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Search Results for " nuclear translocation "

55

抑制剂 & 化合物

12

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T6207	SC144	Apoptosis; Interleukin	Apoptosis; Immunology/Inflammation
	SC144 是一种口服活性 gp130 抑制剂。它结合 gp130，诱导 gp130 磷酸化(S782) 和去糖基化，消除 Stat3 磷酸化和核易位，进一步抑制下游靶基因的表达。它对 gp130 配体触发的信号转导有明显的抑制作用，可诱导人卵巢癌细胞凋亡。
T28362	PF-02413873 PF02413873	Progesterone Receptor	Others
	PF-02413873 是一种非甾体孕酮受体的竞争性拮抗剂，Ki 为 2.6 nM。 PF-02413873 可用于治疗子宫内膜异位症等妇科疾病的研究。
T8730	BMS986260	TGF-beta/Smad	Stem Cells
	BMS986260是一种口服有活力的选择性TGFβR1抑制剂，是免疫肿瘤学药物。它能够抑制 MINK 和 NHLF 细胞系中 TGFβ 介导的 pSMAD2/3 核转位，IC50值分别为 350 nM 和 190 nM。它对 TGFβR1 的选择比 TGFβR2 同功酶高。
T83727	Tat-NTS Peptide TFA Tat-Nuclear Translocation Signal Peptide
	Tat-NTS肽是一种能穿透细胞的肽，由HIV-1 Tat蛋白的转导域与对应于脂联素A1重复III域残基228-237的10个氨基酸肽链接而成，扮演核转运信号（NTS）的角色。它通过阻断脂联素A1与进口素β之间的蛋白质-蛋白质相互作用，阻止脂联素A1在初级鼠海马神经元中的核内转运。Tat-NTS抑制初级鼠海马神经元在葡萄糖-氧剥夺及再灌注诱导的细胞凋亡。在体内，Tat-NTS（10 mg/kg）有效减少了由中脑动脉闭塞（MCAO）引起的缺血-再灌注损伤模型小鼠的梗塞体积和神经元凋亡，并缩短了在Morris水迷宫测试中达到平台的时间。
T2008	LY294002 LY 294002,NSC 697286,SF 1101	Apoptosis; DNA-PK; Casein Kinase; PI3K; Autophagy	Apoptosis; Autophagy; DNA Damage/DNA Repair; Metabolism; PI3K/Akt/mTOR signaling; Stem Cells
	LY294002 (SF 1101) 是一种 PI3K 的广谱抑制剂，抑制 PI3Kα、PI3Kδ 和 PI3Kβ (IC50=0.5/0.57/0.97 μM)。LY294002 也是 DNA-PK 抑制剂 (IC50=1.4 μM) 和 CK2 抑制剂 (IC50=98 nM)。LY294002 可以激活凋亡和自噬。
T4079	LY-294002 hydrochloride SF 1101,LY 294002,NSC 697286	PI3K	PI3K/Akt/mTOR signaling
	LY-294002 hydrochloride (NSC 697286) 是一种合成的 PI3Kα/δ/β 分子抑制剂（IC50：0.5/0.57/0.97 μM，在无细胞试验中）；在溶液中比 Wortmannin 更稳定，也是自噬体形成的阻断剂。
T11886	LTβR-IN-1	Others; NF-κB; LTR	Immunology/Inflammation; NF-κB; Others
	LTβR-IN-1是一种有作用的、具有选择性的淋巴素β受体(LTβR)抑制剂。LTβR-IN-1 对TNF12A 的的 p52 的核易位抑制作用具有选择性，对 TNF-α 受体介导的 p65 的核易位无明显作用，却抑制受 TWEAK 或 Anti-LTβR 刺激的 p52 核易位，IC50为10 μM。LTβR-IN-1通过配体非依赖性方式实现对 NF-kB 信号通路的调节作用。
T6915	Darolutamide ODM-201,BAY-1841788	Androgen Receptor	Endocrinology/Hormones
	Darolutamide (BAY-1841788) 是一种雄激素受体(AR) 拮抗剂，在体内试验中的IC50值为26 nM。
T4657	WHI-P97 4-(3',5'-二溴-4-羟基苯基)氨基-6,7-二甲氧基喹唑啉	JAK	Angiogenesis; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells
	WHI-P97 是一种选择性 JAK-3抑制剂，可用于预防过敏性哮喘的研究。
T6308	Stattic STAT3 Inhibitor V	Apoptosis; STAT	Apoptosis; JAK/STAT signaling; Stem Cells
	Stattic (STAT3 Inhibitor V) 是一种 STAT3 抑制剂 (IC50=5.1 μM)，选择性地抑制 STAT3 活化、二聚化和核转位。Stattic 具有抗肿瘤活性，可诱导细胞凋亡。
T4022	QS11 QS 11	GTPase	GPCR/G Protein
	QS11 是一种ARFGAP1抑制剂(EC50:1.5 µM)。QS 11 能抑制 ARFGAP 过表达的乳腺癌细胞迁移。QS 11 通过影响蛋白质运输来增强 Wnt/β-catenin 信号。
