124
82
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T11917 |
Lys-SMCC-DM1
Lys-Nε-MCC-DM1 |
Microtubule Associated | Cytoskeletal Signaling |
DM1 是一种微管蛋白抑制剂。 Lys-SMCC-DM1 (Lys-Nε-MCC-DM1) 是 DM1 的活性代谢物。 | |||
TQ0018 |
6-Amino-5-azacytidine
|
Antibacterial | Microbiology/Virology |
6-Amino-5-azacytidine 对大肠杆菌的生长有抑制作用。 | |||
T21804 |
GW 610
|
Others | Others |
GW 610 是一种抗肿瘤剂,能够选择性作用于肺癌、结肠癌和乳腺癌细胞系,具有抗癌活性。 | |||
T10104 |
3,4-Dihydroxybenzylamine hydrobromide
NSC 263475 hydrobromide,3,4-二羟基苄胺·氢溴酸 |
Others; DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Others |
3,4-Dihydroxybenzylamine hydrobromide (NSC-263475 hydrobromide) 抑制黑色素瘤细胞中的 DNA 聚合酶活性,并在具有不同程度酪氨酸酶活性的黑色素瘤细胞系中显示出生长抑制活性。 | |||
T16449 |
PD176252
|
Bombesin Receptor | GPCR/G Protein |
PD176252 是一种有效的 BB1 和 BB2 拮抗剂,对 BB1 和 BB2 受体具有抑制作用。PD176252 可当作一种小分子 BB2 抑制剂和 FPR1/FPR2 激动剂可以抑制多种癌细胞的生长和增殖。 | |||
T24897 |
TP0427736
TP427736,TP-0427736,TP-427736 |
TGF-beta/Smad | Stem Cells |
TP0427736 是一种有效的选择性 ALK5 抑制剂,IC50 为 2.72 nM,比对 ALK3 的抑制作用高 300 倍。 TP0427736 可降低人外根鞘细胞中 TGF-β 诱导的生长抑制,并延长小鼠毛囊中的生长期。 | |||
T3567 |
SU 4942
|
Others | Others |
SU-4942 是酪氨酸激酶信号传导调节剂。SU-4942 对 VEGF 和内皮细胞生长因子 (ECGF) 诱导的内皮细胞有丝分裂具有抑制作用。 | |||
TP2236L |
Cortistatin-8 acetate
Cortistatin-8 acetate(485803-62-1 Free base) |
GHSR | GPCR/G Protein |
Cortistatin-8 acetate 是一种皮质抑素类似物,是一种GHS-R拮抗剂,对生长激素促分泌素受体有抑制作用。Cortistatin-8 acetate 是一种合成皮质抑素衍生的生长素释放肽受体配体,不会改变人类对酰化生长素释放肽或海沙瑞林的内分泌反应。 | |||
T4272 |
4-Hydroxyquinoline
4-羟基喹啉,4-Quinolinol,Quinolin-4-Ol |
Antibacterial | Microbiology/Virology |
4-Hydroxyquinoline (4-Quinolinol) 是一种具有抗菌活性的羟基化喹啉衍生物。它显示出对肠道细菌的生长抑制作用。它也可以用作光生氧物质的牺牲清除剂。 | |||
T9573 |
GSK3685032
|
DNA Methyltransferase | Chromatin/Epigenetic |
GSK-3685032 是一种非时间依赖、非共价、选择性的、可逆的DNMT1抑制剂,IC50=0.036 μM。它诱导 DNA 甲基化丧失、转录激活和癌细胞生长抑制。 | |||
TP1410 |
Cecropin A
|
Antibacterial; Antibiotic | Microbiology/Virology |
Cecropin A 是37个氨基酸组成的线性多肽,表现出抗菌、抗炎和抗肿瘤的功效。 | |||
T77437 |
Telisotuzumab
ABT-700,Mab-224G11 |
c-Met/HGFR | Tyrosine Kinase/Adaptors |
Telisotuzumab(ABT-700) 是一种人源化重组抗体,靶向治疗性肝细胞生长因子受体(MET)的抗体,对 c-Met 具有很高的亲和力 。Telisotuzumab 对 c-Met 信号传导具有抑制作用且具有抗肿瘤活性。 | |||
T11800 |
L-803087
|
Somatostatin | GPCR/G Protein |
L-803087 是一种具有高效性和选择性的生长抑素 sst4 受体激动剂,对 sst4 的 Ki 值为 0.7 nM,比其他生长抑素受体的选择性高 280 倍以上。L-803087 在体外诱导 AMPA 介导的海马突触反应,在体内增加了海藻酸盐促使的小鼠癫痫发作。 | |||
T21854 |
Proteasome inhibitor IX
PS-IX,AM114 |
Proteasome | Proteases/Proteasome; Ubiquitination |
Proteasome inhibitor IX (PS-IX) 是 Chalcone 的一种衍生物,对20S 蛋白酶体的胰凝乳蛋白酶样活性有抑制作用,IC50约为 1 μM。它抑制 HCT116 p53+/+细胞生长,IC50为 1.49 μM,显示出有效的抗癌活性。 | |||
T73582 |
EB1
|
MNK | MAPK |
EB1 是一种具有有效性和选择性的 MNK 激酶抑制剂,对 MNK1和 MNK2 具有抑制作用 IC50 分别为 0.69 μM 和 9.4 μM。EB1 抑制癌细胞的生长,促进细胞凋亡,抑制 eIF4E 磷酸化。 | |||
T36310 |
AKT-IN-6
INCB-047775 |
Akt | Cytoskeletal Signaling; PI3K/Akt/mTOR signaling |
AKT-IN-6 (INCB-047775)对ATK 有抑制作用。Akt 是对生长因子、细胞因子和其他细胞刺激的细胞信号传导的重要组成部分。Akt 的异常激活与2型糖尿病和癌症的发生密切相关。 | |||
T39392L |
