NP-MRD: Showing NP-Card for 1-[3-acetyl-2,4,6-trihydroxy-5-(2-hydroxy-3-methylbut-3-en-1-yl)phenyl]-3-methylbutan-1-one (NP0254096)

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Record Information

Version

2.0

Created at

2022-09-07 18:09:14 UTC

Updated at

2022-09-07 18:09:14 UTC

NP-MRD ID

NP0254096

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-[3-acetyl-2,4,6-trihydroxy-5-(2-hydroxy-3-methylbut-3-en-1-yl)phenyl]-3-methylbutan-1-one

Description

Sessiliflorene 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. 1-[3-acetyl-2,4,6-trihydroxy-5-(2-hydroxy-3-methylbut-3-en-1-yl)phenyl]-3-methylbutan-1-one is found in Medicosma sessiliflora. Sessiliflorene is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 48 48  0  0  0  0  0  0  0  0999 V2000
   -3.2000   -1.1400    1.8404 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6822   -1.1407    0.6035 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8825   -2.4499   -0.0801 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9842    0.1599    0.0025 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.3367   -0.0178   -0.4927 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1359    0.6408   -1.1136 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7238    0.9242   -0.7944 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3262    2.1895   -0.4480 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2408    3.2599   -0.4203 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0044    2.4637   -0.1098 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3854    3.8130    0.2490 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7306    4.2768    0.6324 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5658    4.6925    0.2239 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9058    1.4312   -0.1294 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1925    1.5786    0.1761 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5275    0.1057   -0.4848 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5451   -0.9228   -0.4827 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2730   -2.1041   -0.7858 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9642   -0.6824   -0.1321 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7787   -1.9875   -0.2243 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1968   -1.6571    0.1451 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2630   -3.0485    0.6908 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7763   -0.1212   -0.8100 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2254   -1.3723   -1.1707 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9715   -2.0892    2.3008 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0204   -0.2531    2.4193 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1398   -3.1590    0.3366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8825   -2.8599    0.1740 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8158   -2.3682   -1.1831 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1002    0.9397    0.7752 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5330    0.7028   -1.1486 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1011   -0.0842   -1.9720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6418    1.5356   -1.5485 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1973    3.2253   -0.6251 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6995    5.4016    0.7866 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0230    3.7803    1.5622 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4164    4.1485   -0.2058 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9478    2.0203    0.4292 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5022   -0.0032   -0.7994 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0178   -0.4192    0.9338 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7002   -2.2773   -1.3063 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8888   -2.1513   -0.5778 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3766   -0.5450    0.1052 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4174   -2.0721    1.1456 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1346   -3.6576    1.0744 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7390   -2.6679    1.5700 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6482   -3.8105    0.1274 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7864   -2.2276   -1.2587 H   0  0  0  0  0  0  0  0  0  0  0  0
 21 20  1  0
 20 22  1  0
 20 19  1  0
 19 17  1  0
 17 18  2  0
 17 16  1  0
 16 23  2  0
 23 24  1  0
 23  7  1  0
  7  6  1  0
  6  4  1  0
  4  5  1  0
  4  2  1  0
  2  3  1  0
  2  1  2  3
  7  8  2  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  2  0
 10 14  2  0
 14 15  1  0
 14 16  1  0
 21 42  1  0
 21 43  1  0
 21 44  1  0
 20 41  1  0
 22 45  1  0
 22 46  1  0
 22 47  1  0
 19 39  1  0
 19 40  1  0
 24 48  1  0
  6 32  1  0
  6 33  1  0
  4 30  1  1
  5 31  1  0
  3 27  1  0
  3 28  1  0
  3 29  1  0
  1 25  1  0
  1 26  1  0
  9 34  1  0
 12 35  1  0
 12 36  1  0
 12 37  1  0
 15 38  1  0
M  END


  Mrv1533004261513472D          

 24 24  0  0  0  0            999 V2000
   -0.7145    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 O   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
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 O   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
    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 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    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
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    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 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.0000    0.0000 O   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    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 10 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 19 23  2  0  0  0  0
  7 23  1  0  0  0  0
 23 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0254096

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)CC(=O)C1=C(O)C(CC(O)C(C)=C)=C(O)C(C(C)=O)=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C18H24O6/c1-8(2)6-13(21)15-17(23)11(7-12(20)9(3)4)16(22)14(10(5)19)18(15)24/h8,12,20,22-24H,3,6-7H2,1-2,4-5H3

> <INCHI_KEY>
IVCZSTVLAZFXIS-UHFFFAOYSA-N

> <FORMULA>
C18H24O6

> <MOLECULAR_WEIGHT>
336.384

> <EXACT_MASS>
336.157288493

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
48

> <JCHEM_AVERAGE_POLARIZABILITY>
35.41913380705226

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1-[3-acetyl-2,4,6-trihydroxy-5-(2-hydroxy-3-methylbut-3-en-1-yl)phenyl]-3-methylbutan-1-one

