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Search Results for " colony formation "

39

抑制剂 & 化合物

2

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T22089	HPI 1	Hedgehog/Smoothened	GPCR/G Protein; Stem Cells
	HPI 1 是一种刺猬 (Hh) 信号抑制剂。在 Shh-LIGHT2 细胞中抑制 Sonic Hedgehog (Shh)-、SAG- 和 Gli 诱导的 Hh 通路激活（Shh-、SAG-、Gli2- 和 Gli1 诱导的激活的 IC50 值为 1.5、1.5、4 和 6 μM） .
T10723	CDC25B-IN-1 ethyl 3-[(3-methoxynaphthalen-1-yl)amino]benzoate	Phosphatase	Metabolism
	CDC25B-IN-1 是 CDC25B 的抑制剂，Ki 为 8.5 μM。 CDC25B-IN-1 通过抑制细胞增殖和集落形成来增加 G2/M 期。
T2011	RKI1313 RKI 1313,RKI-1313	ROCK	Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells
	RKI1313 (RKI-1313) 是一种选择性抑制剂，可抑制 ROCK 依赖性信号传导、细胞骨架变化、不依赖锚定的集落形成、迁移和侵袭。
T60197	UNC 1025	Others	Others
	UNC1062 is a highly selective tyrosine kinase inhibitor that specifically targets MERTK. This compound effectively suppresses MERTK-mediated downstream signaling, induces apoptosis in cell cultures, reduces colony formation in soft agar, and inhibits invasion of melanoma cells. Notably, UNC1062 demonstrates potent inhibition of MERTK kinase activity, with an IC50 of 1.1 nM and a Morrison Ki of 0.33 nM. It also displays specificity within the TAM family, exhibiting IC50 values of 60 nM for TYRO3 ...
T61722	ZDLD20	Apoptosis	Apoptosis
	ZDLD20 是一种具有口服活性和选择性的CDK4抑制剂，是一种 β-咔啉类化合物，具有抗 HCT116 和抗癌活性，抑制集落形成、抑制侵袭和迁移、诱导细胞凋亡和阻止细胞周期的 G1 期。
T77677	12R-LOX-IN-2	Lipoxygenase	Metabolism
	12R-LOX-IN-2 是一种 12R-脂氧合酶 (12R-LOX) 的抑制剂。12R-LOX-IN-2 抑制咪喹莫特 (IMQ) 诱导银屑病角质形成细胞过度增殖，并抑制细胞集落形成。12R-LOX-IN-2 还降低 IMQ 诱导细胞中 Ki67 的蛋白水平和 IL-17A 的 mRNA 表达。12R-LOX-IN-2 可用于牛皮癣和其他皮肤相关炎症性疾病的研究。
T37518	Diphenyl disulfide Phenyl disulfide	Apoptosis; BCL; Endogenous Metabolite	Apoptosis; Metabolism
	Diphenyl disulfide (Phenyl disulfide) 在乳腺癌细胞系中显示出抗癌活性。Diphenyl disulfide 通过Bax 蛋白水解活化和伴随的自噬来诱导并增强乳腺癌细胞的凋亡。Diphenyl disulfide 以剂量依赖性方式抑制细胞增殖和活力，并减少集落形成。Diphenyl disulfide 可用来治疗乳腺癌。
T23726	WB-308 WB308
	WB-308 is an EGFR inhibitor that acts by decreasing NSCLC cell proliferation and colony formation and causing G2/M arrest and apoptosis.
T28848	SR31527 SR-31527,SR31527 chloride,SR 31527	Kinesin	Cytoskeletal Signaling
	SR31527 (SR31527 chloride) 是一种有效的 KIFC1 抑制剂，对KIFC1的IC50 为 6.6 µM。SR31527 chloride 对细胞活力和集落形成有一定的抑制作用。
T60672	GSD-11
	GSD-11 抑制 Akt/mTOR 信号通路。GSD-11 是一种有效的选择性抗紧缩剂，抑制 PANC-1 细胞的迁移和集落形成，具有用于胰腺癌研究的潜力。
T11691	IV-23	Others	Others
	IV-23, a potent inhibitor of cell growth both in vitro and in vivo, effectively reduces colony formation, arrests the cell cycle at the M phase, and induces apoptosis in esophageal squamous cell carcinoma through Noxa-mediated pathways. This compound emerges as a promising anticancer agent with significant potential.
