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Merck

UC280

酮康唑

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

同義詞:

(±)--1-乙酰基-4-(4-[(2-[2,4-二氯苯基]-2-[1H-咪唑-1-基甲基]-1,3-二氧戊环-4-基)-甲氧基]苯基)哌嗪

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關於此項目

經驗公式(希爾表示法):
C26H28Cl2N4O4
CAS 編號:
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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產品名稱

酮康唑,

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抑制剂
酮康唑作为细胞色素 P450(CYP)抑制剂用于研究其在大鼠胚胎睾丸中的作用[1]。酮康唑也用于筛选杀灭非复制型结核分枝杆菌的抗菌药物 [2]。此外,研究曾将酮康唑用于抗真菌药物敏感性试验 [3],也用作标准抗真菌药物 [4]

Biochem/physiol Actions

抗真菌剂
酮康唑是一种咪唑衍生物。它在对真菌细胞壁中的羊毛固醇转化为麦角固醇的抑制中起着重要作用。酮康唑对皮肤癣菌病、浅部念珠菌病和副球孢子菌病均有疗效。

Features and Benefits

该化合物由 强生公司 开发。如需浏览其他制药公司开发的化合物和批准的药物/候选药物列表,请点击此处
这种化合物是 ADME 毒性研究的特色产品。点击此处查看更多特色 ADME 毒性产品。登录sigma.com/discover-bsm可了解更多关于其他研究领域中关于生物活性小分子的消息。

Packaging

无底玻璃瓶。内含物装在插入式熔锥内。

Preparation Note

酮康唑可溶于 DMSO [1]

signalword

Danger

Hazard Classifications

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

存儲類別/等級

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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分析證明 (COA)

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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.
D Feldman
Endocrine reviews, 7(4), 409-420 (1986-11-01)
Ketoconazole.
Hay, R.
British Medical Journal (Clinical Research ed.), 285(6342), 584-584 (1982)
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
Gökalp Işcan et al.
Journal of agricultural and food chemistry, 50(14), 3943-3946 (2002-06-27)
Essential oils of peppermint Mentha piperita L. (Lamiaceae), which are used in flavors, fragrances, and pharmaceuticals, were investigated for their antimicrobial properties against 21 human and plant pathogenic microorganisms. The bioactivity of the oils menthol and menthone was compared using

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