anti-metastasis

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。

Glabridin (KB-289522) 能够结合并激活PPARγ，EC50值为 6115 nM，是一种从Glycyrrhiza glabra 中分到的异黄烷类天然产物。它具有抗炎、抗菌、抗肾炎、抗氧化、抗肿瘤、抗糖尿病、抗骨质疏松、保护神经、保护心血管、清除自由基等作用。

NMac1 (Nm23 activator 1) 是一种天然产物 cassumunene，从姜科植物 Zingiber cassumunar Roxb.中提取，在东亚传统上用作抗炎剂。NMac1 通过与 Nm23-H1 的 C 端直接相互作用，在体外激活其 NDP 激酶（NDPK）酶活性，具有抗转移潜力，并在体内实验中抑制乳腺癌转移。

20(S)-Ginsenoside Rg3 (Rg3) 是红参的主要成分，通过抑制肿瘤细胞的粘附和侵袭来抑制肿瘤细胞肺转移。它抑制Na+和hKv1.4通道，IC50分别为 32.2±4.5 和 32.6±2.2 μM。它还抑制Aβ，NF-κB 活性和COX-2表达，抑制人脐静脉内皮细胞的增殖并具有抗血管生成活性。

6-Shogaol (6-Shogaol) 是从生姜中分离的一种天然产物，具有抗癌、抗炎和抗氧化的多种生物活性。

AhR modulator-1 is a selective and orally active aryl hydrocarbon receptor (AhR) modulator. It inhibits metastasis, in part, by inhibiting prostatic VEGF production prior to tumor formation. It also possesses anti-estrogenic properties in rat uterus.

Borrelidin(Treponemycin) 是苏糖酰-tRNA 合成酶的抑制剂，是可从 Streptomyces rochei 中分离到的含氮大环内酯类抗生素，具有抗癌、抗真菌和抗血管生成活性，抑制肿瘤生长和肺转移。

possesses anticancer, anti-invasive, anti-metastasis, anti-angiogenic and pro-apoptosis properties with high safety.Frondoside A, a natural glycoside extracted from the sea cucumber, Cucumaria frondosa,

R916562 is an orally active and selective Axl VEGF-R2 inhibitor with IC50s of 136 nM and 24 nM, respectively. R916562 has anti-angiogenesis and anti-metastasis.

YF438 作为一种HDAC抑制剂，展示了显著的体外及体内抗癌效果。它通过阻止HDAC和MDM2的相互作用，引发MDM2-MDMX的解离并加速MDM2的降解，有效抑制了三阴性乳腺癌 (TNBC) 细胞的增长及其转移。

Pixatimod（亦称PG-545）是一种合成糖类改良的肝素硫酸仿生物及Toll样受体9（TLR9）的激动剂，具有潜在的免疫增强、抗肿瘤和抗病毒作用。Pixatimod (PG545) 强效地通过破坏刺突蛋白-ACE2相互作用抑制SARS-CoV-2。此外，Pixatimod阻断多种促癌过程，包括细胞增殖、侵袭、转移、血管生成和上皮-间充质转化。这些作用在多种不同的小鼠癌症模型中展现出强大的效力，包括约30种异种移植模型和20种同种移植模型。Pixatimod已与多种批准的抗癌化合物联合测试，展示了其临床潜力，包括与gemcitabine、paclitaxel、sorafenib、铂类化合物及抗PD-1抗体合用。

Pixatimod（又名PG-545）是一种合成的改性糖类肝素硫酸模拟剂及Toll样受体9（TLR9）的激动剂，具有潜在的免疫刺激、抗肿瘤和抗病毒活性。Pixatimod强效抑制SARS-CoV-2，其通过破坏刺突蛋白-ACE2的相互作用来实现。此外，Pixatimod阻断了多种促癌过程，包括细胞增殖、侵袭、转移、血管生成及上皮-间充质转换。这些活性在多种不同的小鼠癌症模型中显示出强大效果，涵盖约30种异种移植模型和20种同源移植模型。Pixatimod已与多种已获批准的抗癌化合物联合测试，展现其临床潜力，包括与吉西他滨、紫杉醇、索拉非尼、铂类化合物和一种抗PD-1抗体的联合应用。

iHAC 是一种抑制剂-HSP90 锚定嵌合体，通过与 BRD4 配体 (+)-JQ-1 共价结合在HSP90上，可抑制癌细胞增殖。iHAC 能激活抗肿瘤免疫反应，并在小鼠模型中阻止 4T1 乳腺癌的复发和转移。

2-Deoxy-L-ribose 是 2-Deoxy-d-ribose 的立体异构体，并能抑制 2-Deoxy-d-ribose 的抗凋亡活性。2-Deoxy-L-ribose 还可以阻止过表达胸苷磷酸化酶的肿瘤细胞进行转移。

HPH-15 是一种抗细胞迁移化合物，其作用机制包括与hnRNP U结合或抑制TGF-β，从而抑制细胞迁移。此外，HPH-15 能抑制上皮到间充质转化 (EMT)，为抗肿瘤转移和抗纤维化研究提供了潜力。

