NP-MRD: Showing NP-Card for 3-hydroxybenzyl 2-(4-oxo-5,6-dihydro-2H-pyran-3-yl) acetate (NP0009134)

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Record Information

Version

2.0

Created at

2020-12-09 06:34:40 UTC

Updated at

2021-07-15 17:02:24 UTC

NP-MRD ID

NP0009134

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-hydroxybenzyl 2-(4-oxo-5,6-dihydro-2H-pyran-3-yl) acetate

Provided By

NPAtlas

Description

3-Hydroxybenzyl 2-(4-oxo-5,6-dihydro-2H-pyran-3-yl) acetate belongs to the class of organic compounds known as benzyloxycarbonyls. These are organic compounds containing a carbonyl group substituted with a benzyloxyl group. 3-hydroxybenzyl 2-(4-oxo-5,6-dihydro-2H-pyran-3-yl) acetate is found in Penicillium. 3-hydroxybenzyl 2-(4-oxo-5,6-dihydro-2H-pyran-3-yl) acetate was first documented in 2010 (PMID: 20390738). Based on a literature review very few articles have been published on 3-hydroxybenzyl 2-(4-oxo-5,6-dihydro-2H-pyran-3-yl) acetate.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242106323D          

 33 34  0  0  0  0            999 V2000
    0.3579    1.3377    0.2753 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1789    0.3610   -0.2978 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2380    0.6033   -1.2882 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5633    0.3685   -0.6546 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6710   -0.0089    0.6144 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9285   -0.2186    1.1703 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1021    0.3747    0.5983 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.0549    0.1765   -0.9017 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7483    0.5687   -1.4768 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6290    1.0590   -2.6285 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2260   -0.9105    0.0025 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2150   -1.2845    0.9085 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5478   -0.7392    0.5085 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7752   -0.1588   -0.7160 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0440    0.3152   -1.0345 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0720    0.2094   -0.1376 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8319   -0.3714    1.0813 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9027   -0.4625    1.9717 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5928   -0.8402    1.4060 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1458    0.0013   -2.2176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2618    1.6815   -1.6211 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7554   -0.1386    1.1665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1742    1.4601    0.8632 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0068   -0.1968    0.9516 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8409    0.7793   -1.3970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1765   -0.9121   -1.0963 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9524   -0.9416    1.9457 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2898   -2.4010    0.9054 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9515   -0.0760   -1.4411 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1811    0.7721   -2.0237 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0601    0.5940   -0.4233 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0814    0.2707    2.6159 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3938   -1.3017    2.3707 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  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  1  0  0  0  0
  9 10  2  0  0  0  0
  2 11  1  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
 17 19  2  0  0  0  0
  9  4  1  0  0  0  0
 19 13  1  0  0  0  0
  3 20  1  0  0  0  0
  3 21  1  0  0  0  0
  5 22  1  0  0  0  0
  7 23  1  0  0  0  0
  7 24  1  0  0  0  0
  8 25  1  0  0  0  0
  8 26  1  0  0  0  0
 12 27  1  0  0  0  0
 12 28  1  0  0  0  0
 14 29  1  0  0  0  0
 15 30  1  0  0  0  0
 16 31  1  0  0  0  0
 18 32  1  0  0  0  0
 19 33  1  0  0  0  0
M  END

