triene-2,5,6-trione)

PDB for NP0235132 ((1r,7e,9s,11e,13r,14s,16r,17s,18r,19s)-17-ethyl-21-hydroxy-19-[(1r)-1-(1h-indol-3-yl)ethyl]-7,9,16-trimethyl-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]henicosa-7,11,20-triene-2,5,6-trione)

3D PDB for NP0235132 ((1r,7e,9s,11e,13r,14s,16r,17s,18r,19s)-17-ethyl-21-hydroxy-19-[(1r)-1-(1h-indol-3-yl)ethyl]-7,9,16-trimethyl-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]henicosa-7,11,20-triene-2,5,6-trione)

SMILES for NP0235132 ((1r,7e,9s,11e,13r,14s,16r,17s,18r,19s)-17-ethyl-21-hydroxy-19-[(1r)-1-(1h-indol-3-yl)ethyl]-7,9,16-trimethyl-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]henicosa-7,11,20-triene-2,5,6-trione)

INCHI for NP0235132 ((1r,7e,9s,11e,13r,14s,16r,17s,18r,19s)-17-ethyl-21-hydroxy-19-[(1r)-1-(1h-indol-3-yl)ethyl]-7,9,16-trimethyl-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]henicosa-7,11,20-triene-2,5,6-trione)

Structure for NP0235132 ((1r,7e,9s,11e,13r,14s,16r,17s,18r,19s)-17-ethyl-21-hydroxy-19-[(1r)-1-(1h-indol-3-yl)ethyl]-7,9,16-trimethyl-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]henicosa-7,11,20-triene-2,5,6-trione)

3D Structure for NP0235132 ((1r,7e,9s,11e,13r,14s,16r,17s,18r,19s)-17-ethyl-21-hydroxy-19-[(1r)-1-(1h-indol-3-yl)ethyl]-7,9,16-trimethyl-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]henicosa-7,11,20-triene-2,5,6-trione)