Building Blocks

N'-Hydroxy-2-thiophenecarboximidamide is a factor-1 inhibitor that has been shown to inhibit the hypoxia inducible transcription factors (HIF) 1α and HIF2α. These proteins are involved in cellular response to hypoxia, which can lead to metastasis. This drug also inhibits the development of xenograft tumors by inhibiting cellular responses. N'-Hydroxy-2-thiophenecarboximidamide has been shown to be more effective than other inhibitors at preventing tumor growth and angiogenesis. It is also an important advance for cancer therapy as it provides a new target for cancer therapeutics.

Methyl 2-(benzylamino)acetate is a carboxyalkyl compound that is involved in the biosynthesis of β-unsaturated ketones. It can be used as a substrate for the oxidation of molecules such as quinazolines, piperidines and piperazines. Methyl 2-(benzylamino)acetate can also act as an acceptor for hydrogen atoms or electrons from other molecules. The methyl group in this molecule has been shown to be able to donate or accept electrons from other molecules, allowing it to participate in many different reactions. Methyl 2-(benzylamino)acetate is synthesized by bacteria such as Bacillus subtilis.

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

N-Benzyl-N-methylthiourea is an isomeric, bicyclic compound. It has antiaromatic properties and belongs to the thiazole class of compounds. It was isolated from a reaction mixture in which benzyl chloride and methylisothiourea were heated together with sodium amide. It has been reinvestigated as a possible intermediate for heterocyclic synthesis. The substance is stable at room temperature, but decomposes on heating.

Versatile small molecule scaffold

2-(Aminomethylidene)-2,3-dihydro-1H-inden-1-one is a lipophilic drug that is used in pharmaceutical preparations. It is a non-irritating and non-sensitizing agent that does not cause any significant sensitization reactions. It is used as a diagnostic aid for the detection of fatty acid esters in tissue samples, an enhancement agent during cavity preparation, and as pharmaceutical dosage for treatment of depression. This compound has been shown to act as a transporter gene modulator and can be found in tissues such as the brain, heart, kidney, liver, spleen, adrenal gland and pancreas. 2-(Aminomethylidene)-2,3-dihydro-1H-inden-1-one may be conjugated with glutathione or sulfate and excreted into bile. Fatty acids are transported into cells by carriers

5,6,7,8-Tetrahydro-8-quinolinecarbothioamide is a pyridine compound with the molecular formula C4H5N. It is an anti-ulcer agent that has been used in the synthesis of other organic compounds. This compound contains a pyridine ring with a nitrogen atom at position 8 that is substituted with a cyano group. It also contains two hydrocarbon rings and one nitro group at position 5. 5,6,7,8-Tetrahydro-8-quinolinecarbothioamide can be synthesized by reacting 2 equivalents of carbonyl fluoride with 1 equivalent of sodium nitrite in the presence of copper metal.

6-Hydroxy-2H-benzo[b][1,4]oxazin-3(4H)-one is a dermatological active substance that is used in the treatment of skin diseases. It has been shown to be an immunosuppressant in animals and humans and can also be used in the treatment of respiratory disease. It has vasotropic properties and is an antiinflammatory agent. 6-Hydroxy-2H-benzo[b][1,4]oxazin-3(4H)-one is a topoisomerase II inhibitor that binds to DNA and prevents the unwinding of DNA strands by inhibiting the formation of topoisomerases II–DNA complexes. The compound binds to the C1 position on the cyclohexane ring, which contains both unsubstituted alkyl and unsubstituted aryl groups as well as elements such as silver halide.

Versatile small molecule scaffold

Versatile small molecule scaffold

N-Methylthiophene-2-sulfonamide is an inhibitor of arylsulfonamides. It can be used to investigate the conformational and torsional effects of arylsulfonamides and their relationship to the inhibition of sulfonamide. N-Methylthiophene-2-sulfonamide has been shown to have good inhibitory activity against sulfonamide with conformation and torsional effects, which may be due to its ability to bind to the sulfanilamide in the active site. The computational results also show that this compound has potential for use as a drug candidate.