NP-MRD: Showing NP-Card for (2e)-2-methyl-n-[(2r)-1-oxo-1-{[(6z,8z,10z,16z)-3,15,22-trihydroxy-5-methoxy-14,16-dimethyl-2-azabicyclo[18.3.1]tetracosa-1(23),2,6,8,10,16,20(24),21-octaen-13-yl]oxy}propan-2-yl]but-2-enimidic acid (NP0264542)

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Record Information

Version

2.0

Created at

2022-09-08 08:06:21 UTC

Updated at

2022-09-08 08:06:21 UTC

NP-MRD ID

NP0264542

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2e)-2-methyl-n-[(2r)-1-oxo-1-{[(6z,8z,10z,16z)-3,15,22-trihydroxy-5-methoxy-14,16-dimethyl-2-azabicyclo[18.3.1]tetracosa-1(23),2,6,8,10,16,20(24),21-octaen-13-yl]oxy}propan-2-yl]but-2-enimidic acid

Description

Trienomycin F 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. (2e)-2-methyl-n-[(2r)-1-oxo-1-{[(6z,8z,10z,16z)-3,15,22-trihydroxy-5-methoxy-14,16-dimethyl-2-azabicyclo[18.3.1]tetracosa-1(23),2,6,8,10,16,20(24),21-octaen-13-yl]oxy}propan-2-yl]but-2-enimidic acid is found in Streptomyces rishiriensis. Based on a literature review very few articles have been published on Trienomycin F.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082210062D          

 43 44  0  0  1  0            999 V2000
   13.6078    5.7858    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652309082210062D          

 43 44  0  0  1  0            999 V2000
   13.6078    5.7858    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   13.6309    2.0052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2294    1.7266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3903    0.9174    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4482    1.9919    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.8279    1.4480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2733    0.7535    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4942   -0.0414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4709   -0.8660    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2056   -1.6472    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7219   -2.3155    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0627   -2.8115    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2865   -3.0912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4624   -3.1296    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3776   -3.9503    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6245   -4.2872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6636   -2.9235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9610   -2.4910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4287   -3.1213    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4171   -1.8707    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.0802   -1.1176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2556   -1.0944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8633   -0.3686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0387   -0.3454    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2958    0.3340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1205    0.3108    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5127   -0.4150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5049    1.2462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0829    1.8350    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8087    2.2272    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6178    2.3880    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5794    3.2121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4385    2.3032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6446    3.1021    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.1976    1.9803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6301    2.6829    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
  3  5  1  0  0  0  0
  5  6  1  4  0  0  0
  5  7  2  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
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 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
 21 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  2  0  0  0  0
 27 28  1  4  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 28 34  1  0  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  2  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
 40 41  1  0  0  0  0
 40 42  1  0  0  0  0
 13 42  1  0  0  0  0
 42 43  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0264542

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1CC(O)=NC2=CC(O)=CC(CC\C=C(C)/C(O)C(C)C(C\C=C/C=C\C=C/1)OC(=O)[C@@H](C)N=C(O)C(\C)=C\C)=C2

> <INCHI_IDENTIFIER>
InChI=1S/C34H46N2O7/c1-7-22(2)33(40)35-25(5)34(41)43-30-17-12-10-8-9-11-16-29(42-6)21-31(38)36-27-18-26(19-28(37)20-27)15-13-14-23(3)32(39)24(30)4/h7-12,14,16,18-20,24-25,29-30,32,37,39H,13,15,17,21H2,1-6H3,(H,35,40)(H,36,38)/b9-8-,12-10-,16-11-,22-7+,23-14-/t24?,25-,29?,30?,32?/m1/s1

> <INCHI_KEY>
AUGXWJMBIIIAAX-AXRTWXBGSA-N

> <FORMULA>
C34H46N2O7

> <MOLECULAR_WEIGHT>
594.749

> <EXACT_MASS>
594.330501829

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
89

> <JCHEM_AVERAGE_POLARIZABILITY>
65.19830655329258

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2E)-2-methyl-N-[(2R)-1-oxo-1-{[(6Z,8Z,10Z,16Z)-3,15,22-trihydroxy-5-methoxy-14,16-dimethyl-2-azabicyclo[18.3.1]tetracosa-1(23),2,6,8,10,16,20(24),21-octaen-13-yl]oxy}propan-2-yl]but-2-enimidic acid

> <JCHEM_LOGP>
6.580058042666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
6.322316185226333

