NP-MRD: Showing NP-Card for isopetasin (NP0227775)

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Record Information

Version

2.0

Created at

2022-09-06 07:12:55 UTC

Updated at

2022-09-06 07:12:55 UTC

NP-MRD ID

NP0227775

Secondary Accession Numbers

None

Natural Product Identification

Common Name

isopetasin

Description

Isopetasin belongs to the class of organic compounds known as eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids. These are sesquiterpenoids with a structure based either on the eremophilane skeleton, its 8,9-seco derivative, or the furoeremophilane skeleton. Eremophilanes have been shown to be derived from eudesmanes by migration of the methyl group at C-10 to C-5. isopetasin is found in Ligularia dictyoneura, Ligularia sagitta, Ligularia subspicata, Petasites formosanus, Petasites hybridus, Petasites japonicus, Petasites pyrenaicus and Tephroseris integrifolia. isopetasin was first documented in 2020 (PMID: 32486467). Based on a literature review a small amount of articles have been published on Isopetasin (PMID: 35062310) (PMID: 35051554) (PMID: 34252512) (PMID: 33849430).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 51 52  0  0  0  0  0  0  0  0999 V2000
    5.4795    2.6248   -0.8488 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5966    1.2547   -1.4032 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7035    0.3086   -1.2105 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8767   -1.0477   -1.7931 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5184    0.5767   -0.4153 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3317    1.7090    0.0960 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5472   -0.4148   -0.1926 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4005   -0.1852    0.5662 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3549   -1.0582    1.8300 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1452   -0.6194    2.6011 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1142   -0.6370    1.8159 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1452   -1.2125    2.3880 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4228   -1.2813    1.7079 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4348   -1.8195    2.2054 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5007   -0.6887    0.3854 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6726   -0.4331   -0.1506 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9537   -0.7191    0.5291 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6998    0.1780   -1.5188 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2794   -0.3519   -0.3876 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0999   -0.0232    0.4794 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0480    1.4914    0.6339 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1713   -0.5334   -0.2051 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2260   -0.1465   -1.6465 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5647    3.1636   -1.2245 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4651    2.6066    0.2421 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3513    3.2502   -1.1413 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4816    1.0380   -2.0028 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9485   -1.2660   -2.0239 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4865   -1.7686   -1.0214 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2229   -1.1458   -2.6793 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4241    0.8584    0.9220 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2431   -0.7979    2.4328 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3649   -2.1260    1.5860 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0963   -1.2963    3.5044 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3626    0.3807    3.0275 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0909   -1.6591    3.3861 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0913   -1.8092    0.6215 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7990   -0.2641   -0.0581 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9442   -0.2427    1.5137 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4569    1.2534   -1.4285 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7283    0.0775   -1.9468 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0003   -0.2976   -2.2057 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5340    0.5088   -1.0389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0709   -1.2086   -1.0593 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0425    1.9573    0.4279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3426    1.9546   -0.0820 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8108    1.7670    1.6883 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0698   -1.6584   -0.1683 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2134   -0.9585   -2.2947 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3115   -0.1158   -1.9460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2481    0.8270   -1.8370 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  3  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 13 15  1  0
 15 19  1  0
 19 20  1  0
 20 21  1  1
 20 22  1  0
 22 23  1  0
 15 16  2  3
 16 17  1  0
 16 18  1  0
 22  8  1  0
 20 11  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  0
  4 28  1  0
  4 29  1  0
  4 30  1  0
  8 31  1  1
  9 32  1  0
  9 33  1  0
 10 34  1  0
 10 35  1  0
 12 36  1  0
 19 43  1  0
 19 44  1  0
 21 45  1  0
 21 46  1  0
 21 47  1  0
 22 48  1  6
 23 49  1  0
 23 50  1  0
 23 51  1  0
 17 37  1  0
 17 38  1  0
 17 39  1  0
 18 40  1  0
 18 41  1  0
 18 42  1  0
M  END


  Mrv1652309062209122D          

 23 24  0  0  1  0            999 V2000
   -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  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
   -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   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  2  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 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
    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 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   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -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  1  0  0  0  0  0  0  0  0  0
    2.1434   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  1  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
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  8  7  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 15 19  1  0  0  0  0
 19 20  1  0  0  0  0
 11 20  1  0  0  0  0
 20 21  1  1  0  0  0
 20 22  1  0  0  0  0
  8 22  1  0  0  0  0
 22 23  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0227775

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C=C(\C)C(=O)O[C@@H]1CCC2=CC(=O)C(C[C@]2(C)[C@H]1C)=C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C20H28O3/c1-7-13(4)19(22)23-18-9-8-15-10-17(21)16(12(2)3)11-20(15,6)14(18)5/h7,10,14,18H,8-9,11H2,1-6H3/b13-7-/t14-,18+,20+/m0/s1

> <INCHI_KEY>
OFDHBFFGRFCQOW-KSEJUSODSA-N

> <FORMULA>
C20H28O3

> <MOLECULAR_WEIGHT>
316.441

> <EXACT_MASS>
316.203844762

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
51

> <JCHEM_AVERAGE_POLARIZABILITY>
35.92150192185427

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,2R,8aR)-1,8a-dimethyl-6-oxo-7-(propan-2-ylidene)-1,2,3,4,6,7,8,8a-octahydronaphthalen-2-yl (2Z)-2-methylbut-2-enoate

