NP-MRD: Showing NP-Card for (3s,4z,6z,8e)-3-hydroxy-2,2,4-trimethyl-10-(1,3-oxazol-5-yl)deca-4,6,8-trienimidic acid (NP0237774)

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Record Information

Version

2.0

Created at

2022-09-06 21:00:53 UTC

Updated at

2022-09-06 21:00:53 UTC

NP-MRD ID

NP0237774

Secondary Accession Numbers

None

Natural Product Identification

Common Name

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

Description

(3S,4Z,6Z,8E)-2,2,4-Trimethyl-3-hydroxy-10-(5-oxazolyl)-4,6,8-decatrieneamide belongs to the class of organic compounds known as fatty amides. These are carboxylic acid amide derivatives of fatty acids, that are formed from a fatty acid and an amine. Based on a literature review very few articles have been published on (3S,4Z,6Z,8E)-2,2,4-Trimethyl-3-hydroxy-10-(5-oxazolyl)-4,6,8-decatrieneamide.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 43 43  0  0  0  0  0  0  0  0999 V2000
   -3.4027    2.6231    0.4860 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0471    2.0472    1.2551 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0779    0.7851    1.1999 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5640    0.0802    2.3083 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6247    0.0445    0.0320 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3987    0.9916   -0.7848 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6558   -0.9217    0.6579 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5828   -0.7767   -0.5803 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2470   -1.5445   -1.6091 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4527   -0.2177   -1.2369 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4619    0.6334   -2.4688 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2468   -0.4391   -0.7421 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0910   -1.2109    0.4261 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3445   -1.3539    0.8081 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4822   -0.7790    0.1315 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7199   -0.9899    0.6101 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8955   -0.4146   -0.0619 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6279    0.4902    0.8680 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6464    0.1204    1.7217 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9950    1.2643    2.3569 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.2175    2.2628    1.8986 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3991    1.7744    1.0006 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9896    0.2937    3.2045 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0410    1.5995   -0.1066 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7750    1.7695   -1.3068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1207    0.5241   -1.4892 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1386   -1.7557    1.1755 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3418   -0.4002    1.3251 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2231   -1.3726   -0.1823 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2918   -1.5748    0.1053 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6170   -2.2298   -1.9161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2724    1.6936   -2.1902 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4463    0.6448   -2.9594 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6336    0.3697   -3.1589 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6256    0.0151   -1.2749 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6757   -1.6825    1.0146 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5235   -1.9558    1.7073 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4612   -0.1706   -0.7553 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8131   -1.5988    1.5074 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5978    0.1596   -0.9392 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5770   -1.2298   -0.4153 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0663   -0.8556    1.8512 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2450    3.2874    2.2010 H   0  0  0  0  0  0  0  0  0  0  0  0
 11 10  1  0
 10 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 10  8  1  0
  8  9  1  0
  8  5  1  0
  5  6  1  0
  5  7  1  0
  5  3  1  0
  3  4  1  0
  3  2  2  0
 22 18  1  0
 11 32  1  0
 11 33  1  0
 11 34  1  0
 12 35  1  0
 13 36  1  0
 14 37  1  0
 15 38  1  0
 16 39  1  0
 17 40  1  0
 17 41  1  0
 19 42  1  0
 21 43  1  0
  8 30  1  1
  9 31  1  0
  6 24  1  0
  6 25  1  0
  6 26  1  0
  7 27  1  0
  7 28  1  0
  7 29  1  0
  4 23  1  0
  2  1  1  0
M  END


  Mrv1652309062223002D          

 21 21  0  0  1  0            999 V2000
    0.5678    6.0643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1467    5.6518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1467    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 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9803   -0.1553    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.1553   -0.1553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0997    0.6294    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8612    6.0643    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5757    5.6518    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8612    6.8893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0362    6.8893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6862    6.8893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8612    7.7143    0.0000 C   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
   -0.1467    8.1268    0.0000 O   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  0  0  0  0
  4  5  2  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
  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
  9 13  1  0  0  0  0
  2 14  1  0  0  0  0
 14 15  1  6  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>
NP0237774

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C(=C\C=C/C=C/CC1=CN=CO1)[C@H](O)C(C)(C)C(O)=N

