推荐产品
product name
四咪唑 盐酸盐, phosphatase inhibitor
生物源
synthetic (organic)
描述
alkaline phosphatase inhibitor
化驗
≥99% (TLC)
形狀
powder
mp
266-267 °C (lit.)
溶解度
water: 50 mg/mL, clear, colorless
SMILES 字串
Cl[H].C1CN2CC(N=C2S1)c3ccccc3
InChI
1S/C11H12N2S.ClH/c1-2-4-9(5-3-1)10-8-13-6-7-14-11(13)12-10;/h1-5,10H,6-8H2;1H
InChI 密鑰
LAZPBGZRMVRFKY-UHFFFAOYSA-N
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應用
四咪唑衍生物作为碱性磷酸酶抑制剂的结构-活性关系。
适于抑制各种哺乳动物碱性磷酸酶(例如,肝、肾、胎盘、骨和肿瘤)。肠道碱性磷酸酶仅受到轻微的抑制。
其他說明
外消旋形式的左旋咪唑。
相關產品
訊號詞
Warning
危險分類
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
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
個人防護裝備
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
其他客户在看
eLife, 9 (2020-07-10)
Proper positioning of cells is essential for many aspects of development. Daughter cell positions can be specified via orienting the cell division axis during cytokinesis. Rotatory actomyosin flows during division have been implied in specifying and reorienting the cell division
Nature physics, 17(8), 920-925 (2021-11-16)
Oocytes are large cells that develop into an embryo upon fertilization1. As interconnected germ cells mature into oocytes, some of them grow-typically at the expense of others that undergo cell death2-4. We present evidence that in the nematode Caenorhabditis elegans
Kinetics and inhibition of alkaline phosphatases from canine tissues.
Biochimica et biophysica acta, 289(1), 158-168 (1972-11-10)
PLoS computational biology, 17(7), e1009185-e1009185 (2021-07-20)
Complex dendritic trees are a distinctive feature of neurons. Alterations to dendritic morphology are associated with developmental, behavioral and neurodegenerative changes. The highly-arborized PVD neuron of C. elegans serves as a model to study dendritic patterning; however, quantitative, objective and
Genetics, 199(2), 497-509 (2014-12-10)
The L1CAM family of cell adhesion molecules is a conserved set of single-pass transmembrane proteins that play diverse roles required for proper nervous system development and function. Mutations in L1CAMs can cause the neurological L1 syndrome and are associated with
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