NP-MRD: Showing NP-Card for Cladoniamide F (NP0007872)

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Record Information

Version

2.0

Created at

2020-12-09 05:26:40 UTC

Updated at

2021-07-15 16:58:47 UTC

NP-MRD ID

NP0007872

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Cladoniamide F

Provided By

NPAtlas

Description

Cladoniamide F belongs to the class of organic compounds known as beta carbolines. Beta carbolines are compounds containing a 9H-pyrido[3,4-b]indole moiety. Cladoniamide F is found in Streptomyces uncialis. Based on a literature review very few articles have been published on cladoniamide F.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242106043D          

 45 49  0  0  0  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1652306242106043D          

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M  END
> <DATABASE_ID>
NP0007872

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]O[C@@]1(C(=O)N([H])C([H])([H])[H])C2=C(N([H])C3=C([H])C([H])=C(Cl)C([H])=C23)C2=C(OC([H])([H])[H])C3=C([H])C([H])=C([H])C([H])=C3N2C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C21H16ClN3O4/c1-23-19(26)21(28)15-12-9-10(22)7-8-13(12)24-16(15)17-18(29-2)11-5-3-4-6-14(11)25(17)20(21)27/h3-9,24,28H,1-2H3,(H,23,26)/t21-/m1/s1

> <INCHI_KEY>
KKUHRVKGTKCZEO-OAQYLSRUSA-N

> <FORMULA>
C21H16ClN3O4

> <MOLECULAR_WEIGHT>
409.83

> <EXACT_MASS>
409.0829337

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
42.07916213680723

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(11R)-7-chloro-11-hydroxy-20-methoxy-N-methyl-12-oxo-3,13-diazapentacyclo[11.7.0.0^{2,10}.0^{4,9}.0^{14,19}]icosa-1(20),2(10),4,6,8,14,16,18-octaene-11-carboxamide

> <ALOGPS_LOGP>
2.99

> <JCHEM_LOGP>
1.8451686013333335

> <ALOGPS_LOGS>
-4.64

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.429886573825694

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.089467690583001

> <JCHEM_PKA_STRONGEST_BASIC>
-4.92344701069479

> <JCHEM_POLAR_SURFACE_AREA>
96.35000000000002

> <JCHEM_REFRACTIVITY>
106.58100000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.43e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(11R)-7-chloro-11-hydroxy-20-methoxy-N-methyl-12-oxo-3,13-diazapentacyclo[11.7.0.0^{2,10}.0^{4,9}.0^{14,19}]icosa-1(20),2(10),4,6,8,14,16,18-octaene-11-carboxamide

