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Search Results for " vegf "

176

抑制剂 & 化合物

24

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T71944	FGF/PDGF/VEGF RTK Inhibitor
	FGF/PDGF/VEGF RTK Inhibitor is a potent, reversible, atp-competitive inhibitor against pdgfrβ, fgfr-1, and vegfr-2 (ic50 = 20, 90, and 240 nm, respectively) and effectively suppresses vegf-stimulated proliferation of hmvecs (ec50 = 420 nm).
T8496	MAZ51	Apoptosis; VEGFR	Angiogenesis; Apoptosis; Tyrosine Kinase/Adaptors
	MAZ51 是一种 VEGFR-3酪氨酸激酶的选择性抑制剂。它抑制 VEGF-C 诱导的 VEGFR-3 激活，而没有阻断 VEGF-C 介导的 VEGFR2 刺激。它阻止增殖并诱导多种肿瘤细胞凋亡，具有抗肿瘤活性。
T4288	hVEGF-IN-1	VEGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	hVEGF-IN-1 是一种喹唑啉衍生物，可以特异性结合内部核糖体进入位点 A 中富含 G 的序列，并会使 G-四链体结构不稳定。在 SPR 实验中，它与 IRES-A (WT) 结合的Kd 值为 0.928 μM。它能够抑制VEGF-A 蛋白表达，阻止肿瘤细胞迁移，抑制肿瘤生长。
T8574	SPHINX	Others	Others
	SPHINX 是新一代的 SPRK1抑制剂。
T0463	Loxoprofen Loxoprofene,洛索洛芬,Loxoprofeno,Koloxo	COX	Immunology/Inflammation; Neuroscience
	Loxoprofen (Koloxo) 是一种非甾体类抗炎药，具有解热作用，可用于缓解疼痛的研究。它是非选择性COX 抑制剂，对 COX-1 和 COX-2 的IC50分别为 6.5 和 13.5 μM。
T15102	Dexamethasone palmitate 地塞米松棕榈酸酯,DXP	Glucocorticoid Receptor	Endocrinology/Hormones
	Dexamethasone palmitate (DXP) (DXP) 是 Dexamethasone 的前药。Dexamethasone 是糖皮质激素受体激动剂。与Dexamethasone 相比， DXP 对糖皮质激素受体的亲和力低 47 倍。DXP 显示出抗炎活性。
T8657	KYP-2047	Others	Others
	KYP-2047 是一种非常有效的选择性脯氨酰寡肽酶 (POP) 抑制剂。
T9928	Ranibizumab	VEGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	Ranibizumab 是一种人源化单克隆抗体片段，旨在靶向和抑制血管内皮生长因子 (VEGF)，包括 VEGF110、VEGF121 和 VEGF165。 Ranibizumab 选择性靶向和中和 VEGF-A 同工型的能力使其成为湿性年龄相关性黄斑变性 (AMD) 研究和治疗策略的重要组成部分。
T8973	HS-1793	Others	Others
	HS-1793 是 resveratrol 类似物，可以诱导细胞凋亡，在多种癌细胞中有抗肿瘤的能力。
T6182	Tirofiban L700462,Aggrastat,替罗非班,MK383	Integrin	Cytoskeletal Signaling
	Tirofiban (L700462) 是一种非肽类选择性 GPIIb/IIIa 拮抗剂，IC50 为 9 nM，可抑制血小板聚集。
T2537	Tirofiban hydrochloride monohydrate Tirofiban Hydrochloride,盐酸替罗非班水合物,MK-383 Hydrochloride,盐酸替罗非班	ATPase; Integrin	Cytoskeletal Signaling; Membrane transporter/Ion channel
	Tirofiban hydrochloride monohydrate (MK-383 Hydrochloride) 是一种非肽类糖蛋白IIb/IIIa 的拮抗剂。
T72924	VEGFR-3-IN-1	VEGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	VEGFR-3-IN-1 是一种新型有效且具有选择性的 VEGFR3 抑制剂，其 IC50 为 110.4 nM。VEGFR-3-IN-1 具有抗肿瘤活性，可使 VEGFR3 信号通路失活，可抑制 VEGF-C 诱导人真皮淋巴管内皮细胞 (HDLEC)、MDA-MB-231 和 MDA-MB-436 细胞的增殖和迁移，并且能有效抑制乳腺癌的生长。
