NP-MRD: Showing NP-Card for Aspinonediol (NP0007413)

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Record Information

Version

2.0

Created at

2020-12-09 04:17:55 UTC

Updated at

2021-07-15 16:57:31 UTC

NP-MRD ID

NP0007413

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Aspinonediol

Provided By

NPAtlas

Description

Aspinonediol 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. Aspinonediol is found in Aspergillus ostianus. Aspinonediol was first documented in 2007 (PMID: 17994702). Based on a literature review very few articles have been published on aspinonediol.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242118403D          

 26 25  0  0  0  0            999 V2000
   -3.9590    0.2395   -0.5071 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4247   -0.8232    0.4003 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1881   -1.5572    1.0439 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9777   -1.0108    0.5084 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1837   -0.1287   -0.1428 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2010   -0.2334   -0.1264 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3644   -0.3214   -0.1127 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7905   -0.4317   -0.0945 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3731   -0.7678    1.2568 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4613    0.6633   -0.6815 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3742    1.5800   -0.4543 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2715    1.5611   -1.6205 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0351    0.0707   -0.6231 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7359    1.2483   -0.1854 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4901    0.0233   -1.5202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4739   -1.7753    1.0816 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7722    0.6125   -0.6722 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2168   -1.5855    0.5455 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1016   -1.2923   -0.7722 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9864   -0.1647    2.0935 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4607   -0.7798    1.1403 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0715   -1.8250    1.5224 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0008    1.1093    0.0337 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3969    1.6697   -0.3460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1902    1.7845    0.4225 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0971    2.1348   -1.5843 H   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
  2  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  3  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  0  0  0  0
  1 13  1  0  0  0  0
  1 14  1  0  0  0  0
  1 15  1  0  0  0  0
  4 16  1  0  0  0  0
  5 17  1  0  0  0  0
  7 18  1  0  0  0  0
  8 19  1  6  0  0  0
  9 20  1  0  0  0  0
  9 21  1  0  0  0  0
  9 22  1  0  0  0  0
 10 23  1  0  0  0  0
 11 24  1  0  0  0  0
 11 25  1  0  0  0  0
 12 26  1  0  0  0  0
M  END


  Mrv1652306242118403D          

 26 25  0  0  0  0            999 V2000
   -3.9590    0.2395   -0.5071 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4247   -0.8232    0.4003 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1881   -1.5572    1.0439 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9777   -1.0108    0.5084 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1837   -0.1287   -0.1428 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2010   -0.2334   -0.1264 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3644   -0.3214   -0.1127 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7905   -0.4317   -0.0945 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3731   -0.7678    1.2568 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4613    0.6633   -0.6815 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3742    1.5800   -0.4543 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2715    1.5611   -1.6205 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0351    0.0707   -0.6231 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7359    1.2483   -0.1854 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4901    0.0233   -1.5202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4739   -1.7753    1.0816 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7722    0.6125   -0.6722 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2168   -1.5855    0.5455 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1016   -1.2923   -0.7722 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9864   -0.1647    2.0935 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4607   -0.7798    1.1403 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0715   -1.8250    1.5224 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0008    1.1093    0.0337 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3969    1.6697   -0.3460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1902    1.7845    0.4225 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0971    2.1348   -1.5843 H   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
  2  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  3  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  0  0  0  0
  1 13  1  0  0  0  0
  1 14  1  0  0  0  0
  1 15  1  0  0  0  0
  4 16  1  0  0  0  0
  5 17  1  0  0  0  0
  7 18  1  0  0  0  0
  8 19  1  6  0  0  0
  9 20  1  0  0  0  0
  9 21  1  0  0  0  0
  9 22  1  0  0  0  0
 10 23  1  0  0  0  0
 11 24  1  0  0  0  0
 11 25  1  0  0  0  0
 12 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0007413

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC([H])([H])C(\C([H])=C(/[H])C(=O)C([H])([H])[H])=C([H])[C@@]([H])(O[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C9H14O3/c1-7(11)3-4-9(6-10)5-8(2)12/h3-5,8,10,12H,6H2,1-2H3/b4-3+,9-5?/t8-/m0/s1

> <INCHI_KEY>
KZEYOZKGIDUZLU-QLNVLWNGSA-N

> <FORMULA>
C9H14O3

> <MOLECULAR_WEIGHT>
170.208

> <EXACT_MASS>
170.094294311

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
26

> <JCHEM_AVERAGE_POLARIZABILITY>
18.950980027650985

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3E,7S)-7-hydroxy-5-(hydroxymethyl)octa-3,5-dien-2-one

