NP-MRD: Showing NP-Card for (3s,4r,5r,7s,9s,10r,12s,13r,14r,16s,21s,22r,23r,24r)-24-[(1r,2s,3e)-1,2-dihydroxy-3-methylpent-3-en-1-yl]-22,23,28-trihydroxy-5,7,14,21-tetramethyl-11,15,26-trioxa-25-azahexacyclo[23.2.2.0³,¹³.0⁴,⁹.0¹⁰,¹².0¹⁴,¹⁶]nonacos-1(28)-ene-2,27-dione (NP0317722)

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Record Information

Version

2.0

Created at

2022-09-11 17:45:32 UTC

Updated at

2022-09-11 17:45:32 UTC

NP-MRD ID

NP0317722

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3s,4r,5r,7s,9s,10r,12s,13r,14r,16s,21s,22r,23r,24r)-24-[(1r,2s,3e)-1,2-dihydroxy-3-methylpent-3-en-1-yl]-22,23,28-trihydroxy-5,7,14,21-tetramethyl-11,15,26-trioxa-25-azahexacyclo[23.2.2.0³,¹³.0⁴,⁹.0¹⁰,¹².0¹⁴,¹⁶]nonacos-1(28)-ene-2,27-dione

Description

Not Available

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112219452D          

 46 51  0  0  1  0            999 V2000
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M  END

     RDKit          3D

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 20 75  1  6
 23 76  1  0
 23 77  1  0
 23 78  1  0
 24 79  1  6
 25 80  1  1
 27 81  1  1
 28 82  1  6
 29 83  1  0
 29 84  1  0
 30 85  1  6
 31 86  1  0
 31 87  1  0
 31 88  1  0
 32 89  1  0
 32 90  1  0
 33 91  1  6
 34 92  1  0
 34 93  1  0
 34 94  1  0
 35 95  1  6
 36 96  1  1
 41 97  1  0
 42 98  1  0
 42 99  1  0
M  END


  Mrv1652309112219452D          

 46 51  0  0  1  0            999 V2000
   -1.5159   -2.3684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7225   -2.1424    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5215   -1.3422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1140   -0.7681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2719   -1.1162    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8644   -1.6903    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4729   -0.3161    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1195    0.2581    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2663   -0.0901    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1442    0.7534    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3247    0.8485    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4682    1.5766    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7894    2.0456    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1143    2.1624    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7013    2.8766    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9599    2.4353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7852    2.3655    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5327    2.0020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0980    1.3934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4054    0.6220    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.1243    0.2171    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4142   -0.2029    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.0494   -0.7294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1305   -0.9857    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.9405   -1.1426    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.7504   -1.2995    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2095   -1.9225    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.6686   -2.5455    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.9377   -3.3253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3968   -3.9483    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.6658   -4.7282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5869   -3.7914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3178   -3.0115    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5079   -2.8545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8587   -2.3885    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5896   -1.6086    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8431   -2.0254    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3120   -2.6568    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9625   -2.0053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1646   -2.2667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0041   -3.0759    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5434   -1.7346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6190   -0.8988    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4073   -0.6552    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0446   -1.1687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8053   -0.8494    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  1  0  0  0
  5  7  1  0  0  0  0
  7  8  1  6  0  0  0
  9  7  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  1  1  0  0  0
 10 12  1  0  0  0  0
 12 13  1  6  0  0  0
 12 14  1  0  0  0  0
 14 15  1  1  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  6  0  0  0
 21 22  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  1  0  0  0
 24 22  1  1  0  0  0
 24 25  1  0  0  0  0
 25 26  1  6  0  0  0
 27 26  1  6  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  1  0  0  0
 29 30  1  0  0  0  0
 30 31  1  1  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  1  0  0  0
 35 33  1  1  0  0  0
 28 35  1  0  0  0  0
 35 36  1  0  0  0  0
 24 36  1  0  0  0  0
 36 37  1  6  0  0  0
 37 38  2  0  0  0  0
 37 39  1  0  0  0  0
 39 40  2  0  0  0  0
 40 41  1  0  0  0  0
 40 42  1  0  0  0  0
 42 43  1  0  0  0  0
  9 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 39 45  1  0  0  0  0
 45 46  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0317722

