83
23
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T22774L |
eukaryotic translation elongation factor 1 alpha 1 (EEF1A1) (387-394) [Multiple species](TFA)
|
Others | Others |
eukaryotic translation elongation factor 1 alpha 1 (EEF1A1) (387-394) [Multiple species](TFA) 是延伸因子 1 亚基。真核翻译延伸因子 1 alpha 1 (EEF1A1) 编码延伸因子 alpha 亚基的同种型- 1 复合物,负责将氨酰 tRNA 酶促递送至核糖体。这种亚型(α 1)在脑、胎盘、肺、肝、肾和胰腺中表达,另一种亚型(α 2)在脑、心脏和骨骼肌中表达。这种亚型在 66% 的 Felty 综合征患者中被鉴定为自身抗原。已发现该基因在许多染色体上具有多个拷贝,其中一些(如果不是全部)代表不同的假基因。 | |||
TP2247 |
eukaryotic translation initiation factor 3
|
Others | Others |
Eukaryotic initiation factors (eIF) are proteins involved in the initiation phase of eukaryotic translation. Eukaryotic translation initiation factor 3 binds to the ribosome subunit-mRNA complex. It has been implicated in preventing the large ribosomal subunit from binding the small subunit before it is ready to commence elongation. | |||
T22774 |
eukaryotic translation elongation factor 1 alpha 1 (EEF1A1) (387-394) [Multiple species]
|
Others | Others |
eukaryotic translation elongation factor 1 alpha 1 (EEF1A1) encodes an isoform of the alpha subunit of the elongation factor-1 complex, which is responsible for the enzymatic delivery of aminoacyl tRNAs to the ribosome. This isoform (alpha 1) is expressed | |||
T11375 |
GCN2iB
|
Others; Autophagy | Autophagy; Others |
GCN2iB 是一种 ATP 竞争性的一般控制非抑制性 2 抑制剂,IC50 为 2.4 nM。 | |||
T1742 |
4E1rcat
|
PERK; Autophagy | Apoptosis; Autophagy |
4E1RCat 是 cap 依赖性翻译抑制剂,可抑制 eIF4 g 与 eIF4E 的结合,IC50 为 3.2 μM。 | |||
T14044 |
4E2RCat
|
PERK | Apoptosis |
4E2RCat 是一种 eIF4E-eIF4G 相互作用的抑制剂,IC50为13.5 μM。 | |||
T21508 |
Anhydrotetracycline hydrochloride
|
Antibacterial; Antibiotic | Microbiology/Virology |
Anhydrotetracycline hydrochloride 是四环素的生物合成前体,是广谱的、有效的竞争性四环素破坏酶抑制剂。它是真核细胞中四环素控制的基因表达系统的效应子。 | |||
T2665 |
4EGI-1
4EGI 1 |
Apoptosis; PERK; Autophagy | Apoptosis; Autophagy |
4EGI-1 是一种竞争性 eIF4E/eIF4 g 相互作用抑制剂,与 eIF4E 结合,Kd 值为 25 μM。 | |||
T11374 |
GCN2-IN-6
|
Others; PERK | Apoptosis; Others |
GCN2-IN-6 经酶法和细胞分析证实,是一种口服有效GCN2抑制剂,IC50分别为1.8 nM 和9.3 nM。GCN2-IN-6 还是 eIF2α 激酶PERK 抑制剂,在酶法测定和细胞测定中的IC50分别为 0.26 nM 和 230 nM。 | |||
T3207 |
Briciclib
ON 014185 |
CDK; PERK; Autophagy | Apoptosis; Autophagy; Cell Cycle/Checkpoint |
Briciclib (ON 014185) 是一种 ON 013100 衍生物,是一种抑制 Y 细胞中 cyclin D1 积累的小分子。它可靶作用于eIF4E,有抑制实体瘤的潜力。 | |||
T11373 |
GCN2-IN-1
A-92 |
Others | Others |
GCN2-IN-1 (A-92) 是一种有效的一般性调控阻遏蛋白激酶 2 抑制剂,可作为化疗药物用于癌症治疗的研究。 | |||
T9149 |
2BAct
2B-Act,2B Act |
PERK | Apoptosis |
2BAct 是一种具有口服活性的高选择性真核起始因子eIF2B 活化剂,EC50为 33 nM。它可防止由慢性综合应激反应引起的神经系统缺陷。 | |||
T5173 |
SBI-0640756
SBI 0640756,SBI-756 |
PERK; Autophagy | Apoptosis; Autophagy |
SBI-0640756 (SBI-756) 是一种靶向 eIF4G1 并破坏 eIF4F 复合物的抑制剂。 | |||
T28506 |
Rbin-2
|
Phosphatase | Metabolism |
Rbin-2 是一种具有细胞渗透性、强效性、选择性和可逆性的 Midasin(Mdn1) 抑制剂。Rbin-2 直接靶向 AAA+ ATPase Midasin,抑制真核生物核糖体的生成,是研究真核生物核糖体组装过程的强效探针。 | |||
