NP-MRD: Showing NP-Card for (2e,4e)-5-[1,4-dihydroxy-6-(hydroxymethyl)-2,6-dimethylcyclohex-2-en-1-yl]-3-methylpenta-2,4-dienoic acid (NP0214920)

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Record Information

Version

2.0

Created at

2022-09-05 14:21:13 UTC

Updated at

2022-09-05 14:21:13 UTC

NP-MRD ID

NP0214920

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2e,4e)-5-[1,4-dihydroxy-6-(hydroxymethyl)-2,6-dimethylcyclohex-2-en-1-yl]-3-methylpenta-2,4-dienoic acid

Description

Pisumic acid, also known as pisumate, belongs to the class of organic compounds known as abscisic acids and derivatives. These are terpene compounds containing the abscisic acid moiety, which is characterized by a 3-methylpenta-2,4-dienoic acid attached to the C1 carbon of a 4-oxocyclohex-2-ene moiety. Pisumic acid is an extremely weak basic (essentially neutral) compound (based on its pKa). Outside of the human body, Pisumic acid has been detected, but not quantified in, common pea. (2e,4e)-5-[1,4-dihydroxy-6-(hydroxymethyl)-2,6-dimethylcyclohex-2-en-1-yl]-3-methylpenta-2,4-dienoic acid is found in Pisum sativum. This could make pisumic acid a potential biomarker for the consumption of these foods.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 42 42  0  0  0  0  0  0  0  0999 V2000
   -1.3119    3.0304   -0.0069 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7320    1.5973   -0.0297 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9909    1.2514   -0.2199 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4821   -0.1490   -0.2793 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.1322   -0.4295    0.9143 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3638   -1.1043   -0.4968 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0589   -0.4869   -0.9684 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1183   -1.6926   -1.0698 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2664    0.1275   -2.2964 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5592   -0.8158   -3.2925 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7486    0.4594    0.1354 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1832   -0.1311    1.3500 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5535    0.9562    0.2840 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7513    0.6877    0.5535 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6712   -0.2851    0.9157 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3052   -1.6978    1.2698 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9540    0.0548    1.0316 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0073   -0.8015    1.4549 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9177   -1.9837    1.7643 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3095   -0.2493    1.5318 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6414    3.2135   -0.8435 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8466    3.2849    0.9377 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2301    3.6512   -0.2176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7020    2.0909   -0.3323 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2454   -0.2473   -1.0994 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5955    0.3744    1.1839 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1124   -1.5348    0.5348 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6038   -2.0183   -1.0720 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8843   -1.4094   -1.3896 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1836   -2.3307   -0.1743 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5128   -2.3773   -1.8810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0346    0.8893   -2.3069 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3399    0.6280   -2.7065 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3756   -1.3426   -3.1092 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4846   -0.1163    2.0369 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5206    2.0992    0.1379 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2787    1.7290    0.3386 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2014   -1.7286    1.4581 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8042   -1.8643    2.2539 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6620   -2.3785    0.5059 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2253    1.0800    0.7723 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8097   -0.0306    0.6570 H   0  0  0  0  0  0  0  0  0  0  0  0
 16 15  1  0
 15 14  1  0
 14 13  2  0
 13 11  1  0
 11 12  1  1
 11  2  1  0
  2  1  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  4  6  1  0
  6  7  1  0
  7  8  1  6
  7  9  1  0
  9 10  1  0
 15 17  2  0
 17 18  1  0
 18 20  1  0
 18 19  2  0
  7 11  1  0
 16 38  1  0
 16 39  1  0
 16 40  1  0
 14 37  1  0
 13 36  1  0
 12 35  1  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
  3 24  1  0
  4 25  1  6
  5 26  1  0
  6 27  1  0
  6 28  1  0
  8 29  1  0
  8 30  1  0
  8 31  1  0
  9 32  1  0
  9 33  1  0
 10 34  1  0
 17 41  1  0
 20 42  1  0
M  END