T79434	Antitumor agent-103	Apoptosis	Apoptosis
	Antitumor agent-103（compound 24l）是一种诱导凋亡（apoptosis）的化合物，具备抗增殖及抗克隆形成的特性。该化合物能够导致细胞周期在G0/G1期发生阻滞，并且刺激NO的产生，表现出显著的抗肿瘤活性。
T24411	Y08060 Y 08060,Y-08060
	Y08060 is an effective and selective BET Inhibitor for the Treatment of Prostate Cancer. Y08060 effectively suppresses cell growth, colony formation, and expression of androgen receptor (AR), AR regulated genes, and MYC in prostate cancer cell lines. Y08060 has IC50 values of 3.23 and 4.41 μM in inhibition of cell viability in the C4 2B and LNCaP cell lines, respectively.
T79289	Antiproliferative agent-27	Apoptosis	Apoptosis
	Antiproliferative agent-27 (化合物 11) 作为一种有效的抗增殖剂，可显著降低肿瘤细胞的集落数量并诱导细胞凋亡，显示出在癌症研究中的应用潜力。
T74919	QA-68
	QA-68 (QA-68-ZU81) 为一种高效BRD9降解剂。该化合物抑制细胞周期进展与细胞集落生成，对急性髓系白血病（AML）细胞系展现出抗增殖能力。
T69205	GGTI-2166
	GGTI-2166 is a geranylgeranyl transferase I inhibitor. GGTI-2166 inhibit the pOC formation induced by RANKL or TNF-alpha in cultures of both mouse marrow-derived macrophage-colony-stimulating factor (M-CSF) dependent monocytes (MD cells) and the mouse monocyte cell line RAW 264.7 (RAW cells). GGTI-2166 inhibited TRAP activity induced by RANKL or TNF-alpha in both cell cultures and prevented the incorporation of [3H]all-trans geranylgeraniol into prenylated proteins in RAW cells.
T79445	KV1.3-IN-1	Potassium Channel	Membrane transporter/Ion channel
	KV1.3-IN-1 (Compound trans-18) 作为KV1.3通道抑制剂，表现出对Ltk 细胞和PHA激活的T淋巴细胞的IC50值分别为230 nM和26.12 nM。该化合物干扰了细胞内Ca2+信号传导，并能够抑制T细胞的活化、增殖与集落形成。
T78768	HDAC6-IN-16	HDAC	Chromatin/Epigenetic; DNA Damage/DNA Repair
	HDAC6-IN-16（compound 5c）是基于Quinazolin-4(3H)-One的一种HDAC6抑制剂，具备抑制肿瘤细胞集落形成的抗癌活性。该化合物能够引发G2期细胞周期阻滞并诱导细胞凋亡(apoptosis)。
T78746	Mtb-IN-3
	Mtb-IN-3（化合物10c）是针对结核分枝杆菌（Mtb）的选择性抑制剂。该化合物具有有效的体外抗Mtb活性，并且不表现出细胞毒性。在小鼠结核病模型中，Mtb-IN-3可抑制脾脏的集落形成。
T62398	KH-3
	KH-3 是一种 RNA 结合蛋白 Hu 抗原 R (HuR) 的有效抑制剂 (IC50: 0.35 μM)，表现出抗增殖作用。KH-3 能够干扰 HuR–FOXQ1 Mrna 相互作用，抑制乳腺癌细胞侵袭，并延缓肺集落的形成。
T74542	YM458	Histone Methyltransferase	Chromatin/Epigenetic
	YM458为EZH2和BRD4的有效双重抑制剂，IC50值分别为490 nM和34 nM。该化合物能够抑制实体癌细胞的增殖与集落形成，并诱导细胞周期阻滞与细胞凋亡(apoptosis)，适用于抗癌研究领域。
T78880	Tubulin/HDAC-IN-3
	Tubulin/HDAC-IN-3（compound 12a）为一种高效的tubulin/HDAC汇合型抑制剂，能显著破坏微管蛋白聚合（IC50: 5.4 μM），并对HDAC1/8展现强效抑制作用，IC50值分别为0.155 μM和0.177 μM。该化合物通过阻断细胞周期、诱导细胞凋亡（apoptosis）及抑制集落形成以施展其生物学效用。
T64210	ATX inhibitor 13
	ATX inhibitor 13 (compound 10c) 是一种口服具有活力的 ATX 抑制剂 (IC50: 3.4 nM)。ATX inhibitor 13 能够将RAW264.7 细胞的细胞周期阻滞在 G2 期，抑制细胞的增殖和迁移，诱导细胞凋亡。ATX inhibitor 13 对肿瘤细胞集落形成表现出抑制作用。
T79685	PI3Kα-IN-13	PI3K	PI3K/Akt/mTOR signaling
	PI3Kα-IN-13（Compound 18a）是一款高效的PI3Kα抑制剂，具有2.5 nM的IC50值。此化合物能够诱发肿瘤细胞的凋亡，并显著抑制癌细胞的增殖，具体IC50值为MCF-7细胞系0.75 μM、HCT-116细胞系3.79 μM、MDA-MB-231细胞系13.71 μM和SW620细胞系9.85 μM。此外，PI3Kα-IN-13能有效阻止肿瘤细胞集落的形成、迁移以及侵袭。