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 45 49  0  0  0  0  0  0  0  0999 V2000
   -4.0191    2.2404    0.6792 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7729    1.5974    0.3212 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5525    1.0147   -0.9571 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4768    1.0628   -1.8021 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2737    0.3669   -1.2935 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3596   -0.1066   -2.6100 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1723    1.3414   -1.2732 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3361    2.3863   -1.9732 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0232    1.2078   -0.5534 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2153    0.1002    0.1985 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4471    0.1741    0.8163 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0242   -0.7564    1.6710 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8354   -1.7931    1.1312 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9935    1.3729    0.4074 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2029    1.9715    0.7059 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5564    3.1961    0.1784 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6520    3.8111   -0.6672 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4422    3.2367   -0.9801 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0942    2.0152   -0.4515 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1685   -0.9419    0.2470 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0912   -2.1208    0.8960 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0679   -2.7555    0.6457 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6113   -3.9618    1.0606 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8508   -4.3863    0.6440 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5765   -3.5868   -0.2137 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1521   -4.1256   -0.7436 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -3.0315   -2.3865   -0.6242 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7910   -1.9424   -0.2186 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0116   -0.8288   -0.4525 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4381    2.8036   -0.1814 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7629    1.5029    1.0041 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8336    2.9413    1.5219 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9952    1.5612    1.0433 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9766    0.4453   -3.1521 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3058   -2.4318    0.4205 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3182   -2.3559    1.9567 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6584   -1.2977    0.5758 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8860    1.4425    1.3823 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5122    3.6394    0.4318 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9520    4.7732   -1.0697 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7837    3.7695   -1.6456 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8586   -2.4834    1.5202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0575   -4.5978    1.7303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2910   -5.3291    0.9600 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6105   -1.7862   -1.2866 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
  3  5  1  0
  5  6  1  6
  5  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 11 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 10 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 25 27  1  0
 27 28  2  0
 28 29  1  0
 29  5  1  0
 19  9  1  0
 29 20  2  0
 19 14  1  0
 28 22  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  2 33  1  0
  6 34  1  0
 13 35  1  0
 13 36  1  0
 13 37  1  0
 15 38  1  0
 16 39  1  0
 17 40  1  0
 18 41  1  0
 21 42  1  0
 23 43  1  0
 24 44  1  0
 27 45  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      -4.019   2.240   0.679  0.00  0.00           C+0
HETATM    2  N   UNK     0      -2.773   1.597   0.321  0.00  0.00           N+0
HETATM    3  C   UNK     0      -2.553   1.015  -0.957  0.00  0.00           C+0
HETATM    4  O   UNK     0      -3.477   1.063  -1.802  0.00  0.00           O+0
HETATM    5  C   UNK     0      -1.274   0.367  -1.294  0.00  0.00           C+0
HETATM    6  O   UNK     0      -1.360  -0.107  -2.610  0.00  0.00           O+0
HETATM    7  C   UNK     0      -0.172   1.341  -1.273  0.00  0.00           C+0
HETATM    8  O   UNK     0      -0.336   2.386  -1.973  0.00  0.00           O+0
HETATM    9  N   UNK     0       1.023   1.208  -0.553  0.00  0.00           N+0
HETATM   10  C   UNK     0       1.215   0.100   0.199  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.447   0.174   0.816  0.00  0.00           C+0
HETATM   12  O   UNK     0       3.024  -0.756   1.671  0.00  0.00           O+0
HETATM   13  C   UNK     0       3.835  -1.793   1.131  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.994   1.373   0.407  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.203   1.972   0.706  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.556   3.196   0.178  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.652   3.811  -0.667  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.442   3.237  -0.980  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.094   2.015  -0.452  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.169  -0.942   0.247  0.00  0.00           C+0
HETATM   21  N   UNK     0       0.091  -2.121   0.896  0.00  0.00           N+0
HETATM   22  C   UNK     0      -1.068  -2.756   0.646  0.00  0.00           C+0
HETATM   23  C   UNK     0      -1.611  -3.962   1.061  0.00  0.00           C+0
HETATM   24  C   UNK     0      -2.851  -4.386   0.644  0.00  0.00           C+0
HETATM   25  C   UNK     0      -3.576  -3.587  -0.214  0.00  0.00           C+0
HETATM   26 Cl   UNK     0      -5.152  -4.126  -0.744  0.00  0.00          Cl+0
HETATM   27  C   UNK     0      -3.031  -2.386  -0.624  0.00  0.00           C+0
HETATM   28  C   UNK     0      -1.791  -1.942  -0.219  0.00  0.00           C+0
HETATM   29  C   UNK     0      -1.012  -0.829  -0.453  0.00  0.00           C+0
HETATM   30  H   UNK     0      -4.438   2.804  -0.181  0.00  0.00           H+0
HETATM   31  H   UNK     0      -4.763   1.503   1.004  0.00  0.00           H+0
HETATM   32  H   UNK     0      -3.834   2.941   1.522  0.00  0.00           H+0
HETATM   33  H   UNK     0      -1.995   1.561   1.043  0.00  0.00           H+0
HETATM   34  H   UNK     0      -1.977   0.445  -3.152  0.00  0.00           H+0
HETATM   35  H   UNK     0       3.306  -2.432   0.421  0.00  0.00           H+0
HETATM   36  H   UNK     0       4.318  -2.356   1.957  0.00  0.00           H+0
HETATM   37  H   UNK     0       4.658  -1.298   0.576  0.00  0.00           H+0
HETATM   38  H   UNK     0       4.886   1.442   1.382  0.00  0.00           H+0
HETATM   39  H   UNK     0       5.512   3.639   0.432  0.00  0.00           H+0
HETATM   40  H   UNK     0       3.952   4.773  -1.070  0.00  0.00           H+0
HETATM   41  H   UNK     0       1.784   3.769  -1.646  0.00  0.00           H+0
HETATM   42  H   UNK     0       0.859  -2.483   1.520  0.00  0.00           H+0
HETATM   43  H   UNK     0      -1.058  -4.598   1.730  0.00  0.00           H+0
HETATM   44  H   UNK     0      -3.291  -5.329   0.960  0.00  0.00           H+0
HETATM   45  H   UNK     0      -3.611  -1.786  -1.287  0.00  0.00           H+0
CONECT    1    2   30   31   32                                             
CONECT    2    1    3   33                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7   29                                             
CONECT    6    5   34                                                       
CONECT    7    5    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   19                                                  
CONECT   10    9   11   20                                                  
CONECT   11   10   12   14                                                  
CONECT   12   11   13                                                       
CONECT   13   12   35   36   37                                             
CONECT   14   11   15   19                                                  
CONECT   15   14   16   38                                                  
CONECT   16   15   17   39                                                  
CONECT   17   16   18   40                                                  
CONECT   18   17   19   41                                                  
CONECT   19   18    9   14                                                  
CONECT   20   10   21   29                                                  
CONECT   21   20   22   42                                                  
CONECT   22   21   23   28                                                  
CONECT   23   22   24   43                                                  
CONECT   24   23   25   44                                                  
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   45                                                  
CONECT   28   27   29   22                                                  
CONECT   29   28    5   20                                                  
CONECT   30    1                                                            
CONECT   31    1                                                            
CONECT   32    1                                                            
CONECT   33    2                                                            
CONECT   34    6                                                            
CONECT   35   13                                                            
CONECT   36   13                                                            
CONECT   37   13                                                            
CONECT   38   15                                                            
CONECT   39   16                                                            
CONECT   40   17                                                            
CONECT   41   18                                                            
CONECT   42   21                                                            
CONECT   43   23                                                            
CONECT   44   24                                                            
CONECT   45   27                                                            
MASTER        0    0    0    0    0    0    0    0   45    0   98    0
END

