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Search Results for " anti-metastatic "

40

抑制剂 & 化合物

12

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T9582	CLEFMA	NF-κB	NF-κB
	CLEFMA 是一种姜黄素，抑制肿瘤生长与 NF-κB 调节的抗炎和抗转移作用有关，具有抗肿瘤活性。
T8310	MMP-9-IN-1	MMP	Proteases/Proteasome
	MMP-9-IN-1 是特异性的基质金属蛋白酶-9 抑制剂，选择性靶向 MMP-9 的血红素域，对其他 MMP 无影响。
T5125	LY3200882	TGF-beta/Smad	Stem Cells
	LY3200882 是一种高度选择性的、口服活性的、具有 ATP 竞争性的 TGF-β 受体 1 型 (ALK5) 抑制剂(IC50:38.2 nM)。它能够抑制多种促肿瘤活性，可用作免疫调节剂。
T9236	WSB1 Degrader 1	Others; E1/E2/E3 Enzyme	Others; Ubiquitination
	WSB1 Degrader 1 是具有口服活性的 WSB1降解剂，具有抗癌活性。
T62536	S100P-IN-1	Others	Others
	S100P-IN-1 是一种高效的 S100P 抑制剂。S100P-IN-1 对胰腺癌 (pancreatic) 细胞具有抗转移作用。
T17255	WJ460	Others	Others
	WJ460 是一种有效的肌铁蛋白抑制剂。 WJ460 在乳腺癌细胞中显示出抗转移活性。
T9075	BDP-13176	Others	Others
	BDP-13176 是fascin 1抑制剂，Kd=90 nM，IC50=240 nM。它具有成为抗转移剂的潜力。
T26969	CCT365623 CCT-365623,CCT 365623	Monoamine Oxidase	Neuroscience
	CCT365623 是一种口服生物可利用的赖氨酰氧化酶抑制剂，具有良好的抗 LOX 效力、选择性、药代动力学特性以及抗转移功效。
T77374	Ontuxizumab MORAb-004	Others	Others
	Ontuxizumab (MORAb-004) 是一种靶向内髓酸的单克隆抗体，具有抗肿瘤作用。Ontuxizumab 是一种有效的 IgG1/κ 抗内皮素 (TEM-1 或 CD248) 的单克隆抗体，可用于治疗转移性黑色素瘤。
T76750	Cemiplimab REGN-2810,SAR-439684	Others	Others
	Cemiplimab (Anti-Human PD-1) 是一种针对程序性细胞死亡受体 1 （PD-1）的人单克隆抗体，也是一种检查点抑制剂，可阻断 PD-1/PD-L1 介导的 T 细胞抑制，可用于转移性癌症和鳞状细胞皮肤癌研究。
T76828	Sonepcizumab LT 1009	LPL Receptor	GPCR/G Protein
	Sonepcizumab (LT 1009) 是一种完全人源化的抗 S1P 单克隆抗体。Sonepcizumab 具有抗癌活性，可用于研究转移性肾细胞癌 (mRCC) ，可预防青光眼滤过手术后的眼部瘢痕形成。
T76857	Anetumab	Others	Others
	Anetumab 是一种新型全人源抗间皮素 IgG1抗体，是 Anetumab ravtansine的裸抗。Anetumab 可用于合成抗体-活性分子偶联物 Anetumab ravtansine。Anetumab 可用于研究治疗转移性胸膜间皮瘤。
T60616	MPT0G211	HDAC	Chromatin/Epigenetic; DNA Damage/DNA Repair
	MPT0G211 是一种具有高效性选择性和口服活性的 HDAC6 抑制剂 (IC50=0.291 nM)，具有神经保护作用在人乳腺癌细胞中显示出有抗转移活性。MPT0G211 对 HDAC6 的亲和力是其他 HDAC 亚型的 1000 倍。MPT0G211 可以透过血脑屏障，可用于改善阿尔茨海默病模型中 tau 磷酸化和认知缺陷。
T77434	Vopratelimab JTX 2011	Others	Others
	Vopratelimab (JTX-2011) 是一种选择性人源化免疫球蛋白 G1-kappa 单克隆抗体，是一种高效 ICOS 激动剂。Vopratelimab 对诱导型 T 细胞 CO 刺激因子 (ICOS)亲和力较高，对 hICOS 的亲和力为 0.93 nM，对大鼠 ICOS 的亲和力为 3.7 nM，对 mICOS 的亲和力为 0.64 nM。Vopratelimab 具有抗肿瘤免疫作用，可用于改善转移性非小细胞肺癌。
T70226	Amentoflavone hexaacetate
	Amentoflavone hexaacetate is a 3,5-cyclic nucleotide phosphodiesterase inhibitor. It has anti-angiogenic and anti-metastatic effects.
T25593	Labetuzumab govitecan IMMU-130,Labetuzumab-SN38,hMN14-SN38,IMMU130,IMMU 130	Others	Others
	Labetuzumab govitecan is an anti-CEACAM5/SN-38 antibody-drug conjugate for therapy of refractory or relapsing metastatic colorectal cancer.
T72740	n-Octyl caffeate
	n-Octyl caffeate 具有抗癌、诱导凋亡活性。
T62833	Myoferlin inhibitor 1
	Myoferlin inhibitor 1 是一种新型抗胰腺癌转移药物，能够肌球蛋白发挥作用。
T37037	Vinflunine ditartrate
	Vinflunine ditartrate, a fluorinated microtubule inhibitor and member of the Vinca alkaloids family, exhibits anti-angiogenic, vascular-disrupting, and anti-metastatic properties. It presents a potential avenue for studying transitional cell carcinoma of the urothelial tract, non-small cell lung cancer, and breast carcinoma[1][2].
T9901A-009	Anti-MAGEA3 Anti-HIP8
	Anti-MAGEA3 是一种靶向 MAGE-A 的抗体，可用于研究转移性癌和黑色素癌。
T34632	SH-5 SH5 PIA5. LchiroInositol 1deoxy6Omethyl 5(2R)2methoxy3(octadecyloxy)propyl hydrogen phosphate. Akt inhibitor II
	SH-5 是一种AKT抑制剂，通过抑制IκBα激酶激活调节的抗凋亡、增殖和转移基因产物，增强细胞凋亡并抑制侵袭。
T75057	RLA-4842
	RLA-4842，含有抗雄激素性质的铁活化剂，表现出对于转移性去势抵抗性前列腺癌(mCRPC)细胞系的抗增殖活性。
T75058	RLA-5331
	RLA-5331，一种含有抗雄激素的铁活化剂，针对(mCRPC)细胞系显示出抗增殖活性。
T76918	Barecetamab
	Barecetamab (ISU-104) 是一种人源话抗 ErbB3单克隆抗体。Barecetamab 可用于复发/转移性 (R/M) 头颈部鳞状细胞癌 (HNSCC) 的研究。
T77996	iRGD peptide 1 TFA
	iRGD peptide 1 TFA为原型肿瘤组织特异性穿透肽，能深入血管外肿瘤组织传递活性分子，且具备抗转移能力。
T76970	Tagitanlimab
	Tagitanlimab (HBM-9167)，一种人源化抗PD-L1抗体(IgG1κ型)，通过选择性阻断PD-L1与PD-1的相互作用，展现出对研究复发性或转移性鼻咽癌(NPC)的潜力。
T78796	MHJ-627	ERK	MAPK
	MHJ-627，作为一种有效的ERK5(MAPK7)抑制剂（IC50: 0.91 μM），可增强抑癌基因和抗转移基因的mRNA表达，从而促进癌细胞凋亡。
T76689	Margetuximab
	Margetuximab (MGAH22)为优化Fc结构域的嵌合抗HER2单克隆抗体，EC50值为39.33 ng/mL，适用于转移性HER2阳性乳腺癌研究。
T70957	NMac1
	NMac1is a small molecule phenylbutenoid dimer that has novel anti-proliferative effect only under glucose starvation in metastatic breast cancer cells. NMac1 causes significant activation of AMPK by decreasing ATP synthesis, lowers mitochondrial membrane potential (MMP, ΔΨm), and inhibits oxygen consumption rate (OCR) under glucose starvation. These effects of NMac1 are provoked by a consequence of OXPHOS complex I inhibition.
T62945	Aurora A/PKC-IN-1
	Aurora A/PKC-IN-1 (Compound 2e) 是一种有效的 Aurora A (AurA) 和 PKC (α, β1, β2, θ) 双重抑制剂，作用于 AurA (IC50: 6.9 nM) 和 PKCα (IC50: 16.9 nM)。Aurora A/PKC-IN-1 对乳腺癌细胞表现出抗增殖和抗转移作用。
T70344	BJ-2302
	BJ-2302 is a SRC inhibitor. BJ-2302 effectively suppressed MDA-MB-231 cell invasion (Matrigel invasion assay) and metastasis (chorioallantoic membrane assay xenografted with MDA-MB-231-luc2-tdTomato cancer cells). Additionally, BJ-2302 (1 mg/kg) strongly suppressed TNBC cell proliferation in vitro and tumor growth in a xenograft mouse tumor model. The anti-metastatic and anti-tumor effects of BJ-2302 were superior to those of Z-FL-COCHO (1 mg/kg) or batimastat (30 mg/kg), a pan-MMP inhibitor.
