NP-MRD: Showing NP-Card for Diplopyrone (NP0004542)

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Record Information

Version

2.0

Created at

2020-12-09 02:00:34 UTC

Updated at

2021-07-15 16:49:28 UTC

NP-MRD ID

NP0004542

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Diplopyrone

Provided By

NPAtlas

Description

6-[(1S)-1-hydroxyethyl]-2H,4aH,6H,8aH-pyrano[3,2-b]pyran-2-one belongs to the class of organic compounds known as dihydropyranones. Dihydropyranones are compounds containing a hydrogenated pyran ring which bears a ketone, and contains one double bond. Diplopyrone is found in Diplodia mutila. Diplopyrone was first documented in 2003 (PMID: 12608876). Based on a literature review very few articles have been published on 6-[(1S)-1-hydroxyethyl]-2H,4aH,6H,8aH-pyrano[3,2-b]pyran-2-one.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242118073D          

 26 27  0  0  0  0            999 V2000
   -3.3209    0.3994   -0.8884 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3577   -0.3978   -0.0634 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9238   -0.6316    1.1888 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0911    0.4429    0.1209 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5521    0.7107   -1.2401 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6786    0.4148   -1.6259 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5662   -0.2287   -0.6143 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9085    0.2703   -0.7685 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7739   -0.1904    0.2368 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9809   -0.3344   -0.0559 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2458   -0.4803    1.5671 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9621   -0.2957    1.7857 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0660    0.1896    0.7407 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2427   -0.2827    0.9190 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3433    0.0435   -0.6607 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2551    1.4793   -0.5897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0774    0.2781   -1.9488 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0966   -1.3549   -0.5175 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4408   -1.4616    1.1734 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3413    1.4023    0.6315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2243    1.1779   -1.9461 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0393    0.6242   -2.6273 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5321   -1.3203   -0.7003 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9198   -0.8434    2.3550 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5996   -0.5247    2.7914 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9943    1.3202    0.7366 H   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  2  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  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14  4  1  0  0  0  0
 13  7  1  0  0  0  0
  1 15  1  0  0  0  0
  1 16  1  0  0  0  0
  1 17  1  0  0  0  0
  2 18  1  6  0  0  0
  3 19  1  0  0  0  0
  4 20  1  1  0  0  0
  5 21  1  0  0  0  0
  6 22  1  0  0  0  0
  7 23  1  1  0  0  0
 11 24  1  0  0  0  0
 12 25  1  0  0  0  0
 13 26  1  6  0  0  0
M  END


  Mrv1652306242118073D          

 26 27  0  0  0  0            999 V2000
   -3.3209    0.3994   -0.8884 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3577   -0.3978   -0.0634 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9238   -0.6316    1.1888 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0911    0.4429    0.1209 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5521    0.7107   -1.2401 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6786    0.4148   -1.6259 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5662   -0.2287   -0.6143 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9085    0.2703   -0.7685 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7739   -0.1904    0.2368 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9809   -0.3344   -0.0559 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2458   -0.4803    1.5671 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9621   -0.2957    1.7857 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0660    0.1896    0.7407 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2427   -0.2827    0.9190 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3433    0.0435   -0.6607 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2551    1.4793   -0.5897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0774    0.2781   -1.9488 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0966   -1.3549   -0.5175 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4408   -1.4616    1.1734 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3413    1.4023    0.6315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2243    1.1779   -1.9461 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0393    0.6242   -2.6273 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5321   -1.3203   -0.7003 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9198   -0.8434    2.3550 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5996   -0.5247    2.7914 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9943    1.3202    0.7366 H   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  2  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  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14  4  1  0  0  0  0
 13  7  1  0  0  0  0
  1 15  1  0  0  0  0
  1 16  1  0  0  0  0
  1 17  1  0  0  0  0
  2 18  1  6  0  0  0
  3 19  1  0  0  0  0
  4 20  1  1  0  0  0
  5 21  1  0  0  0  0
  6 22  1  0  0  0  0
  7 23  1  1  0  0  0
 11 24  1  0  0  0  0
 12 25  1  0  0  0  0
 13 26  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0004542

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]O[C@@]([H])(C([H])([H])[H])[C@@]1([H])O[C@@]2([H])C([H])=C([H])C(=O)O[C@]2([H])C([H])=C1[H]

> <INCHI_IDENTIFIER>
InChI=1S/C10H12O4/c1-6(11)7-2-3-9-8(13-7)4-5-10(12)14-9/h2-9,11H,1H3/t6-,7-,8-,9+/m0/s1

> <INCHI_KEY>
YMKWNRDVGOVSHY-JUGFDQIVSA-N

> <FORMULA>
C10H12O4

> <MOLECULAR_WEIGHT>
196.202

> <EXACT_MASS>
196.073558866

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
26

> <JCHEM_AVERAGE_POLARIZABILITY>
19.77144983079387

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(4aS,6S,8aR)-6-[(1S)-1-hydroxyethyl]-2H,4aH,6H,8aH-pyrano[3,2-b]pyran-2-one

