NP-MRD: Showing NP-Card for 8-methyl-8-azabicyclo[3.2.1]octan-3-yl 3-hydroxy-2-(3-methoxyphenyl)propanoate (NP0186775)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-04 02:44:34 UTC

Updated at

2022-09-04 02:44:35 UTC

NP-MRD ID

NP0186775

Secondary Accession Numbers

None

Natural Product Identification

Common Name

8-methyl-8-azabicyclo[3.2.1]octan-3-yl 3-hydroxy-2-(3-methoxyphenyl)propanoate

Description

SCHEMBL22311559 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-hydroxy-2-(3-methoxyphenyl)propanoate is found in Datura stramonium. Based on a literature review very few articles have been published on SCHEMBL22311559.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 48 50  0  0  0  0  0  0  0  0999 V2000
    6.3149    2.3536   -0.9148 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5956    1.1864   -1.1900 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4594    0.8029   -0.5024 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9596    1.5766    0.5243 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8175    1.2103    1.2301 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1795    0.0303    0.8749 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6630   -0.7574   -0.1484 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9730   -2.0286   -0.5288 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9259   -2.9143    0.6985 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2580   -3.1468    1.0873 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5948   -1.6794   -0.9444 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2227   -1.9586   -2.1073 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3319   -1.0543   -0.1256 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6420   -0.7282   -0.5372 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7734    0.7799   -0.5476 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1770    1.2505   -0.7247 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.6535    1.7712    0.6359 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8977    0.4968    1.3779 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9630   -0.5757    0.3216 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6992   -1.4084    0.2686 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0501    0.1330   -0.9568 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4046    0.5277   -1.2532 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7935   -0.3617   -0.8217 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9015    3.1966   -1.5055 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3482    2.5724    0.1547 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3668    2.1759   -1.2439 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4252    2.5050    0.8352 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4484    1.8410    2.0340 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3008   -0.2398    1.4270 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4969   -2.5101   -1.3516 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4538   -2.3636    1.5380 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3824   -3.8549    0.4937 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8048   -3.4583    0.3229 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7375   -1.0680   -1.5897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2924    1.1733    0.3759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1660    1.1576   -1.3929 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2829    2.0514   -1.4896 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8145    2.3685    1.0664 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5141    2.4328    0.5531 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0818    0.3486    2.1004 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8373    0.5925    1.9502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8696   -1.2004    0.3876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9954   -2.3729   -0.2370 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3700   -1.7064    1.2841 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0927   -0.3051   -0.9340 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5386    0.6609   -2.3456 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7319    1.4382   -0.7482 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2310   -0.9411   -1.6452 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  7  1  0
  7 23  2  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  8 11  1  0
 11 12  2  0
 11 13  1  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
 19 21  1  0
 21 22  1  0
 23  3  1  0
 20 14  1  0
 21 16  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  4 27  1  0
  5 28  1  0
  6 29  1  0
 23 48  1  0
  8 30  1  6
  9 31  1  0
  9 32  1  0
 10 33  1  0
 14 34  1  6
 15 35  1  0
 15 36  1  0
 16 37  1  6
 17 38  1  0
 17 39  1  0
 18 40  1  0
 18 41  1  0
 19 42  1  1
 20 43  1  0
 20 44  1  0
 22 45  1  0
 22 46  1  0
 22 47  1  0
M  END


  Mrv1652309042204442D          

 23 25  0  0  0  0            999 V2000
   -5.7406    0.1613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0261   -0.2512    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3117    0.1613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3117    0.9863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5972    1.3988    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8827    0.9863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8827    0.1613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1682   -0.2512    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1682   -1.0762    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8827   -1.4887    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4538    0.1613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4538    0.9863    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7393   -0.2512    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0248    0.1613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6568   -0.3034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4452   -0.0602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7466    0.7077    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3341    1.4222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5183    1.5452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0865    0.9840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1824    0.8583    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.8969    1.2708    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5972   -0.2512    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  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  8 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
  7 23  2  0  0  0  0
  3 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0186775

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C18H25NO4/c1-19-13-6-7-14(19)10-16(9-13)23-18(21)17(11-20)12-4-3-5-15(8-12)22-2/h3-5,8,13-14,16-17,20H,6-7,9-11H2,1-2H3

> <INCHI_KEY>
GTQDIPBCLBLDHT-UHFFFAOYSA-N

> <FORMULA>
C18H25NO4

> <MOLECULAR_WEIGHT>
319.401

> <EXACT_MASS>
319.178358289

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
48

> <JCHEM_AVERAGE_POLARIZABILITY>
34.21173853915821

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
8-methyl-8-azabicyclo[3.2.1]octan-3-yl 3-hydroxy-2-(3-methoxyphenyl)propanoate