TQ0137 |
A-484954
A 484954 |
CaMK; Parasite; Autophagy | Autophagy; Microbiology/Virology; Neuroscience |
A-484954 (A 484954) 是一种高度特异性的真核延伸因子-2 抑制剂,其 IC50值为 280 nM。 | |||
T62461 |
Benzyl-piperazine-CO-benzothiazole-4-methylpiperidine
|
Others | Others |
Benzyl-piperazine-CO-benzothiazole-4-methylpiperidine 可用于改变真核生物寿命。 | |||
T22592 |
ATPγS tetralithium salt
ATP-gamma-S tetralithium salt |
PERK | Apoptosis |
ATPγS tetralithium salt 是真核生物翻译起始因子 eIF4A 的核苷酸水解和RNA解链活性的底物,与 p97 突变体和朊病毒相关。 | |||
T67945 |
WAY-620473
|
PARP | Chromatin/Epigenetic; DNA Damage/DNA Repair |
WAY-620473是一种有效的 PARP-1抑制剂,具有抗肿瘤活性,可改变真核生物的寿命。 | |||
T7411 |
Rbin-1
Ribozinoindole-1 |
ATPase; Phosphatase | Membrane transporter/Ion channel; Metabolism |
Rbin-1 (Ribozinoindole-1) 是一种选择性 Midasin 抑制剂,是一种可逆的、特异性真核核糖体生物合成抑制剂,GI50=136 nM。 | |||
T28543 |
RK-9123016
RK9123016,RK 9123016 |
Sirtuin | Chromatin/Epigenetic; DNA Damage/DNA Repair |
RK-9123016是一种SIRT2抑制剂。RK-9123016增加真核翻译起始因子5A(eIF5A)(SIRT2的生理底物)的乙酰化水平,降低人乳腺癌细胞的细胞活力,同时降低c-Myc 表达。 | |||
T15790 |
Lucifer Yellow CH dilithium salt
|
||
Lucifer Yellow CH dilithium salt 是一种荧光染料,可常用于选择性染色和研究光动力破坏真核细胞和亚细胞结构。 | |||
TP1875L |
CDK2 acetate(255064-79-0 free base)
|
Others | Others |
CDK2 acetate(255064-79-0 free base) 是真核生物 S/T 蛋白激酶家族的成员,其功能是催化 ATP γ-磷酸磷酸基转移到蛋白质底物中的丝氨酸或苏氨酸羟基(表示为 S0/T0)。 | |||
T39965 |
NF-κΒ activator 1
|
NF-κB | NF-κB |
NF-κΒ activator 1 可激活NF-κΒ基因,EC50 为 0.9 μM。NF-κB 作为一种调控细胞增殖和细胞存活的基因被真核细胞广泛应用。NF-κΒ activator 1 可诱导超氧化物歧化酶 (SOD)2 mRNA 表达。 | |||
T11372 |
GC7 Sulfate
|
Autophagy | Autophagy |
GC7 Sulfate 是 deoxyhypusine synthase(DHS)有效抑制剂。真核翻译起始因子5A2 (eIF5A2)是DHS 已知的底物,因此GC7通过抑制DHS 活性来抑制eIF5A2的激活。 | |||
T3045 |
Salubrinal
|
Apoptosis; Phosphatase; PERK; Autophagy; HSV | Apoptosis; Autophagy; Metabolism; Microbiology/Virology |
Salubrinal 是一种磷酸酶抑制剂 ,对真核翻译起始因子 2 亚基 (eIF2α) 发挥作用。它作为双特异性磷酸酶 2 抑制剂,抑制抗胶原蛋白抗体诱导的关节炎。它具有抗HSV-1病毒的活性,并抑制由HSV-1蛋白 ICP34.5 介导的eIF2α的去磷酸化。 | |||
T15735 |
Leptomycin B
CI 940,LMB,来普霉素B |
CRM1; Antibiotic; Antifungal | Membrane transporter/Ion channel; Microbiology/Virology |
Leptomycin B (LMB) 是一种抗真菌抗生素,可阻断真核细胞周期,抑制蛋白出核转运。Leptomycin 通过半胱氨酸残基处的共价修饰使 CRM1/exportin 1失活。它 | |||
T38889 |
Thailanstatin A
|
||
Thailanstatin A 是真核 RNA 剪接抑制剂,IC50为650 nM,通过非共价结合到剪接体的 U2 snRNA 亚复合物的 SF3b 亚单位发挥作用。Thailanstatin A 对多种癌细胞系的抑制显示 nM 级别的 IC50。它与 Trastuzumab 上的赖氨酸结合,可产生“无连接子” ADC。 | |||
T27544 |
Hippuristanol
|
||
Hippuristanol is a potent steroid inhibitor of eukaryotic initiation factor 4A (eIF4A). | |||
T34033 |
Phosphohistidine
3-Phosphohistidine |
||
Phosphohistidine is a eukaryotic enzyme dephosphorylating proteins and peptides. | |||
T10848 | CMLD012073 | Others | Others |
CMLD012073 is a potent eukaryotic initiation factor 4A (eIF4A) inhibitor. It inhibits NIH/3T3 cells (IC50: 10 nM). CMLD012073 inhibits eukaryotic translation initiation by modifying the behavior of the RNA helicase (eIF4A). | |||
T10849 |
CMLD012612
|
Others | Others |
CMLD012612 is a potent eukaryotic initiation factor 4A (eIF4A) inhibitor. It inhibits cell translation and is cytotoxic to NIH/3T3 cells (IC50: 2 nM). | |||
T40210 |
eIF4E-IN-3
eIF4E-IN-3 |
||
eIF4E-IN-3 is a highly effective inhibitor of eukaryotic initiation factor 4e (eIF4e), exhibiting noteworthy potential for investigating eIF4e dependent diseases, particularly cancer research (WO2021003157A1, compound 485). | |||
T11171 | eIF4A3-IN-2 | Others | Others |
eIF4A3-IN-2 is a highly selective and noncompetitive eukaryotic initiation factor 4A-3 inhibitor with an IC50 of 110 nM. | |||
T70790 |
Pateamine A
|
||
Pateamine A is a marine macrolide that is isolated from the sponge Mycale hentscheli and exhibits anticancer and antiviral properties. It has a role as a marine metabolite, an antiviral agent, an antineoplastic agent, and a eukaryotic initiation factor 4F inhibitor. It is a macrolide, a member of 1,3-thiazoles, a tertiary amino compound, a primary amino compound, and an olefinic compound. Pateamine A an inhibitor of eukaryotic translation. | |||
T40214 |
eIF4E-IN-2
eIF4E-IN-2 |
||
eIF4E-IN-2 is a highly effective inhibitor of eukaryotic initiation factor 4e (eIF4e). This compound exhibits significant potential in the investigation of eIF4e dependent diseases, particularly in the context of cancer research. | |||
T10847 |
CMLD012072
|
Others | Others |
CMLD012072 is a potent eukaryotic initiation factor 4A (eIF4A) inhibitor with potent anti-neoplastic activity. It can induce RNA clamping of eIF4A1 and eIF4A2. | |||
T69376 |
Viriditoxin
|
||
Viriditoxin is a secondary metabolite isolated from Aspergillus viridinutans that has been shown to inhibit FtsZ, the bacterial homologue of eukaryotic tubulin. | |||
TP1875 |
CDK2
|
||
CDK2 is a member of the eukaryotic S/T protein kinase family and its function is to catalyze the phosphoryl transfer of ATP γ-phosphate to serine or threonine hydroxyl (denoted as S0/T0) in a protein substrate. | |||
T39530 |
eIF4A3-IN-5
eIF4A3-IN-5 |
||
eIF4A3-IN-5 is a highly effective inhibitor of eukaryotic initiation factor 4A (eIF4A), specifically targeting eIF4AI and eIF4AII. With its potent inhibitory properties, eIF4A3-IN-5 shows great potential for advancing research in eIF4A-dependent diseases, including cancer studies. | |||
T26973 |
Cefatrizine
Cephatriazine,BL-S-640,BLS640,S 640P,BL S 640 |
||
Cefatrizine is an inhibitor of eukaryotic elongation factor-2 kinase, a unique calcium/calmodulin-dependent protein kinase, is well known to regulate apoptosis, autophagy and ER stress in many types of human cancers. | |||
T74246 |
Transfectam
|
||
Transfectam为一种阳离子脂质,能与DNA形成复合物,从而高效地将基因转入多种真核细胞。 | |||
T32537 |
LAI-1
LAI 1,Legionella autoinducer-1,Legionella autoinducer 1 |
||
