38
23
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T1635 |
Fenchlorphos
Ronnel,Dermafos,皮蝇磷 |
AChE; Parasite | Microbiology/Virology; Neuroscience |
Fenchlorphos (Dermafos) 是一种有机磷酸盐杀虫剂,是乙酰胆碱酯酶的抑制剂,能够引起线粒体功能障碍。 | |||
T0866 |
Propafenone
Rythmol,普罗帕酮,Propafenonum |
Potassium Channel; MRP; Sodium Channel | Immunology/Inflammation; Membrane transporter/Ion channel |
Propafenone (Propafenonum) 是钠通道阻滞剂,它对 β 受体具有高亲和力 (IC50=32 nM)。它能够阻断瞬时外向钾电流 (Ito) (IC50: 4.9 nM) 和持续延迟整流器K+电流 (Isus) (IC50: 8.6 nM) ,具有抗心律失常的作用。它能够诱导线粒体功能障碍及诱导细胞凋亡,从而抑制食管癌增殖。 | |||
T19663 |
Triheptanoin
UX 007,IND106011,三庚酸甘油脂,UX007,UX-007,IND 106011,IND-106011 |
Others | Others |
Triheptanoin (IND 106011) 是合成的中链甘油三酯 (MCT),由甘油主链上的三个奇数链 7-碳(庚酸)脂肪酸组成,可以用于研究遗传代谢紊乱。 | |||
T20543 |
Flurochloridone
氟咯草酮,R 40244,R-40244,R40244,EPA Pesticide Chemical Code 128401 |
Apoptosis; Reactive Oxygen Species | Apoptosis; Immunology/Inflammation; Metabolism; NF-κB |
Flurochloridone (R 40244) 是一种选择性除草剂。 Flurochloridone 诱导细胞凋亡并受线粒体功能障碍和氧化应激的调节。 | |||
T13267 |
USP30 inhibitor 11
USP30-IN-11 |
DUB | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Ubiquitination |
USP30 inhibitor 11 (USP30-IN-11) 是一个选择性的 USP30 抑制剂(IC50 : 0.01 µΜ),抑制 SVA,可用于研究癌症、线粒体功能障碍和帕金森。 | |||
T24905 |
TT01001
TT-01001,TT 01001,Ethyl 4-(3-(3,5-dichlorophenyl)thioureido)piperidine-1-carboxylate |
Mitochondrial Metabolism | Metabolism |
TT01001 (Ethyl 4-(3-(3,5-dichlorophenyl)thioureido)piperidine-1-carboxylate) 是 mitoNEET 的选择性激动剂,通过改善线粒体功能障碍来减少氧化应激损伤和神经元凋亡。 TT01001可用于治疗 II 型糖尿病的研究。 | |||
T72662 |
NMDAR/TRPM4-IN-2
|
ERK; TRP/TRPV Channel; NMDAR; iGluR | MAPK; Membrane transporter/Ion channel; Neuroscience |
NMDAR/TRPM4-IN-2 是一种有效的 NMDAR/TRPM4 相互作用界面抑制剂。NMDAR/TRPM4-IN-2 保护小鼠免受 MCAO 诱导的脑损伤和 NMDA 诱导的视网膜神经节细胞丢失。NMDAR/TRPM4-IN-2 具有神经保护活性, 可预防 NMDA 诱导的海马神经元细胞死亡和线粒体功能障碍,其 IC50 值为 2.1 μM。 | |||
T38013 |
Sonlicromanol hydrochloride
KH176 hydrochloride |
ROS | Immunology/Inflammation |
Sonlicromanol hydrochloride (KH176 hydrochloride) 是可透过血脑屏障的 ROS-redox 调节剂,具有潜在的抗癌活性, 可改善 iPSC 衍生神经元中与 m.3243A>G 异质相关的神经元网络功能障碍和转录组变化,可用于治疗线粒体疾病。 | |||
T16342 |
KL1333
NQO1 activator 1 |
NADPH; Mitochondrial Metabolism | Metabolism |
KL1333 (NQO1 activator 1) 是口服NAD+调节剂,与 NAD(P)H: 醌氧化还原酶 1 作为底物反应。它改善线粒体脑肌病、乳酸酸中毒和中风样发作成纤维细胞的能量代谢和线粒体功能障碍。它对顺铂诱导的小鼠耳蜗培养耳毒性的保护作用。 | |||
T71997 | CypD-IN-29 | ||
CypD-IN-29 is a non-peptidic inhibitor of cyclophilin D as a neuroprotective agent in Aβ-induced mitochondrial dysfunction. | |||
T14150 |
AKOS-22
|
Others | Others |
