NP-MRD: Showing NP-Card for (-)-Manadomanzamine A (NP0068733)

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Record Information

Version

2.0

Created at

2022-04-28 13:59:46 UTC

Updated at

2022-04-28 13:59:47 UTC

NP-MRD ID

NP0068733

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(-)-Manadomanzamine A

Description

1-[(1R,2S,4R,17R,18R,19S,20S,21R,37Z)-19-hydroxy-5,15,22,32-tetraazaoctacyclo[18.10.10.0¹,²¹.0²,¹⁸.0⁵,¹⁷.0⁸,¹⁶.0⁹,¹⁴.0²⁰,³²]Tetraconta-8(16),9,11,13,27,37-hexaen-4-yl]propan-2-one belongs to the class of organic compounds known as beta carbolines. Beta carbolines are compounds containing a 9H-pyrido[3,4-b]indole moiety. (-)-Manadomanzamine A is found in Acanthostrongylophora sp. Based on a literature review very few articles have been published on 1-[(1R,2S,4R,17R,18R,19S,20S,21R,37Z)-19-hydroxy-5,15,22,32-tetraazaoctacyclo[18.10.10.0¹,²¹.0²,¹⁸.0⁵,¹⁷.0⁸,¹⁶.0⁹,¹⁴.0²⁰,³²]Tetraconta-8(16),9,11,13,27,37-hexaen-4-yl]propan-2-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282215592D          

 45 52  0  0  1  0            999 V2000
    1.4490    1.6768    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8226    1.0936    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1362    0.3305    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0745   -0.2769    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9263    0.1766    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0978    1.1672    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8635    1.4741    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9806    2.2908    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3318    2.8005    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5661    2.4935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4488    3.6171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
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  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  6  0  0  0
  1  6  1  0  0  0  0
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  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  1 10  1  1  0  0  0
  9 11  1  6  0  0  0
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  8 15  1  0  0  0  0
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  7 18  1  1  0  0  0
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M  END

     RDKit          3D

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 21 73  1  0
 23 74  1  0
 23 75  1  0
 24 76  1  0
 24 77  1  0
 25 78  1  0
 26 79  1  0
 27 80  1  0
 27 81  1  0
 28 82  1  0
 28 83  1  0
 29 84  1  0
 29 85  1  0
 30 86  1  0
 30 87  1  0
 31 88  1  0
 32 89  1  6
 33 90  1  1
 44 98  1  0
 44 99  1  0
 43 96  1  0
 43 97  1  0
 35 91  1  0
 37 92  1  0
 38 93  1  0
 39 94  1  0
 40 95  1  0
M  END


  Mrv1652304282215592D          

 45 52  0  0  1  0            999 V2000
    1.4490    1.6768    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8226    1.0936    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1362    0.3305    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0745   -0.2769    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9263    0.1766    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0978    1.1672    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8635    1.4741    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9806    2.2908    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3318    2.8005    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5661    2.4935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4488    3.6171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8001    4.1268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0344    3.8198    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9171    4.9435    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7463    2.5978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3950    2.0881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2780    1.2714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5123    0.9645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5676    0.1413    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.3675   -0.0604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8066    0.6380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6310    0.6070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0164   -0.1225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5773   -0.8209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7529   -0.7899    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5946   -0.3071    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1409   -0.0214    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.1812    0.7609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3503    0.8101    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3801    1.4207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4001    1.0704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3086    0.7020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1433    0.6852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1315   -0.1548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5775   -0.7998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7272   -0.8554    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6161   -0.4075    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6785   -1.2301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0845   -1.5437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6186   -0.9148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5072   -0.7557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8208    0.0074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3167    0.6605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4991    0.5505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0050    1.2036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  6  0  0  0
  1  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
  1 10  1  1  0  0  0
  9 11  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
  8 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
  7 18  1  1  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 17 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 20 25  2  0  0  0  0
  5 26  1  6  0  0  0
  4 27  1  1  0  0  0
 27 28  1  0  0  0  0
  2 28  1  1  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
  4 36  1  0  0  0  0
  3 37  1  1  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  2  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
  2 45  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0068733