  Mrv0541 02241211302D          

 20 20  0  0  0  0            999 V2000
   -2.4987   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4987   -1.1278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7844   -1.5407    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0713   -1.1278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0713   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7844    0.1095    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1972    0.8251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3715    0.8251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2143   -1.5407    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3556   -1.5407    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3556    0.1095    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3571   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0713    0.1095    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7857   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5000    0.1095    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3556   -0.7150    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0713    0.9352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5000    0.9352    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2143   -0.3020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7844    1.5407    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  6  1  0  0  0  0
  2  3  1  0  0  0  0
  2  9  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  4 10  1  0  0  0  0
  5  6  1  0  0  0  0
  5 11  1  0  0  0  0
  5 16  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8 20  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 17  1  0  0  0  0
 14 15  1  0  0  0  0
 15 18  2  0  0  0  0
 15 19  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0214920

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C(\C=C\C1(O)C(C)=CC(O)CC1(C)CO)=C/C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C15H22O5/c1-10(6-13(18)19)4-5-15(20)11(2)7-12(17)8-14(15,3)9-16/h4-7,12,16-17,20H,8-9H2,1-3H3,(H,18,19)/b5-4+,10-6+

> <INCHI_KEY>
GBHKILLDPRFXNU-UMCKCUICSA-N

> <FORMULA>
C15H22O5

> <MOLECULAR_WEIGHT>
282.3322

> <EXACT_MASS>
282.146723814

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_AVERAGE_POLARIZABILITY>
29.885814509011205

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2E,4E)-5-[1,4-dihydroxy-6-(hydroxymethyl)-2,6-dimethylcyclohex-2-en-1-yl]-3-methylpenta-2,4-dienoic acid

> <ALOGPS_LOGP>
0.51

> <JCHEM_LOGP>
0.40116584866666677

> <ALOGPS_LOGS>
-2.51

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
13.348286214337058

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.6435938008452675

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7967183492242045

> <JCHEM_POLAR_SURFACE_AREA>
97.99000000000001

> <JCHEM_REFRACTIVITY>
77.6485

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.82e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2E,4E)-5-[1,4-dihydroxy-6-(hydroxymethyl)-2,6-dimethylcyclohex-2-en-1-yl]-3-methylpenta-2,4-dienoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0      -4.664  -0.564   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.664  -2.105   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.331  -2.876   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.000  -2.105   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.000  -0.564   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -3.331   0.204   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -4.101   1.540   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.560   1.540   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -6.000  -2.876   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -0.664  -2.876   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.664   0.204   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.667  -0.564   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.000   0.204   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.333  -0.564   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.667   0.204   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -0.664  -1.335   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       2.000   1.746   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       4.667   1.746   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       6.000  -0.564   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      -3.331   2.876   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3    9                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   10                                                  
CONECT    5    4    6   11   16                                             
CONECT    6    1    5    7    8                                             
CONECT    7    6                                                            
CONECT    8    6   20                                                       
CONECT    9    2                                                            
CONECT   10    4                                                            
CONECT   11    5   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   17                                                  
CONECT   14   13   15                                                       
CONECT   15   14   18   19                                                  
CONECT   16    5                                                            
CONECT   17   13                                                            
CONECT   18   15                                                            
CONECT   19   15                                                            
CONECT   20    8                                                            
MASTER        0    0    0    0    0    0    0    0   20    0   40    0
END

View in JSmol

Synonyms

Value	Source
Pisumate	Generator
(2E,4E)-5-[1,4-Dihydroxy-6-(hydroxymethyl)-2,6-dimethylcyclohex-2-en-1-yl]-3-methylpenta-2,4-dienoate	Generator

Chemical Formula

C₁₅H₂₂O₅

Average Mass

282.3322 Da

Monoisotopic Mass

282.14672 Da

IUPAC Name

(2E,4E)-5-[1,4-dihydroxy-6-(hydroxymethyl)-2,6-dimethylcyclohex-2-en-1-yl]-3-methylpenta-2,4-dienoic acid

Traditional Name

(2E,4E)-5-[1,4-dihydroxy-6-(hydroxymethyl)-2,6-dimethylcyclohex-2-en-1-yl]-3-methylpenta-2,4-dienoic acid

