NP-MRD: Showing NP-Card for (2s)-2,5-dihydroxy-8,8-dimethyl-10-(3-methylbut-2-en-1-yl)-2h,3h-pyrano[3,2-g]chromen-4-one (NP0218760)

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Record Information

Version

2.0

Created at

2022-09-05 19:31:56 UTC

Updated at

2022-09-05 19:31:57 UTC

NP-MRD ID

NP0218760

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s)-2,5-dihydroxy-8,8-dimethyl-10-(3-methylbut-2-en-1-yl)-2h,3h-pyrano[3,2-g]chromen-4-one

Description

Eriosematin E belongs to the class of organic compounds known as pyranochromenes. These are organic heterocyclic compounds containing a pyran ring fused to a chromene (1-benzopyran) moiety. (2s)-2,5-dihydroxy-8,8-dimethyl-10-(3-methylbut-2-en-1-yl)-2h,3h-pyrano[3,2-g]chromen-4-one was first documented in 2017 (PMID: 28160852). Based on a literature review a small amount of articles have been published on Eriosematin E (PMID: 33086104) (PMID: 30807750).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 46 48  0  0  0  0  0  0  0  0999 V2000
    4.0037    0.0822    0.1036 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1557   -0.9566   -0.5393 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7615   -1.7138   -1.6808 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9265   -1.2411   -0.1713 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3017   -0.5199    0.9369 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0668    0.2016    0.5716 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1042   -0.5007    0.3977 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2211    0.2228    0.0563 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2285    1.5999   -0.1189 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3930    2.1906   -0.4530 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0351    2.2647    0.0640 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1324    1.5693    0.4137 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3337    2.2382    0.5996 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4720    3.5118   -0.0046 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6691    4.1272    0.2676 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2834    4.3525    0.4901 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9195    3.7059   -0.1072 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7985    4.3308   -0.7270 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4491   -0.5221   -0.1282 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4746   -1.8213    0.0263 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2832   -2.6067    0.3909 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5713   -3.4999    1.5904 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0578   -3.5641   -0.8021 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1219   -1.8584    0.5650 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0200    0.0134    1.2126 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0607    0.0096   -0.2645 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6556    1.0728   -0.2712 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1859   -0.9438   -2.3725 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6119   -2.3292   -1.3305 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0410   -2.3607   -2.1826 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3838   -2.0102   -0.6926 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0188    0.1177    1.4931 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9823   -1.2890    1.7025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5778    3.1195   -0.6015 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3184    3.4501   -1.1232 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0680    4.4860   -0.5617 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3903    5.3784    0.0491 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2049    4.3483    1.5783 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3630    0.0331   -0.4020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4483   -2.3244   -0.1303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6737   -3.7002    1.5688 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0063   -4.4300    1.4522 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3432   -2.9282    2.4990 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7150   -2.9513   -1.6876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0036   -4.0701   -1.0853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2596   -4.2843   -0.5914 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  2  0
  7 24  1  0
 24 21  1  0
 21 22  1  0
 21 23  1  0
 21 20  1  0
 20 19  2  0
 19  8  1  0
  8  9  2  0
  9 10  1  0
  9 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 17 18  2  0
 12  6  1  0
  8  7  1  0
 17 11  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  3 28  1  0
  3 29  1  0
  3 30  1  0
  4 31  1  0
  5 32  1  0
  5 33  1  0
 22 41  1  0
 22 42  1  0
 22 43  1  0
 23 44  1  0
 23 45  1  0
 23 46  1  0
 20 40  1  0
 19 39  1  0
 10 34  1  0
 14 35  1  6
 15 36  1  0
 16 37  1  0
 16 38  1  0
M  END


  Mrv1652309052221312D          

 24 26  0  0  1  0            999 V2000
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    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
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    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
    0.7145    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0993    0.1433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5690   -0.7752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    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
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
  6 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 11 17  1  0  0  0  0
 17 18  2  0  0  0  0
  8 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 21 24  1  0  0  0  0
  7 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0218760

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCC1=C2OC(C)(C)C=CC2=C(O)C2=C1O[C@H](O)CC2=O

> <INCHI_IDENTIFIER>
InChI=1S/C19H22O5/c1-10(2)5-6-12-17-11(7-8-19(3,4)24-17)16(22)15-13(20)9-14(21)23-18(12)15/h5,7-8,14,21-22H,6,9H2,1-4H3/t14-/m0/s1

> <INCHI_KEY>
CDFMHPFQZKLTFQ-AWEZNQCLSA-N

> <FORMULA>
C19H22O5

> <MOLECULAR_WEIGHT>
330.38

> <EXACT_MASS>
330.146723808

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
35.66898509965176

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S)-2,5-dihydroxy-8,8-dimethyl-10-(3-methylbut-2-en-1-yl)-2H,3H,4H,8H-pyrano[3,2-g]chromen-4-one

> <JCHEM_LOGP>
3.922964966

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.005836197458814

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.527045553722747

> <JCHEM_PKA_STRONGEST_BASIC>
-4.1049742043797055

> <JCHEM_POLAR_SURFACE_AREA>
75.99

> <JCHEM_REFRACTIVITY>
92.71130000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-2,5-dihydroxy-8,8-dimethyl-10-(3-methylbut-2-en-1-yl)-2H,3H-pyrano[3,2-g]chromen-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.334  -5.390   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       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.335  -0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       4.001   3.850   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       1.334  -0.770   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -1.334  -0.770   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       1.334   3.850   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.002   0.000   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       9.519   0.267   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.529  -1.447   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       6.668  -0.770   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                                                       
CONECT    6    5    7   12                                                  
CONECT    7    6    8   24                                                  
CONECT    8    7    9   19                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   17                                                  
CONECT   12   11    6   13                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   11   18                                                  
CONECT   18   17                                                            
CONECT   19    8   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23   24                                             
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   21    7                                                       
MASTER        0    0    0    0    0    0    0    0   24    0   52    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₂₂O₅

