NP-MRD: Showing NP-Card for (12e,29s)-5,16,21,33,36-pentabromo-12,25-bis(hydroxyimino)-2,18-dioxa-10,27-diazapentacyclo[28.2.2.2¹⁴,¹⁷.1³,⁷.1¹⁹,²³]octatriaconta-1(32),3(38),4,6,10,14,16,19(35),20,22,26,30,33,36-tetradecaene-4,11,20,26,29-pentol (NP0199990)

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Record Information

Version

2.0

Created at

2022-09-04 18:44:13 UTC

Updated at

2022-09-04 18:44:14 UTC

NP-MRD ID

NP0199990

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(12e,29s)-5,16,21,33,36-pentabromo-12,25-bis(hydroxyimino)-2,18-dioxa-10,27-diazapentacyclo[28.2.2.2¹⁴,¹⁷.1³,⁷.1¹⁹,²³]octatriaconta-1(32),3(38),4,6,10,14,16,19(35),20,22,26,30,33,36-tetradecaene-4,11,20,26,29-pentol

Description

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042220442D          

 52 56  0  0  1  0            999 V2000
   15.6833    1.7866    0.0000 O   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


  Mrv1652309042220442D          

 52 56  0  0  1  0            999 V2000
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   15.2769   -0.9037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.6913   -2.5090    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.1303   -3.1738    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3811   -2.7985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3616   -1.9737    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
   12.6602   -3.2034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6387   -4.0403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3784   -4.4395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.1018   -4.0214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.8093   -4.4457    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
   11.7980   -4.2291    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9490   -4.2206    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8668   -5.0415    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   11.5367   -5.5230    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.1216   -4.0620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8666   -4.8466    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.3524   -3.7007    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.7224   -3.1360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2654   -2.4053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8872   -1.6249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0422   -1.5777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6258   -0.8507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8009   -0.8413    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    7.0533   -0.1423    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6352    0.5689    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8897   -0.1130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2757   -0.8720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2937    0.6706    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.8340    1.3544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5811    0.9824    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2943    1.4041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3144    2.2433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5666    2.6297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8481    2.2025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1344    2.6163    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
   11.1564    2.4481    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.0621    3.2677    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.0104    2.4401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8410    2.2723    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   13.6162    1.9334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0275    2.6485    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  2  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
  5 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15 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
 14 20  1  0  0  0  0
 20 21  1  0  0  0  0
 18 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 23 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  2  0  0  0  0
 28 29  1  4  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  2  0  0  0  0
 35 36  1  0  0  0  0
 35 37  1  0  0  0  0
 37 38  2  0  0  0  0
 31 38  1  0  0  0  0
 37 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 41 42  1  0  0  0  0
 42 43  2  0  0  0  0
 43 44  1  0  0  0  0
 44 45  2  0  0  0  0
 40 45  1  0  0  0  0
 45 46  1  0  0  0  0
 43 47  1  0  0  0  0
 47 48  1  6  0  0  0
 47 49  1  0  0  0  0
 50 49  1  4  0  0  0
 50 51  2  0  0  0  0
  3 51  1  0  0  0  0
 51 52  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0199990

> <DATABASE_NAME>
NP-MRD

> <SMILES>
O\N=C1/CC2=CC(Br)=C(OC3=CC(CC(=NO)C(O)=NC[C@@H](O)C4=CC=C(OC5=CC(CCN=C1O)=CC(Br)=C5O)C(Br)=C4)=CC(Br)=C3O)C(Br)=C2

> <INCHI_IDENTIFIER>
InChI=1S/C34H27Br5N4O9/c35-19-13-18-1-2-27(19)51-28-11-15(5-20(36)30(28)45)3-4-40-33(47)24(42-49)9-16-7-22(38)32(23(39)8-16)52-29-12-17(6-21(37)31(29)46)10-25(43-50)34(48)41-14-26(18)44/h1-2,5-8,11-13,26,44-46,49-50H,3-4,9-10,14H2,(H,40,47)(H,41,48)/b42-24+,43-25?/t26-/m1/s1

