NP-MRD: Showing NP-Card for (7e,9s,10s,11s,12e,14s,16e,20s,21s,22e)-31-amino-4,10,14,20,28-pentahydroxy-3,7,9,11,17,21,27-heptamethyl-29-azatricyclo[28.3.1.0⁵,³³]tetratriaconta-1(33),2,4,7,12,16,22,24,26,28,30-undecaene-6,18,32,34-tetrone (NP0215759)

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Record Information

Version

2.0

Created at

2022-09-05 15:28:56 UTC

Updated at

2022-09-05 15:28:56 UTC

NP-MRD ID

NP0215759

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(7e,9s,10s,11s,12e,14s,16e,20s,21s,22e)-31-amino-4,10,14,20,28-pentahydroxy-3,7,9,11,17,21,27-heptamethyl-29-azatricyclo[28.3.1.0⁵,³³]tetratriaconta-1(33),2,4,7,12,16,22,24,26,28,30-undecaene-6,18,32,34-tetrone

Description

Not Available

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052217282D          

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M  END

     RDKit          3D

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 40 89  1  0
 39 88  1  0
 38 87  1  0
 37 84  1  0
 37 85  1  0
 37 86  1  0
 35 83  1  0
 31 81  1  0
 31 82  1  0
 25 80  1  0
 24 77  1  0
 24 78  1  0
 24 79  1  0
 22 76  1  0
 17 73  1  0
 17 74  1  0
 17 75  1  0
 15 72  1  0
 13 68  1  1
 14 69  1  0
 14 70  1  0
 14 71  1  0
 11 66  1  6
 12 67  1  0
  9 62  1  1
 10 63  1  0
 10 64  1  0
 10 65  1  0
  8 61  1  0
  7 60  1  0
  5 58  1  1
  6 59  1  0
  4 56  1  0
  4 57  1  0
  3 55  1  0
  1 52  1  0
  1 53  1  0
  1 54  1  0
 47 98  1  0
 47 99  1  0
 45 96  1  1
 46 97  1  0
M  END


  Mrv1652309052217282D          

 51 53  0  0  1  0            999 V2000
    6.9683    0.3874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3146   -0.3614    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1236   -0.1088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9732   -0.0776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7882   -0.2499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5466   -0.6026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2159   -1.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7479   -1.7910    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.4457   -1.3509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1130   -2.5473    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.8909   -2.2728    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.3022   -3.3597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3092   -4.2034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.1298   -4.2888    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.1273   -5.0338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9084   -5.2992    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7692   -5.7960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2622   -6.4551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6166   -6.9959    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.0741   -7.6824    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.8775   -7.3791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0688   -7.5959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2368   -7.6332    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.1847   -8.4565    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4128   -7.4908    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.1852   -8.2837    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6358   -7.1733    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.2400   -7.8972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9485   -6.6901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4029   -6.0661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7025   -6.5021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0807   -5.2936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8386   -4.9677    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7343   -4.5117    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9095   -4.6806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6546   -5.4652    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3524   -4.0710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5467   -4.2484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6022   -3.2833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4094   -3.0747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9855   -3.6887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8049   -3.4801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3736   -4.0778    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0460   -2.6976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8527   -2.5251    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.4984   -2.0735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9866   -1.3715    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.6046   -0.8104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1050   -0.1539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6689   -2.2725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1085   -1.6670    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
  3  4  1  4  0  0  0
  4  5  2  0  0  0  0
  5  6  1  4  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  8 10  1  0  0  0  0
 10 11  1  1  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  6  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  6  0  0  0
 23 25  1  0  0  0  0
 25 26  1  6  0  0  0
 25 27  1  0  0  0  0
 27 28  1  1  0  0  0
 27 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 32 33  2  0  0  0  0
 32 34  1  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 35 37  1  0  0  0  0
 37 38  1  0  0  0  0
 37 39  2  0  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 34 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  2  0  0  0  0
 42 44  1  0  0  0  0
 44 45  1  0  0  0  0
 44 46  2  0  0  0  0
 47 46  1  4  0  0  0
 47 48  2  0  0  0  0
  2 48  1  0  0  0  0
 48 49  1  0  0  0  0
 46 50  1  0  0  0  0
 40 50  1  0  0  0  0
 50 51  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0215759

