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Search Results for " signalling "

70

抑制剂 & 化合物

18

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T7953	BpV(HOpic) bpV (HOpic)	PTEN	PI3K/Akt/mTOR signaling
	BpV(HOpic) (bpV (HOpic)) 是 PTEN 选择性抑制剂，IC50=14 nM。BpV(HOpic) 具有神经保护作用。
T14327	AS1949490	Phosphatase	Metabolism
	AS1949490 是选择性SHIP-2抑制剂，其IC50=620 nM。它能够通过上调L6肌管GLUT1基因激活葡萄糖代谢。
T50103	NFAT Inhibitor-2	Others	Others
	NFAT Inhibitor-2 是一种化学合成中的砌块。
T23516	VU590	Potassium Channel	Membrane transporter/Ion channel
	VU590 是一种具有高效性和中等选择性的肾外髓质钾 ROMK (Kir1.1) 抑制剂。VU590 抑制 Kir7.1，可调节子宫肌层收缩力和黑皮质素信号传导。
T2261	IM-12 IM 12	GSK-3	PI3K/Akt/mTOR signaling; Stem Cells
	IM-12 是一种 GSK-3β的抑制剂，其 IC50=53 nM，可提高 Wnt 信号传导。
T62356	Mardepodect hydrochloride PF-2545920 HCl,Mardepodect HCl,MP-10 HCl,PF-02545920 HCl	Apoptosis; PDE	Apoptosis; Metabolism
	Mardepodect hydrochloride (Mardepodect HCl) 是一种可穿过血脑屏障且具有口服活性的、选择性和高效性的 PDE10A 抑制剂（IC50 ：0.37 nM）。Mardepodect hydrochloride 可上调编码特定生长因子、转录因子、细胞信号分子和细胞表面蛋白的基因，同时下调广泛的可靶向细胞周期和细胞凋亡相关基因。
T14886	Cbz-B3A	mTOR	PI3K/Akt/mTOR signaling
	Cbz-B3A 是一种具有现在性的 mTORC1 信号转导抑制剂，抑制 eIF4E 结合蛋白 1 （4EBP1）的磷酸化并阻断 68% 的翻译。
T9015	LY900009	Gamma-secretase	Neuroscience; Proteases/Proteasome; Stem Cells
	LY900009 是一种通过选择性抑制 γ-分泌酶蛋白来抑制 Notch 信号传导的小分子抑制剂。
T21890	JLK6	Gamma-secretase	Neuroscience; Proteases/Proteasome; Stem Cells
	JLK-6 是一种γ分泌酶抑制剂，选择性作用于 HEK293细胞的淀粉样β前体蛋白(APP)的γ-分泌酶裂解 APP，抑制 Aβ的生成，但对不 Notch 受体的裂解无影响。
T7201	Nelociguat N-[4,6-二氨基-2-[1-[(2-氟苯基)甲基]-1H-吡唑并[3,4-B]吡啶-3-基]-5-嘧啶]-氨基甲酸甲酯,BAY60-4552	Guanylate cyclase	GPCR/G Protein
	Nelociguat (BAY60-4552) 是一种一氧化氮敏感的可溶性鸟苷酸环化酶刺激剂。
T28497	RA-839 RA 839,RA839	Nrf2	Immunology/Inflammation
	RA-839 是一种有效的小分子 Keap1 的结合剂和选择性 Nrf2 信号传导激活剂，也是 Keap1/Nrf2 相互作用的抑制剂，具有抗癌活性。RA-839 抑制诱导型一氧化氮合酶表达，抑制一氧化氮释放。
T63643	BI-4142	HER	Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors
	BI-4142 是一种具有口服活性、高效和选择性的 HER2 抑制剂，抑制癌细胞增殖，抑制her2依赖性细胞系并抑制下游信号传导。
T23910	Cosalane NSC 658586,NSC-658586,NSC 640067	HIV Protease	Microbiology/Virology; Proteases/Proteasome
	Cosalane (NSC 658586) 是一种 HIV 复制抑制剂，是人和小鼠趋化因子受体 7 （CCR7）信号传导的抑制剂，具有抗病毒活性，可阻断 CCR7 与其天然配体 CCL19 和 CCL21 结合。Cosalane 对多种 HIV-1 株系和 HIV-2 具有活性。
T76795	Xentuzumab BI 836845	Akt; IGF-1R	Cytoskeletal Signaling; PI3K/Akt/mTOR signaling; Tyrosine Kinase/Adaptors
	Xentuzumab (BI836845) 是人源化IGF 配体的重组单克隆抗体，抑制 IGF1 和 IGF2 促生长信号传导，抑制 AKT 的激活，可用于研究实体肿瘤。
T76910	Astegolimab RG 6149,MSTT 1041A	Interleukin	Immunology/Inflammation
	Astegolimab (RG 6149) 是一种人源化靶向 IL-33 受体的 IgG2 单克隆抗体，可抑制 IL-33 信号传导。Astegolimab 可用于研究慢性阻塞性肺疾病 (COPD) 和成人严重哮喘。
T7511	Cyclo(his-pro)	NF-κB; Endogenous Metabolite	Metabolism; NF-κB
	Cyclo(his-pro) 是一种口服具有活力的，结构上与促甲状腺激素释放激素相关的环状二肽。它能够抑制NF-κB 核积累，也能够穿越脑血屏障并影响多种炎症和应激反应。
T77673	7-FluorotryptaMine HCl	GPR; Arrestin	Endocrinology/Hormones; GPCR/G Protein
