NP-MRD: Showing NP-Card for methyl 4-chloro-8,11,15,18,22,25-hexahydroxy-29-methyl-13,20,27-trioxo-6-oxaheptacyclo[15.10.2.0¹,¹⁹.0³,¹⁶.0⁵,¹⁴.0⁷,¹².0²¹,²⁶]nonacosa-3(16),4,11,14,18,21,23,25,28-nonaene-7-carboxylate (NP0250945)

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Record Information

Version

2.0

Created at

2022-09-07 13:57:45 UTC

Updated at

2022-09-07 13:57:46 UTC

NP-MRD ID

NP0250945

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 4-chloro-8,11,15,18,22,25-hexahydroxy-29-methyl-13,20,27-trioxo-6-oxaheptacyclo[15.10.2.0¹,¹⁹.0³,¹⁶.0⁵,¹⁴.0⁷,¹².0²¹,²⁶]nonacosa-3(16),4,11,14,18,21,23,25,28-nonaene-7-carboxylate

Description

Methyl 4-chloro-8,11,15,18,22,25-hexahydroxy-29-methyl-13,20,27-trioxo-6-oxaheptacyclo[15.10.2.0¹,¹⁹.0³,¹⁶.0⁵,¹⁴.0⁷,¹².0²¹,²⁶]Nonacosa-3(16),4,11,14,18,21,23,25,28-nonaene-7-carboxylate belongs to the class of organic compounds known as anthraquinones. These are organic compounds containing either anthracene-9,10-quinone, 1,4-anthraquinone, or 1,2-anthraquinone. methyl 4-chloro-8,11,15,18,22,25-hexahydroxy-29-methyl-13,20,27-trioxo-6-oxaheptacyclo[15.10.2.0¹,¹⁹.0³,¹⁶.0⁵,¹⁴.0⁷,¹².0²¹,²⁶]nonacosa-3(16),4,11,14,18,21,23,25,28-nonaene-7-carboxylate is found in Cercospora beticola. Methyl 4-chloro-8,11,15,18,22,25-hexahydroxy-29-methyl-13,20,27-trioxo-6-oxaheptacyclo[15.10.2.0¹,¹⁹.0³,¹⁶.0⁵,¹⁴.0⁷,¹².0²¹,²⁶]Nonacosa-3(16),4,11,14,18,21,23,25,28-nonaene-7-carboxylate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004161502182D          

 44 50  0  0  0  0            999 V2000
    8.7076    0.0697    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8508    0.8822    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.6260    1.1644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2580    0.6342    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.7692    1.9769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9940    1.6947    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.3619    2.2249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5867    1.9426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4435    1.1302    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    6.9546    2.4729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2171    1.9613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3980    2.3635    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1378    2.6603    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1501    3.4314    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3637    3.6808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5840    4.0681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6820    4.0021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1729    3.2511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3230    3.3624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1035    4.1576    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6620    2.8399    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   11.1764    1.7290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4012    1.4467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7630    0.7052    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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  5  6  1  0  0  0  0
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 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
  5 43  1  0  0  0  0
 43 44  1  0  0  0  0
M  END

     RDKit          3D

 67 73  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1533004161502182D          

 44 50  0  0  0  0            999 V2000
    8.7076    0.0697    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.8719    2.0420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7061    1.8569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8755    1.0495    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2692    4.7163    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0978    3.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8730    3.5676    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0162    4.3801    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5051    3.0374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2803    3.3196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4234    4.1321    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.9123    2.7894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6875    3.0717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8307    3.8842    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.3196    2.5414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1764    1.7290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4012    1.4467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7630    0.7052    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 12 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  2  0  0  0  0
 21 28  1  0  0  0  0
 28 29  1  0  0  0  0
 12 29  1  0  0  0  0
 29 30  2  0  0  0  0
 17 31  1  0  0  0  0
 16 32  1  0  0  0  0
 10 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
  7 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 36 38  1  0  0  0  0
  5 38  1  0  0  0  0
 38 39  2  0  0  0  0
 39 40  1  0  0  0  0
 39 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
  5 43  1  0  0  0  0
 43 44  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0250945

