NP-MRD: Showing NP-Card for methyl 2-[3,3-dimethyl-2-(2,4,5-trihydroxy-3-methylidenepentyl)cyclobutyl]prop-2-enoate (NP0308775)

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Record Information

Version

2.0

Created at

2022-09-11 02:49:14 UTC

Updated at

2022-09-11 02:49:15 UTC

NP-MRD ID

NP0308775

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 2-[3,3-dimethyl-2-(2,4,5-trihydroxy-3-methylidenepentyl)cyclobutyl]prop-2-enoate

Description

Methyl 2-[3,3-dimethyl-2-(2,4,5-trihydroxy-3-methylidenepentyl)cyclobutyl]prop-2-enoate belongs to the class of organic compounds known as fatty alcohols. These are aliphatic alcohols consisting of a chain of a least six carbon atoms. methyl 2-[3,3-dimethyl-2-(2,4,5-trihydroxy-3-methylidenepentyl)cyclobutyl]prop-2-enoate is found in Hebeloma longicaudum. Methyl 2-[3,3-dimethyl-2-(2,4,5-trihydroxy-3-methylidenepentyl)cyclobutyl]prop-2-enoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 47 47  0  0  0  0  0  0  0  0999 V2000
   -1.6913   -3.1579    0.2855 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2510   -2.2725    1.1709 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2921   -1.2367    0.6976 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0691   -1.4307   -0.6570 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7332    0.1696    0.8977 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3183    1.1357    0.4255 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7350    1.0988   -0.9967 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0146    0.5056   -1.3621 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8222   -0.0031   -0.4639 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3991    0.4829   -2.7624 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6543    0.9618   -3.6730 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6210   -0.0795   -3.1291 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0117   -0.1086   -4.5013 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9294    2.6251   -0.8779 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1737    2.5439    0.1764 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0441    3.5086    1.2994 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5089    2.6788   -0.4677 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7032   -2.3628    2.5644 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3365   -1.1599    2.9178 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7035   -3.4614    2.7927 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8837   -3.3080    2.0716 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3523   -3.1185   -0.7641 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3816   -3.9526    0.5315 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6479   -1.3780    1.2690 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9015   -1.1991   -1.1593 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7055    0.4010    0.4170 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8936    0.3595    2.0014 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1657    1.1824    1.1378 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0901    0.9539   -1.7307 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7799   -0.4395   -0.7871 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6590   -0.0508    0.5945 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0756   -0.0923   -5.1074 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5863   -1.0082   -4.7578 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6387    0.7782   -4.6919 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6566    3.1661   -1.7881 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8934    2.8852   -0.4274 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2317    2.9703    2.2454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5134    4.4322    1.1600 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1339    3.6938    1.3798 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3185    2.9460    0.2706 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8200    1.8179   -1.0812 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4572    3.5520   -1.1736 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8452   -2.5581    3.2661 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0451   -0.8811    3.8089 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9334   -3.5644    3.8857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2670   -4.4511    2.4842 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6845   -3.5745    2.6082 H   0  0  0  0  0  0  0  0  0  0  0  0
 13 12  1  0
 12 10  1  0
 10 11  2  0
 10  8  1  0
  8  9  2  3
  8  7  1  0
  7 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 15  6  1  0
  6  5  1  0
  5  3  1  0
  3  4  1  0
  3  2  1  0
  2  1  2  3
  2 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
  6  7  1  0
 13 32  1  0
 13 33  1  0
 13 34  1  0
  9 30  1  0
  9 31  1  0
  7 29  1  6
 14 35  1  0
 14 36  1  0
 16 37  1  0
 16 38  1  0
 16 39  1  0
 17 40  1  0
 17 41  1  0
 17 42  1  0
  6 28  1  1
  5 26  1  0
  5 27  1  0
  3 24  1  1
  4 25  1  0
  1 22  1  0
  1 23  1  0
 18 43  1  1
 19 44  1  0
 20 45  1  0
 20 46  1  0
 21 47  1  0
M  END


  Mrv1533004201501012D          

 21 21  0  0  0  0            999 V2000
   -2.5780    0.1784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7530    0.1784    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3405    0.8929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7530    1.6073    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5155    0.8929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1030    0.1784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1030    1.6073    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3165    2.4042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4804    2.6178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2668    3.4146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2773    2.8313    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6939    1.8209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4084    1.4084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1228    1.8209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1228    2.6459    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8373    1.4084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8373    0.5834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5518    1.8209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5518    2.6459    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2662    1.4084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9807    1.8209    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
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  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
  9 11  1  0  0  0  0
  9 12  1  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0308775

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C(=C)C1CC(C)(C)C1CC(O)C(=C)C(O)CO

> <INCHI_IDENTIFIER>
InChI=1S/C16H26O5/c1-9(15(20)21-5)11-7-16(3,4)12(11)6-13(18)10(2)14(19)8-17/h11-14,17-19H,1-2,6-8H2,3-5H3

> <INCHI_KEY>
AEOAKDQHDIICMZ-UHFFFAOYSA-N

> <FORMULA>
C16H26O5

> <MOLECULAR_WEIGHT>
298.379

> <EXACT_MASS>
298.178023937

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
32.638237710754645

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl 2-[3,3-dimethyl-2-(2,4,5-trihydroxy-3-methylidenepentyl)cyclobutyl]prop-2-enoate

