NP-MRD: Showing NP-Card for (2r,3r,4s,6r)-6-{[(3e,5e,7s,8s,10e,13e,15e,19s)-2-hydroxy-7,11,13,19-tetramethyl-1-azacycloicosa-1,3,5,10,13,15-hexaen-8-yl]oxy}-2,4-dimethyloxane-3,4-diol (NP0281891)

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Record Information

Version

2.0

Created at

2022-09-09 08:30:11 UTC

Updated at

2022-09-09 08:30:12 UTC

NP-MRD ID

NP0281891

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,3r,4s,6r)-6-{[(3e,5e,7s,8s,10e,13e,15e,19s)-2-hydroxy-7,11,13,19-tetramethyl-1-azacycloicosa-1,3,5,10,13,15-hexaen-8-yl]oxy}-2,4-dimethyloxane-3,4-diol

Description

Vicenistatin M 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. Based on a literature review very few articles have been published on Vicenistatin M.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092210302D          

 36 37  0  0  1  0            999 V2000
    6.4302   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -6.6000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2868   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    5.0013   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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    7.1447   -0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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    7.3289    1.8695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3895    1.8695    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.2881    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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    7.8592   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -3.7125    0.0000 C   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
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
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  8  9  1  6  0  0  0
  8 10  1  0  0  0  0
 11 10  1  4  0  0  0
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 14 15  2  0  0  0  0
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 17 18  1  0  0  0  0
 18 19  1  6  0  0  0
 18 20  1  0  0  0  0
 20 21  1  1  0  0  0
 22 21  1  1  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
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 24 27  1  0  0  0  0
 27 28  1  6  0  0  0
 27 29  1  0  0  0  0
 29 30  1  1  0  0  0
 29 31  1  0  0  0  0
 22 31  1  0  0  0  0
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 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
  2 36  1  0  0  0  0
M  END

     RDKit          3D

 83 84  0  0  0  0  0  0  0  0999 V2000
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 18 58  1  1
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 19 60  1  0
 19 61  1  0
M  END


  Mrv1652309092210302D          

 36 37  0  0  1  0            999 V2000
    6.4302   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    8.5737   -0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.2881   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -3.7125    0.0000 C   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
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  8 10  1  0  0  0  0
 11 10  1  4  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  6  0  0  0
 18 20  1  0  0  0  0
 20 21  1  1  0  0  0
 22 21  1  1  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  1  0  0  0
 24 26  1  6  0  0  0
 24 27  1  0  0  0  0
 27 28  1  6  0  0  0
 27 29  1  0  0  0  0
 29 30  1  1  0  0  0
 29 31  1  0  0  0  0
 22 31  1  0  0  0  0
 20 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
  2 36  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0281891

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1O[C@H](C[C@](C)(O)[C@@H]1O)O[C@H]1C\C=C(C)\C\C(C)=C\C=C\CC[C@H](C)CN=C(O)\C=C\C=C\[C@@H]1C

> <INCHI_IDENTIFIER>
InChI=1S/C30H47NO5/c1-21-12-8-7-9-13-23(3)20-31-27(32)15-11-10-14-24(4)26(17-16-22(2)18-21)36-28-19-30(6,34)29(33)25(5)35-28/h7-8,10-12,14-16,23-26,28-29,33-34H,9,13,17-20H2,1-6H3,(H,31,32)/b8-7+,14-10+,15-11+,21-12+,22-16+/t23-,24-,25+,26-,28-,29+,30-/m0/s1

> <INCHI_KEY>
YVXZXDRTHFRUIX-LPLNQVICSA-N

> <FORMULA>
C30H47NO5

> <MOLECULAR_WEIGHT>
501.708

> <EXACT_MASS>
501.345423617

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
83

> <JCHEM_AVERAGE_POLARIZABILITY>
58.126472986248416

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,3R,4S,6R)-6-{[(3E,5E,7S,8S,10E,13E,15E,19S)-2-hydroxy-7,11,13,19-tetramethyl-1-azacycloicosa-1,3,5,10,13,15-hexaen-8-yl]oxy}-2,4-dimethyloxane-3,4-diol

