NP-MRD: Showing NP-Card for n-(3-{3,6,9,12,15,18,21-heptahydroxy-17,20-bis[3-(n-hydroxyacetamido)propyl]-1,4,7,10,13,16,19-heptaazacyclohenicosa-1(21),3,6,9,12,15,18-heptaen-2-yl}propyl)-n-hydroxyacetamide (NP0266448)

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Record Information

Version

2.0

Created at

2022-09-08 10:47:45 UTC

Updated at

2022-09-08 10:47:45 UTC

NP-MRD ID

NP0266448

Secondary Accession Numbers

None

Natural Product Identification

Common Name

n-(3-{3,6,9,12,15,18,21-heptahydroxy-17,20-bis[3-(n-hydroxyacetamido)propyl]-1,4,7,10,13,16,19-heptaazacyclohenicosa-1(21),3,6,9,12,15,18-heptaen-2-yl}propyl)-n-hydroxyacetamide

Description

2,5,8-Tris[3-[(acetyl)(hydroxy)amino]propyl]-1,4,7,10,13,16,19-heptaazacyclohenicosane-3,6,9,12,15,18,21-heptaone belongs to the class of organic compounds known as cyclic peptides. Cyclic peptides are compounds containing a cyclic moiety bearing a peptide backbone. n-(3-{3,6,9,12,15,18,21-heptahydroxy-17,20-bis[3-(n-hydroxyacetamido)propyl]-1,4,7,10,13,16,19-heptaazacyclohenicosa-1(21),3,6,9,12,15,18-heptaen-2-yl}propyl)-n-hydroxyacetamide is found in Tilletia indica. Based on a literature review very few articles have been published on 2,5,8-Tris[3-[(acetyl)(hydroxy)amino]propyl]-1,4,7,10,13,16,19-heptaazacyclohenicosane-3,6,9,12,15,18,21-heptaone.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082212472D          

 52 52  0  0  0  0            999 V2000
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M  END

     RDKit          3D

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  9 10  1  0
 10 11  2  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 26 27  2  0
 27 28  1  0
 27 29  1  0
 36 85  1  0
 36 86  1  0
 36 87  1  0
 34 84  1  0
 32 82  1  0
 32 83  1  0
 31 80  1  0
 31 81  1  0
 30 78  1  0
 30 79  1  0
 29 77  1  6
 40 88  1  0
 41 89  1  1
 42 90  1  0
 42 91  1  0
 43 92  1  0
 43 93  1  0
 44 94  1  0
 44 95  1  0
 46 96  1  0
 48 97  1  0
 48 98  1  0
 48 99  1  0
 52100  1  0
  9 63  1  1
  8 61  1  0
  8 62  1  0
  7 59  1  0
  7 60  1  0
  6 57  1  0
  6 58  1  0
  5 56  1  0
  1 53  1  0
  1 54  1  0
  1 55  1  0
 12 64  1  0
 13 65  1  0
 13 66  1  0
 16 67  1  0
 17 68  1  0
 17 69  1  0
 20 70  1  0
 21 71  1  0
 21 72  1  0
 24 73  1  0
 25 74  1  0
 25 75  1  0
 28 76  1  0
M  END


  Mrv1652309082212472D          

 52 52  0  0  0  0            999 V2000
   -1.1947    8.9800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5497    8.4657    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2183    8.7671    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6726    7.6499    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4406    7.3485    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0276    7.1355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1506    6.3197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4944    5.8053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3715    4.9895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3965    4.6881    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9576    5.2929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    6.0812    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7620    5.1093    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0051    4.3210    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8278    4.2593    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2926    4.9410    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1858    3.5160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7210    2.8344    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1858    2.1527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0085    2.2144    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8278    1.4094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0051    1.3478    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7620    0.5594    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3231   -0.0453    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9576    0.3758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3965    0.9806    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.3715    0.6792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4944   -0.1366    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0165    1.1936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7845    0.8922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4295    1.4066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1974    1.1052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8424    1.6195    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.7195    2.4353    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6104    1.3181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2554    1.8325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7334    0.5023    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8935    2.0094    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6080    2.4219    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3225    2.0094    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6080    3.2469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3225    3.6594    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0369    3.2469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7514    3.6594    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4659    3.2469    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.4659    2.4219    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1803    3.6594    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1803    4.4844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8948    3.2469    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8935    3.6594    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.0165    4.4752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7845    4.7766    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  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
 10  9  1  4  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 14 13  1  4  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 18 17  1  4  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 22 21  1  4  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 26 25  1  4  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  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  1  0  0  0  0
 33 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  2  0  0  0  0
 38 29  1  4  0  0  0
 38 39  2  0  0  0  0
 39 40  1  0  0  0  0
 39 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 45 47  1  0  0  0  0
 47 48  1  0  0  0  0
 47 49  2  0  0  0  0
 50 41  1  4  0  0  0
 50 51  2  0  0  0  0
  9 51  1  0  0  0  0
 51 52  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0266448

