NP-MRD: Showing NP-Card for Phencomycin (NP0023032)

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Record Information

Version

1.0

Created at

2021-01-06 08:10:00 UTC

Updated at

2021-07-15 17:40:39 UTC

NP-MRD ID

NP0023032

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Phencomycin

Provided By

NPAtlas

Description

Phencomycin is found in Streptomyces sp. It was first documented in 1995 (PMID: 8557581). Based on a literature review very few articles have been published on 6-(methoxycarbonyl)phenazine-1-carboxylic acid (PMID: 34383398) (PMID: 34383397) (PMID: 34383396) (PMID: 34384147).

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242105393D          

 31 33  0  0  0  0            999 V2000
    5.2753    1.0207   -0.2824 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3398   -0.0335   -0.3986 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9956    0.2676   -0.2678 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6777    1.4631   -0.0525 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9590   -0.7818   -0.3770 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3741   -2.0751   -0.6140 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3792   -3.0343   -0.7109 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0460   -2.7102   -0.5770 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3291   -1.3940   -0.3386 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.9561    1.7987   -1.0196 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2713    1.4655    0.7504 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4263   -2.3013   -0.7149 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6651   -4.0642   -0.8970 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

 31 33  0  0  0  0  0  0  0  0999 V2000
    5.2753    1.0207   -0.2824 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3398   -0.0335   -0.3986 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9956    0.2676   -0.2678 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6777    1.4631   -0.0525 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9590   -0.7818   -0.3770 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3741   -2.0751   -0.6140 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.6126    3.2458    0.4389 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652306242105393D          

 31 33  0  0  0  0            999 V2000
    5.2753    1.0207   -0.2824 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3398   -0.0335   -0.3986 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9956    0.2676   -0.2678 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6777    1.4631   -0.0525 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9590   -0.7818   -0.3770 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3741   -2.0751   -0.6140 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3792   -3.0343   -0.7109 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0460   -2.7102   -0.5770 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3291   -1.3940   -0.3386 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.3460   -0.4385    0.0614 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END
> <DATABASE_ID>
NP0023032

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC(=O)C1=C2N=C3C([H])=C([H])C([H])=C(C(=O)OC([H])([H])[H])C3=NC2=C([H])C([H])=C1[H]

> <INCHI_IDENTIFIER>
InChI=1S/C15H10N2O4/c1-21-15(20)9-5-3-7-11-13(9)17-10-6-2-4-8(14(18)19)12(10)16-11/h2-7H,1H3,(H,18,19)

> <INCHI_KEY>
YPYRMWFNCMDUIB-UHFFFAOYSA-N

> <FORMULA>
C15H10N2O4

> <MOLECULAR_WEIGHT>
282.255

> <EXACT_MASS>
282.06405681

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
31

> <JCHEM_AVERAGE_POLARIZABILITY>
28.094534795059204

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
6-(methoxycarbonyl)phenazine-1-carboxylic acid

