NP-MRD: Showing NP-Card for (3s,5s)-3-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-5-(2-methylprop-1-en-1-yl)oxolan-2-one (NP0189270)

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Record Information

Version

2.0

Created at

2022-09-04 05:43:40 UTC

Updated at

2022-09-04 05:43:40 UTC

NP-MRD ID

NP0189270

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3s,5s)-3-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-5-(2-methylprop-1-en-1-yl)oxolan-2-one

Description

(+)-Chizhine A belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group. It was first documented in 2022 (PMID: 36051722). Based on a literature review a significant number of articles have been published on (+)-chizhine A (PMID: 36050584) (PMID: 36044365) (PMID: 36043368) (PMID: 36038174) (PMID: 36030880) (PMID: 36029144).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 39 40  0  0  0  0  0  0  0  0999 V2000
    5.4057   -1.3575   -0.5288 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5983   -0.4109    0.2928 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2645    0.6579    1.1066 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2895   -0.5256    0.2946 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4766    0.4050    1.1036 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9971    0.0190    1.0782 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5922    0.4624   -0.2849 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8829    0.7422   -0.4171 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7306   -0.4030   -0.1337 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2063   -1.4981    0.1793 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1608   -0.3094   -0.2039 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9275   -1.4507    0.0780 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3034   -1.4247    0.0260 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9959   -2.6109    0.3225 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9570   -0.2579   -0.3092 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2335    0.8755   -0.5904 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8431    0.8333   -0.5336 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1121    1.9738   -0.8162 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4121    1.6816   -0.4872 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2536    2.5806   -1.3368 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4331    1.6778    0.4530 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3289   -0.8953   -0.9182 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6033   -2.2994    0.0403 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7940   -1.6437   -1.4188 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0184    1.2010    0.4790 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7093    0.1691    1.9861 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5310    1.3893    1.4428 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8136   -1.2884   -0.2863 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8402    0.4929    2.1488 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8448   -1.0486    1.2771 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5090    0.6740    1.8406 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8492   -0.3178   -1.0358 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0966    1.0851   -1.4685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1002    1.5969    0.2395 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4190   -2.3816    0.3451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2456   -2.7539    1.2929 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0519   -0.2752   -0.3404 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7130    1.8024   -0.8554 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5851    2.8329   -1.0636 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 13 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
  7 19  1  0
 19 20  2  0
 19 21  1  0
 21  5  1  0
 17 11  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  3 25  1  0
  3 26  1  0
  3 27  1  0
  4 28  1  0
  5 29  1  1
  6 30  1  0
  6 31  1  0
  7 32  1  6
  8 33  1  0
  8 34  1  0
 12 35  1  0
 14 36  1  0
 15 37  1  0
 16 38  1  0
 18 39  1  0
M  END


  Mrv1652309042207432D          

 21 22  0  0  1  0            999 V2000
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0964   -2.9599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414   -3.7445    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3264   -4.4120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1468   -4.3257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4824   -3.5721    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6318   -4.9932    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4522   -4.9070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9372   -5.5744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7577   -5.4882    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6016   -6.3281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7811   -6.4143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2962   -5.7469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4757   -5.8331    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164   -3.7445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5315   -4.4120    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7615   -2.9599    0.0000 O   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  2  0  0  0  0
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  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
 13 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 11 17  1  0  0  0  0
 17 18  1  0  0  0  0
  7 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
  5 21  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0189270

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=C[C@@H]1C[C@@H](CC(=O)C2=CC(O)=CC=C2O)C(=O)O1

> <INCHI_IDENTIFIER>
InChI=1S/C16H18O5/c1-9(2)5-12-6-10(16(20)21-12)7-15(19)13-8-11(17)3-4-14(13)18/h3-5,8,10,12,17-18H,6-7H2,1-2H3/t10-,12+/m0/s1

> <INCHI_KEY>
QRWTVFKEWNICIM-CMPLNLGQSA-N

> <FORMULA>
C16H18O5

> <MOLECULAR_WEIGHT>
290.315

> <EXACT_MASS>
290.11542368

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
30.13311066482069

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3S,5S)-3-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-5-(2-methylprop-1-en-1-yl)oxolan-2-one

> <JCHEM_LOGP>
3.034986049333333

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.036502449649136

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.205040784201707

> <JCHEM_PKA_STRONGEST_BASIC>
-5.124974437588045

> <JCHEM_POLAR_SURFACE_AREA>
83.83

> <JCHEM_REFRACTIVITY>
77.71629999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(3S,5S)-3-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-5-(2-methylprop-1-en-1-yl)oxolan-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.913  -5.525   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.437  -6.990   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.343  -8.236   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.874  -8.075   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       6.500  -6.668   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       6.779  -9.321   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.311  -9.160   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.216 -10.406   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      10.748 -10.245   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       8.590 -11.812   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.058 -11.973   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.153 -10.727   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       4.621 -10.888   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       1.897  -6.990   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       0.992  -8.236   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       1.421  -5.525   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   21                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   19                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   17                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   11   18                                                  
CONECT   18   17                                                            
CONECT   19    7   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19    5                                                       
MASTER        0    0    0    0    0    0    0    0   21    0   44    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₆H₁₈O₅

