NP-MRD: Showing NP-Card for 17-hydroxy-8,10-dimethyl-5-oxa-12-azatetracyclo[8.6.1.0⁴,⁶.0¹³,¹⁷]heptadec-13-ene-9,11,15-trione (NP0245264)

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Record Information

Version

2.0

Created at

2022-09-07 06:17:05 UTC

Updated at

2022-09-07 06:17:06 UTC

NP-MRD ID

NP0245264

Secondary Accession Numbers

None

Natural Product Identification

Common Name

17-hydroxy-8,10-dimethyl-5-oxa-12-azatetracyclo[8.6.1.0⁴,⁶.0¹³,¹⁷]heptadec-13-ene-9,11,15-trione

Description

17-Hydroxy-8,10-dimethyl-5-oxa-12-azatetracyclo[8.6.1.0⁴,⁶.0¹³,¹⁷]Heptadec-13-ene-9,11,15-trione belongs to the class of organic compounds known as indolines. Indolines are compounds containing an indole moiety, which consists of pyrrolidine ring fused to benzene to form 2,3-dihydroindole. Based on a literature review very few articles have been published on 17-hydroxy-8,10-dimethyl-5-oxa-12-azatetracyclo[8.6.1.0⁴,⁶.0¹³,¹⁷]Heptadec-13-ene-9,11,15-trione.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 44 47  0  0  0  0  0  0  0  0999 V2000
   -2.8199    2.1500    0.4280 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0793    0.7921    0.2926 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0081   -0.1157   -0.3884 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9610   -1.5514   -0.2545 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0969   -1.9443    1.1785 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0872   -2.3922    0.3527 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6851   -2.0879    0.7082 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0433   -1.7662   -0.5742 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3765   -1.1449   -0.4291 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1758   -1.7339    0.7247 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5544   -1.1819    0.5884 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5699   -1.8872    0.6466 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6662    0.2844    0.3744 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6973    0.9636   -0.1698 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4432    2.3205   -0.5208 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.0347    2.5316   -0.5892 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4390    3.5230   -1.0106 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4601    1.2305   -0.0135 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6130    1.4533    1.4644 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9015    1.1534   -0.5149 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1072    1.4070   -1.7017 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4358    0.2922   -0.6089 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3978    0.5582   -2.0125 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3685    2.3221   -0.5190 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4935    2.1298    1.3033 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1001    2.9717    0.5381 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8634    0.5546    1.3480 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0617    0.2283   -0.1398 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9377    0.1467   -1.4923 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8697   -2.0233   -0.7609 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1933   -3.5072    0.1397 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1899   -3.0262    1.1110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5167   -1.3886    1.5211 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1298   -2.7750   -1.0963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6362   -1.2115   -1.2198 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9753   -1.5656   -1.3215 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2506   -2.8217    0.5242 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7264   -1.5961    1.6985 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5517    0.8249    0.6624 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1962    3.0514   -0.6988 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7058    1.3589    1.6876 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3747    2.5295    1.7151 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0135    0.8563    2.1154 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1727    0.0872   -2.3996 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  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
 18 19  1  1
 18 20  1  0
 20 21  2  0
 18 22  1  0
 22 23  1  6
 20  2  1  0
  6  4  1  0
 22  9  1  0
 22 14  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  1
  3 28  1  0
  3 29  1  0
  4 30  1  6
  6 31  1  6
  7 32  1  0
  7 33  1  0
  8 34  1  0
  8 35  1  0
  9 36  1  6
 10 37  1  0
 10 38  1  0
 13 39  1  0
 15 40  1  0
 19 41  1  0
 19 42  1  0
 19 43  1  0
 23 44  1  0
M  END


  Mrv1652309072208172D          

 23 26  0  0  0  0            999 V2000
    5.8519    2.6025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0685    1.8064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8662    1.5959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0827    0.7999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2993    0.0038    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5016    0.2143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7039    0.4248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1228   -0.1608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3251    0.0497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6859   -0.4720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9146   -0.1793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2754   -0.7009    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7824    0.6351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4216    1.1567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4616    1.9807    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2577    2.1973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5758    2.9585    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6897    1.4313    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1939    2.0842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4874    1.2208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1946    0.4495    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1085    0.8457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4805    0.3107    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  1  0  0  0  0
  4  6  1  0  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  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
  2 20  1  0  0  0  0
 20 21  2  0  0  0  0
 18 22  1  0  0  0  0
 14 22  1  0  0  0  0
  9 22  1  0  0  0  0
 22 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0245264

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1CC2OC2CCC2CC(=O)C=C3NC(=O)C(C)(C1=O)C23O

> <INCHI_IDENTIFIER>
InChI=1S/C17H21NO5/c1-8-5-12-11(23-12)4-3-9-6-10(19)7-13-17(9,22)16(2,14(8)20)15(21)18-13/h7-9,11-12,22H,3-6H2,1-2H3,(H,18,21)

> <INCHI_KEY>
NSJVBGMLBQMMIK-UHFFFAOYSA-N

> <FORMULA>
C17H21NO5

> <MOLECULAR_WEIGHT>
319.357

> <EXACT_MASS>
319.14197278

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
44

> <JCHEM_AVERAGE_POLARIZABILITY>
31.83146440189049

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
17-hydroxy-8,10-dimethyl-5-oxa-12-azatetracyclo[8.6.1.0^{4,6}.0^{13,17}]heptadec-13-ene-9,11,15-trione

