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Search Results for " pi3k-akt "

Targets Recommended: Others

93

抑制剂 & 化合物

72

天然产物

4

化合物库

10

重组蛋白

1

同位素标记化合物

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Cat. No.	Product Name
L1300	PI3K/Akt/mTOR 化合物库		420 compounds
	420 种与PI3K/Akt/mTOR 相关的生物活性小分子化合物的特有集合，用于PI3K/Akt/mTOR 相关研究以及高通量、高内涵筛选；
L2193	抗肝癌化合物库		1787 compounds
	1787 种与肝癌相关的化合物，可以用于抗肝癌药物研发和药理研究；
L2195	抗前列腺癌化合物库		2070 compounds
	2070 种与前列腺癌相关的化合物，可以用于高通量和高内涵筛选
L8500	HIF-1化合物库		1336 compounds
	1336 个HIF-1相关小分子的独特集合，可用于缺血性疾病、癌症等相关领域的药物开发和药理研究；

化合物库

PI3K/Akt/mTOR 化合物库

Cat.No: L1300

Compounds: 420

抗肝癌化合物库

Cat.No: L2193

Compounds: 1787

抗前列腺癌化合物库

Cat.No: L2195

Compounds: 2070

HIF-1化合物库

Cat.No: L8500

Compounds: 1336

Cat. No.	Product Name	Target	Signaling Pathways
T71272	PI3K/Akt-IN-C89	Others	Others
	PI3K/Akt-IN-C89 is a novel Inhibitor of the PI3K-Akt Pathway, Inducing Autophagy of Female Germline Stem Cells.
T9393	(E)-Akt inhibitor-IV (E)-AKTIV,CS-1992	Akt	Cytoskeletal Signaling; PI3K/Akt/mTOR signaling
	(E)-Akt inhibitor-IV ((E)-AKTIV) 是PI3K-Akt 抑制剂，表现出明显的细胞毒性。
T60564	PI3K/Akt/mTOR-IN-2	Apoptosis; Akt; PI3K; mTOR	Apoptosis; Cytoskeletal Signaling; PI3K/Akt/mTOR signaling
	PI3K/Akt/mTOR-IN-2 是一种有效的 PI3K/AKT/mTOR 抑制剂。PI3K/Akt/mTOR-IN-2 具有抗癌作用，并对 MDA-MB-231 细胞具有选择性，IC50 为 2.29 μM。PI3K/Akt/mTOR-IN-2 具有抗癌活性，可诱导癌细胞周期阻滞和细胞凋亡 (apoptosis)。
T2423	P7C3-A20	Others	Others
	P7C3-A20 是促神经原性和神经保护活性的 P7C3 衍生物。它具有抗抑郁活性，能够透过血脑屏障，并可用于研究脑损伤。
T13862	Recilisib RECILISIB 钠盐,Ex-RAD,ON 01210	Akt; PI3K	Cytoskeletal Signaling; PI3K/Akt/mTOR signaling
	Recilisib (ON 01210) 是辐射防护剂，能够提高细胞中AKT 和PI3K 的活性。
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。
TP1197	Sincalide SQ19844,辛卡利特,CCK-8,Cholecystokinin octapeptide	Others	Others
	Sincalide (CCK-8) 是一种速效的胆囊收缩素的氨基酸多肽激素类似物，可在胆囊造影术中静脉使用。它的肝胆生理作用是增加胆汁的分泌，使胆囊收缩并使 Oddi 的括约肌松弛，从而使胆汁排入十二指肠。它是一种通过注射促进胆囊收缩并帮助诊断胆囊和胰腺疾病的药物。
T7879	TASP0415914	Akt; PI3K	Cytoskeletal Signaling; PI3K/Akt/mTOR signaling
	TASP0415914 是一种具有口服活性的 PI3Kγ抑制剂，其 IC50=29 nM。它是一种 Akt 抑制剂，其 IC50=294 nM。它可用于研究炎症性疾病。
T1921	Alpelisib BYL-719	PI3K	PI3K/Akt/mTOR signaling
	Alpelisib (BYL-719) 是一种 PI3Kα 抑制剂 (IC50=5 nM)，具有选择性、有效性和口服活性。Alpelisib 以较低活性抑制 PI3Kβ/γ/δ (IC50=250/290/1200 nM)。Alpelisib 具有抗肿瘤活性，对 PIK3CA 突变肿瘤具有靶向性。
T13376	YS-49	RAAS; Akt; PI3K; Adrenergic Receptor	Cytoskeletal Signaling; Endocrinology/Hormones; GPCR/G Protein; Neuroscience; PI3K/Akt/mTOR signaling
	YS-49 是一种PI3K/Akt(RhoA 的下游靶标) 的激活剂，可减少 3-甲基胆碱处理的细胞中 RhoA/PTEN 的激活。它是异喹啉化合物生物碱，因能激活心脏β-adrenoceptors 而具有强烈的正性肌力作用。它能通过诱导血红素加氧酶来抑制血管紧张素 II 刺激 VSMC 细胞的增殖。
T6322	Copanlisib BAY 80-6946,可泮利塞,库潘尼西	Apoptosis; PI3K	Apoptosis; PI3K/Akt/mTOR signaling
	Copanlisib (BAY 80-6946) 是一种选择性的和 ATP 竞争性的泛 I 类PI3K 抑制剂，具有抗肿瘤活性，对PI3Kα，PI3Kδ，PI3Kβ和PI3Kγ的IC50分别为 0.5 nM、0.7 nM、3.7 nM 和 6.4 nM。
T0365	Thioridazine hydrochloride 盐酸硫利达嗪,Mellaril,Aldazine	Apoptosis; Potassium Channel; Dopamine Receptor; 5-HT Receptor; Antibacterial; Adrenergic Receptor; Autophagy	Apoptosis; Autophagy; GPCR/G Protein; Membrane transporter/Ion channel; Microbiology/Virology; Neuroscience
	Thioridazine hydrochloride (Mellaril) 是一种多巴胺受体D2家族蛋白的拮抗剂，有抗精神病和抗焦虑活性。它也是一种PI3K-Akt-mTOR 信号通路的抑制剂，具有抗血管生成作用。它在多种类型的癌细胞中显示出抗增殖和凋亡诱导作用，对靶向癌症干细胞具有特异性。
T14998	Copanlisib dihydrochloride 库潘尼西盐酸,BAY 80-6946 dihydrochloride	Apoptosis; PI3K; mTOR	Apoptosis; PI3K/Akt/mTOR signaling
	Copanlisib dihydrochloride (BAY 80-6946 dihydrochloride) 是一种选择性和 ATP 竞争性的泛 I 类 PI3K 抑制剂。它具有优越的抗肿瘤活性，对除 mTOR 以外的其他脂质和蛋白激酶的选择性也超过 2,000 倍。
T62997	PI3K/AKT-IN-1	Others	Others
	PI3K/AKT-IN-1 是一种有效的、双重的 PI3K/AKT 抑制剂，能够作用于 PI3Kγ (IC50: 6.99 μM)、PI3Kδ (IC50: 4.01 μM) 和 AKT (IC50: 3.36 μM)。PI3K/AKT-IN-1 通过抑制 PI3K/AKT 通路，诱导 caspase 3 依赖性凋亡，表现出抗癌作用。
T72880	PI3K/AKT-IN-2	Others	Others
	PI3K/AKT-IN-2 是一种 PI3K 和 AKT 抑制剂。PI3K/AKT-IN-2 阻断上皮-间质转化 (EMT)，诱导细胞凋亡 (apoptosis)。PI3K/AKT-IN-2 抑制微管蛋白 (tubulin) 的聚合。
T1967	AZD-3463 ALK/IGF1R inhibitor	Apoptosis; IGF-1R; ALK; Autophagy	Angiogenesis; Apoptosis; Autophagy; Tyrosine Kinase/Adaptors
	AZD-3463 (ALK/IGF1R inhibitor) 是一种具有口服活性的ALK/IGF1R 抑制剂，对 ALK 作用的Ki 值为 0.75 nM。它可诱导神经母细胞瘤细胞凋亡和自噬。
T63455	PI3K/Akt/mTOR-IN-3	Others	Others
	PI3K/Akt/mTOR-IN-3 是 PI3K/Akt/mTOR 的有效抑制剂。PI3K/Akt/mTOR-IN-3 能够抑制 MCF-7 细胞 (IC50: 0.77 μM)、HeLa 细胞 (IC50: 1.23 μM) 和 HepG2 细胞(IC50: 4.57 μM)。PI3K/Akt/mTOR-IN-3 在 4 μM 浓度下可抑制 MCF-7 和 HeLa 细胞的迁移。PI3K/Akt/mTOR-IN-3 能够将细胞周期阻滞在 S 期，并诱导细胞凋亡 (apoptosis)。
T72227	PI3K/Akt/CREB activator 1	Others	Others
	PI3K/Akt/CREB activator 1 是一种口服有效的PI3K/Akt/CREB 的激活剂。PI3K/Akt/CREB activator 1 通过 PI3K/Akt/CREB 通路上调脑源性神经营养因子，促进神经元增殖，诱导 Neuro-2a 细胞分化成神经元样形态，加速海马原代神经元轴突-树突极化的建立。PI3K/Akt/CREB activator 1 可用于血管性痴呆 (VaD) 的研究。
T1101	Minocycline hydrochloride Minocycline HCl,盐酸米诺环素,美满霉素	HIF/HIF Prolyl-Hydroxylase; Antibacterial; Antibiotic	Chromatin/Epigenetic; Metabolism; Microbiology/Virology
	Minocycline hydrochloride (Minocycline HCl) 属于四环素类抗生素，具有出色的吸收和组织渗透性。Minocycline hydrochloride 是一种广谱的抗菌剂，可用于多种细菌感染以及痤疮的治疗。
T24573	Ovatodiolide	Others	Others
	Ovatodiolide is a broad anticancer agent that acts by upregulating hsa-miR-155, suppressing the BCR-ABL fusion gene, and dysregulating the PI3K/AKT/mTOR pathway.
T3705	GDC0084 GDC-0084,RG7666,GDC 0084	PI3K; mTOR	PI3K/Akt/mTOR signaling
	GDC0084 (RG7666) 是一种具有潜在抗肿瘤活性的 PI3K 抑制剂。 GDC0084 (RG7666) 特异性抑制 PI3K/AKT 激酶（或蛋白激酶 B）信号通路中的 PI3K，从而抑制 PI3K 信号通路的激活。这可能导致易感肿瘤细胞群中的细胞生长和存活受到抑制。
T1826	PI3K-IN-1 Voxtalisib Analogue,Voxtalisib (SAR245409, XL765) Analogue,XL765,SAR245409	DNA-PK; PI3K	DNA Damage/DNA Repair; PI3K/Akt/mTOR signaling
	PI3K-IN-1 (Voxtalisib Analogue) 是 PI3K 抑制剂，PI3K-IN-1(25 μM) 能够阻断 PI3K/Akt 信号通路。
T7832	Ibrolipim NO-1886	LPL Receptor	GPCR/G Protein
	Ibrolipim (NO-1886) 是口服具有活力的脂蛋白脂肪酶 (LPL) 激活剂。它能够降低血浆甘油三酸酯，增加高密度脂蛋白胆固醇水平，具有肾保护和降血脂的作用。
T37379	Protectin D1 Neuroprotectin D1,NPD1	Akt; PI3K	Cytoskeletal Signaling; PI3K/Akt/mTOR signaling
	Protectin D1 (Neuroprotectin D1) 是神经细胞产生的神经保护素，是一种潜在的心脏保护剂。Protectin D1 通过调节 PI3K/AKT 信号通路缓解心肌缺血/再灌注损伤，抑制咪喹莫特诱导的银屑病样皮肤炎症。
