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Merck

SML0059

Sigma-Aldrich

BLT-1

≥98% (HPLC)

别名:

2-己基-1-环戊酮氨基硫脲, 33M20, BLT1, MIT 9952-53, 阻断脂质转运-1

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About This Item

经验公式(希尔记法):
C12H23N3S
分子量:
241.40
MDL號碼:
分類程式碼代碼:
51111800
PubChem物質ID:
NACRES:
NA.77

品質等級

化驗

≥98% (HPLC)

形狀

powder

顏色

white to tan

溶解度

DMSO: ≥13 mg/mL

儲存溫度

2-8°C

SMILES 字串

CCCCCCC1CCC\C1=N/NC(N)=S

InChI

1S/C12H23N3S/c1-2-3-4-5-7-10-8-6-9-11(10)14-15-12(13)16/h10H,2-9H2,1H3,(H3,13,15,16)/b14-11+

InChI 密鑰

OWGUSBISUVLUJF-SDNWHVSQSA-N

應用

BLT-1可用于研究在胆固醇流入和流出中起作用的细胞信号通路。
BLT-1(阻断脂质转运-1)已被用作SR-BI(清道夫受体,B类,I型)介导的脂质转移的抑制剂,以确定miR-223-3p是否从多形核中性粒细胞(PMN)输出高密度脂蛋白(HDL)依赖于SR-BI介导的脂质通量。它也被用作SR-BI抑制剂,通过SR-B1研究HDL对单核细胞系中骨钙素(OCN)表达的影响。

生化/生理作用

阻断脂质转运-1(BLT-1)是SR-BI(清道夫受体,B类,I型)介导的脂质转移的特异性抑制剂。该化合物抑制HDL胆固醇醚的细胞选择性脂质摄取和细胞胆固醇向HDL的流出。

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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Yue-Hua Feng et al.
Lipids in health and disease, 17(1), 200-200 (2018-08-27)
Scavenger receptor BI (SR-BI) is a classic high-density lipoprotein (HDL) receptor, which mediates selective lipid uptake from HDL cholesterol esters (HDL-C). Apolipoprotein M (ApoM), as a component of HDL particles, could influence preβ-HDL formation and cholesterol efflux. The aim of
Maria C de Beer et al.
Journal of lipids, 2013, 283486-283486 (2013-02-23)
Studies suggest that inflammation impairs reverse cholesterol transport (RCT). We investigated whether serum amyloid A (SAA) contributes to this impairment using an established macrophage-to-feces RCT model. Wild-type (WT) mice and mice deficient in SAA1.1 and SAA2.1 (SAAKO) were injected intraperitoneally
Ivana Halova et al.
Frontiers in immunology, 3, 119-119 (2012-06-02)
Migration of mast cells is essential for their recruitment within target tissues where they play an important role in innate and adaptive immune responses. These processes rely on the ability of mast cells to recognize appropriate chemotactic stimuli and react
High density lipoprotein modulates osteocalcin expression in circulating monocytes: a potential protective mechanism for cardiovascular disease in type 1 diabetes
Maddaloni E, et al.
Cardiovascular Diabetology, 16(1), 1-11 (2017)
Jérôme Robert et al.
Molecular neurodegeneration, 12(1), 60-60 (2017-08-24)
Alzheimer's Disease (AD), characterized by accumulation of beta-amyloid (Aβ) plaques in the brain, can be caused by age-related failures to clear Aβ from the brain through pathways that involve the cerebrovasculature. Vascular risk factors are known to increase AD risk

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