NP-MRD: Showing NP-Card for pterolinus B (NP0035847)

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Record Information

Version

2.0

Created at

2021-06-20 19:10:46 UTC

Updated at

2021-06-30 00:07:07 UTC

NP-MRD ID

NP0035847

Secondary Accession Numbers

None

Natural Product Identification

Common Name

pterolinus B

Provided By

JEOL Database JEOL Logo

Description

Pterolinus B belongs to the class of organic compounds known as 2-arylbenzofuran flavonoids. These are phenylpropanoids containing the 2-phenylbenzofuran moiety. pterolinus B is found in Pterocarpus santalinus. pterolinus B was first documented in 2011 (Wu, S. -F., et al.). Based on a literature review very few articles have been published on Pterolinus B.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306202121103D          

 34 36  0  0  0  0            999 V2000
   -2.6222    2.5132   -4.0207 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2316    1.3060   -3.5756 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6691    0.7056   -2.4746 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5561    1.1747   -1.7731 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1455    0.4105   -0.6778 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0886    0.7046    0.1223 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0122   -0.2647    1.0828 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0651   -0.0857    2.0528 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9081   -0.4750    3.3904 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9466   -0.3040    4.3104 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1467    0.2605    3.8986 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1319    0.4085    4.8287 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3272    0.6614    2.5805 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2860    0.4890    1.6630 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0164   -1.2051    0.8889 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2771   -2.4344    1.6802 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7587   -0.7591   -0.2510 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8769   -1.2228   -0.9657 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3064   -0.4751   -2.0647 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3985   -0.9346   -2.7553 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6782    3.2905   -3.2514 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1809    2.8668   -4.8926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5879    2.3400   -4.3356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0150    2.0741   -2.0297 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0289   -0.8997    3.7395 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8153   -0.6058    5.3457 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9009    0.8207    4.4021 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2591    1.1060    2.2470 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4342    0.8031    0.6314 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8303   -3.1746    1.0935 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8687   -2.1957    2.5695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3413   -2.9048    1.9981 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3985   -2.1306   -0.6823 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5359   -0.2843   -3.4717 H   0  0  0  0  0  0  0  0  0  0  0  0
 11 12  1  0  0  0  0
  9 10  2  0  0  0  0
  8  9  1  0  0  0  0
 19  3  2  0  0  0  0
 10 11  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7 15  2  0  0  0  0
 15 17  1  0  0  0  0
  3  4  1  0  0  0  0
 19 20  1  0  0  0  0
  4  5  2  0  0  0  0
  3  2  1  0  0  0  0
  2  1  1  0  0  0  0
  7  8  1  0  0  0  0
 17 18  2  0  0  0  0
  8 14  2  0  0  0  0
 18 19  1  0  0  0  0
 14 13  1  0  0  0  0
 13 11  2  0  0  0  0
 17  5  1  0  0  0  0
 15 16  1  0  0  0  0
  9 25  1  0  0  0  0
 10 26  1  0  0  0  0
 12 27  1  0  0  0  0
  4 24  1  0  0  0  0
 18 33  1  0  0  0  0
 20 34  1  0  0  0  0
  1 21  1  0  0  0  0
  1 22  1  0  0  0  0
  1 23  1  0  0  0  0
 14 29  1  0  0  0  0
 13 28  1  0  0  0  0
 16 30  1  0  0  0  0
 16 31  1  0  0  0  0
 16 32  1  0  0  0  0
M  END

