NP-MRD: Showing NP-Card for 4,17,21,23-tetrachloropentacyclo[20.2.2.1¹⁰,¹⁴.1¹⁵,¹⁹.0²,⁷]octacosa-1(25),2(7),3,5,10,12,14(28),15(27),16,18,20,22(26),23-tridecaene-5,13,16,24-tetrol (NP0285363)

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Record Information

Version

2.0

Created at

2022-09-09 13:30:39 UTC

Updated at

2022-09-09 13:30:39 UTC

NP-MRD ID

NP0285363

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4,17,21,23-tetrachloropentacyclo[20.2.2.1¹⁰,¹⁴.1¹⁵,¹⁹.0²,⁷]octacosa-1(25),2(7),3,5,10,12,14(28),15(27),16,18,20,22(26),23-tridecaene-5,13,16,24-tetrol

Description

4,17,21,23-Tetrachloropentacyclo[20.2.2.1¹⁰,¹⁴.1¹⁵,¹⁹.0²,⁷]Octacosa-1(24),2,4,6,10(28),11,13,15,17,19(27),20,22,25-tridecaene-5,13,16,24-tetrol belongs to the class of organic compounds known as 1-hydroxy-4-unsubstituted benzenoids. These are phenols that are unsubstituted at the 4-position. 4,17,21,23-tetrachloropentacyclo[20.2.2.1¹⁰,¹⁴.1¹⁵,¹⁹.0²,⁷]octacosa-1(25),2(7),3,5,10,12,14(28),15(27),16,18,20,22(26),23-tridecaene-5,13,16,24-tetrol is found in Bazzania trilobata. 4,17,21,23-Tetrachloropentacyclo[20.2.2.1¹⁰,¹⁴.1¹⁵,¹⁹.0²,⁷]Octacosa-1(24),2,4,6,10(28),11,13,15,17,19(27),20,22,25-tridecaene-5,13,16,24-tetrol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004191516342D          

 36 40  0  0  0  0            999 V2000
    3.5318    0.9589    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3256    0.7343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9082    1.3279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7073    1.1114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9541    0.3078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7818    0.0906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4594   -0.4158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8668   -1.1655    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5316   -0.6771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2871   -1.0086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9519   -0.5202    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.3776   -1.8286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1331   -2.1602    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    8.7128   -2.3171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9573   -1.9855    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5774   -2.8076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8766   -2.3473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1266   -2.6746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9774   -3.4904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0914   -3.4244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3077   -3.0699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7959   -2.3213    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9642   -2.1525    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6228   -1.3757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8046   -1.2698    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
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    6.6903   -3.9542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6157   -4.7758    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    7.4510   -3.6365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1012   -4.1445    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
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 33 35  2  0  0  0  0
 16 35  1  0  0  0  0
 35 36  1  0  0  0  0
M  END

     RDKit          3D

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    2.0848    0.8356   -0.8227 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5012    1.0508   -2.0612 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5259    1.9848   -2.4190 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0113    2.8533   -1.4878 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5675    2.6524   -0.2414 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1011    3.5321    1.3457 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    1.5386    1.7223    0.1203 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8863    1.7858    1.5450 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.9026    5.5134   -2.7273 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -2.3486    3.6013   -1.8375 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8526    2.5222   -0.8996 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8950    3.0006   -0.0724 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4155    2.2900    0.9656 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.2560    1.8140   -3.5424 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.1785    0.7365    2.8355 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.1340   -0.1021    1.3145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8678   -4.4116    1.4177 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2622   -4.0230    1.1375 H   0  0  0  0  0  0  0  0  0  0  0  0
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 27 20  2  0
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  3 38  1  0
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  6 39  1  0
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 16 42  1  0
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 29 47  1  0
M  END


  Mrv1533004191516342D          

 36 40  0  0  0  0            999 V2000
    3.5318    0.9589    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3256    0.7343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9082    1.3279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7073    1.1114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9541    0.3078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7818    0.0906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4594   -0.4158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8668   -1.1655    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5316   -0.6771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2871   -1.0086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9519   -0.5202    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   10.1331   -2.1602    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
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    7.4510   -3.6365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1012   -4.1445    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
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M  END
> <DATABASE_ID>
NP0285363

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC1=CC=C2CCC3=CC(O)=C(Cl)C=C3C3=CC=C(C(Cl)=C3O)C(Cl)=CC3=CC(Cl)=C(O)C(=C3)C1=C2

> <INCHI_IDENTIFIER>
InChI=1S/C28H18Cl4O4/c29-21-9-14-8-20(27(35)23(31)10-14)19-7-13(2-6-24(19)33)1-3-15-11-25(34)22(30)12-18(15)16-4-5-17(21)26(32)28(16)36/h2,4-12,33-36H,1,3H2

