Tolciclate

	WikiDoc Resources for Tolciclate
Articles
Most recent articles on Tolciclate Most cited articles on Tolciclate Review articles on Tolciclate Articles on Tolciclate in N Eng J Med, Lancet, BMJ
Media
Powerpoint slides on Tolciclate Images of Tolciclate Photos of Tolciclate Podcasts & MP3s on Tolciclate Videos on Tolciclate
Evidence Based Medicine
Cochrane Collaboration on Tolciclate Bandolier on Tolciclate TRIP on Tolciclate
Clinical Trials
Ongoing Trials on Tolciclate at Clinical Trials.gov Trial results on Tolciclate Clinical Trials on Tolciclate at Google
Guidelines / Policies / Govt
US National Guidelines Clearinghouse on Tolciclate NICE Guidance on Tolciclate NHS PRODIGY Guidance FDA on Tolciclate CDC on Tolciclate
Books
Books on Tolciclate
News
Tolciclate in the news Be alerted to news on Tolciclate News trends on Tolciclate
Commentary
Blogs on Tolciclate
Definitions
Definitions of Tolciclate
Patient Resources / Community
Patient resources on Tolciclate Discussion groups on Tolciclate Patient Handouts on Tolciclate Directions to Hospitals Treating Tolciclate Risk calculators and risk factors for Tolciclate
Healthcare Provider Resources
Symptoms of Tolciclate Causes & Risk Factors for Tolciclate Diagnostic studies for Tolciclate Treatment of Tolciclate
Continuing Medical Education (CME)
CME Programs on Tolciclate
International
Tolciclate en Espanol Tolciclate en Francais
Business
Tolciclate in the Marketplace Patents on Tolciclate
Experimental / Informatics
List of terms related to Tolciclate

Tolciclate
Clinical data
AHFS/Drugs.com	International Drug Names
ATC code	D01AE19 (WHO) ;
Identifiers
CAS Number	50838-36-3 ;
PubChem CID	5506;
ChemSpider	5305 ;
UNII	T3TZ02X2AZ;
KEGG	D01384 ;
E number	{{#property:P628}}
ECHA InfoCard	{{#property:P2566}}Lua error in Module:EditAtWikidata at line 36: attempt to index field 'wikibase' (a nil value).
Chemical and physical data
Formula	C20H21NOS
Molar mass	323.45 g/mol
3D model (JSmol)	Interactive image;
	SMILES Cc1cccc(c1)N(C)C(=S)Oc2ccc3c(c2)C4CCC3C4;
	InChI InChI=1S/C20H21NOS/c1-13-4-3-5-16(10-13)21(2)20(23)22-17-8-9-18-14-6-7-15(11-14)19(18)12-17/h3-5,8-10,12,14-15H,6-7,11H2,1-2H3 ; Key:CANCCLAKQQHLNK-UHFFFAOYSA-N ;
(what is this?) (verify)

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview[edit | edit source]

Tolciclate is an antifungal.^[1]^[2]

↑ Ryder, N. S.; Frank, I.; Dupont, M. C. (May 1986). "Ergosterol biosynthesis inhibition by the thiocarbamate antifungal agents tolnaftate and tolciclate". Antimicrobial Agents and Chemotherapy. 29 (5): 858–860. doi:10.1128/aac.29.5.858. PMC 284167. PMID 3524433.
↑ Bianchi, A.; Monti, G.; de Carneri, I. (September 1977). "Tolciclate: further antimycotic studies". Antimicrobial Agents and Chemotherapy. 12 (3): 429–430. doi:10.1128/aac.12.3.429. PMC 429931. PMID 907333.

v t e Antifungals (D01 and J02)
Antibiotics	Griseofulvin • polyene antimycotics (Natamycin, Nystatin)
Topical azoles	imidazoles (Bifonazole, Clomidazole, Clotrimazole, Econazole, Fenticonazole, Ketoconazole, Isoconazole, Miconazole, Oxiconazole, Sertaconazole, Sulconazole, Tioconazole) • triazoles (Fluconazole) • benzimidazole (Thiabendazole)
Other topicals	Ciclopirox • Ethylparaben • Flucytosine • Salicylic acid • Selenium sulfide • Tolnaftate • Undecylenic acid • allylamines (Amorolfine, Butenafine, Naftifine, Terbinafine)
For systemic use	Griseofulvin • allylamine (Terbinafine) • polyene antimycotic (Amphotericin B) • triazoles (Itraconazole, Posaconazole, Voriconazole) • echinocandins (Anidulafungin, Caspofungin, Micafungin)
Other	Tea tree oil • citronella oil • lemon grass • orange oil • patchouli • lemon myrtle