> <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-/t14-/m0/s1

> <INCHI_KEY>
MRTUFVRJHFZVOT-FINZEZQYSA-N

> <FORMULA>
C16H22N2O3

> <MOLECULAR_WEIGHT>
290.363

> <EXACT_MASS>
290.163042576

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
43

> <JCHEM_AVERAGE_POLARIZABILITY>
32.450172182991885

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

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

> <JCHEM_LOGP>
-0.5770404462816524

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.235725106675172

> <JCHEM_PKA_STRONGEST_ACIDIC>
-0.900393778581627

> <JCHEM_PKA_STRONGEST_BASIC>
13.218916324431788

> <JCHEM_POLAR_SURFACE_AREA>
90.34000000000002

> <JCHEM_REFRACTIVITY>
95.74210000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(3S,4Z,6Z,8E)-3-hydroxy-2,2,4-trimethyl-10-(1,3-oxazol-5-yl)deca-4,6,8-trienimidic 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       1.060  11.320   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.274  10.550   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.274   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  C   UNK     0       2.306   1.175   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0       1.830  -0.290   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0       0.290  -0.290   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -0.186   1.175   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -1.608  11.320   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -2.941  10.550   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -1.608  12.860   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.068  12.860   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -3.148  12.860   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.608  14.400   0.000  0.00  0.00           C+0
HETATM   20  N   UNK     0      -2.941  15.170   0.000  0.00  0.00           N+0
HETATM   21  O   UNK     0      -0.274  15.170   0.000  0.00  0.00           O+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

Not Available

Chemical Formula

C₁₆H₂₂N₂O₃

Average Mass

290.3630 Da

Monoisotopic Mass

290.16304 Da

IUPAC Name

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

Traditional Name

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

CAS Registry Number

Not Available

SMILES

C\C(=C\C=C/C=C/CC1=CN=CO1)[C@H](O)C(C)(C)C(O)=N

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-/t14-/m0/s1

InChI Key

MRTUFVRJHFZVOT-FINZEZQYSA-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 fatty amides. These are carboxylic acid amide derivatives of fatty acids, that are formed from a fatty acid and an amine.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty amides

Direct Parent

Fatty amides

Alternative Parents

Substituents

Fatty amide
Azole
Oxazole
Heteroaromatic compound
Carboxamide group
Primary carboxylic acid amide
Secondary alcohol
Organoheterocyclic compound
Carboxylic acid derivative
Azacycle
Oxacycle
Organic nitrogen compound
Organic oxide
Organooxygen compound
Organonitrogen compound
Organic oxygen compound
Alcohol
Carbonyl group
Hydrocarbon derivative
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	-0.58	ChemAxon
pKa (Strongest Acidic)	-0.9	ChemAxon
pKa (Strongest Basic)	13.22	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	90.34 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	95.74 m³·mol⁻¹	ChemAxon
Polarizability	32.45 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	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

101851476

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3s,4z,6z,8e)-3-hydroxy-2,2,4-trimethyl-10-(1,3-oxazol-5-yl)deca-4,6,8-trienimidic acid (NP0237774)

MOL for NP0237774 ((3s,4z,6z,8e)-3-hydroxy-2,2,4-trimethyl-10-(1,3-oxazol-5-yl)deca-4,6,8-trienimidic acid)

3D MOL for NP0237774 ((3s,4z,6z,8e)-3-hydroxy-2,2,4-trimethyl-10-(1,3-oxazol-5-yl)deca-4,6,8-trienimidic acid)

3D SDF for NP0237774 ((3s,4z,6z,8e)-3-hydroxy-2,2,4-trimethyl-10-(1,3-oxazol-5-yl)deca-4,6,8-trienimidic acid)

3D-SDF for NP0237774 ((3s,4z,6z,8e)-3-hydroxy-2,2,4-trimethyl-10-(1,3-oxazol-5-yl)deca-4,6,8-trienimidic acid)

PDB for NP0237774 ((3s,4z,6z,8e)-3-hydroxy-2,2,4-trimethyl-10-(1,3-oxazol-5-yl)deca-4,6,8-trienimidic acid)

3D PDB for NP0237774 ((3s,4z,6z,8e)-3-hydroxy-2,2,4-trimethyl-10-(1,3-oxazol-5-yl)deca-4,6,8-trienimidic acid)

SMILES for NP0237774 ((3s,4z,6z,8e)-3-hydroxy-2,2,4-trimethyl-10-(1,3-oxazol-5-yl)deca-4,6,8-trienimidic acid)

INCHI for NP0237774 ((3s,4z,6z,8e)-3-hydroxy-2,2,4-trimethyl-10-(1,3-oxazol-5-yl)deca-4,6,8-trienimidic acid)

Structure for NP0237774 ((3s,4z,6z,8e)-3-hydroxy-2,2,4-trimethyl-10-(1,3-oxazol-5-yl)deca-4,6,8-trienimidic acid)

3D Structure for NP0237774 ((3s,4z,6z,8e)-3-hydroxy-2,2,4-trimethyl-10-(1,3-oxazol-5-yl)deca-4,6,8-trienimidic acid)