Decane-1,10-dithiol is an important raw material and intermediate used in organic synthesis, pharmaceuticals and agrochemicals.

Decanedioic acid aslo know as Sebacic acid. It is produced from castor oil by using sodium hydroxide, sulfuric acid with catalysts including zinc oxide and phenol.[citation needed] Byproducts include glycerol, octanol and polymer residue. Sebacic acid has been used in the synthesis of: biodegradable and elastomeric polyesters [poly(glycerol sebacate)], novel bio-nylon, PA5.10, novel temperature-response hydrogel based on poly(ether-ester anhydride) nanoparticle for drug-delivery applications.

Polytetramethylene sebacate was prepared from dimethyl sebacate. Dimethyl sebacate was used in the biosynthesis of oligomeric sebacates as lubricant oils. Dimethyl sebacate was a convenient starting material for cyclization of N-Succinylglycine dimethyl ester.

Dibenzyl sebacate is a biochemical.

Perfluorosebacic acid (Hexadecafluorosebacic acid) is a perfluoroalkanedicarboxylic acid, useful in the preparation of synthetic polymers.

Rorifone is a biochemical.

2-Methyldecanenitrile is a component in perfume compositionalso. It is also known as frutonile. Frutonile has an intense peach character with lactonic undertones. Frutonile is stable accross the whole pH range, allowing the perfumers to create a stable fruity effect at low concentration in any applications, including bleach system.

Phosphonic acid, P-decyl- is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff. It is used in stabilizing dye-sensitized solar cell.

Decanoic acid is a lipid used in manufacturing of esters for artificial fruit flavors and perfumes.

Tricaprin is used to construct solid lipid nanoparticles (SLNs) as delivery system for bromocriptine (B682600, Mesylate salt). It is also used in cationic SLNs to enhance p53 tumor suppressor gene transfer to lung cancer cells.

Isopropyl caprate is a biochemical.

Monoctanoin component B also is known as 1-Decanoyl-rac-glycerol. It is a monoacylglyecrol with antibacterial activity. Studies show that 1-Decanoyl-rac-glycerol maybe potential apoptotic agents in T-cells.

2-Hydroxydecanoic acid is a fatty acid found in the lipophilic portion of the lipopolysaccharide fraction of P. ovalis, an aerobic bacterium.1 Synthesis of the hydroxy portion of 2-hydroxy decanoic acid occurs through oxygenation by monooxygenase, using molecular O2 as its substrate.

1,3-Didecanoylglycerol is a saturated diacylglycerol with decanoic acid (Item No. 20838) at the sn-1 and sn-3 positions. It has been used in the formation of lipid monolayers in the study of lipases.

3-hydroxydecanoic acid is a medium-chain fatty acid that is decanoic acid substituted at position 3 by a hydroxy group. It has a role as an antimitotic and an Escherichia coli metabolite. It is a 3-hydroxy fatty acid and a medium-chain fatty acid. It derives from a decanoic acid. It is a conjugate acid of a 3-hydroxydecanoate. 3-Hydroxycapric acid is a normally occurring carboxylic acid in human blood plasma. It also induces a reversible shape change of the membrane crenation in human erythrocytes.

Didecanoyltriethylene glycol ester is a biochemical.

Methyl decanoate is an unsaturated biodiesel fuel surrogate. It can also be used as flavor and fragrance ingredients.

Monomethyl sebacate is a biochemical.

Pentyl decanoate is a biochemical.

Propyl caprate is a biochemical.

Sodium decanoate, or sodium caprate, is the sodium salt of caproic acid, a 10-carbon saturated fatty acid. It has amphiphilic character and can form micelles and liquid crystalline phases in aqueous solution. In a chemical model system, sodium caprate has been used in 13C NMR studies of the addition of hydrophilic and hydrophobic molecules to the 1-monooleoyl glycerol/water system, to elucidate the transport of biologically active molecules.

Decanoyl Chloride is used in the synthesis of an effective metalloproteinase inhibitor. Also acts as a reagent in the synthesis of reversible α-ketoheterocycle inhibitors of fatty acid amide hydrolase as potnetial analgesics.

