NP-MRD: Showing NP-Card for Ankalactone (NP0066339)

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Record Information

Version

2.0

Created at

2022-04-28 10:37:13 UTC

Updated at

2022-04-28 10:37:13 UTC

NP-MRD ID

NP0066339

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Ankalactone

Description

Ankalactone belongs to the class of organic compounds known as benzofurans. These are organic compounds containing a benzene ring fused to a furan. Furan is a five-membered aromatic ring with four carbon atoms and one oxygen atom. Ankalactone is found in Monascus anka. Based on a literature review very few articles have been published on Ankalactone.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 50 51  0  0  0  0  0  0  0  0999 V2000
    6.7113   -0.5635    0.1810 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2254   -0.7726    0.3455 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5173    0.5536    0.0432 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0080    0.3678    0.2032 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3388    1.6816   -0.0987 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8450    1.5672    0.0699 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3135    0.5436   -0.8711 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1742    0.3724   -0.8333 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8511    0.6073   -1.9383 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3269    0.4525   -1.9614 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3208    0.8975   -2.6731 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5757    0.3603   -2.1706 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7256    0.6082   -2.6576 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2397   -0.4342   -1.1040 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8804   -0.4718   -0.9251 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3358   -0.0096    0.3774 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8175    1.3784    0.7581 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8305   -0.8869    1.3588 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8381   -0.0520    0.3900 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4461    0.7414    1.4994 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3956   -1.4720    0.6639 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5667   -2.4101   -0.1423 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7592   -1.7932    1.8681 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3385   -3.1225    2.1382 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9372    0.0150   -0.7334 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2470   -1.5373    0.0992 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0840    0.0308    1.0445 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9132   -1.5413   -0.4002 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9954   -1.0876    1.3821 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7589    0.8342   -0.9874 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9173    1.2887    0.7590 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8299    0.0512    1.2379 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7204   -0.4287   -0.5209 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5156    1.8622   -1.2001 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7693    2.5082    0.5057 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6933    1.3341    1.1492 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3889    2.5667   -0.1259 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7774   -0.4535   -0.6646 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6586    0.8178   -1.8909 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3900    0.9151   -2.8560 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1899    1.5829   -3.5277 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4509   -1.5123   -1.0846 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7759    1.6363    0.2892 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0598    2.1491    0.4841 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9287    1.4488    1.8651 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0162   -0.4399    2.2053 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2095    0.1796    2.2640 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7760   -3.1870    2.0646 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8113   -3.7797    1.3763 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6875   -3.3967    3.1562 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 16 18  1  1
 16 19  1  0
 19 20  1  1
 19 21  1  0
 21 22  2  0
 21 23  1  0
 23 24  1  0
 19  8  1  0
 15 10  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  0
  2 29  1  0
  3 30  1  0
  3 31  1  0
  4 32  1  0
  4 33  1  0
  5 34  1  0
  5 35  1  0
  6 36  1  0
  6 37  1  0
  7 38  1  0
  7 39  1  0
  9 40  1  0
 11 41  1  0
 15 42  1  6
 17 43  1  0
 17 44  1  0
 17 45  1  0
 18 46  1  0
 20 47  1  0
 24 48  1  0
 24 49  1  0
 24 50  1  0
M  END


  Mrv1652304282212372D          

 24 25  0  0  1  0            999 V2000
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3149   -3.6945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1354   -3.7807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5479   -4.4952    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4710   -3.0270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8579   -1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1434   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5307   -0.5091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0935    0.1906    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3552   -0.4803    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7425    0.2482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7561   -0.5091    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6824   -1.6212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2951   -0.9504    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  8  7  1  6  0  0  0
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  1 10  1  0  0  0  0
 10 11  1  1  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 10 15  1  6  0  0  0
  9 16  1  6  0  0  0
  9 17  1  1  0  0  0
  1 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 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
M  END
> <DATABASE_ID>
NP0066339

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCC1=CC2=CC(=O)O[C@@H]2[C@@](C)(O)[C@@]1(O)C(=O)OC

> <INCHI_IDENTIFIER>
InChI=1S/C18H26O6/c1-4-5-6-7-8-9-13-10-12-11-14(19)24-15(12)17(2,21)18(13,22)16(20)23-3/h10-11,15,21-22H,4-9H2,1-3H3/t15-,17+,18-/m0/s1

