NP-MRD: Showing NP-Card for 2-(2,4-Dihydroxyphenyl)-5-hydroxy-3-(3-hydroxy-3-methylbutyl)-8,8-dimethyl-4H,8H-benzo[1,2-b:3,4-b']dipyran-4-one (NP0052438)

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Record Information

Version

2.0

Created at

2022-04-27 23:28:58 UTC

Updated at

2022-04-27 23:28:58 UTC

NP-MRD ID

NP0052438

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-(2,4-Dihydroxyphenyl)-5-hydroxy-3-(3-hydroxy-3-methylbutyl)-8,8-dimethyl-4H,8H-benzo[1,2-b:3,4-b']dipyran-4-one

Description

Morusinol, also known as oxyhydromorusin, belongs to the class of organic compounds known as 3-prenylated flavones. These are flavones that features a C5-isoprenoid substituent at the 3-position. Thus, morusinol is considered to be a flavonoid lipid molecule. Morusinol is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral. Outside of the human body, Morusinol has been detected, but not quantified in, fruits. 2-(2,4-Dihydroxyphenyl)-5-hydroxy-3-(3-hydroxy-3-methylbutyl)-8,8-dimethyl-4H,8H-benzo[1,2-b:3,4-b']dipyran-4-one is found in Morus alba , Morus australis and Morus mongolica . This could make morusinol a potential biomarker for the consumption of these foods.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv0541 05061305232D          

 32 35  0  0  0  0            999 V2000
   -2.9980    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1730    0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6465    0.9428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6465   -0.1178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480    1.1270    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
   -0.1105    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1730    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480    3.9849    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    2.5559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -1.7309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105   -1.0164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1730    1.9520    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -0.3020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  2  0  0  0  0
  9  7  1  0  0  0  0
 10  8  2  0  0  0  0
 13  5  1  0  0  0  0
 13 11  2  0  0  0  0
 14  6  1  0  0  0  0
 15  8  1  0  0  0  0
 16  7  1  0  0  0  0
 17 11  1  0  0  0  0
 17 14  2  0  0  0  0
 18 12  2  0  0  0  0
 19 12  1  0  0  0  0
 19 15  2  0  0  0  0
 20 18  1  0  0  0  0
 21 16  1  0  0  0  0
 21 20  1  0  0  0  0
 22 14  1  0  0  0  0
 22 16  2  0  0  0  0
 23 15  1  0  0  0  0
 23 20  2  0  0  0  0
 24  1  1  0  0  0  0
 24  2  1  0  0  0  0
 24  9  1  0  0  0  0
 25  3  1  0  0  0  0
 25  4  1  0  0  0  0
 25 10  1  0  0  0  0
 26 13  1  0  0  0  0
 27 17  1  0  0  0  0
 28 18  1  0  0  0  0
 29 21  2  0  0  0  0
 30 24  1  0  0  0  0
 31 22  1  0  0  0  0
 31 23  1  0  0  0  0
 32 19  1  0  0  0  0
 32 25  1  0  0  0  0
M  END

     RDKit          3D

 58 61  0  0  0  0  0  0  0  0999 V2000
   -5.3764   -1.2845    1.0957 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8767   -1.8347   -0.1937 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4307   -1.0263   -1.3525 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3211   -3.1411   -0.3417 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3510   -1.9077   -0.2833 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7439   -0.5260   -0.1553 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2857   -0.4914   -0.1608 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6044    0.6137    0.2269 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1449    1.8935    0.6921 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2919    2.4530    0.1897 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6900    3.7326    0.5566 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9502    4.4770    1.4309 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3385    5.7672    1.8055 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7979    3.9479    1.9539 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3930    2.6577    1.5889 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7541    2.2301    2.1763 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7304    0.5708    0.2058 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4586   -0.4255   -0.1512 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8385   -0.3747   -0.1474 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5803   -1.4552   -0.5380 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9544   -2.5952   -0.9375 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5503   -2.6639   -0.9478 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0155   -3.8484   -1.3629 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7977   -1.5773   -0.5541 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5734   -1.6242   -0.5639 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1299   -2.6616   -0.9245 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9766   -1.3662   -0.5164 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6851   -0.1857   -0.2774 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3594    0.1548   -1.6224 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7986   -0.4983    0.7018 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8280    0.9278    0.1475 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5156    0.8611    0.2114 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5901   -0.9654    1.8069 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9727   -2.0501    1.6819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1329   -0.4779    0.8930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6871   -0.0141   -0.9560 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7558   -0.9966   -2.2055 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3929   -1.4833   -1.6543 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7679   -3.6323   -1.0320 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0019   -2.5475    0.5190 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1817   -2.2683   -1.3230 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2478    0.0095    0.6557 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1007   -0.0384   -1.1334 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9301    1.9735   -0.5173 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6090    4.1737    0.1489 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0421    6.5903    1.2923 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2233    4.5479    2.6430 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1872    1.3826    2.1108 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5476   -3.4657   -1.2518 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1400   -4.2029   -1.4787 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9530   -0.4618   -2.4491 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2044    1.2403   -1.8478 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4425   -0.0229   -1.5700 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6851   -0.9488    0.1882 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1543    0.4936    1.0963 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5137   -1.2070    1.4870 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3408    1.8516    0.4176 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9241    1.7209    0.5259 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  2  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  8 17  1  0
 17 18  1  0
 18 24  2  0
 24 22  1  0
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 22 21  2  0
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 31 28  1  0
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 28 27  1  0
 24 25  1  0
 25 26  2  0
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 14 12  2  0
 12 13  1  0
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 11 10  2  0
 25  7  1  0
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 19 18  1  0
 27 20  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  3 36  1  0
  3 37  1  0
  3 38  1  0
  4 39  1  0
  5 40  1  0
  5 41  1  0
  6 42  1  0
  6 43  1  0
 23 50  1  0
 21 49  1  0
 32 58  1  0
 31 57  1  0
 29 51  1  0
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 29 53  1  0
 30 54  1  0
 30 55  1  0
 30 56  1  0
 16 48  1  0
 14 47  1  0
 13 46  1  0
 11 45  1  0
 10 44  1  0
M  END


  Mrv0541 05061305232D          

 32 35  0  0  0  0            999 V2000
   -2.9980    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1730    0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6465    0.9428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6465   -0.1178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480    1.1270    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
   -0.1105    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1730    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480    3.9849    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    2.5559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -1.7309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105   -1.0164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1730    1.9520    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -0.3020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  2  0  0  0  0
  9  7  1  0  0  0  0
 10  8  2  0  0  0  0
 13  5  1  0  0  0  0
 13 11  2  0  0  0  0
 14  6  1  0  0  0  0
 15  8  1  0  0  0  0
 16  7  1  0  0  0  0
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 17 14  2  0  0  0  0
 18 12  2  0  0  0  0
 19 12  1  0  0  0  0
 19 15  2  0  0  0  0
 20 18  1  0  0  0  0
 21 16  1  0  0  0  0
 21 20  1  0  0  0  0
 22 14  1  0  0  0  0
 22 16  2  0  0  0  0
 23 15  1  0  0  0  0
 23 20  2  0  0  0  0
 24  1  1  0  0  0  0
 24  2  1  0  0  0  0
 24  9  1  0  0  0  0
 25  3  1  0  0  0  0
 25  4  1  0  0  0  0
 25 10  1  0  0  0  0
 26 13  1  0  0  0  0
 27 17  1  0  0  0  0
 28 18  1  0  0  0  0
 29 21  2  0  0  0  0
 30 24  1  0  0  0  0
 31 22  1  0  0  0  0
 31 23  1  0  0  0  0
 32 19  1  0  0  0  0
 32 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0052438

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)(O)CCC1=C(OC2=C(C(O)=CC3=C2C=CC(C)(C)O3)C1=O)C1=C(O)C=C(O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C25H26O7/c1-24(2,30)9-7-16-21(29)20-18(28)12-19-15(8-10-25(3,4)32-19)23(20)31-22(16)14-6-5-13(26)11-17(14)27/h5-6,8,10-12,26-28,30H,7,9H2,1-4H3

> <INCHI_KEY>
AFOKZNPZDXHDHD-UHFFFAOYSA-N

> <FORMULA>
C25H26O7

> <MOLECULAR_WEIGHT>
438.4697

> <EXACT_MASS>
438.167853186

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_AVERAGE_POLARIZABILITY>
46.71364453678914

