NP-MRD: Showing NP-Card for (+)-Artocommunol CE (NP0079784)

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Record Information

Version

2.0

Created at

2022-04-29 00:50:32 UTC

Updated at

2022-04-29 00:50:32 UTC

NP-MRD ID

NP0079784

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-Artocommunol CE

Description

5-Hydroxy-3-[(1R)-1-hydroxy-3-methylbut-2-en-1-yl]-2-(4-methoxyphenyl)-8,8-dimethyl-4H,8H-pyrano[2,3-f]chromen-4-one 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. (+)-Artocommunol CE is found in Artocarpus communis . Based on a literature review very few articles have been published on 5-hydroxy-3-[(1R)-1-hydroxy-3-methylbut-2-en-1-yl]-2-(4-methoxyphenyl)-8,8-dimethyl-4H,8H-pyrano[2,3-f]chromen-4-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292202502D          

 32 35  0  0  1  0            999 V2000
    3.6020   -0.3020    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
    2.3645    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
    3.6020    1.1270    0.0000 O   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
    4.7429    0.7998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7429    0.0252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    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
    1.1270   -0.3020    0.0000 O   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
   -0.1105    0.4125    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
   -0.1105    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3480    1.1270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480   -0.3020    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
   -2.5855    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5855   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480   -3.1599    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355   -3.8743    0.0000 C   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  2  2  0  0  0  0
  2  3  1  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
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  4  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
  3 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 11 16  1  0  0  0  0
 16 17  2  0  0  0  0
 15 18  1  0  0  0  0
 18 19  1  1  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 14 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 24 29  1  0  0  0  0
 27 30  1  0  0  0  0
 30 31  1  0  0  0  0
 10 32  1  0  0  0  0
M  END

     RDKit          3D

 58 61  0  0  0  0  0  0  0  0999 V2000
    5.4094    4.4564    1.2632 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1476    4.6052    0.6285 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2800    3.5419    0.5159 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6299    2.3157    1.0211 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7433    1.2355    0.9041 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5363    1.3472    0.3021 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5907    0.2785    0.0515 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7001    0.6579   -0.0091 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6716   -0.1593   -0.2200 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9722    0.3378   -0.2637 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9997   -0.5420   -0.4886 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7207   -1.8721   -0.6623 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4158   -2.3968   -0.6224 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2649   -3.7364   -0.8091 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3874   -1.5174   -0.3976 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0960   -1.9748   -0.3512 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2245   -3.1761   -0.5019 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9209   -1.0331   -0.1206 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2945   -1.5825   -0.2490 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3256   -2.1491   -1.5939 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5416   -2.7166    0.6882 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5256   -3.5796    0.5256 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7085   -4.6842    1.5020 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4889   -3.5096   -0.6079 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2835   -0.0263   -0.5280 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6381    1.3175   -0.3604 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.6381    1.3653    0.7972 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3618    1.7887   -1.6292 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5023    2.2304   -0.1206 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2668    1.7518   -0.0795 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2200    2.6215   -0.1990 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0645    3.6942   -0.0982 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9343    3.5521    0.8676 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2506    4.3849    2.3710 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9764    5.3944    1.0350 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5729    2.1337    1.5149 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0629    0.3299    1.3785 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5518   -2.5485   -0.8389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5526   -4.3679   -0.8389 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1156   -0.9016   -0.2511 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4698   -1.3931   -2.2239 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8678   -2.8039    1.5227 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9981   -5.4978    1.2024 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7167   -5.1302    1.4694 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4054   -4.3462    2.5086 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4951   -3.7879   -0.1770 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2194   -4.2696   -1.3926 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5684   -2.5035   -1.0491 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3451    2.2049    0.6731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1162    1.4940    1.7723 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1821    0.3863    0.8616 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5609    2.1874   -2.2969 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8501    0.8938   -2.0588 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0845    2.5489   -1.3218 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7429    3.2755    0.0136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4701    2.4504    0.0974 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2619    2.7581   -0.6875 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8084    4.6663   -0.4874 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  2  0
  6 31  1  0
 31 32  2  0
  6  7  1  0
  7 18  2  0
 18 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  2  3
 22 23  1  0
 22 24  1  0
 18 16  1  0
 16 17  2  0
 16 15  1  0
 15 13  2  0
 13 14  1  0
 13 12  1  0
 12 11  2  0
 11 25  1  0
 25 26  1  0
 26 27  1  1
 26 28  1  0
 26 29  1  0
 29 30  2  0
 30 10  1  0
 10  9  2  0
  9  8  1  0
 32  3  1  0
  8  7  1  0
  9 15  1  0
 10 11  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  4 36  1  0
  5 37  1  0
 31 57  1  0
 32 58  1  0
 19 40  1  6
 20 41  1  0
 21 42  1  0
 23 43  1  0
 23 44  1  0
 23 45  1  0
 24 46  1  0
 24 47  1  0
 24 48  1  0
 14 39  1  0
 12 38  1  0
 27 49  1  0
 27 50  1  0
 27 51  1  0
 28 52  1  0
 28 53  1  0
 28 54  1  0
 29 55  1  0
 30 56  1  0
M  END


