Strictly, a substance intended to kill members of the class Insecta. In common usage, any substance used for preventing, destroying, repelling or controlling insects.
| Member | Definition | Class |
|---|
| 1-hexacosanol | A very long-chain primary fatty alcohol that is hexacosane in which a hydrogen attached to one of the terminal carbons is replaced by a hydroxy group. | hexacosan-1-ol |
| 1-naphthylisothiocyanate | | 1-naphthyl isothiocyanate |
| 4-bromo-2-(4-chlorophenyl)-5-(trifluoromethyl)-1h-pyrrole-3-carbonitrile | A pyrrole resulting from the N-dealkylation of the ethoxymethyl group of chlorfenapyr. It is the active insecticide of the proinsecticide chlorfenapyr. | tralopyril |
| 4-dichlorobenzene | A dichlorobenzene carrying chloro groups at positions 1 and 4. | 1,4-dichlorobenzene |
| afidopyropen | An organic heterotetracyclic compound that is 1,3,4,4a,5,6,6a,12,12a,12b-decahydro-2H,11H-benzo[f]pyrano[4,3-b]chromen-11-one which is substituted by methyl groups at positions 4, 6a, and 12b; hydroxy groups at positions 3, 6, and 9; and a cyclopropycarbonyloxymethyl group and a cyclopropylcarbonyloxy group at positions 17 and 18 respectively, and a pyridin-3-yl group at position 14 (the (3S,4R,4aR,6S,6aS,12R,12aS,12bS stereoisomer). It is an insecticide that is effective against sucking insects on fruit, vegetables and nuts. | afidopyropen |
| allyl alcohol | A propenol in which the C=C bond connects C-2 and C-3. It is has been found in garlic (Allium sativum). Formerly used as a herbicide for the control of various grass and weed seeds. | allyl alcohol |
| amitraz | A tertiary amino compound that is 1,3,5-triazapenta-1,4-diene substituted by a methyl group at position 3 and 2,4-dimethylphenyl groups at positions 1 and 5. | amitraz |
| arsenic trioxide | An arsenic oxide in which arsenic and oxygen atoms are present in the ratio 2:3. | diarsenic trioxide |
| bassianolide | A cyclodepsipeptide consisting of a cyclic tetramer of the depsipeptide D-Hiv-N-methyl-L-leucine (where D-Hiv = D-alpha-hydroxyisovaleric acid). Found in the fungal species Beauveria bassiana and Verticillium lecanii, it has insecticidal properties and is used as a commercial biopesticide to control of insects of agricultural, veterinary and medical significance. For elucidation of the structure, see Suzuki et al., Tetrahedron Lett. 1977 v25, 2167-2170. | bassianolide |
| bpmc | A carbamate ester obtained by the formal condensation of 2-sec-butylphenol with methylcarbamic acid. | fenobucarb |
| cevine | A steroid consisting of cevane having an oxygen bridge between positions 4 and 9 and carrying seven additional hydroxy substituents. | cevine |
| chlordecone | An organochlorine compound with insecticidal activity. | chlordecone |
| chlorpyrifos | An organic thiophosphate that is O,O-diethyl hydrogen phosphorothioate in which the hydrogen of the hydroxy group has been replaced by a 3,5,6-trichloropyridin-2-yl group. | chlorpyrifos |
| chlorpyrifos-methyl | An organic thiophosphate that is O,O-dimethyl hydrogen phosphorothioate in which the hydrogen of the hydroxy group has been replaced by a 3,5,6-trichloropyridin-2-yl group. | chlorpyrifos-methyl |
| cuminaldehyde | A member of the class of benzaldehydes that is benzaldehyde substituted by an isopropyl group at position 4. It is a component of essential oils from Cumin and exhibits insecticidal activities. | cuminaldehyde |