> <JCHEM_LOGP>
5.083313170505196

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.99996255658398

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.047873888290063

> <JCHEM_PKA_STRONGEST_BASIC>
7.089452257146585

> <JCHEM_POLAR_SURFACE_AREA>
91.51000000000002

> <JCHEM_REFRACTIVITY>
150.52810000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3R,4S,6R)-6-{[(3E,5E,7S,8S,10E,13E,15E,19S)-2-hydroxy-7,11,13,19-tetramethyl-1-azacycloicosa-1,3,5,10,13,15-hexaen-8-yl]oxy}-2,4-dimethyloxane-3,4-diol

> <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      12.003  -6.930   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.337  -7.700   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      13.337  -9.240   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      12.003 -10.010   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      12.003 -11.550   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.669 -12.320   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.336 -11.550   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.002 -12.320   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.002 -13.860   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.668 -11.550   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0       6.668 -10.010   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0       8.002  -9.240   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       9.336 -10.010   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       8.002  -7.700   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.336  -6.930   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.336  -5.390   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.669  -4.620   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      10.669  -3.080   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      12.003  -2.310   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      12.003  -0.770   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      13.337  -0.000   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      13.337   1.540   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      14.670   2.310   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      13.681   3.490   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      15.660   3.490   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      16.004   1.540   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      17.338   2.310   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      16.004  -0.000   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      17.338  -0.770   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      14.670  -0.770   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      13.337  -3.080   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      13.337  -4.620   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      14.670  -5.390   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      16.004  -4.620   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      14.670  -6.930   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   36                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   32                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   31                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   26   27                                             
CONECT   25   24                                                            
CONECT   26   24                                                            
CONECT   27   24   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   22                                                       
CONECT   32   20   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34    2                                                       
MASTER        0    0    0    0    0    0    0    0   36    0   74    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₄₇NO₅

Average Mass

501.7080 Da

Monoisotopic Mass

501.34542 Da

IUPAC Name

(2R,3R,4S,6R)-6-{[(3E,5E,7S,8S,10E,13E,15E,19S)-2-hydroxy-7,11,13,19-tetramethyl-1-azacycloicosa-1,3,5,10,13,15-hexaen-8-yl]oxy}-2,4-dimethyloxane-3,4-diol

Traditional Name

(2R,3R,4S,6R)-6-{[(3E,5E,7S,8S,10E,13E,15E,19S)-2-hydroxy-7,11,13,19-tetramethyl-1-azacycloicosa-1,3,5,10,13,15-hexaen-8-yl]oxy}-2,4-dimethyloxane-3,4-diol

CAS Registry Number

Not Available

SMILES

C[C@H]1O[C@H](C[C@](C)(O)[C@@H]1O)O[C@H]1C\C=C(C)\C\C(C)=C\C=C\CC[C@H](C)CN=C(O)\C=C\C=C\[C@@H]1C

InChI Identifier

InChI=1S/C30H47NO5/c1-21-12-8-7-9-13-23(3)20-31-27(32)15-11-10-14-24(4)26(17-16-22(2)18-21)36-28-19-30(6,34)29(33)25(5)35-28/h7-8,10-12,14-16,23-26,28-29,33-34H,9,13,17-20H2,1-6H3,(H,31,32)/b8-7+,14-10+,15-11+,21-12+,22-16+/t23-,24-,25+,26-,28-,29+,30-/m0/s1

InChI Key

YVXZXDRTHFRUIX-LPLNQVICSA-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 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
Hexose monosaccharide
Glycosyl compound
O-glycosyl compound
Sugar acid
Monosaccharide
Oxane
Tertiary alcohol
1,2-diol
Carboxamide group
Lactam
Secondary carboxylic acid amide
Secondary alcohol
Acetal
Carboxylic acid derivative
Oxacycle
Azacycle
Organoheterocyclic compound
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Organic nitrogen compound
Organic oxygen compound
Alcohol
Carbonyl group
Organonitrogen compound
Organooxygen compound
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
logP	5.08	ChemAxon
pKa (Strongest Acidic)	5.05	ChemAxon
pKa (Strongest Basic)	7.09	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	91.51 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	150.53 m³·mol⁻¹	ChemAxon
Polarizability	58.13 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