> <ALOGPS_LOGP>
1.63

> <JCHEM_LOGP>
2.7213156499999998

> <ALOGPS_LOGS>
-3.37

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.6520656887246266

> <JCHEM_PKA_STRONGEST_BASIC>
-1.3623200952321803

> <JCHEM_POLAR_SURFACE_AREA>
89.38

> <JCHEM_REFRACTIVITY>
72.4381

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.22e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6-(methoxycarbonyl)phenazine-1-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 31 33  0  0  0  0  0  0  0  0999 V2000
    5.2753    1.0207   -0.2824 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3398   -0.0335   -0.3986 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9956    0.2676   -0.2678 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6777    1.4631   -0.0525 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.3741   -2.0751   -0.6140 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.0460   -2.7102   -0.5770 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3291   -1.3940   -0.3386 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6342   -1.0598   -0.2048 N   0  0  0  0  0  0  0  0  0  0  0  0
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    5.2713    1.4655    0.7504 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.7556    2.1464    0.5098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9932    3.8622    0.6842 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6126    3.2458    0.4389 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
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 17 30  1  0
 18 31  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0       5.275   1.021  -0.282  0.00  0.00           C+0
HETATM    2  O   UNK     0       4.340  -0.034  -0.399  0.00  0.00           O+0
HETATM    3  C   UNK     0       2.996   0.268  -0.268  0.00  0.00           C+0
HETATM    4  O   UNK     0       2.678   1.463  -0.053  0.00  0.00           O+0
HETATM    5  C   UNK     0       1.959  -0.782  -0.377  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.374  -2.075  -0.614  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.379  -3.034  -0.711  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.046  -2.710  -0.577  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.329  -1.394  -0.339  0.00  0.00           C+0
HETATM   10  N   UNK     0      -1.634  -1.060  -0.205  0.00  0.00           N+0
HETATM   11  C   UNK     0      -1.984   0.236   0.029  0.00  0.00           C+0
HETATM   12  C   UNK     0      -3.320   0.583   0.167  0.00  0.00           C+0
HETATM   13  C   UNK     0      -4.346  -0.439   0.061  0.00  0.00           C+0
HETATM   14  O   UNK     0      -5.552  -0.171   0.178  0.00  0.00           O+0
HETATM   15  O   UNK     0      -3.995  -1.760  -0.177  0.00  0.00           O+0
HETATM   16  C   UNK     0      -3.706   1.894   0.405  0.00  0.00           C+0
HETATM   17  C   UNK     0      -2.702   2.846   0.500  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.385   2.495   0.363  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.990   1.195   0.126  0.00  0.00           C+0
HETATM   20  N   UNK     0       0.318   0.880  -0.005  0.00  0.00           N+0
HETATM   21  C   UNK     0       0.641  -0.421  -0.238  0.00  0.00           C+0
HETATM   22  H   UNK     0       6.297   0.686  -0.551  0.00  0.00           H+0
HETATM   23  H   UNK     0       4.956   1.799  -1.020  0.00  0.00           H+0
HETATM   24  H   UNK     0       5.271   1.466   0.750  0.00  0.00           H+0
HETATM   25  H   UNK     0       3.426  -2.301  -0.715  0.00  0.00           H+0
HETATM   26  H   UNK     0       1.665  -4.064  -0.897  0.00  0.00           H+0
HETATM   27  H   UNK     0      -0.727  -3.462  -0.653  0.00  0.00           H+0
HETATM   28  H   UNK     0      -4.591  -2.379  -0.695  0.00  0.00           H+0
HETATM   29  H   UNK     0      -4.756   2.146   0.510  0.00  0.00           H+0
HETATM   30  H   UNK     0      -2.993   3.862   0.684  0.00  0.00           H+0
HETATM   31  H   UNK     0      -0.613   3.246   0.439  0.00  0.00           H+0
CONECT    1    2   22   23   24                                             
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   21                                                  
CONECT    6    5    7   25                                                  
CONECT    7    6    8   26                                                  
CONECT    8    7    9   27                                                  
CONECT    9    8   10   21                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   19                                                  
CONECT   12   11   13   16                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   28                                                       
CONECT   16   12   17   29                                                  
CONECT   17   16   18   30                                                  
CONECT   18   17   19   31                                                  
CONECT   19   18   20   11                                                  
CONECT   20   19   21                                                       
CONECT   21   20    5    9                                                  
CONECT   22    1                                                            
CONECT   23    1                                                            
CONECT   24    1                                                            
CONECT   25    6                                                            
CONECT   26    7                                                            
CONECT   27    8                                                            
CONECT   28   15                                                            
CONECT   29   16                                                            
CONECT   30   17                                                            
CONECT   31   18                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   66    0
END

RDKit          3D

31 33  0  0  0  0  0  0  0  0999 V2000
    5.2753    1.0207   -0.2824 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3398   -0.0335   -0.3986 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9956    0.2676   -0.2678 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6777    1.4631   -0.0525 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9590   -0.7818   -0.3770 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3741   -2.0751   -0.6140 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3792   -3.0343   -0.7109 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0460   -2.7102   -0.5770 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3291   -1.3940   -0.3386 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6342   -1.0598   -0.2048 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9836    0.2363    0.0288 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3200    0.5829    0.1666 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3460   -0.4385    0.0614 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5522   -0.1711    0.1784 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9952   -1.7602   -0.1766 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7057    1.8943    0.4049 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7020    2.8461    0.5000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3845    2.4948    0.3626 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9898    1.1949    0.1257 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3181    0.8804   -0.0051 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411   -0.4210   -0.2380 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2969    0.6864   -0.5512 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9561    1.7987   -1.0196 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2713    1.4655    0.7504 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4263   -2.3013   -0.7149 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6651   -4.0642   -0.8970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7271   -3.4615   -0.6533 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5910   -2.3794   -0.6949 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7556    2.1464    0.5098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9932    3.8622    0.6842 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6126    3.2458    0.4389 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
  3  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 13 15  1  0
 12 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 21  5  1  0
 21  9  1  0
 19 11  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  6 25  1  0
  7 26  1  0
  8 27  1  0
 15 28  1  0
 16 29  1  0
 17 30  1  0
 18 31  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
6-(Methoxycarbonyl)phenazine-1-carboxylate	Generator
1,5-Phenazinedicarboxylic acid 1-methyl ester	MeSH