	7-FluorotryptaMine HCl 是一种有效的芳香单胺 GPRC5A 激动剂，可诱导 GPRC5A 介导的 β-arrestin 募集。7-FluorotryptaMine HCl 可用于研究与免疫和癌症相关的信号通路。
T6760	APS-2-79 hydrochloride APS-2-79 HCl,APS-2-79	MEK; MAPK	MAPK
	APS-2-79 hydrochloride (APS-2-79 HCl) 是一种 KSR 依赖性的MEK 拮抗剂，可与 ATPbiotin 竞争性地结合到 KSR2-MEK1 复合物内的KSR2。它与 KSR 结合可将 KSR 处于非活性状态，使其无法再结合 RAF 和激活 MEK，从而阻断 Ras-MAPK 信号通路。
T72057	H1k	CDK	Cell Cycle/Checkpoint
	H1k 是一种 eudistomin Y 荧光衍生物和溶酶体靶向抗增殖剂。它可以剂量依赖性地增加自噬信号，下调细胞周期蛋白依赖性激酶(cyclin-dependent kinase, CDK1)和细胞周期蛋白 B1的表达。
T23097	O-1602 O1602,O 1602	Cannabinoid Receptor; Calcium Channel	GPCR/G Protein; Membrane transporter/Ion channel; Metabolism
	O-1602 是一种新型 GPR55 激动剂，是一种非典型大麻素，与中枢神经系统和肥胖有关，是治疗膀胱炎的候选化合物。O-1602通过小鼠GPR55 的 PI3激酶/ Akt / SREBP-1c信号传导促进肝脂肪变性。O-1602以GPR3非依赖性方式诱导Hep55B细胞中的细胞内钙升高。
T60657	(R)-STU104	TNF; MAPK	Apoptosis; MAPK
	(R)-STU104 是一种新型 TAK1-MKK3 蛋白-蛋白相互作用（PPI）抑制剂，抑制 TNF-α，通过与 MKK3 结合并破坏TAK1磷酸化MKK3来抑制TAK1/MKK3/p38/MnK1/MK2/elF4E信号通路。(R)-STU104 是治疗溃疡性结肠炎的候选化合物。
T15300	Fluorofenidone AKF-PD	Others	Others
	Fluorofenidone (AKF-PD) 是 AMR69 的类似物，抗纤维化活性与 AMR69相同，但 Fluorofenidone 的毒性更低，半衰期长。它部分通过 PI3K/Akt 信号通路抑制 NADPH 氧化酶和细胞外基质 (ECM) 的沉积，能够减少肾间质纤维化的发生。
T8656	CAY10404 3-(4-METHYLSULPHONYLPHENYL)-4-PHENYL-5-T	Apoptosis; Akt; COX	Apoptosis; Cytoskeletal Signaling; Immunology/Inflammation; Neuroscience; PI3K/Akt/mTOR signaling
	CAY10404 (3-(4-METHYLSULPHONYLPHENYL)-4-PHENYL-5-T) 是一种有效且高度选择性的 COX-2 和 COX-1 抑制剂。它还是 PKB/Akt 和 MAPK 信号通路的有效抑制剂，可诱导 NSC-LC 细胞凋亡，具有镇痛、抗炎和抗癌活性。
T4564	Ethacrynic acid Edecrin,利尿酸,Etacrynic Acid,Hydromedin	Others; Calcium Channel; NF-κB; GST	Membrane transporter/Ion channel; Metabolism; NF-κB; Others; oxidation-reduction
	Ethacrynic acid (Edecrin) 是谷胱甘肽 S-转移酶抑制剂，也是NF-κB 信号传导途径的有效抑制剂，并且还调节白三烯的形成。它还可抑制 L 型电压依赖性和储存操作的钙通道，从而导致气道平滑肌细胞松弛。它是利尿剂，具有抗炎特性，可减轻类维生素 A 诱导的小鼠耳部水肿。
T12797	RU-SKI 43 RUSKI 43	Hedgehog/Smoothened; Acyltransferase	GPCR/G Protein; Metabolism; Stem Cells
	RU-SKI 43 是一种有效的选择性刺猬酰基转移酶 (Hhat) 抑制剂，IC50 为 850 nM。RU-SKI 43 具有抗癌活性，是治疗肺腺癌的潜在化合物。RU-SKI 43 通过独立于平滑化的非规范信号传导降低 Gli-1 激活，并抑制 Akt 和 mTOR 通路活性。
TP1263	Fz7-21 (Ac)-LPSDDLEFWCHVMY-NH2	Wnt/beta-catenin	Cytoskeletal Signaling; Stem Cells
	Fz7-21 ((Ac)-LPSDDLEFWCHVMY-NH2) 是一种 Frizzled 7 (FZD 7) 受体的肽抑制剂，能够选择性的与FZD7 CRD 亚类结合。它还阻断了WNT3A 介导的β-catenin 在小鼠L 细胞中的稳定作用。它对外源性WNT3A 刺激和转染WNT3A 或WNT1的HEK293细胞Wnt/β-catenin 信号传导有损伤。
T3997	WEHI-345 WEHI345	RIP kinase	Apoptosis; NF-κB
	WEHI-345 是一种选择性RIPK2 激酶抑制剂，IC50值为 0.13 μM。它在寡聚化结构域刺激下可延迟RIPK2的泛素化和NF-κB 的活化。
T29024	TX2-121-1 TX 21211,TX 2-121-1
	TX2-121-1 targets HER3 for proteasome-mediated degradation to inhibit HER3-dependent signalling and growth.
T13344	Wnt/β-catenin agonist 1	Others	Others
	Wnt/β-catenin agonist 1 is an agonist of Wnt/β-catenin signalling pathway(EC50 of 0.27 μM).
T68954	UCB-6876
