NP-MRD: Showing NP-Card for 8-acetyl-8-azabicyclo[3.2.1]octan-3-yl 3,4-dimethoxybenzoate (NP0187068)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-04 03:07:00 UTC

Updated at

2022-09-04 03:07:00 UTC

NP-MRD ID

NP0187068

Secondary Accession Numbers

None

Natural Product Identification

Common Name

8-acetyl-8-azabicyclo[3.2.1]octan-3-yl 3,4-dimethoxybenzoate

Description

8-Acetyl-8-azabicyclo[3.2.1]Octan-3-yl 3,4-dimethoxybenzoate belongs to the class of organic compounds known as p-methoxybenzoic acids and derivatives. These are benzoic acids in which the hydrogen atom at position 4 of the benzene ring is replaced by a methoxy group. 8-acetyl-8-azabicyclo[3.2.1]octan-3-yl 3,4-dimethoxybenzoate is found in Convolvulus subhirsutus. 8-Acetyl-8-azabicyclo[3.2.1]Octan-3-yl 3,4-dimethoxybenzoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 47 49  0  0  0  0  0  0  0  0999 V2000
   -7.1915    1.8381    0.4306 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3122    0.7431    0.4121 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9382    0.8774    0.2598 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3359    2.1005    0.1151 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9576    2.1861   -0.0345 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1568    1.0696   -0.0433 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7186    1.1722   -0.2003 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1896    2.3117   -0.3317 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1245    0.0775   -0.2151 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5336    0.1829   -0.3692 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9037   -0.6015   -1.6022 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3302   -1.1409   -1.4317 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2601   -2.4095   -0.5817 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9122   -2.0514    0.7369 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6505   -0.5398    0.7693 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1546   -0.3763    0.8883 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0151   -0.1807   -0.5869 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.8580    0.8799   -0.9871 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4726    1.7638    0.0351 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1136    1.1100   -2.1961 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7694   -0.1520    0.1023 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1437   -0.2573    0.2527 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7327   -1.5289    0.3993 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8881   -2.6498    0.3861 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9061    2.6633   -0.2268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2033    1.4914    0.0786 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3074    2.2541    1.4576 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9289    3.0310    0.1147 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5433    3.1976   -0.1454 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7562    1.2655   -0.4648 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1928   -1.4241   -1.8235 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9492    0.1166   -2.4481 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8191   -1.3076   -2.3912 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7708   -3.2544   -1.0839 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2053   -2.6968   -0.4142 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0021   -2.2551    0.6572 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4385   -2.5614    1.5970 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2231   -0.0310    1.5373 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9718    0.3779    1.6932 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6529   -1.3074    1.2168 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3577    1.2231    0.4718 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7705    1.9686    0.8866 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8296    2.7201   -0.3795 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2040   -1.0737    0.1050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2940   -2.6925   -0.5703 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1407   -2.5322    1.2099 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4064   -3.5975    0.5360 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  1  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  2  0
 22  3  1  0
 16 10  1  0
 17 12  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  4 28  1  0
  5 29  1  0
 21 44  1  0
 24 45  1  0
 24 46  1  0
 24 47  1  0
 10 30  1  6
 11 31  1  0
 11 32  1  0
 12 33  1  6
 13 34  1  0
 13 35  1  0
 14 36  1  0
 14 37  1  0
 15 38  1  1
 16 39  1  0
 16 40  1  0
 19 41  1  0
 19 42  1  0
 19 43  1  0
M  END


  Mrv1533004251514222D          

 24 26  0  0  0  0            999 V2000
    7.7380    0.6363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3255   -0.0781    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5005   -0.0781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0880   -0.7926    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2630   -0.7926    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8505   -0.0781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2630    0.6363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0880    0.6363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5005    1.3508    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3255    1.3508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0255   -0.0781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6130   -0.7926    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6130    0.6363    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7880    0.6363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4300    1.3796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6257    1.5632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9807    1.0488    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9807    0.2238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6257   -0.2905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4300   -0.1070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3940    0.6363    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5690    0.6363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1565   -0.0781    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1565    1.3508    0.0000 C   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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  6 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 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
 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
 14 20  1  0  0  0  0
 19 21  1  0  0  0  0
 16 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0187068

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C(C=C1OC)C(=O)OC1CC2CCC(C1)N2C(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C18H23NO5/c1-11(20)19-13-5-6-14(19)10-15(9-13)24-18(21)12-4-7-16(22-2)17(8-12)23-3/h4,7-8,13-15H,5-6,9-10H2,1-3H3

> <INCHI_KEY>
HZEOENYXYFFKIU-UHFFFAOYSA-N

> <FORMULA>
C18H23NO5

> <MOLECULAR_WEIGHT>
333.384

> <EXACT_MASS>
333.157622845

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
35.27565515231931

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
8-acetyl-8-azabicyclo[3.2.1]octan-3-yl 3,4-dimethoxybenzoate

