NP-MRD: Showing NP-Card for Benzastatin H (NP0003816)

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Record Information

Version

2.0

Created at

2020-12-09 00:57:37 UTC

Updated at

2021-07-15 16:47:27 UTC

NP-MRD ID

NP0003816

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Benzastatin H

Provided By

NPAtlas

Description

4-Amino-3-[(2E)-7-hydroxy-3-methyl-6-(propan-2-ylidene)hept-2-en-1-yl]benzamide belongs to the class of organic compounds known as aromatic monoterpenoids. These are monoterpenoids containing at least one aromatic ring. Benzastatin H is found in Streptomyces and Streptomyces nitrosporeus. Based on a literature review very few articles have been published on 4-amino-3-[(2E)-7-hydroxy-3-methyl-6-(propan-2-ylidene)hept-2-en-1-yl]benzamide.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242117503D          

 48 48  0  0  0  0            999 V2000
    4.0179   -1.9334    0.7931 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4887   -0.5165    0.7179 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.6404    0.4956    0.6218 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.8124    2.5369   -0.6095 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1877    0.1772    0.5910 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5189    0.6541   -0.6752 C   0  0  1  0  0  0  0  0  0  0  0  0
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 22 48  1  0  0  0  0
M  END

     RDKit          3D

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    4.4887   -0.5165    0.7179 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652306242117503D          

 48 48  0  0  0  0            999 V2000
    4.0179   -1.9334    0.7931 C   0  0  0  0  0  0  0  0  0  0  0  0
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  3 27  1  0  0  0  0
  3 28  1  0  0  0  0
  5 29  1  0  0  0  0
  5 30  1  0  0  0  0
  6 31  1  0  0  0  0
  7 32  1  0  0  0  0
  7 33  1  0  0  0  0
  8 34  1  0  0  0  0
  8 35  1  0  0  0  0
 10 36  1  0  0  0  0
 10 37  1  0  0  0  0
 10 38  1  0  0  0  0
 11 39  1  0  0  0  0
 12 40  1  0  0  0  0
 12 41  1  0  0  0  0
 14 42  1  0  0  0  0
 17 43  1  0  0  0  0
 17 44  1  0  0  0  0
 19 45  1  0  0  0  0
 20 46  1  0  0  0  0
 22 47  1  0  0  0  0
 22 48  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0003816

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC([H])([H])C(=C(C([H])([H])[H])C([H])([H])[H])C([H])([H])C([H])([H])C(=C(/[H])C([H])([H])C1=C([H])C(=C([H])C([H])=C1N([H])[H])C(=O)N([H])[H])\C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C18H26N2O2/c1-12(2)16(11-21)7-5-13(3)4-6-14-10-15(18(20)22)8-9-17(14)19/h4,8-10,21H,5-7,11,19H2,1-3H3,(H2,20,22)/b13-4+

> <INCHI_KEY>
DGLVSNIKVGBYHU-YIXHJXPBSA-N

> <FORMULA>
C18H26N2O2

> <MOLECULAR_WEIGHT>
302.418

> <EXACT_MASS>
302.199428085

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
48

> <JCHEM_AVERAGE_POLARIZABILITY>
35.22756748568139

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-amino-3-[(2E)-7-hydroxy-3-methyl-6-(propan-2-ylidene)hept-2-en-1-yl]benzamide

> <ALOGPS_LOGP>
2.36

> <JCHEM_LOGP>
2.345831545666668

> <ALOGPS_LOGS>
-4.16

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
17.275166754827286

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.24942903687645

> <JCHEM_PKA_STRONGEST_BASIC>
2.708362559465532

> <JCHEM_POLAR_SURFACE_AREA>
89.34

> <JCHEM_REFRACTIVITY>
93.93889999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.08e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-amino-3-[(2E)-7-hydroxy-3-methyl-6-(propan-2-ylidene)hept-2-en-1-yl]benzamide

