NP-MRD: Showing NP-Card for (10e,12s,13r,14s,15e,17s,19e,23s,24s,25e,28e)-7,13,17,23,31-pentahydroxy-6,10,12,14,20,24,30-heptamethyl-34-thia-32-azatetracyclo[28.3.1.1⁴,³³.0³,⁸]pentatriaconta-1(33),3,5,7,10,15,19,25,28,31-decaene-2,9,21,27,35-pentone (NP0330776)

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Record Information

Version

2.0

Created at

2022-09-12 16:27:46 UTC

Updated at

2022-09-12 16:27:46 UTC

NP-MRD ID

NP0330776

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(10e,12s,13r,14s,15e,17s,19e,23s,24s,25e,28e)-7,13,17,23,31-pentahydroxy-6,10,12,14,20,24,30-heptamethyl-34-thia-32-azatetracyclo[28.3.1.1⁴,³³.0³,⁸]pentatriaconta-1(33),3,5,7,10,15,19,25,28,31-decaene-2,9,21,27,35-pentone

Description

Not Available

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122218272D          

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M  END

     RDKit          3D

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 36 83  1  0
 36 84  1  0
 36 85  1  0
 34 82  1  0
 22 77  1  0
 24 78  1  0
 24 79  1  0
 24 80  1  0
 25 81  1  0
 17 74  1  0
 17 75  1  0
 17 76  1  0
 15 73  1  0
 13 69  1  6
 14 70  1  0
 14 71  1  0
 14 72  1  0
 11 67  1  1
 12 68  1  0
  9 63  1  1
 10 64  1  0
 10 65  1  0
 10 66  1  0
  8 62  1  0
  7 61  1  0
  5 59  1  1
  6 60  1  0
  4 57  1  0
  4 58  1  0
  3 56  1  0
  1 53  1  0
  1 54  1  0
  1 55  1  0
 47 96  1  0
 47 97  1  0
 45 94  1  1
 46 95  1  0
M  END


  Mrv1652309122218272D          

 52 55  0  0  1  0            999 V2000
   -0.7786    1.2861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0284    1.1150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2921    1.8968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7289    2.5966    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3153    3.1769    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8071    3.8267    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0198    3.6063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8043    3.8616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6265    3.9292    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6549    4.7537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4422    3.8053    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6599    4.6010    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2072    3.4966    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.6026    4.2207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8805    3.0199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4257    2.4007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1040    2.8703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8134    1.6724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5817    1.9730    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0227    0.8744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7504    1.2631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0311    2.0389    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4509    0.8273    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1786    1.2160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4237    0.0027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6960   -0.3860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9955    0.0499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2678   -0.3388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5673    0.0970    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2406   -1.1634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9411   -1.5992    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9139   -2.4238    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.1862   -2.8125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1590   -3.6370    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4857   -2.3766    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5102   -3.2013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6041   -3.0006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7953   -3.1632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9708   -3.1348    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8469   -3.9505    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1750   -2.9171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4509   -2.5217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8376   -1.9700    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2184   -2.5151    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3679   -1.2917    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3603   -1.6794    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0674   -0.5234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0478    0.2936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8726    0.2739    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5129   -1.5521    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    7.6688   -1.2105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3692   -1.6464    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  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  6  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  6  0  0  0
  9 11  1  0  0  0  0
 11 12  1  1  0  0  0
 11 13  1  0  0  0  0
 13 14  1  1  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 20 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  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  1  0  0  0  0
 37 38  2  0  0  0  0
 38 39  1  0  0  0  0
 39 40  2  0  0  0  0
 39 41  1  0  0  0  0
 41 42  2  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  6  0  0  0
 43 45  1  0  0  0  0
 45 46  1  1  0  0  0
 45 47  1  0  0  0  0
 47 48  1  0  0  0  0
  2 48  1  0  0  0  0
 48 49  2  0  0  0  0
 35 50  1  0  0  0  0
 30 50  1  0  0  0  0
 31 51  1  0  0  0  0
 26 51  1  0  0  0  0
 51 52  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0330776

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1\C=C/C(=O)/C=C\C2(C)SC3=C(N=C2O)C(=O)C2=C(C3=O)C(=C(O)C(C)=C2)C(=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

> <INCHI_IDENTIFIER>
InChI=1S/C40H45NO10S/c1-19-8-11-25(42)13-10-21(3)33(46)22(4)16-23(5)34(47)31-30-27(17-24(6)35(31)48)36(49)32-38(37(30)50)52-40(7,39(51)41-32)15-14-26(43)12-9-20(2)29(45)18-28(19)44/h8-10,12-17,20-22,25,29,33,42,45-46,48H,11,18H2,1-7H3,(H,41,51)/b12-9-,13-10-,15-14-,19-8-,23-16-/t20-,21-,22-,25-,29-,33+,40?/m0/s1