LAI-1 is a regulator of bacterial signaling, modulating gene regulation and cellular responses of eukaryotic cells (amoebae or macrophages) and a variety of processes including pathogen-host cell interactions. | |||
T71815 |
TX-1918
|
||
TX-1918 is a cell-permeable tyrphostin derivative that inhibits eukaryotic elongation factor-2 kinase (eEF-2K). TX-1918 disrupts the proliferation of HepG2 and HCT116 tumor cells. | |||
T19306 |
ELX-02 disulfate
NB-124 disulfate |
Others | Others |
ELX-02 disulfate (also referred to as NB-124 disulfate) is a synthetic eukaryotic ribosome selective glycoside (ERSG). This compound is currently in development as a therapy specifically designed to address genetic diseases resulting from nonsense mutations. | |||
T38766 |
Histone H3 (1-35)
Histone H3 (1-35) |
||
Histone H3 (1-35) is a 35-residue peptide derived from histone H3, which is a key member of the five main histones participating in the formation of chromatin within eukaryotic cells. | |||
T16945 |
Streptolydigin
Portamycin |
Antibacterial | Microbiology/Virology |
Streptolydigin inhibits RNA synthesis by binding to RNA polymerase and does not inhibit eukaryotic RNA polymerases. Streptolydigin is a 3-acetyltetramic acid antibiotic and a potent bacterial RNA polymerase inhibitor (Ki: 18 μM and a Kd: 15 μM). | |||
T32126L |
Hypusine HCl
(+)-Hypusine dihydrochloride,Hypusine dihydrochloride |
||
Hypusine HCl is an unusual amino acid found in all eukaryotes and in some archaea, but not in bacteria. The only known protein containing hypusine is eukaryotic translation initiation factor 5A (eIF5A) and a similar protein found in archaebacteria. | |||
T31616 |
ELX-02
NB-124,NB 124,NB124,ELX02,ELX 02 |
||
ELX-02, also known as NB-124, is a eukaryotic ribosomal selective glycoside (ERSG) designed to increase the read-through activity in patients with nonsense mutations and enable the production of sufficient amounts of full-length functional protein to rest | |||
T63728 |
RAD51-IN-7
|
||
RAD51-IN-7 是 RAD51 的有效抑制剂。其中 RAD51 是一种真核生物基因。RAD51-IN-7 对线粒体缺陷病症表现出研究潜力。 | |||
T15136L |
DiZPK Hydrochloride (1337883-32-5 free base)
DiZPK Hydrochloride |
Others | Others |
DiZPK Hydrochloride is a structural analog of pyrrolysine (Pyl), acting as a photocrosslinker for identifying direct protein-protein interactions in living prokaryotic and eukaryotic cells. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TQ0131 |
Rocaglamide
Rocaglamide A,楝酰胺,Roc-A |
HSP; NF-κB; PERK | Apoptosis; Cytoskeletal Signaling; Metabolism; NF-κB |
Rocaglamide (Roc-A) 是从米仔兰中分离出来的一种天然产物,具有抗癌特性,可用于咳嗽,受伤,哮喘和炎症性皮肤病。它是一种有效的选择性热休克因子 1 活化抑制剂,IC50约为 50 nM。它是 T 细胞中 NF-κB 活化的有效抑制剂,还抑制翻译起始因子eIF4A 的功能。 | |||
T6512 |
G-418 disulfate
Geneticin,G418 Sulfate,Antibiotic G-418 sulfate,遗传霉素,Geneticin sulfate |
Antibacterial; Antibiotic | Microbiology/Virology |
G-418 disulfate (Geneticin sulfate) 属于氨基糖苷类抗生素,是一种蛋白质合成的抑制剂,具有真核细胞选择性。G-418 disulfate 通过抑制肽链的延伸来阻断多肽合成。 | |||
