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Search Results for " hif-1α inhibitor "

50

抑制剂 & 化合物

6

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Cat. No.	Product Name	Target	Signaling Pathways
T3494	LW6 HIF-1α inhibitor,CAY10585,LW8	Apoptosis; Dehydrogenase; HIF/HIF Prolyl-Hydroxylase; HIF	Angiogenesis; Apoptosis; Chromatin/Epigenetic; Metabolism
	LW6 (HIF-1α inhibitor) 是一种新型 HIF-1抑制剂，IC50值为 4.4 μM。它降低 HIF-1α蛋白表达，但不影响 HIF-1β 表达。
T36711	FM19G11 FM19G11,HIF-1alpha/2alpha Inhibitor	HIF	Angiogenesis; Chromatin/Epigenetic
	FM19G11 是一种低氧诱导因子 (HIF) α-亚基抑制剂（在低氧诱导的荧光素酶试验中 IC50 为 80 nM）。
T21653	1,4-DPCA	HIF/HIF Prolyl-Hydroxylase	Chromatin/Epigenetic; Metabolism
	1,4-DPCA 是一种脯氨酰羟化酶抑制剂，对人源包皮成纤维细胞中胶原羟基化的 IC50 为 2.4 μM，对因子抑制 HIF (FIH) 的 IC50 为 60 μM。
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。
T0692	Allopurinol Zyloric,别嘌醇,Zyloprim,Lopurin,别嘌呤醇	ROS; Xanthine Oxidase	Immunology/Inflammation; Metabolism
	Allopurinol (Zyloric) 是一种黄嘌呤氧化酶(XO)抑制剂，IC50=7.82±0.12 μM。
T71659	Indacaterol acetate
	Indacaterol acetate is an ultra-long-acting beta-adrenoceptor agonist.
T6376	Allopurinol Sodium 1H-吡唑并[3,4-D]嘧啶-4-醇单钠盐,Allopurinol sodium salt,Sodium allopurinol	ROS	Immunology/Inflammation
	Allopurinol Sodium 是黄嘌呤氧化酶抑制剂，其IC50= 0.2~50 μM。它能够抗利什曼原虫，也可用于研究痛风以及高尿酸血症。
T71661	HIF-1α inhibitor-1
	HIF-1α inhibitor-1 is a HIF-1 alpha inhibitor.
T67767	HIF-1 inhibitor-4 HIF-1 inhibitor-4	HIF	Angiogenesis; Chromatin/Epigenetic
	HIF-1 inhibitor-4 (HIF-1 inhibitor-4) 是一种 HIF-1 抑制剂 (IC50: 560 nM)。HIF-1 inhibitor-4 减少 HIF-1α 蛋白水平，但不影响 mRNA 水平。
T36290	HIF-1 inhibitor-1
	HIF-1 inhibitor-1 is an aryl carboxamide compound and a potent hypoxia-inducible factor 1 (HIF-1) inhibitor with an IC50 of 0.32 μM for the cancer metastasi[1]. [1]. Liu M, et al. Discovery of Novel Aryl Carboxamide Derivatives as Hypoxia-Inducible Factor 1α Signaling Inhibitors with Potent Activities of Anticancer Metastasis. J Med Chem. 2019 Oct 24;62(20):9299-9314.
T74804	HIF-1 inhibitor-5
	HIF-1 inhibitor-5 (Compound 16e) 是一种有效的 HIF-1抑制剂，其 IC50为 2.38 μM。HIF-1 inhibitor-5 具有抗血管生成潜能。
T61349	HIF-1α-IN-2	HIF	Angiogenesis; Chromatin/Epigenetic
