NP-MRD: Showing NP-Card for 3alpha-(3,4,5-Trimethoxybenzoyloxy)nortropan-6beta-ol (NP0074964)

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Record Information

Version

2.0

Created at

2022-04-28 20:15:17 UTC

Updated at

2022-04-28 20:15:17 UTC

NP-MRD ID

NP0074964

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3alpha-(3,4,5-Trimethoxybenzoyloxy)nortropan-6beta-ol

Description

(1R,3R,5R,6S)-6-hydroxy-8-azabicyclo[3.2.1]Octan-3-yl 3,4,5-trimethoxybenzoate belongs to the class of organic compounds known as gallic acid and derivatives. Gallic acid and derivatives are compounds containing a 3,4,5-trihydroxybenzoic acid moiety. 3alpha-(3,4,5-Trimethoxybenzoyloxy)nortropan-6beta-ol is found in Erythroxylum zambesiacum. Based on a literature review very few articles have been published on (1R,3R,5R,6S)-6-hydroxy-8-azabicyclo[3.2.1]Octan-3-yl 3,4,5-trimethoxybenzoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 47 49  0  0  0  0  0  0  0  0999 V2000
   -1.8982   -1.4120    3.1747 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0446   -0.9420    2.4927 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8631   -0.3923    1.2303 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6272   -0.2955    0.6405 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4794    0.2603   -0.6253 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1573    0.3525   -1.2314 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0396    0.8575   -2.3760 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9478   -0.1129   -0.5471 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2078   -0.0032   -1.1728 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8607   -1.3393   -1.3385 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7352   -1.7197   -0.1640 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1194   -1.1194   -0.2650 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1171    0.0971    0.6389 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7631   -0.1517    1.8504 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6167    0.2701    0.8852 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0448    0.9427   -0.3248 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1975   -1.1024    1.0289 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5937    0.7198   -1.2941 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8374    0.6318   -0.7211 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9725    1.0959   -1.3939 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8204    1.6585   -2.6756 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9513    0.0727    0.5413 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2319   -0.0007    1.0934 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7483    1.0566    1.8806 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1518   -1.7078    4.2142 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4940   -2.3459    2.6907 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1222   -0.6424    3.1714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7355   -0.6509    1.1486 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1319    0.4710   -2.1908 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0711   -2.1260   -1.4604 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5172   -1.3670   -2.2415 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7489   -2.8216   -0.1046 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9096   -1.8444    0.0162 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2366   -0.7467   -1.3131 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5344    0.9978    0.1206 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7294   -0.0606    1.7452 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4402    0.8210    1.8239 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8352    1.3489   -1.0025 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3667    1.7943   -0.0687 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1770   -1.2253    1.1340 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4568    1.1477   -2.2754 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3682    0.9318   -3.3825 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1319    2.5427   -2.5959 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7710    2.0289   -3.0764 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0300    1.8690    1.9994 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6341    1.4809    1.3343 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1480    0.6802    2.8426 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 18  2  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 19 22  2  0
 22 23  1  0
 23 24  1  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 15 17  1  0
 22  3  1  0
 16  9  1  0
 17 11  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  4 28  1  0
 18 41  1  0
 21 42  1  0
 21 43  1  0
 21 44  1  0
 24 45  1  0
 24 46  1  0
 24 47  1  0
  9 29  1  6
 10 30  1  0
 10 31  1  0
 11 32  1  1
 12 33  1  0
 12 34  1  0
 13 35  1  6
 14 36  1  0
 15 37  1  1
 16 38  1  0
 16 39  1  0
 17 40  1  0
M  END


  Mrv1652304282222152D          

 24 26  0  0  1  0            999 V2000
    0.1593    0.4941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1593   -0.3309    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8044   -0.8453    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6087   -0.6617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9666    0.0816    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6087    0.8249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8044    1.0085    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0361    0.0816    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.7916    0.0816    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2041    0.7961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7916    1.5106    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0291    0.7961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4416    1.5106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2666    1.5106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6791    0.7961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2666    0.0816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4416    0.0816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6791   -0.6329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2666   -1.3473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5041    0.7961    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9166    0.0816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6791    2.2250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5041    2.2250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5840   -0.6888    0.0000 O   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
  6  7  1  0  0  0  0
  1  7  1  0  0  0  0
  7  8  1  1  0  0  0
  3  8  1  1  0  0  0
  5  9  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 12 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 15 20  1  0  0  0  0
 20 21  1  0  0  0  0
 14 22  1  0  0  0  0
 22 23  1  0  0  0  0
  2 24  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0074964

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(=CC(OC)=C1OC)C(=O)O[C@@H]1C[C@H]2C[C@H](O)[C@@H](C1)N2

> <INCHI_IDENTIFIER>
InChI=1S/C17H23NO6/c1-21-14-4-9(5-15(22-2)16(14)23-3)17(20)24-11-6-10-7-13(19)12(8-11)18-10/h4-5,10-13,18-19H,6-8H2,1-3H3/t10-,11+,12+,13-/m0/s1

> <INCHI_KEY>
QSSMPCOINVZTOL-LOWDOPEQSA-N

> <FORMULA>
C17H23NO6

> <MOLECULAR_WEIGHT>
337.372

> <EXACT_MASS>
337.152537465

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
35.48667284048876

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,3R,5R,6S)-6-hydroxy-8-azabicyclo[3.2.1]octan-3-yl 3,4,5-trimethoxybenzoate

