首页工具

登录

搜索结果

Search Results for " pc3 "

63

抑制剂 & 化合物

10

天然产物

如果没找到您满意的产品或者您对产品有其他要求，可以联系我们专业顾问为您提供针对性的合理建议。 QQ咨询网站留言咨询

Cat. No.	Product Name	Target	Signaling Pathways
T12928	SK33	Androgen Receptor	Endocrinology/Hormones
	SK33 是一种有效的组织选择性抗雄激素药物，是一种肌醇类似物，能够降低雄激素受体 (AR) 的转录活性。
T1267	Abacavir Epzicom,Ziagen,阿巴卡韦,Abacavir sulfate	Apoptosis; HIV Protease; Reverse Transcriptase	Apoptosis; Microbiology/Virology; Proteases/Proteasome
	Abacavir (Ziagen) 是一种核苷类似物逆转录酶抑制剂。
T6967	RHPS4 RHPS 4 methosulfate,NSC714187	Apoptosis; Telomerase	Apoptosis; DNA Damage/DNA Repair
	RHPS4 (RHPS 4 methosulfate) 是 DNA 损伤诱导剂，是一种有效的亚微摩尔端粒酶抑制剂，IC50为0.33 μM。
T1448	Dasatinib BMS-354825,达沙替尼	Apoptosis; Bcr-Abl; Src; c-Kit; Autophagy	Angiogenesis; Apoptosis; Autophagy; Cytoskeletal Signaling; Tyrosine Kinase/Adaptors
	Dasatinib (BMS-354825) 是一种酪氨酸激酶抑制剂，抑制 Src 和 Bcr-Abl (Ki=16/30 pM)，具有口服活性和 ATP 竞争性。Dasatinib 具有抗肿瘤活性，用于治疗白血病和淋巴瘤等。
T6367	Abacavir sulfate Abacavir Hemisulfate,硫酸阿巴卡韦,1592U89,ABC sulfate,Ziagen	Apoptosis; HIV Protease; Reverse Transcriptase	Apoptosis; Microbiology/Virology; Proteases/Proteasome
	Abacavir sulfate (Ziagen) 是一种核苷类似物逆转录酶抑制剂，可用于 HIV 和 AIDS。
T1448L	Dasatinib monohydrate 达沙替尼,BMS-354825 Monohydrate	Apoptosis; Bcr-Abl; Src; c-Kit; Ephrin Receptor; Autophagy	Angiogenesis; Apoptosis; Autophagy; Cytoskeletal Signaling; Tyrosine Kinase/Adaptors
	Dasatinib monohydrate (BMS-354825 Monohydrate) 是一种具有口服活性的，ATP 竞争性的双重Src/Bcr-Abl 抑制剂，有抗肿瘤活性，还诱导凋亡和自噬。它抑制Src 和Bcr-Abl 的IC50分别为 0.5 nM 和 <1.0 nM，Ki 值分别为 16 pM 和 30 pM。
T61407	TRPC3/6-IN-1
	TRPC3/6-IN-1 is a highly potent and selective inhibitor that specifically blocks the activity of the canonical transient receptor channels TRPC3 and TRPC6. It exhibits a significant blocking potency against the human isoforms hTRPC3 and hTRPC6, with IC50 values of 1260 nM and 500 nM, respectively. This compound, TRPC3/6-IN-1, is particularly valuable for conducting research on chronic models of heart failure [1].
T35071	VPC32179 VPC 32179,VPC-32179
	VPC32179 is a bioactive chemical.
T29113	VPC32183 VPC-32183,VPC 32183
	VPC32183 is a competitive antagonist of LPA1 and LPA3 receptors.
T79054	TRPC3/6-IN-2
	TRPC3/6-IN-2为针对TRPC3及TRPC6的高效抑制剂，IC50分别为16 nM对TRPC3与29.8 nM对TRPC6。
T10657	C75 C-75	Fatty Acid Synthase	Metabolism
	C75 是一种合成脂肪酸合酶 (FASN) 抑制剂，可抑制前列腺癌细胞 PC3 (IC50: 35 μM)。
T35666	PRGL493	Others	Others
	PRGL493为高效、选择性的长链酰基辅酶a合成酶4 (ACSL4) 抑制剂，能在乳腺和前列腺细胞以及动物模型中抑制细胞增殖和肿瘤生长，主要应用于癌症研究。
T29110	VPC-13163 2,3-dihydro-2,3'-Bi-1H-indole,VPC13163,NSC52361,NSC 52361,VPC 13163	Others	Others