> <INCHI_KEY>
XRCOVLHHCDFIHF-BJROWRAMSA-N

> <FORMULA>
C34H27Br5N4O9

> <MOLECULAR_WEIGHT>
1035.129

> <EXACT_MASS>
1029.769493

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
79

> <JCHEM_AVERAGE_POLARIZABILITY>
80.73774878048663

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(12E,29S)-5,16,21,33,36-pentabromo-12,25-bis(hydroxyimino)-2,18-dioxa-10,27-diazapentacyclo[28.2.2.2^{14,17}.1^{3,7}.1^{19,23}]octatriaconta-1(32),3(38),4,6,10,14,16,19(35),20,22,26,30,33,36-tetradecaene-4,11,20,26,29-pentol

> <JCHEM_LOGP>
8.988612696602399

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
2.407103056977971

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.0012871010280535

> <JCHEM_PKA_STRONGEST_BASIC>
3.1523460818610305

> <JCHEM_POLAR_SURFACE_AREA>
209.50999999999996

> <JCHEM_REFRACTIVITY>
209.93189999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(12E,29S)-5,16,21,33,36-pentabromo-12,25-bis(hydroxyimino)-2,18-dioxa-10,27-diazapentacyclo[28.2.2.2^{14,17}.1^{3,7}.1^{19,23}]octatriaconta-1(32),3(38),4,6,10,14,16,19(35),20,22,26,30,33,36-tetradecaene-4,11,20,26,29-pentol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  O   UNK     0      29.275   3.335   0.000  0.00  0.00           O+0
HETATM    2  N   UNK     0      27.793   3.752   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0      26.690   2.678   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      27.608   1.353   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      27.827  -0.241   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      26.269  -0.255   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      25.424  -1.543   0.000  0.00  0.00           C+0
HETATM    8 Br   UNK     0      23.886  -1.482   0.000  0.00  0.00          Br+0
HETATM    9  C   UNK     0      26.163  -2.889   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      25.309  -4.171   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      27.710  -3.055   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      28.517  -1.687   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      27.424  -4.683   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      26.377  -5.924   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      24.978  -5.224   0.000  0.00  0.00           C+0
HETATM   16 Br   UNK     0      24.942  -3.684   0.000  0.00  0.00          Br+0
HETATM   17  C   UNK     0      23.632  -5.980   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      23.592  -7.542   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      24.973  -8.287   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      26.323  -7.507   0.000  0.00  0.00           C+0
HETATM   21 Br   UNK     0      27.644  -8.299   0.000  0.00  0.00          Br+0
HETATM   22  C   UNK     0      22.023  -7.894   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      20.438  -7.878   0.000  0.00  0.00           C+0
HETATM   24  N   UNK     0      20.285  -9.411   0.000  0.00  0.00           N+0
HETATM   25  O   UNK     0      21.535 -10.310   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      18.894  -7.582   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      18.418  -9.047   0.000  0.00  0.00           O+0
HETATM   28  N   UNK     0      17.458  -6.908   0.000  0.00  0.00           N+0
HETATM   29  C   UNK     0      16.282  -5.854   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      15.429  -4.490   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      14.723  -3.033   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      13.145  -2.945   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      12.368  -1.588   0.000  0.00  0.00           C+0
HETATM   34 Br   UNK     0      10.828  -1.570   0.000  0.00  0.00          Br+0
HETATM   35  C   UNK     0      13.166  -0.266   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      12.386   1.062   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      14.727  -0.211   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      15.448  -1.628   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      15.481   1.252   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      16.490   2.528   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      17.885   1.834   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      19.216   2.621   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      19.254   4.187   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      17.858   4.909   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      16.516   4.111   0.000  0.00  0.00           C+0
HETATM   46 Br   UNK     0      15.184   4.884   0.000  0.00  0.00          Br+0
HETATM   47  C   UNK     0      20.825   4.570   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0      20.649   6.100   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0      22.419   4.555   0.000  0.00  0.00           C+0
HETATM   50  N   UNK     0      23.970   4.242   0.000  0.00  0.00           N+0
HETATM   51  C   UNK     0      25.417   3.609   0.000  0.00  0.00           C+0
HETATM   52  O   UNK     0      26.185   4.944   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   51                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   12                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   13                                                  
CONECT   12   11    5                                                       
CONECT   13   11   14                                                       
CONECT   14   13   15   20                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19   22                                                  
CONECT   19   18   20                                                       
CONECT   20   19   14   21                                                  
CONECT   21   20                                                            
CONECT   22   18   23                                                       
CONECT   23   22   24   26                                                  
CONECT   24   23   25                                                       
CONECT   25   24                                                            
CONECT   26   23   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32   38                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35   38   39                                                  
CONECT   38   37   31                                                       
CONECT   39   37   40                                                       
CONECT   40   39   41   45                                                  
CONECT   41   40   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   44   47                                                  
CONECT   44   43   45                                                       
CONECT   45   44   40   46                                                  
CONECT   46   45                                                            
CONECT   47   43   48   49                                                  
CONECT   48   47                                                            
CONECT   49   47   50                                                       
CONECT   50   49   51                                                       
CONECT   51   50    3   52                                                  
CONECT   52   51                                                            
MASTER        0    0    0    0    0    0    0    0   52    0  112    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₄H₂₇Br₅N₄O₉