> <ALOGPS_LOGP>
2.33

> <JCHEM_LOGP>
1.4404123199999994

> <ALOGPS_LOGS>
-2.70

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-1.0335768657373032

> <JCHEM_POLAR_SURFACE_AREA>
65.07000000000001

> <JCHEM_REFRACTIVITY>
87.6134

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.69e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
8-acetyl-8-azabicyclo[3.2.1]octan-3-yl 3,4-dimethoxybenzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0      14.444   1.188   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      13.674  -0.146   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      12.134  -0.146   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.364  -1.480   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.824  -1.480   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.054  -0.146   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.824   1.188   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      11.364   1.188   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      12.134   2.522   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      13.674   2.522   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.514  -0.146   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       6.744  -1.480   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0       6.744   1.188   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       5.204   1.188   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.536   2.575   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.035   2.918   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.831   1.958   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.831   0.418   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.035  -0.542   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.536  -0.200   0.000  0.00  0.00           C+0
HETATM   21  N   UNK     0       2.602   1.188   0.000  0.00  0.00           N+0
HETATM   22  C   UNK     0       1.062   1.188   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       0.292  -0.146   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       0.292   2.522   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   11                                                  
CONECT    7    6    8                                                       
CONECT    8    7    3    9                                                  
CONECT    9    8   10                                                       
CONECT   10    9                                                            
CONECT   11    6   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15   20                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   21                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19   14                                                       
CONECT   21   19   16   22                                                  
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   52    0
END

View in JSmol

Synonyms

Value	Source
8-Acetyl-8-azabicyclo[3.2.1]octan-3-yl 3,4-dimethoxybenzoic acid	Generator

Chemical Formula

C₁₈H₂₃NO₅

Average Mass

333.3840 Da

Monoisotopic Mass

333.15762 Da

IUPAC Name

8-acetyl-8-azabicyclo[3.2.1]octan-3-yl 3,4-dimethoxybenzoate

Traditional Name

8-acetyl-8-azabicyclo[3.2.1]octan-3-yl 3,4-dimethoxybenzoate

CAS Registry Number

Not Available

SMILES

COC1=CC=C(C=C1OC)C(=O)OC1CC2CCC(C1)N2C(C)=O

InChI Identifier

InChI=1S/C18H23NO5/c1-11(20)19-13-5-6-14(19)10-15(9-13)24-18(21)12-4-7-16(22-2)17(8-12)23-3/h4,7-8,13-15H,5-6,9-10H2,1-3H3

InChI Key

HZEOENYXYFFKIU-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
Convolvulus subhirsutus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as p-methoxybenzoic acids and derivatives. These are benzoic acids in which the hydrogen atom at position 4 of the benzene ring is replaced by a methoxy group.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Benzoic acids and derivatives

Direct Parent

P-methoxybenzoic acids and derivatives

Alternative Parents

Substituents

M-methoxybenzoic acid or derivatives
P-methoxybenzoic acid or derivatives
Benzoate ester
Dimethoxybenzene
O-dimethoxybenzene
N-acyl-piperidine
Tropane alkaloid
Anisole
Benzoyl
Phenoxy compound
N-acylpyrrolidine
Phenol ether
Methoxybenzene
Alkyl aryl ether
Piperidine
Tertiary carboxylic acid amide
Pyrrolidine
Acetamide
Carboxamide group
Carboxylic acid ester
Azacycle
Organoheterocyclic compound
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Ether
Carbonyl group
Organic oxygen compound
Organic nitrogen compound
Organic oxide
Organonitrogen compound
Organooxygen compound
Hydrocarbon derivative
Organopnictogen compound
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	2.33	ALOGPS
logP	1.44	ChemAxon
logS	-2.7	ALOGPS
pKa (Strongest Basic)	-1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	65.07 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	87.61 m³·mol⁻¹	ChemAxon
Polarizability	35.28 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

3788763

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 8-acetyl-8-azabicyclo[3.2.1]octan-3-yl 3,4-dimethoxybenzoate (NP0187068)

MOL for NP0187068 (8-acetyl-8-azabicyclo[3.2.1]octan-3-yl 3,4-dimethoxybenzoate)

3D MOL for NP0187068 (8-acetyl-8-azabicyclo[3.2.1]octan-3-yl 3,4-dimethoxybenzoate)

3D SDF for NP0187068 (8-acetyl-8-azabicyclo[3.2.1]octan-3-yl 3,4-dimethoxybenzoate)

3D-SDF for NP0187068 (8-acetyl-8-azabicyclo[3.2.1]octan-3-yl 3,4-dimethoxybenzoate)

PDB for NP0187068 (8-acetyl-8-azabicyclo[3.2.1]octan-3-yl 3,4-dimethoxybenzoate)

3D PDB for NP0187068 (8-acetyl-8-azabicyclo[3.2.1]octan-3-yl 3,4-dimethoxybenzoate)

SMILES for NP0187068 (8-acetyl-8-azabicyclo[3.2.1]octan-3-yl 3,4-dimethoxybenzoate)

INCHI for NP0187068 (8-acetyl-8-azabicyclo[3.2.1]octan-3-yl 3,4-dimethoxybenzoate)

Structure for NP0187068 (8-acetyl-8-azabicyclo[3.2.1]octan-3-yl 3,4-dimethoxybenzoate)

3D Structure for NP0187068 (8-acetyl-8-azabicyclo[3.2.1]octan-3-yl 3,4-dimethoxybenzoate)