C-Type Natriuretic Peptide (CNP) (1-22), human acetate
C-Type Natriuretic Peptide (CNP) (1-22), human acetate(1966153-17-2 Free base) |
Others | Others |
C-Type Natriuretic Peptide (CNP) (1-22), human acetate 是一种利钠肽受体 B (NPR-B) 的激动剂,一种内皮衍生的松弛剂和生长抑制因子。 C-Type Natriuretic Peptide (CNP) (1-22), human acetate 抑制由组胺和 5-HT 或直接由毛喉素刺激的 cAMP 合成。 | |||
T26873 |
BMY-27709
BMY 27709,BMY27709 |
Influenza Virus | Microbiology/Virology |
BMY-27709 是一种流感病毒生长抑制剂,对 A/WSN/33 病毒生长的 IC50 值为 3-8 μM,对流感病毒的部分亚型也展现出抑制活性。BMY-27709 对 H1 和 H2 病毒感染的早期起作用,通过抑制血凝素蛋白展现其抗病毒活性。然而,BMY-27709 对 H3 亚型病毒以及 B 型/Lee/40 流感病毒没有作用。 | |||
T76756 |
Parsatuzumab
RG 7414,Anti-EGFL7,MEGF0444A,MEGF-0444A,RO-5490248,M0444A |
VEGFR | Angiogenesis; Tyrosine Kinase/Adaptors |
Parsatuzumab (RG 7414) 是一种人源化靶向 EGFL7 的单克隆抗体,也可作为一种免疫调节剂使用。Parsatuzumab 选择性抑制 EGFL7 与内皮细胞之间的相互作用,对内皮生长因子 (VEGF) 有抑制作用。Parsatuzumab 长期其他化合物联合联合使用来研究直肠癌 | |||
T64124 |
Sunvozertinib
DZD9008,DZD 9008,DZD-9008 |
EGFR; BTK | Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors |
Sunvozertinib (DZD9008) 是一种有效的 ErbBs 和 BTK 抑制剂,对EGFR、Her2和突变型表皮生长因子有抑制作用。 Sunvozertinib 显示 EGFR 外显子 20 NPH 插入、EGFR 外显子 20 ASV 插入、EGFR L858R 和 T790M 突变以及 Her2 外显子 20 YVMA 和 EGFR WT A431 有抑制作用, IC50 分别为 20.4、20.4、1.1、7.5 和 80.4 nM 。 | |||
T79088 |
Chlamydia pneumoniae-IN-1
|
||
Chlamydia pneumoniae-IN-1 (compound 55),一种抗衣原体的苯并咪唑类化合物,对肺炎衣原体具有高度抑制作用,在10 μM 浓度下能够抑制99%的肺炎衣原体生长,并对宿主细胞的活力产生95%的抑制效果。此外,Chlamydia pneumoniae-IN-1 对CV-6菌株亦显示出明显的抗菌活性,其最小抑菌浓度(MIC)为12.6 μM。 | |||
T21831 |
UCM05
G28UCM |
Fatty Acid Synthase | Metabolism |
UCM05 (G28UCM) (G28UCM) 是一种有效的脂肪酸合酶 (FASN) 抑制剂,对 HER2+ 乳腺癌异种移植物具有作用活性,且在抗 HER2 耐药细胞系中具有活性。UCM05 是一种丝状温度敏感蛋白 Z (FtsZ) 抑制剂,可抑制革兰氏阳性菌B. subtilis 生长,MIC 值为 100 μM,但对革兰氏阴性菌E. coli 缺乏活性。 | |||
T76863 |
Elezanumab
AE12-1Y-QL,ABT-555 |
TGF-beta/Smad | Stem Cells |
Elezanumab(ABT-555) 是一种有效的人抗 RGMa 单克隆抗体。Elezanumab 通过 SMAD1/5/8 通路发挥对 RGMa 介导的 BMP 信号传导的抑制作用,IC50 约为 97 pM。在神经元损伤和脱髓鞘模型中,Elezanumab 促进神经再生、神经保护和神经恢复。Elezanumab 促进皮质脊髓轴突生长为脊髓灰质,并增强腹角的血清素能神经支配,形成颈部病变尾部的突触连接。 | |||
T24457 | Methotrexate-gamma-aspartate | ||
Methotrexate-gamma-aspartate has growth inhibitory effects. It is used in antibody-targeted liposomes. | |||
T24933 |
VCC234718
VCC-234718,VCC 234718 |
||
VCC234718 is an IMPDH inhibitor. VCC234718 showed growth inhibitory activity against Mycobacterium tuberculosis. VCC234718 inhibits Mtb GuaB2 (Ki: 100 nM). | |||
T71875 |
OM-137
|
||
OM137 is an inhibitor of Aurora kinases. which is growth inhibitory to cultured cells when applied at high concentration and potentiates the growth inhibitory effects of subnanomolar concentrations of paclitaxel. | |||
T71312 |
Litophynin C
|
||
Litophynin C is an Insect Growth Inhibitory Diterpenoid from a Soft Coral Litophyton sp. | |||
T10551 | Bithionol sulfoxide | Others | Others |
Bithionol sulfoxide is a clinically approved antiparasitic drug with the inhibitory against solid tumor growth in several preclinical cancer models. | |||
T69511 | Diospyrin | ||
Diospyrin is a plant product that has significant inhibitory effect on the growth of Leishmania donovani promastigotes. | |||
T71414 |
Litophynin A
|
||
Litophynin A is an insect Growth Inhibitory Diterpenoids from the Soft Coral Litophyton sp. | |||
T71862 |
GPR120-IN-1
|
||
GPR120-IN-1 is a novel GPR120 inhibitor, showing ~90% inhibitory effects on cell growth with micromolar affinities against SW480. | |||
T70240 |
Caparratriene
|
||
Caparratriene is a new sesquiterpene hydrocarbon isolated from Ocotea caparrapi with potential for significant growth inhibitory activityagainst CEM leukemia cells | |||
T69260 |
Genistein Diglucuronide
|
||
Genistein Diglucuronide is a metabolite of Genistein which exhibits specific inhibitory activity against tyrosine kinases including autophosphorylation of epidermal growth factor receptor kinase. | |||
T69863 | Dihydrogenistein | ||
Dihydrogenistein is a derivative of Genistein -- a compound that exhibits specific inhibitory activity against tyrosine kinases including autophosphorylation of epidermal growth factor receptor kinase. | |||
T71060 |
IST-622
|
||
IST-622 is a unique topoisomerase inhibitor, showing significant growth-inhibitory effects against large-cell lung cancer (Lu-116) and gastric adenocarcinoma (St-4). | |||
T69209 |
ZK-304709
|
||
ZK-304709 is a potent multi-target tumor growth inhibitor with IC50 = nanomolar inhibitory activity to cyclin-dependent kinases 1, 2, 4, 7 and 9, as well as vascular endothelial growth factor receptor tyrosine kinase 1-3 and of platelet-derived growth factor receptor beta tyrosine kinase. | |||
T70894 | Azamitosene | ||
Azamitosene is a DNA cleaving agent exhibiting G and A base specificity. Azamitosene may exhibit a growth inhibitory effect on human gastric cancer cells. | |||
T36750 |
Didesmethylrocaglamide
|
||
Didesmethylrocaglamide, a Rocaglamide derivative, is a potent eukaryotic initiation factor 4A (eIF4A) inhibitor that exhibits strong growth-inhibitory effects, with an IC50 of 5 nM. It hinders several growth-promoting signaling pathways and triggers apoptosis in tumor cells, demonstrating antitumor activity[1]. | |||
T62802 | Indoluidin E | ||
Indoluidin E 能够选择性地抑制 DHODH,且对癌细胞生长具有抑制作用。 | |||
T69264 |
Aristeromycin diphosphate
|
||
Aristeromycin diphosphate is an inhibitor of S-adenosylhomocysteine hydrolase (AHCY), inducing miR-26a and regulating oncogenic EZH2 expression, showing high inhibitory activity against AHCY, and causing growth inhibition of prostate cancer. | |||
T69293 |
Lasonolide A
|
||
Lasonolide A is a potential anticancer molecule isolated from the marine sponge Forcepia sp., with nanomolar growth inhibitory activity and a unique cytotoxicity profile against the National Cancer Institute 60-cell-line screen | |||
T39001 |
FGFR-IN-1
|
||
FGFR-IN-1 is a highly effective inhibitor targeting the Fibroblast Growth Factor Receptor (FGFR) group, comprising FGFR1, FGFR2, and FGFR3, with an impressive inhibitory concentration (IC 50) of less than 100 nM (US20130338134A1, example 219). | |||
T28007 | MDPD | ||
MDPD is an enhancer of the N-acylethanolamine degrading enzyme, fatty acid amide hydrolase, in Arabidopsis. MDPD alleviates the growth inhibitory effects of NAE 12:0, in part by enhancing the enzymatic activity of Arabidopsis FAAH (AtFAAH). | |||
T39856 |
Purine riboside triphosphate
PTP,Purine riboside triphosphate |
||
Purine riboside triphosphate, a derivative of purine riboside, exhibits structural similarity to adenosine. This naturally occurring base analog possesses inhibitory effects on carcinogenic growth, particularly in cancer ascites cells, by strongly impeding RNA and DNA synthesis. | |||
T41133 |
Ursonic acid methyl ester
|
||
Ursonic acid methyl ester, an esterified derivative of Ursolic acid, exhibits growth inhibitory activity against four tumor cell lines: HL-60, BGC, Bel-7402, and Hela, and the ED50 values for inhibition are >100 μg/ml. | |||
T60555 | Antiproliferative agent-3 | ||
Antiproliferative agent-3 (comp 4) 对 MCF-7 癌细胞表现出良好的活性,IC50值为 0.19 nM。 | |||
T63460 |
Tropesin
|
||
Tropesin 是一种非甾体抗炎剂 (NSAIA),对绿色木霉的生长具有抑制作用。 | |||
T80339 |
Gallin
|
||
Gallin是一种从蛋清提取的抗菌肽,在0.25 µM浓度时能够抑制Escherischia coli的生长。 | |||
T68209 |
Kopsoffinol
|
||
Kopsoffinol is a bisindole alkaloid that has been shown to have in vitro growth inhibitory activity against human PC-3, HCT-116, MCF-7, and A549 cells and moderate effects in reversing multidrug-resistance in vincristine-resistant human KB cells. | |||
T83244 |
7Ethanol-10NH2-11F-Camptothecin
|
||
7Ethanol-10NH2-11F-Camptothecin 是一抗体-活性分子偶联物(ADC),具有抑制肿瘤生长的功能,适用于癌症研究。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN1402 |
Arjungenin
阿江榄仁素,2ALPHA,19ALPHA,23-三羟基齐墩果酸 |
Antifection; Immunology/Inflammation related | Immunology/Inflammation; Microbiology/Virology |
Arjungenin, a triterpene derived from Terminalia arjuna, exhibits insect feeding-deterrent and growth inhibitory properties. | |||
T8283 |
(+)-Bornyl Acetate
Bornyl acetate,1-乙酸冰片酯,(+)-乙酸龙脑酯 |
Others | Others |
(+)-Bornyl Acetate 存在于 Pichtae 精油 (西伯利亚冷杉针油) 中。它能够显著抑制拟南芥幼苗根系生长。 | |||
TN1028 |
Militarine
|
Others | Others |
Militarine 是一种糖苷化合物,分离自 Bletilla striata,能够抑制植物生长。 | |||
T4S0051 |
Coptisine sulfate
|
Indoleamine 2,3-Dioxygenase (IDO) | Metabolism |
Coptisine Sulfate 是一种从黄连中分离到的生物碱,是非竞争性的IDO 抑制剂,Ki=为 5.8 μM,IC50=6.3 μM。 | |||
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)。 | |||
TN1433 | Batatasin III | FAK; Others; Akt | Angiogenesis; Cytoskeletal Signaling; Others; PI3K/Akt/mTOR signaling; Tyrosine Kinase/Adaptors |
Batatasin III 通过抑制上皮间质转化和 FAK-AKT 信号来抑制癌症迁移和侵袭,并具有抗癌活性。 Batatasin III 对整株生长有长期抑制作用,显示出抑制萌发活性。 | |||
TN2347 |
Methylsticin
麻醉椒苦素,Methysticin |
Others | Others |
Methylsticin (Methysticin) 是一种卡瓦内酯,从卡瓦根中分离得到。它能够抑制破骨细胞形成的活性。 | |||
T2978 |
Mogroside V
|