Decanoyl-coenzyme A is a thioester of decanoic acid and CoA. It inhibits the activity of citrate synthase (CS) and glutamate dehydrogenase (GDH) in mitochondria. Decanoyl CoA also binds the fatty acid metabolism regulator protein (FadR) promoter in E. coli. It is produced during isomerase-dependent β-oxidation of oleic acid.

Decanoyllevocarnitine is an ester derivative of L-carnitine (Cay-21489). It increases the formation of C24 fatty acid intermediates, as well as docosapentaenoic and docosahexaenoic acid (Cay-90310) in rat hepatocytes.

3-Hydroxydecanoic acid, (3R)- is active against Bacillus subtilis, Escherichia coli and Staphyllococcus aureus. fungistatic activity against Candida albicans.

3-Hydroxydecanoic acid, (3S)- is a compound useful in organic synthesis.

Decaprenoic acid is a branched carboxylic acid compound for organic synthesis and proteomics research.

Decaphosphenonium bromide is a biochmeical.

Delmopinol can be used in therapeutic use and biological study for its effect and fluoride on acid adaptation and acid production in dental plaque biofilms.

S-Adenosyl-3-methylthiopropylamine is a substrate that is involved in the biosynthesis of polyamines including spermidine, spermine, and thermospermine.

Decarboxyl oflA degradation product of Oflaxacin which is a synthetic broad-spectrum antimicrobial agent.oxacin.

Decarboxy Enrofloxacin (Enrofloxacin EP Impurity F) is an Enrofloxacin (E557800) impurity.

is a compound related to Zolmitriptan (Z639000), which is Serotonin 5HTID-receptor agonist.

Decarboxyl ofloxacin, (S)- is a degradation product of Levofloxacin.

6-Isopropyl-2-decalone is used in the synthesis of 6-Isopropyl-2-decahydronaphthalenol,which is a fragrance raw material, used in the perfumery industry.

N,N-Diphenylamine is an aromatic amine containing two phenyl substituents. It has been used as a fungicide for the treatment of superficial scald in apples and pears, but is no longer approved for this purpose within the European Union. It has a role as a carotogenesis inhibitor, an antioxidant, an EC 1.3.99.29 [phytoene desaturase (zeta-carotene-forming)] inhibitor and an antifungal agrochemical. It is an aromatic amine, a secondary amino compound and a bridged diphenyl fungicide.

TrichloromelamineTrichloromelamine is a solid disinfectant/sanitizer used in many antimicrobial applications. It is an EPA registered active ingredient which is formulated as a food contact surface sanitizer, 3rd sink sanitizer, and hard surface disinfectant. It was first used by the US Military as a fruit and vegetable disinfectant.

sec-Butylamine, (+/-)-2-Aminobutane is an important raw material and intermediate used in organic synthesis, pharmaceuticals and agrochemicals.

Deceth-3 is a non-ionic surfactant.

Deceth-6 is a nonionic surfactant useful for proteomics research.

Dechlorohaloperidol is also known as Haloperidol impurity B.

Dicyclohexylamine nitrite is a biochemical.

Dechloro perphenazine is the dechlorinated analogue of Perphenazine (P291100), an D2 dopamine receptor antagonist; α-adrenergic receptor antagonist and σ-receptor agonist.

Dechlorogriseofulvin is a major photoproduct of Griseofulvin.

Dechlorane plus (abbrev. DDC-CO) is a polychlorinated flame retardant produced by Oxychem. Its log P is 9.3. It is produced by the Diels-Alder reaction of two equivalents of hexachlorocyclopentadiene with one equivalent of cyclooctadiene. The syn and anti isomer are formed in the approximate ratio of 1:3.

Dechlorane 603 is a chlorinated polycyclic compound that acts as an antioxidant with prolonged thermal stability.

Dechloro trazodone is an antipsychotic with potential use as a schizophrenia agent. Trazodone impurity B.

Tafluprost ethyl amide is a prostaglandin derivative. Tafluprost ethyl amide is capable of intraocular pressure (IOP) reduction and influencing eyelash growth. Tafluprost ethyl amide can be used in antiglaucoma ophthalmic compositions or cosmetics.

