NP-MRD: Showing NP-Card for 5-{5,6,11-trihydroxy-3,7,22-trimethyl-13,19,21,26,27-pentaoxaoctacyclo[22.2.1.0¹,¹⁸.0³,¹⁶.0⁴,¹².0⁷,¹¹.0¹²,¹⁴.0²⁰,²⁵]heptacosan-8-yl}pyran-2-one (NP0324604)

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Record Information

Version

2.0

Created at

2022-09-12 04:47:21 UTC

Updated at

2022-09-12 04:47:21 UTC

NP-MRD ID

NP0324604

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-{5,6,11-trihydroxy-3,7,22-trimethyl-13,19,21,26,27-pentaoxaoctacyclo[22.2.1.0¹,¹⁸.0³,¹⁶.0⁴,¹².0⁷,¹¹.0¹²,¹⁴.0²⁰,²⁵]heptacosan-8-yl}pyran-2-one

Description

5-{5,6,11-Trihydroxy-3,7,22-trimethyl-13,19,21,26,27-pentaoxaoctacyclo[22.2.1.0¹,¹⁸.0³,¹⁶.0⁴,¹².0⁷,¹¹.0¹²,¹⁴.0²⁰,²⁵]Heptacosan-8-yl}-2H-pyran-2-one belongs to the class of organic compounds known as bufanolides and derivatives. These are steroid lactones containing a pyran-2-one moiety linked to the C17 atom of a cyclopenta[a]phenanthrene derivative. 5-{5,6,11-trihydroxy-3,7,22-trimethyl-13,19,21,26,27-pentaoxaoctacyclo[22.2.1.0¹,¹⁸.0³,¹⁶.0⁴,¹².0⁷,¹¹.0¹²,¹⁴.0²⁰,²⁵]heptacosan-8-yl}pyran-2-one is found in Cotyledon orbiculata. 5-{5,6,11-Trihydroxy-3,7,22-trimethyl-13,19,21,26,27-pentaoxaoctacyclo[22.2.1.0¹,¹⁸.0³,¹⁶.0⁴,¹².0⁷,¹¹.0¹²,¹⁴.0²⁰,²⁵]Heptacosan-8-yl}-2H-pyran-2-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004161504502D          

 40 48  0  0  0  0            999 V2000
    6.9582   -4.4607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1335   -4.4830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.8113   -5.3330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8936   -5.5588    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3221   -4.6319    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5114   -4.8383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8977   -4.2815    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7288   -5.0891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0609   -3.4728    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8317   -3.1753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4183   -3.7390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1715   -3.3678    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8273   -3.8583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6780   -3.7893    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5298   -4.6351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.4421   -2.9272    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
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  8 10  1  0  0  0  0
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  6 12  1  0  0  0  0
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  2 15  1  0  0  0  0
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  8 22  1  0  0  0  0
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 21 32  1  0  0  0  0
 27 32  1  0  0  0  0
 32 33  1  0  0  0  0
 29 34  1  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 37 39  1  0  0  0  0
 39 40  2  0  0  0  0
 34 40  1  0  0  0  0
M  END

     RDKit          3D

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 39 78  1  1
M  END


  Mrv1533004161504502D          

 40 48  0  0  0  0            999 V2000
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    1.4421   -2.9272    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6602   -3.1902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1218   -3.4532    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4970   -3.9989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1157   -4.5446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9526   -5.3533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5713   -5.8989    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1706   -5.6163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0074   -6.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4481   -5.0706    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6950   -5.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2677   -5.1654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6110   -4.4152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0037   -3.8568    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2850   -4.2619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4648   -3.4568    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6728   -5.8840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4977   -5.8926    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9028   -6.6113    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4830   -7.3214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8881   -8.0401    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6580   -7.3129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2529   -6.5942    0.0000 C   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  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
  6 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
  2 15  1  0  0  0  0
 14 16  1  0  0  0  0
  4 16  1  0  0  0  0
 16 17  1  0  0  0  0
  6 17  1  0  0  0  0
 10 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
  8 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 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
 21 32  1  0  0  0  0
 27 32  1  0  0  0  0
 32 33  1  0  0  0  0
 29 34  1  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 37 39  1  0  0  0  0
 39 40  2  0  0  0  0
 34 40  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0324604

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1CC2OC34CC5(C)C(CC6OC66C5C(O)C(O)C5(C)C(CCC65O)C5=COC(=O)C=C5)CC3OC(O1)C2O4

> <INCHI_IDENTIFIER>
InChI=1S/C30H38O10/c1-13-8-17-22-25(36-13)37-18-9-15-10-19-30(39-19)23(26(15,2)12-28(18,38-17)40-22)21(32)24(33)27(3)16(6-7-29(27,30)34)14-4-5-20(31)35-11-14/h4-5,11,13,15-19,21-25,32-34H,6-10,12H2,1-3H3