T64014	Antitumor agent-58
	Antitumor agent-58 是一种抗肿瘤剂，对 MGC-803 细胞的集落形成和细胞迁移具有有效的抑制作用，并能够诱导 MGC-803 细胞的线粒体功能障碍。Antitumor agent-58 可以激活 p38 和 JNK 信号通路，并诱导 MGC-803 细胞凋亡 (apoptosis)。Antitumor agent-58 对携带 MGC-803 细胞的异种移植模型的肿瘤生长表现出有效的抑制活性。
T83023	Antiproliferative agent-26
	Antiproliferative agent-26 (compound 4g) 是抗增殖药物，(10 μM) 对多种癌细胞如白血病、中枢神经系统肿瘤、黑色素瘤、肾癌和乳腺癌具有抑制效果。该药物能够阻止集落形成，并在(5 μM) 和 (25 μM) 浓度作用下导致细胞周期在G1期/S期停滞。
T28269	ORY-1001 free base RG 6016,ORY-1001,ORY 1001,ORY1001,RG-6016,RG6016
	ORY-1001 is a KDM1A inhibitor (IC50 <20nM) with high selectivity against related FAD dependent aminoxidases (MAO-A/B, IL4I1, KDM1B >100uM, SMOX 7uM). Treatment of THP-1 (MLL-AF9) cells with ORY-1001, results in a time/dose dependent me2H3K4 accumulation a
T36514	QD-394
	QD-394 is an inducer of reactive oxygen species (ROS) production.1It induces lipid peroxidation, increases in intracellular accumulation of reactive oxygen species (ROS), and decreases in the reduced glutathione (GSH) to oxidized GSH (GSSG) ratio in MIA PaCa-2 pancreatic cancer cells when used at concentrations ranging from 0.5 to 10 μM. QD-394 is cytotoxic to MIA PaCa-2, PANC-1, and BxPC-3 cancer cells (IC50s = 0.64, 0.34, and 0.9 μM, respectively). QD-394 acts synergistically with napabucasin ...
T78837	CP-07	CDK	Cell Cycle/Checkpoint
	CP-07为高效的PROTAC CDK9选择性降解剂（DC50：43 nM），能显著抑制22RV1细胞增殖（IC50：62 nM）及集落形成，其作用机制为通过下调Mcl-1与c-Myc。此外，CP-07有效抑制22RV1异种移植肿瘤的生长，有望成为研究前列腺癌的重要化合物。
T64027	ALK-IN-23
	ALK-IN-23 是 ALK 的有效抑制剂，能够作用于 ALKWT (IC50: 1.6 nM)、ALKL1196M (IC50: 0.71 nM) 和 ALKG1202R (IC50: 1.3 nM)。ALK-IN-23 能够诱导细胞凋亡 (apoptosis) 并将细胞阻滞在 G2 期。ALK-IN-23 在体外对癌细胞迁移和集落形成具有抑制作用。在 H2228 异种移植裸鼠模型中，ALK-IN-23 具有良好的抗肿瘤效果且毒性较低。
T60689	ZDLD13
	ZDLD13 是一种 β-咔啉，具有强大的抗 HCT116 活性，包括抑制侵袭和迁移、抑制集落形成、诱导细胞凋亡以及阻止细胞周期的 G1 期。ZDLD13是口服有效的 CDK4/CycD3选择性抑制剂 (IC50 = 0.38 μM)。ZDLD13 在 HCT116 肿瘤异种移植模型中表现出显着的抑制肿瘤生长作用。
T37050	MPS1/TTK Inhibitor MPS1/TTK Inhibitor
	MPS1/TTK inhibitor is an inhibitor of monopolar spindle 1 (MPS1/TTK; IC50 = 5.8 nM), a kinase involved in mitotic spindle checkpoint signaling that is overexpressed in certain cancerous tumors. It inhibits MPS1 phosphorylation of kinetochore scaffold 1 (KNL1) and increases the rate of mitosis and the number of cells entering anaphase within 15 minutes, indicating MPS1 checkpoint inhibition, when used at a concentration of 100 nM. MPS1/TTK inhibitor (50 and 100 nM) increases the number of missegr...
T3512	S49076 HCl S-49076 Hydrochloride	FGFR; c-Met/HGFR; TAM Receptor	Angiogenesis; Tyrosine Kinase/Adaptors
