Terbinafine - 10mM in DMSO , Squalene monooxygenase inhibitor, CAS No.91161-71-6, Squalene monooxygenase inhibitor

CAS: 91161-71-6 Cat. No.: T409060 Molecular Weight: 291.43 EC Number: 618-706-8 PubChem CID: 1549008
AVAILABLE TO ORDER
GRADE & PURITY 10mM in DMSO
Synonyms
SF 86-327 | N-​[(2E)​-​6,​6-​dimethyl-​2-​hepten-​4-​yn-​1-​yl]​-​N-​methyl-1-​naphthalenemethanami​ne
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
1ml
T409060-1ml
2

$85.90

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Why this grade

10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 7 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Information

Terbinafine Terbinafine (SF 86-327) is used to treat infections caused by a fungus. It works by killing the fungus or preventing its growth.
In vitro

Terbinafine (50 μM to 100 μM) inhibits only marginally the metabolism of ethoxycoumarin (CYP1A2), tolbutamide (CYP2C9), or ethynylestradiol, CsA, and cortisol. Terbinafine proves to be a potent inhibitor of the CYP2D6-mediated dextromethorphan O-demethylation and bufuralol 1-hydroxylation with IC50values of 0.2 μM and 0.25 μM, respectively. Terbinafine is highly activ Aspergillus isolates (minimum inhibitory concentration [MIC] 0.01 to 2 mg/mL) with a primary fungicidal action (minimum fungicidal concentration [MFC] 0.02 to 4 mg/mL). Terbinafine inhibits dextromethorphan O-demethylation with an apparent Ki ranging from 28 to 44 nM in human hepatic microsomes and averaging 22.4 nM for the heterologously expressed enzymes. Terbinafine shows a very strong activity in vitro against Penicillium spp., Paecilomyces spp., Trichoderma spp., Acremonium spp. and Arthrographis spp. with GMs <1 mg/L. Terbinafine decreases the levels of phosphorylated extracellular signal-regulated kinase (ERK). Terbinafine might cause a decrease of MEK, which in turn up-regulates p53 through the inhibition of ERK phosphorylation, and finally causes an increase of p21expression and cell-cycle arrest.

In vivo


Cell Data

cell lines:HUVECs

Concentrations:

Incubation Time:

Powder Purity:≥99%

Specifications

Synonyms
SF 86-327 | N-​[(2E)​-​6, ​6-​dimethyl-​2-​hepten-​4-​yn-​1-​yl]​-​N-​methyl-1-​naphthalenemethanami​ne
Specifications & Purity
10mM in DMSO
Biochemical and Physiological Mechanisms
Terbinafine (SF 86-327) is used to treat infections caused by a fungus. It works by killing the fungus or preventing its growth.
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
This product requires cold chain shipping. Ground and other economy services are not available.
Action Type
INHIBITOR
Mechanism of action
Squalene monooxygenase inhibitor
Product Properties
ALogP5.6
Names and Identifiers
Isomeric SMILES CC(C)(C)C#C/C=C/CN(C)CC1=CC=CC2=CC=CC=C21
Alternate CAS 91161-71-6
PubChem CID 1549008
MeSH Entry Terms (E)-N-(6,6-dimethyl-2-heptenynyl)-N-methyl-1-naphthalenementhamin hydrochloride;DA 5505;Lamisil;SF 86 327;SF 86-327;SF 86327;SF-86-327;SF86327;TDT 067;TDT-067;TDT067;terbinafine;terbinafine hydrochloride;Terbinafine, (Z)-;terbinafine, (Z)-isomer
Molecular Weight 291.43

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Associated Targets(Human)
CYP2D6 Tclin Cytochrome P450 2D6 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
SQLE Tchem Squalene monooxygenase (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
SIGMAR1 Tclin Sigma non-opioid intracellular receptor 1 (2 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Chemical and Physical Properties
SolubilitySolubility (25°C) In vitro DMSO: 128 mg/mL (199.49 mM); Water: Insoluble; Ethanol: Insoluble;
Melt Point(°C)43 °C
Documents & Articles
Citations of This Product
References
1. Yue Qun, Meng Jie, Qiu Yue, Yin Miaomiao, Zhang Liwen, Zhou Weiping, An Zhiqiang, Liu Zihe, Yuan Qipeng, Sun Wentao, Li Chun, Zhao Huimin, Molnár István, Xu Yuquan, Shi Shuobo.  (2023)  A polycistronic system for multiplexed and precalibrated expression of multigene pathways in fungi.  Nature Communications,  14  (1): (1-10).  [PMID:37460548] [10.1038/s41467-023-40027-0]
2. Meng Wang, Yanwen Zhou, Zhaohui Wang.  (2023)  Unearth the ultrapotent intrinsic fungicidal efficacy of the surface-piercing CuFeSe2-PVP nano-blade.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2023.142603]
3. Hui Lu, Wanqian Li, Malcolm Whiteway, Hongkang Wang, Shuo Zhu, Zhe Ji, Yanru Feng, Lan Yan, Ting Fang, Liping Li, Tingjunhong Ni, Xiaolong Zhang, Quanzhen Lv, Zichao Ding, Lijuan Qiu, Dazhi Zhang, Yuanying Jiang.  (2022)  A Small Molecule Inhibitor of Erg251 Makes Fluconazole Fungicidal by Inhibiting the Synthesis of the 14α-Methylsterols.  mBio,  14  (1):   [PMID:36475771] [10.1128/mbio.02639-22]
4. Guo Penghao, Chen Jianlong, Tan Yiwei, Xia Li, Zhang Weizheng, Li Xiaojie, Jiang Yujie, Li Ruiying, Chen Chunmei, Liao Kang, Peng Yaqin.  (2022)  Comparison of molecular and MALDI-TOF MS identification and antifungal susceptibility of clinical Fusarium isolates in Southern China.  Frontiers in Microbiology,      [PMID:36386677] [10.3389/fmicb.2022.992582]
5. Xu Xue, Naseri Ali, Houbraken Jos, Akbari Farzaneh, Wang Xiaodong, Zhao Rongfen, Zhang Hong, Najafzadeh Mohammad Javad, Deng Shuwen.  (2021)  Identification and in vitro antifungal susceptibility of causative agents of onychomycosis due to Aspergillus species in Mashhad, Iran.  Scientific Reports,  11  (1): (1-8).  [PMID:33762586] [10.1038/s41598-021-86038-z]
6. Li Wanqian, Whiteway Malcolm, Hang Sijin, Yu Jinhua, Lu Hui, Jiang Yuanying.  (2025)  Impairing the interaction between Erg11 and cytochrome P450 reductase Ncp1 enhances azoles’ antifungal activities.  Nature Communications,  16  (1): (1-18).  [PMID:40707518] [10.1038/s41467-025-62131-z]
7. Ya-Hong Wang, Die Zhu, Dan Wang, Ruo-Cheng Sheng, Li-Chao Wang, Chen-Ning Zhang, Muhammad Faizan Latif, Huan Li, Feng-Mao Chen.  (2026)  The complex subunit VdAP-2α regulates polar growth, ergosterol metabolism, and virulence in Verticillium dahliae.  Virulence,      [PMID:] [10.1080/21505594.2026.2647468]
Solution Calculators
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