NP-MRD: Showing NP-Card for Riccardin B (NP0061379)

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Record Information

Version

2.0

Created at

2022-04-28 06:11:29 UTC

Updated at

2022-04-28 06:11:29 UTC

NP-MRD ID

NP0061379

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Riccardin B

Description

Riccardin B belongs to the class of organic compounds known as lignans, neolignans and related compounds. These are plant products of low molecular weight formed primarily from oxidative coupling of two p-propylphenol moieties. They can also be described as micromolecules with two phenylpropanoid units coupled together. They can be attached in various manners, like C5-C5', C8-C8'. Most known natural lignans are oxidized at C9 and C9´ and, based upon the way in which oxygen is incorporated into the skeleton and on the cyclization patterns, a wide range of lignans of very different structural types can be formed. Riccardin B is found in Asterella angusta and Riccardia multifida. Riccardin B is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241517052D          

 32 36  0  0  0  0            999 V2000
   10.8264    3.9589    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.4284    3.2362    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8688    2.5292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4655    1.7996    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6256    1.7380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2199    0.9691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6294    0.3492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7904    0.1356    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5446    0.9358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7497    1.1591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1355    0.5902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4914    1.1594    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8969    1.7728    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0556    1.7669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6152    2.4739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0186    3.2035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8585    3.2651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2642    4.0341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8547    4.6540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6936    4.8676    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9394    4.0674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7343    3.8440    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3486    4.4129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9926    3.8438    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.5872    3.2304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2127    2.4760    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1232    5.2260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3126    5.4473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2714    2.5271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3608   -0.2228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7786   -0.8073    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1715   -0.4442    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  1  0  0  0  0
  7  8  1  0  0  0  0
  8  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
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
  2 25  1  0  0  0  0
 25 26  2  0  0  0  0
  5 26  1  0  0  0  0
 23 27  1  0  0  0  0
 27 28  2  0  0  0  0
 20 28  1  0  0  0  0
 17 29  2  0  0  0  0
 13 29  1  0  0  0  0
 11 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  2  0  0  0  0
  8 32  1  0  0  0  0
M  END

     RDKit          3D

 56 60  0  0  0  0  0  0  0  0999 V2000
   -0.7930    3.5271   -1.8662 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3560    3.0546   -0.5816 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9952    3.4381   -0.3156 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6271    3.1003    0.8572 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9307    2.3737    1.7836 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4145    2.0071    1.4884 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0680    2.3298    0.3328 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4120    1.9604    0.0413 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0327    0.7531   -0.2887 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4236    0.6164   -1.6252 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0397   -0.4912   -2.1371 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2643   -1.5034   -1.2350 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9009   -1.4426    0.1309 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2897   -0.3118    0.5896 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2679   -2.7064    0.8314 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1537   -3.4327    1.5361 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7443   -3.0824    1.0894 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7881   -2.7940    2.0279 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5348   -2.4545    1.6250 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9065   -2.4020    0.3129 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0571   -2.6942   -0.6032 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3820   -3.0355   -0.2332 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2211   -2.0638   -0.0807 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8635   -0.8600   -0.3368 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0689    0.2009    0.5385 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7308    1.2930    0.0661 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1837    1.3204   -1.2761 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0039    0.2992   -2.1691 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3351   -0.7874   -1.6652 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1468   -1.8556   -2.5794 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1155    2.5797    0.7372 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0501    3.5005    1.1542 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1566    4.0464   -2.4249 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3699    3.9928   -1.2257 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2160    1.9389    2.7980 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8085    1.4393    2.3717 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2829    1.4107   -2.3919 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3355   -0.5779   -3.1786 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7679   -2.4064   -1.6447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9999   -0.1591    1.6899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6247   -3.4930    0.0639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1252   -2.6542    1.4973 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4037   -3.1332    2.5988 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3547   -4.5409    1.4608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7785   -2.7750    3.1570 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1712   -2.2613    2.5329 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0703   -2.7106   -1.7372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9676   -3.2542   -1.1877 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6854    0.0927    1.6113 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7191    2.2085   -1.6701 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3592    0.3421   -3.1904 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4793   -1.8078   -3.5207 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8399    3.1838    0.1077 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7776    2.3586    1.6177 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2284    3.8123    2.2420 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3634    4.5109    0.7070 H   0  0  0  0  0  0  0  0  0  0  0  0
 30 29  1  0
 29 28  2  0
 28 27  1  0
 27 26  2  0
 26 31  1  0
 31 32  1  0
 32  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20 23  1  0
 23 24  1  0
 24 25  2  0
 20 21  1  0
 21 22  2  0
 13 14  2  0
  7  2  1  0
  2  1  1  0
  2  3  2  0
 24 29  1  0
 25 26  1  0
  3  4  1  0
 14  9  1  0
 22 17  1  0
 30 52  1  0
 28 51  1  0
 27 50  1  0
 31 53  1  0
 31 54  1  0
 32 55  1  0
 32 56  1  0
  5 35  1  0
  6 36  1  0
 10 37  1  0
 11 38  1  0
 12 39  1  0
 15 41  1  0
 15 42  1  0
 16 43  1  0
 16 44  1  0
 18 45  1  0
 19 46  1  0
 25 49  1  0
 21 47  1  0
 22 48  1  0
 14 40  1  0
  1 33  1  0
  3 34  1  0
M  END


