NP-MRD: Showing NP-Card for Terrestrol D (NP0007476)

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Record Information

Version

2.0

Created at

2020-12-09 04:20:57 UTC

Updated at

2021-07-15 16:57:42 UTC

NP-MRD ID

NP0007476

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Terrestrol D

Provided By

NPAtlas

Description

Terrestrol D is found in Penicillium terrestre. Based on a literature review very few articles have been published on 2-{[3-chloro-4-hydroxy-5-(hydroxymethyl)phenoxy]methyl}benzene-1,4-diol.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242118403D          

 33 34  0  0  0  0            999 V2000
   -5.1438    1.8963   -1.2547 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5538    0.6473   -1.2606 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3924    0.5199   -0.2976 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1650    1.0681   -0.6200 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0862    0.6336    0.1278 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2745    1.0967   -0.1479 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1931    0.4068    0.6678 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5470    0.1873    0.1473 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0207    0.5326   -1.0732 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2158    0.0359   -1.5472 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6997    0.3624   -2.7924 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9542   -0.8448   -0.7534 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4915   -1.2015    0.5120 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3036   -0.6816    0.9372 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8530   -1.0568    2.2261 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2824   -0.2726    1.1250 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5457   -0.8183    1.4372 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6761   -1.9764    2.7411 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -3.6072   -0.4079    0.7032 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8983   -0.8585    0.9058 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9507    1.8129   -0.5646 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0410    0.6424   -2.3439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2280   -0.1848   -1.2319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0081    1.8186   -1.3627 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2529    0.9541    1.6602 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7757   -0.6206    0.7498 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4618    1.2087   -1.6986 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2866    1.1179   -2.9890 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8753   -1.2483   -1.0829 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0778   -1.9082    1.1526 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9039   -0.7079    2.4748 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4588   -0.5959    1.7932 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1496   -1.5576    1.6300 H   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  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  2  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
  5 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
 19 20  1  0  0  0  0
 19  3  1  0  0  0  0
 14  8  1  0  0  0  0
  1 21  1  0  0  0  0
  2 22  1  0  0  0  0
  2 23  1  0  0  0  0
  4 24  1  0  0  0  0
  7 25  1  0  0  0  0
  7 26  1  0  0  0  0
  9 27  1  0  0  0  0
 11 28  1  0  0  0  0
 12 29  1  0  0  0  0
 13 30  1  0  0  0  0
 15 31  1  0  0  0  0
 16 32  1  0  0  0  0
 20 33  1  0  0  0  0
M  END

     RDKit          3D

 33 34  0  0  0  0  0  0  0  0999 V2000
   -5.1438    1.8963   -1.2547 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5538    0.6473   -1.2606 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3924    0.5199   -0.2976 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1650    1.0681   -0.6200 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0862    0.6336    0.1278 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2745    1.0967   -0.1479 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1931    0.4068    0.6678 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5470    0.1873    0.1473 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0207    0.5326   -1.0732 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2158    0.0359   -1.5472 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6997    0.3624   -2.7924 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9542   -0.8448   -0.7534 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4915   -1.2015    0.5120 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3036   -0.6816    0.9372 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8530   -1.0568    2.2261 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2824   -0.2726    1.1250 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5457   -0.8183    1.4372 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6761   -1.9764    2.7411 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -3.6072   -0.4079    0.7032 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8983   -0.8585    0.9058 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9507    1.8129   -0.5646 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0410    0.6424   -2.3439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2280   -0.1848   -1.2319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0081    1.8186   -1.3627 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2529    0.9541    1.6602 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7757   -0.6206    0.7498 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4618    1.2087   -1.6986 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2866    1.1179   -2.9890 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8753   -1.2483   -1.0829 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0778   -1.9082    1.1526 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9039   -0.7079    2.4748 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4588   -0.5959    1.7932 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1496   -1.5576    1.6300 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
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 10 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
  5 16  2  0
 16 17  1  0
 17 18  1  0
 17 19  2  0
 19 20  1  0
 19  3  1  0
 14  8  1  0
  1 21  1  0
  2 22  1  0
  2 23  1  0
  4 24  1  0
  7 25  1  0
  7 26  1  0
  9 27  1  0
 11 28  1  0
 12 29  1  0
 13 30  1  0
 15 31  1  0
 16 32  1  0
 20 33  1  0
M  END


