NP-MRD: Showing NP-Card for (5s,6s)-1,7-dioxadispiro[4.0.4⁶.2⁵]dodeca-3,9-diene-2,8-dione (NP0247393)

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Record Information

Version

2.0

Created at

2022-09-07 09:14:07 UTC

Updated at

2022-09-07 09:14:08 UTC

NP-MRD ID

NP0247393

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(5s,6s)-1,7-dioxadispiro[4.0.4⁶.2⁵]dodeca-3,9-diene-2,8-dione

Description

Anemone camphor belongs to the class of organic compounds known as butenolides. These are dihydrofurans with a carbonyl group at the C2 carbon atom. (5s,6s)-1,7-dioxadispiro[4.0.4⁶.2⁵]dodeca-3,9-diene-2,8-dione is found in Prumnopitys andina. Based on a literature review very few articles have been published on Anemone camphor.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072211142D          

 14 16  0  0  1  0            999 V2000
    3.3776    2.8292    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2485    2.0144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8319    1.4310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4573    0.6959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6425    0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6425    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8175   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8175    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0026    0.6959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6281    1.4310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2115    2.0144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0824    2.8292    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9465    1.6398    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5134    1.6398    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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  6  0  0  0
  6  7  1  0  0  0  0
  8  7  1  1  0  0  0
  5  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
  8 13  1  0  0  0  0
  5 14  1  0  0  0  0
  2 14  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0247393

> <DATABASE_NAME>
NP-MRD

> <SMILES>
O=C1O[C@@]2(CC[C@@]22OC(=O)C=C2)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C10H8O4/c11-7-1-3-9(13-7)5-6-10(9)4-2-8(12)14-10/h1-4H,5-6H2/t9-,10-/m1/s1

> <INCHI_KEY>
JLUQTCXCAFSSLD-NXEZZACHSA-N

> <FORMULA>
C10H8O4

> <MOLECULAR_WEIGHT>
192.17

> <EXACT_MASS>
192.042258738

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
22

> <JCHEM_AVERAGE_POLARIZABILITY>
17.83350303160058

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(5S,6S)-1,7-dioxadispiro[4.0.4^{6}.2^{5}]dodeca-3,9-diene-2,8-dione

> <JCHEM_LOGP>
1.2745752679999998

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-6.534645713928027

> <JCHEM_POLAR_SURFACE_AREA>
52.6

> <JCHEM_REFRACTIVITY>
47.186400000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(5S,6S)-1,7-dioxadispiro[4.0.4^{6}.2^{5}]dodeca-3,9-diene-2,8-dione

> <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  O   UNK     0       6.305   5.281   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       6.064   3.760   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.153   2.671   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.454   1.299   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.933   1.540   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.933   0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.393  -0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.393   1.540   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.872   1.299   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.172   2.671   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.261   3.760   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       2.020   5.281   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0       3.634   3.061   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0       4.692   3.061   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   14                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    8   14                                             
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    5    9   13                                             
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11    8                                                       
CONECT   14    5    2                                                       
MASTER        0    0    0    0    0    0    0    0   14    0   32    0
END

View in JSmol

Synonyms

Value	Source
Pulsatilla camphor	Kegg

Chemical Formula

C₁₀H₈O₄

Average Mass

192.1700 Da

Monoisotopic Mass

192.04226 Da

IUPAC Name

(5S,6S)-1,7-dioxadispiro[4.0.4^{6}.2^{5}]dodeca-3,9-diene-2,8-dione

Traditional Name

(5S,6S)-1,7-dioxadispiro[4.0.4^{6}.2^{5}]dodeca-3,9-diene-2,8-dione

CAS Registry Number

Not Available

SMILES

O=C1O[C@@]2(CC[C@@]22OC(=O)C=C2)C=C1

InChI Identifier

InChI=1S/C10H8O4/c11-7-1-3-9(13-7)5-6-10(9)4-2-8(12)14-10/h1-4H,5-6H2/t9-,10-/m1/s1

InChI Key

JLUQTCXCAFSSLD-NXEZZACHSA-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
Prumnopitys andina	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

Dicarboxylic acid or derivatives
2-furanone
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Lactone
Carboxylic acid ester
Oxacycle
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

butenolide (CHEBI:80791 )

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	1.27	ChemAxon
pKa (Strongest Basic)	-6.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	52.6 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	47.19 m³·mol⁻¹	ChemAxon
Polarizability	17.83 Å³	ChemAxon
Number of Rings	3	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

C00050531

Chemspider ID

24534169

KEGG Compound ID

C16913

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

46173847

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (5s,6s)-1,7-dioxadispiro[4.0.4⁶.2⁵]dodeca-3,9-diene-2,8-dione (NP0247393)

MOL for NP0247393 ((5s,6s)-1,7-dioxadispiro[4.0.4⁶.2⁵]dodeca-3,9-diene-2,8-dione)

3D MOL for NP0247393 ((5s,6s)-1,7-dioxadispiro[4.0.4⁶.2⁵]dodeca-3,9-diene-2,8-dione)

3D SDF for NP0247393 ((5s,6s)-1,7-dioxadispiro[4.0.4⁶.2⁵]dodeca-3,9-diene-2,8-dione)

3D-SDF for NP0247393 ((5s,6s)-1,7-dioxadispiro[4.0.4⁶.2⁵]dodeca-3,9-diene-2,8-dione)

PDB for NP0247393 ((5s,6s)-1,7-dioxadispiro[4.0.4⁶.2⁵]dodeca-3,9-diene-2,8-dione)

3D PDB for NP0247393 ((5s,6s)-1,7-dioxadispiro[4.0.4⁶.2⁵]dodeca-3,9-diene-2,8-dione)

SMILES for NP0247393 ((5s,6s)-1,7-dioxadispiro[4.0.4⁶.2⁵]dodeca-3,9-diene-2,8-dione)

INCHI for NP0247393 ((5s,6s)-1,7-dioxadispiro[4.0.4⁶.2⁵]dodeca-3,9-diene-2,8-dione)

Structure for NP0247393 ((5s,6s)-1,7-dioxadispiro[4.0.4⁶.2⁵]dodeca-3,9-diene-2,8-dione)

3D Structure for NP0247393 ((5s,6s)-1,7-dioxadispiro[4.0.4⁶.2⁵]dodeca-3,9-diene-2,8-dione)