NP-MRD: Showing NP-Card for (R)-Reticuline (NP0137697)

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Record Information

Version

2.0

Created at

2022-05-31 16:03:52 UTC

Updated at

2022-05-31 16:03:52 UTC

NP-MRD ID

NP0137697

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(R)-Reticuline

Description

(R)-reticuline belongs to the class of organic compounds known as benzylisoquinolines. These are organic compounds containing an isoquinoline to which a benzyl group is attached (R)-reticuline is a primary metabolite. Primary metabolites are metabolically or physiologically essential metabolites. They are directly involved in an organism’s growth, development or reproduction. (R)-Reticuline is found in Annona glabra, Annona purpurea, Argemone gracilenta, Argemone ochroleuca, Artabotrys hexapetalus, Berberis integerrima, Berberis nummularia, Croton celtidifolius, Ficus pachyrrhachis, Fumaria vaillantii, Glaucium fimbrilligerum, Glaucium flavum, Guatteria dumetorum, Isopyrum thalictroides, Licaria triandra, Litsea leefeana, Papaver somniferum, Phylica rogersii, Sassafras albidum, Uvaria dulcis and Xylopia parviflora. (R)-Reticuline was first documented in 2018 (PMID: 29786941). Based on a literature review very few articles have been published on (R)-reticuline.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 47 49  0  0  0  0  0  0  0  0999 V2000
    5.0705    3.0833   -0.8503 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0314    2.8338    0.0729 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3169    1.6434    0.0661 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5489    0.6187   -0.8202 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7942   -0.5330   -0.7608 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7861   -0.7171    0.1714 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9905   -1.9717    0.2085 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2149   -1.8753   -0.6871 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9675   -0.6494   -0.3120 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6218    0.6021   -0.7954 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3475    1.7169   -0.4162 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0341    2.9889   -0.8775 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4172    1.6029    0.4411 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1292    2.7015    0.8127 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2270    2.7316    1.6676 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7429    0.3440    0.9097 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0299   -0.7531    0.5371 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3881   -2.0948    1.0294 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3543   -2.9639   -0.2366 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0431   -2.9826   -0.7402 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7417   -4.0413   -1.6338 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5686    0.3240    1.0531 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3137    1.4786    1.0055 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0669    2.5119    1.9127 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2541    4.1860   -0.9176 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9891    2.5833   -0.4929 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7485    2.7659   -1.8546 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3343    0.7533   -1.5520 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0178   -1.3097   -1.4823 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7275   -2.1359    1.2737 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6626   -2.8112   -0.0662 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1715   -1.6705   -1.7325 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2049    0.7126   -1.4644 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2796    3.1903   -1.5027 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9643    2.6002    2.7372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7361    3.7122    1.5364 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9845    1.9652    1.3711 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6069    0.2872    1.5960 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6021   -2.4550    1.6952 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4012   -2.1292    1.4815 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0515   -2.4897   -0.9782 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7037   -3.9910   -0.0298 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7203   -3.6353   -2.6847 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1868   -4.5745   -1.4677 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5898   -4.7619   -1.6276 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7751    0.2155    1.8097 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3392    2.3932    2.5945 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  7  1  0
  7  6  1  0
  6 22  2  0
 22 23  1  0
 23 24  1  0
 23  3  2  0
  3  2  1  0
  2  1  1  0
  3  4  1  0
  4  5  2  0
  8 20  1  0
 20 21  1  0
 20 19  1  0
 19 18  1  0
 18 17  1  0
 17 16  2  0
 16 13  1  0
 13 14  1  0
 14 15  1  0
 13 11  2  0
 11 12  1  0
 11 10  1  0
 10  9  2  0
  9  8  1  0
  5  6  1  0
  9 17  1  0
  8 32  1  6
  7 30  1  0
  7 31  1  0
 22 46  1  0
 24 47  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  4 28  1  0
  5 29  1  0
 21 43  1  0
 21 44  1  0
 21 45  1  0
 19 41  1  0
 19 42  1  0
 18 39  1  0
 18 40  1  0
 16 38  1  0
 15 35  1  0
 15 36  1  0
 15 37  1  0
 12 34  1  0
 10 33  1  0
M  END


  Mrv1652305312218032D          

 25 27  0  0  1  0            999 V2000
    2.1434   -2.0625    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  1  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  2  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
  4 12  1  0  0  0  0
  2 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 19 22  2  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  2  0  0  0  0
  2 25  1  0  0  0  0
 17 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0137697

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@]1(CC2=CC(O)=C(OC)C=C2)N(C)CCC2=CC(OC)=C(O)C=C12

> <INCHI_IDENTIFIER>
InChI=1S/C19H23NO4/c1-20-7-6-13-10-19(24-3)17(22)11-14(13)15(20)8-12-4-5-18(23-2)16(21)9-12/h4-5,9-11,15,21-22H,6-8H2,1-3H3/t15-/m1/s1

> <INCHI_KEY>
BHLYRWXGMIUIHG-OAHLLOKOSA-N

> <FORMULA>
C19H23NO4

> <MOLECULAR_WEIGHT>
329.396

> <EXACT_MASS>
329.162708225

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
36.254984479585644

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R)-1-[(3-hydroxy-4-methoxyphenyl)methyl]-6-methoxy-2-methyl-1,2,3,4-tetrahydroisoquinolin-7-ol