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)C[C@H]1C[C@H]2[C@@H]([C@H](O)[C@@]34CC\C=C/CCCCN3C[C@@]22CC\C=C/CCCCN[C@@H]42)[C@H]2N1CCC1=C2NC2=CC=CC=C12

> <INCHI_IDENTIFIER>
InChI=1S/C39H54N4O2/c1-27(44)24-28-25-31-33(35-34-30(18-23-43(28)35)29-16-10-11-17-32(29)41-34)36(45)39-20-13-7-3-5-9-15-22-42(39)26-38(31)19-12-6-2-4-8-14-21-40-37(38)39/h2-3,6-7,10-11,16-17,28,31,33,35-37,40-41,45H,4-5,8-9,12-15,18-26H2,1H3/b6-2-,7-3-/t28-,31-,33+,35+,36-,37+,38-,39+/m0/s1

> <INCHI_KEY>
MFDADOYAAWFHON-IHRPDMNKSA-N

> <FORMULA>
C39H54N4O2

> <MOLECULAR_WEIGHT>
610.887

> <EXACT_MASS>
610.424676995

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
99

> <JCHEM_AVERAGE_POLARIZABILITY>
71.33282451477068

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
1-[(1R,2S,4R,17R,18R,19S,20S,21R,27Z,37Z)-19-hydroxy-5,15,22,32-tetraazaoctacyclo[18.10.10.0^{1,21}.0^{2,18}.0^{5,17}.0^{8,16}.0^{9,14}.0^{20,32}]tetraconta-8(16),9,11,13,27,37-hexaen-4-yl]propan-2-one

> <ALOGPS_LOGP>
5.09

> <JCHEM_LOGP>
5.607920399666666

> <ALOGPS_LOGS>
-5.42

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
8

> <JCHEM_PHYSIOLOGICAL_CHARGE>
2

> <JCHEM_PKA>
16.365515538330914

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.029151037520084

> <JCHEM_PKA_STRONGEST_BASIC>
10.680545218318727

> <JCHEM_POLAR_SURFACE_AREA>
71.6

> <JCHEM_REFRACTIVITY>
184.4907

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.30e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-[(1R,2S,4R,17R,18R,19S,20S,21R,27Z,37Z)-19-hydroxy-5,15,22,32-tetraazaoctacyclo[18.10.10.0^{1,21}.0^{2,18}.0^{5,17}.0^{8,16}.0^{9,14}.0^{20,32}]tetraconta-8(16),9,11,13,27,37-hexaen-4-yl]propan-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       2.705   3.130   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.536   2.041   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.121   0.617   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.006  -0.517   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.596   0.330   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.916   2.179   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.345   2.752   0.000  0.00  0.00           C+0
HETATM    8  N   UNK     0       5.564   4.276   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0       4.353   5.228   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.923   4.655   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.571   6.752   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.360   7.703   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       1.931   7.130   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       3.579   9.228   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.993   4.849   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.204   3.898   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.986   2.373   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.556   1.800   0.000  0.00  0.00           C+0
HETATM   19  N   UNK     0       6.659   0.264   0.000  0.00  0.00           N+0
HETATM   20  C   UNK     0       8.153  -0.113   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.972   1.191   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      10.511   1.133   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      11.231  -0.229   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      10.411  -1.532   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       8.872  -1.475   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       4.843  -0.573   0.000  0.00  0.00           O+0
HETATM   27  N   UNK     0       0.263  -0.040   0.000  0.00  0.00           N+0
HETATM   28  C   UNK     0       0.338   1.420   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -0.654   1.512   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       0.709   2.652   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       2.614   1.998   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       4.309   1.310   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       5.867   1.279   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       5.845  -0.289   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       4.811  -1.493   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       3.224  -1.597   0.000  0.00  0.00           C+0
HETATM   37  N   UNK     0       1.150  -0.761   0.000  0.00  0.00           N+0
HETATM   38  C   UNK     0       1.267  -2.296   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      -0.158  -2.882   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      -1.155  -1.708   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -2.813  -1.411   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -3.399   0.014   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      -2.458   1.233   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      -0.932   1.028   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       0.009   2.247   0.000  0.00  0.00           C+0
CONECT    1    2    6   10                                                  
CONECT    2    1    3   28   45                                             
CONECT    3    2    4   37                                                  
CONECT    4    3    5   27   36                                             
CONECT    5    4    6   26                                                  
CONECT    6    5    1    7                                                  
CONECT    7    6    8   18                                                  
CONECT    8    7    9   15                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9    1                                                       
CONECT   11    9   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15    8   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   21                                                  
CONECT   18   17    7   19                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   25                                                  
CONECT   21   20   17   22                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   20                                                       
CONECT   26    5                                                            
CONECT   27    4   28   29                                                  
CONECT   28   27    2                                                       
CONECT   29   27   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35    4                                                       
CONECT   37    3   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43   45                                                       
CONECT   45   44    2                                                       
MASTER        0    0    0    0    0    0    0    0   45    0  104    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₉H₅₄N₄O₂