	HIF-1α-IN-2 是一种新型高效的 HIF-1α 抑制剂，具有抗癌抗肿瘤活性，以剂量依赖的方式抑制 HIF-1α 和 VEGF 的表达，抑制细胞迁移。
T15396	GN44028 N-(2,3-Dihydro-1,4-benzodioxin-6-yl)-1,4-dihydroindeno[1,2-c]pyrazol-3-amine	HIF	Angiogenesis; Chromatin/Epigenetic
	GN44028 (N-(2,3-Dihydro-1,4-benzodioxin-6-yl)-1,4-dihydroindeno[1,2-c]pyrazol-3-amine) 是缺氧诱导因子(HIF)-1的有效抑制剂，其 IC50=14 nM。它可以抑制低氧诱导的 HIF-1α 的转录特性，但不抑制 HIF-1α mRNA 的表达，HIF-1α 蛋白的累积或HIF-1α/HIF-1β 的异缘二聚化。
T19832	Acriflavine Hydrochloride 盐酸吖啶黄,Acriflavine HCl	HIF	Angiogenesis; Chromatin/Epigenetic
	Acriflavine Hydrochloride (Acriflavine HCl) 是一种 HIF-1α 抑制剂。它通过靶向 HIF-1α 介导的途径并在体外和体内降低 PGK1、VEGF 和 HIF-1α 的水平发挥作用。
T60413	HIF-IN-1	HIF	Angiogenesis; Chromatin/Epigenetic
	HIF-IN-1 是一种有效的缺氧诱导因子 (HIF-1) 抑制剂，与肿瘤和癌细胞的增殖有关，对 HIF-1α 蛋白聚集有抑制作用。
T13398	ZINC13466751	HIF	Angiogenesis; Chromatin/Epigenetic
	ZINC13466751 是有效的 HIF-1α/von Hippel-Lindau 相互作用抑制剂，抑制作用的 IC50为 2.0 µM。
T17009	TC-S 7009	HIF	Angiogenesis; Chromatin/Epigenetic
	TC-S 7009是一种有效的和具有选择性的HIF-2α抑制剂(Kd: 81 nM)。TC-S 7009对HIF-2α的亲和力大于HIF-1α (Kd >> 5 μM)。 TC-S 7009破坏HIF-2α异源二聚化，降低HIF-2α靶基因表达，降低dna 结合活性。
T29106	VH032 VH-032,VH 032	Ligand for E3 Ligase	PROTAC
	VH032通常用作 PROTAC 的前体，作为 E3泛素连接酶组件连接 VHL，是一种与 KdPROTACs 相互作用的 VHL/HIF-1α抑制剂，作为von Hippel-Lindau (VHL)的配体招募VHL 蛋白。
T1939	DMOG Dimethyloxalylglycine,Dimethyloxallyl Glycine,Dimethyloxaloylglycine,二甲基草酰甘氨酸	HIF/HIF Prolyl-Hydroxylase; HIF; Autophagy	Angiogenesis; Autophagy; Chromatin/Epigenetic; Metabolism
	DMOG (Dimethyloxalylglycine) 是 α-酮戊二酸辅因子的拮抗剂，是一种 HIF 脯氨酰羟化酶抑制剂，可导致蛋白HIF-1α的积聚和稳定，诱导细胞自噬。它是一种促血管生成剂，在结肠炎和腹泻动物模型中起保护作用。
T1637	Deferoxamine Mesylate desferrioxamine B,Desferrioxamine B mesylate,DFO,DFOM,去铁铵,甲磺酸去铁胺	Mitophagy; Beta Amyloid; Others; Ferroptosis; HIF/HIF Prolyl-Hydroxylase; Autophagy	Apoptosis; Autophagy; Chromatin/Epigenetic; Metabolism; Neuroscience; Others
	Deferoxamine Mesylate (DFOM) 是一种铁螯合剂和铁死亡抑制剂。Deferoxamine Mesylate 可将游离铁结合成稳定的复合物，减少铁的积累。Deferoxamine Mesylate 可以上调 HIF-1α 水平，诱导细胞凋亡。
T6961	PX-478 PX-478 2HCl	HIF/HIF Prolyl-Hydroxylase; HIF; Autophagy	Angiogenesis; Autophagy; Chromatin/Epigenetic; Metabolism