> <INCHI_KEY>
ISIUIMTUNVCMGZ-JQHSSLGASA-N

> <FORMULA>
C18H26O6

> <MOLECULAR_WEIGHT>
338.4

> <EXACT_MASS>
338.172938557

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
50

> <JCHEM_AVERAGE_POLARIZABILITY>
36.657503672844165

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (6R,7R,7aS)-5-heptyl-6,7-dihydroxy-7-methyl-2-oxo-2,6,7,7a-tetrahydro-1-benzofuran-6-carboxylate

> <ALOGPS_LOGP>
2.21

> <JCHEM_LOGP>
2.387470075000001

> <ALOGPS_LOGS>
-3.23

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
11.025883146708988

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.67117582929591

> <JCHEM_PKA_STRONGEST_BASIC>
-3.8848347745216367

> <JCHEM_POLAR_SURFACE_AREA>
93.06000000000002

> <JCHEM_REFRACTIVITY>
88.3763

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.01e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl (6R,7R,7aS)-5-heptyl-6,7-dihydroxy-7-methyl-2-oxo-7aH-1-benzofuran-6-carboxylate

> <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      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.321  -6.896   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -5.853  -7.057   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -6.623  -8.391   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0      -6.479  -5.650   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -5.335  -4.620   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -4.724  -0.950   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -3.908   0.356   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0      -6.263  -0.897   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -6.986   0.463   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -3.278  -0.950   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -6.874  -3.026   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -6.151  -1.774   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
CONECT    1    2   10   18                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    3    9                                                  
CONECT    9    8   10   16   17                                             
CONECT   10    9    1   11   15                                             
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13                                                            
CONECT   15   10                                                            
CONECT   16    9                                                            
CONECT   17    9                                                            
CONECT   18    1   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   50    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₂₆O₆

Average Mass

338.4000 Da

Monoisotopic Mass

338.17294 Da

IUPAC Name

methyl (6R,7R,7aS)-5-heptyl-6,7-dihydroxy-7-methyl-2-oxo-2,6,7,7a-tetrahydro-1-benzofuran-6-carboxylate

Traditional Name

methyl (6R,7R,7aS)-5-heptyl-6,7-dihydroxy-7-methyl-2-oxo-7aH-1-benzofuran-6-carboxylate

CAS Registry Number

Not Available

SMILES

CCCCCCCC1=CC2=CC(=O)O[C@@H]2[C@@](C)(O)[C@@]1(O)C(=O)OC

InChI Identifier

InChI=1S/C18H26O6/c1-4-5-6-7-8-9-13-10-12-11-14(19)24-15(12)17(2,21)18(13,22)16(20)23-3/h10-11,15,21-22H,4-9H2,1-3H3/t15-,17+,18-/m0/s1

InChI Key

ISIUIMTUNVCMGZ-JQHSSLGASA-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
Monascus purpureus	Fungi	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzofurans. These are organic compounds containing a benzene ring fused to a furan. Furan is a five-membered aromatic ring with four carbon atoms and one oxygen atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzofurans

Sub Class

Not Available

Direct Parent

Benzofurans

Alternative Parents

Substituents

Benzofuran
2-furanone
Dicarboxylic acid or derivatives
Dihydrofuran
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Methyl ester
Tertiary alcohol
1,2-diol
Carboxylic acid ester
Lactone
Carboxylic acid derivative
Oxacycle
Hydrocarbon derivative
Alcohol
Carbonyl group
Organic oxide
Organic oxygen compound
Organooxygen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	2.21	ALOGPS
logP	2.39	ChemAxon
logS	-3.2	ALOGPS
pKa (Strongest Acidic)	2.67	ChemAxon
pKa (Strongest Basic)	-3.9	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	93.06 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	88.38 m³·mol⁻¹	ChemAxon
Polarizability	36.66 Å³	ChemAxon
Number of Rings	2	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

C00023724

Chemspider ID

68024598

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

101601480

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Ankalactone (NP0066339)

MOL for NP0066339 (Ankalactone)

3D MOL for NP0066339 (Ankalactone)

3D SDF for NP0066339 (Ankalactone)

3D-SDF for NP0066339 (Ankalactone)

PDB for NP0066339 (Ankalactone)

3D PDB for NP0066339 (Ankalactone)

SMILES for NP0066339 (Ankalactone)

INCHI for NP0066339 (Ankalactone)

Structure for NP0066339 (Ankalactone)

3D Structure for NP0066339 (Ankalactone)