NP-MRD: Showing NP-Card for {[(3r,5s,6r,7s,8e,10s,11s,14e)-6,16,22,26-tetrahydroxy-5,11,25-trimethoxy-3,7,9,15-tetramethyl-20-thia-17,23-diazatricyclo[16.7.1.0¹⁹,²⁴]hexacosa-1(25),8,14,16,18(26),19(24),22-heptaen-10-yl]oxy}methanimidic acid (NP0289738)

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Record Information

Version

2.0

Created at

2022-09-09 20:04:19 UTC

Updated at

2022-09-09 20:04:20 UTC

NP-MRD ID

NP0289738

Secondary Accession Numbers

None

Natural Product Identification

Common Name

{[(3r,5s,6r,7s,8e,10s,11s,14e)-6,16,22,26-tetrahydroxy-5,11,25-trimethoxy-3,7,9,15-tetramethyl-20-thia-17,23-diazatricyclo[16.7.1.0¹⁹,²⁴]hexacosa-1(25),8,14,16,18(26),19(24),22-heptaen-10-yl]oxy}methanimidic acid

Description

{[(3R,5S,6R,7S,10S,11S,14E)-6,16,22,26-tetrahydroxy-5,11,25-trimethoxy-3,7,9,15-tetramethyl-20-thia-17,23-diazatricyclo[16.7.1.0¹⁹,²⁴]Hexacosa-1(26),8,14,16,18,22,24-heptaen-10-yl]oxy}methanimidic acid belongs to the class of organic compounds known as macrolactams. These are cyclic amides of amino carboxylic acids, having a 1-azacycloalkan-2-one structure, or analogues having unsaturation or heteroatoms replacing one or more carbon atoms of the ring. They are nitrogen analogues (the a nitrogen atom replacing the o atom of the cyclic carboxylic acid group ) of the naturally occurring macrolides. {[(3r,5s,6r,7s,8e,10s,11s,14e)-6,16,22,26-tetrahydroxy-5,11,25-trimethoxy-3,7,9,15-tetramethyl-20-thia-17,23-diazatricyclo[16.7.1.0¹⁹,²⁴]hexacosa-1(25),8,14,16,18(26),19(24),22-heptaen-10-yl]oxy}methanimidic acid is found in Streptomyces hygroscopicus. Based on a literature review very few articles have been published on {[(3R,5S,6R,7S,10S,11S,14E)-6,16,22,26-tetrahydroxy-5,11,25-trimethoxy-3,7,9,15-tetramethyl-20-thia-17,23-diazatricyclo[16.7.1.0¹⁹,²⁴]Hexacosa-1(26),8,14,16,18,22,24-heptaen-10-yl]oxy}methanimidic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092222042D          

 44 46  0  0  1  0            999 V2000
   -1.0259   -2.9346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.7864   -1.3333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5439   -1.6601    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
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    0.8018    0.6534    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
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  4 44  1  0  0  0  0
M  END

     RDKit          3D

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 23 70  1  0
M  END


  Mrv1652309092222042D          

 44 46  0  0  1  0            999 V2000
   -1.0259   -2.9346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2551   -2.6404    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1245   -1.8258    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6239   -1.5762    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7286   -0.6795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5321   -0.4925    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2810    0.0135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6907   -0.5138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7864   -1.3333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5439   -1.6601    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2057   -1.1676    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9632   -1.4945    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1100   -0.3482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3526   -0.0213    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    0.8018    0.6534    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5713    0.3557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8071   -0.4348    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4281    0.6402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5769    1.4517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0679    0.1194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8389    0.4131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4787   -0.1078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2496    0.1859    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.3808    1.0004    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1517    1.2941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8895   -0.3349    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.6604   -0.0412    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3002   -0.5620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0712   -0.2683    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.1691   -1.3765    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7583   -1.1494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3981   -1.6702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9874   -1.4431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8562   -2.2576    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.4961   -2.7784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0853   -2.5513    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9541   -3.3658    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4455   -2.0305    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3143   -2.8450    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5434   -3.1387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6745   -2.3242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0347   -1.8033    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1658   -0.9888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2637   -2.0970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  3  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
  8 14  1  0  0  0  0
 15  7  1  4  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  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
 23 24  1  6  0  0  0
 24 25  1  0  0  0  0
 23 26  1  0  0  0  0
 26 27  1  1  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 26 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  6  0  0  0
 34 36  1  0  0  0  0
 36 37  1  1  0  0  0
 36 38  1  0  0  0  0
 38 39  1  6  0  0  0
 39 40  1  0  0  0  0
 38 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  1  0  0  0
 42 44  1  0  0  0  0
  4 44  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0289738