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)N(O)CCCC1N=C(O)C(CCCN(O)C(C)=O)N=C(O)C(CCCN(O)C(C)=O)N=C(O)CN=C(O)CN=C(O)CN=C(O)CN=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C29H48N10O13/c1-17(40)37(50)10-4-7-20-27(47)33-15-25(45)31-13-23(43)30-14-24(44)32-16-26(46)34-21(8-5-11-38(51)18(2)41)28(48)36-22(29(49)35-20)9-6-12-39(52)19(3)42/h20-22,50-52H,4-16H2,1-3H3,(H,30,43)(H,31,45)(H,32,44)(H,33,47)(H,34,46)(H,35,49)(H,36,48)

> <INCHI_KEY>
GDKGUAKTXWFQAS-UHFFFAOYSA-N

> <FORMULA>
C29H48N10O13

> <MOLECULAR_WEIGHT>
744.76

> <EXACT_MASS>
744.340231646

> <JCHEM_ACCEPTOR_COUNT>
20

> <JCHEM_ATOM_COUNT>
100

> <JCHEM_AVERAGE_POLARIZABILITY>
73.938925347847

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
10

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
N-(3-{3,6,9,12,15,18,21-heptahydroxy-17,20-bis[3-(N-hydroxyacetamido)propyl]-1,4,7,10,13,16,19-heptaazacyclohenicosa-1(21),3,6,9,12,15,18-heptaen-2-yl}propyl)-N-hydroxyacetamide

> <JCHEM_LOGP>
-2.5758744946666665

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
3.3486136971783016

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.9185401171549024

> <JCHEM_PKA_STRONGEST_BASIC>
-5.680503513212597

> <JCHEM_POLAR_SURFACE_AREA>
349.75000000000006

> <JCHEM_REFRACTIVITY>
178.51690000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
N-(3-{3,6,9,12,15,18,21-heptahydroxy-17,20-bis[3-(N-hydroxyacetamido)propyl]-1,4,7,10,13,16,19-heptaazacyclohenicosa-1(21),3,6,9,12,15,18-heptaen-2-yl}propyl)-N-hydroxyacetamide

