NP-MRD: Showing NP-Card for Eryvarinol A (NP0001499)

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Record Information

Version

1.0

Created at

2020-08-18 03:26:50 UTC

Updated at

2021-08-10 02:54:47 UTC

NP-MRD ID

NP0001499

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Eryvarinol A

Description

1-Hydroxy-1-(4-hydroxy-2-methoxyphenyl)-3-(4-hydroxyphenyl)propan-2-yl 4-hydroxy-3,5-dimethoxybenzoate belongs to the class of organic compounds known as cinnamylphenols. These are organic compounds containing the 1,3-diphenylpropene moiety with one benzene ring bearing one or more hydroxyl groups. Eryvarinol A is found in Erythrina variegata. Based on a literature review very few articles have been published on 1-hydroxy-1-(4-hydroxy-2-methoxyphenyl)-3-(4-hydroxyphenyl)propan-2-yl 4-hydroxy-3,5-dimethoxybenzoate.

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI


  Mrv1533004251503592D          

 34 36  0  0  0  0            999 V2000
   -3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -3.3000    0.0000 O   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
   -1.4289   -3.3000    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
   -0.7145   -4.5375    0.0000 C   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
   -1.4289   -5.7750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -3.3000    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
    0.0000   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.0625    0.0000 C   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
    0.0000   -0.8250    0.0000 C   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   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    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
    1.4289   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.0625    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
    2.8579   -0.8250    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
    4.2868   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -3.3000    0.0000 O   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
  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  1  0  0  0  0
  8  9  1  0  0  0  0
  7 10  2  0  0  0  0
  3 10  1  0  0  0  0
 10 11  1  0  0  0  0
  5 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 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
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  2  0  0  0  0
 17 23  1  0  0  0  0
 15 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 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
 29 31  1  0  0  0  0
 31 32  2  0  0  0  0
 26 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
M  END

NP0001499
     RDKit          3D

 60 62  0  0  0  0  0  0  0  0999 V2000
   -3.7691    3.0175   -2.6444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0619    2.0589   -1.9157 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5053    2.3988   -0.6880 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6535    3.6729   -0.1979 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1112    4.0421    1.0222 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2838    5.3392    1.4809 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4065    3.1280    1.7733 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2748    1.8535    1.2528 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7940    1.4492    0.0533 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6903    0.1165   -0.5344 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5064    0.1397   -1.9188 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7770   -0.8230    0.1578 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0047   -2.2724   -0.3424 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3490   -2.7594   -0.1045 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6648   -3.3540    1.0974 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9260   -3.8253    1.3203 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8985   -3.7063    0.3324 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1594   -4.2046    0.6209 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6070   -3.1192   -0.8695 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3206   -2.6503   -1.0690 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5919   -0.6248   -0.0382 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5904   -0.5191    0.8786 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2785   -0.6153    2.0921 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9998   -0.3016    0.5417 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9144   -0.2168    1.5655 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2674   -0.0156    1.3581 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1812    0.0684    2.3989 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7388   -0.0529    3.7375 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6738    0.0999    0.0413 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0258    0.3021   -0.1968 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7912    0.0211   -1.0137 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2600    0.1447   -2.3116 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4676    0.0863   -3.4557 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4495   -0.1812   -0.7439 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6548    3.3793   -2.0602 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0852    3.8516   -2.9159 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1484    2.5606   -3.5958 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2118    4.4049   -0.7884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7911    6.0067    0.9465 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9693    3.3885    2.7348 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7298    1.1027    1.8257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7349   -0.3345   -0.4205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3136   -0.0408   -2.4430 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0527   -0.8194    1.2557 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7074   -2.2397   -1.4159 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2555   -2.9047    0.1725 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8830   -3.4399    1.8682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1487   -4.2921    2.2816 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9252   -4.1628   -0.0327 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3532   -3.0300   -1.6222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1364   -2.2007   -2.0381 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6002   -0.3076    2.6126 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5412    0.2207    4.4541 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3122   -1.0458    3.9379 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9112    0.6832    3.9389 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7062    0.3667    0.5253 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8237   -0.7960   -3.5387 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1566    0.1762   -4.3386 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8458    1.0223   -3.4753 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7371   -0.2467   -1.5488 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  1  0
  5  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 17 19  1  0
 19 20  2  0
 12 21  1  0
 21 22  1  0
 22 23  2  0
 22 24  1  0
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 26 27  1  0
 27 28  1  0
 26 29  2  0
 29 30  1  0
 29 31  1  0
 31 32  1  0
 32 33  1  0
 31 34  2  0
  9  3  1  0
 20 14  1  0
 34 24  1  0
  1 35  1  0
  1 36  1  0
  1 37  1  0
  4 38  1  0
  6 39  1  0
  7 40  1  0
  8 41  1  0
 10 42  1  0
 11 43  1  0
 12 44  1  0
 13 45  1  0
 13 46  1  0
 15 47  1  0
 16 48  1  0
 18 49  1  0
 19 50  1  0
 20 51  1  0
 25 52  1  0
 28 53  1  0
 28 54  1  0
 28 55  1  0
 30 56  1  0
 33 57  1  0
 33 58  1  0
 33 59  1  0
 34 60  1  0
M  END