	VPC-13163 (NSC-52361) 对 LNCaP 和耐恩杂鲁胺的前列腺癌细胞系 (MR49F) 具有很强的抗增殖活性，而它不影响 AR 独立 PC3 细胞系的生长。它还抑制 LNCaP 和 MR49F 中的前列腺特异性抗原 (PSA) 并降低 AR 靶基因 PSA 和 TMPRSS2 的表达。这些发现表明 VPC-13566 表现出 AR BF3 特定的作用机制。
TP1895L1	KYL acetate(676657-00-4 free base)	Ephrin Receptor	Tyrosine Kinase/Adaptors
	KYL acetate(676657-00-4 free base) 是EphA4受体酪氨酸激酶抑制剂（Kd = 0.8 μM）；抑制 EphA4-EphrinA5 相互作用 (IC50 = 6.34 μM)。防止 AβO 诱导的突触损伤、树突棘丢失并防止海马 CA3-CA1 传输中 LTP 的阻断。在细胞培养基中表现出较长的半衰期（在 PC3 和 C2C12 培养基中分别为 8 和 12 小时）。它有神经保护作用。
T3989	SMI-16a PIM1/2 Kinase Inhibitor VI	Pim	Chromatin/Epigenetic; JAK/STAT signaling
	SMI-16a (PIM1/2 Kinase Inhibitor VI) 是选择性 Pim 激酶抑制剂，对 Pim1、Pim2 和 PC3 细胞的 IC50值分别为0.15、0.02 和48 μM。
T10656	trans-C75 (±)-C75,反-4-羧基-5-辛基-3-甲基-丁内酯	Others; Fatty Acid Synthase	Metabolism; Others
	trans-C75 ((±)-C75) 是一种 C75 的对映异构体。其中 C75 是一种脂肪酸合成酶 (FASN) 的抑制剂。
T64222	Antitumor agent-55
	Antitumor agent-55 (compound 5q) 是一种有效的抗肿瘤剂，能够有效的抑制PC3 (IC50: 0.91 μM)。Antitumor agent-55 能够将 PC3 的细胞周期阻滞 G1/S 期，诱导其凋亡，抑制细胞迁移，阻碍 PC3 的形成。
T36991	Monascuspiloin
	Monascuspiloin is a fungal metabolite that has been found inM. pilosusM93-fermented rice.1It induces endoplasmic reticulum stress and autophagy in PC3 prostate cancer cells. Monascuspiloin (15-45 μM) decreases viability of PC3 cells and has an additive effect on the reduction in viability of PC3 cells induced by irradiation when used at a concentration of 25 μM. It induces intratumor apoptosis and autophagy and reduces tumor growth in a PC3 mouse xenograft model when administered at doses of 40 ...
T72468	Anticancer agent 25
	Anticancer agent 25对 PC3细胞显示出较强的细胞毒性，IC50值为0.19μM。
T68441	SABRAC
	SABRAC inhibits acid ceramidase in PC3 MC metastatic prostate cancer cells (IC50 = <1 µM), as well as induces accumulation of ceramides in the same cells.
T78980	Pim-1 kinase inhibitor 5	Pim	Chromatin/Epigenetic; JAK/STAT signaling
	Pim-1 kinase inhibitor 5 (Compound 4c)是一种选择性Pim-1激酶抑制剂，具有0.61 μM的半抑制浓度(IC50)。该化合物对HepG2、MCF-7、PC3和HCT-116癌细胞系表现出细胞毒性，其IC50s值介于6.95至20.19 μM之间。
T10924	Cysteine protease inhibitor-2	Cysteine Protease	Proteases/Proteasome
	Cysteine protease inhibitor-2 是半胱氨酸蛋白酶抑制剂。
T83007	Antitumor agent-120
	Antitumor agent-120 (compound 1) 为一类黄酮化合物，来源于葛根提取。本化合物对LNCaP和PC3癌细胞的抑制作用不明显，表现出IC50s均大于50 μM。
T78051	Necrocide 1	Others	Others
	Necrocide 1（化合物(S)-38）是一款有效的抗癌药物，具备显著的抗增殖效果，针对MCF-7和PC3细胞株的IC50值分别为0.48 nM及2 nM。
T35629	ATRA-BA Hybrid
	ATRA-BA hybrid is a mutual prodrug form of all-transretinoic acid and butyric acid .1ATRA-BA hybrid is cleaved to release ATRA and BA in isolated mouse plasma. It inhibits the growth of MDA-MB-231 breast and PC3 prostate cancer cells with GI50values of 0.01 and 1.02 μM, respectively. ATRA-BA (20 μM) has 15-fold greater antiproliferative activity in PC3 cells compared to an equimolar concentration of ATRA and BA. 1.Gediya, L.K., Khandelwal, A., Patel, J., et al.Design, synthesis, and evaluation o...
