PeptideDB

Fasnall

CAS: 929978-58-5 F: C19H22N4S W: 338.47

Fasnall is a selective fatty acid synthase (FASN) inhibitor with an IC50 of 3.71 μM. Fasnall induces apoptosis inHER2+
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Bioactivity Fasnall is a selective fatty acid synthase (FASN) inhibitor with an IC50 of 3.71 μM. Fasnall induces apoptosis in HER2+ breast cancer cell lines. Fasnall shows potent anti-tumor activities[1].
Target IC50: 3.71 μM (human purified FASN activity)
Invitro Fasnall 有效阻断乙酸盐和葡萄糖掺入总脂质中,在 HepG2 细胞中的 IC50 值分别为 147 和 213 nM[1]。Fasnall(50 μM;24-120 小时)抑制乳腺癌细胞系的增殖[1]。Fasnall(25-100 μM;24 小时)诱导 HER2+ 乳腺癌细胞系凋亡[1]。 Cell Proliferation Assay[1] Cell Line:
In Vivo Fasnall(15 mg/kg,腹腔注射,每周两次;3 周)在 HER2+ 乳腺癌的 MMTV-Neu 模型中显示出有效的抗肿瘤活性[1]。 Animal Model:
Name Fasnall
CAS 929978-58-5
Formula C19H22N4S
Molar Mass 338.47
Transport Room temperature in continental US; may vary elsewhere.
Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Reference [1]. Yazan Alwarawrah, et al. Fasnall, a Selective FASN Inhibitor, Shows Potent Anti-tumor Activity in the MMTV-Neu Model of HER2(+) Breast Cancer. Cell Chem Biol. 2016 Jun 23;23(6):678-88.