NP-MRD: Showing NP-Card for 6-(3,5-dihydroxyphenyl)-7,11,19-tris(4-hydroxyphenyl)-8,18-dioxapentacyclo[11.6.1.0²,¹⁰.0⁵,⁹.0¹⁷,²⁰]icosa-2,4,9,11,13,15,17(20)-heptaene-4,15-diol (NP0163266)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-02 21:50:51 UTC

Updated at

2022-09-02 21:50:51 UTC

NP-MRD ID

NP0163266

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6-(3,5-dihydroxyphenyl)-7,11,19-tris(4-hydroxyphenyl)-8,18-dioxapentacyclo[11.6.1.0²,¹⁰.0⁵,⁹.0¹⁷,²⁰]icosa-2,4,9,11,13,15,17(20)-heptaene-4,15-diol

Description

6-(3,5-Dihydroxyphenyl)-7,11,19-tris(4-hydroxyphenyl)-8,18-dioxapentacyclo[11.6.1.0²,¹⁰.0⁵,⁹.0¹⁷,²⁰]Icosa-2,4,9,11,13,15,17(20)-heptaene-4,15-diol belongs to the class of organic compounds known as 2-arylbenzofuran flavonoids. These are phenylpropanoids containing the 2-phenylbenzofuran moiety. 6-(3,5-Dihydroxyphenyl)-7,11,19-tris(4-hydroxyphenyl)-8,18-dioxapentacyclo[11.6.1.0²,¹⁰.0⁵,⁹.0¹⁷,²⁰]Icosa-2,4,9,11,13,15,17(20)-heptaene-4,15-diol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251514592D          

 51 59  0  0  0  0            999 V2000
    9.0199    3.3435    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.3288    2.8929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3735    2.0691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6824    1.6186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9466    1.9918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9020    2.8156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5931    3.2662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2556    1.5412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4848    1.8355    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9668    1.1934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4173    0.5023    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2138    0.7173    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8559    0.1993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6256    0.4963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2677   -0.0218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0373    0.2753    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1401   -0.8368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3704   -1.1339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2428   -1.9489    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7283   -0.6158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0441   -0.2334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4947   -0.9245    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2203   -0.2781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7698    0.4130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9618    0.2461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6561   -0.5201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8328   -0.4661    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6298    0.3335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8997    0.7177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8674    1.5421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1373    1.9263    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5652    1.9823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3446    1.5985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0001    2.0995    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8005    1.8993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3280    2.5336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0426    3.3076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5702    3.9419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3832    3.8021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9108    4.4363    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6687    3.0281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1411    2.3938    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1430    1.1488    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3276    0.7737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0962   -1.2179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9206   -1.1856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3608   -1.8833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9766   -2.6134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4168   -3.3112    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1522   -2.6457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7120   -1.9480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  2  7  1  0  0  0  0
  5  8  1  0  0  0  0
  8  9  1  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
  8 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 13 20  1  0  0  0  0
 11 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 39 40  1  0  0  0  0
 39 41  1  0  0  0  0
 41 42  2  0  0  0  0
 36 42  1  0  0  0  0
 35 43  1  0  0  0  0
 10 43  1  0  0  0  0
 24 43  2  0  0  0  0
 33 44  2  0  0  0  0
 25 44  1  0  0  0  0
 28 44  1  0  0  0  0
 26 45  1  0  0  0  0
 45 46  2  0  0  0  0
 46 47  1  0  0  0  0
 47 48  2  0  0  0  0
 48 49  1  0  0  0  0
 48 50  1  0  0  0  0
 50 51  2  0  0  0  0
 45 51  1  0  0  0  0
M  END