T11760	KIN101 3-(4-Bromophenyl)-7-[(methylsulfonyl)oxy]-4-oxo-4H-chromene,3-(4-溴苯基)-4-氧代-7-[(甲磺酰基)氧基]-4H-色烯	HCV Protease; Influenza Virus; RSV; Antifection	Microbiology/Virology; Proteases/Proteasome
	KIN101 (3-(4-Bromophenyl)-7-[(methylsulfonyl)oxy]-4-oxo-4H-chromene) 是 IRF-3 依赖性信号传导的异黄酮激动剂，可诱导 IRF-3 核易位。它对 RNA 病毒、HCV 和 RSV 具有抗病毒活性。
T61531	NFATc1-IN-1	RANKL/RANK	NF-κB
	NFATc1-IN-1 (also known as compound A04) is a highly effective inhibitor of osteoclast formation induced by RANKL, with an IC50 of 1.57 μM. It exerts its anti-osteoclastogenic effects by attenuating the RANKL-induced nuclear translocation of NFATc1. Due to its remarkable properties, NFATc1-IN-1 holds significant potential for advancing research related to osteoclastic diseases [1].
TP1938L	RS09 2TFA (1449566-36-2 free base) RS09 2TFA 1449566-36-2(free base)	TLR	Immunology/Inflammation
	RS09 2TFA (1449566-36-2 free base) 是一种 TLR4 激动剂。促进 NF-κB 核转位并在体外诱导 RAW264.7 巨噬细胞分泌炎性细胞因子。它在体内充当佐剂并提高 X-15 特异性抗体血清浓度。
T77332	TV 3279	BCL; PKC	Apoptosis; Chromatin/Epigenetic; Cytoskeletal Signaling
	TV 3279是一种新型ChE-MAI 抑制剂，神经保护特性取决于它们诱导抗凋亡蛋白PKC、Bcl-2、Bcl-x 和SOD 的能力，并阻止促凋亡酶甘油醛磷酸脱氢酶在PC-12和神经母细胞瘤细胞中的核易位。
T19710	Ciglitazone Ciglitazona,U 63287,ADD3878,ADD-3878,U-63287,ADD 3878	Apoptosis; p38 MAPK; PPAR	Apoptosis; DNA Damage/DNA Repair; MAPK; Metabolism
	Ciglitazone (ADD 3878) 是一种强效和选择性的PPARγ激动剂(EC50：3μM)和口服降糖药。Ciglitazone 抑制th17细胞的增殖和分化，降低胰岛素水平、血管内皮生长因子的产生和血压，诱导胃癌细胞的细胞周期停止。Ciglitazone 能诱导负鼠肾上皮细胞的凋亡，激活p38 MAPK 和凋亡诱导因子(AIF)的核转位。 Ciglitazone 在肥胖症和高血糖症的动物模型中表现出降血糖活性。
T6964	Resiquimod R848,雷西莫特,S28463	HCV Protease; TLR	Immunology/Inflammation; Microbiology/Virology; Proteases/Proteasome
	Resiquimod (R848) 是一种 Toll 样受体7/8的激动剂，可诱导细胞因子上调。
T60013	GA-017	Others	Others
	GA-017是一种有效的选择性 LATS1和 LATS2(大型肿瘤抑制激酶 1/2) 抑制剂，其 IC50值分别为 4.10 和 3.92 nM。GA-017 是细胞增殖的激活剂。GA-017 促进 YAP/TAZ 激活和核转位。GA-017 在 3D 培养条件下促进细胞生长。GA-017 增强小鼠肠道类器官的离体形成。
T8055	TFEB activator 1 (1E,4E)-1,5-Bis(2-Methoxyphenyl)penta-1,,Curcumin analog compound C1,Curcumin analog C1,(1E,4E)-1,5(2 -甲氧基苯基)-1,4-戊二烯-3-酮,RPN77612	Others; Autophagy	Autophagy; Others
	TFEB activator 1 (Curcumin analog compound C1) 是转录因子 EB 的一种激活剂，有望预防或治疗阿尔茨海默病。
T30868	CH-5137291 CH 5137291,CH5137291
	CH-5137291 is a pure AR antagonist with AR nuclear translocation inhibition activity. It suppresses castration and prevents the growth of prostate cancer cells.
T71842	D719
	D719 is a novel inhibitor of integrase nuclear translocation, showing significant inhibition on virus p24 antigen production.
T30877	CHF-1024 UNII-HPH2L3QA2F
	CH-5137291 is a pure AR antagonist with AR nuclear translocation inhibition activity. It inhibits castration and prevents the growth of prostate cancer cells.