AMPK | Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
Mogroside V 是三萜糖苷,是非糖类甜味剂,甜度比蔗糖甜高300倍。它具有抗氧化,抗糖尿病和抗癌作用。 | |||
T2979 |
DL-Menthol
DL-薄荷醇,Hexahydrothymol,(±)-Menthol,薄荷醇 |
GABA Receptor; AChE | Membrane transporter/Ion channel; Neuroscience |
DL-Menthol ((±)-Menthol) 是单萜醇 (–)-薄荷醇和 (+)-薄荷醇的外消旋混合物,已在大麻中发现。它与 GABAA 受体的激活有关。 | |||
TN1905 |
Magnolioside
七叶苷甲基醚,6-甲氧基香豆素-7-0-BETA-D-吡喃葡萄糖苷 |
Antifection | Microbiology/Virology |
Magnolioside 是分离自Angelica gigas Nakai(Umbelliferae) 中,对谷氨酸诱导的毒性有显著的神经保护作用。 它显示出对金黄色葡萄球菌 CIP 53.154 的中等抗菌活性。它具有抗疟原虫活性,对氯喹敏感的恶性疟原虫菌株具有强烈的生长抑制作用。 | |||
T4S0998 |
Trifolirhizin
红车轴草根甙/三叶豆紫檀苷,三叶豆紫檀苷 |
TNF; Tyrosinase | Apoptosis; Proteases/Proteasome |
Trifolirhizin 是一种从苦参根中分离出的 pterocarpan 黄酮类化合物。它具有酪氨酸酶高抑制活性,IC50=506 μM。它具有抗炎和抗癌的潜能。 | |||
T7028 |
Licochalcone C
LICOCHALCONEC,甘草查尔酮C |
Phosphatase; Antioxidant; Glucosidase | Metabolism; oxidation-reduction |
Licochalcone C (LICOCHALCONEC) 能够抑制 α-葡萄糖苷酶,其对 α-葡萄糖苷酶的 IC50 <100 nM,对蛋白酪氨酸磷酸酶 1B 的 IC50=92.43 μM 。 | |||
T3864 |
Erianin
|
BCL; Antibacterial | Apoptosis; Microbiology/Virology |
Erianin 能抑制吲哚胺-2,3-双加氧酶诱导的肿瘤血管生成,可用作退烧药和止疼剂。 | |||
T3S2312 |
Poncirin
枸橘苷,Isosakuranetin-7-neohesperidoside |
Apoptosis; Others | Apoptosis; Others |
Poncirin (Isosakuranetin-7-neohesperidoside) 是从三叶草中分离出来的一种天然产物,具有抗炎活性。 它防止脂肪生成,增强间充质干细胞中的成骨细胞分化,增加骨矿物质密度,改善小梁微结构,可能反映 GIO 小鼠的骨形成增加和骨吸收减少。 | |||
T3923 |
Calycosin
Cyclosin,3'-Hydroxyformononetin,异黄酮,毛异黄酮 |
Apoptosis; Tyrosinase | Apoptosis; Proteases/Proteasome |
Calycosin (Cyclosin) 是一抗氧化和抗炎症活性天然产物。 | |||
T2S1865 |
Octyl gallate
Gallic acid octyl ester,n-Octylgallate,Octyl 3,4,5-trihydroxybenzoate,Progallin O,Stabilizer GA-8,没食子酸辛酯 |
Antioxidant; Influenza Virus; Reactive Oxygen Species; Antibacterial; Antifungal; HSV | Immunology/Inflammation; Metabolism; Microbiology/Virology; NF-κB; oxidation-reduction |
Octyl gallate (Octyl 3,4,5-trihydroxybenzoate) 具有抗菌、抗氧化作用,有选择性和敏感性的荧光特性,广泛用作食品添加剂。它对 HSV-1,水泡性口炎病毒和脊髓灰质炎病毒有显著的抗病毒作用。 | |||
TL0008 |
Gigantol
|
Wnt/beta-catenin; Glucosidase | Cytoskeletal Signaling; Metabolism; Stem Cells |
Gigantol 是一种联苄基化合物,从几种药用兰花中获得,是一种Wnt/β-catenin 通路抑制剂,具有抗肿瘤活性。 | |||
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。 | |||
T6S1699 |
Shogaol
[6]-Shogaol,姜烯酚,6-姜烯酚,6-Shogaol |
Lipoxygenase; Autophagy | Autophagy; Metabolism |
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。 | |||
T2S0843 |
Negletein
黄芩素-7-甲醚,7-O-Methylbaicalein,Baicalein-7-methylether |
IL Receptor; TNF; NOS; Interleukin | Apoptosis; Immunology/Inflammation |
Negletein (7-O-Methylbaicalein) 一种神经保护剂,可增强神经生长因子的作用并诱导 PC12 细胞中的神经突生长。它通过抑制TNF-α和IL-1β表现出抗炎活性,其 IC50值分别为 16.4 和 10.8 μM。它还具有抗菌、抗缺氧和抗阿尔茨海默病活性。 | |||
T40988 | (+)-Norlirioferine | ||
(+)-Norlirioferine is an alkaloid compound that exhibits cell growth inhibitory effects on macrophages and VERO cells. | |||
TN4603 |
Myricanol
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BCL; VEGFR; Caspase; HIF | Angiogenesis; Apoptosis; Chromatin/Epigenetic; Proteases/Proteasome; Tyrosine Kinase/Adaptors |