	S49076 HCl (S-49076 Hydrochloride) 是 MET、AXL/MER 和 FGFR1/2/3 的有效抑制剂。S49076 HCl 在体外和体内有效阻断 MET、AXL 和 FGFR 的细胞磷酸化并抑制下游信号传导。在细胞模型中，S49076 HCl (S-49076 Hydrochloride) 抑制 MET 和 FGFR2 依赖性胃癌细胞的增殖，阻断 MET 驱动的肺癌细胞迁移，并抑制表达 FGFR1/2 和 AXL 的肝癌细胞的集落形成。在肿瘤异种移植模型中，建立了口服 S49076 HCl (S-49076 Hydrochloride) 后 MET 和 FGFR2 抑制的良好药代动力学/药效学关系，并与对肿瘤生长的影响密切相关。
T69682	AEW541 HCl
	AEW541, also known as NVP-AEW541, is a novel, potent IGF-IR kinase inhibitor. NVP-AEW541 is capable of distinguishing between the IGF-IR (IC50 = 0.086 microM) and the closely related InsR (IC50 = 2.3 microM) in cells. NVP- AEW541 abrogates IGF-I-mediated survival and colony formation in soft agar at concentrations that are consistent with inhibition of IGF-IR autophosphorylation. Note: AEW541 has a Cis-configuration on the cyclobutane ring. Its CAS# is 475489-16-8. Many vendors and Sc-finder sc...
T37873	CAP 3
	CAP 3 is a cholic acid-peptide conjugate (CAP) with antibacterial activity. It is active against the Gram-negative bacteria E. coli, K. pneumoniae, and A. baumanii (MIC99s = 8, 16, and 16 μM, respectively). CAP 3 increases the fluidity of model Gram-negative bacterial membranes and binds to LPS in vitro. It reduces the biomass and number of colony-forming units in E. coli biofilms in a concentration-dependent manner. CAP 3 inhibits E. coli biofilm formation on catheters implanted in mice infecte...
T63590	c-Met-IN-10
	c-Met-IN-10 是高效的 c-Met 激酶抑制剂 (IC50: 16 nM)。c-Met-IN-10 能够抑制癌细胞 A549、H460 和 HT-29 的活性，通过抑制 HT-29 细胞集落形成，进而诱导 HT-29 和 A549 细胞凋亡 apoptosis，抑制 A549 细胞移动。c-Met-IN-10 能够用于抗癌研究。
T78853	PI3K-IN-47	PI3K	PI3K/Akt/mTOR signaling
	PI3K-IN-47 (Compound 27) 是一款高度选择性的二价PI3K抑制剂，对PI3Kα具有极低的半抑制浓度（IC50: 0.44 nM）, 同时对PI3Kβ、PI3Kγ、PI3Kδ也表现出良好的抑制活性（IC50分别为7.18 nM、13.92 nM、22.83 nM）。此化合物能够有效诱导细胞周期在G1期发生暂停，并且在体外抑制集落形成和细胞迁移。对于HGC-27异种移植的小鼠模型，PI3K-IN-47能够显著抑制肿瘤生长。
T83914	Glutaminase C Inhibitor 11
	Glutaminase C inhibitor 11是一种glutaminase C (GAC)的抑制剂。它能够抑制GAC酶的活性（EC50 = 10.64 nM），降低A549非小细胞肺癌(NSCLC)细胞的活力（IC50 = 4.025 nM）。在A549细胞中，Glutaminase C inhibitor 11（0.1和1 µM）能减少细胞集落形成并降低细胞内谷氨酸水平。在体内，Glutaminase C inhibitor 11（100 mg/kg）能够减缓A549小鼠异位瘤模型中的肿瘤生长。
T35955	PAR2 (1-6) amide (human) (trifluoroacetate salt) PAR2 (1-6) amide (human) (trifluoroacetate salt)
	PAR2 (1-6) amide is a synthetic peptide agonist of proteinase-activated receptor 2 (PAR2) that corresponds to residues 1-6 of the amino terminal tethered ligand sequence of human PAR2 and residues 37-42 of the full-length sequence.1It binds to NCTC 2544 cells expressing human PAR2 (Ki= 9.64 μM in a radioligand binding assay) and induces calcium mobilization in the same cells (EC50= 0.075 μM).2PAR2 (1-6) amide (100 μM) reduces colony formation of A549 lung cancer cells.1It induces superoxide prod...

