fendiline

{{Short description|Non-selective calcium channel blocker}}

{{Drugbox

| Verifiedfields = changed

| Watchedfields = changed

| verifiedrevid = 444353505

| IUPAC_name = 3,3-diphenyl-N-(1-phenylethyl)propan-1-amine

| image = Fendiline.png

| tradename =

| pregnancy_AU =

| pregnancy_US =

| pregnancy_category =

| legal_AU =

| legal_CA =

| legal_UK =

| legal_US =

| legal_status =

| routes_of_administration =

| bioavailability =

| protein_bound =

| metabolism =

| elimination_half-life =

| excretion =

| CAS_number_Ref = {{cascite|correct|??}}

| CAS_number = 13042-18-7

| ATC_prefix = C08

| ATC_suffix = EA01

| PubChem = 3336

| DrugBank_Ref = {{drugbankcite|changed|drugbank}}

| DrugBank = DB08980

| ChEMBL_Ref = {{ebicite|changed|EBI}}

| ChEMBL = 254832

| UNII_Ref = {{fdacite|correct|FDA}}

| UNII = S253D559A8

| KEGG_Ref = {{keggcite|correct|kegg}}

| KEGG = D07185

| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}}

| ChemSpiderID = 3219

| C=23 | H=25 | N=1

| smiles = CC(NCCC(c1ccccc1)c2ccccc2)c3ccccc3

| StdInChI_Ref = {{stdinchicite|changed|chemspider}}

| StdInChI = 1S/C23H25N/c1-19(20-11-5-2-6-12-20)24-18-17-23(21-13-7-3-8-14-21)22-15-9-4-10-16-22/h2-16,19,23-24H,17-18H2,1H3

| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}}

| StdInChIKey = NMKSAYKQLCHXDK-UHFFFAOYSA-N

}}

Fendiline is a nonselective calcium channel blocker.{{cite journal | vauthors = Scultéty S, Tamáskovits E | title = Effect of Ca2+ antagonists on isolated rabbit detrusor muscle | journal = Acta Physiologica Hungarica | volume = 77 | issue = 3–4 | pages = 269–78 | year = 1991 | pmid = 1755331 }}{{Cite web|url=https://www.sciencedirect.com/topics/pharmacology-toxicology-and-pharmaceutical-science/fendiline|title = Fendiline - an overview | ScienceDirect Topics}}