NP-MRD: Showing NP-Card for 17-methyl-17-(4-methylpent-3-en-1-yl)-4,12,18-trioxapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-1(21),5,7,9,13,19-hexaene-7,16,20-triol (NP0232262)

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Record Information

Version

2.0

Created at

2022-09-06 13:26:17 UTC

Updated at

2022-09-06 13:26:18 UTC

NP-MRD ID

NP0232262

Secondary Accession Numbers

None

Natural Product Identification

Common Name

17-methyl-17-(4-methylpent-3-en-1-yl)-4,12,18-trioxapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-1(21),5,7,9,13,19-hexaene-7,16,20-triol

Description

17-Methyl-17-(4-methylpent-3-en-1-yl)-4,12,18-trioxapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]Henicosa-1(21),5(10),6,8,13,19-hexaene-7,16,20-triol belongs to the class of organic compounds known as pterocarpans. These are benzo-pyrano-furano-benzene compounds, containing the 6H-[1]benzofuro[3,2-c]chromene skeleton. They are derivatives of isoflavonoids. 17-methyl-17-(4-methylpent-3-en-1-yl)-4,12,18-trioxapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-1(21),5,7,9,13,19-hexaene-7,16,20-triol is found in Lespedeza homoloba. 17-Methyl-17-(4-methylpent-3-en-1-yl)-4,12,18-trioxapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]Henicosa-1(21),5(10),6,8,13,19-hexaene-7,16,20-triol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004231520052D          

 31 35  0  0  0  0            999 V2000
    2.0041    1.6419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7325    1.2546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7613    0.4301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4897    0.0428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5185   -0.7817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2469   -1.1690    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7390   -1.8191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5019   -0.3844    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3089   -0.2129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5638    0.5718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0118    1.1849    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3708    0.7433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9228    0.1302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7478    0.1302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2998    0.7433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1068    0.5718    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.3617   -0.2129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1687   -0.3844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4237   -1.1690    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2306   -1.3405    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.8716   -1.7821    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0647   -1.6106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8097   -0.8259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0027   -0.6544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3353   -1.1393    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6679   -0.6544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8609   -0.8259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6060   -1.6106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7990   -1.7821    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5440   -2.5667    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4321    1.6918    0.0000 C   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
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
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 29 30  1  0  0  0  0
  2 31  1  0  0  0  0
M  END

     RDKit          3D

 59 63  0  0  0  0  0  0  0  0999 V2000
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    1.1060    2.1187    0.9399 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4689    3.0748    0.1544 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6641   -0.0944    0.4252 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5057   -1.1487   -0.0163 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.9194   -0.9432    0.2967 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4755   -1.4395    1.4673 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8053   -1.2533    1.7774 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5811   -0.5488    0.8783 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9496   -0.3080    1.1085 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0404   -0.0541   -0.2822 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7039   -0.2439   -0.5893 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1460    0.2484   -1.7544 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8956   -0.0815   -2.2511 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1794   -1.1711   -1.4887 C   0  0  1  0  0  0  0  0  0  0  0  0
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    3.2049    3.6082    0.2842 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7236    2.5907   -1.1716 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4813   -0.4601   -2.9104 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9585   -1.5298   -3.3021 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5971    0.3308    1.9480 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8173    1.4628    1.5506 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4279    2.6093    1.8715 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6918    4.0002    0.4343 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1714   -2.1442    0.3931 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8643   -1.9998    2.1853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2592   -1.6328    2.6839 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.6329    0.5073   -1.0117 H   0  0  0  0  0  0  0  0  0  0  0  0
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 17 48  1  0
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 19 51  1  0
M  END


  Mrv1533004231520052D          

 31 35  0  0  0  0            999 V2000
    2.0041    1.6419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7325    1.2546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7613    0.4301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4897    0.0428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5185   -0.7817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2469   -1.1690    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7390   -1.8191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5019   -0.3844    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3089   -0.2129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5638    0.5718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0118    1.1849    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3708    0.7433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9228    0.1302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7478    0.1302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2998    0.7433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1068    0.5718    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.3617   -0.2129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1687   -0.3844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4237   -1.1690    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2306   -1.3405    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    9.0647   -1.6106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8097   -0.8259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0027   -0.6544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.8609   -0.8259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6060   -1.6106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7990   -1.7821    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5440   -2.5667    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4321    1.6918    0.0000 C   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
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M  END
> <DATABASE_ID>
NP0232262

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCCC1(C)OC2=C(O)C=C3C4COC5=CC(O)=CC=C5C4OC3=C2CC1O

> <INCHI_IDENTIFIER>
InChI=1S/C25H28O6/c1-13(2)5-4-8-25(3)21(28)11-17-23-16(10-19(27)24(17)31-25)18-12-29-20-9-14(26)6-7-15(20)22(18)30-23/h5-7,9-10,18,21-22,26-28H,4,8,11-12H2,1-3H3

> <INCHI_KEY>
MVDMPADXXDHNOL-UHFFFAOYSA-N

> <FORMULA>
C25H28O6

> <MOLECULAR_WEIGHT>
424.493

> <EXACT_MASS>
424.188588622

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
46.192587036031696

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
17-methyl-17-(4-methylpent-3-en-1-yl)-4,12,18-trioxapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-1(21),5,7,9,13,19-hexaene-7,16,20-triol