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 48 48  0  0  0  0  0  0  0  0999 V2000
    4.0179   -1.9334    0.7931 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4887   -0.5165    0.7179 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9503   -0.2642    0.7533 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6404    0.4956    0.6218 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1677    1.8668    0.5516 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8124    2.5369   -0.6095 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1877    0.1772    0.5910 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5189    0.6541   -0.6752 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0580    0.2436   -0.5248 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6579    0.8097    0.6225 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4721   -0.5531   -1.3834 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8009   -1.0777   -1.4581 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8299   -0.7831   -0.4888 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8713    0.0754   -0.7728 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8477    0.2991    0.1634 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9651    1.1933   -0.0840 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0551    1.8567   -1.3248 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8339    1.3768    0.7801 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8115   -0.3266    1.4058 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7670   -1.1774    1.6692 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7792   -1.4164    0.7483 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7220   -2.3099    1.0666 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.3482   -2.0986    1.6787 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8918   -2.6118    0.8207 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4704   -2.1642   -0.1550 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5180   -1.2237    0.7760 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2073    0.3419    1.6463 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2377    0.3163   -0.1471 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7364    2.4177    1.4333 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2495    1.8586    0.7103 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9478    3.5069   -0.4444 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6654    0.5914    1.4912 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0616   -0.9184    0.6281 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5225    1.7607   -0.7536 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9628    0.1407   -1.5233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6271    1.1876    0.3283 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0969    1.7643    0.9422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6184    0.1996    1.5491 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2268   -0.8886   -2.2069 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2662   -0.8083   -2.4841 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7834   -2.2360   -1.5872 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9330    0.5798   -1.7279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9884    2.0129   -1.7839 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1940    2.1986   -1.7982 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5821   -0.1496    2.1442 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7219   -1.6766    2.6372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1880   -2.3093    1.9492 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4750   -3.0184    0.3422 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  4  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  9 11  2  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 16 18  2  0
 15 19  2  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 21 13  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  3 26  1  0
  3 27  1  0
  3 28  1  0
  5 29  1  0
  5 30  1  0
  6 31  1  0
  7 32  1  0
  7 33  1  0
  8 34  1  0
  8 35  1  0
 10 36  1  0
 10 37  1  0
 10 38  1  0
 11 39  1  0
 12 40  1  0
 12 41  1  0
 14 42  1  0
 17 43  1  0
 17 44  1  0
 19 45  1  0
 20 46  1  0
 22 47  1  0
 22 48  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       4.018  -1.933   0.793  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.489  -0.517   0.718  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.950  -0.264   0.753  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.640   0.496   0.622  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.168   1.867   0.552  0.00  0.00           C+0
HETATM    6  O   UNK     0       3.812   2.537  -0.610  0.00  0.00           O+0
HETATM    7  C   UNK     0       2.188   0.177   0.591  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.519   0.654  -0.675  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.058   0.244  -0.525  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.658   0.810   0.623  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.472  -0.553  -1.383  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.801  -1.078  -1.458  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.830  -0.783  -0.489  0.00  0.00           C+0
HETATM   14  C   UNK     0      -3.871   0.075  -0.773  0.00  0.00           C+0
HETATM   15  C   UNK     0      -4.848   0.299   0.163  0.00  0.00           C+0
HETATM   16  C   UNK     0      -5.965   1.193  -0.084  0.00  0.00           C+0
HETATM   17  N   UNK     0      -6.055   1.857  -1.325  0.00  0.00           N+0
HETATM   18  O   UNK     0      -6.834   1.377   0.780  0.00  0.00           O+0
HETATM   19  C   UNK     0      -4.811  -0.327   1.406  0.00  0.00           C+0
HETATM   20  C   UNK     0      -3.767  -1.177   1.669  0.00  0.00           C+0
