NP-MRD: Showing NP-Card for Hyaluromycin (NP0012439)

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Record Information

Version

2.0

Created at

2021-01-05 21:49:12 UTC

Updated at

2021-07-15 17:11:46 UTC

NP-MRD ID

NP0012439

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Hyaluromycin

Provided By

NPAtlas

Description

(2S)-4,9,10'-trihydroxy-N-(2-hydroxy-5-oxocyclopent-1-en-1-yl)-7-methoxy-5,8,9'-trioxo-4',5,8,9'-tetrahydro-3H,3'H-spiro[naphtho[2,3-b]furan-2,2'-pyrano[3,2-g]isochromene]-7'-carboxamide belongs to the class of organic compounds known as pyranochromenes. These are organic heterocyclic compounds containing a pyran ring fused to a chromene (1-benzopyran) moiety. Hyaluromycin is found in Streptomyces sp. Hyaluromycin was first documented in 2014 (PMID: 24451191). Based on a literature review very few articles have been published on (2S)-4,9,10'-trihydroxy-N-(2-hydroxy-5-oxocyclopent-1-en-1-yl)-7-methoxy-5,8,9'-trioxo-4',5,8,9'-tetrahydro-3H,3'H-spiro[naphtho[2,3-b]furan-2,2'-pyrano[3,2-g]isochromene]-7'-carboxamide.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242117083D          

 65 71  0  0  0  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1652306242117083D          

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   10.6373   -1.1605    2.3462 H   0  0  0  0  0  0  0  0  0  0  0  0
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 44 64  1  0  0  0  0
 44 65  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0012439

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C(N([H])C(=O)C2=C([H])C3=C(C(=O)O2)C(O[H])=C2O[C@]4(OC5=C(C(O[H])=C6C(=O)C([H])=C(OC([H])([H])[H])C(=O)C6=C5O[H])C4([H])[H])C([H])([H])C([H])([H])C2=C3[H])C(=O)C([H])([H])C1([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C30H21NO13/c1-41-16-8-15(34)19-20(23(16)36)25(38)27-12(22(19)35)9-30(44-27)5-4-10-6-11-7-17(28(39)31-21-13(32)2-3-14(21)33)42-29(40)18(11)24(37)26(10)43-30/h6-8,32,35,37-38H,2-5,9H2,1H3,(H,31,39)/t30-/m0/s1

> <INCHI_KEY>
SVUGCIHLYMYXQP-PMERELPUSA-N

> <FORMULA>
C30H21NO13

> <MOLECULAR_WEIGHT>
603.492

> <EXACT_MASS>
603.10128974

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_ATOM_COUNT>
65

> <JCHEM_AVERAGE_POLARIZABILITY>
60.111407848748755

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S)-4,9,10'-trihydroxy-N-(2-hydroxy-5-oxocyclopent-1-en-1-yl)-7-methoxy-5,8,9'-trioxo-4',5,8,9'-tetrahydro-3H,3'H-spiro[naphtho[2,3-b]furan-2,2'-pyrano[3,2-g]isochromene]-7'-carboxamide

> <ALOGPS_LOGP>
2.54

> <JCHEM_LOGP>
3.050117290666666

> <ALOGPS_LOGS>
-4.42

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.697059412668413

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.982048790098026

> <JCHEM_PKA_STRONGEST_BASIC>
-3.8669778736073814

> <JCHEM_POLAR_SURFACE_AREA>
215.21999999999997

> <JCHEM_REFRACTIVITY>
152.09040000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.28e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-4,9,10'-trihydroxy-N-(2-hydroxy-5-oxocyclopent-1-en-1-yl)-7-methoxy-5,8,9'-trioxo-3',4'-dihydro-3H-spiro[naphtho[2,3-b]furan-2,2'-pyrano[3,2-g]isochromene]-7'-carboxamide

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 65 71  0  0  0  0  0  0  0  0999 V2000
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 44 64  1  0
 44 65  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      10.773  -1.534   1.304  0.00  0.00           C+0
HETATM    2  O   UNK     0      10.415  -0.536   0.346  0.00  0.00           O+0
HETATM    3  C   UNK     0       9.132  -0.049   0.348  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.886   1.072   1.042  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.536   1.616   1.066  0.00  0.00           C+0
HETATM    6  O   UNK     0       7.327   2.666   1.722  0.00  0.00           O+0
HETATM    7  C   UNK     0       6.478   0.933   0.336  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.179   1.421   0.335  0.00  0.00           C+0
HETATM    9  O   UNK     0       4.934   2.580   1.056  0.00  0.00           O+0
HETATM   10  C   UNK     0       4.196   0.757  -0.363  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.423  -0.387  -1.078  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.724  -0.877  -1.078  0.00  0.00           C+0
HETATM   13  O   UNK     0       6.020  -2.031  -1.782  0.00  0.00           O+0
HETATM   14  C   UNK     0       6.719  -0.225  -0.385  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.091  -0.736  -0.381  0.00  0.00           C+0
HETATM   16  O   UNK     0       8.296  -1.800  -1.047  0.00  0.00           O+0
HETATM   17  O   UNK     0       3.241  -0.810  -1.664  0.00  0.00           O+0
HETATM   18  C   UNK     0       2.145  -0.251  -0.955  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.862  -1.143   0.208  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.708  -2.100  -0.119  0.00  0.00           C+0
HETATM   21  C   UNK     0      -0.448  -1.236  -0.449  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.712  -1.448   0.044  0.00  0.00           C+0
HETATM   23  C   UNK     0      -2.769  -0.639  -0.273  0.00  0.00           C+0
HETATM   24  C   UNK     0      -4.055  -0.821   0.203  0.00  0.00           C+0
HETATM   25  C   UNK     0      -5.087   0.016  -0.142  0.00  0.00           C+0
HETATM   26  C   UNK     0      -6.453  -0.210   0.389  0.00  0.00           C+0
HETATM   27  O   UNK     0      -6.621  -1.176   1.149  0.00  0.00           O+0
HETATM   28  N   UNK     0      -7.473   0.671   0.008  0.00  0.00           N+0
HETATM   29  C   UNK     0      -8.828   0.655   0.381  0.00  0.00           C+0
HETATM   30  C   UNK     0      -9.454  -0.180   1.165  0.00  0.00           C+0
HETATM   31  O   UNK     0      -8.958  -1.285   1.850  0.00  0.00           O+0
HETATM   32  C   UNK     0     -10.919   0.177   1.291  0.00  0.00           C+0
HETATM   33  C   UNK     0     -10.957   1.643   0.907  0.00  0.00           C+0
HETATM   34  C   UNK     0      -9.834   1.658  -0.094  0.00  0.00           C+0
HETATM   35  O   UNK     0      -9.691   2.325  -1.121  0.00  0.00           O+0
HETATM   36  O   UNK     0      -4.843   1.013  -0.944  0.00  0.00           O+0
HETATM   37  C   UNK     0      -3.624   1.235  -1.432  0.00  0.00           C+0
HETATM   38  O   UNK     0      -3.433   2.213  -2.207  0.00  0.00           O+0
HETATM   39  C   UNK     0      -2.566   0.425  -1.115  0.00  0.00           C+0
HETATM   40  C   UNK     0      -1.285   0.651  -1.622  0.00  0.00           C+0
HETATM   41  O   UNK     0      -1.101   1.726  -2.466  0.00  0.00           O+0
HETATM   42  C   UNK     0      -0.242  -0.170  -1.293  0.00  0.00           C+0
HETATM   43  O   UNK     0       1.053   0.021  -1.778  0.00  0.00           O+0
HETATM   44  C   UNK     0       2.747   1.079  -0.512  0.00  0.00           C+0
HETATM   45  H   UNK     0      10.637  -1.161   2.346  0.00  0.00           H+0
HETATM   46  H   UNK     0      11.838  -1.842   1.166  0.00  0.00           H+0
HETATM   47  H   UNK     0      10.150  -2.459   1.141  0.00  0.00           H+0
HETATM   48  H   UNK     0       9.711   1.555   1.579  0.00  0.00           H+0
HETATM   49  H   UNK     0       3.990   2.933   1.054  0.00  0.00           H+0
HETATM   50  H   UNK     0       5.289  -2.518  -2.297  0.00  0.00           H+0
HETATM   51  H   UNK     0       2.736  -1.783   0.463  0.00  0.00           H+0
HETATM   52  H   UNK     0       1.511  -0.536   1.058  0.00  0.00           H+0
HETATM   53  H   UNK     0       0.988  -2.633  -1.050  0.00  0.00           H+0
HETATM   54  H   UNK     0       0.547  -2.749   0.742  0.00  0.00           H+0
HETATM   55  H   UNK     0      -1.893  -2.274   0.703  0.00  0.00           H+0
HETATM   56  H   UNK     0      -4.235  -1.643   0.859  0.00  0.00           H+0
HETATM   57  H   UNK     0      -7.150   1.457  -0.659  0.00  0.00           H+0
HETATM   58  H   UNK     0      -9.149  -2.237   1.528  0.00  0.00           H+0
HETATM   59  H   UNK     0     -11.245   0.014   2.328  0.00  0.00           H+0
HETATM   60  H   UNK     0     -11.457  -0.422   0.544  0.00  0.00           H+0
HETATM   61  H   UNK     0     -11.902   1.941   0.452  0.00  0.00           H+0
HETATM   62  H   UNK     0     -10.626   2.260   1.757  0.00  0.00           H+0
HETATM   63  H   UNK     0      -0.221   1.962  -2.876  0.00  0.00           H+0
HETATM   64  H   UNK     0       2.285   1.385   0.448  0.00  0.00           H+0
HETATM   65  H   UNK     0       2.662   1.842  -1.302  0.00  0.00           H+0
CONECT    1    2   45   46   47                                             
CONECT    2    1    3                                                       
CONECT    3    2    4   15                                                  
CONECT    4    3    5   48                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   14                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8   49                                                       
CONECT   10    8   11   44                                                  
CONECT   11   10   12   17                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12   50                                                       
CONECT   14   12   15    7                                                  
CONECT   15   14   16    3                                                  
CONECT   16   15                                                            
CONECT   17   11   18                                                       
CONECT   18   17   19   44   43                                             
CONECT   19   18   20   51   52                                             
CONECT   20   19   21   53   54                                             
CONECT   21   20   22   42                                                  
CONECT   22   21   23   55                                                  
CONECT   23   22   24   39                                                  
CONECT   24   23   25   56                                                  
CONECT   25   24   26   36                                                  
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   57                                                  
CONECT   29   28   30   34                                                  
CONECT   30   29   31   32                                                  
CONECT   31   30   58                                                       
CONECT   32   30   33   59   60                                             
CONECT   33   32   34   61   62                                             
CONECT   34   33   35   29                                                  
CONECT   35   34                                                            
CONECT   36   25   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40   23                                                  
CONECT   40   39   41   42                                                  
CONECT   41   40   63                                                       
CONECT   42   40   43   21                                                  
CONECT   43   42   18                                                       
CONECT   44   18   10   64   65                                             
CONECT   45    1                                                            
CONECT   46    1                                                            
CONECT   47    1                                                            
CONECT   48    4                                                            
CONECT   49    9                                                            
CONECT   50   13                                                            
CONECT   51   19                                                            
CONECT   52   19                                                            
CONECT   53   20                                                            
CONECT   54   20                                                            
CONECT   55   22                                                            
CONECT   56   24                                                            
CONECT   57   28                                                            
CONECT   58   31                                                            
CONECT   59   32                                                            
CONECT   60   32                                                            
CONECT   61   33                                                            
CONECT   62   33                                                            
CONECT   63   41                                                            
CONECT   64   44                                                            
CONECT   65   44                                                            
MASTER        0    0    0    0    0    0    0    0   65    0  142    0
END