T7450 |
1-Phenylpropane-1,2-dione
1-Phenyl-1,2-propanedione,Acetyl benzoyl,1-苯基-1,2-丙二酮 |
Others | Others |
1-Phenylpropane-1,2-dione (Acetyl benzoyl) 是麻黄素生物碱的生物合成前体,分离自从嫩麻黄中。 | |||
T19083 |
1-Methylinosine
N1-Methylinosine,Inosine, 1-methyl,1-甲基肌苷 |
Nucleoside Antimetabolite/Analog; Endogenous Metabolite | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism |
1-Methylinosine (N1-Methylinosine) 是在真核生物 tRNA 反密码子 3' 位 tRNA 的 37 位上发现的修饰核苷酸,具有代谢物的作用。 | |||
T3093 |
Spermine tetrahydrochloride
精胺盐酸盐,Spermine Tetrahydrochloride,Neuridine tetrahydrochloride,Musculamine tetrahydrochloride,Gerontine tetrahydrochloride |
Others; Endogenous Metabolite | Metabolism; Others |
Spermine tetrahydrochloride (Musculamine tetrahydrochloride) 是内源性代谢产物的一种。 | |||
T64911 |
Blasticidin S HCl
|
Antibiotic | Microbiology/Virology |
Blasticidin S HCl 是从 Streptomyces griseochromogenes 中分离的肽基核苷类抗生素 (antibiotic),主要通过干扰核糖体中肽键的形成从而抑制原核细胞和真核细胞蛋白的合成。 | |||
T5055 |
For-Met-OH
fMet,N-甲酰甲硫氨酸,N-Formyl-L-methionine |
Others; Endogenous Metabolite | Metabolism; Others |
For-Met-OH (N-Formyl-L-methionine) 是内源性代谢产物的一种。 | |||
T9715 |
Aplidine
|
SARS-CoV; DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology |
Aplidine 是有效的eEF1A2(KD=80 nM) 靶向的抗癌药物。Aplidine 具有抗病毒活性,抑制SARS-CoV-2的 IC90为 0.88 nM。Aplidine 在多发性骨髓瘤,晚期癌症及 COVID-19 领域有研究的价值。 | |||
T3S1729 |
Dihydrolycorine
|
Others | Others |
Dihydrolycorine 是分离自Lycoris radiate 草药中,是一种真核细胞中蛋白质合成的抑制剂。 | |||
T0950 |
Neomycin sulfate
Framycin sulfate,硫酸新霉素 |
Phospholipase; ribosome; Antibacterial; Antibiotic | Metabolism; Microbiology/Virology |
Neomycin sulfate (Framycin sulfate) 是一种广谱的氨基糖苷类抗生素。Neomycin sulfate 可以阻断细菌蛋白质的合成以发挥抗菌活性。Neomycin sulfate 常用于筛选具有 Neo 抗性基因的原核和真核细胞。 | |||
T1022 |
Hygromycin B
潮霉素B,Hygrovetine |
ribosome; Antibacterial; Antibiotic; Antifungal | Microbiology/Virology |
Hygromycin B (Hygrovetine) 是一种氨基糖苷类抗生素,通过干扰易位并导致 70S 核糖体的错误翻译来抑制蛋白质合成。Hygromycin B 可用于筛选转染 hph 或 hyg 抗性基因的原核或者真核细胞。 | |||
T5270 |
5-Methylcytosine
|
Others; DNA/RNA Synthesis; Endogenous Metabolite | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism; Others |
5-Methylcytosine 是一种存在于真核 DNA 中的甲基化核苷酸碱基。它是由 DNA 甲基转移酶作用形成的表观遗传修饰。 | |||
T7961 |
N4-Benzoyl-2′-deoxycytidine
N-苯甲酰-2'-脱氧胞苷 |
Others | Others |
N4-Benzoyl-2′-deoxycytidine 是天然核苷脱氧胞苷(dC)的合成核苷类似物,是一种DNA 聚合酶的竞争性抑制剂。体外研究表明,它可以抑制病毒、细菌和真核细胞的复制。在动物模型中,它也被证明可以抑制肿瘤细胞的生长。 | |||
T5075 |
Phytic acid potassium
植酸二钾盐,Inositol hexakisphosphate dipotassium salt,Phytic acid dipotassium salt,Fytic Acid dipotassium salt,Inositol polyphosphate dipotassium salt |
Others; Endogenous Metabolite | Metabolism; Others |
Phytic acid potassium (Inositol polyphosphate dipotassium salt) 是内源性代谢产物的一种。 | |||
T2924 |
Phloretin
根皮素,Dihydronaringenin,NSC 407292,RJC 02792 |
SGLT; transporter; Endogenous Metabolite | GPCR/G Protein; Metabolism |
