NP-MRD: Showing NP-Card for 3,5-Dihydroxy-4-(3-methylbut-2-enyl)benzene-1,2-dicarbaldehyde (NP0006811)

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Record Information

Version

2.0

Created at

2020-12-09 03:44:20 UTC

Updated at

2021-07-15 16:55:51 UTC

NP-MRD ID

NP0006811

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3,5-Dihydroxy-4-(3-methylbut-2-enyl)benzene-1,2-dicarbaldehyde

Provided By

NPAtlas

Description

3,5-Dihydroxy-4-(3-methylbut-2-en-1-yl)benzene-1,2-dicarbaldehyde belongs to the class of organic compounds known as hydroxybenzaldehydes. These are organic aromatic compounds containing a benzene ring carrying an aldehyde group and a hydroxyl group. 3,5-Dihydroxy-4-(3-methylbut-2-enyl)benzene-1,2-dicarbaldehyde is found in Stereum. 3,5-Dihydroxy-4-(3-methylbut-2-enyl)benzene-1,2-dicarbaldehyde was first documented in 2006 (PMID: 17193259). Based on a literature review very few articles have been published on 3,5-dihydroxy-4-(3-methylbut-2-en-1-yl)benzene-1,2-dicarbaldehyde.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242118353D          

 31 31  0  0  0  0            999 V2000
    3.6553   -1.7154   -0.9459 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9073   -0.5681   -0.3163 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3713    0.7963   -0.6218 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9031   -0.8102    0.4626 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1128    0.2298    1.1217 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3307    0.1616    0.7676 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1479   -0.7954    1.3231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5334   -1.6794    2.2180 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4834   -0.8899    1.0286 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1011   -0.0056    0.1322 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5299   -0.1605   -0.1342 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1696   -1.1033    0.4602 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2938    0.9497   -0.4255 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8553    1.9080   -1.3676 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0518    1.9398   -1.7268 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9263    1.0534   -0.1289 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1002    2.0068   -0.6790 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9640   -1.4236   -1.9713 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5566   -1.8776   -0.3150 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0343   -2.6371   -0.9247 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5746    1.5321   -0.7060 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9233    0.7755   -1.6024 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0553    1.1111    0.2032 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6014   -1.8499    0.6595 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5318    1.2447    0.9844 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1608    0.0791    2.2508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0250   -2.4170    2.6835 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0974   -1.6550    1.4846 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1197    0.4311   -0.7799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2072    2.6750   -1.8158 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3792    2.6941   -1.3190 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
  2  4  2  3  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 10 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 13 16  2  0  0  0  0
 16 17  1  0  0  0  0
 16  6  1  0  0  0  0
  1 18  1  0  0  0  0
  1 19  1  0  0  0  0
  1 20  1  0  0  0  0
  3 21  1  0  0  0  0
  3 22  1  0  0  0  0
  3 23  1  0  0  0  0
  4 24  1  0  0  0  0
  5 25  1  0  0  0  0
  5 26  1  0  0  0  0
  8 27  1  0  0  0  0
  9 28  1  0  0  0  0
 11 29  1  0  0  0  0
 14 30  1  0  0  0  0
 17 31  1  0  0  0  0
M  END