AKOS-22 is a potent mitochondrial protein VDAC1 (voltage-dependent anion channel 1) inhibitor (Kd=15.4 μM). AKOS-22 protects against mitochondrial dysfunction[1]. AKOS-22 interacts with VDAC1 and inhibiting both VDAC1 oligomerization and apoptosis. | |||
TP1947 |
P110
|
||
Dynamin-related protein 1 (Drp1) inhibitor, inhibits Drp1 GTPase activity. Displays no effect on dynamin 1 or other mitochondrial dynamics-related proteins. Inhibits mitochondrial fission, dysfunction and reactive oxygen species (ROS) production in vitro. | |||
T68788 | Ellipticine quinone | ||
Ellipticine quinone, also known as NSC-383230, is a Drp1 inhibitor. rpitor1 and Drpitor1a inhibited the GTPase activity of Drp1 without inhibiting the GTPase of dynamin 1. Ellipticine quinone showed greater potency than the current std. Drp1 GTPase inhibitor, mdivi-1, (IC50 for mitochondrial fragmentation are (0.06, and 10 μM, resp.). Ellipticine quinone suppressed lung cancer tumor growth in a mouse xenograft model. Ellipticine quinone also inhibited mitochondrial ROS prodn., prevented mi... | |||
T73227 |
SH-BC-893
|
||
SH-BC-893是一种具有口服活性的抗肿瘤鞘脂类似物,能够防止神经酰胺引起的线粒体功能障碍并纠正饮食引起的肥胖。适用于癌症和肥胖症的研究。 | |||
T79709 |
PK-10
|
||
PK-10是Fluconazole的协同抗菌剂,具有针对多种Fluconazole耐药白色念珠菌株的强抗真菌活性。联合应用PK-10和Fluconazole能够抑制菌丝生长并诱导活性氧的积累,从而损害线粒体膜电位、降低ATP水平,并最终导致线粒体功能障碍。 | |||
T74571 | TSPO Ligand-Linker Conjugates 1 | ||
TSPO Ligand-Linker Conjugates 1,包含TSPO配体和连接子,用于合成靶向线粒体的AUTAC。该AUTAC能与OMM上TSPO结合,通过mitophagy降解受损线粒体和蛋白质,提升线粒体活性。适用于研究线粒体功能紊乱,包括神经退行性疾病、癌症和糖尿病。 | |||
T80737 |
ZG36
|
||
ZG36是一种人类Caseinolytic protease P(ClpP)激动剂,具有非选择性地降解呼吸链复合物和减少线粒体DNA的能力,从而导致线粒体功能衰竭及白血病细胞死亡。此外,ZG36能够抑制异种移植小鼠模型中急性髓细胞性白血病的发展。 | |||
T83057 |
Anti-inflammatory agent 49
|
||
Anti-inflammatory agent 49 (化合物 SC9),一种Drp1-Fis1相互作用的抑制剂,可用于缓解Fis1介导的线粒体功能障碍。该化合物在体外对GTPase的IC50值为270 nM。 | |||
T37533 |
DOPAL
|
||
DOPAL is an aldehyde product of the oxidative deamination of dopamine by monoamine oxidase.[1] It can be further oxidized to 3,4-dihydroxyphenylacetic acid (DOPAC) by aldehyde dehydrogenase (ALDH) and, to a lesser extent reduced to 3,4-dihydroxyphenyl ethanol (DOPET). DOPAL is toxic to neurons.[2],[3] It can also oligomerize and precipitate α-synuclein, an event associated with Parkinson's disease.[2] Mice lacking cytosolic and mitochondrial forms of ALDH display increased levels of DOPAL as wel... | |||
T73125 |
SMTIN-T140
|
HSP | Cytoskeletal Signaling; Metabolism |
SMTIN-T140(化合物6a)是一种TRAP1(肿瘤坏死因子受体相关蛋白1)的高效抑制剂,IC50值为1.646 μM。该化合物表现出显著的抗癌活性,可引起线粒体功能障碍,增加线粒体ROS产生以及激活AMPK。在PC3前列腺癌细胞异种移植的小鼠模型中,SMTIN-T140有效抑制了肿瘤生长,并显示出良好的体内安全性。 | |||
T78580 | Erythronic acid | Endogenous Metabolite | Metabolism |
Erythronic acid为一糖类内源性代谢物,关键于高尿酸血症发病及其改善过程,且与转醛缩酶缺乏症相关联的线粒体功能障碍相关,常用于代谢性疾病研究。 | |||
