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156361

海因

Name: 海因
Brand: ALDRICH

98%

别名:

2,4-咪唑啉二酮, 海因

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关于此项目

经验公式（希尔记法）:

C₃H₄N₂O₂

化学文摘社编号:

461-72-3

分子量:

100.08

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24849609

EC Number:

207-313-3

Beilstein/REAXYS Number:

110598

MDL number:

MFCD00005259

Assay:

98%

Form:

powder

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属性

Quality Level

100

assay

98%

form

powder

mp

218-220 °C (lit.)

SMILES string

O=C1CNC(=O)N1

InChI

1S/C3H4N2O2/c6-2-1-4-3(7)5-2/h1H2,(H2,4,5,6,7)

InChI key

WJRBRSLFGCUECM-UHFFFAOYSA-N

说明

Application

本产品已被用作底物（在 40℃ 和 pH 9.0 下），以测定红小豆提取物中的 D -海因酶活性。

用于合成以下物质的反应物：
抗癌药物 N-苄基无赖氨酸视蛋白类似物
D-谷氨酸基抑制剂
抗糖尿病铬-2,4-噻唑烷二酮类
具有脑渗透性的GSK-3β抑制剂
作为 15-PGDH 抑制剂的噻唑烷二酮衍生物
放射增敏剂

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存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Asymmetric Synthesis of Adjacent Tri- and Tetrasubstituted Carbon Stereocenters: Organocatalytic Aldol Reaction of an Hydantoin Surrogate with Azaarene 2-Carbaldehydes.

June Izquierdo et al.

Chemistry (Weinheim an der Bergstrasse, Germany), 25(53), 12431-12438 (2019-07-19)

A bifunctional amine/squaramide catalyst promoted direct aldol addition of an hydantoin surrogate to pyridine 2-carbaldehyde N-oxides to afford adducts bearing two vicinal tertiary/quaternary carbons in high diastereo- and enantioselectivity (d.r. up to >20:1; ee up to 98 %) is reported. Acid

Synthesis and SAR of thiazolidinedione derivatives as 15-PGDH inhibitors.

Ying Wu et al.

Bioorganic & medicinal chemistry, 18(4), 1428-1433 (2010-02-04)

Prostaglandins have a short life in vivo because they are metabolized rapidly by oxidation to 15-ketoprostaglandins catalyzed by a cytosolic enzyme known as NAD(+)-dependent 15-hydroxyprostaglandin dehydrogenase (15-PGDH). Previously, CT-8, a thiazolidinedione analogue, was found to be a potent inhibitor of

Synthesis and in vitro screening of novel N-benzyl aplysinopsin analogs as potential anticancer agents.

Narsimha Reddy Penthala et al.

Bioorganic & medicinal chemistry letters, 21(5), 1411-1413 (2011-02-08)

A series of novel substituted (Z)-5-((1-benzyl-1H-indol-3-yl)methylene)imidazolidin-2,4-diones (3a-f) and (Z)-5-((1-benzyl-1H-indol-3-yl)methylene)-2-iminothiazolidin-4-ones (3g-o) have been synthesized utilizing microwave irradiation. These analogs were evaluated for in vitro cytotoxicity against a panel of 60 human tumor cell lines. Compound 3i exhibits potent growth inhibition against

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全球贸易项目编号

货号	GTIN
156361-100G	04061838742667
156361-500G	04061838742674