NP-MRD: Showing NP-Card for n-[(1e,3z,5r)-5-[(2r,4e,6e,10s,11s,12e,14s,18e)-11,14-dihydroxy-10-(c-hydroxycarbonimidoyloxy)-4-methyl-20-oxo-1-oxacycloicosa-4,6,12,18-tetraen-2-yl]-3-methylhexa-1,3-dien-1-yl]-3-methylbut-2-enimidic acid (NP0302308)

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Record Information

Version

2.0

Created at

2022-09-10 15:46:37 UTC

Updated at

2022-09-10 15:46:37 UTC

NP-MRD ID

NP0302308

Secondary Accession Numbers

None

Natural Product Identification

Common Name

n-[(1e,3z,5r)-5-[(2r,4e,6e,10s,11s,12e,14s,18e)-11,14-dihydroxy-10-(c-hydroxycarbonimidoyloxy)-4-methyl-20-oxo-1-oxacycloicosa-4,6,12,18-tetraen-2-yl]-3-methylhexa-1,3-dien-1-yl]-3-methylbut-2-enimidic acid

Description

Palmerolide G 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. n-[(1e,3z,5r)-5-[(2r,4e,6e,10s,11s,12e,14s,18e)-11,14-dihydroxy-10-(c-hydroxycarbonimidoyloxy)-4-methyl-20-oxo-1-oxacycloicosa-4,6,12,18-tetraen-2-yl]-3-methylhexa-1,3-dien-1-yl]-3-methylbut-2-enimidic acid is found in Synoicum adareanum. Based on a literature review very few articles have been published on Palmerolide G.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102217462D          

 42 42  0  0  1  0            999 V2000
    7.9358    5.4101    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1112    5.4352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7206    6.1619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6772    4.7336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8526    4.7586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4619    5.4853    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4185    4.0570    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.5939    4.0821    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1599    3.3805    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3353    3.4055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9447    4.1322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9013    2.7039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2919    1.9772    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1165    1.9522    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    1.2756    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6825    1.2506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0731    0.5239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6391   -0.1777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8977    0.4988    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.0500    0.6492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.2086    1.3257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6427    2.0273    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2520    2.7540    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4673    2.0023    0.0000 O   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
  2  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  4  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
 15 13  1  6  0  0  0
 15 16  1  0  0  0  0
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 17 19  2  0  0  0  0
 19 20  1  0  0  0  0
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 21 22  1  0  0  0  0
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 25 26  1  0  0  0  0
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 38 39  2  0  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 40 42  1  0  0  0  0
 15 42  1  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652309102217462D          

 42 42  0  0  1  0            999 V2000
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    2.9013    2.7039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2919    1.9772    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1165    1.9522    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    1.2756    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6825    1.2506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0731    0.5239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6391   -0.1777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8977    0.4988    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2883   -0.2278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8543   -0.9294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2449   -1.6561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8109   -2.3577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9863   -2.3327    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5523   -3.0343    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7277   -3.0092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2937   -3.7108    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3371   -2.2826    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5957   -1.6060    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0297   -0.9044    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7711   -1.5809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3805   -0.8543    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5559   -0.8292    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1218   -1.5308    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1652   -0.1025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3406   -0.0775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0500    0.6492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3840    1.3508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2086    1.3257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6427    2.0273    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2520    2.7540    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4673    2.0023    0.0000 O   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
  2  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  4  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
 15 13  1  6  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  6  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 24 29  1  0  0  0  0
 29 30  1  6  0  0  0
 29 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  1  0  0  0
 33 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 40 42  1  0  0  0  0
 15 42  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0302308

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H](\C=C(\C)/C=C/N=C(O)C=C(C)C)[C@H]1C\C(C)=C\C=C\CC[C@H](OC(O)=N)[C@@H](O)\C=C\[C@@H](O)CCC\C=C\C(=O)O1

> <INCHI_IDENTIFIER>
InChI=1S/C33H48N2O7/c1-23(2)20-31(38)35-19-18-25(4)21-26(5)30-22-24(3)12-8-6-10-14-29(42-33(34)40)28(37)17-16-27(36)13-9-7-11-15-32(39)41-30/h6,8,11-12,15-21,26-30,36-37H,7,9-10,13-14,22H2,1-5H3,(H2,34,40)(H,35,38)/b8-6+,15-11+,17-16+,19-18+,24-12+,25-21-/t26-,27+,28+,29+,30-/m1/s1