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.0174644256015535

> <JCHEM_PKA_STRONGEST_BASIC>
2.2457513669173874

> <JCHEM_POLAR_SURFACE_AREA>
141.17000000000002

> <JCHEM_REFRACTIVITY>
175.40370000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2E)-2-methyl-N-[(2R)-1-oxo-1-{[(6Z,8Z,10Z,16Z)-3,15,22-trihydroxy-5-methoxy-14,16-dimethyl-2-azabicyclo[18.3.1]tetracosa-1(23),2,6,8,10,16,20(24),21-octaen-13-yl]oxy}propan-2-yl]but-2-enimidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0      25.401  10.800   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      25.702   9.290   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      24.544   8.274   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      23.085   8.770   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      24.844   6.764   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      26.302   6.269   0.000  0.00  0.00           O+0
HETATM    7  N   UNK     0      23.686   5.749   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0      23.986   4.238   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      25.444   3.743   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      22.828   3.223   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      23.129   1.713   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0      21.370   3.718   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      20.212   2.703   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      21.043   1.407   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      21.456  -0.077   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      21.412  -1.617   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      20.917  -3.075   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      20.014  -4.322   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      18.784  -5.248   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      17.335  -5.770   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      15.796  -5.842   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      15.638  -7.374   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      14.232  -8.003   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      14.305  -5.457   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      12.994  -4.650   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      12.000  -5.826   0.000  0.00  0.00           O+0
HETATM   27  N   UNK     0      11.979  -3.492   0.000  0.00  0.00           N+0
HETATM   28  C   UNK     0      11.350  -2.086   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       9.810  -2.043   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       9.078  -0.688   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       7.539  -0.645   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       9.885   0.623   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      11.425   0.580   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      12.157  -0.775   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      12.143   2.326   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      13.221   3.425   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      14.576   4.157   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      16.087   4.458   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      16.015   5.996   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      17.618   4.299   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      18.003   5.791   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0      19.036   3.697   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      19.843   5.008   0.000  0.00  0.00           C+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                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   42                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   24                                                  
CONECT   22   21   23                                                       
CONECT   23   22                                                            
CONECT   24   21   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27   29   34                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33   28                                                       
CONECT   35   33   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40   13   43                                                  
CONECT   43   42                                                            
MASTER        0    0    0    0    0    0    0    0   43    0   88    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₄H₄₆N₂O₇

Average Mass

594.7490 Da

Monoisotopic Mass

594.33050 Da

IUPAC Name

(2E)-2-methyl-N-[(2R)-1-oxo-1-{[(6Z,8Z,10Z,16Z)-3,15,22-trihydroxy-5-methoxy-14,16-dimethyl-2-azabicyclo[18.3.1]tetracosa-1(23),2,6,8,10,16,20(24),21-octaen-13-yl]oxy}propan-2-yl]but-2-enimidic acid

Traditional Name

(2E)-2-methyl-N-[(2R)-1-oxo-1-{[(6Z,8Z,10Z,16Z)-3,15,22-trihydroxy-5-methoxy-14,16-dimethyl-2-azabicyclo[18.3.1]tetracosa-1(23),2,6,8,10,16,20(24),21-octaen-13-yl]oxy}propan-2-yl]but-2-enimidic acid

CAS Registry Number

Not Available

SMILES

COC1CC(O)=NC2=CC(O)=CC(CC\C=C(C)/C(O)C(C)C(C\C=C/C=C\C=C/1)OC(=O)[C@@H](C)N=C(O)C(\C)=C\C)=C2

InChI Identifier

InChI=1S/C34H46N2O7/c1-7-22(2)33(40)35-25(5)34(41)43-30-17-12-10-8-9-11-16-29(42-6)21-31(38)36-27-18-26(19-28(37)20-27)15-13-14-23(3)32(39)24(30)4/h7-12,14,16,18-20,24-25,29-30,32,37,39H,13,15,17,21H2,1-6H3,(H,35,40)(H,36,38)/b9-8-,12-10-,16-11-,22-7+,23-14-/t24?,25-,29?,30?,32?/m1/s1

InChI Key

AUGXWJMBIIIAAX-AXRTWXBGSA-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 rishiriensis	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

Alpha-amino acid ester
Macrolactam
N-acyl-alpha amino acid or derivatives
Alanine or derivatives
Alpha-amino acid or derivatives
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Benzenoid
N-acyl-amine
Carboxamide group
Carboxylic acid ester
Lactam
Secondary carboxylic acid amide
Secondary alcohol
Carboxylic acid derivative
Dialkyl ether
Ether
Azacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Organic nitrogen compound
Hydrocarbon derivative
Alcohol
Organic oxygen compound
Carbonyl group
Organic oxide
Organooxygen compound
Organonitrogen compound
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
logP	6.58	ChemAxon
pKa (Strongest Acidic)	5.02	ChemAxon
pKa (Strongest Basic)	2.25	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	141.17 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	175.4 m³·mol⁻¹	ChemAxon
Polarizability	65.2 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

