NP-MRD: Showing NP-Card for n-methyl{1-[4-(10-hydroxy-8-methoxy-3,7,9,13,15,17,20,23-octamethyl-24-oxo-18-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1-oxacyclotetracosa-4,6,11,13,15,19,22-heptaen-2-yl)-1,3-thiazol-2-yl]-3-methylbutoxy}carboximidic acid (NP0197375)

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Record Information

Version

2.0

Created at

2022-09-04 15:37:43 UTC

Updated at

2022-09-04 15:37:43 UTC

NP-MRD ID

NP0197375

Secondary Accession Numbers

None

Natural Product Identification

Common Name

n-methyl{1-[4-(10-hydroxy-8-methoxy-3,7,9,13,15,17,20,23-octamethyl-24-oxo-18-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1-oxacyclotetracosa-4,6,11,13,15,19,22-heptaen-2-yl)-1,3-thiazol-2-yl]-3-methylbutoxy}carboximidic acid

Description

N-methyl{1-[4-(10-hydroxy-8-methoxy-3,7,9,13,15,17,20,23-octamethyl-24-oxo-18-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1-oxacyclotetracosa-4,6,11,13,15,19,22-heptaen-2-yl)-1,3-thiazol-2-yl]-3-methylbutoxy}carboximidic acid belongs to the class of organic compounds known as macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members. Based on a literature review very few articles have been published on N-methyl{1-[4-(10-hydroxy-8-methoxy-3,7,9,13,15,17,20,23-octamethyl-24-oxo-18-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1-oxacyclotetracosa-4,6,11,13,15,19,22-heptaen-2-yl)-1,3-thiazol-2-yl]-3-methylbutoxy}carboximidic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042217372D          

 63 65  0  0  0  0            999 V2000
   -2.6577   -5.0457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9432   -4.6332    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9432   -3.8082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6577   -3.3957    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2288   -3.3957    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2288   -2.5707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5143   -2.1582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2002   -2.5707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2002   -3.3957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9146   -2.1582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9432   -2.1582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0295   -1.3377    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8364   -1.1662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1720   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6569   -1.0799    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4774   -0.9937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.6334   -0.1538    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3046    1.3536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.4908    3.5283    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.7306    6.1119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9101    6.0256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4252    6.6931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.7541    5.1857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.7172    1.5898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2022    0.9224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8666    0.1687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.7995   -1.1118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2489   -1.8806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6969   -2.4937    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  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
  8 10  1  0  0  0  0
  6 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 20 21  1  4  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  2  0  0  0  0
 24 25  1  4  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
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 32 33  1  0  0  0  0
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 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 27 36  1  0  0  0  0
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 14 60  1  0  0  0  0
 60 61  1  0  0  0  0
 13 62  2  0  0  0  0
 62 63  1  0  0  0  0
 11 63  1  0  0  0  0
M  END

     RDKit          3D

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M  END


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M  END
> <DATABASE_ID>
NP0197375

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1C(C)C(O)C=CC(C)=CC(C)=CC(C)C(OC2OC(CO)C(O)C(O)C2O)C=C(C)CC=C(C)C(=O)OC(C(C)C=CC=C1C)C1=CSC(=N1)C(CC(C)C)OC(O)=NC

> <INCHI_IDENTIFIER>
InChI=1S/C48H72N2O12S/c1-26(2)20-38(61-48(57)49-11)45-50-35(25-63-45)44-31(7)15-13-14-30(6)43(58-12)34(10)36(52)19-17-27(3)21-29(5)22-33(9)37(23-28(4)16-18-32(8)46(56)62-44)59-47-42(55)41(54)40(53)39(24-51)60-47/h13-15,17-19,21-23,25-26,31,33-34,36-44,47,51-55H,16,20,24H2,1-12H3,(H,49,57)

