55
24
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T9232 |
Mitochondrial fusion promoter M1
|
Mitochondrial Metabolism | Metabolism |
Mitochondrial fusion promoter M1 是一种线粒体动态调节剂,能够保持线粒体功能并促进细胞呼吸,减轻心肌缺血/再灌注大鼠的心脏损伤和大脑损伤。 | |||
T13829 |
Oiligodendrocyte differentiation promoter 1
|
Others | Others |
Oiligodendrocyte differentiation promoter 1 is a promoter of oiligodendrocyte differentiation . | |||
T8536 |
Filastatin
|
Antifungal | Microbiology/Virology |
Filastatin 是一种长效的白色念珠菌丝状体抑制剂,具有强大的抗真菌作用。它抑制真菌与聚苯乙烯和人类细胞的粘附,从酵母到菌丝的形态转变,抑制菌丝特异性 HWP1 启动子。 | |||
T6793 |
BRD7552
|
Others | Others |
BRD7552 是PDX1转录因子诱导剂,它能够上调人类原代胰岛和导管细胞中 PDX1 的表达,诱导 PDX1 启动子的表观遗传变化与转录激活一致,提高胰岛素表达。其中 PDX1 是参与胰腺发育和β细胞功能的关键转录因子。 | |||
T21867 |
BI-6015
2-甲基-1-(2-甲基-5-硝基苯基磺酰基)-1H-苯并[D]咪唑 |
Others | Others |
BI 6015 是肝细胞核因子 4α (HNF4α) 拮抗剂,可抑制已知 HNF4α 靶基因的表达。它利用 HNF4α 拮抗作用,降低胰岛素启动子活性,可用于研究癌症和糖尿病。 | |||
T8926 |
Salcaprozate sodium
8-(2-羟基苯甲酰胺基)辛酸钠,SNAC |
Others | Others |
Salcaprozate sodium (SNAC) 是口服吸收促进剂,有作为口服形式的肝素和胰岛素递送剂的潜力。它可提高非共价大分子络合引起的亲脂性,从而增加小肠上皮细胞的被动跨细胞渗透。 | |||
T19849L |
2-PADQZ hydrochloride
2-PADQZ hydrochloride (60547-97-9 Free base) |
Antiviral; Influenza Virus | Immunology/Inflammation; Microbiology/Virology |
2-PADQZ hydrochloride 显示出抗病毒活性并靶向甲型流感病毒 RNA 启动子。 | |||
T19853 |
Dimethoxycurcumin
Veratrylcurcuminoid,二甲氧基姜黄素 |
Others | Others |
Dimethoxycurcumin (Veratrylcurcuminoid) 是 curcumin 衍生物,拥有抗氧化及抗炎作用。 | |||
T8340 |
Quinocetone
|
Others; Antibacterial; Antibiotic | Microbiology/Virology; Others |
Quinocetone 是一种合成的强效抗菌剂,可用于提高饲料用动物饲料效率和控制痢疾。 | |||
T4028 |
ML329
|
TRP/TRPV Channel | Membrane transporter/Ion channel |
ML329 是小眼畸形相关转录因子抑制剂,它抑制 TRPM-1 启动子活性(IC50:1.2 μM)。 | |||
T60028 | MM41 | DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
MM41 是一种人类端粒和基因启动子 DNA 四链体稳定剂,对 MIA PaCa-2 胰腺癌细胞系的 IC50 <10 nM。 | |||
T2454 |
Dacinostat
NVP-LAQ824,达西司特,LAQ824 |
HDAC; Autophagy | Autophagy; Chromatin/Epigenetic; DNA Damage/DNA Repair |
Dacinostat (NVP-LAQ824) 是一种新型 HDAC 抑制剂,IC50 为 32 nM,是 p21 启动子的激活剂。它也可抑制HDAC1的活性,IC50值为 9 nM,主要用于癌症研究。 | |||
T13974 |
ZL0580
|
Epigenetic Reader Domain; HIV Protease | Chromatin/Epigenetic; Microbiology/Virology; Proteases/Proteasome |
ZL0580 通过抑制 Tat 反式激活和转录延伸以及通过在 HIV 启动子处诱导抑制性染色质结构来诱导 HIV 抑制。 | |||
T31597 |
Ecabapide
DQ2511,DQ 2511,DQ-2511 |
Others | Others |
Ecabapide (DQ-2511) 是一种新型促胃肠蠕动剂,能显著增强SHRSP的胃排空能力。Ecabapide 可激活的兔胃壁细胞中的环状 GMP 依赖性管家 Cl- 通道。 | |||
T9049 |
Difurazon hydrochloride
|
Others | Others |
Difurazon hydrochloride 是一种致突变药物。它可能已用于治疗细菌性痢疾。它是动物饲料中的抗菌促生长剂。 | |||
T13613 |
ChX710
|
STING | Immunology/Inflammation |
ChX710可以引发 I 型干扰素对细胞溶质 DNA 的反应,其特异性细胞干扰素刺激基因 (ISG) 诱导 ISRE 启动子序列和干扰素调节因子 (IRF) 3 的磷酸化。 | |||
T5321 |
Itaconic anhydride
|
Others | Others |
Itaconic anhydride 是一种从可再生资源中获得的生物基材料。广泛用于金属助粘剂、合成树脂改良剂、酯化剂、除草剂、杀虫剂。 | |||
T2019 |
OAC2
|
OCT | Membrane transporter/Ion channel |
OAC2 是一种 Oct4 激活剂,通过 Oct4 基因启动子激活表达, 通过提高胚胎成纤维细胞诱导多能干细胞的产生速率来提高重编程效率,是 OAC1 的类似物。 | |||
