107
21
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
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。 | |||
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。 | |||
T14994 |
Coelenterazine h
腔肠素-H,2-Deoxycoelenterazine,CLZN-h |
Others | Others |
Coelenterazine h (CLZN-h) 是一种 Coelenterazine 的衍生物。它对 Ca2+比它的天然复合物更敏感,是一种能够测量 Ca2+浓度的微小变化的有效工具。 | |||
T14057 |
6-CFDA
6-羧基荧光素二醋酸,6-Carboxyfluorescein diacetate |
Others | Others |
6-CFDA (6-Carboxyfluorescein diacetate) 是可用于流式细胞术和荧光显微镜的荧光探针,也可以用于活体多光子显微镜研究动物肝胆代谢。 | |||
T68165 |
Trapencaine
|
||
Trapencaine 是一种新合成的氨基甲酸型局部麻醉剂,诱导的肥大细胞膜上钠通道的构象变化。 | |||
T9325 |
2-(2-Aminothiazole-4-yl)-2-methoxyiminoa
|
Others | Others |
2-(2-Aminothiazole-4-yl)-2-methoxyiminoa 是一种蛋白质酪氨酸磷酸酶的抑制剂,蛋白质酪氨酸磷酸酶可以导致细胞信号通路的变化,从而影响细胞的行为。 | |||
T2011 |
RKI1313
RKI 1313,RKI-1313 |
ROCK | Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells |
RKI1313 (RKI-1313) 是一种选择性抑制剂,可抑制 ROCK 依赖性信号传导、细胞骨架变化、不依赖锚定的集落形成、迁移和侵袭。 | |||
T77556 |
2-(4-Hydroxyphenylazo)benzoicacid
|
||
2-(4-Hydroxyphenylazo)benzoicacid 是一种分光光度法探针,可显示与蛋白质结合时的吸收光谱变化,可与牛血清蛋白结合。 | |||
T4683 |
Alovudine
3'-Deoxy-3'-fluorothymidine,3'-脱氧-3-氟胸苷 |
Antiviral | Immunology/Inflammation |
Alovudine (3'-Deoxy-3'-fluorothymidine) 是一种 DNA 合成的标志物。与18F-Fluorodeoxyglucose (FDG) 相比,它不易受炎症变化的影响,在胰腺癌中,它是更好的生物标志物。 | |||
T5104 |
BTSA1
|
Apoptosis; BCL | Apoptosis |
BTSA1 是一种有口服活性的 BAX 激活剂,IC50为 250 nM,EC50为 144 nM。它以高亲和力和特异性与 N 末端激活位点结合,并诱导 BAX 发生构象变化,从而导致BAX 介导的细胞凋亡。 | |||
T22229 |
Acid Yellow 36
Metanil Yellow,酸性黄36 |
Others | Others |
Acid Yellow 36 (Metanil Yellow) 是一种偶氮染料和 pH 指示剂,当 pH 值从 1.2 到 2.3 时,发生由红色到黄色的颜色转变。它是 P-450 特异性同工酶和胞浆酶的双功能诱导剂,可用于皮革、造纸和纺织工业。 | |||
T6760 |
APS-2-79 hydrochloride
APS-2-79 HCl,APS-2-79 |
MEK; MAPK | MAPK |
APS-2-79 hydrochloride (APS-2-79 HCl) 是一种 KSR 依赖性的MEK 拮抗剂,可与 ATPbiotin 竞争性地结合到 KSR2-MEK1 复合物内的KSR2。它与 KSR 结合可将 KSR 处于非活性状态,使其无法再结合 RAF 和激活 MEK,从而阻断 Ras-MAPK 信号通路。 | |||
T24076 |
FzM1
FzM 1,FzM-1 |
Wnt/beta-catenin | Cytoskeletal Signaling; Stem Cells |
FzM1 是卷曲蛋白受体 FZD4 的负变构调节剂 (NAM)。 FzM1减少 WNT5A 依赖的 WNT 反应元件 (WRE) 活性 (log EC50inh=-6.2)。 FzM1 与位于 FZD4 细胞内环 3 (ICL3) 的变构结合位点结合并改变受体的构象,从而抑制 WNT/β-连环蛋白级联反应。 | |||
T33613 |
NCGC00135472
NCGC 00135472,DRV1 (GPR32) agonist C2A,C2A,NCGC-00135472 |
Others | Others |
NCGC00135472 (DRV1 (GPR32) agonist C2A)是具有促分解功能的人Resolvin D1受体激动剂,可在β阻滞素和 cAMP 测定中激活人溶解蛋白 D1 受体 DRV1/GPR32 受体,EC50 分别为 0.37 uM 和 0.05 uM。NCGC00135472在过表达重组DRV1的细胞中引起快速阻抗变化,刺激血清处理的酶聚糖的吞噬作用。 | |||
T63971 |
Canocapavir
ZM-H1505R |
HBV | Microbiology/Virology |
Canocapavir (ZM-H1505R)是一种新型可口服的 HBV 衣壳蛋白调节剂,具有抗病毒活性,可诱导 HBV 核心蛋白连接子区域的构象变化,可用于治疗乙型肝炎病毒。 | |||
T22694 |
CRANAD 2
|
Others | Others |
CRANAD 2 是一种特异性近红外 (NIR) 荧光探针,可用于检测 Aβ 斑块。它可透过血脑屏障,且对 Aβ 聚集体有高亲和性,其 Kd=38 nM。 | |||
T3126 |
Bethanechol chloride
(±)-Bethanechol,Urecholine,Myocholine,氯贝胆碱,Carbamyl-β-methylcholine chloride |
AChR | Neuroscience |
Bethanechol chloride (Carbamyl-β-methylcholine chloride) 是一种拟副交感神经剂,是毒蕈碱型受体 (mAChR) 激动剂,通过直接刺激副交感神经系统的 mAChR 发挥作用。 | |||
T4364 |
Aftin-4
Aftin 4,Aftin4 |