T80067	Uroguanylin (human)	Guanylate cyclase	GPCR/G Protein
	Uroguanylin (human) 作为一种在转移性结直肠癌肿瘤中表达的观音酰环化酶(GCC)受体的天然配体，Guanylyl Cyclase 在人类结肠癌动物模型中展现出抗肿瘤活性。
T76879	Vesencumab
	Vesencumab (MNRP-1685A)是一种针对neuropilin-1 (NRP-1)的IG1抗体。通过与NRP-1结合，Vesencumab 阻断了NRP-1与VEGFR-2的偶联，展现出抗血管生成和抗肿瘤的活性。此化合物适用于转移性实体瘤，如卵巢癌的研究。
T61753	MPT0G211 mesylate
	MPT0G211 mesylate is a powerful and selective HDAC6 inhibitor (IC50 = 0.291 nM), with high oral bioavailability. It exhibits remarkable selectivity for HDAC6 over other HDAC isoforms (>1000-fold selectivity). Additionally, MPT0G211 mesylate can effectively cross the blood-brain barrier. In preclinical studies using an Alzheimer's disease model, MPT0G211 mesylate has shown promising results in reducing tau phosphorylation and cognitive deficits. Furthermore, this compound exhibits anti-metastatic...
T79919	S-Adenosyl-L-methionine (1,4-butanedisulfonate) Ademetionine (1,4-butanedisulfonate),S-Adenosyl methionine (1,4-butanedisulfonate),AdoMet (1,4-butanedisulfonate)	Endogenous Metabolite	Metabolism
	S-Adenosyl-L-methionine (S-Adenosyl methionine) 1,4-butanedisulfonate 作为一种口服活性的甲基供体，它是一种膳食补充剂，对抗抑郁和缓解疼痛具有显著功效。此化合物在癌症治疗中显示了抗增殖、促进凋亡和阻止转移的潜在作用。同时，S-Adenosyl-L-methionine 1,4-butanedisulfonate 也用于肝病和骨关节炎的相关研究。
T79599	Anti-inflammatory agent 53	COX	Immunology/Inflammation; Neuroscience
	Anti-inflammatory agent 53（compound 7c）是口服有效及选择性的COX-2抑制剂。Anti-inflammatory agent 52展现了抗HT29细胞迁移的特性，能够促使细胞周期在S期与G2/M期停滞。此外，该化合物对大鼠胃肠道安全，对炎症具有中等程度的抑制效应。在携带艾利希实体瘤的小鼠模型中，Anti-inflammatory agent 52能够抑制肿瘤生长，显示出潜在的抗癌活性。
T76997	Socazolimab
	Socazolimab (ZKAB001) 是一种针对PD-L1的单克隆抗体，在治疗复发或转移性宫颈癌方面展现了持久的安全性和有效性。此外，Socazolimab 也被认为在小细胞肺癌、食管鳞状细胞癌 (ESCC)、晚期尿路上皮癌及骨肉瘤治疗中具有潜在应用价值。
T73547	CPUL1
	CPUL1 是一种TrxR 抑制剂，对 A549 细胞显示出增殖抑制和抗转移活性。CPUL1 通过抑制TrxR1酶活性来诱导 ROS 介导的ERK/JNK 信号传导从而影响上皮-间质转化 (EMT)。CPUL1 与α-Lipoic Acid 或Dithiodipropionic acid 联合使用效果更好。
T64022	Antitumor agent-37
	Antitumor agent-37 表现出有效的抗增殖和抗转移效果。Antitumor agent-37 能够诱导严重的 DNA 损伤，进而导致 γ-H2AX 和 p53 的高表达。Antitumor agent-37 可利用线粒体凋亡通路 Bcl-2/Bax/caspase3，诱导肿瘤细胞凋亡 (apoptosis)。Antitumor agent-37 可以抑制 PD-L1 的表达，提高肿瘤组织中 CD3+ 和 CD8+ T 浸润细胞，明显改善免疫反应。
T62090	(Rac)-Tanomastat
	Rac)-Tanomastat ((Rac)-BAY 12-9566) 是 Tanomastat 的外消旋体。其中 Tanomastat (BAY 12-9566) 是一种口服具有活力的、含锌羧基的非肽联苯基质金属蛋白酶(MMPs)抑制剂，能够抑制 MMP-2 (Ki: 11 nM)、MMP-3 (Ki: 143 nM)、MMP-9 (Ki: 301 nM)、MMP-13 (Ki: 1470 nM)。在几种实验性肿瘤模型中，Tanomastat 表现出抗侵袭和抗转移作用。

