NP-MRD: Showing NP-Card for 5-methyl-3,7-dioxo-2,8-dioxa-13-azatricyclo[8.5.1.0¹³,¹⁶]hexadec-10-en-5-yl acetate (NP0168246)

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Record Information

Version

2.0

Created at

2022-09-03 04:00:04 UTC

Updated at

2022-09-03 04:00:04 UTC

NP-MRD ID

NP0168246

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-methyl-3,7-dioxo-2,8-dioxa-13-azatricyclo[8.5.1.0¹³,¹⁶]hexadec-10-en-5-yl acetate

Description

5-Methyl-3,7-dioxo-2,8-dioxa-13-azatricyclo[8.5.1.0¹³,¹⁶]Hexadec-10-en-5-yl acetate belongs to the class of organic compounds known as tricarboxylic acids and derivatives. These are carboxylic acids containing exactly three carboxyl groups. 5-methyl-3,7-dioxo-2,8-dioxa-13-azatricyclo[8.5.1.0¹³,¹⁶]hexadec-10-en-5-yl acetate is found in Crotalaria lachnosema. 5-Methyl-3,7-dioxo-2,8-dioxa-13-azatricyclo[8.5.1.0¹³,¹⁶]Hexadec-10-en-5-yl acetate is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 44 46  0  0  0  0  0  0  0  0999 V2000
    5.9516    0.4645   -1.0338 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7645    0.2428   -0.1589 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8170    0.2647    1.0818 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5668    0.0050   -0.7713 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3291   -0.2256   -0.1311 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3488   -1.4109    0.7707 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2865   -0.3298   -1.2428 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7804   -1.7257   -1.2746 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6842   -2.6112   -1.3971 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5467   -1.9718   -1.1777 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4520   -1.7753   -0.1478 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5497   -0.8243   -0.4800 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8356   -1.0746   -0.7155 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5960    0.1706   -1.0120 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6961    1.1738   -0.5105 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9911    1.3533    0.8918 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7436    0.9515    1.6518 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7117    1.3117    0.5631 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4518    1.1871    0.8631 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6628    0.8162    1.3962 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8662    0.2671    2.5395 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9694    1.0091    0.6589 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3441    0.6181   -0.5987 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.6326    0.8384   -2.0223 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5308    1.2893   -0.5553 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5450   -0.4545   -1.1194 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0441   -2.2109    0.4365 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6010   -1.0871    1.8213 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3430   -1.8487    0.8195 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7491   -0.0611   -2.2413 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4751    0.4134   -1.1300 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8667   -2.8027    0.0933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0181   -1.4538    0.8181 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3338   -2.0565   -0.7068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5118    0.1450   -0.3925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8143    0.2786   -2.0919 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8789    0.8019    1.2314 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1041    2.4595    1.0510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7325   -0.1243    1.8360 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5854    1.5698    2.5513 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9471    2.4141    0.3874 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7730    1.2986    1.3486 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8789    1.8372   -0.0716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8889    0.8676   -1.5711 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  5  4  1  6
  5  6  1  0
  5  7  1  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
 18 23  1  0
 22  5  1  0
 23 12  1  0
 23 15  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  6 27  1  0
  6 28  1  0
  6 29  1  0
  7 30  1  0
  7 31  1  0
 11 32  1  0
 11 33  1  0
 13 34  1  0
 14 35  1  0
 14 36  1  0
 16 37  1  0
 16 38  1  0
 17 39  1  0
 17 40  1  0
 18 41  1  6
 22 42  1  0
 22 43  1  0
 23 44  1  6
M  END


  Mrv1533004161521302D          

 23 25  0  0  0  0            999 V2000
    7.9759    0.2334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5243    0.9238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8965    1.6601    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7006    0.8780    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2491    1.5685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0121    1.8822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5998    0.9412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5068    0.1214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1153   -0.4357    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6984   -0.0434    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2918    0.6745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4488    0.9974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6621    0.7490    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1827    1.4205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6731    2.0839    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6800    2.9088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4667    3.1573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9016    2.3527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6841    2.0913    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3017    2.6383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1369    3.4466    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0842    2.3768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2840    1.8058    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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 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
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
  5 22  1  0  0  0  0
 18 23  1  0  0  0  0
 12 23  1  0  0  0  0
 15 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0168246

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC1(C)CC(=O)OCC2=CCN3CCC(OC(=O)C1)C23

> <INCHI_IDENTIFIER>
InChI=1S/C16H21NO6/c1-10(18)23-16(2)7-13(19)21-9-11-3-5-17-6-4-12(15(11)17)22-14(20)8-16/h3,12,15H,4-9H2,1-2H3

> <INCHI_KEY>
BNGPHQUXXYPQBM-UHFFFAOYSA-N

> <FORMULA>
C16H21NO6

> <MOLECULAR_WEIGHT>
323.345

> <EXACT_MASS>
323.1368874

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
44

> <JCHEM_AVERAGE_POLARIZABILITY>
32.71058160910512

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5-methyl-3,7-dioxo-2,8-dioxa-13-azatricyclo[8.5.1.0¹³,¹⁶]hexadec-10-en-5-yl acetate