T68986	ZINC08383544
	ZINC08383544 is a specific pyruvate kinase M2 activator which promotes the formation of PKM2 tetramer. ZINC08383544 effectively blocks PKM2 nuclear translocation, and inhibits the growth of tumor.
T36535	SEC
	SEC activates ANXA7 GTPase through the AMPK/mTORC1/STAT3 signaling pathway. It selectively induces apoptosis in cancer cells expressing high levels of ITGB4 by promoting ITGB4 nuclear translocation [1][2].
T26936	C188 Cpd188,STAT3-IN-C188,Cpd-188,C 188,C-188
	C188 is a cell-permeable naphthol compound and a STAT3 inhibitor. C188 inhibits IL-6-stimulated STAT3 Tyr705 phosphorylation and nuclear translocation in HepG2 cells by targeting STAT3 SH2 domain peptide-binding pocket, while exhibiting little effect agai
T38460	SN52
	SN52 is a powerful, competitive, and cell-permeable inhibitor of NF-κB2. It is a variant of the SN50 peptide. SN52 effectively prevents the nuclear translocation of p52-RelB heterodimers, exhibiting a robust radiosensitization effect on prostate cancer cells. This compound holds significant potential for cancer research purposes.
TP1938	RS 09	TLR	Immunology/Inflammation
	RS 09 是一种 LPS 肽模拟物，是 TLR4 激动剂佐剂，可在疫苗环境中增加抗体产量。
T70399	TTC-352
	TTC-352 is an orally bioavailable selective human estrogen receptor alpha (ERalpha; ESR1; ERa) partial agonist (ShERPA), with potential antineoplastic activity. Upon administration, TTC-352 mimics the naturally-occurring 17beta-estradiol (E2) and targets and binds to ERa located in the nucleus. This causes translocation of ERa to extranuclear sites. Nuclear export of ERa prevents normal ER-mediated signaling and inhibits proliferation of ER-positive tumor cells.
T35429	AC-4-130
	AC-4-130, a powerful inhibitor of the SH2 domain of STAT5, effectively hinders STAT5 activation, dimerization, nuclear translocation, and transcription of genes reliant on STAT5. This compound directly binds to STAT5, ultimately leading to cell cycle arrest and apoptosis in FLT3-ITD-driven leukemic cells. AC-4-130 exhibits notable anti-cancer properties and effectively suppresses abnormal STAT5 activity in acute myeloid leukemia (AML), making it a promising therapeutic option [1].
T78846	EP12	Apoptosis	Apoptosis
	EP12是一种c-Myc抑制剂及c-MycG4稳定剂，能够诱导多发性骨髓瘤细胞的细胞凋亡(apoptosis)及DNA损伤，并通过干扰NF-κB信号通路破坏P65/P50的核转位，从而抑制多发性骨髓瘤的生长。
T69401	MIND4-17
	MIND4-17为一种NRF2激活剂，通过共价修饰Keap1的C151残基发挥作用。该化合物能破坏Keap1-Nrf2之间的结合，进而促进Nrf2蛋白的稳定性及其向核内的迁移，显示出显著的抗氧化活性。
TP2157L	TAT-DEF-Elk-1 TFA (1220751-16-5 free base) TDE TFA,TAT-DEF-Elk-1 TFA	Others	Others