     RDKit          3D

 34 36  0  0  0  0  0  0  0  0999 V2000
   -2.6222    2.5132   -4.0207 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2316    1.3060   -3.5756 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6691    0.7056   -2.4746 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5561    1.1747   -1.7731 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1455    0.4105   -0.6778 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0886    0.7046    0.1223 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0122   -0.2647    1.0828 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0651   -0.0857    2.0528 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9081   -0.4750    3.3904 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9466   -0.3040    4.3104 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1467    0.2605    3.8986 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1319    0.4085    4.8287 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3272    0.6614    2.5805 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2860    0.4890    1.6630 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0164   -1.2051    0.8889 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2771   -2.4344    1.6802 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7587   -0.7591   -0.2510 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8769   -1.2228   -0.9657 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3064   -0.4751   -2.0647 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3985   -0.9346   -2.7553 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6782    3.2905   -3.2514 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1809    2.8668   -4.8926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5879    2.3400   -4.3356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0150    2.0741   -2.0297 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0289   -0.8997    3.7395 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8153   -0.6058    5.3457 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9009    0.8207    4.4021 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2591    1.1060    2.2470 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4342    0.8031    0.6314 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8303   -3.1746    1.0935 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8687   -2.1957    2.5695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3413   -2.9048    1.9981 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3985   -2.1306   -0.6823 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5359   -0.2843   -3.4717 H   0  0  0  0  0  0  0  0  0  0  0  0
 11 12  1  0
  9 10  2  0
  8  9  1  0
 19  3  2  0
 10 11  1  0
  5  6  1  0
  6  7  1  0
  7 15  2  0
 15 17  1  0
  3  4  1  0
 19 20  1  0
  4  5  2  0
  3  2  1  0
  2  1  1  0
  7  8  1  0
 17 18  2  0
  8 14  2  0
 18 19  1  0
 14 13  1  0
 13 11  2  0
 17  5  1  0
 15 16  1  0
  9 25  1  0
 10 26  1  0
 12 27  1  0
  4 24  1  0
 18 33  1  0
 20 34  1  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
 14 29  1  0
 13 28  1  0
 16 30  1  0
 16 31  1  0
 16 32  1  0
M  END


  Mrv1652306202121103D          

 34 36  0  0  0  0            999 V2000
   -2.6222    2.5132   -4.0207 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2316    1.3060   -3.5756 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6691    0.7056   -2.4746 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5561    1.1747   -1.7731 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1455    0.4105   -0.6778 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0886    0.7046    0.1223 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0122   -0.2647    1.0828 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0651   -0.0857    2.0528 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9081   -0.4750    3.3904 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9466   -0.3040    4.3104 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1467    0.2605    3.8986 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1319    0.4085    4.8287 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3272    0.6614    2.5805 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2860    0.4890    1.6630 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0164   -1.2051    0.8889 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2771   -2.4344    1.6802 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7587   -0.7591   -0.2510 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8769   -1.2228   -0.9657 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3064   -0.4751   -2.0647 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3985   -0.9346   -2.7553 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6782    3.2905   -3.2514 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1809    2.8668   -4.8926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5879    2.3400   -4.3356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0150    2.0741   -2.0297 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0289   -0.8997    3.7395 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8153   -0.6058    5.3457 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9009    0.8207    4.4021 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2591    1.1060    2.2470 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4342    0.8031    0.6314 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8303   -3.1746    1.0935 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8687   -2.1957    2.5695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3413   -2.9048    1.9981 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3985   -2.1306   -0.6823 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5359   -0.2843   -3.4717 H   0  0  0  0  0  0  0  0  0  0  0  0
 11 12  1  0  0  0  0
  9 10  2  0  0  0  0
  8  9  1  0  0  0  0
 19  3  2  0  0  0  0
 10 11  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7 15  2  0  0  0  0
 15 17  1  0  0  0  0
  3  4  1  0  0  0  0
 19 20  1  0  0  0  0
  4  5  2  0  0  0  0
  3  2  1  0  0  0  0
  2  1  1  0  0  0  0
  7  8  1  0  0  0  0
 17 18  2  0  0  0  0
  8 14  2  0  0  0  0
 18 19  1  0  0  0  0
 14 13  1  0  0  0  0
 13 11  2  0  0  0  0
 17  5  1  0  0  0  0
 15 16  1  0  0  0  0
  9 25  1  0  0  0  0
 10 26  1  0  0  0  0
 12 27  1  0  0  0  0
  4 24  1  0  0  0  0
 18 33  1  0  0  0  0
 20 34  1  0  0  0  0
  1 21  1  0  0  0  0
  1 22  1  0  0  0  0
  1 23  1  0  0  0  0
 14 29  1  0  0  0  0
 13 28  1  0  0  0  0
 16 30  1  0  0  0  0
 16 31  1  0  0  0  0
 16 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0035847

