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Merck

L6545

Sigma-Aldrich

来曲唑

≥98% (HPLC), powder, non-steroidal aromatase inhibitor

别名:

4,4′-(1H-1,2,4-三唑-1-基亚甲基)双苄腈

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About This Item

经验公式(希尔记法):
C17H11N5
分子量:
285.30
MDL號碼:
分類程式碼代碼:
51111800
PubChem物質ID:
NACRES:
NA.77

product name

来曲唑, ≥98% (HPLC)

化驗

≥98% (HPLC)

形狀

powder

顏色

white to off-white

溶解度

DMSO: >50 mg/mL

起源

Novartis

儲存溫度

2-8°C

SMILES 字串

N#CC(C=C1)=CC=C1C(N2C=NC=N2)C3=CC=C(C#N)C=C3

InChI

1S/C17H11N5/c18-9-13-1-5-15(6-2-13)17(22-12-20-11-21-22)16-7-3-14(10-19)4-8-16/h1-8,11-12,17H

InChI 密鑰

HPJKCIUCZWXJDR-UHFFFAOYSA-N

基因資訊

human ... CYP19A1(1588)

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應用

来曲唑已用于:
  • 在类器官生长试验中测定其抑制力(48)
  • 研究类固醇受体共激活因子1(SRC-1)介导的海马PSD-95内源性雌激素调节作用(49)
  • 研究其对肿瘤诱导的痛觉过敏的作用 (50)
  • 对大鼠进行激素干预(51)研究其对脂质运载蛋白-2(Lcn2)的作用(52)研究其对机械痛觉过敏和芳香化酶表达的作用(53)

生化/生理作用

来曲唑是一种佐剂,可用于治疗乳腺癌。
来曲唑是第三代非甾体芳香酶抑制剂。 它是芳香酶系统的竞争性抑制剂,因此可抑制雄激素向雌激素转化。来曲唑通过竞争性结合到该酶的细胞色素P450亚基的血红素上而抑制芳香酶,导致所有组织中雌激素的生物合成减少。

特點和優勢

该化合物是受体分类及信号转导手册上核受体(类固醇)页面上的特色化合物。想要浏览手册的其他页面, 请单击此处
该化合物是由 Novartis开发。浏览其他医药开发的化合物和已批准的药物/候选药物清单,请点击此处

象形圖

Health hazard

訊號詞

Warning

危險聲明

危險分類

Repr. 2 - STOT RE 2

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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访问文档库

Bianca Posocco et al.
PloS one, 15(2), e0228822-e0228822 (2020-02-08)
A novel LC-MS/MS method was developed for the quantification of the new cyclin dependent kinase inhibitors (CDKIs) palbociclib and ribociclib and the aromatase inhibitor letrozole used in combinatory regimen. The proposed method is appropriate to be applied in clinical practice
Natalia Lagunas et al.
Frontiers in neuroanatomy, 16, 902218-902218 (2022-07-12)
Sex steroid hormones, such as androgens and estrogens, are known to exert organizational action at perinatal periods and activational effects during adulthood on the brain and peripheral tissues. These organizational effects are essential for the establishment of biological axes responsible
Drugs for Pregnant and Lactating Women E-Book (2009)
Zahra Shaaban et al.
Iranian journal of basic medical sciences, 25(1), 110-120 (2022-06-04)
Despite prevalence of polycystic ovary syndrome (PCOS) among childbearing women and development of many animal models for this syndrome, information on its etiology is still scarce. The intrauterine hyperandrogenic environment may underlie changes at the level of hypothalamus, pituitary, ovary
Lijun Tan et al.
Cancers, 14(19) (2022-10-15)
Antiestrogen therapy (AET) is an alternative to cytotoxic chemotherapy for recurrent ovarian cancer, yet the often short duration of response suggests mechanisms of resistance. We previously demonstrated that tumor microenvironment interleukin-6/leukemia inhibitory factor (IL6/LIF) cytokines induce tumor cell JAK-STAT signaling

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