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1\C=C/C=CC=C(C)C(O)=NC2=C(N)C(=O)C3=C(C=C(C)C(O)=C3C(=O)\C(C)=C/[C@H](C)[C@@H](O)[C@@H](C)\C=C/[C@@H](O)C\C=C(C)/C(=O)C[C@@H]1O)C2=O

> <INCHI_IDENTIFIER>
InChI=1S/C40H48N2O9/c1-20-11-9-8-10-12-23(4)40(51)42-34-33(41)39(50)31-28(38(34)49)18-26(7)37(48)32(31)36(47)25(6)17-24(5)35(46)22(3)14-16-27(43)15-13-21(2)30(45)19-29(20)44/h8-14,16-18,20,22,24,27,29,35,43-44,46,48H,15,19,41H2,1-7H3,(H,42,51)/b10-8?,11-9-,16-14-,21-13-,23-12?,25-17-/t20-,22-,24-,27-,29-,35-/m0/s1

> <INCHI_KEY>
JUWFHSXVGJIUPA-ZFODYLJOSA-N

> <FORMULA>
C40H48N2O9

> <MOLECULAR_WEIGHT>
700.829

> <EXACT_MASS>
700.335981134

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
99

> <JCHEM_AVERAGE_POLARIZABILITY>
76.02152503225511

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(7E,9S,10S,11S,12E,14S,16E,20S,21S,22E)-31-amino-4,10,14,20,28-pentahydroxy-3,7,9,11,17,21,27-heptamethyl-29-azatricyclo[28.3.1.0^{5,33}]tetratriaconta-1(33),2,4,7,12,16,22,24,26,28,30-undecaene-6,18,32,34-tetrone

> <JCHEM_LOGP>
4.895325238333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
5.870998844697787

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.043815489676501

> <JCHEM_PKA_STRONGEST_BASIC>
0.7477373439470357

> <JCHEM_POLAR_SURFACE_AREA>
207.81000000000003

> <JCHEM_REFRACTIVITY>
204.9497000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(7E,9S,10S,11S,12E,14S,16E,20S,21S,22E)-31-amino-4,10,14,20,28-pentahydroxy-3,7,9,11,17,21,27-heptamethyl-29-azatricyclo[28.3.1.0^{5,33}]tetratriaconta-1(33),2,4,7,12,16,22,24,26,28,30-undecaene-6,18,32,34-tetrone

