NP-MRD: Showing NP-Card for Bis-(7-hydroxygirinimbine) A (NP0067002)

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Record Information

Version

2.0

Created at

2022-04-28 11:12:08 UTC

Updated at

2022-04-28 11:12:08 UTC

NP-MRD ID

NP0067002

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Bis-(7-hydroxygirinimbine) A

Description

15-{14-Hydroxy-5,5,8-trimethyl-6-oxa-17-azatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]Heptadeca-1,3,7,9,11(16),12,14-heptaen-15-yl}-5,5,8-trimethyl-6-oxa-17-azatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]Heptadeca-1,3,7,9,11(16),12,14-heptaen-14-ol belongs to the class of organic compounds known as carbazoles. Carbazoles are compounds containing a three ring system containing a pyrrole ring fused on either side to a benzene ring. Bis-(7-hydroxygirinimbine) A is found in Murraya euchrestifolia. 15-{14-Hydroxy-5,5,8-trimethyl-6-oxa-17-azatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]Heptadeca-1,3,7,9,11(16),12,14-heptaen-15-yl}-5,5,8-trimethyl-6-oxa-17-azatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]Heptadeca-1,3,7,9,11(16),12,14-heptaen-14-ol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171502322D          

 42 49  0  0  0  0            999 V2000
    2.9063    4.8102    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2773    4.0733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1010    4.0262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4720    3.2893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2678    3.0720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9619    3.5180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6951    3.1399    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7343    2.3158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4676    1.9377    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0403    1.8698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0795    1.0457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8128    0.6677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5068    1.1137    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8520   -0.1564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.4246   -0.2243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6530   -0.5163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
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  8 10  2  0  0  0  0
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  4 34  2  0  0  0  0
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 41 42  1  0  0  0  0
  2 42  1  0  0  0  0
 35 42  2  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1533004171502322D          

 42 49  0  0  0  0            999 V2000
    2.9063    4.8102    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.3215    0.0023    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1369    0.1274    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5896    0.8171    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.3854    0.5998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3070    2.2479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5354    1.9560    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.0193    2.5996    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1956    2.6467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7430    1.9570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9193    2.0042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5483    2.7410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8871    2.2477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9477    3.3066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0010    3.4308    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8246    3.3836    0.0000 C   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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 12 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
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 23 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 21 28  2  0  0  0  0
 28 29  1  0  0  0  0
 17 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 11 31  1  0  0  0  0
 16 31  2  0  0  0  0
 10 32  1  0  0  0  0
  5 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
  4 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
 38 41  1  0  0  0  0
 41 42  1  0  0  0  0
  2 42  1  0  0  0  0
 35 42  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0067002

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=CC2=C(NC3=C2C=CC(O)=C3C2=C(O)C=CC3=C2NC2=C3C=C(C)C3=C2C=CC(C)(C)O3)C2=C1OC(C)(C)C=C2

> <INCHI_IDENTIFIER>
InChI=1S/C36H32N2O4/c1-17-15-23-19-7-9-25(39)27(31(19)37-29(23)21-11-13-35(3,4)41-33(17)21)28-26(40)10-8-20-24-16-18(2)34-22(30(24)38-32(20)28)12-14-36(5,6)42-34/h7-16,37-40H,1-6H3

> <INCHI_KEY>
VHEPPYVPQJDUCC-UHFFFAOYSA-N

> <FORMULA>
C36H32N2O4

> <MOLECULAR_WEIGHT>
556.662

> <EXACT_MASS>
556.236207518

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
74

> <JCHEM_AVERAGE_POLARIZABILITY>
64.54580366000442

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
15-{9-hydroxy-3,3,5-trimethyl-3H,11H-pyrano[3,2-a]carbazol-10-yl}-5,5,8-trimethyl-6-oxa-17-azatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]heptadeca-1(10),2(7),3,8,11(16),12,14-heptaen-14-ol

