NP-MRD: Showing NP-Card for isosinomenine (NP0306861)

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Record Information

Version

2.0

Created at

2022-09-10 23:36:27 UTC

Updated at

2022-09-10 23:36:28 UTC

NP-MRD ID

NP0306861

Secondary Accession Numbers

None

Natural Product Identification

Common Name

isosinomenine

Description

Isosinomenine, also known as milonine, belongs to the class of organic compounds known as morphinans. These are polycyclic compounds with a four-ring skeleton with three condensed six-member rings forming a partially hydrogenated phenanthrene moiety, one of which is aromatic while the two others are alicyclic. isosinomenine was first documented in 2014 (PMID: 24593266). Based on a literature review very few articles have been published on Isosinomenine.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 47 50  0  0  0  0  0  0  0  0999 V2000
   -3.1104    3.8326   -0.6852 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8015    3.5263   -0.2555 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4672    2.1953   -0.0267 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8389    1.5116   -0.9603 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4953    0.0917   -0.6815 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2884   -0.6500   -2.0134 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9613   -1.9801   -2.0459 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8275   -2.7305   -0.8260 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7215   -3.8716   -0.9152 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1528   -1.9947    0.3498 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0137   -1.9887    1.3046 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0075   -1.0007    0.9627 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2526   -1.0835    1.6300 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2258   -0.1732    1.3317 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0210    0.8188    0.3991 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9855    1.7549    0.0750 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2581    1.8127    0.6373 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7866    0.8884   -0.2521 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5802    1.8851   -1.1897 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7823   -0.0290    0.0374 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6304   -0.6043    0.0043 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1247    0.1098    1.2443 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7994    1.5411    1.2251 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8080    2.1963    2.2806 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1465    4.9470   -0.8020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2356    3.3788   -1.7018 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8716    3.4788    0.0313 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5978    2.0053   -1.9089 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7928   -0.7109   -2.2693 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7611   -0.0182   -2.7914 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4747   -2.5812   -2.8496 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0363   -1.9149   -2.3418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2332   -4.7120   -1.4480 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6367   -3.5227   -1.4392 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0667   -4.1979    0.1063 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0243   -2.4569    0.9110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3400   -1.8114    2.3702 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4407   -3.0046    1.3069 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3846   -1.8668    2.3521 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1797   -0.2202    1.8291 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9920    1.1250    0.1805 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2517    1.6670    1.7365 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6550    2.8492    0.4688 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3264    2.5352   -1.3785 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4631   -0.7062   -0.7146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7467   -0.3542    2.1716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2473    0.0332    1.3066 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
  5  4  1  6
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 15 18  1  0
 18 19  1  0
 18 20  2  0
 10 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  2  0
 23  3  1  0
 20  5  1  0
 21  5  1  0
 20 12  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  4 28  1  0
  6 29  1  0
  6 30  1  0
  7 31  1  0
  7 32  1  0
  9 33  1  0
  9 34  1  0
  9 35  1  0
 10 36  1  1
 11 37  1  0
 11 38  1  0
 13 39  1  0
 14 40  1  0
 17 41  1  0
 17 42  1  0
 17 43  1  0
 19 44  1  0
 21 45  1  6
 22 46  1  0
 22 47  1  0
M  END


  Mrv1652309112201362D          

 24 27  0  0  1  0            999 V2000
    3.9603    2.0694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9319    1.2448    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4356    0.8835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5038    1.2939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7756    0.9062    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9559    0.8129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4423    0.1672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5356   -0.6525    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1860   -1.0524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1813   -1.1661    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0010   -1.0727    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5410   -0.6590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2711   -0.7562    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9343   -0.2655    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8410    0.5542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5042    1.0449    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2608    0.7159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0845    0.8832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9911    1.7030    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4212    0.3926    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7473    0.0817    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4472   -0.3551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1754    0.0326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7061   -0.5991    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  2  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
 10  8  1  6  0  0  0
 10 11  1  0  0  0  0
 11 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  1  0  0  0  0
 15 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 12 20  1  0  0  0  0
  5 20  1  0  0  0  0
 10 21  1  0  0  0  0
  5 21  1  0  0  0  0
 21 22  1  6  0  0  0
 22 23  1  0  0  0  0
  3 23  1  0  0  0  0
 23 24  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0306861

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C[C@@]23CCN(C)[C@@H](CC4=CC=C(OC)C(O)=C24)[C@H]3CC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C19H23NO4/c1-20-7-6-19-10-16(24-3)14(21)9-12(19)13(20)8-11-4-5-15(23-2)18(22)17(11)19/h4-5,10,12-13,22H,6-9H2,1-3H3/t12-,13+,19-/m1/s1

> <INCHI_KEY>
OWDQPILTDJLGCN-QHRIQVFBSA-N

> <FORMULA>
C19H23NO4

> <MOLECULAR_WEIGHT>
329.396

> <EXACT_MASS>
329.162708225

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
34.848761389188866

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,9S,10S)-3-hydroxy-4,13-dimethoxy-17-methyl-17-azatetracyclo[7.5.3.0^{1,10}.0^{2,7}]heptadeca-2,4,6,13-tetraen-12-one

