T6638
托萘酯
别名:
甲基-(3-间甲苯基)硫代氨基甲酸-2-萘酯
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关于此项目
经验公式（希尔记法）:
C19H17NOS
化学文摘社编号:
分子量:
307.41
NACRES:
NA.85
PubChem Substance ID:
UNSPSC Code:
51302004
EC Number:
219-266-6
MDL number:
InChI key
FUSNMLFNXJSCDI-UHFFFAOYSA-N
InChI
1S/C19H17NOS/c1-14-6-5-9-17(12-14)20(2)19(22)21-18-11-10-15-7-3-4-8-16(15)13-18/h3-13H,1-2H3
SMILES string
CN(C(=S)Oc1ccc2ccccc2c1)c3cccc(C)c3
form
powder
storage condition
(Keep container tightly closed in a dry and well-ventilated place.)
color
white to off-white
solubility
chloroform: soluble 50 mg/mL
antibiotic activity spectrum
fungi
mode of action
enzyme | inhibits
storage temp.
2-8°C
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Application
甲苯磺酸盐用于研究角鲨烯环氧酶抑制的限速步骤中，麦角甾醇（甾醇）的生物合成机理。 甲苯磺酸盐在临床上用于治疗皮肤感染，例如脚癣、股癣和癣菌。它也被用作抗真菌功效研究的比较化合物。
Biochem/physiol Actions
甲苯磺酸盐通过抑制角鲨烯环氧酶来防止麦角固醇生物合成。也有报道称其会扭曲菌丝并阻碍易感生物体中的菌丝生长。甲苯磺酸盐可抑制黄曲霉毒素的生物合成。
Packaging
1G,5G
Other Notes
保存于密闭容器内，置于干燥通风处。
存储类别
13 - Non Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Andrew E Czeizel et al.
Reproductive toxicology (Elmsford, N.Y.), 18(3), 443-444 (2004-04-15)
Teratogenic studies of tolnaftate, an antifungal agent, in humans have not been published. The population-based data set of the Hungarian Case-Control Surveillance of Congenital Abnormalities, 1980-1996 contained 22843 fetuses or newborns with congenital abnormalities and 38151 matched controls without congenital
Tang Bo et al.
The journal of physical chemistry. B, 110(17), 8877-8884 (2006-04-28)
Based on the fact that tolnaftate degrade to beta-naphthol sodium (RONa) at 5.00 mol/L NaOH solution and RO(-) was protonated to ROH after being acidified and adjusted to the pH 4.50 by acetic acid-sodium acetate buffer solution, we studied and
D Arul Dhas et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 79(5), 993-1003 (2011-05-14)
Vibrational analysis of the thionocarbamate fungicide tolnaftate which is antidermatophytic, antitrichophytic and antimycotic agent, primarily inhibits the ergosterol biosynthesis in the fungus, was carried out using NIR FT-Raman and FTIR spectroscopic techniques. The equilibrium geometry, various bonding features, harmonic vibrational
S T Patil et al.
Fresenius' journal of analytical chemistry, 367(1), 91-93 (2001-03-03)
Tolnaftate, an antifungal drug (TF) and related impurities arising from synthesis, viz., N-methyl-m-toluidine (NMmT) and beta-naphthol-1-chlorothio carbamate (beta-NCTC) can be determined by supercritical fluid chromatography. Even though it was possible to elute TF completely with neat SCF CO2, the peaks
J Pannu et al.
Antimicrobial agents and chemotherapy, 53(8), 3273-3279 (2009-05-13)
NB-002 is an oil-in-water emulsion designed for use for the treatment of skin, hair, and nail infections. The activity of NB-002 was compared to the activities of the available antifungal drugs against the major dermatophytes responsible for cutaneous infections, Trichophyton
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