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55

抑制剂 & 化合物

24

天然产物

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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。

化合物

Mitochondrial fusion promoter M1
Cat.No: T9232
Synonym:
Target: Mitochondrial Metabolism
Oiligodendrocyte differentiation promoter 1
Cat.No: T13829
Synonym:
Target: Others
Filastatin
Cat.No: T8536
Synonym:
Target: Antifungal
BRD7552
Cat.No: T6793
Synonym:
Target: Others
BI-6015
Cat.No: T21867
Synonym: 2-甲基-1-(2-甲基-5-硝基苯基磺酰基)-1H-苯并[D]咪唑
Target: Others
Salcaprozate sodium
Cat.No: T8926
Synonym: 8-(2-羟基苯甲酰胺基)辛酸钠,SNAC
Target: Others
2-PADQZ hydrochloride
Cat.No: T19849L
Synonym: 2-PADQZ hydrochloride (60547-97-9 Free base)
Target: Antiviral, Influenza Virus
Dimethoxycurcumin
Cat.No: T19853
Synonym: Veratrylcurcuminoid,二甲氧基姜黄素
Target: Others
Quinocetone
Cat.No: T8340
Synonym:
Target: Others, Antibacterial, Antibiotic
ML329
Cat.No: T4028
Synonym:
Target: TRP/TRPV Channel
MM41
Cat.No: T60028
Synonym:
Target: DNA/RNA Synthesis
Dacinostat
Cat.No: T2454
Synonym: NVP-LAQ824,达西司特,LAQ824
Target: HDAC, Autophagy
ZL0580
Cat.No: T13974
Synonym:
Target: Epigenetic Reader Domain, HIV Protease
Ecabapide
Cat.No: T31597
Synonym: DQ2511,DQ 2511,DQ-2511
Target: Others
Difurazon hydrochloride
Cat.No: T9049
Synonym:
Target: Others
ChX710
Cat.No: T13613
Synonym:
Target: STING
Itaconic anhydride
Cat.No: T5321
Synonym:
Target: Others
OAC2
Cat.No: T2019
Synonym:
Target: OCT
TD52 dihydrochloride
Cat.No: T35528L
Synonym: TD52 dihydrochloride(1798328-24-1 Free base),TD52 2HCl
Target: Others
Protein kinase inhibitor H-7 dihydrochloride
Cat.No: T22831
Synonym: H-7 dihydrochloride
Target: PKC
Schnurri-3 inhibitor-1
Cat.No: T60554
Synonym:
Target: Others
Bis-T-23
Cat.No: T30479
Synonym: Bis T-23,Bis-T 23,AG1717
Target: HIV Protease
RJW100
Cat.No: T38680
Synonym:
Target: Others
AP-1/NF-κB activation inhibitor 1
Cat.No: T9656
Synonym:
Target: NF-κB, DNA/RNA Synthesis
L 665871
Cat.No: T24318
Synonym: L-665,871,L-665871,L665,871,L665871,L 665,871
Target:
Phorbol 12,13-dibutyrate
Cat.No: T16526
Synonym: PDBu,Phorbol dibutyrate
Target: PKC
Xylarianaphthol-1
Cat.No: T70371
Synonym:
Target:
Pseudobactin
Cat.No: T34174
Synonym: Ferric pseudobactin
Target:
Veledimex
Cat.No: T13293L
Synonym: RG-115932,INXN-1001
Target: Others
D153249
Cat.No: T31168
Synonym: D 153249,D-153249
Target:
AZ-27
Cat.No: T70502
Synonym:
Target:
VSWRAPTA
Cat.No: T35075
Synonym:
Target:
6,2',4'-Trimethoxyflavone
Cat.No: T22528
Synonym:
Target: Others
Veledimex (S enantiomer)
Cat.No: T13294
Synonym: RG-115932 S enantiome,INXN-1001 S enantiome
Target: Others
CL67
Cat.No: T25255
Synonym: CL-67,CL 67
Target:
YM-155 hydrochloride
Cat.No: T21834
Synonym:
Target:
IBS008738
Cat.No: T40481
Synonym:
Target:
T3SS-IN-1
Cat.No: T78930
Synonym:
Target:
Multiflorenol
Cat.No: T36412
Synonym:
Target:
TD52
Cat.No: T35528
Synonym:
Target: Apoptosis, Phosphatase, Akt
Isonanangenine B
Cat.No: T71925
Synonym:
Target:
Geninthiocin A
Cat.No: T38150
Synonym:
Target:
T7 RNA polymerase
Cat.No: T79923
Synonym:
Target: DNA/RNA Synthesis
DNA Gyrase-IN-1
Cat.No: T63681
Synonym:
Target:
Okadaic acid ammonium salt
Cat.No: T39183
Synonym:
Target:
hnRNPK-IN-1
Cat.No: T37036
Synonym:
Target:
Antidiabetic agent 2
Cat.No: T79644
Synonym:
Target: Glucosidase
Dot1L-IN-1 TFA
Cat.No: T73637
Synonym:
Target:
WAY-255348
Cat.No: T68473
Synonym:
Target:
PPM-18
Cat.No: T21693
Synonym:
Target:
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