     RDKit          3D

 31 31  0  0  0  0  0  0  0  0999 V2000
    3.6553   -1.7154   -0.9459 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9073   -0.5681   -0.3163 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3713    0.7963   -0.6218 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9031   -0.8102    0.4626 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1128    0.2298    1.1217 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3307    0.1616    0.7676 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1479   -0.7954    1.3231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5334   -1.6794    2.2180 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4834   -0.8899    1.0286 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1011   -0.0056    0.1322 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5299   -0.1605   -0.1342 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1696   -1.1033    0.4602 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2938    0.9497   -0.4255 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8553    1.9080   -1.3676 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0518    1.9398   -1.7268 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9263    1.0534   -0.1289 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1002    2.0068   -0.6790 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9640   -1.4236   -1.9713 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5566   -1.8776   -0.3150 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0343   -2.6371   -0.9247 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5746    1.5321   -0.7060 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9233    0.7755   -1.6024 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0553    1.1111    0.2032 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6014   -1.8499    0.6595 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5318    1.2447    0.9844 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1608    0.0791    2.2508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0250   -2.4170    2.6835 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0974   -1.6550    1.4846 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1197    0.4311   -0.7799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2072    2.6750   -1.8158 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3792    2.6941   -1.3190 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  7  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 10 13  1  0
 13 14  1  0
 14 15  2  0
 13 16  2  0
 16 17  1  0
 16  6  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  3 21  1  0
  3 22  1  0
  3 23  1  0
  4 24  1  0
  5 25  1  0
  5 26  1  0
  8 27  1  0
  9 28  1  0
 11 29  1  0
 14 30  1  0
 17 31  1  0
M  END


  Mrv1652306242118353D          

 31 31  0  0  0  0            999 V2000
    3.6553   -1.7154   -0.9459 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9073   -0.5681   -0.3163 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3713    0.7963   -0.6218 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9031   -0.8102    0.4626 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1128    0.2298    1.1217 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3307    0.1616    0.7676 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1479   -0.7954    1.3231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5334   -1.6794    2.2180 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4834   -0.8899    1.0286 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1011   -0.0056    0.1322 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5299   -0.1605   -0.1342 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1696   -1.1033    0.4602 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2938    0.9497   -0.4255 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8553    1.9080   -1.3676 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0518    1.9398   -1.7268 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9263    1.0534   -0.1289 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1002    2.0068   -0.6790 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9640   -1.4236   -1.9713 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5566   -1.8776   -0.3150 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0343   -2.6371   -0.9247 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5746    1.5321   -0.7060 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9233    0.7755   -1.6024 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0553    1.1111    0.2032 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6014   -1.8499    0.6595 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5318    1.2447    0.9844 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1608    0.0791    2.2508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0250   -2.4170    2.6835 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0974   -1.6550    1.4846 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1197    0.4311   -0.7799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2072    2.6750   -1.8158 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3792    2.6941   -1.3190 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
  2  4  2  3  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 10 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 13 16  2  0  0  0  0
 16 17  1  0  0  0  0
 16  6  1  0  0  0  0
  1 18  1  0  0  0  0
  1 19  1  0  0  0  0
  1 20  1  0  0  0  0
  3 21  1  0  0  0  0
  3 22  1  0  0  0  0
  3 23  1  0  0  0  0
  4 24  1  0  0  0  0
  5 25  1  0  0  0  0
  5 26  1  0  0  0  0
  8 27  1  0  0  0  0
  9 28  1  0  0  0  0
 11 29  1  0  0  0  0
 14 30  1  0  0  0  0
 17 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0006811

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C13H14O4/c1-8(2)3-4-10-12(16)5-9(6-14)11(7-15)13(10)17/h3,5-7,16-17H,4H2,1-2H3

> <INCHI_KEY>
PTTDDDIGARBEKV-UHFFFAOYSA-N

> <FORMULA>
C13H14O4

> <MOLECULAR_WEIGHT>
234.251

> <EXACT_MASS>
234.089208931

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
31

> <JCHEM_AVERAGE_POLARIZABILITY>
24.376278064243227

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3,5-dihydroxy-4-(3-methylbut-2-en-1-yl)benzene-1,2-dicarbaldehyde

> <ALOGPS_LOGP>
2.19

> <JCHEM_LOGP>
3.169686861333333

> <ALOGPS_LOGS>
-2.95

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.49120932468305

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.748326165928538

> <JCHEM_PKA_STRONGEST_BASIC>
-5.780281154957353

> <JCHEM_POLAR_SURFACE_AREA>
74.6

> <JCHEM_REFRACTIVITY>
67.4306

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.64e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3,5-dihydroxy-4-(3-methylbut-2-en-1-yl)benzene-1,2-dicarbaldehyde

