NP-MRD: Showing NP-Card for 4-{[(2s)-3,3-dimethyloxiran-2-yl]methyl}-2-(4-hydroxybenzoyl)-5-methoxy-6-(3-methylbut-2-en-1-yl)benzene-1,3-diol (NP0208569)

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Record Information

Version

2.0

Created at

2022-09-05 05:37:30 UTC

Updated at

2022-09-05 05:37:30 UTC

NP-MRD ID

NP0208569

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-{[(2s)-3,3-dimethyloxiran-2-yl]methyl}-2-(4-hydroxybenzoyl)-5-methoxy-6-(3-methylbut-2-en-1-yl)benzene-1,3-diol

Description

Vismiaphenone G belongs to the class of organic compounds known as benzophenones. These are organic compounds containing a ketone attached to two phenyl groups. 4-{[(2s)-3,3-dimethyloxiran-2-yl]methyl}-2-(4-hydroxybenzoyl)-5-methoxy-6-(3-methylbut-2-en-1-yl)benzene-1,3-diol is found in Vismia cayennensis. Based on a literature review very few articles have been published on Vismiaphenone G.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052207372D          

 30 32  0  0  1  0            999 V2000
    5.0013   -2.5388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.3638    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -3.7763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.6013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -5.0138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.6013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -5.0138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -4.6013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -5.8388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.0138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.8388    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.6013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -5.0138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -5.8388    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.6013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -5.0138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.6013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -3.7763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.3638    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.3638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -3.7763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -3.7763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.3638    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.3638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.5388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.1263    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1118   -2.1263    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6993   -1.4118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2261   -0.7360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1725   -0.7360    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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  4 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 15 21  1  0  0  0  0
 12 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  2  0  0  0  0
  3 24  1  0  0  0  0
 24 25  1  0  0  0  0
 26 25  1  1  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
M  END

     RDKit          3D

 58 60  0  0  0  0  0  0  0  0999 V2000
    2.2156    2.6927    0.2989 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2185    2.1540    1.1169 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2832    1.2685    0.6444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9119    1.7689    0.1588 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3022    3.1796    0.1297 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4224    4.1735    0.6876 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0038    5.2111   -0.0383 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9091    6.2502    0.5293 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4768    5.3068   -1.4443 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8568    0.8810   -0.3102 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0723    1.3112   -0.8111 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6675   -0.5100   -0.3187 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7195   -1.3346   -0.8928 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4436   -0.8390   -1.8273 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0135   -2.6636   -0.4821 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8498   -3.0536    0.8289 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1239   -4.3433    1.2312 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5691   -5.2495    0.2964 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8530   -6.5631    0.6816 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7433   -4.8918   -1.0204 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4671   -3.6110   -1.4004 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4853   -1.0062    0.1569 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1837   -2.3116    0.1801 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4960   -0.0799    0.6451 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7587   -0.6829    1.0947 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8218   -0.7898    0.0276 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4296   -1.6054   -1.1154 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4226   -2.0846   -0.2744 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1739   -3.2299    0.6604 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8256   -2.1181   -0.8982 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0390    2.5894   -0.7826 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2255    2.2517    0.5212 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3704    3.7705    0.5708 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5836    3.4001   -0.9501 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3076    3.2658    0.6498 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0756    4.1096    1.7082 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9109    6.2462    1.6264 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5016    7.2403    0.2204 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9261    6.1898    0.1028 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5797    5.4577   -1.5142 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0035    6.2014   -1.8944 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1475    4.3996   -1.9912 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2635    2.2958   -0.8305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5024   -2.3528    1.5979 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9816   -4.5981    2.2562 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7294   -6.8378    1.6423 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0953   -5.6428   -1.7130 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5969   -3.2976   -2.4441 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4219   -3.1893   -0.0262 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5340   -1.7159    1.4567 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1674   -0.1366    1.9766 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3120    0.1394   -0.3084 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1675   -3.6507    0.5531 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9056   -4.0686    0.4917 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -2.9066    1.7195 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5680   -1.6422   -0.2425 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8451   -1.5665   -1.8650 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0740   -3.1815   -1.0662 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  2  3
  7  8  1  0
  7  9  1  0
  4 10  1  0
 10 11  1  0
 10 12  2  0
 12 13  1  0
 13 14  2  0
 13 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 18 20  1  0
 20 21  2  0
 12 22  1  0
 22 23  1  0
 22 24  2  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 28 30  1  0
 24  3  1  0
 28 26  1  0
 21 15  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  5 34  1  0
  5 35  1  0
  6 36  1  0
  8 37  1  0
  8 38  1  0
  8 39  1  0
  9 40  1  0
  9 41  1  0
  9 42  1  0
 11 43  1  0
 16 44  1  0
 17 45  1  0
 19 46  1  0
 20 47  1  0
 21 48  1  0
 23 49  1  0
 25 50  1  0
 25 51  1  0
 26 52  1  6
 29 53  1  0
 29 54  1  0
 29 55  1  0
 30 56  1  0
 30 57  1  0
 30 58  1  0
M  END