T74299	MS5033
	MS5033 是一种有效的基于 PROTAC 的 AKT 降解剂，在 PC3 细胞中的 DC50值为 430 nM。
T70792	SPR519
	SPR519 is a potent dual inhibitor of PI3Kα and mTOR kinases with IC50 (PI3Kalpha) = 30 nM and IC50 (mTOR) = 10 nM. SPR519 exhibits an EC50 of low sub-micromolar range among various tested cancer cell lines such as A2780 (0.23 μM), PC3 (0.48 μM), and SKOV3 (0.50 μM).
T61902	Anticancer agent 69
	Anticancer agent 69 (Compound 34) 是有效的选择性抗癌剂，对人前列腺癌细胞系 PC3 具有选择性抑制作用(IC50=26 nM)。Anticancer agent 69 可以增加ROS 水平，下调EGFR，从而诱导细胞凋亡apoptosis。
T35940	Darinaparsin Dimethylarsinic glutathione,Darinaparsin
	Darinaparsin is a dimethylated arsenic linked to glutathione. It is cytotoxic to DU145, LNCaP, and PC3 prostate cancer cells (IC50s = 5-10 &#181M) and patient-derived primary prostate cancer cells (IC50s = 2.5-20 &#181M), as well as Jurkat T cell lymphoma and L540 Hodgkin lymphoma cells (IC50s = 2.7 and 1.3 &#181M, respectively). [1][2] It decreases the tumor-initiating subpopulation in DU145 and PC3 cells and halts the cell cycle in the G2/M phase. Darinaparsin decreases transcription of Gli-2,...
T74300	MS143
	MS143 是一种有效的AKT 降解剂，在 PC3 细胞中DC50=46 nM，GI50=0.8 µM。MS143 通过劫持泛素-蛋白酶体系统，以浓度和时间依赖性的方式诱导快速、稳定的AKT 降解。MS143 能抑制癌细胞生长。
T79202	Anticancer agent 118
	Anticanceragent 118是一种N-酰化环丙沙星衍生物，展现了针对革兰氏阳性(bacterial)菌株的高度活性，以及对前列腺癌PC3细胞的抗增殖能力，适用于抗肿瘤研究。
T35855	AAA
	AAA is an antagonist of G protein-coupled receptor 75 (GPR75).1It increases basal GPR75 protein levels and inhibits 20-HETE-induced reductions in GPR75 protein levels in PC3 cells. AAA (5 and 10 μM) also reduces 20-HETE-induced phosphorylation of EGFR, NF-κB, and Akt in, and cell migration of, PC3 cells.In vivo, AAA (10 mg/kg per day) reduces systolic blood pressure, albuminuria, renal angiotensin II levels, and cardiac hypertrophy in a Cyp1a1-Ren-2 transgenic rat model of malignant hypertension...
T36628	PROTAC BRD4 Degrader-8 PROTAC BRD4 Degrader-8
	PROTAC BRD4 Degrader-8 is a potent BRD4 inhibitor, with IC50s of 1.1 nM and 1.4 nM for BRD4 BD1 and BD2, respectively. PROTAC BRD4 Degrader-8 is capable of potently degrading the BRD4 protein in PC3 prostate cancer cells[1]. PROTAC BRD4 Degrader-8 (compound 8; 6 days) inhibits the proliferation of PC3 prostate cancer cells, with an IC50 of 28 nM[1].PROTAC BRD4 Degrader-8 (4 h) suppresses MYC gene transcript in MV4-11 AML cells, with an IC50 of 11 nM[1].PROTAC BRD4 Degrader-8 (4 h) potently degra...