| diallyl trisulfide | An organic trisulfide that is trisulfane in which both of the hydrogens are replaced by allyl groups. A component of the essential oil of garlic and a major component of the traditional Chinese medicine allitridium, it exhibits antifungal, antitumour and antioxidant activity | diallyl trisulfide |
| dimethoate | A monocarboxylic acid amide that is N-methylacetamide in which one of the hydrogens of the methyl group attached to the carbonyl moiety is replaced by a (dimethoxyphosphorothioyl)sulfanediyl group. | dimethoate |
| dodecanol | A primary alcohol that is dodecane in which a hydrogen from one of the methyl groups is replaced by a hydroxy group. It is registered for use in apple and pear orchards as a Lepidopteran pheromone/sex attractant, used to disrupt the mating behaviour of certain moths whose larvae destroy crops. | dodecan-1-ol |
| epoxyazadiradione | A limonoid that is azadiradione with an epoxy group across positions 14 and 15. Isolated from Azadirachta indica it exhibits insecticidal activitry against mosquitoes. | epoxyazadiradione |
| ethion | An organic thiophosphate that is S,S'-methanediyl bis[dihydrogen (phosphorodithioate)] in which all the hydroxy groups have been converted to their corresponding ethyl esters respectively. Ethion is an organophosphate insecticide with inhibitory activity towards the enzyme acetylcholinesterase ( EC 3.1.1.7). | ethion |
| euonine | A sesquiterpene alkaloid that has been isolated from Tripterygium wilfordii and exhibits immunosuppressive and insecticidal properties. It was found to be identical with euonine, previously isolated from Euonymous sieboldiana. | wilformine |
| fenitrothion | An organic thiophosphate that is O,O-dimethyl O-phenyl phosphorothioate substituted by a methyl group at position 3 and a nitro group at position 4. | fenitrothion |
| fenoxycarb | A carbamate ester that is the O-ethyl carbamate of 2-(4-phenoxyphenoxy)ethylamine. | fenoxycarb |
| fenthion | An organic thiophosphate that is O,O-dimethyl hydrogen phosphorothioate in which the hydrogen atom of the hydroxy group is replaced by a 3-methyl-4-(methylsulfanyl)phenyl group. It exhibits acaricidal and insecticidal activities. | fenthion |
| flonicamid | A pyridinecarboxamide that is nicotinamide substituted by a trifluoromethyl group at position 4 and a cyanomethyl group at the carbamoyl nitrogen atom. | flonicamid |
| flupyradifurone | A tertiary amino compound that is ammonia in which the nitrogens have been replaced by (6-chloropyridin-3-yl)methyl, 2,2-difluoroethyl, and 5-oxo-2,5-dihydrofuran-3-yl groups, respectively. A nicotinic acetylcholine receptor (AChR) agonist, it is used as an insecticide to control sucking pests in a variety of crops. | flupyradifurone |
| germacrone | A germacrane sesquiterpenoid that has formula C15H22O. It is a natural product found in traditional medicinal plants of the family Zingiberaceae. The compound exhibits a range of pharmacological activities including anti-inflammatory, anticancer, antiviral, anti-androgenic, antioxidant, antimicrobial, antifungal, neuroprotective and insecticidal activities. | (E,E)-germacrone |
| isoprothiolane | A malonate ester that is diisopropyl malonate in which the two methylene hydrogens at position 2 are replaced by a 1,3-dithiolan-2-ylidene group. An insecticide and fungicide used to control a range of diseases including Pyricularia oryzae, Helminthosporium sigmoideum and Fusarium nivale. | isoprothiolane |