> <INCHI_KEY>
IUSQHZMTRKEVLT-UHFFFAOYSA-N

> <FORMULA>
C30H38O10

> <MOLECULAR_WEIGHT>
558.624

> <EXACT_MASS>
558.246497424

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
78

> <JCHEM_AVERAGE_POLARIZABILITY>
57.93476925450436

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
5-{5,6,11-trihydroxy-3,7,22-trimethyl-13,19,21,26,27-pentaoxaoctacyclo[22.2.1.0¹,¹⁸.0³,¹⁶.0⁴,¹².0⁷,¹¹.0¹²,¹⁴.0²⁰,²⁵]heptacosan-8-yl}-2H-pyran-2-one

> <ALOGPS_LOGP>
1.39

> <JCHEM_LOGP>
0.8924982489999991

> <ALOGPS_LOGS>
-2.99

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
9

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.66512722272886

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.97450389284386

> <JCHEM_PKA_STRONGEST_BASIC>
-3.3136637180085176

> <JCHEM_POLAR_SURFACE_AREA>
136.44000000000003

> <JCHEM_REFRACTIVITY>
136.18390000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.73e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-{5,6,11-trihydroxy-3,7,22-trimethyl-13,19,21,26,27-pentaoxaoctacyclo[22.2.1.0¹,¹⁸.0³,¹⁶.0⁴,¹².0⁷,¹¹.0¹²,¹⁴.0²⁰,²⁵]heptacosan-8-yl}pyran-2-one

> <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      12.989  -8.327   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      11.449  -8.368   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.643  -9.754   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.981  -9.955   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       7.268 -10.376   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       6.201  -8.646   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.688  -9.032   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.542  -7.992   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.227  -9.500   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.847  -6.483   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.286  -5.927   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.381  -6.979   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       7.787  -6.287   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       9.011  -7.202   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      10.599  -7.073   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       8.456  -8.652   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       6.897  -9.415   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       2.692  -5.464   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.232  -5.955   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -0.227  -6.446   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       0.928  -7.465   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.083  -8.483   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.778  -9.993   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       2.933 -11.011   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       0.318 -10.484   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       0.014 -11.993   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -0.837  -9.465   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -1.297 -10.935   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -2.366  -9.642   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -3.007  -8.242   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -1.874  -7.199   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -0.532  -7.956   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      -0.868  -6.453   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      -3.123 -10.984   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -4.662 -10.999   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      -5.419 -12.341   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      -4.635 -13.667   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      -5.391 -15.008   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0      -3.095 -13.651   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      -2.339 -12.309   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   15                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   16                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   12   17                                             
CONECT    7    6    8                                                       
CONECT    8    7    9   10   22                                             
CONECT    9    8                                                            
CONECT   10    8   11   18                                                  
CONECT   11   10   12                                                       
CONECT   12   11    6   13                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14    2                                                       
CONECT   16   14    4   17                                                  
CONECT   17   16    6                                                       
CONECT   18   10   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19   21                                                       
CONECT   21   20   19   22   32                                             
CONECT   22   21    8   23                                                  
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   29   32                                             
CONECT   28   27                                                            
CONECT   29   27   30   34                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   21   27   33                                             
CONECT   33   32                                                            
CONECT   34   29   35   40                                                  
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40                                                       
CONECT   40   39   34                                                       
MASTER        0    0    0    0    0    0    0    0   40    0   96    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₃₈O₁₀

Average Mass

558.6240 Da

Monoisotopic Mass

558.24650 Da

IUPAC Name

5-{5,6,11-trihydroxy-3,7,22-trimethyl-13,19,21,26,27-pentaoxaoctacyclo[22.2.1.0¹,¹⁸.0³,¹⁶.0⁴,¹².0⁷,¹¹.0¹²,¹⁴.0²⁰,²⁵]heptacosan-8-yl}-2H-pyran-2-one

Traditional Name

5-{5,6,11-trihydroxy-3,7,22-trimethyl-13,19,21,26,27-pentaoxaoctacyclo[22.2.1.0¹,¹⁸.0³,¹⁶.0⁴,¹².0⁷,¹¹.0¹²,¹⁴.0²⁰,²⁵]heptacosan-8-yl}pyran-2-one

CAS Registry Number

Not Available

SMILES

CC1CC2OC34CC5(C)C(CC6OC66C5C(O)C(O)C5(C)C(CCC65O)C5=COC(=O)C=C5)CC3OC(O1)C2O4

InChI Identifier

InChI=1S/C30H38O10/c1-13-8-17-22-25(36-13)37-18-9-15-10-19-30(39-19)23(26(15,2)12-28(18,38-17)40-22)21(32)24(33)27(3)16(6-7-29(27,30)34)14-4-5-20(31)35-11-14/h4-5,11,13,15-19,21-25,32-34H,6-10,12H2,1-3H3

InChI Key

IUSQHZMTRKEVLT-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
Cotyledon orbiculata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as bufanolides and derivatives. These are steroid lactones containing a pyran-2-one moiety linked to the C17 atom of a cyclopenta[a]phenanthrene derivative.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroid lactones