     RDKit          3D

 33 34  0  0  0  0  0  0  0  0999 V2000
    0.3579    1.3377    0.2753 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1789    0.3610   -0.2978 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2380    0.6033   -1.2882 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5633    0.3685   -0.6546 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6710   -0.0089    0.6144 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9285   -0.2186    1.1703 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1021    0.3747    0.5983 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0549    0.1765   -0.9017 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7483    0.5687   -1.4768 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6290    1.0590   -2.6285 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2260   -0.9105    0.0025 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2150   -1.2845    0.9085 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5478   -0.7392    0.5085 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7752   -0.1588   -0.7160 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0440    0.3152   -1.0345 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0720    0.2094   -0.1376 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8319   -0.3714    1.0813 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9027   -0.4625    1.9717 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5928   -0.8402    1.4060 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1458    0.0013   -2.2176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2618    1.6815   -1.6211 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7554   -0.1386    1.1665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1742    1.4601    0.8632 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0068   -0.1968    0.9516 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8409    0.7793   -1.3970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1765   -0.9121   -1.0963 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9524   -0.9416    1.9457 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2898   -2.4010    0.9054 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9515   -0.0760   -1.4411 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1811    0.7721   -2.0237 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0601    0.5940   -0.4233 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0814    0.2707    2.6159 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3938   -1.3017    2.3707 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
  2 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 17 19  2  0
  9  4  1  0
 19 13  1  0
  3 20  1  0
  3 21  1  0
  5 22  1  0
  7 23  1  0
  7 24  1  0
  8 25  1  0
  8 26  1  0
 12 27  1  0
 12 28  1  0
 14 29  1  0
 15 30  1  0
 16 31  1  0
 18 32  1  0
 19 33  1  0
M  END


  Mrv1652306242106323D          

 33 34  0  0  0  0            999 V2000
    0.3579    1.3377    0.2753 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1789    0.3610   -0.2978 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2380    0.6033   -1.2882 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5633    0.3685   -0.6546 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6710   -0.0089    0.6144 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9285   -0.2186    1.1703 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1021    0.3747    0.5983 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.0549    0.1765   -0.9017 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7483    0.5687   -1.4768 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6290    1.0590   -2.6285 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2260   -0.9105    0.0025 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2150   -1.2845    0.9085 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5478   -0.7392    0.5085 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7752   -0.1588   -0.7160 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0440    0.3152   -1.0345 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0720    0.2094   -0.1376 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8319   -0.3714    1.0813 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9027   -0.4625    1.9717 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5928   -0.8402    1.4060 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1458    0.0013   -2.2176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2618    1.6815   -1.6211 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7554   -0.1386    1.1665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1742    1.4601    0.8632 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0068   -0.1968    0.9516 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8409    0.7793   -1.3970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1765   -0.9121   -1.0963 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9524   -0.9416    1.9457 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2898   -2.4010    0.9054 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9515   -0.0760   -1.4411 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1811    0.7721   -2.0237 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0601    0.5940   -0.4233 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0814    0.2707    2.6159 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3938   -1.3017    2.3707 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  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  1  0  0  0  0
  9 10  2  0  0  0  0
  2 11  1  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
 17 19  2  0  0  0  0
  9  4  1  0  0  0  0
 19 13  1  0  0  0  0
  3 20  1  0  0  0  0
  3 21  1  0  0  0  0
  5 22  1  0  0  0  0
  7 23  1  0  0  0  0
  7 24  1  0  0  0  0
  8 25  1  0  0  0  0
  8 26  1  0  0  0  0
 12 27  1  0  0  0  0
 12 28  1  0  0  0  0
 14 29  1  0  0  0  0
 15 30  1  0  0  0  0
 16 31  1  0  0  0  0
 18 32  1  0  0  0  0
 19 33  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0009134

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C14H14O5/c15-12-3-1-2-10(6-12)8-19-14(17)7-11-9-18-5-4-13(11)16/h1-3,6,9,15H,4-5,7-8H2

> <INCHI_KEY>
AWBGMZRVRSBJQZ-UHFFFAOYSA-N

> <FORMULA>
C14H14O5

> <MOLECULAR_WEIGHT>
262.261

> <EXACT_MASS>
262.084123551

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
33

> <JCHEM_AVERAGE_POLARIZABILITY>
26.556631926618753

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3-hydroxyphenyl)methyl 2-(4-oxo-3,4-dihydro-2H-pyran-5-yl)acetate