  Mrv1533004241517052D          

 32 36  0  0  0  0            999 V2000
   10.8264    3.9589    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.4284    3.2362    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8688    2.5292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4655    1.7996    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6256    1.7380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2199    0.9691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6294    0.3492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7904    0.1356    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5446    0.9358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7497    1.1591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1355    0.5902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4914    1.1594    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8969    1.7728    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0556    1.7669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6152    2.4739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0186    3.2035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8585    3.2651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2642    4.0341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8547    4.6540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6936    4.8676    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9394    4.0674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7343    3.8440    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3486    4.4129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9926    3.8438    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.5872    3.2304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2127    2.4760    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1232    5.2260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3126    5.4473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2714    2.5271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3608   -0.2228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7786   -0.8073    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1715   -0.4442    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  1  0  0  0  0
  7  8  1  0  0  0  0
  8  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
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
  2 25  1  0  0  0  0
 25 26  2  0  0  0  0
  5 26  1  0  0  0  0
 23 27  1  0  0  0  0
 27 28  2  0  0  0  0
 20 28  1  0  0  0  0
 17 29  2  0  0  0  0
 13 29  1  0  0  0  0
 11 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  2  0  0  0  0
  8 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0061379

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC1=CC=C2CCC3=CC=C(OC4=CC=CC(CCC5=CC=C(OC1=C2)C=C5)=C4)C(O)=C3

> <INCHI_IDENTIFIER>
InChI=1S/C28H24O4/c29-25-14-10-22-7-6-21-11-15-27(26(30)17-21)32-24-3-1-2-20(16-24)5-4-19-8-12-23(13-9-19)31-28(25)18-22/h1-3,8-18,29-30H,4-7H2

> <INCHI_KEY>
UJIJNWKXNAZKOA-UHFFFAOYSA-N

> <FORMULA>
C28H24O4

> <MOLECULAR_WEIGHT>
424.496

> <EXACT_MASS>
424.167459253

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
44.83741868675072

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2,14-dioxapentacyclo[20.2.2.2¹⁰,¹³.1³,⁷.1¹⁵,¹⁹]triaconta-1(24),3(30),4,6,10(29),11,13(28),15,17,19(27),22,25-dodecaene-4,12-diol

