NP-MRD: Showing NP-Card for Litebamine (NP0070052)

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Record Information

Version

2.0

Created at

2022-04-28 15:19:43 UTC

Updated at

2022-04-28 15:19:44 UTC

NP-MRD ID

NP0070052

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Litebamine

Description

Litebamine belongs to the class of organic compounds known as phenanthrols. Phenanthrols are compounds containing a phenanthrene (or its hydrogenated derivative) to which a hydroxyl group is attached. Litebamine is a very strong basic compound (based on its pKa). Outside of the human body, litebamine has been detected, but not quantified in, fruits. Litebamine is found in Litsea cubeba . This could make litebamine a potential biomarker for the consumption of these foods.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 46 49  0  0  0  0  0  0  0  0999 V2000
   -4.8153    0.1517    2.2255 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1539    0.2757    0.8682 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1802    0.3007   -0.1074 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8444    0.1971    0.3195 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8417    0.2141   -0.6065 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1436    0.3391   -1.9680 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1430    0.3995   -2.9078 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1652    0.3342   -2.4909 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4635    0.2073   -1.1540 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7955    0.1575   -0.7780 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1551    0.0429    0.5357 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1682   -0.0273    1.4922 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5303   -0.1431    2.8237 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1940    0.0178    1.1455 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0358   -0.0777    2.2190 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3466   -1.3851    2.7805 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5106    0.1397   -0.1668 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5952    0.0140    0.8575 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2499   -0.7368   -0.2042 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.6116   -1.0482    0.1541 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2013    0.0070   -1.4502 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8016    0.2260   -1.9078 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4758    0.4423   -2.3841 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4693    0.4199   -1.4376 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7850    0.5214   -1.8613 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2240   -0.7857    2.4035 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7218    0.1798    2.8613 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1672    1.0228    2.4961 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6624    0.1590    1.3512 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4031    0.4976   -3.9620 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9607    0.3907   -3.2258 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4817   -0.1665    3.0918 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4759   -1.8253    3.2598 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1188   -1.1927    3.5380 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7061   -1.9741    1.9113 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8716   -0.4383    1.8048 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9373    1.0924    0.7843 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0297   -0.2362    0.8079 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5747   -1.9552    0.8048 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2510   -1.2709   -0.7017 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7321    0.9863   -1.3683 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7650   -0.5882   -2.1976 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6926    1.2009   -2.4129 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5463   -0.6008   -2.6270 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6477    0.5347   -3.4390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5140    0.5058   -1.1774 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3 24  2  0
 24 25  1  0
 24 23  1  0
 23  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 22  1  0
 22 21  1  0
 21 19  1  0
 19 20  1  0
 19 18  1  0
 18 11  1  0
 11 12  2  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 14 17  2  0
 17  5  1  0
  5  4  2  0
  4  3  1  0
  5  6  1  0
 17  9  1  0
 11 10  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
 25 46  1  0
 23 45  1  0
  7 30  1  0
  8 31  1  0
 22 43  1  0
 22 44  1  0
 21 41  1  0
 21 42  1  0
 20 38  1  0
 20 39  1  0
 20 40  1  0
 18 36  1  0
 18 37  1  0
 13 32  1  0
 16 33  1  0
 16 34  1  0
 16 35  1  0
  4 29  1  0
M  END


  Mrv0541 05061310332D          

 25 28  0  0  0  0            999 V2000
    8.2588   -1.1368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0477   -2.8518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4782   -3.3196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9381    0.4223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7482    0.2664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3685   -0.0454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1786   -0.2014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5878   -0.0454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1279   -1.6046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9086   -1.6046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3980   -0.2014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8284   -0.6691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0182   -0.5132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6680   -0.9809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0984   -1.4486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0477   -0.6691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3178   -1.4486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4782   -1.1368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5583   -2.0723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7482   -1.9164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4486   -0.9809    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2376   -0.5132    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8284   -2.8518    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7777   -2.0723    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2081   -2.5400    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  5  4  2  0  0  0  0
  7  6  1  0  0  0  0
 11  4  1  0  0  0  0
 11  8  2  0  0  0  0
 12  6  1  0  0  0  0
 13  5  1  0  0  0  0
 13 12  2  0  0  0  0
 14  9  2  0  0  0  0
 14 11  1  0  0  0  0
 15 10  1  0  0  0  0
 15 12  1  0  0  0  0
 16  8  1  0  0  0  0
 17  9  1  0  0  0  0
 17 16  2  0  0  0  0
 18 13  1  0  0  0  0
 18 14  1  0  0  0  0
 19 15  2  0  0  0  0
 20 18  2  0  0  0  0
 20 19  1  0  0  0  0
 21  1  1  0  0  0  0
 21  7  1  0  0  0  0
 21 10  1  0  0  0  0
 22 16  1  0  0  0  0
 23 19  1  0  0  0  0
 24  2  1  0  0  0  0
 24 17  1  0  0  0  0
 25  3  1  0  0  0  0
 25 20  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0070052

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(O)C=C2C=CC3=C4CCN(C)CC4=C(O)C(OC)=C3C2=C1

> <INCHI_IDENTIFIER>
InChI=1S/C20H21NO4/c1-21-7-6-12-13-5-4-11-8-16(22)17(24-2)9-14(11)18(13)20(25-3)19(23)15(12)10-21/h4-5,8-9,22-23H,6-7,10H2,1-3H3

> <INCHI_KEY>
QOWFEPGZJDCIKG-UHFFFAOYSA-N

> <FORMULA>
C20H21NO4

> <MOLECULAR_WEIGHT>
339.385

> <EXACT_MASS>
339.147058165

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_AVERAGE_POLARIZABILITY>
36.926689401350735

