33
14
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T3934 |
Isavuconazonium sulfate
|
Antifungal | Microbiology/Virology |
Isavuconazonium sulfate 是一种口服活性抗真菌药,是活性三唑类抗真菌药物 Isavuconazole 的前药,可用于侵袭性曲霉菌病和毛霉菌病。 | |||
T9211 |
Mito-LND
Mito-Loidamine |
OXPHOS; Reactive Oxygen Species; Mitochondrial Metabolism; Autophagy | Apoptosis; Autophagy; Immunology/Inflammation; Metabolism; NF-κB |
Mito-LND (Mito-Loidamine) 是一种有口服活性和靶向线粒体的氧化磷酸化抑制剂。它抑制线粒体生物能,刺激活性氧的形成,并诱导肺癌细胞自噬细胞死亡。 | |||
T5519 |
Bivalirudin
BG-8967,比伐卢定,Hirulog-1 |
Thrombin | Proteases/Proteasome |
Bivalirudin (BG-8967) 是一种直接凝血酶(thrombin)抑制剂,是一种肽类抗凝剂,可在侵入性心脏病,特别是在经皮冠状动脉介入中用于抗凝。 | |||
T14322 |
ARP-100
MMP-2 Inhibitor III |
MMP | Proteases/Proteasome |
ARP-100 (MMP-2 Inhibitor III) 是选择性基质金属蛋白酶MMP-2抑制剂 (IC50=12 nM)。它对 MMP-1 (>50 μM),MMP-3 (4.5 μM),MMP-7 (>50 μM) 和MMP-9 (0.2 μM) 的抑制活性较小。它与 MMP-2 的 S1'口袋相互作用,并在体外对基质胶的侵袭模型中显示抗侵袭特性。 | |||
T1898 |
RKI-1447
RKI1447 |
ROCK | Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells |
RKI-1447 是一种高效的ROCK1和ROCK2的小分子抑制剂,IC50值分别为14.5和6.2 nM。 | |||
T21483 |
Tricaine methanesulfonate
3-氨基苯甲酸乙酯甲基磺酸盐,MS-222 |
Others | Others |
Tricaine methanesulfonate (MS-222) 常用于固定鱼的标记和运输,并能抑制入侵过程中的感觉系统。 | |||
T17239 |
VU0155069
CAY10593 |
Phospholipase | Metabolism |
VU0155069 在 transwell 试验中强烈抑制几种癌细胞系的侵袭性迁移。 VU0155069 是一种选择性磷脂酶 D1 抑制剂(体外 IC50:46 nM)。 | |||
T25384 |
Erbulozole
R-55104,R55104,R 55104 |
Microtubule Associated | Cytoskeletal Signaling |
Erbulozole (R 55104) 是一种有效的合成微管抑制剂,具有抗侵袭、抗肿瘤和放射增敏活性,可诱发 Wernicke 脑病样神经毒性。 | |||
T64695 |
IR-808
MHI-148 |
||
IR-808 (MHI-148) 是一种近红外菁染料,可用于无创癌症成像、诊断和成像引导光热治疗。 | |||
T9912 |
Trastuzumab
|
EGFR | Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors |
Trastuzumab 是人源化单克隆抗体,以高亲和力与HER2选择性结合,可用于 HER2 阳性转移性乳腺癌和 HER2 阳性胃癌的研究。 | |||
TQ0223 |
Lusutrombopag
芦曲泊帕,鲁索曲波帕,S-888711,Mulpleta |
Thrombin; Thrombopoietin Receptor | Immunology/Inflammation; Proteases/Proteasome |
Lusutrombopag (Mulpleta) 是一种口服生物可利用的小分子血小板生成素 (TPO) 受体激动剂,用于选择性侵入性手术前患有血小板减少症的慢性肝病的患者。 | |||
T60952 |
Fluridone
EL-171 |
Others | Others |
Fluridone (EL-171) 是 一种有效的合成脱落酸 (ABA) 的抑制剂,抑制 AchnFAR 和 TF 基因的表达,减少伯醇的形成。Fluridone 常作为水生除草剂用于控制入侵植物,也被用来控制水螅和欧亚水螅等物种。 | |||
T30040 |
Amphocil
Amphotericin B cholesteryl sulfate |
||
Amphocil is used to treat patients with invasive fungal infection. | |||
T40861 |
Nerindocianine
|
||