RDKit          3D

65 71  0  0  0  0  0  0  0  0999 V2000
   10.7731   -1.5335    1.3037 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4155   -0.5364    0.3457 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -9.6906    2.3248   -1.1206 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.6235    1.2346   -1.4320 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4329    2.2133   -2.2066 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5662    0.4252   -1.1145 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2845    0.6509   -1.6223 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.7466    1.0795   -0.5120 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6373   -1.1605    2.3462 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.8380   -1.8418    1.1661 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1496   -2.4588    1.1405 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7108    1.5550    1.5786 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.5111   -0.5358    1.0582 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9884   -2.6332   -1.0499 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.2346   -1.6434    0.8594 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1504    1.4570   -0.6588 H   0  0  0  0  0  0  0  0  0  0  0  0
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  -11.9018    1.9408    0.4523 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.6260    2.2600    1.7573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2206    1.9624   -2.8757 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2851    1.3846    0.4484 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6624    1.8422   -1.3020 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
  4  5  1  0
  5  6  2  0
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  7  8  2  0
  8  9  1  0
  8 10  1  0
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 14  7  1  0
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  1 45  1  0
  1 46  1  0
  1 47  1  0
  4 48  1  0
  9 49  1  0
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 41 63  1  0
 44 64  1  0
 44 65  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₃₀H₂₁NO₁₃

