NP-MRD: Showing NP-Card for Tenacibactin B (NP0006931)

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Record Information

Version

2.0

Created at

2020-12-09 03:50:51 UTC

Updated at

2021-07-15 16:56:11 UTC

NP-MRD ID

NP0006931

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Tenacibactin B

Provided By

NPAtlas

Description

Tenacibactin B belongs to the class of organic compounds known as branched fatty acids. These are fatty acids containing a branched chain. Tenacibactin B is found in Tenacibaculum. Based on a literature review very few articles have been published on tenacibactin B.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242118363D          

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M  END

     RDKit          3D

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 18 45  1  0  0  0  0
 18 46  1  0  0  0  0
 21 47  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0006931

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]ON(C(=O)C([H])([H])C([H])(C([H])([H])[H])C([H])([H])[H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])N([H])C(=O)C([H])([H])C([H])([H])C(=O)O[H]

> <INCHI_IDENTIFIER>
InChI=1S/C14H26N2O5/c1-11(2)10-13(18)16(21)9-5-3-4-8-15-12(17)6-7-14(19)20/h11,21H,3-10H2,1-2H3,(H,15,17)(H,19,20)

> <INCHI_KEY>
BMWAAYSPJQJFIA-UHFFFAOYSA-N

> <FORMULA>
C14H26N2O5

> <MOLECULAR_WEIGHT>
302.371

> <EXACT_MASS>
302.184171945

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
32.39535580696381

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-{[5-(N-hydroxy-3-methylbutanamido)pentyl]carbamoyl}propanoic acid