	PX-478 是一种 HIF-1α 抑制剂，具有选择性、口服活性和血脑屏障渗透性。PX-478 具有抗肿瘤活性，还可以保护糖尿病中的胰腺 β 细胞功能，用于 2 型糖尿病的研究。
T67836	AT-533	HSP; HSV	Cytoskeletal Signaling; Metabolism; Microbiology/Virology
	AT-533 是有效的 HSV 和 Hsp90 抑制剂。AT-533 可以阻断 HIF-1α/VEGF/VEGFR-2 信号通路，从而抑制血管生成和肿瘤生长。AT-533 也抑制下游通路的激活，包括 Erk1/2, FAK, Akt/mTOR/p70S6K。AT-533 抑制人脐静脉内皮细胞 (HUVEC) 的细胞迁移、侵袭和管形成。
T4381	Lificiguat 利非西呱,YC-1	Others; Guanylate cyclase; HIF	Angiogenesis; Chromatin/Epigenetic; GPCR/G Protein; Others
	Lificiguat (YC-1) 是一种不依赖一氧化氮的可溶性鸟苷酸环化酶激活剂和低氧诱导因子 1α 的抑制剂。
T2309	Ganetespib STA-9090	Apoptosis; HSP; HIF	Angiogenesis; Apoptosis; Chromatin/Epigenetic; Cytoskeletal Signaling; Metabolism
	Ganetespib (STA-9090) 是一种热休克蛋白 90 抑制剂，通过抑制 HIF-1α 和 STAT3 对大肠癌具有抗血管生成作用。它还具有细胞毒性。
T2283	PX-12 2-[(1-甲基丙基)二硫代]-1H-咪唑,IV-2,PX12	Thioredoxin	Metabolism
	PX-12 (PX12) 是一种可逆的硫氧还蛋白-1(Trx-1)抑制剂，能够抑制 MCF-7 细胞(IC50:1.9 μM)和HT-29 细胞(IC50:2.9 μM)的生长。
T70788	KST012174 HCl
	KST012174 is a HIF-1α inhibitor. KST012174 involves in the HIF-1α/p300 protein−protein interaction.
T68718	103D5R
	103D5R is a novel selective inhibitor of hif-1α, markedly decreasing hif-1α protein levels induced by hypoxia or cobaltous ions in a dose- and time-dependent manner
T82595	DEALA-Hyp-YIPD
	DEALA-Hyp-YIPD为HIF-1α抑制剂，阻断VHL/HIF-1α相互作用，显示IC50值为0.91 μM，Kd为180 nM。
T82198	HIF-1α-IN-6	HIF/HIF Prolyl-Hydroxylase	Chromatin/Epigenetic; Metabolism
	HIF-1α-IN-6 (compound 3s) 为HIF-1α抑制剂，MiaPaCa-2 和 MDA-MB-231 细胞中IC50分别为 0.6 nM 和 53.3 nM。它通过减少HIF-1α mRNA水平来抑制HIF-1α表达。
T60398	Dimethyl-bisphenol A
	Dimethyl-bisphenol A (DMBPA) 是有效的HIF-1α抑制剂，通过从 HIF-1α 解离 Hsp90 促进 HIF-1α 蛋白的降解。Dimethyl-bisphenol A 可降低 Vegfa mRNA 的表达。
T61161	HIF-1α-IN-3
	HIF-1α-IN-3, also known as Compound (S)-3f, is a hypoxia-selective inhibitor of HIF-1α. It exhibits potent antiestrogenic activity [1].
T6804	Chetomin Chaetomin,NSC289491,BRN0077366	Apoptosis; HSP; HIF	Angiogenesis; Apoptosis; Chromatin/Epigenetic; Cytoskeletal Signaling; Metabolism
	Chetomin (BRN0077366) 是球毛壳菌的活性成分，是一种无毒的非小细胞肺癌干细胞靶向分子。它是一种热休克蛋白90/缺氧诱导因子1α 途径的抑制剂。
T10258	AFP464 free base NSC710464 free base	HIF	Angiogenesis; Chromatin/Epigenetic