  Mrv1652309052207372D          

 30 32  0  0  1  0            999 V2000
    5.0013   -2.5388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.3638    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -3.7763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.6013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -5.0138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.6013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -5.0138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -4.6013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -5.8388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.0138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.8388    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.6013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -5.0138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -5.8388    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.6013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -5.0138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.6013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -3.7763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.3638    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.3638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -3.7763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -3.7763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.3638    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.3638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.5388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.1263    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1118   -2.1263    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6993   -1.4118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2261   -0.7360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1725   -0.7360    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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  4 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 15 21  1  0  0  0  0
 12 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  2  0  0  0  0
  3 24  1  0  0  0  0
 24 25  1  0  0  0  0
 26 25  1  1  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0208569

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(CC=C(C)C)C(O)=C(C(=O)C2=CC=C(O)C=C2)C(O)=C1C[C@@H]1OC1(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C24H28O6/c1-13(2)6-11-16-21(27)19(20(26)14-7-9-15(25)10-8-14)22(28)17(23(16)29-5)12-18-24(3,4)30-18/h6-10,18,25,27-28H,11-12H2,1-5H3/t18-/m0/s1

> <INCHI_KEY>
HONWZIFLOYHCME-SFHVURJKSA-N

> <FORMULA>
C24H28O6

> <MOLECULAR_WEIGHT>
412.482

> <EXACT_MASS>
412.188588622

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
44.51869472149586

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4-{[(2S)-3,3-dimethyloxiran-2-yl]methyl}-2-(4-hydroxybenzoyl)-5-methoxy-6-(3-methylbut-2-en-1-yl)benzene-1,3-diol

> <JCHEM_LOGP>
6.142630382999999

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
7.782260205348761

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.993695474631494

> <JCHEM_PKA_STRONGEST_BASIC>
-4.136319023680303

> <JCHEM_POLAR_SURFACE_AREA>
99.52000000000001

> <JCHEM_REFRACTIVITY>
116.36250000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
4-{[(2S)-3,3-dimethyloxiran-2-yl]methyl}-2-(4-hydroxybenzoyl)-5-methoxy-6-(3-methylbut-2-en-1-yl)benzene-1,3-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0       9.336  -4.739   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       9.336  -6.279   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       8.002  -7.049   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.002  -8.589   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.336  -9.359   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.669  -8.589   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      12.003  -9.359   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      13.337  -8.589   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      12.003 -10.899   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.668  -9.359   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       6.668 -10.899   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       5.335  -8.589   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.001  -9.359   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       4.001 -10.899   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       2.667  -8.589   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.334  -9.359   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.000  -8.589   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.000  -7.049   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -1.334  -6.279   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       1.334  -6.279   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.667  -7.049   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.335  -7.049   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       4.001  -6.279   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       6.668  -6.279   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.668  -4.739   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.002  -3.969   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       9.542  -3.969   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       8.772  -2.635   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       7.889  -1.374   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       9.655  -1.374   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   24                                                  
CONECT    4    3    5   10                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    4   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   22                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   21                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   15                                                       
CONECT   22   12   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22    3   25                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26   28                                                       
CONECT   28   27   26   29   30                                             
CONECT   29   28                                                            
CONECT   30   28                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₂₈O₆

Average Mass

412.4820 Da

Monoisotopic Mass

412.18859 Da

IUPAC Name

4-{[(2S)-3,3-dimethyloxiran-2-yl]methyl}-2-(4-hydroxybenzoyl)-5-methoxy-6-(3-methylbut-2-en-1-yl)benzene-1,3-diol