Sodium thiosulfate is applied in a widely useful thiosulfate-assisted biochemical used for synthesis of a variety of diamine-CuCN complexes.

Lodelaben is a human neutrophil elastase inhibitor, the inhibition of human neutrophil elastase (HNE) by Lodelaben is non-competetive.

Declenperon acts as a reagent for antimalarial drug lead identification. The are also used in the chemical development of selective and specific serotonin S2-antagonists.

Decloxizine hydrochloride is a biochemical.

Decursinol may be a beneficial antimetastatic agent, targeting MMPs and its upstream signaling molecules; it inhibits the proliferation and invasion of CT-26 colon carcinoma cells, might via downregulated ERK and JNK phosphorylation.

Decursinol angelate has anti-tumor, anti-inflammatory, anti-oxidant, and hepatoprotective activities, it inhibits VEGF-induced angiogenesis via suppression of the VEGFR-2-signaling pathway; it also suppresses invasion and inflammatory activation of cancer cells through modulation of PI3K/AKT, ERK and NF-kappaB, its anti-inflammatory activity may contribute to its anti-cancer activity.Decursinol angelate has protective effects against amyloid β-protein-induced oxidative stress in the PC12 cell line. It improves wound healing by upregulating the expression of genes encoding extracellular matrix remodeling proteins, inflammatory cytokines, and growth factors. Decursinol angelate has in vitro and in vivo antifungal activity against Magnaporthe oryzae, the causal agent of rice blast.

Amantanium bromide is a quaternary ammonium compound, which is used as an antiseptic/disinfectant for therapeutic fuction.

Decyl borate is a biochemical.

Decyl glucoside synthesized by direct glucosidation of d-glucose over zeolite catalysts has estrogenicity. It is non-endocrine disruptive surfactant.

Undecanol, also known by its IUPAC name 1-undecanol or undecan-1-ol, and by its trivial names undecyl alcohol and hendecanol, is a fatty alcohol. Undecanol is a colorless, water-insoluble liquid of melting point 19 °C and boiling point 243 °C.

Decyl cyanoacetate is a biochemical.

Decyl chloroformate is an n-alkyl chloroformate derivative that can be prepared by reacting decyl alcohol with triphosgene. Decyl chloroformate may be used in the preparation of (S)-(+)-N-decoxycarbonyl-leucine, a chiral surfactant. It may also be used to synthesize decyl chloride via decarboxylation in the presence of dimethylformamide.

Decyl disulfide is a biochemical.

Decyl acetate is found in citrus. Decyl acetate is a flavouring agent. Decyl acetate is present in citrus peels, apple, melon, strawberry, celery and other foodstuffs. Decyl acetate is used in apple, orange and rum flavours.

Sulfachlorpyridazine, also known as Sonilyn, Cluricol, Durasulf, and Ba 10370, is an antibacterial agent typically used in agricultural practices.

Oxprenolol hydrochloride is a non-selective beta-adrenergic blocking agent that also possesses intrinsic sympathomimetic activity (ISA) and membrane stabilizing effects. Oxprenolol hydrochloride undergoes first pass metabolism with only 30% of an oral dose reaching the systemic circulation. The drug is approximately 80% protein bound and is eliminated primarily by glucuronidation in the liver. Less than 4% of oxprenolol hydrochloride is excreted unchanged in the urine. Oxprenolol hydrochloride may reduce the heart rate and prolong the effective and functional atrioventricular nodal refractory period. It appears to be comparable to other beta blockers in the treatment of hypertension and angina pectoris with no additional adverse reactions.

Benazolin is a synthetically produced chemical compound from the group of thiazolinones (thiazolines with a keto group) or benzothiazolinones. The colorless, crystalline solid is used predominantly as a herbicide agent.

Xipamide is a sulfamoylbenzamide analog of Clopamide. It is a diuretic as well as a saluretic with antihypertensive activity. It is bound to plasma proteins, thus has a delayed onset and prolonged action.

Cystamine, also known as Aminoethyl-SS-ethylamine, is a cleavable PEG Linker and radiation-protective agent that interferes with sulfhydryl enzymes. It may also protect against carbon tetrachloride liver damage.