	TAT-DEF-Elk-1 TFA is a cell-penetrating peptide Elk-1 inhibitor, mimics and specifically interferes with the DEF domain of Elk-1. TAT-DEF-Elk-1 blocks Elk-1 phosphorylation and prevents Elk-1 nuclear translocation without interfering with ERK nor MSK1 act
T83047	Anti-inflammatory agent 65	STING	Immunology/Inflammation
	Anti-inflammatory agent 65（compound 29）是一种从常春藤酸衍生且具有有效抗炎活性的化合物。它能够抑制一氧化氮（NO）的释放，阻止IRF3和p65的核转位，破坏STING/IRF3/NF-κB信号通路，有效减弱炎症反应。
T78640	Z-LLF-CHO Z-Leu-Leu-Phe-CHO	Proteasome	Proteases/Proteasome; Ubiquitination
	Z-LLF-CHO（Z-Leu-Leu-Phe-CHO）为垂体多催化蛋白酶复合物所具有的胰凝乳蛋白酶样活性提供有效抑制，具有Ki值为460 nM。此外，Z-LLF-CHO同样作为NF-κB核转位的抑制剂。
T79465	Anticancer agent 135	Androgen Receptor	Endocrinology/Hormones
	Anticanceragent 135（compound 26h）为一有效的雄激素受体（AR）拮抗剂，能够阻断AR核转位并抑制AR/AR-V7异二聚化，以抑制下游基因转录。该化合物在前列腺癌异种移植模型中展现出显著疗效。
T60988	Androgen receptor antagonist 4
	Androgen receptor antagonist 4 (Compound AT2) 表现出抗癌活性。Androgen receptor antagonist 4 有效拮抗 AR 的转录活性，抑制 AR 的下游靶基因，并阻断 DHT 诱导的 AR 核转位。它是雄激素受体 (AR) 的拮抗剂 (IC50 = 0.15 μM)。
T75952	RS 09 TFA
	RS 09 TFA是一种TLR4激动剂，能在体外RAW264.7巨噬细胞中促进NF-κB核易位并诱导炎性细胞因子的分泌。作为体内佐剂，与X-15-KLH联用时，RS 09 TFA能在小鼠中提高X-15特异性抗体的血清浓度。
T68393	SNX-7081
	NX-7081 is a novel small molecule inhibitor of Hsp90, which blocks components of inflammation, including cytokine production, protein kinase activity, and angiogenic signaling. SNX-7081 showed strong binding affinity to Hsp90 and expected induction of Hsp70. NF-kappaB nuclear translocation was blocked by SNX-7081 at nanomolar concentrations, and cytokine production was potently inhibited. Growth factor activation of ERK and JNK signaling was significantly reduced by SNX-7081. NO production was a...
T71361	CHS-828 nicotinate
	CHS-828 nicotinate is a CHS-828 salt with Nicotinic acid.. CHS-828 also known as GMX-1778, is a potent and selective NAMPT inhibitor. CHS-828 inhibits cellular synthesis of NAD. CHS 828 kill tumour cells by inhibiting the nuclear factor-kappaB translocation but unlikely through down-regulation of proteasome. CHS 828 has shown promising anticancer activity in experimental tumor models and primary cultures of cancer cells from patients. CHS 828 showed a synergistic effect with melphalan in 67%, ...
T5339	YZ129
	YZ129 是一种抗胶质母细胞瘤的HSP90-磷酸酶-NFAT 通路的抑制剂，直接与热休克蛋白 (HSP90)结合，对NFAT 核易位的IC50值为820 nM。YZ129 在 G2/M 期诱导GBM 细胞周期阻滞，促进细胞凋亡，抑制肿瘤细胞增值和迁移。
T41260	SC144 hydrochloride
	SC144 hydrochloride 是首创的口服活性gp130 (IL6-beta)抑制剂。SC144 hydrochloride 结合 gp130，诱导 gp130 磷酸化(S782) 和去糖基化，消除 Stat3 磷酸化和核易位，进而抑制下游靶基因的表达。SC144 hydrochloride 对 gp130 配体触发的信号转导显示有效的抑制作用。SC144 hydrochloride 诱导人卵巢癌细胞凋亡。