Myricanol can elicit growth inhibitory and cytotoxic effects on lung cancer cells, it can significantly decelerate tumor growth in vivo by inducing apoptosis. | |||
T2S0606 |
Bakkenolide A
|
IL Receptor; IκB/IKK; GSK-3; TNF; Akt; Caspase; PI3K; HDAC | Apoptosis; Chromatin/Epigenetic; Cytoskeletal Signaling; DNA Damage/DNA Repair; Immunology/Inflammation; NF-κB; PI3K/Akt/mTOR signaling; Proteases/Proteasome; Stem Cells |
Bakkenolide A has antifeedant and growth inhibitory effects on neonate variegated cutworms, it inhibits leukemia by regulation of HDAC3 and PI3K/Akt-related signaling pathways. | |||
TN3113 |
5-Heptadecylresorcinol
芒果 |
Others | Others |
5-Heptadecylresorcinol has strong inhibitory property against the growth of PC3 cells. | |||
T5527 |
Anigorufone
|
Antifection | Microbiology/Virology |
Anigorufone is a phytoalexin, it shows striking antinematode activity. Anigorufone has shown inhibitory activity on the growth of the germinative tube of Fusarium oxysporum f. sp. cubense race 4. | |||
TN3837 |
Desmethoxycentaureidin
|
Others | Others |
Desmethoxycentaureidin shows high inhibitory activity against HeLa cell growth (GI50 9 microM). | |||
T72805 |
(±)-Hydnocarpin
|
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(±)-Hydnocarpin 是一种黄酮木脂素。(±)-Hydnocarpin 可以抑制S. aureus 的生长,MIC50值为 3.1 μM。 | |||
TN3280 |
8-Hydroxy-4-cadinen-3-one
|
Others | Others |
8-Hydroxy-4-cadinen-3-one shows significant inhibitory activity against A.thaliana seedling root growth. | |||
T40440 |
Isobyakangelicol
Isobyakangelicol,Anhydrobyakangelicin |
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Isobyakangelicol, a coumarin compound present in Angelica dahurica roots, exhibits inhibitory effects on the growth of HeLa and HepG2 cells, with IC50 values of 70.04 μM and 17.97 μM, respectively. | |||
T40866 |
8-Methylsulfinyloctyl isothiocyanate
|
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8-Methylsulfinyloctyl isothiocyanate is a compound with antimicrobial activity and notable inhibitory effects on plant growth. It also exhibits COX-2-mediated inflammatory response impairment in LPS-stimulated raw macrophages. | |||
T4366 |
Quinovic acid
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NF-κB; Caspase | Apoptosis; NF-κB; Proteases/Proteasome |
Quinovic acid shows some anti-tumour activities, quinovic acid glycosides have a potent inhibitory effect on the growth of human bladder cancer cell lines by inducing apoptosis through modulation of NF-κB. | |||
TN3563 |
Caesalmin B
|
Antifection | Microbiology/Virology |
Caesalmin B shows significant dose-dependent inhibitory effects on Plasmodium falciparum FCR-3/A2 growth in vitro. | |||
TN3902 |
Durantoside I
|
Others | Others |
Durantoside I has inhibitory activity on the growth of lettuce seedling. It also displays DPPH scavenging activity. | |||
TN2837 |