Chlorpropham is an agricultural chemical that acts as a plant growth regulator and herbicide.

Befunolol is a beta blocker with intrinsic sympathomimetic activity used in the management of open-angle glaucoma. It also acts as a β adrenoreceptor partial agonist.

Bemegride is a central nervous system stimulant that is used to induce convulsions in experimental animals. It has also been used as a respiratory stimulant and in the treatment of barbiturate overdose.

Benalaxyl is an agricultural chemical typically used as a fungicide.

Flurtamone is an agricultural chemical mainly used as an herbicide.

Fenbutatin oxide, also known as Vendex, is an organometallic insecticide chemical mainly used in agricultural practices to kill ticks and mites.

Acibenzolar-S-methyl is a fungicide that works by activating a plant's own defense system by increasing the transcription of W-box controlled genes such as CAD1, NPR1 and PR2.

Salicylamide is a non-steroidal anti-inflammatory agent with analgesic and antipyretic properties. Its medicinal uses are similar to those of aspirin.

Khellin is a vasodilator that also has bronchodilatory action. It has been employed in the treatment of angina pectoris, in the treatment of asthma, and in conjunction with ultraviolet light A, has been tried in the treatment of vitiligo.

Dichlorvos is an organophosphorus insecticide that inhibits acetylcholinesterase.

Tralomethrin is an agricultural chemical used as a pyrethroid insecticide. It kills by modifying the gating kinetics of the sodium channels in neurons, increasing the length of time the channel remains open after a stimulus, thereby depolarizing the neuron for a longer period of time. This leads to uncontrolled spasms, paralysis, and eventual death.

Myrtenal is a natural monoterpene that occurs in plants such as cumin, pepper, mint and eucalyptus. It was found to attenuate diethylnitrosamine-induced hepatocellular carcinoma in rats by stabilizing intrinsic antioxidants and modulating apoptotic and anti-apoptotic cascades. Myrtenal has also shown activity as an inhibiting agent of acetylcholinesterase, a known Alzheimer target.

Benodanil is an agricultural chemical primarily used as a fungicide, bactericide, and wood preservative.

Benoxacor is an inert agricultural chemical that acts as an herbicide safener to protect crops from herbicide toxicity.

Brodifacoum is a highly lethal 4-hydroxycoumarin vitamin K antagonist anticoagulant poison. In recent years, it has become one of the world's most widely used pesticides. It is typically used as a rodenticide but is also used to control larger pests such as possum. Brodifacoum has an especially long half-life in the body, which ranges to several months, requiring prolonged treatment with antidotal vitamin K for both human and pet poisonings. It has one of the highest risks of secondary poisoning to both mammals and birds.

Herkinorin is an opioid analgesic that is an analogue of the natural product Salvinorin A. Unlike Salvinorin A which is a selective κ-opioid agonist with no significant μ-opioid receptor affinity, herkinorin is a μ-opioid agonist with more than 100x higher μ-opioid affinity and 50x lower κ-opioid affinity compared to Salvinorin A. Herkinorin is a semi-synthetic compound, made from Salvinorin B, which is most conveniently made from Salvinorin A by deacetylation, as while both Salvinorin A and Salvinorin B are found in the plant Salvia divinorum, Salvinorin A is present in larger quantities.

Tribenoside in conjunction with lidocaine can be used to treat hemorrhoids.

BGC 20-761 is a selective, high affinity SR-6 antagonist.

Dalapon is a selective herbicide used to control perennial grasses. The major use of dalapon is on food crops including sugarcane and sugar beets. Its use is no longer authorized in France. The National Institute for Occupational Safety and Health in the United States has identified it as a potential workplace hazard. The recommended time-weighted average exposure limit is 6 milligrams per cubic meter during a 10-hour workday. Exposure to dalapon affects the eyes, central nervous system, digestive system, respiratory system, and skin. Dalapon can be absorbed through inhalation, eye contact, skin contact, or by ingesting it. The symptoms of dalapon exposure include eye irritation, central nervous system depression, bradycardia, vomiting, diarrhea, loss of appetite, fatigue, burn, upper respiratory irritation, and skin irritation. First aid measures for exposure include artificial respiration, immediate eye irrigation, and immediate washing with water. Immediate medical attention should be sought if dalapon is ingested.