	UCB-6876 is a novel inhibitor of TNF signalling by stabilising an asymmetric form of the trimer, displaying a concentration-dependent response curve and selectivity over the TNFR1 extracellular domain and control proteins.
T71807	UCB-6786
	UCB-6786 is a novel inhibitor of TNF signalling by stabilising an asymmetric form of the trimer, displaying a concentration-dependent response curve and selectivity over the TNFR1 extracellular domain and control proteins.
T70647	CD2019
	CD2019 is a retinoic acid receptor beta (rarbeta) agonist, overcoming inhibition of axonal outgrowth via phosphoinositide 3-kinase signalling in the injured adult spinal cord.
T28113	MS-1020 MS 1020
	MS-1020 is a JAK3 and STAT3 inhibitor. MS-1020 selectively blocks constitutively-active JAK3 and consistently suppressed interleukin-2-induced JAK3/STAT5 signalling. MS-1020 potently inhibits persistently-active STAT3 in a cell type-specific manner.
T62322	(S)-MALT1-IN-5
	(S)-MALT1-IN-5 是一种 MALT1 蛋白酶的有效抑制剂。(S)-MALT1-IN-5 能够抑制 MALT1 的活性，有潜力改善由 T 细胞受体信号或 B 细胞受体信号异常导致的 MALT1 活性增强，以及由 MALT1 活性引起的癌症或炎症性疾病。(S)-MALT1-IN-5 具有潜力进行 MALT1 相关疾病的研究。
T27189	DL-threo dihydrosphingosine DL-Safingol,DTD,DL threo dihydrosphingosine
	DL-threo dihydrosphingosine is a cell-permeable inhibitor of the extracellular signal-regulated kinase (ERK) signalling cassette in mammalian cells. DL-threo dihydrosphingosine is effective against both growth factor- and G-protein-dependent activation of
T62803	STAT3-IN-12
	STAT3-IN-12 是一种 STAT3 的有效信号抑制剂，对 IL-6 诱导的 JAK/STAT3 信号通路的激活具有抑制作用。STAT3-IN-12 对癌细胞生长、迁移具有抑制作用，可阻滞细胞周期并诱导细胞凋亡。STAT3-IN-12 能够用于癌症的相关研究（如肝细胞癌 (HCC) 、食管癌）。
T68471	(+/-)- Adomeglivant
	(+/-)- Adomeglivant, also known as LY2409021, is a potent and selective glucagon receptor antagonist. LY2409021 lowers blood glucose in healthy people and in those with type 2 diabetes. Blockade of glucagon signalling in patients with type 2 diabetes is well tolerated and results in substantial reduction of fasting and postprandial glucose with minimal hypoglycaemia, but with reversible increases in aminotransferases. Inhibition of glucagon signalling by LY2409021 is a promising potential treatm...
T29161	STOCK2S-26016 WNK IN B,WNK-IN-B,Compound B
	WNK-IN-B is an inhibitor of Wnk signalling. WNK-IN-B is a cell-permeable diaminoacridine derivative that targets the CCT domain of SPAK and OSR1 via reversible binding. WNK-IN-B selectively suppress hypotonic shock-induced WNK signaling pathway activation
T62078	Akt/NF-κB/JNK-IN-1
	Akt/NF-κB/JNK-IN-1 (Compound 2i) 是一种 Akt、NF-κB 和 JNK 信号通路抑制剂。Akt/NF-κB/JNK-IN-1 对一氧化氮的产生表现出抑制作用 (IC50: 3.15 μM)，表现出抗炎效果。
T34811	Terrein NSC 291308,土曲霉酮,Terrain,(+)Terrein,NSC291308,NSC-291308
	Terrain, also known as NSC 291308, is a fungal metabolite with diverse biological activities. Terrein reduces age-related inflammation induced by oxidative stress through Nrf2/ERK1/2/HO-1 signalling in aged HDF cells. (+)-terrein suppresses interleukin-6/