| lead arsenate | An inorganic lead salt composed from lead(2+) and arsenate dianion. It was widely used in the United States in the 1950's as an insecticide to control pests in fruit orchards, specifically apples and cherries. | lead arsenate |
| maysin | A flavone C-glycoside that is luteolin attached to a disaccharide residue at position 6. It has been isolated from natural product Petrorhagia velutina and Zea mays and exhibits insecticidal and neuroprotective activities. | maysin |
| methiocarb | A carbamate ester obtained by the formal condensation of the phenolic group of 3,5-dimethyl-4-(methylsulfanyl)phenol with the carboxy group of methylcarbamic acid. | methiocarb |
| methomyl | A carbamate ester obtained by the formal condensation of methylcarbamic acid with the hydroxy group of 1-(methylsulfanyl)acetaldoxime. | methomyl |
| methoxyfenozide | A carbohydrazide that is hydrazine in which the amino hydrogens have been replaced by 3-methoxy-2-methylbenzoyl, 3,5-dimethylbenzoyl, and tert-butyl groups respectively. | methoxyfenozide |
| methyl formate | A formate ester resulting from the formal condensation of formic acid with methanol. A low-boiling (31.5 degreeC) colourless, flammable liquid, it has been used as a fumigant and larvicide for tobacco and food crops. | methyl formate |
| nereistoxin | Toxin isolated from marine segmented worm, Lumbriconereis heterodopa. It is also the active insecticide of the proinsecticide thiocyclam. | nereistoxin |
| pirimicarb | An aminopyrimidine that is N,N,4,5-tetramethylpyrimidin-2-amine substituted by a (dimethylcarbamoyl)oxy group at position 4. | pirimicarb |
| pirimiphos methyl | An organic thiophosphate that is O,O-dimethyl O-pyrimidin-4-yl phosphorothioate substituted by a methyl group at position 6 and a diethylamino group at position 2. | pirimiphos-methyl |
| prothiophos | An organic thiophosphate that is the 2,4-dichlorophenyl ester of O-ethyl S-propyl dithiophosphoric acid. | prothiofos |
| pyrazophos | A member of the class of pyrazolopyrimidines that is the ethyl ester of 2-[(diethoxyphosphorothioyl)oxy]-5-methylpyrazolo[1,5-a]pyrimidine-6-carboxylic acid. A profungicide (by hydrolysis of the thionophosphate group to afford the corresponding 2-hydroxypyrazolopyrimidine fungicide), it is used to control Erysiphe, Helminthosporium and Rhynchospium in cereals. | pyrazophos |
| rediocide a | A diterpenoid of the class of daphnane-type terpenes. It is isolated from Trigonostemon reidioides and has been shown to exhibit insecticidal activity. | rediocide A |
| safrole | A member of the class of benzodioxoles that is 1,3-benzodioxole which is substituted by an allyl group at position 5. It is found in several plants, including black pepper, cinnamon and nutmeg, and is present in several essential oils, notably that of sassafras. It has insecticidal properties and has been used as a topical antiseptic. Although not thought to pose a significant carcinogenic risk to humans, findings of weak carcinogenicity in rats have resulted in the banning of its (previously widespread) use in perfumes and soaps, and as a food additive. | safrole |
| sodium arsenite | An inoganic sodium salt with formula with formula NaAsO2. | sodium arsenite |
| spiromesifen | A butenolide that is but-2-en-4-olide bearing a 2,4,6-trimethylphenyl group at position 3, a 3,3-dimethylbutyryloxy group at position 4 and a spiro-fused cyclopentyl ring at position 5. | spiromesifen |