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C=C(/C)[C@H](O)[C@H](O)[C@H]1[C@@H](O)[C@H](O)[C@@H](C)CCCC[C@@H]2O[C@]2(C)[C@H]2[C@@H]3O[C@@H]3[C@H]3C[C@@H](C)C[C@@H](C)[C@H]3[C@@H]2C(=O)C2=C(O)CN1OC2=O

> <INCHI_IDENTIFIER>
InChI=1S/C35H53NO10/c1-7-16(3)27(38)30(41)26-31(42)28(39)17(4)10-8-9-11-21-35(6,45-21)25-24(29(40)23-20(37)14-36(26)46-34(23)43)22-18(5)12-15(2)13-19(22)32-33(25)44-32/h7,15,17-19,21-22,24-28,30-33,37-39,41-42H,8-14H2,1-6H3/b16-7+/t15-,17-,18+,19-,21-,22+,24-,25+,26-,27-,28+,30+,31+,32+,33-,35-/m0/s1

> <INCHI_KEY>
ZEXKBCGEARGIOX-IGRLKBMTSA-N

> <FORMULA>
C35H53NO10

> <MOLECULAR_WEIGHT>
647.806

> <EXACT_MASS>
647.366946911

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
99

> <JCHEM_AVERAGE_POLARIZABILITY>
70.26483345479414

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3S,4R,5R,7S,9S,10R,12S,13R,14R,16S,21S,22R,23R,24R)-24-[(1R,2S,3E)-1,2-dihydroxy-3-methylpent-3-en-1-yl]-22,23,28-trihydroxy-5,7,14,21-tetramethyl-11,15,26-trioxa-25-azahexacyclo[23.2.2.0^{3,13}.0^{4,9}.0^{10,12}.0^{14,16}]nonacos-1(28)-ene-2,27-dione

> <JCHEM_LOGP>
2.738993875666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
12.944115495844809

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.8665701280680316

> <JCHEM_PKA_STRONGEST_BASIC>
0.40443943246627284

> <JCHEM_POLAR_SURFACE_AREA>
172.82

> <JCHEM_REFRACTIVITY>
168.71840000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(3S,4R,5R,7S,9S,10R,12S,13R,14R,16S,21S,22R,23R,24R)-24-[(1R,2S,3E)-1,2-dihydroxy-3-methylpent-3-en-1-yl]-22,23,28-trihydroxy-5,7,14,21-tetramethyl-11,15,26-trioxa-25-azahexacyclo[23.2.2.0^{3,13}.0^{4,9}.0^{10,12}.0^{14,16}]nonacos-1(28)-ene-2,27-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0      -2.830  -4.421   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.349  -3.999   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.973  -2.506   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.079  -1.434   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.508  -2.084   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       1.614  -3.155   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       0.883  -0.590   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -0.223   0.482   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       2.364  -0.168   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.136   1.406   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       0.606   1.584   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       2.741   2.943   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       1.474   3.818   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       3.947   4.037   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.176   5.370   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.525   4.546   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.066   4.416   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.461   3.737   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.516   2.601   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.090   1.161   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      11.432   0.405   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      10.107  -0.379   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      11.292  -1.362   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.577  -1.840   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      11.089  -2.133   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      12.601  -2.426   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      11.591  -3.589   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      10.581  -4.752   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      11.084  -6.207   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      10.074  -7.370   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      10.576  -8.826   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       8.562  -7.077   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       8.060  -5.621   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       6.548  -5.328   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       9.070  -4.459   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       8.567  -3.003   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       7.174  -3.781   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       6.182  -4.959   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       5.530  -3.743   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       4.041  -4.231   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       3.741  -5.742   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       2.881  -3.238   0.000  0.00  0.00           C+0
HETATM   43  N   UNK     0       3.022  -1.678   0.000  0.00  0.00           N+0
HETATM   44  O   UNK     0       4.494  -1.223   0.000  0.00  0.00           O+0
HETATM   45  C   UNK     0       5.683  -2.182   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0       7.103  -1.586   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   43                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20   22                                                       
CONECT   22   21   20   23   24                                             
CONECT   23   22                                                            
CONECT   24   22   25   36                                                  
CONECT   25   24   26   27                                                  
CONECT   26   25   27                                                       
CONECT   27   26   25   28                                                  
CONECT   28   27   29   35                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   28   36                                                  
CONECT   36   35   24   37                                                  
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40   45                                                  
CONECT   40   39   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40   43                                                       
CONECT   43   42    9   44                                                  
CONECT   44   43   45                                                       
CONECT   45   44   39   46                                                  
CONECT   46   45                                                            
MASTER        0    0    0    0    0    0    0    0   46    0  102    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₅H₅₃NO₁₀

