NP-MRD: Showing NP-Card for N,N’-diacetyl-Z-L-fusarinine A (NP0351085)

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Record Information

Version

2.0

Created at

2025-05-29 23:26:23 UTC

Updated at

2025-05-30 00:00:52 UTC

NP-MRD ID

NP0351085

Natural Product DOI

https://doi.org/10.57994/4074

Secondary Accession Numbers

None

Natural Product Identification

Common Name

N,N’-diacetyl-Z-L-fusarinine A

Description

Not Available

Structure

MOL SDF PDB SMILES InChI


  Mrv2104 03122301502D          

 41 40  0  0  0  0            999 V2000
   -2.9092   -4.0954    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1947   -4.5079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1947   -5.3329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4802   -4.0954    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7658   -4.5079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0513   -4.0954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6632   -4.5079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3776   -4.0954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0921   -4.5079    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.0921   -5.3329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8066   -4.0954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8066   -3.2704    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5211   -4.5079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2355   -4.0954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9500   -4.5079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2355   -3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9500   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6645   -3.2704    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3789   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3789   -2.0329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0934   -3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8079   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5224   -3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2368   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9513   -3.2704    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.9513   -4.0954    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.6658   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6658   -2.0329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.3802   -3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0947   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8092   -3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0947   -2.0329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8092   -1.6204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5237   -2.0329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0934   -4.0954    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.8079   -4.5079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5224   -4.0954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8079   -5.3329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7658   -5.3329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0513   -5.7454    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4802   -5.7454    0.0000 O   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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 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
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 21 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  2  0  0  0  0
  5 39  1  0  0  0  0
 39 40  2  0  0  0  0
 39 41  1  0  0  0  0
M  END


  Mrv2104 03122301502D          

 41 40  0  0  0  0            999 V2000
   -2.9092   -4.0954    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1947   -4.5079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1947   -5.3329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4802   -4.0954    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7658   -4.5079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0513   -4.0954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6632   -4.5079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3776   -4.0954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0921   -4.5079    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.0921   -5.3329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8066   -4.0954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8066   -3.2704    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5211   -4.5079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2355   -4.0954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9500   -4.5079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2355   -3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9500   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6645   -3.2704    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3789   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3789   -2.0329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0934   -3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8079   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5224   -3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2368   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9513   -3.2704    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.9513   -4.0954    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.6658   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6658   -2.0329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.3802   -3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0947   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8092   -3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0947   -2.0329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8092   -1.6204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5237   -2.0329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0934   -4.0954    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.8079   -4.5079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5224   -4.0954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8079   -5.3329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7658   -5.3329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0513   -5.7454    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4802   -5.7454    0.0000 O   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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 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
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 21 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  2  0  0  0  0
  5 39  1  0  0  0  0
 39 40  2  0  0  0  0
 39 41  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0351085

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)NC(CCCN(O)C(=O)\C=C(\C)CCOC(=O)C(CCCN(O)C(=O)\C=C(\C)CCO)NC(C)=O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1/C26H42N4O11/c1-17(9-13-31)15-23(34)30(40)12-6-8-22(28-20(4)33)26(38)41-14-10-18(2)16-24(35)29(39)11-5-7-21(25(36)37)27-19(3)32/h15-16,21-22,31,39-40H,5-14H2,1-4H3,(H,27,32)(H,28,33)(H,36,37)/b17-15-,18-16-

> <INCHI_KEY>
ILNVNOICNGPWQY-IQRFGFHNNA-N

> <FORMULA>
C26H42N4O11

> <MOLECULAR_WEIGHT>
586.639

> <EXACT_MASS>
586.285008188

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
83

> <JCHEM_AVERAGE_POLARIZABILITY>
60.92801385252515

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
5-[(2Z)-5-({5-[(2Z)-N,5-dihydroxy-3-methylpent-2-enamido]-2-acetamidopentanoyl}oxy)-N-hydroxy-3-methylpent-2-enamido]-2-acetamidopentanoic acid

> <JCHEM_LOGP>
-1.5885086106666653

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.502528289977551

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.589249586217568

> <JCHEM_PKA_STRONGEST_BASIC>
-1.4994833286900837

> <JCHEM_POLAR_SURFACE_AREA>
223.10999999999999

> <JCHEM_REFRACTIVITY>
146.495

> <JCHEM_ROTATABLE_BOND_COUNT>
20

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
5-[(2Z)-5-({5-[(2Z)-N,5-dihydroxy-3-methylpent-2-enamido]-2-acetamidopentanoyl}oxy)-N-hydroxy-3-methylpent-2-enamido]-2-acetamidopentanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-MAR-23   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-MAR-23         0                                  
HETATM    1  O   UNK     0      -5.430  -7.645   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      -4.097  -8.415   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.097  -9.955   0.000  0.00  0.00           C+0
HETATM    4  N   UNK     0      -2.763  -7.645   0.000  0.00  0.00           N+0
HETATM    5  C   UNK     0      -1.429  -8.415   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.096  -7.645   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.238  -8.415   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.572  -7.645   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0       3.905  -8.415   0.000  0.00  0.00           N+0
HETATM   10  O   UNK     0       3.905  -9.955   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       5.239  -7.645   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       5.239  -6.105   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       6.573  -8.415   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.906  -7.645   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.240  -8.415   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.906  -6.105   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.240  -5.335   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      10.574  -6.105   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      11.907  -5.335   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      11.907  -3.795   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      13.241  -6.105   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      14.575  -5.335   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      15.908  -6.105   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      17.242  -5.335   0.000  0.00  0.00           C+0
HETATM   25  N   UNK     0      18.576  -6.105   0.000  0.00  0.00           N+0
HETATM   26  O   UNK     0      18.576  -7.645   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      19.909  -5.335   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      19.909  -3.795   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      21.243  -6.105   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      22.577  -5.335   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      23.910  -6.105   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      22.577  -3.795   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      23.910  -3.025   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      25.244  -3.795   0.000  0.00  0.00           O+0
HETATM   35  N   UNK     0      13.241  -7.645   0.000  0.00  0.00           N+0
HETATM   36  C   UNK     0      14.575  -8.415   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      15.908  -7.645   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      14.575  -9.955   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0      -1.429  -9.955   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      -0.096 -10.725   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0      -2.763 -10.725   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   39                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   35                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33                                                            
CONECT   35   21   36                                                       
CONECT   36   35   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36                                                            
CONECT   39    5   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39                                                            
MASTER        0    0    0    0    0    0    0    0   41    0   80    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₆H₄₂N₄O₁₁

