NP-MRD: Showing NP-Card for 1-formyl-8-methyl-8-azabicyclo[3.2.1]octan-3-yl (2s)-3-hydroxy-2-phenylpropanoate (NP0266675)

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Record Information

Version

2.0

Created at

2022-09-08 11:05:52 UTC

Updated at

2022-09-08 11:05:52 UTC

NP-MRD ID

NP0266675

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-formyl-8-methyl-8-azabicyclo[3.2.1]octan-3-yl (2s)-3-hydroxy-2-phenylpropanoate

Description

Hyoscyamal 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. 1-formyl-8-methyl-8-azabicyclo[3.2.1]octan-3-yl (2s)-3-hydroxy-2-phenylpropanoate is found in Hyoscyamus niger. 1-formyl-8-methyl-8-azabicyclo[3.2.1]octan-3-yl (2s)-3-hydroxy-2-phenylpropanoate was first documented in 2009 (PMID: 19401911). Based on a literature review very few articles have been published on hyoscyamal.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 46 48  0  0  0  0  0  0  0  0999 V2000
   -4.6174    0.0424    1.3254 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2708   -0.0752    0.8473 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1424   -1.0272   -0.2405 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4838   -0.2673   -1.5059 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2464    1.1748   -1.1635 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7393    1.1239    0.2714 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1589    2.3460    0.9653 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7651    3.4188    0.5591 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2333    0.9765    0.2017 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8774   -0.2007   -0.6635 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4814   -0.5622   -0.4922 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4102   -0.5368   -1.5091 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0129   -0.1695   -2.6473 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8239   -0.9255   -1.2784 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9269   -2.3939   -0.8698 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2622   -2.6872   -0.6721 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4955   -0.0960   -0.2771 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6273    0.6266   -0.6041 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2811    1.4153    0.3146 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8150    1.5015    1.5937 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6876    0.7910    1.9472 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0551    0.0176    1.0275 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6904   -1.4425   -0.2877 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1790   -0.8717    0.9840 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1245    0.9658    1.0469 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6081   -0.0152    2.4338 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7739   -1.9072   -0.1067 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8809   -0.6012   -2.3771 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5608   -0.4194   -1.7330 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5024    1.6540   -1.8305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1954    1.7556   -1.1643 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8087    2.3222    1.8285 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7632    0.8441    1.1797 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8332    1.8875   -0.2869 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0566    0.0938   -1.7126 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3741   -0.8423   -2.2364 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5095   -2.9681   -1.7295 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3097   -2.5316    0.0206 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3168   -3.4622   -0.0517 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0288    0.5843   -1.6108 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1602    1.9627    0.0195 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3149    2.1235    2.3526 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2982    0.8476    2.9697 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1694   -0.5458    1.2892 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4755   -2.2251   -1.0156 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3730   -1.7016    0.7480 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  9  1  0
  9 10  1  0
 10 23  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 14 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
  6  7  1  1
  7  8  2  0
  6  2  1  0
 22 17  1  0
 23  3  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  3 27  1  1
  4 28  1  0
  4 29  1  0
  5 30  1  0
  5 31  1  0
  9 33  1  0
  9 34  1  0
 10 35  1  6
 23 45  1  0
 23 46  1  0
 14 36  1  6
 15 37  1  0
 15 38  1  0
 16 39  1  0
 18 40  1  0
 19 41  1  0
 20 42  1  0
 21 43  1  0
 22 44  1  0
  7 32  1  0
M  END


  Mrv1652309082213052D          

 23 25  0  0  1  0            999 V2000
    0.3528    4.2361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4542    4.4076    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1914    5.3262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0072    5.2032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4197    4.4887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1183    3.7208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6794    3.1160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4837    3.2996    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3299    3.4776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3517    3.9423    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0662    3.5298    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0662    2.7048    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3517    2.2923    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7807    2.2923    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4951    2.7048    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2096    2.2923    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7807    1.4673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4951    1.0548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4951    0.2298    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7807   -0.1827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0662    0.2298    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0662    1.0548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4134    4.7650    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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  2  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  6  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  2  0  0  0  0
 14 12  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 14 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 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
 17 22  1  0  0  0  0
 10 23  1  0  0  0  0
  3 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0266675

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CN1C2CCC1(CC(C2)OC(=O)[C@H](CO)C1=CC=CC=C1)C=O

> <INCHI_IDENTIFIER>
InChI=1S/C18H23NO4/c1-19-14-7-8-18(19,12-21)10-15(9-14)23-17(22)16(11-20)13-5-3-2-4-6-13/h2-6,12,14-16,20H,7-11H2,1H3/t14?,15?,16-,18?/m1/s1

> <INCHI_KEY>
PHYDFSZUNLSCDZ-LMBQMVEXSA-N

> <FORMULA>
C18H23NO4

> <MOLECULAR_WEIGHT>
317.385

> <EXACT_MASS>
317.162708225

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
33.21326805883871

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1-formyl-8-methyl-8-azabicyclo[3.2.1]octan-3-yl (2S)-3-hydroxy-2-phenylpropanoate