Siccanin, also known as NSC 135048, is an antifungal antibiotic with antidermatophytic properties.

Bicyclomycin (Bicozamycin) is a broad spectrum antibiotic active against Gram-negative bacteria and the Gram-positive bacterium, Micrococcus luteusn that was isolated from Streptomyces sapporonesis and Streptomyces aizumenses in 1972. It belongs to a class of naturally occurring 2,5-diketopiperazines, that are among the most numerous of all the naturally occurring peptide antibiotics. This clinically useful antibiotic is rapidly absorbed in man when given intramuscularly, has low toxicity and has been used to treat diarrhea in humans and bacterial diarrhea in calves and pigs.

Cefadroxil, also known as Duricef, is an antibiotic effective against pyodermic skin diseases, such as Staphylococcus aureus and Streptococcus pyogenes.

Bikaverin, also known as Lycopersin, is a reddish pigment produced by different fungal species, most of them from the genus Fusarium, with antibiotic properties against certain protozoa and fungi. The biological properties of bikaverin include antitumoral activity against different cancer cell lines.

Beclometasone, also known as Beclomethasone, is an anti-inflammatory, synthetic glucocorticoid. It is used topically as an anti-inflammatory agent and in aerosol form for the treatment of asthma.

Ambroxol is a metabolite of Bromhexine that stimulates mucociliary action and clears the air passages in the respiratory tract. It is usually administered as the hydrochloride.

Bropirimine is an immunostimulant that has an antitumor effect on superficial transitional cell carcinoma of the bladder.

Butamirate, particularly Butamirate citrate, is a cough suppressant that works by acting centrally through the receptors in the brainstem. It has a very beneficial effect, because it reduces the resistance in the airways by inhibiting bronchospasm and anti-inflammatory effect.

Phostriecin, also known as Sultriecin, is an antifungal and antitumor antibiotic from Streptomyces roseiscleroticus.

Carbutamide is a sulfonylurea antidiabetic agent with similar actions and uses to chlorpropamide.

Niceritrol is an ester of nicotinic acid that lowers cholesterol and triglycerides in total plasma and in the VLD- and LD-lipoprotein fractions.

Xenalipin is a hypolipidemic that reduces blood cholesterol and triglycerides in rats.

Methisazone is an antiviral agent effective against pox viruses.

BW245C has potent platelet anti-aggregating actions following parenteral or oral administration which makes this hydantoin a potentially-useful anti-thrombotic prostaglandin analogue.

Phenobarbital is a barbituric acid derivative that acts as a nonselective central nervous system depressant. It potentiates GAMMA-AMINOBUTYRIC ACID action on GABA-A RECEPTORS, and modulates chloride currents through receptor channels. It also inhibits glutamate induced depolarizations. Phenobarbital is discontinued.

Carazolol is a beta1/beta2 adrenoceptor antagonist of high potency used in the treatment of hypertension. Its affinity for the beta 3-adrenoceptor was determined in Chinese hamster ovary cells transfected with the gene of the human or the murine beta 3-adrenoceptor. Carazolol is recognized with a nanomolar affinity, which positions it among the best ligands for beta 3-adrenoceptors.

Cefapirin is an antibiotic effective against gram-negative and gram-positive organisms.

Ocinaplon appears to be a well-tolerated and effective treatment for GAD. It produces a rapid onset of anxiolytic action absent the side effects (e.g., dizziness, sedation) typically reported following anxiolytic doses of benzodiazepines.

Leucovorin is the active metabolite of folic acid. Leucovorin is used principally as its calcium salt as an antidote to folic acid antagonists which block the conversion of folic acid to folinic acid.

Paramethasone is a glucocorticoid with the general properties of corticosteroids. It has been used by mouth in the treatment of all conditions in which corticosteroid therapy is indicated except adrenal-deficiency states for which its lack of sodium-retaining properties makes it less suitable than Hydrocortisone with supplementary Fludrocortisone.

Curcumenol is a sesquiterpene isolated from Curcuma zedoaria is known to possess a variety of health and medicinal values which includes neuroprotection, anti-inflammatory, anti-tumor and hepatoprotective activities.