	AFP464 (NSC710464) free base is an active HIF-1α inhibitor (IC50: 0.25 μM) and a potent aryl hydrocarbon receptor (AhR) activator.
T60532	HIF-1α-IN-5
	HIF-1α-IN-5 是 HIF-1α的抑制剂，在 HEK293T 细胞中的 IC50值为 24 nM，也可抑制 MAO-A 的活性。在缺氧条件下， HIF-1α-IN-5可下调 VEGF 和 PDK1 mRNA 的表达。HIF-1α-IN-5 具有用于癌症研究的潜力。
T24148	HPCG
	HPCG is an inhibitor of HIF-1α prolyl hydroxylase.
T23988	DHPCG
	DHPCG is an inhibitor of HIF-1α prolyl hydroxylase.
T60524	HIF-1α-IN-4
	HIF-1α-IN-4 是 HIF-1α抑制剂，在 HEK293T 细胞中的IC50值为 24 nM，具有潜在的抗肿瘤作用。 HIF-1α-IN-4 在缺氧条件下下调 VEGF 和 PDK1 mRNA 的表达。
T27866	LXY6090 LXY 6090,LXY-6090
	LXY6090 is a HIF-1 inhibitor. LXY6090 inhibited the activity of HIF-1 and downregulated the protein level of HIF-1α in breast cancer cells. LXY6090 showed in vivo anticancer efficacy by decreasing the HIF-1α expression in nude mice bearing MX-1 tumor xeno
T26573	AG311 AG 311,AG-311
	AG311 is an inhibitor of complex I and hypoxia-induced HIF-1α stabilization. In vitro, AG311 induces rapid necrosis in numerous cancer cell lines. Within minutes, exposure to AG311 also results in mitochondrial depolarization, superoxide production, and i
T78123	HIF-1α-IN-2 hydrochloride	HIF/HIF Prolyl-Hydroxylase	Chromatin/Epigenetic; Metabolism
	HIF-1α-IN-2 hydrochloride 是一款有效的 HIF-1α 抑制剂，对抗癌活性显著，其在MDA-MB-231细胞和MiaPaCa-2细胞中的IC50值分别为28 nM和15 nM。该化合物主要通过抑制转录和阻碍蛋白质合成来下调HIF-1α的表达。
T61442	HIF-1/2α-IN-1
	HIF-1/2α-IN-1, an orally active compound, functions as an inhibitor of HIF-2α. Its inhibitory effect on HIF-2α activity is significant, with an IC 50 value of 0.92 μM. Furthermore, HIF-1/2α-IN-1 has the ability to decrease HIF-1α levels. This compound is particularly valuable for research on clear cell renal cell carcinoma (ccRCC) [1].
T71116	MPT0B098
	MPT0B098 is a potent microtubule inhibitor through binding to the colchicine-binding site of tubulin. MPT0B098 is active against the growth of various human cancer cells, including chemoresistant cells with IC50 values ranging from 70 to 150 nmol/L. MPT0B098 arrests cells in the G2Â–M phase and subsequently induces cell apoptosis. In addition, MPT0B098 effectively suppresses VEGF-induced cell migration and capillary-like tube formation of HUVECs. Distinguished from other microtubule inhibitors, ...