T13773 |
Mito-apocynin (C11)
|
Others | Others |
Mito-apocynin (C11)是一种线粒体靶向抗氧化剂,通过靶向和中和细胞呼吸过程中产生的活性氧(ROS)发挥作用。三苯基溴化鏻已被发现能有效预防线粒体功能障碍,线粒体功能障碍是衰老过程和各种疾病的主要原因。它具有抗炎、抗凋亡和抗氧化活性。 | |||
T60528 | PDPOB | ||
PDPOB 是一种苯基羧酸衍生物,具有用于脑缺血研究的潜力。PDPOB 被证明可以防止 SH-SY5Y 细胞中 OGD/R 诱发的多方面神经元退化,减轻的线粒体功能障碍、氧化应激和细胞凋亡证明了这一点。 | |||
T60510 |
Perhexiline
|
||
Perhexiline 是一种口服活性的 CPT1和 CPT2抑制剂,可降低脂肪酸的代谢。Perhexiline 可以穿过血脑屏障 (BBB)具有抗癌活性。Perhexiline 诱导肝细胞中的线粒体功能障碍和细胞凋亡。因此,Perhexiline 可用于研究癌症和心绞痛等心血管疾病。 | |||
T37679 |
3-hydroxy Palmitic Acid
|
||
3-hydroxy Palmitic acid is a form of the 16:0 lipid palmitic acid . The lipid A part of lipopolysaccharides contain various 3-hydroxy fatty acids, making oxylipins such as 3-hydroxy palmitic acid useful as chemical markers of endotoxins. In R. solanacearum, 3-hydroxy palmitic acid is converted by an S-adenosyl methionine-dependent methyltransferase to 3-hydroxy palmitic acid methyl ester, which acts as a quorum sensing signal molecule for post-transcriptional modulation of genes involved in viru... | |||
T37516 |
[(3R)-3-Hydroxydodecanoyl]-L-carnitine
|
||
[(3R)-3-Hydroxydodecanoyl]-L-carnitine is an endogenous metabolite[1]. [1]. Hunter WG, et al. Metabolomic Profiling Identifies Novel Circulating Biomarkers of Mitochondrial Dysfunction Differentially Elevated in Heart Failure With Preserved Versus Reduced Ejection Fraction: Evidence for Shared Metabolic Impairments in Clinical Heart Failure. J Am Heart Assoc. 2016;5(8):e003190. Published 2016 Jul 29. | |||
T62445 | Tubulin inhibitor 22 | ||
Tubulin inhibitor 22 (compound 4c) 是一种 tubulin 的有效抑制剂,表现出抗血管生成和抗癌活性。Tubulin inhibitor 22 能够将 MGC-803 细胞的细胞周期阻滞在 G2/M 期。Tubulin inhibitor 22 剂量依赖性地通过线粒体功能障碍引起 Caspase 诱导的 MGC-803 细胞凋亡 (apoptosis)。 | |||
T64014 | Antitumor agent-58 | ||
Antitumor agent-58 是一种抗肿瘤剂,对 MGC-803 细胞的集落形成和细胞迁移具有有效的抑制作用,并能够诱导 MGC-803 细胞的线粒体功能障碍。Antitumor agent-58 可以激活 p38 和 JNK 信号通路,并诱导 MGC-803 细胞凋亡 (apoptosis)。Antitumor agent-58 对携带 MGC-803 细胞的异种移植模型的肿瘤生长表现出有效的抑制活性。 | |||
T79601 | SPC-180002 | Sirtuin | Chromatin/Epigenetic; DNA Damage/DNA Repair |
SPC-180002是一种针对SIRT1/3的双重抑制剂,IC50值分别为1.13 μM和5.41 μM。该化合物可通过诱导ROS产生干扰氧化还原平衡,进而增强p21蛋白的稳定性并引起线粒体功能障碍,同时显著抑制细胞周期进程及癌细胞的增殖,并能激活Nrf2信号通路。 | |||
T79284 |
IR-251
|
||
IR-251是一种线粒体靶向的近红外荧光探针,通过OATP导向线粒体,诱导肿瘤细胞中线粒体损伤。IR-251抑制PPARγ,从而引发ROS的过量生成,进而抑制β-catenin信号通路及相关细胞周期和转移的下游蛋白,有效抑止肿瘤的增殖和转移。 | |||
T80286 |
TP4 (Nile tilapia piscidin)
|
Necroptosis | Apoptosis |
TP4(Nile tilapia piscidin)是一种piscidin样的抗菌肽,其口服活性被证实。此化合物对多种革兰氏阳性及阴性菌株均有效(MIC: 0.03-10 μg/mL),并展现了溶血性。TP4还能增强免疫响应、提升抗氧化能力和改善肠道健康,助于防御细菌感染。除此之外,TP4显示抗肿瘤效果,并可通过激发癌细胞线粒体功能障碍导致坏死(necrosis)。 | |||