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CO[C@H]1C[C@H](C)CC2=C(OC)C3=C(SCC(O)=N3)C(N=C(O)\C(C)=C\CC[C@H](OC)[C@@H](OC(O)=N)\C(C)=C\[C@H](C)[C@H]1O)=C2O

> <INCHI_IDENTIFIER>
InChI=1S/C31H45N3O9S/c1-15-11-19-26(37)23(29-24(28(19)42-7)33-22(35)14-44-29)34-30(38)16(2)9-8-10-20(40-5)27(43-31(32)39)18(4)13-17(3)25(36)21(12-15)41-6/h9,13,15,17,20-21,25,27,36-37H,8,10-12,14H2,1-7H3,(H2,32,39)(H,33,35)(H,34,38)/b16-9+,18-13+/t15-,17+,20+,21+,25-,27+/m1/s1

> <INCHI_KEY>
QGZAKVRVQXKUBI-KDEKQAKKSA-N

> <FORMULA>
C31H45N3O9S

> <MOLECULAR_WEIGHT>
635.77

> <EXACT_MASS>
635.287651215

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
89

> <JCHEM_AVERAGE_POLARIZABILITY>
67.55988812335872

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
{[(3R,5S,6R,7S,8E,10S,11S,14E)-6,16,22,26-tetrahydroxy-5,11,25-trimethoxy-3,7,9,15-tetramethyl-20-thia-17,23-diazatricyclo[16.7.1.0^{19,24}]hexacosa-1(25),8,14,16,18(26),19(24),22-heptaen-10-yl]oxy}methanimidic acid

> <JCHEM_LOGP>
2.328806782987558

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
-0.2646923775583394

> <JCHEM_PKA_STRONGEST_ACIDIC>
-4.163966300127147

> <JCHEM_PKA_STRONGEST_BASIC>
15.03372051132217

> <JCHEM_POLAR_SURFACE_AREA>
186.64

> <JCHEM_REFRACTIVITY>
184.87590000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
{[(3R,5S,6R,7S,8E,10S,11S,14E)-6,16,22,26-tetrahydroxy-5,11,25-trimethoxy-3,7,9,15-tetramethyl-20-thia-17,23-diazatricyclo[16.7.1.0^{19,24}]hexacosa-1(25),8,14,16,18(26),19(24),22-heptaen-10-yl]oxy}methanimidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.915  -5.478   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -0.476  -4.929   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -0.232  -3.408   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.165  -2.942   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.360  -1.268   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       2.860  -0.919   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       0.525   0.025   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.289  -0.959   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.468  -2.489   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0      -2.882  -3.099   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0      -4.117  -2.180   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -5.531  -2.790   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -3.939  -0.650   0.000  0.00  0.00           C+0
HETATM   14  S   UNK     0      -2.525  -0.040   0.000  0.00  0.00           S+0
HETATM   15  N   UNK     0       1.497   1.220   0.000  0.00  0.00           N+0
HETATM   16  C   UNK     0       2.933   0.664   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       3.373  -0.812   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       4.532   1.195   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.810   2.710   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.727   0.223   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.166   0.771   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.360  -0.201   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.799   0.347   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      10.044   1.868   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      11.483   2.416   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      10.994  -0.625   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      12.433  -0.077   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      13.627  -1.049   0.000  0.00  0.00           C+0
HETATM   29  N   UNK     0      15.066  -0.501   0.000  0.00  0.00           N+0
HETATM   30  O   UNK     0      13.382  -2.570   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      10.749  -2.146   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      11.943  -3.118   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       9.310  -2.694   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       9.065  -4.214   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      10.259  -5.186   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       7.626  -4.762   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       7.381  -6.283   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       6.432  -3.790   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       6.187  -5.311   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       4.748  -5.859   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       4.992  -4.338   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       3.798  -3.366   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       4.043  -1.846   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       2.359  -3.914   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    9                                                  
CONECT    4    3    5   44                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   15                                                  
CONECT    8    7    9   14                                                  
CONECT    9    8    3   10                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13    8                                                       
CONECT   15    7   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                                                       
CONECT   23   22   24   26                                                  
CONECT   24   23   25                                                       
CONECT   25   24                                                            
CONECT   26   23   27   31                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28                                                            
CONECT   31   26   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34                                                       
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   39   41                                                  
CONECT   39   38   40                                                       
CONECT   40   39                                                            
CONECT   41   38   42                                                       
CONECT   42   41   43   44                                                  
CONECT   43   42                                                            
CONECT   44   42    4                                                       
MASTER        0    0    0    0    0    0    0    0   44    0   92    0
END