Cynaropicrin is the first plant natural product with in vivo activity against Trypanosoma brucei.

Cyclobendazole is an antihelmintic; benzimidazole derivative related to mebendazole.

Cyheptamide is an anticonvulsant.

Alminoprofen is a nonsteroidal anti-inflammatory agent that was found to significantly suppress passive anaphylactic bronchoconstrictions at 30 mg/kg given intraduodenally, while ibuprofen did not at the same doses.

Levcromakalim, also known as Lemakalim, is an anti-asthmatic, antihypertensive, and potassium-ATP channel opener.

Oxethazaine is a surface anesthetic used mainly orally in chronic gastritis & heartburn to analgize the gastric mucosa.

Spiroxatrine is a potent dopamine antagonist that most likely functions as an agonist at the 5-HT1A receptor. This compound is similar to buspirone in that it has a prominent dopamine antagonist component and has been found to produce greater anxiolytic effects when combined with buspirone.

Esmolol is a short acting hyperselective β-adrenergic blocker effective in blunting adrenergic response to several perioperative stimuli and so it might interfere in the effect of the anesthetic drugs on the brain. Esmolol is effective not only in attenuating intraoperative hemodynamic changes related to sympathetic overdrive but also in minimizing significant propofol and sevoflurane requirements without compromising the hemodynamic status.

Piribedil is a dopamine D2 agonist. It is used in the treatment of Parkinson disease, particularly for alleviation of tremor. It has also been used for circulatory disorders and in other applications as a D2 agonist.

Syrosingopine has been found to potentiate the anticancer activity of widely used diabetic drug metformin by sensitizing cancer cells to metformin.

Chlorhexidine is a disinfectant and topical anti-infective agent used also as mouthwash to prevent oral plaque.

Norgestrel is a synthetic progestational agent with actions similar to those of PROGESTERONE. This racemic or (±)-form has about half the potency of the levo form (LEVONORGESTREL). Norgestrel is used as a contraceptive, ovulation inhibitor, and for the control of menstrual disorders and endometriosis.

Sulindac sulfone is an mTORC1 pathway inhibitor and a metabolite of Sulindac. Sulindac sulfone inhibits colon cancer cell growth and induces cell cycle arrest. Sulindac sulfone is used in cancer research.

Fucosterol has been reported to have antioxidant, antidiabetic, and anti-inflammatory effects. In one study, fucosterol exhibited a protective effect on LPS-induced acute lung injury with a possible mechanism inhibiting NF-κB activation, thereby inhibiting LPS-induced inflammatory response.

Fasudil, a Rho-kinase inhibitor, has been shown to reduce portal venous pressure in cirrhotic rats.

Clemastine is an FDA approved antimuscarinic compound that has been found to rescue impaired myelination and reverse social avoidance behavior in mice.

XY 018 is a RORγ antagonist that suppresses androgen receptor expression in prostate cancer cell lines and inhibits growth of tumors in androgen receptor-positive xenograft models.

Cinnamamide is an amide of trans-cinnamic acid and a metabolite of Streptomyces that reduced tumor weight in a mouse model of C26 murine colon carcinoma, in vivo.

Helecin is the O-glucoside of salicylaldehyde, which is a key precursor to a variety chelating agents.

Phenibut, a GABA analogue, is a central nervous system depressant with anxiolytic and sedative effects.

WEHI-539 has high affinity (IC50=1.1 nM) and selectivity for BCL-XL and potently kills cells by selectively antagonizing its prosurvival activity. It has more than a 400-fold higher affinity for BCL-XL versus other prosurvival BCL-2 family members.

Cefazedone is a semisynthetic first-generation cephalosporin with antibacterial activity.

Iproniazid is a non-selective, irreversible monoamine oxidase (MAO) inhibitor (MAOI) that is used as an antidepressive agent.

A 127722 is highly potent and a selective ETA endothelin receptor antagonist (IC50 values are 0.11 nM and 98 nM for human ETA and ETB receptors, respectively)that attenuates hypoxia-induced pulmonary hypertension in rats.

