NP-MRD: Showing NP-Card for methyl 16-ethenyl-22-(3-ethoxy-3-oxopropyl)-11-ethyl-3,4-dihydroxy-12,17,21,26-tetramethyl-7,23,24,25-tetraazahexacyclo[18.2.1.1⁵,⁸.1¹⁰,¹³.1¹⁵,¹⁸.0²,⁶]hexacosa-1,4,6,8(26),9,11,13(25),14,16,18(24),19-undecaene-3-carboxylate (NP0149309)

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Record Information

Version

2.0

Created at

2022-09-02 05:10:52 UTC

Updated at

2022-09-02 05:10:52 UTC

NP-MRD ID

NP0149309

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 16-ethenyl-22-(3-ethoxy-3-oxopropyl)-11-ethyl-3,4-dihydroxy-12,17,21,26-tetramethyl-7,23,24,25-tetraazahexacyclo[18.2.1.1⁵,⁸.1¹⁰,¹³.1¹⁵,¹⁸.0²,⁶]hexacosa-1,4,6,8(26),9,11,13(25),14,16,18(24),19-undecaene-3-carboxylate

Description

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022207102D          

 47 52  0  0  0  0            999 V2000
   10.2918   -1.6175    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    9.3016    0.3563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8602    0.9634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4821    0.4513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1384   -0.2987    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.7455   -0.8573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    7.9055   -2.4828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1555   -2.1391    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652309022207102D          

 47 52  0  0  0  0            999 V2000
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    8.4875   -1.8981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9055   -2.4828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1555   -2.1391    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.5969   -2.7462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5561   -2.4882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9714   -1.9062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1862   -1.6531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5199   -2.1396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1843   -0.8281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6978   -0.1618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8728   -0.1637    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1812    0.5068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5150    1.2612    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4658    0.9176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7522    0.5034    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4638    1.7426    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1774    2.1568    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9664    0.2536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5480    1.0279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2980    0.6842    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.8566    1.2913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8974    1.0333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4518    2.0102    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7955    2.7602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6430    1.8474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0359    2.4060    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2161    3.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6090    3.7697    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8217    3.5232    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7892    4.5747    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1821    5.1333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3623    5.9384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9683   -0.5714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4548   -1.2377    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.0017   -3.4651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6580   -4.2151    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1357   -4.8878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8105   -3.3023    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4176   -3.8609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  3  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  4  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  4  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 20 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30  6  1  4  0  0  0
 29 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 27 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 36 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 26 41  1  0  0  0  0
 17 41  1  0  0  0  0
 41 42  2  0  0  0  0
 14 42  1  0  0  0  0
 12 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 43 46  2  0  0  0  0
 10 46  1  0  0  0  0
 46 47  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0149309

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCOC(=O)CCC1C(C)C2=CC3=NC(=CC4=NC(=CC5=C(C)C6=C(O)C(O)(C(=O)OC)\C(=C1\N2)C6=N5)C(CC)=C4C)C(C=C)=C3C

> <INCHI_IDENTIFIER>
InChI=1S/C37H40N4O6/c1-9-21-17(4)24-14-26-19(6)23(12-13-30(42)47-11-3)33(40-26)32-34-31(35(43)37(32,45)36(44)46-8)20(7)27(41-34)16-29-22(10-2)18(5)25(39-29)15-28(21)38-24/h9,14-16,19,23,40,43,45H,1,10-13H2,2-8H3/b26-14?,28-15?,29-16?,33-32+

> <INCHI_KEY>
WYMUMUWSXFAWNX-VLKYNKRASA-N

> <FORMULA>
C37H40N4O6

> <MOLECULAR_WEIGHT>
636.749

> <EXACT_MASS>
636.294785024

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
87

> <JCHEM_AVERAGE_POLARIZABILITY>
73.45284067813137

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl 16-ethenyl-22-(3-ethoxy-3-oxopropyl)-11-ethyl-3,4-dihydroxy-12,17,21,26-tetramethyl-7,23,24,25-tetraazahexacyclo[18.2.1.1^{5,8}.1^{10,13}.1^{15,18}.0^{2,6}]hexacosa-1,4,6,8(26),9,11,13(25),14,16,18(24),19-undecaene-3-carboxylate