T37078	VEGFR-2-IN-6	VEGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	VEGFR-2-IN-6 (WO 02/059110, example 64) is a potent inhibitor of VEGFR2, a crucial receptor involved in the regulation of angiogenesis [1].
T2056	VEGFR-2-IN-5 2, 4-Pyrimidinediamine with linker,UNC0064-12,2,4-Pyrimidinediamine with linker	VEGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	VEGFR-2-IN-5 (UNC0064-12) 是 VEGFR2 抑制剂。
T79860	TIE-2/VEGFR-2 kinase-IN-5	VEGFR; Tie-2	Angiogenesis; Tyrosine Kinase/Adaptors
	TIE-2/VEGFR-2 kinase-IN-5 是一种高效的 TIE-2 和 VEGFR-2 酪氨酸激酶受体抑制剂，具有的抗血管生成活性，常用于血管生成相关的生物医学研究领域。
T9724	VEGFR2-IN-2	Others	Others
	VEGFR2-IN-2 具有抗炎和镇痛活性。
T9979	VEGFR-2-IN-29	VEGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	VEGFR-2-IN-29是一种 VEGFR2抑制剂。
T10123	VEGFR-2-IN-9 KDR-in-4	VEGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	VEGFR-2-IN-9 (KDR-in-4) 是一种高效的 KDR/VEGFR2 抑制剂（IC50：7 nM）,可用于研究乳腺癌。
T61899	VEGFR2-IN-1	VEGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	VEGFR2-IN-1 是一种具有选择性和高效性的 VEGFR2 抑制剂，具有抗肿瘤活性，可抑制细胞的增殖和迁移，可用于研究乳腺癌。
T61038	VEGFR-2-IN-10
	VEGFR-2-IN-10 对 VEGF 诱导的VEGFR2磷酸化表现出增强的抗血管生成效力，IC50值为 0.7 μM，而无细胞毒性作用。
T37079	VEGFR2 Kinase Inhibitor II
	Vascular endothelial growth factor receptor 2 (VEGFR2, also known as KDR and FLK1) is a receptor tyrosine kinase that regulates angiogenesis, vascular development, and embryonic hematopoiesis in response to VEGF isoforms A, C, and D. VEGFR2 kinase inhibitor II is a reversible, cell-permeable inhibitor of VEGFR2's kinase activity (IC50 = 70 nM). It less potently inhibits the platelet-derived growth factor receptor β (PDGFRβ; IC50 = 920 nM) and related receptor and non-receptor tyrosine kinases. V...
T80873	VEGFR2/HDAC1-IN-1	VEGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	VEGFR2/HDAC1-IN-1（compound 13）是一款有效的VEGFR-2和HDAC双重抑制剂，其IC50值分别为57.83 nM 和9.82 nM 。该化合物能够阻滞细胞周期于S期及G2期，并能诱导HeLa细胞发生凋亡，同时具有抗血管生成的特性。
T63112	VEGFR-IN-3
	VEGFR-IN-3 (compound 3f) 是 VEGFR 抑制剂。VEGFR-IN-3 抑制 OVCAR-4 和 MDA-MB-468 癌细胞的生长，其 IC50值分别为 0.29 和 0.35 μM。VEGFR-IN-3 可用于癌症的研究。
T79540	hCA/VEGFR-2-IN-1	Carbonic Anhydrase	Metabolism
	hCA/VEGFR-2-IN-1 是一种高效的双靶点抑制剂，对 hCA IX 和 hCA XII 两种碳酸酐酶（CA）具有极低的Ki值，分别为8.3 nM和4.7 nM。同时，hCA/VEGFR-2-IN-1 也是一种有效的 VEGFR-2 抑制剂，其 IC50 值仅为26.3 nM，并且显示出抗癌活性。
T72713	PI3K/VEGFR2-IN-1	PI3K	PI3K/Akt/mTOR signaling