Nerindocianine is a hydrophilic, fluorescent diagnostic contrast agent that is predominantly metabolized by the kidneys, enabling non-invasive, intraoperative ureteral imaging. | |||
T68425 |
Saracatinib difumarate
|
||
Saracatinib difumarate is an orally available dual-specific inhibitor of Src and Abl with anti-invasive and anti-tumor activities. | |||
T25925 |
p-DDAP
pDDAP,p-Dodecylaminophenol |
||
p-DDAP is an anti-invasive agent that acts by significantly suppressing cell invasion, and the activity and mRNA expression of matrix metalloproteinase-9 (MMP-9). | |||
T11325 | Frondoside A | Others | Others |
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, | |||
T70703 |
DK-139
|
||
DK-139 is an inhibitor of NF-kappaB-mediated GROalpha expression, suppressing the TNFalpha-induced invasive capability of MDA-MB-231 human breast cancer cells. | |||
T69769 |
BDP8900
|
||
BDP8900 is a potent and selective MRCK inhibitor, reducing substrate phosphorylation. BDP8900 leads to morphological changes in cancer cells along with inhibition of their motility and invasive character. | |||
T71965 |
KRIBB3
|
||
KRIBB3 is novel and potent microtubule inhibitor with potential anticancer activity. KRIBB3 has anti-migratory and anti-invasive activities in MDA-MB-231 cells. KRIBB3 inhibits tumor cell migration and invasion by blocking protein kinase C-dependent phosphorylation of Hsp27 through its direct binding to Hsp27. | |||
T35368 |
N-butyl-N-(4-hydroxybutyl) nitrosamine
4-Hydroxybutylbutylnitrosamine,N-Nitrosobutylbutanolamine,OH-BBN,N-butyl-N-(4-hydroxybutyl) nitrosamine,BBN,N-Butyl-N-(4-hydroxybutyl)nitrosamine,4-(Butylnitrosamino)-1-butanol |
Others | Others |
N-butyl-N-(4-hydroxybutyl) nitrosamine (N-Nitrosobutylbutanolamine) (BBN, OH-BBN) 是一种模型化合物,可诱导膀胱中的高级别侵袭性肿瘤。 | |||
T74959 | Antifungal agent 41 | ||
Antifungal agent 41 (compound B01) 是一种抗真菌剂。Antifungal agent 41 在体内外表现出对白假丝酵母菌的抗性。Antifungal agent 41 可以用于侵袭性真菌感染的研究。 | |||
TD0087L |
Sulfo-Cy5.5 Trifluoroacetate
|
Others | Others |
Sulfo-Cy5.5 Trifluoroacetate 是一种氰基染料,非常适用于无创体内近红外成像,适用于需要低荧光背景的应用。 | |||
T11314 |
Fosmanogepix
APX001,E1211 |
Others | Others |
Fosmanogepix (APX001) is a first-in-class, orally available broad-spectrum antifungal agent. It acts as an N-phosphonooxymethyl prodrug that undergoes rapid and complete metabolism by systemic alkaline phosphatases. This metabolism leads to the formation of the active moiety, APX001A. Fosmanogepix (APX001), with its ability to target the highly conserved Gwt1 fungal enzyme, holds great potential for the development of treatments against invasive fungal infections. | |||