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C([H])C([H])=C(C([H])=C1[H])C1=C(C2=C([H])C(O[H])=C(OC([H])([H])[H])C([H])=C2O1)C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C16H14O4/c1-9-12-7-13(18)15(19-2)8-14(12)20-16(9)10-3-5-11(17)6-4-10/h3-8,17-18H,1-2H3

> <INCHI_KEY>
CQFHUONRLJIEPG-UHFFFAOYSA-N

> <FORMULA>
C16H14O4

> <MOLECULAR_WEIGHT>
270.284

> <EXACT_MASS>
270.089208931

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
34

> <JCHEM_AVERAGE_POLARIZABILITY>
29.520412390989314

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-(4-hydroxyphenyl)-6-methoxy-3-methyl-1-benzofuran-5-ol

> <ALOGPS_LOGP>
3.52

> <JCHEM_LOGP>
3.448215182666666

> <ALOGPS_LOGS>
-3.49

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.641224517323412

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.992233996558957

> <JCHEM_PKA_STRONGEST_BASIC>
-2.744385739141898

> <JCHEM_POLAR_SURFACE_AREA>
62.83

> <JCHEM_REFRACTIVITY>
75.379

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.65e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-(4-hydroxyphenyl)-6-methoxy-3-methyl-1-benzofuran-5-ol

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 34 36  0  0  0  0  0  0  0  0999 V2000
   -2.6222    2.5132   -4.0207 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2316    1.3060   -3.5756 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6691    0.7056   -2.4746 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5561    1.1747   -1.7731 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1455    0.4105   -0.6778 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0886    0.7046    0.1223 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0122   -0.2647    1.0828 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0651   -0.0857    2.0528 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9081   -0.4750    3.3904 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9466   -0.3040    4.3104 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1467    0.2605    3.8986 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1319    0.4085    4.8287 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3272    0.6614    2.5805 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2860    0.4890    1.6630 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0164   -1.2051    0.8889 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2771   -2.4344    1.6802 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7587   -0.7591   -0.2510 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8769   -1.2228   -0.9657 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3064   -0.4751   -2.0647 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3985   -0.9346   -2.7553 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6782    3.2905   -3.2514 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1809    2.8668   -4.8926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5879    2.3400   -4.3356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0150    2.0741   -2.0297 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0289   -0.8997    3.7395 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8153   -0.6058    5.3457 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9009    0.8207    4.4021 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2591    1.1060    2.2470 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4342    0.8031    0.6314 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8303   -3.1746    1.0935 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8687   -2.1957    2.5695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3413   -2.9048    1.9981 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3985   -2.1306   -0.6823 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5359   -0.2843   -3.4717 H   0  0  0  0  0  0  0  0  0  0  0  0
 11 12  1  0
  9 10  2  0
  8  9  1  0
 19  3  2  0
 10 11  1  0
  5  6  1  0
  6  7  1  0
  7 15  2  0
 15 17  1  0
  3  4  1  0
 19 20  1  0
  4  5  2  0
  3  2  1  0
  2  1  1  0
  7  8  1  0
 17 18  2  0
  8 14  2  0
 18 19  1  0
 14 13  1  0
 13 11  2  0
 17  5  1  0
 15 16  1  0
  9 25  1  0
 10 26  1  0
 12 27  1  0
  4 24  1  0
 18 33  1  0
 20 34  1  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
 14 29  1  0
 13 28  1  0
 16 30  1  0
 16 31  1  0
 16 32  1  0
M  END

