NP-MRD: Showing NP-Card for 8-methyl-8-azabicyclo[3.2.1]octan-3-yl 3-(acetyloxy)-2-phenylpropanoate (NP0319288)

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Record Information

Version

2.0

Created at

2022-09-11 20:14:34 UTC

Updated at

2022-09-11 20:14:34 UTC

NP-MRD ID

NP0319288

Secondary Accession Numbers

None

Natural Product Identification

Common Name

8-methyl-8-azabicyclo[3.2.1]octan-3-yl 3-(acetyloxy)-2-phenylpropanoate

Description

Atropine acetate belongs to the class of organic compounds known as tropane alkaloids. These are organic compounds containing the nitrogenous bicyclic alkaloid parent N-Methyl-8-azabicyclo[3.2.1]Octane. 8-methyl-8-azabicyclo[3.2.1]octan-3-yl 3-(acetyloxy)-2-phenylpropanoate is found in Datura stramonium. Based on a literature review very few articles have been published on Atropine acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 49 51  0  0  0  0  0  0  0  0999 V2000
   -6.2003    1.6884   -1.1305 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7669    1.4439   -1.4427 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3654    1.0540   -2.5560 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8357    1.6592   -0.4514 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4643    1.4833   -0.5649 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0512    0.0799   -0.9143 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5625    0.0397   -1.0024 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0293   -0.1850   -2.0641 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1966    0.2589    0.1323 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5931    0.2458    0.1711 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2046    1.5611    0.5545 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7140    1.4184    0.3930 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0754    0.7592   -0.9150 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0415   -0.7083   -0.6400 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6758   -0.8393    0.8073 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1779   -0.8254    1.0407 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1769    0.4300    1.3567 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.6134    0.4199    1.4636 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5470   -0.9284    0.0178 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1926   -0.8653    1.3590 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6754   -1.8311    2.2164 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4972   -2.8468    1.7595 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8485   -2.9023    0.4086 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3719   -1.9427   -0.4571 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5169    2.7155   -1.3181 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4056    1.4705   -0.0475 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8150    0.9315   -1.6937 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0792    2.1461   -1.3821 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9880    1.8076    0.3812 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4407   -0.1249   -1.9298 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9331    0.0269   -0.8807 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8062    2.3957   -0.0273 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0141    1.7212    1.6423 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2417    2.3749    0.5512 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4427    1.0834   -1.7571 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1149    1.1206   -1.1681 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0947   -1.0958   -0.7437 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4261   -1.2959   -1.3216 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1756   -1.6899    1.3089 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7822   -1.8278    0.8533 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0549   -0.5795    2.1276 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8846    1.0566    2.3240 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1277    0.8264    0.5814 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9753   -0.6148    1.6253 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5499   -0.0496    1.6526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3802   -1.7559    3.2645 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8615   -3.5884    2.4455 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4971   -3.7165    0.0861 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6593   -2.0050   -1.5104 H   0  0  0  0  0  0  0  0  0  0  0  0
 18 17  1  0
 17 15  1  0
 15 14  1  0
 14 13  1  0
 13 12  1  0
 12 11  1  0
 11 10  1  0
 10 16  1  0
 10  9  1  0
  9  7  1  0
  7  8  2  0
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
  6 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  2  0
 12 17  1  0
 24 19  1  0
 16 15  1  0
 18 42  1  0
 18 43  1  0
 18 44  1  0
 15 39  1  1
 14 37  1  0
 14 38  1  0
 13 35  1  0
 13 36  1  0
 12 34  1  1
 11 32  1  0
 11 33  1  0
 10 31  1  6
 16 40  1  0
 16 41  1  0
  6 30  1  6
  5 28  1  0
  5 29  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
 20 45  1  0
 21 46  1  0
 22 47  1  0
 23 48  1  0
 24 49  1  0
M  END


  Mrv1652309112222142D          

 24 26  0  0  0  0            999 V2000
   -5.0221   -0.1444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3077    0.2681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3077    1.0931    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5932   -0.1444    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8787    0.2681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1643   -0.1444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4498    0.2681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4498    1.0931    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7353   -0.1444    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0208    0.2681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6608   -0.1966    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4492    0.0465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7506    0.8145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3381    1.5290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5223    1.6520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0825    1.0908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1864    0.9651    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9009    1.3776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1643   -0.9694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4498   -1.3819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4498   -2.2069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1643   -2.6194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8787   -2.2069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8787   -1.3819    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
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  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  1  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
 10 16  1  0  0  0  0
 15 17  1  0  0  0  0
 12 17  1  0  0  0  0
 17 18  1  0  0  0  0
  6 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 19 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0319288

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CN1C2CCC1CC(C2)OC(=O)C(COC(C)=O)C1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C19H25NO4/c1-13(21)23-12-18(14-6-4-3-5-7-14)19(22)24-17-10-15-8-9-16(11-17)20(15)2/h3-7,15-18H,8-12H2,1-2H3

> <INCHI_KEY>
FFTQFHULPHYOIS-UHFFFAOYSA-N

> <FORMULA>
C19H25NO4

> <MOLECULAR_WEIGHT>
331.412

> <EXACT_MASS>
331.178358289

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
49

> <JCHEM_AVERAGE_POLARIZABILITY>
35.49443910464442

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
8-methyl-8-azabicyclo[3.2.1]octan-3-yl 3-(acetyloxy)-2-phenylpropanoate

