NP-MRD: Showing NP-Card for 7,22-dihydroxy-8-{[5-({4-hydroxy-5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-4-methoxy-6-methyloxan-2-yl]oxy}-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.0⁴,¹³.0⁵,¹⁰.0¹⁹,²²]docosa-1(21),10-dien-14-one (NP0228984)

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Record Information

Version

2.0

Created at

2022-09-06 08:51:37 UTC

Updated at

2022-09-06 08:51:37 UTC

NP-MRD ID

NP0228984

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7,22-dihydroxy-8-{[5-({4-hydroxy-5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-4-methoxy-6-methyloxan-2-yl]oxy}-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.0⁴,¹³.0⁵,¹⁰.0¹⁹,²²]docosa-1(21),10-dien-14-one

Description

7,22-Dihydroxy-8-{[5-({4-hydroxy-5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-4-methoxy-6-methyloxan-2-yl]oxy}-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.0⁴,¹³.0⁵,¹⁰.0¹⁹,²²]Docosa-1(21),10-dien-14-one belongs to the class of organic compounds known as oligosaccharides. These are carbohydrates made up of 3 to 10 monosaccharide units linked to each other through glycosidic bonds. 7,22-dihydroxy-8-{[5-({4-hydroxy-5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-4-methoxy-6-methyloxan-2-yl]oxy}-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.0⁴,¹³.0⁵,¹⁰.0¹⁹,²²]docosa-1(21),10-dien-14-one is found in Vincetoxicum atratum. 7,22-Dihydroxy-8-{[5-({4-hydroxy-5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-4-methoxy-6-methyloxan-2-yl]oxy}-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.0⁴,¹³.0⁵,¹⁰.0¹⁹,²²]Docosa-1(21),10-dien-14-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171520352D          

 57 64  0  0  0  0            999 V2000
    2.9926   -3.6643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8125   -3.7560    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1430   -4.5119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9629   -4.6037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2934   -5.3596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1133   -5.4513    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6026   -4.7871    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4225   -4.8788    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7530   -5.6347    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9119   -4.2146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5814   -3.4587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0707   -2.7945    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7402   -2.0386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9203   -1.9469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4310   -2.6111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5898   -1.1910    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  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
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 18 19  1  0  0  0  0
 13 19  1  0  0  0  0
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 20 21  1  0  0  0  0
 17 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
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 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
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M  END

     RDKit          3D

119126  0  0  0  0  0  0  0  0999 V2000
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M  END


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M  END
> <DATABASE_ID>
NP0228984

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1CC(OC2C(O)CC(OC3C(C)OC(CC3OC)OC3CC4=CCC5C(CCC6=COC7(C)OCC(OC5=O)C67O)C4(C)CC3O)OC2C)OC(C)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C41H62O16/c1-19-35(44)29(47-6)14-34(51-19)56-36-20(2)52-32(13-26(36)42)57-37-21(3)53-33(15-30(37)48-7)54-28-12-22-8-10-24-25(39(22,4)16-27(28)43)11-9-23-17-49-40(5)41(23,46)31(18-50-40)55-38(24)45/h8,17,19-21,24-37,42-44,46H,9-16,18H2,1-7H3

> <INCHI_KEY>
JMLUQNLKDNOKLQ-UHFFFAOYSA-N

> <FORMULA>
C41H62O16

> <MOLECULAR_WEIGHT>
810.931

> <EXACT_MASS>
810.403785916

> <JCHEM_ACCEPTOR_COUNT>
15

> <JCHEM_ATOM_COUNT>
119

> <JCHEM_AVERAGE_POLARIZABILITY>
87.04760501183847

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
7,22-dihydroxy-8-{[5-({4-hydroxy-5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-4-methoxy-6-methyloxan-2-yl]oxy}-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.0⁴,¹³.0⁵,¹⁰.0¹⁹,²²]docosa-1(21),10-dien-14-one