T35528L |
TD52 dihydrochloride
TD52 dihydrochloride(1798328-24-1 Free base),TD52 2HCl |
Others | Others |
TD52 dihydrochloride (TD52 2HCl), a derivative of Erlotinib, is a potent and orally active inhibitor of protein phosphatase 2A (CIP2A). It exhibits strong anti-cancer properties by regulating the CIP2A/PP2A/p-Akt signaling pathway, resulting in the induction of apoptosis in triple-negative breast cancer (TNBC) cells. Mechanistically, TD52 dihydrochloride disrupts the binding of Elk1 to the CIP2A promoter, effectively reducing CIP2A levels. Notably, TD52 dihydrochloride demonstrates powerful anti... | |||
T22831 |
Protein kinase inhibitor H-7 dihydrochloride
H-7 dihydrochloride |
PKC | Chromatin/Epigenetic; Cytoskeletal Signaling |
Protein kinase inhibitor H-7 dihydrochloride(H-7 dihydrochloride0) 是一种有效的蛋白激酶 C(PKC)抑制剂。Protein kinase inhibitor H-7 dihydrochloride(100 μM)显著抑制 TPA (皮肤肿瘤启动子,12-O-tetradecanoylphorbol-13-acetate) 和磷脂酶 C 促使的 ODC (鸟氨酸脱羧酶),抑制 PMA 诱导的混杂细胞溶解活性。 | |||
T60554 |
Schnurri-3 inhibitor-1
|
Others | Others |
Schnurri-3 inhibitor-1 是有效的 schnurri-3 抑制剂,schnurri-3是成人骨形成的重要调节因子。在成骨细胞系 Shn3FFL 中,Schnurri-3 inhibitor-1 通过 EF1alpha 启动子抑制 Shn3 蛋白表达 (AC50= 2.09 μM)。Schnurri-3 inhibitor-1 可用于骨质疏松症相关的研究。 | |||
T30479 |
Bis-T-23
Bis T-23,Bis-T 23,AG1717 |
HIV Protease | Microbiology/Virology; Proteases/Proteasome |
Bis-T-23是一种肌动蛋白依赖性达纳敏低聚物的促进剂,是一种 HIV-I 整合酶抑制剂,是泰尔普斯丁衍生物。Bis-T-23可以促进肌动蛋白依赖性的dynamin 寡聚化。Bis-T-23可用于HIV 和慢性肾脏疾病(CKD)的研究。 | |||
T38680 |
RJW100
|
Others | Others |
RJW100是一种化合物,作为肝受体同源体1(LRH-1, NR5A2)和类固醇生成因子-1(SF-1, NR5A1)的强效激动剂,分别展现出6.6和7.5的pEC50值。此外,RJW100能强力激活miR-200c(miRNA-200c, microRNA-200c)启动子。 | |||
T9656 |
AP-1/NF-κB activation inhibitor 1
|
NF-κB; DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; NF-κB |
AP-1/NF-κB activation inhibitor 1 是一种有效的 AP-1和 NF-κB 介导的转录激活抑制剂(IC50=1 μM),不阻断 β-actin 启动子驱动的基础转录。AP-1/NF-κB activation inhibitor 1 对受刺激细胞中 IL-2和 IL-8的产生水平有相似的抑制作用。 | |||
T24318 |
L 665871
L-665,871,L-665871,L665,871,L665871,L 665,871 |
||
L 665871 is used as a beta-agonist. It works as a potential swine growth promoter. | |||
T16526 |
Phorbol 12,13-dibutyrate
PDBu,Phorbol dibutyrate |
PKC | Chromatin/Epigenetic; Cytoskeletal Signaling |
Phorbol 12,13-dibutyrate is a PKC activator. It also is a potent skin tumor promoter. | |||
T70371 |
Xylarianaphthol-1
|
||
Xylarianaphthol-1 is an activator of p21 promoter in a p53-independent manner. | |||
T34174 |
Pseudobactin
Ferric pseudobactin |
||
Pseudobactin is a linear hexapeptide fluorescent iron transport agent (siderophore) from plant growth promoter Pseudomonas B10. | |||
T13293L |
Veledimex
RG-115932,INXN-1001 |
Others | Others |
Veledimex is an oral activator ligand for a proprietary gene therapy promoter system. It is also a moderate inhibitor of and substrate for CYP3A4/5. | |||
T31168 |
D153249
D 153249,D-153249 |
||
D153249 is a promoter of spinal muscular atrophy (SMA). | |||