T79558 |
fac-[Re(CO)3(L3)(H2O)][NO3]
|
||
fac-[Re(CO)3(L3)(H2O)][NO3](简称compound 3),是一种与线粒体功能障碍相关的抗前列腺癌剂。这种铼(I)三羰基水配合物对前列腺癌细胞系(PC-3)表现出显著的细胞毒性,其IC50值为0.32 μM。研究表明,fac-[Re(CO)3(L3)(H2O)][NO3]主要在线粒体中积聚,能够降低PC-3细胞的ATP生成,进而触发细胞副凋亡(paraptosis)机制,而不通过引发坏死、凋亡或自噬途径作用。 | |||
T37297 |
Ru360
|
||
Ru360, an oxygen-bridged dinuclear ruthenium amine complex, is a selective mitochondrial calcium uptake inhibitor. Ru360 potently inhibits Ca2+ uptake into mitochondria with an IC50 of 0.184 nM. Ru360 binds to mitochondria with high affinity (Kd of 0.34 nM). Ru360 has antiarrhythmic and cardioprotective effects[1][2]. Ru360 permeates slowly into the cell, and specifically inhibits mitochondrial calcium uptake in intact cardiomyocytes and in isolated heart. 1 μm Ru360 is taken up by myocardial ce... | |||
T36490 | AZT triphosphate TEA | ||
AZT triphosphate TFA (3'-Azido-3'-deoxythymidine-5'-triphosphate TFA) is a active triphosphate metabolite of Zidovudine (AZT). AZT triphosphate TFA exhibits antiretroviral activity and inhibits replication of HIV. AZT triphosphate TFA also inhibits the DNA polymerase of HBV. AZT triphosphate TFA activates the mitochondria-mediated apoptosis pathway[1][2][3]. Treatment with 100 μM Zidovudine (AZT) for 48h disrupts the mitochondrial tubular network via accumulation of AZT triphosphate (AZT-TP) in ... | |||
T35712 |
Debutyldronedarone hydrochloride
SR35021 hydrochloride |
||
N-Desbutyl dronedarone is an active metabolite of the antiarrhythmic agent dronedarone .1,2,3It is formed from dronedarone by cytochrome P450s (CYPs) and monoamine oxidase (MAO) in human hepatocyte preparations.4N-Desbutyl dronedarone inhibits the binding of 3,3’,5-triiodo-L-thyronine to the thyroid hormone receptors TRα1and TRβ1(IC50s = 59 and 280 μM for the chicken and human receptors, respectively).1It inhibits CYP2J2-mediated formation of 14,15-EET from arachidonic acid and soluble epoxide h... | |||
T36903 |
Rasagiline-13C3 (mesylate)
Rasagiline-13C3 (mesylate) |
||
Rasagiline-13C3is intended for use as an internal standard for the quantification of rasagiline by GC- or LC-MS. Rasagiline is an inhibitor of monoamine oxidase B (MAO-B; IC50= 4.43 nM for the rat brain enzyme).1It is selective for MAO-B over MAO-A (IC50= 412 nM for the rat brain enzyme). It inhibits serum and NGF withdrawal-induced apoptosis of PC12 cells when used at concentrations ranging from 0.01 to 100 μM.2Rasagiline inhibits rat brain MAO-Bin vivo(ED50= 0.1 mg/kg).1It reduces cerebral ede... | |||
T38284 |
C24 dihydro 1-Deoxyceramide (m18:0/24:0)
C24 dihydro 1-Deoxyceramide (m18:0/24:0) |