Average Mass

1035.1290 Da

Monoisotopic Mass

1029.76949 Da

IUPAC Name

(12E,29S)-5,16,21,33,36-pentabromo-12,25-bis(hydroxyimino)-2,18-dioxa-10,27-diazapentacyclo[28.2.2.2^{14,17}.1^{3,7}.1^{19,23}]octatriaconta-1(32),3(38),4,6,10,14,16,19(35),20,22,26,30,33,36-tetradecaene-4,11,20,26,29-pentol

Traditional Name

CAS Registry Number

Not Available

SMILES

O\N=C1/CC2=CC(Br)=C(OC3=CC(CC(=NO)C(O)=NC[C@@H](O)C4=CC=C(OC5=CC(CCN=C1O)=CC(Br)=C5O)C(Br)=C4)=CC(Br)=C3O)C(Br)=C2

InChI Identifier

InChI=1S/C34H27Br5N4O9/c35-19-13-18-1-2-27(19)51-28-11-15(5-20(36)30(28)45)3-4-40-33(47)24(42-49)9-16-7-22(38)32(23(39)8-16)52-29-12-17(6-21(37)31(29)46)10-25(43-50)34(48)41-14-26(18)44/h1-2,5-8,11-13,26,44-46,49-50H,3-4,9-10,14H2,(H,40,47)(H,41,48)/b42-24+,43-25?/t26-/m1/s1

InChI Key

XRCOVLHHCDFIHF-BJROWRAMSA-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
Ianthella basta	LOTUS Database	35616633

Chemical Taxonomy

Classification

Not classified

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	8.99	ChemAxon
pKa (Strongest Acidic)	1	ChemAxon
pKa (Strongest Basic)	3.15	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	209.51 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	209.93 m³·mol⁻¹	ChemAxon
Polarizability	80.74 Å³	ChemAxon
Number of Rings	5	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

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (12e,29s)-5,16,21,33,36-pentabromo-12,25-bis(hydroxyimino)-2,18-dioxa-10,27-diazapentacyclo[28.2.2.2¹⁴,¹⁷.1³,⁷.1¹⁹,²³]octatriaconta-1(32),3(38),4,6,10,14,16,19(35),20,22,26,30,33,36-tetradecaene-4,11,20,26,29-pentol (NP0199990)

MOL for NP0199990 ((12e,29s)-5,16,21,33,36-pentabromo-12,25-bis(hydroxyimino)-2,18-dioxa-10,27-diazapentacyclo[28.2.2.2¹⁴,¹⁷.1³,⁷.1¹⁹,²³]octatriaconta-1(32),3(38),4,6,10,14,16,19(35),20,22,26,30,33,36-tetradecaene-4,11,20,26,29-pentol)