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0      -2.230  16.763   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.026  15.803   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       0.407  16.365   0.000  0.00  0.00           O+0
HETATM    4  N   UNK     0      -1.256  14.280   0.000  0.00  0.00           N+0
HETATM    5  O   UNK     0      -2.689  13.717   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -0.052  13.320   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.281  11.797   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.923  10.837   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.693   9.314   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0      -0.740   8.751   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0      -1.788   9.880   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -1.334  11.352   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -3.289   9.537   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0      -3.743   8.066   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0      -5.279   7.951   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -6.146   9.223   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -5.947   6.563   0.000  0.00  0.00           C+0
HETATM   18  N   UNK     0      -5.079   5.291   0.000  0.00  0.00           N+0
HETATM   19  C   UNK     0      -5.947   4.018   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -7.482   4.134   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -5.279   2.631   0.000  0.00  0.00           C+0
HETATM   22  N   UNK     0      -3.743   2.516   0.000  0.00  0.00           N+0
HETATM   23  C   UNK     0      -3.289   1.044   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -4.336  -0.085   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -1.788   0.702   0.000  0.00  0.00           C+0
HETATM   26  N   UNK     0      -0.740   1.830   0.000  0.00  0.00           N+0
HETATM   27  C   UNK     0       0.693   1.268   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       0.923  -0.255   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       1.897   2.228   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       3.331   1.665   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.535   2.626   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       5.969   2.063   0.000  0.00  0.00           C+0
HETATM   33  N   UNK     0       7.173   3.023   0.000  0.00  0.00           N+0
HETATM   34  O   UNK     0       6.943   4.546   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       8.606   2.461   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       9.810   3.421   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       8.836   0.938   0.000  0.00  0.00           O+0
HETATM   38  N   UNK     0       1.668   3.751   0.000  0.00  0.00           N+0
HETATM   39  C   UNK     0       3.002   4.521   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       4.335   3.751   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       3.002   6.061   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       4.335   6.831   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       5.669   6.061   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       7.003   6.831   0.000  0.00  0.00           C+0
HETATM   45  N   UNK     0       8.336   6.061   0.000  0.00  0.00           N+0
HETATM   46  O   UNK     0       8.336   4.521   0.000  0.00  0.00           O+0
HETATM   47  C   UNK     0       9.670   6.831   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       9.670   8.371   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0      11.004   6.061   0.000  0.00  0.00           O+0
HETATM   50  N   UNK     0       1.668   6.831   0.000  0.00  0.00           N+0
HETATM   51  C   UNK     0       1.897   8.354   0.000  0.00  0.00           C+0
HETATM   52  O   UNK     0       3.331   8.916   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   51                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   38                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35                                                            
CONECT   38   29   39                                                       
CONECT   39   38   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   42   50                                                  
CONECT   42   41   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43   45                                                       
CONECT   45   44   46   47                                                  
CONECT   46   45                                                            
CONECT   47   45   48   49                                                  
CONECT   48   47                                                            
CONECT   49   47                                                            
CONECT   50   41   51                                                       
CONECT   51   50    9   52                                                  
CONECT   52   51                                                            
MASTER        0    0    0    0    0    0    0    0   52    0  104    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₉H₄₈N₁₀O₁₃

Average Mass

744.7600 Da

Monoisotopic Mass

744.34023 Da

IUPAC Name

N-(3-{3,6,9,12,15,18,21-heptahydroxy-17,20-bis[3-(N-hydroxyacetamido)propyl]-1,4,7,10,13,16,19-heptaazacyclohenicosa-1(21),3,6,9,12,15,18-heptaen-2-yl}propyl)-N-hydroxyacetamide

Traditional Name

N-(3-{3,6,9,12,15,18,21-heptahydroxy-17,20-bis[3-(N-hydroxyacetamido)propyl]-1,4,7,10,13,16,19-heptaazacyclohenicosa-1(21),3,6,9,12,15,18-heptaen-2-yl}propyl)-N-hydroxyacetamide

CAS Registry Number

Not Available

SMILES

CC(=O)N(O)CCCC1N=C(O)C(CCCN(O)C(C)=O)N=C(O)C(CCCN(O)C(C)=O)N=C(O)CN=C(O)CN=C(O)CN=C(O)CN=C1O

InChI Identifier

InChI=1S/C29H48N10O13/c1-17(40)37(50)10-4-7-20-27(47)33-15-25(45)31-13-23(43)30-14-24(44)32-16-26(46)34-21(8-5-11-38(51)18(2)41)28(48)36-22(29(49)35-20)9-6-12-39(52)19(3)42/h20-22,50-52H,4-16H2,1-3H3,(H,30,43)(H,31,45)(H,32,44)(H,33,47)(H,34,46)(H,35,49)(H,36,48)

InChI Key

GDKGUAKTXWFQAS-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, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, 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
Tilletia indica	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cyclic peptides. Cyclic peptides are compounds containing a cyclic moiety bearing a peptide backbone.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Cyclic peptides