> <JCHEM_LOGP>
1.4135697509999998

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.126771169018937

> <JCHEM_PKA_STRONGEST_BASIC>
9.385561837076581

> <JCHEM_POLAR_SURFACE_AREA>
59.00000000000001

> <JCHEM_REFRACTIVITY>
87.2796

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
8-methyl-8-azabicyclo[3.2.1]octan-3-yl 3-hydroxy-2-(3-methoxyphenyl)propanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0     -10.716   0.301   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -9.382  -0.469   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -8.048   0.301   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -8.048   1.841   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -6.715   2.611   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -5.381   1.841   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -5.381   0.301   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -4.047  -0.469   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -4.047  -2.009   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -5.381  -2.779   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -2.714   0.301   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -2.714   1.841   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0      -1.380  -0.469   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -0.046   0.301   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.226  -0.566   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.698  -0.112   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.260   1.321   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.490   2.655   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.967   2.884   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.161   1.837   0.000  0.00  0.00           C+0
HETATM   21  N   UNK     0       2.207   1.602   0.000  0.00  0.00           N+0
HETATM   22  C   UNK     0       3.541   2.372   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -6.715  -0.469   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   23                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   23                                                  
CONECT    8    7    9   11                                                  
CONECT    9    8   10                                                       
CONECT   10    9                                                            
CONECT   11    8   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                                                            
CONECT   23    7    3                                                       
MASTER        0    0    0    0    0    0    0    0   23    0   50    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₂₅NO₄

Average Mass

319.4010 Da

Monoisotopic Mass

319.17836 Da

IUPAC Name

8-methyl-8-azabicyclo[3.2.1]octan-3-yl 3-hydroxy-2-(3-methoxyphenyl)propanoate

Traditional Name

8-methyl-8-azabicyclo[3.2.1]octan-3-yl 3-hydroxy-2-(3-methoxyphenyl)propanoate

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C18H25NO4/c1-19-13-6-7-14(19)10-16(9-13)23-18(21)17(11-20)12-4-3-5-15(8-12)22-2/h3-5,8,13-14,16-17,20H,6-7,9-11H2,1-2H3

InChI Key

GTQDIPBCLBLDHT-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
Phenoxy compound
Phenol ether
Anisole
Methoxybenzene
Alkyl aryl ether
Beta-hydroxy acid
Piperidine
Monocyclic benzene moiety
N-alkylpyrrolidine
Benzenoid
Hydroxy acid
Pyrrolidine
Amino acid or derivatives
Tertiary amine
Tertiary aliphatic amine
Carboxylic acid ester
Carboxylic acid derivative
Azacycle
Ether
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Amine
Organic nitrogen compound
Alcohol
Carbonyl group
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Organopnictogen compound
Organonitrogen compound
Organooxygen compound
Primary alcohol
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	1.41	ChemAxon
pKa (Strongest Acidic)	15.13	ChemAxon
pKa (Strongest Basic)	9.39	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	59 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	87.28 m³·mol⁻¹	ChemAxon
Polarizability	34.21 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

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

123970977

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-hydroxy-2-(3-methoxyphenyl)propanoate (NP0186775)

MOL for NP0186775 (8-methyl-8-azabicyclo[3.2.1]octan-3-yl 3-hydroxy-2-(3-methoxyphenyl)propanoate)

3D MOL for NP0186775 (8-methyl-8-azabicyclo[3.2.1]octan-3-yl 3-hydroxy-2-(3-methoxyphenyl)propanoate)

3D SDF for NP0186775 (8-methyl-8-azabicyclo[3.2.1]octan-3-yl 3-hydroxy-2-(3-methoxyphenyl)propanoate)

3D-SDF for NP0186775 (8-methyl-8-azabicyclo[3.2.1]octan-3-yl 3-hydroxy-2-(3-methoxyphenyl)propanoate)

PDB for NP0186775 (8-methyl-8-azabicyclo[3.2.1]octan-3-yl 3-hydroxy-2-(3-methoxyphenyl)propanoate)

3D PDB for NP0186775 (8-methyl-8-azabicyclo[3.2.1]octan-3-yl 3-hydroxy-2-(3-methoxyphenyl)propanoate)

SMILES for NP0186775 (8-methyl-8-azabicyclo[3.2.1]octan-3-yl 3-hydroxy-2-(3-methoxyphenyl)propanoate)

INCHI for NP0186775 (8-methyl-8-azabicyclo[3.2.1]octan-3-yl 3-hydroxy-2-(3-methoxyphenyl)propanoate)

Structure for NP0186775 (8-methyl-8-azabicyclo[3.2.1]octan-3-yl 3-hydroxy-2-(3-methoxyphenyl)propanoate)

3D Structure for NP0186775 (8-methyl-8-azabicyclo[3.2.1]octan-3-yl 3-hydroxy-2-(3-methoxyphenyl)propanoate)