> <INCHI_KEY>
HEOKDDVDVGNHMR-YRFNEGEBSA-N

> <FORMULA>
C33H48N2O7

> <MOLECULAR_WEIGHT>
584.754

> <EXACT_MASS>
584.346151894

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
90

> <JCHEM_AVERAGE_POLARIZABILITY>
63.28069692631031

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
N-[(1E,3Z,5R)-5-[(2R,4E,6E,10S,11S,12E,14S,18E)-11,14-dihydroxy-10-(C-hydroxycarbonimidoyloxy)-4-methyl-20-oxo-1-oxacycloicosa-4,6,12,18-tetraen-2-yl]-3-methylhexa-1,3-dien-1-yl]-3-methylbut-2-enimidic acid

> <JCHEM_LOGP>
3.2226165805138542

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
5.403133967856867

> <JCHEM_PKA_STRONGEST_ACIDIC>
-4.091250444673128

> <JCHEM_PKA_STRONGEST_BASIC>
10.935061274618764

> <JCHEM_POLAR_SURFACE_AREA>
152.66000000000003

> <JCHEM_REFRACTIVITY>
182.33840000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
N-[(1E,3Z,5R)-5-[(2R,4E,6E,10S,11S,12E,14S,18E)-11,14-dihydroxy-10-(C-hydroxycarbonimidoyloxy)-4-methyl-20-oxo-1-oxacycloicosa-4,6,12,18-tetraen-2-yl]-3-methylhexa-1,3-dien-1-yl]-3-methylbut-2-enimidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0      14.813  10.099   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.274  10.146   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      12.545  11.502   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      12.464   8.836   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.925   8.883   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      10.196  10.239   0.000  0.00  0.00           O+0
HETATM    7  N   UNK     0      10.115   7.573   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0       8.575   7.620   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.765   6.310   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.226   6.357   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.497   7.713   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.416   5.047   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.145   3.691   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.684   3.644   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.335   2.381   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.874   2.334   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.603   0.978   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.793  -0.332   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.142   0.931   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.872  -0.425   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.061  -1.735   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       9.791  -3.091   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.980  -4.401   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       7.441  -4.354   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       6.631  -5.664   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       5.092  -5.617   0.000  0.00  0.00           C+0
HETATM   27  N   UNK     0       4.282  -6.927   0.000  0.00  0.00           N+0
HETATM   28  O   UNK     0       4.363  -4.261   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       6.712  -2.998   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       7.522  -1.688   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       5.173  -2.951   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       4.444  -1.595   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       2.904  -1.548   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       2.094  -2.858   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       2.175  -0.191   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       0.636  -0.145   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -0.093   1.212   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       0.717   2.521   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       2.256   2.475   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       3.066   3.784   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       2.337   5.141   0.000  0.00  0.00           O+0
HETATM   42  O   UNK     0       4.606   3.738   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   42                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   29                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26                                                            
CONECT   29   24   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40   15                                                       
MASTER        0    0    0    0    0    0    0    0   42    0   84    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₃H₄₈N₂O₇

Average Mass

584.7540 Da

Monoisotopic Mass

584.34615 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@H](\C=C(\C)/C=C/N=C(O)C=C(C)C)[C@H]1C\C(C)=C\C=C\CC[C@H](OC(O)=N)[C@@H](O)\C=C\[C@@H](O)CCC\C=C\C(=O)O1

InChI Identifier

InChI=1S/C33H48N2O7/c1-23(2)20-31(38)35-19-18-25(4)21-26(5)30-22-24(3)12-8-6-10-14-29(42-33(34)40)28(37)17-16-27(36)13-9-7-11-15-32(39)41-30/h6,8,11-12,15-21,26-30,36-37H,7,9-10,13-14,22H2,1-5H3,(H2,34,40)(H,35,38)/b8-6+,15-11+,17-16+,19-18+,24-12+,25-21-/t26-,27+,28+,29+,30-/m1/s1

InChI Key

HEOKDDVDVGNHMR-YRFNEGEBSA-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
Synoicum adareanum	LOTUS Database	35616633

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
N-acyl-amine
Carbamic acid ester
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Carboxamide group
Carboxylic acid ester
Lactone
Secondary alcohol
Secondary carboxylic acid amide
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Alcohol
Organooxygen compound
Organonitrogen compound
Organic oxygen compound
Organic nitrogen compound
Carbonyl group
Organic oxide
Hydrocarbon derivative
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic 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

