NP-MRD: Showing NP-Card for 3-hydroxy-4-[(2r)-2,6,6-trimethyloxan-2-yl]benzoic acid (NP0237353)

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Record Information

Version

1.0

Created at

2022-09-06 20:28:18 UTC

Updated at

2022-09-06 20:28:18 UTC

NP-MRD ID

NP0237353

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-hydroxy-4-[(2r)-2,6,6-trimethyloxan-2-yl]benzoic acid

Description

UNII-8UAK634V59 belongs to the class of organic compounds known as hydroxybenzoic acid derivatives. Hydroxybenzoic acid derivatives are compounds containing a hydroxybenzoic acid (or a derivative), which is a benzene ring bearing a carboxyl and a hydroxyl groups. 3-hydroxy-4-[(2r)-2,6,6-trimethyloxan-2-yl]benzoic acid is found in Aspergillus austroafricanus and Dichotella gemmacea. Based on a literature review very few articles have been published on UNII-8UAK634V59.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 39 40  0  0  0  0  0  0  0  0999 V2000
   -1.9620    1.7248   -0.0182 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2428    0.4886   -0.8023 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8862    0.9338   -2.1242 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2306   -0.3592   -0.0261 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5471   -0.8577    1.1923 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0671   -0.6632    1.2498 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4478   -0.8420   -0.0980 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3758   -2.3571   -0.3381 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9190   -0.3268   -0.2320 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2391    0.5362   -1.2605 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5010    1.0499   -1.4396 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4881    0.6957   -0.5652 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8448    1.2146   -0.7130 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0831    1.9906   -1.6579 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8191    0.8432    0.1792 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1872   -0.1794    0.4873 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9122   -0.6731    0.6342 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6010   -1.5332    1.6628 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1890   -0.2916   -1.1305 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4794    1.7037    0.9869 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8855    1.9534    0.1026 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3920    2.6533   -0.5008 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5510    0.1668   -2.5272 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0848    1.1739   -2.8743 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4555    1.8812   -1.9863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1495    0.2276    0.1803 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4861   -1.2143   -0.6849 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8363   -1.9407    1.3355 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0312   -0.3501    2.0791 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7470    0.2496    1.7844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6968   -1.5141    1.8978 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6582   -2.6809   -0.1212 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6203   -2.5929   -1.3964 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0345   -2.9108    0.3618 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4766    0.8332   -1.9673 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7087    1.7315   -2.2701 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6380    1.4627    0.2732 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9930   -0.4313    1.1511 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3296   -1.7960    2.3101 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  6
  7 19  1  0
  7  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 16  1  0
 16 17  2  0
 17 18  1  0
 12 13  1  0
 13 15  1  0
 13 14  2  0
 19  2  1  0
 17  9  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
  3 23  1  0
  3 24  1  0
  3 25  1  0
  4 26  1  0
  4 27  1  0
  5 28  1  0
  5 29  1  0
  6 30  1  0
  6 31  1  0
  8 32  1  0
  8 33  1  0
  8 34  1  0
 10 35  1  0
 11 36  1  0
 16 38  1  0
 18 39  1  0
 15 37  1  0
M  END


  Mrv1652309062222282D          

 19 20  0  0  1  0            999 V2000
    1.7751   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2448   -1.0445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9592   -1.4570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9592   -2.2820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2448   -2.6945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5303   -2.2820    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2481   -3.0572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2822   -2.1387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8125   -2.7707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6249   -2.6275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9071   -1.8522    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7196   -1.7089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2499   -2.3409    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0017   -0.9337    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3768   -1.2202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5643   -1.3635    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0340   -0.7315    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5303   -1.4570    0.0000 O   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  1  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  1  0  0  0
  7  9  1  6  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 12 16  1  0  0  0  0
 16 17  2  0  0  0  0
  9 17  1  0  0  0  0
 17 18  1  0  0  0  0
  7 19  1  0  0  0  0
  2 19  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0237353

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)CCC[C@@](C)(O1)C1=CC=C(C=C1O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C15H20O4/c1-14(2)7-4-8-15(3,19-14)11-6-5-10(13(17)18)9-12(11)16/h5-6,9,16H,4,7-8H2,1-3H3,(H,17,18)/t15-/m1/s1

> <INCHI_KEY>
PPKSRWBBMMEDGG-OAHLLOKOSA-N

> <FORMULA>
C15H20O4

> <MOLECULAR_WEIGHT>
264.321

> <EXACT_MASS>
264.136159124

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
28.58110958043543

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-hydroxy-4-[(2R)-2,6,6-trimethyloxan-2-yl]benzoic acid