	PI3K/VEGFR2-IN-1是一种具有双重抑制效应的化合物，对PI3K和VEGFR2的IC50分别为2.21 μM和68 μM，能够诱导细胞凋亡(apoptosis)，在癌症研究中应用。
T61631	VEGFR-2-IN-23
	VEGFR-2-IN-23 (compound 11b) is a highly potent and selective inhibitor of VEGFR-2, with an impressive IC 50 value of 0.34 nM. This compound exhibits notable antitumor activity, capable of inducing apoptosis and cell cycle arrest specifically at the G1 phase [1].
T61943	VEGFR-2-IN-5 hydrochloride
	VEGFR-2-IN-5 hydrochloride 是有效的VEGFR2抑制剂。
T62763	VEGFR-2-IN-12
	VEGFR-2-IN-12 (compound 6g) 是一种 2-oxoquinoxalinyl-1,2,4-triazole，是一种 VEGFR-2 的有效抑制剂 (IC50: 0.037 μM)。VEGFR-2-IN-12 能够高度抑制 MCF-7 细胞的生长 (GI50: 1.6 μM)。VEGFR-2-IN-12 具有抗肿瘤作用。
T62071	VEGFR-2-IN-16
	VEGFR-2-IN-16 (Compound 15b) 是一种 VEGFR-2 的有效抑制剂 (IC50: 86.36 nM)，表现出抗肿瘤效果。
T61542	VEGFR-2-IN-17
	VEGFR-2-IN-17 (Compound 15a) is a highly potent inhibitor of Vascular Endothelial Growth Factor Receptor 2 (VEGFR-2), with an IC50 value of 67.25 nM. This compound exhibits significant antitumor properties [1].
T72890	VEGFR-2-IN-30
	VEGFR-2-IN-30为一种针对VEGFR-2的抑制剂（IC50：66 nM），同时对PDGFR、EGFR及FGFR1亦有一定抑制作用，其IC50s分别为180、98、82 nM。此外，VEGFR-2-IN-30能够阻止癌细胞在S期的进展并诱导早期以及晚期的细胞凋亡（apoptosis）。
T79591	hCA/VEGFR-2-IN-4	VEGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	hCA/VEGFR-2-IN-4 (化合物15b) 是一种具有癌症治疗潜力的吲哚酮基苯磺酰胺类双重抑制剂，旨在抑制与癌症相关的hCA IX/XII 和VEGFR-2。该化合物对VEGFR-2具有较强的抑制能力（IC50=0.811 μM），并对hCAs展现高亲和性，其Ki值分别为hCA XII的3.8 nM，hCA IX的6.2 nM，hCA II的19.8 nM，以及hCA I的35.5 nM。此外，hCA/VEGFR-2-IN-4 对于VEGFR-2过表达的乳腺癌细胞有抗增殖作用。
T79400	VEGFR-2-IN-35	VEGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	VEGFR-2-IN-35（compound 7）作为 VEGFR-2 抑制剂，展示出37 nM 的IC50值；同时，该化合物对MCF-7 和 HCT 116 癌细胞的抑制效果显著，IC50值分别为10.56 μM 和7.07 μM。
T78759	VEGFR2-IN-4	VEGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	VEGFR2-IN-4（化合物25）为一种针对VEGFR2激酶的有效且选择性抑制剂，其GI50为0.7 nM。该化合物表现出抗血管生成活性，可用于类风湿关节炎研究领域。
T78819	VEGFR-2-IN-33	VEGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	VEGFR-2-IN-33（Compound 4d）为一种有效的VEGFR抑制剂，其IC50值为61.04 nM。该化合物在抑制HepG2细胞增殖方面表现出更高的效力，IC50仅为4.31 nM，因此常用于肝细胞癌（HCC）研究领域。
T63722	VEGFR-2-IN-24
	VEGFR-2-IN-24 是 VEGFR-2 的有效抑制剂 (IC50: 0.22 μM)，能够用于研究肿瘤。
T8817	TIE-2/VEGFR-2 kinase-IN-1
	TIE-2/VEGFR-2 kinase-IN-1 用于合成TIE-2或者VEGFR-2抑制剂，可用于研究不适当的血管生成的相关疾病。
T61861	VEGFR-2-IN-20
	VEGFR-2-IN-20 (Compound 7) is a highly effective VEGFR inhibitor with significant potential for cancer research [1].
