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貨號(hào) 產(chǎn)品名 純度
A851897 現(xiàn)貨 Maribavir/馬立巴韋

Maribavir是一種有效的野生型pUL97催化的組蛋白磷酸化抑制劑,IC50為3 nM。它對(duì)HCMV和Epstein-Barr病毒(EBV)具有強(qiáng)效的抗病毒活性。

≥99%
A733173 現(xiàn)貨 Zerumbone/球姜酮

Zerumbone是一種從 Zingiber zerumbet Smith 根莖中分離的單環(huán)倍半萜化合物,能夠強(qiáng)效抑制 Epstein-Barr 病毒的激活,IC50 為 0.14 mM。Zerumbone 具有抗癌、抗氧化、抗炎和抗增殖作用。

≥99%
A2240182 現(xiàn)貨 VK-2019

VK-2019作為首個(gè)進(jìn)入臨床的EBNA1(Epstein-Barr病毒核抗原1)抑制劑,通過(guò)抑制EBNA1的DNA結(jié)合能力,阻斷病毒基因組的復(fù)制和轉(zhuǎn)錄,導(dǎo)致EBV DNA拷貝數(shù)顯著減少。在EBV感染的鼻咽癌細(xì)胞和小鼠模型中,VK-2019顯著抑制腫瘤生長(zhǎng),效果優(yōu)于傳統(tǒng)放療或化療。

≥99%
A689625 現(xiàn)貨 Paederoside/雞矢藤苷

Paederoside is extracted from paederia scandense with high anti-tumor promoting activity.

≥99%
A225120 現(xiàn)貨 Narcissin/水仙苷

Narcissoside exhibits protection against mitochondrial induced oxidative stress. It is a flavonol glycoside isolated and purified from the bulbus of Narcissus tazettaL. var. chinensis Roem.

≥99%
A2476872 EBV lytic cycle inducer-1

EBV lytic cycle inducer-1是一種類(lèi)似鐵螯合物的化合物,能與 HDAC 抑制劑 Romidespin 和 SAHA 協(xié)同誘導(dǎo) EBV 裂解周期,并通過(guò)激活 ERK1/2-自噬軸重新激活 EBV 裂解周期。

≥95%
A1680325 EBNA1-IN-SC7

99%
A1371238 BRL44385

BRL44385 is a potent and selective inhibitor of the replication of herpes simplex virus types 1 and 2 (HSV-1 and HSV2), varicella zoster virus (VZV) and Epstein-Barr virus (EBV).

98+%
A487855 Eritoran

Eritoran is a TLR4 receptor antagonist.

99+%
A994666 2α,19α-Dihydroxy-3-oxo-urs-12-en-28-oic acid

98%
A1145788 Rubropunctamine/潘紅胺

95%
A990406 Minumicrolin

Minumicrolin, a natural potential anti-tumor agent isolated and purified from the herbs of Murraya exotica L., shows mild butyrylcholinesterase inhibition activity and exhibits cytotoxicity against cholangiocarcinoma cell line, KKU-100.

98+%
A2423120 VK-1727

98%
A459015 α-Toxicarol

alpha-Toxicarol is a natural product isolated and purified from the herbs of Derris trifoliata Lour. exhibiting a marked inhibitory effect on mouse skin tumor promotion in an in vivo two-stage carcinogenesis test.

98+%
A1702846 L-I-OddU

98%
A754627 α-Cembrenediol

VEGFR inhibitor TC1 acts in angiogenesis inhibitory in multiple breast cancer cell lines by significantly reducing the activated VEGFR2 levels.

98+%
A1006787 3,29-O-Dibenzoyloxykarounidiol

99%
A1340212 Azadirachtin B/印楝素 B

99%
A1249530 GSK983

99%
A2419512 LMP2A (426-434)

96%
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