> <ALOGPS_LOGP>
-0.04

> <JCHEM_LOGP>
-0.12518253366666643

> <ALOGPS_LOGS>
-1.36

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.516957410040973

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.88650525422117

> <JCHEM_PKA_STRONGEST_BASIC>
-2.679185922217978

> <JCHEM_POLAR_SURFACE_AREA>
57.53

> <JCHEM_REFRACTIVITY>
49.0848

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.50e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3E,7S)-7-hydroxy-5-(hydroxymethyl)octa-3,5-dien-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0      -3.959   0.240  -0.507  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.425  -0.823   0.400  0.00  0.00           C+0
HETATM    3  O   UNK     0      -4.188  -1.557   1.044  0.00  0.00           O+0
HETATM    4  C   UNK     0      -1.978  -1.011   0.508  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.184  -0.129  -0.143  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.201  -0.233  -0.126  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.364  -0.321  -0.113  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.791  -0.432  -0.095  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.373  -0.768   1.257  0.00  0.00           C+0
HETATM   10  O   UNK     0       3.461   0.663  -0.682  0.00  0.00           O+0
HETATM   11  C   UNK     0       0.374   1.580  -0.454  0.00  0.00           C+0
HETATM   12  O   UNK     0      -0.272   1.561  -1.621  0.00  0.00           O+0
HETATM   13  H   UNK     0      -5.035   0.071  -0.623  0.00  0.00           H+0
HETATM   14  H   UNK     0      -3.736   1.248  -0.185  0.00  0.00           H+0
HETATM   15  H   UNK     0      -3.490   0.023  -1.520  0.00  0.00           H+0
HETATM   16  H   UNK     0      -1.474  -1.775   1.082  0.00  0.00           H+0
HETATM   17  H   UNK     0      -1.772   0.613  -0.672  0.00  0.00           H+0
HETATM   18  H   UNK     0       1.217  -1.585   0.546  0.00  0.00           H+0
HETATM   19  H   UNK     0       3.102  -1.292  -0.772  0.00  0.00           H+0
HETATM   20  H   UNK     0       2.986  -0.165   2.094  0.00  0.00           H+0
HETATM   21  H   UNK     0       4.461  -0.780   1.140  0.00  0.00           H+0
HETATM   22  H   UNK     0       3.071  -1.825   1.522  0.00  0.00           H+0
HETATM   23  H   UNK     0       4.001   1.109   0.034  0.00  0.00           H+0
HETATM   24  H   UNK     0       1.397   1.670  -0.346  0.00  0.00           H+0
HETATM   25  H   UNK     0      -0.190   1.785   0.423  0.00  0.00           H+0
HETATM   26  H   UNK     0      -1.097   2.135  -1.584  0.00  0.00           H+0
CONECT    1    2   13   14   15                                             
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   16                                                  
CONECT    5    4    6   17                                                  
CONECT    6    5    7   11                                                  
CONECT    7    6    8   18                                                  
CONECT    8    7    9   10   19                                             
CONECT    9    8   20   21   22                                             
CONECT   10    8   23                                                       
CONECT   11    6   12   24   25                                             
CONECT   12   11   26                                                       
CONECT   13    1                                                            
CONECT   14    1                                                            
CONECT   15    1                                                            
CONECT   16    4                                                            
CONECT   17    5                                                            
CONECT   18    7                                                            
CONECT   19    8                                                            
CONECT   20    9                                                            
CONECT   21    9                                                            
CONECT   22    9                                                            
CONECT   23   10                                                            
CONECT   24   11                                                            
CONECT   25   11                                                            
CONECT   26   12                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   50    0
END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₉H₁₄O₃

Average Mass

170.2080 Da

Monoisotopic Mass

170.09429 Da

IUPAC Name

(3E,7S)-7-hydroxy-5-(hydroxymethyl)octa-3,5-dien-2-one

Traditional Name

(3E,7S)-7-hydroxy-5-(hydroxymethyl)octa-3,5-dien-2-one

CAS Registry Number

Not Available

SMILES

C[C@H](O)\C=C(/CO)\C=C\C(C)=O

InChI Identifier

InChI=1S/C9H14O3/c1-7(11)3-4-9(6-10)5-8(2)12/h3-5,8,10,12H,6H2,1-2H3/b4-3+,9-5-/t8-/m0/s1

InChI Key

KZEYOZKGIDUZLU-QLNVLWNGSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Aspergillus ostianus	NPAtlas	17994702

Species Where Detected

Species Name	Source	Reference
Aspergillus ostianus strain 01F313	KNApSAcK Database	22123792

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
Alpha,beta-unsaturated ketone
Enone
Acryloyl-group
Secondary alcohol
Ketone
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic 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	-0.04	ALOGPS
logP	-0.13	ChemAxon
logS	-1.4	ALOGPS
pKa (Strongest Acidic)	14.89	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	57.53 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	49.08 m³·mol⁻¹	ChemAxon
Polarizability	18.95 Å³	ChemAxon
Number of Rings	0	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

NPAtlas ID

NPA013668

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00038523

Chemspider ID

23076708

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

24762997

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Kito K, Ookura R, Yoshida S, Namikoshi M, Ooi T, Kusumi T: Pentaketides relating to aspinonene and dihydroaspyrone from a marine-derived fungus, Aspergillus ostianus. J Nat Prod. 2007 Dec;70(12):2022-5. doi: 10.1021/np070301n. Epub 2007 Nov 10. [PubMed:17994702 ]

Showing NP-Card for Aspinonediol (NP0007413)

MOL for NP0007413 (Aspinonediol)

3D MOL for NP0007413 (Aspinonediol)

3D SDF for NP0007413 (Aspinonediol)

3D-SDF for NP0007413 (Aspinonediol)

PDB for NP0007413 (Aspinonediol)

3D PDB for NP0007413 (Aspinonediol)

SMILES for NP0007413 (Aspinonediol)

INCHI for NP0007413 (Aspinonediol)

Structure for NP0007413 (Aspinonediol)

3D Structure for NP0007413 (Aspinonediol)