NP-MRD: Showing NP-Card for 17-Hydroxytacamonine (NP0067886)

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Record Information

Version

2.0

Created at

2022-04-28 12:43:22 UTC

Updated at

2022-04-28 12:43:22 UTC

NP-MRD ID

NP0067886

Secondary Accession Numbers

None

Natural Product Identification

Common Name

17-Hydroxytacamonine

Description

(13R,15S,16S,19R)-13-ethyl-16-hydroxy-1,11-diazapentacyclo[9.6.2.0²,⁷.0⁸,¹⁸.0¹⁵,¹⁹]Nonadeca-2,4,6,8(18)-tetraen-17-one belongs to the class of organic compounds known as tacaman alkaloids. These are alkaloids containing the pentacyclic tacaman skeleton, which consists of a pyrido[1,2-a]indole fused to a quinolizine. Tacaman alkaloids are obtained from a precursor to a pseudoaspidospermidine (type II skeleton) derivative, by the formation of new bonds at C-20/C-3 and C-140/C-17. 17-Hydroxytacamonine is found in Tabernaemontana eglandulosa Stapf. Based on a literature review very few articles have been published on (13R,15S,16S,19R)-13-ethyl-16-hydroxy-1,11-diazapentacyclo[9.6.2.0²,⁷.0⁸,¹⁸.0¹⁵,¹⁹]Nonadeca-2,4,6,8(18)-tetraen-17-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 45 49  0  0  0  0  0  0  0  0999 V2000
    4.7519    1.2760   -0.6148 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9399    0.8620    0.5920 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9510   -0.2078    0.1786 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0064    0.2965   -0.8931 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9881   -0.8364   -1.1065 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2312   -0.7152   -2.3608 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8072    0.3051   -3.1523 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2073   -0.4188   -2.2301 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9356   -0.4754   -3.2535 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8161   -0.0688   -0.9919 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1171   -0.3380    0.1050 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8448    0.0623    1.1754 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0519    0.6066    0.7515 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1628    1.1610    1.3480 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2411    1.6283    0.6235 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1615    1.5152   -0.7686 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0589    0.9641   -1.3787 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9959    0.5049   -0.6365 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2769   -0.1280    2.5346 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0920   -0.7442    2.4537 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8620   -0.3135    1.3077 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2094   -0.7650    1.3792 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2250   -0.9676    0.1493 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3657    2.2010   -1.0851 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8246    1.4349   -0.3662 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6780    0.4569   -1.3808 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4564    1.7439    1.0103 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6419    0.4379    1.3350 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5173   -1.0494   -0.2790 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6018    0.4810   -1.7940 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4607    1.1846   -0.5319 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6436   -1.7558   -1.1976 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3008   -1.6380   -3.0047 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0949    0.6859   -3.7268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1603    1.2181    2.4222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1167    2.0650    1.0905 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0267    1.8918   -1.3191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0465    0.9000   -2.4519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9064   -0.8070    3.1473 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1552    0.8687    3.0162 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6408   -0.6111    3.4065 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0562   -1.8504    2.3302 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6921   -0.4881    2.3392 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2030   -1.8916    1.3639 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1525   -2.0510    0.4639 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  7  1  0
  6  8  1  0
  8  9  2  0
  8 10  1  0
 10 18  1  0
 18 17  2  0
 17 16  1  0
 16 15  2  0
 15 14  1  0
 14 13  2  0
 13 12  1  0
 12 11  2  0
 11 23  1  0
 23 21  1  0
 21 20  1  0
 20 19  1  0
 21 22  1  0
 22  3  1  0
 23  5  1  0
 11 10  1  0
 13 18  1  0
 19 12  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  0
  2 28  1  0
  3 29  1  6
  4 30  1  0
  4 31  1  0
  5 32  1  6
  6 33  1  6
  7 34  1  0
 17 38  1  0
 16 37  1  0
 15 36  1  0
 14 35  1  0
 23 45  1  1
 20 41  1  0
 20 42  1  0
 19 39  1  0
 19 40  1  0
 22 43  1  0
 22 44  1  0
M  END


  Mrv1652304282214432D          

 23 27  0  0  1  0            999 V2000
    6.5058    0.7906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4665   -0.0335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7333   -0.4116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0392    0.0344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0784    0.8585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8117    1.2366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1617    1.2437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7907    0.5068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2434   -0.1829    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8724   -0.9198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3250   -1.6095    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0487   -0.9670    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5961   -0.2772    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9671    0.4596    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5144    1.1494    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8854    1.8863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7091    1.9334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6908    1.1022    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3198    0.3654    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7724   -0.3244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4961    0.3182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1251   -0.4187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6777   -1.7038    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  4  9  1  0  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  1  0  0  0  0
 13 14  1  0  0  0  0
 14  8  1  1  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
  7 17  1  0  0  0  0
 15 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 13 20  1  1  0  0  0
 19 21  1  1  0  0  0
 21 22  1  0  0  0  0
 12 23  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0067886

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@@H]1C[C@@H]2[C@H](O)C(=O)N3C4=CC=CC=C4C4=C3[C@@H]2N(CC4)C1

> <INCHI_IDENTIFIER>
InChI=1S/C19H22N2O2/c1-2-11-9-14-16-17-13(7-8-20(16)10-11)12-5-3-4-6-15(12)21(17)19(23)18(14)22/h3-6,11,14,16,18,22H,2,7-10H2,1H3/t11-,14+,16-,18+/m1/s1