     RDKit          3D

 81 89  0  0  0  0  0  0  0  0999 V2000
   -1.8977    6.6109    0.8558 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2019    5.4502    0.4770 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4155    5.4420   -0.6393 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2537    4.3033   -0.9949 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1769    3.1082   -0.2578 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0785    2.0738   -0.6862 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3438    2.5417   -0.7284 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5672    1.8647   -1.1095 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7023    2.6366   -1.0296 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9421    2.0992   -1.2454 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0572    2.8997   -1.1599 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0976    0.7427   -1.5532 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9416   -0.0179   -1.6291 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7005    0.5450   -1.4143 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7403   -0.5307   -1.7007 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3503   -0.3341   -1.4323 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6537   -1.4725   -1.7790 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7073   -1.5791   -1.7500 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3880   -2.7453   -2.1070 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4672   -0.5167   -1.3592 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8118    0.6489   -0.9952 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5755    0.7696   -1.0209 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8092    1.5745   -0.6330 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9805    0.8420   -0.2639 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9222    0.4255    1.1468 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0626    0.6317    1.9372 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0874    0.2688    3.2543 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9794   -0.3095    3.8233 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9925   -0.6784    5.1461 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8624   -0.5160    3.0647 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8355   -0.1539    1.7476 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9229   -0.2314   -1.2818 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.8200   -1.3529   -1.2271 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6833   -1.5742   -2.3164 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5717   -2.6171   -2.3789 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4130   -2.8106   -3.4690 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6586   -3.5216   -1.3432 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8268   -3.3260   -0.2715 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8727   -4.2044    0.7955 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9253   -2.2611   -0.2172 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4667   -1.7515   -1.3333 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6503   -2.0541    0.0788 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0828   -3.2345    0.5930 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1966   -3.6026    1.9121 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8785   -2.8226    2.7952 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9849   -3.2102    4.1293 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4507   -1.6593    2.3402 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3271   -1.2992    1.0017 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7663   -1.3933   -1.8992 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6123    3.1471    0.8517 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2984    4.3048    1.2188 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4333    7.2631    1.4757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3407    6.3425   -1.2187 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8847    4.3088   -1.8981 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4695    3.5856   -0.4320 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6193    3.7035   -0.7887 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3589    3.3597   -2.0162 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0723    0.3083   -1.7238 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7979   -0.5597   -2.8910 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1956   -2.3752   -2.1075 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8143   -3.5267   -2.3951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8836    1.5146   -0.3977 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9312    1.0839    1.4957 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9829    0.4305    3.8749 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7103   -0.0688    5.9104 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9599   -0.9758    3.4882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9181   -0.3433    1.1809 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1420    0.3508   -2.2745 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6567   -0.8987   -3.1507 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1109   -3.3767   -4.2485 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3468   -4.3506   -1.3635 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2363   -5.0139    0.7267 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2956   -2.1714    0.6503 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1648   -2.6561   -1.9256 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5234   -3.9075   -0.0525 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7472   -4.5264    2.2939 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7479   -3.7853    4.4598 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9896   -1.0456    3.0443 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8019   -0.3711    0.7379 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6602    2.2872    1.4918 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9093    4.2640    2.1109 H   0  0  0  0  0  0  0  0  0  0  0  0
 46 45  1  0
 45 44  2  0
 44 43  1  0
 43 42  2  0
 42 48  1  0
 48 47  2  0
 42 41  1  0
 41 49  1  0
 49 13  1  0
 13 12  2  0
 12 10  1  0
 10 11  1  0
 10  9  2  0
  9  8  1  0
  8 14  2  0
 14 15  1  0
 15 16  1  0
 16 22  2  0
 22 21  1  0
 21 20  2  0
 20 32  1  0
 32 24  1  0
 24 23  1  0
 24 25  1  0
 25 26  2  0
 26 27  1  0
 27 28  2  0
 28 29  1  0
 28 30  1  0
 30 31  2  0
 32 33  1  0
 33 34  2  0
 34 35  1  0
 35 36  1  0
 35 37  2  0
 37 38  1  0
 38 39  1  0
 38 40  2  0
 20 18  1  0
 18 19  1  0
 18 17  2  0
 22  6  1  0
  6  7  2  0
  6  5  1  0
  5  4  2  0
  4  3  1  0
  3  2  2  0
  2  1  1  0
  2 51  1  0
 51 50  2  0
 47 45  1  0
 15 41  1  0
 17 16  1  0
 50  5  1  0
 14 13  1  0
 23 21  1  0
 31 25  1  0
 40 33  1  0
  7  8  1  0
 46 77  1  0
 44 76  1  0
 43 75  1  0
 48 79  1  0
 47 78  1  0
 41 74  1  6
 12 58  1  0
 11 57  1  0
  9 56  1  0
 15 59  1  6
 32 68  1  6
 24 62  1  1
 26 63  1  0
 27 64  1  0
 29 65  1  0
 30 66  1  0
 31 67  1  0
 34 69  1  0
 36 70  1  0
 37 71  1  0
 39 72  1  0
 40 73  1  0
 19 61  1  0
 17 60  1  0
  7 55  1  0
  4 54  1  0
  3 53  1  0
  1 52  1  0
 51 81  1  0
 50 80  1  0
M  END