> <INCHI_KEY>
DCUUIFQQELZBFD-UHFFFAOYSA-N

> <FORMULA>
C48H72N2O12S

> <MOLECULAR_WEIGHT>
901.17

> <EXACT_MASS>
900.48059694

> <JCHEM_ACCEPTOR_COUNT>
13

> <JCHEM_ATOM_COUNT>
135

> <JCHEM_AVERAGE_POLARIZABILITY>
99.08664201395949

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
N-methyl{1-[4-(10-hydroxy-8-methoxy-3,7,9,13,15,17,20,23-octamethyl-24-oxo-18-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1-oxacyclotetracosa-4,6,11,13,15,19,22-heptaen-2-yl)-1,3-thiazol-2-yl]-3-methylbutoxy}carboximidic acid

> <JCHEM_LOGP>
6.864839566960445

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.207772290115596

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.922249844511569

> <JCHEM_PKA_STRONGEST_BASIC>
2.3922585766068822

> <JCHEM_POLAR_SURFACE_AREA>
209.85

> <JCHEM_REFRACTIVITY>
248.9021000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
N-methyl{1-[4-(10-hydroxy-8-methoxy-3,7,9,13,15,17,20,23-octamethyl-24-oxo-18-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1-oxacyclotetracosa-4,6,11,13,15,19,22-heptaen-2-yl)-1,3-thiazol-2-yl]-3-methylbutoxy}carboximidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0      -4.961  -9.419   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0      -3.627  -8.649   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0      -3.627  -7.109   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -4.961  -6.339   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0      -2.294  -6.339   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -2.294  -4.799   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.960  -4.029   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.374  -4.799   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.374  -6.339   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.707  -4.029   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -3.627  -4.029   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0      -3.788  -2.497   0.000  0.00  0.00           N+0
HETATM   13  C   UNK     0      -5.295  -2.177   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -5.921  -0.770   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -6.826  -2.016   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -8.358  -1.855   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -9.263  -3.101   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -8.984  -0.448   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0     -10.927   0.221   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -8.079   0.798   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -8.705   2.205   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -7.800   3.451   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -6.269   3.290   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -8.427   4.857   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -7.521   6.103   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -9.053   6.264   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -9.958   5.018   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -9.332   3.612   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0     -10.237   2.366   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -9.611   0.959   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0     -10.516  -0.287   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0     -11.769   2.527   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0     -12.674   1.281   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0     -12.395   3.934   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0     -13.926   4.094   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0     -11.490   5.179   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0     -12.116   6.586   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      -8.148   7.510   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      -9.679   7.671   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      -7.243   8.756   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -7.869  10.163   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -9.401  10.324   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      -6.964  11.409   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      -5.432  11.248   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      -4.527  12.494   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      -4.806   9.841   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      -3.274   9.680   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      -2.648   8.273   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0      -1.116   8.112   0.000  0.00  0.00           O+0
HETATM   50  C   UNK     0      -3.553   7.027   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      -5.085   7.188   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      -2.927   5.620   0.000  0.00  0.00           C+0
HETATM   53  O   UNK     0      -1.395   5.459   0.000  0.00  0.00           O+0
HETATM   54  C   UNK     0      -0.769   4.053   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0      -3.832   4.375   0.000  0.00  0.00           C+0
HETATM   56  C   UNK     0      -5.363   4.535   0.000  0.00  0.00           C+0
HETATM   57  C   UNK     0      -3.206   2.968   0.000  0.00  0.00           C+0
HETATM   58  C   UNK     0      -4.111   1.722   0.000  0.00  0.00           C+0
HETATM   59  C   UNK     0      -3.484   0.315   0.000  0.00  0.00           C+0
HETATM   60  C   UNK     0      -4.390  -0.931   0.000  0.00  0.00           C+0
HETATM   61  C   UNK     0      -3.359  -2.075   0.000  0.00  0.00           C+0
HETATM   62  C   UNK     0      -6.065  -3.511   0.000  0.00  0.00           C+0
HETATM   63  S   UNK     0      -5.034  -4.655   0.000  0.00  0.00           S+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7   11                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    6   12   63                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   62                                                  
CONECT   14   13   15   60                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26   38                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   36                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30   32                                                  
CONECT   30   29   31                                                       
CONECT   31   30                                                            
CONECT   32   29   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   27   37                                                  
CONECT   37   36                                                            
CONECT   38   25   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38   41                                                       
CONECT   41   40   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41   44                                                       
CONECT   44   43   45   46                                                  
CONECT   45   44                                                            
CONECT   46   44   47                                                       
CONECT   47   46   48                                                       
CONECT   48   47   49   50                                                  
CONECT   49   48                                                            
CONECT   50   48   51   52                                                  
CONECT   51   50                                                            
CONECT   52   50   53   55                                                  
CONECT   53   52   54                                                       
CONECT   54   53                                                            
CONECT   55   52   56   57                                                  
CONECT   56   55                                                            
CONECT   57   55   58                                                       
CONECT   58   57   59                                                       
CONECT   59   58   60                                                       
CONECT   60   59   14   61                                                  
CONECT   61   60                                                            
CONECT   62   13   63                                                       
CONECT   63   62   11                                                       
MASTER        0    0    0    0    0    0    0    0   63    0  130    0
END