Beta Amyloid; Gamma-secretase | Neuroscience; Proteases/Proteasome; Stem Cells |
Aftin-4 是一种 β-淀粉样蛋白42(Aβ42) 的诱导剂。 | |||
T36008 |
Nebentan potassium
|
||
Nebentan potassium (YM598) is a potent, selective and orally active non-peptide endothelin ETA receptor antagonist through the modification of Bosentan . Nebentan potassium inhibits [125I] endothelin-1 binding to cloned human endothelin ETA and ETB receptor, with Ki of 0.697 nM and 569 nM, respectively[1]. YM598 can ameliorate the progression of cor pulmonale and myocardial infarction in vivo[2]. Nebentan potassium inhibits the specific binding of [125I] endothelin-1 to endothelin ETA and ETB re... | |||
T32681 |
Leukotriene F-4 sulfone
Ltf4 sulfone |
||
Leukotriene F-4 sulfone induces vascular permeability changes. | |||
T19476 |
NHC-triphosphate
|
Others | Others |
NHC-triphosphate is a weak alternative substrate for the viral polymerase and changes the mobility of the product in polyacrylamide electrophoresis gels. | |||
T68327 | Dexnafenodone Free Base | ||
Dexnafenodone Free Base is a potent inhibitor of noradrenaline, and to a lesser degree of serotonin reuptake, induced changes in the pattern of sleep which are comparable to those of non‐sedating tricyclic antidepressants. | |||
T26395 |
6-Benzylthioinosine
6-BT,6Benzylthioinosine,6-Bn-thioinosine |
||
6-Benzylthioinosine, a broad-spectrum metabolic inhibitor, inhibits glucose uptake, decreases glycolysis and ATP concentration with minimal changes in ROS and mitochondrial respiration. | |||
T23697 |
AL-8417
J1.090.276B,AL8417,(2R)-AL-5898 |
||
AL-8417 is an enzyme inhibitor. It acting as an antioxidant, anti-inflammatory, and cytostatic agent. It also has the ability to suppress vitrectomy-induced posterior lens fiber changes. | |||
T18973 |
Di-8-ANEPPS
|
Others | Others |
Di-8-ANEPPS, a voltage-sensitive dye, demonstrates shifts in both its fluorescence excitation and emission spectra in response to changes in membrane potential (Vm). | |||
T69017 | Ibotenic acid hydrate | ||
Ibotenic acid hydrate is a neurotoxic isoxazole (similar to Kainic acid and Muscimol) found in Amanita mushrooms. It causes motor depression, ataxia, and changes in mood, perceptions and feelings, and is a potent excitatory amino acid agonist. | |||
T33417 |
MK 410
MK-410,MK410 |
||
MK 410 is an indomethacin analogue and anti-inflammatory agent that induces changes in the immune system by inhibiting plasma neutral protease activity. | |||
T12934 |
SMAP-2
DT-1154 |
Phosphatase | Metabolism |
SMAP-2 is an orally bioavailable activator of phosphatase 2A (PP2A) which binds to the PP2A Aα scaffold subunit to drive conformational changes in PP2A. It inhibits the growth of KRAS-mutant lung cancers . | |||
T31088 |
CPX-351
Cytarabine/daunonubicin,Vyxeos,CPX 351,Daunonubicin/cytarabine |
||
CPX-351 is a Liposomal-encapsulated combination of daunorubicin and cytarabine for the treatment of newly diagnosed tAML or AML with myelodysplasia-related changes (AML-MRCs). | |||
T18884 |