T74124	PROTAC BRD4 Degrader-11
	PROTACBRD4Degrader-11 (compound 9a) 是一种有效的由von Hippel-Lindau 配体和BRD4配体相连的PROTAC。PROTACBRD4Degrader-11 可与 STEAP1 和 CLL1 抗体偶联从而降解 PC3 前列腺癌细胞中的BRD4蛋白，DC50值分别为 0.23 nM 和 0.38 nM。
T40073	PROTAC BRD4 Degrader-10 PROTAC BRD4 Degrader-10
	PROTAC BRD4 Degrader-10, also known as compound 8b, is a dual ligand-based PROTAC that combines ligands for von Hippel-Lindau and BRD4. To degrade the BRD4 protein in PC3 prostate cancer cells, PROTAC BRD4 Degrader-10 can be conjugated with STEAP1 and CLL1 antibodies, with respective DC 50 values of 1.3 nM and 18 nM.
T70962	MHY219
	MHY219 is a novel HDAC inhibitor. MHY219 induces apoptosis via up-regulation of androgen receptor expression in human prostate cancer cells. MHY219 was shown to enhance the cytotoxicity on DU145 cells (IC50, 0.36 μM) when compared with LNCaP (IC50, 0.97 μM) and PC3 cells (IC50, 5.12 μM). MHY219 showed a potent inhibition of total HDAC activity when compared with SAHA. MHY219 increased histone H3 hyperacetylation and reduced the expression of class I HDACs (1, 2 and 3) in prostate cancer cells. M...
T40072	PROTAC BRD4 Degrader-9 PROTAC BRD4 Degrader-9
	PROTAC BRD4 Degrader-9 (compound 8a) is a novel chemical compound consisting of ligands for von Hippel-Lindau and BRD4, connected by a PROTAC moiety. This compound can effectively degrade the BRD4 protein in PC3 prostate cancer cells. When conjugated with STEAP1 and CLL1 antibodies, PROTAC BRD4 Degrader-9 exhibits potent activity, with respective DC50 values of 0.86 nM and 7.6 nM.
T62278	Anticancer agent 36
	Anticancer agent 36 (compound 11) 是一种有效的抗微生物剂和抗癌剂，是一种磺酰脲类衍生物。Anticancer agent 36 对蕈状芽孢杆菌、大肠杆菌和白色念珠菌的微生物生长有抑制作用 (MIC: 0.156 - 0.039 mg/mL)。Anticancer agent 36 能够抑制 A549 细胞 (IC50: 19.7 μg/mL)、PC3 细胞 (IC50: 11.9 μg/mL) 生长。
T74126	PROTAC BRD4 Degrader-14
	PROTACBRD4Degrader-14 是一种由 von Hippel-Lindau 配体和 BRD4配体相连的 PROTAC，对 BRD4BD1和 BD2的 IC50值分别为 1.8 nM 和 1.7 nM。PROTACBRD4Degrader-14 能够有效降解 PC3 前列腺癌细胞中的 BRD4蛋白。
T82089	ICMT-IN-53
	ICMT-IN-53 (compound 12)是ICMT抑制剂，IC50值为0.96 μM，展现出PAMPA渗透性及抗增殖效果。该化合物在抑制MDA-MB-231与PC3细胞增殖方面的IC50s分别为5.14 μM与5.88 μM。
T40074	PROTAC BRD4 Degrader-15 PROTAC BRD4 Degrader-15
	PROTAC BRD4 Degrader-15 is a chemical compound consisting of a PROteolysis TArgeting Chimera (PROTAC) linked to ligands specific to von Hippel-Lindau and BRD4. It exhibits an IC50 of 7.2 nM for BRD4 BD1 and 8.1 nM for BRD4 BD2. Additionally, PROTAC BRD4 Degrader-15 demonstrates potent degradation activity against the BRD4 protein in PC3 prostate cancer cells.
T74125	PROTAC BRD4 Degrader-12
