ri-2

RI-2 是一种可逆的RAD51抑制剂，IC50值为 44.17 μM，可抑制人体细胞中的同源重组修复。

PNRI-299 is a selective inhibitor of AP-1 transcription(IC50 of 20 uM ).

SRI-29132 is potent; highly permeant of the blood-brain barrier; and selective for LRRK2 kinase activity, therefore effective in attenuating pro-inflammatory responses in macrophages and in rescuing neurite retraction phenotypes in neurons.

SRI-29329 是一种有效的、特异性的 CDC 样激酶抑制剂，对 CLK1、CLK2 和 CLK4 的 IC50 分别为 78 nM、16 nM 和 86 nM。

SRI-29574 是一种作用于多巴胺转运体 (DAT) 的别构调节剂,能部分抑制 DAT 的摄取 (IC50=2.3 nM),同时也对羟色胺转运体 (SERT) 与去甲肾上腺素转运体 (NET) 的摄取有一定的抑制作用.该化合物可用于探究 DAT 的功能及其调控机制,是研究中的重要工具.

Tri(2-butoxyethyl) phosphate (Phosflex T-bep) 是一种塑料增塑剂和阻燃剂，是一种从奶粉中提取得到的有机磷酸酯。

Imidazole mustard is an inhibitor of purine nucleoside synthesis.

TSRI265 is a novel αvβ3 ligand, disrupting the integrin-MMP2 interaction and showing antiangiogenic activit, inhibiting angiogenesis and tumor growth in vivo.

RI(dl)-2 TFA 是一种有效的选择性 RAD51 介导的 D 环形成 (RAD51-mediated D-loop formation) 抑制剂，IC50为 11.1 μM，并抑制人细胞中的同源重组 (HR) 活性，IC50为 3.0 μM。

STAD-2 is a cell permeable akap disruptor, selectively binding to pka-rii and blocking the interaction of pka-ri with akap

5’-O-TBDMS-dG is a modified nucleoside. 5’-O-DMT-2’-O-TBDMS-rI can be used in the synthesis of deoxyribonucleic acid or nucleic acid.

5'-O-DMT-2'-O-TBDMS-rI is a modified nucleoside utilized in the synthetic process of deoxyribonucleic acid (DNA) or nucleic acid.

5'-O-DMT-2'-O-TBDMS-rI, a modified nucleoside, finds application in deoxyribonucleic acid (DNA) or nucleic acid synthesis.

AKAP disruptor. Selectively binds PKA-RI with high affinity (KD values are 6.2 and 12.1 nM for the RIα and β subunits, respectively) and blocks its interaction with AKAP. Inhibits type I PKA-mediated phosphorylation in live cells. Cell permeable.