Metipranolol (hydrochloride) is a non-selective β-adrenergic receptor (β-AR) antagonist. Formulations containing metipranolol have been used in the treatment of elevated IOP in patients with ocular hypertension or glaucoma.

Lymecycline is a semisynthetic antibiotic related to TETRACYCLINE.

Sulfaquinoxaline is an antiprotozoal agent used to combat coccidial infections of swine, cattle, fowl, and other veterinary animals. Also used in controlling outbreaks of fowl typhoid and fowl cholera and in treatment of infectious enteritis.

Azidamfenicol is a broad-spectrum chloramphenicol-like antibiotic that is active against Gram-negative and Gram-positive bacteria. It inhibits ribosomal peptidyltransferase.

Cycloechinulin is a diketopiperazine fungal metabolite originally isolated from A. ochraceus. It reduces weight gain of corn earworms by 33% compared to controls when used at a dose of 100 ppm in the diet.

Ginkgetin is a biflavonoid that has been isolated from G. biloba and has diverse biological activities, including pro-apoptotic, antiproliferative, anti-inflammatory, anti-atherosclerosis, and neuroprotective properties.

Valpromide is an antiepileptic drug, derivative of Valproic acid (VPA), used as a mood-stabilizer in bipolar disorder.

Cloflucarban is a disinfectant agent.

TC KHNS 11 is a potent and selective PI 3-kinase δ inhibitor that is orally bioavailable.

ML 351 is a selective 12/15 LOX inhibitor that is active in vivo.

3CAI is an inhibitor of Akt1 and Akt2 with anticancer activity.

Leriglitazone is a peroxisome proliferator activated receptor (PPAR) gamma agonist.

TL4-12 is a potent MAP4K2 (GCK) inhibitor that inhibits IL-1 and TGFβ-induced p38 MAPK phosphorylation, in vitro.

Flonicamid is a pyridinecarboxamide insecticide. Flonicamid inhibits aphid (M. persicae) salivation and sap ingestion during feeding on Japanese radish leaves. It induces toxicity in the aphid species A. gossypii, R. padi, S. graminum, and L. erysimi and rats. Formulations containing flonicamid have been used for the control of pest insects in agriculture.

Spirotetramat is an insecticide active against C. pyri nymphs in vitro.

Allolactose is a disaccharide similar to lactose. It is an inducer of the lac operon in Escherichia coli and many other enteric bacteria.

Idramantone is an immunostimulant, a derivative of adamantine, and used in the treatment of pulmonary tuberculosis patients.

AZ 5704 is a potent and selective ATM kinase inhibitor.

KT 1 decreased aortic pressure, renal blood flow, left ventricular enddiastolic pressure and resistances of total peripheral, vertebral, coronary and renal vasculatures and increased aortic blood flow, vertebral blood flow, coronary blood flow, peak positive left ventricular dP/dt and heart rate in anesthetized open-chest dogs.

Fludioxonil is a phenylpyrrole fungicide that inhibits the growth of B. cinerea isolates from strawberry and blackberry crops.

Trifloxystrobin is a fungicide that inhibits the growth of R. solani isolates from sugar beet crops.

MGK-264 is a dicarboxamide synergist used to enhance the effects of pesticides. It also decreases the fecundity of adult L. acuminata and reduces survival of the offspring after hatching when used in combination with sublethal doses of a variety of plant-derived molluscicides.

Jedi2 is a Piezo1 channel activator that promotes Ca2+ influx into HEK293 cells expressing Piezo1 channels and elicits responses in mouse Piezo1-transfected, but not Piezo2-transfected cells.

Lufenuron is a chitin-synthesis inhibitor.

Lynestrenol is a synthetic progestational hormone used often in mixtures with estrogens as an oral contraceptive.

C3 is a selective microsomal prostaglandin E synthase 1 (mPGES-1) inhibitor.

ML-226 is an inhibitor of α/β hydrolase domain-containing protein 11 (ABHD11) that inhibits ABHD11 in vitro and in situ.

Piperitenone is a monoterpene that has been found in various plants, has antioxidant activity and inhibits peroxidation of linoleic acid

(+)-Gallocatechin is a polyphenol and flavonoid that has been isolated from the leaves of tea plants and has diverse biological activities.