T72687	Keap1-Nrf2-IN-11
	Keap1-Nrf2-IN-11为Keap1-Nrf2抑制剂，KD2值达0.21 nM。该化合物可有效抑制ROS及NO的生成，并降低TNF-α的表达。通过促进Nrf2的核内转移，Keap1-Nrf2-IN-11对炎症具有调节作用，适用于抗炎研究。
T78716	MKA031
	MKA031（compound 6y）作为一种非竞争性MIF抑制剂，展现出1.7 μM的IC50。该化合物能够阻断MIF/AIF相互作用、抑制MIF核内转移，并干预MNNG所诱发的细胞死亡。MKA031主要用于研究慢性丙型肝炎病毒感染。
T62111	Antioxidant agent-5
	Antioxidant agent-5 (compound D-6) 是一种有效的抗氧化剂。Antioxidant agent-5 能够抑制 oxLDL 诱导的 ROS 水平升高和 NF-κB 核转位。Antioxidant agent-5 对 oxLDL (氧化型低密度脂蛋白)诱导的 VECs 细胞凋亡 (apoptosis) 及 ICAM-1 和 VCAM-1 的表达表现出抑制作用。Antioxidant agent-5 可以激活 Nrf2/HO-1 抗氧化通路，对 oxLDL 诱导的内皮损伤表现出保护活性。
T36645	CAY10763 CAY10763
	CAY10763 is a dual inhibitor of indolamine 2,3-dioxygenase 1 (IDO1; IC50= 46 nM) and STAT3 activation.1It binds to STAT3 (Kd= 530 nM) and selectively reduces the levels of STAT3 phosphorylated at the tyrosine in position 705 (STAT3Y705) over phosphorylated STAT3S727, STAT1, and STAT5 in SKOV3 cells when used at a concentration of 500 nM. It also inhibits STAT3 nuclear translocation in SKOV3 cells. CAY10763 is cytotoxic to HCT116, SKOV3, A549, and HepG2 cancer cells (IC50s = 37, 28, 33, and 12 nM...
T79662	STAT3-IN-20	STAT	JAK/STAT signaling; Stem Cells
	STAT3-IN-20（Compound 40）是一种选择性地靶向STAT3的SH2结构域，展现了在DU145和MDA-MB-231癌细胞中的抗增殖效果（IC50分别为2.97 μM和3.26 μM），并诱导细胞周期停滞与细胞凋亡。该抑制剂有效抑制了STAT3的磷酸化、核内易位及其下游基因的转录活性（IC50: 0.65 μM）。
T69288	CEP-7055
	CEP-18770 is an orally bioavailable synthetic P2 threonine boronic acid inhibitor of the chymotrypsin-like activity of the proteasome, with potential antineoplastic activity. Proteasome inhibitor CEP 18770 represses the proteasomal degradation of a variety of proteins, including inhibitory kappaBalpha (IkappaBalpha), resulting in the cytoplasmic sequestration of the transcription factor NF-kappaB; inhibition of NF-kappaB nuclear translocation and transcriptional up-regulation of a variety of cel...
T81038	TAT-DEF-Elk-1 TFA TDE TFA
	TAT-DEF-Elk-1 TFA (TDE TFA) 是一种Elk-1的细胞穿透性肽抑制剂，通过模仿Elk-1的DEF域并特异性地阻断其功能来抑制Elk-1。该化合物能够抑制Elk-1的磷酸化作用，阻止其核内转位，同时不影响ERK和MSK1的活化。TAT-DEF-Elk-1 TFA作为一种研究工具，对于探究神经元可塑性及Elk-1在该进程中的角色具有重要价值。
T83661	17(R,S)-Benzo-Resolvin D1 17(R,S)-Benzo-RvD1,Benzo-RvD1
	17(R,S)-Benzo-resolvin D1 (benzo-RvD1) 是专门的分辨介质 (SPM) RvD1 的衍生物。在10和100 nM的浓度下，它能减少PDGF-BB诱导的人类血管平滑肌细胞 (VSMCs) 的细胞骨架变化，并抑制PDGF诱导的这些细胞的迁移。Benzo-RvD1 (10 nM) 抑制人脐静脉内皮细胞 (HUVECs) 中的p65核转位。它还提高了RAW 264.7对S. aureus和zymosan颗粒的吞噬作用。
T78698	Aβ-IN-6
	Aβ-IN-6降低小胶质细胞释放的促炎细胞因子，能有效促进Nrf2核转位并抑制Aβ寡聚体的形成。通过调节体内氧化应激的氧化还原敏感信号通路，Aβ-IN-6展现出一致的神经保护效应。具有口服活性的Aβ-IN-6表现出抗炎、抗氧化和抗寡聚特性，并显示出作为阿尔茨海默病(AD)治疗研究潜力。