T2078	Fimepinostat CUDC-907,PI3K/HDAC Inhibitor,CUDC 907	Apoptosis; PI3K; HDAC	Apoptosis; Chromatin/Epigenetic; DNA Damage/DNA Repair; PI3K/Akt/mTOR signaling
	Fimepinostat (CUDC 907) 是一种 I 型PI3K 及 I 和 II 型HDAC 酶抑制剂，作用于 PI3Kα/PI3Kβ/PI3Kδ 和 HDAC1/HDAC2/HDAC3/HDAC10 ，IC50分别为 19/54/39 nM 和 1.7/5.0/1.8/2.8 nM。
T83658	SQLE-IN-1	Antifungal	Microbiology/Virology
	SQLE-IN-1 是一种角鲨烯环氧化酶 (SQLE) 抑制剂，具有抗肿瘤活性，可抑制肝癌细胞系 Huh7 的增殖和迁移能力，抑制细胞胆固醇的生成，增加抑癌基因PTEN的表达，抑制PI3K和AKT的蛋白表达。
T67965	Torbafylline	cAMP; PI3K; PDE	GPCR/G Protein; Metabolism; PI3K/Akt/mTOR signaling
	Torbafylline 是黄嘌呤衍生物，是磷酸二酯酶（PDE）抑制剂，通过激活 PDE4/cAMP/EPAC/PI3K/Akt 途径减弱烧伤诱导的大鼠骨骼肌蛋白水解，抑制癌症和败血症大鼠增强的骨骼肌泛素 - 蛋白酶体依赖性蛋白水解。
T12777	RTC-5 TRC-382	EGFR	Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors
	RTC-5 (TRC-382) 是一种特别增强了抗癌活性的Phenothiazine 化合物，对EGFR驱动的癌症异种移植模型表现出显著的效果。其作用机制归因于同时抑制PI3K-AKT和RAS-ERK信号通路。
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。
T3467	Miransertib ARQ-092,AKT inhibitor 2	Akt; Parasite	Cytoskeletal Signaling; Microbiology/Virology; PI3K/Akt/mTOR signaling
	Miransertib (ARQ-092) 是一种具有口服活性的，选择性和变构性Akt 抑制剂。它有效抑制利什曼原虫，还是 AKT1-E17K 突变蛋白抑制剂，可研究PI3K/AKT 驱动的肿瘤和 Proteus 综合征。
T14214	AMG 511	PI3K	PI3K/Akt/mTOR signaling
	AMG 511 是一种高效的、口服有效的 I 类 pan-PI3K 抑制剂，对 PI3Kα, β, δ 和 γ 作用的 Ki 值分别为 4 nM, 6 nM, 2 nM 和 1 nM。它它显著抑制了 PI3K 信号，减少 p-Akt (Ser473)。它在小鼠胶质母细胞瘤移植瘤模型中具有抗肿瘤作用。
T5485	OSU-T315 OSU-T315 (1,5-regioisomer),ILK-IN-2	Apoptosis; Integrin; Autophagy	Apoptosis; Autophagy; Cytoskeletal Signaling
	OSU-T315 (OSU-T315 (1,5-regioisomer)) 是一种整联蛋白连接激酶抑制剂，通过去磷酸化 AKT-Ser473 和其他 ILK 靶标抑制 PI3K/AKT 信号传导。它阻止 AKT 转位到脂筏消除 AKT 的活化，并以 ILK 非依赖性方式触发 Caspase 依赖性细胞凋亡。它通过自噬和凋亡导致细胞死亡。
T6070	(E/Z)-Rigosertib sodium N-[2-甲氧基-5-[[[2-(2,4,6-三甲氧基苯基)乙烯基]磺酰]甲基]苯基]甘氨酸钠盐,(E/Z) ON-01910 sodium	PLK	Cell Cycle/Checkpoint
	ON-01910 是一种非 ATP 竞争性 PLK1 抑制剂（IC50 为 9 nM，在无细胞试验中）。它对 Plk2 的选择性高出 30 倍，对 Plk3 没有活性。 Rigosertib 抑制 PI3K/Akt 通路并激活氧化应激信号。 Rigosertib 可诱导多种癌细胞凋亡。它是一种合成的苄基苯乙烯基砜类似物，具有潜在的抗肿瘤活性。
T5092	AIM-100 AIM100	ACK	Tyrosine Kinase/Adaptors
	AIM-100 是选择性的 Ack1 抑制剂 (IC50:21.58 nM)。它还抑制 Tyr267磷酸化，但不抑制其他激酶，包括 PI3K 和 AKT 亚家族成员。它具有抗癌活性。
T6334	Ridaforolimus AP23573,Deforolimus,MK-8669	mTOR; Autophagy	Autophagy; PI3K/Akt/mTOR signaling
	Ridaforolimus (AP23573) 是亲脂性大环内酯类抗生素雷帕霉素的小分子非前药类似物，具有潜在的抗肿瘤活性。它是一种有效和选择性的 mTOR 抑制剂，在 HT-1080 细胞中抑制 S6 磷酸化的 IC50值为 0.2 nM。
T16750	Rigosertib ON-01910,瑞格色替	Apoptosis; FLT; PLK; PI3K; Bcr-Abl; CDK; PDGFR; Src	Angiogenesis; Apoptosis; Cell Cycle/Checkpoint; Cytoskeletal Signaling; PI3K/Akt/mTOR signaling; Tyrosine Kinase/Adaptors
	Rigosertib (ON-01910) 是一种多激酶抑制剂和选择性抗癌剂，通过抑制 PI3K/Akt 途径诱导细胞凋亡，促进组蛋白 H2AX 的磷酸化并诱导细胞周期中的 G2/M 期停滞。它是一种选择性的非 ATP 竞争性PLK1抑制剂，IC50值为 9 nM。
T16923	SPP-86	c-RET	Apoptosis; Tyrosine Kinase/Adaptors
	SPP-86 是有效的、选择性的RET 酪氨酸激酶抑制剂，其IC50=8 nM。它能够抑制 MCF7 细胞中 RET 诱导激活的 PI3K/Akt 和 MAPK 信号通路，也能抑制 RET 诱导的 ERα 磷酸化。
T4325	COTI-2 COTI 2,COTI2	Apoptosis; p53	Apoptosis
	COTI-2是一种具有口服活性的低毒性抗癌药物，是 p53 突变体激活剂。它通过激活突变型 p53 和抑制PI3K/AKT/mTOR 途径发挥作用，通过 p53 依赖和非依赖机制在 HNSCC 中具有抗肿瘤活性。它诱导多种人肿瘤细胞凋亡，可将突变型 p53 转化为野生型构象。
T5818	Rigosertib sodium Rigosertib,Estybon,ON-01910	Apoptosis; PLK; PI3K	Apoptosis; Cell Cycle/Checkpoint; PI3K/Akt/mTOR signaling
	Rigosertib sodium (ON-01910) 是一种选择性的非 ATP 竞争性PLK1抑制剂，IC50值为 9 nM。它是一种多激酶抑制剂和选择性抗癌剂，通过抑制PI3K/Akt 途径诱导细胞凋亡，促进组蛋白 H2AX 的磷酸化并诱导细胞周期中的 G2/M 期停滞。
T71188	LY2780301	Others	Others
	LY2780301 is an orally bioavailable inhibitor of the serine/threonine protein kinase Akt (protein kinase B) with potential antineoplastic activity. Akt inhibitor LY2780301 binds to and inhibits the activity of Akt, which may result in inhibition of the PI3K/Akt signaling pathway, thereby leading to inhibition of cell proliferation and the induction of apoptosis in tumor cells. Activation of the PI3K/Akt signaling pathway is frequently associated with tumorigenesis and dysregulated PI3K/Akt signa...
T63957	PI3K-IN-29	Others	Others
	PI3K-IN-29 是一种有效的 PI3K 抑制剂。PI3K-IN-29 对 U87MG、HeLa 和 HL60 细胞具有较好的抑制作用，IC50值分别为 0.264、2.04 和 1.14 µM。PI3K-IN-29 通过抑制PI3K 催化的Akt 的磷酸化来抑制PI3K/Akt 通路。
T24715	RLX THA-Q,PD-139530,THA Q,PD 139530,PD139530	Others	Others
	RLX is a PI3K/Akt/FoxO3a signaling inhibitor in experimental colon cancer.
T34778	Talaumidin	Others	Others
	Talaumidin is a natural neurotrophic agent which promotes neurite outgrowth from neurons through the PI3K/Akt pathway.
T29165	XC-302 free base XC 302,Puquitinib,XC-302,XC302	Others	Others
	XC-302 is a multi-targeted inhibitor, it induces autophagy of nasopharyngeal cancer cells via inhibiting the PI3K/AKT/mTOR signaling pathway.
T68464	PABA/NO	Others	Others
	PABA/NO is a novel glutathione-S-transferase-p-activated nitric oxide donor, inhibiting proliferation and inducing apoptosis by targeting PI3K/AKT/mTOR and MEK/ERK pathways in hepatocellular carcinoma cells.
T79701	PI3K-IN-48	Akt	Cytoskeletal Signaling; PI3K/Akt/mTOR signaling
	PI3K-IN-48，PI3K抑制剂，对A549细胞系表现出1.55 ± 0.18 μM的IC50值。该化合物能够诱导G0/G1期细胞周期阻滞与细胞凋亡，并可下调p-PI3K与p-Akt的表达水平，适用于人类肺癌研究。
T13376L	YS-49 monohydrate (132836-42-1 free base) YS-49 monohydrate	Others	Others
	YS-49 (monohydrate) is an activator of PI3K/Akt (a downstream target of RhoA).
T70152	Miransertib mesylate	Others	Others
	Miransertib mesylate is a selective AKT inhibitor that binds to and inhibits the activity of AKT in a non-ATP competitive manner, which may result in the inhibition of the PI3K/AKT signaling pathway. This may result in reduction in tumor cell proliferation and the induction of tumor cell apoptosis.
T64041	PI3K/mTOR Inhibitor-7	Others	Others
	PI3K/mTOR Inhibitor-7 是有效的 PI3K/mTOR 双重抑制剂。PI3K/mTOR Inhibitor-7 的作用比 gedatolisib 高 4.7 倍，他们的 IC50 值分别为 1.4 μM 和 0.3 μM。10 μM 的 PI3K/mTOR Inhibitor-7 能够明显抑制 PI3K/Akt/mTOR 信号通路。PI3K/mTOR Inhibitor-7 对癌症疾病表现出研究潜力。
T39929	MS21	PROTACs	PROTAC
	MS21 is a unique AKT degrader that selectively hampers the proliferation of cancers with mutations in the PI3K/PTEN pathway, alongside wild-type KRAS and BRAF.

化合物

PI3K/Akt-IN-C89

Cat.No: T71272

Target: Others

(E)-Akt inhibitor-IV

Cat.No: T9393

Synonym: (E)-AKTIV,CS-1992

Target: Akt

PI3K/Akt/mTOR-IN-2

Cat.No: T60564

Target: Apoptosis, Akt, PI3K, mTOR

Cat.No: T2423

Target: Others

Cat.No: T13862

Synonym: RECILISIB 钠盐,Ex-RAD,ON 01210

Target: Akt, PI3K

Cat.No: T7953

Synonym: bpV (HOpic)

Target: PTEN

Cat.No: TP1197

Synonym: SQ19844,辛卡利特,CCK-8,Cholecystokinin octapeptide

Target: Others

Cat.No: T7879

Target: Akt, PI3K

Cat.No: T1921

Synonym: BYL-719

Target: PI3K

Cat.No: T13376

Target: RAAS, Akt, PI3K, Adrenergic Receptor

Cat.No: T6322

Synonym: BAY 80-6946,可泮利塞,库潘尼西

Target: Apoptosis, PI3K

Thioridazine hydrochloride

Cat.No: T0365

Synonym: 盐酸硫利达嗪,Mellaril,Aldazine

Target: Apoptosis, Potassium Channel, Dopamine Receptor, 5-HT Receptor, Antibacterial, Adrenergic Receptor, Autophagy

Copanlisib dihydrochloride

Cat.No: T14998

Synonym: 库潘尼西盐酸,BAY 80-6946 dihydrochloride

Target: Apoptosis, PI3K, mTOR

PI3K/AKT-IN-1

Cat.No: T62997

Target: Others

PI3K/AKT-IN-2

Cat.No: T72880

Target: Others

Cat.No: T1967

Synonym: ALK/IGF1R inhibitor

Target: Apoptosis, IGF-1R, ALK, Autophagy

PI3K/Akt/mTOR-IN-3

Cat.No: T63455

Target: Others

PI3K/Akt/CREB activator 1

Cat.No: T72227

Target: Others

Minocycline hydrochloride

Cat.No: T1101

Synonym: Minocycline HCl,盐酸米诺环素,美满霉素

Target: HIF/HIF Prolyl-Hydroxylase, Antibacterial, Antibiotic

Cat.No: T24573

Target: Others

Cat.No: T3705

Synonym: GDC-0084,RG7666,GDC 0084

Target: PI3K, mTOR

Cat.No: T1826

Synonym: Voxtalisib Analogue,Voxtalisib (SAR245409, XL765) Analogue,XL765,SAR245409