  Mrv1652306242118403D          

 33 34  0  0  0  0            999 V2000
   -5.1438    1.8963   -1.2547 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5538    0.6473   -1.2606 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3924    0.5199   -0.2976 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1650    1.0681   -0.6200 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0862    0.6336    0.1278 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2745    1.0967   -0.1479 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1931    0.4068    0.6678 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5470    0.1873    0.1473 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0207    0.5326   -1.0732 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2158    0.0359   -1.5472 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6997    0.3624   -2.7924 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9542   -0.8448   -0.7534 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4915   -1.2015    0.5120 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3036   -0.6816    0.9372 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8530   -1.0568    2.2261 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2824   -0.2726    1.1250 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5457   -0.8183    1.4372 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6761   -1.9764    2.7411 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -3.6072   -0.4079    0.7032 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8983   -0.8585    0.9058 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9507    1.8129   -0.5646 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0410    0.6424   -2.3439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2280   -0.1848   -1.2319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0081    1.8186   -1.3627 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2529    0.9541    1.6602 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7757   -0.6206    0.7498 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4618    1.2087   -1.6986 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2866    1.1179   -2.9890 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8753   -1.2483   -1.0829 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0778   -1.9082    1.1526 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9039   -0.7079    2.4748 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4588   -0.5959    1.7932 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1496   -1.5576    1.6300 H   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  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  2  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
  5 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
 19 20  1  0  0  0  0
 19  3  1  0  0  0  0
 14  8  1  0  0  0  0
  1 21  1  0  0  0  0
  2 22  1  0  0  0  0
  2 23  1  0  0  0  0
  4 24  1  0  0  0  0
  7 25  1  0  0  0  0
  7 26  1  0  0  0  0
  9 27  1  0  0  0  0
 11 28  1  0  0  0  0
 12 29  1  0  0  0  0
 13 30  1  0  0  0  0
 15 31  1  0  0  0  0
 16 32  1  0  0  0  0
 20 33  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0007476

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C14H13ClO5/c15-12-5-11(4-8(6-16)14(12)19)20-7-9-3-10(17)1-2-13(9)18/h1-5,16-19H,6-7H2

> <INCHI_KEY>
WTDORBLYOHYLPZ-UHFFFAOYSA-N

> <FORMULA>
C14H13ClO5

> <MOLECULAR_WEIGHT>
296.7

> <EXACT_MASS>
296.0451512

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
33

> <JCHEM_AVERAGE_POLARIZABILITY>
29.60659754392346

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-{[3-chloro-4-hydroxy-5-(hydroxymethyl)phenoxy]methyl}benzene-1,4-diol

> <ALOGPS_LOGP>
1.96

> <JCHEM_LOGP>
2.4660466116666666

> <ALOGPS_LOGS>
-3.71

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.469590537901446

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.685330150738762

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0067120087879564

> <JCHEM_POLAR_SURFACE_AREA>
90.15

> <JCHEM_REFRACTIVITY>
74.6972

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.82e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
terrestrol D

