Ambeed.cn

首页 / 抑制剂/激动剂 / 抗体-药物偶联物 / 连接子-载荷偶联物

货号 产品名 纯度
A309085 现货 Monomethyl Auristatin F

MMAF can inhibit tubulin polymerization used in ADCs, with lower cytotoxic activity than MMAE.

99%+
A144786 现货 Topotecan/拓扑替康

Topotecan is an inhibitor of topoisomerase I and the IC50 values in cancer cells are less than 6 μM.

98%
A1369554 现货 FL118

FL118是一种口服有效的Survivin抑制剂,通过结合DDX5(p68)蛋白并诱导其去磷酸化与降解,展示了在癌症治疗中的潜力,主要用于肿瘤细胞增殖和存活机制的研究。

98%
A537376 现货 Exatecan mesylate/依喜替康甲磺酸盐

Exatecan mesylate is a totally synthetic analogue of the topoisomerase I-inhibitor camptothecin, which was synthesised to impart increased aqueous solubility, greater tumour efficacy, and less toxicity than camptothecin itself.

98%
A348562 现货 DM4

Maytansinoid DM4 is a tubulin inhibitor, inhibits the assemblyof microtubules by binding to tubulin, with a linker structure can create an antibody-drug conjugate (ADC).

99%+
A106511 现货 Monomethyl Auristatin D

MMAD, a potent tubulin inhibitor, is a toxin payload in antibody drug conjugate.

99%+
A880207 现货 Maytansinol

Maytansinol (Ansamitocin P-0) 是从 Maytansine 衍生出的,具有阻止微管聚合和触发细胞凋亡的能力,具有抗肿瘤潜力。

99%+
A155153 现货 (s)-10-hydroxycamptothecin/(S)-10-羟基喜树碱

(S)-10-hydroxycamptothecin is an inhibitor of DNA topoisomerase I with antitumor activity.

98+%
A516438 现货 Auristatin F/澳瑞他汀 F

Auristatin F is a cytotoxic tubulin modifier with potent and selective antitumor activity, and it is MMAF analog and cytotoxin in antibody-drug conjugates.

99%+
A366170 现货 SN-38/7-乙基-10羟基喜树碱

SN-38 is an active metabolite of CPT-11 that inhibits DNA topoisomerase I, DNA synthesis and causes frequent DNA single-strand breaks.

98%
A172961 现货 Monomethyl auristatin E/一甲基澳瑞他汀 E

Monomethyl auristatin E(MMAE;SGD-1010)是杜氏素10的合成衍生物,通过抑制微管蛋白聚合而起到强效有丝分裂抑制剂的作用。MMAE广泛用于抗体-药物结合物(ADC)的细胞毒性成分,以治疗各种癌症。

99%+
A686559 现货 DM1

DM1(Mertansine)是一种微管抑制剂和抗体可结合的美坦新类物质,旨在克服美坦新的全身毒性并增强肿瘤特异性递送。美坦新可以通过连接子附着到单克隆抗体上,以形成抗体-药物结合物(ADC)。

99%+
A432426 现货 9-Aminocamptothecin/9-氨基喜树碱

9-Aminocamptothecin, a natural product isolated and purified from the barks of Camptotheca acuminata Decne, is an active derivative of camptothecin, which belongs to the general group of chemotherapy drugs called topoisomerase inhibitors. 9-Aminocamptothecin is an inhibitor of Topo I.

99%+
A932860 现货 Mc-MMAE

Mc-MMAE is a protective group (maleimidocaproyl)-conjugated MMAE.

98%
A759395 现货 Rubitecan/鲁比替康

Rubitecan is an oral topoisomerase inhibitor.

99%+
A238238 现货 Paclitaxel/紫杉醇

Paclitaxel 是一种天然抗肿瘤药物,能稳定微管蛋白 (tubulin) 的聚合,导致有丝分裂停滞和诱导细胞凋亡 (apoptosis),最终导致细胞死亡。Paclitaxel 还可诱导细胞自噬 (autophagy)。

99%
A1365430 现货 Mc-VC-PAB-SN38

99%+
A700623 现货 MMAF-OMe/MMAF-Ome甲酯

MMAF-OMe is a synthetic antineoplastic agent and also used as a part of some experimental anti-cancer antibody-drug conjugates such as vorsetuzumab mafodotin and SGN-CD19A.

99%+
A1463319 现货 Mc-Phe-Lys(Boc)-PAB

TKN8718 is a hydrolyzable ADC linker.

98%
A866930 现货 DM1-SMe

DM1-SMe 是 IMGN901 中 Maytansinoid 的非结合形式。在一组人类肿瘤细胞系中,DM1-SMe 比母体 Maytansinoid 强效约 3-10 倍,IC50 值在 0.003 到 0.01 nM 之间

98%+
Ambeed 相关网站 Ambeed.cn Ambeed.com
Ambeed
关于我们
联系我们
资讯中心
网站地图
产品手册
  • 批次文件查询
  • 客户支持
    技术支持
    专业术语
    缩略词释义
    质量手册
    产品咨询
    计算器
    活动政策
    订购方法
    积分商城
    活动声明
    联系我们
    400-920-2911 sales@ambeed.cn tech@ambeed.cn
    Ambeed 只为有资质的科研机构、医药企业基于科学研究或药证申报的用途提供医药研发服务,不为任何个人或者非科研性质用途提供服务。