> <ALOGPS_LOGP>
2.17

> <JCHEM_LOGP>
4.765658099333334

> <ALOGPS_LOGS>
-2.75

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.71191120228234

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.599715093747384

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0550544167629683

> <JCHEM_POLAR_SURFACE_AREA>
115.06000000000002

> <JCHEM_REFRACTIVITY>
91.26859999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.99e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-[3-acetyl-2,4,6-trihydroxy-5-(2-hydroxy-3-methylbut-3-en-1-yl)phenyl]-3-methylbutan-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 26-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   26-APR-15         0                                  
HETATM    1  C   UNK     0      -1.334   6.930   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.000   6.160   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.334   6.930   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       2.667   4.620   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       4.001   2.310   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.335  -0.000   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       5.335   1.540   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.002  -0.000   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -2.667   0.000   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -1.334   2.310   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    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   23                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   17                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17   10   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   23                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   19    7   24                                                  
CONECT   24   23                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   48    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₂₄O₆

Average Mass

336.3840 Da

Monoisotopic Mass

336.15729 Da

IUPAC Name

1-[3-acetyl-2,4,6-trihydroxy-5-(2-hydroxy-3-methylbut-3-en-1-yl)phenyl]-3-methylbutan-1-one

Traditional Name

1-[3-acetyl-2,4,6-trihydroxy-5-(2-hydroxy-3-methylbut-3-en-1-yl)phenyl]-3-methylbutan-1-one

CAS Registry Number

Not Available

SMILES

CC(C)CC(=O)C1=C(O)C(CC(O)C(C)=C)=C(O)C(C(C)=O)=C1O

InChI Identifier

InChI=1S/C18H24O6/c1-8(2)6-13(21)15-17(23)11(7-12(20)9(3)4)16(22)14(10(5)19)18(15)24/h8,12,20,22-24H,3,6-7H2,1-2,4-5H3

InChI Key

IVCZSTVLAZFXIS-UHFFFAOYSA-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
Medicosma sessiliflora	LOTUS Database	35616633

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
Acylphloroglucinol derivative
Butyrophenone
Acetophenone
Benzenetriol
Phloroglucinol derivative
Benzoyl
Aryl alkyl ketone
Phenol
Benzenoid
Monocyclic benzene moiety
Vinylogous acid
Secondary alcohol
Polyol
Hydrocarbon derivative
Organic oxide
Alcohol
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic 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	2.17	ALOGPS
logP	4.77	ChemAxon
logS	-2.8	ALOGPS
pKa (Strongest Acidic)	7.6	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	115.06 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	91.27 m³·mol⁻¹	ChemAxon
Polarizability	35.42 Å³	ChemAxon
Number of Rings	1	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

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

503991

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1-[3-acetyl-2,4,6-trihydroxy-5-(2-hydroxy-3-methylbut-3-en-1-yl)phenyl]-3-methylbutan-1-one (NP0254096)

MOL for NP0254096 (1-[3-acetyl-2,4,6-trihydroxy-5-(2-hydroxy-3-methylbut-3-en-1-yl)phenyl]-3-methylbutan-1-one)

3D MOL for NP0254096 (1-[3-acetyl-2,4,6-trihydroxy-5-(2-hydroxy-3-methylbut-3-en-1-yl)phenyl]-3-methylbutan-1-one)

3D SDF for NP0254096 (1-[3-acetyl-2,4,6-trihydroxy-5-(2-hydroxy-3-methylbut-3-en-1-yl)phenyl]-3-methylbutan-1-one)

3D-SDF for NP0254096 (1-[3-acetyl-2,4,6-trihydroxy-5-(2-hydroxy-3-methylbut-3-en-1-yl)phenyl]-3-methylbutan-1-one)

PDB for NP0254096 (1-[3-acetyl-2,4,6-trihydroxy-5-(2-hydroxy-3-methylbut-3-en-1-yl)phenyl]-3-methylbutan-1-one)

3D PDB for NP0254096 (1-[3-acetyl-2,4,6-trihydroxy-5-(2-hydroxy-3-methylbut-3-en-1-yl)phenyl]-3-methylbutan-1-one)

SMILES for NP0254096 (1-[3-acetyl-2,4,6-trihydroxy-5-(2-hydroxy-3-methylbut-3-en-1-yl)phenyl]-3-methylbutan-1-one)

INCHI for NP0254096 (1-[3-acetyl-2,4,6-trihydroxy-5-(2-hydroxy-3-methylbut-3-en-1-yl)phenyl]-3-methylbutan-1-one)

Structure for NP0254096 (1-[3-acetyl-2,4,6-trihydroxy-5-(2-hydroxy-3-methylbut-3-en-1-yl)phenyl]-3-methylbutan-1-one)

3D Structure for NP0254096 (1-[3-acetyl-2,4,6-trihydroxy-5-(2-hydroxy-3-methylbut-3-en-1-yl)phenyl]-3-methylbutan-1-one)