> <ALOGPS_LOGP>
3.76

> <JCHEM_LOGP>
4.050031336999999

> <ALOGPS_LOGS>
-4.34

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.401019828959964

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.372749600197015

> <JCHEM_PKA_STRONGEST_BASIC>
-3.3463761398992986

> <JCHEM_POLAR_SURFACE_AREA>
88.38000000000001

> <JCHEM_REFRACTIVITY>
117.0967

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.95e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
17-methyl-17-(4-methylpent-3-en-1-yl)-4,12,18-trioxapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-1(21),5,7,9,13,19-hexaene-7,16,20-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 23-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-APR-15         0                                  
HETATM    1  C   UNK     0       3.741   3.065   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.101   2.342   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.154   0.803   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.514   0.080   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.568  -1.459   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.928  -2.182   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.980  -3.396   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       8.404  -0.718   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       9.910  -0.397   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.386   1.067   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       9.355   2.212   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      11.892   1.387   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      12.923   0.243   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      14.463   0.243   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      15.493   1.387   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      16.999   1.067   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      17.475  -0.397   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      18.982  -0.718   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      19.457  -2.182   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      20.964  -2.502   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      18.427  -3.327   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      16.921  -3.006   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      16.445  -1.542   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      14.938  -1.222   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      13.693  -2.127   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      12.447  -1.222   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      10.940  -1.542   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      10.464  -3.006   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       8.958  -3.327   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       8.482  -4.791   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       6.407   3.158   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   31                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8   29                                             
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10   27                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   26                                                  
CONECT   14   13   15   24                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   23                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   17   24                                                  
CONECT   24   23   14   25                                                  
CONECT   25   24   26                                                       
CONECT   26   25   13   27                                                  
CONECT   27   26    9   28                                                  
CONECT   28   27   29                                                       
CONECT   29   28    6   30                                                  
CONECT   30   29                                                            
CONECT   31    2                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   70    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₂₈O₆

Average Mass

424.4930 Da

Monoisotopic Mass

424.18859 Da

IUPAC Name

17-methyl-17-(4-methylpent-3-en-1-yl)-4,12,18-trioxapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-1(21),5,7,9,13,19-hexaene-7,16,20-triol

Traditional Name

17-methyl-17-(4-methylpent-3-en-1-yl)-4,12,18-trioxapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-1(21),5,7,9,13,19-hexaene-7,16,20-triol

CAS Registry Number

Not Available

SMILES

CC(C)=CCCC1(C)OC2=C(O)C=C3C4COC5=CC(O)=CC=C5C4OC3=C2CC1O

InChI Identifier

InChI=1S/C25H28O6/c1-13(2)5-4-8-25(3)21(28)11-17-23-16(10-19(27)24(17)31-25)18-12-29-20-9-14(26)6-7-15(20)22(18)30-23/h5-7,9-10,18,21-22,26-28H,4,8,11-12H2,1-3H3

InChI Key

MVDMPADXXDHNOL-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
Lespedeza homoloba	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pterocarpans. These are benzo-pyrano-furano-benzene compounds, containing the 6H-[1]benzofuro[3,2-c]chromene skeleton. They are derivatives of isoflavonoids.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Isoflavonoids

Sub Class

Furanoisoflavonoids

Direct Parent

Pterocarpans

Alternative Parents

Substituents

Pterocarpan
Isoflavanol
Neolignan skeleton
Isoflavan
Chromane
Benzopyran
1-benzopyran
Coumaran
Benzofuran
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Benzenoid
Secondary alcohol
Oxacycle
Organoheterocyclic compound
Ether
Polyol
Alcohol
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	3.76	ALOGPS
logP	4.05	ChemAxon
logS	-4.3	ALOGPS
pKa (Strongest Acidic)	9.37	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	88.38 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	117.1 m³·mol⁻¹	ChemAxon
Polarizability	46.19 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

101040109

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 17-methyl-17-(4-methylpent-3-en-1-yl)-4,12,18-trioxapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-1(21),5,7,9,13,19-hexaene-7,16,20-triol (NP0232262)

MOL for NP0232262 (17-methyl-17-(4-methylpent-3-en-1-yl)-4,12,18-trioxapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-1(21),5,7,9,13,19-hexaene-7,16,20-triol)

3D MOL for NP0232262 (17-methyl-17-(4-methylpent-3-en-1-yl)-4,12,18-trioxapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-1(21),5,7,9,13,19-hexaene-7,16,20-triol)

3D SDF for NP0232262 (17-methyl-17-(4-methylpent-3-en-1-yl)-4,12,18-trioxapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-1(21),5,7,9,13,19-hexaene-7,16,20-triol)

3D-SDF for NP0232262 (17-methyl-17-(4-methylpent-3-en-1-yl)-4,12,18-trioxapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-1(21),5,7,9,13,19-hexaene-7,16,20-triol)

PDB for NP0232262 (17-methyl-17-(4-methylpent-3-en-1-yl)-4,12,18-trioxapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-1(21),5,7,9,13,19-hexaene-7,16,20-triol)

3D PDB for NP0232262 (17-methyl-17-(4-methylpent-3-en-1-yl)-4,12,18-trioxapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-1(21),5,7,9,13,19-hexaene-7,16,20-triol)

SMILES for NP0232262 (17-methyl-17-(4-methylpent-3-en-1-yl)-4,12,18-trioxapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-1(21),5,7,9,13,19-hexaene-7,16,20-triol)

INCHI for NP0232262 (17-methyl-17-(4-methylpent-3-en-1-yl)-4,12,18-trioxapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-1(21),5,7,9,13,19-hexaene-7,16,20-triol)

Structure for NP0232262 (17-methyl-17-(4-methylpent-3-en-1-yl)-4,12,18-trioxapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-1(21),5,7,9,13,19-hexaene-7,16,20-triol)

3D Structure for NP0232262 (17-methyl-17-(4-methylpent-3-en-1-yl)-4,12,18-trioxapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-1(21),5,7,9,13,19-hexaene-7,16,20-triol)