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Merck
CN

K4394

PKF118-310

≥98% (HPLC)

别名:

1,6-二甲基-嘧啶 [5,4-e]-1,2,4-三嗪-5,7 (1H,6H)-二酮, 毒性黄素, 黄丝菌素

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关于此项目

经验公式(希尔记法):
C7H7N5O2
化学文摘社编号:
分子量:
193.16
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352200
MDL number:
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InChI

1S/C7H7N5O2/c1-11-6(13)4-5(10-7(11)14)12(2)9-3-8-4/h3H,1-2H3

SMILES string

CN1N=CN=C(C1=N2)C(N(C)C2=O)=O

InChI key

SLGRAIAQIAUZAQ-UHFFFAOYSA-N

assay

≥98% (HPLC)

form

powder

color

white to light brown

solubility

H2O: 10 mg/mL, clear

storage temp.

2-8°C

Quality Level

Biochem/physiol Actions

PKF118-310 是 Tcf4/β-连环蛋白信号通路的拮抗剂。该化合物破坏 Tcf4/β-连环蛋白复合物并抑制 Tcf4 应答基因的表达。PKF118-310 抑制肝细胞癌、结肠肿瘤和淋巴细胞白血病细胞系中生存素的表达并诱导细胞凋亡。
PKF118-310 是一种 Tcf4/β-连环蛋白拮抗剂。

pictograms

Skull and crossbones

signalword

Danger

hcodes

Hazard Classifications

Acute Tox. 2 Oral

存储类别

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

涉药品监管产品
此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Jinwoo Kim et al.
Molecular microbiology, 54(4), 921-934 (2004-11-04)
Burkholderia glumae BGR1 produces a broad-host range phytotoxin, called toxoflavin, which is a key pathogenicity factor in rice grain rot and wilt in many field crops. Our molecular and genetic analyses of toxoflavin-deficient mutants demonstrated that gene clusters for toxoflavin
Phyllis S Y Chong et al.
Oncogene, 38(9), 1508-1519 (2018-10-12)
Aberrant activation of Wnt/β-catenin signaling pathway is essential for the development of AML; however, the mechanistic basis for this dysregulation is unclear. PRL-3 is an oncogenic phosphatase implicated in the development of LSCs. Here, we identified Leo1 as a direct
Boknam Jung et al.
Nature communications, 9(1), 31-31 (2018-01-04)
Bacterial-fungal interactions are widely found in distinct environments and contribute to ecosystem processes. Previous studies of these interactions have mostly been performed in soil, and only limited studies of aerial plant tissues have been conducted. Here we show that a
T Nagamatsu et al.
Chemical & pharmaceutical bulletin, 41(2), 362-368 (1993-02-01)
6-Phenyl analogs of toxoflavin (1-methyl-6-phenylpyrimido[5,4-e]-1,2,4-triazine-5,7(1H,6H)-diones ) (7a--f) and their 4-oxides (8a-f) were synthesized by nitrosative or nitrative cyclization of the aldehyde hydrazones (6a-f) of 6-(1-methylhydrazino)-3-phenyluracil (5). Both sets of compounds, 7a-f and 8a-f, gave the corresponding 1-demethyl derivatives (10a-f) upon
K A Buckle et al.
The Journal of applied bacteriology, 68(6), 571-576 (1990-06-01)
Tempe bongkrek was prepared from partially defatted coconut by fermentation with the mould Rhizopus oligosporus. The addition of 2% sodium chloride decreased but did not inhibit formation of bongkrek acid by Pseudomonas cocovenenans strain ITB in either coconut culture medium

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Cell cycle phases (G1, S, G2, M) regulate cell growth, DNA replication, and division in proliferating cells.

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