HETATM   21  C   UNK     0      -2.779  -1.416   0.748  0.00  0.00           C+0
HETATM   22  N   UNK     0      -1.722  -2.310   1.067  0.00  0.00           N+0
HETATM   23  H   UNK     0       3.348  -2.099   1.679  0.00  0.00           H+0
HETATM   24  H   UNK     0       4.892  -2.612   0.821  0.00  0.00           H+0
HETATM   25  H   UNK     0       3.470  -2.164  -0.155  0.00  0.00           H+0
HETATM   26  H   UNK     0       6.518  -1.224   0.776  0.00  0.00           H+0
HETATM   27  H   UNK     0       6.207   0.342   1.646  0.00  0.00           H+0
HETATM   28  H   UNK     0       6.238   0.316  -0.147  0.00  0.00           H+0
HETATM   29  H   UNK     0       3.736   2.418   1.433  0.00  0.00           H+0
HETATM   30  H   UNK     0       5.250   1.859   0.710  0.00  0.00           H+0
HETATM   31  H   UNK     0       3.948   3.507  -0.444  0.00  0.00           H+0
HETATM   32  H   UNK     0       1.665   0.591   1.491  0.00  0.00           H+0
HETATM   33  H   UNK     0       2.062  -0.918   0.628  0.00  0.00           H+0
HETATM   34  H   UNK     0       1.523   1.761  -0.754  0.00  0.00           H+0
HETATM   35  H   UNK     0       1.963   0.141  -1.523  0.00  0.00           H+0
HETATM   36  H   UNK     0      -1.627   1.188   0.328  0.00  0.00           H+0
HETATM   37  H   UNK     0      -0.097   1.764   0.942  0.00  0.00           H+0
HETATM   38  H   UNK     0      -0.618   0.200   1.549  0.00  0.00           H+0
HETATM   39  H   UNK     0       0.227  -0.889  -2.207  0.00  0.00           H+0
HETATM   40  H   UNK     0      -2.266  -0.808  -2.484  0.00  0.00           H+0
HETATM   41  H   UNK     0      -1.783  -2.236  -1.587  0.00  0.00           H+0
HETATM   42  H   UNK     0      -3.933   0.580  -1.728  0.00  0.00           H+0
HETATM   43  H   UNK     0      -6.988   2.013  -1.784  0.00  0.00           H+0
HETATM   44  H   UNK     0      -5.194   2.199  -1.798  0.00  0.00           H+0
HETATM   45  H   UNK     0      -5.582  -0.150   2.144  0.00  0.00           H+0
HETATM   46  H   UNK     0      -3.722  -1.677   2.637  0.00  0.00           H+0
HETATM   47  H   UNK     0      -1.188  -2.309   1.949  0.00  0.00           H+0
HETATM   48  H   UNK     0      -1.475  -3.018   0.342  0.00  0.00           H+0
CONECT    1    2   23   24   25                                             
CONECT    2    1    3    4                                                  
CONECT    3    2   26   27   28                                             
CONECT    4    2    5    7                                                  
CONECT    5    4    6   29   30                                             
CONECT    6    5   31                                                       
CONECT    7    4    8   32   33                                             
CONECT    8    7    9   34   35                                             
CONECT    9    8   10   11                                                  
CONECT   10    9   36   37   38                                             
CONECT   11    9   12   39                                                  
CONECT   12   11   13   40   41                                             
CONECT   13   12   14   21                                                  
CONECT   14   13   15   42                                                  
CONECT   15   14   16   19                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16   43   44                                                  
CONECT   18   16                                                            
CONECT   19   15   20   45                                                  
CONECT   20   19   21   46                                                  
CONECT   21   20   22   13                                                  
CONECT   22   21   47   48                                                  
CONECT   23    1                                                            
CONECT   24    1                                                            
CONECT   25    1                                                            
CONECT   26    3                                                            
CONECT   27    3                                                            
CONECT   28    3                                                            
CONECT   29    5                                                            
CONECT   30    5                                                            
CONECT   31    6                                                            
CONECT   32    7                                                            
CONECT   33    7                                                            
CONECT   34    8                                                            
CONECT   35    8                                                            
CONECT   36   10                                                            
CONECT   37   10                                                            
CONECT   38   10                                                            
CONECT   39   11                                                            
CONECT   40   12                                                            
CONECT   41   12                                                            
CONECT   42   14                                                            
CONECT   43   17                                                            
CONECT   44   17                                                            
CONECT   45   19                                                            
CONECT   46   20                                                            
CONECT   47   22                                                            
CONECT   48   22                                                            
MASTER        0    0    0    0    0    0    0    0   48    0   96    0
END

