NP-MRD: Showing NP-Card for (5z)-5-[(2e)-4-hydroxybut-2-en-1-ylidene]-3-[(1e)-3-hydroxyprop-1-en-1-yl]furan-2-one (NP0158665)

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Record Information

Version

2.0

Created at

2022-09-02 16:17:46 UTC

Updated at

2022-09-02 16:17:46 UTC

NP-MRD ID

NP0158665

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(5z)-5-[(2e)-4-hydroxybut-2-en-1-ylidene]-3-[(1e)-3-hydroxyprop-1-en-1-yl]furan-2-one

Description

Lissoclinolide belongs to the class of organic compounds known as butenolides. These are dihydrofurans with a carbonyl group at the C2 carbon atom. (5z)-5-[(2e)-4-hydroxybut-2-en-1-ylidene]-3-[(1e)-3-hydroxyprop-1-en-1-yl]furan-2-one is found in Diplosoma virens. (5z)-5-[(2e)-4-hydroxybut-2-en-1-ylidene]-3-[(1e)-3-hydroxyprop-1-en-1-yl]furan-2-one was first documented in 2004 (PMID: 14962505). Based on a literature review very few articles have been published on Lissoclinolide.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022218172D          

 15 15  0  0  0  0            999 V2000
    0.5678    1.9393    0.0000 O   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
    1.4652   -0.8227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2857   -0.7365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7706   -1.4039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5911   -1.3177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0760   -1.9851    0.0000 O   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 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8843    0.8843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0558    1.6913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8405    1.9462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4535    1.3942    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  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
  4 10  1  0  0  0  0
 10 11  2  0  0  0  0
  2 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0158665

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C11H12O4/c12-6-2-1-5-10-8-9(4-3-7-13)11(14)15-10/h1-5,8,12-13H,6-7H2/b2-1+,4-3+,10-5-

> <INCHI_KEY>
ZYNGLDJNLYFSIV-CZFMBXACSA-N

> <FORMULA>
C11H12O4

> <MOLECULAR_WEIGHT>
208.213

> <EXACT_MASS>
208.073558866

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
27

> <JCHEM_AVERAGE_POLARIZABILITY>
22.324156839705275

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(5Z)-5-[(2E)-4-hydroxybut-2-en-1-ylidene]-3-[(1E)-3-hydroxyprop-1-en-1-yl]-2,5-dihydrofuran-2-one

> <ALOGPS_LOGP>
1.02

> <JCHEM_LOGP>
0.031895928000000434

> <ALOGPS_LOGS>
-2.29

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
16.496924667034513

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.894617492121128

> <JCHEM_PKA_STRONGEST_BASIC>
-2.271237610355631

> <JCHEM_POLAR_SURFACE_AREA>
66.76

> <JCHEM_REFRACTIVITY>
60.22730000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.06e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(5Z)-5-[(2E)-4-hydroxybut-2-en-1-ylidene]-3-[(1E)-3-hydroxyprop-1-en-1-yl]furan-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  O   UNK     0       1.060   3.620   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       1.060   2.080   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       2.306   1.175   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       1.830  -0.290   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.735  -1.536   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.267  -1.375   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.172  -2.621   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.703  -2.460   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       7.609  -3.706   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       0.290  -0.290   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.186   1.175   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.651   1.651   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.971   3.157   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -3.436   3.633   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -4.580   2.602   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   11                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   10                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8                                                            
CONECT   10    4   11                                                       
CONECT   11   10    2   12                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14                                                            
MASTER        0    0    0    0    0    0    0    0   15    0   30    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₁H₁₂O₄

Average Mass

208.2130 Da

Monoisotopic Mass

208.07356 Da

IUPAC Name

(5Z)-5-[(2E)-4-hydroxybut-2-en-1-ylidene]-3-[(1E)-3-hydroxyprop-1-en-1-yl]-2,5-dihydrofuran-2-one

