KP 103

KP 103 Struktur
164650-44-6
CAS-Nr.
164650-44-6
Englisch Name:
KP 103
Synonyma:
Efinaconazole;Jublia;Efinaconzole;JUBLIA; KP 103; KP103;(alphaR,betaR)-alpha-(2,4-Difluorophenyl)-beta-methyl-4-methylene-alpha-(1H-1,2,4-triazol-1-ylmethyl)-1-piperidineethanol;KP 103;Efluconazole;KP 103 USP/EP/BP;Efinaconazole 13CD2;Efinaconazole 13CD6
CBNumber:
CB21313343
Summenformel:
C18H22F2N4O
Molgewicht:
348.39
MOL-Datei:
164650-44-6.mol

KP 103 Eigenschaften

Schmelzpunkt:
192-195°C
Siedepunkt:
512.2±60.0 °C(Predicted)
Dichte
1.26±0.1 g/cm3(Predicted)
storage temp. 
-20°C
Löslichkeit
Chloroform (Slightly), Methanol (Slightly)
pka
12.11±0.29(Predicted)
Aggregatzustand
powder
Farbe
white to beige
Optische Aktivität
[α]/D -85 to -95°, c = 1 in chloroform
Sicherheit
  • Risiko- und Sicherheitserklärung
  • Gefahreninformationscode (GHS)
Bildanzeige (GHS) GHS hazard pictograms
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H361 Kann vermutlich die Fruchtbarkeit beeinträchtigen oder das Kind im Mutterleib schädigen. Reproduktionstoxizität Kategorie 2 Warnung P201, P202, P281, P308+P313, P405,P501
Sicherheit
P201 Vor Gebrauch besondere Anweisungen einholen.
P308+P313 BEI Exposition oder falls betroffen: Ärztlichen Rat einholen/ärztliche Hilfe hinzuziehen.

KP 103 Chemische Eigenschaften,Einsatz,Produktion Methoden

Beschreibung

In October 2013, efinaconazole (also known as KP-103) was approved in Canada as a 10% topical solution for the treatment of onychomycosis. Like other azole antifungal agents, efinaconazole acts by disrupting fungal cell membranes through inhibition of sterol 14α-demethylase, an enzyme involved in the biosynthesis of ergosterol, which is a key component of the fungal cell membrane. Efinaconazole has potent antifungal activity against clinical isolates of dermatophytes, including Trichophyton mentagrophyes (MIC80 =0.125 μg/mL) and Trichophyton rubrum (MIC80 =0.25 μg/mL), as well as against Candida and Malassezia species. Unlike other antifungal agents, efinaconazole retains activity in the presence of keratin, indicating that more unbound drug is available at the site of action. Efinaconazole is efficacious in guinea-pig models of fungal infection. Efinaconazole is prepared by reaction of an epoxide intermediate with 4-methylenepiperidine.

Verwenden

Efinaconazole has been used as:
  • a topical anti-onychomycosis drug to determine its effects on Trichophyton rubrum and Trichophyton interdigitale
  • as an anti-fungal agent to study its permeability into the nail lysates
  • as an anti-fungal agent to study its effects on Candida africana and Candida dubliniensis

Definition

ChEBI: A member of the class of triazoles that is butan-2-ol which is substituted at positions 1, 2, and 3 by 1,2,4-triazol-1-yl, 2,4-difluorophenyl, and 4-methylenepiperidin-1-yl groups, respectively (the 2R,3R stereoisomer). It is an antifungal drug used for the topical treatment of onychomycosis (a nail infection caused mainly by dermatophytes).

KP 103 Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


KP 103 Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 322)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Jinan Qinmu Fine Chemical Co.,Ltd.
+8618660799346
sales@qinmuchem.com China 1009 58
Guangzhou TongYi biochemistry technology Co.,LTD
+8613073028829
mack@tongyon.com China 2996 58
Anhui Dexinjia Biopharm Co., Ltd
+86-531-82375887 +86-15064153060
sales01@ahdxj.com China 292 58
Sinoway Industrial co., ltd.
0592-5800732; +8613806035118
xie@china-sinoway.com China 992 58
Firsky International Trade (Wuhan) Co., Ltd
+8615387054039
admin@firsky-cn.com China 436 58
Zhengzhou Anbu Chem Co.,Ltd
+86-0371-88006763; +8615988602810
sales@anbuchem.com China 3000 58
Zibo Hangyu Biotechnology Development Co., Ltd
+86-0533-2185556 +8617865335152
Mandy@hangyubiotech.com China 11013 58
Anhui Ruihan Technology Co., Ltd
+8617756083858
daisy@anhuiruihan.com China 994 58
Capot Chemical Co.,Ltd.
571-85586718 +8613336195806
sales@capotchem.com China 29797 60
Beijing Cooperate Pharmaceutical Co.,Ltd
010-60279497
sales01@cooperate-pharm.com CHINA 1811 55

164650-44-6()Verwandte Suche:


  • KP 103
  • KP 103 (pharmaceutical)
  • (2R,3R)-2-(2,4-Difluorophenyl)-3-(4-methylenepiperidin-1-yl)-1-(1,2,4-triazol-1-yl)-2-butanol
  • Efinaconazole(KP 103)
  • (R,R)-2-(2,4-Difluorophenyl)-3-(4-methylenepiperidin-1-yl)-1-(1,2,4-triazol-1-yl)-2-butanol
  • (αR,βR)-α-(2,4-Difluorophenyl)-β-methyl-4-methylene-α-(1H-1,2,4-triazol-1-ylmethyl)-1-piperidineethanol
  • 1-Piperidineethanol, α-(2,4-difluorophenyl)-β-methyl-4-methylene-α-(1H-1,2,4-triazol-1-ylmethyl)-, (αR,βR)-
  • Efinaconazole (Jublia)
  • KP 103 USP/EP/BP
  • EfinaconazoleQ: What is Efinaconazole Q: What is the CAS Number of Efinaconazole Q: What is the storage condition of Efinaconazole Q: What are the applications of Efinaconazole
  • Efinaconazole 13CD2
  • Efinaconazole 13CD6
  • Efinaconazole D4Q: What is Efinaconazole D4 Q: What is the CAS Number of Efinaconazole D4
  • Efinaconazole
  • (alphaR,betaR)-alpha-(2,4-Difluorophenyl)-beta-methyl-4-methylene-alpha-(1H-1,2,4-triazol-1-ylmethyl)-1-piperidineethanol
  • Jublia
  • JUBLIA; KP 103; KP103
  • Efinaconzole
  • Efluconazole
  • (2R,3R)-2-(2,4-Difluorophenyl)-3-(4-methylenepiperidin-1-yl)-1-(1H-1,2,4-triazol-1-yl)butan-2-ol (Efinaconazole)
  • Efinaconazole In-House
  • 164650-44-6
  • 1644650-44-6
  • 164650-44-7
  • C18H22F2N4O
  • Inhibitors
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