| sulfluramid | A sulfonamide obtained by the formal condensation of perfluorooctane-1-sulfonic acid with ethylamine. | sulfluramid |
| teflubenzuron | A N-acylurea that is N-carbamoyl-2,6-difluorobenzamide substituted by a 3,5-dichloro-2,4-difluorophenyl group at the terminal nitrogen atom. | teflubenzuron |
| thallium sulfate | A metal sulfate in which the counterion is thallium and the ratio of thallium to sulfate is 2:1. It is a rodenticide used to control rats, squirrels, mice, moles, prairie dogs, ants and cockroaches. It is no longer registered for pesticide use in the United States. | thallium sulfate |
| trichlorfon | A phosphonic ester that is dimethyl phosphonate in which the hydrogen atom attched to the phosphorous is substituted by a 2,2,2-trichloro-1-hydroxyethyl group. | trichlorfon |
| xanthone | The parent compound of the xanthone class consisting of xanthene bearing a single oxo substituent at position 9. | xanthone |
| Protein | Taxonomy | Measurement | Average (mM) | Bioassay(s) | Drugs |
|---|
| 15-hydroxyprostaglandin dehydrogenase [NAD(+)] isoform 1 | Homo sapiens (human) | Potency | 22.5833 | 1 | 3 |
| 15-lipoxygenase, partial | Homo sapiens (human) | Potency | 28.2073 | 1 | 4 |
| 67.9K protein | Vaccinia virus | Potency | 11.2202 | 1 | 1 |
| acetylcholinesterase | Homo sapiens (human) | Potency | 38.7255 | 4 | 39 |
| activating transcription factor 6 | Homo sapiens (human) | Potency | 38.5808 | 2 | 9 |
| aldehyde dehydrogenase 1 family, member A1 | Homo sapiens (human) | Potency | 32.3070 | 1 | 8 |
| alpha-galactosidase | Homo sapiens (human) | Potency | 31.8326 | 2 | 2 |
| Alpha-synuclein | Homo sapiens (human) | Potency | 10.0000 | 1 | 1 |
| apical membrane antigen 1, AMA1 | Plasmodium falciparum 3D7 | Potency | 22.3872 | 1 | 1 |
| AR protein | Homo sapiens (human) | Potency | 34.1382 | 11 | 100 |
| aryl hydrocarbon receptor | Homo sapiens (human) | Potency | 34.5542 | 3 | 40 |
| ATAD5 protein, partial | Homo sapiens (human) | Potency | 0.2310 | 1 | 1 |
| Ataxin-2 | Homo sapiens (human) | Potency | 52.1486 | 1 | 3 |
| ATPase family AAA domain-containing protein 5 | Homo sapiens (human) | Potency | 52.1486 | 1 | 3 |
| bromodomain adjacent to zinc finger domain 2B | Homo sapiens (human) | Potency | 75.0594 | 1 | 2 |
| caspase 7, apoptosis-related cysteine protease | Homo sapiens (human) | Potency | 46.4213 | 1 | 3 |
| caspase-1 isoform alpha precursor | Homo sapiens (human) | Potency | 25.1189 | 1 | 1 |
| caspase-3 | Cricetulus griseus (Chinese hamster) | Potency | 65.7816 | 1 | 4 |
| caspase-3 | Homo sapiens (human) | Potency | 46.4213 | 1 | 3 |
| Caspase-7 | Cricetulus griseus (Chinese hamster) | Potency | 65.7816 | 1 | 4 |
| Caspase-7 | Homo sapiens (human) | Potency | 25.1189 | 1 | 1 |
| Cellular tumor antigen p53 | Homo sapiens (human) | Potency | 58.1651 | 3 | 21 |
| cellular tumor antigen p53 isoform a | Homo sapiens (human) | Potency | 15.9370 | 2 | 2 |
| Chain A, 2-oxoglutarate Oxygenase | Homo sapiens (human) | Potency | 28.1838 | 1 | 1 |
| Chain A, Beta-lactamase | Escherichia coli K-12 | Potency | 39.8107 | 1 | 1 |
| Chain A, Cruzipain | Trypanosoma cruzi | Potency | 31.6228 | 1 | 1 |
| Chain A, Ferritin light chain | Equus caballus (horse) | Potency | 29.8816 | 1 | 2 |
| Chain A, HADH2 protein | Homo sapiens (human) | Potency | 22.5276 | 2 | 5 |
| Chain A, JmjC domain-containing histone demethylation protein 3A | Homo sapiens (human) | Potency | 65.5694 | 1 | 5 |