化合物

Cat.No: T22089

Target: Hedgehog/Smoothened

Cat.No: T10723

Synonym: ethyl 3-[(3-methoxynaphthalen-1-yl)amino]benzoate

Target: Phosphatase

Cat.No: T2011

Synonym: RKI 1313,RKI-1313

Target: ROCK

Cat.No: T60197

Target: Others

Cat.No: T61722

Target: Apoptosis

Cat.No: T77677

Target: Lipoxygenase

Diphenyl disulfide

Cat.No: T37518

Synonym: Phenyl disulfide

Target: Apoptosis, BCL, Endogenous Metabolite

Cat.No: T23726

Synonym: WB308

Cat.No: T28848

Synonym: SR-31527,SR31527 chloride,SR 31527

Target: Kinesin

Cat.No: T60672

Cat.No: T11691

Target: Others

Antitumor agent-103

Cat.No: T79434

Target: Apoptosis

Cat.No: T24411

Synonym: Y 08060,Y-08060

Antiproliferative agent-27

Cat.No: T79289

Target: Apoptosis

Cat.No: T74919

Cat.No: T69205

Cat.No: T79445

Target: Potassium Channel

Cat.No: T78768

Target: HDAC

Cat.No: T78746

Cat.No: T62398

Cat.No: T74542

Target: Histone Methyltransferase

Tubulin/HDAC-IN-3

Cat.No: T78880

ATX inhibitor 13

Cat.No: T64210

Cat.No: T79685

Target: PI3K

Antitumor agent-58

Cat.No: T64014

Antiproliferative agent-26

Cat.No: T83023

ORY-1001 free base

Cat.No: T28269

Synonym: RG 6016,ORY-1001,ORY 1001,ORY1001,RG-6016,RG6016

Cat.No: T36514

Cat.No: T78837

Target: CDK

Cat.No: T64027

Cat.No: T60689

MPS1/TTK Inhibitor

Cat.No: T37050

Synonym: MPS1/TTK Inhibitor

Cat.No: T3512

Synonym: S-49076 Hydrochloride

Target: FGFR, c-Met/HGFR, TAM Receptor

Cat.No: T69682

Cat.No: T37873

Cat.No: T63590

Cat.No: T78853

Target: PI3K

Glutaminase C Inhibitor 11

Cat.No: T83914

PAR2 (1-6) amide (human) (trifluoroacetate salt)

Cat.No: T35955

Synonym: PAR2 (1-6) amide (human) (trifluoroacetate salt)

Cat. No.	Product Name	Target	Signaling Pathways
TN2269	Tetramethylcurcumin	Apoptosis; STAT	Apoptosis; JAK/STAT signaling; Stem Cells
	Tetramethylcurcumin 是一种新型姜黄素类似物，是一种有效的 STAT3 磷酸化、DNA 结合活性和体外反式激活抑制剂。它具有抗炎和抗癌作用。
T26358	(-)-Agelastatin A
	(-)-Agelastatin A inhibits osteopontin-mediated adhesion, invasion, and colony formation.

天然产物

Tetramethylcurcumin

Cat.No: TN2269

Target: Apoptosis, STAT

(-)-Agelastatin A

Cat.No: T26358

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