	PROTACBRD4Degrader-12 (compound 9c) 是一种由 von Hippel-Lindau 配体和 BRD4配体相连的 PROTAC。PROTACBRD4Degrader-12 可与 STEAP1 和 CLL1 抗体偶联从而降解 PC3 前列腺癌细胞中的 BRD4蛋白，DC50值分别为 0.39 nM 和 0.24 nM。
T35561	MS351
	MS351 is an antagonist of chromobox 7 (CBX7) that acts by binding the CBX7 chromodomain. It enhances the binding of long noncoding RNA to the CBX7 chromodomain when used at 25 μM. MS351 induces transcriptional derepression of CBX7 target genes, including p16 (INK4a), in mouse embryonic stem cells and human prostate cancer PC3 cells.
T62754	Anticancer agent 34
	Anticancer agent 34 (compound 9) 是一种磺酰脲类衍生物，也是一种有效的抗微生物剂和抗癌剂。Anticancer agent 34 对蕈状芽孢杆菌、大肠杆菌和白色念珠菌的微生物生长表现出抑制作用 (MIC: 0.039-0.156 mg/ml)。Anticancer agent 34 能够抑制 A549 细胞 (IC50: 8.4 μg/ml)、PC3 细胞 (IC50: 7.8 μg/ml) 的生长。
T73125	SMTIN-T140	HSP	Cytoskeletal Signaling; Metabolism
	SMTIN-T140（化合物6a）是一种TRAP1（肿瘤坏死因子受体相关蛋白1）的高效抑制剂，IC50值为1.646 μM。该化合物表现出显著的抗癌活性，可引起线粒体功能障碍，增加线粒体ROS产生以及激活AMPK。在PC3前列腺癌细胞异种移植的小鼠模型中，SMTIN-T140有效抑制了肿瘤生长，并显示出良好的体内安全性。
T63947	GRPR antagonist-1
	GRPR antagonist-1 是胃泌素释放肽受体 (GRPR) 的有效拮抗剂，对某些癌细胞具有细胞毒性 (能够作用于 PC3 细胞 (IC50: 4.97 μM)、Pan02 细胞 (IC50: 4.36 μM)、HGC-27 细胞 (IC50: 3.40 μM))。GRPR antagonist-1 能够减少 Bcl-2 水平、提高 Bax 水平，进而抑制 HGC-27 细胞活力，使细胞凋亡，表现出抗癌效果。
T79557	fac-[Re(CO)3(L6)(H2O)][NO3]	Apoptosis	Apoptosis
	fac-[Re(CO)3(L6)(H2O)][NO3]（compound 6）是一种具有针对线粒体功能失调的抗癌活性的铼(I)三羰基水配合物。该化合物对前列腺癌细胞展现出显著的细胞毒性，具有50 nM的IC50值（PC-3细胞）。fac-[Re(CO)3(L6)(H2O)][NO3]能够主要集中在细胞核，抑制PC3细胞的ATP生成并诱导细胞凋亡，而不触发坏死、焦亡或自噬过程。
T15205	EL-102 EL102	Microtubule Associated; HIF	Angiogenesis; Chromatin/Epigenetic; Cytoskeletal Signaling
	EL-102 是一种 HIF1α 抑制剂，具有抗癌活性，可抑制微管蛋白聚合，可用于研究前列腺癌。
T37018	OH-Chol
	OH-Chol is a cationic cholesterol derivative.1 OH-Chol, as a component of lipoplexes with DOPE , has been used for siRNA delivery and gene silencing in MCF-7 cells, as well as in mice via intravenous injection, resulting in lipoplex accumulation in the liver. It has also been used in cationic nanoparticles in combination with Tween 80 to transfect pDNA and siRNA into PC3 mouse xenografts via intratumoral injection and with Tween 80 and folate-PEG2000-DSPE in a KB mouse xenograft model for intrat...
T69758	Flutamide-d7
	Flutamide-d7 is intended for use as an internal standard for the quantification of flutamide by GC- or LC-MS. Flutamide is an androgen receptor antagonist and prodrug form of 2-hydroxy flutamide. Flutamide is converted to 2-hydroxy flutamide by the cytochrome P450 (CYP) isoform CYP1A2 in human liver microsomes. It is cytotoxic to PC3 and LNCaP prostate cancer cells with IC50 values of 98.8 and 81.8 µM, respectively. Flutamide (50 mg/kg per day) reduces tumor growth in a PC-82 mouse xenograft mo...