  Mrv1652304292202502D          

 32 35  0  0  1  0            999 V2000
    3.6020   -0.3020    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
    2.3645    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
    3.6020    1.1270    0.0000 O   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
    4.7429    0.7998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7429    0.0252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    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
    1.1270   -0.3020    0.0000 O   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
   -0.1105    0.4125    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
   -0.1105    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3480    1.1270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480   -0.3020    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
   -2.5855    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5855   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480   -3.1599    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355   -3.8743    0.0000 C   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  2  2  0  0  0  0
  2  3  1  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
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  4  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
  3 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 11 16  1  0  0  0  0
 16 17  2  0  0  0  0
 15 18  1  0  0  0  0
 18 19  1  1  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 14 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 24 29  1  0  0  0  0
 27 30  1  0  0  0  0
 30 31  1  0  0  0  0
 10 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0079784

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C(C=C1)C1=C([C@H](O)C=C(C)C)C(=O)C2=C(O)C=C3OC(C)(C)C=CC3=C2O1

> <INCHI_IDENTIFIER>
InChI=1S/C26H26O6/c1-14(2)12-18(27)21-23(29)22-19(28)13-20-17(10-11-26(3,4)32-20)25(22)31-24(21)15-6-8-16(30-5)9-7-15/h6-13,18,27-28H,1-5H3/t18-/m1/s1

> <INCHI_KEY>
AEULKVUZCRFRBV-GOSISDBHSA-N

> <FORMULA>
C26H26O6

> <MOLECULAR_WEIGHT>
434.488

> <EXACT_MASS>
434.172938557

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
47.56242614935901

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5-hydroxy-3-[(1R)-1-hydroxy-3-methylbut-2-en-1-yl]-2-(4-methoxyphenyl)-8,8-dimethyl-4H,8H-pyrano[2,3-f]chromen-4-one

