NP-MRD: Showing NP-Card for 1-[2,4-dihydroxy-5-(2-methylpropanoyl)phenyl]-2-{2-ethyl-4,8-dihydroxy-1,5-dioxaspiro[2.5]octan-6-yl}-3-methylpentan-1-one (NP0266682)

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Record Information

Version

2.0

Created at

2022-09-08 11:06:22 UTC

Updated at

2022-09-08 11:06:22 UTC

NP-MRD ID

NP0266682

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-[2,4-dihydroxy-5-(2-methylpropanoyl)phenyl]-2-{2-ethyl-4,8-dihydroxy-1,5-dioxaspiro[2.5]octan-6-yl}-3-methylpentan-1-one

Description

1-[2,4-Dihydroxy-5-(2-methylpropanoyl)phenyl]-2-{2-ethyl-4,8-dihydroxy-1,5-dioxaspiro[2.5]Octan-6-yl}-3-methylpentan-1-one belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group. Based on a literature review very few articles have been published on 1-[2,4-dihydroxy-5-(2-methylpropanoyl)phenyl]-2-{2-ethyl-4,8-dihydroxy-1,5-dioxaspiro[2.5]Octan-6-yl}-3-methylpentan-1-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082213062D          

 32 34  0  0  0  0            999 V2000
    2.8875   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8875    0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3164    0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0309   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454    0.1105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0309   -1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3164   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3164   -2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8875   -2.3645    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -3.6020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8875   -4.0145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3164   -4.0145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0309   -2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0309   -3.6020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4599   -1.1270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3164    0.9355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020    1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020    2.1730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8875    2.5855    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3164    2.5855    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9039    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7289    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4434    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4434    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0309    2.1730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454    2.5855    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0309    1.3480    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  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 10 16  2  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
  8 19  1  0  0  0  0
 19 20  1  0  0  0  0
  5 21  1  0  0  0  0
 21 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
 26 27  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 25 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 21 32  1  0  0  0  0
M  END

     RDKit          3D

 66 68  0  0  0  0  0  0  0  0999 V2000
   -0.7834   -3.4396    2.4304 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1425   -2.1513    1.6763 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6514   -2.3194    0.2475 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2904   -3.4831   -0.4397 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.4641   -0.1938   -0.1583 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0918    0.8332    0.5433 O   0  0  0  0  0  0  0  0  0  0  0  0
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    4.1116    0.5932    0.0172 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9453    1.5822    0.6812 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3202    2.4858    1.3437 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4002    1.6567    0.6834 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1157    0.5559    1.3954 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8431    2.9818    1.3233 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6605   -0.4183   -0.7544 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0195   -0.5331   -0.9635 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8176   -1.3383   -1.3342 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4247   -1.2856   -1.1711 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6618   -2.2427   -1.7927 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9886   -0.3775   -0.6604 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9010    0.9014   -1.4917 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3669    1.2047   -1.8510 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8888    0.0406   -2.4063 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0618    1.4817   -0.5470 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6321    2.8331   -0.0727 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9992    2.5685   -0.4790 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.9507    2.8213    0.6365 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9169    1.6718    0.8533 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7991    0.4805    0.5077 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.7429   -0.5690    0.3941 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5724   -0.0868    0.5618 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5119   -4.2301    2.2600 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.2116   -2.0081    1.7816 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4304   -2.6140    0.4111 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.3512   -3.3281   -0.6923 H   0  0  0  0  0  0  0  0  0  0  0  0
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    2.3291    1.4105    0.7606 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8329    1.7263   -0.3488 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6308    0.9585    2.3159 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9466    0.1881    0.7682 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4854   -0.3133    1.6634 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4796    3.7923    0.6625 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3563    3.0333    2.3131 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9326    3.0239    1.3871 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3696   -1.2790   -1.5276 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2340   -2.1424   -1.9449 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1072   -2.9565   -2.3426 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7143   -1.0230   -1.2018 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3431    0.6473   -2.3992 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4769    1.7064   -0.8956 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4435    2.0050   -2.5797 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6311    0.2319   -3.0337 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.4511    3.0972    1.6119 H   0  0  0  0  0  0  0  0  0  0  0  0
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 19  8  1  0
 27 25  1  0
  1 33  1  0
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  9 43  1  0
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 15 50  1  0
 17 51  1  0
 18 52  1  0
 20 53  1  0
M  END


