NP-MRD: Showing NP-Card for 4,5-dihydroxy-6-({5-methoxy-4-phenyl-[1,1'-biphenyl]-6-yl}oxy)-5,6-dihydro-4h-pyran-2-carboxylic acid (NP0282009)

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Record Information

Version

2.0

Created at

2022-09-09 08:40:31 UTC

Updated at

2022-09-09 08:40:31 UTC

NP-MRD ID

NP0282009

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4,5-dihydroxy-6-({5-methoxy-4-phenyl-[1,1'-biphenyl]-6-yl}oxy)-5,6-dihydro-4h-pyran-2-carboxylic acid

Description

3,4-Dihydroxy-2-({6-methoxy-4-phenyl-[1,1'-biphenyl]-5-yl}oxy)-3,4-dihydro-2H-pyran-6-carboxylic acid belongs to the class of organic compounds known as p-terphenyls. These are terphenyls with a structure containing the 1,4-diphenylbenzene skeleton. Based on a literature review very few articles have been published on 3,4-dihydroxy-2-({6-methoxy-4-phenyl-[1,1'-biphenyl]-5-yl}oxy)-3,4-dihydro-2H-pyran-6-carboxylic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092210402D          

 33 36  0  0  0  0            999 V2000
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  5 10  1  0  0  0  0
  4 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 16 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 14 23  1  0  0  0  0
 23 24  1  0  0  0  0
 12 25  1  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
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 26 31  1  0  0  0  0
 25 32  2  0  0  0  0
  3 32  1  0  0  0  0
 32 33  1  0  0  0  0
M  END

     RDKit          3D

 55 58  0  0  0  0  0  0  0  0999 V2000
   -4.8840   -0.2890   -1.1023 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1885   -0.0474    0.0968 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8021    0.1388    0.0779 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9580   -0.9428    0.2132 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4832   -2.2795    0.3739 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0024   -3.3274   -0.3704 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4904   -4.6167   -0.2360 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5052   -4.8175    0.6966 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0073   -3.7854    1.4574 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4865   -2.5067    1.2892 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5899   -0.6844    0.1864 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0905    0.6051    0.0302 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2262    0.9303   -0.0021 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2622    0.0396    0.1906 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2643    0.5202    1.0562 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4337   -0.1970    1.1997 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3987    0.0907    2.2594 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1285    1.0303    3.0621 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5771   -0.6052    2.4274 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6764   -1.1759    0.3404 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7878   -1.5692   -0.7747 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8659   -2.5412   -0.3685 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9617   -0.3272   -1.1268 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9918   -0.6308   -2.0569 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9916    1.6641   -0.1032 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4795    3.0124   -0.2652 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0401    3.4739   -1.5114 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4450    4.7475   -1.6896 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5014    5.5981   -0.6100 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0797    5.1777    0.6227 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4024    3.9020    0.7843 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3276    1.4147   -0.0770 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2300    2.4631   -0.2086 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2391   -0.2144   -1.9994 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2719   -1.3238   -1.0713 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7450    0.4138   -1.2128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2067   -3.1393   -1.0978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1041   -5.4232   -0.8256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8976   -5.8374    0.8081 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8060   -3.9999    2.1776 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9215   -1.7373    1.9159 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0763   -1.5333    0.2881 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9073   -0.9344    0.5976 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5602   -1.5988    2.5504 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6056   -1.7531    0.4449 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3979   -1.8585   -1.6276 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1228   -2.9548    0.4964 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5795    0.4909   -1.5076 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2457   -0.4784   -2.9893 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0925    2.7921   -2.3416 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7875    5.1094   -2.6578 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8820    6.6238   -0.7155 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1372    5.8817    1.4688 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7325    3.5817    1.7637 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9264    3.4281   -0.3268 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 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 20  2  0
 20 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 16 17  1  0
 17 19  1  0
 17 18  2  0
 12 25  1  0
 25 32  2  0
 32 33  1  0
 25 26  1  0
 26 27  2  0
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 28 29  2  0
 29 30  1  0
 30 31  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 32  3  1  0
 31 26  1  0
 10  5  1  0
 23 14  1  0
  1 34  1  0
  1 35  1  0
  1 36  1  0
 11 42  1  0
 14 43  1  1
 20 45  1  0
 21 46  1  6
 22 47  1  0
 23 48  1  6
 24 49  1  0
 19 44  1  0
 33 55  1  0
 27 50  1  0
 28 51  1  0
 29 52  1  0
 30 53  1  0
 31 54  1  0
  6 37  1  0
  7 38  1  0
  8 39  1  0
  9 40  1  0
 10 41  1  0
M  END