化合物

Cat.No: T9582

Target: NF-κB

Cat.No: T8310

Target: MMP

Cat.No: T5125

Target: TGF-beta/Smad

WSB1 Degrader 1

Cat.No: T9236

Target: Others, E1/E2/E3 Enzyme

Cat.No: T62536

Target: Others

Cat.No: T17255

Target: Others

Cat.No: T9075

Target: Others

Cat.No: T26969

Synonym: CCT-365623,CCT 365623

Target: Monoamine Oxidase

Cat.No: T77374

Synonym: MORAb-004

Target: Others

Cat.No: T76750

Synonym: REGN-2810,SAR-439684

Target: Others

Cat.No: T76828

Synonym: LT 1009

Target: LPL Receptor

Cat.No: T76857

Target: Others

Cat.No: T60616

Target: HDAC

Cat.No: T77434

Synonym: JTX 2011

Target: Others

Amentoflavone hexaacetate

Cat.No: T70226

Labetuzumab govitecan

Cat.No: T25593

Synonym: IMMU-130,Labetuzumab-SN38,hMN14-SN38,IMMU130,IMMU 130

Target: Others

n-Octyl caffeate

Cat.No: T72740

Myoferlin inhibitor 1

Cat.No: T62833

Vinflunine ditartrate

Cat.No: T37037

Cat.No: T9901A-009

Synonym: Anti-HIP8

Cat.No: T34632

Synonym: SH5 PIA5. LchiroInositol 1deoxy6Omethyl 5(2R)2methoxy3(octadecyloxy)propyl hydrogen phosphate. Akt inhibitor II

Cat.No: T75057

Cat.No: T75058

Cat.No: T76918

iRGD peptide 1 TFA

Cat.No: T77996

Cat.No: T76970

Cat.No: T78796

Target: ERK

Cat.No: T76689

Cat.No: T70957

Aurora A/PKC-IN-1

Cat.No: T62945

Cat.No: T70344

Uroguanylin (human)