  Mrv1533004251503592D          

 34 36  0  0  0  0            999 V2000
   -3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -3.3000    0.0000 O   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
   -1.4289   -3.3000    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
   -0.7145   -4.5375    0.0000 C   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
   -1.4289   -5.7750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -3.3000    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
    0.0000   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.0625    0.0000 C   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
    0.0000   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    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
    1.4289   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.0625    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
    2.8579   -0.8250    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
    4.2868   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -3.3000    0.0000 O   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
  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  1  0  0  0  0
  8  9  1  0  0  0  0
  7 10  2  0  0  0  0
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 31 32  2  0  0  0  0
 26 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0001499

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(=CC(OC)=C1O)C(=O)OC(CC1=CC=C(O)C=C1)C(O)C1=CC=C(O)C=C1OC

> <INCHI_IDENTIFIER>
InChI=1S/C25H26O9/c1-31-19-13-17(27)8-9-18(19)23(28)22(10-14-4-6-16(26)7-5-14)34-25(30)15-11-20(32-2)24(29)21(12-15)33-3/h4-9,11-13,22-23,26-29H,10H2,1-3H3

> <INCHI_KEY>
ISBPEYMYDJMZGH-UHFFFAOYSA-N

> <FORMULA>
C25H26O9

> <MOLECULAR_WEIGHT>
470.474

> <EXACT_MASS>
470.157682417

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
47.80677532311206

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1-hydroxy-1-(4-hydroxy-2-methoxyphenyl)-3-(4-hydroxyphenyl)propan-2-yl 4-hydroxy-3,5-dimethoxybenzoate

> <ALOGPS_LOGP>
2.80

> <JCHEM_LOGP>
3.7600525856666667

> <ALOGPS_LOGS>
-4.72

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.216408508158038

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.357526383712981

> <JCHEM_PKA_STRONGEST_BASIC>
-3.5745010995652677

> <JCHEM_POLAR_SURFACE_AREA>
134.91

> <JCHEM_REFRACTIVITY>
123.02850000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.89e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-hydroxy-1-(4-hydroxy-2-methoxyphenyl)-3-(4-hydroxyphenyl)propan-2-yl 4-hydroxy-3,5-dimethoxybenzoate