  Mrv1652309092210402D          

 33 36  0  0  0  0            999 V2000
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  5 10  1  0  0  0  0
  4 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 16 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 14 23  1  0  0  0  0
 23 24  1  0  0  0  0
 12 25  1  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
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 26 31  1  0  0  0  0
 25 32  2  0  0  0  0
  3 32  1  0  0  0  0
 32 33  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0282009

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(C=C(OC2OC(=CC(O)C2O)C(O)=O)C(=C1O)C1=CC=CC=C1)C1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C25H22O8/c1-31-23-16(14-8-4-2-5-9-14)12-18(20(22(23)28)15-10-6-3-7-11-15)32-25-21(27)17(26)13-19(33-25)24(29)30/h2-13,17,21,25-28H,1H3,(H,29,30)

> <INCHI_KEY>
DWAQMWPHCVWJMI-UHFFFAOYSA-N

> <FORMULA>
C25H22O8

> <MOLECULAR_WEIGHT>
450.443

> <EXACT_MASS>
450.131467668

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
45.63116167013704

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3,4-dihydroxy-2-({5-methoxy-4-phenyl-[1,1'-biphenyl]-6-yl}oxy)-3,4-dihydro-2H-pyran-6-carboxylic acid

> <JCHEM_LOGP>
3.2940298373333334

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
9.641006101910262

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.3496426318878947

> <JCHEM_PKA_STRONGEST_BASIC>
-3.4548202748775276

> <JCHEM_POLAR_SURFACE_AREA>
125.68000000000002

> <JCHEM_REFRACTIVITY>
119.12820000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
4,5-dihydroxy-6-({5-methoxy-4-phenyl-[1,1'-biphenyl]-6-yl}oxy)-5,6-dihydro-4H-pyran-2-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       1.334  -0.770   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.335  -0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       1.334  -6.930   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       4.001  -6.930   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       6.668  -5.390   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       8.002  -7.700   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       5.335  -9.240   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.001 -10.010   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       4.001 -11.550   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       2.667  -9.240   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       1.334 -10.010   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      -1.334  -2.310   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   32                                                  
CONECT    4    3    5   11                                                  
CONECT    5    4    6   10                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9    5                                                       
CONECT   11    4   12                                                       
CONECT   12   11   13   25                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   23                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   20                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   16   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   14   24                                                  
CONECT   24   23                                                            
CONECT   25   12   26   32                                                  
CONECT   26   25   27   31                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   26                                                       
CONECT   32   25    3   33                                                  
CONECT   33   32                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   72    0
END

View in JSmol

Synonyms

Value	Source
3,4-Dihydroxy-2-({6-methoxy-4-phenyl-[1,1'-biphenyl]-5-yl}oxy)-3,4-dihydro-2H-pyran-6-carboxylate	Generator

Chemical Formula

C₂₅H₂₂O₈

Average Mass

450.4430 Da

Monoisotopic Mass

450.13147 Da

IUPAC Name

3,4-dihydroxy-2-({5-methoxy-4-phenyl-[1,1'-biphenyl]-6-yl}oxy)-3,4-dihydro-2H-pyran-6-carboxylic acid

Traditional Name

4,5-dihydroxy-6-({5-methoxy-4-phenyl-[1,1'-biphenyl]-6-yl}oxy)-5,6-dihydro-4H-pyran-2-carboxylic acid