T70502 |
AZ-27
|
||
AZ-27 is a respiratory syncytial virus inhibitor which differentially inhibits different polymerase activities at the promoter. | |||
T35075 | VSWRAPTA | ||
VSWRAPTA is a promoter of neuronal branching via transcellular activation of the focal adhesion kinase (FAK) and the ERK1/2 signaling pathway in vitro. | |||
T22528 |
6,2',4'-Trimethoxyflavone
|
Others | Others |
The compound is an Aryl hydrocarbon receptor antagonist (EC50 = 0.9 μM). It also has no short term agonist activity and no species or promoter dependence. | |||
T13294 |
Veledimex (S enantiomer)
RG-115932 S enantiome,INXN-1001 S enantiome |
Others | Others |
Veledimex S enantiomer is the S enantiomer of veledimex. Veledimex is an oral activator ligand for a proprietary gene therapy promoter system and CYP3A4/5 inhibitor. | |||
T25255 |
CL67
CL-67,CL 67 |
||
CL67 is a hypoxia-inducible factor pathway inhibitor. It acts by binding to a G-quadruplex higher-order structure in the HIF promoter sequence in vitro. | |||
T21834 |
YM-155 hydrochloride
|
||
Sepantronium hydrochloride (YM-155 hydrochloride) 是一种新型survivin 抑制剂,抑制survivin 启动子的IC50为 0.54 nM。 | |||
T40481 | IBS008738 | ||
IBS008738, a potent TAZ activator, stabilizes TAZ, elevates the unphosphorylated TAZ level, enhances the interaction of MyoD with the myogenin promoter, upregulates gene transcription regulated by MyoD, and competes with myostatin in C2C12 cells. Additionally, IBS008738 promotes myogenesis in C2C12 cells and facilitates muscle repair in a model of muscle injury. | |||
T78930 |
T3SS-IN-1
|
||
T3SS-IN-1 (compound B9)为高效的III型分泌系统 (T3SS) 抑制剂,能够抑制hpa1启动子活性及harpin蛋白表达,但不干扰细菌生长。 | |||
T36412 |
Multiflorenol
|
||
Multiflorenol is a triterpene that has been found in T. kirilowii seeds.1 It inhibits in vitro activation of Epstein-Barr virus early antigen (EBV-EA) induced by the tumor promoter phorbol 12-myristate 13-acetate in a concentration-dependent manner. |1. Akihisa, T., Tokuda, H., Ichiishi, E., et al. Anti-tumor promoting effects of multiflorane-type triterpenoids and cytotoxic activity of karounidiol against human cancer cell lines. Cancer Lett. 173(1), 9-14 (2001). | |||
T35528 |
TD52
|
Apoptosis; Phosphatase; Akt | Apoptosis; Cytoskeletal Signaling; Metabolism; PI3K/Akt/mTOR signaling |
TD52 是 PP2A (CIP2A) 癌性抑制剂的口服活性抑制剂。 TD52 是厄洛替尼衍生物,通过干扰 Elk1 与 CIP2A 启动子的结合间接降低了 CIP2A。 | |||
T71925 |
Isonanangenine B
|
||
Isonanangenine B is a drimane sesquiterpene lactone that has been found in Aspergillus. It decreases survivin mRNA expression in a reporter assay when used at concentrations of 13.6, 18.42, and 26.31 µM. Isonanagenine B (18.42 µM) inhibits STAT3 and NF-κB binding to the survivin promoter in chromatin immunoprecipitation (ChIP) assays. It also induces apoptosis in COLO 320DM cells. | |||
T38150 |
Geninthiocin A
|
||