  Mrv1533004251514592D          

 51 59  0  0  0  0            999 V2000
    9.0199    3.3435    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.3288    2.8929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3735    2.0691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6824    1.6186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9466    1.9918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9020    2.8156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5931    3.2662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2556    1.5412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4848    1.8355    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9668    1.1934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4173    0.5023    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2138    0.7173    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8559    0.1993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6256    0.4963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2677   -0.0218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0373    0.2753    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1401   -0.8368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3704   -1.1339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2428   -1.9489    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7283   -0.6158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0441   -0.2334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4947   -0.9245    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2203   -0.2781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7698    0.4130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9618    0.2461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6561   -0.5201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8328   -0.4661    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6298    0.3335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8997    0.7177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8674    1.5421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1373    1.9263    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5652    1.9823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3446    1.5985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0001    2.0995    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8005    1.8993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3280    2.5336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0426    3.3076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5702    3.9419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3832    3.8021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9108    4.4363    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6687    3.0281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1411    2.3938    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1430    1.1488    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3276    0.7737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0962   -1.2179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9206   -1.1856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3608   -1.8833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9766   -2.6134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4168   -3.3112    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1522   -2.6457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7120   -1.9480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  2  7  1  0  0  0  0
  5  8  1  0  0  0  0
  8  9  1  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
  8 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 13 20  1  0  0  0  0
 11 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 39 40  1  0  0  0  0
 39 41  1  0  0  0  0
 41 42  2  0  0  0  0
 36 42  1  0  0  0  0
 35 43  1  0  0  0  0
 10 43  1  0  0  0  0
 24 43  2  0  0  0  0
 33 44  2  0  0  0  0
 25 44  1  0  0  0  0
 28 44  1  0  0  0  0
 26 45  1  0  0  0  0
 45 46  2  0  0  0  0
 46 47  1  0  0  0  0
 47 48  2  0  0  0  0
 48 49  1  0  0  0  0
 48 50  1  0  0  0  0
 50 51  2  0  0  0  0
 45 51  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0163266

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC1=CC=C(C=C1)C1OC2=CC(O)=CC3=C2C1C1=C(C2=C(C(C(O2)C2=CC=C(O)C=C2)C2=CC(O)=CC(O)=C2)C(O)=C1)C(=C3)C1=CC=C(O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C42H30O9/c43-25-7-1-20(2-8-25)31-16-24-15-30(48)18-34-35(24)38(41(50-34)22-5-11-27(45)12-6-22)32-19-33(49)39-36(23-13-28(46)17-29(47)14-23)40(51-42(39)37(31)32)21-3-9-26(44)10-4-21/h1-19,36,38,40-41,43-49H

> <INCHI_KEY>
AYDHZBQRJGDSHM-UHFFFAOYSA-N

> <FORMULA>
C42H30O9

> <MOLECULAR_WEIGHT>
678.693

> <EXACT_MASS>
678.188982546

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
81

> <JCHEM_AVERAGE_POLARIZABILITY>
72.27541780967488

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
6-(3,5-dihydroxyphenyl)-7,11,19-tris(4-hydroxyphenyl)-8,18-dioxapentacyclo[11.6.1.0²,¹⁰.0⁵,⁹.0¹⁷,²⁰]icosa-2(10),3,5(9),11,13(20),14,16-heptaene-4,15-diol

