al-1

AL-1 is a GLYCOINOSITOL PHOSPHOLIPID MEMBRANE ANCHOR containing ephrin found in developing tectum. It can mediate the bundling of cortical axons and repel the axonal growth of retinal ganglia axons. It exists in a variety of adult tissues of BRAIN; HEART;

Phos-tag Acrylamide AAL-107 是一种丙烯酰胺悬垂物，可用作可视化磷酸化蛋白质的工具。

CAL-130 is a PI3Kδ and PI3Kγ inhibitor (IC50s: 1.3 and 6.1 nM).

CAL-130 Hydrochloride is a PI3Kδ and PI3Kγ inhibitor (IC50s: 1.3 and 6.1 nM).

CAL-130 Racemate is the racemate of CAL-130. CAL-130 is a PI3Kδ and PI3Kγ inhibitor (IC50s: 1.3 and 6.1 nM).

a-Santal-10-en-12-oic acid 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 T124279，CAS号为 74642-79-8。

AAL-149 是 FTY720 的类似物和一种 TRPM7 抑制剂 (IC50= 1.081 μM)，具有多重抗炎作用，不靶向 S1P 受体，适用于抗炎研究。

SirReal-1 is an effective and selective inhibitor of Sirt2.

AL-16049 is an FP-Class prostaglandin analog which may be useful in the treatment of glaucoma and ocular hypertension.

CYMAL-1 在生命科学相关研究中具有广泛的应用。

KP136 (AL136) 是一种具有口服活性的抗过敏化合物，抑制组胺释放，可用于研究哮喘和过敏性水肿。

AL 1965 具有抗神经病作用。

Alconil (Al 1567) 是一种醛糖还原酶抑制剂，可用于研究慢性阻塞性肺疾病（COPD）和糖尿病。

Idelalisib (GS-1101) 是 PI3K 催化亚基 p110δ 的小分子抑制剂，IC50为 2.5 nM，对 p110δ 的选择性是 p110α β γ 的 40 到 300 倍。

Acalisib (CAL-120) 是一种PI3Kδ的选择性抑制剂，其 IC50=12.7 nM。

iKIX1 是一种 Pdr1 依赖性基因激活。 它在体外和在播散性和泌尿道光滑念珠菌感染的动物模型中使耐药的光滑念珠菌对唑类抗真菌剂重新敏感。它可研究多药耐药性和光滑念珠菌感染。

Potent and selective CLK inhibitor (IC50 values are 28, 88 and 510 nM for CLK4, 1 and 2, respectively). Exhibits no significant activity at CLK3, DYRK, CDK or GSK3 at a concentration of 10 μM. Inhibits growth of a range of cancer cell lines in vitro at subnanomolar concentrations. Walter et al (2018) Molecular structures of cdc2-like kinases in complex with a new inhibitor chemotype. PLoS One 13 e0196761 PMID:29723265

LYPLAL1-IN-1 is a selective covalent small-molecule inhibitor of Lysophospholipase-like 1 (IC50: 0.006 μM). LYPLAL1-IN-1 also enhances glucose production.

SirReal1-O-propargyl is a selective and highly potent Sirtuin 2 (Sirt2) inhibitor, with an IC50 of 2.4 μM. SirReal1-O-propargyl, the SirReal1-based moiety, binds to the cereblon ligand via a linker to form PROTAC to degrade Sirt2[1].

Methamnetamine (PAL-1046) hydrochloride 是一种苯丙胺类精神活性化合物，能够引起过量血清素的释放。

AL 1612 is a bio-active chemical.

AL12180 is a bioactive chemical.

Decanal, 10-fluoro- is a biochemical.

Heptanal 1,3-glyceryl acetal is a bioactive chemical.