> <ALOGPS_LOGP>
0.89

> <JCHEM_LOGP>
1.0254031223333326

> <ALOGPS_LOGS>
-2.20

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.641683470192625

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.668932174649601

> <JCHEM_PKA_STRONGEST_BASIC>
-2.959673206980213

> <JCHEM_POLAR_SURFACE_AREA>
86.99000000000001

> <JCHEM_REFRACTIVITY>
79.3201

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.87e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl 2-[3,3-dimethyl-2-(2,4,5-trihydroxy-3-methylidenepentyl)cyclobutyl]prop-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 20-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-APR-15         0                                  
HETATM    1  C   UNK     0      -4.812   0.333   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -3.272   0.333   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -2.502   1.667   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -3.272   3.000   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -0.962   1.667   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.192   0.333   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.192   3.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.591   4.488   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.897   4.886   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.498   6.374   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.384   5.285   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.295   3.399   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.629   2.629   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.963   3.399   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       3.963   4.939   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       5.296   2.629   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.296   1.089   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.630   3.399   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       6.630   4.939   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       7.964   2.629   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       9.297   3.399   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   12                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11   12                                             
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    9    7   13                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   42    0
END

View in JSmol

Synonyms

Value	Source
Methyl 2-[3,3-dimethyl-2-(2,4,5-trihydroxy-3-methylidenepentyl)cyclobutyl]prop-2-enoic acid	Generator

Chemical Formula

C₁₆H₂₆O₅

Average Mass

298.3790 Da

Monoisotopic Mass

298.17802 Da

IUPAC Name

methyl 2-[3,3-dimethyl-2-(2,4,5-trihydroxy-3-methylidenepentyl)cyclobutyl]prop-2-enoate

Traditional Name

methyl 2-[3,3-dimethyl-2-(2,4,5-trihydroxy-3-methylidenepentyl)cyclobutyl]prop-2-enoate

CAS Registry Number

Not Available

SMILES

COC(=O)C(=C)C1CC(C)(C)C1CC(O)C(=C)C(O)CO

InChI Identifier

InChI=1S/C16H26O5/c1-9(15(20)21-5)11-7-16(3,4)12(11)6-13(18)10(2)14(19)8-17/h11-14,17-19H,1-2,6-8H2,3-5H3

InChI Key

AEOAKDQHDIICMZ-UHFFFAOYSA-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
Hebeloma longicaudum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as fatty alcohols. These are aliphatic alcohols consisting of a chain of a least six carbon atoms.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty alcohols

Direct Parent

Fatty alcohols

Alternative Parents

Substituents

Fatty alcohol
Methyl ester
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Carboxylic acid ester
Secondary alcohol
Polyol
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Primary alcohol
Organooxygen compound
Organic oxygen compound
Alcohol
Carbonyl group
Organic oxide
Hydrocarbon derivative
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	0.89	ALOGPS
logP	1.03	ChemAxon
logS	-2.2	ALOGPS
pKa (Strongest Acidic)	13.67	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	86.99 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	79.32 m³·mol⁻¹	ChemAxon
Polarizability	32.64 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

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KEGG Compound ID

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BioCyc ID

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BiGG ID

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Wikipedia Link

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METLIN ID

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PubChem Compound

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PDB ID

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ChEBI ID

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Good Scents ID

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References

General References

LOTUS database [Link]

Showing NP-Card for methyl 2-[3,3-dimethyl-2-(2,4,5-trihydroxy-3-methylidenepentyl)cyclobutyl]prop-2-enoate (NP0308775)

MOL for NP0308775 (methyl 2-[3,3-dimethyl-2-(2,4,5-trihydroxy-3-methylidenepentyl)cyclobutyl]prop-2-enoate)

3D MOL for NP0308775 (methyl 2-[3,3-dimethyl-2-(2,4,5-trihydroxy-3-methylidenepentyl)cyclobutyl]prop-2-enoate)

3D SDF for NP0308775 (methyl 2-[3,3-dimethyl-2-(2,4,5-trihydroxy-3-methylidenepentyl)cyclobutyl]prop-2-enoate)

3D-SDF for NP0308775 (methyl 2-[3,3-dimethyl-2-(2,4,5-trihydroxy-3-methylidenepentyl)cyclobutyl]prop-2-enoate)

PDB for NP0308775 (methyl 2-[3,3-dimethyl-2-(2,4,5-trihydroxy-3-methylidenepentyl)cyclobutyl]prop-2-enoate)

3D PDB for NP0308775 (methyl 2-[3,3-dimethyl-2-(2,4,5-trihydroxy-3-methylidenepentyl)cyclobutyl]prop-2-enoate)

SMILES for NP0308775 (methyl 2-[3,3-dimethyl-2-(2,4,5-trihydroxy-3-methylidenepentyl)cyclobutyl]prop-2-enoate)

INCHI for NP0308775 (methyl 2-[3,3-dimethyl-2-(2,4,5-trihydroxy-3-methylidenepentyl)cyclobutyl]prop-2-enoate)

Structure for NP0308775 (methyl 2-[3,3-dimethyl-2-(2,4,5-trihydroxy-3-methylidenepentyl)cyclobutyl]prop-2-enoate)

3D Structure for NP0308775 (methyl 2-[3,3-dimethyl-2-(2,4,5-trihydroxy-3-methylidenepentyl)cyclobutyl]prop-2-enoate)