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-(2,4-dihydroxyphenyl)-5-hydroxy-3-(3-hydroxy-3-methylbutyl)-8,8-dimethyl-4H,8H-pyrano[2,3-h]chromen-4-one

> <ALOGPS_LOGP>
4.19

> <JCHEM_LOGP>
4.152473431333333

> <ALOGPS_LOGS>
-4.72

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.80549005005522

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.050507870044008

> <JCHEM_PKA_STRONGEST_BASIC>
-1.2104495481600797

> <JCHEM_POLAR_SURFACE_AREA>
116.45

> <JCHEM_REFRACTIVITY>
121.85209999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.29e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
oxydihydromorusin

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0      -5.596   2.104   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.056   0.564   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.673   1.760   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.673  -0.220   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.516   4.771   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.746   3.437   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.746   0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.184   2.104   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.516   2.104   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.724   2.104   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.206   6.105   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.414  -1.897   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.746   6.105   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.206   3.437   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.414   0.770   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.206   0.770   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.564   4.771   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.874  -1.897   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.184  -0.564   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.104  -0.564   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.564  -0.564   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.564   2.104   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.874   0.770   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -4.056   2.104   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       7.494   0.770   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -2.516   7.438   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       2.104   4.771   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       2.104  -3.231   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      -0.206  -1.897   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      -4.056   3.644   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       2.104   2.104   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       6.724  -0.564   0.000  0.00  0.00           O+0
CONECT    1   24                                                            
CONECT    2   24                                                            
CONECT    3   25                                                            
CONECT    4   25                                                            
CONECT    5    6   13                                                       
CONECT    6    5   14                                                       
CONECT    7    9   16                                                       
CONECT    8   10   15                                                       
CONECT    9    7   24                                                       
CONECT   10    8   25                                                       
CONECT   11   13   17                                                       
CONECT   12   18   19                                                       
CONECT   13    5   11   26                                                  
CONECT   14    6   17   22                                                  
CONECT   15    8   19   23                                                  
CONECT   16    7   21   22                                                  
CONECT   17   11   14   27                                                  
CONECT   18   12   20   28                                                  
CONECT   19   12   15   32                                                  
CONECT   20   18   21   23                                                  
CONECT   21   16   20   29                                                  
CONECT   22   14   16   31                                                  
CONECT   23   15   20   31                                                  
CONECT   24    1    2    9   30                                             
CONECT   25    3    4   10   32                                             
CONECT   26   13                                                            
CONECT   27   17                                                            
CONECT   28   18                                                            
CONECT   29   21                                                            
CONECT   30   24                                                            
CONECT   31   22   23                                                       
CONECT   32   19   25                                                       
MASTER        0    0    0    0    0    0    0    0   32    0   70    0
END

View in JSmol

Synonyms

Value	Source
Oxyhydromorusin	Kegg
2-(2,4-Dihydroxyphenyl)-5-hydroxy-3-(3-hydroxy-3-methylbutyl)-8,8-dimethyl-4H,8H-benzo[1,2-b:3,4-b']dipyran-4-one	HMDB
2-(2,4-Dihydroxyphenyl)-5-hydroxy-3-(3-hydroxy-3-methylbutyl)-8,8-dimethyl-4H,8H-benzo[1,2-b:3,4-b']dipyran-4-one, 9ci	HMDB
Oxydihydromorusin	HMDB

Chemical Formula

C₂₅H₂₆O₇

Average Mass

438.4697 Da

Monoisotopic Mass

438.16785 Da

IUPAC Name

2-(2,4-dihydroxyphenyl)-5-hydroxy-3-(3-hydroxy-3-methylbutyl)-8,8-dimethyl-4H,8H-pyrano[2,3-h]chromen-4-one

Traditional Name

oxydihydromorusin

CAS Registry Number

Not Available

SMILES

CC(C)(O)CCC1=C(OC2=C(C(O)=CC3=C2C=CC(C)(C)O3)C1=O)C1=C(O)C=C(O)C=C1

InChI Identifier

InChI=1S/C25H26O7/c1-24(2,30)9-7-16-21(29)20-18(28)12-19-15(8-10-25(3,4)32-19)23(20)31-22(16)14-6-5-13(26)11-17(14)27/h5-6,8,10-12,26-28,30H,7,9H2,1-4H3