Average Mass

603.4920 Da

Monoisotopic Mass

603.10129 Da

IUPAC Name

(2S)-4,9,10'-trihydroxy-N-(2-hydroxy-5-oxocyclopent-1-en-1-yl)-7-methoxy-5,8,9'-trioxo-4',5,8,9'-tetrahydro-3H,3'H-spiro[naphtho[2,3-b]furan-2,2'-pyrano[3,2-g]isochromene]-7'-carboxamide

Traditional Name

(2S)-4,9,10'-trihydroxy-N-(2-hydroxy-5-oxocyclopent-1-en-1-yl)-7-methoxy-5,8,9'-trioxo-3',4'-dihydro-3H-spiro[naphtho[2,3-b]furan-2,2'-pyrano[3,2-g]isochromene]-7'-carboxamide

CAS Registry Number

Not Available

SMILES

COC1=CC(=O)C2=C(C(O)=C3O[C@]4(CC3=C2O)CCC2=C(O4)C(O)=C3C(=O)OC(=CC3=C2)C(=O)NC2=C(O)CCC2=O)C1=O

InChI Identifier

InChI=1S/C30H21NO13/c1-41-16-8-15(34)19-20(23(16)36)25(38)27-12(22(19)35)9-30(44-27)5-4-10-6-11-7-17(28(39)31-21-13(32)2-3-14(21)33)42-29(40)18(11)24(37)26(10)43-30/h6-8,32,35,37-38H,2-5,9H2,1H3,(H,31,39)/t30-/m0/s1

InChI Key

SVUGCIHLYMYXQP-PMERELPUSA-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	24451191

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyranochromenes. These are organic heterocyclic compounds containing a pyran ring fused to a chromene (1-benzopyran) moiety.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

Pyranochromenes

Alternative Parents

Substituents

Pyranochromene
Naphthofuran
Naphthoquinone
Isocoumarin
Naphthalene
2-benzopyran
Coumaran
2-heteroaryl carboxamide
Quinone
Aryl ketone
Ketal
1-hydroxy-4-unsubstituted benzenoid
Pyranone
Pyran
Benzenoid
Vinylogous acid
Vinylogous ester
Heteroaromatic compound
Cyclic ketone
Carboxamide group
Secondary carboxylic acid amide
Ketone
Lactone
Carboxylic acid derivative
Oxacycle
Polyol
Acetal
Organic oxygen compound
Organic nitrogen compound
Organonitrogen compound
Organooxygen compound
Hydrocarbon derivative
Organopnictogen compound
Carbonyl group
Organic oxide
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	2.54	ALOGPS
logP	3.05	ChemAxon
logS	-4.4	ALOGPS
pKa (Strongest Acidic)	7.98	ChemAxon
pKa (Strongest Basic)	-3.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	12	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	215.22 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	152.09 m³·mol⁻¹	ChemAxon
Polarizability	60.11 Å³	ChemAxon
Number of Rings	7	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

NPAtlas ID

NPA001696

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

32674747

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Harunari E, Imada C, Igarashi Y, Fukuda T, Terahara T, Kobayashi T: Hyaluromycin, a new hyaluronidase inhibitor of polyketide origin from marine Streptomyces sp. Mar Drugs. 2014 Jan 21;12(1):491-507. doi: 10.3390/md12010491. [PubMed:24451191 ]

Showing NP-Card for Hyaluromycin (NP0012439)

MOL for NP0012439 (Hyaluromycin)

3D MOL for NP0012439 (Hyaluromycin)

3D SDF for NP0012439 (Hyaluromycin)

3D-SDF for NP0012439 (Hyaluromycin)

PDB for NP0012439 (Hyaluromycin)

3D PDB for NP0012439 (Hyaluromycin)

SMILES for NP0012439 (Hyaluromycin)

INCHI for NP0012439 (Hyaluromycin)

Structure for NP0012439 (Hyaluromycin)

3D Structure for NP0012439 (Hyaluromycin)