> <ALOGPS_LOGP>
0.68

> <JCHEM_LOGP>
-0.15185634700000106

> <ALOGPS_LOGS>
-0.88

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_BASIC>
7.14571863522708

> <JCHEM_POLAR_SURFACE_AREA>
82.14000000000001

> <JCHEM_REFRACTIVITY>
79.22830000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.28e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-methyl-3,7-dioxo-2,8-dioxa-13-azatricyclo[8.5.1.0¹³,¹⁶]hexadec-10-en-5-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0      14.888   0.436   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      14.045   1.724   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      14.740   3.099   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      12.508   1.639   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      11.665   2.928   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      13.089   3.514   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.453   1.757   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      10.279   0.227   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      11.415  -0.813   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0       8.770  -0.081   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       8.011   1.259   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.438   1.862   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.969   1.398   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.074   2.652   0.000  0.00  0.00           C+0
HETATM   15  N   UNK     0       4.990   3.890   0.000  0.00  0.00           N+0
HETATM   16  C   UNK     0       5.003   5.430   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.471   5.894   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.283   4.392   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       8.744   3.904   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       9.897   4.925   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       9.589   6.434   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      11.357   4.437   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.130   3.371   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6    7   22                                             
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   23                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   23                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   23                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20    5                                                       
CONECT   23   18   12   15                                                  
MASTER        0    0    0    0    0    0    0    0   23    0   50    0
END

View in JSmol

Synonyms

Value	Source
5-Methyl-3,7-dioxo-2,8-dioxa-13-azatricyclo[8.5.1.0,]hexadec-10-en-5-yl acetic acid	Generator
5-Methyl-3,7-dioxo-2,8-dioxa-13-azatricyclo[8.5.1.0¹³,¹⁶]hexadec-10-en-5-yl acetic acid	Generator

Chemical Formula

C₁₆H₂₁NO₆

Average Mass

323.3450 Da

Monoisotopic Mass

323.13689 Da

IUPAC Name

5-methyl-3,7-dioxo-2,8-dioxa-13-azatricyclo[8.5.1.0¹³,¹⁶]hexadec-10-en-5-yl acetate

Traditional Name

5-methyl-3,7-dioxo-2,8-dioxa-13-azatricyclo[8.5.1.0¹³,¹⁶]hexadec-10-en-5-yl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)OC1(C)CC(=O)OCC2=CCN3CCC(OC(=O)C1)C23

InChI Identifier

InChI=1S/C16H21NO6/c1-10(18)23-16(2)7-13(19)21-9-11-3-5-17-6-4-12(15(11)17)22-14(20)8-16/h3,12,15H,4-9H2,1-2H3

InChI Key

BNGPHQUXXYPQBM-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

Species Name	Source	Reference
Crotalaria lachnosema	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tricarboxylic acids and derivatives. These are carboxylic acids containing exactly three carboxyl groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Tricarboxylic acids and derivatives

Direct Parent

Tricarboxylic acids and derivatives

Alternative Parents

Substituents

Tricarboxylic acid or derivatives
Pyrrolizine
N-alkylpyrrolidine
Pyrrolidine
Pyrroline
Amino acid or derivatives
Carboxylic acid ester
Lactone
Tertiary amine
Tertiary aliphatic amine
Organoheterocyclic compound
Azacycle
Oxacycle
Amine
Carbonyl group
Organopnictogen compound
Organic oxygen compound
Organic nitrogen compound
Organooxygen compound
Organonitrogen compound
Organic oxide
Hydrocarbon derivative
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	0.68	ALOGPS
logP	-0.15	ChemAxon
logS	-0.88	ALOGPS
pKa (Strongest Basic)	7.15	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	82.14 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	79.23 m³·mol⁻¹	ChemAxon
Polarizability	32.71 Å³	ChemAxon
Number of Rings	3	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

14109794

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 5-methyl-3,7-dioxo-2,8-dioxa-13-azatricyclo[8.5.1.0¹³,¹⁶]hexadec-10-en-5-yl acetate (NP0168246)

MOL for NP0168246 (5-methyl-3,7-dioxo-2,8-dioxa-13-azatricyclo[8.5.1.0¹³,¹⁶]hexadec-10-en-5-yl acetate)

3D MOL for NP0168246 (5-methyl-3,7-dioxo-2,8-dioxa-13-azatricyclo[8.5.1.0¹³,¹⁶]hexadec-10-en-5-yl acetate)

3D SDF for NP0168246 (5-methyl-3,7-dioxo-2,8-dioxa-13-azatricyclo[8.5.1.0¹³,¹⁶]hexadec-10-en-5-yl acetate)

3D-SDF for NP0168246 (5-methyl-3,7-dioxo-2,8-dioxa-13-azatricyclo[8.5.1.0¹³,¹⁶]hexadec-10-en-5-yl acetate)

PDB for NP0168246 (5-methyl-3,7-dioxo-2,8-dioxa-13-azatricyclo[8.5.1.0¹³,¹⁶]hexadec-10-en-5-yl acetate)

3D PDB for NP0168246 (5-methyl-3,7-dioxo-2,8-dioxa-13-azatricyclo[8.5.1.0¹³,¹⁶]hexadec-10-en-5-yl acetate)

SMILES for NP0168246 (5-methyl-3,7-dioxo-2,8-dioxa-13-azatricyclo[8.5.1.0¹³,¹⁶]hexadec-10-en-5-yl acetate)

INCHI for NP0168246 (5-methyl-3,7-dioxo-2,8-dioxa-13-azatricyclo[8.5.1.0¹³,¹⁶]hexadec-10-en-5-yl acetate)

Structure for NP0168246 (5-methyl-3,7-dioxo-2,8-dioxa-13-azatricyclo[8.5.1.0¹³,¹⁶]hexadec-10-en-5-yl acetate)

3D Structure for NP0168246 (5-methyl-3,7-dioxo-2,8-dioxa-13-azatricyclo[8.5.1.0¹³,¹⁶]hexadec-10-en-5-yl acetate)