> <JCHEM_LOGP>
3.0909017016666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
9.076052748268992

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.830757217683816

> <JCHEM_PKA_STRONGEST_BASIC>
-4.236329974434966

> <JCHEM_POLAR_SURFACE_AREA>
66.76

> <JCHEM_REFRACTIVITY>
72.3696

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
3-hydroxy-4-[(2R)-2,6,6-trimethyloxan-2-yl]benzoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0       3.313  -0.770   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.324  -1.950   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.657  -2.720   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.657  -4.260   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.324  -5.030   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.990  -4.260   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.463  -5.707   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.527  -3.992   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.517  -5.172   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -3.033  -4.905   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -3.560  -3.457   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -5.077  -3.190   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -6.066  -4.370   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0      -5.603  -1.743   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -2.570  -2.278   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.053  -2.545   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -0.064  -1.365   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       0.990  -2.720   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4   19                                             
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9   19                                             
CONECT    8    7                                                            
CONECT    9    7   10   17                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   16                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13                                                            
CONECT   16   12   17                                                       
CONECT   17   16    9   18                                                  
CONECT   18   17                                                            
CONECT   19    7    2                                                       
MASTER        0    0    0    0    0    0    0    0   19    0   40    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₂₀O₄

Average Mass

264.3210 Da

Monoisotopic Mass

264.13616 Da

IUPAC Name

3-hydroxy-4-[(2R)-2,6,6-trimethyloxan-2-yl]benzoic acid

Traditional Name

3-hydroxy-4-[(2R)-2,6,6-trimethyloxan-2-yl]benzoic acid

CAS Registry Number

Not Available

SMILES

CC1(C)CCC[C@@](C)(O1)C1=CC=C(C=C1O)C(O)=O

InChI Identifier

InChI=1S/C15H20O4/c1-14(2)7-4-8-15(3,19-14)11-6-5-10(13(17)18)9-12(11)16/h5-6,9,16H,4,7-8H2,1-3H3,(H,17,18)/t15-/m1/s1

InChI Key

PPKSRWBBMMEDGG-OAHLLOKOSA-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, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, 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
Aspergillus austroafricanus	LOTUS Database	35616633
Dichotella gemmacea	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hydroxybenzoic acid derivatives. Hydroxybenzoic acid derivatives are compounds containing a hydroxybenzoic acid (or a derivative), which is a benzene ring bearing a carboxyl and a hydroxyl groups.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Benzoic acids and derivatives

Direct Parent

Hydroxybenzoic acid derivatives

Alternative Parents

Substituents

Hydroxybenzoic acid
Benzoic acid
Benzoyl
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Oxane
Carboxylic acid derivative
Carboxylic acid
Dialkyl ether
Ether
Monocarboxylic acid or derivatives
Organoheterocyclic compound
Oxacycle
Hydrocarbon derivative
Organic oxygen compound
Organooxygen compound
Organic oxide
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	3.09	ChemAxon
pKa (Strongest Acidic)	3.83	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	66.76 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	72.37 m³·mol⁻¹	ChemAxon
Polarizability	28.58 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

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

9911851

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11737144

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-hydroxy-4-[(2r)-2,6,6-trimethyloxan-2-yl]benzoic acid (NP0237353)

MOL for NP0237353 (3-hydroxy-4-[(2r)-2,6,6-trimethyloxan-2-yl]benzoic acid)

3D MOL for NP0237353 (3-hydroxy-4-[(2r)-2,6,6-trimethyloxan-2-yl]benzoic acid)

3D SDF for NP0237353 (3-hydroxy-4-[(2r)-2,6,6-trimethyloxan-2-yl]benzoic acid)

3D-SDF for NP0237353 (3-hydroxy-4-[(2r)-2,6,6-trimethyloxan-2-yl]benzoic acid)

PDB for NP0237353 (3-hydroxy-4-[(2r)-2,6,6-trimethyloxan-2-yl]benzoic acid)

3D PDB for NP0237353 (3-hydroxy-4-[(2r)-2,6,6-trimethyloxan-2-yl]benzoic acid)

SMILES for NP0237353 (3-hydroxy-4-[(2r)-2,6,6-trimethyloxan-2-yl]benzoic acid)

INCHI for NP0237353 (3-hydroxy-4-[(2r)-2,6,6-trimethyloxan-2-yl]benzoic acid)

Structure for NP0237353 (3-hydroxy-4-[(2r)-2,6,6-trimethyloxan-2-yl]benzoic acid)

3D Structure for NP0237353 (3-hydroxy-4-[(2r)-2,6,6-trimethyloxan-2-yl]benzoic acid)