T63822	VEGFR-2-IN-22
	VEGFR-2-IN-22 (Compound 25) 是 VEGFR-2 和 β-tubulin 聚合抑制剂，对 VEGFR-2 的 IC50=19.82 nM。VEGFR-2-IN-22 能够诱导细胞凋亡 (apoptosis)。
T63168	VEGFR-2-IN-26
	VEGFR-2-IN-26 (compound 5h) 是一种 VEGFR-2 的高效抑制剂 (IC50: 15.5 nM)。VEGFR-2-IN-26 对白血病、中枢神经系统、非小肺、卵巢、肾、前列腺和乳腺癌细胞表现出良好的抗增殖作用。
T80874	VEGFR-2/c-Met-IN-1	VEGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	VEGFR-2/c-Met-IN-1为VEGFR-2及c-Met的双重抑制剂，IC50值为138 nM和74 nM，显示出抗肿瘤活性。
T23504	VEGFR-IN-1 VEGFR Tyrosine Kinase Inhibitor II	Others	Others
	VEGFR inhibitor
T61561	VEGFR-2-IN-18
	VEGFR-2-IN-18 (Compound 15d) is a high-potency inhibitor of VEGFR-2, with an IC 50 value of 60 nM. This compound effectively initiates cell apoptosis and demonstrates significant antitumor properties [1].
T61137	VEGFR-2-IN-19
	VEGFR-2-IN-19 (Compound 15b) is a highly efficacious inhibitor of VEGFR2, a receptor involved in angiogenesis. Its mechanism of action involves the induction of cellular apoptosis and elevation of intracellular reactive oxygen species. Due to these properties, VEGFR-2-IN-19 holds promise as an effective anticancer agent [1].
T61229	VEGFR-2/DHFR-IN-2
	VEGFR-2/DHFR-IN-2 (compound 5b) is a dual inhibitor targeting VEGFR-2 and DHFR, with respective IC50 values of 0.623 μM and 9.085 μM. It demonstrates potent cytotoxicity against C26, HepG2, and MCF7 cancer cell lines, with IC50 values ranging from 3.59 μM to 8.38 μM. VEGFR-2/DHFR-IN-2 holds promise for cancer research [1].
T61489	VEGFR-2/DHFR-IN-1
	VEGFR-2/DHFR-IN-1 (compound 8b) 是 VEGFR-2和DHFR 的抑制剂，其IC50值分别为 0.384 和 7.881 μM。VEGFR-2/DHFR-IN-1 对大肠埃希菌，粪链球菌，肠沙门氏菌，金黄色酿脓葡萄球菌，MSSA 和MRSA 显示了良好的抗菌活性，MIC 值分别为 16，16，16，8 和 16 μg/mL。VEGFR-2/DHFR-IN-1 对 C26，HepG2 和 CF7 癌细胞系具有良好的细胞毒性，IC50值为 2.97-7.12 μM。VEGFR-2/DHFR-IN-1 可用于癌症的研究。
T79859	TIE-2/VEGFR-2 kinase-IN-4
	TIE-2/VEGFR-2 kinase-IN-4，一种苯并咪唑衍生物，作为有效的TIE-2和VEGFR-2酪氨酸激酶受体抑制剂，其IC50值分别为5.2 nM和5.1 nM，适用于血管生成相关研究。
T78845	FGFR1/VEGFR2-IN-1	VEGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	FGFR1/VEGFR2-IN-1 (compound 2b) 为FGFR1/VEGFR2抑制剂，适用于癌症研究。
T62901	VEGFR-2-IN-27
	VEGFR-2-IN-27 (compound 7a) 是一种 VEGFR-2 的高效抑制剂 (IC50: 14.8 nM)，能够用于抗癌研究。
T72607	VEGFR-2/BRAF-IN-1
	VEGFR-2/BRAF-IN-1 是一种 VEGFR-2和 BRAF 双重抑制剂，对 VEGFR-2、BRAFV600E 和BRAFWT 的IC50分别为 0.049、0.063 和 0.005 µM。VEGFR-2/BRAF-IN-1 诱导细胞凋亡，在 G1/S 期阻滞细胞周期。