Target: DNA-PK, PI3K

Cat.No: T7832

Synonym: NO-1886

Target: LPL Receptor

Cat.No: T37379

Synonym: Neuroprotectin D1,NPD1

Target: Akt, PI3K

Cat.No: T2078

Synonym: CUDC-907,PI3K/HDAC Inhibitor,CUDC 907

Target: Apoptosis, PI3K, HDAC

Cat.No: T83658

Target: Antifungal

Cat.No: T67965

Target: cAMP, PI3K, PDE

Cat.No: T12777

Synonym: TRC-382

Target: EGFR

Cat.No: T15300

Synonym: AKF-PD

Target: Others

Cat.No: T3467

Synonym: ARQ-092,AKT inhibitor 2

Target: Akt, Parasite

Cat.No: T14214

Target: PI3K

Cat.No: T5485

Synonym: OSU-T315 (1,5-regioisomer),ILK-IN-2

Target: Apoptosis, Integrin, Autophagy

(E/Z)-Rigosertib sodium

Cat.No: T6070

Synonym: N-[2-甲氧基-5-[[[2-(2,4,6-三甲氧基苯基)乙烯基]磺酰]甲基]苯基]甘氨酸钠盐,(E/Z) ON-01910 sodium

Target: PLK

Cat.No: T5092

Synonym: AIM100

Target: ACK

Cat.No: T6334

Synonym: AP23573,Deforolimus,MK-8669

Target: mTOR, Autophagy

Cat.No: T16750

Synonym: ON-01910,瑞格色替

Target: Apoptosis, FLT, PLK, PI3K, Bcr-Abl, CDK, PDGFR, Src

Cat.No: T16923

Target: c-RET

Cat.No: T4325

Synonym: COTI 2,COTI2

Target: Apoptosis, p53

Rigosertib sodium

Cat.No: T5818

Synonym: Rigosertib,Estybon,ON-01910

Target: Apoptosis, PLK, PI3K

Cat.No: T71188

Target: Others

Cat.No: T63957

Target: Others

Cat.No: T24715

Synonym: THA-Q,PD-139530,THA Q,PD 139530,PD139530

Target: Others

Cat.No: T34778

Target: Others

XC-302 free base

Cat.No: T29165

Synonym: XC 302,Puquitinib,XC-302,XC302

Target: Others

Cat.No: T68464

Target: Others

Cat.No: T79701

Target: Akt

YS-49 monohydrate (132836-42-1 free base)

