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Merck
CN

D9766

双嘧达莫

≥98% (HPLC), powder, phosphodiesterase V inhibitor

别名:

NSC 515776, NSC 619103

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关于此项目

经验公式(希尔记法):
C24H40N8O4
化学文摘社编号:
分子量:
504.63
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
41106305
EC Number:
200-374-7
MDL number:
Assay:
≥98% (HPLC)
Form:
powder
Quality level:
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产品名称

双嘧达莫, ≥98% (HPLC)

Quality Level

assay

≥98% (HPLC)

form

powder

color

yellow

mp

165-166 °C (lit.)

solubility

DMSO: soluble, ethanol: soluble

originator

Boehringer Ingelheim

storage temp.

room temp

SMILES string

OCCN(CCO)c1nc(N2CCCCC2)c3nc(nc(N4CCCCC4)c3n1)N(CCO)CCO

InChI

1S/C24H40N8O4/c33-15-11-31(12-16-34)23-26-20-19(21(27-23)29-7-3-1-4-8-29)25-24(32(13-17-35)14-18-36)28-22(20)30-9-5-2-6-10-30/h33-36H,1-18H2

InChI key

IZEKFCXSFNUWAM-UHFFFAOYSA-N

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General description

双嘧达莫阻止细胞摄取腺苷。作为一种平衡核苷转运蛋白 1 (ENT1) 抑制剂发挥作用。

Application

双嘧达莫已用于:
  • 进行体外生长抑制试验 (40)
  • 测定其预防子宫肌层收缩的能力 (41)
  • 确定其对烟酰胺腺嘌呤二核苷酸 (NAD +) 诱导的细胞内三磷酸腺苷 (ATP) 水平增加的作用 (42)
  • ,防止烟酰胺核苷 (NR) 诱导的轴突保护作用 (43)

Biochem/physiol Actions

磷酸二酯酶 V 选择性抑制剂 (PDE 5);强效冠脉扩张药物;腺苷转运抑制剂;血小板聚集抑制剂。

Features and Benefits

该化合物是受体分类及信号转导手册上磷酸二酯酶页面上的特色化合物。想要浏览手册的其他页面, 请单击此处
该化合物由 Boehringer Ingelheim 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
这种化合物是环核苷酸研究的特色产品。点击此处发现更多特色环核苷酸产品。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。

存储类别

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Jiwen Li et al.
The Journal of experimental medicine, 218(6) (2021-04-24)
Previous studies implicated the neuronal guidance molecule netrin-1 in attenuating myocardial ischemia-reperfusion injury. However, the tissue-specific sources and receptor signaling events remain elusive. Neutrophils are among the first cells responding to an ischemic insult and can be associated with tissue
Terence B Beghyn et al.
Journal of medicinal chemistry, 54(9), 3222-3240 (2011-04-21)
The dominant strategy for discovery of new antimalarial drugs relies on cell-free assays on specific biochemical pathways of Plasmodium falciparum . However, it appears that screening directly on the parasite is a more rewarding approach. The "drug to genome to
M Sundaram et al.
The Journal of biological chemistry, 273(34), 21519-21525 (1998-08-15)
We have recently isolated cDNAs from human placenta and rat jejunum encoding the prototypic human and rat equilibrative nitrobenzylthioinosine (NBMPR)-sensitive nucleoside transporters hENT1 and rENT1. The two proteins (456 and 457 residues, Mr 50,000) are 78% identical in amino acid
Tochukwu C Okwuosa et al.
Pharmaceutical research, 33(11), 2704-2712 (2016-08-11)
The fabrication of ready-to-use immediate release tablets via 3D printing provides a powerful tool to on-demand individualization of dosage form. This work aims to adapt a widely used pharmaceutical grade polymer, polyvinylpyrrolidone (PVP), for instant on-demand production of immediate release
The Top 100 Drugs e-book: Clinical Pharmacology and Practical Prescribing (2014)

商品

Cyclic nucleotides like cAMP modulate cell function via PKA activation and ion channels.

全球贸易项目编号

货号GTIN
D9766-10G04061832897882
D9766-25G04061832897899
D9766-5G04061833591109
D9766-1G04061826682494

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