T70403	VUF14480
	VUF14480 is a covalent partial agonist that interacts with cysteine 98(3.36) of the human histamine H₄ receptor. VUF14480 was shown to be a partial agonist of hH4 receptor-mediated G protein signalling and β-arrestin2 recruitment. VUF14480 bound covalently to the hH₄ receptor with submicromolar affinity. Serine substitution of C98(3.36) prevented this covalent interaction.
T70421	VCP746
	VCP-746 is a potent adenosine A2B receptor agonist that stimulates anti-fibrotic signalling. VCP746 reduces hypertrophy in a rat neonatal cardiac myocyte model. VCP746 is a hybrid molecule consisting of an adenosine moiety linked to an adenosine A1 receptor (A1AR) allosteric modulator moiety. At the A1AR, VCP746 mediated cardioprotection in the absence of haemodynamic side effects such as bradycardia.
T21964	KP372-1
	KP372-1是一种 Akt 的抑制剂，通过阻断 PI3K 通路信号，抑制细胞增殖，同时诱导癌细胞凋亡，可用于头颈部鳞状细胞癌的研究。
T64059	G12Si-5
	G12Si-5 是一种共价的 K-RasG12S 突变体抑制剂，其 Ki 值为 26 μM。G12Si-5 能够结合 S-IIP 结构域，抑制致癌信号。G12Si-5 能够减少 KRAS G12S 突变细胞中的 ERK 磷酸化水平。
T62293	CDK8-IN-11 hydrochloride
	CDK8-IN-11 hydrochloride 是一种选择性、有效的 CDK8 抑制剂 (IC50: 46 nM)。CDK8-IN-11 hydrochloride 对 WNT/β-catenin 信号通路具有抑制作用。CDK8-IN-11 hydrochloride 能够用于研究结肠癌。
T71176	Atiprimod (free base)
	Atiprimod is an orally bioavailable small molecule belonging to the azaspirane class of cationic amphiphilic agents with anti-inflammatory, antineoplastic, and antiangiogenic properties. Atiprimod inhibits the phosphorylation of signal transducer and activator of transcription 3 (STAT3), blocking the signalling pathways of interleukin-6 and vascular endothelial growth factor (VEGF) and downregulating the anti-apoptotic proteins Bcl-2, Bcl-XL, and Mcl-1, thereby inhibiting cell proliferation, ind...
T38070	Arachidonic Acid-biotin
	Virtually all cellular arachidonic acid is esterified in membrane phospholipids where its presence is tightly regulated through multiple interconnected pathways. Free arachidonic acid is a transient, critical substrate for the biosynthesis of eicosanoid second messengers. Receptor-stimulated release, metabolism, and re-uptake of free arachidonate are all important aspects of cell signalling and inflammation. Arachidonic acid-biotin was designed to allow arachidonic acid to be detected in complex...
T63914	Estrogen receptor antagonist 3
	Estrogen receptor antagonist 3 是雌激素受体 (ER) 的有效降解剂。雌激素信号系统在调节细胞生长、分化和凋亡 (apoptosis) 中发挥着重要作用。Estrogen receptor antagonist 4 对癌症疾病表现出研究潜力。
T62132	S-777469
	S-777469 是一种选择性的、口服具有活力的大麻素 2 型受体(CB2)激动剂 (Ki: 36 nM)。S-777469 能够剂量依赖性地明显抑制化合物 48/80 诱导的小鼠抓挠行为。S-777469 兴奋 CB2，抑制瘙痒信号的传递，显示出止痒效果。
T63038	WAY-181187 oxalate
	WAY-181187 (SAX-187) oxalate 是一种选择性的、有效的 5-HT6 受体的激动剂 (Ki: 2.2 nM; EC50: 6.6 nM)。WAY-181187 oxalate 是一种特异性激动剂，介导 5-HT6 受体依赖性信号通路（如 cAMP，Fyn 和 ERK1/2 激酶）。