> <ALOGPS_LOGP>
5.81

> <JCHEM_LOGP>
7.978550815333332

> <ALOGPS_LOGS>
-5.72

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
9

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.003010145366364

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.615277151318288

> <JCHEM_PKA_STRONGEST_BASIC>
-4.906185891565048

> <JCHEM_POLAR_SURFACE_AREA>
160.07

> <JCHEM_REFRACTIVITY>
200.11819999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.30e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6-(3,5-dihydroxyphenyl)-7,11,19-tris(4-hydroxyphenyl)-8,18-dioxapentacyclo[11.6.1.0²,¹⁰.0⁵,⁹.0¹⁷,²⁰]icosa-2(10),3,5(9),11,13(20),14,16-heptaene-4,15-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  O   UNK     0      16.837   6.241   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      15.547   5.400   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      15.631   3.862   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      14.340   3.021   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      12.967   3.718   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      12.884   5.256   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      14.174   6.097   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      11.677   2.877   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      10.238   3.426   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       9.271   2.228   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.112   0.938   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      11.599   1.339   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      12.798   0.372   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      14.234   0.926   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      15.433  -0.041   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      16.870   0.514   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      15.195  -1.562   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      13.758  -2.117   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      13.520  -3.638   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      12.560  -1.150   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.416  -0.436   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      10.257  -1.726   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       7.878  -0.519   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       7.037   0.771   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.529   0.459   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.958  -0.971   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       3.421  -0.870   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       3.042   0.623   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       1.679   1.340   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       1.619   2.879   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       0.256   3.596   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       2.922   3.700   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       4.377   2.984   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       5.600   3.919   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       7.094   3.545   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       8.079   4.729   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       7.546   6.174   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       8.531   7.358   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      10.049   7.097   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      11.034   8.281   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      10.582   5.652   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       9.597   4.468   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       7.734   2.144   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       4.345   1.444   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       5.780  -2.273   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       7.318  -2.213   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       8.140  -3.516   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       7.423  -4.878   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0       8.245  -6.181   0.000  0.00  0.00           O+0
HETATM   50  C   UNK     0       5.884  -4.939   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0       5.062  -3.636   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    8                                                  
CONECT    6    5    7                                                       
CONECT    7    6    2                                                       
CONECT    8    5    9   12                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   43                                                  
CONECT   11   10   12   21                                                  
CONECT   12   11    8   13                                                  
CONECT   13   12   14   20                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   13                                                       
CONECT   21   11   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25   43                                                  
CONECT   25   24   26   44                                                  
CONECT   26   25   27   45                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29   44                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33                                                       
CONECT   33   32   34   44                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36   43                                                  
CONECT   36   35   37   42                                                  
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   42                                                       
CONECT   42   41   36                                                       
CONECT   43   35   10   24                                                  
CONECT   44   33   25   28                                                  
CONECT   45   26   46   51                                                  
CONECT   46   45   47                                                       
CONECT   47   46   48                                                       
CONECT   48   47   49   50                                                  
CONECT   49   48                                                            
CONECT   50   48   51                                                       
CONECT   51   50   45                                                       
MASTER        0    0    0    0    0    0    0    0   51    0  118    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₂H₃₀O₉

Average Mass

678.6930 Da

Monoisotopic Mass

678.18898 Da

IUPAC Name

6-(3,5-dihydroxyphenyl)-7,11,19-tris(4-hydroxyphenyl)-8,18-dioxapentacyclo[11.6.1.0²,¹⁰.0⁵,⁹.0¹⁷,²⁰]icosa-2(10),3,5(9),11,13(20),14,16-heptaene-4,15-diol

Traditional Name

6-(3,5-dihydroxyphenyl)-7,11,19-tris(4-hydroxyphenyl)-8,18-dioxapentacyclo[11.6.1.0²,¹⁰.0⁵,⁹.0¹⁷,²⁰]icosa-2(10),3,5(9),11,13(20),14,16-heptaene-4,15-diol

CAS Registry Number

Not Available

SMILES

OC1=CC=C(C=C1)C1OC2=CC(O)=CC3=C2C1C1=C(C2=C(C(C(O2)C2=CC=C(O)C=C2)C2=CC(O)=CC(O)=C2)C(O)=C1)C(=C3)C1=CC=C(O)C=C1

InChI Identifier

InChI=1S/C42H30O9/c43-25-7-1-20(2-8-25)31-16-24-15-30(48)18-34-35(24)38(41(50-34)22-5-11-27(45)12-6-22)32-19-33(49)39-36(23-13-28(46)17-29(47)14-23)40(51-42(39)37(31)32)21-3-9-26(44)10-4-21/h1-19,36,38,40-41,43-49H

InChI Key

AYDHZBQRJGDSHM-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 2-arylbenzofuran flavonoids. These are phenylpropanoids containing the 2-phenylbenzofuran moiety.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

