NP-MRD: Showing NP-Card for Dimeroperatic acid (NP0064968)

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Record Information

Version

2.0

Created at

2022-04-28 09:15:58 UTC

Updated at

2022-04-28 09:15:58 UTC

NP-MRD ID

NP0064968

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Dimeroperatic acid

Description

Dimeroperatic acid, also known as dimeroperatate, belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety. Dimeroperatic acid is found in Dimerostemma asperatum. Based on a literature review very few articles have been published on Dimeroperatic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 52 52  0  0  0  0  0  0  0  0999 V2000
   -5.5546    2.3744   -0.2142 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1734    1.1027   -0.9640 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5257    0.2091   -0.2556 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0860   -1.0667   -0.8102 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6042   -1.2467   -0.9801 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8467   -1.1355    0.2707 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7555    0.0969    1.0966 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1451   -2.2020    0.7188 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3294   -2.1847    1.9477 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1207   -2.4493    1.6806 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7017   -1.4268    0.7969 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2360   -1.2284   -0.5873 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6959   -0.6950    1.2829 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3161    0.3437    0.4465 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8055    0.0433    0.2356 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4096    1.1145   -0.6173 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3902    1.8907   -0.2541 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7270    2.8144   -1.3222 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6171    3.7140   -1.3466 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8726    2.5413   -2.3703 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0304    1.4894   -1.9830 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5241    1.0049   -2.3562 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2319    0.0354   -3.0572 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2205    2.0387   -2.9521 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3380    2.9209   -0.7585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6510    2.9856   -0.1062 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9345    2.0530    0.7627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3481    0.4707    0.8068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6615   -1.4792   -1.6360 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3314   -1.8360    0.0391 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1841   -0.5716   -1.7595 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4822   -2.2802   -1.4200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3623   -0.0570    2.0025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6618    0.2418    1.3223 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1168    1.0053    0.5568 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2214   -3.1099    0.1076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4845   -1.2735    2.5718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6657   -3.0140    2.6537 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2536   -3.4529    1.1913 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7085   -2.5424    2.6300 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6963   -0.2730   -0.7523 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5897   -2.0399   -0.9795 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1200   -1.2205   -1.2864 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0646   -0.8582    2.3136 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3076    1.3232    1.0144 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7877    0.4926   -0.4891 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3031    0.0646    1.2207 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8730   -0.9547   -0.2478 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9077    1.8749    0.7097 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1824    0.6656   -2.7185 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9536    1.7748   -2.0308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2302    1.9115   -3.1076 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  3  1  0
  3  2  2  0
  2  1  1  0
  2 22  1  0
 22 24  1  0
 22 23  2  0
  6  8  2  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  0
 21 16  1  0
  7 33  1  0
  7 34  1  0
  7 35  1  0
  5 31  1  0
  5 32  1  0
  4 29  1  0
  4 30  1  0
  3 28  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
 24 52  1  0
  8 36  1  0
  9 37  1  0
  9 38  1  0
 10 39  1  0
 10 40  1  0
 12 41  1  0
 12 42  1  0
 12 43  1  0
 13 44  1  0
 14 45  1  0
 14 46  1  0
 15 47  1  0
 15 48  1  0
 17 49  1  0
 21 50  1  0
 21 51  1  0
M  END


  Mrv1652304282211152D          

 24 24  0  0  0  0            999 V2000
    0.5678    1.1143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5678    1.9393    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2352    0.6294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9803   -0.1553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1553   -0.1553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0997    0.6294    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4652   -0.8227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1296   -1.5764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6145   -2.2438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2790   -2.9975    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7639   -3.6649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4284   -4.4186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9133   -5.0860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5777   -5.8397    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0626   -6.5072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8831   -6.4209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3680   -7.0884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1885   -7.0021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6734   -7.6696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5241   -6.2484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3446   -6.1622    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0392   -5.5810    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7572   -5.9259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4585   -3.0837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  1  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  4  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 14 23  1  0  0  0  0
 10 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0064968

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C(CC\C=C(\C)C(O)=O)=C/CC\C(C)=C\CCC1=CC(=O)OC1

> <INCHI_IDENTIFIER>
InChI=1S/C20H28O4/c1-15(9-5-11-17(3)20(22)23)7-4-8-16(2)10-6-12-18-13-19(21)24-14-18/h7,10-11,13H,4-6,8-9,12,14H2,1-3H3,(H,22,23)/b15-7+,16-10+,17-11-