化合物

Cat.No: T7953

Synonym: bpV (HOpic)

Target: PTEN

Cat.No: T14327

Target: Phosphatase

NFAT Inhibitor-2

Cat.No: T50103

Target: Others

Cat.No: T23516

Target: Potassium Channel

Cat.No: T2261

Synonym: IM 12

Target: GSK-3

Mardepodect hydrochloride

Cat.No: T62356

Synonym: PF-2545920 HCl,Mardepodect HCl,MP-10 HCl,PF-02545920 HCl

Target: Apoptosis, PDE

Cat.No: T14886

Target: mTOR

Cat.No: T9015

Target: Gamma-secretase

Cat.No: T21890

Target: Gamma-secretase

Cat.No: T7201

Synonym: N-[4,6-二氨基-2-[1-[(2-氟苯基)甲基]-1H-吡唑并[3,4-B]吡啶-3-基]-5-嘧啶]-氨基甲酸甲酯,BAY60-4552

Target: Guanylate cyclase

Cat.No: T28497

Synonym: RA 839,RA839

Target: Nrf2

Cat.No: T63643

Target: HER

Cat.No: T23910

Synonym: NSC 658586,NSC-658586,NSC 640067

Target: HIV Protease

Cat.No: T76795

Synonym: BI 836845

Target: Akt, IGF-1R

Cat.No: T76910

Synonym: RG 6149,MSTT 1041A

Target: Interleukin

Cat.No: T7511

Target: NF-κB, Endogenous Metabolite

7-FluorotryptaMine HCl

Cat.No: T77673

Target: GPR, Arrestin

APS-2-79 hydrochloride

Cat.No: T6760

Synonym: APS-2-79 HCl,APS-2-79

Target: MEK, MAPK

Cat.No: T72057

Target: CDK

Cat.No: T23097

Synonym: O1602,O 1602

Target: Cannabinoid Receptor, Calcium Channel

Cat.No: T60657

Target: TNF, MAPK

Cat.No: T15300

Synonym: AKF-PD

Target: Others

Cat.No: T8656

Synonym: 3-(4-METHYLSULPHONYLPHENYL)-4-PHENYL-5-T

Target: Apoptosis, Akt, COX

Ethacrynic acid

Cat.No: T4564

Synonym: Edecrin,利尿酸,Etacrynic Acid,Hydromedin

Target: Others, Calcium Channel, NF-κB, GST

Cat.No: T12797

Synonym: RUSKI 43

Target: Hedgehog/Smoothened, Acyltransferase

Cat.No: TP1263

Synonym: (Ac)-LPSDDLEFWCHVMY-NH2

Target: Wnt/beta-catenin

Cat.No: T3997

Synonym: WEHI345

Target: RIP kinase

Cat.No: T29024

Synonym: TX 21211,TX 2-121-1

Wnt/β-catenin agonist 1

Cat.No: T13344

Target: Others

Cat.No: T68954

Cat.No: T71807

Cat.No: T70647

Cat.No: T28113

Synonym: MS 1020

Cat.No: T62322

DL-threo dihydrosphingosine

Cat.No: T27189

Synonym: DL-Safingol,DTD,DL threo dihydrosphingosine

Cat.No: T62803

(+/-)- Adomeglivant

Cat.No: T68471

Cat.No: T29161

Synonym: WNK IN B,WNK-IN-B,Compound B

Akt/NF-κB/JNK-IN-1

Cat.No: T62078

Cat.No: T34811

Synonym: NSC 291308,土曲霉酮,Terrain,(+)Terrein,NSC291308,NSC-291308

Cat.No: T70403

Cat.No: T70421

Cat.No: T21964

Cat.No: T64059

CDK8-IN-11 hydrochloride

Cat.No: T62293

Atiprimod (free base)

