NP-MRD: Showing NP-Card for Boldine (NP0137203)

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Record Information

Version

2.0

Created at

2022-05-30 16:45:00 UTC

Updated at

2022-05-30 16:45:00 UTC

NP-MRD ID

NP0137203

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Boldine

Description

(S)-Boldine belongs to the class of organic compounds known as aporphines. These are quinoline alkaloids containing the dibenzo[de,g]quinoline ring system or a dehydrogenated derivative thereof (S)-Boldine is a very strong basic compound (based on its pKa). Outside of the human body, (S)-boldine has been detected, but not quantified in, sweet bay. Boldine is found in Actinodaphne pruinosa, Beilschmiedia alloiophylla, Beilschmiedia kunstleri, Hedycarya angustifolia, Licaria triandra, Lindera glauca, Litsea glutinosa, Litsea leefeana, Litsea wightiana, Neolitsea dealbata, Neolitsea konishii, Peumus boldus, Phoebe grandis, Sassafras albidum, Siparuna pauciflora and Xylopia parviflora. This could make (S)-boldine a potential biomarker for the consumption of these foods.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 45 48  0  0  0  0  0  0  0  0999 V2000
    4.9798    1.0190    0.3701 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7130   -0.3704    0.3841 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3976   -0.7762    0.2095 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3582    0.1487    0.0244 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0948   -0.3103   -0.1395 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8012   -1.6713   -0.1356 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8549   -2.5768    0.0527 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1387   -2.1244    0.2232 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1927   -3.0184    0.4114 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5457   -2.2028   -0.4441 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5760   -1.2771    0.0893 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3326    0.0911   -0.3247 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3880    0.8896   -0.6369 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1636    2.2243   -0.8709 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8974    2.7454   -0.7893 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6798    4.0951   -1.0242 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2041    1.9387   -0.4693 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4071    2.5884   -0.4126 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6528    3.2880    0.8390 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0293    0.6176   -0.2476 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7522    0.3793   -0.7388 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8597   -1.1083   -0.7133 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8985   -1.7860    0.0285 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3388   -2.4876    1.1934 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0374    1.2458    0.5918 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3428    1.4855    1.1723 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6296    1.4933   -0.5807 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6484    1.1486    0.0017 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6139   -3.6503    0.0581 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9591   -3.9999    0.4145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6360   -3.2382   -0.0380 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6666   -2.2814   -1.5700 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3556   -1.2663    1.2273 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9879    2.9050   -1.1281 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3928    4.7493   -1.2574 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5188    2.6113    1.6959 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6757    3.6831    0.8131 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9561    4.1336    0.9539 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3634    0.8576    0.0680 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1870    0.7748   -1.6955 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8694   -1.4710   -1.7703 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8834   -1.3549   -0.3181 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4270   -2.6792    1.1000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8711   -3.5139    1.2594 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0753   -1.9481    2.1234 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  8  2  0
  8  9  1  0
  8  7  1  0
  7  6  2  0
  6 10  1  0
 10 11  1  0
 11 23  1  0
 23 24  1  0
 23 22  1  0
 22 21  1  0
 21 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 18 19  1  0
 17 20  2  0
 20  5  1  0
  5  4  2  0
 20 12  1  0
  4  3  1  0
  5  6  1  0
 12 11  1  0
 12 13  2  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  9 30  1  0
  7 29  1  0
 10 31  1  0
 10 32  1  0
 11 33  1  1
 24 43  1  0
 24 44  1  0
 24 45  1  0
 22 41  1  0
 22 42  1  0
 21 39  1  0
 21 40  1  0
 14 34  1  0
 16 35  1  0
 19 36  1  0
 19 37  1  0
 19 38  1  0
  4 28  1  0
M  END


  Mrv0541 05061310502D          

 24 27  0  0  0  0            999 V2000
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.8250    0.0000 C   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
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   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
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    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
    3.5724   -1.2375    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
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    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
    5.0013   -0.4125    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
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  5  4  1  0  0  0  0
 10  4  1  0  0  0  0
 10  7  2  0  0  0  0
 11  6  1  0  0  0  0
 11  8  2  0  0  0  0
 12  9  2  0  0  0  0
 12 11  1  0  0  0  0
 13  6  1  0  0  0  0
 14  8  1  0  0  0  0
 15  7  1  0  0  0  0
 16  9  1  0  0  0  0
 16 14  2  0  0  0  0
 17 10  1  0  0  0  0
 17 13  1  0  0  0  0
 18 12  1  0  0  0  0
 18 17  2  0  0  0  0
 19 15  2  0  0  0  0
 19 18  1  0  0  0  0
 20  1  1  0  0  0  0
 20  5  1  0  0  0  0
 20 13  1  0  0  0  0
 21 14  1  0  0  0  0
 22 15  1  0  0  0  0
 23  2  1  0  0  0  0
 23 16  1  0  0  0  0
 24  3  1  0  0  0  0
 24 19  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0137203

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(O)C=C2CC3N(C)CCC4=CC(O)=C(OC)C(C2=C1)=C34

> <INCHI_IDENTIFIER>
InChI=1S/C19H21NO4/c1-20-5-4-10-7-15(22)19(24-3)18-12-9-16(23-2)14(21)8-11(12)6-13(20)17(10)18/h7-9,13,21-22H,4-6H2,1-3H3

> <INCHI_KEY>
LZJRNLRASBVRRX-UHFFFAOYSA-N

> <FORMULA>
C19H21NO4

> <MOLECULAR_WEIGHT>
327.3743

> <EXACT_MASS>
327.147058165

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_AVERAGE_POLARIZABILITY>
35.347607692268554