RDKit          3D

45 49  0  0  0  0  0  0  0  0999 V2000
   -4.0191    2.2404    0.6792 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7729    1.5974    0.3212 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5525    1.0147   -0.9571 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4768    1.0628   -1.8021 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2737    0.3669   -1.2935 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3596   -0.1066   -2.6100 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1723    1.3414   -1.2732 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3361    2.3863   -1.9732 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0232    1.2078   -0.5534 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2153    0.1002    0.1985 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4471    0.1741    0.8163 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0242   -0.7564    1.6710 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8354   -1.7931    1.1312 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9935    1.3729    0.4074 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2029    1.9715    0.7059 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5564    3.1961    0.1784 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6520    3.8111   -0.6672 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4422    3.2367   -0.9801 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0942    2.0152   -0.4515 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1685   -0.9419    0.2470 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0912   -2.1208    0.8960 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0679   -2.7555    0.6457 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6113   -3.9618    1.0606 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8508   -4.3863    0.6440 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5765   -3.5868   -0.2137 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1521   -4.1256   -0.7436 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -3.0315   -2.3865   -0.6242 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7910   -1.9424   -0.2186 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0116   -0.8288   -0.4525 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4381    2.8036   -0.1814 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7629    1.5029    1.0041 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8336    2.9413    1.5219 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9952    1.5612    1.0433 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9766    0.4453   -3.1521 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3058   -2.4318    0.4205 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3182   -2.3559    1.9567 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6584   -1.2977    0.5758 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8860    1.4425    1.3823 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5122    3.6394    0.4318 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9520    4.7732   -1.0697 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7837    3.7695   -1.6456 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8586   -2.4834    1.5202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0575   -4.5978    1.7303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2910   -5.3291    0.9600 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6105   -1.7862   -1.2866 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
  3  5  1  0
  5  6  1  6
  5  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 11 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 10 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 25 27  1  0
 27 28  2  0
 28 29  1  0
 29  5  1  0
 19  9  1  0
 29 20  2  0
 19 14  1  0
 28 22  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  2 33  1  0
  6 34  1  0
 13 35  1  0
 13 36  1  0
 13 37  1  0
 15 38  1  0
 16 39  1  0
 17 40  1  0
 18 41  1  0
 21 42  1  0
 23 43  1  0
 24 44  1  0
 27 45  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₂₁H₁₆ClN₃O₄

