psam

PSEM 89S TFA 是一种脑渗透性和选择性离子通道激动剂，分别对 Q79G 和 L141F 具有正交选择性。

Lycopsamine N-oxide 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 T123864。

7-O-Acetyllycopsamine N-oxide 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 T124402。

Psammaplysene A is a FOXO1a nuclear export inhibitor.

Psammaplysene B is a FOXO1a nuclear export inhibitor.

Lycopsamine is a bioactive chemical.

Lycopsamine `1-acetate is a bioactive chemical.

Psammaplin A, a marine metabolite, functions as a robust inhibitor of HDAC and DNA methyltransferases, displaying notable potency and selectivity as a DAC1 inhibitor, with an IC50 value of 0.9 nM. It exhibits antimicrobial effects against Gram-positive bacteria and inhibits both DNA synthesis and DNA gyrase activity, also demonstrating antitumor activity[1][2].

7-Acetyllycopsamine (Standard) 是 7-Acetyllycopsamine 的标准品。适用于定量分析、质量控制及生化实验等相关研究。Lycopsamine `1-acetate is a bioactive chemical.

Lycopsamine (Standard) 是 Lycopsamine 的标准品。适用于定量分析、质量控制及生化实验等相关研究。Lycopsamine is a bioactive chemical.

Napsamycin C是一种抗生素，对铜绿假单胞菌以及其他假单胞菌表现出显著的抗菌活性，但其对其他革兰氏阳性菌和革兰氏阴性菌的抗菌效力较弱。

Napsamycin D 是一种抗生素，具有对铜绿假单胞菌及其他假单胞菌的抗菌活性，但对其他革兰氏阳性菌和阴性菌的抗菌活性较弱。

Napsamycin A 是一种抗生素，主要对铜绿假单胞菌和其他假单胞菌表现出抗菌活性，但对其他革兰氏阳性和阴性菌的抗菌作用较弱。

Napsamycin B 是一种抗生素。Napsamycin D 对铜绿假单胞菌及其他假单胞菌表现出抗菌活性，而对其他革兰氏阳性菌和阴性菌的抗菌效果较弱。

BRK inhibitor P21d hydrochloride is a highly potent inhibitor of breast tumor kinase (BRK/PTK6), displaying an IC50 of 30 nM. Additionally, it effectively suppresses p-SAM68 with an IC50 value of 52 nM. This compound, BRK inhibitor P21d hydrochloride, serves as a valuable tool for evaluating the efficacy of BRK inhibitors in xenograft breast tumor models, enabling the assessment of their in vivo activity.

Sp-cAMPS-AM, 作为cAMP的一个类似物，主要通过渗透细胞并释放其母体极性结构Sp-cAMPS来发挥功能，进而诱导PKA激活和CREB磷酸化。

18:1-12:0 Biotin PS 是一种经生物素化的脂质。

PSAM (pharmacologically selective actuator module) agonist. Activates PSAML141F-GlyR chimeric ion channels. Inhibits activity of neurons expressing PSAML141F-GlyR in vivo and activates locus coeruleus noradrenergic neurons expressing PSAML141F,Y115F-5-HT3 ion channels. Recommended concentration for use in mice is 5 mg/kg or lower. Plasmid vectors for the transfection of cells with PSAML141F-GlyR and PSAML141F,Y115F-5-HT3 are available from Addgene. Lovett-Barron et al (2012) Regulation of neuronal input transformations by tunable dendritic inhibition. Nat.Neurosci. 15 423 PMID:22246433 |Satoh et al (2016) Context-dependent gait choice elicited by EphA4 mutation in Lbx1 spinal interneurons. Neuron 89 1046 PMID:26924434 |Atasoy et al (2012) Deconstruction of a neural circuit for hunger. Nature 488 172 PMID:22801496 |Hirschberg et al (2017) Functional dichotomy in spinal- vs prefrontal-projecting locus coeruleus modules splits descending noradrenergic analgesia from ascending aversion and anxiety in rats. Elife 6 e29808 PMID:29027903