3D MOL for NP0199990 ((12e,29s)-5,16,21,33,36-pentabromo-12,25-bis(hydroxyimino)-2,18-dioxa-10,27-diazapentacyclo[28.2.2.2¹⁴,¹⁷.1³,⁷.1¹⁹,²³]octatriaconta-1(32),3(38),4,6,10,14,16,19(35),20,22,26,30,33,36-tetradecaene-4,11,20,26,29-pentol)

3D SDF for NP0199990 ((12e,29s)-5,16,21,33,36-pentabromo-12,25-bis(hydroxyimino)-2,18-dioxa-10,27-diazapentacyclo[28.2.2.2¹⁴,¹⁷.1³,⁷.1¹⁹,²³]octatriaconta-1(32),3(38),4,6,10,14,16,19(35),20,22,26,30,33,36-tetradecaene-4,11,20,26,29-pentol)

3D-SDF for NP0199990 ((12e,29s)-5,16,21,33,36-pentabromo-12,25-bis(hydroxyimino)-2,18-dioxa-10,27-diazapentacyclo[28.2.2.2¹⁴,¹⁷.1³,⁷.1¹⁹,²³]octatriaconta-1(32),3(38),4,6,10,14,16,19(35),20,22,26,30,33,36-tetradecaene-4,11,20,26,29-pentol)

PDB for NP0199990 ((12e,29s)-5,16,21,33,36-pentabromo-12,25-bis(hydroxyimino)-2,18-dioxa-10,27-diazapentacyclo[28.2.2.2¹⁴,¹⁷.1³,⁷.1¹⁹,²³]octatriaconta-1(32),3(38),4,6,10,14,16,19(35),20,22,26,30,33,36-tetradecaene-4,11,20,26,29-pentol)

3D PDB for NP0199990 ((12e,29s)-5,16,21,33,36-pentabromo-12,25-bis(hydroxyimino)-2,18-dioxa-10,27-diazapentacyclo[28.2.2.2¹⁴,¹⁷.1³,⁷.1¹⁹,²³]octatriaconta-1(32),3(38),4,6,10,14,16,19(35),20,22,26,30,33,36-tetradecaene-4,11,20,26,29-pentol)

SMILES for NP0199990 ((12e,29s)-5,16,21,33,36-pentabromo-12,25-bis(hydroxyimino)-2,18-dioxa-10,27-diazapentacyclo[28.2.2.2¹⁴,¹⁷.1³,⁷.1¹⁹,²³]octatriaconta-1(32),3(38),4,6,10,14,16,19(35),20,22,26,30,33,36-tetradecaene-4,11,20,26,29-pentol)

INCHI for NP0199990 ((12e,29s)-5,16,21,33,36-pentabromo-12,25-bis(hydroxyimino)-2,18-dioxa-10,27-diazapentacyclo[28.2.2.2¹⁴,¹⁷.1³,⁷.1¹⁹,²³]octatriaconta-1(32),3(38),4,6,10,14,16,19(35),20,22,26,30,33,36-tetradecaene-4,11,20,26,29-pentol)

Structure for NP0199990 ((12e,29s)-5,16,21,33,36-pentabromo-12,25-bis(hydroxyimino)-2,18-dioxa-10,27-diazapentacyclo[28.2.2.2¹⁴,¹⁷.1³,⁷.1¹⁹,²³]octatriaconta-1(32),3(38),4,6,10,14,16,19(35),20,22,26,30,33,36-tetradecaene-4,11,20,26,29-pentol)

3D Structure for NP0199990 ((12e,29s)-5,16,21,33,36-pentabromo-12,25-bis(hydroxyimino)-2,18-dioxa-10,27-diazapentacyclo[28.2.2.2¹⁴,¹⁷.1³,⁷.1¹⁹,²³]octatriaconta-1(32),3(38),4,6,10,14,16,19(35),20,22,26,30,33,36-tetradecaene-4,11,20,26,29-pentol)