View in JSmol

Synonyms

Value	Source
N-Methyl{1-[4-(10-hydroxy-8-methoxy-3,7,9,13,15,17,20,23-octamethyl-24-oxo-18-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1-oxacyclotetracosa-4,6,11,13,15,19,22-heptaen-2-yl)-1,3-thiazol-2-yl]-3-methylbutoxy}carboximidate	Generator

Chemical Formula

C₄₈H₇₂N₂O₁₂S

Average Mass

901.1700 Da

Monoisotopic Mass

900.48060 Da

IUPAC Name

Traditional Name

CAS Registry Number

Not Available

SMILES

COC1C(C)C(O)C=CC(C)=CC(C)=CC(C)C(OC2OC(CO)C(O)C(O)C2O)C=C(C)CC=C(C)C(=O)OC(C(C)C=CC=C1C)C1=CSC(=N1)C(CC(C)C)OC(O)=NC

InChI Identifier

InChI=1S/C48H72N2O12S/c1-26(2)20-38(61-48(57)49-11)45-50-35(25-63-45)44-31(7)15-13-14-30(6)43(58-12)34(10)36(52)19-17-27(3)21-29(5)22-33(9)37(23-28(4)16-18-32(8)46(56)62-44)59-47-42(55)41(54)40(53)39(24-51)60-47/h13-15,17-19,21-23,25-26,31,33-34,36-44,47,51-55H,16,20,24H2,1-12H3,(H,49,57)

InChI Key

DCUUIFQQELZBFD-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Macrolides and analogues

Sub Class

Not Available

Direct Parent

Macrolides and analogues

Alternative Parents

Substituents

Macrolide
Hexose monosaccharide
O-glycosyl compound
Glycosyl compound
2,4-disubstituted 1,3-thiazole
Oxane
Monosaccharide
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Carbamic acid ester
Thiazole
Azole
Heteroaromatic compound
Carboxylic acid ester
Carbonic acid derivative
Secondary alcohol
Lactone
Acetal
Carboxylic acid derivative
Dialkyl ether
Ether
Oxacycle
Azacycle
Monocarboxylic acid or derivatives
Organoheterocyclic compound
Polyol
Organic oxide
Hydrocarbon derivative
Organic oxygen compound
Carbonyl group
Organic nitrogen compound
Organopnictogen compound
Primary alcohol
Alcohol
Organonitrogen compound
Organooxygen compound
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic 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	6.86	ChemAxon
pKa (Strongest Acidic)	3.92	ChemAxon
pKa (Strongest Basic)	2.39	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	13	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	209.85 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	248.9 m³·mol⁻¹	ChemAxon
Polarizability	99.09 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	Yes	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

