关于 "Insulin Receptor" 的结果21+ 个结果

An insulin receptor tyrosine kinase inhibitor

S961 is a biosynthetic insulin receptor antagonist that inhibits cellular proliferation and colony formation in breast tumour cells.

S961 is a biosynthetic insulin receptor antagonist that inhibits cellular proliferation and colony formation in breast tumour cells.

MID-1 is a disruptor of MG53-IRS-1 (Mitsugumin 53-insulin receptor substrate-1) interaction, which can disrupts molecular association of MG53 with IRS-1 and abolishes MG53-induced IRS-1 ubiquitination and degradation in skeletal muscle, leading to elevated IRS-1 expression level and increased insulin signaling and glucose uptake.

胰岛素是一种由21个和30个氨基酸组成的激素蛋白质。

Insulin degludec 是一种超长效形式的胰岛素，用于治疗 1 型和 2 型糖尿病引起的高血糖。Insulin degludec 结合胰岛素受体的 IC50 值为 19.59 nM/L。Insulin degludec 可用于 1 型和 2 型糖尿病的研究。

Insulin glargine 是一种长效胰岛素类似物。Insulin glargine 可用于研究糖尿病。

Insulin glulisine（HMR 1964）是一种速效胰岛素类似物，它模拟了生理性人胰岛素的药代动力学和药效学特征。

Insulinlevelsmodulator可用于治疗糖尿病。

Insulin efsitora alfa (LY-3209590)是胰岛素受体（IR）的选择性激动剂。

cFMS Receptor Inhibitor IV (Compound 42) 是一种有效的 cFMS 抑制剂，IC50 为 0.017 μM。

cFMSReceptorInhibitorII是一种CSF1R激酶抑制剂。CSF-1是一种细胞因子。

A selective antagonist of the EGFR

ALW-II-41-27 是一种 Eph 家族酪氨酸激酶抑制剂，抑制 Eph2 的 IC50 为 11 nM。

An inhibitor of EGFR, PDGFβ, FGF, and c-Src

BLU-782 是一种口服精准疗法，专门设计用于选择性靶向突变体 ALK2。

A natural insulin mimic

MSDC-0602K is a insulin sensitizer that modulates the mitochondrial pyruvate carrier (MPC).

A potent and selective VEGF receptor inhibitor

An inhibitor of VEGF receptor tyrosine kinases

A multi-targeted receptor tyrosine kinase inhibitor