NP-MRD: Showing NP-Card for (+/-)-Tangutorine (NP0068671)

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Record Information

Version

2.0

Created at

2022-04-28 13:56:11 UTC

Updated at

2022-04-28 13:56:11 UTC

NP-MRD ID

NP0068671

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+/-)-Tangutorine

Description

3,4,4Aalpha,6,7,12,12balpha,13,14,14abeta-Decahydrobenzo[f]indolo[2,3-a]quinolizine-2-methanol belongs to the class of organic compounds known as beta carbolines. Beta carbolines are compounds containing a 9H-pyrido[3,4-b]indole moiety. (+/-)-Tangutorine is found in Nitraria tangutorum. Based on a literature review very few articles have been published on 3,4,4aalpha,6,7,12,12balpha,13,14,14abeta-Decahydrobenzo[f]indolo[2,3-a]quinolizine-2-methanol.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 47 51  0  0  0  0  0  0  0  0999 V2000
   -6.2581    0.6832   -0.2435 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7364   -0.4712    0.2863 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2986   -0.6046   -0.0808 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6654    0.2967   -0.8179 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2368    0.0320   -1.1027 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5967    1.0782   -1.9709 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1189    0.6797   -2.0904 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4601    0.7559   -0.7196 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9324    0.5446   -0.7117 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9031    0.3992   -1.5999 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.0839    0.2342   -0.9506 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3795    0.0454   -1.3729 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3804   -0.0919   -0.4446 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1604   -0.0509    0.9171 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8611    0.1384    1.3419 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8446    0.2779    0.4091 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5096    0.4705    0.5619 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5689    0.6134    1.7005 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4021   -0.2844    1.4553 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1289   -0.2437    0.1351 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5641   -0.1496    0.2131 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1116   -1.3963    0.8595 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4791   -1.7688    0.3564 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9906    1.5050    0.2117 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8240   -0.5088    1.4089 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2894   -1.3353   -0.1347 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1379    1.1749   -1.1979 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1475   -0.9418   -1.6655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0929    1.0458   -2.9610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6306    2.0808   -1.5061 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4217    1.3588   -2.7868 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0801   -0.3795   -2.4277 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2411    1.7841   -0.3188 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7665    0.4116   -2.6447 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5586    0.0123   -2.4524 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3966   -0.2401   -0.8028 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9964   -0.1662    1.5954 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6320    0.1786    2.3958 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0255    0.3339    2.6706 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2572    1.6922    1.7312 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7601   -1.3403    1.6369 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3833   -0.1319    2.2474 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8531    0.7057    0.8630 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4442   -2.2760    0.6120 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0685   -1.3364    1.9676 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3936   -2.4309   -0.5550 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0115   -2.3844    1.1127 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  6  1  0
  6  7  1  0
  7  8  1  0
  8 20  1  0
 20 19  1  0
 19 18  1  0
 18 17  1  0
 17  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23  3  1  0
 21  5  1  0
  9  8  1  0
 16 11  1  0
 16 17  1  0
  1 24  1  0
  2 25  1  0
  2 26  1  0
  4 27  1  0
  5 28  1  6
  6 29  1  0
  6 30  1  0
  7 31  1  0
  7 32  1  0
  8 33  1  1
 19 41  1  0
 19 42  1  0
 18 39  1  0
 18 40  1  0
 10 34  1  0
 12 35  1  0
 13 36  1  0
 14 37  1  0
 15 38  1  0
 21 43  1  1
 22 44  1  0
 22 45  1  0
 23 46  1  0
 23 47  1  0
M  END


  Mrv1652304282215562D          

 23 27  0  0  1  0            999 V2000
    6.0859    1.0803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4220    0.3269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9376   -0.3409    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1171   -0.2553    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7810    0.4981    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2654    1.1659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9604    0.5837    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4760   -0.0841    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8121   -0.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6327   -0.9231    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6554    0.0015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3193    0.7549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8037    1.4227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6243    1.3371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4989    0.6680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3280   -0.1391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0428   -0.5510    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5436   -0.3946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0700    0.1570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1010    0.9641    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8854    1.2196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2426    0.2413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7270    0.9091    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  4  3  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  4 10  1  0  0  0  0
  8 11  1  6  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
  7 14  1  0  0  0  0
 12 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 11 17  1  0  0  0  0
 16 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
 15 21  2  0  0  0  0
  2 22  1  0  0  0  0
 22 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0068671

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OCC1=C[C@H]2CC[C@H]3N(CCC4=C3NC3=CC=CC=C43)[C@@H]2CC1

> <INCHI_IDENTIFIER>
InChI=1S/C20H24N2O/c23-12-13-5-7-18-14(11-13)6-8-19-20-16(9-10-22(18)19)15-3-1-2-4-17(15)21-20/h1-4,11,14,18-19,21,23H,5-10,12H2/t14-,18-,19-/m1/s1

