NP-MRD: Showing NP-Card for Neo-S-petasin (NP0061579)

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Record Information

Version

2.0

Created at

2022-04-28 06:20:51 UTC

Updated at

2022-04-28 06:20:51 UTC

NP-MRD ID

NP0061579

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Neo-S-petasin

Description

S-Neopetasin 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. Neo-S-petasin is found in Petasites fragrans, Petasites hybridus and Petasites japonicus. Based on a literature review very few articles have been published on S-Neopetasin.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 49 50  0  0  0  0  0  0  0  0999 V2000
   -3.4632    2.9707    1.1015 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5693    2.1107    0.1014 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6917    2.3396   -0.8720 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6822    0.9503   -0.1379 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6460    0.9038    0.9454 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7577   -0.2988    0.9139 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3531   -0.5850    2.3672 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4006   -1.5259    0.3820 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6534   -1.5424   -0.0576 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4681   -0.3069   -0.0317 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7089   -0.3779    0.0726 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6216   -2.7642    0.3418 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7995   -2.5712   -0.1001 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3985   -1.2661    0.3565 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7026   -1.0754   -0.1033 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8238   -1.0014    0.6683 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6781   -1.1146    1.9126 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1123   -0.7990    0.0330 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1755   -0.6908   -1.2725 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7384   -0.7795   -2.3408 S   0  0  0  0  0  0  0  0  0  0  0  0
    3.7470    0.7422   -3.3545 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4872   -0.1148    0.0569 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1223    1.2180    0.2186 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6643    2.8310    1.8178 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1133    3.8008    1.2563 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6484    2.3381   -0.2777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7209    1.5797   -1.6572 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5635    3.3755   -1.2481 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2374    0.9656   -1.1566 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2305    0.8630    1.9143 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0562    1.8220    0.9721 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2213   -1.6444    2.5720 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5310    0.0463    2.6405 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1774   -0.2292    3.0197 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0927   -2.4494   -0.4360 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6204   -3.2214    1.3516 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0629   -3.5393   -0.3308 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3819   -3.4361    0.2609 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8500   -2.5880   -1.2112 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4713   -1.3441    1.4815 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0374   -0.7344    0.6229 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1300   -0.5402   -1.7535 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6770    0.8269   -3.9455 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6777    1.6011   -2.6425 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8904    0.7704   -4.0549 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1427   -0.2269   -0.9992 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5792    1.9330   -0.4658 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1541    1.1644   -0.1854 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1170    1.6139    1.2535 H   0  0  0  0  0  0  0  0  0  0  0  0
 21 20  1  0
 20 19  1  0
 19 18  2  0
 18 16  1  0
 16 17  2  0
 16 15  1  0
 15 14  1  0
 14 13  1  0
 13 12  1  0
 12  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 10  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  1
  6 22  1  0
 22 23  1  0
  4  2  1  0
  2  3  1  0
  2  1  2  3
 22 14  1  0
  6  8  1  0
 21 43  1  0
 21 44  1  0
 21 45  1  0
 19 42  1  0
 18 41  1  0
 14 40  1  1
 13 38  1  0
 13 39  1  0
 12 36  1  0
 12 37  1  0
  9 35  1  0
  4 29  1  6
  5 30  1  0
  5 31  1  0
  7 32  1  0
  7 33  1  0
  7 34  1  0
 22 46  1  6
 23 47  1  0
 23 48  1  0
 23 49  1  0
  3 26  1  0
  3 27  1  0
  3 28  1  0
  1 24  1  0
  1 25  1  0
M  END


  Mrv1652304282208202D          

 23 24  0  0  1  0            999 V2000
    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  2  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  2  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
    2.1434   -2.0625    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
    0.0000   -1.6500    0.0000 O   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
   -0.7145   -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   -4.1250    0.0000 S   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
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  4 10  1  0  0  0  0
 10 11  1  0  0  0  0
  1 11  1  0  0  0  0
 11 12  1  1  0  0  0
 10 13  1  1  0  0  0
  8 14  1  1  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
  1 17  1  6  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0061579

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C19H26O3S/c1-12(2)15-11-19(4)13(3)17(22-18(21)8-9-23-5)7-6-14(19)10-16(15)20/h8-10,13,15,17H,1,6-7,11H2,2-5H3/b9-8-/t13-,15+,17+,19+/m0/s1