Average Mass

647.8060 Da

Monoisotopic Mass

647.36695 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C\C=C(/C)[C@H](O)[C@H](O)[C@H]1[C@@H](O)[C@H](O)[C@@H](C)CCCC[C@@H]2O[C@]2(C)[C@H]2[C@@H]3O[C@@H]3[C@H]3C[C@@H](C)C[C@@H](C)[C@H]3[C@@H]2C(=O)C2=C(O)CN1OC2=O

InChI Identifier

InChI=1S/C35H53NO10/c1-7-16(3)27(38)30(41)26-31(42)28(39)17(4)10-8-9-11-21-35(6,45-21)25-24(29(40)23-20(37)14-36(26)46-34(23)43)22-18(5)12-15(2)13-19(22)32-33(25)44-32/h7,15,17-19,21-22,24-28,30-33,37-39,41-42H,8-14H2,1-6H3/b16-7+/t15-,17-,18+,19-,21-,22+,24-,25+,26-,27-,28+,30+,31+,32+,33-,35-/m0/s1

InChI Key

ZEXKBCGEARGIOX-IGRLKBMTSA-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

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Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
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Predicted Properties

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General References

LOTUS database [Link]

Showing NP-Card for (3s,4r,5r,7s,9s,10r,12s,13r,14r,16s,21s,22r,23r,24r)-24-[(1r,2s,3e)-1,2-dihydroxy-3-methylpent-3-en-1-yl]-22,23,28-trihydroxy-5,7,14,21-tetramethyl-11,15,26-trioxa-25-azahexacyclo[23.2.2.0³,¹³.0⁴,⁹.0¹⁰,¹².0¹⁴,¹⁶]nonacos-1(28)-ene-2,27-dione (NP0317722)

MOL for NP0317722 ((3s,4r,5r,7s,9s,10r,12s,13r,14r,16s,21s,22r,23r,24r)-24-[(1r,2s,3e)-1,2-dihydroxy-3-methylpent-3-en-1-yl]-22,23,28-trihydroxy-5,7,14,21-tetramethyl-11,15,26-trioxa-25-azahexacyclo[23.2.2.0³,¹³.0⁴,⁹.0¹⁰,¹².0¹⁴,¹⁶]nonacos-1(28)-ene-2,27-dione)

3D MOL for NP0317722 ((3s,4r,5r,7s,9s,10r,12s,13r,14r,16s,21s,22r,23r,24r)-24-[(1r,2s,3e)-1,2-dihydroxy-3-methylpent-3-en-1-yl]-22,23,28-trihydroxy-5,7,14,21-tetramethyl-11,15,26-trioxa-25-azahexacyclo[23.2.2.0³,¹³.0⁴,⁹.0¹⁰,¹².0¹⁴,¹⁶]nonacos-1(28)-ene-2,27-dione)

3D SDF for NP0317722 ((3s,4r,5r,7s,9s,10r,12s,13r,14r,16s,21s,22r,23r,24r)-24-[(1r,2s,3e)-1,2-dihydroxy-3-methylpent-3-en-1-yl]-22,23,28-trihydroxy-5,7,14,21-tetramethyl-11,15,26-trioxa-25-azahexacyclo[23.2.2.0³,¹³.0⁴,⁹.0¹⁰,¹².0¹⁴,¹⁶]nonacos-1(28)-ene-2,27-dione)