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 33 34  0  0  0  0  0  0  0  0999 V2000
   -5.1438    1.8963   -1.2547 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5538    0.6473   -1.2606 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3924    0.5199   -0.2976 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1650    1.0681   -0.6200 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0862    0.6336    0.1278 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2745    1.0967   -0.1479 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1931    0.4068    0.6678 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5470    0.1873    0.1473 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0207    0.5326   -1.0732 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2158    0.0359   -1.5472 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6997    0.3624   -2.7924 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9542   -0.8448   -0.7534 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4915   -1.2015    0.5120 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3036   -0.6816    0.9372 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8530   -1.0568    2.2261 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2824   -0.2726    1.1250 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5457   -0.8183    1.4372 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6761   -1.9764    2.7411 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -3.6072   -0.4079    0.7032 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8983   -0.8585    0.9058 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9507    1.8129   -0.5646 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0410    0.6424   -2.3439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2280   -0.1848   -1.2319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0081    1.8186   -1.3627 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2529    0.9541    1.6602 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7757   -0.6206    0.7498 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4618    1.2087   -1.6986 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2866    1.1179   -2.9890 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8753   -1.2483   -1.0829 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0778   -1.9082    1.1526 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9039   -0.7079    2.4748 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4588   -0.5959    1.7932 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1496   -1.5576    1.6300 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
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 10 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
  5 16  2  0
 16 17  1  0
 17 18  1  0
 17 19  2  0
 19 20  1  0
 19  3  1  0
 14  8  1  0
  1 21  1  0
  2 22  1  0
  2 23  1  0
  4 24  1  0
  7 25  1  0
  7 26  1  0
  9 27  1  0
 11 28  1  0
 12 29  1  0
 13 30  1  0
 15 31  1  0
 16 32  1  0
 20 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      -5.144   1.896  -1.255  0.00  0.00           O+0
HETATM    2  C   UNK     0      -4.554   0.647  -1.261  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.392   0.520  -0.298  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.165   1.068  -0.620  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.086   0.634   0.128  0.00  0.00           C+0
HETATM    6  O   UNK     0       0.275   1.097  -0.148  0.00  0.00           O+0
HETATM    7  C   UNK     0       1.193   0.407   0.668  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.547   0.187   0.147  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.021   0.533  -1.073  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.216   0.036  -1.547  0.00  0.00           C+0
HETATM   11  O   UNK     0       4.700   0.362  -2.792  0.00  0.00           O+0
HETATM   12  C   UNK     0       4.954  -0.845  -0.753  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.492  -1.202   0.512  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.304  -0.682   0.937  0.00  0.00           C+0
HETATM   15  O   UNK     0       2.853  -1.057   2.226  0.00  0.00           O+0
HETATM   16  C   UNK     0      -1.282  -0.273   1.125  0.00  0.00           C+0
HETATM   17  C   UNK     0      -2.546  -0.818   1.437  0.00  0.00           C+0
HETATM   18 Cl   UNK     0      -2.676  -1.976   2.741  0.00  0.00          Cl+0
HETATM   19  C   UNK     0      -3.607  -0.408   0.703  0.00  0.00           C+0
HETATM   20  O   UNK     0      -4.898  -0.859   0.906  0.00  0.00           O+0
HETATM   21  H   UNK     0      -5.951   1.813  -0.565  0.00  0.00           H+0
HETATM   22  H   UNK     0      -4.041   0.642  -2.344  0.00  0.00           H+0
HETATM   23  H   UNK     0      -5.228  -0.185  -1.232  0.00  0.00           H+0
HETATM   24  H   UNK     0      -2.008   1.819  -1.363  0.00  0.00           H+0
HETATM   25  H   UNK     0       1.253   0.954   1.660  0.00  0.00           H+0
HETATM   26  H   UNK     0       0.776  -0.621   0.750  0.00  0.00           H+0
HETATM   27  H   UNK     0       2.462   1.209  -1.699  0.00  0.00           H+0
HETATM   28  H   UNK     0       5.287   1.118  -2.989  0.00  0.00           H+0
HETATM   29  H   UNK     0       5.875  -1.248  -1.083  0.00  0.00           H+0
HETATM   30  H   UNK     0       5.078  -1.908   1.153  0.00  0.00           H+0
HETATM   31  H   UNK     0       1.904  -0.708   2.475  0.00  0.00           H+0
HETATM   32  H   UNK     0      -0.459  -0.596   1.793  0.00  0.00           H+0
HETATM   33  H   UNK     0      -5.150  -1.558   1.630  0.00  0.00           H+0
CONECT    1    2   21                                                       
CONECT    2    1    3   22   23                                             
CONECT    3    2    4   19                                                  
CONECT    4    3    5   24                                                  
CONECT    5    4    6   16                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   25   26                                             
CONECT    8    7    9   14                                                  
CONECT    9    8   10   27                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10   28                                                       
CONECT   12   10   13   29                                                  
CONECT   13   12   14   30                                                  
CONECT   14   13   15    8                                                  
CONECT   15   14   31                                                       
CONECT   16    5   17   32                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20    3                                                  
CONECT   20   19   33                                                       
CONECT   21    1                                                            
CONECT   22    2                                                            
CONECT   23    2                                                            
CONECT   24    4                                                            
CONECT   25    7                                                            
CONECT   26    7                                                            
CONECT   27    9                                                            
CONECT   28   11                                                            
CONECT   29   12                                                            
CONECT   30   13                                                            
CONECT   31   15                                                            
CONECT   32   16                                                            
CONECT   33   20                                                            
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
   -5.1438    1.8963   -1.2547 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5538    0.6473   -1.2606 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3924    0.5199   -0.2976 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1650    1.0681   -0.6200 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0862    0.6336    0.1278 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2745    1.0967   -0.1479 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1931    0.4068    0.6678 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5470    0.1873    0.1473 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0207    0.5326   -1.0732 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2158    0.0359   -1.5472 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6997    0.3624   -2.7924 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9542   -0.8448   -0.7534 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4915   -1.2015    0.5120 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3036   -0.6816    0.9372 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8530   -1.0568    2.2261 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2824   -0.2726    1.1250 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5457   -0.8183    1.4372 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6761   -1.9764    2.7411 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -3.6072   -0.4079    0.7032 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8983   -0.8585    0.9058 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9507    1.8129   -0.5646 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0410    0.6424   -2.3439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2280   -0.1848   -1.2319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0081    1.8186   -1.3627 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2529    0.9541    1.6602 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7757   -0.6206    0.7498 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4618    1.2087   -1.6986 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2866    1.1179   -2.9890 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8753   -1.2483   -1.0829 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0778   -1.9082    1.1526 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9039   -0.7079    2.4748 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4588   -0.5959    1.7932 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1496   -1.5576    1.6300 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
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 10 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
  5 16  2  0
 16 17  1  0
 17 18  1  0
 17 19  2  0
 19 20  1  0
 19  3  1  0
 14  8  1  0
  1 21  1  0
  2 22  1  0
  2 23  1  0
  4 24  1  0
  7 25  1  0
  7 26  1  0
  9 27  1  0
 11 28  1  0
 12 29  1  0
 13 30  1  0
 15 31  1  0
 16 32  1  0
 20 33  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₁₄H₁₃ClO₅