RDKit          3D

48 48  0  0  0  0  0  0  0  0999 V2000
    4.0179   -1.9334    0.7931 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4887   -0.5165    0.7179 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9503   -0.2642    0.7533 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6404    0.4956    0.6218 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1677    1.8668    0.5516 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8124    2.5369   -0.6095 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1877    0.1772    0.5910 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5189    0.6541   -0.6752 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0580    0.2436   -0.5248 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6579    0.8097    0.6225 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4721   -0.5531   -1.3834 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8009   -1.0777   -1.4581 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8299   -0.7831   -0.4888 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8713    0.0754   -0.7728 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8477    0.2991    0.1634 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9651    1.1933   -0.0840 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0551    1.8567   -1.3248 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8339    1.3768    0.7801 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8115   -0.3266    1.4058 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7670   -1.1774    1.6692 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7792   -1.4164    0.7483 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7220   -2.3099    1.0666 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.3482   -2.0986    1.6787 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8918   -2.6118    0.8207 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4704   -2.1642   -0.1550 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5180   -1.2237    0.7760 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2073    0.3419    1.6463 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2377    0.3163   -0.1471 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7364    2.4177    1.4333 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2495    1.8586    0.7103 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9478    3.5069   -0.4444 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6654    0.5914    1.4912 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0616   -0.9184    0.6281 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5225    1.7607   -0.7536 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9628    0.1407   -1.5233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6271    1.1876    0.3283 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0969    1.7643    0.9422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6184    0.1996    1.5491 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2268   -0.8886   -2.2069 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2662   -0.8083   -2.4841 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7834   -2.2360   -1.5872 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9330    0.5798   -1.7279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9884    2.0129   -1.7839 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1940    2.1986   -1.7982 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5821   -0.1496    2.1442 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7219   -1.6766    2.6372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1880   -2.3093    1.9492 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4750   -3.0184    0.3422 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  4  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  9 11  2  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 16 18  2  0
 15 19  2  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 21 13  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  3 26  1  0
  3 27  1  0
  3 28  1  0
  5 29  1  0
  5 30  1  0
  6 31  1  0
  7 32  1  0
  7 33  1  0
  8 34  1  0
  8 35  1  0
 10 36  1  0
 10 37  1  0
 10 38  1  0
 11 39  1  0
 12 40  1  0
 12 41  1  0
 14 42  1  0
 17 43  1  0
 17 44  1  0
 19 45  1  0
 20 46  1  0
 22 47  1  0
 22 48  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
Benzastatin I	MeSH

Chemical Formula

C₁₈H₂₆N₂O₂

Average Mass

302.4180 Da

Monoisotopic Mass

302.19943 Da

IUPAC Name

4-amino-3-[(2E)-7-hydroxy-3-methyl-6-(propan-2-ylidene)hept-2-en-1-yl]benzamide

Traditional Name

4-amino-3-[(2E)-7-hydroxy-3-methyl-6-(propan-2-ylidene)hept-2-en-1-yl]benzamide

CAS Registry Number

Not Available

SMILES

CC(C)=C(CO)CC\C(C)=C\CC1=C(N)C=CC(=C1)C(N)=O

InChI Identifier

InChI=1S/C18H26N2O2/c1-12(2)16(11-21)7-5-13(3)4-6-14-10-15(18(20)22)8-9-17(14)19/h4,8-10,21H,5-7,11,19H2,1-3H3,(H2,20,22)/b13-4+

InChI Key

DGLVSNIKVGBYHU-YIXHJXPBSA-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	NPAtlas	11513042
Streptomyces nitrosporeus	LOTUS Database	35616633

Species Where Detected

Species Name	Source	Reference
Streptomyces nitrosporeus 30643	KNApSAcK Database	22123792

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as aromatic monoterpenoids. These are monoterpenoids containing at least one aromatic ring.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Monoterpenoids

Direct Parent

Aromatic monoterpenoids

Alternative Parents

Substituents

Aminobenzamide
Aminobenzoic acid or derivatives
Aromatic monoterpenoid
Monocyclic monoterpenoid
Benzamide
Benzoic acid or derivatives
Aniline or substituted anilines
Benzoyl
Benzenoid
Monocyclic benzene moiety
Amino acid or derivatives
Primary carboxylic acid amide
Carboxamide group
Carboxylic acid derivative
Alcohol
Primary alcohol
Primary amine
Amine
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Organic nitrogen compound
Organooxygen compound
Organonitrogen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic 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	2.36	ALOGPS
logP	2.35	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	15.25	ChemAxon
pKa (Strongest Basic)	2.71	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	89.34 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	93.94 m³·mol⁻¹	ChemAxon
Polarizability	35.23 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

NPAtlas ID

NPA020554

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00015957

Chemspider ID

8623082

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10447663

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Benzastatin H (NP0003816)

MOL for NP0003816 (Benzastatin H)

3D MOL for NP0003816 (Benzastatin H)

3D SDF for NP0003816 (Benzastatin H)

3D-SDF for NP0003816 (Benzastatin H)

PDB for NP0003816 (Benzastatin H)

3D PDB for NP0003816 (Benzastatin H)

SMILES for NP0003816 (Benzastatin H)

INCHI for NP0003816 (Benzastatin H)

Structure for NP0003816 (Benzastatin H)

3D Structure for NP0003816 (Benzastatin H)