29-Nor-20-oxolupeol
|
Others | Others |
29-Nor-20-oxolupeol(3 beta-Hydroxy-30-norlupan-20-one) has growth inhibitory effects on HL-60 cells. | |||
TN3711 |
Corylifol C
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ERK; EGFR; p38 MAPK; MEK | Angiogenesis; JAK/STAT signaling; MAPK; Tyrosine Kinase/Adaptors |
Corylifol C and, to a lesser extent, xanthoangelol are potent protein kinase inhibitors (inhibitory concentration 50% values for epidermal growth factor receptor (EGFR): 1.1 and 4.4 × 10(-6) μg/ml, respectively). | |||
TN4743 |
Paucinervin A
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Others | Others |
Paucinervin A has inhibitory effect against HeLa cell growth, with the IC50 value of 29.5 microM. | |||
T83246 |
7-Deoxynarciclasine
|
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7-Deoxynarciclasine,一种可从Hymenocallis littoralis中提取的化合物,具有抑制癌细胞生长的作用。 | |||
T28379 |
PF-1163B
PF1163B,(-)-PF1163B,PF 1163B |
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PF-1163B is an antifungal agent form Penicillium sp. II. PF-1163B inhibits ergosterol (ERG) synthesis with IC50 value of 34 ng/ml. PF-1163B showed potent growth inhibitory activity against pathogenic fungal strain Candida albicans but did not show cytotox | |||
TN2747 |
2-Acetoxy-3-deacetoxycaesaldekarin E
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Antifection | Microbiology/Virology |
2-Acetoxy-3-deacetoxycaesaldekarin E shows significant dose-dependent inhibitory effects on Plasmodium falciparum FCR-3/A2 growth in vitro. | |||
TN2219 |
Sophoraisoflavone A
鲁冰花,砂生槐异黄酮 A |
MRP; Antifection | Immunology/Inflammation; Microbiology/Virology |
Sophoraisoflavone A is a potential MRP inhibitor; it is also an inhibitor of germ tube growth in the AM fungus Gigaspora margarita, it strongly inhibited germ tube growth at 1.25 ug/disc. Sophoraisoflavone A shows inhibitory effects on copper-induced prot | |||
TN2515 |
1,7-Bis(4-hydroxyphenyl)hepta-4,6-dien-3-one
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Antifection | Microbiology/Virology |
(4Z,6E)-5-hydroxy-1,7-bis(4-hydroxyphenyl)hepta-4,6-dien-3-one shows growth inhibitory activity in vitro versus bloodstream forms of African trypanosomes, with the IC(50) value in the range of 1-3 microg/mL. | |||
TN2504 |
1,5-Dihydroxyxanthone
|
EGFR; AChR | Angiogenesis; JAK/STAT signaling; Neuroscience; Tyrosine Kinase/Adaptors |
1,5-Dihydroxyxanthone exhibits the epidermal growth factor receptor (EGFR) -tyrosine kinase inhibitory activity, with the IC50 value of 90.34 nM. It may have anticholinesterase activity on acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) enzym | |||
TN4443 |
Lipiferolide
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Telomerase; Antifection | DNA Damage/DNA Repair; Microbiology/Virology |