T74530	GEM-5
	GEM-5为基于吉西他滨且含HIF-1α抑制剂(YC-1)的偶联物，IC50值为30 nM。此化合物能有效降低HIF-1α表达，并提高肿瘤抑制因子p53的表达量。GEM-5可诱导A2780细胞的凋亡(apoptosis)，进而抑制肿瘤生长。
T63035	Izilendustat hydrochloride
	Izilendustat (hydrochloride) 是一种脯氨酰羟化酶 (prolyl hydroxylase) 的有效抑制剂，能够稳定缺氧诱导因子-1 α (HIF-1α) 和缺氧诱导因子-2 (HIF-2)。Izilendustat (hydrochloride) 具有潜力进行 HIF-1α 相关疾病的研究（包括外周血管疾病（PVD）、心力衰竭、冠状动脉疾病（CAD）、缺血、贫血、结肠炎和其他炎症性肠病）。
T75943	TAT-cyclo-CLLFVY TFA
	TAT-cyclo-CLLFVY TFA 是一种 HIF-1异二聚化的环肽抑制剂，可抑制癌细胞中的缺氧信号传导。TAT-cyclo-CLLFVY TFA 破坏 HIF-1α/HIF-1β蛋白相互作用，IC50为 1.3 μM。
T79720	VHL-IN-1	HIF/HIF Prolyl-Hydroxylase	Chromatin/Epigenetic; Metabolism
	VHL-IN-1 (compound 30) 为泛素 E3 连接酶 von Hippel-Lindau (VHL) 的抑制剂，其解离常数 Kd 为 37 nM，能够稳定并激活 HIF-1α 转录功能。此化合物具备作为 HIF-1α 稳定剂以及蛋白水解靶向嵌合体(PROTACs) 降解剂的应用潜力。
TP2046	TAT-cyclo-CLLFVY
	Selective HIF-1 dimerization inhibitor. Blocks protein-protein interaction of recombinant HIF-1α, but not HIF-2α, with HIF-1β (IC50 = 1.3 μM). Inhibits hypoxia-induced HIF-1 activity, and decreases VEGF and CAIX expression in osteosarcoma and breast cance
T60539	KG-548
	KG-548 是一种ARNT/TACC3干扰剂以及HIF-1α抑制剂。KG-548 通过 ARNT 的 PAS-B 结构域与 TACC3 竞争性结合，直接干扰ARNT/TACC3复合物的形成。ARNT 是芳基烃受体核转运蛋白，也称为 HIF-β。
T18667	(S,R,S)-AHPC-C5-COOH VH032-C5-COOH	Others	Others
	(S,R,S)-AHPC-C5-COOH (VH032-C5-COOH) is a synthesized E3 ligase ligand-linker conjugate, contains the VH032 VHL-based ligand and a linker to form PROTACs. VH-032 is a selective and potent inhibitor of VHL/HIF-1α interaction with a Kd of 185 nM, has the potential for the study of anemia and ischemic diseases[1].
T69966	Roxadustat-d5
	Roxadustat-d5 is intended for use as an internal standard for the quantification of roxadustat by GC- or LC-MS. Roxadustat is an inhibitor of hypoxia-inducible factor prolyl hydroxylase (HIF-PH; IC50s = 1.4, 1.26, and 1.32 µM for HIF-PH1, HIF-PH2, and HIF-PH3, respectively). It is selective for HIF-PH over other 2-oxoglutarate-dependent dioxygenases, including lysine-specific demethylase 5A (KDM5A), KDM5B, -5C, -5D, and -6B (IC50s = >100 µM for all). Roxadustat (10-200 µM) stabilizes HIF-1α and ...

