chemical inhibits protein chemical inhibits in vitro invasion of virus has role has role is conjugate base of EC 2.1.1.8 (histamine N-methyltransferase) inhibitor amodiaquine(1+) anticoronaviral agent amodiaquine InChI=1S/C20H22ClN3O/c1-3-24(4-2)13-14-11-16(6-8-20(14)25)23-18-9-10-22-19-12-15(21)5-7-17(18)19/h5-12,25H,3-4,13H2,1-2H3,(H,22,23) PMID:8885219 amodiaquinum C20H22ClN3O KEGG:D02922 355.14514 CAS:86-42-0 chebi_ontology Drug_Central:186 Amodiaquine OVCDSSHSILBFBN-UHFFFAOYSA-N PMID:11044276 CCN(CC)Cc1cc(Nc2ccnc3cc(Cl)ccc23)ccc1O PMID:17222819 PMID:27031231 4-[(7-chloroquinolin-4-yl)amino]-2-[(diethylamino)methyl]phenol Beilstein:300962 0 PMID:26647924 Wikipedia:Amodiaquine PMID:26851641 PMID:26735991 KEGG:C07626 PMID:19245687 PMID:18419816 DrugBank:DB00613 CHEBI:2674 LINCS:LSM-4042 PMID:26900802 PMID:26597254 PMID:17046445 PDBeChem:CQA A quinoline having a chloro group at the 7-position and an aryl amino group at the 4-position. PMID:26206402 PMID:26930583 PMID:19024339 PMID:11971651 Reaxys:300962 https://www.drugbank.ca/drugs/DB00613 PMID:18855526 355.86100 PMID: 32366720; PMID: 30700611 amodiaquine Patent:US2474821 amodiaquina phenols non-steroidal anti-inflammatory drug organochlorine compound aminoquinoline antimalarial prodrug secondary amino compound tertiary amino compound drug allergen Severe acute respiratory syndrome-related coronavirus histamine N-methyltransferase (human)