Geninthiocin A is a cyclic thiopeptide bacterial metabolite originally isolated from Streptomyces sp. DD84. It is active against a variety of Gram-positive bacteria (MICs = 0.2-4 μg/ml), the Gram-negative bacterium C. violaceum (MIC = 19 μg/ml), and the fungus M. hiemalis (MIC = 38 μg/ml). Geninthiocin A also induces tipA promoter transcription with a minimum induction concentration of 1.2 ng/ml. | |||
T79923 |
T7 RNA polymerase
|
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
T7 RNA polymerase是一种由大肠杆菌表达的聚合酶,由T7噬菌体的RNA聚合酶基因编码。它在合成mRNA体外转录(IVT)过程中显示出高度专一性。T7 RNA polymerase能在Mg2+的作用下,针对含有T7启动子序列的单链或双链DNA模板,使用NTP作为底物进行RNA合成,产生的RNA与DNA模板的启动子下游区域互补。 | |||
T63681 | DNA Gyrase-IN-1 | ||
DNA Gyrase-IN-1 是有效的、选择性的 DNA 促旋酶抑制剂 (IC50: 2.6 μM)。DNA Gyrase-IN-1 能够较好的抑制结核分枝杆菌 (Mtb) 的活性 (MIC: 0.49 μM)。DNA Gyrase-IN-1 能够用于研究结核病。 | |||
T39183 |
Okadaic acid ammonium salt
|
||
Okadaic acid ammonium salt, a marine toxin, serves as an inhibitor of protein phosphatases (PP), displaying a higher affinity for PP2A (IC 50 =0.1-0.3 nM) alongside inhibitory effects on PP1 (IC 50 =15-50 nM), PP3 (IC 50 =3.7-4 nM), PP4 (IC 50 =0.1 nM), and PP5 (IC 50 =3.5 nM), but does not affect PP2C. By inhibiting PPs, this compound promotes protein phosphorylation and acts as a tumor promoter. Additionally, it is involved in inducing tau phosphorylation. | |||
T37036 |
hnRNPK-IN-1
|
||
hnRNPK-IN-1 is a specific ligand that binds to the heterogeneous nuclear ribonucleoprotein K (hnRNPK) with high affinity, evidenced by Kd values of 4.6 μM and 2.6 μM determined using surface plasmon resonance (SPR) and microscale thermophoresis (MST), respectively. This binding event leads to the disruption of hnRNPK's interaction with the c-myc promoter, resulting in the inhibition of c-myc transcription. Additionally, hnRNPK-IN-1 induces apoptosis in Hela cells and exhibits potent anti-tumor a... | |||
T79644 |
Antidiabetic agent 2
|
Glucosidase | Metabolism |
Antidiabetic agent 2 (Compound 56) 作为一种葡萄糖摄取促进剂,能有效地抑制DPP-4, PTP-1B, α-淀粉酶和α-葡萄糖苷酶,其IC50s分别达到0.036、0.042、0.241、0.185 μM,表现出显著的降血糖作用。 | |||
T73637 | Dot1L-IN-1 TFA | ||
Dot1L-IN-1 TFA 是一种高效选择性Dot1L抑制剂,具有2 pM的Ki值和小于0.1 nM的IC50值。在HeLa细胞中,它能有效抑制H3K79的二甲基化(IC50=3 nM),同时也能在Molm-13细胞中抑制HoxA9启动子的活性(IC50=17 nM)。 | |||
T68473 |
WAY-255348
|
||
WAY-255348 is a potent nonsteroidal progesterone receptor (PR) antagonist. WAY-255348 inhibits the activity of progesterone. WAY-255348 achieves antagonist activity by binding to and subsequently preventing progesterone-induced nuclear accumulation, phosphorylation and promoter interactions of the PR. WAY-255348 bound PR conformation was similar to that of a progesterone agonist-bound PR and distinct from steroidal antagonist-bound PR conformations. WAY-255348 inhibits PR action through a novel ... | |||
T21693 |
PPM-18
|
||
PPM-18 (NSC 73233) 是一种有效的抗炎剂,可抑制一氧化氮合酶的表达。PPM-18 是有效的 iNOS 表达抑制剂,可阻断 NF-κB 与启动子的结合。PPM-18 是维生素 K 的类似物,通过 ROS 和 AMPK 信号通路诱导膀胱癌细胞自噬和凋亡。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T6S1423 |
Praeruptorin B
|