> <ALOGPS_LOGP>
4.17

> <JCHEM_LOGP>
0.7612591795831408

> <ALOGPS_LOGS>
-4.33

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.921801159339728

> <JCHEM_PKA_STRONGEST_ACIDIC>
-9.74148212486222

> <JCHEM_PKA_STRONGEST_BASIC>
16.07126013963095

> <JCHEM_POLAR_SURFACE_AREA>
142.17000000000002

> <JCHEM_REFRACTIVITY>
187.94890000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.98e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl 16-ethenyl-22-(3-ethoxy-3-oxopropyl)-11-ethyl-3,4-dihydroxy-12,17,21,26-tetramethyl-7,23,24,25-tetraazahexacyclo[18.2.1.1^{5,8}.1^{10,13}.1^{15,18}.0^{2,6}]hexacosa-1,4,6,8(26),9,11,13(25),14,16,18(24),19-undecaene-3-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0      19.211  -3.019   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      19.067  -1.486   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      17.667  -0.845   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      17.363   0.665   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      18.406   1.798   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      15.833   0.842   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0      15.192  -0.558   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0      16.325  -1.600   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      15.843  -3.543   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      14.757  -4.635   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0      13.357  -3.993   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0      12.314  -5.126   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.371  -4.645   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.280  -3.558   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.814  -3.086   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.570  -3.994   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.811  -1.546   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.903  -0.302   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       5.363  -0.306   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       7.805   0.946   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       8.428   2.354   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       6.469   1.713   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       5.138   0.940   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       6.466   3.253   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       7.798   4.026   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       9.271   0.473   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      10.356   1.919   0.000  0.00  0.00           C+0
HETATM   28  N   UNK     0      11.756   1.277   0.000  0.00  0.00           N+0
HETATM   29  C   UNK     0      12.799   2.411   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      14.742   1.929   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      12.043   3.752   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      12.685   5.152   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      10.534   3.448   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       9.400   4.491   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       9.737   5.994   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       8.603   7.037   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       7.134   6.577   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0       8.940   8.540   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       7.807   9.582   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       8.143  11.085   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       9.274  -1.067   0.000  0.00  0.00           C+0
HETATM   42  N   UNK     0      10.182  -2.310   0.000  0.00  0.00           N+0
HETATM   43  C   UNK     0      13.070  -6.468   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      12.428  -7.868   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      13.320  -9.124   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      14.580  -6.164   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      15.713  -7.207   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7   30                                                  
CONECT    7    6    8                                                       
CONECT    8    7    3    9                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   46                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   43                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   42                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   41                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   22   26                                             
CONECT   21   20                                                            
CONECT   22   20   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24                                                            
CONECT   26   20   27   41                                                  
CONECT   27   26   28   33                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29    6                                                       
CONECT   31   29   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   27   34                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39                                                            
CONECT   41   26   17   42                                                  
CONECT   42   41   14                                                       
CONECT   43   12   44   46                                                  
CONECT   44   43   45                                                       
CONECT   45   44                                                            
CONECT   46   43   10   47                                                  
CONECT   47   46                                                            
MASTER        0    0    0    0    0    0    0    0   47    0  104    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₇H₄₀N₄O₆

Average Mass

636.7490 Da

Monoisotopic Mass

636.29479 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CCOC(=O)CCC1C(C)C2=CC3=NC(=CC4=NC(=CC5=C(C)C6=C(O)C(O)(C(=O)OC)\C(=C1\N2)C6=N5)C(CC)=C4C)C(C=C)=C3C

InChI Identifier

InChI=1S/C37H40N4O6/c1-9-21-17(4)24-14-26-19(6)23(12-13-30(42)47-11-3)33(40-26)32-34-31(35(43)37(32,45)36(44)46-8)20(7)27(41-34)16-29-22(10-2)18(5)25(39-29)15-28(21)38-24/h9,14-16,19,23,40,43,45H,1,10-13H2,2-8H3/b26-14?,28-15?,29-16?,33-32+

InChI Key

WYMUMUWSXFAWNX-VLKYNKRASA-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
Usnea diffracta	LOTUS Database	35616633

Chemical Taxonomy

Classification

Not classified

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	4.17	ALOGPS
logS	-4.3	ALOGPS

External Links

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 16-ethenyl-22-(3-ethoxy-3-oxopropyl)-11-ethyl-3,4-dihydroxy-12,17,21,26-tetramethyl-7,23,24,25-tetraazahexacyclo[18.2.1.1⁵,⁸.1¹⁰,¹³.1¹⁵,¹⁸.0²,⁶]hexacosa-1,4,6,8(26),9,11,13(25),14,16,18(24),19-undecaene-3-carboxylate (NP0149309)

