跳转至内容

尊敬的客户：

目前国际形势复杂多变，关税政策尚不明朗，这可能对我们的产品价格产生一定影响。在此情况下，我们希望就订单事宜与您进行友好沟通。

基于当前的不确定性，如果您选择在此期间下单，我们将保留根据实际情况调整价格的权利。同时，我们也理解市场变化可能给您带来的困扰，因此如果在订单实际发货前因关税政策变动导致价格出现较大波动，默克将与您进行协商讨论并视情况对订单进行调整或取消。

Merck
CN
所有图片(2)

主要文件

查看所有文档

C4522

Sigma-Aldrich

西咪替丁

别名:

SKF-92334

登录查看公司和协议定价

选择尺寸

5 G
¥1,135.44
10 G
¥1,592.51
25 G
¥3,483.43

¥1,135.44

预计发货时间2025年4月27日详情

获取大包装报价
所有图片(2)

选择尺寸

变更视图
5 G
¥1,135.44
10 G
¥1,592.51
25 G
¥3,483.43

About This Item

经验公式（希尔记法）:
C10H16N6S
CAS号:
51481-61-9
分子量:
252.34
EC 号:
257-232-2
MDL编号:
MFCD00133296
UNSPSC代码:
12352200
PubChem化学物质编号:
24277766
NACRES:
NA.77

¥1,135.44

预计发货时间2025年4月27日详情

获取大包装报价

表单

powder

质量水平

200

创始人

GlaxoSmithKline

储存温度

2-8°C

SMILES字符串

CN\C(NC#N)=N\CCSCc1nc[nH]c1C

InChI

1S/C10H16N6S/c1-8-9(16-7-15-8)5-17-4-3-13-10(12-2)14-6-11/h7H,3-5H2,1-2H3,(H,15,16)(H2,12,13,14)

InChI key

AQIXAKUUQRKLND-UHFFFAOYSA-N

基因信息

human ... ABCB1(5243) , CYP1A2(1544) , CYP3A4(1576) , HRH2(3274) , SLC9A2(6549) , SLC9A5(6553)
mouse ... Abcb1a(18671) , Abcb1b(18669)
rat ... Slc9a1(24782) , Slc9a3(24784) , Slc9a5(192215)

正在寻找类似产品? 访问 产品对比指南

相关类别

比较类似商品

查看完整比较结果

显示差异

1 of 4

此商品
PHR1075SML1493E2535
西咪替丁

C4522

西咪替丁

西咪替丁 Pharmaceutical Secondary Standard; Certified Reference Material

PHR1075

西咪替丁

Suprafenacine ≥98% (HPLC)

SML1493

Suprafenacine

Eprosartan mesylate ≥98% (HPLC)

E2535

Eprosartan mesylate

form

powder

form

-

form

powder

form

powder

Quality Level

200

Quality Level

300

Quality Level

-

Quality Level

100

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

room temp

originator

GlaxoSmithKline

originator

-

originator

-

originator

Abbott

Gene Information

human ... ABCB1(5243), CYP1A2(1544), CYP3A4(1576), HRH2(3274), SLC9A2(6549), SLC9A5(6553)
mouse ... Abcb1a(18671), Abcb1b(18669)
rat ... Slc9a1(24782), Slc9a3(24784), Slc9a5(192215)

Gene Information

human ... HRH2(3274)

Gene Information

-

Gene Information

human ... AGTR1(185)

生化/生理作用

H2组胺受体拮抗剂；I1咪唑啉受体激动剂；抗溃疡剂。通过抑制内皮细胞表面上E-选择蛋白的表达来阻断癌症转移，从而阻断肿瘤细胞的粘附。

特点和优势

该化合物由 GlaxoSmithKline 开发。想要浏览其他由制药公司开发的化合物以及已批准药物/候选药物清单，请单击此处。
这种化合物是 ADME 毒性研究的特色产品。点击此处发现更多特色 ADME 毒性产品。在sigma.com/discover-bsm可了解更多关于生物活性小分子的其他研究领域。

储存分类代码

11 - Combustible Solids

WGK

WGK 3

个人防护装备

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges

  • 技术规格说明书

    • 历史批次信息供参考:

    分析证书(COA)

    Lot/Batch Number
    WXBF4105V
    BCCG8282
    BCCC3082
    BCBT1578
    BCBP2916V

    没有发现合适的版本？

    如果您需要特殊版本，可通过批号或批次号查找具体证书。

    搜索COA

    已有该产品？

    在文件库中查找您最近购买产品的文档。

    访问文档库

    K Kobayashi et al.
    Cancer research, 60(14), 3978-3984 (2000-08-05)
    Although the beneficial effect of cimetidine on survival in cancer has been clinically demonstrated in colorectal cancer patients, the mode of action of cimetidine has not been elucidated. In this report, we have demonstrated for the first time that cimetidine
    Huan Yang et al.
    Molecular medicine (Cambridge, Mass.), 28(1), 57-57 (2022-05-17)
    Severe COVID-19 is characterized by pro-inflammatory cytokine release syndrome (cytokine storm) which causes high morbidity and mortality. Recent observational and clinical studies suggest famotidine, a histamine 2 receptor (H2R) antagonist widely used to treat gastroesophageal reflux disease, attenuates the clinical
    Sarit Pal et al.
    Biology open, 11(7) (2022-07-02)
    Histamine exerts its physiological functions through its four receptor subtypes. In this work, we report the subcellular localization of histamine receptor 2 (H2R), a G protein-coupled receptor (GPCR), which is expressed in a wide variety of cell and tissue types.
    H van der Goot et al.
    European journal of medicinal chemistry, 35(1), 5-20 (2000-03-25)
    In this review the histaminergic ligands for the histamine H(1), H(2) and H(3) receptors, which are currently used as tools in pharmacological studies, are described. To study interactions with the histamine H(1) receptor, the H(1) agonist 2-aminoethylthiazole has long since
    Hiroki Shimizu et al.
    ChemMedChem, 17(16), e202200204-e202200204 (2022-06-14)
    We synthesized and experimentally tested the passive permeability of more than thirty tetrapeptides mimicking the N-terminus of the pro-apoptotic protein Smac (Second mitochondria-derived activator of caspases). Each peptide bore one or two unnatural Hydrogen Bond Acceptor-bearing Amino Acid (HBA-AA) residues
    查看所有相关文献

    商品

    Discover Bioactive Small Molecules for ADME/Tox

    Discover Bioactive Small Molecules for ADME/Tox

    我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

    联系客户支持