化合物

FGF/PDGF/VEGF RTK Inhibitor

Cat.No: T71944

Cat.No: T8496

Target: Apoptosis, VEGFR

Cat.No: T4288

Target: VEGFR

Cat.No: T8574

Target: Others

Cat.No: T0463

Synonym: Loxoprofene,洛索洛芬,Loxoprofeno,Koloxo

Target: COX

Dexamethasone palmitate

Cat.No: T15102

Synonym: 地塞米松棕榈酸酯,DXP

Target: Glucocorticoid Receptor

Cat.No: T8657

Target: Others

Cat.No: T9928

Target: VEGFR

Cat.No: T8973

Target: Others

Cat.No: T6182

Synonym: L700462,Aggrastat,替罗非班,MK383

Target: Integrin

Tirofiban hydrochloride monohydrate

Cat.No: T2537

Synonym: Tirofiban Hydrochloride,盐酸替罗非班水合物,MK-383 Hydrochloride,盐酸替罗非班

Target: ATPase, Integrin

Cat.No: T72924

Target: VEGFR

Cat.No: T37078

Target: VEGFR

Cat.No: T2056

Synonym: 2, 4-Pyrimidinediamine with linker,UNC0064-12,2,4-Pyrimidinediamine with linker

Target: VEGFR

TIE-2/VEGFR-2 kinase-IN-5

Cat.No: T79860

Target: VEGFR, Tie-2

Cat.No: T9724

Target: Others

VEGFR-2-IN-29

Cat.No: T9979

Target: VEGFR

Cat.No: T10123

Synonym: KDR-in-4

Target: VEGFR

Cat.No: T61899

Target: VEGFR

VEGFR-2-IN-10

Cat.No: T61038

VEGFR2 Kinase Inhibitor II

Cat.No: T37079

VEGFR2/HDAC1-IN-1

Cat.No: T80873

Target: VEGFR

Cat.No: T63112

hCA/VEGFR-2-IN-1

Cat.No: T79540

Target: Carbonic Anhydrase

PI3K/VEGFR2-IN-1

Cat.No: T72713

Target: PI3K

VEGFR-2-IN-23

Cat.No: T61631

VEGFR-2-IN-5 hydrochloride

Cat.No: T61943

VEGFR-2-IN-12

Cat.No: T62763

VEGFR-2-IN-16

Cat.No: T62071

VEGFR-2-IN-17

Cat.No: T61542

VEGFR-2-IN-30

Cat.No: T72890

hCA/VEGFR-2-IN-4

Cat.No: T79591

Target: VEGFR

VEGFR-2-IN-35

Cat.No: T79400

Target: VEGFR

Cat.No: T78759

Target: VEGFR

VEGFR-2-IN-33

Cat.No: T78819

Target: VEGFR

VEGFR-2-IN-24

Cat.No: T63722

TIE-2/VEGFR-2 kinase-IN-1

Cat.No: T8817

VEGFR-2-IN-20

Cat.No: T61861

VEGFR-2-IN-22

Cat.No: T63822

VEGFR-2-IN-26

Cat.No: T63168

VEGFR-2/c-Met-IN-1

Cat.No: T80874

Target: VEGFR

Cat.No: T23504

Synonym: VEGFR Tyrosine Kinase Inhibitor II

Target: Others

VEGFR-2-IN-18

Cat.No: T61561

VEGFR-2-IN-19

Cat.No: T61137

VEGFR-2/DHFR-IN-2

Cat.No: T61229

VEGFR-2/DHFR-IN-1

Cat.No: T61489

TIE-2/VEGFR-2 kinase-IN-4

Cat.No: T79859

FGFR1/VEGFR2-IN-1

Cat.No: T78845

Target: VEGFR

VEGFR-2-IN-27

Cat.No: T62901

VEGFR-2/BRAF-IN-1

Cat.No: T72607

Cat. No.	Product Name	Target	Signaling Pathways
T9715	Aplidine	SARS-CoV; DNA/RNA Synthesis	Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology
	Aplidine 是有效的eEF1A2(KD=80 nM) 靶向的抗癌药物。Aplidine 具有抗病毒活性，抑制SARS-CoV-2的 IC90为 0.88 nM。Aplidine 在多发性骨髓瘤，晚期癌症及 COVID-19 领域有研究的价值。
T1152	Albendazole SKF-62979,阿苯达唑	HIF/HIF Prolyl-Hydroxylase; Microtubule Associated; Antibiotic; Parasite	Chromatin/Epigenetic; Cytoskeletal Signaling; Metabolism; Microbiology/Virology
	Albendazole (SKF-62979) 是一种广谱抗寄生虫剂，具有高效，低宿主毒性的特点。它用于研究人类和动物的胃肠道寄生虫。