Average Mass

290.3150 Da

Monoisotopic Mass

290.11542 Da

IUPAC Name

(3S,5S)-3-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-5-(2-methylprop-1-en-1-yl)oxolan-2-one

Traditional Name

(3S,5S)-3-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-5-(2-methylprop-1-en-1-yl)oxolan-2-one

CAS Registry Number

Not Available

SMILES

CC(C)=C[C@@H]1C[C@@H](CC(=O)C2=CC(O)=CC=C2O)C(=O)O1

InChI Identifier

InChI=1S/C16H18O5/c1-9(2)5-12-6-10(16(20)21-12)7-15(19)13-8-11(17)3-4-14(13)18/h3-5,8,10,12,17-18H,6-7H2,1-2H3/t10-,12+/m0/s1

InChI Key

QRWTVFKEWNICIM-CMPLNLGQSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbonyl compounds

Direct Parent

Alkyl-phenylketones

Alternative Parents

Substituents

Alkyl-phenylketone
Benzoyl
Hydroquinone
Aryl alkyl ketone
1-hydroxy-2-unsubstituted benzenoid
Phenol
Monocyclic benzene moiety
Gamma butyrolactone
Benzenoid
Oxolane
Vinylogous acid
Lactone
Carboxylic acid ester
Oxacycle
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organoheterocyclic compound
Hydrocarbon derivative
Organic oxide
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic 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	3.03	ChemAxon
pKa (Strongest Acidic)	9.21	ChemAxon
pKa (Strongest Basic)	-5.1	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	4	ChemAxon
Refractivity	77.72 m³·mol⁻¹	ChemAxon
Polarizability	30.13 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

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

78440935

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

101905607

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Wako M, Kono H, Koyama K, Fujimaki T, Furuya N, Haro H: The Anatomical Position of Graf's Standard Plane and Its Relationship With Pelvic Morphology: A Computed Tomography-Based Study. Cureus. 2022 Jul 28;14(7):e27424. doi: 10.7759/cureus.27424. eCollection 2022 Jul. [PubMed:36051722 ]
Jayroe M, Aguilar DR, Porter A, Cima M, Chai S, Hayman K: Transmission Analysis of COVID-19 Outbreaks Associated with Places of Worship, Arkansas, May 2020-December 2020. J Relig Health. 2022 Sep 1. pii: 10.1007/s10943-022-01653-y. doi: 10.1007/s10943-022-01653-y. [PubMed:36050584 ]
Belik AA, Khalyavin DD, Matsushita Y, Yamaura K: Triple A-Site Cation Ordering in the Ferrimagnetic Y2CuGaMn4O12 Perovskite. Inorg Chem. 2022 Sep 12;61(36):14428-14435. doi: 10.1021/acs.inorgchem.2c02343. Epub 2022 Aug 31. [PubMed:36044365 ]
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LOTUS database [Link]

Showing NP-Card for (3s,5s)-3-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-5-(2-methylprop-1-en-1-yl)oxolan-2-one (NP0189270)

MOL for NP0189270 ((3s,5s)-3-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-5-(2-methylprop-1-en-1-yl)oxolan-2-one)

3D MOL for NP0189270 ((3s,5s)-3-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-5-(2-methylprop-1-en-1-yl)oxolan-2-one)

3D SDF for NP0189270 ((3s,5s)-3-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-5-(2-methylprop-1-en-1-yl)oxolan-2-one)

3D-SDF for NP0189270 ((3s,5s)-3-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-5-(2-methylprop-1-en-1-yl)oxolan-2-one)

PDB for NP0189270 ((3s,5s)-3-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-5-(2-methylprop-1-en-1-yl)oxolan-2-one)

3D PDB for NP0189270 ((3s,5s)-3-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-5-(2-methylprop-1-en-1-yl)oxolan-2-one)

SMILES for NP0189270 ((3s,5s)-3-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-5-(2-methylprop-1-en-1-yl)oxolan-2-one)

INCHI for NP0189270 ((3s,5s)-3-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-5-(2-methylprop-1-en-1-yl)oxolan-2-one)

Structure for NP0189270 ((3s,5s)-3-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-5-(2-methylprop-1-en-1-yl)oxolan-2-one)

3D Structure for NP0189270 ((3s,5s)-3-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-5-(2-methylprop-1-en-1-yl)oxolan-2-one)