CAS Registry Number

Not Available

SMILES

COC1=C(C=C(OC2OC(=CC(O)C2O)C(O)=O)C(=C1O)C1=CC=CC=C1)C1=CC=CC=C1

InChI Identifier

InChI=1S/C25H22O8/c1-31-23-16(14-8-4-2-5-9-14)12-18(20(22(23)28)15-10-6-3-7-11-15)32-25-21(27)17(26)13-19(33-25)24(29)30/h2-13,17,21,25-28H,1H3,(H,29,30)

InChI Key

DWAQMWPHCVWJMI-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 p-terphenyls. These are terphenyls with a structure containing the 1,4-diphenylbenzene skeleton.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Terphenyls

Direct Parent

P-terphenyls

Alternative Parents

Substituents

Para-terphenyl
Biphenyl
Methoxyphenol
Phenoxy compound
Methoxybenzene
Phenol ether
Anisole
1-hydroxy-4-unsubstituted benzenoid
Phenol
Alkyl aryl ether
Secondary alcohol
1,2-diol
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Ether
Carboxylic acid
Carboxylic acid derivative
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	3.29	ChemAxon
pKa (Strongest Acidic)	3.35	ChemAxon
pKa (Strongest Basic)	-3.5	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	125.68 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	119.13 m³·mol⁻¹	ChemAxon
Polarizability	45.63 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	Yes	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

163057559

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4,5-dihydroxy-6-({5-methoxy-4-phenyl-[1,1'-biphenyl]-6-yl}oxy)-5,6-dihydro-4h-pyran-2-carboxylic acid (NP0282009)

MOL for NP0282009 (4,5-dihydroxy-6-({5-methoxy-4-phenyl-[1,1'-biphenyl]-6-yl}oxy)-5,6-dihydro-4h-pyran-2-carboxylic acid)

3D MOL for NP0282009 (4,5-dihydroxy-6-({5-methoxy-4-phenyl-[1,1'-biphenyl]-6-yl}oxy)-5,6-dihydro-4h-pyran-2-carboxylic acid)

3D SDF for NP0282009 (4,5-dihydroxy-6-({5-methoxy-4-phenyl-[1,1'-biphenyl]-6-yl}oxy)-5,6-dihydro-4h-pyran-2-carboxylic acid)

3D-SDF for NP0282009 (4,5-dihydroxy-6-({5-methoxy-4-phenyl-[1,1'-biphenyl]-6-yl}oxy)-5,6-dihydro-4h-pyran-2-carboxylic acid)

PDB for NP0282009 (4,5-dihydroxy-6-({5-methoxy-4-phenyl-[1,1'-biphenyl]-6-yl}oxy)-5,6-dihydro-4h-pyran-2-carboxylic acid)

3D PDB for NP0282009 (4,5-dihydroxy-6-({5-methoxy-4-phenyl-[1,1'-biphenyl]-6-yl}oxy)-5,6-dihydro-4h-pyran-2-carboxylic acid)

SMILES for NP0282009 (4,5-dihydroxy-6-({5-methoxy-4-phenyl-[1,1'-biphenyl]-6-yl}oxy)-5,6-dihydro-4h-pyran-2-carboxylic acid)

INCHI for NP0282009 (4,5-dihydroxy-6-({5-methoxy-4-phenyl-[1,1'-biphenyl]-6-yl}oxy)-5,6-dihydro-4h-pyran-2-carboxylic acid)

Structure for NP0282009 (4,5-dihydroxy-6-({5-methoxy-4-phenyl-[1,1'-biphenyl]-6-yl}oxy)-5,6-dihydro-4h-pyran-2-carboxylic acid)

3D Structure for NP0282009 (4,5-dihydroxy-6-({5-methoxy-4-phenyl-[1,1'-biphenyl]-6-yl}oxy)-5,6-dihydro-4h-pyran-2-carboxylic acid)