> <INCHI_KEY>
SCJFFZAHMFLMSW-YCPBSIBJSA-N

> <FORMULA>
C40H45NO10S

> <MOLECULAR_WEIGHT>
731.86

> <EXACT_MASS>
731.276417827

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
97

> <JCHEM_AVERAGE_POLARIZABILITY>
78.92942862937214

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(10E,12S,13R,14S,15E,17S,19E,23S,24S,25E,28E)-7,13,17,23,31-pentahydroxy-6,10,12,14,20,24,30-heptamethyl-34-thia-32-azatetracyclo[28.3.1.1^{4,33}.0^{3,8}]pentatriaconta-1(33),3,5,7,10,15,19,25,28,31-decaene-2,9,21,27,35-pentone

> <JCHEM_LOGP>
5.504778901666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
5.61182284591989

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.347864641006336

> <JCHEM_PKA_STRONGEST_BASIC>
-0.5262112983543242

> <JCHEM_POLAR_SURFACE_AREA>
198.85999999999999

> <JCHEM_REFRACTIVITY>
207.15240000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(10E,12S,13R,14S,15E,17S,19E,23S,24S,25E,28E)-7,13,17,23,31-pentahydroxy-6,10,12,14,20,24,30-heptamethyl-34-thia-32-azatetracyclo[28.3.1.1^{4,33}.0^{3,8}]pentatriaconta-1(33),3,5,7,10,15,19,25,28,31-decaene-2,9,21,27,35-pentone

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.453   2.401   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.053   2.081   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.545   3.541   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.361   4.847   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.455   5.930   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       1.507   7.143   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       3.770   6.732   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.235   7.208   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.769   7.334   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.822   8.874   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.292   7.103   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       8.698   8.589   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       9.720   6.527   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.458   7.879   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.977   5.637   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      11.995   4.481   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      13.261   5.358   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      12.718   3.122   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      14.153   3.683   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      13.109   1.632   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      14.467   2.358   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      14.991   3.806   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      15.775   1.544   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      17.133   2.270   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      15.724   0.005   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      14.366  -0.720   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      13.058   0.093   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      11.700  -0.632   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      10.392   0.181   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      11.649  -2.172   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      12.957  -2.985   0.000  0.00  0.00           C+0
HETATM   32  N   UNK     0      12.906  -4.524   0.000  0.00  0.00           N+0
HETATM   33  C   UNK     0      11.548  -5.250   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      11.497  -6.789   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      10.240  -4.436   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      10.286  -5.976   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       8.594  -5.601   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       7.085  -5.905   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       5.545  -5.852   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       5.314  -7.374   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       4.060  -5.445   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       2.708  -4.707   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       1.563  -3.677   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       0.408  -4.695   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       0.687  -2.411   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0      -0.673  -3.135   0.000  0.00  0.00           O+0
HETATM   47  C   UNK     0       0.126  -0.977   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      -0.089   0.548   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0      -1.629   0.511   0.000  0.00  0.00           O+0
HETATM   50  S   UNK     0      10.291  -2.897   0.000  0.00  0.00           S+0
HETATM   51  C   UNK     0      14.315  -2.260   0.000  0.00  0.00           C+0
HETATM   52  O   UNK     0      15.623  -3.073   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    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   27                                                  
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   27   51                                                  
CONECT   27   26   20   28                                                  
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31   50                                                  
CONECT   31   30   32   51                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   36   37   50                                             
CONECT   36   35                                                            
CONECT   37   35   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   44   45                                                  
CONECT   44   43                                                            
CONECT   45   43   46   47                                                  
CONECT   46   45                                                            
CONECT   47   45   48                                                       
CONECT   48   47    2   49                                                  
CONECT   49   48                                                            
CONECT   50   35   30                                                       
CONECT   51   31   26   52                                                  
CONECT   52   51                                                            
MASTER        0    0    0    0    0    0    0    0   52    0  110    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₀H₄₅NO₁₀S

Average Mass

731.8600 Da

Monoisotopic Mass

731.27642 Da

IUPAC Name

(10E,12S,13R,14S,15E,17S,19E,23S,24S,25E,28E)-7,13,17,23,31-pentahydroxy-6,10,12,14,20,24,30-heptamethyl-34-thia-32-azatetracyclo[28.3.1.1^{4,33}.0^{3,8}]pentatriaconta-1(33),3,5,7,10,15,19,25,28,31-decaene-2,9,21,27,35-pentone

Traditional Name

CAS Registry Number

Not Available

SMILES

C[C@H]1\C=C/C(=O)/C=C\C2(C)SC3=C(N=C2O)C(=O)C2=C(C3=O)C(=C(O)C(C)=C2)C(=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

InChI Identifier

InChI=1S/C40H45NO10S/c1-19-8-11-25(42)13-10-21(3)33(46)22(4)16-23(5)34(47)31-30-27(17-24(6)35(31)48)36(49)32-38(37(30)50)52-40(7,39(51)41-32)15-14-26(43)12-9-20(2)29(45)18-28(19)44/h8-10,12-17,20-22,25,29,33,42,45-46,48H,11,18H2,1-7H3,(H,41,51)/b12-9-,13-10-,15-14-,19-8-,23-16-/t20-,21-,22-,25-,29-,33+,40?/m0/s1