> <JCHEM_VEBER_RULE>
0

$$$$

NP0001499
     RDKit          3D

 60 62  0  0  0  0  0  0  0  0999 V2000
   -3.7691    3.0175   -2.6444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0619    2.0589   -1.9157 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5053    2.3988   -0.6880 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6535    3.6729   -0.1979 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1112    4.0421    1.0222 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2838    5.3392    1.4809 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4065    3.1280    1.7733 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2748    1.8535    1.2528 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7940    1.4492    0.0533 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6903    0.1165   -0.5344 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5064    0.1397   -1.9188 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7770   -0.8230    0.1578 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0047   -2.2724   -0.3424 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3490   -2.7594   -0.1045 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6648   -3.3540    1.0974 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9260   -3.8253    1.3203 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8985   -3.7063    0.3324 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1594   -4.2046    0.6209 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6070   -3.1192   -0.8695 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3206   -2.6503   -1.0690 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5919   -0.6248   -0.0382 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5904   -0.5191    0.8786 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2785   -0.6153    2.0921 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9998   -0.3016    0.5417 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9144   -0.2168    1.5655 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2674   -0.0156    1.3581 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1812    0.0684    2.3989 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7388   -0.0529    3.7375 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6738    0.0999    0.0413 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0258    0.3021   -0.1968 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7912    0.0211   -1.0137 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2600    0.1447   -2.3116 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4676    0.0863   -3.4557 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4495   -0.1812   -0.7439 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6548    3.3793   -2.0602 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0852    3.8516   -2.9159 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1484    2.5606   -3.5958 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2118    4.4049   -0.7884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7911    6.0067    0.9465 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9693    3.3885    2.7348 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7298    1.1027    1.8257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7349   -0.3345   -0.4205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3136   -0.0408   -2.4430 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0527   -0.8194    1.2557 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7074   -2.2397   -1.4159 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2555   -2.9047    0.1725 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8830   -3.4399    1.8682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1487   -4.2921    2.2816 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9252   -4.1628   -0.0327 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3532   -3.0300   -1.6222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1364   -2.2007   -2.0381 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6002   -0.3076    2.6126 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5412    0.2207    4.4541 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3122   -1.0458    3.9379 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9112    0.6832    3.9389 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7062    0.3667    0.5253 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8237   -0.7960   -3.5387 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1566    0.1762   -4.3386 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8458    1.0223   -3.4753 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7371   -0.2467   -1.5488 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  1  0
  5  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 17 19  1  0
 19 20  2  0
 12 21  1  0
 21 22  1  0
 22 23  2  0
 22 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 26 29  2  0
 29 30  1  0
 29 31  1  0
 31 32  1  0
 32 33  1  0
 31 34  2  0
  9  3  1  0
 20 14  1  0
 34 24  1  0
  1 35  1  0
  1 36  1  0
  1 37  1  0
  4 38  1  0
  6 39  1  0
  7 40  1  0
  8 41  1  0
 10 42  1  0
 11 43  1  0
 12 44  1  0
 13 45  1  0
 13 46  1  0
 15 47  1  0
 16 48  1  0
 18 49  1  0
 19 50  1  0
 20 51  1  0
 25 52  1  0
 28 53  1  0
 28 54  1  0
 28 55  1  0
 30 56  1  0
 33 57  1  0
 33 58  1  0
 33 59  1  0
 34 60  1  0
M  END

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  C   UNK     0      -6.668  -6.930   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -5.335  -6.160   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -4.001  -6.930   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.667  -6.160   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.334  -8.470   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.667  -9.240   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -2.667 -10.780   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -4.001 -11.550   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -4.001  -8.470   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -5.335  -9.240   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       0.000  -6.160   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  O   UNK     0       0.000  -4.620   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       1.334  -3.850   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.000  -1.540   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -2.667  -1.540   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -4.001   0.770   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -1.334   0.770   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       2.667  -6.160   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       4.001  -3.850   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       5.335  -1.540   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       8.002  -1.540   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       6.668  -3.850   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       5.335  -6.160   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   10                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   12                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   10                                                  
CONECT    8    7    9                                                       
CONECT    9    8                                                            
CONECT   10    7    3   11                                                  
CONECT   11   10                                                            
CONECT   12    5   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16   24                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   23                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   17                                                       
CONECT   24   15   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   32                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32                                                       
CONECT   32   31   26   33                                                  
CONECT   33   32   34                                                       
CONECT   34   33                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   72    0
END