Others | Others |
Praeruptorin B 在体外能抑制促癌因子诱导的现象。 | |||
T4037 |
Phorbol
4β-Phorbol,佛波醇,(+)-Phorbol |
PKC | Chromatin/Epigenetic; Cytoskeletal Signaling |
Phorbol (4β-Phorbol) 是具有毒性的二萜类化合物,其酯类具有强大的生物活性。 | |||
T3S1916 |
Heteroclitin D
异型南五味子丁素,异南五味子丁素;异型南五味子丁素 |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Heteroclitin D 是异形南五味子中的一种木脂素,可抑制 L 型钙通道,具有抗脂质过氧化作用。 | |||
T2838 |
Naringenin
柚皮素,Naringetol,S-Dihydrogenistein,Pelargidanon,Salipurol,NSC 11855,NSC 34875 |
P450; Influenza Virus; Reactive Oxygen Species; Endogenous Metabolite; PPAR | DNA Damage/DNA Repair; Immunology/Inflammation; Metabolism; Microbiology/Virology; NF-κB |
Naringenin (NSC-11855) 是葡萄柚中主要的黄烷酮,可作为抗氧化剂、自由基清除剂、抗炎剂、碳水化合物代谢促进剂、免疫系统调节剂。 | |||
TN1031 |
Poricoic acid B
茯苓酸B,茯苓新酸 B |
Others | Others |
Poricoic acid B 是提取自 Poria cocos 中,拥有抗肿瘤作用。 | |||
TN1025 |
3,29-O-Dibenzoyloxykarounidiol
|
Others | Others |
3,29-O-Dibenzoyloxykarounidiol 是一种苯甲酸三萜烯酯,从 Momordica grosvenori 果实中提取。它能够抑制肿瘤启动子 TPA 诱导的 EB 病毒早期抗原活化。 | |||
T3674 |
Hydroxysafflor yellow A
藏红花,羟基红花黄色素A,HSYA,Safflomin A |
TGF-beta/Smad | Stem Cells |
Hydroxysafflor yellow A (Safflomin A) 是一种黄酮类天然产物,从中药红花中分离得到,具有抗癌作用。 | |||
T4S0145 |
Corylifol A
Corylinin,补骨脂异黄酮A |
hCE; STAT; UGT | JAK/STAT signaling; Metabolism; Stem Cells |
Corylifol A (Corylinin) 是补骨脂中的一种天然产物,可抑制IL-6 诱导的STAT3激活和磷酸化,IC50值为0.81 μM。 | |||
T3S0209 |
Vincristine
|
ERK; p38 MAPK; NF-κB; Akt; JNK; mTOR | Cytoskeletal Signaling; MAPK; NF-κB; PI3K/Akt/mTOR signaling |
Vincristine 与微管蛋白结合并抑制微管的形成,从而抑制癌细胞的有丝分裂。 Vincristine 可用作微管去稳定剂,用于研究治疗血液系统癌症,如白血病和淋巴瘤以及儿童肉瘤的相关研究。 | |||
TN1354 | Aaptamine | c-Myc; TNF; p53 | Apoptosis; Cell Cycle/Checkpoint |
Aaptamine functions as a proteasome inhibitor, it activates p21 promoter in a p53-independent manner. | |||
TN3309 |
9alpha,13alpha-Epidioxyabiet-8(14)-en-18-oic acid
|
Others | Others |
9alpha,13alpha-Epidioxyabiet-8(14)-en-18-oic acid shows potent inhibitory effects on Epstein-Barr virus early antigen (EBV-EA) activation induced by the tumor promoter 12-O-tetradecanoylphorbol 13-acetate. | |||
TMA0237 | Carlinoside | Nrf2 | Immunology/Inflammation |
Carlinoside could be a worthy choice to intervene hyperbilirubinemia due to liver dysfunction. Carlinoside upregulates Nrf2 gene expression, increases its nuclear translocation and stimulates UGT1A1 promoter activity. | |||
T78469 |
α-Copaene
|
||
α-Copaene,一种倍半萜烃,具有水果挥发物性质,可作为橄榄实蝇(Bactrocera oleae)的产卵促进剂。 | |||
TN4421 |
Latisxanthone C
|
Others | Others |
Latisxanthone C shows inhibitory effects on Epstein-Barr virus early antigen (EBV-EA) activation induced by 12-O-tetradecanoylphorbol-13-acetate (TPA) in Raji cells, it may be a valuable antitumor promoter. | |||
T73815 |
TMC-205
|
||
TMC-205,一种具抗肿瘤细胞增殖活性的天然真菌代谢产物,为SV40启动子的转录上调因子。 | |||
TN2926 |
3-Epicabraleahydroxylactone
|
Others | Others |
3-Epicabraleahydroxylactone has anti-tumor promoting effect, it has anti-carcinogenic activity by the inhibitory effect on the induction of Epstein-Barr virus early antigen(EBV-EA) by the tumor promoter. | |||
