NP-MRD: Showing NP-Card for (8e)-3-hydroxy-2,2,4-trimethyl-10-(1,3-oxazol-5-yl)deca-4,6,8-trienimidic acid (NP0204462)

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Record Information

Version

2.0

Created at

2022-09-05 00:08:16 UTC

Updated at

2022-09-05 00:08:16 UTC

NP-MRD ID

NP0204462

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(8e)-3-hydroxy-2,2,4-trimethyl-10-(1,3-oxazol-5-yl)deca-4,6,8-trienimidic acid

Description

(8E)-3-hydroxy-2,2,4-trimethyl-10-(1,3-oxazol-5-yl)deca-4,6,8-trienimidic acid belongs to the class of organic compounds known as oxazoles. Oxazoles are compounds containing an oxazole ring, which is a five-membered aromatic heterocycle with one oxygen, one nitrogen, and three carbon atoms. Isomers include 1,2-oxazole and 1,3-oxazole (8E)-3-hydroxy-2,2,4-trimethyl-10-(1,3-oxazol-5-yl)deca-4,6,8-trienimidic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 43 43  0  0  0  0  0  0  0  0999 V2000
   -1.9710    1.1606    1.6166 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5949   -0.0909    0.9257 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3376   -0.2873    0.5796 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6991    0.7515    0.8754 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8979    0.5310    0.5290 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2062    0.2905    0.1510 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5682   -0.8765   -0.4593 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9645   -1.1402   -0.8697 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8169    0.0568   -0.5743 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5045    0.2818    0.5983 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1446    1.4606    0.4658 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.8489    1.9279   -0.7500 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0566    1.0779   -1.3549 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6175   -1.0831    0.5310 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4199   -1.4533    1.5973 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5452   -0.4995   -0.5219 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8091   -0.0892   -1.7566 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4666   -1.6524   -0.9503 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4220    0.5729   -0.0165 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4987    0.3870    0.8864 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2377    1.7630   -0.3892 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3876    1.2694    2.5857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7385    2.0721    1.0666 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0187    1.0622    1.9571 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0242   -1.1654    0.0818 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3196    1.6425    1.3906 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2506    1.8268    0.9866 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0751    0.9456    0.2731 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7595   -1.5703   -0.6082 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3378   -2.0265   -0.3485 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9527   -1.2579   -1.9674 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5025   -0.4005    1.4500 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1954    2.8665   -1.1996 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1331   -1.9853    0.1061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0154   -1.2662    2.4856 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2251    0.8902   -2.1421 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7181   -0.0335   -1.5661 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9484   -0.8063   -2.6179 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9297   -2.4877   -1.3967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9516   -1.9755    0.0185 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2700   -1.2639   -1.6205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3513   -0.0815    0.4515 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5170    0.6563    1.8805 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
  2 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 16 18  1  0
 16 19  1  0
 19 20  1  0
 19 21  2  0
 13  9  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  3 25  1  0
  4 26  1  0
  5 27  1  0
  6 28  1  0
  7 29  1  0
  8 30  1  0
  8 31  1  0
 10 32  1  0
 12 33  1  0
 14 34  1  6
 15 35  1  0
 17 36  1  0
 17 37  1  0
 17 38  1  0
 18 39  1  0
 18 40  1  0
 18 41  1  0
 20 42  1  0
 20 43  1  0
M  END


  Mrv1533004171520092D          

 21 21  0  0  0  0            999 V2000
   -0.8612    6.0643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5757    5.6518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5757    4.8268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8612    4.4143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8612    3.5893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1467    3.1768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1467    2.3518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5678    1.9393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5678    1.1143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2352    0.6294    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9803   -0.1553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1553   -0.1553    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0997    0.6294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2901    6.0643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0046    5.6518    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2901    6.8893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4651    6.8893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1151    6.8893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2901    7.7143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0046    8.1268    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5757    8.1268    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  4  0  0  0
  4  5  2  0  0  0  0
  5  6  1  4  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  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
  9 13  2  0  0  0  0
  2 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 16 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0204462

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=CC=C\C=C\CC1=CN=CO1)C(O)C(C)(C)C(N)=O

> <INCHI_IDENTIFIER>
InChI=1S/C16H22N2O3/c1-12(14(19)16(2,3)15(17)20)8-6-4-5-7-9-13-10-18-11-21-13/h4-8,10-11,14,19H,9H2,1-3H3,(H2,17,20)/b6-4?,7-5+,12-8?

