您好,欢迎来到易推广 请登录 免费注册

上海陶术生物科技有限公司 主营产品:生物试剂,实验服务等

当前位置:易推广 > 上海陶术生物科技有限公司 > 产品展示

企业档案

会员类型:会员

已获得易推广信誉   等级评定
139成长值

(0 -40)基础信誉积累,可浏览访问

(41-90)良好信誉积累,可接洽商谈

(91+  )优质信誉积累,可持续信赖

易推广会员:5

工商认证 【已认证】

最后认证时间:

注册号: 【已认证】

法人代表: 【已认证】

企业类型:生产商 【已认证】

注册资金:人民币万 【已认证】

产品数:86101

参观次数:3615285

手机网站:http://m.yituig.com/c135739/

旗舰版地址:http://tsbiochem.app17.com

自主品牌

已选条件

  • T68681Casuarinin;化合物 CasuarininCasuarinin

    Casuarinin is an ellagitannin. It is found in the pericarp of pomegranates. It is also found in Casuarina and Stachyurus species and in Alnus sieboldiana. It is an isomer of casuarictin. It is a highly active carbonic anhydrase inhibitor. It is a compound that causes the contraction of body tissues, typically used to reduce bleeding from minor abrasions.

    价 格:¥电议型 号:T68681产 地:中国大陆

  • T68680CP-53631;化合物 CP-53631CP-53631

    CP-53631 is a selective serotonin reuptake inhibitor (SSRI)

    价 格:¥电议型 号:T68680产 地:中国大陆

  • T6868KYA1797K;化合物KYA1797KKYA1797K

    KYA1797K is a highly potent and selective inhibitor. Wnt/β-catenin IC50 is 0.75 μM through TOPflash assay.

    价 格:¥电议型 号:T6868产 地:中国大陆

  • T68679VPC 32183 (S);化合物 VPC 32183 (S)VPC 32183 (S)

    VPC 32183 (S) is a competitive antagonist at the LPA1 and LPA3 receptors. VPC 32183 is devoid of agonist activity at the human LPA1, LPA2 and LPA3 receptors, and, presumably, at other mammalian LPA receptors.

    价 格:¥电议型 号:T68679产 地:中国大陆

  • T68678VPC 24191;化合物 VPC 24191VPC 24191

    VPC 24191 is a sphingosine 1-phosphate (S1P1/3) receptor agonist.

    价 格:¥电议型 号:T68678产 地:中国大陆

  • T68677D-87503;化合物 D-87503D-87503

    D-87503 is a dual extracellular signaling-related kinase (ERK)/PI3K inhibitor.

    价 格:¥电议型 号:T68677产 地:中国大陆

  • T68676Ciladopa (free base);化合物 Ciladopa (free base)Ciladopa (free base)

    Ciladopa (free base) is a dopamine agonist with a similar chemical structure to dopamine. It was under investigation as an antiparkinsonian agent but was discontinued due to concerns of tumorogenesis in rodents.

    价 格:¥电议型 号:T68676产 地:中国大陆

  • T68675Porfiromycin;化合物 PorfiromycinPorfiromycin

    Porfiromycin is a n N-methyl derivative of the antineoplastic antibiotic mitomycin C isolated from the bacterium Streptomyces ardus and other Streptomyces bacterial species. Bioreduced porfiromycin generates oxygen radicals and alkylates DNA, producing interstrand cross-links and single-strand breaks, thereby inhibiting DNA synthesis. Porfiromycin is preferentially toxic to hypoxic cells.

    价 格:¥电议型 号:T68675产 地:中国大陆

  • T68674Vincapusine;化合物 VincapusineVincapusine

    Vincapusine is a natural inhibitor of 3C-like protease (3CLpro), targeting SARS-CoV-2 3CLpro, SARS-CoV 3CLpro and MERS-CoV 3CLpro.

    价 格:¥电议型 号:T68674产 地:中国大陆

  • T68673Amsacrine gluconate;化合物 Amsacrine gluconateAmsacrine gluconate

    Amsacrine gluconate is an aminoacridine derivative with potential antineoplastic activity. Although its mechanism of action is incompletely defined, amsacrine may intercalate into DNA and inhibit topoisomerase II, resulting in DNA double-strand breaks, arrest of the S/G2 phase of the cell cycle, and cell death.

