The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature. Application In Synthesis of 8-(Phenylamino)naphthalene-1-sulfonic acid, 82-76-8, Name is 8-(Phenylamino)naphthalene-1-sulfonic acid, SMILES is O=S(C1=C2C(NC3=CC=CC=C3)=CC=CC2=CC=C1)(O)=O, in an article , author is Guare, JP, once mentioned of 82-76-8.
A series of 5-aminosubstituted 4-fluorobenzyl-8-hydroxy-[1,6]naphthyridine-7-carboxamide HIV-1 integrase inhibitors
A series of 5-amino derivatives of 8-hydroxy[1,6]-naphthyridine-7-carboxamide exhibiting sub-micromolar potency against replication of HIV-1 in cell culture was identified. One of these analogs, compound 12, displayed excellent pharmacokinetic properties when dosed orally in rats and in monkeys. This compound was demonstrated to be efficacious against replication of simian-human immunodeficiency virus (SHIV) 89.6P in infected rhesus macaques. (c) 2006 Elsevier Ltd. All rights reserved.
But sometimes, even after several years of basic chemistry education, it is not easy to form a clear picture on how they govern reactivity! 82-76-8, you can contact me at any time and look forward to more communication. Application In Synthesis of 8-(Phenylamino)naphthalene-1-sulfonic acid.
Reference:
1,8-Naphthyridine – Wikipedia,
,1,8-Naphthyridine | C8H6N2 – PubChem