化合物

Cat.No: T6207

Target: Apoptosis, Interleukin

Cat.No: T28362

Synonym: PF02413873

Target: Progesterone Receptor

Cat.No: T8730

Target: TGF-beta/Smad

Tat-NTS Peptide TFA

Cat.No: T83727

Synonym: Tat-Nuclear Translocation Signal Peptide

Cat.No: T2008

Synonym: LY 294002,NSC 697286,SF 1101

Target: Apoptosis, DNA-PK, Casein Kinase, PI3K, Autophagy

LY-294002 hydrochloride

Cat.No: T4079

Synonym: SF 1101,LY 294002,NSC 697286

Target: PI3K

Cat.No: T11886

Target: Others, NF-κB, LTR

Cat.No: T6915

Synonym: ODM-201,BAY-1841788

Target: Androgen Receptor

Cat.No: T4657

Synonym: 4-(3',5'-二溴-4-羟基苯基)氨基-6,7-二甲氧基喹唑啉

Target: JAK

Cat.No: T6308

Synonym: STAT3 Inhibitor V

Target: Apoptosis, STAT

Cat.No: T4022

Synonym: QS 11

Target: GTPase

Cat.No: T11760

Synonym: 3-(4-Bromophenyl)-7-[(methylsulfonyl)oxy]-4-oxo-4H-chromene,3-(4-溴苯基)-4-氧代-7-[(甲磺酰基)氧基]-4H-色烯

Target: HCV Protease, Influenza Virus, RSV, Antifection

Cat.No: T61531

Target: RANKL/RANK

RS09 2TFA (1449566-36-2 free base)

Cat.No: TP1938L

Synonym: RS09 2TFA 1449566-36-2(free base)

Target: TLR

Cat.No: T77332

Target: BCL, PKC

Cat.No: T19710

Synonym: Ciglitazona,U 63287,ADD3878,ADD-3878,U-63287,ADD 3878

Target: Apoptosis, p38 MAPK, PPAR

Cat.No: T6964

Synonym: R848,雷西莫特,S28463

Target: HCV Protease, TLR

Cat.No: T60013

Target: Others

TFEB activator 1

Cat.No: T8055

Synonym: (1E,4E)-1,5-Bis(2-Methoxyphenyl)penta-1,,Curcumin analog compound C1,Curcumin analog C1,(1E,4E)-1,5(2 -甲氧基苯基)-1,4-戊二烯-3-酮,RPN77612