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
9,13-dimethoxy-5-methyl-5-azatetracyclo[8.8.0.0²,⁷.0¹¹,¹⁶]octadeca-1,7,9,11,13,15,17-heptaene-8,14-diol

> <ALOGPS_LOGP>
3.04

> <JCHEM_LOGP>
2.806824756684445

> <ALOGPS_LOGS>
-3.74

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
9.811700591417347

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.98829515483833

> <JCHEM_PKA_STRONGEST_BASIC>
7.457172527070641

> <JCHEM_POLAR_SURFACE_AREA>
62.16000000000001

> <JCHEM_REFRACTIVITY>
97.69889999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.13e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
9,13-dimethoxy-5-methyl-5-azatetracyclo[8.8.0.0²,⁷.0¹¹,¹⁶]octadeca-1,7,9,11,13,15,17-heptaene-8,14-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      15.416  -2.122   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.822  -5.323   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.359  -6.197   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.351   0.788   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.863   0.497   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      11.888  -0.085   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      13.400  -0.376   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.831  -0.085   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.839  -2.995   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      12.896  -2.995   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.343  -0.376   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.880  -1.249   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.367  -0.958   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.847  -1.831   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      11.384  -2.704   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.822  -1.249   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.327  -2.704   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.359  -2.122   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      10.375  -3.868   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.863  -3.577   0.000  0.00  0.00           C+0
HETATM   21  N   UNK     0      13.904  -1.831   0.000  0.00  0.00           N+0
HETATM   22  O   UNK     0       2.310  -0.958   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      10.880  -5.323   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       3.318  -3.868   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       7.855  -4.741   0.000  0.00  0.00           O+0
CONECT    1   21                                                            
CONECT    2   24                                                            
CONECT    3   25                                                            
CONECT    4    5   11                                                       
CONECT    5    4   13                                                       
CONECT    6    7   12                                                       
CONECT    7    6   21                                                       
CONECT    8   11   16                                                       
CONECT    9   14   17                                                       
CONECT   10   15   21                                                       
CONECT   11    4    8   14                                                  
CONECT   12    6   13   15                                                  
CONECT   13    5   12   18                                                  
CONECT   14    9   11   18                                                  
CONECT   15   10   12   19                                                  
CONECT   16    8   17   22                                                  
CONECT   17    9   16   24                                                  
CONECT   18   13   14   20                                                  
CONECT   19   15   20   23                                                  
CONECT   20   18   19   25                                                  
CONECT   21    1    7   10                                                  
CONECT   22   16                                                            
CONECT   23   19                                                            
CONECT   24    2   17                                                       
CONECT   25    3   20                                                       
MASTER        0    0    0    0    0    0    0    0   25    0   56    0
END

View in JSmol

Synonyms

Value	Source
1,2,3,4-Tetrahydro-9,11-dimethoxy-2-methylnaphth[2,1-F]isoquinoline-8,12-diol, 9ci	HMDB
Litebamine	MeSH

Chemical Formula

C₂₀H₂₁NO₄

Average Mass

339.3850 Da

Monoisotopic Mass

339.14706 Da

IUPAC Name

9,13-dimethoxy-5-methyl-5-azatetracyclo[8.8.0.0²,⁷.0¹¹,¹⁶]octadeca-1,7,9,11,13,15,17-heptaene-8,14-diol

Traditional Name

9,13-dimethoxy-5-methyl-5-azatetracyclo[8.8.0.0²,⁷.0¹¹,¹⁶]octadeca-1,7,9,11,13,15,17-heptaene-8,14-diol

CAS Registry Number

Not Available

SMILES

COC1=C(O)C=C2C=CC3=C4CCN(C)CC4=C(O)C(OC)=C3C2=C1

InChI Identifier

InChI=1S/C20H21NO4/c1-21-7-6-12-13-5-4-11-8-16(22)17(24-2)9-14(11)18(13)20(25-3)19(23)15(12)10-21/h4-5,8-9,22-23H,6-7,10H2,1-3H3

InChI Key

QOWFEPGZJDCIKG-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
Litsea cubeba	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenanthrols. Phenanthrols are compounds containing a phenanthrene (or its hydrogenated derivative) to which a hydroxyl group is attached.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Phenanthrenes and derivatives

Sub Class

Phenanthrols

Direct Parent

Phenanthrols

Alternative Parents

Substituents

Phenanthrol
2-naphthol
Naphthalene
Tetrahydroisoquinoline
Anisole
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
Aralkylamine
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	3.04	ALOGPS
logP	2.81	ChemAxon
logS	-3.7	ALOGPS
pKa (Strongest Acidic)	8.99	ChemAxon
pKa (Strongest Basic)	7.46	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	97.7 m³·mol⁻¹	ChemAxon
Polarizability	36.93 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

HMDB0038629

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB018023

KNApSAcK ID

C00028482

Chemspider ID

170528

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

196885

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Litebamine (NP0070052)

MOL for NP0070052 (Litebamine)

3D MOL for NP0070052 (Litebamine)

3D SDF for NP0070052 (Litebamine)

3D-SDF for NP0070052 (Litebamine)

PDB for NP0070052 (Litebamine)

3D PDB for NP0070052 (Litebamine)

SMILES for NP0070052 (Litebamine)

INCHI for NP0070052 (Litebamine)

Structure for NP0070052 (Litebamine)

3D Structure for NP0070052 (Litebamine)