NP-MRD: Showing NP-Card for (2s)-4-(4-benzoyl-3,5-dihydroxyphenoxy)-2-methylbutanoic acid (NP0297882)

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Record Information

Version

2.0

Created at

2022-09-10 08:38:11 UTC

Updated at

2022-09-10 08:38:12 UTC

NP-MRD ID

NP0297882

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s)-4-(4-benzoyl-3,5-dihydroxyphenoxy)-2-methylbutanoic acid

Description

(2S)-4-(4-benzoyl-3,5-dihydroxyphenoxy)-2-methylbutanoic acid belongs to the class of organic compounds known as benzophenones. These are organic compounds containing a ketone attached to two phenyl groups. (2s)-4-(4-benzoyl-3,5-dihydroxyphenoxy)-2-methylbutanoic acid is found in Helichrysum asperum. Based on a literature review very few articles have been published on (2S)-4-(4-benzoyl-3,5-dihydroxyphenoxy)-2-methylbutanoic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 42 43  0  0  0  0  0  0  0  0999 V2000
    3.3933    0.0073   -0.9644 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4215    0.3719    0.0464 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8968    0.8496    1.3734 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0585    2.0790    1.2222 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9484    1.9025    0.4550 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8304    1.1468    0.5483 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5330    0.3022    1.5687 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6299   -0.4255    1.5727 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9116   -1.2904    2.6390 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5329   -0.3139    0.5293 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7069   -1.1379    0.5494 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6748   -2.1675    1.3401 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9182   -0.9373   -0.2186 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5729   -2.0631   -0.7403 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7587   -1.9070   -1.4171 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3389   -0.6613   -1.6053 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6813    0.4294   -1.0854 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4825    0.3023   -0.3967 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2546    0.5329   -0.5160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1030    0.6907   -1.5973 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0829    1.2587   -0.5069 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3455   -0.7852    0.2992 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4548   -1.2841    1.4507 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0868   -1.3188   -0.7207 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9171    0.8898   -1.4040 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8952   -0.5212   -1.8289 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6514   -0.7304   -0.6037 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0618    1.1897   -0.3515 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4454    0.0403    1.9644 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8349    1.1252    1.9692 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6516    2.9292    0.7834 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7932    2.4576    2.2437 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1835    0.1712    2.4209 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2722   -1.3856    3.4032 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1072   -3.0318   -0.5857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2479   -2.7912   -1.8122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2750   -0.5714   -2.1444 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1321    1.4130   -1.2300 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0561    1.2311    0.0041 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8614    1.3166   -2.3335 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1265    1.9252   -1.3355 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0713   -1.2386   -0.8440 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  8 10  2  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 10 19  1  0
 19 20  1  0
 19 21  2  0
  2 22  1  0
 22 24  1  0
 22 23  2  0
 21  6  1  0
 18 13  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  6
  3 29  1  0
  3 30  1  0
  4 31  1  0
  4 32  1  0
  7 33  1  0
  9 34  1  0
 14 35  1  0
 15 36  1  0
 16 37  1  0
 17 38  1  0
 18 39  1  0
 20 40  1  0
 21 41  1  0
 24 42  1  0
M  END


  Mrv1652309102210382D          

 24 25  0  0  1  0            999 V2000
    5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -2.4750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 O   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
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  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
  8  9  1  0  0  0  0
  8 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 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  2  0  0  0  0
 13 18  1  0  0  0  0
 10 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
  6 21  1  0  0  0  0
  2 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0297882

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H](CCOC1=CC(O)=C(C(=O)C2=CC=CC=C2)C(O)=C1)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C18H18O6/c1-11(18(22)23)7-8-24-13-9-14(19)16(15(20)10-13)17(21)12-5-3-2-4-6-12/h2-6,9-11,19-20H,7-8H2,1H3,(H,22,23)/t11-/m0/s1

> <INCHI_KEY>
VKSQXENFIXPPPN-NSHDSACASA-N

> <FORMULA>
C18H18O6

> <MOLECULAR_WEIGHT>
330.336

> <EXACT_MASS>
330.1103383

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
34.08633633808563

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S)-4-(4-benzoyl-3,5-dihydroxyphenoxy)-2-methylbutanoic acid