化合物

Cat.No: T3494

Synonym: HIF-1α inhibitor,CAY10585,LW8

Target: Apoptosis, Dehydrogenase, HIF/HIF Prolyl-Hydroxylase, HIF

Cat.No: T36711

Synonym: FM19G11,HIF-1alpha/2alpha Inhibitor

Target: HIF

Cat.No: T21653

Target: HIF/HIF Prolyl-Hydroxylase

Cat.No: T8973

Target: Others

Cat.No: T0692

Synonym: Zyloric,别嘌醇,Zyloprim,Lopurin,别嘌呤醇

Target: ROS, Xanthine Oxidase

Indacaterol acetate

Cat.No: T71659

Allopurinol Sodium

Cat.No: T6376

Synonym: 1H-吡唑并[3,4-D]嘧啶-4-醇单钠盐,Allopurinol sodium salt,Sodium allopurinol

Target: ROS

HIF-1α inhibitor-1

Cat.No: T71661

HIF-1 inhibitor-4

Cat.No: T67767

Synonym: HIF-1 inhibitor-4

Target: HIF

HIF-1 inhibitor-1

Cat.No: T36290

HIF-1 inhibitor-5

Cat.No: T74804

Cat.No: T61349

Target: HIF

Cat.No: T15396

Synonym: N-(2,3-Dihydro-1,4-benzodioxin-6-yl)-1,4-dihydroindeno[1,2-c]pyrazol-3-amine

Target: HIF

Acriflavine Hydrochloride

Cat.No: T19832

Synonym: 盐酸吖啶黄,Acriflavine HCl

Target: HIF

Cat.No: T60413

Target: HIF

Cat.No: T13398

Target: HIF

Cat.No: T17009

Target: HIF

Cat.No: T29106

Synonym: VH-032,VH 032

Target: Ligand for E3 Ligase

Cat.No: T1939

Synonym: Dimethyloxalylglycine,Dimethyloxallyl Glycine,Dimethyloxaloylglycine,二甲基草酰甘氨酸

Target: HIF/HIF Prolyl-Hydroxylase, HIF, Autophagy

Deferoxamine Mesylate

Cat.No: T1637

Synonym: desferrioxamine B,Desferrioxamine B mesylate,DFO,DFOM,去铁铵,甲磺酸去铁胺

Target: Mitophagy, Beta Amyloid, Others, Ferroptosis, HIF/HIF Prolyl-Hydroxylase, Autophagy