COMPND    NP0001499
HETATM    1  C1  UNL     1      -3.769   3.018  -2.644  1.00  0.00           C  
HETATM    2  O1  UNL     1      -3.062   2.059  -1.916  1.00  0.00           O  
HETATM    3  C2  UNL     1      -2.505   2.399  -0.688  1.00  0.00           C  
HETATM    4  C3  UNL     1      -2.654   3.673  -0.198  1.00  0.00           C  
HETATM    5  C4  UNL     1      -2.111   4.042   1.022  1.00  0.00           C  
HETATM    6  O2  UNL     1      -2.284   5.339   1.481  1.00  0.00           O  
HETATM    7  C5  UNL     1      -1.407   3.128   1.773  1.00  0.00           C  
HETATM    8  C6  UNL     1      -1.275   1.853   1.253  1.00  0.00           C  
HETATM    9  C7  UNL     1      -1.794   1.449   0.053  1.00  0.00           C  
HETATM   10  C8  UNL     1      -1.690   0.117  -0.534  1.00  0.00           C  
HETATM   11  O3  UNL     1      -1.506   0.140  -1.919  1.00  0.00           O  
HETATM   12  C9  UNL     1      -0.777  -0.823   0.158  1.00  0.00           C  
HETATM   13  C10 UNL     1      -1.005  -2.272  -0.342  1.00  0.00           C  
HETATM   14  C11 UNL     1      -2.349  -2.759  -0.105  1.00  0.00           C  
HETATM   15  C12 UNL     1      -2.665  -3.354   1.097  1.00  0.00           C  
HETATM   16  C13 UNL     1      -3.926  -3.825   1.320  1.00  0.00           C  
HETATM   17  C14 UNL     1      -4.899  -3.706   0.332  1.00  0.00           C  
HETATM   18  O4  UNL     1      -6.159  -4.205   0.621  1.00  0.00           O  
HETATM   19  C15 UNL     1      -4.607  -3.119  -0.869  1.00  0.00           C  
HETATM   20  C16 UNL     1      -3.321  -2.650  -1.069  1.00  0.00           C  
HETATM   21  O5  UNL     1       0.592  -0.625  -0.038  1.00  0.00           O  
HETATM   22  C17 UNL     1       1.590  -0.519   0.879  1.00  0.00           C  
HETATM   23  O6  UNL     1       1.279  -0.615   2.092  1.00  0.00           O  
HETATM   24  C18 UNL     1       3.000  -0.302   0.542  1.00  0.00           C  
HETATM   25  C19 UNL     1       3.914  -0.217   1.565  1.00  0.00           C  
HETATM   26  C20 UNL     1       5.267  -0.016   1.358  1.00  0.00           C  
HETATM   27  O7  UNL     1       6.181   0.068   2.399  1.00  0.00           O  
HETATM   28  C21 UNL     1       5.739  -0.053   3.738  1.00  0.00           C  
HETATM   29  C22 UNL     1       5.674   0.100   0.041  1.00  0.00           C  
HETATM   30  O8  UNL     1       7.026   0.302  -0.197  1.00  0.00           O  
HETATM   31  C23 UNL     1       4.791   0.021  -1.014  1.00  0.00           C  
HETATM   32  O9  UNL     1       5.260   0.145  -2.312  1.00  0.00           O  
HETATM   33  C24 UNL     1       4.468   0.086  -3.456  1.00  0.00           C  
HETATM   34  C25 UNL     1       3.449  -0.181  -0.744  1.00  0.00           C  
HETATM   35  H1  UNL     1      -4.655   3.379  -2.060  1.00  0.00           H  