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

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

Praeruptorin B
Cat.No: T6S1423
Synonym:
Target: Others
Phorbol
Cat.No: T4037
Synonym: 4β-Phorbol,佛波醇,(+)-Phorbol
Target: PKC
Heteroclitin D
Cat.No: T3S1916
Synonym: 异型南五味子丁素,异南五味子丁素;异型南五味子丁素
Target: Calcium Channel
Naringenin
Cat.No: T2838
Synonym: 柚皮素,Naringetol,S-Dihydrogenistein,Pelargidanon,Salipurol,NSC 11855,NSC 34875
Target: P450, Influenza Virus, Reactive Oxygen Species, Endogenous Metabolite, PPAR
Poricoic acid B
Cat.No: TN1031
Synonym: 茯苓酸B,茯苓新酸 B
Target: Others
3,29-O-Dibenzoyloxykarounidiol
Cat.No: TN1025
Synonym:
Target: Others
Hydroxysafflor yellow A
Cat.No: T3674
Synonym: 藏红花,羟基红花黄色素A,HSYA,Safflomin A
Target: TGF-beta/Smad
Corylifol A
Cat.No: T4S0145
Synonym: Corylinin,补骨脂异黄酮A
Target: hCE, STAT, UGT
Vincristine
Cat.No: T3S0209
Synonym:
Target: ERK, p38 MAPK, NF-κB, Akt, JNK, mTOR
Aaptamine
Cat.No: TN1354
Synonym:
Target: c-Myc, TNF, p53
9alpha,13alpha-Epidioxyabiet-8(14)-en-18-oic acid
Cat.No: TN3309
Synonym:
Target: Others
Carlinoside
Cat.No: TMA0237
Synonym:
Target: Nrf2
α-Copaene
Cat.No: T78469
Synonym:
Target:
Latisxanthone C
Cat.No: TN4421
Synonym:
Target: Others
TMC-205
Cat.No: T73815
Synonym:
Target:
3-Epicabraleahydroxylactone
Cat.No: TN2926
Synonym:
Target: Others
Cycloart-25-ene-3,24-diol
Cat.No: TN3736
Synonym:
Target: Others
Karavilagenin D
Cat.No: TN4380
Synonym:
Target: Others
Flavoglaucin
Cat.No: TN4064
Synonym:
Target: Phosphatase, IL Receptor, TNF, NOS, NF-κB, COX, Nrf2, Prostaglandin Receptor, Autophagy
Abieta-8,11,13-triene-7,15,18-triol
Cat.No: TN5578
Synonym:
Target:
Niazimicin
Cat.No: TN4652
Synonym:
Target: NF-κB, PI3K, AChR, Antifection
9,13-Epidioxy-8(14)-abieten-18-oic acid
Cat.No: T5157
Synonym:
Target: Others
Hyptadienic acid
Cat.No: TN4241
Synonym:
Target:
Herboxidiene
Cat.No: T36749
Synonym:
Target:
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