> <INCHI_KEY>
VBZXBFNXHOZDBI-AEPYBEDWSA-N

> <FORMULA>
C20H28O4

> <MOLECULAR_WEIGHT>
332.44

> <EXACT_MASS>
332.198759382

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
38.746677322925336

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2Z,6E,10E)-2,6,10-trimethyl-13-(5-oxo-2,5-dihydrofuran-3-yl)trideca-2,6,10-trienoic acid

> <ALOGPS_LOGP>
4.97

> <JCHEM_LOGP>
4.950812284333335

> <ALOGPS_LOGS>
-4.91

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
7.433812269359907

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.069269371900448

> <JCHEM_PKA_STRONGEST_BASIC>
-6.822615127547263

> <JCHEM_POLAR_SURFACE_AREA>
63.60000000000001

> <JCHEM_REFRACTIVITY>
98.65439999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.05e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2Z,6E,10E)-2,6,10-trimethyl-13-(5-oxo-2H-furan-3-yl)trideca-2,6,10-trienoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

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       1.060   2.080   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       1.060   3.620   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       2.306   1.175   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.830  -0.290   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.290  -0.290   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -0.186   1.175   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       2.735  -1.536   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.109  -2.943   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.014  -4.188   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.387  -5.595   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.293  -6.841   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.666  -8.248   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.571  -9.494   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.945 -10.901   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.850 -12.147   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.382 -11.986   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.287 -13.232   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.819 -13.071   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.724 -14.317   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.445 -11.664   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       9.977 -11.503   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       7.540 -10.418   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       1.414 -11.062   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.856  -5.756   0.000  0.00  0.00           C+0
CONECT    1    2    3    6                                                  
CONECT    2    1                                                            
CONECT    3    1    4                                                       
CONECT    4    3    5    7                                                  
CONECT    5    4    6                                                       
CONECT    6    5    1                                                       
CONECT    7    4    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   24                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   23                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   14                                                            
CONECT   24   10                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   48    0
END

View in JSmol

Synonyms

Value	Source
Dimeroperatate	Generator

Chemical Formula

C₂₀H₂₈O₄

Average Mass

332.4400 Da

Monoisotopic Mass

332.19876 Da

IUPAC Name

(2Z,6E,10E)-2,6,10-trimethyl-13-(5-oxo-2,5-dihydrofuran-3-yl)trideca-2,6,10-trienoic acid

Traditional Name

(2Z,6E,10E)-2,6,10-trimethyl-13-(5-oxo-2H-furan-3-yl)trideca-2,6,10-trienoic acid

CAS Registry Number

Not Available

SMILES

C\C(CC\C=C(\C)C(O)=O)=C/CC\C(C)=C\CCC1=CC(=O)OC1

InChI Identifier

InChI=1S/C20H28O4/c1-15(9-5-11-17(3)20(22)23)7-4-8-16(2)10-6-12-18-13-19(21)24-14-18/h7,10-11,13H,4-6,8-9,12,14H2,1-3H3,(H,22,23)/b15-7+,16-10+,17-11-

InChI Key

VBZXBFNXHOZDBI-AEPYBEDWSA-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
Dimerostemma asperatum	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Diterpene lactones

Alternative Parents

Substituents

Diterpene lactone
Diterpenoid
Long-chain fatty acid
Branched fatty acid
Methyl-branched fatty acid
Heterocyclic fatty acid
2-furanone
Dicarboxylic acid or derivatives
Fatty acyl
Fatty acid
Unsaturated fatty acid
Dihydrofuran
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Carboxylic acid ester
Lactone
Carboxylic acid derivative
Carboxylic acid
Oxacycle
Organoheterocyclic compound
Hydrocarbon derivative
Organic oxygen compound
Organic oxide
Carbonyl group
Organooxygen compound
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic 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	4.97	ALOGPS
logP	4.95	ChemAxon
logS	-4.9	ALOGPS
pKa (Strongest Acidic)	5.07	ChemAxon
pKa (Strongest Basic)	-6.8	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	63.6 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	98.65 m³·mol⁻¹	ChemAxon
Polarizability	38.75 Å³	ChemAxon
Number of Rings	1	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

C00022042

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

101277244

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Dimeroperatic acid (NP0064968)

MOL for NP0064968 (Dimeroperatic acid)

3D MOL for NP0064968 (Dimeroperatic acid)

3D SDF for NP0064968 (Dimeroperatic acid)

3D-SDF for NP0064968 (Dimeroperatic acid)

PDB for NP0064968 (Dimeroperatic acid)

3D PDB for NP0064968 (Dimeroperatic acid)

SMILES for NP0064968 (Dimeroperatic acid)

INCHI for NP0064968 (Dimeroperatic acid)

Structure for NP0064968 (Dimeroperatic acid)

3D Structure for NP0064968 (Dimeroperatic acid)