| Chain A, MAJOR APURINIC/APYRIMIDINIC ENDONUCLEASE | Homo sapiens (human) | Potency | 27.1947 | 1 | 5 |
| Chain A, Putative fructose-1,6-bisphosphate aldolase | Giardia intestinalis | Potency | 12.5594 | 1 | 1 |
| Chain A, TYROSYL-DNA PHOSPHODIESTERASE | Homo sapiens (human) | Potency | 56.7973 | 1 | 4 |
| Chain B, HADH2 protein | Homo sapiens (human) | Potency | 22.5276 | 2 | 5 |
| chromobox protein homolog 1 | Homo sapiens (human) | Potency | 89.7164 | 1 | 4 |
| cytochrome P450 2C9, partial | Homo sapiens (human) | Potency | 3.8902 | 1 | 1 |
| cytochrome P450 2D6 | Homo sapiens (human) | Potency | 36.2898 | 1 | 2 |
| cytochrome P450 3A4 isoform 1 | Homo sapiens (human) | Potency | 18.2158 | 2 | 18 |
| cytochrome P450 family 3 subfamily A polypeptide 4 | Homo sapiens (human) | Potency | 20.9790 | 1 | 4 |
| cytochrome P450, family 19, subfamily A, polypeptide 1, isoform CRA_a | Homo sapiens (human) | Potency | 47.2385 | 1 | 11 |
| DNA polymerase kappa isoform 1 | Homo sapiens (human) | Potency | 23.7781 | 1 | 2 |
| estrogen nuclear receptor alpha | Homo sapiens (human) | Potency | 35.4860 | 12 | 118 |
| estrogen receptor 2 (ER beta) | Homo sapiens (human) | Potency | 44.9971 | 3 | 20 |
| estrogen-related nuclear receptor alpha | Homo sapiens (human) | Potency | 37.7998 | 6 | 73 |
| euchromatic histone-lysine N-methyltransferase 2 | Homo sapiens (human) | Potency | 32.3105 | 1 | 2 |
| farnesoid X nuclear receptor | Homo sapiens (human) | Potency | 36.0382 | 4 | 14 |
| G | Vesicular stomatitis virus | Potency | 3.8902 | 1 | 1 |
| GABA theta subunit | Rattus norvegicus (Norway rat) | Potency | 18.2158 | 1 | 9 |
| Gamma-aminobutyric acid receptor subunit alpha-1 | Rattus norvegicus (Norway rat) | Potency | 18.2158 | 1 | 9 |
| Gamma-aminobutyric acid receptor subunit alpha-2 | Rattus norvegicus (Norway rat) | Potency | 18.2158 | 1 | 9 |
| Gamma-aminobutyric acid receptor subunit alpha-3 | Rattus norvegicus (Norway rat) | Potency | 18.2158 | 1 | 9 |
| Gamma-aminobutyric acid receptor subunit alpha-4 | Rattus norvegicus (Norway rat) | Potency | 18.2158 | 1 | 9 |
| Gamma-aminobutyric acid receptor subunit alpha-5 | Rattus norvegicus (Norway rat) | Potency | 18.2158 | 1 | 9 |
| Gamma-aminobutyric acid receptor subunit alpha-6 | Rattus norvegicus (Norway rat) | Potency | 18.2158 | 1 | 9 |
| Gamma-aminobutyric acid receptor subunit beta-1 | Rattus norvegicus (Norway rat) | Potency | 18.2158 | 1 | 9 |
| Gamma-aminobutyric acid receptor subunit beta-2 | Rattus norvegicus (Norway rat) | Potency | 18.2158 | 1 | 9 |
| Gamma-aminobutyric acid receptor subunit beta-3 | Rattus norvegicus (Norway rat) | Potency | 18.2158 | 1 | 9 |
| Gamma-aminobutyric acid receptor subunit delta | Rattus norvegicus (Norway rat) | Potency | 18.2158 | 1 | 9 |
| Gamma-aminobutyric acid receptor subunit epsilon | Rattus norvegicus (Norway rat) | Potency | 18.2158 | 1 | 9 |
| Gamma-aminobutyric acid receptor subunit gamma-1 | Rattus norvegicus (Norway rat) | Potency | 18.2158 | 1 | 9 |
| Gamma-aminobutyric acid receptor subunit gamma-2 | Rattus norvegicus (Norway rat) | Potency | 18.2158 | 1 | 9 |
| Gamma-aminobutyric acid receptor subunit gamma-3 | Rattus norvegicus (Norway rat) | Potency | 18.2158 | 1 | 9 |
| Gamma-aminobutyric acid receptor subunit pi | Rattus norvegicus (Norway rat) | Potency | 18.2158 | 1 | 9 |
| geminin | Homo sapiens (human) | Potency | 12.4151 | 2 | 6 |