> <ALOGPS_LOGP>
1.75

> <JCHEM_LOGP>
1.410008733666667

> <ALOGPS_LOGS>
-2.94

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
18.241416439164105

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.373723543809344

> <JCHEM_PKA_STRONGEST_BASIC>
-4.75907466354444

> <JCHEM_POLAR_SURFACE_AREA>
72.83000000000001

> <JCHEM_REFRACTIVITY>
67.69780000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.01e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3-hydroxyphenyl)methyl (4-oxo-5,6-dihydropyran-3-yl)acetate

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 33 34  0  0  0  0  0  0  0  0999 V2000
    0.3579    1.3377    0.2753 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1789    0.3610   -0.2978 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2380    0.6033   -1.2882 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5633    0.3685   -0.6546 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6710   -0.0089    0.6144 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9285   -0.2186    1.1703 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1021    0.3747    0.5983 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0549    0.1765   -0.9017 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7483    0.5687   -1.4768 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6290    1.0590   -2.6285 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2260   -0.9105    0.0025 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2150   -1.2845    0.9085 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5478   -0.7392    0.5085 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7752   -0.1588   -0.7160 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0440    0.3152   -1.0345 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0720    0.2094   -0.1376 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8319   -0.3714    1.0813 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9027   -0.4625    1.9717 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5928   -0.8402    1.4060 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1458    0.0013   -2.2176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2618    1.6815   -1.6211 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7554   -0.1386    1.1665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1742    1.4601    0.8632 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0068   -0.1968    0.9516 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8409    0.7793   -1.3970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1765   -0.9121   -1.0963 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9524   -0.9416    1.9457 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2898   -2.4010    0.9054 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9515   -0.0760   -1.4411 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1811    0.7721   -2.0237 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0601    0.5940   -0.4233 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0814    0.2707    2.6159 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3938   -1.3017    2.3707 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
  2 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 17 19  2  0
  9  4  1  0
 19 13  1  0
  3 20  1  0
  3 21  1  0
  5 22  1  0
  7 23  1  0
  7 24  1  0
  8 25  1  0
  8 26  1  0
 12 27  1  0
 12 28  1  0
 14 29  1  0
 15 30  1  0
 16 31  1  0
 18 32  1  0
 19 33  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  O   UNK     0       0.358   1.338   0.275  0.00  0.00           O+0
HETATM    2  C   UNK     0      -0.179   0.361  -0.298  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.238   0.603  -1.288  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.563   0.369  -0.655  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.671  -0.009   0.614  0.00  0.00           C+0
HETATM    6  O   UNK     0      -3.929  -0.219   1.170  0.00  0.00           O+0
HETATM    7  C   UNK     0      -5.102   0.375   0.598  0.00  0.00           C+0
HETATM    8  C   UNK     0      -5.055   0.177  -0.902  0.00  0.00           C+0
HETATM    9  C   UNK     0      -3.748   0.569  -1.477  0.00  0.00           C+0
HETATM   10  O   UNK     0      -3.629   1.059  -2.628  0.00  0.00           O+0
HETATM   11  O   UNK     0       0.226  -0.911   0.003  0.00  0.00           O+0
HETATM   12  C   UNK     0       1.215  -1.285   0.909  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.548  -0.739   0.508  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.775  -0.159  -0.716  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.044   0.315  -1.034  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.072   0.209  -0.138  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.832  -0.371   1.081  0.00  0.00           C+0
HETATM   18  O   UNK     0       5.903  -0.463   1.972  0.00  0.00           O+0
HETATM   19  C   UNK     0       3.593  -0.840   1.406  0.00  0.00           C+0
HETATM   20  H   UNK     0      -1.146   0.001  -2.218  0.00  0.00           H+0
HETATM   21  H   UNK     0      -1.262   1.682  -1.621  0.00  0.00           H+0
HETATM   22  H   UNK     0      -1.755  -0.139   1.167  0.00  0.00           H+0
HETATM   23  H   UNK     0      -5.174   1.460   0.863  0.00  0.00           H+0
HETATM   24  H   UNK     0      -6.007  -0.197   0.952  0.00  0.00           H+0
HETATM   25  H   UNK     0      -5.841   0.779  -1.397  0.00  0.00           H+0
HETATM   26  H   UNK     0      -5.176  -0.912  -1.096  0.00  0.00           H+0
HETATM   27  H   UNK     0       0.952  -0.942   1.946  0.00  0.00           H+0
HETATM   28  H   UNK     0       1.290  -2.401   0.905  0.00  0.00           H+0
HETATM   29  H   UNK     0       1.952  -0.076  -1.441  0.00  0.00           H+0
HETATM   30  H   UNK     0       4.181   0.772  -2.024  0.00  0.00           H+0
HETATM   31  H   UNK     0       6.060   0.594  -0.423  0.00  0.00           H+0
HETATM   32  H   UNK     0       6.081   0.271   2.616  0.00  0.00           H+0
HETATM   33  H   UNK     0       3.394  -1.302   2.371  0.00  0.00           H+0
CONECT    1    2                                                            
CONECT    2    1    3   11                                                  
CONECT    3    2    4   20   21                                             
CONECT    4    3    5    9                                                  
CONECT    5    4    6   22                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   23   24                                             
CONECT    8    7    9   25   26                                             
CONECT    9    8   10    4                                                  
CONECT   10    9                                                            
CONECT   11    2   12                                                       
CONECT   12   11   13   27   28                                             
CONECT   13   12   14   19                                                  
CONECT   14   13   15   29                                                  
CONECT   15   14   16   30                                                  
CONECT   16   15   17   31                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17   32                                                       
CONECT   19   17   13   33                                                  
CONECT   20    3                                                            
CONECT   21    3                                                            
CONECT   22    5                                                            
CONECT   23    7                                                            
CONECT   24    7                                                            
CONECT   25    8                                                            
CONECT   26    8                                                            
CONECT   27   12                                                            
CONECT   28   12                                                            
CONECT   29   14                                                            
CONECT   30   15                                                            
CONECT   31   16                                                            
CONECT   32   18                                                            
CONECT   33   19                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   68    0
END