TN3736 | Cycloart-25-ene-3,24-diol | Others | Others |
(24R)-Cycloart-25-ene-3beta,24-diol may be an anti-tumor promoter, it exhibits inhibitory effects on both Epstein-Barr virus early antigen (EBV-EA) and (+/-)-(E)-methtyl-2-[(E)-hydroxyimino]-5-nitro-6-methoxy-3- hexemide (NOR 1) activation. | |||
TN4380 | Karavilagenin D | Others | Others |
Karavilagenin D exhibits inhibitory effects on skin-tumor promotion in an in vivo two-stage mouse skin carcinogenesis test based on 7,12-dimethylbenz[a]anthracene (DMBA) as initiator, and with TPA as a promoter. It exhibits inhibition effect against human | |||
TN4064 |
Flavoglaucin
|
Phosphatase; IL Receptor; TNF; NOS; NF-κB; COX; Nrf2; Prostaglandin Receptor; Autophagy | Apoptosis; Autophagy; GPCR/G Protein; Immunology/Inflammation; Metabolism; Neuroscience; NF-κB |
Flavoglaucin exhibits significant inhibitory effects on PTP1B, the IC50 value of 13.4, micrometer; it also shows good binding affinity for human opioid or cannabinoid receptors. Flavoglaucin appears to be an antitumor promoter, it also has anti-inflammato | |||
TN5578 | Abieta-8,11,13-triene-7,15,18-triol | ||
Abieta-8,11,13-triene-7alpha,15,18-triol,7alpha,8alpha,13beta,14beta-diepoxyabietan-18-oic acid, and 18-nor-abieta-8,11,13-triene-4alpha,7alpha,15-triol may have inhibitory effects on Epstein-Barr virus early antigen (EBV-EA) activation induced by the tum | |||
TN4652 | Niazimicin | NF-κB; PI3K; AChR; Antifection | Microbiology/Virology; Neuroscience; NF-κB; PI3K/Akt/mTOR signaling |
Niazimicin are NF-B and PI3K inhibitors, which shows antimicrobial, hypotensive and spasmolytic activities. Niazimicin has potent antitumor promoting activity in the two-stage carcinogenesis in mouse skin using 7,12-dimethylbenz(a)anthracene (DMBA) as ini | |||
T5157 |
9,13-Epidioxy-8(14)-abieten-18-oic acid
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Others | Others |
9,13β-Epidioxy-8(14)-abieten-18-oic acid has anti-inflammatory activities, it exhibits moderate activities on NO levels in LPS-stimulated murine microglia BV2 cells, with IC50 values of 57.3 ± 0.2 uM. It is also a potential antitumor-promoting diterpenoid, it shows potent inhibitory effects on Epstein-Barr virus early antigen (EBV-EA) activation induced by the tumor promoter 12-O-tetradecanoylphorbol 13-acetate. 9 α ,13 β -Epidioxyabeit-8(14)en-18-oic acid may contribute to the growth inhibitory... | |||
TN4241 | Hyptadienic acid | ||
Hyptadienic acid exhibits moderate cytotoxicity against HepG2 cells.It also shows a marked anti-inflammatory effect, it also exhibits strong antitumor-promoting activity in an in vivo two-stage carcinogenesis test of mouse tumor by using 7,12-dimethylbenz | |||
T36749 |
Herboxidiene
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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... |