3D-SDF for NP0317722 ((3s,4r,5r,7s,9s,10r,12s,13r,14r,16s,21s,22r,23r,24r)-24-[(1r,2s,3e)-1,2-dihydroxy-3-methylpent-3-en-1-yl]-22,23,28-trihydroxy-5,7,14,21-tetramethyl-11,15,26-trioxa-25-azahexacyclo[23.2.2.0³,¹³.0⁴,⁹.0¹⁰,¹².0¹⁴,¹⁶]nonacos-1(28)-ene-2,27-dione)

PDB for NP0317722 ((3s,4r,5r,7s,9s,10r,12s,13r,14r,16s,21s,22r,23r,24r)-24-[(1r,2s,3e)-1,2-dihydroxy-3-methylpent-3-en-1-yl]-22,23,28-trihydroxy-5,7,14,21-tetramethyl-11,15,26-trioxa-25-azahexacyclo[23.2.2.0³,¹³.0⁴,⁹.0¹⁰,¹².0¹⁴,¹⁶]nonacos-1(28)-ene-2,27-dione)

3D PDB for NP0317722 ((3s,4r,5r,7s,9s,10r,12s,13r,14r,16s,21s,22r,23r,24r)-24-[(1r,2s,3e)-1,2-dihydroxy-3-methylpent-3-en-1-yl]-22,23,28-trihydroxy-5,7,14,21-tetramethyl-11,15,26-trioxa-25-azahexacyclo[23.2.2.0³,¹³.0⁴,⁹.0¹⁰,¹².0¹⁴,¹⁶]nonacos-1(28)-ene-2,27-dione)

SMILES for NP0317722 ((3s,4r,5r,7s,9s,10r,12s,13r,14r,16s,21s,22r,23r,24r)-24-[(1r,2s,3e)-1,2-dihydroxy-3-methylpent-3-en-1-yl]-22,23,28-trihydroxy-5,7,14,21-tetramethyl-11,15,26-trioxa-25-azahexacyclo[23.2.2.0³,¹³.0⁴,⁹.0¹⁰,¹².0¹⁴,¹⁶]nonacos-1(28)-ene-2,27-dione)

INCHI for NP0317722 ((3s,4r,5r,7s,9s,10r,12s,13r,14r,16s,21s,22r,23r,24r)-24-[(1r,2s,3e)-1,2-dihydroxy-3-methylpent-3-en-1-yl]-22,23,28-trihydroxy-5,7,14,21-tetramethyl-11,15,26-trioxa-25-azahexacyclo[23.2.2.0³,¹³.0⁴,⁹.0¹⁰,¹².0¹⁴,¹⁶]nonacos-1(28)-ene-2,27-dione)

Structure for NP0317722 ((3s,4r,5r,7s,9s,10r,12s,13r,14r,16s,21s,22r,23r,24r)-24-[(1r,2s,3e)-1,2-dihydroxy-3-methylpent-3-en-1-yl]-22,23,28-trihydroxy-5,7,14,21-tetramethyl-11,15,26-trioxa-25-azahexacyclo[23.2.2.0³,¹³.0⁴,⁹.0¹⁰,¹².0¹⁴,¹⁶]nonacos-1(28)-ene-2,27-dione)

3D Structure for NP0317722 ((3s,4r,5r,7s,9s,10r,12s,13r,14r,16s,21s,22r,23r,24r)-24-[(1r,2s,3e)-1,2-dihydroxy-3-methylpent-3-en-1-yl]-22,23,28-trihydroxy-5,7,14,21-tetramethyl-11,15,26-trioxa-25-azahexacyclo[23.2.2.0³,¹³.0⁴,⁹.0¹⁰,¹².0¹⁴,¹⁶]nonacos-1(28)-ene-2,27-dione)