RDKit          3D

33 34  0  0  0  0  0  0  0  0999 V2000
    0.3579    1.3377    0.2753 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1789    0.3610   -0.2978 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2380    0.6033   -1.2882 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5633    0.3685   -0.6546 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6710   -0.0089    0.6144 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9285   -0.2186    1.1703 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1021    0.3747    0.5983 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0549    0.1765   -0.9017 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7483    0.5687   -1.4768 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6290    1.0590   -2.6285 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2260   -0.9105    0.0025 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2150   -1.2845    0.9085 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5478   -0.7392    0.5085 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7752   -0.1588   -0.7160 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0440    0.3152   -1.0345 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0720    0.2094   -0.1376 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8319   -0.3714    1.0813 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9027   -0.4625    1.9717 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5928   -0.8402    1.4060 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1458    0.0013   -2.2176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2618    1.6815   -1.6211 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7554   -0.1386    1.1665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1742    1.4601    0.8632 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0068   -0.1968    0.9516 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8409    0.7793   -1.3970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1765   -0.9121   -1.0963 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9524   -0.9416    1.9457 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2898   -2.4010    0.9054 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9515   -0.0760   -1.4411 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1811    0.7721   -2.0237 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0601    0.5940   -0.4233 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0814    0.2707    2.6159 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3938   -1.3017    2.3707 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
  2 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 17 19  2  0
  9  4  1  0
 19 13  1  0
  3 20  1  0
  3 21  1  0
  5 22  1  0
  7 23  1  0
  7 24  1  0
  8 25  1  0
  8 26  1  0
 12 27  1  0
 12 28  1  0
 14 29  1  0
 15 30  1  0
 16 31  1  0
 18 32  1  0
 19 33  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
3-Hydroxybenzyl 2-(4-oxo-5,6-dihydro-2H-pyran-3-yl) acetic acid	Generator
(3-Hydroxyphenyl)methyl 2-(4-oxo-3,4-dihydro-2H-pyran-5-yl)acetic acid	Generator