化合物

Cat.No: T12928

Target: Androgen Receptor

Cat.No: T1267

Synonym: Epzicom,Ziagen,阿巴卡韦,Abacavir sulfate

Target: Apoptosis, HIV Protease, Reverse Transcriptase

Cat.No: T6967

Synonym: RHPS 4 methosulfate,NSC714187

Target: Apoptosis, Telomerase

Cat.No: T1448

Synonym: BMS-354825,达沙替尼

Target: Apoptosis, Bcr-Abl, Src, c-Kit, Autophagy

Abacavir sulfate

Cat.No: T6367

Synonym: Abacavir Hemisulfate,硫酸阿巴卡韦,1592U89,ABC sulfate,Ziagen

Target: Apoptosis, HIV Protease, Reverse Transcriptase

Dasatinib monohydrate

Cat.No: T1448L

Synonym: 达沙替尼,BMS-354825 Monohydrate

Target: Apoptosis, Bcr-Abl, Src, c-Kit, Ephrin Receptor, Autophagy

Cat.No: T61407

Cat.No: T35071

Synonym: VPC 32179,VPC-32179

Cat.No: T29113

Synonym: VPC-32183,VPC 32183

Cat.No: T79054

Cat.No: T10657

Synonym: C-75

Target: Fatty Acid Synthase

Cat.No: T35666

Target: Others

Cat.No: T29110

Synonym: 2,3-dihydro-2,3'-Bi-1H-indole,VPC13163,NSC52361,NSC 52361,VPC 13163

Target: Others

KYL acetate(676657-00-4 free base)

Cat.No: TP1895L1

Target: Ephrin Receptor

Cat.No: T3989

Synonym: PIM1/2 Kinase Inhibitor VI

Target: Pim

Cat.No: T10656

Synonym: (±)-C75,反-4-羧基-5-辛基-3-甲基-丁内酯

Target: Others, Fatty Acid Synthase

Antitumor agent-55

Cat.No: T64222

Cat.No: T36991

Anticancer agent 25

Cat.No: T72468

Cat.No: T68441

Pim-1 kinase inhibitor 5

Cat.No: T78980

Target: Pim

Cysteine protease inhibitor-2

Cat.No: T10924

Target: Cysteine Protease

Antitumor agent-120

Cat.No: T83007

Cat.No: T78051

Target: Others

Cat.No: T35629

Cat.No: T74299

Cat.No: T70792

Anticancer agent 69

Cat.No: T61902

Cat.No: T35940

Synonym: Dimethylarsinic glutathione,Darinaparsin

Cat.No: T74300

Anticancer agent 118

Cat.No: T79202

Cat.No: T35855

PROTAC BRD4 Degrader-8

Cat.No: T36628

Synonym: PROTAC BRD4 Degrader-8

PROTAC BRD4 Degrader-11

Cat.No: T74124

PROTAC BRD4 Degrader-10

Cat.No: T40073

Synonym: PROTAC BRD4 Degrader-10

Cat.No: T70962

PROTAC BRD4 Degrader-9

Cat.No: T40072

Synonym: PROTAC BRD4 Degrader-9

Anticancer agent 36

Cat.No: T62278

PROTAC BRD4 Degrader-14

Cat.No: T74126

Cat.No: T82089

PROTAC BRD4 Degrader-15

Cat.No: T40074

Synonym: PROTAC BRD4 Degrader-15

PROTAC BRD4 Degrader-12

Cat.No: T74125

Cat.No: T35561

Anticancer agent 34

Cat.No: T62754

Cat.No: T73125

Target: HSP

GRPR antagonist-1

Cat.No: T63947

fac-[Re(CO)3(L6)(H2O)][NO3]