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4,16-dimethoxy-10-methyl-10-azatetracyclo[7.7.1.0²,⁷.0¹³,¹⁷]heptadeca-1(17),2,4,6,13,15-hexaene-5,15-diol

> <ALOGPS_LOGP>
2.33

> <JCHEM_LOGP>
2.7789388529999997

> <ALOGPS_LOGS>
-2.99

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
7.690712008032604

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.674202396319299

> <JCHEM_PKA_STRONGEST_BASIC>
12.345130218305792

> <JCHEM_POLAR_SURFACE_AREA>
62.16000000000001

> <JCHEM_REFRACTIVITY>
92.91449999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.34e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4,16-dimethoxy-10-methyl-10-azatetracyclo[7.7.1.0²,⁷.0¹³,¹⁷]heptadeca-1(17),2,4,6,13,15-hexaene-5,15-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.669   1.540   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.002  -3.080   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.002   0.000   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.336  -0.770   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       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   20  N   UNK     0       2.667  -3.080   0.000  0.00  0.00           N+0
HETATM   21  O   UNK     0      10.669  -3.080   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       4.001   3.850   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      10.669   0.000   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       6.668   2.310   0.000  0.00  0.00           O+0
CONECT    1   20                                                            
CONECT    2   23                                                            
CONECT    3   24                                                            
CONECT    4    5   10                                                       
CONECT    5    4   20                                                       
CONECT    6   11   13                                                       
CONECT    7   10   15                                                       
CONECT    8   11   14                                                       
CONECT    9   12   16                                                       
CONECT   10    4    7   17                                                  
CONECT   11    6    8   12                                                  
CONECT   12    9   11   18                                                  
CONECT   13    6   17   20                                                  
CONECT   14    8   16   21                                                  
CONECT   15    7   19   22                                                  
CONECT   16    9   14   23                                                  
CONECT   17   10   13   18                                                  
CONECT   18   12   17   19                                                  
CONECT   19   15   18   24                                                  
CONECT   20    1    5   13                                                  
CONECT   21   14                                                            
CONECT   22   15                                                            
CONECT   23    2   16                                                       
CONECT   24    3   19                                                       
MASTER        0    0    0    0    0    0    0    0   24    0   54    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₂₁NO₄

Average Mass

327.3743 Da

Monoisotopic Mass

327.14706 Da

IUPAC Name

4,16-dimethoxy-10-methyl-10-azatetracyclo[7.7.1.0²,⁷.0¹³,¹⁷]heptadeca-1(17),2,4,6,13,15-hexaene-5,15-diol

Traditional Name

4,16-dimethoxy-10-methyl-10-azatetracyclo[7.7.1.0²,⁷.0¹³,¹⁷]heptadeca-1(17),2,4,6,13,15-hexaene-5,15-diol

CAS Registry Number

Not Available

SMILES

COC1=C(O)C=C2CC3N(C)CCC4=CC(O)=C(OC)C(C2=C1)=C34

InChI Identifier

InChI=1S/C19H21NO4/c1-20-5-4-10-7-15(22)19(24-3)18-12-9-16(23-2)14(21)8-11(12)6-13(20)17(10)18/h7-9,13,21-22H,4-6H2,1-3H3

InChI Key

LZJRNLRASBVRRX-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
Actinodaphne pruinosa	LOTUS Database	35616633
Beilschmiedia alloiophylla	LOTUS Database	35616633
Beilschmiedia kunstleri	LOTUS Database	35616633
Hedycarya angustifolia	LOTUS Database	35616633
Licaria triandra	LOTUS Database	35616633
Lindera glauca	LOTUS Database	35616633
Litsea glutinosa	LOTUS Database	35616633
Litsea leefeana	LOTUS Database	35616633
Litsea wightiana	LOTUS Database	35616633
Neolitsea dealbata	LOTUS Database	35616633
Neolitsea konishii	LOTUS Database	35616633
Peumus boldus	LOTUS Database	35616633
Phoebe grandis	LOTUS Database	35616633
Sassafras albidum	LOTUS Database	35616633
Siparuna pauciflora	LOTUS Database	35616633
Xylopia parviflora	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as aporphines. These are quinoline alkaloids containing the dibenzo[de,g]quinoline ring system or a dehydrogenated derivative thereof.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Aporphines

Sub Class

Not Available

Direct Parent

Aporphines

Alternative Parents

Substituents

Aporphine
Benzoquinoline
Phenanthrene
2-naphthol
Naphthalene
Quinoline
Tetrahydroisoquinoline
Anisole
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
Aralkylamine
Benzenoid
Tertiary amine
Tertiary aliphatic amine
Azacycle
Ether
Organoheterocyclic compound
Organic nitrogen compound
Organooxygen compound
Organonitrogen compound
Hydrocarbon derivative
Organopnictogen compound
Organic oxygen compound
Amine
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	2.78	ChemAxon
logS	-3	ALOGPS
pKa (Strongest Acidic)	6.67	ChemAxon
pKa (Strongest Basic)	12.35	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	62.16 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	92.91 m³·mol⁻¹	ChemAxon
Polarizability	35.35 Å³	ChemAxon
Number of Rings	4	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

HMDB0039085

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB018587

KNApSAcK ID

Not Available

Chemspider ID

217564

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

248507

PDB ID

Not Available

ChEBI ID

95169

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Boldine (NP0137203)

MOL for NP0137203 (Boldine)

3D MOL for NP0137203 (Boldine)

3D SDF for NP0137203 (Boldine)

3D-SDF for NP0137203 (Boldine)

PDB for NP0137203 (Boldine)

3D PDB for NP0137203 (Boldine)

SMILES for NP0137203 (Boldine)

INCHI for NP0137203 (Boldine)

Structure for NP0137203 (Boldine)

3D Structure for NP0137203 (Boldine)