Traditional Name

4-{[(2S)-3,3-dimethyloxiran-2-yl]methyl}-2-(4-hydroxybenzoyl)-5-methoxy-6-(3-methylbut-2-en-1-yl)benzene-1,3-diol

CAS Registry Number

Not Available

SMILES

COC1=C(CC=C(C)C)C(O)=C(C(=O)C2=CC=C(O)C=C2)C(O)=C1C[C@@H]1OC1(C)C

InChI Identifier

InChI=1S/C24H28O6/c1-13(2)6-11-16-21(27)19(20(26)14-7-9-15(25)10-8-14)22(28)17(23(16)29-5)12-18-24(3,4)30-18/h6-10,18,25,27-28H,11-12H2,1-5H3/t18-/m0/s1

InChI Key

HONWZIFLOYHCME-SFHVURJKSA-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
Vismia cayennensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzophenones. These are organic compounds containing a ketone attached to two phenyl groups.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Benzophenones

Direct Parent

Benzophenones

Alternative Parents

Substituents

Benzophenone
Aryl-phenylketone
Diphenylmethane
Methoxyphenol
Phenoxy compound
Anisole
Benzoyl
Methoxybenzene
Phenol ether
Resorcinol
Aryl ketone
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
Phenol
Vinylogous acid
Ketone
Oxacycle
Ether
Oxirane
Dialkyl ether
Organoheterocyclic compound
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic 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	6.14	ChemAxon
pKa (Strongest Acidic)	6.99	ChemAxon
pKa (Strongest Basic)	-4.1	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	99.52 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	116.36 m³·mol⁻¹	ChemAxon
Polarizability	44.52 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	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

C00049334

Chemspider ID

416451

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

474317

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4-{[(2s)-3,3-dimethyloxiran-2-yl]methyl}-2-(4-hydroxybenzoyl)-5-methoxy-6-(3-methylbut-2-en-1-yl)benzene-1,3-diol (NP0208569)

MOL for NP0208569 (4-{[(2s)-3,3-dimethyloxiran-2-yl]methyl}-2-(4-hydroxybenzoyl)-5-methoxy-6-(3-methylbut-2-en-1-yl)benzene-1,3-diol)

3D MOL for NP0208569 (4-{[(2s)-3,3-dimethyloxiran-2-yl]methyl}-2-(4-hydroxybenzoyl)-5-methoxy-6-(3-methylbut-2-en-1-yl)benzene-1,3-diol)

3D SDF for NP0208569 (4-{[(2s)-3,3-dimethyloxiran-2-yl]methyl}-2-(4-hydroxybenzoyl)-5-methoxy-6-(3-methylbut-2-en-1-yl)benzene-1,3-diol)

3D-SDF for NP0208569 (4-{[(2s)-3,3-dimethyloxiran-2-yl]methyl}-2-(4-hydroxybenzoyl)-5-methoxy-6-(3-methylbut-2-en-1-yl)benzene-1,3-diol)

PDB for NP0208569 (4-{[(2s)-3,3-dimethyloxiran-2-yl]methyl}-2-(4-hydroxybenzoyl)-5-methoxy-6-(3-methylbut-2-en-1-yl)benzene-1,3-diol)

3D PDB for NP0208569 (4-{[(2s)-3,3-dimethyloxiran-2-yl]methyl}-2-(4-hydroxybenzoyl)-5-methoxy-6-(3-methylbut-2-en-1-yl)benzene-1,3-diol)

SMILES for NP0208569 (4-{[(2s)-3,3-dimethyloxiran-2-yl]methyl}-2-(4-hydroxybenzoyl)-5-methoxy-6-(3-methylbut-2-en-1-yl)benzene-1,3-diol)

INCHI for NP0208569 (4-{[(2s)-3,3-dimethyloxiran-2-yl]methyl}-2-(4-hydroxybenzoyl)-5-methoxy-6-(3-methylbut-2-en-1-yl)benzene-1,3-diol)

Structure for NP0208569 (4-{[(2s)-3,3-dimethyloxiran-2-yl]methyl}-2-(4-hydroxybenzoyl)-5-methoxy-6-(3-methylbut-2-en-1-yl)benzene-1,3-diol)

3D Structure for NP0208569 (4-{[(2s)-3,3-dimethyloxiran-2-yl]methyl}-2-(4-hydroxybenzoyl)-5-methoxy-6-(3-methylbut-2-en-1-yl)benzene-1,3-diol)