View in JSmol

Synonyms

Value	Source
{[(3R,5S,6R,7S,10S,11S,14E)-6,16,22,26-tetrahydroxy-5,11,25-trimethoxy-3,7,9,15-tetramethyl-20-thia-17,23-diazatricyclo[16.7.1.0,]hexacosa-1(26),8,14,16,18,22,24-heptaen-10-yl]oxy}methanimidate	Generator

Chemical Formula

C₃₁H₄₅N₃O₉S

Average Mass

635.7700 Da

Monoisotopic Mass

635.28765 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CO[C@H]1C[C@H](C)CC2=C(OC)C3=C(SCC(O)=N3)C(N=C(O)\C(C)=C\CC[C@H](OC)[C@@H](OC(O)=N)\C(C)=C\[C@H](C)[C@H]1O)=C2O

InChI Identifier

InChI=1S/C31H45N3O9S/c1-15-11-19-26(37)23(29-24(28(19)42-7)33-22(35)14-44-29)34-30(38)16(2)9-8-10-20(40-5)27(43-31(32)39)18(4)13-17(3)25(36)21(12-15)41-6/h9,13,15,17,20-21,25,27,36-37H,8,10-12,14H2,1-7H3,(H2,32,39)(H,33,35)(H,34,38)/b16-9+,18-13+/t15-,17+,20+,21+,25-,27+/m1/s1

InChI Key

QGZAKVRVQXKUBI-KDEKQAKKSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Streptomyces hygroscopicus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as macrolactams. These are cyclic amides of amino carboxylic acids, having a 1-azacycloalkan-2-one structure, or analogues having unsaturation or heteroatoms replacing one or more carbon atoms of the ring. They are nitrogen analogues (the a nitrogen atom replacing the o atom of the cyclic carboxylic acid group ) of the naturally occurring macrolides.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Macrolactams

Sub Class

Not Available

Direct Parent

Macrolactams

Alternative Parents

Substituents

Macrolactam
Benzothiazine
Anisole
Aryl thioether
Phenol ether
Alkyl aryl ether
Phenol
Alkylarylthioether
Para-thiazine
Benzenoid
Carbamic acid ester
Secondary carboxylic acid amide
Secondary alcohol
Carboxamide group
Lactam
Thioether
Azacycle
Organoheterocyclic compound
Carboxylic acid derivative
Dialkyl ether
Ether
Hydrocarbon derivative
Organopnictogen compound
Organonitrogen compound
Organooxygen compound
Carbonyl group
Organic oxygen compound
Organic nitrogen compound
Organic oxide
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic 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

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

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FoodDB ID

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KNApSAcK ID

Not Available

Chemspider ID

28289318

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

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Wikipedia Link

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METLIN ID

Not Available

PubChem Compound

53380950

PDB ID

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ChEBI ID

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Good Scents ID

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References

General References

LOTUS database [Link]

Showing NP-Card for {[(3r,5s,6r,7s,8e,10s,11s,14e)-6,16,22,26-tetrahydroxy-5,11,25-trimethoxy-3,7,9,15-tetramethyl-20-thia-17,23-diazatricyclo[16.7.1.0¹⁹,²⁴]hexacosa-1(25),8,14,16,18(26),19(24),22-heptaen-10-yl]oxy}methanimidic acid (NP0289738)