  Mrv1652309082213062D          

 32 34  0  0  0  0            999 V2000
    2.8875   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8875    0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3164    0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0309   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454    0.1105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0309   -1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3164   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3164   -2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8875   -2.3645    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    5.0309   -2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0309   -3.6020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4599   -1.1270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3164    0.9355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020    1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020    2.1730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8875    2.5855    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3164    2.5855    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9039    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7289    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4434    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4434    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0309    2.1730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454    2.5855    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0309    1.3480    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  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
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 25 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 21 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0266682

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC(C)C(C1CC(O)C2(OC2CC)C(O)O1)C(=O)C1=CC(C(=O)C(C)C)=C(O)C=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C24H34O8/c1-6-12(5)20(17-10-18(27)24(23(30)31-17)19(7-2)32-24)22(29)14-8-13(21(28)11(3)4)15(25)9-16(14)26/h8-9,11-12,17-20,23,25-27,30H,6-7,10H2,1-5H3

> <INCHI_KEY>
NWYMHIQKVQKIAG-UHFFFAOYSA-N

> <FORMULA>
C24H34O8

> <MOLECULAR_WEIGHT>
450.528

> <EXACT_MASS>
450.225368055

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
66

> <JCHEM_AVERAGE_POLARIZABILITY>
47.94130597678375

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1-[2,4-dihydroxy-5-(2-methylpropanoyl)phenyl]-2-{2-ethyl-4,8-dihydroxy-1,5-dioxaspiro[2.5]octan-6-yl}-3-methylpentan-1-one

> <JCHEM_LOGP>
4.464741967666665

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.404607076133638

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.15615552970968

> <JCHEM_PKA_STRONGEST_BASIC>
-3.380858873241171

> <JCHEM_POLAR_SURFACE_AREA>
136.82000000000002

> <JCHEM_REFRACTIVITY>
116.6408

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
1-[2,4-dihydroxy-5-(2-methylpropanoyl)phenyl]-2-{2-ethyl-4,8-dihydroxy-1,5-dioxaspiro[2.5]octan-6-yl}-3-methylpentan-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0       5.390  -2.874   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.724  -2.104   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.724  -0.564   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.390   0.206   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.057   0.206   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.391  -0.564   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      10.725   0.206   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       9.391  -2.104   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.057  -2.874   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.057  -4.414   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.724  -5.184   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       5.390  -4.414   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       6.724  -6.724   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.390  -7.494   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.057  -7.494   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.391  -5.184   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       9.391  -6.724   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      10.725  -4.414   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      10.725  -2.874   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      12.058  -2.104   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       8.057   1.746   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.724   2.516   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.724   4.056   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       5.390   4.826   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       8.057   4.826   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       7.287   6.160   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       8.827   6.160   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      10.161   6.930   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      10.161   8.470   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       9.391   4.056   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      10.725   4.826   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       9.391   2.516   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   21                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   19                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   16                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13                                                            
CONECT   16   10   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18    8   20                                                  
CONECT   20   19                                                            
CONECT   21    5   22   32                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   27   30                                             
CONECT   26   25   27                                                       
CONECT   27   26   25   28                                                  
CONECT   28   27   29                                                       
CONECT   29   28                                                            
CONECT   30   25   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   21                                                       
MASTER        0    0    0    0    0    0    0    0   32    0   68    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₃₄O₈

Average Mass

450.5280 Da

Monoisotopic Mass

450.22537 Da

IUPAC Name

1-[2,4-dihydroxy-5-(2-methylpropanoyl)phenyl]-2-{2-ethyl-4,8-dihydroxy-1,5-dioxaspiro[2.5]octan-6-yl}-3-methylpentan-1-one

Traditional Name

1-[2,4-dihydroxy-5-(2-methylpropanoyl)phenyl]-2-{2-ethyl-4,8-dihydroxy-1,5-dioxaspiro[2.5]octan-6-yl}-3-methylpentan-1-one

