7-ketolithocholic acid

7-Ketolithocholic acid (3α-Hydroxy-7-oxo-5β-cholanic acid) (3α-Hydroxy-7-oxo-5β-cholanic acid) is capable of absorption and serves to suppress the production of endogenous bile acid and the secretion of biliary cholesterol.

7-Chlorokynurenic acid (7-chloro-4-hydroxy-2-carboxyquinoline) is an effecitve and selective antagonist of NMDA receptor with IC50 of 0.56 μM for the glycine B coagonist site. 7-Chlorokynurenic acid inhibits the reuptake of glutamate into synaptic vesicles with a Ki of 0.59 μM and shows antinociceptive actions after neuraxial delivery.

3-Oxo-7-hydroxychol-4-enoic acid, an endogenous metabolite, is potentially a significant prognostic marker for adverse outcomes in hepatobiliary disease [1].

6-hydroxyl kaempherol-3,6-O-diglucosyl-7-O-Glucuronic acid is a natural product from Carthamus tinctorius Linn.

7-Hydroxyaristolochic acid A is a natural product from Aristolochia debilis Sieb.

Scutellarin-7-diglucosidic acid, a natural flavone, is isolated from the purple leaves of Perilla ocimoides var. crispa [1].

7-Methyluric Acid is a natural product for research related to life sciences. The catalog number is T37856 and the CAS number is 612-37-3.

7-keto-deoxycholic acid is converted from Lactobacillus and Bifidobacterium with specific condition and from cholic acid in vitro.

7-Methoxy-β-carboline-1-propionic acid (compound 46), known for its cytotoxic and antimalarial properties, is derived from the roots of Eurycoma longifolia [1].

15-Hydroxy-7-oxodehydroabietic acid is a natural product of Pinus, Pinaceae. The catalog number is TN2638 and the CAS number is 95416-25-4. 15-Hydroxy-7-oxodehydroabietic acid can be used as a reference standard.

7-Amino-4-methylcoumarin-3-acetic acid (7-Amino-4-methylcoumarin) is more suitable as a substrate for enteropeptidase than GD(4)K-NA.

7-Aminocephalosporanic acid is an HSP90β inhibitor used in the synthesis of cephalosporin antibiotics and their intermediates.

(±)-7-epiJasmonic acid, the primary metabolite in the 12-oxo phytodienoic acid pathway of 13(S)-hydroperoxy linolenic acid metabolism in plants, is synthesized initially as the more active (+)-7-epijasmonic acid. It quickly epimerizes to the more stable (−)-7-jasmonic acid isomer, demonstrating its biological relevance. Acting as a plant growth regulator, (±)-7-epiJasmonic acid triggers various signal transduction pathways, which can either promote growth or inhibit it, likely as a response to stress conditions.