> <ALOGPS_LOGP>
0.80

> <JCHEM_LOGP>
0.5251011663333329

> <ALOGPS_LOGS>
-2.54

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.549646704239134

> <JCHEM_PKA_STRONGEST_BASIC>
10.317488076103425

> <JCHEM_POLAR_SURFACE_AREA>
86.25000000000001

> <JCHEM_REFRACTIVITY>
85.82860000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.70e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,3R,5R,6S)-6-hydroxy-8-azabicyclo[3.2.1]octan-3-yl 3,4,5-trimethoxybenzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       0.297   0.922   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.297  -0.618   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.501  -1.578   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.003  -1.235   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.671   0.152   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.003   1.540   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.501   1.883   0.000  0.00  0.00           C+0
HETATM    8  N   UNK     0       1.934   0.152   0.000  0.00  0.00           N+0
HETATM    9  O   UNK     0       5.211   0.152   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       5.981   1.486   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       5.211   2.820   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       7.521   1.486   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.291   2.820   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.831   2.820   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.601   1.486   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.831   0.152   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.291   0.152   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      10.601  -1.181   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       9.831  -2.515   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      12.141   1.486   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      12.911   0.152   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      10.601   4.153   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      12.141   4.153   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -1.090  -1.286   0.000  0.00  0.00           O+0
CONECT    1    2    7                                                       
CONECT    2    1    3   24                                                  
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    9                                                  
CONECT    6    5    7                                                       
CONECT    7    6    1    8                                                  
CONECT    8    7    3                                                       
CONECT    9    5   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   22                                                  
CONECT   15   14   16   20                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16   12                                                       
CONECT   18   16   19                                                       
CONECT   19   18                                                            
CONECT   20   15   21                                                       
CONECT   21   20                                                            
CONECT   22   14   23                                                       
CONECT   23   22                                                            
CONECT   24    2                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   52    0
END

View in JSmol

Synonyms

Value	Source
(1R,3R,5R,6S)-6-Hydroxy-8-azabicyclo[3.2.1]octan-3-yl 3,4,5-trimethoxybenzoic acid	Generator

Chemical Formula

C₁₇H₂₃NO₆

Average Mass

337.3720 Da

Monoisotopic Mass

337.15254 Da

IUPAC Name

(1R,3R,5R,6S)-6-hydroxy-8-azabicyclo[3.2.1]octan-3-yl 3,4,5-trimethoxybenzoate

Traditional Name

(1R,3R,5R,6S)-6-hydroxy-8-azabicyclo[3.2.1]octan-3-yl 3,4,5-trimethoxybenzoate

CAS Registry Number

Not Available

SMILES

COC1=CC(=CC(OC)=C1OC)C(=O)O[C@@H]1C[C@H]2C[C@H](O)[C@@H](C1)N2

InChI Identifier

InChI=1S/C17H23NO6/c1-21-14-4-9(5-15(22-2)16(14)23-3)17(20)24-11-6-10-7-13(19)12(8-11)18-10/h4-5,10-13,18-19H,6-8H2,1-3H3/t10-,11+,12+,13-/m0/s1

InChI Key

QSSMPCOINVZTOL-LOWDOPEQSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Erythroxylum zambesiacum	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as gallic acid and derivatives. Gallic acid and derivatives are compounds containing a 3,4,5-trihydroxybenzoic acid moiety.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Benzoic acids and derivatives

Direct Parent

Gallic acid and derivatives

Alternative Parents

Substituents

Gallic acid or derivatives
P-methoxybenzoic acid or derivatives
M-methoxybenzoic acid or derivatives
Benzoate ester
Tropane alkaloid
Phenoxy compound
Methoxybenzene
Phenol ether
Benzoyl
Anisole
Alkyl aryl ether
Piperidine
Pyrrolidine
Cyclic alcohol
Secondary alcohol
Carboxylic acid ester
Amino acid or derivatives
1,2-aminoalcohol
Azacycle
Organoheterocyclic compound
Secondary amine
Monocarboxylic acid or derivatives
Ether
Secondary aliphatic amine
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Amine
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	0.8	ALOGPS
logP	0.53	ChemAxon
logS	-2.5	ALOGPS
pKa (Strongest Acidic)	14.55	ChemAxon
pKa (Strongest Basic)	10.32	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	86.25 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	85.83 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

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

163075584

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 3alpha-(3,4,5-Trimethoxybenzoyloxy)nortropan-6beta-ol (NP0074964)

MOL for NP0074964 (3alpha-(3,4,5-Trimethoxybenzoyloxy)nortropan-6beta-ol)

3D MOL for NP0074964 (3alpha-(3,4,5-Trimethoxybenzoyloxy)nortropan-6beta-ol)

3D SDF for NP0074964 (3alpha-(3,4,5-Trimethoxybenzoyloxy)nortropan-6beta-ol)

3D-SDF for NP0074964 (3alpha-(3,4,5-Trimethoxybenzoyloxy)nortropan-6beta-ol)

PDB for NP0074964 (3alpha-(3,4,5-Trimethoxybenzoyloxy)nortropan-6beta-ol)

3D PDB for NP0074964 (3alpha-(3,4,5-Trimethoxybenzoyloxy)nortropan-6beta-ol)

SMILES for NP0074964 (3alpha-(3,4,5-Trimethoxybenzoyloxy)nortropan-6beta-ol)

INCHI for NP0074964 (3alpha-(3,4,5-Trimethoxybenzoyloxy)nortropan-6beta-ol)

Structure for NP0074964 (3alpha-(3,4,5-Trimethoxybenzoyloxy)nortropan-6beta-ol)

3D Structure for NP0074964 (3alpha-(3,4,5-Trimethoxybenzoyloxy)nortropan-6beta-ol)