MOL for NP0149309 (methyl 16-ethenyl-22-(3-ethoxy-3-oxopropyl)-11-ethyl-3,4-dihydroxy-12,17,21,26-tetramethyl-7,23,24,25-tetraazahexacyclo[18.2.1.1⁵,⁸.1¹⁰,¹³.1¹⁵,¹⁸.0²,⁶]hexacosa-1,4,6,8(26),9,11,13(25),14,16,18(24),19-undecaene-3-carboxylate)

3D MOL for NP0149309 (methyl 16-ethenyl-22-(3-ethoxy-3-oxopropyl)-11-ethyl-3,4-dihydroxy-12,17,21,26-tetramethyl-7,23,24,25-tetraazahexacyclo[18.2.1.1⁵,⁸.1¹⁰,¹³.1¹⁵,¹⁸.0²,⁶]hexacosa-1,4,6,8(26),9,11,13(25),14,16,18(24),19-undecaene-3-carboxylate)

3D SDF for NP0149309 (methyl 16-ethenyl-22-(3-ethoxy-3-oxopropyl)-11-ethyl-3,4-dihydroxy-12,17,21,26-tetramethyl-7,23,24,25-tetraazahexacyclo[18.2.1.1⁵,⁸.1¹⁰,¹³.1¹⁵,¹⁸.0²,⁶]hexacosa-1,4,6,8(26),9,11,13(25),14,16,18(24),19-undecaene-3-carboxylate)

3D-SDF for NP0149309 (methyl 16-ethenyl-22-(3-ethoxy-3-oxopropyl)-11-ethyl-3,4-dihydroxy-12,17,21,26-tetramethyl-7,23,24,25-tetraazahexacyclo[18.2.1.1⁵,⁸.1¹⁰,¹³.1¹⁵,¹⁸.0²,⁶]hexacosa-1,4,6,8(26),9,11,13(25),14,16,18(24),19-undecaene-3-carboxylate)

PDB for NP0149309 (methyl 16-ethenyl-22-(3-ethoxy-3-oxopropyl)-11-ethyl-3,4-dihydroxy-12,17,21,26-tetramethyl-7,23,24,25-tetraazahexacyclo[18.2.1.1⁵,⁸.1¹⁰,¹³.1¹⁵,¹⁸.0²,⁶]hexacosa-1,4,6,8(26),9,11,13(25),14,16,18(24),19-undecaene-3-carboxylate)

3D PDB for NP0149309 (methyl 16-ethenyl-22-(3-ethoxy-3-oxopropyl)-11-ethyl-3,4-dihydroxy-12,17,21,26-tetramethyl-7,23,24,25-tetraazahexacyclo[18.2.1.1⁵,⁸.1¹⁰,¹³.1¹⁵,¹⁸.0²,⁶]hexacosa-1,4,6,8(26),9,11,13(25),14,16,18(24),19-undecaene-3-carboxylate)

SMILES for NP0149309 (methyl 16-ethenyl-22-(3-ethoxy-3-oxopropyl)-11-ethyl-3,4-dihydroxy-12,17,21,26-tetramethyl-7,23,24,25-tetraazahexacyclo[18.2.1.1⁵,⁸.1¹⁰,¹³.1¹⁵,¹⁸.0²,⁶]hexacosa-1,4,6,8(26),9,11,13(25),14,16,18(24),19-undecaene-3-carboxylate)

INCHI for NP0149309 (methyl 16-ethenyl-22-(3-ethoxy-3-oxopropyl)-11-ethyl-3,4-dihydroxy-12,17,21,26-tetramethyl-7,23,24,25-tetraazahexacyclo[18.2.1.1⁵,⁸.1¹⁰,¹³.1¹⁵,¹⁸.0²,⁶]hexacosa-1,4,6,8(26),9,11,13(25),14,16,18(24),19-undecaene-3-carboxylate)

Structure for NP0149309 (methyl 16-ethenyl-22-(3-ethoxy-3-oxopropyl)-11-ethyl-3,4-dihydroxy-12,17,21,26-tetramethyl-7,23,24,25-tetraazahexacyclo[18.2.1.1⁵,⁸.1¹⁰,¹³.1¹⁵,¹⁸.0²,⁶]hexacosa-1,4,6,8(26),9,11,13(25),14,16,18(24),19-undecaene-3-carboxylate)

3D Structure for NP0149309 (methyl 16-ethenyl-22-(3-ethoxy-3-oxopropyl)-11-ethyl-3,4-dihydroxy-12,17,21,26-tetramethyl-7,23,24,25-tetraazahexacyclo[18.2.1.1⁵,⁸.1¹⁰,¹³.1¹⁵,¹⁸.0²,⁶]hexacosa-1,4,6,8(26),9,11,13(25),14,16,18(24),19-undecaene-3-carboxylate)