Average Mass

330.3800 Da

Monoisotopic Mass

330.14672 Da

IUPAC Name

(2S)-2,5-dihydroxy-8,8-dimethyl-10-(3-methylbut-2-en-1-yl)-2H,3H,4H,8H-pyrano[3,2-g]chromen-4-one

Traditional Name

(2S)-2,5-dihydroxy-8,8-dimethyl-10-(3-methylbut-2-en-1-yl)-2H,3H-pyrano[3,2-g]chromen-4-one

CAS Registry Number

Not Available

SMILES

CC(C)=CCC1=C2OC(C)(C)C=CC2=C(O)C2=C1O[C@H](O)CC2=O

InChI Identifier

InChI=1S/C19H22O5/c1-10(2)5-6-12-17-11(7-8-19(3,4)24-17)16(22)15-13(20)9-14(21)23-18(12)15/h5,7-8,14,21-22H,6,9H2,1-4H3/t14-/m0/s1

InChI Key

CDFMHPFQZKLTFQ-AWEZNQCLSA-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 pyranochromenes. These are organic heterocyclic compounds containing a pyran ring fused to a chromene (1-benzopyran) moiety.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

Pyranochromenes

Alternative Parents

Substituents

Pyranochromene
2,2-dimethyl-1-benzopyran
Chromone
Aryl alkyl ketone
Aryl ketone
Alkyl aryl ether
Phenol
Benzenoid
Vinylogous acid
Ketone
Hemiacetal
Oxacycle
Ether
Hydrocarbon derivative
Organooxygen compound
Organic oxide
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	3.92	ChemAxon
pKa (Strongest Acidic)	8.53	ChemAxon
pKa (Strongest Basic)	-4.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	75.99 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	92.71 m³·mol⁻¹	ChemAxon
Polarizability	35.67 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

Not Available

Chemspider ID

9005573

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10830273

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Parmar KM, Sinha SK, Prasad RS, Jogi MS, Laloo D, Dhobi M, Gurav SS, Prasad SK: Identifying the mechanism of eriosematin E from Eriosema chinense Vogel. for its antidiarrhoeal potential against Shigella flexneri-induced diarrhoea using in vitro, in vivo and in silico models. Microb Pathog. 2020 Dec;149:104582. doi: 10.1016/j.micpath.2020.104582. Epub 2020 Oct 18. [PubMed:33086104 ]
Parmar KM, Bhagwat DS, Sinha SK, Katare NT, Prasad SK: The potency of eriosematin E from Eriosema chinense Vogel. against enteropathogenic Escherichia coli induced diarrhoea using preclinical and molecular docking studies. Acta Trop. 2019 May;193:84-91. doi: 10.1016/j.actatropica.2019.02.025. Epub 2019 Feb 23. [PubMed:30807750 ]
Prasad SK, Parmar KM, Danta CC, Laloo D, Hemalatha S: Antidiarrhoeal activity of eriosematin E isolated from the roots of Eriosema chinense Vogel. Phytomedicine. 2017 Jan 15;24:127-133. doi: 10.1016/j.phymed.2016.11.022. Epub 2016 Dec 1. [PubMed:28160852 ]
LOTUS database [Link]

Showing NP-Card for (2s)-2,5-dihydroxy-8,8-dimethyl-10-(3-methylbut-2-en-1-yl)-2h,3h-pyrano[3,2-g]chromen-4-one (NP0218760)

MOL for NP0218760 ((2s)-2,5-dihydroxy-8,8-dimethyl-10-(3-methylbut-2-en-1-yl)-2h,3h-pyrano[3,2-g]chromen-4-one)

3D MOL for NP0218760 ((2s)-2,5-dihydroxy-8,8-dimethyl-10-(3-methylbut-2-en-1-yl)-2h,3h-pyrano[3,2-g]chromen-4-one)

3D SDF for NP0218760 ((2s)-2,5-dihydroxy-8,8-dimethyl-10-(3-methylbut-2-en-1-yl)-2h,3h-pyrano[3,2-g]chromen-4-one)

3D-SDF for NP0218760 ((2s)-2,5-dihydroxy-8,8-dimethyl-10-(3-methylbut-2-en-1-yl)-2h,3h-pyrano[3,2-g]chromen-4-one)

PDB for NP0218760 ((2s)-2,5-dihydroxy-8,8-dimethyl-10-(3-methylbut-2-en-1-yl)-2h,3h-pyrano[3,2-g]chromen-4-one)

3D PDB for NP0218760 ((2s)-2,5-dihydroxy-8,8-dimethyl-10-(3-methylbut-2-en-1-yl)-2h,3h-pyrano[3,2-g]chromen-4-one)

SMILES for NP0218760 ((2s)-2,5-dihydroxy-8,8-dimethyl-10-(3-methylbut-2-en-1-yl)-2h,3h-pyrano[3,2-g]chromen-4-one)

INCHI for NP0218760 ((2s)-2,5-dihydroxy-8,8-dimethyl-10-(3-methylbut-2-en-1-yl)-2h,3h-pyrano[3,2-g]chromen-4-one)

Structure for NP0218760 ((2s)-2,5-dihydroxy-8,8-dimethyl-10-(3-methylbut-2-en-1-yl)-2h,3h-pyrano[3,2-g]chromen-4-one)

3D Structure for NP0218760 ((2s)-2,5-dihydroxy-8,8-dimethyl-10-(3-methylbut-2-en-1-yl)-2h,3h-pyrano[3,2-g]chromen-4-one)