||
C24 dihydro 1-Deoxyceramide (m18:0/24:0) is a very long-chain atypical ceramide containing a 1-deoxysphinganine backbone. 1-Deoxysphingolipids are formed when serine palmitoyltransferase condenses palmitoyl-CoA with alanine instead of serine during sphingolipid synthesis.1,2 C24 dihydro 1-Deoxyceramide (m18:0/24:0) has been found in mouse embryonic fibroblasts (MEFs) following application of 1-deoxysphinganine alkyne or 1-deoxysphinganine-d3.3 It has also been found in mouse brain, spinal cord, ... | |||
T38280 |
C22 dihydro 1-Deoxyceramide (m18:0/22:0)
C22 dihydro 1-Deoxyceramide (m18:0/22:0) |
||
C22 dihydro 1-Deoxyceramide (m18:0/22:0) is a very long-chain atypical ceramide containing a 1-deoxysphinganine backbone. 1-Deoxysphingolipids are formed when serine palmitoyltransferase condenses palmitoyl-CoA with alanine instead of serine during sphingolipid synthesis.1,2 C22 dihydro 1-Deoxyceramide (m18:0/22:0) has been found in mouse embryonic fibroblasts (MEFs) following application of 1-deoxysphinganine alkyne or 1-deoxysphinganine-d3.3 It has also been found as the most prevalent dihydro... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T11685 |
Isolongifolene
异长叶烯,(-)-Isolongifolene |
Apoptosis; Others | Apoptosis; Others |
Isolongifolene ((-)-Isolongifolene) 是一种从调料九里香中分离的三环倍半萜烯,具有抗氧化,抗炎,抗癌和神经保护的特性。它通过调节 PI3K/AKT/GSK-3β 信号通路来减轻鱼藤酮诱导的氧化应激,线粒体功能障碍和细胞凋亡。 | |||
T5645 |
Nerol
Cis-Geraniol,橙花醇,Neryl alcohol |
Apoptosis; Reactive Oxygen Species; Mitochondrial Metabolism; Endogenous Metabolite; Antifungal | Apoptosis; Immunology/Inflammation; Metabolism; Microbiology/Virology; NF-κB |
Nerol (Neryl alcohol) 是橙花油的一种单萜, 它通过增强 Ca2+和ROS 来触发线粒体功能障碍并诱导凋亡,具有抗真菌活性。它可减轻哺乳动物心脏中哇巴因引发的心律失常的严重程度。 | |||
T3410 |
Momordin Ic
地肤子皂苷Ic,地肤子皂苷 Ic,Momordin 1c |
Apoptosis; MAPK; PI3K | Apoptosis; MAPK; PI3K/Akt/mTOR signaling |
Momordin Ic (Momordin 1c) 是山茱萸的主要皂苷成分,通过氧化应激调控线粒体功能障碍诱导细胞凋亡,具有抗癌活性。 | |||
T3916 |
Ginsenoside F2
人参皂苷F2 |
Apoptosis; Endogenous Metabolite; Autophagy | Apoptosis; Autophagy; Metabolism |
Ginsenoside F2 是 Ginsenoside Rb1 的代谢物,通过激活内在的凋亡途径和线粒体功能障碍来诱导乳腺的凋亡,对乳腺癌干细胞具有抗增殖活性。 | |||
T5255 |
5-Hydroxymethyluracil
5-(Hydroxymethyl)uracil,5-羟甲基脲嘧啶,Hydroxymethyl Uracil,a-Hydroxythymine |
Others; Endogenous Metabolite | Metabolism; Others |
5-Hydroxymethyluracil (a-Hydroxythymine) 是一种氧化性 DNA 损伤的产物,能够增强或抑制细菌 RNA 聚合酶转录的潜在表观遗传标记。 | |||
TN1461 |
(-)-Butin
Butin,漆黄素 ( 紫铆素) |
Akt; PI3K; Nrf2 | Cytoskeletal Signaling; Immunology/Inflammation; PI3K/Akt/mTOR signaling |
(-)-Butin (Butin) 是 Butin 的 S 对映体。其中 Butin 是一种分离自黄檀的心材中的生物活性黄酮类化合物,具有显著的抗血小板、抗氧化、抗炎作用。 | |||
T3895 |