TWA2417	Sodium taurocholate 牛黄胆酸钠(牛胆酸钠，牛胆酸钠盐，牛磺膽酸鈉，牛磺胆酸钠，牛磺胆酸钠盐，牛胆酸钠水合物，水合牛磺胆酸钠，牛胆酸钠(混合物)，牛黄胆酸钠(水合)，牛磺胆酸钠(标准品)),Taurocholate Sodium	Others	Others
	Sodium taurocholate (Taurocholate Sodium) hydrate 具有显著的生物学效应，例如通过上调 VEGF-A 的表达抑制肝动脉结扎所致的胆道损伤。对免疫系统具有一定的调节作用。
T17280	(Z)-Guggulsterone	Apoptosis; VEGFR; Akt	Angiogenesis; Apoptosis; Cytoskeletal Signaling; PI3K/Akt/mTOR signaling; Tyrosine Kinase/Adaptors
	(Z)-Guggulsterone 是印度阿育吠陀药用植物Commiphora mukul 的成分，可通过引起细胞凋亡来抑制人前列腺癌细胞的生长，还可通过抑制VEGF-VEGF-R2-Akt 信号传导轴来抑制血管生成。
TC0036	Compound Lup-20(29)-en-3-yl acetate	IL Receptor; VEGFR; Others; TNF; COX	Angiogenesis; Apoptosis; Immunology/Inflammation; Neuroscience; Others; Tyrosine Kinase/Adaptors
	Lup-20(29)-en-3-yl acetate 是 Lupeol 的衍生物，通过下调 TNF-α、IL-1β、MCP-1、COX-2、VEGF 和颗粒酶 B 来抑制类风湿性关节炎的进展。
TQ0169	Inulicin 1-O-Acetylbritannilactone,旋覆花内酯	FAK; NF-κB; COX; Src	Angiogenesis; Cytoskeletal Signaling; Immunology/Inflammation; Neuroscience; NF-κB; Tyrosine Kinase/Adaptors
	Inulicin (1-O-Acetylbritannilactone) 是从欧亚旋覆花中提取的一种天然产物，可抑制 VEGF 介导的Src 和FAK 活化，抑制NF-κB 活化和易位，以及抑制 LPS 诱导的PGE2产生和COX-2表达。
T3250	Royal Jelly acid 10-羟基-2-癸烯酸(10-HAD),蜂王浆酸,王浆酸,10-Hydroxy-trans-2-decenoic acid,10-Hydroxy-2-decenoic acid,10H2DA,10-Hydroxy-2-decylenic acid,Queen Bee Acid,(E)-10-Hydroxy-2-decenoic acid	VEGFR; Endogenous Metabolite	Angiogenesis; Metabolism; Tyrosine Kinase/Adaptors
	Royal Jelly acid (Queen Bee Acid) 是一种蜂王浆中的主要脂肪酸，可促进神经元的生长和保护，减少焦虑。
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。
T7203	Oglufanide 奥谷法奈,L-Glutamyl-L-tryptophan,H-Glu-Trp-OH	VEGFR; HCV Protease; Endogenous Metabolite	Angiogenesis; Metabolism; Microbiology/Virology; Proteases/Proteasome; Tyrosine Kinase/Adaptors
	Oglufanide (H-Glu-Trp-OH) 是一种从小牛胸腺中分离出来的二肽免疫调节剂，可抑制血管内皮生长因子，可刺激细胞内细菌感染和对丙型肝炎病毒的免疫反应。
T3S0335	Soyasaponin Bb Soyasaponin I,大豆皂苷Bb	NF-κB; Caspase	Apoptosis; NF-κB; Proteases/Proteasome
	Soyasaponin Bb (Soyasaponin I) 是一种分离自菜豆科中的大豆皂苷，可用作醛糖还原酶差异抑制剂。
T5429	Theaflavin 3,3'-digallate 茶黄素-3,3'-双没食子酸,8-Gingerol,TFDG	Virus Protease; Antioxidant; HIV Protease; HSV	Microbiology/Virology; oxidation-reduction; Proteases/Proteasome
	Theaflavin 3,3'-digallate (8-Gingerol) 是一种寨卡病毒蛋白酶抑制剂，IC50为 2.3 μM。它直接与 ZIKVpro 结合并抑制 ZIKV 复制，可抑制 gp41 和 NS2B-3 蛋白酶的活性，并具有抗 HSV 和 HIV-1病毒活性。它是红茶中的主要多酚，有抗肿瘤作用。
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。
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。
T2906	Tanshinone IIA 丹参酮IIA,Tanshinone B,Dan Shen ketone	VEGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	Tanshinone IIA (Tanshinone B) 是红根丹参根系中的一种主要组合物。它能够利用靶向 VEGF/VEGFR2的蛋白激酶结构域，抑制血管生成。
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。
T4S1551	Cinnamaldehyde Cinnamic Aldehyde,肉桂醛	HIF	Angiogenesis; Chromatin/Epigenetic
