NP-MRD: Showing NP-Card for (1s)-2-methyl-4-oxo-3-[(2e)-penta-2,4-dien-1-yl]cyclopent-2-en-1-yl (1r,3r)-3-[(1z)-3-methoxy-2-methyl-3-oxoprop-1-en-1-yl]-2,2-dimethylcyclopropane-1-carboxylate (NP0316401)

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Record Information

Version

2.0

Created at

2022-09-11 15:34:29 UTC

Updated at

2022-09-11 15:34:29 UTC

NP-MRD ID

NP0316401

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s)-2-methyl-4-oxo-3-[(2e)-penta-2,4-dien-1-yl]cyclopent-2-en-1-yl (1r,3r)-3-[(1z)-3-methoxy-2-methyl-3-oxoprop-1-en-1-yl]-2,2-dimethylcyclopropane-1-carboxylate

Description

ZINC3875843 belongs to the class of organic compounds known as pyrethrins. These are pyrethroids with a structure based on a skeleton that is characterized by the presence of a chrysanthemic acid esterified with a cyclopentenone derivative. (1s)-2-methyl-4-oxo-3-[(2e)-penta-2,4-dien-1-yl]cyclopent-2-en-1-yl (1r,3r)-3-[(1z)-3-methoxy-2-methyl-3-oxoprop-1-en-1-yl]-2,2-dimethylcyclopropane-1-carboxylate is found in Tanacetum cinerariifolium. Based on a literature review very few articles have been published on ZINC3875843.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112217342D          

 27 28  0  0  1  0            999 V2000
    3.6229   -2.3369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2873   -1.5832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4668   -1.4970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1313   -0.7433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3108   -0.6571    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
    0.1682    0.2681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4448   -0.2839    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0820    1.0886    0.0000 C   0  0  1  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
   -1.3469    1.0886    0.0000 C   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
   -2.0614    1.5011    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8864    1.5011    0.0000 C   0  0  1  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
   -3.6009    0.2636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3153   -0.1489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8864   -0.1489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1719    0.2636    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8864   -0.9739    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6009   -1.3864    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
   -2.9471    2.8914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0007    2.8914    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
    2.2082    0.8973    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  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
  7  9  1  0  0  0  0
  9 10  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 13 11  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  1  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 14 22  1  0  0  0  0
 13 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
  9 25  1  0  0  0  0
 25 26  1  0  0  0  0
  6 26  1  0  0  0  0
 26 27  2  0  0  0  0
M  END

     RDKit          3D

 55 56  0  0  0  0  0  0  0  0999 V2000
    8.4222    2.4043    0.6402 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3974    1.8673    0.9790 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2012    1.2264    1.3811 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0057    1.8738    1.1534 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7114    1.3314    1.5237 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8135    1.1169    0.3140 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1597   -0.0083    0.0861 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1172   -1.1632    0.9806 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4489    0.0849   -1.2297 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0445    0.0073   -1.1187 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6278   -1.1937   -1.3991 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1117   -2.1508   -1.7080 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.5475    2.1168    0.7884 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9315    3.3995    0.6868 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7425   -2.5863   -1.3550 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1045   -3.9375   -1.1133 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0467   -2.6900   -2.1122 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9817    1.2764   -1.9262 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5985    2.0356   -0.7811 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8901    3.2582   -0.7526 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2884    2.8727    0.3470 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7734    3.5492    0.2318 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1585    0.7518    1.3751 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0553    0.2919    1.8578 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1050    2.8353    0.6806 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2234    1.9513    2.2864 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9061    0.3277    1.9968 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3657   -1.9315    0.6911 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1155   -1.6682    1.0035 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9240   -0.8502    2.0510 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8058   -0.8679   -1.7413 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5928   -0.3674   -1.7383 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9737   -2.0455    0.7348 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.6464   -0.8579    0.4318 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.0124   -0.7513    2.1312 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9487    3.7039   -0.3652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9260    3.4233    1.1690 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5722    4.0832    1.2719 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4962   -4.6624   -1.8803 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0277   -3.9817   -1.1523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5506   -4.3316   -0.1479 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0639   -3.6279   -2.7275 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9477   -2.5309   -1.5238 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0093   -1.8767   -2.8823 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2838    1.8706   -2.5137 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8822    1.0109   -2.5658 H   0  0  0  0  0  0  0  0  0  0  0  0
 21 20  1  0
 20 18  1  0
 18 19  2  0
 18 16  1  0
 16 17  1  0
 16 15  2  0
 15 14  1  0
 14 13  1  0
 13 11  1  0
 11 12  2  0
 11 10  1  0
 10  9  1  0
  9 25  1  0
 25 26  1  0
 26 27  2  0
 26  6  1  0
  6  5  1  0
  5  4  1  0
  4  3  2  0
  3  2  1  0
  2  1  2  0
  6  7  2  0
  7  8  1  0
 13 22  1  0
 22 23  1  0
 22 24  1  0
 22 14  1  0
  7  9  1  0
 21 45  1  0
 21 46  1  0
 21 47  1  0
 17 42  1  0
 17 43  1  0
 17 44  1  0
 15 41  1  0
 14 40  1  1
 13 39  1  6
  9 38  1  6
 25 54  1  0
 25 55  1  0
  5 33  1  0
  5 34  1  0
  4 32  1  0
  3 31  1  0
  2 30  1  0
  1 28  1  0
  1 29  1  0
  8 35  1  0
  8 36  1  0
  8 37  1  0
 23 48  1  0
 23 49  1  0
 23 50  1  0
 24 51  1  0
 24 52  1  0
 24 53  1  0
M  END