> <ALOGPS_LOGP>
7.02

> <JCHEM_LOGP>
8.076709864

> <ALOGPS_LOGS>
-6.44

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
8

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.774730365898815

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.946450171538277

> <JCHEM_PKA_STRONGEST_BASIC>
-4.6181728188125515

> <JCHEM_POLAR_SURFACE_AREA>
90.49999999999999

> <JCHEM_REFRACTIVITY>
168.85360000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.01e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
15-{9-hydroxy-3,3,5-trimethyl-11H-pyrano[3,2-a]carbazol-10-yl}-5,5,8-trimethyl-6-oxa-17-azatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]heptadeca-1(10),2(7),3,8,11(16),12,14-heptaen-14-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0       5.425   8.979   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.118   7.604   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.655   7.516   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.348   6.140   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.833   5.734   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      11.129   6.567   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      12.498   5.861   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      12.571   4.323   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      13.940   3.617   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      11.275   3.490   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      11.348   1.952   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      12.717   1.246   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      14.013   2.079   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      12.790  -0.292   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      11.495  -1.124   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.126  -0.419   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.686  -0.964   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.127  -2.399   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.605  -2.632   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.046  -4.067   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.641  -1.431   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       4.119  -1.664   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       3.156  -0.463   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.140  -1.620   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.840   0.337   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.715   0.972   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.237   1.206   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.200   0.004   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       7.722   0.238   0.000  0.00  0.00           C+0
HETATM   30  N   UNK     0       8.567   1.525   0.000  0.00  0.00           N+0
HETATM   31  C   UNK     0      10.053   1.120   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       9.906   4.196   0.000  0.00  0.00           C+0
HETATM   33  N   UNK     0       8.466   3.651   0.000  0.00  0.00           N+0
HETATM   34  C   UNK     0       7.503   4.853   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       5.965   4.941   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       5.120   3.653   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       3.583   3.741   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       2.890   5.117   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       1.656   4.196   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       1.769   6.172   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       3.735   6.404   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       5.273   6.316   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   42                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   34                                                  
CONECT    5    4    6   32                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   32                                                  
CONECT   11   10   12   31                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   31                                                  
CONECT   17   16   18   29                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   28                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   25   26                                             
CONECT   24   23                                                            
CONECT   25   23                                                            
CONECT   26   23   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   21   29                                                  
CONECT   29   28   17   30                                                  
CONECT   30   29   31                                                       
CONECT   31   30   11   16                                                  
CONECT   32   10    5   33                                                  
CONECT   33   32   34                                                       
CONECT   34   33    4   35                                                  
CONECT   35   34   36   42                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39   40   41                                             
CONECT   39   38                                                            
CONECT   40   38                                                            
CONECT   41   38   42                                                       
CONECT   42   41    2   35                                                  
MASTER        0    0    0    0    0    0    0    0   42    0   98    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₆H₃₂N₂O₄

Average Mass

556.6620 Da

Monoisotopic Mass

556.23621 Da

IUPAC Name

15-{9-hydroxy-3,3,5-trimethyl-3H,11H-pyrano[3,2-a]carbazol-10-yl}-5,5,8-trimethyl-6-oxa-17-azatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]heptadeca-1(10),2(7),3,8,11(16),12,14-heptaen-14-ol

Traditional Name

15-{9-hydroxy-3,3,5-trimethyl-11H-pyrano[3,2-a]carbazol-10-yl}-5,5,8-trimethyl-6-oxa-17-azatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]heptadeca-1(10),2(7),3,8,11(16),12,14-heptaen-14-ol

CAS Registry Number

Not Available

SMILES

CC1=CC2=C(NC3=C2C=CC(O)=C3C2=C(O)C=CC3=C2NC2=C3C=C(C)C3=C2C=CC(C)(C)O3)C2=C1OC(C)(C)C=C2

InChI Identifier

InChI=1S/C36H32N2O4/c1-17-15-23-19-7-9-25(39)27(31(19)37-29(23)21-11-13-35(3,4)41-33(17)21)28-26(40)10-8-20-24-16-18(2)34-22(30(24)38-32(20)28)12-14-36(5,6)42-34/h7-16,37-40H,1-6H3

InChI Key

VHEPPYVPQJDUCC-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, 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
Murraya euchrestifolia	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as carbazoles. Carbazoles are compounds containing a three ring system containing a pyrrole ring fused on either side to a benzene ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Carbazoles

Direct Parent

Carbazoles

Alternative Parents

Substituents

Carbazole
2,2-dimethyl-1-benzopyran
Benzopyran
1-benzopyran
Hydroxyindole
Indole
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
Benzenoid
Heteroaromatic compound
Pyrrole
Oxacycle
Azacycle
Ether
Organopnictogen compound
Organic oxygen compound
Organooxygen compound
Organonitrogen compound
Organic nitrogen compound
Hydrocarbon derivative
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	7.02	ALOGPS
logP	8.08	ChemAxon
logS	-6.4	ALOGPS
pKa (Strongest Acidic)	8.95	ChemAxon
pKa (Strongest Basic)	-4.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	90.5 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	168.85 m³·mol⁻¹	ChemAxon
Polarizability	64.55 Å³	ChemAxon
Number of Rings	8	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

14892682

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Bis-(7-hydroxygirinimbine) A (NP0067002)

MOL for NP0067002 (Bis-(7-hydroxygirinimbine) A)

3D MOL for NP0067002 (Bis-(7-hydroxygirinimbine) A)

3D SDF for NP0067002 (Bis-(7-hydroxygirinimbine) A)

3D-SDF for NP0067002 (Bis-(7-hydroxygirinimbine) A)

PDB for NP0067002 (Bis-(7-hydroxygirinimbine) A)

3D PDB for NP0067002 (Bis-(7-hydroxygirinimbine) A)

SMILES for NP0067002 (Bis-(7-hydroxygirinimbine) A)

INCHI for NP0067002 (Bis-(7-hydroxygirinimbine) A)

Structure for NP0067002 (Bis-(7-hydroxygirinimbine) A)

3D Structure for NP0067002 (Bis-(7-hydroxygirinimbine) A)