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Cat. No. | Product Name | Target | Signaling Pathways |
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T74217 | Angiogenesis agent 1 | HIF/HIF Prolyl-Hydroxylase | Chromatin/Epigenetic; Metabolism |
Angiogenesis agent 1 (compound C-31) 为红景天苷衍生的糖苷类似物,能激活 HIF-1α 通路。该化合物有助于研究糖尿病所致后肢缺血。 | |||
T83116 |
Angiogenesis inhibitor 4
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Angiogenesis Inhibitor 4为一种高效血管生成抑制剂,主要应用于癌症研究领域。 | |||
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]. | |||
T75667 |
Neamine
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Neamine,新霉素降解产物,为广谱氨基糖苷类抗生素。作为抗血管生成剂,针对血管生成素 (angiogenin),展现抗菌、抗肿瘤及神经保护活性。 | |||
T78064 |
Synstatin (92-119)
SSTN92-119 |
Integrin | Cytoskeletal Signaling |
Synstatin (92-119)为一种抗肿瘤化合物,它能够抑制血管生成与癌细胞侵袭,通过下调整合素αvβ3,降低VEGF与FGF-2的活化。 | |||
T70273 |
APTO-253 HCl
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APTO-253, also known as LOR-253, LT-253, is a small molecule inhibitor of human metal-regulatory transcription factor 1 (MTF-1) with potential antitumor activity. MTF-1 inhibitor LOR-253 inhibits MTF-1 activity and thereby induces the expression of MTF-1 dependent tumor suppressor factor Kruppel like factor 4 (KLF4). This subsequently leads to the downregulation of cyclin D1, blocking cell cycle progression and proliferation. This agent also causes decreased expression of genes involved in tumor... | |||
T70706 |
APTO-253 isomer
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APTO-253 isomer is an isomer of APTO-253 with the Fluoro-atom in 6-position. APTO-253 also known as LOR-253, LT-253, is a small molecule inhibitor of human metal-regulatory transcription factor 1 (MTF-1) with potential antitumor activity. MTF-1 inhibitor LOR-253 inhibits MTF-1 activity and thereby induces the expression of MTF-1 dependent tumor suppressor factor Kruppel like factor 4 (KLF4). This subsequently leads to the downregulation of cyclin D1, blocking cell cycle progression and prolifer... | |||
T79699 | anti-TNBC agent-2 | Apoptosis | Apoptosis |
Anti-TNBC agent-2(3j)是一款针对三阴性乳腺癌(TNBC)的嘌呤衍生化合物。它能够引导MDA-MB-231细胞走向凋亡(apoptosis),阻碍其迁移和血管生成能力,并在TNBC异种移植模型中,抑制肿瘤生长与转移,同时下调Ki67和CD31蛋白的表达水平。Anti-TNBC agent-2主要用于三阴性乳腺癌的科研领域。 | |||
T80130 |
SDF-1α (human)
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CXCR | Autophagy; GPCR/G Protein; Immunology/Inflammation |
SDF-1α (human) 是一种能够与CXCR4受体相结合的单核细胞趋化剂,它在心肌梗死模型中的干细胞归巢、维持、生存、增殖、心肌细胞修复、血管形成以及心室重构过程扮演关键角色。SDF-1α (human) 常用于心血管病研究。 | |||
T60292 |
Ibuprofen sodium
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Ibuprofen ((±)-Ibuprofen) sodium 是一种口服活性的选择性COX-1抑制剂,IC50值为 13 μM。Ibuprofen sodium 抑制细胞增殖、血管生成,并诱导细胞凋亡 (apoptosis)。Ibuprofen sodium 是一种非甾体抗炎剂和一氧化氮 (NO) 供体。Ibuprofen sodium 可用于疼痛、肿胀、炎症、感染、免疫学、癌症的研究。 | |||
T83680 |
Azurin (50-77) (P. aeruginosa) TFA
Azurin p28,p28 |
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Azurin (50-77)是一种含铜细菌蛋白azurin的肽段,存在于P. aeruginosa中,具有细胞周期停滞、抑制癌细胞增殖和调节血管生成活性。作为VEGFR2的抑制剂(IC20约为10.7 µM),Azurin (50-77)(20 µM)能在MCF-7乳腺癌细胞中诱导G2/M期的细胞周期停滞。在50 µM的浓度下,减少MCF-7和ZR-75-1乳腺癌细胞的增殖。Azurin (50-77)以25 µM的浓度减少VEGF-A诱导的毛细管管腔形成(IC50 = 12 µM),降低人脐静脉内皮细胞(HUVECs)中与细胞膜相关的F-actin、焦点粘附激酶(FAK)和paxillin的水平,并增加胞外的血小板内皮细胞粘附分子-1(PECAM-1)的水平。在体内,Azurin (50-77)(每日10 mg/kg)在MCF-7小鼠异种移植模型中减少肿瘤体积。 |
Cat. No. | Product Name | Target | Signaling Pathways |
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T6S1487 |
Ginsenoside Rg5
人参皂苷Rg5,人参皂甙 Rg5 |
NF-κB; COX; IGF-1R | Immunology/Inflammation; Neuroscience; NF-κB; Tyrosine Kinase/Adaptors |
Ginsenoside Rg5 是红参的主要成分,可阻断IGF-1与其受体的结合,IC50约为90 nM。它还通过抑制NF-κB p65的 DNA 结合活性来抑制COX-2的 mRNA 表达。它可促进血管生成和改善高血压,具有抗炎和治疗阿尔茨海默病的潜力。 |