NP-MRD: Showing NP-Card for n-methyl[(1s)-1-{4-[(2r,3r,4e,6e,8r,9r,10r,11e,13e,15z,17r,18s,19e,22e)-10,18-dihydroxy-8-methoxy-3,7,9,13,15,17,20,23-octamethyl-24-oxo-1-oxacyclotetracosa-4,6,11,13,15,19,22-heptaen-2-yl]-1,3-thiazol-2-yl}-3-methylbutoxy]carboximidic acid (NP0211074)

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Record Information

Version

2.0

Created at

2022-09-05 09:10:58 UTC

Updated at

2022-09-05 09:10:58 UTC

NP-MRD ID

NP0211074

Secondary Accession Numbers

None

Natural Product Identification

Common Name

n-methyl[(1s)-1-{4-[(2r,3r,4e,6e,8r,9r,10r,11e,13e,15z,17r,18s,19e,22e)-10,18-dihydroxy-8-methoxy-3,7,9,13,15,17,20,23-octamethyl-24-oxo-1-oxacyclotetracosa-4,6,11,13,15,19,22-heptaen-2-yl]-1,3-thiazol-2-yl}-3-methylbutoxy]carboximidic acid

Description

N-methyl[(1S)-1-{4-[(2R,3R,6E,8R,9R,10R,11E,13E,15Z,17R,18S,19E,22E)-10,18-dihydroxy-8-methoxy-3,7,9,13,15,17,20,23-octamethyl-24-oxo-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[(1S)-1-{4-[(2R,3R,6E,8R,9R,10R,11E,13E,15Z,17R,18S,19E,22E)-10,18-dihydroxy-8-methoxy-3,7,9,13,15,17,20,23-octamethyl-24-oxo-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


  Mrv1652309052211102D          

 52 53  0  0  1  0            999 V2000
   -4.0866    4.2207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3722    3.8082    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6577    4.2207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6577    5.0457    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9432    3.8082    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9432    2.9832    0.0000 C   0  0  1  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    2.9832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5143    3.8082    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
   -2.6577    2.5707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7439    1.7502    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5509    1.5787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8865    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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   -3.7371   -0.5961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5576   -0.6824    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.7438   -2.8571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0492   -2.2759    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.8697   -2.3622    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.8931   -1.4360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1985   -0.8548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.0425   -0.0149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7070    0.7388    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.1919    1.4062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9634    2.2931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4114    2.9062    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
  6  5  1  1  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
 14 13  1  6  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  0  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  0  0  0  0
 25 26  1  6  0  0  0
 25 27  1  0  0  0  0
 27 28  1  6  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
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  1  0  0  0
 37 39  1  0  0  0  0
 39 40  1  6  0  0  0
 39 41  1  0  0  0  0
 41 42  1  1  0  0  0
 42 43  1  0  0  0  0
 41 44  1  0  0  0  0
 44 45  1  0  0  0  0
 44 46  2  0  0  0  0
 46 47  1  0  0  0  0
 47 48  2  0  0  0  0
 48 49  1  0  0  0  0
 14 49  1  0  0  0  0
 49 50  1  1  0  0  0
 13 51  2  0  0  0  0
 51 52  1  0  0  0  0
 11 52  1  0  0  0  0
M  END

     RDKit          3D

114115  0  0  0  0  0  0  0  0999 V2000
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    0.8806   -4.1753   -2.8724 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5073   -4.2327   -0.9314 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.2390    1.7317   -0.1488 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1227   -1.1014    3.6194 H   0  0  0  0  0  0  0  0  0  0  0  0
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  1 54  1  0
  1 55  1  0
M  END


  Mrv1652309052211102D          

 52 53  0  0  1  0            999 V2000
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   -4.2589   -3.5246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9535   -4.1058    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2890   -4.8595    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1095   -4.9457    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8041   -5.5269    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9836   -5.4407    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1396   -6.2806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9601   -6.3668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2957   -7.1205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4451   -5.6994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2655   -5.7856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6011   -6.5393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7505   -5.1182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4149   -4.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.7438   -2.8571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0492   -2.2759    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.8697   -2.3622    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3546   -1.6947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7136   -1.5223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.1985   -0.8548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8630   -0.1011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0425   -0.0149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7070    0.7388    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.1919    1.4062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9634    2.2931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4114    2.9062    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
  6  5  1  1  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
 14 13  1  6  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  0  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  0  0  0  0
 25 26  1  6  0  0  0
 25 27  1  0  0  0  0
 27 28  1  6  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
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  1  0  0  0
 37 39  1  0  0  0  0
 39 40  1  6  0  0  0
 39 41  1  0  0  0  0
 41 42  1  1  0  0  0
 42 43  1  0  0  0  0
 41 44  1  0  0  0  0
 44 45  1  0  0  0  0
 44 46  2  0  0  0  0
 46 47  1  0  0  0  0
 47 48  2  0  0  0  0
 48 49  1  0  0  0  0
 14 49  1  0  0  0  0
 49 50  1  1  0  0  0
 13 51  2  0  0  0  0
 51 52  1  0  0  0  0
 11 52  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0211074

