NP-MRD: Showing NP-Card for pyrethrin (NP0195340)

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Record Information

Version

1.0

Created at

2022-09-04 13:11:16 UTC

Updated at

2022-09-04 13:11:16 UTC

NP-MRD ID

NP0195340

Secondary Accession Numbers

None

Natural Product Identification

Common Name

pyrethrin

Description

Allethrin, also known as pynamin or duocide, belongs to the class of organic compounds known as pyrethroids. These are organic compounds similar to the pyrethrins. Some pyrethroids containing a chrysanthemic acid esterified with a cyclopentenone (pyrethrins), or with a phenoxybenzyl group. Allethrin is an extremely weak basic (essentially neutral) compound (based on its pKa). pyrethrin is found in Tanacetum parthenifolium. Allethrin is a potentially toxic compound.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 48 49  0  0  0  0  0  0  0  0999 V2000
    6.2419    0.4291   -1.8590 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8640   -0.0397   -0.6774 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5639    0.8498    0.4380 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1946    0.7631    0.9796 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1946    0.0145    0.6204 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1406   -0.9864   -0.4620 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9949    0.2893    1.4887 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9128    0.4947    0.6043 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1991   -0.3263    0.5429 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2531   -1.3103    1.3150 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2890   -0.0350   -0.4173 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7187   -0.2003    0.0445 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.7455    0.7482   -0.4026 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9501    0.7255    0.1231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2777   -0.2676    1.1790 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0269    1.6811   -0.3095 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1429   -1.1167   -0.9540 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9698   -2.5506   -0.5061 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5275   -1.0034   -2.4212 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3085    1.5413    2.2355 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7831    1.6042    2.1044 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5051    2.2927    2.8735 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4722   -0.1970   -2.7069 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3255    1.4989   -1.9852 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7839   -1.1111   -0.5525 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7396    1.9219    0.1475 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2513    0.6946    1.3188 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0797   -1.2482   -0.7268 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5893   -0.5993   -1.3913 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5925   -1.9665   -0.1824 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8646   -0.5993    2.1321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1499    0.8620   -1.0617 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8055   -0.5555    1.0905 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4447    1.4567   -1.1839 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3517   -0.2271    1.4542 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6496   -0.0354    2.0663 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0407   -1.2709    0.7639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3232    2.2928    0.5752 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9311    1.0809   -0.5663 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7031    2.3041   -1.1514 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8796   -3.0999   -0.8916 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1102   -3.0483   -0.9760 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0152   -2.6661    0.5934 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8889   -1.7513   -2.9578 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6002   -1.2197   -2.5698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2308   -0.0092   -2.8296 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8054    2.4106    1.7328 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0167    1.4850    3.3187 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 14  1  0
 14 16  1  0
 14 13  2  3
 13 12  1  0
 12 11  1  0
 11  9  1  0
  9 10  2  0
  9  8  1  0
  8  7  1  0
  7 20  1  0
 20 21  1  0
 21 22  2  0
 21  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  2  3
  4  5  2  0
  5  6  1  0
 11 17  1  0
 17 18  1  0
 17 19  1  0
 17 12  1  0
  5  7  1  0
 15 35  1  0
 15 36  1  0
 15 37  1  0
 16 38  1  0
 16 39  1  0
 16 40  1  0
 13 34  1  0
 12 33  1  1
 11 32  1  6
  7 31  1  1
 20 47  1  0
 20 48  1  0
  3 26  1  0
  3 27  1  0
  2 25  1  0
  1 23  1  0
  1 24  1  0
  6 28  1  0
  6 29  1  0
  6 30  1  0
 18 41  1  0
 18 42  1  0
 18 43  1  0
 19 44  1  0
 19 45  1  0
 19 46  1  0
M  END


