NP-MRD: Showing NP-Card for 4-[(1e)-8-hydroxynon-1-en-1-yl]-3-methyl-5h-furan-2-one (NP0156888)

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Record Information

Version

2.0

Created at

2022-09-02 14:09:54 UTC

Updated at

2022-09-02 14:09:54 UTC

NP-MRD ID

NP0156888

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-[(1e)-8-hydroxynon-1-en-1-yl]-3-methyl-5h-furan-2-one

Description

Appenolide B 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. 4-[(1e)-8-hydroxynon-1-en-1-yl]-3-methyl-5h-furan-2-one is found in Podospora appendiculata. Based on a literature review very few articles have been published on Appenolide B.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 39 39  0  0  0  0  0  0  0  0999 V2000
   -5.5196   -0.8887   -0.1223 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1388    0.3578    0.6267 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8950    0.6623    0.9329 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7085   -0.1579    0.5942 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5064    0.2406    0.9494 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2753   -0.5651    0.6237 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6087    0.3353   -0.2371 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8552   -0.4974   -0.5596 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7370    0.3888   -1.4132 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0084   -0.2822   -1.8172 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8369   -0.6872   -0.6086 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1873    0.5394    0.2062 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0228   -1.2644   -1.0566 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9143    1.9440    1.6590 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2511    2.3253    1.7324 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0360    1.3884    1.1160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2978    1.3876    0.9803 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6475   -1.7174    0.5819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8016   -1.1036   -0.9385 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5036   -0.6790   -0.5875 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8056   -1.0800    0.0599 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4182    1.1724    1.4881 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5443   -1.4596    0.0294 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2886   -0.8307    1.5376 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9221    1.2299    0.3030 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1232    0.5840   -1.1909 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3174   -0.8217    0.3699 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4893   -1.3754   -1.1117 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9630    1.3449   -0.9017 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1620    0.6244   -2.3265 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6113    0.4523   -2.3876 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8433   -1.1413   -2.4839 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3084   -1.4358    0.0048 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4761    0.6495    1.0745 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2257    0.4687    0.5393 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1106    1.4531   -0.4497 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9946   -2.2412   -0.9489 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3931    2.7452    1.0695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4352    1.8395    2.6628 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 11  1  0
 11 13  1  0
 11 10  1  0
 10  9  1  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  4  2  0
  4  3  1  0
  3  2  2  0
  2  1  1  0
  2 16  1  0
 16 17  2  0
 16 15  1  0
 15 14  1  0
 14  3  1  0
 12 34  1  0
 12 35  1  0
 12 36  1  0
 11 33  1  1
 13 37  1  0
 10 31  1  0
 10 32  1  0
  9 29  1  0
  9 30  1  0
  8 27  1  0
  8 28  1  0
  7 25  1  0
  7 26  1  0
  6 23  1  0
  6 24  1  0
  5 22  1  0
  4 21  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
 14 38  1  0
 14 39  1  0
M  END


  Mrv1652309022216092D          

 17 17  0  0  0  0            999 V2000
   -6.6253    0.8438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4538    0.0368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7001   -0.2987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9856    0.1138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2712   -0.2987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5567    0.1138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8422   -0.2987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1278    0.1138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4133   -0.2987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6988    0.1138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0157   -0.2987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7301    0.1138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0157   -1.1237    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7863   -1.1192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5933   -1.2907    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0058   -0.5763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8263   -0.4900    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  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
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
  3 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  2 16  1  0  0  0  0
 16 17  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0156888

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(O)CCCCC\C=C\C1=C(C)C(=O)OC1

> <INCHI_IDENTIFIER>
InChI=1S/C14H22O3/c1-11(15)8-6-4-3-5-7-9-13-10-17-14(16)12(13)2/h7,9,11,15H,3-6,8,10H2,1-2H3/b9-7+

> <INCHI_KEY>
XJNVZUVIGOZMFT-VQHVLOKHSA-N

> <FORMULA>
C14H22O3

> <MOLECULAR_WEIGHT>
238.327

> <EXACT_MASS>
238.156894568

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
28.48238254980949

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-[(1E)-8-hydroxynon-1-en-1-yl]-3-methyl-2,5-dihydrofuran-2-one

