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Details

Stereochemistry ABSOLUTE
Molecular Formula C20H14Cl3F6N3O3S
Molecular Weight 596.758
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LOTILANER

SMILES

CC1=C(SC(=C1)C2=NO[C@@](C2)(C3=CC(Cl)=C(Cl)C(Cl)=C3)C(F)(F)F)C(=O)NCC(=O)NCC(F)(F)F

InChI

InChIKey=HDKWFBCPLKNOCK-SFHVURJKSA-N
InChI=1S/C20H14Cl3F6N3O3S/c1-8-2-13(36-16(8)17(34)30-6-14(33)31-7-19(24,25)26)12-5-18(35-32-12,20(27,28)29)9-3-10(21)15(23)11(22)4-9/h2-4H,5-7H2,1H3,(H,30,34)(H,31,33)/t18-/m0/s1

HIDE SMILES / InChI

Molecular Formula C20H14Cl3F6N3O3S
Molecular Weight 596.758
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Lotilaner is a member of the isoxazoline family, a novel class of parasiticides that targets the nerve receptors of ticks and fleas. This veterinary medicinal product provides immediate and persistent killing activity for 1 month for fleas (Ctenocephalides felis and C. canis) and ticks (Rhipicephalus sanguineus, Ixodes ricinus, I. hexagonus and Dermacentor reticulatus). The veterinary medicinal product can be used as part of a treatment strategy for the control of flea allergy dermatitis. During clinical testing, no interactions between Lotilaner chewable tablets and routinely used veterinary medicinal products were observed.

Approval Year

Patents

Patents

Sample Use Guides

20 to 43 mg lotilaner/kg bodyweight
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Sat Dec 16 16:55:29 GMT 2023
Edited
by admin
on Sat Dec 16 16:55:29 GMT 2023
Record UNII
HEH4938D7K
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LOTILANER
INN   USAN  
USAN   INN  
Official Name English
LOTILANER [GREEN BOOK]
Common Name English
LOTILANER (EMA EPAR: VETERINARY)
Common Name English
lotilaner [INN]
Common Name English
XDEMVY
Brand Name English
LOTILANER [USAN]
Common Name English
LOTILANER [MI]
Common Name English
CREDELIO
Brand Name English
2-THIOPHENECARBOXAMIDE, 5-((5S)-4,5-DIHYDRO-5-(3,4,5-TRICHLOROPHENYL)-5-(TRIFLUOROMETHYL)-3-ISOXAZOLYL)-3-METHYL-N-(2-OXO-2-((2,2,2-TRIFLUOROETHYL)AMINO)ETHYL)-
Systematic Name English
3-METHYI-N-(2-OXO-2-((2,2,2-TRIFLUOROETHYL)AMINO)ETHYL)-5-((55)-5-(3,4,5-TRICHLOROPHENYL)-5-(TRIFLUOROMETHYL)-4,5-DIHYDRO-1,2-OXAZOL-3-YL)THIOPHENE-2-CARBOXAMIDE
Systematic Name English
Classification Tree Code System Code
EMA VETERINARY ASSESSMENT REPORTS CREDELIO (AUTHORISED)
Created by admin on Sat Dec 16 16:55:29 GMT 2023 , Edited by admin on Sat Dec 16 16:55:29 GMT 2023
Code System Code Type Description
SMS_ID
300000023732
Created by admin on Sat Dec 16 16:55:29 GMT 2023 , Edited by admin on Sat Dec 16 16:55:29 GMT 2023
PRIMARY
EPA CompTox
DTXSID70102755
Created by admin on Sat Dec 16 16:55:29 GMT 2023 , Edited by admin on Sat Dec 16 16:55:29 GMT 2023
PRIMARY
ALANWOOD
lotilaner
Created by admin on Sat Dec 16 16:55:29 GMT 2023 , Edited by admin on Sat Dec 16 16:55:29 GMT 2023
PRIMARY
USAN
CD-84
Created by admin on Sat Dec 16 16:55:29 GMT 2023 , Edited by admin on Sat Dec 16 16:55:29 GMT 2023
PRIMARY
WIKIPEDIA
Lotilaner
Created by admin on Sat Dec 16 16:55:29 GMT 2023 , Edited by admin on Sat Dec 16 16:55:29 GMT 2023
PRIMARY
FDA UNII
HEH4938D7K
Created by admin on Sat Dec 16 16:55:29 GMT 2023 , Edited by admin on Sat Dec 16 16:55:29 GMT 2023
PRIMARY
PUBCHEM
76959255
Created by admin on Sat Dec 16 16:55:29 GMT 2023 , Edited by admin on Sat Dec 16 16:55:29 GMT 2023
PRIMARY
DAILYMED
HEH4938D7K
Created by admin on Sat Dec 16 16:55:29 GMT 2023 , Edited by admin on Sat Dec 16 16:55:29 GMT 2023
PRIMARY
INN
9867
Created by admin on Sat Dec 16 16:55:29 GMT 2023 , Edited by admin on Sat Dec 16 16:55:29 GMT 2023
PRIMARY
MERCK INDEX
m12039
Created by admin on Sat Dec 16 16:55:29 GMT 2023 , Edited by admin on Sat Dec 16 16:55:29 GMT 2023
PRIMARY
NCI_THESAURUS
C170132
Created by admin on Sat Dec 16 16:55:29 GMT 2023 , Edited by admin on Sat Dec 16 16:55:29 GMT 2023
PRIMARY
ChEMBL
CHEMBL3707310
Created by admin on Sat Dec 16 16:55:29 GMT 2023 , Edited by admin on Sat Dec 16 16:55:29 GMT 2023
PRIMARY
RXCUI
1998841
Created by admin on Sat Dec 16 16:55:29 GMT 2023 , Edited by admin on Sat Dec 16 16:55:29 GMT 2023
PRIMARY
CAS
1369852-71-0
Created by admin on Sat Dec 16 16:55:29 GMT 2023 , Edited by admin on Sat Dec 16 16:55:29 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY