Preferred Name |
Chloroquine |
|
Synonyms |
chloroquinum InChIKey=WHTVZRBIWZFKQO-UHFFFAOYSA-N Nivaquine B N(4)-(7-chloro-4-quinolinyl)-N(1),N(1)-diethyl-1,4-pentanediamine InChI=1S/C18H26ClN3/c1-4-22(5-2)12-6-7-14(3)21-17-10-11-20-18-13-15(19)8-9-16(17)18/h8-11,13-14H,4-7,12H2,1-3H3,(H,20,21) chloroquine CCN(CC)CCCC(C)Nc1ccnc2cc(Cl)ccc12 Aralen Artrichin Bemaphate C18H26ClN3 Capquin Chlorochin Resoquine Reumachlor Sanoquin cloroquina Chloroquine N(4)-(7-chloroquinolin-4-yl)-N(1),N(1)-diethylpentane-1,4-diamine |
|
Definitions |
A quinoline alkaloid that has formula C18H26ClN3. An aminoquinoline that is quinoline which is substituted at position 4 by a [5-(diethylamino)pentan-2-yl]amino group at at position 7 by chlorine. It is used for the treatment of malaria, hepatic amoebiasis, lupus erythematosus, light-sensitive skin eruptions, and rheumatoid arthritis. |
|
ID |
http://purl.obolibrary.org/obo/CHEBI_3638 |
|
alternative term |
chloroquinum InChIKey=WHTVZRBIWZFKQO-UHFFFAOYSA-N Nivaquine B N(4)-(7-chloro-4-quinolinyl)-N(1),N(1)-diethyl-1,4-pentanediamine InChI=1S/C18H26ClN3/c1-4-22(5-2)12-6-7-14(3)21-17-10-11-20-18-13-15(19)8-9-16(17)18/h8-11,13-14H,4-7,12H2,1-3H3,(H,20,21) chloroquine CCN(CC)CCCC(C)Nc1ccnc2cc(Cl)ccc12 Aralen Artrichin Bemaphate C18H26ClN3 Capquin Chlorochin Resoquine Reumachlor Sanoquin cloroquina Chloroquine N(4)-(7-chloroquinolin-4-yl)-N(1),N(1)-diethylpentane-1,4-diamine |
|
capable of inhibiting activity of | ||
charge |
0 |
|
chemical effective in vitro against virus |
http://purl.obolibrary.org/obo/NCBITaxon_694009 |
|
chemical has protein target |
http://purl.obolibrary.org/obo/PR_Q9BYF1 http://purl.obolibrary.org/obo/PR_P09210 http://purl.obolibrary.org/obo/PR_Q8MU52 http://purl.obolibrary.org/obo/PR_P09429 |
|
chemical inhibits in vitro invasion of virus |
http://purl.obolibrary.org/obo/NCBITaxon_694009 |
|
chemical inhibits in vitro replication of virus |
http://purl.obolibrary.org/obo/NCBITaxon_694009 |
|
chemical inhibits protein |
http://purl.obolibrary.org/obo/PR_P09210 http://purl.obolibrary.org/obo/PR_Q8MU52 http://purl.obolibrary.org/obo/PR_P09429 |
|
database_cross_reference |
Patent:DE683692 PMID:18052874 Beilstein:482809 LINCS:LSM-1901 PMID:19426658 PDBeChem:CLQ NIST Chemistry WebBook:54-05-7 Wikipedia:Chloroquine PMID:17594118 PMID:23580861 Patent:US2233970 CAS:54-05-7 KEGG:D02366 PMID:23644906 KEGG DRUG:D02366 PMID:23706562 PMID:23891850 PMID:23635029 Drug_Central:607 ChemIDplus:54-05-7 KEGG COMPOUND:C07625 KEGG COMPOUND:54-05-7 PMID:23852712 DrugBank:DB00608 HMDB:HMDB0014746 Reaxys:482809 PMID:23288916 KEGG:C07625 PMID:11198399 Gmelin:781126 PMID:25285162 |
|
definition source |
https://www.drugbank.ca/drugs/DB00608 PMID: 16837072; PMID: 27344959; PMID: 27916837; PMID: 32150618; PMID: 32020029 |
|
formula |
C18H26ClN3 |
|
has exact synonym |
Chloroquine N(4)-(7-chloroquinolin-4-yl)-N(1),N(1)-diethylpentane-1,4-diamine |
|
has role |
http://purl.obolibrary.org/obo/CHEBI_149553 http://purl.obolibrary.org/obo/CHEBI_88230 http://purl.obolibrary.org/obo/CHEBI_50177 |
|
has_obo_namespace |
chebi_ontology |
|
has_related_synonym |
chloroquinum InChIKey=WHTVZRBIWZFKQO-UHFFFAOYSA-N Nivaquine B N(4)-(7-chloro-4-quinolinyl)-N(1),N(1)-diethyl-1,4-pentanediamine InChI=1S/C18H26ClN3/c1-4-22(5-2)12-6-7-14(3)21-17-10-11-20-18-13-15(19)8-9-16(17)18/h8-11,13-14H,4-7,12H2,1-3H3,(H,20,21) chloroquine CCN(CC)CCCC(C)Nc1ccnc2cc(Cl)ccc12 Aralen Artrichin Bemaphate C18H26ClN3 Capquin Chlorochin Resoquine Reumachlor Sanoquin cloroquina |
|
has_RxCUI |
2393 |
|
id |
CHEBI:3638 |
|
imported from | ||
in subset | ||
inchi |
InChI=1S/C18H26ClN3/c1-4-22(5-2)12-6-7-14(3)21-17-10-11-20-18-13-15(19)8-9-16(17)18/h8-11,13-14H,4-7,12H2,1-3H3,(H,20,21) |
|
inchikey |
WHTVZRBIWZFKQO-UHFFFAOYSA-N |
|
is conjugate base of | ||
label |
Chloroquine chloroquine |
|
mass |
319.87200 |
|
monoisotopicmass |
319.18153 |
|
notation |
CHEBI:3638 |
|
prefLabel |
Chloroquine |
|
smiles |
CCN(CC)CCCC(C)Nc1ccnc2cc(Cl)ccc12 |
|
textual definition |
A quinoline alkaloid that has formula C18H26ClN3. An aminoquinoline that is quinoline which is substituted at position 4 by a [5-(diethylamino)pentan-2-yl]amino group at at position 7 by chlorine. It is used for the treatment of malaria, hepatic amoebiasis, lupus erythematosus, light-sensitive skin eruptions, and rheumatoid arthritis. |
|
subClassOf |
http://purl.obolibrary.org/obo/CHEBI_50995 http://purl.obolibrary.org/obo/CHEBI_36709 http://purl.obolibrary.org/obo/CHEBI_36683 |
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