Cat.No: T13376L

Synonym: YS-49 monohydrate

Target: Others

Miransertib mesylate

Cat.No: T70152

Target: Others

PI3K/mTOR Inhibitor-7

Cat.No: T64041

Target: Others

Cat.No: T39929

Target: PROTACs

Cat. No.	Product Name	Target	Signaling Pathways
T5654	Musk ketone	Others	Others
	Musk ketone 可诱导癌细胞生长抑制和凋亡。它增加谷胱甘肽 S-转移酶的活性，因此可能被证明是有用的癌症化学保护剂。
TN1891	Lupiwighteone	Apoptosis; BCL; PARP; Caspase	Apoptosis; Chromatin/Epigenetic; DNA Damage/DNA Repair; Proteases/Proteasome
	Lupiwighteone 是一种广泛存在于野生植物中的异黄酮。它通过抑制 PI3K/Akt/mTOR 通路，诱导人乳腺癌细胞 caspase 依赖性和非依赖性凋亡，具有抗氧化、抗菌和抗癌作用。
TN1079	Deoxyelephantopin	NF-κB	NF-κB
	Deoxyelephantopin 是来自Elephantopus scaber 的，具有生物活性的天然倍半萜烯内酯，能够抑制NF-κB，MAPK，PI3K/Akt 和β-catenin 信号传导。它可广泛用于癌症方面的研究。
T6677	Sophocarpine	ERK; p38 MAPK; NF-κB; TLR; COX; HER; JNK; STAT	Angiogenesis; Immunology/Inflammation; JAK/STAT signaling; MAPK; Neuroscience; NF-κB; Stem Cells; Tyrosine Kinase/Adaptors
	Sophocarpine 是一种从传统草药苦参中提取的重要生物碱。苦参具有抗病毒、抗肿瘤和抗炎等多种药理作用。它通过多种机制显著抑制癌细胞的生长，具有抗肿瘤活性。
T5S1982	Periplocin Periplocoside,杠柳毒苷	Apoptosis; Others	Apoptosis; Others
	Periplocin (Periplocoside) 是从黑龙骨中分离出的一种强心类固醇。它可促进肿瘤细胞凋亡并抑制肿瘤生长。它通过激活 Na/K-ATPase 介导的 Src/ERK 和 PI3K/Akt 途径，具有促进伤口愈合的潜力。
TN1644	Flavanomarein	Others	Others
	Flavanomarein 是Coreopsis tinctoria Nutt 的主要黄酮类化合物，对糖尿病性肾病具有保护作用。它具有很好的抗氧化，降糖，降压和降血脂作用。
TL0006	Cichoric Acid 菊苣酸,Dicaffeoyltartaric acid,Chicoric Acid	Reactive Oxygen Species; HIV Protease	Immunology/Inflammation; Metabolism; Microbiology/Virology; NF-κB; Proteases/Proteasome
	Cichoric Acid (Dicaffeoyltartaric acid) 是一种天然化合物，具有抗氧化作用。
T2791	Pectolinarin 柳穿鱼叶苷,大蓟苷	Apoptosis; Others; NO Synthase; Prostaglandin Receptor; Interleukin	Apoptosis; GPCR/G Protein; Immunology/Inflammation; Others
	Pectolinarin 抑制 IL-6和 IL-8分泌以及 PGE2和 NO 产生，可通过抑制 PI3K/Akt 途径来抑制细胞增殖和炎症反应并诱导凋亡，具有抗炎活性。
T2798	Esculetin 秦皮乙素,二羟基香豆素,Aesculetin,Cichorigenin	Lipoxygenase; Akt; PI3K	Cytoskeletal Signaling; Metabolism; PI3K/Akt/mTOR signaling
	Esculetin (Cichorigenin) 是主要提取自水曲柳的树皮中的活性成分。它能够抑制PI3K/Akt 途径，阻碍血小板衍生生长因子诱导的气道平滑肌细胞表型转换。它具有抗氧化，抗炎和抗肿瘤的活性。
TN4761	Phellamurin	P-gp	Membrane transporter/Ion channel; Neuroscience
	Phellamurin 是一种来自黄檗叶的黄酮糖苷，可诱导细胞凋亡，具有抗肿瘤活性。它抑制肠道 P-糖蛋白，还抑制凤蝶的产卵。
T2746	Sophocarpine monohydrate 槐果碱,Sophocarpine,槐果碱水合物	Apoptosis; Influenza Virus; Akt; PI3K; AMPK; Autophagy	Apoptosis; Autophagy; Chromatin/Epigenetic; Cytoskeletal Signaling; Microbiology/Virology; PI3K/Akt/mTOR signaling
	Sophocarpine monohydrate 是从传统草药苦参中提取的一种重要生物碱，具有抗肿瘤活性，可用于肝细胞癌，前列腺癌和结肠直肠癌。苦参具有抗病毒，抗肿瘤和抗炎等多种药理作用。
TN1405	Arnicolide D 山金车内酯 D,山金车内酯D	Akt; Caspase; PI3K; STAT; mTOR	Apoptosis; Cytoskeletal Signaling; JAK/STAT signaling; PI3K/Akt/mTOR signaling; Proteases/Proteasome; Stem Cells
	Arnicolide D 是从石胡荽中分离出的一种倍半萜内酯，以浓度和时间依赖性方式抑制鼻咽癌细胞活力。它调节细胞周期，激活 caspase 信号通路并抑制 PI3K/AKT/mTOR 和 STAT3 信号通路。
T4S0498	Glaucocalyxin A 蓝萼甲素,Wangzaozin B,Leukamenin F	Apoptosis; Akt; Caspase; PI3K	Apoptosis; Cytoskeletal Signaling; PI3K/Akt/mTOR signaling; Proteases/Proteasome
	Glaucocalyxin A (Leukamenin F) 是来自日本黑纹病菌的一种对映型月桂基二萜，具有抗肿瘤作用。它通过调节PI3K/Akt 信号通路抑制 GLI1 的核易位，诱导骨肉瘤凋亡。
T3826	Polygalasaponin F 异牡荆苷,瓜子金皂苷己	NF-κB; TLR; Akt; PI3K	Cytoskeletal Signaling; Immunology/Inflammation; NF-κB; PI3K/Akt/mTOR signaling
	Polygalasaponin F 是从瓜子金中提取的齐墩果烷型三萜皂苷，可通过调节TLR4-PI3K/AKT-NF-kB 信号通路减少神经炎症细胞因子的分泌，能降低炎性细胞因子肿瘤坏死因子 α 的释放。
T5740	25(R,S)-Ruscogenin (25RS)鲁斯可皂苷元,(25RS)-Ruscogenin	Others; HIF	Angiogenesis; Chromatin/Epigenetic; Others
	25(R,S)-Ruscogenin 能够调节 PI3K/Akt/mTOR 信号通路，抑制 MMP-2、MMP-9、uPA、VEGF 和 HIF-1α 的表达，阻碍肝癌转移。它能够抑制 TLR4信号通路，减轻 LPS 诱导的肺内皮细胞凋亡。
T8160	EGCG Octaacetate 乙酰化表没食子儿茶素没食子酸酯,乙酰化EGCG	Others; Antibacterial	Microbiology/Virology; Others
	EGCG Octaacetate 是表没食子儿茶素没食子酸酯的前药，对革兰氏阳性菌和革兰氏阴性菌有潜在抗菌可能。它可下调 PI3K/Akt/NFκB 磷酸化和 p65 乙酰化来降低促炎介质水平，减少小鼠结肠炎引起的结肠癌。
TN3500	beta-Amyrone β-Amyron,β-香树脂酮	COX; AChR; PPAR; Antifection	DNA Damage/DNA Repair; Immunology/Inflammation; Metabolism; Microbiology/Virology; Neuroscience
	beta-Amyrone (β-Amyron) 对基孔肯雅病毒复制具有抗真菌活性，EC50 为 86 uM。 beta-Amyrone 通过抑制 COX-2 的表达而具有抗炎活性。 beta-Amyrone 表现出抗α-葡萄糖苷酶抑制活性和中等 AChE 活性。 β-Amyrone 可用于炎症、感染和肥胖等疾病的研究。
T2P2806	Hederacolchiside A1 黑海常春藤苷A1,革叶常春藤皂苷 A1,Raddeanoside R13	Apoptosis; ERK; MEK; Akt; PI3K; Parasite; mTOR	Apoptosis; Cytoskeletal Signaling; MAPK; Microbiology/Virology; PI3K/Akt/mTOR signaling
	Hederacolchiside A1 (Raddeanoside R13) 是从白头翁中分离的一种有抗利什曼原虫和抗肿瘤增殖活性的天然产物。
T3P2904	α-Linolenic acid Alpha-Linolenic Acid,Linolenic acid,α-亚麻酸	Akt; PI3K	Cytoskeletal Signaling; PI3K/Akt/mTOR signaling
	α-Linolenic acid (Alpha-Linolenic Acid) 是一种必需脂肪酸，人体无法合成，从种子油中分离得到。它可调节 PI3K/Akt 信号传导，影响血栓形成过程。它具有抗心律失常的特性，并且与心血管疾病和癌症等有关。
T2163	Dihydrocapsaicin CCRIS1589,二氢辣椒素,6,7-Dihydrocapsaicin,8-Methyl-N-vanillylnonanamide	Others; TRP/TRPV Channel	Membrane transporter/Ion channel; Others
	Dihydrocapsaicin (CCRIS1589) 是一种天然来源的辣椒素，是TRPV1的选择性激动剂，同时可以增加 p-Akt 水平。它可以增强低温诱导的神经保护。
T5736	1,3-Dicaffeoylquinic acid CYNARIN,1,3-二咖啡酰奎宁酸,Cyclohexanecarboxylic acid, 1,3-bis[[3-(3,4-dihydroxyphenyl)-1-oxo-2-propen-1-yl]oxy]-4,5-dihydroxy-, (1S,3R,4R,5R)-,1,3-O-Dicaffeoylquinic acid,1,5-Dicaffeoylquinic acid	Reactive Oxygen Species; Akt; PI3K	Cytoskeletal Signaling; Immunology/Inflammation; Metabolism; NF-κB; PI3K/Akt/mTOR signaling
	1,3-Dicaffeoylquinic acid (CYNARIN) 是一种咖啡酰奎宁酸衍生物，具有抗氧化、自由基清除作用。
T6817	Deguelin 鱼藤素,(-)-Deguelin,(-)-cis-Deguelin,魚藤素	Apoptosis; Akt; PI3K; Autophagy	Apoptosis; Autophagy; Cytoskeletal Signaling; PI3K/Akt/mTOR signaling
	Deguelin ((-)-Deguelin) 是一种 PI3K/AKT 抑制剂，从 Mundulea sericea 家族植物中分离出来的鱼藤酮类天然产物。
TN1507	Clematichinenoside AR	TNF; Autophagy	Apoptosis; Autophagy
	Clematichinenoside AR 是从中药威灵仙中提取的一种天然产物，具有抗炎和免疫抑制特性，对 PI3K/Akt 信号通路和与胶原诱导的关节炎相关的 TNF-α± 具有抗关节炎作用。
T16324	Nimbolide	Apoptosis; NF-κB; CDK	Apoptosis; Cell Cycle/Checkpoint; NF-κB
	Nimbolide 是源自印楝叶和花的一种三萜。它抑制CDK4/CDK6激酶活性。它抑制 NF-κB，Wnt，PI3K-Akt，MAPK 和 JAK-STAT 信号通路。它通过抑制NF-κB 而诱导肿瘤细胞凋亡。
T3890	Verbenalin Verbenalol β-D-glucopyranoside,马鞭草苷,Verbenaloside,Verbenalol glucoside,Cornin	Others	Others
