ho 1

L-Perillaldehyde 是紫苏草精油的主要成分，吸入后经由嗅觉神经功能表现出抗抑郁功能。

Nrf2 HO-1 activator 3 (Compound C3a) 是一种激活 Nrf2 信号通路的化合物，能促进 Nrf2 的核易位并上调血红素加氧酶-1（HO-1）的表达。在 H2O2 或高糖刺激的 H9c2 心肌细胞中，Nrf2 HO-1 activator 3 能抑制 ROS 和 MDA 的过度表达，抑制细胞活力及细胞克隆形成，从而展现其抗氧化活性。

Nrf2 HO-1-IN-1 是一种有效的 Nrf2 HO-1抑制剂，对 NO 的 IC50为 0.38 μM。Nrf2 HO-1-IN-1 可显著降低细胞中 ROS 水平。Nrf2 HO-1-IN-1 可用于抗炎研究。

Nrf2 HO-1 activator 2 (compound 13m), a difluoro-substituted derivative, is a highly potent activator of Nrf2 HO-1. It exhibits substantial neuroprotective and antioxidant properties by activating the Nrf2 HO-1 pathway through phosphorylation of ERK1 2, JNK, or Akt in PC12 cells. This compound finds utility in the investigation of Parkinson's disease (PD) [1].

Nrf2 HO-1 activator 1 (Compound 24) 作为一种有效的Nrf2 HO-1激活剂及神经保护剂，展现了神经保护和抗氧化活性，适用于帕金森病 (PD) 研究。

HO-PEG1-benzyl ester is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

VK3-OCH3 (2-[(2-Methoxy)ethylthio]-3-methyl-1,4-na) 是一种通过血红素加氧酶(HO-1) 相关机制的选择性抗肿瘤剂；维生素 K3 类似物。

Latifolin is a strong DPPH-scavenger, it attenuates inflammatory responses by inhibiting NF-κB activation via Nrf2-mediated heme oxygenase-1 expression. Latifolin displays potent anticarcinogenic phase II marker enzyme, quinone reductase (QR) inducing activity and high chemopreventive indices. Latifolin also shows antifungal activity against white- and brown-rot fungi.

Cudraflavone B has anti-proliferative activity, mouse brain monoamine oxidase (MAO) inhibitory effects, apoptotic actions in human gastric carcinoma cells and mouse melanoma cells, and hepatoprotective activity. It may be a lead for the development of a potential candidate for human oral squamous cell carcinoma cells.

Dehydroglyasperin C is a potent NAD(P)H:oxidoquinone reductase (NQO1) and phase 2 enzyme inducer. Dehydroglyasperin C possesses potent antioxidant, cancer chemopreventive, and neuroprotective activities, it has protective effects against chronic diseases

Physalin H is an Hh signaling inhibitor blocks GLI1-DNA-complex formation, it also strong quinone reductase induction activity with IR (Induction ratio, QR induction activity) value of 3.74±0.02. Physalin H shows immunosuppressive effects on T cells both

Eupatolide 是从 Inula japonica 的花中分离出来的，具有抗炎活性。 Eupatolide 可用于研究乳腺癌细胞对 TRAIL 的耐药性。

YHO-13351 free base 是 YHO-13177 的水溶性前药，YHO-13177 是 BCRP 的抑制剂。

Tin-protoporphyrin IX dichloride (SnPPIX dichloride) 是血红素加氧酶-1 (HO-1) 抑制剂，具有抗病毒活性，抑制登革热和黄热病病毒，可改善肝部分切除术后的肝脏再生。

NLRP3-IN-72 (Compound 2) 是一种苯并咪唑衍生物，具有抗炎和抗氧化活性，其对NLRP3IL-1β的IC50是0.3 μM，能够通过对细胞焦亡(pyroptosis)的保护显示PD50为0.4 μM，并可诱导HO-1的EC50达0.6 μM。

Tricetin 是一种从石榴中分离出的类黄酮。Tricetin 是 Keap1-Nrf2 蛋白相互作用（PPI）的强效竞争性抑制剂，通过激活 Nrf2 HO-1 信号通路和阻止线粒体依赖性细胞凋亡通路，保护帕金森病患免受 6-OHDA 诱导的神经毒性的影响。Tricetin 通过 Akt GSK-1β途径抑制鼻咽癌的迁移和指示性蛋白酶早老素-1（PS-1）表达。Tricetin 抑制由Egr-1介导的氧化LDL 诱导的内皮炎症，保护大鼠软骨细胞免受IL-1β诱导的炎症和细胞凋亡。

2,9-Dihydroxy-7-methoxy-4-methylnaphtho[1,2-b]fura 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 T125732，CAS号为 1558053-97-6。

YHO-13351 是多药物转运蛋白 （ABCG2） 抑制剂，是丙烯腈衍生物，诱导癌症干细胞 起始样侧群体细胞对伊立替康敏感。

YHO-13177 是高活性乳腺癌耐药蛋白多药转运通道（BCRP）抑制剂，可增强SN-38活性。

SHO1122147 (Compound 7m) 通过影响线粒体电子传递链展现出线粒体解偶联活性（EC50=3.6 μM），提升细胞耗氧率（OCR=69%）并促进细胞呼吸。SHO1122147 具备口服活性，适用于肥胖和代谢功能障碍相关脂肪性肝炎 (MASH) 的研究。

3,4-Dihydro-2,2-dimethyl-2H-naphtho_1,2-b_pyran是一种天然产物，属于茜草科拉拉藤属，其产品编号为 TN2874，CAS号为 16274-33-2。3,4-Dihydro-2,2-dimethyl-2H-naphtho_1,2-b_pyran可用作对照参考。

GSK429286A (RHO-15) 是一种选择性ROCK1 2抑制剂，IC50值为14 和 63 nM。

DCP-Rho1 is a fluorescent probe for the detection of sulfenic acid-containing proteins.1,2 It displays excitation emission maxima of 560 581 nm, respectively, and has been used to visualize protein oxidation sites in situ. |1. Klomsiri, C., Rogers, L.C., Soito, L., et al. Endosomal H2O2 production leads to localized cysteine sulfenic acid formation on proteins during lysophosphatidic acid-mediated cell signaling. Free Rad. Biol. Med. 71, 49-60 (2014).|2. Holmila, R.J., Vance, S.A., Chen, X., et al. Mitochondria-targeted probes for imaging protein sulfenylation. Sci. Rep. 8(1), 6635 (2018).

DCG066 是一种赖氨酸甲基转移酶 G9a 的抑制剂，具有抗癌活性，通过 Nrf2 HO-1 通路抑制 MM 细胞的增殖并诱导铁死亡，可用于研究白血病。