Cat.No: T71176

Arachidonic Acid-biotin

Cat.No: T38070

Estrogen receptor antagonist 3

Cat.No: T63914

Cat.No: T62132

WAY-181187 oxalate

Cat.No: T63038

Cat. No.	Product Name	Target	Signaling Pathways
T6S0923	Hypericin Hypericine,金丝桃素,Cyclosan	Apoptosis; Antiviral; Influenza Virus; Tyrosine Kinases; Antibacterial; PKC	Apoptosis; Chromatin/Epigenetic; Cytoskeletal Signaling; Immunology/Inflammation; Microbiology/Virology; Tyrosine Kinase/Adaptors
	Hypericin (Cyclosan) 是贯叶连翘的提取物，有抗菌、抗病毒、抗肿瘤和抗抑郁作用。
T8200	Ginkgolide K 银杏内酯 K,银杏内酯K	AMPK; Autophagy	Autophagy; Chromatin/Epigenetic; PI3K/Akt/mTOR signaling
	Ginkgolide K 是从银杏中分离得到的一种二萜类天然产物，有神经保护活性，可通过 AMPK/mTOR/ULK1信号通路诱导保护性自噬。
T5S0168	Atractylenolide II 2-Atractylenolide,Asterolide,苍术内酯II	Apoptosis; ERK; p38 MAPK; Akt; STAT	Apoptosis; Cytoskeletal Signaling; JAK/STAT signaling; MAPK; PI3K/Akt/mTOR signaling; Stem Cells
	Atractylenolide II (2-Atractylenolide) 是一种从白术干燥根茎分离的倍半萜类天然产物，具有抗增殖活性。
T4S1540	Myrislignan	Apoptosis; NF-κB	Apoptosis; NF-κB
	Myrislignan 是一种木酚素，从Myristica fragransHoutt 分离得到，具有抗炎作用。它通过抑制NF-kB 信号通路的激活，减轻LPS 诱导的小鼠巨噬细胞炎症反应。
TN2085	Piperlonguminine	Anti-infection; Antibacterial; Antifungal	Microbiology/Virology
	Piperlonguminine 是一种从 Piper 中分离出的生物碱酰胺。它具有多种生物活性，如神经保护、抗炎、抗肿瘤、抗血小板、抗黑素生成、抗真菌和抗菌活性。
T19529	Proteinase	Others	Others
	Proteinase 是一种催化蛋白质分解的酶。它们通过水解作用来裂解蛋白质内的肽键，将蛋白质分解成更小的多肽或单个氨基酸。Proteinase 参与许多生物功能，包括消化进食的蛋白质、旧蛋白质的分解，以及细胞信号传递。它们同时促进新的蛋白质产物的形成
TN2080	Pinoresinol 松脂酚，松脂素,(+)-Pinoresinol	Apoptosis; NF-κB; CDK; p53	Apoptosis; Cell Cycle/Checkpoint; NF-κB
	Pinoresinol ((+)-Pinoresinol) 是一种植物来源的木质素，具有抗炎、保肝和杀真菌活性。它导致 CDK 抑制剂 p21(WAF1/Cip1) 在 mRNA 和蛋白质水平上调，抑制 NF-kappaB 和激活蛋白 1 。
T5S0754	Isoquercetin 3-Glucosylquercetin,Hirsutrin,Isoquercitrin,异槲皮苷,Quercetin 3-o-glucopyranoside,槲皮素-3-葡萄糖苷	NF-κB; Wnt/beta-catenin; NO Synthase	Cytoskeletal Signaling; Immunology/Inflammation; NF-κB; Stem Cells
	Isoquercetin (3-Glucosylquercetin) 是天然存在的多酚，具有抗氧化，抗增殖和抗炎特性。它通过调节核因子-κB 转录调节系统调节一氧化氮合酶 2 的表达。它通过 Nrf2/ARE 抗氧化剂信号传导途径减轻乙醇诱导的肝毒性，氧化应激和炎症反应。它具有高生物利用度和低毒性，是预防糖尿病妊娠出生缺陷的有希望的候选药物。
T5S0055	Chelidonine Helidonine,Khelidonin,白屈菜碱,Stylophorin	Apoptosis; Others; Influenza Virus	Apoptosis; Microbiology/Virology; Others
	Chelidonine (Stylophorin) 是白屈菜中的一种异喹啉生物碱，有抗肿瘤和抗病毒作用。它可导致细胞周期 G2/M 停滞，诱导 caspase 依赖和非依赖性的细胞凋亡。
T5S1632	Barlerin 8-O-乙酰山栀苷甲酯,8-O-Acetylshanzhiside methyl ester,ND01	VEGFR; TNF; NF-κB; Akt; Caspase	Angiogenesis; Apoptosis; Cytoskeletal Signaling; NF-κB; PI3K/Akt/mTOR signaling; Proteases/Proteasome; Tyrosine Kinase/Adaptors
	Barlerin (8-O-Acetylshanzhiside methyl ester) 是一种环孢菌素葡萄糖苷，从中国西藏民间药用植物中分离得到，能够抑制NF-κB 活性。
T38373	2-heptyl-3-hydroxy-4(1H)-Quinolone 2-heptyl-3-hydroxy-4(1H)-Quinolone,PQS,Pseudomonas Quinolone Signal	Others	Others
	2-heptyl-3-hydroxy-4(1H)-Quinolone (Pseudomonas Quinolone Signal) 是一种铜绿假单胞菌为应对细胞密度增加而产生的一种法定人数感应信号分子。它增加了铜绿假单胞菌中lasB 基因的表达，增加代谢物焦蓝蛋白和凝集素PA-IL 的分泌，以及增加铜绿假单胞菌种群的生物膜生产。当使用浓度为40 μM 时，它还会降低铜绿假单胞菌生长介质中的铁含量，并在硫酸铁溶液中充当一种铁螯合剂。