Target: Others, Autophagy

Cat.No: T30868

Synonym: CH 5137291,CH5137291

Cat.No: T71842

Cat.No: T30877

Synonym: UNII-HPH2L3QA2F

Cat.No: T68986

Cat.No: T36535

Cat.No: T26936

Synonym: Cpd188,STAT3-IN-C188,Cpd-188,C 188,C-188

Cat.No: T38460

Cat.No: TP1938

Target: TLR

Cat.No: T70399

Cat.No: T35429

Cat.No: T78846

Target: Apoptosis

Cat.No: T69401

TAT-DEF-Elk-1 TFA (1220751-16-5 free base)

Cat.No: TP2157L

Synonym: TDE TFA,TAT-DEF-Elk-1 TFA

Target: Others

Anti-inflammatory agent 65

Cat.No: T83047

Target: STING

Cat.No: T78640

Synonym: Z-Leu-Leu-Phe-CHO

Target: Proteasome

Anticancer agent 135

Cat.No: T79465

Target: Androgen Receptor

Androgen receptor antagonist 4

Cat.No: T60988

Cat.No: T75952

Cat.No: T68393

CHS-828 nicotinate

Cat.No: T71361

Cat.No: T5339

SC144 hydrochloride

Cat.No: T41260

Keap1-Nrf2-IN-11

Cat.No: T72687

Cat.No: T78716

Antioxidant agent-5

Cat.No: T62111

Cat.No: T36645

Synonym: CAY10763

Cat.No: T79662

Target: STAT

Cat.No: T69288

TAT-DEF-Elk-1 TFA

Cat.No: T81038

Synonym: TDE TFA

17(R,S)-Benzo-Resolvin D1

Cat.No: T83661

Synonym: 17(R,S)-Benzo-RvD1,Benzo-RvD1

Cat.No: T78698

Cat. No.	Product Name	Target	Signaling Pathways
T5689	20-DEOXYINGENOL	Others; Autophagy	Autophagy; Others
	20-Deoxyingenol 是从甘遂的根中分离出的一种二萜类天然产物。它可通过促进体外转录因子 EB 的核易位来促进自噬和溶酶体生物发生，可研究骨关节炎。
T19768	γ-Tocotrienol gamma Tocotrienol,gammaTocotrienol,gamma-Tocotrienol,D-gamma-Tocotrienol,Plastochromanol,γ-生育三烯酚	Others	Others
	γ-Tocotrienol (Plastochromanol) 是一种维生素 E 的活性形式。
T5701	OPHIOPOGONIN D 麦冬皂苷 D,麦冬皂苷D	RAAS; Calcium Channel; NF-κB; PPAR	DNA Damage/DNA Repair; Endocrinology/Hormones; Membrane transporter/Ion channel; Metabolism; NF-κB
	Ophiopogonin D 是从麦冬的块茎中分离的一种天然产物，是罕见的天然存在的 C29甾体糖苷。它是一种 CYP2J3 诱导剂，用于炎症和心血管疾病的相关研究。
T4237	Rubiadin-1-methyl ether Rubiadin 1-methyl ether,3-羟基-1-甲氧基-2-甲基蒽醌	Anti-infection; NF-κB	Microbiology/Virology; NF-κB
	Rubiadin-1-methyl ether (Rubiadin 1-methyl ether) 是一种巴戟天中的蒽醌类化合物，能够抑制 NF-κB p65 的磷酸化和 IκBα 的降解以及减少 p65 的核转位，阻碍破骨细胞的骨吸收。
T2836	Isorhamnetin 3-methylquercetin,3'-Methylquercetin,Isorhamnetol,异鼠李素,3'-Methoxyquercetin	MEK; PI3K; Endogenous Metabolite	MAPK; Metabolism; PI3K/Akt/mTOR signaling
	Isorhamnetin (3-methylquercetin) 是从中草药沙棘中提取的一种类黄酮，可通过抑制MEK1和PI3K 来抑制皮肤癌。
T0798	Triamcinolone Fluoxyprednisolone,曲安西龙,Aristocort,Rodinolone	Glucocorticoid Receptor; COX	Endocrinology/Hormones; Immunology/Inflammation; Neuroscience
	Triamcinolone (Aristocort) 是一种皮质类固醇激素受体激动剂，也是一种合成的长效糖皮质激素，具有抗炎活性。
TMA0237	Carlinoside	Nrf2	Immunology/Inflammation
	Carlinoside could be a worthy choice to intervene hyperbilirubinemia due to liver dysfunction. Carlinoside upregulates Nrf2 gene expression, increases its nuclear translocation and stimulates UGT1A1 promoter activity.