| GLI family zinc finger 3 | Homo sapiens (human) | Potency | 29.6464 | 3 | 37 |
| glp-1 receptor, partial | Homo sapiens (human) | Potency | 10.1578 | 1 | 2 |
| glucocerebrosidase | Homo sapiens (human) | Potency | 25.1189 | 1 | 1 |
| glucocorticoid receptor [Homo sapiens] | Homo sapiens (human) | Potency | 41.8359 | 5 | 18 |
| Glutamate receptor 2 | Rattus norvegicus (Norway rat) | Potency | 41.3456 | 1 | 12 |
| GTP-binding nuclear protein Ran isoform 1 | Homo sapiens (human) | Potency | 0.4109 | 1 | 1 |
| Guanine nucleotide-binding protein G | Homo sapiens (human) | Potency | 50.1187 | 1 | 1 |
| heat shock protein beta-1 | Homo sapiens (human) | Potency | 35.8314 | 2 | 16 |
| Histamine H2 receptor | Cavia porcellus (domestic guinea pig) | Potency | 31.6228 | 1 | 2 |
| histone acetyltransferase KAT2A isoform 1 | Homo sapiens (human) | Potency | 23.5079 | 1 | 3 |
| histone deacetylase 9 isoform 3 | Homo sapiens (human) | Potency | 20.9874 | 2 | 3 |
| Histone H2A.x | Cricetulus griseus (Chinese hamster) | Potency | 93.1799 | 2 | 15 |
| HLA class I histocompatibility antigen, B alpha chain | Homo sapiens (human) | Potency | 3.8902 | 1 | 1 |
| hypoxia-inducible factor 1 alpha subunit | Homo sapiens (human) | Potency | 42.8626 | 2 | 19 |
| hypoxia-inducible factor 1, alpha subunit (basic helix-loop-helix transcription factor) | Homo sapiens (human) | Potency | 40.8708 | 1 | 2 |
| IDH1 | Homo sapiens (human) | Potency | 16.3601 | 1 | 1 |
| importin subunit beta-1 isoform 1 | Homo sapiens (human) | Potency | 44.7680 | 2 | 2 |
| Inositol hexakisphosphate kinase 1 | Homo sapiens (human) | Potency | 3.8902 | 1 | 2 |
| Integrin alpha-IIb | Homo sapiens (human) | Potency | 0.2512 | 1 | 1 |
| Integrin beta-3 | Homo sapiens (human) | Potency | 0.2512 | 1 | 1 |
| Interferon beta | Homo sapiens (human) | Potency | 3.8902 | 1 | 1 |
| interleukin 8 | Homo sapiens (human) | Potency | 74.9780 | 1 | 2 |
| lamin isoform A-delta10 | Homo sapiens (human) | Potency | 23.6545 | 1 | 3 |
| lethal factor (plasmid) | Bacillus anthracis str. A2012 | Potency | 21.7470 | 1 | 3 |
| lethal(3)malignant brain tumor-like protein 1 isoform I | Homo sapiens (human) | Potency | 31.6228 | 1 | 1 |
| Luciferase | Photinus pyralis (common eastern firefly) | Potency | 54.1003 | 2 | 15 |
| Microtubule-associated protein tau | Homo sapiens (human) | Potency | 23.2047 | 2 | 7 |
| mitogen-activated protein kinase 1 | Homo sapiens (human) | Potency | 39.8107 | 1 | 1 |
| muscleblind-like protein 1 isoform 1 | Homo sapiens (human) | Potency | 0.3162 | 1 | 1 |
| nonstructural protein 1 | Influenza A virus (A/WSN/1933(H1N1)) | Potency | 22.3872 | 1 | 1 |
| nuclear factor erythroid 2-related factor 2 isoform 1 | Homo sapiens (human) | Potency | 38.2813 | 4 | 52 |
| nuclear factor erythroid 2-related factor 2 isoform 2 | Homo sapiens (human) | Potency | 14.5810 | 1 | 1 |
| nuclear factor NF-kappa-B p105 subunit isoform 1 | Homo sapiens (human) | Potency | 43.4228 | 1 | 3 |
| nuclear factor of kappa light polypeptide gene enhancer in B-cells 1 (p105), isoform CRA_a | Homo sapiens (human) | Potency | 41.5102 | 2 | 17 |
| Nuclear receptor ROR-gamma | Homo sapiens (human) | Potency | 17.8405 | 1 | 3 |
| nuclear receptor ROR-gamma isoform 1 | Mus musculus (house mouse) | Potency | 21.3905 | 2 | 6 |
| nuclear receptor subfamily 1, group I, member 3 | Homo sapiens (human) | Potency | 29.0568 | 3 | 66 |
| parathyroid hormone/parathyroid hormone-related peptide receptor precursor | Homo sapiens (human) | Potency | 100.0000 | 1 | 1 |