> <ALOGPS_LOGP>
3.20

> <JCHEM_LOGP>
2.9054827559999996

> <ALOGPS_LOGS>
-3.00

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
17.683061040328337

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.467196978851025

> <JCHEM_PKA_STRONGEST_BASIC>
-1.6252267405100467

> <JCHEM_POLAR_SURFACE_AREA>
46.53

> <JCHEM_REFRACTIVITY>
69.5576

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.37e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-[(1E)-8-hydroxynon-1-en-1-yl]-3-methyl-5H-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  C   UNK     0     -12.367   1.575   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -12.047   0.069   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -10.640  -0.558   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -9.307   0.212   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -7.973  -0.558   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -6.639   0.212   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -5.305  -0.558   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -3.972   0.212   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.638  -0.558   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.304   0.212   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.029  -0.558   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.363   0.212   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       0.029  -2.098   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0     -10.801  -2.089   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0     -12.308  -2.409   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0     -13.078  -1.076   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0     -14.609  -0.915   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   16                                                  
CONECT    3    2    4   14                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14    3   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15    2   17                                                  
CONECT   17   16                                                            
MASTER        0    0    0    0    0    0    0    0   17    0   34    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₄H₂₂O₃

Average Mass

238.3270 Da

Monoisotopic Mass

238.15689 Da

IUPAC Name

4-[(1E)-8-hydroxynon-1-en-1-yl]-3-methyl-2,5-dihydrofuran-2-one

Traditional Name

4-[(1E)-8-hydroxynon-1-en-1-yl]-3-methyl-5H-furan-2-one

CAS Registry Number

Not Available

SMILES

CC(O)CCCCC\C=C\C1=C(C)C(=O)OC1

InChI Identifier

InChI=1S/C14H22O3/c1-11(15)8-6-4-3-5-7-9-13-10-17-14(16)12(13)2/h7,9,11,15H,3-6,8,10H2,1-2H3/b9-7+

InChI Key

XJNVZUVIGOZMFT-VQHVLOKHSA-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
Podospora appendiculata	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
2-furanone
Dihydrofuran
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Carboxylic acid ester
Lactone
Secondary alcohol
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Hydrocarbon derivative
Organic oxide
Alcohol
Organic oxygen compound
Carbonyl group
Organooxygen compound
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	3.2	ALOGPS
logP	2.91	ChemAxon
logS	-3	ALOGPS
pKa (Strongest Acidic)	13.47	ChemAxon
pKa (Strongest Basic)	-1.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	46.53 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	69.56 m³·mol⁻¹	ChemAxon
Polarizability	28.48 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

4940927

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

6436280

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4-[(1e)-8-hydroxynon-1-en-1-yl]-3-methyl-5h-furan-2-one (NP0156888)

MOL for NP0156888 (4-[(1e)-8-hydroxynon-1-en-1-yl]-3-methyl-5h-furan-2-one)

3D MOL for NP0156888 (4-[(1e)-8-hydroxynon-1-en-1-yl]-3-methyl-5h-furan-2-one)

3D SDF for NP0156888 (4-[(1e)-8-hydroxynon-1-en-1-yl]-3-methyl-5h-furan-2-one)

3D-SDF for NP0156888 (4-[(1e)-8-hydroxynon-1-en-1-yl]-3-methyl-5h-furan-2-one)

PDB for NP0156888 (4-[(1e)-8-hydroxynon-1-en-1-yl]-3-methyl-5h-furan-2-one)

3D PDB for NP0156888 (4-[(1e)-8-hydroxynon-1-en-1-yl]-3-methyl-5h-furan-2-one)

SMILES for NP0156888 (4-[(1e)-8-hydroxynon-1-en-1-yl]-3-methyl-5h-furan-2-one)

INCHI for NP0156888 (4-[(1e)-8-hydroxynon-1-en-1-yl]-3-methyl-5h-furan-2-one)

Structure for NP0156888 (4-[(1e)-8-hydroxynon-1-en-1-yl]-3-methyl-5h-furan-2-one)

3D Structure for NP0156888 (4-[(1e)-8-hydroxynon-1-en-1-yl]-3-methyl-5h-furan-2-one)