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

27025771

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

54764674

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for n-[(1e,3z,5r)-5-[(2r,4e,6e,10s,11s,12e,14s,18e)-11,14-dihydroxy-10-(c-hydroxycarbonimidoyloxy)-4-methyl-20-oxo-1-oxacycloicosa-4,6,12,18-tetraen-2-yl]-3-methylhexa-1,3-dien-1-yl]-3-methylbut-2-enimidic acid (NP0302308)

MOL for NP0302308 (n-[(1e,3z,5r)-5-[(2r,4e,6e,10s,11s,12e,14s,18e)-11,14-dihydroxy-10-(c-hydroxycarbonimidoyloxy)-4-methyl-20-oxo-1-oxacycloicosa-4,6,12,18-tetraen-2-yl]-3-methylhexa-1,3-dien-1-yl]-3-methylbut-2-enimidic acid)

3D MOL for NP0302308 (n-[(1e,3z,5r)-5-[(2r,4e,6e,10s,11s,12e,14s,18e)-11,14-dihydroxy-10-(c-hydroxycarbonimidoyloxy)-4-methyl-20-oxo-1-oxacycloicosa-4,6,12,18-tetraen-2-yl]-3-methylhexa-1,3-dien-1-yl]-3-methylbut-2-enimidic acid)

3D SDF for NP0302308 (n-[(1e,3z,5r)-5-[(2r,4e,6e,10s,11s,12e,14s,18e)-11,14-dihydroxy-10-(c-hydroxycarbonimidoyloxy)-4-methyl-20-oxo-1-oxacycloicosa-4,6,12,18-tetraen-2-yl]-3-methylhexa-1,3-dien-1-yl]-3-methylbut-2-enimidic acid)

3D-SDF for NP0302308 (n-[(1e,3z,5r)-5-[(2r,4e,6e,10s,11s,12e,14s,18e)-11,14-dihydroxy-10-(c-hydroxycarbonimidoyloxy)-4-methyl-20-oxo-1-oxacycloicosa-4,6,12,18-tetraen-2-yl]-3-methylhexa-1,3-dien-1-yl]-3-methylbut-2-enimidic acid)

PDB for NP0302308 (n-[(1e,3z,5r)-5-[(2r,4e,6e,10s,11s,12e,14s,18e)-11,14-dihydroxy-10-(c-hydroxycarbonimidoyloxy)-4-methyl-20-oxo-1-oxacycloicosa-4,6,12,18-tetraen-2-yl]-3-methylhexa-1,3-dien-1-yl]-3-methylbut-2-enimidic acid)

3D PDB for NP0302308 (n-[(1e,3z,5r)-5-[(2r,4e,6e,10s,11s,12e,14s,18e)-11,14-dihydroxy-10-(c-hydroxycarbonimidoyloxy)-4-methyl-20-oxo-1-oxacycloicosa-4,6,12,18-tetraen-2-yl]-3-methylhexa-1,3-dien-1-yl]-3-methylbut-2-enimidic acid)

SMILES for NP0302308 (n-[(1e,3z,5r)-5-[(2r,4e,6e,10s,11s,12e,14s,18e)-11,14-dihydroxy-10-(c-hydroxycarbonimidoyloxy)-4-methyl-20-oxo-1-oxacycloicosa-4,6,12,18-tetraen-2-yl]-3-methylhexa-1,3-dien-1-yl]-3-methylbut-2-enimidic acid)

INCHI for NP0302308 (n-[(1e,3z,5r)-5-[(2r,4e,6e,10s,11s,12e,14s,18e)-11,14-dihydroxy-10-(c-hydroxycarbonimidoyloxy)-4-methyl-20-oxo-1-oxacycloicosa-4,6,12,18-tetraen-2-yl]-3-methylhexa-1,3-dien-1-yl]-3-methylbut-2-enimidic acid)

Structure for NP0302308 (n-[(1e,3z,5r)-5-[(2r,4e,6e,10s,11s,12e,14s,18e)-11,14-dihydroxy-10-(c-hydroxycarbonimidoyloxy)-4-methyl-20-oxo-1-oxacycloicosa-4,6,12,18-tetraen-2-yl]-3-methylhexa-1,3-dien-1-yl]-3-methylbut-2-enimidic acid)

3D Structure for NP0302308 (n-[(1e,3z,5r)-5-[(2r,4e,6e,10s,11s,12e,14s,18e)-11,14-dihydroxy-10-(c-hydroxycarbonimidoyloxy)-4-methyl-20-oxo-1-oxacycloicosa-4,6,12,18-tetraen-2-yl]-3-methylhexa-1,3-dien-1-yl]-3-methylbut-2-enimidic acid)