Polyphyllin I
重楼皂苷I,重楼皂甙 |
Apoptosis; Akt; JNK; PDK; mTOR; Autophagy | Apoptosis; Autophagy; Cytoskeletal Signaling; MAPK; PI3K/Akt/mTOR signaling |
Polyphyllin I 是从七叶一枝花中提取的生物活性成分,具有很强的抗肿瘤活性。它是 JNK 信号通路的激活剂,也是 PDK1/Akt/mTOR 信号传导的抑制剂。它诱导自噬,G2/M 期阻滞和细胞凋亡。 | |||
T3S1068 |
Oxyresveratrol
trans-Oxyresveratrol,2,3',4,5'-tetrahydroxystilbene,氧化白藜芦醇,Tetrahydroxystilbene |
Tyrosinase; Autophagy; HSV | Autophagy; Microbiology/Virology; Proteases/Proteasome |
Oxyresveratrol (trans-Oxyresveratrol) 是非竞争性酪氨酸酶抑制剂,对蘑菇酪氨酸酶的 IC50值为 1.2 µM。它抑制HSV-1,HSV-2和水痘带状疱疹病毒,具有神经保护作用。它是天然抗氧化剂和自由基清除剂。 | |||
T6S0735 |
Flavokawain B
黄卡瓦胡椒素B,Flavokavain B,Flavokawin B,2'-Hydroxy-4',6'-Dimethoxychalcone |
Apoptosis; Others | Apoptosis; Others |
Flavokawain B (Flavokavain B) 是从卡瓦醉椒的根提取物中,分离出的查尔酮。它是一种凋亡诱导剂,可抑制各种癌细胞株生长。它以极低的无毒浓度抑制人脑内皮细胞的迁移和血管形成,具有抗血管生成活性。 | |||
T19496 |
Oleuroside
|
Others | Others |
Oleuroside can protect against mitochondrial dysfunction in models of early Alzheimer's disease and brain ageing. | |||
TN6608 |
Cyanidin-3-O-arabinoside chloride
|
||
Cyanidin-3-O-arabinoside chloride has antioxidant activity. It reduces the peroxynitrite-induced suppression of mitochondrial respiration, DNA damage, PARS activation and vascular dysfunction in HUVECs. | |||
TN3618 |
Cedrin
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Beta Amyloid; BCL; Caspase | Apoptosis; Neuroscience; Proteases/Proteasome |
Cedrin has protective effects on PC12 cells against the neurotoxicity induced by amyloid β1-42, the protective effect is related to the inhibition of oxidative stress, improvement of mitochondrial dysfunction and suppression of apoptosis. | |||
TN5013 |
Shizukaol D
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AMPK | Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
Shizukaol D exerts a growth inhibition effect on liver cancer cells in a dose- and time-dependent manner by modulating wnt signalling pathway. Shizukaol D may be used to treat metabolic syndrome, it induces mitochondrial dysfunction by depolarizing the mitochondrial membrane and suppressing energy production, which may result in AMPK activation. | |||
TN1093 |
Ginsenoside F4
人参皂苷F4 |
MMP; IL Receptor; BCL | Apoptosis; Immunology/Inflammation; Proteases/Proteasome |
Ginsenoside F4 has inhibitory effect on human lymphocytoma JK cell by inducing its apoptosis, the mechanism is related to the mitochondrial dysfunction and the increase of Bax expression and decrease of Bcl-2 expression. | |||
TN1086 |
Dehydrotrametenolic acid
Dehydroeburicoic acid,去氢齿孔酸,松苓新酸 |
Apoptosis; TNF; NOS; Caspase; NO Synthase | Apoptosis; Immunology/Inflammation; Proteases/Proteasome |