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 31 31  0  0  0  0  0  0  0  0999 V2000
    3.6553   -1.7154   -0.9459 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9073   -0.5681   -0.3163 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3713    0.7963   -0.6218 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9031   -0.8102    0.4626 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1128    0.2298    1.1217 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3307    0.1616    0.7676 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1479   -0.7954    1.3231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5334   -1.6794    2.2180 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4834   -0.8899    1.0286 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1011   -0.0056    0.1322 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5299   -0.1605   -0.1342 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1696   -1.1033    0.4602 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2938    0.9497   -0.4255 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8553    1.9080   -1.3676 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0518    1.9398   -1.7268 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9263    1.0534   -0.1289 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1002    2.0068   -0.6790 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9640   -1.4236   -1.9713 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5566   -1.8776   -0.3150 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0343   -2.6371   -0.9247 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5746    1.5321   -0.7060 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9233    0.7755   -1.6024 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0553    1.1111    0.2032 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6014   -1.8499    0.6595 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5318    1.2447    0.9844 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1608    0.0791    2.2508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0250   -2.4170    2.6835 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0974   -1.6550    1.4846 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1197    0.4311   -0.7799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2072    2.6750   -1.8158 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3792    2.6941   -1.3190 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  7  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 10 13  1  0
 13 14  1  0
 14 15  2  0
 13 16  2  0
 16 17  1  0
 16  6  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  3 21  1  0
  3 22  1  0
  3 23  1  0
  4 24  1  0
  5 25  1  0
  5 26  1  0
  8 27  1  0
  9 28  1  0
 11 29  1  0
 14 30  1  0
 17 31  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  C   UNK     0       3.655  -1.715  -0.946  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.907  -0.568  -0.316  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.371   0.796  -0.622  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.903  -0.810   0.463  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.113   0.230   1.122  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.331   0.162   0.768  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.148  -0.795   1.323  0.00  0.00           C+0
HETATM    8  O   UNK     0      -0.533  -1.679   2.218  0.00  0.00           O+0
HETATM    9  C   UNK     0      -2.483  -0.890   1.029  0.00  0.00           C+0
HETATM   10  C   UNK     0      -3.101  -0.006   0.132  0.00  0.00           C+0
HETATM   11  C   UNK     0      -4.530  -0.161  -0.134  0.00  0.00           C+0
HETATM   12  O   UNK     0      -5.170  -1.103   0.460  0.00  0.00           O+0
HETATM   13  C   UNK     0      -2.294   0.950  -0.426  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.855   1.908  -1.368  0.00  0.00           C+0
HETATM   15  O   UNK     0      -4.052   1.940  -1.727  0.00  0.00           O+0
HETATM   16  C   UNK     0      -0.926   1.053  -0.129  0.00  0.00           C+0
HETATM   17  O   UNK     0      -0.100   2.007  -0.679  0.00  0.00           O+0
HETATM   18  H   UNK     0       3.964  -1.424  -1.971  0.00  0.00           H+0
HETATM   19  H   UNK     0       4.557  -1.878  -0.315  0.00  0.00           H+0
HETATM   20  H   UNK     0       3.034  -2.637  -0.925  0.00  0.00           H+0
HETATM   21  H   UNK     0       2.575   1.532  -0.706  0.00  0.00           H+0
HETATM   22  H   UNK     0       3.923   0.776  -1.602  0.00  0.00           H+0
HETATM   23  H   UNK     0       4.055   1.111   0.203  0.00  0.00           H+0
HETATM   24  H   UNK     0       1.601  -1.850   0.660  0.00  0.00           H+0
HETATM   25  H   UNK     0       1.532   1.245   0.984  0.00  0.00           H+0
HETATM   26  H   UNK     0       1.161   0.079   2.251  0.00  0.00           H+0
HETATM   27  H   UNK     0      -1.025  -2.417   2.684  0.00  0.00           H+0
HETATM   28  H   UNK     0      -3.097  -1.655   1.485  0.00  0.00           H+0
HETATM   29  H   UNK     0      -5.120   0.431  -0.780  0.00  0.00           H+0
HETATM   30  H   UNK     0      -2.207   2.675  -1.816  0.00  0.00           H+0
HETATM   31  H   UNK     0      -0.379   2.694  -1.319  0.00  0.00           H+0
CONECT    1    2   18   19   20                                             
CONECT    2    1    3    4                                                  
CONECT    3    2   21   22   23                                             
CONECT    4    2    5   24                                                  
CONECT    5    4    6   25   26                                             
CONECT    6    5    7   16                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7   27                                                       
CONECT    9    7   10   28                                                  
CONECT   10    9   11   13                                                  
CONECT   11   10   12   29                                                  
CONECT   12   11                                                            
CONECT   13   10   14   16                                                  
CONECT   14   13   15   30                                                  
CONECT   15   14                                                            
CONECT   16   13   17    6                                                  
CONECT   17   16   31                                                       
CONECT   18    1                                                            
CONECT   19    1                                                            
CONECT   20    1                                                            
CONECT   21    3                                                            
CONECT   22    3                                                            
CONECT   23    3                                                            
CONECT   24    4                                                            
CONECT   25    5                                                            
CONECT   26    5                                                            
CONECT   27    8                                                            
CONECT   28    9                                                            
CONECT   29   11                                                            
CONECT   30   14                                                            
CONECT   31   17                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   62    0
END