> <JCHEM_LOGP>
5.014352119333335

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
17.4224958741692

> <JCHEM_PKA_STRONGEST_BASIC>
-4.3671873781156645

> <JCHEM_POLAR_SURFACE_AREA>
43.370000000000005

> <JCHEM_REFRACTIVITY>
94.35050000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,8aR)-1,8a-dimethyl-6-oxo-7-(propan-2-ylidene)-2,3,4,8-tetrahydro-1H-naphthalen-2-yl (2Z)-2-methylbut-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0      -2.667  -3.080   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      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       1.334  -5.390   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       0.000  -3.080   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+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  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       8.002  -0.000   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.002  -3.080   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.001  -3.850   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   22                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   20                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   19                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   15   20                                                       
CONECT   20   19   11   21   22                                             
CONECT   21   20                                                            
CONECT   22   20    8   23                                                  
CONECT   23   22                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   48    0
END

View in JSmol

Synonyms

Value	Source
S-Isopetasin	MeSH

Chemical Formula

C₂₀H₂₈O₃

Average Mass

316.4410 Da

Monoisotopic Mass

316.20384 Da

IUPAC Name

(1R,2R,8aR)-1,8a-dimethyl-6-oxo-7-(propan-2-ylidene)-1,2,3,4,6,7,8,8a-octahydronaphthalen-2-yl (2Z)-2-methylbut-2-enoate

Traditional Name

(1R,2R,8aR)-1,8a-dimethyl-6-oxo-7-(propan-2-ylidene)-2,3,4,8-tetrahydro-1H-naphthalen-2-yl (2Z)-2-methylbut-2-enoate

CAS Registry Number

Not Available

SMILES

C\C=C(\C)C(=O)O[C@@H]1CCC2=CC(=O)C(C[C@]2(C)[C@H]1C)=C(C)C

InChI Identifier

InChI=1S/C20H28O3/c1-7-13(4)19(22)23-18-9-8-15-10-17(21)16(12(2)3)11-20(15,6)14(18)5/h7,10,14,18H,8-9,11H2,1-6H3/b13-7-/t14-,18+,20+/m0/s1

InChI Key

OFDHBFFGRFCQOW-KSEJUSODSA-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
Ligularia dictyoneura	LOTUS Database	35616633
Ligularia sagitta	LOTUS Database	35616633
Ligularia subspicata	LOTUS Database	35616633
Petasites formosanus	LOTUS Database	35616633
Petasites hybridus	LOTUS Database	35616633
Petasites japonicus	LOTUS Database	35616633
Petasites pyrenaicus	LOTUS Database	35616633
Tephroseris integrifolia	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids. These are sesquiterpenoids with a structure based either on the eremophilane skeleton, its 8,9-seco derivative, or the furoeremophilane skeleton. Eremophilanes have been shown to be derived from eudesmanes by migration of the methyl group at C-10 to C-5.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids

Alternative Parents

Substituents

Eremophilane sesquiterpenoid
O-quinomethane
Quinomethane
Fatty acid ester
Cyclohexenone
Fatty acyl
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Cyclic ketone
Ketone
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxygen compound
Carbonyl group
Organooxygen compound
Organic oxide
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic 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	5.01	ChemAxon
pKa (Strongest Acidic)	17.42	ChemAxon
pKa (Strongest Basic)	-4.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	43.37 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	94.35 m³·mol⁻¹	ChemAxon
Polarizability	35.92 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	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

C00050978

Chemspider ID

4477154

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5318627

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Urda L, Kreuter MH, Drewe J, Boonen G, Butterweck V, Klimkait T: The Petasites hybridus CO(2) Extract (Ze 339) Blocks SARS-CoV-2 Replication In Vitro. Viruses. 2022 Jan 7;14(1):106. doi: 10.3390/v14010106. [PubMed:35062310 ]
Uesugi S, Hakozaki M, Kanno Y, Shiraishi A, Suzuki M, Kimura KI, Shiono Y, Yano A: Petasin is the main component responsible for the anti-adipogenic effect of Petasites japonicus. Fitoterapia. 2022 Mar;157:105130. doi: 10.1016/j.fitote.2022.105130. Epub 2022 Jan 18. [PubMed:35051554 ]
Kodjadjiku U, Nagele B, Halbsguth C, Butterweck V: Extract matrix composition does not affect in vitro leukotriene inhibitory effects of the Petasites hybridus extract Ze 339. Fitoterapia. 2021 Sep;153:104986. doi: 10.1016/j.fitote.2021.104986. Epub 2021 Jul 10. [PubMed:34252512 ]
Kleeberg-Hartmann J, Vogler B, Messlinger K: Petasin and isopetasin reduce CGRP release from trigeminal afferents indicating an inhibitory effect on TRPA1 and TRPV1 receptor channels. J Headache Pain. 2021 Apr 13;22(1):23. doi: 10.1186/s10194-021-01235-5. [PubMed:33849430 ]
Mihajilov-Krstev T, Jovanovic B, Zlatkovic B, Matejic J, Vitorovic J, Cvetkovic V, Ilic B, Dordevic L, Jokovic N, Miladinovic D, Jaksic T, Stankovic N, Stankov Jovanovic V, Bernstein N: Phytochemistry, Toxicology and Therapeutic Value of Petasites hybridus Subsp. Ochroleucus (Common Butterbur) from the Balkans. Plants (Basel). 2020 May 31;9(6):700. doi: 10.3390/plants9060700. [PubMed:32486467 ]
LOTUS database [Link]

Showing NP-Card for isopetasin (NP0227775)

MOL for NP0227775 (isopetasin)

3D MOL for NP0227775 (isopetasin)

3D SDF for NP0227775 (isopetasin)

3D-SDF for NP0227775 (isopetasin)

PDB for NP0227775 (isopetasin)

3D PDB for NP0227775 (isopetasin)

SMILES for NP0227775 (isopetasin)

INCHI for NP0227775 (isopetasin)

Structure for NP0227775 (isopetasin)

3D Structure for NP0227775 (isopetasin)