> <ALOGPS_LOGP>
0.09

> <JCHEM_LOGP>
0.7511050330000003

> <ALOGPS_LOGS>
-0.55

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
18.113173057005614

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.450368257289217

> <JCHEM_PKA_STRONGEST_BASIC>
-3.039163744619697

> <JCHEM_POLAR_SURFACE_AREA>
55.760000000000005

> <JCHEM_REFRACTIVITY>
50.36220000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.51e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(4aS,6S,8aR)-6-[(1S)-1-hydroxyethyl]-4aH,6H,8aH-pyrano[3,2-b]pyran-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      -3.321   0.399  -0.888  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.358  -0.398  -0.063  0.00  0.00           C+0
HETATM    3  O   UNK     0      -2.924  -0.632   1.189  0.00  0.00           O+0
HETATM    4  C   UNK     0      -1.091   0.443   0.121  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.552   0.711  -1.240  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.679   0.415  -1.626  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.566  -0.229  -0.614  0.00  0.00           C+0
HETATM    8  O   UNK     0       2.909   0.270  -0.769  0.00  0.00           O+0
HETATM    9  C   UNK     0       3.774  -0.190   0.237  0.00  0.00           C+0
HETATM   10  O   UNK     0       4.981  -0.334  -0.056  0.00  0.00           O+0
HETATM   11  C   UNK     0       3.246  -0.480   1.567  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.962  -0.296   1.786  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.066   0.190   0.741  0.00  0.00           C+0
HETATM   14  O   UNK     0      -0.243  -0.283   0.919  0.00  0.00           O+0
HETATM   15  H   UNK     0      -4.343   0.044  -0.661  0.00  0.00           H+0
HETATM   16  H   UNK     0      -3.255   1.479  -0.590  0.00  0.00           H+0
HETATM   17  H   UNK     0      -3.077   0.278  -1.949  0.00  0.00           H+0
HETATM   18  H   UNK     0      -2.097  -1.355  -0.518  0.00  0.00           H+0
HETATM   19  H   UNK     0      -3.441  -1.462   1.173  0.00  0.00           H+0
HETATM   20  H   UNK     0      -1.341   1.402   0.632  0.00  0.00           H+0
HETATM   21  H   UNK     0      -1.224   1.178  -1.946  0.00  0.00           H+0
HETATM   22  H   UNK     0       1.039   0.624  -2.627  0.00  0.00           H+0
HETATM   23  H   UNK     0       1.532  -1.320  -0.700  0.00  0.00           H+0
HETATM   24  H   UNK     0       3.920  -0.843   2.355  0.00  0.00           H+0
HETATM   25  H   UNK     0       1.600  -0.525   2.791  0.00  0.00           H+0
HETATM   26  H   UNK     0       0.994   1.320   0.737  0.00  0.00           H+0
CONECT    1    2   15   16   17                                             
CONECT    2    1    3    4   18                                             
CONECT    3    2   19                                                       
CONECT    4    2    5   14   20                                             
CONECT    5    4    6   21                                                  
CONECT    6    5    7   22                                                  
CONECT    7    6    8   13   23                                             
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   24                                                  
CONECT   12   11   13   25                                                  
CONECT   13   12   14    7   26                                             
CONECT   14   13    4                                                       
CONECT   15    1                                                            
CONECT   16    1                                                            
CONECT   17    1                                                            
CONECT   18    2                                                            
CONECT   19    3                                                            
CONECT   20    4                                                            
CONECT   21    5                                                            
CONECT   22    6                                                            
CONECT   23    7                                                            
CONECT   24   11                                                            
CONECT   25   12                                                            
CONECT   26   13                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   54    0
END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₁₀H₁₂O₄

Average Mass

196.2020 Da

Monoisotopic Mass

196.07356 Da

IUPAC Name

(4aS,6S,8aR)-6-[(1S)-1-hydroxyethyl]-2H,4aH,6H,8aH-pyrano[3,2-b]pyran-2-one

Traditional Name

(4aS,6S,8aR)-6-[(1S)-1-hydroxyethyl]-4aH,6H,8aH-pyrano[3,2-b]pyran-2-one

CAS Registry Number

Not Available

SMILES

C[C@H](O)C1OC2C=CC(=O)OC2C=C1

InChI Identifier

InChI=1S/C10H12O4/c1-6(11)7-2-3-9-8(13-7)4-5-10(12)14-9/h2-9,11H,1H3/t6-,7?,8?,9?/m0/s1

InChI Key

YMKWNRDVGOVSHY-JUGFDQIVSA-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
Diplodia mutila	NPAtlas	12608876

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as dihydropyranones. Dihydropyranones are compounds containing a hydrogenated pyran ring which bears a ketone, and contains one double bond.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Pyrans

Sub Class

Pyranones and derivatives

Direct Parent

Dihydropyranones

Alternative Parents

Substituents

Dihydropyranone
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Carboxylic acid ester
Lactone
Secondary alcohol
Monocarboxylic acid or derivatives
Ether
Dialkyl ether
Carboxylic acid derivative
Oxacycle
Carbonyl group
Organooxygen compound
Organic oxygen compound
Alcohol
Organic oxide
Hydrocarbon derivative
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
logP	0.09	ALOGPS
logP	0.75	ChemAxon
logS	-0.55	ALOGPS
pKa (Strongest Acidic)	14.45	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	55.76 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	50.36 m³·mol⁻¹	ChemAxon
Polarizability	19.77 Å³	ChemAxon
Number of Rings	2	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

NPA003874

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

9270694

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11095552

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Evidente A, Maddau L, Spanu E, Franceschini A, Lazzaroni S, Motta A: Diplopyrone, a new phytotoxic tetrahydropyranpyran-2-one produced by Diplodia mutila, a fungus pathogen of cork oak. J Nat Prod. 2003 Feb;66(2):313-5. doi: 10.1021/np020367c. [PubMed:12608876 ]

Showing NP-Card for Diplopyrone (NP0004542)

MOL for NP0004542 (Diplopyrone)

3D MOL for NP0004542 (Diplopyrone)

3D SDF for NP0004542 (Diplopyrone)

3D-SDF for NP0004542 (Diplopyrone)

PDB for NP0004542 (Diplopyrone)

3D PDB for NP0004542 (Diplopyrone)

SMILES for NP0004542 (Diplopyrone)

INCHI for NP0004542 (Diplopyrone)

Structure for NP0004542 (Diplopyrone)

3D Structure for NP0004542 (Diplopyrone)