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C12OC3=C(Cl)C4=C(C5C(C)=CC6(C4)C(=O)C4=C(O)C=CC(O)=C4C(=O)C6=C5O)C(O)=C3C(=O)C1=C(O)CCC2O

> <INCHI_IDENTIFIER>
InChI=1S/C31H23ClO12/c1-9-7-30-8-10-16(15(9)24(38)21(30)25(39)17-11(33)3-4-12(34)18(17)28(30)41)23(37)19-26(40)20-13(35)5-6-14(36)31(20,29(42)43-2)44-27(19)22(10)32/h3-4,7,14-15,33-38H,5-6,8H2,1-2H3

> <INCHI_KEY>
ULWZYHBPNXOUKA-UHFFFAOYSA-N

> <FORMULA>
C31H23ClO12

> <MOLECULAR_WEIGHT>
622.96

> <EXACT_MASS>
622.0878039

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
67

> <JCHEM_AVERAGE_POLARIZABILITY>
59.31769303838742

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl 4-chloro-8,11,15,18,22,25-hexahydroxy-29-methyl-13,20,27-trioxo-6-oxaheptacyclo[15.10.2.0¹,¹⁹.0³,¹⁶.0⁵,¹⁴.0⁷,¹².0²¹,²⁶]nonacosa-3(16),4,11,14,18,21,23,25,28-nonaene-7-carboxylate

> <ALOGPS_LOGP>
2.40

> <JCHEM_LOGP>
3.458471609666667

> <ALOGPS_LOGS>
-3.59

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
7.919364438034788

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.158428317557592

> <JCHEM_PKA_STRONGEST_BASIC>
-3.4038421474496436

> <JCHEM_POLAR_SURFACE_AREA>
208.11999999999995

> <JCHEM_REFRACTIVITY>
154.93549999999993

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.62e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl 4-chloro-8,11,15,18,22,25-hexahydroxy-29-methyl-13,20,27-trioxo-6-oxaheptacyclo[15.10.2.0¹,¹⁹.0³,¹⁶.0⁵,¹⁴.0⁷,¹².0²¹,²⁶]nonacosa-3(16),4,11,14,18,21,23,25,28-nonaene-7-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0      16.254   0.130   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      16.521   1.647   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      17.969   2.174   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      19.148   1.184   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      18.236   3.690   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      16.789   3.163   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      15.609   4.153   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      14.162   3.626   0.000  0.00  0.00           C+0
HETATM    9 Cl   UNK     0      13.895   2.110   0.000  0.00  0.00          Cl+0
HETATM   10  C   UNK     0      12.982   4.616   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      11.605   3.661   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.076   4.412   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      11.457   4.966   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      11.480   6.405   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.012   6.871   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      12.290   7.594   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.606   7.470   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.656   6.069   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.070   6.276   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       7.660   7.761   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       6.836   5.301   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.350   5.706   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       4.958   7.196   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       4.256   4.623   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.648   3.133   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.134   2.728   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       6.525   1.238   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       7.227   3.812   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       8.785   3.466   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       9.101   1.959   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       9.836   8.804   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      13.249   6.133   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      14.696   6.660   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      14.964   8.176   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      15.876   5.670   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      17.323   6.197   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      17.590   7.713   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      18.503   5.207   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      19.950   5.734   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      20.217   7.250   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      21.130   4.744   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      20.863   3.227   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      19.416   2.701   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0      20.091   1.316   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   38   43                                             
CONECT    6    5    7                                                       
CONECT    7    6    8   35                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   32                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   18   29                                             
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   32                                                  
CONECT   17   16   18   31                                                  
CONECT   18   17   12   19                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   28                                                  
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   21   29                                                  
CONECT   29   28   12   30                                                  
CONECT   30   29                                                            
CONECT   31   17                                                            
CONECT   32   16   10   33                                                  
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33    7   36                                                  
CONECT   36   35   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36    5   39                                                  
CONECT   39   38   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42    5   44                                                  
CONECT   44   43                                                            
MASTER        0    0    0    0    0    0    0    0   44    0  100    0
END