MOL for NP0289738 ({[(3r,5s,6r,7s,8e,10s,11s,14e)-6,16,22,26-tetrahydroxy-5,11,25-trimethoxy-3,7,9,15-tetramethyl-20-thia-17,23-diazatricyclo[16.7.1.0¹⁹,²⁴]hexacosa-1(25),8,14,16,18(26),19(24),22-heptaen-10-yl]oxy}methanimidic acid)

3D MOL for NP0289738 ({[(3r,5s,6r,7s,8e,10s,11s,14e)-6,16,22,26-tetrahydroxy-5,11,25-trimethoxy-3,7,9,15-tetramethyl-20-thia-17,23-diazatricyclo[16.7.1.0¹⁹,²⁴]hexacosa-1(25),8,14,16,18(26),19(24),22-heptaen-10-yl]oxy}methanimidic acid)

3D SDF for NP0289738 ({[(3r,5s,6r,7s,8e,10s,11s,14e)-6,16,22,26-tetrahydroxy-5,11,25-trimethoxy-3,7,9,15-tetramethyl-20-thia-17,23-diazatricyclo[16.7.1.0¹⁹,²⁴]hexacosa-1(25),8,14,16,18(26),19(24),22-heptaen-10-yl]oxy}methanimidic acid)

3D-SDF for NP0289738 ({[(3r,5s,6r,7s,8e,10s,11s,14e)-6,16,22,26-tetrahydroxy-5,11,25-trimethoxy-3,7,9,15-tetramethyl-20-thia-17,23-diazatricyclo[16.7.1.0¹⁹,²⁴]hexacosa-1(25),8,14,16,18(26),19(24),22-heptaen-10-yl]oxy}methanimidic acid)

PDB for NP0289738 ({[(3r,5s,6r,7s,8e,10s,11s,14e)-6,16,22,26-tetrahydroxy-5,11,25-trimethoxy-3,7,9,15-tetramethyl-20-thia-17,23-diazatricyclo[16.7.1.0¹⁹,²⁴]hexacosa-1(25),8,14,16,18(26),19(24),22-heptaen-10-yl]oxy}methanimidic acid)

3D PDB for NP0289738 ({[(3r,5s,6r,7s,8e,10s,11s,14e)-6,16,22,26-tetrahydroxy-5,11,25-trimethoxy-3,7,9,15-tetramethyl-20-thia-17,23-diazatricyclo[16.7.1.0¹⁹,²⁴]hexacosa-1(25),8,14,16,18(26),19(24),22-heptaen-10-yl]oxy}methanimidic acid)

SMILES for NP0289738 ({[(3r,5s,6r,7s,8e,10s,11s,14e)-6,16,22,26-tetrahydroxy-5,11,25-trimethoxy-3,7,9,15-tetramethyl-20-thia-17,23-diazatricyclo[16.7.1.0¹⁹,²⁴]hexacosa-1(25),8,14,16,18(26),19(24),22-heptaen-10-yl]oxy}methanimidic acid)

INCHI for NP0289738 ({[(3r,5s,6r,7s,8e,10s,11s,14e)-6,16,22,26-tetrahydroxy-5,11,25-trimethoxy-3,7,9,15-tetramethyl-20-thia-17,23-diazatricyclo[16.7.1.0¹⁹,²⁴]hexacosa-1(25),8,14,16,18(26),19(24),22-heptaen-10-yl]oxy}methanimidic acid)

Structure for NP0289738 ({[(3r,5s,6r,7s,8e,10s,11s,14e)-6,16,22,26-tetrahydroxy-5,11,25-trimethoxy-3,7,9,15-tetramethyl-20-thia-17,23-diazatricyclo[16.7.1.0¹⁹,²⁴]hexacosa-1(25),8,14,16,18(26),19(24),22-heptaen-10-yl]oxy}methanimidic acid)

3D Structure for NP0289738 ({[(3r,5s,6r,7s,8e,10s,11s,14e)-6,16,22,26-tetrahydroxy-5,11,25-trimethoxy-3,7,9,15-tetramethyl-20-thia-17,23-diazatricyclo[16.7.1.0¹⁹,²⁴]hexacosa-1(25),8,14,16,18(26),19(24),22-heptaen-10-yl]oxy}methanimidic acid)