Average Mass

296.7000 Da

Monoisotopic Mass

296.04515 Da

IUPAC Name

2-{[3-chloro-4-hydroxy-5-(hydroxymethyl)phenoxy]methyl}benzene-1,4-diol

Traditional Name

terrestrol D

CAS Registry Number

Not Available

SMILES

OCC1=CC(OCC2=C(O)C=CC(O)=C2)=CC(Cl)=C1O

InChI Identifier

InChI=1S/C14H13ClO5/c15-12-5-11(4-8(6-16)14(12)19)20-7-9-3-10(17)1-2-13(9)18/h1-5,16-19H,6-7H2

InChI Key

WTDORBLYOHYLPZ-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 terrestre	NPAtlas	18163588

Chemical Taxonomy

Description

This compound belongs to the class of organic compounds known as 4-alkoxyphenols. These are phenols that carry an alkoxy group at the 4-position of the benzene ring.

Kingdom

Super Class

Class

Sub Class

Direct Parent

Alternative Parents

Substituents

4-alkoxyphenol
Benzyl alcohol
2-halophenol
Hydroquinone
2-chlorophenol
Phenol ether
Phenoxy compound
1-hydroxy-2-unsubstituted benzenoid
Chlorobenzene
Halobenzene
Alkyl aryl ether
Aryl halide
Monocyclic benzene moiety
Aryl chloride
Ether
Organooxygen compound
Organohalogen compound
Alcohol
Primary alcohol
Aromatic alcohol
Hydrocarbon derivative
Organic oxygen compound
Organochloride
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	1.96	ALOGPS
logP	2.47	ChemAxon
logS	-3.7	ALOGPS
pKa (Strongest Acidic)	8.69	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	90.15 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	74.7 m³·mol⁻¹	ChemAxon
Polarizability	29.61 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

NPA011892

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00040467

Chemspider ID

23314363

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

24770504

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Terrestrol D (NP0007476)

MOL for NP0007476 (Terrestrol D)

3D MOL for NP0007476 (Terrestrol D)

3D SDF for NP0007476 (Terrestrol D)

3D-SDF for NP0007476 (Terrestrol D)

PDB for NP0007476 (Terrestrol D)

3D PDB for NP0007476 (Terrestrol D)

SMILES for NP0007476 (Terrestrol D)

INCHI for NP0007476 (Terrestrol D)

Structure for NP0007476 (Terrestrol D)

3D Structure for NP0007476 (Terrestrol D)