Cat.No: T80067

Target: Guanylate cyclase

Cat.No: T76879

MPT0G211 mesylate

Cat.No: T61753

S-Adenosyl-L-methionine (1,4-butanedisulfonate)

Cat.No: T79919

Synonym: Ademetionine (1,4-butanedisulfonate),S-Adenosyl methionine (1,4-butanedisulfonate),AdoMet (1,4-butanedisulfonate)

Target: Endogenous Metabolite

Anti-inflammatory agent 53

Cat.No: T79599

Target: COX

Cat.No: T76997

Cat.No: T73547

Antitumor agent-37

Cat.No: T64022

(Rac)-Tanomastat

Cat.No: T62090

Cat. No.	Product Name	Target	Signaling Pathways
T5S0803	Columbamine 非洲防己碱,Columbamin,Dehydroisocorypalmine	Others	Others
	Columbamine (Columbamin) 是一种从植物中提取的季异喹啉生物碱。
T7927	β-Ionone 乙位紫罗兰酮,β-紫罗兰酮,β-lonone	Apoptosis; Others	Apoptosis; Others
	β-Ionone (β-lonone) 是β-类胡萝卜素的端环类似物，广泛存在于水果和蔬菜中，可有效诱导胃腺癌细胞 SGC7901 凋亡，具有抗增殖、抗转移和抗肿瘤作用。
T1082	Benzyl isothiocyanate Benzoylthiocarbimide,苄基异硫氰酸酯,异硫氰酸苯甲酯,Isothiocyanic Acid Benzoyl Ester	Apoptosis; Antibacterial; Antibiotic	Apoptosis; Microbiology/Virology
	Benzyl isothiocyanate (Benzoylthiocarbimide) 是一种具有杀菌活性的天然异硫氰酸酯，最初存在于十字花科蔬菜中。它显示出免疫调节、抗寄生虫、抗生素、抗氧化、抗动脉粥样硬化、抗血管生成、抗转移、抗癌化疗和化学预防活性。
T20578	Maclurin Fustic extract,Morintannic acid,NSC 83240	Free radical scavengers; Reactive Oxygen Species	Immunology/Inflammation; Metabolism; NF-κB; oxidation-reduction
	Maclurin (NSC-83240) 是桑枝的酚类成分，具有抗转移作用。 Maclurin 可有效防止 OH 诱导的 DNA 和 MSCs 损伤，可用于预防多种疾病或 MSCs 移植的研究。
T5S0053	Coptisine 黄连碱,Coptisin	Indoleamine 2,3-Dioxygenase (IDO)	Metabolism
	Coptisine (Coptisin) 是一种从黄连中分离到的生物碱，是非竞争性的IDO 抑制剂，Ki=为 5.8 μM，IC50=6.3 μM。
T5S2358	Dehydrocorydaline Dehydrocorydalin,脱氢紫堇碱,13-Methylpalmatine	BCL; PARP; p38 MAPK; Caspase; Parasite; Autophagy	Apoptosis; Autophagy; Chromatin/Epigenetic; DNA Damage/DNA Repair; MAPK; Microbiology/Virology; Proteases/Proteasome
	Dehydrocorydaline (13-Methylpalmatine) 是一种生物碱。它调节Bax，Bcl-2蛋白表达，激活caspase-7，caspase-8，并使PARP 失活。它能增强p38 MAPK 活化，具有抗炎、抗癌等功效。它具有强大的抗疟疾作用，并具低细胞毒性。
TN1867	Licoricidin	MMP; VEGFR; ROS	Angiogenesis; Immunology/Inflammation; Proteases/Proteasome; Tyrosine Kinase/Adaptors
	Licoricidin, is a potent anti-metastatic agent, which can markedly inhibit the metastatic and invasive capacity of malignant prostate cancer cells.
T13472	α-Carotene	Others	Others
	α-Carotene is isolated from yellow-orange and dark-green vegetables. α-Carotene is used as an anti-metastatic agent or as an adjuvant for anti-cancer drugs.
TN3517	Bisacurone	IL Receptor; IκB/IKK; TNF; NF-κB; ROS; Akt; PKC	Apoptosis; Chromatin/Epigenetic; Cytoskeletal Signaling; Immunology/Inflammation; NF-κB; PI3K/Akt/mTOR signaling
	Bisacurone has anti-oxidant, anti-inflammatory, and anti-metastatic activities, it may have a protective effect against ethanol-induced liver injury by suppressing hepatic oxidation and inflammation.
TN4101	Ganoderenic acid H	Others	Others
	Ganoderenic acid H is one compound of triterpenoids isolated from Ganoderma lucidum, triterpenoids exhibit a broad spectrum of anti-cancer properties, including anti-proliferative, anti-metastatic and anti-angiogenic activities.
T16035	Meleagrin	Others	Others
	Meleagrin, a roquefortine C-derived alkaloid produced by Penicillium fungi, serves as both a class of FabI inhibitors and a lead c-Met inhibitory entity for controlling c-Met-dependent metastatic and invasive breast malignancies. It exhibits antimicrobial and anti-proliferative activities.
TN4046	Excisanin A	MMP; FAK; PARP; GSK-3; NF-κB; Wnt/beta-catenin; Akt; Caspase; PI3K; Prostaglandin Receptor; JNK	Angiogenesis; Apoptosis; Chromatin/Epigenetic; Cytoskeletal Signaling; DNA Damage/DNA Repair; GPCR/G Protein; Immunology/Inflammation; MAPK; NF-κB; PI3K/Akt/mTOR signaling; Proteases/Proteasome; Stem Cells; Tyrosine Kinase/Adaptors
	ExcisaninA may be a potent inhibitor of AKT signaling pathway in tumor cells, it can inhibit invasion by suppressing MMP-2 and MMP-9 expression, it may be a potential anti-metastatic chemotherapeutic agent for the treatment of breast cancer. Excisanin A shows comparable inhibitory effects on the LPS-induced production of NO and PGE2, and activation of NF-kappaB without affecting cell viability.Excisanin A induces apoptosis in colon cancer cell line SW620 as determined by Annexin V staining, the ...

