NP-MRD: Showing NP-Card for 7,8-dimethoxy-2,5-dimethyl-2-(4,8,12,16,20,24,28,32-octamethyltritriaconta-3,7,11,15,19,23,27,31-octaen-1-yl)chromen-6-ol (NP0297452)

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Record Information

Version

2.0

Created at

2022-09-10 07:48:25 UTC

Updated at

2022-09-10 07:48:25 UTC

NP-MRD ID

NP0297452

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7,8-dimethoxy-2,5-dimethyl-2-(4,8,12,16,20,24,28,32-octamethyltritriaconta-3,7,11,15,19,23,27,31-octaen-1-yl)chromen-6-ol

Description

7,8-Dimethoxy-2,5-dimethyl-2-(4,8,12,16,20,24,28,32-octamethyltritriaconta-3,7,11,15,19,23,27,31-octaen-1-yl)-2H-chromen-6-ol belongs to the class of organic compounds known as polyterpenoids. These are terpenoids consisting of more than eight isoprene units. 7,8-dimethoxy-2,5-dimethyl-2-(4,8,12,16,20,24,28,32-octamethyltritriaconta-3,7,11,15,19,23,27,31-octaen-1-yl)chromen-6-ol is found in Dioscorea alata. 7,8-Dimethoxy-2,5-dimethyl-2-(4,8,12,16,20,24,28,32-octamethyltritriaconta-3,7,11,15,19,23,27,31-octaen-1-yl)-2H-chromen-6-ol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004161514392D          

 58 59  0  0  0  0            999 V2000
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.0761   -4.0520    0.0000 C   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  2  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
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 13 14  1  0  0  0  0
 15 14  1  4  0  0  0
 15 16  2  0  0  0  0
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 16 18  1  0  0  0  0
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 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 30 29  1  4  0  0  0
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 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
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  3 56  1  0  0  0  0
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M  END

     RDKit          3D

140141  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1533004161514392D          

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M  END
> <DATABASE_ID>
NP0297452

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(O)C(C)=C2C=CC(C)(CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)C)OC2=C1OC

> <INCHI_IDENTIFIER>
InChI=1S/C54H82O4/c1-40(2)22-14-23-41(3)24-15-25-42(4)26-16-27-43(5)28-17-29-44(6)30-18-31-45(7)32-19-33-46(8)34-20-35-47(9)36-21-38-54(11)39-37-49-48(10)50(55)52(56-12)53(57-13)51(49)58-54/h22,24,26,28,30,32,34,36-37,39,55H,14-21,23,25,27,29,31,33,35,38H2,1-13H3

> <INCHI_KEY>
JVDNGAORBIPFTO-UHFFFAOYSA-N

> <FORMULA>
C54H82O4

> <MOLECULAR_WEIGHT>
795.246

> <EXACT_MASS>
794.62131112

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
140

> <JCHEM_AVERAGE_POLARIZABILITY>
103.19017647103578

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
7,8-dimethoxy-2,5-dimethyl-2-(4,8,12,16,20,24,28,32-octamethyltritriaconta-3,7,11,15,19,23,27,31-octaen-1-yl)-2H-chromen-6-ol

> <ALOGPS_LOGP>
9.83

> <JCHEM_LOGP>
16.124050684333334

> <ALOGPS_LOGS>
-6.67

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.703192601207077

> <JCHEM_PKA_STRONGEST_BASIC>
-4.4898550259080245

> <JCHEM_POLAR_SURFACE_AREA>
47.92

> <JCHEM_REFRACTIVITY>
260.7437000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
26

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.70e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
7,8-dimethoxy-2,5-dimethyl-2-(4,8,12,16,20,24,28,32-octamethyltritriaconta-3,7,11,15,19,23,27,31-octaen-1-yl)chromen-6-ol

> <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      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       0.000  -3.080   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.185  -2.043   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.195  -3.757   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.205  -4.937   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.732  -6.384   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.742  -7.564   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.225  -7.296   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.269  -9.011   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.279 -10.191   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.806 -11.638   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.816 -12.817   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.299 -12.550   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.342 -14.264   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.352 -15.444   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.879 -16.891   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.889 -18.071   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.373 -17.804   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.416 -19.518   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.426 -20.698   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       3.953 -22.145   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       2.963 -23.325   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       1.446 -23.057   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       3.490 -24.772   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       2.500 -25.952   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       3.026 -27.399   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       2.037 -28.578   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       0.520 -28.311   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       2.563 -30.025   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       1.573 -31.205   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       2.100 -32.652   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       1.110 -33.832   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -0.406 -33.565   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       1.637 -35.279   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       0.647 -36.459   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       1.174 -37.906   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       0.184 -39.086   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      -1.333 -38.818   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       0.711 -40.533   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      -0.279 -41.713   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0       0.247 -43.160   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      -0.743 -44.339   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      -0.216 -45.786   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0      -2.259 -44.072   0.000  0.00  0.00           C+0
HETATM   54  O   UNK     0       5.335  -3.080   0.000  0.00  0.00           O+0
HETATM   55  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   56  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   57  O   UNK     0       2.667  -4.620   0.000  0.00  0.00           O+0
HETATM   58  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   56                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   55                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13   54                                             
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41   44                                                       
CONECT   44   43   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   47   48                                                  
CONECT   47   46                                                            
CONECT   48   46   49                                                       
CONECT   49   48   50                                                       
CONECT   50   49   51                                                       
CONECT   51   50   52   53                                                  
CONECT   52   51                                                            
CONECT   53   51                                                            
CONECT   54   11   55                                                       
CONECT   55   54    8   56                                                  
CONECT   56   55    3   57                                                  
CONECT   57   56   58                                                       
CONECT   58   57                                                            
MASTER        0    0    0    0    0    0    0    0   58    0  118    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₅₄H₈₂O₄