T79789 |
DT-6
|
TGF-beta/Smad | Stem Cells |
DT-6为一有效TGF-β1抑制剂,能够抑制M2巨噬细胞诱导的上皮至间质转化(Epithelial-Mesenchymal Transition, EMT)及癌细胞侵袭性迁移,可用于癌症相关疾病研究。 | |||
T74956 | Chitin synthase inhibitor 10 | ||
Chitin synthase inhibitor 10为一种高效的几丁质合酶(CHS)抑制剂,具有0.11 mM的IC50,表现出显著的CHS抑制活性。作为抗真菌剂,该化合物对包括C. albicans和C. neoformans在内的耐药真菌变体有效,适合用于侵袭性真菌感染(IFI)研究。 | |||
T80591 |
Efungumab
|
||
Efungumab为一种单克隆抗体,对抗真菌(fungal)活性。该化合物通过与HSP90结合,抑制对真菌生存必需的构象变化。Efungumab主要用于侵袭性念珠菌感染(IC)的研究。 | |||
T72569 |
Cathepsin L/S-IN-1
|
||
CathepsinL/S-IN-1 是 Cathepsin L 和 Cathepsin S 的双重抑制剂,IC50分别为 4.10 μM 和 1.79 μM。CathepsinL/S-IN-1 对胰腺癌 BxPC-3 和 PANC-1 细胞具有显著的抗转移和侵袭作用。 | |||
T69269 |
DMGF
|
||
DMGF, also known as 7,7-dimethoxyagastisfavone, is a biflavonoid isolated from Taxus × media cv. Hicksii. DMGF induces apoptotic and autophagic cell death. DMGF could effectively attenuate the motility of B16F10 cells, and the results of real-time PCR revealed that DMGF also suppressed the expressions of matrix metalloproteinase-2 (MMP-2). MGF can inhibit the metastasis of highly invasive melanoma cancer cells through the down-regulation of F-actin polymerization DMGF may be further developed to... | |||
T63077 |
Chitin synthase inhibitor 12
|
||
Chitin synthase inhibitor 12 是一种几丁质合酶 (CHS) 抑制剂,具有优异的 CHS 抑制作用 (IC50: 0.16 mM)。Chitin synthase inhibitor 12 也是一种广谱抗真菌剂,对耐药真菌变体(如 C. albicans、C. neoformans)具有抗性。Chitin synthase inhibitor 12 能够用于研究侵袭性真菌感染 (IFIs)。 | |||
T75363 |
Fluorescein Di-β-D-Glucuronide
|
||
Fluorescein Di-β-D-Glucuronide 作为一款荧光探针,以其非侵入性的优势被广泛应用于裸鼠肠道细菌β-葡萄糖醛酸酶(βG)活性成像研究中。该探针通过成像技术有效揭示了肠道细菌β-葡萄糖醛酸酶在体内外的活性,进而为特定细菌β-葡萄糖醛酸酶抑制剂的药效学评估提供了重要工具。 | |||
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。 | |||
T30783 |
CDy9
CDy 9,CDy-9 |
||
CDy9 is a highly selective fluorescent probe for the detection and isolation of mESC using fluorescence microscopy and flow cytometry. CDy9 allows the detection and isolation of intact stem cells with marginal impact on their function and capabilities. CD |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T5834 |
Myrcene
|
Others | Others |
Myrcene 是具有可挥发性的芳香族化合物,对 TNFα 诱导的 NF-κB 具有抑制作用,且具有抗侵袭的能力。 | |||
T13509 |
4-Vinylphenol
|
Apoptosis; Endogenous Metabolite | Apoptosis; Metabolism |