> <JCHEM_LOGP>
1.1187552216666659

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.145739869561332

> <JCHEM_PKA_STRONGEST_BASIC>
7.4962261161791055

> <JCHEM_POLAR_SURFACE_AREA>
66.84

> <JCHEM_REFRACTIVITY>
86.01540000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
1-formyl-8-methyl-8-azabicyclo[3.2.1]octan-3-yl (2S)-3-hydroxy-2-phenylpropanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0       0.659   7.907   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0      -0.848   8.228   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0      -0.357   9.942   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.880   9.713   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.650   8.379   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.087   6.945   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -3.135   5.817   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -4.636   6.159   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -0.616   6.492   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.657   7.359   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       1.990   6.589   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       1.990   5.049   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       0.657   4.279   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       3.324   4.279   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.658   5.049   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       5.991   4.279   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       3.324   2.739   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.658   1.969   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.658   0.429   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.324  -0.341   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.990   0.429   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.990   1.969   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.772   8.895   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    6                                                  
CONECT    3    2    4   23                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    2    7    9                                             
CONECT    7    6    8                                                       
CONECT    8    7                                                            
CONECT    9    6   10                                                       
CONECT   10    9   11   23                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   17                                                  
CONECT   15   14   16                                                       
CONECT   16   15                                                            
CONECT   17   14   18   22                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   17                                                       
CONECT   23   10    3                                                       
MASTER        0    0    0    0    0    0    0    0   23    0   50    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₂₃NO₄

Average Mass

317.3850 Da

Monoisotopic Mass

317.16271 Da

IUPAC Name

1-formyl-8-methyl-8-azabicyclo[3.2.1]octan-3-yl (2S)-3-hydroxy-2-phenylpropanoate

Traditional Name

1-formyl-8-methyl-8-azabicyclo[3.2.1]octan-3-yl (2S)-3-hydroxy-2-phenylpropanoate

CAS Registry Number

Not Available

SMILES

CN1C2CCC1(CC(C2)OC(=O)[C@H](CO)C1=CC=CC=C1)C=O

InChI Identifier

InChI=1S/C18H23NO4/c1-19-14-7-8-18(19,12-21)10-15(9-14)23-17(22)16(11-20)13-5-3-2-4-6-13/h2-6,12,14-16,20H,7-11H2,1H3/t14?,15?,16-,18?/m1/s1

InChI Key

PHYDFSZUNLSCDZ-LMBQMVEXSA-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
Hyoscyamus niger	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
Beta-hydroxy acid
Benzenoid
N-alkylpyrrolidine
Piperidine
Hydroxy acid
Monocyclic benzene moiety
Pyrrolidine
Tertiary aliphatic amine
Tertiary amine
Carboxylic acid ester
Amino acid or derivatives
Azacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Organonitrogen compound
Carbonyl group
Amine
Aldehyde
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	1.12	ChemAxon
pKa (Strongest Acidic)	15.15	ChemAxon
pKa (Strongest Basic)	7.5	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	66.84 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	86.02 m³·mol⁻¹	ChemAxon
Polarizability	33.21 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

129880591

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Begum AS, Verma S, Sahai M, Schneider K, Sussmuth R: Hyoscyamal, a new tetrahydrofurano lignan from Hyoscyamus niger Linn. Nat Prod Res. 2009;23(7):595-600. doi: 10.1080/14786410802113961. [PubMed:19401911 ]
LOTUS database [Link]

Showing NP-Card for 1-formyl-8-methyl-8-azabicyclo[3.2.1]octan-3-yl (2s)-3-hydroxy-2-phenylpropanoate (NP0266675)

MOL for NP0266675 (1-formyl-8-methyl-8-azabicyclo[3.2.1]octan-3-yl (2s)-3-hydroxy-2-phenylpropanoate)

3D MOL for NP0266675 (1-formyl-8-methyl-8-azabicyclo[3.2.1]octan-3-yl (2s)-3-hydroxy-2-phenylpropanoate)

3D SDF for NP0266675 (1-formyl-8-methyl-8-azabicyclo[3.2.1]octan-3-yl (2s)-3-hydroxy-2-phenylpropanoate)

3D-SDF for NP0266675 (1-formyl-8-methyl-8-azabicyclo[3.2.1]octan-3-yl (2s)-3-hydroxy-2-phenylpropanoate)

PDB for NP0266675 (1-formyl-8-methyl-8-azabicyclo[3.2.1]octan-3-yl (2s)-3-hydroxy-2-phenylpropanoate)

3D PDB for NP0266675 (1-formyl-8-methyl-8-azabicyclo[3.2.1]octan-3-yl (2s)-3-hydroxy-2-phenylpropanoate)

SMILES for NP0266675 (1-formyl-8-methyl-8-azabicyclo[3.2.1]octan-3-yl (2s)-3-hydroxy-2-phenylpropanoate)

INCHI for NP0266675 (1-formyl-8-methyl-8-azabicyclo[3.2.1]octan-3-yl (2s)-3-hydroxy-2-phenylpropanoate)

Structure for NP0266675 (1-formyl-8-methyl-8-azabicyclo[3.2.1]octan-3-yl (2s)-3-hydroxy-2-phenylpropanoate)

3D Structure for NP0266675 (1-formyl-8-methyl-8-azabicyclo[3.2.1]octan-3-yl (2s)-3-hydroxy-2-phenylpropanoate)