NP-MRD: Showing NP-Card for 3,4-Dihydrolactucin (NP0084637)

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Record Information

Version

2.0

Created at

2022-04-29 05:19:14 UTC

Updated at

2022-04-29 05:19:14 UTC

NP-MRD ID

NP0084637

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3,4-Dihydrolactucin

Description

3,4-Dihydrolactucin is found in Cichorium intybus . Based on a literature review very few articles have been published on (3aR,4S,9aS,9bR)-4-hydroxy-9-(hydroxymethyl)-6-methyl-3-methylidene-2H,3H,3aH,4H,5H,7H,8H,9H,9aH,9bH-azuleno[4,5-b]furan-2,7-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 38 40  0  0  0  0  0  0  0  0999 V2000
   -3.5015   -2.1026    0.8830 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3585   -1.8246    0.2679 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7969   -2.6384   -0.8332 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4170   -3.4686   -1.5422 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4450   -2.2556   -0.8761 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4008   -0.8911   -0.6054 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9218   -0.3944   -0.0699 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8678    1.1005   -0.1835 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0049    1.9265    0.3540 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2508    3.3545    0.0305 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1539    1.5968    1.2233 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0415    0.6469    0.4466 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3232    0.6518    0.9716 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4196   -0.7222    0.5017 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9845    1.5077   -1.0300 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1023    2.5815   -1.6393 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9597    0.3942   -1.0282 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0843   -0.8050   -0.9003 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7766   -1.9701   -0.1994 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1776   -1.6441    1.0834 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0902   -2.9576    0.6012 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8755   -1.4862    1.6824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7124   -0.3359   -1.5131 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0039   -0.6615    0.9865 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2875    3.6521    0.2704 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0490    3.5219   -1.0415 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4414    3.9952    0.6138 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7140    1.0762    2.1232 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7390    2.4758    1.5048 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0497    0.9908   -0.6275 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6579    1.5954    0.8907 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8816   -0.8725    1.4699 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6844    0.5420   -0.2300 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4272    0.3836   -2.0348 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7363   -1.1726   -1.8878 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0347   -2.7863   -0.1208 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6439   -2.3172   -0.7927 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0226   -0.6869    1.2509 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  1  0
  5  3  1  0
  3  4  2  0
  3  2  1  0
  2  1  2  3
  2 14  1  0
 14 12  1  0
 12 13  1  0
 12 11  1  0
 11  9  1  0
  9 10  1  0
  9  8  2  0
  8 15  1  0
 15 16  2  0
 15 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 18  7  1  0
 14  6  1  0
  7  8  1  0
  7  6  1  0
  6 23  1  6
  1 21  1  0
  1 22  1  0
 14 32  1  1
 12 30  1  6
 13 31  1  0
 11 28  1  0
 11 29  1  0
 10 25  1  0
 10 26  1  0
 10 27  1  0
 17 33  1  0
 17 34  1  0
 18 35  1  6
 19 36  1  0
 19 37  1  0
 20 38  1  0
  7 24  1  1
M  END


  Mrv1652304292207192D          

 23 25  0  0  1  0            999 V2000
    5.6412   -1.0466    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9527   -0.5921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9157    0.2321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1204    0.4515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8305    1.2239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0167    1.3591    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6659   -0.2370    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3080   -0.9803    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1803   -0.8820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9967   -1.6863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6417   -2.2007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2534   -2.0443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5101   -1.6863    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8651   -2.2007    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3265   -0.8820    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5541   -0.5921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8656   -1.0466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1309   -1.0656    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8409   -0.2370    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2319    0.4895    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3864    0.4515    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5912    0.2321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9461    0.7464    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  1  0  0  0  0
  5  6  1  0  0  0  0
  4  7  1  0  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
  2  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 15 18  1  6  0  0  0
 15 19  1  0  0  0  0
  7 19  1  0  0  0  0
 19 20  1  1  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 16 22  1  0  0  0  0
 22 23  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0084637

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@]12OC(=O)C(=C)[C@]1([H])[C@@H](O)CC(C)=C1C(=O)CC(CO)[C@]21[H]

> <INCHI_IDENTIFIER>
InChI=1S/C15H18O5/c1-6-3-9(17)12-7(2)15(19)20-14(12)13-8(5-16)4-10(18)11(6)13/h8-9,12-14,16-17H,2-5H2,1H3/t8?,9-,12+,13-,14-/m0/s1

> <INCHI_KEY>
LDPVWKYIHKNNQW-ZNOOKKGSSA-N

> <FORMULA>
C15H18O5

> <MOLECULAR_WEIGHT>
278.304

> <EXACT_MASS>
278.11542368

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
38

> <JCHEM_AVERAGE_POLARIZABILITY>
28.60683937888055

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3aR,4S,9aS,9bR)-4-hydroxy-9-(hydroxymethyl)-6-methyl-3-methylidene-2H,3H,3aH,4H,5H,7H,8H,9H,9aH,9bH-azuleno[4,5-b]furan-2,7-dione