InChI Key

AFOKZNPZDXHDHD-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Morus alba	Plant	KNApSAcK
Morus australis	Plant	KNApSAcK
Morus mongolica	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 3-prenylated flavones. These are flavones that features a C5-isoprenoid substituent at the 3-position.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavones

Direct Parent

3-prenylated flavones

Alternative Parents

Substituents

3-prenylated flavone
Pyranoflavonoid
4'-hydroxyflavonoid
5-hydroxyflavonoid
Hydroxyflavonoid
Pyranochromene
2,2-dimethyl-1-benzopyran
Chromone
Benzopyran
1-benzopyran
Resorcinol
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Pyranone
Phenol
Benzenoid
Pyran
Monocyclic benzene moiety
Heteroaromatic compound
Vinylogous acid
Tertiary alcohol
Ether
Organoheterocyclic compound
Oxacycle
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Flavones and Flavonols (LMPK12110919 )

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	4.19	ALOGPS
logP	4.15	ChemAxon
logS	-4.7	ALOGPS
pKa (Strongest Acidic)	8.05	ChemAxon
pKa (Strongest Basic)	-1.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	116.45 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	121.85 m³·mol⁻¹	ChemAxon
Polarizability	46.71 Å³	ChemAxon
Number of Rings	4	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

HMDB0030620

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

KNApSAcK ID

Chemspider ID

KEGG Compound ID

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5481968

PDB ID

Not Available

ChEBI ID

1200679

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 2-(2,4-Dihydroxyphenyl)-5-hydroxy-3-(3-hydroxy-3-methylbutyl)-8,8-dimethyl-4H,8H-benzo[1,2-b:3,4-b']dipyran-4-one (NP0052438)

MOL for NP0052438 (2-(2,4-Dihydroxyphenyl)-5-hydroxy-3-(3-hydroxy-3-methylbutyl)-8,8-dimethyl-4H,8H-benzo[1,2-b:3,4-b']dipyran-4-one)

3D MOL for NP0052438 (2-(2,4-Dihydroxyphenyl)-5-hydroxy-3-(3-hydroxy-3-methylbutyl)-8,8-dimethyl-4H,8H-benzo[1,2-b:3,4-b']dipyran-4-one)

3D SDF for NP0052438 (2-(2,4-Dihydroxyphenyl)-5-hydroxy-3-(3-hydroxy-3-methylbutyl)-8,8-dimethyl-4H,8H-benzo[1,2-b:3,4-b']dipyran-4-one)

3D-SDF for NP0052438 (2-(2,4-Dihydroxyphenyl)-5-hydroxy-3-(3-hydroxy-3-methylbutyl)-8,8-dimethyl-4H,8H-benzo[1,2-b:3,4-b']dipyran-4-one)

PDB for NP0052438 (2-(2,4-Dihydroxyphenyl)-5-hydroxy-3-(3-hydroxy-3-methylbutyl)-8,8-dimethyl-4H,8H-benzo[1,2-b:3,4-b']dipyran-4-one)

3D PDB for NP0052438 (2-(2,4-Dihydroxyphenyl)-5-hydroxy-3-(3-hydroxy-3-methylbutyl)-8,8-dimethyl-4H,8H-benzo[1,2-b:3,4-b']dipyran-4-one)

SMILES for NP0052438 (2-(2,4-Dihydroxyphenyl)-5-hydroxy-3-(3-hydroxy-3-methylbutyl)-8,8-dimethyl-4H,8H-benzo[1,2-b:3,4-b']dipyran-4-one)

INCHI for NP0052438 (2-(2,4-Dihydroxyphenyl)-5-hydroxy-3-(3-hydroxy-3-methylbutyl)-8,8-dimethyl-4H,8H-benzo[1,2-b:3,4-b']dipyran-4-one)

Structure for NP0052438 (2-(2,4-Dihydroxyphenyl)-5-hydroxy-3-(3-hydroxy-3-methylbutyl)-8,8-dimethyl-4H,8H-benzo[1,2-b:3,4-b']dipyran-4-one)

3D Structure for NP0052438 (2-(2,4-Dihydroxyphenyl)-5-hydroxy-3-(3-hydroxy-3-methylbutyl)-8,8-dimethyl-4H,8H-benzo[1,2-b:3,4-b']dipyran-4-one)