Chemical Formula

C₁₅H₁₀N₂O₄

Average Mass

282.2550 Da

Monoisotopic Mass

282.06406 Da

IUPAC Name

6-(methoxycarbonyl)phenazine-1-carboxylic acid

Traditional Name

6-(methoxycarbonyl)phenazine-1-carboxylic acid

CAS Registry Number

Not Available

SMILES

COC(=O)C1=CC=CC2=NC3=C(C=CC=C3N=C12)C(O)=O

InChI Identifier

InChI=1S/C15H10N2O4/c1-21-15(20)9-5-3-7-11-13(9)17-10-6-2-4-8(14(18)19)12(10)16-11/h2-7H,1H3,(H,18,19)

InChI Key

YPYRMWFNCMDUIB-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
Streptomyces sp.	NPAtlas	8557581

Species Where Detected

Species Name	Source	Reference
Streptomyces HIL Y-9031725	KNApSAcK Database	22123792

Chemical Taxonomy

Description

This compound belongs to the class of organic compounds known as phenazines and derivatives. These are polycyclic aromatic compounds containing a phenazine moiety, which is a linear tricyclic system that consists of a two benzene rings joined by a pyrazine ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Diazanaphthalenes

Sub Class

Benzodiazines

Direct Parent

Phenazines and derivatives

Alternative Parents

Substituents

Phenazine
Benzenoid
Pyrazine
Heteroaromatic compound
Methyl ester
Carboxylic acid ester
Carboxylic acid derivative
Carboxylic acid
Azacycle
Organic nitrogen compound
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Organic oxide
Organic oxygen compound
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	1.63	ALOGPS
logP	2.72	ChemAxon
logS	-3.4	ALOGPS
pKa (Strongest Acidic)	3.65	ChemAxon
pKa (Strongest Basic)	-1.4	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	89.38 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	72.44 m³·mol⁻¹	ChemAxon
Polarizability	28.09 Å³	ChemAxon
Number of Rings	3	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

NPAtlas ID

NPA008067

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00016610

Chemspider ID

8214960

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10039396

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Chatterjee S, Vijayakumar EK, Franco CM, Maurya R, Blumbach J, Ganguli BN: Phencomycin, a new antibiotic from a Streptomyces species HIL Y-9031725. J Antibiot (Tokyo). 1995 Nov;48(11):1353-4. doi: 10.7164/antibiotics.48.1353. [PubMed:8557581 ]
Mitchell PM: The cost-effectiveness of what in health and care?. 2021 Feb. [PubMed:34383398 ]
Authors unspecified: Ozanimod. 2012. [PubMed:34383397 ]
Authors unspecified: Ponesimod. 2012. [PubMed:34383396 ]
Lee J, Cho Y, Choi KH, Hwang I, Oh YL: Metastatic leiomyosarcoma of the thyroid gland: cytologic findings and differential diagnosis. J Pathol Transl Med. 2021 Aug 13. pii: jptm.2021.06.23. doi: 10.4132/jptm.2021.06.23. [PubMed:34384147 ]

Showing NP-Card for Phencomycin (NP0023032)

MOL for NP0023032 (Phencomycin)

3D MOL for NP0023032 (Phencomycin)

3D SDF for NP0023032 (Phencomycin)

3D-SDF for NP0023032 (Phencomycin)

PDB for NP0023032 (Phencomycin)

3D PDB for NP0023032 (Phencomycin)

SMILES for NP0023032 (Phencomycin)

INCHI for NP0023032 (Phencomycin)

Structure for NP0023032 (Phencomycin)

3D Structure for NP0023032 (Phencomycin)