CAS Registry Number

Not Available

SMILES

C\C(\C=C\C1(O)C(C)=CC(O)CC1(C)CO)=C/C(O)=O

InChI Identifier

InChI=1S/C15H22O5/c1-10(6-13(18)19)4-5-15(20)11(2)7-12(17)8-14(15,3)9-16/h4-7,12,16-17,20H,8-9H2,1-3H3,(H,18,19)/b5-4+,10-6+

InChI Key

GBHKILLDPRFXNU-UMCKCUICSA-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
Pisum sativum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as abscisic acids and derivatives. These are terpene compounds containing the abscisic acid moiety, which is characterized by a 3-methylpenta-2,4-dienoic acid attached to the C1 carbon of a 4-oxocyclohex-2-ene moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Abscisic acids and derivatives

Alternative Parents

Substituents

Abscisic acid
Medium-chain fatty acid
Branched fatty acid
Hydroxy fatty acid
Methyl-branched fatty acid
Fatty acyl
Fatty acid
Unsaturated fatty acid
Tertiary alcohol
Secondary alcohol
Carboxylic acid derivative
Carboxylic acid
Monocarboxylic acid or derivatives
Hydrocarbon derivative
Alcohol
Organic oxygen compound
Carbonyl group
Organic oxide
Organooxygen compound
Primary alcohol
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic 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	0.51	ALOGPS
logP	0.4	ChemAxon
logS	-2.5	ALOGPS
pKa (Strongest Acidic)	4.64	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	97.99 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	77.65 m³·mol⁻¹	ChemAxon
Polarizability	29.89 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

HMDB0039241

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB018778

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

131752585

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

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References

General References

LOTUS database [Link]

Showing NP-Card for (2e,4e)-5-[1,4-dihydroxy-6-(hydroxymethyl)-2,6-dimethylcyclohex-2-en-1-yl]-3-methylpenta-2,4-dienoic acid (NP0214920)

MOL for NP0214920 ((2e,4e)-5-[1,4-dihydroxy-6-(hydroxymethyl)-2,6-dimethylcyclohex-2-en-1-yl]-3-methylpenta-2,4-dienoic acid)

3D MOL for NP0214920 ((2e,4e)-5-[1,4-dihydroxy-6-(hydroxymethyl)-2,6-dimethylcyclohex-2-en-1-yl]-3-methylpenta-2,4-dienoic acid)

3D SDF for NP0214920 ((2e,4e)-5-[1,4-dihydroxy-6-(hydroxymethyl)-2,6-dimethylcyclohex-2-en-1-yl]-3-methylpenta-2,4-dienoic acid)

3D-SDF for NP0214920 ((2e,4e)-5-[1,4-dihydroxy-6-(hydroxymethyl)-2,6-dimethylcyclohex-2-en-1-yl]-3-methylpenta-2,4-dienoic acid)

PDB for NP0214920 ((2e,4e)-5-[1,4-dihydroxy-6-(hydroxymethyl)-2,6-dimethylcyclohex-2-en-1-yl]-3-methylpenta-2,4-dienoic acid)

3D PDB for NP0214920 ((2e,4e)-5-[1,4-dihydroxy-6-(hydroxymethyl)-2,6-dimethylcyclohex-2-en-1-yl]-3-methylpenta-2,4-dienoic acid)

SMILES for NP0214920 ((2e,4e)-5-[1,4-dihydroxy-6-(hydroxymethyl)-2,6-dimethylcyclohex-2-en-1-yl]-3-methylpenta-2,4-dienoic acid)

INCHI for NP0214920 ((2e,4e)-5-[1,4-dihydroxy-6-(hydroxymethyl)-2,6-dimethylcyclohex-2-en-1-yl]-3-methylpenta-2,4-dienoic acid)

Structure for NP0214920 ((2e,4e)-5-[1,4-dihydroxy-6-(hydroxymethyl)-2,6-dimethylcyclohex-2-en-1-yl]-3-methylpenta-2,4-dienoic acid)

3D Structure for NP0214920 ((2e,4e)-5-[1,4-dihydroxy-6-(hydroxymethyl)-2,6-dimethylcyclohex-2-en-1-yl]-3-methylpenta-2,4-dienoic acid)