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0      13.007   0.723   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.654  -0.675   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      15.164  -0.203   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      16.750  -0.145   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      18.271  -0.467   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      19.687  -1.125   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      20.936  -2.104   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      21.929  -3.343   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      23.232  -2.522   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      22.611  -4.755   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      24.063  -4.243   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      22.964  -6.271   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      22.977  -7.846   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      24.509  -8.006   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      22.638  -9.396   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      24.096  -9.892   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      21.969 -10.819   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      21.023 -12.050   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      19.818 -13.059   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      20.672 -14.341   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      18.438 -13.774   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      16.928 -14.179   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      15.375 -14.249   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      15.278 -15.786   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      13.837 -13.983   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      13.412 -15.463   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      12.387 -13.390   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      11.648 -14.741   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      11.104 -12.488   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      10.085 -11.323   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       8.778 -12.137   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       9.484  -9.881   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      10.899  -9.273   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       8.837  -8.422   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       7.298  -8.737   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       6.822 -10.202   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       6.258  -7.599   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       4.754  -7.930   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       6.724  -6.129   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       8.231  -5.740   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       9.306  -6.886   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      10.836  -6.496   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      11.897  -7.612   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      11.286  -5.035   0.000  0.00  0.00           C+0
HETATM   45  N   UNK     0      12.792  -4.713   0.000  0.00  0.00           N+0
HETATM   46  C   UNK     0      10.264  -3.870   0.000  0.00  0.00           C+0
HETATM   47  N   UNK     0      11.175  -2.560   0.000  0.00  0.00           N+0
HETATM   48  C   UNK     0      12.329  -1.513   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0      11.396  -0.287   0.000  0.00  0.00           O+0
HETATM   50  C   UNK     0       8.715  -4.242   0.000  0.00  0.00           C+0
HETATM   51  O   UNK     0       7.669  -3.112   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   48                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   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   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35   41                                                  
CONECT   35   34   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40                                                       
CONECT   40   39   41   50                                                  
CONECT   41   40   34   42                                                  
CONECT   42   41   43   44                                                  
CONECT   43   42                                                            
CONECT   44   42   45   46                                                  
CONECT   45   44                                                            
CONECT   46   44   47   50                                                  
CONECT   47   46   48                                                       
CONECT   48   47    2   49                                                  
CONECT   49   48                                                            
CONECT   50   46   40   51                                                  
CONECT   51   50                                                            
MASTER        0    0    0    0    0    0    0    0   51    0  106    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₀H₄₈N₂O₉

Average Mass

700.8290 Da

Monoisotopic Mass

700.33598 Da

IUPAC Name

(7E,9S,10S,11S,12E,14S,16E,20S,21S,22E)-31-amino-4,10,14,20,28-pentahydroxy-3,7,9,11,17,21,27-heptamethyl-29-azatricyclo[28.3.1.0^{5,33}]tetratriaconta-1(33),2,4,7,12,16,22,24,26,28,30-undecaene-6,18,32,34-tetrone

Traditional Name

CAS Registry Number

Not Available

SMILES

C[C@H]1\C=C/C=CC=C(C)C(O)=NC2=C(N)C(=O)C3=C(C=C(C)C(O)=C3C(=O)\C(C)=C/[C@H](C)[C@@H](O)[C@@H](C)\C=C/[C@@H](O)C\C=C(C)/C(=O)C[C@@H]1O)C2=O

InChI Identifier

InChI=1S/C40H48N2O9/c1-20-11-9-8-10-12-23(4)40(51)42-34-33(41)39(50)31-28(38(34)49)18-26(7)37(48)32(31)36(47)25(6)17-24(5)35(46)22(3)14-16-27(43)15-13-21(2)30(45)19-29(20)44/h8-14,16-18,20,22,24,27,29,35,43-44,46,48H,15,19,41H2,1-7H3,(H,42,51)/b10-8?,11-9-,16-14-,21-13-,23-12?,25-17-/t20-,22-,24-,27-,29-,35-/m0/s1

InChI Key

JUWFHSXVGJIUPA-ZFODYLJOSA-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

Not Available

Chemical Taxonomy

Classification

Not classified

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	4.9	ChemAxon
pKa (Strongest Acidic)	5.04	ChemAxon
pKa (Strongest Basic)	0.75	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	207.81 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	204.95 m³·mol⁻¹	ChemAxon
Polarizability	76.02 Å³	ChemAxon
Number of Rings	3	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

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (7e,9s,10s,11s,12e,14s,16e,20s,21s,22e)-31-amino-4,10,14,20,28-pentahydroxy-3,7,9,11,17,21,27-heptamethyl-29-azatricyclo[28.3.1.0⁵,³³]tetratriaconta-1(33),2,4,7,12,16,22,24,26,28,30-undecaene-6,18,32,34-tetrone (NP0215759)