Oxysophocarpine 是提取自海藻的生物碱。它对中枢神经系统和周围神经系统具有神经保护作用和抗伤害感受作用。

Xanthone (Xanthenone) 是一种从山竹果中分离得到的天然产物，具有抗炎，抗氧化，抗肿瘤，抗过敏，抗细菌，抗真菌和抗病毒活性。在癌变的不同阶段可控制细胞分裂和生长，凋亡，炎症和转移。

Epitalon is a synthetic tetrapeptide with anti-aging properties.1,2,3,4 Dietary administration of epitalon (0.00001% w w) reduces levels of lipid peroxidation products in aged D. melanogaster tissue homogenates.1 Epitalon (1 μg animal) delays age-related estrous shutdown and decreases the frequency of bone marrow cell chromosomal aberrations in female mice.2 It decreases spontaneous mammary gland and ovarian tumor development and metastasis in aged female mice.3 Epitalon also stimulates melatonin synthesis and normalizes the circadian rhythm of cortisol secretion in senescent female M. mulatta monkeys.4References1. Khavinson, V.K., and Myl'nikov, S.V. Effect of epithalone on the age-specific changes in the time course of lipid peroxidation in Drosophila melanogaster. Bull. Exp. Biol. Med. 130(11), 1116-1119 (2000).2. Anisimov, V.N., Khavinson, V.K., Popovich, I.G., et al. Effect of Epitalon on biomarkers of aging, life span and spontaneous tumor incidence in female Swiss-derived SHR mice. Biogerontology 4(4), 193-202 (2003).3. Kossoy, G., Anisimov, V.N., Ben-Hur, H., et al. Effect of the synthetic pineal peptide epitalon on spontaneous carcinogenesis in female C3H He mice. In Vivo 20(2), 253-257 (2006).4. Khavinson, V., Goncharova, N., and Lapin, B. Synthetic tetrapeptide epitalon restores disturbed neuroendocrine regulation in senescent monkeys. Neuro. Endocrinol. Lett. 22(4), 251-254 (2001). Epitalon is a synthetic tetrapeptide with anti-aging properties.1,2,3,4 Dietary administration of epitalon (0.00001% w w) reduces levels of lipid peroxidation products in aged D. melanogaster tissue homogenates.1 Epitalon (1 μg animal) delays age-related estrous shutdown and decreases the frequency of bone marrow cell chromosomal aberrations in female mice.2 It decreases spontaneous mammary gland and ovarian tumor development and metastasis in aged female mice.3 Epitalon also stimulates melatonin synthesis and normalizes the circadian rhythm of cortisol secretion in senescent female M. mulatta monkeys.4 References1. Khavinson, V.K., and Myl'nikov, S.V. Effect of epithalone on the age-specific changes in the time course of lipid peroxidation in Drosophila melanogaster. Bull. Exp. Biol. Med. 130(11), 1116-1119 (2000).2. Anisimov, V.N., Khavinson, V.K., Popovich, I.G., et al. Effect of Epitalon on biomarkers of aging, life span and spontaneous tumor incidence in female Swiss-derived SHR mice. Biogerontology 4(4), 193-202 (2003).3. Kossoy, G., Anisimov, V.N., Ben-Hur, H., et al. Effect of the synthetic pineal peptide epitalon on spontaneous carcinogenesis in female C3H He mice. In Vivo 20(2), 253-257 (2006).4. Khavinson, V., Goncharova, N., and Lapin, B. Synthetic tetrapeptide epitalon restores disturbed neuroendocrine regulation in senescent monkeys. Neuro. Endocrinol. Lett. 22(4), 251-254 (2001).

CCG-203971 是一种Rho MRTF SRF 通路抑制剂，具有潜在的抗转移作用。它有效靶向 RhoA C 激活的 SRE 荧光素酶，IC50为 6.4 μM。它抑制 PC-3 细胞迁移，IC50为 4.2 μM。

Obtusifolin 是分离自决明子的种子中，能够抑制NF-kB 通路，调节气道上皮细胞中 MUC5AC 粘蛋白的基因表达和产生。它通过靶向甲状旁腺激素相关蛋白来抑制邻苯二甲酸酯诱导的乳腺癌骨转移。

Escin IA (Escin IA;Aescin IA);Aescin IA 是从马蹄中七叶树分离出的一种三萜皂苷，抑制HIV-1蛋白酶，IC50值为 35 μM。它具有抗 TNBC 转移活性，其作用机制涉及通过下调 LOXL2 表达抑制上皮-间质转化过程。

Lasofoxifene (CP-336156) 是一种选择性的、口服具有活力的雌激素受体调节剂 (SERM)。Lasofoxifene 对原生肿瘤的生长和转移具有抑制作用，也能够抗骨质疏松。Lasofoxifene 能够用于研究乳腺癌和绝经后骨质疏松症。

EGFR kinase inhibitor 1 是 EGFR 的有效抑制剂，能够作用于 WT (IC50: 37 nM)，l885R T790M (IC50: 1.7 nM)，L858R T790M C797S (IC50>300 nM)。EGFR kinase inhibitor 1 能够将细胞周期阻滞在 G0 G1 期，诱导细胞凋亡 (apoptosis)，对细胞转移显示出抑制作用。EGFR kinase inhibitor 1 表现出抗增殖和抗肿瘤效果。

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.