> <INCHI_KEY>
OHANKWLYFDFHOJ-OXRZYUPZSA-N

> <FORMULA>
C19H26O3S

> <MOLECULAR_WEIGHT>
334.47

> <EXACT_MASS>
334.160265871

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
49

> <JCHEM_AVERAGE_POLARIZABILITY>
36.62465624289551

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,2R,7R,8aR)-1,8a-dimethyl-6-oxo-7-(prop-1-en-2-yl)-1,2,3,4,6,7,8,8a-octahydronaphthalen-2-yl (2Z)-3-(methylsulfanyl)prop-2-enoate

> <ALOGPS_LOGP>
4.01

> <JCHEM_LOGP>
4.311197077333334

> <ALOGPS_LOGS>
-5.20

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
18.874165079856926

> <JCHEM_PKA_STRONGEST_ACIDIC>
17.09377283675959

> <JCHEM_PKA_STRONGEST_BASIC>
-5.022897852901604

> <JCHEM_POLAR_SURFACE_AREA>
43.370000000000005

> <JCHEM_REFRACTIVITY>
96.33719999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.09e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,7R,8aR)-1,8a-dimethyl-6-oxo-7-(prop-1-en-2-yl)-1,2,3,4,7,8-hexahydronaphthalen-2-yl (2Z)-3-(methylsulfanyl)prop-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       8.002  -0.000   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.001  -3.850   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.002  -3.080   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       0.000  -3.080   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       1.334  -5.390   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   22  S   UNK     0       0.000  -7.700   0.000  0.00  0.00           S+0
HETATM   23  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
CONECT    1    2   11   17                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   10                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   14                                                  
CONECT    9    8   10                                                       
CONECT   10    9    4   11   13                                             
CONECT   11   10    1   12                                                  
CONECT   12   11                                                            
CONECT   13   10                                                            
CONECT   14    8   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17    1   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   48    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₂₆O₃S

Average Mass

334.4700 Da

Monoisotopic Mass

334.16027 Da

IUPAC Name

(1R,2R,7R,8aR)-1,8a-dimethyl-6-oxo-7-(prop-1-en-2-yl)-1,2,3,4,6,7,8,8a-octahydronaphthalen-2-yl (2Z)-3-(methylsulfanyl)prop-2-enoate

Traditional Name

(1R,2R,7R,8aR)-1,8a-dimethyl-6-oxo-7-(prop-1-en-2-yl)-1,2,3,4,7,8-hexahydronaphthalen-2-yl (2Z)-3-(methylsulfanyl)prop-2-enoate

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C19H26O3S/c1-12(2)15-11-19(4)13(3)17(22-18(21)8-9-23-5)7-6-14(19)10-16(15)20/h8-10,13,15,17H,1,6-7,11H2,2-5H3/b9-8-/t13-,15+,17+,19+/m0/s1

InChI Key

OHANKWLYFDFHOJ-OXRZYUPZSA-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
Petasites fragrans	Plant	KNApSAcK
Petasites hybridus	LOTUS Database	35616633
Petasites japonicus	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
Cyclohexenone
Vinylogous thioester
Acrylic acid or derivatives
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Carboxylic acid ester
Ketone
Thioenolether
Cyclic ketone
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Sulfenyl compound
Organooxygen compound
Carbonyl group
Organic oxide
Organic oxygen compound
Organosulfur compound
Hydrocarbon derivative
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	4.01	ALOGPS
logP	4.31	ChemAxon
logS	-5.2	ALOGPS
pKa (Strongest Acidic)	17.09	ChemAxon
pKa (Strongest Basic)	-5	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	5	ChemAxon
Refractivity	96.34 m³·mol⁻¹	ChemAxon
Polarizability	36.62 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

52083606

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

91800184

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Neo-S-petasin (NP0061579)

MOL for NP0061579 (Neo-S-petasin)

3D MOL for NP0061579 (Neo-S-petasin)

3D SDF for NP0061579 (Neo-S-petasin)

3D-SDF for NP0061579 (Neo-S-petasin)

PDB for NP0061579 (Neo-S-petasin)

3D PDB for NP0061579 (Neo-S-petasin)

SMILES for NP0061579 (Neo-S-petasin)

INCHI for NP0061579 (Neo-S-petasin)

Structure for NP0061579 (Neo-S-petasin)

3D Structure for NP0061579 (Neo-S-petasin)