2-arylbenzofuran flavonoids

Sub Class

Not Available

Direct Parent

2-arylbenzofuran flavonoids

Alternative Parents

Substituents

2-arylbenzofuran flavonoid
Linear 1,7-diphenylheptane skeleton
1-phenylcoumaran
Dibenzocycloheptene
Stilbene
Coumaran
Resorcinol
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
1-hydroxy-4-unsubstituted benzenoid
Phenol
Monocyclic benzene moiety
Benzenoid
Oxacycle
Ether
Organoheterocyclic compound
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	5.81	ALOGPS
logP	7.98	ChemAxon
logS	-5.7	ALOGPS
pKa (Strongest Acidic)	8.62	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	160.07 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	200.12 m³·mol⁻¹	ChemAxon
Polarizability	72.28 Å³	ChemAxon
Number of Rings	9	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

74835147

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 6-(3,5-dihydroxyphenyl)-7,11,19-tris(4-hydroxyphenyl)-8,18-dioxapentacyclo[11.6.1.0²,¹⁰.0⁵,⁹.0¹⁷,²⁰]icosa-2,4,9,11,13,15,17(20)-heptaene-4,15-diol (NP0163266)

MOL for NP0163266 (6-(3,5-dihydroxyphenyl)-7,11,19-tris(4-hydroxyphenyl)-8,18-dioxapentacyclo[11.6.1.0²,¹⁰.0⁵,⁹.0¹⁷,²⁰]icosa-2,4,9,11,13,15,17(20)-heptaene-4,15-diol)

3D MOL for NP0163266 (6-(3,5-dihydroxyphenyl)-7,11,19-tris(4-hydroxyphenyl)-8,18-dioxapentacyclo[11.6.1.0²,¹⁰.0⁵,⁹.0¹⁷,²⁰]icosa-2,4,9,11,13,15,17(20)-heptaene-4,15-diol)

3D SDF for NP0163266 (6-(3,5-dihydroxyphenyl)-7,11,19-tris(4-hydroxyphenyl)-8,18-dioxapentacyclo[11.6.1.0²,¹⁰.0⁵,⁹.0¹⁷,²⁰]icosa-2,4,9,11,13,15,17(20)-heptaene-4,15-diol)

3D-SDF for NP0163266 (6-(3,5-dihydroxyphenyl)-7,11,19-tris(4-hydroxyphenyl)-8,18-dioxapentacyclo[11.6.1.0²,¹⁰.0⁵,⁹.0¹⁷,²⁰]icosa-2,4,9,11,13,15,17(20)-heptaene-4,15-diol)

PDB for NP0163266 (6-(3,5-dihydroxyphenyl)-7,11,19-tris(4-hydroxyphenyl)-8,18-dioxapentacyclo[11.6.1.0²,¹⁰.0⁵,⁹.0¹⁷,²⁰]icosa-2,4,9,11,13,15,17(20)-heptaene-4,15-diol)

3D PDB for NP0163266 (6-(3,5-dihydroxyphenyl)-7,11,19-tris(4-hydroxyphenyl)-8,18-dioxapentacyclo[11.6.1.0²,¹⁰.0⁵,⁹.0¹⁷,²⁰]icosa-2,4,9,11,13,15,17(20)-heptaene-4,15-diol)

SMILES for NP0163266 (6-(3,5-dihydroxyphenyl)-7,11,19-tris(4-hydroxyphenyl)-8,18-dioxapentacyclo[11.6.1.0²,¹⁰.0⁵,⁹.0¹⁷,²⁰]icosa-2,4,9,11,13,15,17(20)-heptaene-4,15-diol)

INCHI for NP0163266 (6-(3,5-dihydroxyphenyl)-7,11,19-tris(4-hydroxyphenyl)-8,18-dioxapentacyclo[11.6.1.0²,¹⁰.0⁵,⁹.0¹⁷,²⁰]icosa-2,4,9,11,13,15,17(20)-heptaene-4,15-diol)

Structure for NP0163266 (6-(3,5-dihydroxyphenyl)-7,11,19-tris(4-hydroxyphenyl)-8,18-dioxapentacyclo[11.6.1.0²,¹⁰.0⁵,⁹.0¹⁷,²⁰]icosa-2,4,9,11,13,15,17(20)-heptaene-4,15-diol)

3D Structure for NP0163266 (6-(3,5-dihydroxyphenyl)-7,11,19-tris(4-hydroxyphenyl)-8,18-dioxapentacyclo[11.6.1.0²,¹⁰.0⁵,⁹.0¹⁷,²⁰]icosa-2,4,9,11,13,15,17(20)-heptaene-4,15-diol)