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Merck

UC280

ケトコナゾール

≥99% (HPLC), Cytochrome P450c17 inhibitor, solid

別名:

(±)-cis-1-アセチル-4-(4-[(2-[2,4-ジクロロフェニル]-2-[1H-イミダゾール-1-イルメチル]-1,3-ジオキソラン-4-イル)-メトキシ]フェニル)ピペラジン

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この商品について

実験式(ヒル表記法):
C26H28Cl2N4O4
CAS番号:
分子量:
531.43
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12161501
EC Number:
265-667-4
MDL number:
Assay:
≥99% (HPLC)
Form:
solid

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製品名

ケトコナゾール,

assay

≥99% (HPLC)

form

solid

color

white to light yellow

solubility

DMSO: soluble

antibiotic activity spectrum

fungi, yeast

mode of action

enzyme | inhibits

originator

Johnson & Johnson

storage temp.

2-8°C

SMILES string

CC(=O)N1CCN(CC1)c2ccc(OC[C@H]3CO[C@@](Cn4ccnc4)(O3)c5ccc(Cl)cc5Cl)cc2

InChI

1S/C26H28Cl2N4O4/c1-19(33)31-10-12-32(13-11-31)21-3-5-22(6-4-21)34-15-23-16-35-26(36-23,17-30-9-8-29-18-30)24-7-2-20(27)14-25(24)28/h2-9,14,18,23H,10-13,15-17H2,1H3/t23-,26-/m0/s1

InChI key

XMAYWYJOQHXEEK-OZXSUGGESA-N

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Application

CYP3A4インヒビタ-
Ketoconazole has been used as a cytochrome P450 (CYP) inhibitor to study its functions in embryonic testes of rats[1]. Ketoconazole has also been used for the screening of antimicrobial agents against nonreplicating M. tuberculosis[2]. Furthermore, studies have used ketoconazole for antifungal susceptibility testing[3] and also as a standard antifungal agent[4].

Biochem/physiol Actions

抗真菌薬
Ketoconazole is an imidazole derivative. It plays an important role in inhibiting the conversion of lanosterol to ergosterol in the cell wall of fungi. Ketoconazole has therapeutic effects against dermatophytosis, superficial candidiasis, and paracoccidioidomycosis.

Features and Benefits

This compound is a featured product for ADME Tox research. Click here to discover more featured ADME Tox products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm.
This compound was developed by Johnson & Johnson. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.

Packaging

底の開いたガラス瓶内容物は内部に挿入され接着された円錐部に入っています。

Preparation Note

Ketoconazole is soluble in DMSO[1].

signalword

Danger

Hazard Classifications

Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Repr. 1B - STOT RE 2

保管分類

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges


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文書ライブラリで、最近購入した製品の文書を検索できます。

文書ライブラリにアクセスする

Po-Ren Hsueh et al.
Antimicrobial agents and chemotherapy, 49(2), 512-517 (2005-01-28)
The susceptibilities of nonduplicate isolates to six antifungal agents were determined for 391 blood isolates of seven Candida species, 70 clinical isolates (from blood or cerebrospinal fluid) of Cryptococcus neoformans, and 96 clinical isolates of four Aspergillus species, which were
Ketoconazole and other imidazole derivatives as inhibitors of steroidogenesis
Feldman, David
Endocrine Reviews, 7(4), 409-420 (1986)
Ketoconazole.
Hay, R.
British Medical Journal (Clinical Research ed.), 285(6342), 584-584 (1982)
Ketoconazole and other imidazole derivatives as inhibitors of steroidogenesis.
D Feldman
Endocrine reviews, 7(4), 409-420 (1986-11-01)
Bhaskar Das et al.
Frontiers in pharmacology, 13, 990926-990926 (2023-01-24)
Mollugo oppositifolia Linn. is traditionally used in neurological complications. The study aimed to investigate in-vitro neuroprotective effect of the plant extracts through testing against acetylcholinesterase (AChE), butyrylcholinesterase (BChE), and β-secretase linked to Alzheimer's disease (AD). To understand the safety aspects

資料

Discover Bioactive Small Molecules for ADME/Tox

グローバルトレードアイテム番号

カタログ番号GTIN
UC280-5MG04061832932118
UC280-10MG04061832932101

質問

レビュー

評価値なし

アクティブなフィルタ

ライフサイエンス、有機合成、材料科学、クロマトグラフィー、分析など、あらゆる分野の研究に経験のあるメンバーがおります。.

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