Cat.No: T6961

Synonym: PX-478 2HCl

Target: HIF/HIF Prolyl-Hydroxylase, HIF, Autophagy

Cat.No: T67836

Target: HSP, HSV

Cat.No: T4381

Synonym: 利非西呱,YC-1

Target: Others, Guanylate cyclase, HIF

Cat.No: T2309

Synonym: STA-9090

Target: Apoptosis, HSP, HIF

Cat.No: T2283

Synonym: 2-[(1-甲基丙基)二硫代]-1H-咪唑,IV-2,PX12

Target: Thioredoxin

Cat.No: T70788

Cat.No: T68718

Cat.No: T82595

Cat.No: T82198

Target: HIF/HIF Prolyl-Hydroxylase

Dimethyl-bisphenol A

Cat.No: T60398

Cat.No: T61161

Cat.No: T6804

Synonym: Chaetomin,NSC289491,BRN0077366

Target: Apoptosis, HSP, HIF

AFP464 free base

Cat.No: T10258

Synonym: NSC710464 free base

Target: HIF

Cat.No: T60532

Cat.No: T24148

Cat.No: T23988

Cat.No: T60524

Cat.No: T27866

Synonym: LXY 6090,LXY-6090

Cat.No: T26573

Synonym: AG 311,AG-311

HIF-1α-IN-2 hydrochloride

Cat.No: T78123

Target: HIF/HIF Prolyl-Hydroxylase

HIF-1/2α-IN-1

Cat.No: T61442

Cat.No: T71116

Cat.No: T74530

Izilendustat hydrochloride

Cat.No: T63035

TAT-cyclo-CLLFVY TFA

Cat.No: T75943

Cat.No: T79720

Target: HIF/HIF Prolyl-Hydroxylase

TAT-cyclo-CLLFVY

Cat.No: TP2046

Cat.No: T60539

(S,R,S)-AHPC-C5-COOH

Cat.No: T18667

Synonym: VH032-C5-COOH

Target: Others

Cat.No: T69966

Cat. No.	Product Name	Target	Signaling Pathways
T3860	Isoliquiritin apioside	MMP; p38 MAPK; NF-κB	MAPK; NF-κB; Proteases/Proteasome
	Isoliquiritin apioside 可抑制癌细胞和内皮细胞的侵袭和血管生成，显著降低 PMA 诱导的MMP9活性增加，并抑制 PMA 诱导的MAPK 和NF-κB 活化。
T11589	Hydroxycitric acid tripotassium hydrate 柠檬酸钾一水合物,三水合钾柠檬酸,Potassium citrate monohydrate	ATP Citrate Lyase; HIF/HIF Prolyl-Hydroxylase; HIF	Angiogenesis; Chromatin/Epigenetic; Metabolism
	Hydroxycitric acid tripotassium hydrate (Potassium citrate monohydrate) 是一种藤黄果的主要活性成分，也是一种柠檬酸的衍生物。它可竞争性抑制柠檬酸裂解酶 (ATP citrate lyase) ，并具有减肥作用。它有效抑制结石形成，并抑制HIF，具有抗氧化，抗炎和抗肿瘤活性。
T0256	Citric acid trilithium salt tetrahydrate Lithium citrate tribasic tetrahydrate,柠檬酸三锂盐四水合物,Trilithium citrate tetrahydrate	Dehydrogenase; GSK-3; HIF/HIF Prolyl-Hydroxylase; Antibacterial; GluR	Chromatin/Epigenetic; Metabolism; Microbiology/Virology; Neuroscience; PI3K/Akt/mTOR signaling; Stem Cells
	Citric acid trilithium salt tetrahydrate (Lithium citrate tribasic tetrahydrate) 是一种用于治疗精神疾病的药物。它也是一种医药和建筑材料, 可用于氨基酸定量分析时的梯度洗脱。
T1123	Camptothecin NSC-100880,Campathecin,喜树碱,(S)-(+)-Camptothecin,CPT	Apoptosis; Influenza Virus; Topoisomerase; Antibiotic; Antifungal	Apoptosis; DNA Damage/DNA Repair; Microbiology/Virology
	Camptothecin (CPT) 属于生物碱类天然产物，是一种 DNA 拓扑异构酶 I (Topo I) 的抑制剂 (IC50=679 nM)，具有特异性。Camptothecin 具有抗肿瘤活性，可以诱导细胞凋亡。
T3816	Velutin	NF-κB; HIF/HIF Prolyl-Hydroxylase	Chromatin/Epigenetic; Metabolism; NF-κB
	Velutin 是一种苷元，提取自槲寄生中，能够抑制黑色素生物合成。它利用 NF-κB 途径减少破骨细胞分化和下调 HIF-1α。
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。

天然产物

Isoliquiritin apioside

Cat.No: T3860

Target: MMP, p38 MAPK, NF-κB

Hydroxycitric acid tripotassium hydrate

Cat.No: T11589

Synonym: 柠檬酸钾一水合物,三水合钾柠檬酸,Potassium citrate monohydrate

Target: ATP Citrate Lyase, HIF/HIF Prolyl-Hydroxylase, HIF

Citric acid trilithium salt tetrahydrate

Cat.No: T0256

Synonym: Lithium citrate tribasic tetrahydrate,柠檬酸三锂盐四水合物,Trilithium citrate tetrahydrate

Target: Dehydrogenase, GSK-3, HIF/HIF Prolyl-Hydroxylase, Antibacterial, GluR

Cat.No: T1123

Synonym: NSC-100880,Campathecin,喜树碱,(S)-(+)-Camptothecin,CPT

Target: Apoptosis, Influenza Virus, Topoisomerase, Antibiotic, Antifungal

Cat.No: T3816

Target: NF-κB, HIF/HIF Prolyl-Hydroxylase

7-Hydroxyneolamellarin A

Cat.No: T75487

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