> <INCHI_KEY>
CFGWIGBXBJVRDV-ZHPMQELBSA-N

> <FORMULA>
C19H22N2O2

> <MOLECULAR_WEIGHT>
310.397

> <EXACT_MASS>
310.168127956

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
34.76812638900085

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(13R,15S,16S,19R)-13-ethyl-16-hydroxy-1,11-diazapentacyclo[9.6.2.0^{2,7}.0^{8,18}.0^{15,19}]nonadeca-2,4,6,8(18)-tetraen-17-one

> <ALOGPS_LOGP>
2.70

> <JCHEM_LOGP>
1.895914255333333

> <ALOGPS_LOGS>
-2.60

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
16.064742507758602

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.60807800293449

> <JCHEM_PKA_STRONGEST_BASIC>
6.3495210675768785

> <JCHEM_POLAR_SURFACE_AREA>
45.47

> <JCHEM_REFRACTIVITY>
88.51710000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.80e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(13R,15S,16S,19R)-13-ethyl-16-hydroxy-1,11-diazapentacyclo[9.6.2.0^{2,7}.0^{8,18}.0^{15,19}]nonadeca-2,4,6,8(18)-tetraen-17-one

> <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      12.144   1.476   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.071  -0.063   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.702  -0.768   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.407   0.064   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.480   1.603   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.849   2.308   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.769   2.322   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.076   0.946   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0       7.921  -0.341   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0       7.228  -1.717   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       8.073  -3.004   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       5.691  -1.805   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.846  -0.517   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.539   0.858   0.000  0.00  0.00           C+0
HETATM   15  N   UNK     0       4.694   2.146   0.000  0.00  0.00           N+0
HETATM   16  C   UNK     0       5.386   3.521   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.924   3.609   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.156   2.057   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.464   0.682   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.309  -0.606   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.926   0.594   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.234  -0.782   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       4.998  -3.180   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    9                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8   17                                                  
CONECT    8    7    9   14                                                  
CONECT    9    8    4   10                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   23                                                  
CONECT   13   12   14   20                                                  
CONECT   14   13    8   15                                                  
CONECT   15   14   16   18                                                  
CONECT   16   15   17                                                       
CONECT   17   16    7                                                       
CONECT   18   15   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19   13                                                       
CONECT   21   19   22                                                       
CONECT   22   21                                                            
CONECT   23   12                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   54    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₂₂N₂O₂

Average Mass

310.3970 Da

Monoisotopic Mass

310.16813 Da

IUPAC Name

(13R,15S,16S,19R)-13-ethyl-16-hydroxy-1,11-diazapentacyclo[9.6.2.0^{2,7}.0^{8,18}.0^{15,19}]nonadeca-2,4,6,8(18)-tetraen-17-one

Traditional Name

(13R,15S,16S,19R)-13-ethyl-16-hydroxy-1,11-diazapentacyclo[9.6.2.0^{2,7}.0^{8,18}.0^{15,19}]nonadeca-2,4,6,8(18)-tetraen-17-one

CAS Registry Number

Not Available

SMILES

CC[C@@H]1C[C@@H]2[C@H](O)C(=O)N3C4=CC=CC=C4C4=C3[C@@H]2N(CC4)C1

InChI Identifier

InChI=1S/C19H22N2O2/c1-2-11-9-14-16-17-13(7-8-20(16)10-11)12-5-3-4-6-15(12)21(17)19(23)18(14)22/h3-6,11,14,16,18,22H,2,7-10H2,1H3/t11-,14+,16-,18+/m1/s1

InChI Key

CFGWIGBXBJVRDV-ZHPMQELBSA-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
Tabernaemontana eglandulosa	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tacaman alkaloids. These are alkaloids containing the pentacyclic tacaman skeleton, which consists of a pyrido[1,2-a]indole fused to a quinolizine. Tacaman alkaloids are obtained from a precursor to a pseudoaspidospermidine (type II skeleton) derivative, by the formation of new bonds at C-20/C-3 and C-140/C-17.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Tacaman alkaloids

Sub Class

Not Available

Direct Parent

Tacaman alkaloids

Alternative Parents

Substituents

Tacaman alkaloid
Indolo[3,2-1de][1,5]naphthyridine
Beta-carboline
Pyridoindole
Naphthyridine
3-alkylindole
Indole
Indole or derivatives
Aralkylamine
Benzenoid
Piperidine
Heteroaromatic compound
Pyrrole
Lactam
Tertiary aliphatic amine
Tertiary amine
Secondary alcohol
Azacycle
Organoheterocyclic compound
Organooxygen compound
Organonitrogen compound
Alcohol
Amine
Hydrocarbon derivative
Organic oxygen compound
Organic nitrogen compound
Organic oxide
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	2.7	ALOGPS
logP	1.9	ChemAxon
logS	-2.6	ALOGPS
pKa (Strongest Acidic)	12.61	ChemAxon
pKa (Strongest Basic)	6.35	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	45.47 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	88.52 m³·mol⁻¹	ChemAxon
Polarizability	34.77 Å³	ChemAxon
Number of Rings	5	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

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

9100199

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10924954

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 17-Hydroxytacamonine (NP0067886)

MOL for NP0067886 (17-Hydroxytacamonine)

3D MOL for NP0067886 (17-Hydroxytacamonine)

3D SDF for NP0067886 (17-Hydroxytacamonine)

3D-SDF for NP0067886 (17-Hydroxytacamonine)

PDB for NP0067886 (17-Hydroxytacamonine)

3D PDB for NP0067886 (17-Hydroxytacamonine)

SMILES for NP0067886 (17-Hydroxytacamonine)

INCHI for NP0067886 (17-Hydroxytacamonine)

Structure for NP0067886 (17-Hydroxytacamonine)

3D Structure for NP0067886 (17-Hydroxytacamonine)