Average Mass

409.8300 Da

Monoisotopic Mass

409.08293 Da

IUPAC Name

(11R)-7-chloro-11-hydroxy-20-methoxy-N-methyl-12-oxo-3,13-diazapentacyclo[11.7.0.0^{2,10}.0^{4,9}.0^{14,19}]icosa-1(20),2(10),4,6,8,14,16,18-octaene-11-carboxamide

Traditional Name

(11R)-7-chloro-11-hydroxy-20-methoxy-N-methyl-12-oxo-3,13-diazapentacyclo[11.7.0.0^{2,10}.0^{4,9}.0^{14,19}]icosa-1(20),2(10),4,6,8,14,16,18-octaene-11-carboxamide

CAS Registry Number

Not Available

SMILES

CNC(=O)[C@]1(O)C2=C(NC3=C2C=C(Cl)C=C3)C2=C(OC)C3=CC=CC=C3N2C1=O

InChI Identifier

InChI=1S/C21H16ClN3O4/c1-23-19(26)21(28)15-12-9-10(22)7-8-13(12)24-16(15)17-18(29-2)11-5-3-4-6-14(11)25(17)20(21)27/h3-9,24,28H,1-2H3,(H,23,26)/t21-/m1/s1

InChI Key

KKUHRVKGTKCZEO-OAQYLSRUSA-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 uncialis	NPAtlas	18646774

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as beta carbolines. Beta carbolines are compounds containing a 9H-pyrido[3,4-b]indole moiety.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Pyridoindoles

Direct Parent

Beta carbolines

Alternative Parents

Substituents

Beta-carboline
3-alkylindole
Indole
Alkyl aryl ether
Aryl chloride
Aryl halide
Benzenoid
Substituted pyrrole
Heteroaromatic compound
Pyrrole
Tertiary alcohol
Carboxamide group
Lactam
Secondary carboxylic acid amide
Ether
Carboxylic acid derivative
Azacycle
Organonitrogen compound
Organochloride
Organohalogen compound
Organic nitrogen compound
Hydrocarbon derivative
Alcohol
Carbonyl group
Organic oxide
Organopnictogen compound
Organic oxygen compound
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

tertiary alcohol (CHEBI:84371 )
organochlorine compound (CHEBI:84371 )
organic heteropentacyclic compound (CHEBI:84371 )
lactam (CHEBI:84371 )
carboxamide (CHEBI:84371 )
cladoniamide (CHEBI:84371 )

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	2.99	ALOGPS
logP	1.85	ChemAxon
logS	-4.6	ALOGPS
pKa (Strongest Acidic)	10.09	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	96.35 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	106.58 m³·mol⁻¹	ChemAxon
Polarizability	42.08 Å³	ChemAxon
Number of Rings	5	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

NPA012664

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

34448993

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

25053218

PDB ID

Not Available

ChEBI ID

84371

Good Scents ID

Not Available

References

General References

Showing NP-Card for Cladoniamide F (NP0007872)

MOL for NP0007872 (Cladoniamide F)

3D MOL for NP0007872 (Cladoniamide F)

3D SDF for NP0007872 (Cladoniamide F)

3D-SDF for NP0007872 (Cladoniamide F)

PDB for NP0007872 (Cladoniamide F)

3D PDB for NP0007872 (Cladoniamide F)

SMILES for NP0007872 (Cladoniamide F)

INCHI for NP0007872 (Cladoniamide F)

Structure for NP0007872 (Cladoniamide F)

3D Structure for NP0007872 (Cladoniamide F)