> <JCHEM_LOGP>
3.1049593069999997

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
10.36995691314734

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.763064568264014

> <JCHEM_PKA_STRONGEST_BASIC>
7.810592585816691

> <JCHEM_POLAR_SURFACE_AREA>
62.16000000000001

> <JCHEM_REFRACTIVITY>
93.83630000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(-)-reticuline

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 31-MAY-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   31-MAY-22         0                                  
HETATM    1  H   UNK     0       4.001  -3.850   0.000  0.00  0.00           H+0
HETATM    2  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.000  -7.700   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       0.000  -9.240   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -2.667  -7.700   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0       1.334  -2.310   0.000  0.00  0.00           N+0
HETATM   14  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       8.002  -0.000   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       8.002  -3.080   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   13   25                                             
CONECT    3    2    4                                                       
CONECT    4    3    5   12                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   11                                                  
CONECT    9    8   10                                                       
CONECT   10    9                                                            
CONECT   11    8   12                                                       
CONECT   12   11    4                                                       
CONECT   13    2   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   25                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   22                                                  
CONECT   20   19   21                                                       
CONECT   21   20                                                            
CONECT   22   19   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24    2   17                                                  
MASTER        0    0    0    0    0    0    0    0   25    0   54    0
END

View in JSmol

Synonyms

Value	Source
(-)-Reticuline	ChEBI
(1R)-1,2,3,4-Tetrahydro-1-[(3-hydroxy-4-methoxyphenyl)methyl]-6-methoxy-2-methyl-7-isoquinolinol	ChEBI
(R)-(-)-Reticuline	ChEBI

Chemical Formula

C₁₉H₂₃NO₄

Average Mass

329.3960 Da

Monoisotopic Mass

329.16271 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

3968-19-2

SMILES

[H][C@]1(CC2=CC(O)=C(OC)C=C2)N(C)CCC2=CC(OC)=C(O)C=C12

InChI Identifier

InChI=1S/C19H23NO4/c1-20-7-6-13-10-19(24-3)17(22)11-14(13)15(20)8-12-4-5-18(23-2)16(21)9-12/h4-5,9-11,15,21-22H,6-8H2,1-3H3/t15-/m1/s1

InChI Key

BHLYRWXGMIUIHG-OAHLLOKOSA-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
Annona glabra	LOTUS Database	35616633
Annona purpurea	LOTUS Database	35616633
Argemone gracilenta Greene	LOTUS Database	35616633
Argemone ochroleuca	LOTUS Database	35616633
Artabotrys hexapetalus	LOTUS Database	35616633
Berberis integerrima	LOTUS Database	35616633
Berberis nummularia	LOTUS Database	35616633
Croton celtidifolius	LOTUS Database	35616633
Ficus pachyrrhachis	LOTUS Database	35616633
Fumaria vaillantii	LOTUS Database	35616633
Glaucium fimbrilligerum	LOTUS Database	35616633
Glaucium flavum	LOTUS Database	35616633
Guatteria dumetorum	LOTUS Database	35616633
Isopyrum thalictroides	LOTUS Database	35616633
Licaria triandra	LOTUS Database	35616633
Litsea leefeana	LOTUS Database	35616633
Papaver somniferum	LOTUS Database	35616633
Phylica rogersii	LOTUS Database	35616633
Sassafras albidum	LOTUS Database	35616633
Uvaria dulcis	LOTUS Database	35616633
Xylopia parviflora	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzylisoquinolines. These are organic compounds containing an isoquinoline to which a benzyl group is attached.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Isoquinolines and derivatives

Sub Class

Benzylisoquinolines

Direct Parent

Benzylisoquinolines

Alternative Parents

Substituents

Benzylisoquinoline
Methoxyphenol
Tetrahydroisoquinoline
Phenoxy compound
Anisole
Methoxybenzene
Phenol ether
Alkyl aryl ether
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Aralkylamine
Phenol
Monocyclic benzene moiety
Benzenoid
Tertiary aliphatic amine
Tertiary amine
Ether
Azacycle
Amine
Organic nitrogen compound
Hydrocarbon derivative
Organopnictogen compound
Organic oxygen compound
Organonitrogen compound
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

reticuline (CHEBI:17428 )
Isoquinoline alkaloids (C05178 )

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

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00051969

Chemspider ID

389485

KEGG Compound ID

C05178

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Reticuline

METLIN ID

Not Available

PubChem Compound

440586

PDB ID

Not Available

ChEBI ID

17428

Good Scents ID

Not Available

References

General References

Lipp A, Ferenc D, Gutz C, Geffe M, Vierengel N, Schollmeyer D, Schafer HJ, Waldvogel SR, Opatz T: A Regio- and Diastereoselective Anodic Aryl-Aryl Coupling in the Biomimetic Total Synthesis of (-)-Thebaine. Angew Chem Int Ed Engl. 2018 Aug 20;57(34):11055-11059. doi: 10.1002/anie.201803887. Epub 2018 Jun 14. [PubMed:29786941 ]

Showing NP-Card for (R)-Reticuline (NP0137697)

MOL for NP0137697 ((R)-Reticuline)

3D MOL for NP0137697 ((R)-Reticuline)

3D SDF for NP0137697 ((R)-Reticuline)

3D-SDF for NP0137697 ((R)-Reticuline)

PDB for NP0137697 ((R)-Reticuline)

3D PDB for NP0137697 ((R)-Reticuline)

SMILES for NP0137697 ((R)-Reticuline)

INCHI for NP0137697 ((R)-Reticuline)

Structure for NP0137697 ((R)-Reticuline)

3D Structure for NP0137697 ((R)-Reticuline)