InChI Key

SCJFFZAHMFLMSW-YCPBSIBJSA-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	5.5	ChemAxon
pKa (Strongest Acidic)	3.35	ChemAxon
pKa (Strongest Basic)	-0.53	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	198.86 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	207.15 m³·mol⁻¹	ChemAxon
Polarizability	78.93 Å³	ChemAxon
Number of Rings	4	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 (10e,12s,13r,14s,15e,17s,19e,23s,24s,25e,28e)-7,13,17,23,31-pentahydroxy-6,10,12,14,20,24,30-heptamethyl-34-thia-32-azatetracyclo[28.3.1.1⁴,³³.0³,⁸]pentatriaconta-1(33),3,5,7,10,15,19,25,28,31-decaene-2,9,21,27,35-pentone (NP0330776)

MOL for NP0330776 ((10e,12s,13r,14s,15e,17s,19e,23s,24s,25e,28e)-7,13,17,23,31-pentahydroxy-6,10,12,14,20,24,30-heptamethyl-34-thia-32-azatetracyclo[28.3.1.1⁴,³³.0³,⁸]pentatriaconta-1(33),3,5,7,10,15,19,25,28,31-decaene-2,9,21,27,35-pentone)

3D MOL for NP0330776 ((10e,12s,13r,14s,15e,17s,19e,23s,24s,25e,28e)-7,13,17,23,31-pentahydroxy-6,10,12,14,20,24,30-heptamethyl-34-thia-32-azatetracyclo[28.3.1.1⁴,³³.0³,⁸]pentatriaconta-1(33),3,5,7,10,15,19,25,28,31-decaene-2,9,21,27,35-pentone)

3D SDF for NP0330776 ((10e,12s,13r,14s,15e,17s,19e,23s,24s,25e,28e)-7,13,17,23,31-pentahydroxy-6,10,12,14,20,24,30-heptamethyl-34-thia-32-azatetracyclo[28.3.1.1⁴,³³.0³,⁸]pentatriaconta-1(33),3,5,7,10,15,19,25,28,31-decaene-2,9,21,27,35-pentone)

3D-SDF for NP0330776 ((10e,12s,13r,14s,15e,17s,19e,23s,24s,25e,28e)-7,13,17,23,31-pentahydroxy-6,10,12,14,20,24,30-heptamethyl-34-thia-32-azatetracyclo[28.3.1.1⁴,³³.0³,⁸]pentatriaconta-1(33),3,5,7,10,15,19,25,28,31-decaene-2,9,21,27,35-pentone)

PDB for NP0330776 ((10e,12s,13r,14s,15e,17s,19e,23s,24s,25e,28e)-7,13,17,23,31-pentahydroxy-6,10,12,14,20,24,30-heptamethyl-34-thia-32-azatetracyclo[28.3.1.1⁴,³³.0³,⁸]pentatriaconta-1(33),3,5,7,10,15,19,25,28,31-decaene-2,9,21,27,35-pentone)

3D PDB for NP0330776 ((10e,12s,13r,14s,15e,17s,19e,23s,24s,25e,28e)-7,13,17,23,31-pentahydroxy-6,10,12,14,20,24,30-heptamethyl-34-thia-32-azatetracyclo[28.3.1.1⁴,³³.0³,⁸]pentatriaconta-1(33),3,5,7,10,15,19,25,28,31-decaene-2,9,21,27,35-pentone)

SMILES for NP0330776 ((10e,12s,13r,14s,15e,17s,19e,23s,24s,25e,28e)-7,13,17,23,31-pentahydroxy-6,10,12,14,20,24,30-heptamethyl-34-thia-32-azatetracyclo[28.3.1.1⁴,³³.0³,⁸]pentatriaconta-1(33),3,5,7,10,15,19,25,28,31-decaene-2,9,21,27,35-pentone)

INCHI for NP0330776 ((10e,12s,13r,14s,15e,17s,19e,23s,24s,25e,28e)-7,13,17,23,31-pentahydroxy-6,10,12,14,20,24,30-heptamethyl-34-thia-32-azatetracyclo[28.3.1.1⁴,³³.0³,⁸]pentatriaconta-1(33),3,5,7,10,15,19,25,28,31-decaene-2,9,21,27,35-pentone)

Structure for NP0330776 ((10e,12s,13r,14s,15e,17s,19e,23s,24s,25e,28e)-7,13,17,23,31-pentahydroxy-6,10,12,14,20,24,30-heptamethyl-34-thia-32-azatetracyclo[28.3.1.1⁴,³³.0³,⁸]pentatriaconta-1(33),3,5,7,10,15,19,25,28,31-decaene-2,9,21,27,35-pentone)

3D Structure for NP0330776 ((10e,12s,13r,14s,15e,17s,19e,23s,24s,25e,28e)-7,13,17,23,31-pentahydroxy-6,10,12,14,20,24,30-heptamethyl-34-thia-32-azatetracyclo[28.3.1.1⁴,³³.0³,⁸]pentatriaconta-1(33),3,5,7,10,15,19,25,28,31-decaene-2,9,21,27,35-pentone)