Dodecyl maltoside is a surfactant.

Cetyl glycol is used in cosmetics.

RO8191 is an activator of JAK/STAT that induces IFN-like signals.

Peonidin 3-O-glucoside is a metabolite of cyanidin 3-glucoside and an anthocyanin with antioxidant, anti-inflammatory, antiproliferative, and anti-metastatic properties. Peonidin 3-O-glucoside inhibits IL-1β-induced phosphorylation of IKKα, IκBα, and ERK in human articular chondrocytes. Peonidin 3-O-glucoside inhibits the growth of Hs578T human breast cancer cells in vitro in a concentration-dependent manner and decreases pulmonary metastasis in a mouse model of Lewis lung carcinoma.

Creatinolfosfate, also known as Creatinol Phosphate or creatinol-O-phosphate, is a biochemical which may affect heart contractility.

Toltrazuril (Tol) is a broad-spectrum anticoccidiosis drug that is widely used in the prevention and treatment of coccidiosis infection in poultry and mammals.

17A-Hydroxyprogesterone is a metabolite of progesterone. It serves as an intermediate in the biosynthesis of hydrocortisone and gonadal steroid hormones.

Amino-PEG4-amine is a PEG derivative containing two amino groups. The amino groups are reactive with carboxylic acids, activated NHS esters, carbonyls (ketone, aldehyde) etc. PEG Linkers may be useful in the development of antibody drug conjugates and drug delivery methods.

FD&C Blue No. 1 aluminum lake is a dye.

Hadacidin is an inhibitor of AMP synthesis. Hadacidin and hadacidin analogues have anticancer activity and activity against adenylosuccinate synthetase.

Benziodarone is a vasodilator. Results suggest that benziodarone has an amiodarone-like action.

Dipyrone, also known as Metamizole Sodium, is a drug that has analgesic, anti-inflammatory, and antipyretic properties. It is the sodium sulfonate of AMINOPYRINE.

Piroctone olamine is an ethanolamine salt of the hydroxamic acid derivative piroctone used to treat fungal infections.

Lipofundin S is an emulsion containing soy bean oil, soy phosphatides & glycerol.

Tributyl borate is a biochemical.

SPL-334 is an inhibitor of S-nitrosoglutathione reductase. SPL-334 prevents weight loss, attenuating lung inflammation and fibrosis in a bleomycin injury model of interstitial lung disease in mice.

Sophoridin is an anticancer agent, with a promising anti-rumor effect and lower toxicity. Anti-inflammatory.

AM 6201, also known as Reductiomycin, is an alkaloid originally derived from Streptomyces xanthochromogenus that has been shown to exhibit antitumor activity against Ehrlich ascites carcinomas in mice.

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.

6-PNG is a Cav3.2 (T-type) calcium channel blocker.

Buserelin Acetate is a Gonadotropin-releasing hormone agonist (GnRH agonist).

SPDP acid is a non-PEG crosslinker.

Dodecyl benzene sulfonic acid, Dopant for conducting polymers strong acid catalyst for amino cross-linked coatings.

Cilostamide is a selective inhibitor of type III phosphodiesterase (PDE3).

DSS crosslinker, or Disuccinimidyl suberate, is a homobifunctional crosslinker that is cell membrane permeable. DSS crosslinker has amine-reactive NHS esters at both ends of an 8-atom (11.4 angstrom) spacer arm that are used to conjugate proteins. DSS crosslinker can be used to conjugate or crosslink intracellular proteins.

Rugulotrosin A is an antibiotic active against the Gram-positive bacteria E. faecalis, B. cereus, B. subtilis, and S. aureus. Rugulotrosin A is inactive against Gram-negative bacteria.

4-oxo Withaferin A is a derivative of the steroidal lactone withaferin A that has anticancer activity. It is cytotoxic to A2780 ovarian cancer cells and carboplatin-resistant A2780 (A2780/CP70) cells and is 4.4-fold selective for A2780 cells over non-cancerous ARPE19 cells.

Arotinolol (INN, marketed under the tradename Almarl) is a medication in the class of mixed alpha/beta blockers. It also acts as a β3 receptor agonist. A 1979 publication suggests arotinolol as having first been described in the scientific literature by Sumitomo Chemical as "β-adrenergic blocking, antiarrhythmic compound S-596".

Micheliolide is a natural, irreversible activator of pyruvate kinase M2, and a suppressor of leukemia cells.

Bitriben is an anthelmintic agent.