Lipiferolide is an inhibitor of farnesyl protein transferase(FPTase), it inhibits the FPTase activity in a dose-dependent manner, and shows cell growth inhibitory activity against several tumor cells, it possesses cytotoxic activity against KB cells. Liriodenine also has antiplasmodial activity. | |||
TN4132 |
Germanicol
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Germanicol induces selective growth inhibitory effects in human colon HCT-116 and HT29 cancer cells through induction of apoptosis, cell cycle arrest and inhibition of cell migration. Germanicol may have anti-inflammatory effects . | |||
TN4387 | Khellactone | Antifection | Microbiology/Virology |
Khellactone shows antitumor activity,it can suppress the growth of NCI-H460 tumor cells. (+)-4'-cis-Khellactone and (+)-3'-cis-khellactone have antiplasmodial activities, they show notable inhibitory activity against -sensitive strains of with IC(50) values from 1.5 and 2.4 microM. | |||
TN3318 | 9-Hydroxy-alpha-lapachone | Antifection | Microbiology/Virology |
9-Hydroxy-alpha-lapachone can highly inhibit the growth of H. pylori, it exhibits potent inhibitory activity against H. pylori Cystathionine gamma-synthase, with IC(50) values of 4.64 microM. It may have anti-inflammatory activity, it exhibits potent inhi | |||
TN5061 |
Stephanine
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Adrenergic Receptor; Antifection | GPCR/G Protein; Microbiology/Virology; Neuroscience |
l-Stephanine is a potent and highly selective alpha 1 adrenoceptor blocker, inhibits anococcygeus muscle contraction induced by phenylephrine with pA2 values of 6.76. Stephanine shows significant antiplasmodial activities with IC(50) ranged from 1.2 uM to 52.3 uM. Stephanine and crebanine have high inhibitory activity against gram-positive animal pathogenic bacteria, with MIC values of 0.078-0.312g/l, but low inhibitory activity against gram-negative animal pathogenic bacteria, they also inhibit... | |||
T79995 |
(+)-Epieudesmin
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(+)-Epieudesmin,一种具抗肿瘤特性的化合物,对癌细胞系展现轻微抑制作用,亦能抑制革兰氏阴性病原菌生长。 | |||
TN4308 |
Isolupalbigenin
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Antifection | Microbiology/Virology |
Isolupalbigenin shows promising cytotoxic effects toward HL-60 cells (IC50 4.3 ± 0.7 to 18.0 ± 1.7 uM), it also shows in vitro inhibitory activity toward human glyoxalase I. Isolupalbigenin shows two different antibacterial activities against MRSA: direct growth inhibition and intensification of methicillin sensitivity, it could lead to the development of compounds for new approaches against MRSA infection. | |||
TN3973 |
Epinodosin
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Others | Others |
Epinodosin induces significant DNA damage to HepG2 cells in a time- and dose-dependent manner.Epinodosin has a biphasic, dose-dependent effect on root growth and a strong inhibitory effect on root hair development in Lactuca sativa L. seedlings. | |||
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