> <ALOGPS_LOGP>
1.39

> <JCHEM_LOGP>
2.142171292999998

> <ALOGPS_LOGS>
-3.59

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
8

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.107723302646704

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.369079598432851

> <JCHEM_PKA_STRONGEST_BASIC>
-3.1682437888326174

> <JCHEM_POLAR_SURFACE_AREA>
199.51999999999998

> <JCHEM_REFRACTIVITY>
196.35440000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.06e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
7,22-dihydroxy-8-{[5-({4-hydroxy-5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-4-methoxy-6-methyloxan-2-yl]oxy}-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.0⁴,¹³.0⁵,¹⁰.0¹⁹,²²]docosa-1(21),10-dien-14-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0       5.586  -6.840   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       7.117  -7.011   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       7.734  -8.422   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.264  -8.593   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.881 -10.004   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      11.411 -10.176   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      12.325  -8.936   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      13.855  -9.107   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      14.472 -10.518   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      14.769  -7.867   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      14.152  -6.456   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      15.065  -5.216   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      14.448  -3.805   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      12.918  -3.634   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      12.004  -4.874   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      12.301  -2.223   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      13.214  -0.983   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      14.745  -1.155   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      15.362  -2.566   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      16.892  -2.737   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      17.509  -4.148   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      12.598   0.428   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      11.067   0.599   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      10.450   2.010   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       8.920   2.181   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.303   3.592   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.772   3.763   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       5.859   2.523   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.476   1.112   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       6.041  -0.365   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.759  -1.218   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       3.228  -1.046   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       2.323  -2.418   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       0.832  -2.036   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       0.734  -0.499   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -0.697  -1.066   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -0.248   0.687   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       0.577   1.988   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       2.069   1.605   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       2.982   2.845   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       4.479   3.208   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       4.650   4.738   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0       2.166   0.068   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0       3.577   0.685   0.000  0.00  0.00           O+0
HETATM   45  C   UNK     0       8.006   0.941   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       7.093  -0.299   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       8.623  -0.470   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      10.154  -0.641   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0      10.771  -2.052   0.000  0.00  0.00           O+0
HETATM   50  O   UNK     0      12.621  -6.285   0.000  0.00  0.00           O+0
HETATM   51  C   UNK     0      11.708  -7.525   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      10.178  -7.354   0.000  0.00  0.00           C+0
HETATM   53  O   UNK     0       8.967 -11.244   0.000  0.00  0.00           O+0
HETATM   54  C   UNK     0       7.437 -11.073   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0       6.524 -12.313   0.000  0.00  0.00           C+0
HETATM   56  C   UNK     0       6.820  -9.662   0.000  0.00  0.00           C+0
HETATM   57  O   UNK     0       5.290  -9.491   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   56                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   53                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   51                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   50                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   19                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18   22                                                  
CONECT   18   17   19                                                       
CONECT   19   18   13   20                                                  
CONECT   20   19   21                                                       
CONECT   21   20                                                            
CONECT   22   17   23                                                       
CONECT   23   22   24   48                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   45                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   41                                                  
CONECT   29   28   30   45                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33   43                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36   37   43                                             
CONECT   36   35                                                            
CONECT   37   35   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40   43                                                  
CONECT   40   39   41                                                       
CONECT   41   40   28   42                                                  
CONECT   42   41                                                            
CONECT   43   39   32   35   44                                             
CONECT   44   43                                                            
CONECT   45   29   25   46   47                                             
CONECT   46   45                                                            
CONECT   47   45   48                                                       
CONECT   48   47   23   49                                                  
CONECT   49   48                                                            
CONECT   50   11   51                                                       
CONECT   51   50    7   52                                                  
CONECT   52   51                                                            
CONECT   53    5   54                                                       
CONECT   54   53   55   56                                                  
CONECT   55   54                                                            
CONECT   56   54    3   57                                                  
CONECT   57   56                                                            
MASTER        0    0    0    0    0    0    0    0   57    0  128    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₁H₆₂O₁₆

Average Mass

810.9310 Da

Monoisotopic Mass

810.40379 Da

IUPAC Name

Traditional Name

CAS Registry Number

Not Available

SMILES

COC1CC(OC2C(O)CC(OC3C(C)OC(CC3OC)OC3CC4=CCC5C(CCC6=COC7(C)OCC(OC5=O)C67O)C4(C)CC3O)OC2C)OC(C)C1O

InChI Identifier

InChI=1S/C41H62O16/c1-19-35(44)29(47-6)14-34(51-19)56-36-20(2)52-32(13-26(36)42)57-37-21(3)53-33(15-30(37)48-7)54-28-12-22-8-10-24-25(39(22,4)16-27(28)43)11-9-23-17-49-40(5)41(23,46)31(18-50-40)55-38(24)45/h8,17,19-21,24-37,42-44,46H,9-16,18H2,1-7H3

