IBL-302

目录号：SY-109288

IBL-302 (AMU302) 是一种口服有效的PIM和PI3K/AKT/mTOR双信号抑制剂，具有抗乳腺癌和成神经细胞瘤的活性。在裸鼠异种移植模型中，IBL-302 显示出体内效力，并能抑制曲妥珠单抗的耐药性问题。此外，IBL-302 还能增强顺铂、阿霉素和依托泊苷等常见细胞毒性化疗药物的效果。

¥3003.00

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Ack1 inhibitor 1

目录号：SY-109289

Ack1 inhibitor1 是一种有效的、选择性的、具有口服活性的ACK1激酶抑制剂，其IC50值为2.1 nM，能抑制ACK1的磷酸化和下游AKT的激活，具有抗肿瘤活性。

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Biotin-Crosstide

目录号：SY-109290

Biotin-Crosstide 是一种带有生物素标记的Crosstide。

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Chaetominine

目录号：SY-109291

Chaetominine is a type of cytotoxic alkaloid obtained from endophytic Chaetomium sp. IFB-E015.

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Communic acid

目录号：SY-109292

Communic acid has antibacterial activity, including against mycobacterial. trans-Communic acid has potential to be utilized as anti-wrinkling agents and cosmetic ingredients, as they suppress UVB-induced MMP-1 expression.

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Kanosamine hydrochloride

目录号：SY-109293

Kanosamine hydrochloride is an antibiotic which inhibits the growth of plant-pathogenic oomycetes, certain fungi and a few bacterial species. Kanosamine inhibits Phytophthora medicaginis M2913 and Aphanomyces euteiches WI-98 with MICs of 25 and 60 μg/mL, respectively.

¥1357.00

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TX2-121-1

目录号：SY-109294

TX2-121-1 targets HER3 for proteasome-mediated degradation to inhibit HER3-dependent signalling and growth.

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2,3-Dihydro-3-methoxywithaferin A

目录号：SY-109295

2,3-Dihydro-3-methoxywithaferin A is a natural withanolide , is cytotoxic to human cancer cells, and is a candidate anticancer natural compound. It protects normal cells against stress.

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MS21

目录号：SY-109296

MS21 is a unique AKT degrader that selectively hampers the proliferation of cancers with mutations in the PI3K/PTEN pathway, alongside wild-type KRAS and BRAF.

¥3465.00

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