Chemical Formula

C₁₄H₁₄O₅

Average Mass

262.2610 Da

Monoisotopic Mass

262.08412 Da

IUPAC Name

(3-hydroxyphenyl)methyl 2-(4-oxo-3,4-dihydro-2H-pyran-5-yl)acetate

Traditional Name

(3-hydroxyphenyl)methyl (4-oxo-5,6-dihydropyran-3-yl)acetate

CAS Registry Number

Not Available

SMILES

OC1=CC=CC(COC(=O)CC2=COCCC2=O)=C1

InChI Identifier

InChI=1S/C14H14O5/c15-12-3-1-2-10(6-12)8-19-14(17)7-11-9-18-5-4-13(11)16/h1-3,6,9,15H,4-5,7-8H2

InChI Key

AWBGMZRVRSBJQZ-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
Penicillium	NPAtlas	20390738

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzyloxycarbonyls. These are organic compounds containing a carbonyl group substituted with a benzyloxyl group.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Benzyloxycarbonyls

Direct Parent

Benzyloxycarbonyls

Alternative Parents

Substituents

Benzyloxycarbonyl
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Dihydropyranone
Phenol
Vinylogous ester
Carboxylic acid ester
Ketone
Cyclic ketone
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Hydrocarbon derivative
Organooxygen compound
Organic oxygen compound
Organic oxide
Carbonyl group
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	1.75	ALOGPS
logP	1.41	ChemAxon
logS	-2.9	ALOGPS
pKa (Strongest Acidic)	9.37	ChemAxon
pKa (Strongest Basic)	-4.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	72.83 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	67.7 m³·mol⁻¹	ChemAxon
Polarizability	26.56 Å³	ChemAxon
Number of Rings	2	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

NPAtlas ID

NPA018527

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

27024791

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139588250

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Wu HH, Tian L, Feng BM, Li ZF, Zhang QH, Pei YH: Three new compounds from the marine fungus Penicillium sp. J Asian Nat Prod Res. 2010 Jan;12(1):15-9. doi: 10.1080/10286020903442020. [PubMed:20390738 ]

Showing NP-Card for 3-hydroxybenzyl 2-(4-oxo-5,6-dihydro-2H-pyran-3-yl) acetate (NP0009134)

MOL for NP0009134 (3-hydroxybenzyl 2-(4-oxo-5,6-dihydro-2H-pyran-3-yl) acetate)

3D MOL for NP0009134 (3-hydroxybenzyl 2-(4-oxo-5,6-dihydro-2H-pyran-3-yl) acetate)

3D SDF for NP0009134 (3-hydroxybenzyl 2-(4-oxo-5,6-dihydro-2H-pyran-3-yl) acetate)

3D-SDF for NP0009134 (3-hydroxybenzyl 2-(4-oxo-5,6-dihydro-2H-pyran-3-yl) acetate)

PDB for NP0009134 (3-hydroxybenzyl 2-(4-oxo-5,6-dihydro-2H-pyran-3-yl) acetate)

3D PDB for NP0009134 (3-hydroxybenzyl 2-(4-oxo-5,6-dihydro-2H-pyran-3-yl) acetate)

SMILES for NP0009134 (3-hydroxybenzyl 2-(4-oxo-5,6-dihydro-2H-pyran-3-yl) acetate)

INCHI for NP0009134 (3-hydroxybenzyl 2-(4-oxo-5,6-dihydro-2H-pyran-3-yl) acetate)

Structure for NP0009134 (3-hydroxybenzyl 2-(4-oxo-5,6-dihydro-2H-pyran-3-yl) acetate)

3D Structure for NP0009134 (3-hydroxybenzyl 2-(4-oxo-5,6-dihydro-2H-pyran-3-yl) acetate)