Protogracillin is a steroid saponin originally isolated from T. terrestris. It is cytotoxic to K562 cells.

Sitostanol is a saturated sterol found in a variety of plants, including corn, wheat, and rice and reduces cholesterol uptake in rats and rabbits.

ARN14686 is an activity-based affinity probe for the detection of N-acylethanolamine acid amidase (NAAA) using click chemistry.

Hexazinone is an organic compound that is used as a broad spectrum herbicide.

Luxabendazole is a benzimidazole carbamate broad spectrum anthelmintic agent, which has proved to be effective against adult and immature stages of the major gastrointestinal nematodes, trematodes and cestodes.

Chlorindanol is a spermaticide.

Nomifensine is an isoquinoline derivative that prevents dopamine reuptake into synaptosomes. The maleate was formerly used in the treatment of depression.

CBM 301940 is a potent malonyl-CoA decarboxylase inhibitor that is orally bioavailable.

Secologanin is a monoterpene that has been found in V. rosea and is an intermediate in the synthesis of monoterpene indole alkaloids from geraniol.

MEGA-9 is a nonionic detergent that can be used to solubilize membrane proteins.

Lethane 384 is an outdated pesticide.

Furanone C-30 is a synthetic furanone bacterial quorum sensing inhibitor.

Fluo-4 AM is a cell-permeable, fluorescent Ca2+ indicator.

Aloin B is an anthraquinone found in Aloe vera and a component of racemic aloin.

Sabinene is a bicyclic monoterpene found in a variety of plants that has antifungal and anti-inflammatory properties.

Rhodamine 700 is an organic perchlorate salt and has a role as a fluorochrome.

Cefalothin is a β-lactam cephalosporin antibiotic. It inhibits the growth of various Gram-positive and Gram-negative bacteria, including several strains of S. pyogenes, S. aureus, C. tetani, N. gonorrhoeae, Salmonella, and Shigella,

m 15 liquid crystals are a member of the oxycyanobiphenyl family. They exhibit liquid crystalline phase in the temperature range of 47-67.5oC. H NMR of the phase transitions has been studied.

Diflufenican induces inhibition of phytoene desaturase gene expression in carrot cell cultures that results in an increased production of phytoene.

Mahanimbine is a major carbazole alkaloid from Murraya koenigii (curry leaves) that may alleviate development of HFD-induced metabolic alterations.

TC 2559 (fumarate) is a CNS-selective partial agonist for α4β2 subunit-containing nicotinic acetylcholine receptors (nAChRs) with an EC50 value of 0.18 μM for calcium signaling in HEK293 cells expressing human recombinant nAChRs.

R 121919 hydrochloride is a high affinity CRF1 antagonist and is orally bioavailable.

TM N1324 is a potent and selective GPR39 agonist and is orally bioavailable.

AP C5 is a potent and selective PKG2 inhibitor.

MM 47755 is a new benz[a]anthracene antibiotic from a streptomycete.

MB 05032 is a potent FBPase inhibitor that promotes HSC expansion.

Moexiprilat completely inhibits estrone-induced cardiac fibroblast growth.

Mofebutazone inhibits the immunological release of prostaglandins as well as leukotrienes.

Homosalate is an ultraviolet (UV) filtering agent used in sunscreens and other cosmetics for skin protection purposes.

Totarol is a diterpene originally isolated from P. totara that has diverse biological activities, including antibacterial, antioxidant, and neuroprotective properties.

Mitraphylline is isolated from Uncaria tomentosa and has potential anti-inflammatory activity.

A 410099.1 is a high affinity XIAP antagonist that is active in vivo.

4-HOBA has been used as a negative control for the activity of 2-HOBA and related compounds in a mouse model of hypertension.

Netivudine is an inhibitor of varicella zoster virus.

Nevadensin is a natural basil flavonoid that protects against a methyleugenol-induced marker of hepatocarcinogenicity in male F344 rat.

Negletein is a neuroprotectant.

Neocuproine is a copper(I) chelator.

Nifurpirinol is a nitroaromatic antibiotic.

Neoquassine is a CYP1A1 inhibitor isolated from Picrasma excelsa.