Traditional Name

(5Z)-5-[(2E)-4-hydroxybut-2-en-1-ylidene]-3-[(1E)-3-hydroxyprop-1-en-1-yl]furan-2-one

CAS Registry Number

Not Available

SMILES

OC\C=C\C=C1/OC(=O)C(\C=C\CO)=C1

InChI Identifier

InChI=1S/C11H12O4/c12-6-2-1-5-10-8-9(4-3-7-13)11(14)15-10/h1-5,8,12-13H,6-7H2/b2-1+,4-3+,10-5-

InChI Key

ZYNGLDJNLYFSIV-CZFMBXACSA-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
Diplosoma virens	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as butenolides. These are dihydrofurans with a carbonyl group at the C2 carbon atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Dihydrofurans

Sub Class

Furanones

Direct Parent

Butenolides

Alternative Parents

Substituents

2-furanone
Enol ester
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Carboxylic acid ester
Lactone
Carboxylic acid derivative
Oxacycle
Monocarboxylic acid or derivatives
Hydrocarbon derivative
Organic oxide
Alcohol
Carbonyl group
Organic oxygen compound
Organooxygen compound
Primary alcohol
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic 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	1.02	ALOGPS
logP	0.032	ChemAxon
logS	-2.3	ALOGPS
pKa (Strongest Acidic)	15.89	ChemAxon
pKa (Strongest Basic)	-2.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	66.76 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	60.23 m³·mol⁻¹	ChemAxon
Polarizability	22.32 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

4582666

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5472800

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Richardson AD, Ireland CM: A profile of the in vitro antitumor activity of lissoclinolide. Toxicol Appl Pharmacol. 2004 Feb 15;195(1):55-61. doi: 10.1016/j.taap.2003.10.004. [PubMed:14962505 ]
LOTUS database [Link]

Showing NP-Card for (5z)-5-[(2e)-4-hydroxybut-2-en-1-ylidene]-3-[(1e)-3-hydroxyprop-1-en-1-yl]furan-2-one (NP0158665)

MOL for NP0158665 ((5z)-5-[(2e)-4-hydroxybut-2-en-1-ylidene]-3-[(1e)-3-hydroxyprop-1-en-1-yl]furan-2-one)

3D MOL for NP0158665 ((5z)-5-[(2e)-4-hydroxybut-2-en-1-ylidene]-3-[(1e)-3-hydroxyprop-1-en-1-yl]furan-2-one)

3D SDF for NP0158665 ((5z)-5-[(2e)-4-hydroxybut-2-en-1-ylidene]-3-[(1e)-3-hydroxyprop-1-en-1-yl]furan-2-one)

3D-SDF for NP0158665 ((5z)-5-[(2e)-4-hydroxybut-2-en-1-ylidene]-3-[(1e)-3-hydroxyprop-1-en-1-yl]furan-2-one)

PDB for NP0158665 ((5z)-5-[(2e)-4-hydroxybut-2-en-1-ylidene]-3-[(1e)-3-hydroxyprop-1-en-1-yl]furan-2-one)

3D PDB for NP0158665 ((5z)-5-[(2e)-4-hydroxybut-2-en-1-ylidene]-3-[(1e)-3-hydroxyprop-1-en-1-yl]furan-2-one)

SMILES for NP0158665 ((5z)-5-[(2e)-4-hydroxybut-2-en-1-ylidene]-3-[(1e)-3-hydroxyprop-1-en-1-yl]furan-2-one)

INCHI for NP0158665 ((5z)-5-[(2e)-4-hydroxybut-2-en-1-ylidene]-3-[(1e)-3-hydroxyprop-1-en-1-yl]furan-2-one)

Structure for NP0158665 ((5z)-5-[(2e)-4-hydroxybut-2-en-1-ylidene]-3-[(1e)-3-hydroxyprop-1-en-1-yl]furan-2-one)

3D Structure for NP0158665 ((5z)-5-[(2e)-4-hydroxybut-2-en-1-ylidene]-3-[(1e)-3-hydroxyprop-1-en-1-yl]furan-2-one)