HETATM   36  H2  UNL     1      -3.085   3.852  -2.916  1.00  0.00           H  
HETATM   37  H3  UNL     1      -4.148   2.561  -3.596  1.00  0.00           H  
HETATM   38  H4  UNL     1      -3.212   4.405  -0.788  1.00  0.00           H  
HETATM   39  H5  UNL     1      -2.791   6.007   0.946  1.00  0.00           H  
HETATM   40  H6  UNL     1      -0.969   3.389   2.735  1.00  0.00           H  
HETATM   41  H7  UNL     1      -0.730   1.103   1.826  1.00  0.00           H  
HETATM   42  H8  UNL     1      -2.735  -0.335  -0.421  1.00  0.00           H  
HETATM   43  H9  UNL     1      -2.314  -0.041  -2.443  1.00  0.00           H  
HETATM   44  H10 UNL     1      -1.053  -0.819   1.256  1.00  0.00           H  
HETATM   45  H11 UNL     1      -0.707  -2.240  -1.416  1.00  0.00           H  
HETATM   46  H12 UNL     1      -0.255  -2.905   0.172  1.00  0.00           H  
HETATM   47  H13 UNL     1      -1.883  -3.440   1.868  1.00  0.00           H  
HETATM   48  H14 UNL     1      -4.149  -4.292   2.282  1.00  0.00           H  
HETATM   49  H15 UNL     1      -6.925  -4.163  -0.033  1.00  0.00           H  
HETATM   50  H16 UNL     1      -5.353  -3.030  -1.622  1.00  0.00           H  
HETATM   51  H17 UNL     1      -3.136  -2.201  -2.038  1.00  0.00           H  
HETATM   52  H18 UNL     1       3.600  -0.308   2.613  1.00  0.00           H  
HETATM   53  H19 UNL     1       6.541   0.221   4.454  1.00  0.00           H  
HETATM   54  H20 UNL     1       5.312  -1.046   3.938  1.00  0.00           H  
HETATM   55  H21 UNL     1       4.911   0.683   3.939  1.00  0.00           H  
HETATM   56  H22 UNL     1       7.706   0.367   0.525  1.00  0.00           H  
HETATM   57  H23 UNL     1       3.824  -0.796  -3.539  1.00  0.00           H  
HETATM   58  H24 UNL     1       5.157   0.176  -4.339  1.00  0.00           H  
HETATM   59  H25 UNL     1       3.846   1.022  -3.475  1.00  0.00           H  
HETATM   60  H26 UNL     1       2.737  -0.247  -1.549  1.00  0.00           H  
CONECT    1    2   35   36   37
CONECT    2    3
CONECT    3    4    4    9
CONECT    4    5   38
CONECT    5    6    7    7
CONECT    6   39
CONECT    7    8   40
CONECT    8    9    9   41
CONECT    9   10
CONECT   10   11   12   42
CONECT   11   43
CONECT   12   13   21   44
CONECT   13   14   45   46
CONECT   14   15   15   20
CONECT   15   16   47
CONECT   16   17   17   48
CONECT   17   18   19
CONECT   18   49
CONECT   19   20   20   50
CONECT   20   51
CONECT   21   22
CONECT   22   23   23   24
CONECT   24   25   25   34
CONECT   25   26   52
CONECT   26   27   29   29
CONECT   27   28
CONECT   28   53   54   55
CONECT   29   30   31
CONECT   30   56
CONECT   31   32   34   34
CONECT   32   33
CONECT   33   57   58   59
CONECT   34   60
END