Alternative Parents

Substituents

Cyclic alpha peptide
Acetohydroxamic acid
Acetamide
Cyclic carboximidic acid
Hydroxamic acid
Azacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Polyol
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic 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	-2.6	ChemAxon
pKa (Strongest Acidic)	2.92	ChemAxon
pKa (Strongest Basic)	-5.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	20	ChemAxon
Hydrogen Donor Count	10	ChemAxon
Polar Surface Area	349.75 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	178.52 m³·mol⁻¹	ChemAxon
Polarizability	73.94 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

102576133

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for n-(3-{3,6,9,12,15,18,21-heptahydroxy-17,20-bis[3-(n-hydroxyacetamido)propyl]-1,4,7,10,13,16,19-heptaazacyclohenicosa-1(21),3,6,9,12,15,18-heptaen-2-yl}propyl)-n-hydroxyacetamide (NP0266448)

MOL for NP0266448 (n-(3-{3,6,9,12,15,18,21-heptahydroxy-17,20-bis[3-(n-hydroxyacetamido)propyl]-1,4,7,10,13,16,19-heptaazacyclohenicosa-1(21),3,6,9,12,15,18-heptaen-2-yl}propyl)-n-hydroxyacetamide)

3D MOL for NP0266448 (n-(3-{3,6,9,12,15,18,21-heptahydroxy-17,20-bis[3-(n-hydroxyacetamido)propyl]-1,4,7,10,13,16,19-heptaazacyclohenicosa-1(21),3,6,9,12,15,18-heptaen-2-yl}propyl)-n-hydroxyacetamide)

3D SDF for NP0266448 (n-(3-{3,6,9,12,15,18,21-heptahydroxy-17,20-bis[3-(n-hydroxyacetamido)propyl]-1,4,7,10,13,16,19-heptaazacyclohenicosa-1(21),3,6,9,12,15,18-heptaen-2-yl}propyl)-n-hydroxyacetamide)

3D-SDF for NP0266448 (n-(3-{3,6,9,12,15,18,21-heptahydroxy-17,20-bis[3-(n-hydroxyacetamido)propyl]-1,4,7,10,13,16,19-heptaazacyclohenicosa-1(21),3,6,9,12,15,18-heptaen-2-yl}propyl)-n-hydroxyacetamide)

PDB for NP0266448 (n-(3-{3,6,9,12,15,18,21-heptahydroxy-17,20-bis[3-(n-hydroxyacetamido)propyl]-1,4,7,10,13,16,19-heptaazacyclohenicosa-1(21),3,6,9,12,15,18-heptaen-2-yl}propyl)-n-hydroxyacetamide)

3D PDB for NP0266448 (n-(3-{3,6,9,12,15,18,21-heptahydroxy-17,20-bis[3-(n-hydroxyacetamido)propyl]-1,4,7,10,13,16,19-heptaazacyclohenicosa-1(21),3,6,9,12,15,18-heptaen-2-yl}propyl)-n-hydroxyacetamide)

SMILES for NP0266448 (n-(3-{3,6,9,12,15,18,21-heptahydroxy-17,20-bis[3-(n-hydroxyacetamido)propyl]-1,4,7,10,13,16,19-heptaazacyclohenicosa-1(21),3,6,9,12,15,18-heptaen-2-yl}propyl)-n-hydroxyacetamide)

INCHI for NP0266448 (n-(3-{3,6,9,12,15,18,21-heptahydroxy-17,20-bis[3-(n-hydroxyacetamido)propyl]-1,4,7,10,13,16,19-heptaazacyclohenicosa-1(21),3,6,9,12,15,18-heptaen-2-yl}propyl)-n-hydroxyacetamide)

Structure for NP0266448 (n-(3-{3,6,9,12,15,18,21-heptahydroxy-17,20-bis[3-(n-hydroxyacetamido)propyl]-1,4,7,10,13,16,19-heptaazacyclohenicosa-1(21),3,6,9,12,15,18-heptaen-2-yl}propyl)-n-hydroxyacetamide)

3D Structure for NP0266448 (n-(3-{3,6,9,12,15,18,21-heptahydroxy-17,20-bis[3-(n-hydroxyacetamido)propyl]-1,4,7,10,13,16,19-heptaazacyclohenicosa-1(21),3,6,9,12,15,18-heptaen-2-yl}propyl)-n-hydroxyacetamide)