162982033

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for n-methyl{1-[4-(10-hydroxy-8-methoxy-3,7,9,13,15,17,20,23-octamethyl-24-oxo-18-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1-oxacyclotetracosa-4,6,11,13,15,19,22-heptaen-2-yl)-1,3-thiazol-2-yl]-3-methylbutoxy}carboximidic acid (NP0197375)

MOL for NP0197375 (n-methyl{1-[4-(10-hydroxy-8-methoxy-3,7,9,13,15,17,20,23-octamethyl-24-oxo-18-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1-oxacyclotetracosa-4,6,11,13,15,19,22-heptaen-2-yl)-1,3-thiazol-2-yl]-3-methylbutoxy}carboximidic acid)

3D MOL for NP0197375 (n-methyl{1-[4-(10-hydroxy-8-methoxy-3,7,9,13,15,17,20,23-octamethyl-24-oxo-18-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1-oxacyclotetracosa-4,6,11,13,15,19,22-heptaen-2-yl)-1,3-thiazol-2-yl]-3-methylbutoxy}carboximidic acid)

3D SDF for NP0197375 (n-methyl{1-[4-(10-hydroxy-8-methoxy-3,7,9,13,15,17,20,23-octamethyl-24-oxo-18-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1-oxacyclotetracosa-4,6,11,13,15,19,22-heptaen-2-yl)-1,3-thiazol-2-yl]-3-methylbutoxy}carboximidic acid)

3D-SDF for NP0197375 (n-methyl{1-[4-(10-hydroxy-8-methoxy-3,7,9,13,15,17,20,23-octamethyl-24-oxo-18-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1-oxacyclotetracosa-4,6,11,13,15,19,22-heptaen-2-yl)-1,3-thiazol-2-yl]-3-methylbutoxy}carboximidic acid)

PDB for NP0197375 (n-methyl{1-[4-(10-hydroxy-8-methoxy-3,7,9,13,15,17,20,23-octamethyl-24-oxo-18-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1-oxacyclotetracosa-4,6,11,13,15,19,22-heptaen-2-yl)-1,3-thiazol-2-yl]-3-methylbutoxy}carboximidic acid)

3D PDB for NP0197375 (n-methyl{1-[4-(10-hydroxy-8-methoxy-3,7,9,13,15,17,20,23-octamethyl-24-oxo-18-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1-oxacyclotetracosa-4,6,11,13,15,19,22-heptaen-2-yl)-1,3-thiazol-2-yl]-3-methylbutoxy}carboximidic acid)

SMILES for NP0197375 (n-methyl{1-[4-(10-hydroxy-8-methoxy-3,7,9,13,15,17,20,23-octamethyl-24-oxo-18-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1-oxacyclotetracosa-4,6,11,13,15,19,22-heptaen-2-yl)-1,3-thiazol-2-yl]-3-methylbutoxy}carboximidic acid)

INCHI for NP0197375 (n-methyl{1-[4-(10-hydroxy-8-methoxy-3,7,9,13,15,17,20,23-octamethyl-24-oxo-18-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1-oxacyclotetracosa-4,6,11,13,15,19,22-heptaen-2-yl)-1,3-thiazol-2-yl]-3-methylbutoxy}carboximidic acid)

Structure for NP0197375 (n-methyl{1-[4-(10-hydroxy-8-methoxy-3,7,9,13,15,17,20,23-octamethyl-24-oxo-18-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1-oxacyclotetracosa-4,6,11,13,15,19,22-heptaen-2-yl)-1,3-thiazol-2-yl]-3-methylbutoxy}carboximidic acid)

3D Structure for NP0197375 (n-methyl{1-[4-(10-hydroxy-8-methoxy-3,7,9,13,15,17,20,23-octamethyl-24-oxo-18-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1-oxacyclotetracosa-4,6,11,13,15,19,22-heptaen-2-yl)-1,3-thiazol-2-yl]-3-methylbutoxy}carboximidic acid)