3,3'-Dihexyloxacarbocyanine iodide
DiOC6(3) iodide |
Others | Others |
3,3'-Dihexyloxacarbocyanine iodide is a carbocyanine dye. It is used to monitor changes in mitochondrial membrane potential. | |||
TP1311 |
RGD peptide (GRGDNP) (TFA) (114681-65-1 free base)
RGD peptide (GRGDNP) (TFA) |
||
RGD peptide (GRGDNP) (TFA) promote apoptosis through activation of conformation changes that enhance pro-caspase-3 activation and autoprocessing. | |||
T13746 |
KMG-301AM
|
Others | Others |
KMG-301AM, the acetoxy methyl esterified form of KMG-301, facilitates the acquisition of time-course and pseudo-colored images depicting the changes in mitochondrial fluorescence when stained with KMG-301. | |||
T68898 |
Dequalinium Bromide
|
||
Dequalinium Bromide is a HIV-1 fusion inhibitor, targeting the membrane-proximal external region of Env spikes, specifically inhibiting the HIV-1 envelope-mediated membrane fusion by blocking CD4-induced conformational changes. | |||
TP1105 |
α-Factor Mating Pheromone, yeast (TFA)
α-Factor Mating Pheromone, yeast (TFA)(59401-28-4,FREE),Mating Factor α (TFA) |
||
The alpha factor pheromone arrests yeast in the G1 phase of their cell cycle. Alpha Factor Mating Pheromone induces the expression of mating genes, changes in nuclear architecture, and polarzes growth toward the mating partner. | |||
T68600 | Enoximone sulfoxide | ||
Enoximone sulfoxide is a selective phosphodiesterase III (PDE3) inhibitor with vasodilating and positive inotropic activity that does not cause changes in myocardial oxygen consumption. Enoximone prevents the degradation of cAMP by PDE, which prolongs signal transduction and its subsequent effects. It is used in patients with congestive heart failure. | |||
T36081 |
Trehalose 6-phosphate (potassium salt hydrate)
|
||
Trehalose is a natural non-reducing disaccharide found in plants, invertebrates, fungi, and bacteria.1,2In addition to roles as an energy source and stress protectant, trehalose can function as a signaling molecule.3,4Trehalose 6-phosphate is an intermediate in the biosynthesis of trehalose. It is generated from UDP-glucose and glucose 6-phosphate by trehalose 6-phosphate synthase (TPS or otsA).5In plants, changes in trehalose 6-phosphate levels positively correlate with diurnal changes in sucro... | |||
T29453 |
5-Formylcytosine
|
||
5-formylcytosine (5FC) is a rare base found in mammalian DNA. It participates in active DNA demethylation, changes DNA double helix structure, and reduces the transcription rate and substrate specificity of RNA polymerase II. | |||
T80322 |
Mastoparan B
|
||
Mastoparan B,源自黄蜂Vespa的抗菌肽,可引起红细胞形态由常规盘形转变为锯齿状。 | |||
T69769 |
BDP8900
|
||
BDP8900 is a potent and selective MRCK inhibitor, reducing substrate phosphorylation. BDP8900 leads to morphological changes in cancer cells along with inhibition of their motility and invasive character. | |||
T26821 | BIPM | ||