> <INCHI_KEY>
ZIKRKRUIEOVRGS-NIKGAXFTSA-N

> <FORMULA>
C20H24N2O

> <MOLECULAR_WEIGHT>
308.425

> <EXACT_MASS>
308.188863401

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
37.0957668624778

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
[(1R,14R,19R)-3,13-diazapentacyclo[11.8.0.0^{2,10}.0^{4,9}.0^{14,19}]henicosa-2(10),4,6,8,17-pentaen-17-yl]methanol

> <ALOGPS_LOGP>
3.17

> <JCHEM_LOGP>
2.7690088743333323

> <ALOGPS_LOGS>
-3.58

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
16.82812848694787

> <JCHEM_PKA_STRONGEST_ACIDIC>
16.3747941390427

> <JCHEM_PKA_STRONGEST_BASIC>
7.255596675332554

> <JCHEM_POLAR_SURFACE_AREA>
39.260000000000005

> <JCHEM_REFRACTIVITY>
94.07300000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.21e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,14R,19R)-3,13-diazapentacyclo[11.8.0.0^{2,10}.0^{4,9}.0^{14,19}]henicosa-2(10),4,6,8,17-pentaen-17-ylmethanol

> <JCHEM_VEBER_RULE>
1

$$$$

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      11.360   2.017   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      11.988   0.610   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      11.084  -0.636   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.552  -0.477   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.924   0.930   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.829   2.176   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0       7.393   1.090   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0       6.489  -0.157   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.116  -1.563   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.648  -1.723   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.957   0.003   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.329   1.409   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.234   2.656   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.765   2.496   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.798   1.247   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.479  -0.260   0.000  0.00  0.00           C+0
HETATM   17  N   UNK     0       3.813  -1.029   0.000  0.00  0.00           N+0
HETATM   18  C   UNK     0       1.015  -0.737   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.131   0.293   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.188   1.800   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.653   2.277   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      13.520   0.450   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      14.424   1.697   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3   22                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   10                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8   14                                                  
CONECT    8    7    9   11                                                  
CONECT    9    8   10                                                       
CONECT   10    9    4                                                       
CONECT   11    8   12   17                                                  
CONECT   12   11   13   15                                                  
CONECT   13   12   14                                                       
CONECT   14   13    7                                                       
CONECT   15   12   16   21                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16   11                                                       
CONECT   18   16   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   15                                                       
CONECT   22    2   23                                                       
CONECT   23   22                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   54    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₄N₂O

Average Mass

308.4250 Da

Monoisotopic Mass

308.18886 Da

IUPAC Name

[(1R,14R,19R)-3,13-diazapentacyclo[11.8.0.0^{2,10}.0^{4,9}.0^{14,19}]henicosa-2(10),4,6,8,17-pentaen-17-yl]methanol

Traditional Name

(1R,14R,19R)-3,13-diazapentacyclo[11.8.0.0^{2,10}.0^{4,9}.0^{14,19}]henicosa-2(10),4,6,8,17-pentaen-17-ylmethanol

CAS Registry Number

Not Available

SMILES

OCC1=C[C@H]2CC[C@H]3N(CCC4=C3NC3=CC=CC=C43)[C@@H]2CC1

InChI Identifier

InChI=1S/C20H24N2O/c23-12-13-5-7-18-14(11-13)6-8-19-20-16(9-10-22(18)19)15-3-1-2-4-17(15)21-20/h1-4,11,14,18-19,21,23H,5-10,12H2/t14-,18-,19-/m1/s1

InChI Key

ZIKRKRUIEOVRGS-NIKGAXFTSA-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
Nitraria tangutorum	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as beta carbolines. Beta carbolines are compounds containing a 9H-pyrido[3,4-b]indole moiety.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Pyridoindoles

Direct Parent

Beta carbolines

Alternative Parents

Substituents

Beta-carboline
3-alkylindole
Indole
Aralkylamine
Piperidine
Benzenoid
Heteroaromatic compound
Pyrrole
Tertiary aliphatic amine
Tertiary amine
Azacycle
Primary alcohol
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Organic oxygen compound
Organic nitrogen 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	3.17	ALOGPS
logP	2.77	ChemAxon
logS	-3.6	ALOGPS
pKa (Strongest Acidic)	16.37	ChemAxon
pKa (Strongest Basic)	7.26	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	39.26 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	94.07 m³·mol⁻¹	ChemAxon
Polarizability	37.1 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	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

9395617

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11220563

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for (+/-)-Tangutorine (NP0068671)

MOL for NP0068671 ((+/-)-Tangutorine)

3D MOL for NP0068671 ((+/-)-Tangutorine)

3D SDF for NP0068671 ((+/-)-Tangutorine)

3D-SDF for NP0068671 ((+/-)-Tangutorine)

PDB for NP0068671 ((+/-)-Tangutorine)

3D PDB for NP0068671 ((+/-)-Tangutorine)

SMILES for NP0068671 ((+/-)-Tangutorine)

INCHI for NP0068671 ((+/-)-Tangutorine)

Structure for NP0068671 ((+/-)-Tangutorine)

3D Structure for NP0068671 ((+/-)-Tangutorine)