View in JSmol

Synonyms

Value	Source
Methyl 4-chloro-8,11,15,18,22,25-hexahydroxy-29-methyl-13,20,27-trioxo-6-oxaheptacyclo[15.10.2.0,.0,.0,.0,.0,]nonacosa-3(16),4,11,14,18,21,23,25,28-nonaene-7-carboxylic acid	Generator
Methyl 4-chloro-8,11,15,18,22,25-hexahydroxy-29-methyl-13,20,27-trioxo-6-oxaheptacyclo[15.10.2.0¹,¹⁹.0³,¹⁶.0⁵,¹⁴.0⁷,¹².0²¹,²⁶]nonacosa-3(16),4,11,14,18,21,23,25,28-nonaene-7-carboxylic acid	Generator

Chemical Formula

C₃₁H₂₃ClO₁₂

Average Mass

622.9600 Da

Monoisotopic Mass

622.08780 Da

IUPAC Name

Traditional Name

CAS Registry Number

Not Available

SMILES

COC(=O)C12OC3=C(Cl)C4=C(C5C(C)=CC6(C4)C(=O)C4=C(O)C=CC(O)=C4C(=O)C6=C5O)C(O)=C3C(=O)C1=C(O)CCC2O

InChI Identifier

InChI=1S/C31H23ClO12/c1-9-7-30-8-10-16(15(9)24(38)21(30)25(39)17-11(33)3-4-12(34)18(17)28(30)41)23(37)19-26(40)20-13(35)5-6-14(36)31(20,29(42)43-2)44-27(19)22(10)32/h3-4,7,14-15,33-38H,5-6,8H2,1-2H3

InChI Key

ULWZYHBPNXOUKA-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
Cercospora beticola	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as anthraquinones. These are organic compounds containing either anthracene-9,10-quinone, 1,4-anthraquinone, or 1,2-anthraquinone.

Kingdom

Super Class

Class

Sub Class

Direct Parent

Alternative Parents

Substituents

9,10-anthraquinone
Anthraquinone
Xanthone
Dibenzopyran
Xanthene
Chromone
Chromane
Benzopyran
Naphthalene
Tetralin
1-benzopyran
Quinone
Aryl alkyl ketone
Aryl ketone
Beta-hydroxy acid
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
Aryl halide
Hydroxy acid
Aryl chloride
Vinylogous acid
Methyl ester
Secondary alcohol
Carboxylic acid ester
Ketone
Enol
Ether
Monocarboxylic acid or derivatives
Polyol
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Organic oxygen compound
Carbonyl group
Alcohol
Organic oxide
Hydrocarbon derivative
Organohalogen compound
Organochloride
Organooxygen 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	2.4	ALOGPS
logP	3.46	ChemAxon
logS	-3.6	ALOGPS
pKa (Strongest Acidic)	7.16	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	208.12 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	154.94 m³·mol⁻¹	ChemAxon
Polarizability	59.32 Å³	ChemAxon
Number of Rings	7	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 methyl 4-chloro-8,11,15,18,22,25-hexahydroxy-29-methyl-13,20,27-trioxo-6-oxaheptacyclo[15.10.2.0¹,¹⁹.0³,¹⁶.0⁵,¹⁴.0⁷,¹².0²¹,²⁶]nonacosa-3(16),4,11,14,18,21,23,25,28-nonaene-7-carboxylate (NP0250945)

MOL for NP0250945 (methyl 4-chloro-8,11,15,18,22,25-hexahydroxy-29-methyl-13,20,27-trioxo-6-oxaheptacyclo[15.10.2.0¹,¹⁹.0³,¹⁶.0⁵,¹⁴.0⁷,¹².0²¹,²⁶]nonacosa-3(16),4,11,14,18,21,23,25,28-nonaene-7-carboxylate)

