PeptideDB

BAY 36-7620

CAS: 232605-26-4 F: C19H18O2 W: 278.35

BAY 36-7620 is a potent and noncompetitive antagonist of mGlu1 Receptor (IC50=0.16 μM) with inverse agonist activity. B
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Bioactivity BAY 36-7620 is a potent and noncompetitive antagonist of mGlu1 Receptor (IC50=0.16 μM) with inverse agonist activity. BAY 36-7620 inhibits tumor growth and prolongs the survival of mice with tumors by inhibiting mGlu1 receptor. BAY 36-7620 suppresses AKT phosphorylation in A549 tumors. BAY 36-762 has neuroprotective effect in acute subdural hematoma rat model.BAY 36-7620 is used in non-small cell lung cancer and breast cancer research[1][2][3][4].
Invitro BAY 36-7620 (0.1-10 μM) 在浓度 10 μM 时完全抑制了 HEK 293 细胞中的 mGlu1 受体[1] 0 --> BAY 36-7620 相关抗体: Western Blot Analysis[2] Cell Line:
In Vivo BAY 36-7620 (5-10 mg/kg,腹腔注射;每日 1 次,连续 24 天) 抑制了胸腺裸鼠模型的肿瘤生长,延长了肺癌肿瘤小鼠的寿命[2]。BAY 36-7620 (0.01-0.03 mg/kg,静脉注射;4 小时) 对急性硬膜下血肿大鼠模型具有神经保护作用[4]。 Animal Model:
Name BAY 36-7620
CAS 232605-26-4
Formula C19H18O2
Molar Mass 278.35
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]. Carroll FY, et al. BAY36-7620: a potent non-competitive mGlu1 receptor antagonist with inverse agonist activity. Mol Pharmacol. 2001 May;59(5):965-73. [2]. Xia H, et al. Inhibition of metabotropic glutamate receptor 1 suppresses tumor growth and angiogenesis in experimental non-small cell lung cancer. Eur J Pharmacol. 2016 Jul 15;783:103-11. [3]. Dolfi SC, et al. Riluzole exerts distinct antitumor effects from a metabotropic glutamate receptor 1-specific inhibitor on breast cancer cells. Oncotarget. 2017 Jul 4;8(27):44639-44653. [4]. De Vry J, et al. Neuroprotective and behavioral effects of the selective metabotropic glutamate mGlu(1) receptor antagonist BAY 36-7620. Eur J Pharmacol. 2001 Oct 5;428(2):203-14.