  Mrv1652309112217342D          

 27 28  0  0  1  0            999 V2000
    3.6229   -2.3369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2873   -1.5832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4668   -1.4970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1313   -0.7433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3108   -0.6571    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
    0.1682    0.2681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4448   -0.2839    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0820    1.0886    0.0000 C   0  0  1  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
   -1.3469    1.0886    0.0000 C   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
   -2.0614    1.5011    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8864    1.5011    0.0000 C   0  0  1  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
   -3.6009    0.2636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3153   -0.1489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8864   -0.1489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1719    0.2636    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8864   -0.9739    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6009   -1.3864    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
   -2.9471    2.8914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0007    2.8914    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
    2.2082    0.8973    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  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
  7  9  1  0  0  0  0
  9 10  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 13 11  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  1  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 14 22  1  0  0  0  0
 13 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
  9 25  1  0  0  0  0
 25 26  1  0  0  0  0
  6 26  1  0  0  0  0
 26 27  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0316401

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C(\C)=C/[C@@H]1[C@@H](C(=O)O[C@H]2CC(=O)C(C\C=C\C=C)=C2C)C1(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C22H28O5/c1-7-8-9-10-15-14(3)18(12-17(15)23)27-21(25)19-16(22(19,4)5)11-13(2)20(24)26-6/h7-9,11,16,18-19H,1,10,12H2,2-6H3/b9-8+,13-11-/t16-,18+,19+/m1/s1

> <INCHI_KEY>
VJFUPGQZSXIULQ-HIORVMPYSA-N

> <FORMULA>
C22H28O5

> <MOLECULAR_WEIGHT>
372.461

> <EXACT_MASS>
372.193674002

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
41.443841332536294

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S)-2-methyl-4-oxo-3-[(2E)-penta-2,4-dien-1-yl]cyclopent-2-en-1-yl (1R,3R)-3-[(1Z)-3-methoxy-2-methyl-3-oxoprop-1-en-1-yl]-2,2-dimethylcyclopropane-1-carboxylate

> <JCHEM_LOGP>
4.1543261393333335

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.088143422797106

> <JCHEM_PKA_STRONGEST_BASIC>
-5.899382667890335

> <JCHEM_POLAR_SURFACE_AREA>
69.67000000000002

> <JCHEM_REFRACTIVITY>
105.51489999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S)-2-methyl-4-oxo-3-[(2E)-penta-2,4-dien-1-yl]cyclopent-2-en-1-yl (1R,3R)-3-[(1Z)-3-methoxy-2-methyl-3-oxoprop-1-en-1-yl]-2,2-dimethylcyclopropane-1-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0       6.763  -4.362   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.136  -2.955   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.605  -2.794   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.978  -1.388   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.447  -1.227   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.820   0.180   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.314   0.500   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.830  -0.530   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.153   2.032   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -1.181   2.802   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -2.514   2.032   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -2.514   0.492   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -3.848   2.802   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      -6.722   2.032   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -6.722   0.492   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -8.055  -0.278   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -5.388  -0.278   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -4.054   0.492   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      -5.388  -1.818   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -6.722  -2.588   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -4.618   4.136   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -5.501   5.397   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -3.735   5.397   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.560   2.658   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.590   1.514   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       4.122   1.675   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   26                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   25                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   22                                                  
CONECT   14   13   15   22                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20                                                            
CONECT   22   14   13   23   24                                             
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25    9   26                                                       
CONECT   26   25    6   27                                                  
CONECT   27   26                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₂₈O₅

Average Mass

372.4610 Da

Monoisotopic Mass

372.19367 Da

IUPAC Name

(1S)-2-methyl-4-oxo-3-[(2E)-penta-2,4-dien-1-yl]cyclopent-2-en-1-yl (1R,3R)-3-[(1Z)-3-methoxy-2-methyl-3-oxoprop-1-en-1-yl]-2,2-dimethylcyclopropane-1-carboxylate

Traditional Name

(1S)-2-methyl-4-oxo-3-[(2E)-penta-2,4-dien-1-yl]cyclopent-2-en-1-yl (1R,3R)-3-[(1Z)-3-methoxy-2-methyl-3-oxoprop-1-en-1-yl]-2,2-dimethylcyclopropane-1-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)C(\C)=C/[C@@H]1[C@@H](C(=O)O[C@H]2CC(=O)C(C\C=C\C=C)=C2C)C1(C)C