RDKit          3D

31 31  0  0  0  0  0  0  0  0999 V2000
    3.6553   -1.7154   -0.9459 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9073   -0.5681   -0.3163 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3713    0.7963   -0.6218 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9031   -0.8102    0.4626 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1128    0.2298    1.1217 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3307    0.1616    0.7676 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1479   -0.7954    1.3231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5334   -1.6794    2.2180 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4834   -0.8899    1.0286 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1011   -0.0056    0.1322 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5299   -0.1605   -0.1342 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1696   -1.1033    0.4602 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2938    0.9497   -0.4255 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8553    1.9080   -1.3676 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0518    1.9398   -1.7268 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9263    1.0534   -0.1289 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1002    2.0068   -0.6790 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9640   -1.4236   -1.9713 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5566   -1.8776   -0.3150 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0343   -2.6371   -0.9247 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5746    1.5321   -0.7060 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9233    0.7755   -1.6024 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0553    1.1111    0.2032 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6014   -1.8499    0.6595 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5318    1.2447    0.9844 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1608    0.0791    2.2508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0250   -2.4170    2.6835 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0974   -1.6550    1.4846 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1197    0.4311   -0.7799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2072    2.6750   -1.8158 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3792    2.6941   -1.3190 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  7  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 10 13  1  0
 13 14  1  0
 14 15  2  0
 13 16  2  0
 16 17  1  0
 16  6  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  3 21  1  0
  3 22  1  0
  3 23  1  0
  4 24  1  0
  5 25  1  0
  5 26  1  0
  8 27  1  0
  9 28  1  0
 11 29  1  0
 14 30  1  0
 17 31  1  0
M  END

View in JSmol View NMR Assignments View DFT Assignments 3D Conformers

Synonyms

Not Available

Chemical Formula

C₁₃H₁₄O₄

Average Mass

234.2510 Da

Monoisotopic Mass

234.08921 Da

IUPAC Name

3,5-dihydroxy-4-(3-methylbut-2-en-1-yl)benzene-1,2-dicarbaldehyde

Traditional Name

3,5-dihydroxy-4-(3-methylbut-2-en-1-yl)benzene-1,2-dicarbaldehyde

CAS Registry Number

Not Available

SMILES

CC(C)=CCC1=C(O)C=C(C=O)C(C=O)=C1O

InChI Identifier

InChI=1S/C13H14O4/c1-8(2)3-4-10-12(16)5-9(6-14)11(7-15)13(10)17/h3,5-7,16-17H,4H2,1-2H3

