Cytidine 5'-diphosphate disodium is a substrate of CDP (nucleoside diphosphate) kinase (2.7.4.6). It has been shown to produce CTP in support of DNA and RNA biosynthesis and of ribonucleotide reductase to produce dCMP.

SXT1596 is a novel inhibitor of the SS18-SSX/TLE1 interaction. SXT1596 decreases cell viability and reactivates EGR1 expression in synovial sarcoma.

(L)-Canavanine has antimutagenic activity.

4β-Hydroxywithanolide E is a withanolide steroidal lactone that has anti-inflammatory and anticancer activities. It inhibits LPS-induced nitric oxide (NO) production and TNF-α-induced NF-κB activity. 4β-Hydroxywithanolide E inhibits LPS-induced increases in inducible nitric oxide synthase (iNOS) and COX-2 levels and Akt and STAT1 phosphorylation. It inhibits Wnt signaling in HCT116 and SW480 colorectal cancer cells (IC50s = 1.85 and 2.67 μM, respectively).3 4β-Hydroxywithanolide E inhibits the proliferation of HCT116, SW480, HT-29, and LoVo cells.

Aceturic acid is a derivative of the amino acid glycine. Its salts are called aceturates.

Cellocidin is a potent growth inhibitor for gammaherpesvirus-associated B-lymphomas that acts through activation of both the NF-κB and c-Myc-mediated signaling pathways.

Heptaminol hydrochloride is an amino alcohol used as a myocardial stimulant, vasodilator, and to relieve bronchospasm. Its most common therapeutic use is in orthostatic hypotension. The mechanism of heptaminol's therapeutic actions is not well understood although it has been suggested to affect catecholamine release or calcium metabolism.

Fluprostenol, (+)-, is an analog of Prostaglandin F2α with potent FP receptor agonist activity.

3-Benzoylpyridine is a decomposition product of the soman antidote HGG-12.

C.I. 21010 is a dye.

Vicriviroc Malate is a potent, highly selective, and orally bioavailable CCR5 antagonist.

Aminooxy-PEG2-methane is a PEG derivative containing an aminooxy group and a methane group. The aminooxy group can be used in bioconjugation. It reacts with an aldehyde to form an oxime bond. If a reductant is used, it will form a hydroxylamine linkage. PEG Linkers may be useful in the development of antibody drug conjugates and drug delivery methods.

Senecioic acid is a crystalline unsaturated fatty acid found in the pheromones of mealybug species.

Acid red 73 is a red dye.

Decamethylcyclopentasiloxane is a cyclic volatile methylsiloxane.

p-Chlorobenzyl acetate is a biochemical.

Albendazole oxide is a Antiparasitic Agent.

Vinformide is a potent cytostatic agent.

5-Chloro-m-Salicylic Acid is a biochemical.

NP-313 is an antithrombotic agent with dual inhibition of thromboxane A2 synthesis and calcium entry.

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.

Ambazone is an antiseptic agent with potential antibacterial and antileukemic activity. Although the exact mechanism of action remains unclear, ambazone appears to interfere with the membrane-bound nucleotide system by increasing the intracellular concentration of cAMP in leukemia cells and macrophages, which potentially contributes to this agent's antineoplastic activity.

DCC Crosslinker, N,N'-dicyclohexylcarbodiimide, is a zero-length crosslinker that is often employed in peptide synthesis and organic synthesis. DCC's carbodiimide is useful for coupling amines and carboxylates without the insertion of spacer atoms. DCC crosslinker is commonly used in the synthesis of active ester-containing reagents.

Butyl cinnamate is a mosquito repellent.

Dibenzylideneacetone is a synthetic curcumin analog leads to apoptotic cell death in Leishmania donovani.

Benzylideneaniline is a biochemical.

2-Arachidonoylglycerol is an endocannabinoid, an endogenous agonist of the CB1 receptor. At a concentration of 0.3nM, 2-Arachidonoylglycerol induces a rapid, transient increase in intracellular free calcium in NG108-15 neuroblastoma X glioma cells through a CB1 receptor-dependent mechanism.

Benzylurea is a competitive inhibitor of cytokinin oxidase/dehydrogenase.

Tenellin is a fungal metabolite that inhibits Mg2±, Ca2±, and Na+/K±ATPase activities in erythrocytes. Tenellin is cytotoxic to Sf9 and Sf21 insect cells.

Diallylcyanamide Hydrosilylation Cross-Linking of Siloxane Polymers