InChI Identifier

InChI=1S/C22H28O5/c1-7-8-9-10-15-14(3)18(12-17(15)23)27-21(25)19-16(22(19,4)5)11-13(2)20(24)26-6/h7-9,11,16,18-19H,1,10,12H2,2-6H3/b9-8+,13-11-/t16-,18+,19+/m1/s1

InChI Key

VJFUPGQZSXIULQ-HIORVMPYSA-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
Chrysanthemum cinerariaefolium	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyrethrins. These are pyrethroids with a structure based on a skeleton that is characterized by the presence of a chrysanthemic acid esterified with a cyclopentenone derivative.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acid esters

Direct Parent

Pyrethrins

Alternative Parents

Substituents

Pyrethrin-backbone
Monocyclic monoterpenoid
Monoterpenoid
Carbocyclic fatty acid
Cyclopropanecarboxylic acid or derivatives
Dicarboxylic acid or derivatives
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Methyl ester
Carboxylic acid ester
Ketone
Cyclic ketone
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
Organooxygen compound
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic 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	4.15	ChemAxon
pKa (Strongest Acidic)	18.09	ChemAxon
pKa (Strongest Basic)	-5.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	69.67 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	105.51 m³·mol⁻¹	ChemAxon
Polarizability	41.44 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

4947136

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

6443099

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s)-2-methyl-4-oxo-3-[(2e)-penta-2,4-dien-1-yl]cyclopent-2-en-1-yl (1r,3r)-3-[(1z)-3-methoxy-2-methyl-3-oxoprop-1-en-1-yl]-2,2-dimethylcyclopropane-1-carboxylate (NP0316401)

MOL for NP0316401 ((1s)-2-methyl-4-oxo-3-[(2e)-penta-2,4-dien-1-yl]cyclopent-2-en-1-yl (1r,3r)-3-[(1z)-3-methoxy-2-methyl-3-oxoprop-1-en-1-yl]-2,2-dimethylcyclopropane-1-carboxylate)

3D MOL for NP0316401 ((1s)-2-methyl-4-oxo-3-[(2e)-penta-2,4-dien-1-yl]cyclopent-2-en-1-yl (1r,3r)-3-[(1z)-3-methoxy-2-methyl-3-oxoprop-1-en-1-yl]-2,2-dimethylcyclopropane-1-carboxylate)

3D SDF for NP0316401 ((1s)-2-methyl-4-oxo-3-[(2e)-penta-2,4-dien-1-yl]cyclopent-2-en-1-yl (1r,3r)-3-[(1z)-3-methoxy-2-methyl-3-oxoprop-1-en-1-yl]-2,2-dimethylcyclopropane-1-carboxylate)

3D-SDF for NP0316401 ((1s)-2-methyl-4-oxo-3-[(2e)-penta-2,4-dien-1-yl]cyclopent-2-en-1-yl (1r,3r)-3-[(1z)-3-methoxy-2-methyl-3-oxoprop-1-en-1-yl]-2,2-dimethylcyclopropane-1-carboxylate)

PDB for NP0316401 ((1s)-2-methyl-4-oxo-3-[(2e)-penta-2,4-dien-1-yl]cyclopent-2-en-1-yl (1r,3r)-3-[(1z)-3-methoxy-2-methyl-3-oxoprop-1-en-1-yl]-2,2-dimethylcyclopropane-1-carboxylate)

3D PDB for NP0316401 ((1s)-2-methyl-4-oxo-3-[(2e)-penta-2,4-dien-1-yl]cyclopent-2-en-1-yl (1r,3r)-3-[(1z)-3-methoxy-2-methyl-3-oxoprop-1-en-1-yl]-2,2-dimethylcyclopropane-1-carboxylate)

SMILES for NP0316401 ((1s)-2-methyl-4-oxo-3-[(2e)-penta-2,4-dien-1-yl]cyclopent-2-en-1-yl (1r,3r)-3-[(1z)-3-methoxy-2-methyl-3-oxoprop-1-en-1-yl]-2,2-dimethylcyclopropane-1-carboxylate)

INCHI for NP0316401 ((1s)-2-methyl-4-oxo-3-[(2e)-penta-2,4-dien-1-yl]cyclopent-2-en-1-yl (1r,3r)-3-[(1z)-3-methoxy-2-methyl-3-oxoprop-1-en-1-yl]-2,2-dimethylcyclopropane-1-carboxylate)

Structure for NP0316401 ((1s)-2-methyl-4-oxo-3-[(2e)-penta-2,4-dien-1-yl]cyclopent-2-en-1-yl (1r,3r)-3-[(1z)-3-methoxy-2-methyl-3-oxoprop-1-en-1-yl]-2,2-dimethylcyclopropane-1-carboxylate)

3D Structure for NP0316401 ((1s)-2-methyl-4-oxo-3-[(2e)-penta-2,4-dien-1-yl]cyclopent-2-en-1-yl (1r,3r)-3-[(1z)-3-methoxy-2-methyl-3-oxoprop-1-en-1-yl]-2,2-dimethylcyclopropane-1-carboxylate)