BIPM is a potent inhibitor of Rho-associated protein kinase 2 (ROCK2). Exposure of SH-SY5Y cells to BIPM led to significant changes in cell migration, actin stress fibers and neurite length. BIPM significantly inhibits phosphorylation of cofilin, a regula | |||
T20256 |
Sorbitol, L-
L-Glucitol |
||
Sorbitol, L- is a sugar alcohol. It can be obtained by the reduction of glucose, which changes the aldehyde group to a hydroxyl group. It is converted to fructose by sorbitol-6-phosphate 2-dehydrogenase. Sorbitol is an isomer of mannitol, another sugar al | |||
T35820 |
CAY10685
|
||
CAY10685 is a cell-active analog of the lysine acetyltransferase inhibitor CPTH2 that contains an alkyne moiety for use in click chemistry reactions. Its ability to inhibit N-acetyltransferase 10 activity has been used to modulate chromatin organization in order to study changes in nuclear architecture associated with cancer and certain laminopathies. | |||
T15180 |
Duocarmycin A
|
Caspase | Apoptosis; Proteases/Proteasome |
Duocarmycin A, an antitumor antibiotic, is a DNA alkylator and efficiently alkylates adenine N3 at the 3′ end of AT-rich sequences in the DNA. Duocarmycin A, as a chemotherapeutic agent, results in HLC-2 cells typically apoptotic changes. | |||
T61702 | SRI-37240 | ||
SRI-37240 is a powerful inhibitor of premature termination codons (PTCs). It effectively suppresses CFTR nonsense mutations and induces changes in cellular translation termination at PTCs in HEK293T cells. Additionally, when combined with G418, SRI-37240 restores CFTR function in primary bronchial epithelial cells [1]. | |||
T81337 |
Pyrromethene 650
PM650 |
||
Pyrromethene 650 (PM650)为一种绿色荧光偏振示踪染料,常用于膜融合、裂解及隙缝结通讯的研究,并可检测细胞或脂质体的体积变化。 | |||
TD0052 |
Fluo-3, pentasodium salt
|
||
Calcium measurement is critical for numerous biological investigations. Fluorescent probes that show spectral responses upon binding calcium have enabled researchers to investigate changes in intracellular free calcium concentrations by using fluorescence microscopy, flow cytometry, fluorescence spectroscopy and fluorescence microplate readers. Fluo-3, pentasodium salt is most commonly used among the visible light-excitable calcium indicators. | |||
TD0054 |
Fluo-3, pentaammonium salt
|
||
Calcium measurement is critical for numerous biological investigations. Fluorescent probes that show spectral responses upon binding calcium have enabled researchers to investigate changes in intracellular free calcium concentrations by using fluorescence microscopy, flow cytometry, fluorescence spectroscopy and fluorescence microplate readers. Fluo-3, pentaammonium salt is most commonly used among the visible light-excitable calcium indicators. | |||
TD0053 |
Fluo-3, pentapotassium salt
|
||
Calcium measurement is critical for numerous biological investigations. Fluorescent probes that show spectral responses upon binding calcium have enabled researchers to investigate changes in intracellular free calcium concentrations by using fluorescence microscopy, flow cytometry, fluorescence spectroscopy and fluorescence microplate readers. Fluo-3, pentapotassium salt is most commonly used among the visible light-excitable calcium indicators. | |||