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CO[C@@H]1[C@H](C)[C@H](O)\C=C\C(\C)=C\C(\C)=C/[C@@H](C)[C@H](O)\C=C(C)\C\C=C(C)\C(=O)O[C@H]([C@H](C)\C=C\C=C1/C)C1=CSC(=N1)[C@H](CC(C)C)OC(O)=NC

> <INCHI_IDENTIFIER>
InChI=1S/C42H62N2O7S/c1-25(2)20-37(50-42(48)43-11)40-44-34(24-52-40)39-30(7)15-13-14-29(6)38(49-12)33(10)35(45)19-17-26(3)21-28(5)22-32(9)36(46)23-27(4)16-18-31(8)41(47)51-39/h13-15,17-19,21-25,30,32-33,35-39,45-46H,16,20H2,1-12H3,(H,43,48)/b15-13+,19-17+,26-21+,27-23+,28-22-,29-14+,31-18+/t30-,32-,33-,35-,36-,37+,38+,39-/m1/s1

> <INCHI_KEY>
CUYVVUGLFUIZAZ-AYEGRPHTSA-N

> <FORMULA>
C42H62N2O7S

> <MOLECULAR_WEIGHT>
739.03

> <EXACT_MASS>
738.427773518

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
114

> <JCHEM_AVERAGE_POLARIZABILITY>
84.06918778281522

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
N-methyl[(1S)-1-{4-[(2R,3R,4E,6E,8R,9R,10R,11E,13E,15Z,17R,18S,19E,22E)-10,18-dihydroxy-8-methoxy-3,7,9,13,15,17,20,23-octamethyl-24-oxo-1-oxacyclotetracosa-4,6,11,13,15,19,22-heptaen-2-yl]-1,3-thiazol-2-yl}-3-methylbutoxy]carboximidic acid

> <JCHEM_LOGP>
8.635655284917004

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.483399620748546

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.922253050784344

> <JCHEM_PKA_STRONGEST_BASIC>
2.3923639286213585

> <JCHEM_POLAR_SURFACE_AREA>
130.70000000000002

> <JCHEM_REFRACTIVITY>
216.48880000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
N-methyl[(1S)-1-{4-[(2R,3R,4E,6E,8R,9R,10R,11E,13E,15Z,17R,18S,19E,22E)-10,18-dihydroxy-8-methoxy-3,7,9,13,15,17,20,23-octamethyl-24-oxo-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                                 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      -7.628   7.879   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0      -6.295   7.109   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0      -4.961   7.879   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -4.961   9.419   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0      -3.627   7.109   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -3.627   5.569   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.294   4.799   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.960   5.569   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.960   7.109   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.374   4.799   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -4.961   4.799   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0      -5.122   3.267   0.000  0.00  0.00           N+0
HETATM   13  C   UNK     0      -6.628   2.947   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -7.255   1.540   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -6.350   0.294   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -6.976  -1.113   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -8.507  -1.274   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -6.071  -2.359   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -4.539  -2.198   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -6.697  -3.765   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -5.792  -5.011   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -6.418  -6.418   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -7.950  -6.579   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -5.513  -7.664   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -6.139  -9.071   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -7.671  -9.232   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -5.234 -10.317   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -3.703 -10.156   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -5.861 -11.724   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -7.392 -11.885   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -8.019 -13.292   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -8.297 -10.639   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -9.829 -10.800   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0     -10.455 -12.207   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0     -10.734  -9.554   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0     -10.108  -8.147   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0     -11.013  -6.901   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0     -12.545  -7.062   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0     -10.387  -5.494   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      -8.855  -5.333   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0     -11.292  -4.248   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0     -12.823  -4.409   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0     -13.729  -3.164   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0     -10.665  -2.842   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      -9.134  -2.681   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0     -11.571  -1.596   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0     -10.944  -0.189   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      -9.413  -0.028   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      -8.786   1.379   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      -9.692   2.625   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      -7.398   4.281   0.000  0.00  0.00           C+0
HETATM   52  S   UNK     0      -6.368   5.425   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   52                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   51                                                  
CONECT   14   13   15   49                                                  
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   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                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   42   44                                                  
CONECT   42   41   43                                                       
CONECT   43   42                                                            
CONECT   44   41   45   46                                                  
CONECT   45   44                                                            
CONECT   46   44   47                                                       
CONECT   47   46   48                                                       
CONECT   48   47   49                                                       
CONECT   49   48   14   50                                                  
CONECT   50   49                                                            
CONECT   51   13   52                                                       
CONECT   52   51   11                                                       
MASTER        0    0    0    0    0    0    0    0   52    0  106    0
END