> <INCHI_KEY>
MRTUFVRJHFZVOT-UOFHNPOQSA-N

> <FORMULA>
C16H22N2O3

> <MOLECULAR_WEIGHT>
290.363

> <EXACT_MASS>
290.163042576

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
43

> <JCHEM_AVERAGE_POLARIZABILITY>
32.28557051867213

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(8E)-3-hydroxy-2,2,4-trimethyl-10-(1,3-oxazol-5-yl)deca-4,6,8-trienamide

> <ALOGPS_LOGP>
2.22

> <JCHEM_LOGP>
1.2482791350000007

> <ALOGPS_LOGS>
-3.69

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
16.657776879602153

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.940721991886733

> <JCHEM_PKA_STRONGEST_BASIC>
0.3742459760507889

> <JCHEM_POLAR_SURFACE_AREA>
89.35000000000001

> <JCHEM_REFRACTIVITY>
84.8055

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.95e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(8E)-3-hydroxy-2,2,4-trimethyl-10-(1,3-oxazol-5-yl)deca-4,6,8-trienamide

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0      -1.608  11.320   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.941  10.550   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.941   9.010   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.608   8.240   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.608   6.700   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.274   5.930   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.274   4.390   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.060   3.620   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.060   2.080   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       2.306   1.175   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       1.830  -0.290   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0       0.290  -0.290   0.000  0.00  0.00           N+0
HETATM   13  C   UNK     0      -0.186   1.175   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -4.275  11.320   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -5.609  10.550   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -4.275  12.860   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -2.735  12.860   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -5.815  12.860   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -4.275  14.400   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -5.609  15.170   0.000  0.00  0.00           O+0
HETATM   21  N   UNK     0      -2.941  15.170   0.000  0.00  0.00           N+0
CONECT    1    2                                                            
CONECT    2    1    3   14                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   13                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12    9                                                       
CONECT   14    2   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   18   19                                             
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   16   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   42    0
END

View in JSmol

Synonyms

Value	Source
(8E)-3-Hydroxy-2,2,4-trimethyl-10-(1,3-oxazol-5-yl)deca-4,6,8-trienimidate	Generator

Chemical Formula

C₁₆H₂₂N₂O₃

Average Mass

290.3630 Da

Monoisotopic Mass

290.16304 Da

IUPAC Name

(8E)-3-hydroxy-2,2,4-trimethyl-10-(1,3-oxazol-5-yl)deca-4,6,8-trienamide

Traditional Name

(8E)-3-hydroxy-2,2,4-trimethyl-10-(1,3-oxazol-5-yl)deca-4,6,8-trienamide

CAS Registry Number

Not Available

SMILES

CC(=CC=C\C=C\CC1=CN=CO1)C(O)C(C)(C)C(N)=O

InChI Identifier

InChI=1S/C16H22N2O3/c1-12(14(19)16(2,3)15(17)20)8-6-4-5-7-9-13-10-18-11-21-13/h4-8,10-11,14,19H,9H2,1-3H3,(H2,17,20)/b6-4?,7-5+,12-8?

InChI Key

MRTUFVRJHFZVOT-UOFHNPOQSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oxazoles. Oxazoles are compounds containing an oxazole ring, which is a five-membered aromatic heterocycle with one oxygen, one nitrogen, and three carbon atoms. Isomers include 1,2-oxazole and 1,3-oxazole.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Azoles

Sub Class

Oxazoles

Direct Parent

Oxazoles

Alternative Parents

Substituents

Heteroaromatic compound
Oxazole
Secondary alcohol
Oxacycle
Azacycle
Carboximidic acid derivative
Carboximidic acid
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Alcohol
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	2.22	ALOGPS
logP	1.25	ChemAxon
logS	-3.7	ALOGPS
pKa (Strongest Acidic)	13.94	ChemAxon
pKa (Strongest Basic)	0.37	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	89.35 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	84.81 m³·mol⁻¹	ChemAxon
Polarizability	32.29 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

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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (8e)-3-hydroxy-2,2,4-trimethyl-10-(1,3-oxazol-5-yl)deca-4,6,8-trienimidic acid (NP0204462)

MOL for NP0204462 ((8e)-3-hydroxy-2,2,4-trimethyl-10-(1,3-oxazol-5-yl)deca-4,6,8-trienimidic acid)

3D MOL for NP0204462 ((8e)-3-hydroxy-2,2,4-trimethyl-10-(1,3-oxazol-5-yl)deca-4,6,8-trienimidic acid)

3D SDF for NP0204462 ((8e)-3-hydroxy-2,2,4-trimethyl-10-(1,3-oxazol-5-yl)deca-4,6,8-trienimidic acid)

3D-SDF for NP0204462 ((8e)-3-hydroxy-2,2,4-trimethyl-10-(1,3-oxazol-5-yl)deca-4,6,8-trienimidic acid)

PDB for NP0204462 ((8e)-3-hydroxy-2,2,4-trimethyl-10-(1,3-oxazol-5-yl)deca-4,6,8-trienimidic acid)

3D PDB for NP0204462 ((8e)-3-hydroxy-2,2,4-trimethyl-10-(1,3-oxazol-5-yl)deca-4,6,8-trienimidic acid)

SMILES for NP0204462 ((8e)-3-hydroxy-2,2,4-trimethyl-10-(1,3-oxazol-5-yl)deca-4,6,8-trienimidic acid)

INCHI for NP0204462 ((8e)-3-hydroxy-2,2,4-trimethyl-10-(1,3-oxazol-5-yl)deca-4,6,8-trienimidic acid)

Structure for NP0204462 ((8e)-3-hydroxy-2,2,4-trimethyl-10-(1,3-oxazol-5-yl)deca-4,6,8-trienimidic acid)

3D Structure for NP0204462 ((8e)-3-hydroxy-2,2,4-trimethyl-10-(1,3-oxazol-5-yl)deca-4,6,8-trienimidic acid)