InChI Key

PTTDDDIGARBEKV-UHFFFAOYSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 125 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, 50 MHz, Acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 150 MHz, Acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 250 MHz, Acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 175 MHz, Acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 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	¹³C NMR Spectrum (1D, 225 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	¹³C NMR Spectrum (1D, 25 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	¹H 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, 700 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	¹H 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, 1000 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	¹H 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, 600 MHz, Acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

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
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, acetone, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 150 MHz, acetone, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 250 MHz, acetone, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 175 MHz, acetone, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, acetone, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, acetone, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 225 MHz, acetone, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, acetone, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 125 MHz, acetone, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, acetone, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, acetone, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, acetone, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, acetone, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, acetone, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, acetone, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, acetone, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, acetone, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, acetone, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, acetone, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, acetone, 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
Stereum	NPAtlas	17193259

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hydroxybenzaldehydes. These are organic aromatic compounds containing a benzene ring carrying an aldehyde group and a hydroxyl group.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbonyl compounds

Direct Parent

Hydroxybenzaldehydes

Alternative Parents

Substituents

Hydroxybenzaldehyde
Resorcinol
Benzoyl
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Benzenoid
Monocyclic benzene moiety
Vinylogous acid
Organic oxide
Hydrocarbon derivative
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	2.19	ALOGPS
logP	3.17	ChemAxon
logS	-3	ALOGPS
pKa (Strongest Acidic)	6.75	ChemAxon
pKa (Strongest Basic)	-5.8	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	74.6 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	67.43 m³·mol⁻¹	ChemAxon
Polarizability	24.38 Å³	ChemAxon
Number of Rings	1	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

NPA018304

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

78435746

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

91521754

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Li GH, Li L, Duan M, Zhang KQ: The chemical constituents of the fungus Stereum sp. Chem Biodivers. 2006 Feb;3(2):210-6. doi: 10.1002/cbdv.200690024. [PubMed:17193259 ]

Showing NP-Card for 3,5-Dihydroxy-4-(3-methylbut-2-enyl)benzene-1,2-dicarbaldehyde (NP0006811)

MOL for NP0006811 (3,5-Dihydroxy-4-(3-methylbut-2-enyl)benzene-1,2-dicarbaldehyde)

3D MOL for NP0006811 (3,5-Dihydroxy-4-(3-methylbut-2-enyl)benzene-1,2-dicarbaldehyde)

3D SDF for NP0006811 (3,5-Dihydroxy-4-(3-methylbut-2-enyl)benzene-1,2-dicarbaldehyde)

3D-SDF for NP0006811 (3,5-Dihydroxy-4-(3-methylbut-2-enyl)benzene-1,2-dicarbaldehyde)

PDB for NP0006811 (3,5-Dihydroxy-4-(3-methylbut-2-enyl)benzene-1,2-dicarbaldehyde)

3D PDB for NP0006811 (3,5-Dihydroxy-4-(3-methylbut-2-enyl)benzene-1,2-dicarbaldehyde)

SMILES for NP0006811 (3,5-Dihydroxy-4-(3-methylbut-2-enyl)benzene-1,2-dicarbaldehyde)

INCHI for NP0006811 (3,5-Dihydroxy-4-(3-methylbut-2-enyl)benzene-1,2-dicarbaldehyde)

Structure for NP0006811 (3,5-Dihydroxy-4-(3-methylbut-2-enyl)benzene-1,2-dicarbaldehyde)

3D Structure for NP0006811 (3,5-Dihydroxy-4-(3-methylbut-2-enyl)benzene-1,2-dicarbaldehyde)