Average Mass

610.8870 Da

Monoisotopic Mass

610.42468 Da

IUPAC Name

1-[(1R,2S,4R,17R,18R,19S,20S,21R,27Z,37Z)-19-hydroxy-5,15,22,32-tetraazaoctacyclo[18.10.10.0^{1,21}.0^{2,18}.0^{5,17}.0^{8,16}.0^{9,14}.0^{20,32}]tetraconta-8(16),9,11,13,27,37-hexaen-4-yl]propan-2-one

Traditional Name

CAS Registry Number

Not Available

SMILES

CC(=O)C[C@H]1C[C@H]2[C@@H]([C@H](O)[C@@]34CC\C=C/CCCCN3C[C@@]22CC\C=C/CCCCN[C@@H]42)[C@H]2N1CCC1=C2NC2=CC=CC=C12

InChI Identifier

InChI=1S/C39H54N4O2/c1-27(44)24-28-25-31-33(35-34-30(18-23-43(28)35)29-16-10-11-17-32(29)41-34)36(45)39-20-13-7-3-5-9-15-22-42(39)26-38(31)19-12-6-2-4-8-14-21-40-37(38)39/h2-3,6-7,10-11,16-17,28,31,33,35-37,40-41,45H,4-5,8-9,12-15,18-26H2,1H3/b6-2-,7-3-/t28-,31-,33+,35+,36-,37+,38-,39+/m0/s1

InChI Key

MFDADOYAAWFHON-IHRPDMNKSA-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
Acanthostrongylophora sp.	-	KNApSAcK

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
Azepane
Aralkylamine
Beta-aminoketone
Piperidine
N-alkylpyrrolidine
Benzenoid
Cyclic alcohol
Pyrrole
Pyrrolidine
Heteroaromatic compound
Secondary alcohol
Tertiary aliphatic amine
Tertiary amine
1,2-aminoalcohol
Ketone
Secondary amine
Azacycle
Secondary aliphatic amine
Amine
Organic oxide
Organonitrogen compound
Organooxygen compound
Carbonyl group
Organopnictogen compound
Organic oxygen compound
Organic nitrogen compound
Hydrocarbon derivative
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	5.09	ALOGPS
logP	5.61	ChemAxon
logS	-5.4	ALOGPS
pKa (Strongest Acidic)	14.03	ChemAxon
pKa (Strongest Basic)	10.68	ChemAxon
Physiological Charge	2	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	71.6 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	184.49 m³·mol⁻¹	ChemAxon
Polarizability	71.33 Å³	ChemAxon
Number of Rings	8	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

9505914

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11330964

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (-)-Manadomanzamine A (NP0068733)

MOL for NP0068733 ((-)-Manadomanzamine A)

3D MOL for NP0068733 ((-)-Manadomanzamine A)

3D SDF for NP0068733 ((-)-Manadomanzamine A)

3D-SDF for NP0068733 ((-)-Manadomanzamine A)

PDB for NP0068733 ((-)-Manadomanzamine A)

3D PDB for NP0068733 ((-)-Manadomanzamine A)

SMILES for NP0068733 ((-)-Manadomanzamine A)

INCHI for NP0068733 ((-)-Manadomanzamine A)

Structure for NP0068733 ((-)-Manadomanzamine A)

3D Structure for NP0068733 ((-)-Manadomanzamine A)