Lobenzarit

Independent reference data for Lobenzarit (CAS 63329-53-3), compiled from public chemistry databases.

Registry identifiers across databases

Computed descriptors

Documented uses on record

Substances that augment, stimulate, activate, potentiate, or modulate the immune response at either the cellular or humoral level. The classical agents (Freund's adjuvant, BCG, Corynebacterium parvum, et al.) contain bacterial antigens. Some are endogenous (e.g., histamine, interferon, transfer factor, tuftsin, interleukin-1). Their mode of action is either non-specific, resulting in increased immune responsiveness to a wide variety of antigens, or antigen-specific, i.e., affecting a restricted type of immuneAnti-inflammatory agents that are non-steroidal in nature. In addition to anti-inflammatory actions, they have analgesic, antipyretic, and platelet-inhibitory actions. They act by blocking the synthesis of prostaglandins by inhibiting cyclooxygenase, which converts arachidonic acid to cyclic endoperoxides, precursors of prostaglandins. Inhibition of prostaglandin synthesis accounts for their analgesic, antipyretic, and platelet-inhibitory actions; other mechanisms may contribute to their anti-inflammatory effects.

Synonyms and trade names

Lobenzarit; 63329-53-3; Lobenzaritum; 2-((2-carboxyphenyl)amino)-4-chlorobenzoic acid; 2-[(2-carboxyphenyl)amino]-4-chlorobenzoic acid; 915EE91P39; Benzoic acid, 2-((2-carboxyphenyl)amino)-4-chloro-; DTXSID20212709; lobenzart; CCA lobenzarit; 4-chloro-2,2'-iminodibenzoic acid; lobenzarit, disodium salt; N-(2-carboxyphenyl)-4-chloroanthranilic acid; RefChem:153876; DTXCID00135200; 2-(2-carboxyanilino)-4-chlorobenzoic acid

What the public record says

Lobenzarit · CAS 63329-53-3 · C14H10ClNO4. UNII 915EE91P39.

Source: PubChem / Wikidata; the batch COA governs where values differ.