NP-MRD: Showing NP-Card for [(1r,2z,4s)-1,6,6-trimethyl-7-oxabicyclo[2.2.1]heptan-2-ylidene]acetic acid (NP0240811)

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Record Information

Version

2.0

Created at

2022-09-07 00:43:28 UTC

Updated at

2022-09-07 00:43:28 UTC

NP-MRD ID

NP0240811

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[(1r,2z,4s)-1,6,6-trimethyl-7-oxabicyclo[2.2.1]heptan-2-ylidene]acetic acid

Description

Ficusic acid, also known as ficusate, belongs to the class of organic compounds known as tetrahydrofurans. These are heterocyclic compounds containing a saturated, aliphatic, five-membered ring where a carbon is replaced by an oxygen. [(1r,2z,4s)-1,6,6-trimethyl-7-oxabicyclo[2.2.1]heptan-2-ylidene]acetic acid is found in Euphorbia helioscopia, Ficus microcarpa and Sargassum pallidum. [(1r,2z,4s)-1,6,6-trimethyl-7-oxabicyclo[2.2.1]heptan-2-ylidene]acetic acid was first documented in 2014 (PMID: 24946546). Based on a literature review very few articles have been published on Ficusic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 30 31  0  0  0  0  0  0  0  0999 V2000
   -0.7265   -0.5169    1.8179 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0889    0.2024    0.5792 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5379    0.1090    0.2588 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7181    1.6984    0.6512 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3723    1.9816   -0.7811 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1363    1.7386   -0.9684 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1139    0.2665   -0.5259 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2412   -0.2860   -0.1531 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3181   -1.6384    0.2770 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3879   -2.4225    0.3681 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5998   -2.1150    0.6353 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2469   -0.1553   -0.6428 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5949   -1.4506   -1.2736 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8134    0.8732   -1.4972 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9056   -1.6033    1.6432 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3221   -0.3853    2.1371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3836   -0.1699    2.6412 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7920    0.8812   -0.5220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8854   -0.8866   -0.0209 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1081    0.4461    1.1660 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1595    1.7432    1.3321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5628    2.3030    0.9959 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6946    2.9354   -1.1637 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3899    1.7838   -2.0368 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7314    2.3456   -0.2957 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1806    0.3448   -0.1781 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0555   -2.8291    0.0647 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0175   -2.1608   -0.5613 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4148   -1.2257   -2.0568 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2270   -1.8073   -1.8903 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 11  1  0
  9 10  2  0
  7 12  1  0
 12 13  1  6
 12 14  1  0
 12  2  1  0
 14  5  1  0
  1 15  1  0
  1 16  1  0
  1 17  1  0
  3 18  1  0
  3 19  1  0
  3 20  1  0
  4 21  1  0
  4 22  1  0
  5 23  1  6
  6 24  1  0
  6 25  1  0
  8 26  1  0
 11 27  1  0
 13 28  1  0
 13 29  1  0
 13 30  1  0
M  END


  Mrv1652309072202432D          

 14 15  0  0  1  0            999 V2000
   -0.6489    0.3985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1635    0.5418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1186    1.3170    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1635   -0.2832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8780   -0.6957    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5925   -0.2832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5925    0.5418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3069    0.9543    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3069    1.7793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5925    2.1918    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0214    2.1918    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8780    0.9543    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8780    1.7793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6717    0.1293    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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
  7 12  1  0  0  0  0
  2 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
  5 14  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0240811

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)C[C@H]2C\C(=C\C(O)=O)[C@]1(C)O2

> <INCHI_IDENTIFIER>
InChI=1S/C11H16O3/c1-10(2)6-8-4-7(5-9(12)13)11(10,3)14-8/h5,8H,4,6H2,1-3H3,(H,12,13)/b7-5-/t8-,11+/m1/s1

> <INCHI_KEY>
WDJWXGLOUVSXDG-MPQUNQFKSA-N

> <FORMULA>
C11H16O3

> <MOLECULAR_WEIGHT>
196.246

> <EXACT_MASS>
196.109944375

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
30

> <JCHEM_AVERAGE_POLARIZABILITY>
20.746549053395547

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-[(1R,2Z,4S)-1,6,6-trimethyl-7-oxabicyclo[2.2.1]heptan-2-ylidene]acetic acid