> <JCHEM_LOGP>
2.0123664269999995

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_BASIC>
9.385562625165845

> <JCHEM_POLAR_SURFACE_AREA>
55.84000000000001

> <JCHEM_REFRACTIVITY>
89.96790000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
8-methyl-8-azabicyclo[3.2.1]octan-3-yl 3-(acetyloxy)-2-phenylpropanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0      -9.375  -0.270   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -8.041   0.500   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -8.041   2.040   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      -6.707  -0.270   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -5.374   0.500   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -4.040  -0.270   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.706   0.500   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -2.706   2.040   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0      -1.373  -0.270   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -0.039   0.500   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.234  -0.367   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.705   0.087   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.268   1.520   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.498   2.854   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.975   3.084   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.154   2.036   0.000  0.00  0.00           C+0
HETATM   17  N   UNK     0       2.215   1.802   0.000  0.00  0.00           N+0
HETATM   18  C   UNK     0       3.548   2.572   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -4.040  -1.810   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -2.706  -2.580   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -2.706  -4.120   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -4.040  -4.890   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -5.374  -4.120   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -5.374  -2.580   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                                                       
CONECT    6    5    7   19                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11   16                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15   10                                                       
CONECT   17   15   12   18                                                  
CONECT   18   17                                                            
CONECT   19    6   20   24                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   19                                                       
MASTER        0    0    0    0    0    0    0    0   24    0   52    0
END

View in JSmol

Synonyms

Value	Source
Atropine acetic acid	Generator

Chemical Formula

C₁₉H₂₅NO₄

Average Mass

331.4120 Da

Monoisotopic Mass

331.17836 Da

IUPAC Name

8-methyl-8-azabicyclo[3.2.1]octan-3-yl 3-(acetyloxy)-2-phenylpropanoate

Traditional Name

8-methyl-8-azabicyclo[3.2.1]octan-3-yl 3-(acetyloxy)-2-phenylpropanoate

CAS Registry Number

Not Available

SMILES

CN1C2CCC1CC(C2)OC(=O)C(COC(C)=O)C1=CC=CC=C1

InChI Identifier

InChI=1S/C19H25NO4/c1-13(21)23-12-18(14-6-4-3-5-7-14)19(22)24-17-10-15-8-9-16(11-17)20(15)2/h3-7,15-18H,8-12H2,1-2H3

InChI Key

FFTQFHULPHYOIS-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
Datura stramonium	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tropane alkaloids. These are organic compounds containing the nitrogenous bicyclic alkaloid parent N-Methyl-8-azabicyclo[3.2.1]Octane.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Tropane alkaloids

Sub Class

Not Available

Direct Parent

Tropane alkaloids

Alternative Parents

Substituents

Tropane alkaloid
Monocyclic benzene moiety
Dicarboxylic acid or derivatives
Piperidine
N-alkylpyrrolidine
Benzenoid
Pyrrolidine
Amino acid or derivatives
Carboxylic acid ester
Tertiary amine
Tertiary aliphatic amine
Carboxylic acid derivative
Azacycle
Organoheterocyclic compound
Organic oxide
Organopnictogen compound
Organooxygen compound
Organonitrogen compound
Organic oxygen compound
Amine
Carbonyl group
Organic nitrogen compound
Hydrocarbon derivative
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	2.01	ChemAxon
pKa (Strongest Basic)	9.39	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	55.84 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	89.97 m³·mol⁻¹	ChemAxon
Polarizability	35.49 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	Yes	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

16156075

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

15558241

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 8-methyl-8-azabicyclo[3.2.1]octan-3-yl 3-(acetyloxy)-2-phenylpropanoate (NP0319288)

MOL for NP0319288 (8-methyl-8-azabicyclo[3.2.1]octan-3-yl 3-(acetyloxy)-2-phenylpropanoate)

3D MOL for NP0319288 (8-methyl-8-azabicyclo[3.2.1]octan-3-yl 3-(acetyloxy)-2-phenylpropanoate)

3D SDF for NP0319288 (8-methyl-8-azabicyclo[3.2.1]octan-3-yl 3-(acetyloxy)-2-phenylpropanoate)

3D-SDF for NP0319288 (8-methyl-8-azabicyclo[3.2.1]octan-3-yl 3-(acetyloxy)-2-phenylpropanoate)

PDB for NP0319288 (8-methyl-8-azabicyclo[3.2.1]octan-3-yl 3-(acetyloxy)-2-phenylpropanoate)

3D PDB for NP0319288 (8-methyl-8-azabicyclo[3.2.1]octan-3-yl 3-(acetyloxy)-2-phenylpropanoate)

SMILES for NP0319288 (8-methyl-8-azabicyclo[3.2.1]octan-3-yl 3-(acetyloxy)-2-phenylpropanoate)

INCHI for NP0319288 (8-methyl-8-azabicyclo[3.2.1]octan-3-yl 3-(acetyloxy)-2-phenylpropanoate)

Structure for NP0319288 (8-methyl-8-azabicyclo[3.2.1]octan-3-yl 3-(acetyloxy)-2-phenylpropanoate)

3D Structure for NP0319288 (8-methyl-8-azabicyclo[3.2.1]octan-3-yl 3-(acetyloxy)-2-phenylpropanoate)