  Mrv1652307282022232D          

 22 23  0  0  0  0            999 V2000
    3.5136    0.3161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0298    1.0886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3153    2.3261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0072    2.2311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1059    2.7459    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8419    2.7459    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6931    0.2299    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2082    0.8973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6009    1.0886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1682    0.2681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3153    1.5011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8357    1.4242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3877    0.8111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8864    1.5011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9752    0.0966    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0820    1.0886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0614    1.5011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3469    1.0886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4739    2.2156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3108   -0.6571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3469    0.2636    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6325    1.5011    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  7  1  2  0  0  0  0
  8  7  1  0  0  0  0
 11  2  1  0  0  0  0
 11  3  1  0  0  0  0
 11  9  2  0  0  0  0
 12  4  1  0  0  0  0
 13  8  1  0  0  0  0
 13 12  2  0  0  0  0
 14  9  1  0  0  0  0
 15 10  1  0  0  0  0
 15 13  1  0  0  0  0
 16 10  1  0  0  0  0
 16 12  1  0  0  0  0
 17 14  1  0  0  0  0
 18 17  1  0  0  0  0
 19  5  1  0  0  0  0
 19  6  1  0  0  0  0
 19 14  1  0  0  0  0
 19 17  1  0  0  0  0
 20 15  2  0  0  0  0
 21 18  2  0  0  0  0
 22 16  1  0  0  0  0
 22 18  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0195340

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CC1C(C(=O)OC2CC(=O)C(CC=C)=C2C)C1(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C19H26O3/c1-7-8-13-12(4)16(10-15(13)20)22-18(21)17-14(9-11(2)3)19(17,5)6/h7,9,14,16-17H,1,8,10H2,2-6H3

> <INCHI_KEY>
ZCVAOQKBXKSDMS-UHFFFAOYSA-N

> <FORMULA>
C19H26O3

> <MOLECULAR_WEIGHT>
302.4079

> <EXACT_MASS>
302.188194698

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
48

> <JCHEM_AVERAGE_POLARIZABILITY>
34.5588698944844

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-methyl-4-oxo-3-(prop-2-en-1-yl)cyclopent-2-en-1-yl 2,2-dimethyl-3-(2-methylprop-1-en-1-yl)cyclopropane-1-carboxylate

> <ALOGPS_LOGP>
3.58

> <JCHEM_LOGP>
4.056190477666667

> <ALOGPS_LOGS>
-4.18

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.088175488996406

> <JCHEM_PKA_STRONGEST_BASIC>
-5.948486023212152

> <JCHEM_POLAR_SURFACE_AREA>
43.370000000000005

> <JCHEM_REFRACTIVITY>
88.70999999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.00e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
pyrethrin

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-JUL-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-JUL-20         0                                  
HETATM    1  C   UNK     0       6.559   0.590   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -9.389   2.032   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -8.055   4.342   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.880   4.165   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -5.798   5.126   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -3.438   5.126   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.027   0.429   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.122   1.675   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -6.722   2.032   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.314   0.500   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -8.055   2.802   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.560   2.659   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.590   1.514   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -5.388   2.802   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.820   0.180   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.153   2.032   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -3.848   2.802   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.514   2.032   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -4.618   4.136   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       2.447  -1.227   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      -2.514   0.492   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      -1.181   2.802   0.000  0.00  0.00           O+0
CONECT    1    7                                                            
CONECT    2   11                                                            
CONECT    3   11                                                            
CONECT    4   12                                                            
CONECT    5   19                                                            
CONECT    6   19                                                            
CONECT    7    1    8                                                       
CONECT    8    7   13                                                       
CONECT    9   11   14                                                       
CONECT   10   15   16                                                       
CONECT   11    2    3    9                                                  
CONECT   12    4   13   16                                                  
CONECT   13    8   12   15                                                  
CONECT   14    9   17   19                                                  
CONECT   15   10   13   20                                                  
CONECT   16   10   12   22                                                  
CONECT   17   14   18   19                                                  
CONECT   18   17   21   22                                                  
CONECT   19    5    6   14   17                                             
CONECT   20   15                                                            
CONECT   21   18                                                            
CONECT   22   16   18                                                       
MASTER        0    0    0    0    0    0    0    0   22    0   46    0
END