> <ALOGPS_LOGP>
4.26

> <JCHEM_LOGP>
4.592564405666667

> <ALOGPS_LOGS>
-4.95

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.919587740961255

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.5323353371836905

> <JCHEM_PKA_STRONGEST_BASIC>
-3.2721415316987637

> <JCHEM_POLAR_SURFACE_AREA>
85.22000000000001

> <JCHEM_REFRACTIVITY>
124.72890000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.87e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-hydroxy-3-[(1R)-1-hydroxy-3-methylbut-2-en-1-yl]-2-(4-methoxyphenyl)-8,8-dimethylpyrano[2,3-f]chromen-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0       6.724  -0.564   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.184  -0.564   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.414   0.770   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.184   2.104   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       6.724   2.104   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       7.494   0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.853   1.493   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.853   0.047   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.414   3.437   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.874   3.437   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.104   2.104   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.874   0.770   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       2.104  -0.564   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       0.564  -0.564   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.206   0.770   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.564   2.104   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -0.206   3.437   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -1.746   0.770   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -2.516   2.104   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -2.516  -0.564   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -4.056  -0.564   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -4.826   0.770   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -4.826  -1.897   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.206  -1.897   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.564  -3.231   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -0.206  -4.565   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -1.746  -4.565   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -2.516  -3.231   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -1.746  -1.897   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -2.516  -5.898   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      -1.746  -7.232   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       2.104   4.771   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   12                                                  
CONECT    4    3    5    9                                                  
CONECT    5    4    6                                                       
CONECT    6    5    1    7    8                                             
CONECT    7    6                                                            
CONECT    8    6                                                            
CONECT    9    4   10                                                       
CONECT   10    9   11   32                                                  
CONECT   11   10   12   16                                                  
CONECT   12   11    3   13                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   24                                                  
CONECT   15   14   16   18                                                  
CONECT   16   15   11   17                                                  
CONECT   17   16                                                            
CONECT   18   15   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   14   25   29                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   30                                                  
CONECT   28   27   29                                                       
CONECT   29   28   24                                                       
CONECT   30   27   31                                                       
CONECT   31   30                                                            
CONECT   32   10                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   70    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₆H₂₆O₆

Average Mass

434.4880 Da

Monoisotopic Mass

434.17294 Da

IUPAC Name

5-hydroxy-3-[(1R)-1-hydroxy-3-methylbut-2-en-1-yl]-2-(4-methoxyphenyl)-8,8-dimethyl-4H,8H-pyrano[2,3-f]chromen-4-one

Traditional Name

5-hydroxy-3-[(1R)-1-hydroxy-3-methylbut-2-en-1-yl]-2-(4-methoxyphenyl)-8,8-dimethylpyrano[2,3-f]chromen-4-one

CAS Registry Number

Not Available

SMILES

COC1=CC=C(C=C1)C1=C([C@H](O)C=C(C)C)C(=O)C2=C(O)C=C3OC(C)(C)C=CC3=C2O1

InChI Identifier

InChI=1S/C26H26O6/c1-14(2)12-18(27)21-23(29)22-19(28)13-20-17(10-11-26(3,4)32-20)25(22)31-24(21)15-6-8-16(30-5)9-7-15/h6-13,18,27-28H,1-5H3/t18-/m1/s1

InChI Key

AEULKVUZCRFRBV-GOSISDBHSA-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
Artocarpus altilis	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
4p-methoxyflavonoid-skeleton
Hydroxyflavonoid
5-hydroxyflavonoid
Pyranochromene
2,2-dimethyl-1-benzopyran
Chromone
Benzopyran
1-benzopyran
Phenoxy compound
Phenol ether
Anisole
Methoxybenzene
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Pyranone
Pyran
Monocyclic benzene moiety
Benzenoid
Heteroaromatic compound
Vinylogous acid
Secondary alcohol
Oxacycle
Organoheterocyclic compound
Ether
Organic oxide
Organic oxygen compound
Hydrocarbon derivative
Aromatic alcohol
Organooxygen compound
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	4.26	ALOGPS
logP	4.59	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Acidic)	7.53	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	85.22 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	124.73 m³·mol⁻¹	ChemAxon
Polarizability	47.56 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

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

162851665

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (+)-Artocommunol CE (NP0079784)

MOL for NP0079784 ((+)-Artocommunol CE)

3D MOL for NP0079784 ((+)-Artocommunol CE)

3D SDF for NP0079784 ((+)-Artocommunol CE)

3D-SDF for NP0079784 ((+)-Artocommunol CE)

PDB for NP0079784 ((+)-Artocommunol CE)

3D PDB for NP0079784 ((+)-Artocommunol CE)

SMILES for NP0079784 ((+)-Artocommunol CE)

INCHI for NP0079784 ((+)-Artocommunol CE)

Structure for NP0079784 ((+)-Artocommunol CE)

3D Structure for NP0079784 ((+)-Artocommunol CE)