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Search Results for " atp synthase "

16

抑制剂 & 化合物

3

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T10404	ATP synthase inhibitor 1	ATPase	Membrane transporter/Ion channel
	ATP synthase inhibitor 1 是 F1/FO-ATP 合酶复合物 c 亚基的有效抑制剂，抑制线粒体通透性转换孔的开放。
T15373	Gboxin	ATPase; Mitochondrial Metabolism	Membrane transporter/Ion channel; Metabolism
	Gboxin 是一种氧化磷酸化抑制剂，可靶向抑制胶质母细胞瘤生长，还抑制 F0F1 ATP 合成，具有抗肿瘤活性。
T1940	BTB06584	RAAS; ATPase	Endocrinology/Hormones; Membrane transporter/Ion channel
	BTB06584 是选择性依赖 IF1 的线粒体F1Fo-ATPase 抑制剂，可延迟缺血性细胞死亡。
T24111	GSK3i XIII GSK3 inhibitor XIII,GSK3iXIII,GSK3i-XIII	GSK-3	PI3K/Akt/mTOR signaling; Stem Cells
	GSK3i XIII (GSK3 inhibitor XIII) 是ATP 竞争性GSK-3抑制剂(Ki: 24 nM)。
T61649	ATP synthase inhibitor 2
	ATP synthase inhibitor2 是一个铜绿假单胞菌 (PA)ATP synthase 抑制剂 (IC50=10 μg/mL)，在 128 μg/mL 时可完全抑制铜绿假单胞菌 (PA) 的 ATP 合成活性。
T60877	Mtb ATP synthase-IN-1
	Mtb ATP synthase-IN-1 (compound 6ab) 可用于研究抗结核分枝杆菌。Mtb ATP synthase-IN-1 具有低细胞毒性 (Vero IC50> 64 μg/mL)和可接受的口服生物利用度，具有良好的代谢稳定性。Mtb ATP synthase-IN-1 是结核分枝杆菌 (Mtb) ATP 合成酶的有效抑制剂（MIC 值为 0.452 ~ 0.499 μg/mL）。
T79004	ATP synthase inhibitor 2 TFA
	ATP synthase inhibitor2 (Compound 22) TFA 为针对铜绿假单胞菌 (PA) ATP synthase 的抑制剂，具IC50值为10 μg/mL，在浓度达到128 μg/mL 时能够全面阻断铜绿假单胞菌 (PA) ATP的合成活性。
T6820	D-α-Hydroxyglutaric acid disodium D-alpha-Hydroxyglutaric acid disodium salt,(R)-2-羟基戊二酸二钠盐,Disodium (R)-2-Hydroxyglutarate	ATPase; Others; Reactive Oxygen Species; Endogenous Metabolite; mTOR	Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism; NF-κB; Others; PI3K/Akt/mTOR signaling
	D-α-Hydroxyglutaric acid disodium (Disodium (R)-2-Hydroxyglutarate) 是神经代谢疾病 D-2-羟基戊二酸尿症中积累的主要代谢产物，可增加活性氧的产生。它是 α-酮戊二酸 (α-KG) 的弱竞争拮抗剂，可抑制多种α-KG 依赖性双加氧酶，Ki 为 10.87 mM。
T21023	Bedaquiline fumarate TMC 207,R403323,TMC-207,TMC207,R-403323,贝达喹啉富马酸盐,R 403323	Antibacterial; Antibiotic	Microbiology/Virology
	Bedaquiline fumarate (TMC207) 是二芳基喹啉抗生素，作用于 ATP 合成酶，常用于结核杆菌感染的研究。
T3067	Tideglusib NP-12,NP031112	GSK-3	PI3K/Akt/mTOR signaling; Stem Cells
	Tideglusib (NP031112) 是不可逆的 GSK-3抑制剂，能够抑制 GSK-3βWT (IC50:5 nM) 和 GSK-3βC199A (IC50:60 nM)。
T36624L	α-Hydroxyglutaric Acid Lithium α-Hydroxyglutaric Acid Lithium(2889-31-8 Free base)	Decarboxylase; Endogenous Metabolite; mTOR	Metabolism; Others; PI3K/Akt/mTOR signaling
	α-Hydroxyglutaric Acid Lithium 在微生物和动物体内有谷氨酸转化而来，是 α-酮戊二酸依赖性双加氧酶和 5-甲基胞嘧啶羟化酶抑制剂，对 ATP 合酶和 mTOR 信号传导有抑制作用。
T14066	9-ING-41	Apoptosis; GSK-3; Autophagy	Apoptosis; Autophagy; PI3K/Akt/mTOR signaling; Stem Cells
	9-ING-41 是基于马来酰亚胺的 ATP 竞争性和选择性的糖原合酶激酶-3β 抑制剂，IC50为 0.71 μM。它显著导致癌细胞的细胞周期停滞，自噬和凋亡，具有增强化疗药物抗肿瘤作用的潜力，有抗癌活性。
T26843	BMS-199264 hydrochloride
	BMS-199264 hydrochloride potently inhibits the ATP hydrolase activity of mitochondrial F1F0 ATP synthase.
T38231	Isoapoptolidin
	Isoapoptolidin is a stable derivative of apoptolidin that demonstrates 10-fold reduced F1FO-ATP synthase inhibitory activity compared to apoptolidin (IC50s = 17 and 0.7 μM, respectively).
T74033	6-Me-ATP
	6-Me-ATP（N6-Methyl-ATP）为ATP的N6修饰衍生物。该化合物与GSK3β结合亲和力显著，能有效作为GSK3β催化底物肽磷酸化的磷酸基团供体。
T35560	SAR502250
	SAR502250 is a potent, selective, ATP competitive, orally active and brain-penetrant inhibitor of GSK3, with an IC50 of 12 nM for human GSK-3β. SAR502250 displays antidepressant-like activity. SAR502250 can be used for the research of Alzheimer’s disease (AD)[1][2]. SAR502250 (0.01-1 μM; 36 h) attenuates the Aβ25-35-induced cell death in rat embryonic hippocampal neurons[2]. SAR502250 (1-100 mg/kg; a single p.o,) attenuates tau hyperphosphorylation in the cortex and spinal cord of transgenic mic...