HEADER    PROTEIN                                 20-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-JUN-21         0                                  
HETATM    1  C   UNK     0      -2.622   2.513  -4.021  0.00  0.00           C+0
HETATM    2  O   UNK     0      -3.232   1.306  -3.576  0.00  0.00           O+0
HETATM    3  C   UNK     0      -2.669   0.706  -2.475  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.556   1.175  -1.773  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.145   0.411  -0.678  0.00  0.00           C+0
HETATM    6  O   UNK     0      -0.089   0.705   0.122  0.00  0.00           O+0
HETATM    7  C   UNK     0      -0.012  -0.265   1.083  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.065  -0.086   2.053  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.908  -0.475   3.390  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.947  -0.304   4.310  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.147   0.261   3.899  0.00  0.00           C+0
HETATM   12  O   UNK     0       4.132   0.409   4.829  0.00  0.00           O+0
HETATM   13  C   UNK     0       3.327   0.661   2.580  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.286   0.489   1.663  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.016  -1.205   0.889  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.277  -2.434   1.680  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.759  -0.759  -0.251  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.877  -1.223  -0.966  0.00  0.00           C+0
HETATM   19  C   UNK     0      -3.306  -0.475  -2.065  0.00  0.00           C+0
HETATM   20  O   UNK     0      -4.399  -0.935  -2.755  0.00  0.00           O+0
HETATM   21  H   UNK     0      -2.678   3.291  -3.251  0.00  0.00           H+0
HETATM   22  H   UNK     0      -3.181   2.867  -4.893  0.00  0.00           H+0
HETATM   23  H   UNK     0      -1.588   2.340  -4.336  0.00  0.00           H+0
HETATM   24  H   UNK     0      -1.015   2.074  -2.030  0.00  0.00           H+0
HETATM   25  H   UNK     0      -0.029  -0.900   3.740  0.00  0.00           H+0
HETATM   26  H   UNK     0       1.815  -0.606   5.346  0.00  0.00           H+0
HETATM   27  H   UNK     0       4.901   0.821   4.402  0.00  0.00           H+0
HETATM   28  H   UNK     0       4.259   1.106   2.247  0.00  0.00           H+0
HETATM   29  H   UNK     0       2.434   0.803   0.631  0.00  0.00           H+0
HETATM   30  H   UNK     0      -1.830  -3.175   1.093  0.00  0.00           H+0
HETATM   31  H   UNK     0      -1.869  -2.196   2.570  0.00  0.00           H+0
HETATM   32  H   UNK     0      -0.341  -2.905   1.998  0.00  0.00           H+0
HETATM   33  H   UNK     0      -3.398  -2.131  -0.682  0.00  0.00           H+0
HETATM   34  H   UNK     0      -4.536  -0.284  -3.472  0.00  0.00           H+0
CONECT    1    2   21   22   23                                             
CONECT    2    3    1                                                       
CONECT    3   19    4    2                                                  
CONECT    4    3    5   24                                                  
CONECT    5    6    4   17                                                  
CONECT    6    5    7                                                       
CONECT    7    6   15    8                                                  
CONECT    8    9    7   14                                                  
CONECT    9   10    8   25                                                  
CONECT   10    9   11   26                                                  
CONECT   11   12   10   13                                                  
CONECT   12   11   27                                                       
CONECT   13   14   11   28                                                  
CONECT   14    8   13   29                                                  
CONECT   15    7   17   16                                                  
CONECT   16   15   30   31   32                                             
CONECT   17   15   18    5                                                  
CONECT   18   17   19   33                                                  
CONECT   19    3   20   18                                                  
CONECT   20   19   34                                                       
CONECT   21    1                                                            
CONECT   22    1                                                            
CONECT   23    1                                                            
CONECT   24    4                                                            
CONECT   25    9                                                            
CONECT   26   10                                                            
CONECT   27   12                                                            
CONECT   28   13                                                            
CONECT   29   14                                                            
CONECT   30   16                                                            
CONECT   31   16                                                            
CONECT   32   16                                                            
CONECT   33   18                                                            
CONECT   34   20                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   72    0
END