> <JCHEM_LOGP>
1.4316598478185054

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
18.347004761294805

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.8110905567932

> <JCHEM_PKA_STRONGEST_BASIC>
8.31799925655313

> <JCHEM_POLAR_SURFACE_AREA>
59.00000000000001

> <JCHEM_REFRACTIVITY>
92.99739999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,9S,10S)-3-hydroxy-4,13-dimethoxy-17-methyl-17-azatetracyclo[7.5.3.0^{1,10}.0^{2,7}]heptadeca-2,4,6,13-tetraen-12-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0       7.393   3.863   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       7.340   2.324   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       6.413   1.649   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.674   2.415   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.315   1.692   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.784   1.517   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.826   0.312   0.000  0.00  0.00           C+0
HETATM    8  N   UNK     0       1.000  -1.218   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0      -0.347  -1.964   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.205  -2.177   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.735  -2.002   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.743  -1.230   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.106  -1.411   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.344  -0.496   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.170   1.035   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       8.408   1.950   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       9.820   1.336   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.758   1.649   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       5.583   3.179   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       4.520   0.733   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.262   0.152   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.568  -0.663   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.927   0.061   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       6.918  -1.118   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   23                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   20   21                                             
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   21                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   20                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   18                                                  
CONECT   16   15   17                                                       
CONECT   17   16                                                            
CONECT   18   15   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   12    5                                                  
CONECT   21   10    5   22                                                  
CONECT   22   21   23                                                       
CONECT   23   22    3   24                                                  
CONECT   24   23                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   54    0
END

View in JSmol

Synonyms

Value	Source
Milonine	MeSH

Chemical Formula

C₁₉H₂₃NO₄

Average Mass

329.3960 Da

Monoisotopic Mass

329.16271 Da

IUPAC Name

(1S,9S,10S)-3-hydroxy-4,13-dimethoxy-17-methyl-17-azatetracyclo[7.5.3.0^{1,10}.0^{2,7}]heptadeca-2,4,6,13-tetraen-12-one

Traditional Name

(1S,9S,10S)-3-hydroxy-4,13-dimethoxy-17-methyl-17-azatetracyclo[7.5.3.0^{1,10}.0^{2,7}]heptadeca-2,4,6,13-tetraen-12-one

CAS Registry Number

Not Available

SMILES

COC1=C[C@@]23CCN(C)[C@@H](CC4=CC=C(OC)C(O)=C24)[C@H]3CC1=O

InChI Identifier

InChI=1S/C19H23NO4/c1-20-7-6-19-10-16(24-3)14(21)9-12(19)13(20)8-11-4-5-15(23-2)18(22)17(11)19/h4-5,10,12-13,22H,6-9H2,1-3H3/t12-,13+,19-/m1/s1

InChI Key

OWDQPILTDJLGCN-QHRIQVFBSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as morphinans. These are polycyclic compounds with a four-ring skeleton with three condensed six-member rings forming a partially hydrogenated phenanthrene moiety, one of which is aromatic while the two others are alicyclic.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Morphinans

Sub Class

Not Available

Direct Parent

Morphinans

Alternative Parents

Substituents

Morphinan
Phenanthrene
Benzazocine
Isoquinolone
Tetralin
Anisole
Alkyl aryl ether
1-hydroxy-4-unsubstituted benzenoid
Cyclohexenone
Aralkylamine
Piperidine
Benzenoid
Ketone
Tertiary amine
Tertiary aliphatic amine
Cyclic ketone
Azacycle
Ether
Organoheterocyclic compound
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Organic oxide
Organic nitrogen compound
Organopnictogen compound
Carbonyl group
Amine
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

morphinane alkaloid (CHEBI:81369 )

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	1.43	ChemAxon
pKa (Strongest Acidic)	9.81	ChemAxon
pKa (Strongest Basic)	8.32	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	59 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	93 m³·mol⁻¹	ChemAxon
Polarizability	34.85 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

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00025266

Chemspider ID

30791564

KEGG Compound ID

C17899

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11551643

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Ghavimi B, Magnus P: Total synthesis of 8,14-dihydromorphinandienone alkaloids. Org Lett. 2014 Mar 21;16(6):1708-11. doi: 10.1021/ol500368p. Epub 2014 Mar 5. [PubMed:24593266 ]
LOTUS database [Link]

Showing NP-Card for isosinomenine (NP0306861)

MOL for NP0306861 (isosinomenine)

3D MOL for NP0306861 (isosinomenine)

3D SDF for NP0306861 (isosinomenine)

3D-SDF for NP0306861 (isosinomenine)

PDB for NP0306861 (isosinomenine)

3D PDB for NP0306861 (isosinomenine)

SMILES for NP0306861 (isosinomenine)

INCHI for NP0306861 (isosinomenine)

Structure for NP0306861 (isosinomenine)

3D Structure for NP0306861 (isosinomenine)