	Verbenalin (Verbenaloside) 是马鞭草苷，具有抗炎、抗真菌、抗病毒等活性。它能减轻脑缺血再灌注损伤。它可用于前列腺炎的研究。
T3385	Gypenoside XVII GP-17,Gynosaponin S,七叶胆苷XVII	Estrogen Receptor/ERR; GSK-3; Endogenous Metabolite	Endocrinology/Hormones; Metabolism; PI3K/Akt/mTOR signaling; Stem Cells
	Gypenoside XVII (Gynosaponin S) 是一种绞股蓝皂甙类的新型植物雌激素，能够激活雌激素受体。
TN1346	Oxypalmatine 8-Oxypalmatine	Apoptosis	Apoptosis
	Oxypalmatine (8-Oxypalmatine) 是在 Phellodendron amurense 中分离出来的小檗碱型生物碱，通过抑制 PI3K/AKT 信号传导及其对乳腺癌类器官的功效来调节乳腺癌细胞的增殖和凋亡。
T2S0410	Euphorbia factor L1 Euphorbiasteroid,大戟因子L1,大戟因子 L1	Apoptosis; P-gp	Apoptosis; Membrane transporter/Ion channel; Neuroscience
	Euphorbia factor L1 (Euphorbiasteroid) 可降低 Bcl-2，PI3K，AKT 和 mTOR 蛋白和 mRNA 水平，上调 caspase-9 and caspase-3 蛋白水平。它可诱导自噬，具有抗癌、抗脂肪生成、抗破骨细胞生成和多重耐药调节作用。
T6S1844	Tenacissoside H Tenacissimoside C,通关藤苷H	Others	Others
	Tenacissoside H (Tenacissimoside C) 是一种分离自通关藤中的天然产物，具有抗肿瘤作用。
T2S2382	3'-Hydroxypterostilbene 3’-羟基紫檀茋,3'-羟基紫檀茋,3'-HPT	Apoptosis; Autophagy	Apoptosis; Autophagy
	3'-Hydroxypterostilbene (3'-HPT) 是天然紫檀芪类似物，通过诱导细胞凋亡和自噬，有效抑制人结肠癌细胞的生长。它抑制 PI3K/Akt/mTOR/p70S6K 和 p38MAPK 途径并激活 ERK1/2，JNK1/2 MAPK 途径。
T11685	Isolongifolene 异长叶烯,(-)-Isolongifolene	Apoptosis; Others	Apoptosis; Others
	Isolongifolene ((-)-Isolongifolene) 是一种从调料九里香中分离的三环倍半萜烯，具有抗氧化，抗炎，抗癌和神经保护的特性。它通过调节 PI3K/AKT/GSK-3β 信号通路来减轻鱼藤酮诱导的氧化应激，线粒体功能障碍和细胞凋亡。
T4S1796	Heterophyllin B	PI3K	PI3K/Akt/mTOR signaling
	Heterophyllin B 是一种活性环肽，从 Pseudostellaria heterophylla 中分离得到，可用于研究食管癌。
T3330	trans-Trimethoxyresveratrol trans-trismethoxy Resveratrol,E-Resveratrol Trimethyl Ether,MR-3,Tri-O-methylresveratrol,白藜芦醇三甲醚,3,4',5-Trimethoxy-trans-stilbene,Trimethoxystilbene	Reactive Oxygen Species	Immunology/Inflammation; Metabolism; NF-κB
	trans-Trimethoxyresveratrol (MR-3) 是一种 Resveratrol(RSV) 的衍生物，与Resveratrol(RSV)相比，它可能是一个更有效的抗炎、抗血管新生的化合物。
TN2091	Polygalacin D	Apoptosis; IAP	Apoptosis
	Polygalacin D 是从桔梗中分离的一种天然产物，具有抗癌和抗增殖特性。它通过 PI3K/Akt 途径诱导凋亡。它抑制 IAP 蛋白家族的表达，并通过抑制 GSK3β，Akt 的磷酸化和 PI3K 的表达来阻断 PI3K/Akt 途径。
T5S1331	Herbacetin	c-Met/HGFR; Akt	Cytoskeletal Signaling; PI3K/Akt/mTOR signaling; Tyrosine Kinase/Adaptors
	Herbacetin 是一种亚麻籽中的天然类黄酮，具有多种药理活性，如抗氧化、抗炎、抗癌作用。它是鸟氨酸脱羧酶Ornithine decarboxylase (ODC)变构抑制剂，能够直接与 ODC 上的 Asp44，Asp243 和 Glu384 结合。其中鸟氨酸脱羧酶是多胺生物合成中的限速酶。
TL0008	Gigantol	Wnt/beta-catenin; Glucosidase	Cytoskeletal Signaling; Metabolism; Stem Cells
	Gigantol 是一种联苄基化合物，从几种药用兰花中获得，是一种Wnt/β-catenin 通路抑制剂，具有抗肿瘤活性。
TN1461	(-)-Butin Butin,漆黄素 ( 紫铆素)	Akt; PI3K; Nrf2	Cytoskeletal Signaling; Immunology/Inflammation; PI3K/Akt/mTOR signaling
	(-)-Butin (Butin) 是 Butin 的 S 对映体。其中 Butin 是一种分离自黄檀的心材中的生物活性黄酮类化合物，具有显著的抗血小板、抗氧化、抗炎作用。
T16165	Myriocin ISP-I,Thermozymocidin	HCV Protease; Antifungal	Microbiology/Virology; Proteases/Proteasome
	Myriocin (Thermozymocidin) 是一种从 Myriococcum albomyces 中得到的代谢产物，是一种丝氨酸-棕榈酰转移酶 (SPT) 抑制剂,具有潜在的抗肿瘤抗癌和抗寄生虫活性，通过 PI3K/Akt/mTOR 通路调节巨噬细胞极化和功能来抑制肿瘤生长。Myriocin 抑制 HCV 感染，可用于研究神经病变和真菌感染。
T4672	Brevilin A	Apoptosis; Anti-infection; JAK; STAT; Autophagy	Angiogenesis; Apoptosis; Autophagy; Chromatin/Epigenetic; JAK/STAT signaling; Microbiology/Virology; Stem Cells
	Brevilin A 是从Centipeda minima 中分离的倍半萜内酯，具有抗癌活性。它通过线粒体途径和 PI3K/AKT/mTOR 失活诱导结肠腺癌细胞 CT26 的凋亡和自噬。它是一种选择性JAK-STAT 信号通路抑制剂，通过减弱 JAK 信号和阻塞 STAT3 信号起作用。
T5S0896	Loureirin A 龙血素 A,龙血素A	Akt; PI3K	Cytoskeletal Signaling; PI3K/Akt/mTOR signaling
	Loureirin A 是一种黄酮类物质，从龙血树中分离得到，能够降低Akt 的磷酸化，具有抗血小板聚集作用。
T4S1545	Licarin B (-)-Licarin B,Licarine B,(-)-利卡灵B	transporter; Antibacterial; PPAR	DNA Damage/DNA Repair; Metabolism; Microbiology/Virology
	Licarin B (Licarine B) 是来源于肉豆蔻种子的一种天然产物，是 NO 生成抑制剂，可通过激活 IRS-1/PI3K/AKT 通路中的PPARγ和GLUT4 改善胰岛素敏感性。
T3752	4-Hydroxybenzyl alcohol 4-Methylolphenol,P-Methylolphenol,对羟基苯甲醇	Apoptosis; Endogenous Metabolite	Apoptosis; Metabolism
	4-Hydroxybenzyl alcohol (P-Methylolphenol) 是广泛分布于各种植物中的一种酚类天然产物，具有抗炎、抗氧化和抗伤害感受活性。它抑制肿瘤血管生成和生长，有神经保护作用。
TN1013	Cucurbitacin D	Apoptosis	Apoptosis
	Cucurbitacin D 是一种从 Ecballium elaterium （L.）分离出来的三萜类化合物，具有抗癌抗肿瘤活性，抑制转移性 PrC 中的葡萄糖摄取和乳酸产生，诱导独立于 ERK1/2 激活的炎症小体激活。 Cucurbitacin D 是巨噬细胞中的一种新的炎症小体激活剂，通过调节 JAK/STAT3、PI3K/Akt/mTOR 和 MAPK 信号通路抑制 HepG2 细胞增殖并诱导细胞凋亡，可用于研究宫颈癌、白血病和前列腺癌。
T3729	Ethyl gallate Nipagallin A,Phyllemblin,gallic acid ethyl ester,没食子酸乙酯	MMP; NF-κB; Akt; Antibacterial	Cytoskeletal Signaling; Microbiology/Virology; NF-κB; PI3K/Akt/mTOR signaling; Proteases/Proteasome
	Ethyl gallate (gallic acid ethyl ester) 是一种非类黄酮酚过氧化氢清除剂。
T6S0653	Linarin Buddleoflavonoloside,Buddleoside,Acacetin-7-O-rutinoside,Acaciin,Linarine,蒙花苷	TNF; AChE	Apoptosis; Neuroscience
	Linarin (Acacetin-7-O-rutinoside) 是一种选择性的乙酰胆碱酯酶 (AChE) 抑制剂，从薄荷花提取物中分离得到。
TN2063	Physalin B NSC-287088	Apoptosis; NF-κB; Akt; PI3K; Nrf2; NOD	Apoptosis; Cytoskeletal Signaling; Immunology/Inflammation; NF-κB; PI3K/Akt/mTOR signaling
	Physalin B 是茄科植物的主要活性化合物之一，具有广泛的生物活性，可用于治疗炎症湿疹和疱疹等疾病。Physalin B 通过激活 PI3K/Akt 通路抑制 NF-κB 和 NLRP3，从而改善脂多糖诱导的急性肺损伤造成的炎症反应。Physalin B 通过激活 Nrf2 通路抑制 PDGF-BB 诱导的 VSMC 增殖、迁移和表型转化。Physalin B 通过抑制 LAP2α-HDAC1 介导的胶质瘤相关癌基因 1 的去乙酰化和肝星状细胞活化来发挥抗肿瘤活性。
T2808	Bilobalide 白果内酯,银杏内酯,(-)-Bilobalide	Apoptosis; Endogenous Metabolite; Autophagy	Apoptosis; Autophagy; Metabolism
	Bilobalide ((-)-Bilobalide) 是银杏叶中的的一种倍半萜三内酯成分，抑制 NMDA 诱导的胆碱流出，IC50值为 2.3 µM。它通过激活 SH-SY5Y 细胞中的 PI3K/Akt 通路来防止细胞凋亡。对神经元发挥保护和营养作用。
T3780	Oroxin B Hypocretin-2,木蝴蝶苷B	Apoptosis; PTEN; Antioxidant; PI3K; Autophagy	Apoptosis; Autophagy; oxidation-reduction; PI3K/Akt/mTOR signaling
	Oroxin B (Hypocretin-2) 是从传统中草药木蝴蝶中分离出来的黄酮类天然产物，在恶性淋巴瘤细胞中诱导肿瘤抑制性 ER 应激。它通过上调 PTEN，下调 COX-2，VEGF，PI3K 和 p-AKT，对肝癌细胞具有明显的抑制作用，诱导细胞早期凋亡。
TN1557	Decursinol angelate	ERK; VEGFR; PKC; JNK	Angiogenesis; Chromatin/Epigenetic; Cytoskeletal Signaling; MAPK; Tyrosine Kinase/Adaptors
	Decursinol angelate 是从朝鲜当归根部分离得到的一种天然产物，是 PKC 激酶的激活剂，有细胞毒性，抗肿瘤和抗炎活性。
T3923	Calycosin Cyclosin,3'-Hydroxyformononetin,异黄酮,毛异黄酮	Apoptosis; Tyrosinase	Apoptosis; Proteases/Proteasome
	Calycosin (Cyclosin) 是一抗氧化和抗炎症活性天然产物。
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天然产物