3D MOL for NP0250945 (methyl 4-chloro-8,11,15,18,22,25-hexahydroxy-29-methyl-13,20,27-trioxo-6-oxaheptacyclo[15.10.2.0¹,¹⁹.0³,¹⁶.0⁵,¹⁴.0⁷,¹².0²¹,²⁶]nonacosa-3(16),4,11,14,18,21,23,25,28-nonaene-7-carboxylate)

3D SDF for NP0250945 (methyl 4-chloro-8,11,15,18,22,25-hexahydroxy-29-methyl-13,20,27-trioxo-6-oxaheptacyclo[15.10.2.0¹,¹⁹.0³,¹⁶.0⁵,¹⁴.0⁷,¹².0²¹,²⁶]nonacosa-3(16),4,11,14,18,21,23,25,28-nonaene-7-carboxylate)

3D-SDF for NP0250945 (methyl 4-chloro-8,11,15,18,22,25-hexahydroxy-29-methyl-13,20,27-trioxo-6-oxaheptacyclo[15.10.2.0¹,¹⁹.0³,¹⁶.0⁵,¹⁴.0⁷,¹².0²¹,²⁶]nonacosa-3(16),4,11,14,18,21,23,25,28-nonaene-7-carboxylate)

PDB for NP0250945 (methyl 4-chloro-8,11,15,18,22,25-hexahydroxy-29-methyl-13,20,27-trioxo-6-oxaheptacyclo[15.10.2.0¹,¹⁹.0³,¹⁶.0⁵,¹⁴.0⁷,¹².0²¹,²⁶]nonacosa-3(16),4,11,14,18,21,23,25,28-nonaene-7-carboxylate)

3D PDB for NP0250945 (methyl 4-chloro-8,11,15,18,22,25-hexahydroxy-29-methyl-13,20,27-trioxo-6-oxaheptacyclo[15.10.2.0¹,¹⁹.0³,¹⁶.0⁵,¹⁴.0⁷,¹².0²¹,²⁶]nonacosa-3(16),4,11,14,18,21,23,25,28-nonaene-7-carboxylate)

SMILES for NP0250945 (methyl 4-chloro-8,11,15,18,22,25-hexahydroxy-29-methyl-13,20,27-trioxo-6-oxaheptacyclo[15.10.2.0¹,¹⁹.0³,¹⁶.0⁵,¹⁴.0⁷,¹².0²¹,²⁶]nonacosa-3(16),4,11,14,18,21,23,25,28-nonaene-7-carboxylate)

INCHI for NP0250945 (methyl 4-chloro-8,11,15,18,22,25-hexahydroxy-29-methyl-13,20,27-trioxo-6-oxaheptacyclo[15.10.2.0¹,¹⁹.0³,¹⁶.0⁵,¹⁴.0⁷,¹².0²¹,²⁶]nonacosa-3(16),4,11,14,18,21,23,25,28-nonaene-7-carboxylate)

Structure for NP0250945 (methyl 4-chloro-8,11,15,18,22,25-hexahydroxy-29-methyl-13,20,27-trioxo-6-oxaheptacyclo[15.10.2.0¹,¹⁹.0³,¹⁶.0⁵,¹⁴.0⁷,¹².0²¹,²⁶]nonacosa-3(16),4,11,14,18,21,23,25,28-nonaene-7-carboxylate)

3D Structure for NP0250945 (methyl 4-chloro-8,11,15,18,22,25-hexahydroxy-29-methyl-13,20,27-trioxo-6-oxaheptacyclo[15.10.2.0¹,¹⁹.0³,¹⁶.0⁵,¹⁴.0⁷,¹².0²¹,²⁶]nonacosa-3(16),4,11,14,18,21,23,25,28-nonaene-7-carboxylate)