Average Mass

795.2460 Da

Monoisotopic Mass

794.62131 Da

IUPAC Name

7,8-dimethoxy-2,5-dimethyl-2-(4,8,12,16,20,24,28,32-octamethyltritriaconta-3,7,11,15,19,23,27,31-octaen-1-yl)-2H-chromen-6-ol

Traditional Name

7,8-dimethoxy-2,5-dimethyl-2-(4,8,12,16,20,24,28,32-octamethyltritriaconta-3,7,11,15,19,23,27,31-octaen-1-yl)chromen-6-ol

CAS Registry Number

Not Available

SMILES

COC1=C(O)C(C)=C2C=CC(C)(CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)C)OC2=C1OC

InChI Identifier

InChI=1S/C54H82O4/c1-40(2)22-14-23-41(3)24-15-25-42(4)26-16-27-43(5)28-17-29-44(6)30-18-31-45(7)32-19-33-46(8)34-20-35-47(9)36-21-38-54(11)39-37-49-48(10)50(55)52(56-12)53(57-13)51(49)58-54/h22,24,26,28,30,32,34,36-37,39,55H,14-21,23,25,27,29,31,33,35,38H2,1-13H3

InChI Key

JVDNGAORBIPFTO-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
Dioscorea alata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as polyterpenoids. These are terpenoids consisting of more than eight isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Polyterpenoids

Direct Parent

Polyterpenoids

Alternative Parents

Substituents

Polyterpenoid
1-benzopyran
Benzopyran
Anisole
Alkyl aryl ether
Benzenoid
Oxacycle
Organoheterocyclic compound
Ether
Organic oxygen compound
Hydrocarbon derivative
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	9.83	ALOGPS
logP	16.12	ChemAxon
logS	-6.7	ALOGPS
pKa (Strongest Acidic)	10.7	ChemAxon
pKa (Strongest Basic)	-4.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	47.92 Å²	ChemAxon
Rotatable Bond Count	26	ChemAxon
Refractivity	260.74 m³·mol⁻¹	ChemAxon
Polarizability	103.19 Å³	ChemAxon
Number of Rings	2	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

74072107

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 7,8-dimethoxy-2,5-dimethyl-2-(4,8,12,16,20,24,28,32-octamethyltritriaconta-3,7,11,15,19,23,27,31-octaen-1-yl)chromen-6-ol (NP0297452)

MOL for NP0297452 (7,8-dimethoxy-2,5-dimethyl-2-(4,8,12,16,20,24,28,32-octamethyltritriaconta-3,7,11,15,19,23,27,31-octaen-1-yl)chromen-6-ol)

3D MOL for NP0297452 (7,8-dimethoxy-2,5-dimethyl-2-(4,8,12,16,20,24,28,32-octamethyltritriaconta-3,7,11,15,19,23,27,31-octaen-1-yl)chromen-6-ol)

3D SDF for NP0297452 (7,8-dimethoxy-2,5-dimethyl-2-(4,8,12,16,20,24,28,32-octamethyltritriaconta-3,7,11,15,19,23,27,31-octaen-1-yl)chromen-6-ol)

3D-SDF for NP0297452 (7,8-dimethoxy-2,5-dimethyl-2-(4,8,12,16,20,24,28,32-octamethyltritriaconta-3,7,11,15,19,23,27,31-octaen-1-yl)chromen-6-ol)

PDB for NP0297452 (7,8-dimethoxy-2,5-dimethyl-2-(4,8,12,16,20,24,28,32-octamethyltritriaconta-3,7,11,15,19,23,27,31-octaen-1-yl)chromen-6-ol)

3D PDB for NP0297452 (7,8-dimethoxy-2,5-dimethyl-2-(4,8,12,16,20,24,28,32-octamethyltritriaconta-3,7,11,15,19,23,27,31-octaen-1-yl)chromen-6-ol)

SMILES for NP0297452 (7,8-dimethoxy-2,5-dimethyl-2-(4,8,12,16,20,24,28,32-octamethyltritriaconta-3,7,11,15,19,23,27,31-octaen-1-yl)chromen-6-ol)

INCHI for NP0297452 (7,8-dimethoxy-2,5-dimethyl-2-(4,8,12,16,20,24,28,32-octamethyltritriaconta-3,7,11,15,19,23,27,31-octaen-1-yl)chromen-6-ol)

Structure for NP0297452 (7,8-dimethoxy-2,5-dimethyl-2-(4,8,12,16,20,24,28,32-octamethyltritriaconta-3,7,11,15,19,23,27,31-octaen-1-yl)chromen-6-ol)

3D Structure for NP0297452 (7,8-dimethoxy-2,5-dimethyl-2-(4,8,12,16,20,24,28,32-octamethyltritriaconta-3,7,11,15,19,23,27,31-octaen-1-yl)chromen-6-ol)