Cat.No: T5654

Target: Others

Cat.No: TN1891

Target: Apoptosis, BCL, PARP, Caspase

Deoxyelephantopin

Cat.No: TN1079

Target: NF-κB

Cat.No: T6677

Target: ERK, p38 MAPK, NF-κB, TLR, COX, HER, JNK, STAT

Cat.No: T5S1982

Synonym: Periplocoside,杠柳毒苷

Target: Apoptosis, Others

Cat.No: TN1644

Target: Others

Cat.No: TL0006

Synonym: 菊苣酸,Dicaffeoyltartaric acid,Chicoric Acid

Target: Reactive Oxygen Species, HIV Protease

Cat.No: T2791

Synonym: 柳穿鱼叶苷,大蓟苷

Target: Apoptosis, Others, NO Synthase, Prostaglandin Receptor, Interleukin

Cat.No: T2798

Synonym: 秦皮乙素,二羟基香豆素,Aesculetin,Cichorigenin

Target: Lipoxygenase, Akt, PI3K

Cat.No: TN4761

Target: P-gp

Sophocarpine monohydrate

Cat.No: T2746

Synonym: 槐果碱,Sophocarpine,槐果碱水合物

Target: Apoptosis, Influenza Virus, Akt, PI3K, AMPK, Autophagy

Cat.No: TN1405

Synonym: 山金车内酯 D,山金车内酯D

Target: Akt, Caspase, PI3K, STAT, mTOR

Glaucocalyxin A

Cat.No: T4S0498

Synonym: 蓝萼甲素,Wangzaozin B,Leukamenin F

Target: Apoptosis, Akt, Caspase, PI3K

Polygalasaponin F

Cat.No: T3826

Synonym: 异牡荆苷,瓜子金皂苷己

Target: NF-κB, TLR, Akt, PI3K

25(R,S)-Ruscogenin

Cat.No: T5740

Synonym: (25RS)鲁斯可皂苷元,(25RS)-Ruscogenin

Target: Others, HIF

EGCG Octaacetate

Cat.No: T8160

Synonym: 乙酰化表没食子儿茶素没食子酸酯,乙酰化EGCG

Target: Others, Antibacterial

Cat.No: TN3500

Synonym: β-Amyron,β-香树脂酮

Target: COX, AChR, PPAR, Antifection

Hederacolchiside A1

Cat.No: T2P2806

Synonym: 黑海常春藤苷A1,革叶常春藤皂苷 A1,Raddeanoside R13

Target: Apoptosis, ERK, MEK, Akt, PI3K, Parasite, mTOR

α-Linolenic acid

Cat.No: T3P2904

Synonym: Alpha-Linolenic Acid,Linolenic acid,α-亚麻酸

Target: Akt, PI3K

Dihydrocapsaicin

Cat.No: T2163

Synonym: CCRIS1589,二氢辣椒素,6,7-Dihydrocapsaicin,8-Methyl-N-vanillylnonanamide

Target: Others, TRP/TRPV Channel

1,3-Dicaffeoylquinic acid

Cat.No: T5736

Synonym: CYNARIN,1,3-二咖啡酰奎宁酸,Cyclohexanecarboxylic acid, 1,3-bis[[3-(3,4-dihydroxyphenyl)-1-oxo-2-propen-1-yl]oxy]-4,5-dihydroxy-, (1S,3R,4R,5R)-,1,3-O-Dicaffeoylquinic acid,1,5-Dicaffeoylquinic acid

Target: Reactive Oxygen Species, Akt, PI3K

Cat.No: T6817

Synonym: 鱼藤素,(-)-Deguelin,(-)-cis-Deguelin,魚藤素

Target: Apoptosis, Akt, PI3K, Autophagy

Clematichinenoside AR

Cat.No: TN1507

Target: TNF, Autophagy

Cat.No: T16324

Target: Apoptosis, NF-κB, CDK

Cat.No: T3890

Synonym: Verbenalol β-D-glucopyranoside,马鞭草苷,Verbenaloside,Verbenalol glucoside,Cornin

Target: Others

Gypenoside XVII

Cat.No: T3385

Synonym: GP-17,Gynosaponin S,七叶胆苷XVII

Target: Estrogen Receptor/ERR, GSK-3, Endogenous Metabolite

Cat.No: TN1346

Synonym: 8-Oxypalmatine

Target: Apoptosis

Euphorbia factor L1

Cat.No: T2S0410

Synonym: Euphorbiasteroid,大戟因子L1,大戟因子 L1

Target: Apoptosis, P-gp

Tenacissoside H

Cat.No: T6S1844

Synonym: Tenacissimoside C,通关藤苷H

Target: Others

3'-Hydroxypterostilbene

Cat.No: T2S2382

Synonym: 3’-羟基紫檀茋,3'-羟基紫檀茋,3'-HPT

Target: Apoptosis, Autophagy

Cat.No: T11685

Synonym: 异长叶烯,(-)-Isolongifolene

Target: Apoptosis, Others

Heterophyllin B

Cat.No: T4S1796

Target: PI3K

trans-Trimethoxyresveratrol

Cat.No: T3330

Synonym: trans-trismethoxy Resveratrol,E-Resveratrol Trimethyl Ether,MR-3,Tri-O-methylresveratrol,白藜芦醇三甲醚,3,4',5-Trimethoxy-trans-stilbene,Trimethoxystilbene

Target: Reactive Oxygen Species

Cat.No: TN2091

Target: Apoptosis, IAP

Cat.No: T5S1331

Target: c-Met/HGFR, Akt

Cat.No: TL0008

Target: Wnt/beta-catenin, Glucosidase

Cat.No: TN1461

Synonym: Butin,漆黄素 ( 紫铆素)

Target: Akt, PI3K, Nrf2

Cat.No: T16165

Synonym: ISP-I,Thermozymocidin

Target: HCV Protease, Antifungal

Cat.No: T4672

Target: Apoptosis, Anti-infection, JAK, STAT, Autophagy

Cat.No: T5S0896

Synonym: 龙血素 A,龙血素A

Target: Akt, PI3K

Cat.No: T4S1545

Synonym: (-)-Licarin B,Licarine B,(-)-利卡灵B

Target: transporter, Antibacterial, PPAR

4-Hydroxybenzyl alcohol

Cat.No: T3752

Synonym: 4-Methylolphenol,P-Methylolphenol,对羟基苯甲醇

Target: Apoptosis, Endogenous Metabolite

Cat.No: TN1013

Target: Apoptosis

Cat.No: T3729

Synonym: Nipagallin A,Phyllemblin,gallic acid ethyl ester,没食子酸乙酯

Target: MMP, NF-κB, Akt, Antibacterial

Cat.No: T6S0653

Synonym: Buddleoflavonoloside,Buddleoside,Acacetin-7-O-rutinoside,Acaciin,Linarine,蒙花苷