化合物

ATP synthase inhibitor 1

Cat.No: T10404

Target: ATPase

Cat.No: T15373

Target: ATPase, Mitochondrial Metabolism

Cat.No: T1940

Target: RAAS, ATPase

Cat.No: T24111

Synonym: GSK3 inhibitor XIII,GSK3iXIII,GSK3i-XIII

Target: GSK-3

ATP synthase inhibitor 2

Cat.No: T61649

Mtb ATP synthase-IN-1

Cat.No: T60877

ATP synthase inhibitor 2 TFA

Cat.No: T79004

D-α-Hydroxyglutaric acid disodium

Cat.No: T6820

Synonym: D-alpha-Hydroxyglutaric acid disodium salt,(R)-2-羟基戊二酸二钠盐,Disodium (R)-2-Hydroxyglutarate

Target: ATPase, Others, Reactive Oxygen Species, Endogenous Metabolite, mTOR

Bedaquiline fumarate

Cat.No: T21023

Synonym: TMC 207,R403323,TMC-207,TMC207,R-403323,贝达喹啉富马酸盐,R 403323

Target: Antibacterial, Antibiotic

Cat.No: T3067

Synonym: NP-12,NP031112

Target: GSK-3

α-Hydroxyglutaric Acid Lithium

Cat.No: T36624L

Synonym: α-Hydroxyglutaric Acid Lithium(2889-31-8 Free base)

Target: Decarboxylase, Endogenous Metabolite, mTOR

Cat.No: T14066

Target: Apoptosis, GSK-3, Autophagy

BMS-199264 hydrochloride

Cat.No: T26843

Cat.No: T38231

Cat.No: T74033

Cat.No: T35560

Cat. No.	Product Name	Target	Signaling Pathways
T6323	Oligomycin A MCH 32,寡霉素A	ATPase; Antibiotic; Antifungal	Membrane transporter/Ion channel; Microbiology/Virology
	Oligomycin A (MCH 32) 是从链霉菌属中得到的一种线粒体F0F1-ATPase 抑制剂，抑制氧化磷酸化和线粒体偶联膜上发生的所有 ATP 依赖性过程。
T4861	trans-Aconitic acid	ATPase; Endogenous Metabolite	Membrane transporter/Ion channel; Metabolism
	trans-Aconitic acid 是反式丙酮酸2-甲基转移酶的底物，存在于正常人尿液中，大量存在于 Reye 综合征和有机酸尿症。
T12298	Oligomycin B	Others	Others
	Oligomycin B is an antibiotic isolated from marine Streptomyces, is an eukaryotic ATP synthase inhibitor, induces apoptosis.

天然产物

Cat.No: T6323

Synonym: MCH 32,寡霉素A

Target: ATPase, Antibiotic, Antifungal

trans-Aconitic acid

Cat.No: T4861

Target: ATPase, Endogenous Metabolite

Cat.No: T12298

Target: Others

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