Average Mass

586.6390 Da

Monoisotopic Mass

586.28501 Da

IUPAC Name

5-[(2Z)-5-({5-[(2Z)-N,5-dihydroxy-3-methylpent-2-enamido]-2-acetamidopentanoyl}oxy)-N-hydroxy-3-methylpent-2-enamido]-2-acetamidopentanoic acid

Traditional Name

5-[(2Z)-5-({5-[(2Z)-N,5-dihydroxy-3-methylpent-2-enamido]-2-acetamidopentanoyl}oxy)-N-hydroxy-3-methylpent-2-enamido]-2-acetamidopentanoic acid

CAS Registry Number

Not Available

SMILES

CC(=O)NC(CCCN(O)C(=O)\C=C(\C)CCOC(=O)C(CCCN(O)C(=O)\C=C(\C)CCO)NC(C)=O)C(O)=O

InChI Identifier

InChI=1/C26H42N4O11/c1-17(9-13-31)15-23(34)30(40)12-6-8-22(28-20(4)33)26(38)41-14-10-18(2)16-24(35)29(39)11-5-7-21(25(36)37)27-19(3)32/h15-16,21-22,31,39-40H,5-14H2,1-4H3,(H,27,32)(H,28,33)(H,36,37)/b17-15-,18-16-

InChI Key

ILNVNOICNGPWQY-IQRFGFHNNA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
COSY NMR	[¹H, ¹H] NMR Spectrum (2D, 400 MHz, C2D6OS, experimental)	[email protected]	Not Available	Mariana Montanares	2025-05-28	View Spectrum
HSQC NMR	[¹H, ¹³C] NMR Spectrum (2D, 400 MHz, C2D6OS, experimental)	[email protected]	Not Available	Mariana Montanares	2025-05-28	View Spectrum
HMBC NMR	[¹H, ¹³C] NMR Spectrum (2D, 400 MHz, C2D6OS, experimental)	[email protected]	Not Available	Mariana Montanares	2025-05-28	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, C2D6OS, experimental)	[email protected]	Not Available	Mariana Montanares	2025-05-28	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, C2D6OS, experimental)	[email protected]	Not Available	Mariana Montanares	2025-05-28	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, C2D6OS, experimental)	[email protected]	Not Available	Mariana Montanares	2025-05-28	View Spectrum
HSQC NMR	[¹H, ¹³C] NMR Spectrum (2D, 400 MHz, CD3OD, experimental)	[email protected]	Not Available	Mariana Montanares	2025-05-28	View Spectrum
HMBC NMR	[¹H, ¹³C] NMR Spectrum (2D, 400 MHz, CD3OD, experimental)	[email protected]	Not Available	Mariana Montanares	2025-05-28	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, CD3OD, experimental)	[email protected]	Not Available	Mariana Montanares	2025-05-28	View Spectrum
COSY NMR	[¹H, ¹H] NMR Spectrum (2D, 400 MHz, CD3OD, experimental)	[email protected]	Not Available	Mariana Montanares	2025-05-28	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, CD3OD, experimental)	[email protected]	Not Available	Mariana Montanares	2025-05-28	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CD3OD, experimental)	[email protected]	Not Available	Mariana Montanares	2025-05-28	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Pseugogymnoascus verrucosus		Not Available
Pseugogymnoascus verrucosus		Not Available

Chemical Taxonomy

Classification

Not classified

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	-1.6	ChemAxon
pKa (Strongest Acidic)	3.59	ChemAxon
pKa (Strongest Basic)	-1.5	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	223.11 Å²	ChemAxon
Rotatable Bond Count	20	ChemAxon
Refractivity	146.5 m³·mol⁻¹	ChemAxon
Polarizability	60.93 Å³	ChemAxon
Number of Rings	0	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

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for N,N’-diacetyl-Z-L-fusarinine A (NP0351085)

MOL for NP0351085 (N,N’-diacetyl-Z-L-fusarinine A)

3D MOL for NP0351085 (N,N’-diacetyl-Z-L-fusarinine A)

3D SDF for NP0351085 (N,N’-diacetyl-Z-L-fusarinine A)

3D-SDF for NP0351085 (N,N’-diacetyl-Z-L-fusarinine A)

PDB for NP0351085 (N,N’-diacetyl-Z-L-fusarinine A)

3D PDB for NP0351085 (N,N’-diacetyl-Z-L-fusarinine A)

SMILES for NP0351085 (N,N’-diacetyl-Z-L-fusarinine A)

INCHI for NP0351085 (N,N’-diacetyl-Z-L-fusarinine A)

Structure for NP0351085 (N,N’-diacetyl-Z-L-fusarinine A)

3D Structure for NP0351085 (N,N’-diacetyl-Z-L-fusarinine A)