View in JSmol

Synonyms

Value	Source
N-Methyl[(1S)-1-{4-[(2R,3R,6E,8R,9R,10R,11E,13E,15Z,17R,18S,19E,22E)-10,18-dihydroxy-8-methoxy-3,7,9,13,15,17,20,23-octamethyl-24-oxo-1-oxacyclotetracosa-4,6,11,13,15,19,22-heptaen-2-yl]-1,3-thiazol-2-yl}-3-methylbutoxy]carboximidate	Generator

Chemical Formula

C₄₂H₆₂N₂O₇S

Average Mass

739.0300 Da

Monoisotopic Mass

738.42777 Da

IUPAC Name

N-methyl[(1S)-1-{4-[(2R,3R,4E,6E,8R,9R,10R,11E,13E,15Z,17R,18S,19E,22E)-10,18-dihydroxy-8-methoxy-3,7,9,13,15,17,20,23-octamethyl-24-oxo-1-oxacyclotetracosa-4,6,11,13,15,19,22-heptaen-2-yl]-1,3-thiazol-2-yl}-3-methylbutoxy]carboximidic acid

Traditional Name

CAS Registry Number

Not Available

SMILES

CO[C@@H]1[C@H](C)[C@H](O)\C=C\C(\C)=C\C(\C)=C/[C@@H](C)[C@H](O)\C=C(C)\C\C=C(C)\C(=O)O[C@H]([C@H](C)\C=C\C=C1/C)C1=CSC(=N1)[C@H](CC(C)C)OC(O)=NC

InChI Identifier

InChI=1S/C42H62N2O7S/c1-25(2)20-37(50-42(48)43-11)40-44-34(24-52-40)39-30(7)15-13-14-29(6)38(49-12)33(10)35(45)19-17-26(3)21-28(5)22-32(9)36(46)23-27(4)16-18-31(8)41(47)51-39/h13-15,17-19,21-25,30,32-33,35-39,45-46H,16,20H2,1-12H3,(H,43,48)/b15-13+,19-17+,26-21+,27-23+,28-22-,29-14+,31-18+/t30-,32-,33-,35-,36-,37+,38+,39-/m1/s1

InChI Key

CUYVVUGLFUIZAZ-AYEGRPHTSA-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
2,4-disubstituted 1,3-thiazole
Heteroaromatic compound
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Thiazole
Azole
Secondary alcohol
Lactone
Carboxylic acid ester
Oxacycle
Azacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Monocarboxylic acid or derivatives
Ether
Dialkyl ether
Carboxylic acid derivative
Carboximidic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Imine
Carbonyl group
Alcohol
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	8.64	ChemAxon
pKa (Strongest Acidic)	3.92	ChemAxon
pKa (Strongest Basic)	2.39	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	130.7 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	216.49 m³·mol⁻¹	ChemAxon
Polarizability	84.07 Å³	ChemAxon
Number of Rings	2	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

162904358

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[(1s)-1-{4-[(2r,3r,4e,6e,8r,9r,10r,11e,13e,15z,17r,18s,19e,22e)-10,18-dihydroxy-8-methoxy-3,7,9,13,15,17,20,23-octamethyl-24-oxo-1-oxacyclotetracosa-4,6,11,13,15,19,22-heptaen-2-yl]-1,3-thiazol-2-yl}-3-methylbutoxy]carboximidic acid (NP0211074)

MOL for NP0211074 (n-methyl[(1s)-1-{4-[(2r,3r,4e,6e,8r,9r,10r,11e,13e,15z,17r,18s,19e,22e)-10,18-dihydroxy-8-methoxy-3,7,9,13,15,17,20,23-octamethyl-24-oxo-1-oxacyclotetracosa-4,6,11,13,15,19,22-heptaen-2-yl]-1,3-thiazol-2-yl}-3-methylbutoxy]carboximidic acid)