T11042 |
Dihydrocytochalasin B
|
Others | Others |
Dihydrocytochalasin B (H2CB) is a cell division inhibitor that changes the morphology of cells, similar to cytochalasin B. Does not inhibit glucose transport. Dihydrocytochalasin B (H2CB) disrupts the structure of actin and inhibits the ability of growth | |||
T30242 |
AY 31906
AY-31,906 |
||
AY 31906 is a high ceiling diuretic with a relative potassium-sparing effect. AY 31906 has been shown to produce significant increases in the fractional excretion of sodium and chloride in dogs at a dose that produces no statistically significant changes |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T2803 |
Monocrotaline
野百合碱,Crotaline |
TGF-beta/Smad | Stem Cells |
Monocrotaline (Crotaline) 是一种吡咯里西啶生物碱,从猪屎豆植物的种子中提取得到,可诱导啮齿动物产生肺动脉高血压。 | |||
TF0083 |
POPE
|
||
POPE 是从大肠杆菌中发现的化合物,是细胞膜的一部分,可用来研究改变细胞膜通透性。 | |||
TN6779 |
Clausine E
|
Others | Others |
Clausine E 是脂肪量和肥胖相关蛋白 (FTO) 脱甲基酶活性的抑制剂。 Clausine E 与 FTO 的结合是由正熵和负焓变化驱动的。 | |||
T4732 |
L-Carnosine
Karnozin,L-肌肽,beta-Alanyl-L-histidine |
Antioxidant; Endogenous Metabolite | Metabolism; oxidation-reduction |
L-Carnosine (Karnozin) 是 由beta-丙氨酸和组氨酸组成的二肽,具有抑制衰老的作用。 | |||
T10023 |
1-Naphthol
NSC 9586,Nako TRB,1-萘酚,Furro ER |
Endogenous Metabolite | Metabolism |
1-Naphthol (Furro ER) 是激发态质子转移荧光分子探针。 | |||
TN1248 |
3-Epioleanolic acid
|
AChR | Neuroscience |
3-Epioleanolic acid 是一种分离自马鞭草的有效成分,具有抗炎作用。 | |||
TN7117 |
regaloside I
|
Others | Others |
Regaloside I 是百合中的单体成分,可能是保护人类皮肤成纤维细胞免受 UVA 诱导的形态变化的主要成分。 | |||
T5968 |
DL-Homocysteine thiolactone hydrochloride
DL-Homocysteinethiolactone hydrochloride,DL-高半胱氨酸硫内酯盐酸盐 |
Endogenous Metabolite | Metabolism |
DL-Homocysteine thiolactone hydrochloride (DL-Homocysteinethiolactone hydrochloride) 是具有根生长抑制特性的环状氨基酸衍生物。 | |||
T4939 |
Indole-3-pyruvic acid
3-(3-吲哚基)-2-氧代丙酸,3-(3-Indolyl)-2-oxopropanoic acid |
Others | Others |
Indole-3-pyruvic acid (3-(3-Indolyl)-2-oxopropanoic acid) 是一种参与Indole-3-acetic acid 生物合成的化合物,Indole-3-acetic acid 是一种植物激素,在调节生长和对环境变化的反应中起重要作用。 | |||
T5061 |
Lumichrome
7,8-Dimethylalloxazine,光色素 |
Others | Others |
Lumichrome (7,8-Dimethylalloxazine) 是人类体内的内源性化合物,由核黄素光降解产生。它利用 p53 依赖机制抑制人肺癌细胞生长并诱导凋亡。 | |||
T35455 |
N-Nitrosodiethylamine
Diethylnitrosamine,NDEA |
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
N-Nitrosodiethylamine (NDEA) 是致癌物质二烷基硝胺。它主要存在于水、烟草烟雾、腌制食品、油炸食品以及许多酒精饮料中。它与 DNA 修复/复制相关的核酶的变化相关。 | |||
T2S2173 |
(E)-Naringenin chalcone
Isosalipurpol,柚皮苷查尔酮,Chalconaringenin,trans-2'4'6'4-tetrahydroxychalcone,柚皮素查耳酮 |
Others | Others |
Naringenin chalcone (Isosalipurpol) 是一种黄酮醇生物合成的中间体,在查耳酮异构酶的作用下,自发代谢成柚皮素。它具有抗炎和抗过敏活性。 | |||
T1311 |
4-aminobenzoic acid
PABA,Vitamin H1,Vitamin Bx,para-Aminobenzoic acid,对氨基苯甲酸 |
Endogenous Metabolite | Metabolism |
4-aminobenzoic acid (para-Aminobenzoic acid) 是一种具有紫外线吸收和抗纤维化特性的有机酸。当暴露在光线下时,4-aminobenzoic acid 吸收紫外线并通过光化学反应释放多余的能量,这可能会对DNA造成损害。4-aminobenzoic acid 还可以增加组织水平的摄氧量,并可能增强单胺氧化酶(MAO)活性以促进血清素的降解,过量可能导致纤维化变化。 | |||