C00015921

Chemspider ID

8566766

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10391324

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r,3r,4s,6r)-6-{[(3e,5e,7s,8s,10e,13e,15e,19s)-2-hydroxy-7,11,13,19-tetramethyl-1-azacycloicosa-1,3,5,10,13,15-hexaen-8-yl]oxy}-2,4-dimethyloxane-3,4-diol (NP0281891)

MOL for NP0281891 ((2r,3r,4s,6r)-6-{[(3e,5e,7s,8s,10e,13e,15e,19s)-2-hydroxy-7,11,13,19-tetramethyl-1-azacycloicosa-1,3,5,10,13,15-hexaen-8-yl]oxy}-2,4-dimethyloxane-3,4-diol)

3D MOL for NP0281891 ((2r,3r,4s,6r)-6-{[(3e,5e,7s,8s,10e,13e,15e,19s)-2-hydroxy-7,11,13,19-tetramethyl-1-azacycloicosa-1,3,5,10,13,15-hexaen-8-yl]oxy}-2,4-dimethyloxane-3,4-diol)

3D SDF for NP0281891 ((2r,3r,4s,6r)-6-{[(3e,5e,7s,8s,10e,13e,15e,19s)-2-hydroxy-7,11,13,19-tetramethyl-1-azacycloicosa-1,3,5,10,13,15-hexaen-8-yl]oxy}-2,4-dimethyloxane-3,4-diol)

3D-SDF for NP0281891 ((2r,3r,4s,6r)-6-{[(3e,5e,7s,8s,10e,13e,15e,19s)-2-hydroxy-7,11,13,19-tetramethyl-1-azacycloicosa-1,3,5,10,13,15-hexaen-8-yl]oxy}-2,4-dimethyloxane-3,4-diol)

PDB for NP0281891 ((2r,3r,4s,6r)-6-{[(3e,5e,7s,8s,10e,13e,15e,19s)-2-hydroxy-7,11,13,19-tetramethyl-1-azacycloicosa-1,3,5,10,13,15-hexaen-8-yl]oxy}-2,4-dimethyloxane-3,4-diol)

3D PDB for NP0281891 ((2r,3r,4s,6r)-6-{[(3e,5e,7s,8s,10e,13e,15e,19s)-2-hydroxy-7,11,13,19-tetramethyl-1-azacycloicosa-1,3,5,10,13,15-hexaen-8-yl]oxy}-2,4-dimethyloxane-3,4-diol)

SMILES for NP0281891 ((2r,3r,4s,6r)-6-{[(3e,5e,7s,8s,10e,13e,15e,19s)-2-hydroxy-7,11,13,19-tetramethyl-1-azacycloicosa-1,3,5,10,13,15-hexaen-8-yl]oxy}-2,4-dimethyloxane-3,4-diol)

INCHI for NP0281891 ((2r,3r,4s,6r)-6-{[(3e,5e,7s,8s,10e,13e,15e,19s)-2-hydroxy-7,11,13,19-tetramethyl-1-azacycloicosa-1,3,5,10,13,15-hexaen-8-yl]oxy}-2,4-dimethyloxane-3,4-diol)

Structure for NP0281891 ((2r,3r,4s,6r)-6-{[(3e,5e,7s,8s,10e,13e,15e,19s)-2-hydroxy-7,11,13,19-tetramethyl-1-azacycloicosa-1,3,5,10,13,15-hexaen-8-yl]oxy}-2,4-dimethyloxane-3,4-diol)

3D Structure for NP0281891 ((2r,3r,4s,6r)-6-{[(3e,5e,7s,8s,10e,13e,15e,19s)-2-hydroxy-7,11,13,19-tetramethyl-1-azacycloicosa-1,3,5,10,13,15-hexaen-8-yl]oxy}-2,4-dimethyloxane-3,4-diol)