> <INCHI_KEY>
VKYRQUNAQLLRJK-UHFFFAOYSA-N

> <FORMULA>
C28H18Cl4O4

> <MOLECULAR_WEIGHT>
560.25

> <EXACT_MASS>
557.9959199

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
54.565557160770496

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4,17,21,23-tetrachloropentacyclo[20.2.2.1¹⁰,¹⁴.1¹⁵,¹⁹.0²,⁷]octacosa-1(25),2,4,6,10,12,14(28),15(27),16,18,20,22(26),23-tridecaene-5,13,16,24-tetrol

> <ALOGPS_LOGP>
7.17

> <JCHEM_LOGP>
8.922590292666666

> <ALOGPS_LOGS>
-6.43

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
7.576264945809877

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.040251899204366

> <JCHEM_PKA_STRONGEST_BASIC>
-5.5676313154281845

> <JCHEM_POLAR_SURFACE_AREA>
80.92

> <JCHEM_REFRACTIVITY>
147.1196

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.09e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4,17,21,23-tetrachloropentacyclo[20.2.2.1¹⁰,¹⁴.1¹⁵,¹⁹.0²,⁷]octacosa-1(25),2,4,6,10,12,14(28),15(27),16,18,20,22(26),23-tridecaene-5,13,16,24-tetrol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 19-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-APR-15         0                                  
HETATM    1  O   UNK     0       6.593   1.790   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       8.075   1.371   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.162   2.479   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.654   2.075   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      11.114   0.575   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      12.659   0.169   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      13.924  -0.776   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      14.685  -2.176   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      15.926  -1.264   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      17.336  -1.883   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      18.577  -0.971   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      17.505  -3.413   0.000  0.00  0.00           C+0
HETATM   13 Cl   UNK     0      18.915  -4.032   0.000  0.00  0.00          Cl+0
HETATM   14  C   UNK     0      16.264  -4.325   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      14.854  -3.706   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      14.144  -5.241   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      12.836  -4.382   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      11.436  -4.993   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      11.158  -6.515   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.504  -6.392   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.041  -5.731   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.086  -4.333   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.533  -4.018   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.896  -2.568   0.000  0.00  0.00           C+0
HETATM   25 Cl   UNK     0       3.369  -2.370   0.000  0.00  0.00          Cl+0
HETATM   26  C   UNK     0       5.855  -1.361   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       5.240   0.051   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       7.419  -1.483   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       7.933  -3.003   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       8.428  -0.174   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       9.964  -0.493   0.000  0.00  0.00           C+0
HETATM   32 Cl   UNK     0       9.124  -7.885   0.000  0.00  0.00          Cl+0
HETATM   33  C   UNK     0      12.489  -7.381   0.000  0.00  0.00           C+0
HETATM   34 Cl   UNK     0      12.349  -8.915   0.000  0.00  0.00          Cl+0
HETATM   35  C   UNK     0      13.909  -6.788   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      15.122  -7.736   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   30                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   31                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   15                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14    8   16                                                  
CONECT   16   15   17   35                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   33                                                  
CONECT   20   19   21   32                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   29                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   30                                                  
CONECT   29   28   22                                                       
CONECT   30   28    2   31                                                  
CONECT   31   30    5                                                       
CONECT   32   20                                                            
CONECT   33   19   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   16   36                                                  
CONECT   36   35                                                            
MASTER        0    0    0    0    0    0    0    0   36    0   80    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₈H₁₈Cl₄O₄

Average Mass

560.2500 Da

Monoisotopic Mass

557.99592 Da

IUPAC Name

4,17,21,23-tetrachloropentacyclo[20.2.2.1¹⁰,¹⁴.1¹⁵,¹⁹.0²,⁷]octacosa-1(25),2,4,6,10,12,14(28),15(27),16,18,20,22(26),23-tridecaene-5,13,16,24-tetrol

Traditional Name

4,17,21,23-tetrachloropentacyclo[20.2.2.1¹⁰,¹⁴.1¹⁵,¹⁹.0²,⁷]octacosa-1(25),2,4,6,10,12,14(28),15(27),16,18,20,22(26),23-tridecaene-5,13,16,24-tetrol

CAS Registry Number

Not Available

SMILES

OC1=CC=C2CCC3=CC(O)=C(Cl)C=C3C3=CC=C(C(Cl)=C3O)C(Cl)=CC3=CC(Cl)=C(O)C(=C3)C1=C2

InChI Identifier

InChI=1S/C28H18Cl4O4/c29-21-9-14-8-20(27(35)23(31)10-14)19-7-13(2-6-24(19)33)1-3-15-11-25(34)22(30)12-18(15)16-4-5-17(21)26(32)28(16)36/h2,4-12,33-36H,1,3H2