| Parkin | Homo sapiens (human) | Potency | 39.8107 | 1 | 1 |
| peripheral myelin protein 22 | Rattus norvegicus (Norway rat) | Potency | 2.8695 | 1 | 1 |
| peroxisome proliferator activated receptor gamma | Homo sapiens (human) | Potency | 45.8225 | 5 | 24 |
| Peroxisome proliferator-activated receptor alpha | Homo sapiens (human) | Potency | 39.8107 | 1 | 1 |
| peroxisome proliferator-activated receptor delta | Homo sapiens (human) | Potency | 35.6770 | 5 | 12 |
| phosphopantetheinyl transferase | Bacillus subtilis | Potency | 35.9499 | 1 | 6 |
| PINK1 | Homo sapiens (human) | Potency | 39.8107 | 1 | 1 |
| polyunsaturated fatty acid lipoxygenase ALOX12 | Homo sapiens (human) | Potency | 31.0990 | 1 | 2 |
| Polyunsaturated fatty acid lipoxygenase ALOX15B | Homo sapiens (human) | Potency | 31.6228 | 1 | 1 |
| potassium voltage-gated channel subfamily H member 2 isoform d | Homo sapiens (human) | Potency | 25.4251 | 1 | 6 |
| pregnane X nuclear receptor | Homo sapiens (human) | Potency | 33.2732 | 2 | 30 |
| pregnane X receptor | Rattus norvegicus (Norway rat) | Potency | 54.1221 | 1 | 7 |
| progesterone receptor | Homo sapiens (human) | Potency | 27.6634 | 2 | 23 |
| Rap guanine nucleotide exchange factor 3 | Homo sapiens (human) | Potency | 28.1838 | 1 | 1 |
| Rap guanine nucleotide exchange factor 4 | Homo sapiens (human) | Potency | 11.2202 | 1 | 1 |
| RAR-related orphan receptor gamma | Mus musculus (house mouse) | Potency | 25.2153 | 2 | 30 |
| regulator of G-protein signaling 4 | Homo sapiens (human) | Potency | 50.1187 | 1 | 1 |
| retinoic acid nuclear receptor alpha variant 1 | Homo sapiens (human) | Potency | 39.4288 | 3 | 51 |
| retinoid X nuclear receptor alpha | Homo sapiens (human) | Potency | 26.3046 | 4 | 37 |
| serine-protein kinase ATM isoform a | Homo sapiens (human) | Potency | 39.8107 | 1 | 1 |
| serine/threonine-protein kinase PLK1 | Homo sapiens (human) | Potency | 28.3072 | 1 | 2 |
| SMAD family member 2 | Homo sapiens (human) | Potency | 25.2841 | 2 | 7 |
| SMAD family member 3 | Homo sapiens (human) | Potency | 25.2841 | 2 | 7 |
| Smad3 | Homo sapiens (human) | Potency | 25.4830 | 1 | 3 |
| snurportin-1 | Homo sapiens (human) | Potency | 44.7680 | 2 | 2 |
| survival motor neuron protein isoform d | Homo sapiens (human) | Potency | 12.5893 | 1 | 1 |
| TDP1 protein | Homo sapiens (human) | Potency | 21.8218 | 2 | 6 |
| thioredoxin reductase | Rattus norvegicus (Norway rat) | Potency | 50.0500 | 1 | 2 |
| thyroid hormone receptor beta isoform 2 | Rattus norvegicus (Norway rat) | Potency | 45.1050 | 3 | 27 |
| thyroid hormone receptor beta isoform a | Homo sapiens (human) | Potency | 29.1126 | 2 | 10 |
| thyroid stimulating hormone receptor | Homo sapiens (human) | Potency | 27.5293 | 6 | 44 |
| thyrotropin-releasing hormone receptor | Homo sapiens (human) | Potency | 26.3477 | 2 | 6 |
| USP1 protein, partial | Homo sapiens (human) | Potency | 39.8107 | 1 | 1 |
| v-jun sarcoma virus 17 oncogene homolog (avian) | Homo sapiens (human) | Potency | 33.2362 | 2 | 27 |
| vitamin D (1,25- dihydroxyvitamin D3) receptor | Homo sapiens (human) | Potency | 34.7583 | 5 | 20 |
| vitamin D3 receptor isoform VDRA | Homo sapiens (human) | Potency | 48.7602 | 1 | 10 |
| Voltage-dependent calcium channel gamma-2 subunit | Mus musculus (house mouse) | Potency | 41.3456 | 1 | 12 |
| Vpr | Human immunodeficiency virus 1 | Potency | 31.6228 | 1 | 1 |