> <JCHEM_LOGP>
1.6006479743333335

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.7440028226087

> <JCHEM_PKA_STRONGEST_BASIC>
-4.22178595655948

> <JCHEM_POLAR_SURFACE_AREA>
46.53

> <JCHEM_REFRACTIVITY>
52.4305

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
[(1R,2Z,4S)-1,6,6-trimethyl-7-oxabicyclo[2.2.1]heptan-2-ylidene]acetic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.211   0.744   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.305   1.011   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.221   2.458   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.305  -0.529   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.639  -1.299   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.973  -0.529   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.973   1.011   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.306   1.781   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.306   3.321   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       2.973   4.091   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0       5.640   4.091   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       1.639   1.781   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.639   3.321   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       1.254   0.241   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4   12                                             
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   14                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   12                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    7    2   13   14                                             
CONECT   13   12                                                            
CONECT   14   12    5                                                       
MASTER        0    0    0    0    0    0    0    0   14    0   30    0
END

View in JSmol

Synonyms

Value	Source
Ficusate	Generator

Chemical Formula

C₁₁H₁₆O₃

Average Mass

196.2460 Da

Monoisotopic Mass

196.10994 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC1(C)C[C@H]2C\C(=C\C(O)=O)[C@]1(C)O2

InChI Identifier

InChI=1S/C11H16O3/c1-10(2)6-8-4-7(5-9(12)13)11(10,3)14-8/h5,8H,4,6H2,1-3H3,(H,12,13)/b7-5-/t8-,11+/m1/s1

InChI Key

WDJWXGLOUVSXDG-MPQUNQFKSA-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
Euphorbia helioscopia	LOTUS Database	35616633
Ficus microcarpa	LOTUS Database	35616633
Sargassum pallidum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tetrahydrofurans. These are heterocyclic compounds containing a saturated, aliphatic, five-membered ring where a carbon is replaced by an oxygen.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Tetrahydrofurans

Sub Class

Not Available

Direct Parent

Tetrahydrofurans

Alternative Parents

Substituents

Tetrahydrofuran
Oxacycle
Monocarboxylic acid or derivatives
Ether
Dialkyl ether
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic 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

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00039214

Chemspider ID

75143327

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

100955862

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Li SH, Deng Q, Zhu L, Lai CH, Wang HS, Tan QG: [Terpenoids and sterols from Ricinus communis and their activities against diabetes]. Zhongguo Zhong Yao Za Zhi. 2014 Feb;39(3):448-52. [PubMed:24946546 ]
LOTUS database [Link]

Showing NP-Card for [(1r,2z,4s)-1,6,6-trimethyl-7-oxabicyclo[2.2.1]heptan-2-ylidene]acetic acid (NP0240811)

MOL for NP0240811 ([(1r,2z,4s)-1,6,6-trimethyl-7-oxabicyclo[2.2.1]heptan-2-ylidene]acetic acid)

3D MOL for NP0240811 ([(1r,2z,4s)-1,6,6-trimethyl-7-oxabicyclo[2.2.1]heptan-2-ylidene]acetic acid)

3D SDF for NP0240811 ([(1r,2z,4s)-1,6,6-trimethyl-7-oxabicyclo[2.2.1]heptan-2-ylidene]acetic acid)

3D-SDF for NP0240811 ([(1r,2z,4s)-1,6,6-trimethyl-7-oxabicyclo[2.2.1]heptan-2-ylidene]acetic acid)

PDB for NP0240811 ([(1r,2z,4s)-1,6,6-trimethyl-7-oxabicyclo[2.2.1]heptan-2-ylidene]acetic acid)

3D PDB for NP0240811 ([(1r,2z,4s)-1,6,6-trimethyl-7-oxabicyclo[2.2.1]heptan-2-ylidene]acetic acid)

SMILES for NP0240811 ([(1r,2z,4s)-1,6,6-trimethyl-7-oxabicyclo[2.2.1]heptan-2-ylidene]acetic acid)

INCHI for NP0240811 ([(1r,2z,4s)-1,6,6-trimethyl-7-oxabicyclo[2.2.1]heptan-2-ylidene]acetic acid)

Structure for NP0240811 ([(1r,2z,4s)-1,6,6-trimethyl-7-oxabicyclo[2.2.1]heptan-2-ylidene]acetic acid)

3D Structure for NP0240811 ([(1r,2z,4s)-1,6,6-trimethyl-7-oxabicyclo[2.2.1]heptan-2-ylidene]acetic acid)