> <ALOGPS_LOGP>
0.68

> <JCHEM_LOGP>
0.49094623500000006

> <ALOGPS_LOGS>
-2.46

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.38784620217602

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.465116586646297

> <JCHEM_PKA_STRONGEST_BASIC>
-1.674585125523294

> <JCHEM_POLAR_SURFACE_AREA>
106.94000000000001

> <JCHEM_REFRACTIVITY>
77.30160000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.05e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-{[5-(N-hydroxy-3-methylbutanamido)pentyl]carbamoyl}propanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 47 46  0  0  0  0  0  0  0  0999 V2000
   -5.4318   -0.9616   -2.0638 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7168   -0.6714   -0.7401 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6105   -1.9620    0.0018 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4033   -0.0464   -1.0939 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6158    0.2805    0.1599 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0092   -0.6734    0.7011 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6062    1.5846    0.6333 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3474    2.5283   -0.0419 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8690    2.0582    1.7533 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5310    2.5787    1.3602 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4053    1.5834    0.7991 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7564    0.5599    1.8419 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6827   -0.5108    1.3320 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9405    0.0488    0.8646 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9589   -0.7870    0.3424 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7607   -2.0200    0.2882 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2351   -0.2280   -0.1328 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1796   -1.2530   -0.7012 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6244   -1.9515   -1.8688 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9539   -2.9944   -1.7852 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8523   -1.4318   -3.1347 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6685   -1.3520   -2.7552 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7596    0.0427   -2.4453 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2888   -1.6416   -1.9083 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2797    0.0493   -0.1226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9637   -1.9363    0.8913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3283   -2.8169   -0.6636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6447   -2.1943    0.3920 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5993    0.8867   -1.6366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7697   -0.7086   -1.6919 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6880    3.2268   -0.2976 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4748    2.8933    2.2275 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7993    1.2918    2.5753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0743    3.1835    2.1896 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7285    3.3398    0.5405 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3310    2.1201    0.4703 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0712    1.0597   -0.0510 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2756    1.1319    2.6887 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1110    0.1176    2.2975 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1988   -1.1675    0.5844 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9295   -1.1635    2.2000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1248    1.0738    0.9012 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0292    0.4956   -0.9753 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7243    0.3299    0.7055 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0794   -0.6588   -1.0460 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5472   -1.9599    0.0826 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8007   -1.3742   -3.4788 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 19 21  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  2 25  1  0
  3 26  1  0
  3 27  1  0
  3 28  1  0
  4 29  1  0
  4 30  1  0
  8 31  1  0
  9 32  1  0
  9 33  1  0
 10 34  1  0
 10 35  1  0
 11 36  1  0
 11 37  1  0
 12 38  1  0
 12 39  1  0
 13 40  1  0
 13 41  1  0
 14 42  1  0
 17 43  1  0
 17 44  1  0
 18 45  1  0
 18 46  1  0
 21 47  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      -5.432  -0.962  -2.064  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.717  -0.671  -0.740  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.611  -1.962   0.002  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.403  -0.046  -1.094  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.616   0.281   0.160  0.00  0.00           C+0
HETATM    6  O   UNK     0      -2.009  -0.673   0.701  0.00  0.00           O+0
HETATM    7  N   UNK     0      -2.606   1.585   0.633  0.00  0.00           N+0
HETATM    8  O   UNK     0      -3.347   2.528  -0.042  0.00  0.00           O+0
HETATM    9  C   UNK     0      -1.869   2.058   1.753  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.531   2.579   1.360  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.405   1.583   0.799  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.756   0.560   1.842  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.683  -0.511   1.332  0.00  0.00           C+0
HETATM   14  N   UNK     0       2.941   0.049   0.865  0.00  0.00           N+0
HETATM   15  C   UNK     0       3.959  -0.787   0.342  0.00  0.00           C+0
HETATM   16  O   UNK     0       3.761  -2.020   0.288  0.00  0.00           O+0
HETATM   17  C   UNK     0       5.235  -0.228  -0.133  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.180  -1.253  -0.701  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.624  -1.952  -1.869  0.00  0.00           C+0
HETATM   20  O   UNK     0       4.954  -2.994  -1.785  0.00  0.00           O+0
HETATM   21  O   UNK     0       5.852  -1.432  -3.135  0.00  0.00           O+0
HETATM   22  H   UNK     0      -4.668  -1.352  -2.755  0.00  0.00           H+0
HETATM   23  H   UNK     0      -5.760   0.043  -2.445  0.00  0.00           H+0
HETATM   24  H   UNK     0      -6.289  -1.642  -1.908  0.00  0.00           H+0
HETATM   25  H   UNK     0      -5.280   0.049  -0.123  0.00  0.00           H+0
HETATM   26  H   UNK     0      -3.964  -1.936   0.891  0.00  0.00           H+0
HETATM   27  H   UNK     0      -4.328  -2.817  -0.664  0.00  0.00           H+0
HETATM   28  H   UNK     0      -5.645  -2.194   0.392  0.00  0.00           H+0
HETATM   29  H   UNK     0      -3.599   0.887  -1.637  0.00  0.00           H+0
HETATM   30  H   UNK     0      -2.770  -0.709  -1.692  0.00  0.00           H+0
HETATM   31  H   UNK     0      -2.688   3.227  -0.298  0.00  0.00           H+0
HETATM   32  H   UNK     0      -2.475   2.893   2.228  0.00  0.00           H+0
HETATM   33  H   UNK     0      -1.799   1.292   2.575  0.00  0.00           H+0
HETATM   34  H   UNK     0      -0.074   3.184   2.190  0.00  0.00           H+0
HETATM   35  H   UNK     0      -0.729   3.340   0.541  0.00  0.00           H+0
HETATM   36  H   UNK     0       1.331   2.120   0.470  0.00  0.00           H+0
HETATM   37  H   UNK     0      -0.071   1.060  -0.051  0.00  0.00           H+0
HETATM   38  H   UNK     0       1.276   1.132   2.689  0.00  0.00           H+0
HETATM   39  H   UNK     0      -0.111   0.118   2.297  0.00  0.00           H+0
HETATM   40  H   UNK     0       1.199  -1.167   0.584  0.00  0.00           H+0
HETATM   41  H   UNK     0       1.930  -1.163   2.200  0.00  0.00           H+0
HETATM   42  H   UNK     0       3.125   1.074   0.901  0.00  0.00           H+0
HETATM   43  H   UNK     0       5.029   0.496  -0.975  0.00  0.00           H+0
HETATM   44  H   UNK     0       5.724   0.330   0.706  0.00  0.00           H+0
HETATM   45  H   UNK     0       7.079  -0.659  -1.046  0.00  0.00           H+0
HETATM   46  H   UNK     0       6.547  -1.960   0.083  0.00  0.00           H+0
HETATM   47  H   UNK     0       6.801  -1.374  -3.479  0.00  0.00           H+0
CONECT    1    2   22   23   24                                             
CONECT    2    1    3    4   25                                             
CONECT    3    2   26   27   28                                             
CONECT    4    2    5   29   30                                             
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8    9                                                  
CONECT    8    7   31                                                       
CONECT    9    7   10   32   33                                             
CONECT   10    9   11   34   35                                             
CONECT   11   10   12   36   37                                             
CONECT   12   11   13   38   39                                             
CONECT   13   12   14   40   41                                             
CONECT   14   13   15   42                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   43   44                                             
CONECT   18   17   19   45   46                                             
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   47                                                       
CONECT   22    1                                                            
CONECT   23    1                                                            
CONECT   24    1                                                            
CONECT   25    2                                                            
CONECT   26    3                                                            
CONECT   27    3                                                            
CONECT   28    3                                                            
CONECT   29    4                                                            
CONECT   30    4                                                            
CONECT   31    8                                                            
CONECT   32    9                                                            
CONECT   33    9                                                            
CONECT   34   10                                                            
CONECT   35   10                                                            
CONECT   36   11                                                            
CONECT   37   11                                                            
CONECT   38   12                                                            
CONECT   39   12                                                            
CONECT   40   13                                                            
CONECT   41   13                                                            
CONECT   42   14                                                            
CONECT   43   17                                                            
CONECT   44   17                                                            
CONECT   45   18                                                            
CONECT   46   18                                                            
CONECT   47   21                                                            
MASTER        0    0    0    0    0    0    0    0   47    0   92    0
END