TN5013	Shizukaol D	AMPK	Chromatin/Epigenetic; PI3K/Akt/mTOR signaling
	Shizukaol D exerts a growth inhibition effect on liver cancer cells in a dose- and time-dependent manner by modulating wnt signalling pathway. Shizukaol D may be used to treat metabolic syndrome, it induces mitochondrial dysfunction by depolarizing the mitochondrial membrane and suppressing energy production, which may result in AMPK activation.
TN4604	Myricanone	BCL; HSP; NF-κB; ROS; Caspase; STAT	Apoptosis; Cytoskeletal Signaling; Immunology/Inflammation; JAK/STAT signaling; Metabolism; NF-κB; Proteases/Proteasome; Stem Cells
	Myricanone has antioxidant, and anticancer activities, it has apoptosis-promoting ability by triggering caspase activation, and suppression of cell proliferation by down-regulation of NF-ÎºB and STAT3 signalling cascades. Myricanone shows in vitro testost
T19882	Bryonolic acid UNII-J7YR6A878I,20-epi-Bryonolic acid	Apoptosis; Antioxidant; Calcium Channel	Apoptosis; Membrane transporter/Ion channel; Metabolism; oxidation-reduction
	Bryonolic acid (20-epi-Bryonolic acid) 是一种从 Sandoricum indicum 提取的三萜类化合物，具有免疫调节、抗炎，抗氧化和抗癌等活性，通过抑制Ca2+内流和调节Ca2+-CaMKII-CREB信号通路中的基因表达来避免PC12细胞免受NMDA诱导的细胞凋亡反应。
TMA0291	Dehydroglyasperin D	GSK-3; p38 MAPK; ROS; Akt; COX; PI3K; DNA/RNA Synthesis; Prostaglandin Receptor; JNK	Cell Cycle/Checkpoint; Cytoskeletal Signaling; DNA Damage/DNA Repair; GPCR/G Protein; Immunology/Inflammation; MAPK; Neuroscience; PI3K/Akt/mTOR signaling; Stem Cells
	Dehydroglyasperin D exhibits anticancer, anti-inflammatory, anti-obesity, antioxidant and anti-aldose reductase effects, it inhibits the proliferation of HT-29 human colorectal cancer cells through direct interaction with phosphatidylinositol 3-kinase; it also mediates suppression of both COX-2 expression and the MLK3 signalling pathway through direct binding and inhibition of MLK3. Dehydroglyasperin D shows strong ferric reducing activities and effectively scavenged DPPH, ABTS(+), and singlet o...
TN2328	Zeylenone	Apoptosis; ERK; MAPK; Akt; PI3K; mTOR	Apoptosis; Cytoskeletal Signaling; MAPK; PI3K/Akt/mTOR signaling
	Zeylenone 是一种来自 Uvaria grandiflora的环己烯氧化物，具有抗肿瘤和抗癌细胞增殖活性，通过 PI3K/AKT/mTOR 和 MAPK/ERK 信号通路抑制宫颈癌细胞增殖，诱导细胞凋亡 (apoptosis)。
T20232	Kazinol B	Akt; NO Synthase; AMPK	Chromatin/Epigenetic; Cytoskeletal Signaling; Immunology/Inflammation; PI3K/Akt/mTOR signaling
	Kazinol B 是一氧化氮（NO）产生的抑制剂，是一种具有二甲基吡喃环的异戊烯化黄烷。Kazinol B 通过激活胰岛素-Akt 信号途径和AMPK，增强葡萄糖摄取，从而改善胰岛素敏感性。Kazinol B 刺激脂肪素的基因表达和分泌，可用于研究糖尿病。
T11201	Enniatin A1 恩镰孢菌素 A1	ERK	MAPK
	Enniatin A1 possesses anticarcinogenic properties by induction of apoptosis and disruption of ERK signalling pathway. Enniatin A1 inhibits ACAT with an IC50 of 49 μM in rat liver microsomes. Enniatin A1 isolated from Fusarium mycotoxins is a cyclic hexadepsipeptide consisting of alternating D-α-hydroxyisovaleric acids and N-methyl-L-amino acids.

