Others

Sulisobenzone is an ingredient in some sunscreens which protects the skin from damage by UVB and short-wave UVA ultraviolet light.

Glutathione acts as an antioxidant, a free radical scavenger and a detoxifying agent.

L-tyrosine is a non-essential amino acid. In animals it is synthesized from Ephenylalanine.

ON-013100 is a cell cycle inhibitor and is potentially useful for the treatment of mantle cell lymphoma.

Eprodisate is an orally available disodium salt form of eprodisate, a negatively charged sulfonated inhibitor of fibrillogenesis, that can be used in the treatment of amyloid A (AA) amyloidosis.

SCH00013 is a cardiotonic agent that primarily acts via an increase in myofibrillar Ca++ sensitivity, have a significant Ca(2+)sensitizing effect at pH 7.2 to 7.4.

Valbenazine is a potent and selective VMAT2 inhibitor.

SecinH3 is a selective cytohesin inhibitor with IC50 of 2.4 μM, 5.4 μM, 5.4 μM, 5.6 μM, 5.6 μM, and 65 μM for hCyh2, hCyh1, mCyh3, hCyh3, drosophila steppke, and yGea2-S7, respectively.

3,3'-Diindolylmethane(DIM) is a major digestive product of indole-3-carbinol, a potential anticancer component of cruciferous vegetables.

HMN-176 is a stilbene derivative which inhibits mitosis without significant effect on tubulin polymerization.

HTHQ, which is a hydroquinone monoalkyl ether, is a potent anti-oxidative agent, even at low dose levels.

2-Aminoheptane is a nasal decongestant drug which is a sympathomimetic stimulant and vasoconstrictor.

4-Aminohippuric acid is a typical substrate of organic anion transport systems.

6-Acetamidohexanoic acid is a pharmaceutical intermediate.

Aceglutamide is a psychostimulant, nootropic agent which functions as a prodrug to glutamine with improved potency and stability.

Acesulfame potassium is a non-nutritive sweetener.

Acetylleucine is a drug used in the treatment of vertigo.

Aminoguanidine is a diamine oxidase and nitric oxide synthase inhibitor. It acts to reduce levels of advanced glycation end products (AGEs) through interacting with 3-deoxyglucosone.

Antimony potassium tartrate trihydrate is a powerful emetic, also used in the treatment of schistosomiasis and leishmaniasis.

Azaguanine-8 is a purine analogs showing antineoplastic activity by competing with guanine in the metabolism.

Carbazochrome sodium sulfonate (AC-17) is an antihemorrhagic for use in the treatment of hemorrhoids.

Carbimazole is an imidazole antithyroid agent.

Carzenide is an organic synthesis intermediate, used for synthetic drug.

Chromocarb is a synthetic vasoprotectant.

Cinchophen is an analgesic drug that is frequently used to treat gout.

Citiolone is a derivative of the amino acid cysteine, used in liver therapy.

Cysteamine is an agent for the treatment of nephropathic cystinosis and an antioxidant.

Cytidine is a nucleoside molecule that is formed when cytosine is attached to a ribose ring, cytidine is a component of RNA.

Nicaraven is a novel chemically synthesized hydroxyl radical-specific scavenger.

Amcasertib (BBI503), a first-in-class cancer stemness kinase inhibitor, is claimed to inhibit Nanog and other CSC pathways by targeting kinases with potential anticancer activity.

meta-Topolin is an aromatic cytokinin, first isolated from leaves of Populus x robusta. Cytokinins (CTKs) are a class of growth-regulating hormones involved in various physiological and developmental processes.

NSC139021 (ERGi-USU) is a highly selective inhibitor for the growth of ERG-positive cancer cells with IC50s ranging from 30 to 400 nM.

VI-16832 is a broad spectrum type-I kinase inhibitor

LOXL2-IN-1 HCl is a selective LOXL2 inhibitor with an IC50 of 126 nM.

Nifenazone is a drug used as an analgesic for a number of rheumatic conditions.

Neurotoxin Inhibitor is a neurotoxin inhibitor.

FDI-6 is an inhibitor of FOXM1. FDI-6 binds directly to FOXM1 protein, to displace FOXM1 from genomic targets in MCF-7 breast cancer cells, and induce concomitant transcriptional down-regulation.

Guancydine (Guancidine) is an antihypertensive agent.

DSP-4 hydrochloride (Neurotoxin DSP 4 hydrochloride) is a highly selective neurotoxin and readily passes the blood-brain barrier with neurotoxic effects on noradrenergic neurons of adult and developing rats, can be used for the temporary selective degradation of the central and peripheral noradrenergic neurons, mainly those from the locus coeruleus (LC).

N-alpha-Tosyl-L-lysine chloromethyl ketone (TLCK), a trypsin like protease inhibitor, sensitizes HeLa cells to Fas-mediated cell death.

24-norursodeoxycholic acid (norUDCA) is a side chain-shortened C23 homologue of UDCA and has shown potent anti-cholestatic, anti-inflammatory and anti-fibrotic properties.

Macropa-NH2 is the precursor of Macropa-NCS. Macropa-NCS is conjugated to trastuzumab as well as to the prostate-specific membrane antigen-targeting compound RPS-070 and is a promising therapeutic radionuclide applied in the treatment of soft-tissue metastases.

SMS2-IN-2 is a potent, highly selective and orally active sphingomyelin synthase 2 (SMS2) inhibitor, with IC50s of 100 nM and 56 μM for SMS2 and SMS1, respectively. Anti-chronic inflammatory activity.

Anti-Heart Failure Agent 1 an orally available compound suitable for the treatment of heart failure without inducing nausea, vomiting and restlessness.

DS-1040 Tosylate is an inhibitor of the activated thrombin-activatable fibrinolysis inhibitor (TAFIa), used for the treatment of acute ischemic stroke (AIS).

Ketoisophorone (4-Oxoisophorone) is a key intermediate in the synthesis of carotenoids and flavouring agents. Ketoisophorone is an industrially important cyclic endione.

5-Acetylsalicylic acid has anti-inflammatory and is considered to be the active agent in inflammatory bowel disease (IBD).

Melinamide, an amide derivative of an unsaturated long-chain fatty acid, is an inhibitor of cholesterol absorption with an IC50 of 20.9 μM.

Ethyl vanillin acetate is acectate form of ethyl vanillin. Ethyl vanillin acetate is a flavorant used in chocolate or candy.

L-Pyrrolysine is the 22nd genetically encoded amino acid.