> <ALOGPS_LOGP>
6.43

> <JCHEM_LOGP>
7.466169106666667

> <ALOGPS_LOGS>
-5.91

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.955815612185159

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.322822560369426

> <JCHEM_PKA_STRONGEST_BASIC>
-3.42309741381021

> <JCHEM_POLAR_SURFACE_AREA>
58.92

> <JCHEM_REFRACTIVITY>
125.11980000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.26e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2,14-dioxapentacyclo[20.2.2.2¹⁰,¹³.1³,⁷.1¹⁵,¹⁹]triaconta-1(24),3(30),4,6,10(29),11,13(28),15,17,19(27),22,25-dodecaene-4,12-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  O   UNK     0      20.209   7.390   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      19.466   6.041   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      20.288   4.721   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      19.536   3.359   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      17.968   3.244   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      17.210   1.809   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      16.108   0.652   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      14.542   0.253   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      14.083   1.747   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      12.599   2.164   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      11.453   1.102   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      10.251   2.164   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       9.141   3.309   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.571   3.298   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.748   4.618   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.501   5.980   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.069   6.095   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.827   7.530   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      10.929   8.687   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      12.495   9.086   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      12.954   7.592   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      14.437   7.176   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      15.584   8.237   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      16.786   7.175   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      17.896   6.030   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      17.197   4.622   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      15.163   9.755   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      13.650  10.168   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       9.840   4.717   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      11.874  -0.416   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      10.787  -1.507   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      13.387  -0.829   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   25                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   26                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   32                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   30                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   29                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   29                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   28                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   27                                                  
CONECT   24   23   25                                                       
CONECT   25   24    2   26                                                  
CONECT   26   25    5                                                       
CONECT   27   23   28                                                       
CONECT   28   27   20                                                       
CONECT   29   17   13                                                       
CONECT   30   11   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30    8                                                       
MASTER        0    0    0    0    0    0    0    0   32    0   72    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₈H₂₄O₄

Average Mass

424.4960 Da

Monoisotopic Mass

424.16746 Da

IUPAC Name

2,14-dioxapentacyclo[20.2.2.2¹⁰,¹³.1³,⁷.1¹⁵,¹⁹]triaconta-1(24),3(30),4,6,10(29),11,13(28),15,17,19(27),22,25-dodecaene-4,12-diol

Traditional Name

2,14-dioxapentacyclo[20.2.2.2¹⁰,¹³.1³,⁷.1¹⁵,¹⁹]triaconta-1(24),3(30),4,6,10(29),11,13(28),15,17,19(27),22,25-dodecaene-4,12-diol

CAS Registry Number

Not Available

SMILES

OC1=CC=C2CCC3=CC=C(OC4=CC=CC(CCC5=CC=C(OC1=C2)C=C5)=C4)C(O)=C3

InChI Identifier

InChI=1S/C28H24O4/c29-25-14-10-22-7-6-21-11-15-27(26(30)17-21)32-24-3-1-2-20(16-24)5-4-19-8-12-23(13-9-19)31-28(25)18-22/h1-3,8-18,29-30H,4-7H2

InChI Key

UJIJNWKXNAZKOA-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
Asterella angusta	Plant	KNApSAcK
Riccardia multifida	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as lignans, neolignans and related compounds. These are plant products of low molecular weight formed primarily from oxidative coupling of two p-propylphenol moieties. They can also be described as micromolecules with two phenylpropanoid units coupled together. They can be attached in various manners, like C5-C5', C8-C8'. Most known natural lignans are oxidized at C9 and C9´ and, based upon the way in which oxygen is incorporated into the skeleton and on the cyclization patterns, a wide range of lignans of very different structural types can be formed.

Kingdom

Organic compounds

Super Class

Lignans, neolignans and related compounds

Class

Not Available

Sub Class

Not Available

Direct Parent

Lignans, neolignans and related compounds

Alternative Parents

Substituents

Oxyneolignan skeleton
Diaryl ether
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Benzenoid
Oxacycle
Organoheterocyclic compound
Ether
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	6.43	ALOGPS
logP	7.47	ChemAxon
logS	-5.9	ALOGPS
pKa (Strongest Acidic)	8.32	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	58.92 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	125.12 m³·mol⁻¹	ChemAxon
Polarizability	44.84 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	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

14016887

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Riccardin B (NP0061379)

MOL for NP0061379 (Riccardin B)

3D MOL for NP0061379 (Riccardin B)

3D SDF for NP0061379 (Riccardin B)

3D-SDF for NP0061379 (Riccardin B)

PDB for NP0061379 (Riccardin B)

3D PDB for NP0061379 (Riccardin B)

SMILES for NP0061379 (Riccardin B)

INCHI for NP0061379 (Riccardin B)

Structure for NP0061379 (Riccardin B)

3D Structure for NP0061379 (Riccardin B)