MOL for NP0215759 ((7e,9s,10s,11s,12e,14s,16e,20s,21s,22e)-31-amino-4,10,14,20,28-pentahydroxy-3,7,9,11,17,21,27-heptamethyl-29-azatricyclo[28.3.1.0⁵,³³]tetratriaconta-1(33),2,4,7,12,16,22,24,26,28,30-undecaene-6,18,32,34-tetrone)

3D MOL for NP0215759 ((7e,9s,10s,11s,12e,14s,16e,20s,21s,22e)-31-amino-4,10,14,20,28-pentahydroxy-3,7,9,11,17,21,27-heptamethyl-29-azatricyclo[28.3.1.0⁵,³³]tetratriaconta-1(33),2,4,7,12,16,22,24,26,28,30-undecaene-6,18,32,34-tetrone)

3D SDF for NP0215759 ((7e,9s,10s,11s,12e,14s,16e,20s,21s,22e)-31-amino-4,10,14,20,28-pentahydroxy-3,7,9,11,17,21,27-heptamethyl-29-azatricyclo[28.3.1.0⁵,³³]tetratriaconta-1(33),2,4,7,12,16,22,24,26,28,30-undecaene-6,18,32,34-tetrone)

3D-SDF for NP0215759 ((7e,9s,10s,11s,12e,14s,16e,20s,21s,22e)-31-amino-4,10,14,20,28-pentahydroxy-3,7,9,11,17,21,27-heptamethyl-29-azatricyclo[28.3.1.0⁵,³³]tetratriaconta-1(33),2,4,7,12,16,22,24,26,28,30-undecaene-6,18,32,34-tetrone)

PDB for NP0215759 ((7e,9s,10s,11s,12e,14s,16e,20s,21s,22e)-31-amino-4,10,14,20,28-pentahydroxy-3,7,9,11,17,21,27-heptamethyl-29-azatricyclo[28.3.1.0⁵,³³]tetratriaconta-1(33),2,4,7,12,16,22,24,26,28,30-undecaene-6,18,32,34-tetrone)

3D PDB for NP0215759 ((7e,9s,10s,11s,12e,14s,16e,20s,21s,22e)-31-amino-4,10,14,20,28-pentahydroxy-3,7,9,11,17,21,27-heptamethyl-29-azatricyclo[28.3.1.0⁵,³³]tetratriaconta-1(33),2,4,7,12,16,22,24,26,28,30-undecaene-6,18,32,34-tetrone)

SMILES for NP0215759 ((7e,9s,10s,11s,12e,14s,16e,20s,21s,22e)-31-amino-4,10,14,20,28-pentahydroxy-3,7,9,11,17,21,27-heptamethyl-29-azatricyclo[28.3.1.0⁵,³³]tetratriaconta-1(33),2,4,7,12,16,22,24,26,28,30-undecaene-6,18,32,34-tetrone)

INCHI for NP0215759 ((7e,9s,10s,11s,12e,14s,16e,20s,21s,22e)-31-amino-4,10,14,20,28-pentahydroxy-3,7,9,11,17,21,27-heptamethyl-29-azatricyclo[28.3.1.0⁵,³³]tetratriaconta-1(33),2,4,7,12,16,22,24,26,28,30-undecaene-6,18,32,34-tetrone)

Structure for NP0215759 ((7e,9s,10s,11s,12e,14s,16e,20s,21s,22e)-31-amino-4,10,14,20,28-pentahydroxy-3,7,9,11,17,21,27-heptamethyl-29-azatricyclo[28.3.1.0⁵,³³]tetratriaconta-1(33),2,4,7,12,16,22,24,26,28,30-undecaene-6,18,32,34-tetrone)

3D Structure for NP0215759 ((7e,9s,10s,11s,12e,14s,16e,20s,21s,22e)-31-amino-4,10,14,20,28-pentahydroxy-3,7,9,11,17,21,27-heptamethyl-29-azatricyclo[28.3.1.0⁵,³³]tetratriaconta-1(33),2,4,7,12,16,22,24,26,28,30-undecaene-6,18,32,34-tetrone)