msi

Ro 08-2750 是一种非肽和可逆的神经生长因子 (NGF) 抑制剂，与 NGF 结合，IC50 约为 1 µM。它是一种选择性 MSI RNA 结合活性抑制剂，IC50 为 2.7 μM。它选择性抑制 NGF 与 p75NTR 的结合，而不是 TRKA。

MSI-1436 is a selective, non-competitive the enzyme protein-tyrosine phosphatase 1B (PTB1B)inhibitor(IC50 of appr 1 μM)

MSI-1701 is an analogue of MSI-1436.

MSI-1436 lactate is a selective, non-competitive the enzyme protein-tyrosine phosphatase 1B (PTB1B)inhibitor(IC50 of appr 1 μM)

Squalamine is an aminosterol compound, with potent broad spectrum antiviral activity.

Squalamine lactate is an aminosterol compound discovered in the tissues of the dogfish shark, with antimicrobial activity.

Gimsilumab (MORAb-022) 是一种靶向粒细胞巨噬细胞集落刺激因子的人源化单克隆抗体，可用于研究 COVID-19 引起的炎症和低氧血症。

Extensumside H 是一种有用的有机化合物，可用于生命科学领域的相关研究。其产品编号为 T125381，CAS号为 2079912-14-2。

Extensumside F 是一种有用的有机化合物，可用于生命科学领域的相关研究。其产品编号为 T125382，CAS号为 2079912-12-0。

Extensumside E 是一种有用的有机化合物，可用于生命科学领域的相关研究。其产品编号为 T125383，CAS号为 2079912-11-9。

Extensumside C 是一种有用的有机化合物，可用于生命科学领域的相关研究。其产品编号为 T125384，CAS号为 2079912-09-5。

Amsilarotene (TAC101) 是口服有活性的合成类视黄醇，对视黄酸受体 α (RAR-α) 具有选择性亲和力，对 RAR-α 和 RAR-β 的 Ki=为 2.4 nM 和 400 nM。它可造成人胃癌、卵巢癌细胞及肝细胞癌的凋亡，可用于研究癌症。

Temsirolimus (CCI-779) 是一种mTOR 抑制剂，IC50值为 1.76 μM。它能激活自噬，可防止心脏功能恶化。

Camsirubicin is a drug candidate of antineoplastic.

Trimetaphan camsilate is a drug that counteracts cholinergic transmission at the ganglion type of nicotinic receptors of the autonomic ganglia and therefore blocks both the sympathetic nervous system and the parasympathetic nervous system. It acts as a non-depolarizing competitive antagonist at the nicotinic acetylcholine receptor, is short-acting, and is given intravenously.

Camsirubicin, also known as GPX-150, MNPR-201, and CNDO1011, is a synthetic non-cardiotoxic analogue of the anthracycline antibiotic doxorubicin with potential antineoplastic activity. Anthracycline analogue GPX-150 intercalates DNA and impedes the activity of topoisomerase II, inducing single and double-stranded breaks in DNA; inhibiting DNA replication and or repair, transcription, and protein synthesis; and activating tumor cell apoptosis.

Imsidolimab (ANB 019) 是一种人源化的抗 IL-36R 单克隆抗体，抑制 IL-36 信号传导，可用于研究全身性脓疱型银屑病。

mSIRK (G-Protein βγ Binding Peptide) 是一种细胞渗透性 ERK1 和 ERK2 双重激活剂，是一种由15个氨基酸组成的多肽，可促进α亚基解离。

c-Fms-IN-1 是 c-FMS 激酶的抑制剂 (IC50 = 0.8 nM)。

c-Fms-IN-3 是一种新型 c-FMS 激酶抑制剂，可用于抗风湿和抗炎疾病的研究。

c-Fms-IN-2 是一种 c-FMS 激酶抑制剂 (IC50 = 24 nM)。

c-Fms-IN-13 (compound 14) 是有效的 FMS 激酶抑制剂（IC50= 17 nM）。c-Fms-IN-13 是一种作抗炎剂。

c-Fms-IN-10 is the derivative of thieno [3,2-d] pyrimidine, a kinase inhibitor of FMS (Colony-stimulating factor-1 receptor, CSF-1R; IC50: 2 nM) with anti-tumor activity.

c-Fms-IN-6 is a potent inhibitor of c-FMS (IC50 ≤10 nM for unphosphorylated c-FMS) and also weakly inhibits unphosphorylated c-KIT and PDGFR (IC50: > 1 μM).