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Efinaconazole - 99%, high purity , Lanosterol 14-alpha demethylase inhibitor, CAS No.164650-44-6, Lanosterol 14-alpha demethylase inhibitor

  • ≥99%
Item Number
E413214
Grouped product items
SKUSizeAvailabilityPrice Qty
E413214-100mg
100mg
In stock
$314.90
E413214-250mg
250mg
In stock
$708.90
E413214-1g
1g
In stock
$2,551.90
E413214-5g
5g
In stock
$11,481.90

Fungal Inhibitors

Basic Description

SynonymsEFINACONAZOLE|164650-44-6|(2R,3R)-2-(2,4-difluorophenyl)-3-(4-methylenepiperidin-1-yl)-1-(1H-1,2,4-triazol-1-yl)butan-2-ol|KP-103|JUBLIA|Clenafin|efinaconazol|efinaconazolum|IDP-108|UNII-J82SB7FXWB|J82SB7FXWB|KP103|CHEBI:82718|HSDB 8341|DTXSID40167787|(2R
Specifications & Purity99%
Storage TempStore at -20°C
Shipped InDry ice
Action TypeINHIBITOR
Mechanism of actionLanosterol 14-alpha demethylase inhibitor
Product Description

Information

Efinaconazole Efinaconazole (KP-103) is an inhibitor of 14 alpha-demethylase which is involved in the biosynthesis of ergosterol, a constituent of fungal cell membranes.


Targets

14 alpha-demethylase


In vitro

In in vitro antifungal susceptibility tests, efinaconazole shows lower minimum inhibitory concentration (MIC) than terbinafine, ciclopirox, itraconazole and amorolfine.


In vivo

Efinaconazole is a topical antifungal, so it has relatively low systemic accumulation. The plasma half-life after 10 days of administration is 29.9 h. It has high plasma protein-binding affinity from 95.8 to 96.5%; primarily to albumin, a1-acid glycoprotein and γ-globulin. Efinaconazole is metabolized extensively through oxidative and reductive processes resulting in a sole H3 metabolite. It may also undergo glucuronidation. Efinaconazole does not have significant interactions with CYP450 enzymes in the liver. CYP2C8, CYP2C9, CYP2C19 and CYP3A4 are inhibited by efinaconazole at concentrations higher than the systemic concentrations achieved clinically.

Product Properties

ALogP2

Names and Identifiers

IUPAC Name (2R,3R)-2-(2,4-difluorophenyl)-3-(4-methylidenepiperidin-1-yl)-1-(1,2,4-triazol-1-yl)butan-2-ol
INCHI InChI=1S/C18H22F2N4O/c1-13-5-7-23(8-6-13)14(2)18(25,10-24-12-21-11-22-24)16-4-3-15(19)9-17(16)20/h3-4,9,11-12,14,25H,1,5-8,10H2,2H3/t14-,18-/m1/s1
InChi Key NFEZZTICAUWDHU-RDTXWAMCSA-N
Canonical SMILES CC(C(CN1C=NC=N1)(C2=C(C=C(C=C2)F)F)O)N3CCC(=C)CC3
Isomeric SMILES C[C@H]([C@](CN1C=NC=N1)(C2=C(C=C(C=C2)F)F)O)N3CCC(=C)CC3
PubChem CID 489181
Molecular Weight 348.39

Certificates

Certificate of Analysis(COA)

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4 results found

Lot NumberCertificate TypeDateItem
K2229433Certificate of AnalysisOct 10, 2022 E413214
K2229434Certificate of AnalysisOct 10, 2022 E413214
K2229438Certificate of AnalysisOct 10, 2022 E413214
K2229443Certificate of AnalysisOct 10, 2022 E413214

Chemical and Physical Properties

SolubilitySolubility (25°C) In vitro DMSO: 69 mg/mL (198.05 mM); Ethanol: 69 mg/mL (198.05 mM); Water: Insoluble;
Specific Rotation[α][α]/D -85 to -95°, c = 1 in chloroform

Safety and Hazards(GHS)

Pictogram(s) GHS08
Signal Warning
Hazard Statements

H361:Suspected of damaging fertility or the unborn child

Precautionary Statements

P280:Wear protective gloves/protective clothing/eye protection/face protection.

P201:Obtain special instructions before use.

P308+P313:IF exposed or concerned: Get medical advice/attention.

P202:Do not handle until all safety precautions have been read and understood.

RIDADR NONHforallmodesoftransport

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