InChI Key

JMLUQNLKDNOKLQ-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
Vincetoxicum atratum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oligosaccharides. These are carbohydrates made up of 3 to 10 monosaccharide units linked to each other through glycosidic bonds.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Oligosaccharides

Alternative Parents

Substituents

Oligosaccharide
Glycosyl compound
O-glycosyl compound
Furofuran
Ketal
Oxane
Cyclic alcohol
Dihydrofuran
Tetrahydrofuran
Tertiary alcohol
Lactone
Carboxylic acid ester
Secondary alcohol
Oxacycle
Monocarboxylic acid or derivatives
Ether
Dialkyl ether
Acetal
Carboxylic acid derivative
Organoheterocyclic compound
Hydrocarbon derivative
Organic oxide
Alcohol
Carbonyl group
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	1.39	ALOGPS
logP	2.14	ChemAxon
logS	-3.6	ALOGPS
pKa (Strongest Acidic)	11.37	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	15	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	199.52 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	196.35 m³·mol⁻¹	ChemAxon
Polarizability	87.05 Å³	ChemAxon
Number of Rings	8	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

72750090

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 7,22-dihydroxy-8-{[5-({4-hydroxy-5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-4-methoxy-6-methyloxan-2-yl]oxy}-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.0⁴,¹³.0⁵,¹⁰.0¹⁹,²²]docosa-1(21),10-dien-14-one (NP0228984)

MOL for NP0228984 (7,22-dihydroxy-8-{[5-({4-hydroxy-5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-4-methoxy-6-methyloxan-2-yl]oxy}-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.0⁴,¹³.0⁵,¹⁰.0¹⁹,²²]docosa-1(21),10-dien-14-one)

3D MOL for NP0228984 (7,22-dihydroxy-8-{[5-({4-hydroxy-5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-4-methoxy-6-methyloxan-2-yl]oxy}-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.0⁴,¹³.0⁵,¹⁰.0¹⁹,²²]docosa-1(21),10-dien-14-one)

3D SDF for NP0228984 (7,22-dihydroxy-8-{[5-({4-hydroxy-5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-4-methoxy-6-methyloxan-2-yl]oxy}-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.0⁴,¹³.0⁵,¹⁰.0¹⁹,²²]docosa-1(21),10-dien-14-one)

3D-SDF for NP0228984 (7,22-dihydroxy-8-{[5-({4-hydroxy-5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-4-methoxy-6-methyloxan-2-yl]oxy}-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.0⁴,¹³.0⁵,¹⁰.0¹⁹,²²]docosa-1(21),10-dien-14-one)

PDB for NP0228984 (7,22-dihydroxy-8-{[5-({4-hydroxy-5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-4-methoxy-6-methyloxan-2-yl]oxy}-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.0⁴,¹³.0⁵,¹⁰.0¹⁹,²²]docosa-1(21),10-dien-14-one)

3D PDB for NP0228984 (7,22-dihydroxy-8-{[5-({4-hydroxy-5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-4-methoxy-6-methyloxan-2-yl]oxy}-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.0⁴,¹³.0⁵,¹⁰.0¹⁹,²²]docosa-1(21),10-dien-14-one)

SMILES for NP0228984 (7,22-dihydroxy-8-{[5-({4-hydroxy-5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-4-methoxy-6-methyloxan-2-yl]oxy}-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.0⁴,¹³.0⁵,¹⁰.0¹⁹,²²]docosa-1(21),10-dien-14-one)

INCHI for NP0228984 (7,22-dihydroxy-8-{[5-({4-hydroxy-5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-4-methoxy-6-methyloxan-2-yl]oxy}-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.0⁴,¹³.0⁵,¹⁰.0¹⁹,²²]docosa-1(21),10-dien-14-one)

Structure for NP0228984 (7,22-dihydroxy-8-{[5-({4-hydroxy-5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-4-methoxy-6-methyloxan-2-yl]oxy}-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.0⁴,¹³.0⁵,¹⁰.0¹⁹,²²]docosa-1(21),10-dien-14-one)

3D Structure for NP0228984 (7,22-dihydroxy-8-{[5-({4-hydroxy-5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-4-methoxy-6-methyloxan-2-yl]oxy}-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.0⁴,¹³.0⁵,¹⁰.0¹⁹,²²]docosa-1(21),10-dien-14-one)