天然产物

Cat.No: T6S0923

Synonym: Hypericine,金丝桃素,Cyclosan

Target: Apoptosis, Antiviral, Influenza Virus, Tyrosine Kinases, Antibacterial, PKC

Cat.No: T8200

Synonym: 银杏内酯 K,银杏内酯K

Target: AMPK, Autophagy

Atractylenolide II

Cat.No: T5S0168

Synonym: 2-Atractylenolide,Asterolide,苍术内酯II

Target: Apoptosis, ERK, p38 MAPK, Akt, STAT

Cat.No: T4S1540

Target: Apoptosis, NF-κB

Piperlonguminine

Cat.No: TN2085

Target: Anti-infection, Antibacterial, Antifungal

Cat.No: T19529

Target: Others

Cat.No: TN2080

Synonym: 松脂酚，松脂素,(+)-Pinoresinol

Target: Apoptosis, NF-κB, CDK, p53

Cat.No: T5S0754

Synonym: 3-Glucosylquercetin,Hirsutrin,Isoquercitrin,异槲皮苷,Quercetin 3-o-glucopyranoside,槲皮素-3-葡萄糖苷

Target: NF-κB, Wnt/beta-catenin, NO Synthase

Cat.No: T5S0055

Synonym: Helidonine,Khelidonin,白屈菜碱,Stylophorin

Target: Apoptosis, Others, Influenza Virus

Cat.No: T5S1632

Synonym: 8-O-乙酰山栀苷甲酯,8-O-Acetylshanzhiside methyl ester,ND01

Target: VEGFR, TNF, NF-κB, Akt, Caspase

2-heptyl-3-hydroxy-4(1H)-Quinolone

Cat.No: T38373

Synonym: 2-heptyl-3-hydroxy-4(1H)-Quinolone,PQS,Pseudomonas Quinolone Signal

Target: Others

Cat.No: TN5013

Target: AMPK

Cat.No: TN4604

Target: BCL, HSP, NF-κB, ROS, Caspase, STAT

Cat.No: T19882

Synonym: UNII-J7YR6A878I,20-epi-Bryonolic acid

Target: Apoptosis, Antioxidant, Calcium Channel

Dehydroglyasperin D

Cat.No: TMA0291

Target: GSK-3, p38 MAPK, ROS, Akt, COX, PI3K, DNA/RNA Synthesis, Prostaglandin Receptor, JNK

Cat.No: TN2328

Target: Apoptosis, ERK, MAPK, Akt, PI3K, mTOR

Cat.No: T20232

Target: Akt, NO Synthase, AMPK

Cat.No: T11201

Synonym: 恩镰孢菌素 A1

Target: ERK

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