	Cinnamaldehyde (Cinnamic Aldehyde) 具有解热作用。它是镇静剂。它抑制MDA-MB-435S 细胞的侵袭能力与下调miR-27a 的表达有关。它诱导活性氧的产生，发挥血管扩张和抗癌作用。它似乎是一种有希望的候选药物，可作为与 5-氟尿嘧啶 (5-FU) 和奥沙利铂 (OXA) 这两种用于 CRC 治疗的化疗药物联合治疗的辅助剂。其作用的可能机制可能涉及药物代谢基因的调节。它在抑制黑色素瘤的发生和发展方面具有一定的作用，其作用机制可能表现为抑制VEGF 和HIF-α的表达，从而使血管模拟和黑色素瘤细胞新生血管的形成，促进肿瘤的生长。
T3S2344	β,β-Dimethylacrylshikonin β,β-二甲基丙烯酰紫草素,Dimethylacrylshikonin,β, β-Dimethylacrylshikonin	ERK; HIF/HIF Prolyl-Hydroxylase	Chromatin/Epigenetic; MAPK; Metabolism
	β,β-Dimethylacrylshikonin (Dimethylacrylshikonin) 是一种萘醌衍生物，从 Arnebia nobilis 中提取得到。它利用 PI3K 通路诱导 eNOS、VEGF 和 HIF-1α 的表达，促进血管生成，具有抗肿瘤活性。
TN3139	5α-Hydroxycostic acid 5alpha-Hydroxycostic acid	ERK; FAK; Phospholipase; NOS; Akt; Src	Angiogenesis; Cytoskeletal Signaling; Immunology/Inflammation; MAPK; Metabolism; PI3K/Akt/mTOR signaling; Tyrosine Kinase/Adaptors
	5alpha-Hydroxycostic acid possesses anti-angiogenic ability by interfering the VEGF- and Ang2-related pathways, and it may be a good drug candidate.
TN1874	Liriodendrin 鹅掌楸苦素	ATPase; Potassium Channel; Prostaglandin Receptor	GPCR/G Protein; Immunology/Inflammation; Membrane transporter/Ion channel
	Liriodendrin 调节肺部炎症、NF-kB (p65) 的磷酸化和血管内皮生长因子 (VEGF) 的表达。Liriodendrin 具有抗炎、镇痛、降血糖活性，在脓毒症引起的急性肺损伤中起保护作用。
T14055	5Z-7-Oxozeaenol FR148083,L783279,LL-Z 1640-2	VEGFR; FLT; MEK; MAPK; PDGFR; Antibiotic; Src	Angiogenesis; MAPK; Microbiology/Virology; Tyrosine Kinase/Adaptors
	5Z-7-Oxozeaenol (FR148083) 是一种天然抗原生动物抑制剂，不可逆的选择性抑制 TAK1和 VEGF-R2，IC50值分别为 8 nM 和 52 nM。
TN5942	Dammarenediol II 达玛烯二醇II,Dammar-24-ene-3,20-diol
	Dammarenediol II may have the ability to prevent diabetic microvascular complications, including diabetic retinopathy, it can inhibit vascular endothelial growth factor (VEGF)-induced intracellular reactive oxygen species generation and stress fiber forma
TN4356	Jolkinolide A	Akt; STAT; mTOR	Cytoskeletal Signaling; JAK/STAT signaling; PI3K/Akt/mTOR signaling; Stem Cells
	Jolkinolide A has anti-tumor activity. It inhibited VEGF expression in A549 cells through the inhibition of the Akt-STAT3-mTOR signaling pathway, and directly inhibited the proliferation and migration of HUVECs.
T75487	7-Hydroxyneolamellarin A
	7-Hydroxyneolamellarin A，一种从海绵Dendrilla nigra 提取的天然产物，是高效的缺氧诱导因子 1α (HIF-1α) 抑制剂。该化合物能够减弱HIF-1α蛋白的积累，并抑制血管表皮生长因子 (VEGF) 的转录活性，因而在癌症研究中有应用价值。
T36749	Herboxidiene
	Herboxidiene is a polyketide originally isolated from S. chromofuscus that has diverse biological activities.[1],[2,][3],[4],[5] It inhibits growth of HeLa S3, SK-MEL-2, PC3, A549, and EBC-1 cells with GI50 values ranging from 7.4 to 62 nM.3 Herboxidiene is cytostatic against human umbilical vein endothelial cells (HUVECs; (IC50 = 26 nM)) and inhibits VEGF-induced invasion and tube formation of serum-starved HUVECs in a concentration-dependent manner, indicating antiangiogenic activity.[4] Herbo...