> <JCHEM_LOGP>
0.42701113733333307

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.33575141545061

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.362666580369268

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6993318333033267

> <JCHEM_POLAR_SURFACE_AREA>
96.00000000000001

> <JCHEM_REFRACTIVITY>
81.41819999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
17-hydroxy-8,10-dimethyl-5-oxa-12-azatetracyclo[8.6.1.0^{4,6}.0^{13,17}]heptadec-13-ene-9,11,15-trione

> <JCHEM_VEBER_RULE>
0

$$$$

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      10.924   4.858   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      11.328   3.372   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      12.817   2.979   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      13.221   1.493   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      13.625   0.007   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      12.136   0.400   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.647   0.793   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.563  -0.300   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.074   0.093   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.880  -0.881   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.441  -0.335   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       4.248  -1.308   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       5.194   1.185   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.387   2.159   0.000  0.00  0.00           C+0
HETATM   15  N   UNK     0       6.462   3.697   0.000  0.00  0.00           N+0
HETATM   16  C   UNK     0       7.948   4.102   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       8.542   5.523   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       8.754   2.672   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.695   3.891   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.243   2.279   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       9.697   0.839   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       7.669   1.579   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       6.497   0.580   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   20                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4    6                                                       
CONECT    6    5    4    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   22                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15   22                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20   22                                             
CONECT   19   18                                                            
CONECT   20   18    2   21                                                  
CONECT   21   20                                                            
CONECT   22   18   14    9   23                                             
CONECT   23   22                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   52    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₇H₂₁NO₅

Average Mass

319.3570 Da

Monoisotopic Mass

319.14197 Da

IUPAC Name

17-hydroxy-8,10-dimethyl-5-oxa-12-azatetracyclo[8.6.1.0^{4,6}.0^{13,17}]heptadec-13-ene-9,11,15-trione

Traditional Name

17-hydroxy-8,10-dimethyl-5-oxa-12-azatetracyclo[8.6.1.0^{4,6}.0^{13,17}]heptadec-13-ene-9,11,15-trione

CAS Registry Number

Not Available

SMILES

CC1CC2OC2CCC2CC(=O)C=C3NC(=O)C(C)(C1=O)C23O

InChI Identifier

InChI=1S/C17H21NO5/c1-8-5-12-11(23-12)4-3-9-6-10(19)7-13-17(9,22)16(2,14(8)20)15(21)18-13/h7-9,11-12,22H,3-6H2,1-2H3,(H,18,21)

InChI Key

NSJVBGMLBQMMIK-UHFFFAOYSA-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 indolines. Indolines are compounds containing an indole moiety, which consists of pyrrolidine ring fused to benzene to form 2,3-dihydroindole.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Indolines

Direct Parent

Indolines

Alternative Parents

Substituents

Dihydroindole
Cyclohexenone
2-pyrrolidone
Pyrrolidone
Vinylogous amide
Tertiary alcohol
Pyrrolidine
Cyclic ketone
Secondary carboxylic acid amide
Lactam
Ketone
Carboxamide group
Oxacycle
Azacycle
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	0.43	ChemAxon
pKa (Strongest Acidic)	12.36	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	96 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	81.42 m³·mol⁻¹	ChemAxon
Polarizability	31.83 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

162814911

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 17-hydroxy-8,10-dimethyl-5-oxa-12-azatetracyclo[8.6.1.0⁴,⁶.0¹³,¹⁷]heptadec-13-ene-9,11,15-trione (NP0245264)

MOL for NP0245264 (17-hydroxy-8,10-dimethyl-5-oxa-12-azatetracyclo[8.6.1.0⁴,⁶.0¹³,¹⁷]heptadec-13-ene-9,11,15-trione)

3D MOL for NP0245264 (17-hydroxy-8,10-dimethyl-5-oxa-12-azatetracyclo[8.6.1.0⁴,⁶.0¹³,¹⁷]heptadec-13-ene-9,11,15-trione)

3D SDF for NP0245264 (17-hydroxy-8,10-dimethyl-5-oxa-12-azatetracyclo[8.6.1.0⁴,⁶.0¹³,¹⁷]heptadec-13-ene-9,11,15-trione)

3D-SDF for NP0245264 (17-hydroxy-8,10-dimethyl-5-oxa-12-azatetracyclo[8.6.1.0⁴,⁶.0¹³,¹⁷]heptadec-13-ene-9,11,15-trione)

PDB for NP0245264 (17-hydroxy-8,10-dimethyl-5-oxa-12-azatetracyclo[8.6.1.0⁴,⁶.0¹³,¹⁷]heptadec-13-ene-9,11,15-trione)

3D PDB for NP0245264 (17-hydroxy-8,10-dimethyl-5-oxa-12-azatetracyclo[8.6.1.0⁴,⁶.0¹³,¹⁷]heptadec-13-ene-9,11,15-trione)

SMILES for NP0245264 (17-hydroxy-8,10-dimethyl-5-oxa-12-azatetracyclo[8.6.1.0⁴,⁶.0¹³,¹⁷]heptadec-13-ene-9,11,15-trione)

INCHI for NP0245264 (17-hydroxy-8,10-dimethyl-5-oxa-12-azatetracyclo[8.6.1.0⁴,⁶.0¹³,¹⁷]heptadec-13-ene-9,11,15-trione)

Structure for NP0245264 (17-hydroxy-8,10-dimethyl-5-oxa-12-azatetracyclo[8.6.1.0⁴,⁶.0¹³,¹⁷]heptadec-13-ene-9,11,15-trione)

3D Structure for NP0245264 (17-hydroxy-8,10-dimethyl-5-oxa-12-azatetracyclo[8.6.1.0⁴,⁶.0¹³,¹⁷]heptadec-13-ene-9,11,15-trione)