Dehydrotrametenolic acid (Dehydroeburicoic acid) 是从茯苓的菌核中分离的一种甾醇,具有抗肿瘤活性、抗炎和抗糖尿病作用。它通过 caspase-3途径诱导细胞凋亡。 | |||
TN5440 |
Catechin-7-O-xyloside
Catechin 7-O-β-D-xylopyranoside |
Others | Others |
Catechin-7-O-xyloside(C7Ox)具有抗癌活性,它通过内质网应激和线粒体功能障碍诱导人非小细胞肺癌H1299细胞凋亡。 | |||
TN5456 |
Isoerysenegalensein E
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Isoerysenegalensein E shows anti-estrogenic activity comparable to that of 4-hydroxytamoxifen, a typical estrogen receptor antagonist. It shows significant cytotoxicity against HL-60 cells, it induces apoptosis in HL-60 cells through activation of the cas | |||
T78466 |
Erythronic acid potassium
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Endogenous Metabolite | Metabolism |
Erythronic acid potassium为糖类内源性代谢物,关键作用于高尿酸血症发病及改善过程,并与转醛缩酶缺乏症相关的线粒体功能障碍有关,常用于代谢性疾病研究。 | |||
TN5264 |
Xanthoxyletin
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TNF; NOS; ROS; COX; Antifection | Apoptosis; Immunology/Inflammation; Microbiology/Virology; Neuroscience |
Xanthoxyletin shows potent antibacterial, fungicidal, and algicidal properties, it also has anticancer, and anti-inflammatory activities. It shows an inhibitory effect on iNOS protein expression at 10 microM, it also can inhibit the synthesis of nitric oxide and the protein expression of tumor necrosis factor-alpha and cyclooxygenase-2. Xanthoxyletin induces S phase arrest and apoptosis in human gastric adenocarcinoma SGC-7901 cells, the effects are associated with the DNA damage, apoptosis thro... | |||
T82773 |
Catechin 7-O-β-D-glucopyranoside
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Catechin 7-O-beta-D-glucopyranoside 是发现于Ulmus davidiana和Paeonia obovata的具有口服活性的天然化合物。该化合物显示出明显的抗氧化与抗炎活性,能改善线粒体功能障碍,有望成为肠道炎症性疾病研究中的潜在用途。 | |||
T73068 |
Mammea A/BA
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Mammea A/BA 对克氏锥虫 (T. cruzi) 显示出有效抗性。通过诱导线粒体功能障碍、产生活性氧 (ROS)、DNA 片段化以及增加酸性液泡数量,Mammea A/BA 触发细胞死亡机制,包括细胞凋亡 (apoptosis)、细胞自噬 (autophagy) 和细胞坏死,对于南美锥虫病的研究具有潜在应用价值。 | |||
T37974 |
(S)-Coriolic acid
13(S)-HODE |
Lipoxygenase; Mitochondrial Metabolism; PPAR | DNA Damage/DNA Repair; Metabolism |
(S)-Coriolic acid (13(S)-HODE) 是一种重要的细胞内信号剂,是亚油酸与植物和哺乳动物脂氧合酶反应生成的,在各种生物系统中参与细胞增殖和分化。(S)-Coriolic acid 在 1 μM 左右时,它能抑制肿瘤细胞与血管内皮的粘附,能下调 IRGpIIb/IIIa 受体的表达。(S)-Coriolic acid 是15-脂氧合酶 (15-LOX) 代谢产物,常作为内源性配体激活 PPARγ。(S)-Coriolic acid 诱导线粒体功能障碍 和气道上皮损伤。 | |||
TN1094 |
Ginsenoside Rg6
人参皂苷Rg6,人参皂苷 Rg6 |
Apoptosis; NF-κB | Apoptosis; NF-κB |
Ginsenoside Rg6 抑制人淋巴瘤 JK 细胞增殖并诱导其凋亡,在 HepG2 细胞中抑制 TNF-α 诱导的 NF-κB 转录活性,IC50为 29.34 μM。 |