NP0001499
     RDKit          3D

60 62  0  0  0  0  0  0  0  0999 V2000
   -3.7691    3.0175   -2.6444 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

View in JSmol

Synonyms

Value	Source
1-Hydroxy-1-(4-hydroxy-2-methoxyphenyl)-3-(4-hydroxyphenyl)propan-2-yl 4-hydroxy-3,5-dimethoxybenzoic acid	Generator
(1S,2R)-1-Hydroxy-1-(4-hydroxy-2-methoxyphenyl)-3-(4-hydroxyphenyl)-2-propanyl 4-hydroxy-3,5-dimethoxybenzoate	MeSH
1-(4-Hydroxy-2-methoxyphenyl)-2-(4-hydroxy-3,5-dimethoxybenzoyloxy)-3-(4-hydroxyphenyl)propan-1-ol	MeSH
Eryvarinol a	MeSH

Chemical Formula

C₂₅H₂₆O₉

Average Mass

470.4740 Da

Monoisotopic Mass

470.15768 Da

IUPAC Name

1-hydroxy-1-(4-hydroxy-2-methoxyphenyl)-3-(4-hydroxyphenyl)propan-2-yl 4-hydroxy-3,5-dimethoxybenzoate

Traditional Name

1-hydroxy-1-(4-hydroxy-2-methoxyphenyl)-3-(4-hydroxyphenyl)propan-2-yl 4-hydroxy-3,5-dimethoxybenzoate

CAS Registry Number

Not Available

SMILES

COC1=CC(=CC(OC)=C1O)C(=O)OC(CC1=CC=C(O)C=C1)C(O)C1=CC=C(O)C=C1OC

InChI Identifier

InChI=1S/C25H26O9/c1-31-19-13-17(27)8-9-18(19)23(28)22(10-14-4-6-16(26)7-5-14)34-25(30)15-11-20(32-2)24(29)21(12-15)33-3/h4-9,11-13,22-23,26-29H,10H2,1-3H3

InChI Key

ISBPEYMYDJMZGH-UHFFFAOYSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹H NMR Spectrum (1D, 600Mz MHz, Acetone, experimental)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹H NMR Spectrum (1D, 600Mz, Acetone, simulated)	Rgf8b			2020-08-18	View Spectrum

Species

Species of Origin

Species Name	Source	Reference
Erythrina variegata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cinnamylphenols. These are organic compounds containing the 1,3-diphenylpropene moiety with one benzene ring bearing one or more hydroxyl groups.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Linear 1,3-diarylpropanoids

Sub Class

Cinnamylphenols

Direct Parent

Cinnamylphenols

Alternative Parents

Substituents

Cinnamylphenol
Gallic acid or derivatives
P-hydroxybenzoic acid alkyl ester
P-hydroxybenzoic acid ester
M-methoxybenzoic acid or derivatives
Benzoate ester
Methoxyphenol
M-dimethoxybenzene
Dimethoxybenzene
Benzoic acid or derivatives
Anisole
Phenoxy compound
Benzoyl
Phenol ether
Methoxybenzene
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Phenol
Monocyclic benzene moiety
Benzenoid
Carboxylic acid ester
Secondary alcohol
Ether
Carboxylic acid derivative
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Alcohol
Aromatic alcohol
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic 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	2.8	ALOGPS
logP	3.76	ChemAxon
logS	-4.7	ALOGPS
pKa (Strongest Acidic)	8.36	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	134.91 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	123.03 m³·mol⁻¹	ChemAxon
Polarizability	47.81 Å³	ChemAxon
Number of Rings	3	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

20057648

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

22297779

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Eryvarinol A (NP0001499)

MOL for NP0001499 (Eryvarinol A)

3D MOL for NP0001499 (Eryvarinol A)

3D SDF for NP0001499 (Eryvarinol A)

3D-SDF for NP0001499 (Eryvarinol A)

PDB for NP0001499 (Eryvarinol A)

3D PDB for NP0001499 (Eryvarinol A)

SMILES for NP0001499 (Eryvarinol A)

INCHI for NP0001499 (Eryvarinol A)

Structure for NP0001499 (Eryvarinol A)

3D Structure for NP0001499 (Eryvarinol A)