天然产物

Cat.No: T9715

Target: SARS-CoV, DNA/RNA Synthesis

Cat.No: T1152

Synonym: SKF-62979,阿苯达唑

Target: HIF/HIF Prolyl-Hydroxylase, Microtubule Associated, Antibiotic, Parasite

Sodium taurocholate

Cat.No: TWA2417

Synonym: 牛黄胆酸钠(牛胆酸钠，牛胆酸钠盐，牛磺膽酸鈉，牛磺胆酸钠，牛磺胆酸钠盐，牛胆酸钠水合物，水合牛磺胆酸钠，牛胆酸钠(混合物)，牛黄胆酸钠(水合)，牛磺胆酸钠(标准品)),Taurocholate Sodium

Target: Others

(Z)-Guggulsterone

Cat.No: T17280

Target: Apoptosis, VEGFR, Akt

Compound Lup-20(29)-en-3-yl acetate

Cat.No: TC0036

Target: IL Receptor, VEGFR, Others, TNF, COX

Cat.No: TQ0169

Synonym: 1-O-Acetylbritannilactone,旋覆花内酯

Target: FAK, NF-κB, COX, Src

Royal Jelly acid

Cat.No: T3250

Synonym: 10-羟基-2-癸烯酸(10-HAD),蜂王浆酸,王浆酸,10-Hydroxy-trans-2-decenoic acid,10-Hydroxy-2-decenoic acid,10H2DA,10-Hydroxy-2-decylenic acid,Queen Bee Acid,(E)-10-Hydroxy-2-decenoic acid

Target: VEGFR, Endogenous Metabolite

Cat.No: T3890

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

Target: Others

Cat.No: T7203

Synonym: 奥谷法奈,L-Glutamyl-L-tryptophan,H-Glu-Trp-OH

Target: VEGFR, HCV Protease, Endogenous Metabolite

Cat.No: T3S0335

Synonym: Soyasaponin I,大豆皂苷Bb

Target: NF-κB, Caspase

Theaflavin 3,3'-digallate

Cat.No: T5429

Synonym: 茶黄素-3,3'-双没食子酸,8-Gingerol,TFDG

Target: Virus Protease, Antioxidant, HIV Protease, HSV

Decursinol angelate

Cat.No: TN1557

Target: ERK, VEGFR, PKC, JNK

25(R,S)-Ruscogenin

Cat.No: T5740

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

Target: Others, HIF

Cat.No: T2906

Synonym: 丹参酮IIA,Tanshinone B,Dan Shen ketone

Target: VEGFR

Cat.No: T3780

Synonym: Hypocretin-2,木蝴蝶苷B

Target: Apoptosis, PTEN, Antioxidant, PI3K, Autophagy

Cat.No: T4S1551

Synonym: Cinnamic Aldehyde,肉桂醛

Target: HIF

β,β-Dimethylacrylshikonin

Cat.No: T3S2344

Synonym: β,β-二甲基丙烯酰紫草素,Dimethylacrylshikonin,β, β-Dimethylacrylshikonin

Target: ERK, HIF/HIF Prolyl-Hydroxylase

5α-Hydroxycostic acid

Cat.No: TN3139

Synonym: 5alpha-Hydroxycostic acid

Target: ERK, FAK, Phospholipase, NOS, Akt, Src

Cat.No: TN1874

Synonym: 鹅掌楸苦素

Target: ATPase, Potassium Channel, Prostaglandin Receptor

5Z-7-Oxozeaenol

Cat.No: T14055

Synonym: FR148083,L783279,LL-Z 1640-2

Target: VEGFR, FLT, MEK, MAPK, PDGFR, Antibiotic, Src

Dammarenediol II

Cat.No: TN5942

Synonym: 达玛烯二醇II,Dammar-24-ene-3,20-diol

Cat.No: TN4356

Target: Akt, STAT, mTOR

7-Hydroxyneolamellarin A

Cat.No: T75487

Cat.No: T36749

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