4-Vinylphenol 是酒中乳酸菌对香豆酸和阿魏酸的代谢产物,在白花蛇舌草中发现。 4-Vinylphenol 在体内诱导细胞凋亡。 | |||
T8193 |
α-Thujone
Thujone,ALPHA-(-)-THUJONE,α-侧柏酮,(-)-α-侧柏酮 |
Apoptosis; Reactive Oxygen Species; GABA Receptor; AChR; Parasite; Autophagy | Apoptosis; Autophagy; Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism; Microbiology/Virology; Neuroscience; NF-κB |
α-Thujone 是一种从西方金钟柏精油中分离出来的单萜,可穿透血脑屏障。它是 GABAA 受体的可逆调节剂,在抑制 GABA 诱导的电流时,它的 IC50为 21 μM。它诱导 ROS 依赖性细胞毒性,还诱导细胞凋亡和自噬。它具有抗伤害,抗肿瘤、杀虫和驱虫活性。 | |||
T5S0689 |
Demethylwedelolactone
去甲蟛蜞菊内酯,去甲基蟛蜞内酯 |
Serine Protease | Proteases/Proteasome |
Demethylwedelolactone 是一种分离自 Eclipta alba 中的 coumestan 天然产物。它能抑制乳腺癌细胞的移动和侵袭,是一种有效的trypsin 抑制剂(IC50:3.0 μM)。 | |||
T13741 |
Isoviolanthin
异佛莱心苷,异佛来心苷 |
Others | Others |
Isoviolanthin 是一种黄酮类苷类化合物,提取自铁皮石斛叶中。它能减少 TGF-β1 处理的 HCC 细胞的迁移和入侵能力,对正常细胞没有毒性影响,对转移性肝癌晚期具有潜在的研究价值。 | |||
T2787 |
Picroside I
6'-Cinnamoylcatalpol,胡黄连苦苷I |
MMP; STAT | JAK/STAT signaling; Proteases/Proteasome; Stem Cells |
Picroside I (6'-Cinnamoylcatalpol) 是胡黄连的一种天然产物,是有肝脏保护作用的代谢成分,可用于哮喘研究,有减轻炎症作用,还下调 pSTAT6 和 GATA3 表达。 | |||
T5S0055 |
Chelidonine
Helidonine,Khelidonin,白屈菜碱,Stylophorin |
Apoptosis; Others; Influenza Virus | Apoptosis; Microbiology/Virology; Others |
Chelidonine (Stylophorin) 是白屈菜中的一种异喹啉生物碱,有抗肿瘤和抗病毒作用。它可导致细胞周期 G2/M 停滞,诱导 caspase 依赖和非依赖性的细胞凋亡。 | |||
T3S0737 |
Flavokawain A
2'-羟基-4,4',6'-三甲氧基查耳酮,Flavokavain A |
Apoptosis; p38 MAPK | Apoptosis; MAPK |
Flavokawain A (Flavokavain A) 是 kava 提取物中的查耳酮,是一种抗癌试剂,具有抗肿瘤活性。它通过 Bax 蛋白依赖和线粒体依赖的凋亡途径诱导细胞凋亡,有潜力用于膀胱癌的相关研究。 | |||
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。 | |||
T3794 |
Pentagalloylglucose
Penta-O-galloyl-β-D-glucose,1,2,3,4,6-O-Pentagalloylglucose,1,2,3,4,6-Penta-O-galloyl-beta-D-glucopyranose,1,2,3,4,6-五没食子酰葡萄糖 |
Influenza Virus | Microbiology/Virology |
1,2,3,4,6-O-Pentagalloylglucose (Penta-O-galloyl-β-D-glucose) 存在于多种植物中,具有重要的药理作用。Pentagalloylglucose 表现出显著的抗狂犬病病毒 (RABV) 活性。 | |||
T12403 |
Penitrem A
|
Others | Others |
Penitrem A is a selective antagonist of BK channel with antiproliferative and anti-invasive activities against multiple malignancies. | |||
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. | |||
TN1881 |
Lucidenic acid C
赤芝酸 C,赤芝酸C |
MMP | Proteases/Proteasome |
Lucidenic acid C has anti-invasive effect, it shows significant inhibitory effects on PMA-induced MMP-9 activity and invasion of HepG(2 )cells. | |||
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. |