Cat.No: T79557

Target: Apoptosis

Cat.No: T15205

Synonym: EL102

Target: Microtubule Associated, HIF

Cat.No: T37018

Cat.No: T69758

Cat. No.	Product Name	Target	Signaling Pathways
T8188	Podophyllotoxone	Others; Microtubule Associated	Cytoskeletal Signaling; Others
	Podophyllotoxone 是从八角莲根中分离得到的一种天然产物，能抑制微管蛋白聚合，具有抗癌活性。
TN2054	Periplocymarin	Calcium Channel	Membrane transporter/Ion channel; Metabolism
	Periplocymarin 是一种强心苷，从 Periploca sepium 和 Periploca graeca 中分离得到，具有抗癌潜力。
TN1198	19-Hydroxybufalin	Others	Others
	19-Hydroxybufalin 是蟾二烯羟酸内酯，能够阻碍上皮间质转化，抑制 PC3 细胞的迁移和侵袭。
TN6638	(E)-6-O-(p-coumaroyl)scandoside methyl ester
	(E)-6-O-(p-coumaroyl)scandoside methyl ester shows moderate anti-proliferation effect on PC3 human androgen-independent prostate cancer cells.
TN3113	5-Heptadecylresorcinol 芒果	Others	Others
	5-Heptadecylresorcinol has strong inhibitory property against the growth of PC3 cells.
T36489	Malformin A
	Malformin A is a cyclopentapeptide fungal metabolite that has been found in A. niger and has diverse biological activities. It is a plant growth regulator that induces malformations in plant structure. Malformin A inhibits replication of tobacco mosaic virus (TMV) in local lesion and leaf-disc assays (IC50s = 19.7 and 45.4 μg/ml, respectively). It is cytotoxic to NCI-H460, MIA PaCa-2, MCF-7, SF-268, and WI-38 cancer cells (IC50s = 70, 50, 100, 70, and 100 nM, respectively), inhibits proliferati...
TN6059	Demethoxyfumitremorgin C
	Demethoxyfumitremorgin C and tryprostatin B are fungal inhibitors of mammalian cell cycle progression at the G(2)/M transition. Demethoxyfumitremorgin C inhibits the proliferation of PC3 human prostate cancer cells via the intrinsic (mitochondrial) and ex
T37442	Aspergillin PZ
	Aspergillin PZ is a fungal metabolite originally isolated from A. awamori. It induces morphological deformation of P. oryzae conidia when used at a concentration of 89 nM. Aspergillin PZ is active against S. epidermidis (MIC = 20 μM) but not S. aureus, E. coli, or B. cereus (MICs = >20 μM). It is cytotoxic to HL-60 promyelocytic leukemia cells (IC50 = 56.61 μM) but not THP-1 acute monocytic leukemia or PC3 prostate cancer cells (IC50s = >80 μM).
T37452	Stephacidin B
	Stephacidin B is a fungal metabolite that has been found inA. ochraceus.1Dimeric stephacidin B is rapidly converted to a monomer, avrainvillamide ,in vitro.2Stephacidin B is cytotoxic to a variety of cancer cells, including testosterone-independent PC3 and -sensitive LNCaP prostate cancer cells (IC50s = 0.37 and 0.06 μM, respectively) and estradiol-independent SK-BR-3 and -sensitive MCF-7 breast cancer cells (IC50s = 0.32 and 0.27 μM, respectively).1It induces apoptosis in HepG2 and Huh7 hepatoc...
T36749	Herboxidiene
	Herboxidiene is a polyketide originally isolated from S. chromofuscus that has diverse biological activities.[1],[2,][3],[4],[5] It inhibits growth of HeLa S3, SK-MEL-2, PC3, A549, and EBC-1 cells with GI50 values ranging from 7.4 to 62 nM.3 Herboxidiene is cytostatic against human umbilical vein endothelial cells (HUVECs; (IC50 = 26 nM)) and inhibits VEGF-induced invasion and tube formation of serum-starved HUVECs in a concentration-dependent manner, indicating antiangiogenic activity.[4] Herbo...

天然产物

Podophyllotoxone

Cat.No: T8188

Target: Others, Microtubule Associated

Cat.No: TN2054

Target: Calcium Channel

19-Hydroxybufalin

Cat.No: TN1198

Target: Others

(E)-6-O-(p-coumaroyl)scandoside methyl ester

Cat.No: TN6638

5-Heptadecylresorcinol

Cat.No: TN3113

Synonym: 芒果

Target: Others

Cat.No: T36489

Demethoxyfumitremorgin C

Cat.No: TN6059

Cat.No: T37442

Cat.No: T37452

Cat.No: T36749

我们的所有产品和服务仅用于科学研究，不能被用于人体，我们也不向个人提供产品和服务。

Copyright © 2015-2024 TargetMol Chemicals Inc. All rights reserved. 沪ICP备20019793号-4

沪公网安备 31010602006700号

沪公网安备 31010602006700号

TargetMol Loading

联系我们

电话：

400-820-0310

邮箱：

service@tsbiochem.com

QQ：

2881945090（终端用户）

2885109491（经销商）

经销：

终端：

地址：

上海市静安区江场三路238号8楼