RDKit          3D

47 46  0  0  0  0  0  0  0  0999 V2000
   -5.4318   -0.9616   -2.0638 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7168   -0.6714   -0.7401 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6105   -1.9620    0.0018 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4033   -0.0464   -1.0939 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6158    0.2805    0.1599 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0092   -0.6734    0.7011 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6062    1.5846    0.6333 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3474    2.5283   -0.0419 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8690    2.0582    1.7533 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5310    2.5787    1.3602 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4053    1.5834    0.7991 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7564    0.5599    1.8419 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6827   -0.5108    1.3320 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9405    0.0488    0.8646 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9589   -0.7870    0.3424 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7607   -2.0200    0.2882 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2351   -0.2280   -0.1328 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1796   -1.2530   -0.7012 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6244   -1.9515   -1.8688 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9539   -2.9944   -1.7852 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8523   -1.4318   -3.1347 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6685   -1.3520   -2.7552 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7596    0.0427   -2.4453 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2888   -1.6416   -1.9083 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2797    0.0493   -0.1226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9637   -1.9363    0.8913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3283   -2.8169   -0.6636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6447   -2.1943    0.3920 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5993    0.8867   -1.6366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7697   -0.7086   -1.6919 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6880    3.2268   -0.2976 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4748    2.8933    2.2275 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7993    1.2918    2.5753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0743    3.1835    2.1896 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7285    3.3398    0.5405 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3310    2.1201    0.4703 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0712    1.0597   -0.0510 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2756    1.1319    2.6887 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1110    0.1176    2.2975 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1988   -1.1675    0.5844 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9295   -1.1635    2.2000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1248    1.0738    0.9012 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0292    0.4956   -0.9753 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7243    0.3299    0.7055 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0794   -0.6588   -1.0460 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5472   -1.9599    0.0826 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8007   -1.3742   -3.4788 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
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 15 16  2  0
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 18 19  1  0
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  1 22  1  0
  1 23  1  0
  1 24  1  0
  2 25  1  0
  3 26  1  0
  3 27  1  0
  3 28  1  0
  4 29  1  0
  4 30  1  0
  8 31  1  0
  9 32  1  0
  9 33  1  0
 10 34  1  0
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 17 44  1  0
 18 45  1  0
 18 46  1  0
 21 47  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
3-{[5-(N-hydroxy-3-methylbutanamido)pentyl]-C-hydroxycarbonimidoyl}propanoate	Generator

Chemical Formula

C₁₄H₂₆N₂O₅

Average Mass

302.3710 Da

Monoisotopic Mass

302.18417 Da

IUPAC Name

3-{[5-(N-hydroxy-3-methylbutanamido)pentyl]carbamoyl}propanoic acid

Traditional Name

3-{[5-(N-hydroxy-3-methylbutanamido)pentyl]carbamoyl}propanoic acid

CAS Registry Number

Not Available

SMILES

CC(C)CC(=O)N(O)CCCCCNC(=O)CCC(O)=O

InChI Identifier

InChI=1S/C14H26N2O5/c1-11(2)10-13(18)16(21)9-5-3-4-8-15-12(17)6-7-14(19)20/h11,21H,3-10H2,1-2H3,(H,15,17)(H,19,20)

InChI Key

BMWAAYSPJQJFIA-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
Tenacibaculum	NPAtlas	17319723

Species Where Detected

Species Name	Source	Reference
Tenacibaculum sp. A4K-17	KNApSAcK Database	22123792

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as branched fatty acids. These are fatty acids containing a branched chain.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acids and conjugates

Direct Parent

Branched fatty acids

Alternative Parents

Substituents

Branched fatty acid
Fatty amide
N-acyl-amine
Carboxamide group
Hydroxamic acid
Secondary carboxylic acid amide
Carboxylic acid derivative
Carboxylic acid
Monocarboxylic acid or derivatives
Hydrocarbon derivative
Organic oxide
Organic nitrogen compound
Organic oxygen compound
Carbonyl group
Organooxygen compound
Organonitrogen compound
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic 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	0.68	ALOGPS
logP	0.49	ChemAxon
logS	-2.5	ALOGPS
pKa (Strongest Acidic)	4.47	ChemAxon
pKa (Strongest Basic)	-1.7	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	106.94 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	77.3 m³·mol⁻¹	ChemAxon
Polarizability	32.4 Å³	ChemAxon
Number of Rings	0	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

NPA008312

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00040459

Chemspider ID

17214510

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

16216155

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Tenacibactin B (NP0006931)

MOL for NP0006931 (Tenacibactin B)

3D MOL for NP0006931 (Tenacibactin B)

3D SDF for NP0006931 (Tenacibactin B)

3D-SDF for NP0006931 (Tenacibactin B)

PDB for NP0006931 (Tenacibactin B)

3D PDB for NP0006931 (Tenacibactin B)

SMILES for NP0006931 (Tenacibactin B)

INCHI for NP0006931 (Tenacibactin B)

Structure for NP0006931 (Tenacibactin B)

3D Structure for NP0006931 (Tenacibactin B)