> <JCHEM_LOGP>
4.514440472333333

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
6.921525074519693

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.4922992201898775

> <JCHEM_PKA_STRONGEST_BASIC>
-4.874377226164014

> <JCHEM_POLAR_SURFACE_AREA>
104.06000000000002

> <JCHEM_REFRACTIVITY>
87.17200000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-4-(4-benzoyl-3,5-dihydroxyphenoxy)-2-methylbutanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0      10.669  -3.080   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.669  -4.620   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.336  -5.390   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       6.668  -5.390   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       1.334  -5.390   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       0.000  -3.080   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       4.001  -0.770   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      12.003  -5.390   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      13.337  -4.620   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0      12.003  -6.930   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   22                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   21                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   19                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   18                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   13                                                       
CONECT   19   10   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19    6                                                       
CONECT   22    2   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   50    0
END

View in JSmol

Synonyms

Value	Source
(2S)-4-(4-Benzoyl-3,5-dihydroxyphenoxy)-2-methylbutanoate	Generator

Chemical Formula

C₁₈H₁₈O₆

Average Mass

330.3360 Da

Monoisotopic Mass

330.11034 Da

IUPAC Name

(2S)-4-(4-benzoyl-3,5-dihydroxyphenoxy)-2-methylbutanoic acid

Traditional Name

(2S)-4-(4-benzoyl-3,5-dihydroxyphenoxy)-2-methylbutanoic acid

CAS Registry Number

Not Available

SMILES

C[C@@H](CCOC1=CC(O)=C(C(=O)C2=CC=CC=C2)C(O)=C1)C(O)=O

InChI Identifier

InChI=1S/C18H18O6/c1-11(18(22)23)7-8-24-13-9-14(19)16(15(20)10-13)17(21)12-5-3-2-4-6-12/h2-6,9-11,19-20H,7-8H2,1H3,(H,22,23)/t11-/m0/s1

InChI Key

VKSQXENFIXPPPN-NSHDSACASA-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
Helichrysum asperum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzophenones. These are organic compounds containing a ketone attached to two phenyl groups.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Benzophenones

Direct Parent

Benzophenones

Alternative Parents

Substituents

Benzophenone
Diphenylmethane
Aryl-phenylketone
Phenoxy compound
Benzoyl
Phenol ether
Resorcinol
Aryl ketone
Phenol
Alkyl aryl ether
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Vinylogous acid
Ketone
Monocarboxylic acid or derivatives
Ether
Carboxylic acid
Carboxylic acid derivative
Carbonyl group
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
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	4.51	ChemAxon
pKa (Strongest Acidic)	3.49	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	104.06 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	87.17 m³·mol⁻¹	ChemAxon
Polarizability	34.09 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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

162869511

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2s)-4-(4-benzoyl-3,5-dihydroxyphenoxy)-2-methylbutanoic acid (NP0297882)

MOL for NP0297882 ((2s)-4-(4-benzoyl-3,5-dihydroxyphenoxy)-2-methylbutanoic acid)

3D MOL for NP0297882 ((2s)-4-(4-benzoyl-3,5-dihydroxyphenoxy)-2-methylbutanoic acid)

3D SDF for NP0297882 ((2s)-4-(4-benzoyl-3,5-dihydroxyphenoxy)-2-methylbutanoic acid)

3D-SDF for NP0297882 ((2s)-4-(4-benzoyl-3,5-dihydroxyphenoxy)-2-methylbutanoic acid)

PDB for NP0297882 ((2s)-4-(4-benzoyl-3,5-dihydroxyphenoxy)-2-methylbutanoic acid)

3D PDB for NP0297882 ((2s)-4-(4-benzoyl-3,5-dihydroxyphenoxy)-2-methylbutanoic acid)

SMILES for NP0297882 ((2s)-4-(4-benzoyl-3,5-dihydroxyphenoxy)-2-methylbutanoic acid)

INCHI for NP0297882 ((2s)-4-(4-benzoyl-3,5-dihydroxyphenoxy)-2-methylbutanoic acid)

Structure for NP0297882 ((2s)-4-(4-benzoyl-3,5-dihydroxyphenoxy)-2-methylbutanoic acid)

3D Structure for NP0297882 ((2s)-4-(4-benzoyl-3,5-dihydroxyphenoxy)-2-methylbutanoic acid)