InChI Key

VKYRQUNAQLLRJK-UHFFFAOYSA-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
Bazzania trilobata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 1-hydroxy-4-unsubstituted benzenoids. These are phenols that are unsubstituted at the 4-position.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Phenols

Sub Class

1-hydroxy-4-unsubstituted benzenoids

Direct Parent

1-hydroxy-4-unsubstituted benzenoids

Alternative Parents

Substituents

1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Aryl halide
Aryl chloride
Chloroalkene
Haloalkene
Vinyl halide
Vinyl chloride
Polyol
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Organochloride
Organohalogen compound
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic 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	7.17	ALOGPS
logP	8.92	ChemAxon
logS	-6.4	ALOGPS
pKa (Strongest Acidic)	7.04	ChemAxon
pKa (Strongest Basic)	-5.6	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	80.92 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	147.12 m³·mol⁻¹	ChemAxon
Polarizability	54.57 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

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4,17,21,23-tetrachloropentacyclo[20.2.2.1¹⁰,¹⁴.1¹⁵,¹⁹.0²,⁷]octacosa-1(25),2(7),3,5,10,12,14(28),15(27),16,18,20,22(26),23-tridecaene-5,13,16,24-tetrol (NP0285363)

MOL for NP0285363 (4,17,21,23-tetrachloropentacyclo[20.2.2.1¹⁰,¹⁴.1¹⁵,¹⁹.0²,⁷]octacosa-1(25),2(7),3,5,10,12,14(28),15(27),16,18,20,22(26),23-tridecaene-5,13,16,24-tetrol)

3D MOL for NP0285363 (4,17,21,23-tetrachloropentacyclo[20.2.2.1¹⁰,¹⁴.1¹⁵,¹⁹.0²,⁷]octacosa-1(25),2(7),3,5,10,12,14(28),15(27),16,18,20,22(26),23-tridecaene-5,13,16,24-tetrol)

3D SDF for NP0285363 (4,17,21,23-tetrachloropentacyclo[20.2.2.1¹⁰,¹⁴.1¹⁵,¹⁹.0²,⁷]octacosa-1(25),2(7),3,5,10,12,14(28),15(27),16,18,20,22(26),23-tridecaene-5,13,16,24-tetrol)

3D-SDF for NP0285363 (4,17,21,23-tetrachloropentacyclo[20.2.2.1¹⁰,¹⁴.1¹⁵,¹⁹.0²,⁷]octacosa-1(25),2(7),3,5,10,12,14(28),15(27),16,18,20,22(26),23-tridecaene-5,13,16,24-tetrol)

PDB for NP0285363 (4,17,21,23-tetrachloropentacyclo[20.2.2.1¹⁰,¹⁴.1¹⁵,¹⁹.0²,⁷]octacosa-1(25),2(7),3,5,10,12,14(28),15(27),16,18,20,22(26),23-tridecaene-5,13,16,24-tetrol)

3D PDB for NP0285363 (4,17,21,23-tetrachloropentacyclo[20.2.2.1¹⁰,¹⁴.1¹⁵,¹⁹.0²,⁷]octacosa-1(25),2(7),3,5,10,12,14(28),15(27),16,18,20,22(26),23-tridecaene-5,13,16,24-tetrol)

SMILES for NP0285363 (4,17,21,23-tetrachloropentacyclo[20.2.2.1¹⁰,¹⁴.1¹⁵,¹⁹.0²,⁷]octacosa-1(25),2(7),3,5,10,12,14(28),15(27),16,18,20,22(26),23-tridecaene-5,13,16,24-tetrol)

INCHI for NP0285363 (4,17,21,23-tetrachloropentacyclo[20.2.2.1¹⁰,¹⁴.1¹⁵,¹⁹.0²,⁷]octacosa-1(25),2(7),3,5,10,12,14(28),15(27),16,18,20,22(26),23-tridecaene-5,13,16,24-tetrol)

Structure for NP0285363 (4,17,21,23-tetrachloropentacyclo[20.2.2.1¹⁰,¹⁴.1¹⁵,¹⁹.0²,⁷]octacosa-1(25),2(7),3,5,10,12,14(28),15(27),16,18,20,22(26),23-tridecaene-5,13,16,24-tetrol)

3D Structure for NP0285363 (4,17,21,23-tetrachloropentacyclo[20.2.2.1¹⁰,¹⁴.1¹⁵,¹⁹.0²,⁷]octacosa-1(25),2(7),3,5,10,12,14(28),15(27),16,18,20,22(26),23-tridecaene-5,13,16,24-tetrol)