C00015657

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

101693189

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2e)-2-methyl-n-[(2r)-1-oxo-1-{[(6z,8z,10z,16z)-3,15,22-trihydroxy-5-methoxy-14,16-dimethyl-2-azabicyclo[18.3.1]tetracosa-1(23),2,6,8,10,16,20(24),21-octaen-13-yl]oxy}propan-2-yl]but-2-enimidic acid (NP0264542)

MOL for NP0264542 ((2e)-2-methyl-n-[(2r)-1-oxo-1-{[(6z,8z,10z,16z)-3,15,22-trihydroxy-5-methoxy-14,16-dimethyl-2-azabicyclo[18.3.1]tetracosa-1(23),2,6,8,10,16,20(24),21-octaen-13-yl]oxy}propan-2-yl]but-2-enimidic acid)

3D MOL for NP0264542 ((2e)-2-methyl-n-[(2r)-1-oxo-1-{[(6z,8z,10z,16z)-3,15,22-trihydroxy-5-methoxy-14,16-dimethyl-2-azabicyclo[18.3.1]tetracosa-1(23),2,6,8,10,16,20(24),21-octaen-13-yl]oxy}propan-2-yl]but-2-enimidic acid)

3D SDF for NP0264542 ((2e)-2-methyl-n-[(2r)-1-oxo-1-{[(6z,8z,10z,16z)-3,15,22-trihydroxy-5-methoxy-14,16-dimethyl-2-azabicyclo[18.3.1]tetracosa-1(23),2,6,8,10,16,20(24),21-octaen-13-yl]oxy}propan-2-yl]but-2-enimidic acid)

3D-SDF for NP0264542 ((2e)-2-methyl-n-[(2r)-1-oxo-1-{[(6z,8z,10z,16z)-3,15,22-trihydroxy-5-methoxy-14,16-dimethyl-2-azabicyclo[18.3.1]tetracosa-1(23),2,6,8,10,16,20(24),21-octaen-13-yl]oxy}propan-2-yl]but-2-enimidic acid)

PDB for NP0264542 ((2e)-2-methyl-n-[(2r)-1-oxo-1-{[(6z,8z,10z,16z)-3,15,22-trihydroxy-5-methoxy-14,16-dimethyl-2-azabicyclo[18.3.1]tetracosa-1(23),2,6,8,10,16,20(24),21-octaen-13-yl]oxy}propan-2-yl]but-2-enimidic acid)

3D PDB for NP0264542 ((2e)-2-methyl-n-[(2r)-1-oxo-1-{[(6z,8z,10z,16z)-3,15,22-trihydroxy-5-methoxy-14,16-dimethyl-2-azabicyclo[18.3.1]tetracosa-1(23),2,6,8,10,16,20(24),21-octaen-13-yl]oxy}propan-2-yl]but-2-enimidic acid)

SMILES for NP0264542 ((2e)-2-methyl-n-[(2r)-1-oxo-1-{[(6z,8z,10z,16z)-3,15,22-trihydroxy-5-methoxy-14,16-dimethyl-2-azabicyclo[18.3.1]tetracosa-1(23),2,6,8,10,16,20(24),21-octaen-13-yl]oxy}propan-2-yl]but-2-enimidic acid)

INCHI for NP0264542 ((2e)-2-methyl-n-[(2r)-1-oxo-1-{[(6z,8z,10z,16z)-3,15,22-trihydroxy-5-methoxy-14,16-dimethyl-2-azabicyclo[18.3.1]tetracosa-1(23),2,6,8,10,16,20(24),21-octaen-13-yl]oxy}propan-2-yl]but-2-enimidic acid)

Structure for NP0264542 ((2e)-2-methyl-n-[(2r)-1-oxo-1-{[(6z,8z,10z,16z)-3,15,22-trihydroxy-5-methoxy-14,16-dimethyl-2-azabicyclo[18.3.1]tetracosa-1(23),2,6,8,10,16,20(24),21-octaen-13-yl]oxy}propan-2-yl]but-2-enimidic acid)

3D Structure for NP0264542 ((2e)-2-methyl-n-[(2r)-1-oxo-1-{[(6z,8z,10z,16z)-3,15,22-trihydroxy-5-methoxy-14,16-dimethyl-2-azabicyclo[18.3.1]tetracosa-1(23),2,6,8,10,16,20(24),21-octaen-13-yl]oxy}propan-2-yl]but-2-enimidic acid)