Phloretin (NSC-407292) 是从苹果树叶中提取的一种查耳酮,具有抗炎、抗氧化和抗癌活性。它是真核尿素转运蛋白抑制剂,可阻断 VacA 介导的尿素和离子转运,有潜力用于类风湿性关节炎和过敏性气道炎症的相关研究。 | |||
T2830 |
Betulinic acid
白桦脂酸,桦木酸,ALS-357,Lupatic acid,Betulic acid |
Apoptosis; Mitophagy; NF-κB; HIV Protease; Topoisomerase; Endogenous Metabolite; Aminopeptidase; Autophagy | Apoptosis; Autophagy; DNA Damage/DNA Repair; Metabolism; Microbiology/Virology; NF-κB; Proteases/Proteasome |
Betulinic acid (ALS-357) 是从白桦树皮中分离出来的一种五环三萜类天然产物,是真核细胞拓扑异构酶 I 的抑制剂,IC50值为 5 μM,具有抗逆转录病毒、抗疟疾、抗癌和抗炎特性。 | |||
T16884 |
Silvestrol
(-)-Silvestrol |
Others | Others |
Silvestrol is a eukaryotic translation initiation factor 4A inhibitor. Silvestrol causes autophagy and caspase-mediated apoptosis. | |||
T12298 |
Oligomycin B
|
Others | Others |
Oligomycin B is an antibiotic isolated from marine Streptomyces, is an eukaryotic ATP synthase inhibitor, induces apoptosis. | |||
T15094 | Dehydroaltenusin | DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Dehydroaltenusin is a selective eukaryotic DNA polymerase α inhibitor and a type of antibiotic produced by a fungus (IC50: 0.68 μM). Dehydroaltenusin inhibits mammalian pol α activity. | |||
T15703 | Lactimidomycin | Others | Others |
Lactimidomycin, isolated from Streptomyces, is an inhibitor of eukaryotic translation elongation. It is also a potent and non-toxic inhibitor of dengue virus 2 and other RNA viruses. Lactimidomycin has an antiproliferative effect on tumor cell lines. It i | |||
TN4623 | Nagilactone C | Antifection | Microbiology/Virology |
Nagilactone C and phyllanthoside are novel protein synthesis inhibitors, they are specific for the eukaryotic translation apparatus, function in vivo and in vitro, and interfere with translation elongation. Nagilactone C shows high insecticidal activity against second-instar nymphs of Eocanthecona furcellata. Nagilactone C possesses potent antiproliferative activity against human fibrosarcoma and murine colon carcinoma tumor cell lines exhibiting ED50 values of 2.3 and 1.2 microg/ml, respectivel... | |||
T73602 |
Phosphorylcholine
Phosphocholine |
Endogenous Metabolite | Metabolism |
Phosphorylcholine 广泛存在于生物界,是存在于真核生物膜中的磷脂,也存在于与真核生物相关联的共生菌或致病菌中。Phosphorylcholine 具有免疫调节特性,可用于研究动脉粥样硬化。 | |||
TN2977 |
3-O-trans-p-Coumaroyltormentic acid
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Caspase; Antifection | Apoptosis; Microbiology/Virology; Proteases/Proteasome |
3-O-(E)-p-coumaroyl tormentic acid may be promising lead compound for developing an effective drug for treatment of leukemia, it induces apoptotic cell death in human leukemia (HL60) via mainly mitochondrial pathway by, at least in part, Topo I inhibition. 3-O-trans-p-coumaroyltormentic acid shows cytotoxicity against four human tumor cell lines (A549, SK-OV-3, SK-MEL-2, and HCT-15) in vitro, the IC50 values of 13.72, 14.29,14.61, 14.04 uM, respectively. 3beta-O-cis-p-Coumaroyltormentic acid, an... |