    价 格:¥电议型 号:T68673产 地:中国大陆

  • T68672Amsacrine lactate;化合物 Amsacrine lactateAmsacrine lactate

    Amsacrine lactate is an aminoacridine derivative with potential antineoplastic activity. Although its mechanism of action is incompletely defined, amsacrine may intercalate into DNA and inhibit topoisomerase II, resulting in DNA double-strand breaks, arrest of the S/G2 phase of the cell cycle, and cell death.

    价 格:¥电议型 号:T68672产 地:中国大陆

  • T68671Amsacrine Isothionate;化合物 Amsacrine IsothionateAmsacrine Isothionate

    Amsacrine Isothionate is an aminoacridine derivative with potential antineoplastic activity. Although its mechanism of action is incompletely defined, amsacrine may intercalate into DNA and inhibit topoisomerase II, resulting in DNA double-strand breaks, arrest of the S/G2 phase of the cell cycle, and cell death.

    价 格:¥电议型 号:T68671产 地:中国大陆

  • T68670Panuramine;化合物 PanuraminePanuramine

    Panuramine is an antidepressant which was synthesized in 1981 by Wyeth. It acts as a potent and selective serotonin reuptake inhibitor (SSRI).

    价 格:¥电议型 号:T68670产 地:中国大陆

  • T6867Belumosudil化合物KD025KD025|||Rezurock|||ROCK inhibitor|||SLx-2119

    Belumosudil (Rezurock) is an orally available, and specific ROCK2 inhibitor (IC50/Ki: 60/41 nM).

    价 格:¥电议型 号:T6867产 地:中国大陆

  • T68669Quinpirole;化合物 QuinpiroleQuinpirole

    Quinpirole is a dopamine D2/D3 receptor agonist.

    价 格:¥电议型 号:T68669产 地:中国大陆

  • T68668AZ-1;化合物 AZ-1AZ-1

    AZ-1 is an inducer of ABCA1 and apoE. It enhances ABCA1 activity and decreases P2X7 receptor activity. AZ-1 activates endogenous LXR signaling but shows no direct LXRα or LXRβ agonist activity.

    价 格:¥电议型 号:T68668产 地:中国大陆

  • T68667Oxanosine;化合物 OxanosineOxanosine

    Oxanosine is an analog of guanosine that has been found in S. capreolus and has diverse biological activities, including antibacterial, antiviral, and anticancer properties. It is active against a variety of bacteria, including S. flexneri, P. mirabilis, and E. coli (MICs = 6.25, 12.5, 25 ?g/ml, respectively, on peptone, but not nutrient, agar). Oxanosine inhibits replication of the HIV-1 strain IIIb in infected CEM and U937, but not H9, cells (EC50s = 7, 27, and >500 ?g/ml, respectively). It al

    价 格:¥电议型 号:T68667产 地:中国大陆

  • T68666Benfluron Hydrochloride;化合物 Benfluron HydrochlorideBenfluron Hydrochloride

    Benfluron Hydrochloride is an inhibitor of HIV-1 Rev function which also acts as a cytostatic agent with substantial antiretroviral activity.

    价 格:¥电议型 号:T68666产 地:中国大陆

  • T68665Yonkenafil;化合物 Tunodafil (free base)Tunodafil;Tunodafil

    Yonkenafil (Tunodafil), a novel phosphodiesterase 5 (PDE5) inhibitor, effectively reduces cerebral infarction, neurological deficits, edema, and neuronal damage in the infarcted area. It potentially enhances cognitive function through neurogenesis modulation and may have therapeutic effects on Alzheimer´s disease.

    价 格:¥电议型 号:T68665产 地:中国大陆

  • T68664Epostane;环氧司坦Win-32729;Win-32729

    Epostane (Win-32729) is a 3β-hydroxysteroid dehydrogenase inhibitor that acts by inhibiting the enzyme 3β-hydroxysteroid dehydrogenase, blocking progesterone production.

    价 格:¥电议型 号:T68664产 地:中国大陆

快速导航

在线咨询

提交