View in JSmol

Synonyms

Value	Source
2,2-Dimethyl-3-(2-methyl-1-propenyl)cyclopropanecarboxylic acid 2-methyl-4-oxo-3-(2-propenyl)-2-cyclopenten-1-yl ester	ChEBI
3-Allyl-2-methyl-4-oxo-2-cyclopenten-1-yl chrysanthemate	ChEBI
3-Allyl-2-methyl-4-oxocyclopent-2-en-1-yl 2,2-dimethyl-3-(2-methylprop-1-en-1-yl)cyclopropanecarboxylate	ChEBI
3-Allyl-4-keto-2-methylcyclopentenyl chrysanthemum monocarboxylate	ChEBI
Bioallethrin	ChEBI
Pynamin	ChEBI
Duocide	Kegg
2,2-Dimethyl-3-(2-methyl-1-propenyl)cyclopropanecarboxylate 2-methyl-4-oxo-3-(2-propenyl)-2-cyclopenten-1-yl ester	Generator
3-Allyl-2-methyl-4-oxo-2-cyclopenten-1-yl chrysanthemic acid	Generator
3-Allyl-2-methyl-4-oxocyclopent-2-en-1-yl 2,2-dimethyl-3-(2-methylprop-1-en-1-yl)cyclopropanecarboxylic acid	Generator
3-Allyl-4-keto-2-methylcyclopentenyl chrysanthemum monocarboxylic acid	Generator
Allethrins	MeSH

Chemical Formula

C₁₉H₂₆O₃

Average Mass

302.4079 Da

Monoisotopic Mass

302.18819 Da

IUPAC Name

2-methyl-4-oxo-3-(prop-2-en-1-yl)cyclopent-2-en-1-yl 2,2-dimethyl-3-(2-methylprop-1-en-1-yl)cyclopropane-1-carboxylate

Traditional Name

pyrethrin

CAS Registry Number

Not Available

SMILES

CC(C)=CC1C(C(=O)OC2CC(=O)C(CC=C)=C2C)C1(C)C

InChI Identifier

InChI=1S/C19H26O3/c1-7-8-13-12(4)16(10-15(13)20)22-18(21)17-14(9-11(2)3)19(17,5)6/h7,9,14,16-17H,1,8,10H2,2-6H3

InChI Key

ZCVAOQKBXKSDMS-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
Tanacetum partheniifolium	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyrethroids. These are organic compounds similar to the pyrethrins. Some pyrethroids containing a chrysanthemic acid esterified with a cyclopentenone (pyrethrins), or with a phenoxybenzyl group.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acid esters

Direct Parent

Pyrethroids

Alternative Parents

Substituents

Pyrethroid skeleton
Monoterpenoid
Monocyclic monoterpenoid
Cyclopropanecarboxylic acid or derivatives
Cyclic ketone
Ketone
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic homomonocyclic compounds

External Descriptors

cyclopropanes (CHEBI:34572 )
Cyclopropane and cyclobutane monoterpenoids (C14337 )
Pyrethroid insecticides (C14337 )

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	3.58	ALOGPS
logP	4.06	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	18.09	ChemAxon
pKa (Strongest Basic)	-5.9	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	6	ChemAxon
Refractivity	88.71 m³·mol⁻¹	ChemAxon
Polarizability	34.56 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

Not Available

KEGG Compound ID

C14337

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Allethrins

METLIN ID

Not Available

PubChem Compound

11442

PDB ID

Not Available

ChEBI ID

34572

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for pyrethrin (NP0195340)

MOL for NP0195340 (pyrethrin)

3D MOL for NP0195340 (pyrethrin)

3D SDF for NP0195340 (pyrethrin)

3D-SDF for NP0195340 (pyrethrin)

PDB for NP0195340 (pyrethrin)

3D PDB for NP0195340 (pyrethrin)

SMILES for NP0195340 (pyrethrin)

INCHI for NP0195340 (pyrethrin)

Structure for NP0195340 (pyrethrin)

3D Structure for NP0195340 (pyrethrin)