3D MOL for NP0211074 (n-methyl[(1s)-1-{4-[(2r,3r,4e,6e,8r,9r,10r,11e,13e,15z,17r,18s,19e,22e)-10,18-dihydroxy-8-methoxy-3,7,9,13,15,17,20,23-octamethyl-24-oxo-1-oxacyclotetracosa-4,6,11,13,15,19,22-heptaen-2-yl]-1,3-thiazol-2-yl}-3-methylbutoxy]carboximidic acid)

3D SDF for NP0211074 (n-methyl[(1s)-1-{4-[(2r,3r,4e,6e,8r,9r,10r,11e,13e,15z,17r,18s,19e,22e)-10,18-dihydroxy-8-methoxy-3,7,9,13,15,17,20,23-octamethyl-24-oxo-1-oxacyclotetracosa-4,6,11,13,15,19,22-heptaen-2-yl]-1,3-thiazol-2-yl}-3-methylbutoxy]carboximidic acid)

3D-SDF for NP0211074 (n-methyl[(1s)-1-{4-[(2r,3r,4e,6e,8r,9r,10r,11e,13e,15z,17r,18s,19e,22e)-10,18-dihydroxy-8-methoxy-3,7,9,13,15,17,20,23-octamethyl-24-oxo-1-oxacyclotetracosa-4,6,11,13,15,19,22-heptaen-2-yl]-1,3-thiazol-2-yl}-3-methylbutoxy]carboximidic acid)

PDB for NP0211074 (n-methyl[(1s)-1-{4-[(2r,3r,4e,6e,8r,9r,10r,11e,13e,15z,17r,18s,19e,22e)-10,18-dihydroxy-8-methoxy-3,7,9,13,15,17,20,23-octamethyl-24-oxo-1-oxacyclotetracosa-4,6,11,13,15,19,22-heptaen-2-yl]-1,3-thiazol-2-yl}-3-methylbutoxy]carboximidic acid)

3D PDB for NP0211074 (n-methyl[(1s)-1-{4-[(2r,3r,4e,6e,8r,9r,10r,11e,13e,15z,17r,18s,19e,22e)-10,18-dihydroxy-8-methoxy-3,7,9,13,15,17,20,23-octamethyl-24-oxo-1-oxacyclotetracosa-4,6,11,13,15,19,22-heptaen-2-yl]-1,3-thiazol-2-yl}-3-methylbutoxy]carboximidic acid)

SMILES for NP0211074 (n-methyl[(1s)-1-{4-[(2r,3r,4e,6e,8r,9r,10r,11e,13e,15z,17r,18s,19e,22e)-10,18-dihydroxy-8-methoxy-3,7,9,13,15,17,20,23-octamethyl-24-oxo-1-oxacyclotetracosa-4,6,11,13,15,19,22-heptaen-2-yl]-1,3-thiazol-2-yl}-3-methylbutoxy]carboximidic acid)

INCHI for NP0211074 (n-methyl[(1s)-1-{4-[(2r,3r,4e,6e,8r,9r,10r,11e,13e,15z,17r,18s,19e,22e)-10,18-dihydroxy-8-methoxy-3,7,9,13,15,17,20,23-octamethyl-24-oxo-1-oxacyclotetracosa-4,6,11,13,15,19,22-heptaen-2-yl]-1,3-thiazol-2-yl}-3-methylbutoxy]carboximidic acid)

Structure for NP0211074 (n-methyl[(1s)-1-{4-[(2r,3r,4e,6e,8r,9r,10r,11e,13e,15z,17r,18s,19e,22e)-10,18-dihydroxy-8-methoxy-3,7,9,13,15,17,20,23-octamethyl-24-oxo-1-oxacyclotetracosa-4,6,11,13,15,19,22-heptaen-2-yl]-1,3-thiazol-2-yl}-3-methylbutoxy]carboximidic acid)

3D Structure for NP0211074 (n-methyl[(1s)-1-{4-[(2r,3r,4e,6e,8r,9r,10r,11e,13e,15z,17r,18s,19e,22e)-10,18-dihydroxy-8-methoxy-3,7,9,13,15,17,20,23-octamethyl-24-oxo-1-oxacyclotetracosa-4,6,11,13,15,19,22-heptaen-2-yl]-1,3-thiazol-2-yl}-3-methylbutoxy]carboximidic acid)