> <ALOGPS_LOGP>
-0.33

> <JCHEM_LOGP>
-0.049860514666666106

> <ALOGPS_LOGS>
-1.47

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.503018662021514

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.635596362260902

> <JCHEM_PKA_STRONGEST_BASIC>
-2.6107439855083294

> <JCHEM_POLAR_SURFACE_AREA>
83.83000000000001

> <JCHEM_REFRACTIVITY>
71.1154

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.38e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3aR,4S,9aS,9bR)-4-hydroxy-9-(hydroxymethyl)-6-methyl-3-methylidene-3aH,4H,5H,8H,9H,9aH,9bH-azuleno[4,5-b]furan-2,7-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  O   UNK     0      10.530  -1.954   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       9.245  -1.105   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.176   0.433   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.691   0.843   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.150   2.285   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       5.631   2.537   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       6.843  -0.442   0.000  0.00  0.00           C+0
HETATM    8  H   UNK     0       6.175  -1.830   0.000  0.00  0.00           H+0
HETATM    9  C   UNK     0       7.803  -1.646   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.461  -3.148   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.665  -4.108   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.073  -3.816   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.686  -3.148   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       3.482  -4.108   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       4.343  -1.646   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.901  -1.105   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.616  -1.954   0.000  0.00  0.00           C+0
HETATM   18  H   UNK     0       5.844  -1.989   0.000  0.00  0.00           H+0
HETATM   19  C   UNK     0       5.303  -0.442   0.000  0.00  0.00           C+0
HETATM   20  H   UNK     0       6.033   0.914   0.000  0.00  0.00           H+0
HETATM   21  O   UNK     0       4.455   0.843   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       2.970   0.433   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       1.766   1.393   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    9                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    7                                                  
CONECT    5    4    6                                                       
CONECT    6    5                                                            
CONECT    7    4    8    9   19                                             
CONECT    8    7                                                            
CONECT    9    7    2   10                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   18   19                                             
CONECT   16   15   17   22                                                  
CONECT   17   16                                                            
CONECT   18   15                                                            
CONECT   19   15    7   20   21                                             
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   16   23                                                  
CONECT   23   22                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   50    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₁₈O₅

Average Mass

278.3040 Da

Monoisotopic Mass

278.11542 Da

IUPAC Name

(3aR,4S,9aS,9bR)-4-hydroxy-9-(hydroxymethyl)-6-methyl-3-methylidene-2H,3H,3aH,4H,5H,7H,8H,9H,9aH,9bH-azuleno[4,5-b]furan-2,7-dione

Traditional Name

(3aR,4S,9aS,9bR)-4-hydroxy-9-(hydroxymethyl)-6-methyl-3-methylidene-3aH,4H,5H,8H,9H,9aH,9bH-azuleno[4,5-b]furan-2,7-dione

CAS Registry Number

Not Available

SMILES

[H][C@]12OC(=O)C(=C)[C@]1([H])[C@@H](O)CC(C)=C1C(=O)CC(CO)[C@]21[H]

InChI Identifier

InChI=1S/C15H18O5/c1-6-3-9(17)12-7(2)15(19)20-14(12)13-8(5-16)4-10(18)11(6)13/h8-9,12-14,16-17H,2-5H2,1H3/t8?,9-,12+,13-,14-/m0/s1

InChI Key

LDPVWKYIHKNNQW-ZNOOKKGSSA-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
Cichorium intybus	Plant	KNApSAcK

Chemical Taxonomy

Classification

Not classified

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	-0.33	ALOGPS
logP	-0.05	ChemAxon
logS	-1.5	ALOGPS
pKa (Strongest Acidic)	14.64	ChemAxon
pKa (Strongest Basic)	-2.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	83.83 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	71.12 m³·mol⁻¹	ChemAxon
Polarizability	28.61 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

C00054156

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

163184184

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 3,4-Dihydrolactucin (NP0084637)

MOL for NP0084637 (3,4-Dihydrolactucin)

3D MOL for NP0084637 (3,4-Dihydrolactucin)

3D SDF for NP0084637 (3,4-Dihydrolactucin)

3D-SDF for NP0084637 (3,4-Dihydrolactucin)

PDB for NP0084637 (3,4-Dihydrolactucin)

3D PDB for NP0084637 (3,4-Dihydrolactucin)

SMILES for NP0084637 (3,4-Dihydrolactucin)

INCHI for NP0084637 (3,4-Dihydrolactucin)

Structure for NP0084637 (3,4-Dihydrolactucin)

3D Structure for NP0084637 (3,4-Dihydrolactucin)