Direct Parent

Bufanolides and derivatives

Alternative Parents

Substituents

Bufanolide-skeleton
Dioxolopyran
Ketal
1,4-dioxepane
Dioxepane
Oxepane
Pyranone
Para-dioxane
Oxane
Pyran
Meta-dioxolane
Cyclic alcohol
Heteroaromatic compound
Tertiary alcohol
Lactone
Secondary alcohol
Ether
Oxirane
Oxacycle
Dialkyl ether
Organoheterocyclic compound
Acetal
Polyol
Organooxygen compound
Organic oxide
Organic oxygen compound
Hydrocarbon derivative
Alcohol
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	1.39	ALOGPS
logP	0.89	ChemAxon
logS	-3	ALOGPS
pKa (Strongest Acidic)	12.97	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	136.44 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	136.18 m³·mol⁻¹	ChemAxon
Polarizability	57.93 Å³	ChemAxon
Number of Rings	9	ChemAxon
Bioavailability	Yes	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 5-{5,6,11-trihydroxy-3,7,22-trimethyl-13,19,21,26,27-pentaoxaoctacyclo[22.2.1.0¹,¹⁸.0³,¹⁶.0⁴,¹².0⁷,¹¹.0¹²,¹⁴.0²⁰,²⁵]heptacosan-8-yl}pyran-2-one (NP0324604)

MOL for NP0324604 (5-{5,6,11-trihydroxy-3,7,22-trimethyl-13,19,21,26,27-pentaoxaoctacyclo[22.2.1.0¹,¹⁸.0³,¹⁶.0⁴,¹².0⁷,¹¹.0¹²,¹⁴.0²⁰,²⁵]heptacosan-8-yl}pyran-2-one)

3D MOL for NP0324604 (5-{5,6,11-trihydroxy-3,7,22-trimethyl-13,19,21,26,27-pentaoxaoctacyclo[22.2.1.0¹,¹⁸.0³,¹⁶.0⁴,¹².0⁷,¹¹.0¹²,¹⁴.0²⁰,²⁵]heptacosan-8-yl}pyran-2-one)

3D SDF for NP0324604 (5-{5,6,11-trihydroxy-3,7,22-trimethyl-13,19,21,26,27-pentaoxaoctacyclo[22.2.1.0¹,¹⁸.0³,¹⁶.0⁴,¹².0⁷,¹¹.0¹²,¹⁴.0²⁰,²⁵]heptacosan-8-yl}pyran-2-one)

3D-SDF for NP0324604 (5-{5,6,11-trihydroxy-3,7,22-trimethyl-13,19,21,26,27-pentaoxaoctacyclo[22.2.1.0¹,¹⁸.0³,¹⁶.0⁴,¹².0⁷,¹¹.0¹²,¹⁴.0²⁰,²⁵]heptacosan-8-yl}pyran-2-one)

PDB for NP0324604 (5-{5,6,11-trihydroxy-3,7,22-trimethyl-13,19,21,26,27-pentaoxaoctacyclo[22.2.1.0¹,¹⁸.0³,¹⁶.0⁴,¹².0⁷,¹¹.0¹²,¹⁴.0²⁰,²⁵]heptacosan-8-yl}pyran-2-one)

3D PDB for NP0324604 (5-{5,6,11-trihydroxy-3,7,22-trimethyl-13,19,21,26,27-pentaoxaoctacyclo[22.2.1.0¹,¹⁸.0³,¹⁶.0⁴,¹².0⁷,¹¹.0¹²,¹⁴.0²⁰,²⁵]heptacosan-8-yl}pyran-2-one)

SMILES for NP0324604 (5-{5,6,11-trihydroxy-3,7,22-trimethyl-13,19,21,26,27-pentaoxaoctacyclo[22.2.1.0¹,¹⁸.0³,¹⁶.0⁴,¹².0⁷,¹¹.0¹²,¹⁴.0²⁰,²⁵]heptacosan-8-yl}pyran-2-one)

INCHI for NP0324604 (5-{5,6,11-trihydroxy-3,7,22-trimethyl-13,19,21,26,27-pentaoxaoctacyclo[22.2.1.0¹,¹⁸.0³,¹⁶.0⁴,¹².0⁷,¹¹.0¹²,¹⁴.0²⁰,²⁵]heptacosan-8-yl}pyran-2-one)

Structure for NP0324604 (5-{5,6,11-trihydroxy-3,7,22-trimethyl-13,19,21,26,27-pentaoxaoctacyclo[22.2.1.0¹,¹⁸.0³,¹⁶.0⁴,¹².0⁷,¹¹.0¹²,¹⁴.0²⁰,²⁵]heptacosan-8-yl}pyran-2-one)

3D Structure for NP0324604 (5-{5,6,11-trihydroxy-3,7,22-trimethyl-13,19,21,26,27-pentaoxaoctacyclo[22.2.1.0¹,¹⁸.0³,¹⁶.0⁴,¹².0⁷,¹¹.0¹²,¹⁴.0²⁰,²⁵]heptacosan-8-yl}pyran-2-one)