Target: TNF, AChE

Cat.No: TN2063

Synonym: NSC-287088

Target: Apoptosis, NF-κB, Akt, PI3K, Nrf2, NOD

Cat.No: T2808

Synonym: 白果内酯,银杏内酯,(-)-Bilobalide

Target: Apoptosis, Endogenous Metabolite, Autophagy

Cat.No: T3780

Synonym: Hypocretin-2,木蝴蝶苷B

Target: Apoptosis, PTEN, Antioxidant, PI3K, Autophagy

Decursinol angelate

Cat.No: TN1557

Target: ERK, VEGFR, PKC, JNK

Cat.No: T3923

Synonym: Cyclosin,3'-Hydroxyformononetin,异黄酮,毛异黄酮

Target: Apoptosis, Tyrosinase

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Species：

Expression System：

Tag：

Cat. No.	Product Name	Species	Expression System
TMPJ-00059	IL-7 Protein, Human, Recombinant (His) Interleukin-7,IL7,白细胞介素,IL-7,白介素	Human	HEK293 Cells
	Human Interleukin 7 (IL-7) is a potent lymphoid cell growth factor stimulating the proliferation of lymphoid progenitors. IL7 can associate with the hepatocyte growth factor (HGF) to form a hybrid cytokine that functions as a pre-pro-B cell growth-stimulating factor. Human IL7 cDNA encodes a 177 amino acid precursor protein containing a 25 amino acid signal peptide and a 152 amino acid mature protein. Human and mouse IL7 share 65% sequence identity in the mature region and both exhibit cross-spe...
TMPH-01348	FSHR Protein, Human, Recombinant (His) Follitropin receptor,FSHR,Follicle-stimulating horm...	Human	HEK293 Cells
	G protein-coupled receptor for follitropin, the follicle-stimulating hormone. Through cAMP production activates the downstream PI3K-AKT and ERK1/ERK2 signaling pathways. FSHR Protein, Human, Recombinant (His) is expressed in HEK293 mammalian cells with N-6xHis tag. The predicted molecular weight is 43.5 kDa and the accession number is P23945.
TMPH-03365	REG3A Protein, Rat, Recombinant (E.coli, His) Lithostathine 3,Reg3a,RegIII,Regenerating islet-derived prot...	Rat	E. coli
	Bactericidal C-type lectin. Regulates keratinocyte proliferation and differentiation after skin injury via activation of EXTL3-PI3K-AKT signaling pathway. REG3A Protein, Rat, Recombinant (E.coli, His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 20.5 kDa and the accession number is P35231.
TMPH-01347	FSHR Protein, Human, Recombinant (E. coli, His) Follicle-stimulating hormone receptor,Follitropin r...	Human	E. coli
	G protein-coupled receptor for follitropin, the follicle-stimulating hormone. Through cAMP production activates the downstream PI3K-AKT and ERK1/ERK2 signaling pathways. FSHR Protein, Human, Recombinant (E. coli, His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 44.0 kDa and the accession number is P23945.
TMPH-02019	REG3A Protein, Human, Recombinant (GST) Regenerating islet-derived protein 3-alpha,REG3A,Regeneratin...	Human	E. coli
	Bactericidal C-type lectin which acts exclusively against Gram-positive bacteria and mediates bacterial killing by binding to surface-exposed carbohydrate moieties of peptidoglycan. Regulates keratinocyte proliferation and differentiation after skin injury via activation of EXTL3-PI3K-AKT signaling pathway. REG3A Protein, Human, Recombinant (GST) is expressed in E. coli expression system with N-GST tag. The predicted molecular weight is 43.6 kDa and the accession number is Q06141.
TMPK-01034	SEMA4B Protein, Mouse, Recombinant (His) SEMA4B,SemC,Semaphorin-C,MGC131831,Semaphorin-4B,KIAA1745,SE...	Mouse	HEK293 Cells
	Semaphorin 4B (SEMA4B) inhibits the invasion of non-small cell lung cancer (NSCLC) through PI3K-dependent suppression of MMP9 activation. SEMA4B may induce FoxO1 nuclear retention through suppressing PI3K/Akt signaling pathway, which subsequently inhibited cell growth through the direct nuclear target of FoxO1, p21. A role of SEMA4B in suppressing NSCLC growth, besides its role in inhibiting cell metastasis, and highlights SEMA4B as a promising therapeutic target for NSCLC.
TMPK-00136	ULBP-2 Protein, Human, Recombinant (His & Avi) ALCAN-α,RAET1L,NKG2D ligand 2,ALCAN-alpha,N2DL2,ULBP-2/5/6,R...	Human	HEK293 Cells
	ULBPs activate multiple signaling pathways in primary NK cells, resulting in the production of cytokines and chemokines. Binding of ULBPs ligands to NKG2D induces calcium mobilization and activation of the JAK2, STAT5, ERK and PI3K kinase/Akt signal transduction pathway, mediating natural killer cell cytotoxicity.
TMPJ-00181	PD-1 Protein, Human, Recombinant (His & Avi), Biotinylated Programmed cell death protein 1,PDCD1,CD279,hPD-1	Human	HEK293 Cells
	Programmed cell death protein 1(PDCD1) is a single-pass type I membrane protein and contains 1 Ig-like V-type domain. PD-1 is a member of the extended CD28/CTLA-4 family of T cell regulators. PDCD1 inhibits the T-cell proliferation and production of related cytokines including IL-1, IL-4, IL-10 and IFN-γ by suppressing the activation and transduction of PI3K/AKT pathway. In addition, coligation of PDCD1 inhibits BCR-mediating signal by dephosphorylating key signal transducer. PDCD1 has been sugg...
TMPY-05250	CLEC3A Protein, Mouse, Recombinant (His) C-type lectin domain family 3, member A,Gm796,1110019O10Rik,...	Mouse	Baculovirus Insect Cells
	C-type lectin domain family 3 member A (CLEC3A) is a poorly characterized protein belonging to the superfamily of C-type lectins. Elevated CLEC3A expression may correlate with breast IDC metastatic potential and indicated a poor prognosis in breast IDC. CLEC3A knockdown inhibited BC cell growth and metastasis might be through suppressing PI3K/AKT signaling activity. That CLEC3A is a promising therapeutic target for BC in the future. Matrilysin (MMP-7) plays important roles in tumor progression. ...
TMPY-03795	EIF5A2 Protein, Human, Recombinant (His) eIF5AII,eukaryotic translation initiation factor 5A2,EIF-5A2	Human	E. coli
	Eukaryotic translation initiation factor 5A2 (EIF5A2) has been demonstrated to be upregulated in numerous types of human cancer and is associated with cancer progression. Silencing of EIF5A2 in the NSCLC cells resulted in the downregulation of the tumorigenic proteins, apoptosis regulator Bcl-2 and myc proto-oncogene protein, and upregulation of E-cadherin, suggesting that EIF5A2 promotes proliferation and metastasis through these proteins. EIF5A2 may therefore serve as a novel therapeutic targe...

重组蛋白

IL-7 Protein, Human, Recombinant (His)

Cat.No: TMPJ-00059

Species: Human

Expression System: HEK293 Cells

FSHR Protein, Human, Recombinant (His)

Cat.No: TMPH-01348

Species: Human

Expression System: HEK293 Cells

REG3A Protein, Rat, Recombinant (E.coli, His)

Cat.No: TMPH-03365

Species: Rat

Expression System: E. coli

FSHR Protein, Human, Recombinant (E. coli, His)

Cat.No: TMPH-01347

Species: Human

Expression System: E. coli

REG3A Protein, Human, Recombinant (GST)

Cat.No: TMPH-02019

Species: Human

Expression System: E. coli

SEMA4B Protein, Mouse, Recombinant (His)

Cat.No: TMPK-01034

Species: Mouse

Expression System: HEK293 Cells

ULBP-2 Protein, Human, Recombinant (His & Avi)

Cat.No: TMPK-00136

Species: Human

Expression System: HEK293 Cells

PD-1 Protein, Human, Recombinant (His & Avi), Biotinylated

Cat.No: TMPJ-00181

Species: Human

Expression System: HEK293 Cells

CLEC3A Protein, Mouse, Recombinant (His)

Cat.No: TMPY-05250

Species: Mouse

Expression System: Baculovirus Insect Cells

EIF5A2 Protein, Human, Recombinant (His)

Cat.No: TMPY-03795

Species: Human

Expression System: E. coli

Cat. No.	Product Name	Target	Signaling Pathways
T35519	Aflatoxin B2-13C17 Aflatoxin B2-13C17
	Aflatoxin B2-13C17(AFB2-13C17) is intended for use as an internal standard for the quantification of AFB2by GC- or LC-MS. AFB2is a mycotoxin that has been found inA. terricola.1It induces hepatic autophagy and apoptosis in broiler chickens when administered at doses of 0.2, 0.4, and 0.8 mg/kg.2AFB2(0.5 and 1 mg/animal) also induces parenchymal cell hyperplasia in rats.3 1.Moubasher, A.H., el-Kady, I.A., and Shoriet, A.Toxigenic Aspergilli isolated from different sources in EgyptAnn. Nutr. Alimen...

同位素标记化合物

Aflatoxin B2-13C17

Cat.No: T35519

Synonym: Aflatoxin B2-13C17

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