TN2178	Sanggenone H	IL Receptor; TNF; NF-κB	Apoptosis; Immunology/Inflammation; NF-κB
	Sanggenone H may have antiphlogistic activity, it attenuated the secretion of TNF-α± and IL-1α² and inhibited the NF-κB nuclear translocation in LPS-stimulated macrophages.
TN6394	Alisol B acetate
	Alisol B acetate can induce Bax nuclear translocation and apoptosis in human hormone-resistant prostate cancer PC-3 cells, the Bax activation and translocation from the cytosol to nucleus might be a crucial response to the apoptotic effect. Alisol B aceta
T40611	(E)-Dehydrodiconiferyl alcohol
	(E)-Dehydrodiconiferyl alcohol is a potent dual inhibitor of hCA IX and hCA XII, effectively impeding the catalytic activity of both carbonic anhydrase isoforms. Additionally, (E)-Dehydrodiconiferyl alcohol exerts inhibitory effects on the nuclear translocation of NF-κB in the connective tissue of the healing area.
TN1009	Epimagnolin B	NF-κB; NO Synthase; Prostaglandin Receptor	GPCR/G Protein; Immunology/Inflammation; NF-κB
	Epimagnolin B 是一种双环氧木质素，分离自木兰中。它能够抑制 LPS 激活的小胶质细胞中 NO 的产生。它具有抗过敏以及抗炎作用。
TN4635	Neoechinulin A	NADPH-oxidase; Beta Amyloid; ASK; IκB/IKK; p38 MAPK; TNF; NOS; NF-κB; COX; Prostaglandin Receptor	Apoptosis; GPCR/G Protein; Immunology/Inflammation; MAPK; Neuroscience; NF-κB
	Neoechinulin A has anti-inflammatory effect against LPS-stimulated RAW264.7 macrophages through inhibition of the NF-ÎºB and p38 MAPK pathways, it may block the phosphorylation of mitogen-activated protein kinase (MAPK) molecule p38, apoptosis signal-regu

天然产物

20-DEOXYINGENOL

Cat.No: T5689

Target: Others, Autophagy

Cat.No: T19768

Synonym: gamma Tocotrienol,gammaTocotrienol,gamma-Tocotrienol,D-gamma-Tocotrienol,Plastochromanol,γ-生育三烯酚

Target: Others

Cat.No: T5701

Synonym: 麦冬皂苷 D,麦冬皂苷D

Target: RAAS, Calcium Channel, NF-κB, PPAR

Rubiadin-1-methyl ether

Cat.No: T4237

Synonym: Rubiadin 1-methyl ether,3-羟基-1-甲氧基-2-甲基蒽醌

Target: Anti-infection, NF-κB

Cat.No: T2836

Synonym: 3-methylquercetin,3'-Methylquercetin,Isorhamnetol,异鼠李素,3'-Methoxyquercetin

Target: MEK, PI3K, Endogenous Metabolite

Cat.No: T0798

Synonym: Fluoxyprednisolone,曲安西龙,Aristocort,Rodinolone

Target: Glucocorticoid Receptor, COX

Cat.No: TMA0237

Target: Nrf2

Cat.No: TN2178

Target: IL Receptor, TNF, NF-κB

Alisol B acetate

Cat.No: TN6394

(E)-Dehydrodiconiferyl alcohol

Cat.No: T40611

Cat.No: TN1009

Target: NF-κB, NO Synthase, Prostaglandin Receptor

Cat.No: TN4635

Target: NADPH-oxidase, Beta Amyloid, ASK, IκB/IKK, p38 MAPK, TNF, NOS, NF-κB, COX, Prostaglandin Receptor

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