CAS Registry Number

Not Available

SMILES

CCC(C)C(C1CC(O)C2(OC2CC)C(O)O1)C(=O)C1=CC(C(=O)C(C)C)=C(O)C=C1O

InChI Identifier

InChI=1S/C24H34O8/c1-6-12(5)20(17-10-18(27)24(23(30)31-17)19(7-2)32-24)22(29)14-8-13(21(28)11(3)4)15(25)9-16(14)26/h8-9,11-12,17-20,23,25-27,30H,6-7,10H2,1-5H3

InChI Key

NWYMHIQKVQKIAG-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbonyl compounds

Direct Parent

Alkyl-phenylketones

Alternative Parents

Substituents

Alkyl-phenylketone
Butyrophenone
Phenylpropane
Aryl alkyl ketone
Resorcinol
Benzoyl
1-hydroxy-2-unsubstituted benzenoid
Phenol
Benzenoid
Oxane
Monocyclic benzene moiety
Vinylogous acid
Secondary alcohol
Hemiacetal
Oxacycle
Organoheterocyclic compound
Ether
Oxirane
Dialkyl ether
Organic oxide
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	4.46	ChemAxon
pKa (Strongest Acidic)	7.16	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	136.82 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	116.64 m³·mol⁻¹	ChemAxon
Polarizability	47.94 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

163061286

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1-[2,4-dihydroxy-5-(2-methylpropanoyl)phenyl]-2-{2-ethyl-4,8-dihydroxy-1,5-dioxaspiro[2.5]octan-6-yl}-3-methylpentan-1-one (NP0266682)

MOL for NP0266682 (1-[2,4-dihydroxy-5-(2-methylpropanoyl)phenyl]-2-{2-ethyl-4,8-dihydroxy-1,5-dioxaspiro[2.5]octan-6-yl}-3-methylpentan-1-one)

3D MOL for NP0266682 (1-[2,4-dihydroxy-5-(2-methylpropanoyl)phenyl]-2-{2-ethyl-4,8-dihydroxy-1,5-dioxaspiro[2.5]octan-6-yl}-3-methylpentan-1-one)

3D SDF for NP0266682 (1-[2,4-dihydroxy-5-(2-methylpropanoyl)phenyl]-2-{2-ethyl-4,8-dihydroxy-1,5-dioxaspiro[2.5]octan-6-yl}-3-methylpentan-1-one)

3D-SDF for NP0266682 (1-[2,4-dihydroxy-5-(2-methylpropanoyl)phenyl]-2-{2-ethyl-4,8-dihydroxy-1,5-dioxaspiro[2.5]octan-6-yl}-3-methylpentan-1-one)

PDB for NP0266682 (1-[2,4-dihydroxy-5-(2-methylpropanoyl)phenyl]-2-{2-ethyl-4,8-dihydroxy-1,5-dioxaspiro[2.5]octan-6-yl}-3-methylpentan-1-one)

3D PDB for NP0266682 (1-[2,4-dihydroxy-5-(2-methylpropanoyl)phenyl]-2-{2-ethyl-4,8-dihydroxy-1,5-dioxaspiro[2.5]octan-6-yl}-3-methylpentan-1-one)

SMILES for NP0266682 (1-[2,4-dihydroxy-5-(2-methylpropanoyl)phenyl]-2-{2-ethyl-4,8-dihydroxy-1,5-dioxaspiro[2.5]octan-6-yl}-3-methylpentan-1-one)

INCHI for NP0266682 (1-[2,4-dihydroxy-5-(2-methylpropanoyl)phenyl]-2-{2-ethyl-4,8-dihydroxy-1,5-dioxaspiro[2.5]octan-6-yl}-3-methylpentan-1-one)

Structure for NP0266682 (1-[2,4-dihydroxy-5-(2-methylpropanoyl)phenyl]-2-{2-ethyl-4,8-dihydroxy-1,5-dioxaspiro[2.5]octan-6-yl}-3-methylpentan-1-one)

3D Structure for NP0266682 (1-[2,4-dihydroxy-5-(2-methylpropanoyl)phenyl]-2-{2-ethyl-4,8-dihydroxy-1,5-dioxaspiro[2.5]octan-6-yl}-3-methylpentan-1-one)