天然产物

Cat.No: T5S0803

Synonym: 非洲防己碱,Columbamin,Dehydroisocorypalmine

Target: Others

Cat.No: T7927

Synonym: 乙位紫罗兰酮,β-紫罗兰酮,β-lonone

Target: Apoptosis, Others

Benzyl isothiocyanate

Cat.No: T1082

Synonym: Benzoylthiocarbimide,苄基异硫氰酸酯,异硫氰酸苯甲酯,Isothiocyanic Acid Benzoyl Ester

Target: Apoptosis, Antibacterial, Antibiotic

Cat.No: T20578

Synonym: Fustic extract,Morintannic acid,NSC 83240

Target: Free radical scavengers, Reactive Oxygen Species

Cat.No: T5S0053

Synonym: 黄连碱,Coptisin

Target: Indoleamine 2,3-Dioxygenase (IDO)

Dehydrocorydaline

Cat.No: T5S2358

Synonym: Dehydrocorydalin,脱氢紫堇碱,13-Methylpalmatine

Target: BCL, PARP, p38 MAPK, Caspase, Parasite, Autophagy

Cat.No: TN1867

Target: MMP, VEGFR, ROS

Cat.No: T13472

Target: Others

Cat.No: TN3517

Target: IL Receptor, IκB/IKK, TNF, NF-κB, ROS, Akt, PKC

Ganoderenic acid H

Cat.No: TN4101

Target: Others

Cat.No: T16035

Target: Others

Cat.No: TN4046

Target: MMP, FAK, PARP, GSK-3, NF-κB, Wnt/beta-catenin, Akt, Caspase, PI3K, Prostaglandin Receptor, JNK

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