T4719 |
1,4-D-Gulonolactone
D-Gulonic acid γ-lactone,D-(-)-古洛糖酸-1,4-内酯 |
Others; Endogenous Metabolite | Metabolism; Others |
1,4-D-Gulonolactone (D-Gulonic acid γ-lactone) (也称为还原性抗坏血酸,RAA) 是 L-gulono-1,4-lactone oxidoreductase (EC 1.1.3.8)的底物,催化植物和动物中l -抗坏血酸(维生素C)生物合成的最后一步。enzyme L-Gulono-1,4-lactone oxidase 在容易患坏血病、缺乏维生素c的动物(如人类)中缺失。1,4-D-Gulonolactone 存在于人体血液中,并被用作比较运动引起的氧化应激变化的标志物之一。 | |||
T8098 |
γ-Hexalactone
γ-caprolactone,gamma-己内酯,γ-己内酯 |
Others | Others |
γ-Hexalactone (γ-caprolactone) 是一种存在成熟水果中的 gamma 内酯。它会导致 DNA 损伤,可用作对氧磷酶 1 的底物 (PON1)。 | |||
T26545 |
Acanthoic acid
NP1302,NP 1302: NP-1302 |
||
Acanthoic acid is a pimaradiene diterpene isolated from Acanthopanax koreanum with anti-inflammatory activities. Acanthoic acid downregulates LPS-induced IL-1β, IL-6 and TNF-α production in BALF, attenuates lung histopathologic changes, and inhibits infla | |||
T15949 |
Mahanimbine
|
AChE | Neuroscience |
Mahanimbine 存在于Murraya koenigii 的根、叶和茎中,是从Murraya koenigii 中的提取的一种具有口服活性的生物碱。Mahanimbine 具有乙酰胆碱酯酶抑制活性,可抑制了高脂肪饮食(HFD)引起的小鼠代谢并发症的发展,对科尼氏分枝杆菌叶对链脲佐菌素诱导的糖尿病大鼠胰腺β细胞组织病理学变化有作用。 | |||
TN4582 |
Moracin T
|
c-Myc; COX | Cell Cycle/Checkpoint; Immunology/Inflammation; Neuroscience |
Moracin treatment can inhibit the double 12-O-tetradecanoylphorbol 13-acetate (TPA) treatment-induced morphological changes reflecting inflammatory response, including leucocyte infiltration, hyperplasia and cell proliferation; moracin treatment furthermo | |||
TN4585 |
Moronic acid
|
HIV Protease; Antifection; HSV | Microbiology/Virology; Proteases/Proteasome |
Moronic acid shows oral therapeutic efficacy in HSV-infected mice and possessed novel anti-HSV activity. It also shows significant anti-HIV activity (EC(50) 186) and was modified to develop more potent anti-AIDS agents. Moronic acid is a new structural lead for anti-EBV drug development, can substantially reduce the numbers of EBV particles produced by the cells after lytic induction. Morolic and moronic acids have shown sustained antidiabetic and antihyperglycemic action possibly mediated by an... | |||
TN4584 |
Morolic acid
|
IL Receptor; COX; HIV Protease | Immunology/Inflammation; Microbiology/Virology; Neuroscience; Proteases/Proteasome |
Morolic acid and moronic acid have shown sustained antidiabetic and antihyperglycemic action possibly mediated by an insulin sensitization with consequent changes of glucose, cholesterol and triglycerides, in part mediated by inhibition of 11β-HSD 1. Moro | |||
TN4394 |
Kobophenol A
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MMP; BCL; p38 MAPK; NF-κB; ROS; DNA/RNA Synthesis; CDK; JNK | Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Immunology/Inflammation; MAPK; NF-κB; Proteases/Proteasome |
Kobophenol A has antimicrobial, and anti-inflammatory activities, it might be a candidate for treatment of inflammatory bone diseases relevant to osteoblast cell death. Kobophenol A inhibits AChE activity in a dose-dependent manner, and the IC50 value is |