RDKit          3D

34 36  0  0  0  0  0  0  0  0999 V2000
   -2.6222    2.5132   -4.0207 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2316    1.3060   -3.5756 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6691    0.7056   -2.4746 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5561    1.1747   -1.7731 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1455    0.4105   -0.6778 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0886    0.7046    0.1223 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0122   -0.2647    1.0828 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0651   -0.0857    2.0528 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9081   -0.4750    3.3904 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9466   -0.3040    4.3104 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1467    0.2605    3.8986 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1319    0.4085    4.8287 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3272    0.6614    2.5805 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2860    0.4890    1.6630 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0164   -1.2051    0.8889 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2771   -2.4344    1.6802 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7587   -0.7591   -0.2510 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8769   -1.2228   -0.9657 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3064   -0.4751   -2.0647 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3985   -0.9346   -2.7553 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6782    3.2905   -3.2514 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1809    2.8668   -4.8926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5879    2.3400   -4.3356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0150    2.0741   -2.0297 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0289   -0.8997    3.7395 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8153   -0.6058    5.3457 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9009    0.8207    4.4021 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2591    1.1060    2.2470 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4342    0.8031    0.6314 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8303   -3.1746    1.0935 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8687   -2.1957    2.5695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3413   -2.9048    1.9981 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3985   -2.1306   -0.6823 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5359   -0.2843   -3.4717 H   0  0  0  0  0  0  0  0  0  0  0  0
 11 12  1  0
  9 10  2  0
  8  9  1  0
 19  3  2  0
 10 11  1  0
  5  6  1  0
  6  7  1  0
  7 15  2  0
 15 17  1  0
  3  4  1  0
 19 20  1  0
  4  5  2  0
  3  2  1  0
  2  1  1  0
  7  8  1  0
 17 18  2  0
  8 14  2  0
 18 19  1  0
 14 13  1  0
 13 11  2  0
 17  5  1  0
 15 16  1  0
  9 25  1  0
 10 26  1  0
 12 27  1  0
  4 24  1  0
 18 33  1  0
 20 34  1  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
 14 29  1  0
 13 28  1  0
 16 30  1  0
 16 31  1  0
 16 32  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₆H₁₄O₄

Average Mass

270.2840 Da

Monoisotopic Mass

270.08921 Da

IUPAC Name

2-(4-hydroxyphenyl)-6-methoxy-3-methyl-1-benzofuran-5-ol

Traditional Name

2-(4-hydroxyphenyl)-6-methoxy-3-methyl-1-benzofuran-5-ol

CAS Registry Number

Not Available

SMILES

[H]OC1=C([H])C([H])=C(C([H])=C1[H])C1=C(C2=C([H])C(O[H])=C(OC([H])([H])[H])C([H])=C2O1)C([H])([H])[H]

InChI Identifier

InChI=1S/C16H14O4/c1-9-12-7-13(18)15(19-2)8-14(12)20-16(9)10-3-5-11(17)6-4-10/h3-8,17-18H,1-2H3

InChI Key

CQFHUONRLJIEPG-UHFFFAOYSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Pterocarpus santalinus	JEOL database	Wu, S. -F., et al, J. Nat. Prod. 74, 989 (2011)

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
2-phenylbenzofuran
Phenylbenzofuran
Benzofuran
Anisole
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Phenol
Monocyclic benzene moiety
Benzenoid
Furan
Heteroaromatic compound
Ether
Oxacycle
Organoheterocyclic compound
Organooxygen compound
Organic oxygen compound
Hydrocarbon derivative
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

aromatic ether (CHEBI:67382 )
1-benzofurans (CHEBI:67382 )
polyphenol (CHEBI:67382 )

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	3.52	ALOGPS
logP	3.45	ChemAxon
logS	-3.5	ALOGPS
pKa (Strongest Acidic)	8.99	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	62.83 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	75.38 m³·mol⁻¹	ChemAxon
Polarizability	29.52 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	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

26629958

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

53262811

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Wu, S. -F., et al. (2011). Wu, S. -F., et al, J. Nat. Prod. 74, 989 (2011). J. Nat. Prod..

Showing NP-Card for pterolinus B (NP0035847)

MOL for NP0035847 (pterolinus B)

3D MOL for NP0035847 (pterolinus B)

3D SDF for NP0035847 (pterolinus B)

3D-SDF for NP0035847 (pterolinus B)

PDB for NP0035847 (pterolinus B)

3D PDB for NP0035847 (pterolinus B)

SMILES for NP0035847 (pterolinus B)

INCHI for NP0035847 (pterolinus B)

Structure for NP0035847 (pterolinus B)

3D Structure for NP0035847 (pterolinus B)