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Search Results for " nitric oxide production-in-1 "

23

抑制剂 & 化合物

21

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T79981	Nitric oxide production-IN-1	NO Synthase	Immunology/Inflammation
	Nitric oxide production-IN-1（Compound 1）是从Tupistra chinensis中提取的一种NO产生抑制剂，能够抑制脂多糖诱导的大鼠腹腔巨噬细胞NO产量。
T61157	ABAI-30
	ABAI-30 is a highly potent and orally bioavailable anti-inflammatory compound that efficiently suppresses nitric oxide (NO) production in lipopolysaccharide (LPS) activated RAW264.7 cells [1].
T83049	Anti-inflammatory agent 63
	Anti-inflammatory agent 63，在RAW264.7细胞中对脂多糖 (LPS) 诱导的一氧化氮 (NO) 产生显示最佳抑制效果，其半抑制浓度(EC50)为5.33±0.57 μM。
T78229	Aminoguanidine hemisulfate	Reactive Oxygen Species	Immunology/Inflammation; Metabolism; NF-κB
	Aminoguanidine hemisulfate 作为NOS及ROS的抑制剂，能够在体外有效清除ANE诱导的ROS生成，因此它被广泛应用于癌症研究领域。
T83052	Anti-inflammatory agent 60	NF-κB	NF-κB
	Anti-inflammatory agent 60 (compound 21) 的 IC50 值针对一氧化氮生成为 12.95 μM。此化合物通过浓度依赖性方式降低 iNOS、phosphorylated p65 以及 β-catenin 的表达。
T62078	Akt/NF-κB/JNK-IN-1
	Akt/NF-κB/JNK-IN-1 (Compound 2i) 是一种 Akt、NF-κB 和 JNK 信号通路抑制剂。Akt/NF-κB/JNK-IN-1 对一氧化氮的产生表现出抑制作用 (IC50: 3.15 μM)，表现出抗炎效果。
T61821	COX-2-IN-16
	COX-2-IN-16 (compound 2b)为一种口服活性高、选择性强的COX-2抑制剂，其IC50为102 μM，能有效抑制NO产生并具备抗炎活性。
T78439	1,2-Diaminoanthraquinone
	1,2-Diaminoanthraquinone是一种敏感、特异且无毒的一氧化氮(NO)荧光探针，适用于活细胞和生物体内NO生成的检测。该化合物的λmax约为540 nm，对NO的检测极限达到5 μM。
T83002	Antitumor agent-49
	Antitumor agent-49 (Compound 10) 是一款 Harmine 和呋喃杂化的衍生物，带有 NO 供体且表现出抗肿瘤特性。该化合物对 HepG2 细胞线展现出显著的细胞毒性，其 IC50 值为 1.79 µM，并且能在体外产生大量的 NO。
T35864	T-5342126
	T-5342126 is a toll-like receptor 4 (TLR4) antagonist.1It reduces LPS-induced production of nitric oxide (NO) in RAW 264.7 cells (IC50= 27.8 μM), as well as decreases LPS-induced IL-8, TNF-α, and IL-6 production in isolated human whole blood (IC50s = 110.5, 315.6, and 318.4 μM, respectively). T-5342126 (82 mg/kg) reduces ethanol intake and the abundance of ionized calcium-binding adapter molecule 1 (Iba1), a marker of microglial activation, in the central nucleus of the amygdala in ethanol-depen...
T79478	Anti-inflammatory agent 45	Apoptosis	Apoptosis
	Anti-inflammatory agent 45（化合物2v）作为一种抗癌剂，直接抑制多种血癌细胞系（如白血病、淋巴瘤、骨髓瘤）的生长。该化合物能够诱导HL60白血病细胞发生凋亡，并可抑制NO生成，其半抑制浓度（IC50）为14.7 μM。
T79304	Semapimod CPSI-2364,CNI-1493 free base
	Semapimod是一种抑制促炎细胞因子产生的化合物，具有抑制TNF-α、IL-1β和IL-6功能。它通过抑制巨噬细胞的p38 MAPK以及一氧化氮的生成发挥作用，并且能够抑制TLR4信号传导（IC50约为0.3 μM）。Semapimod对于治疗各类炎症和自身免疫性疾病显示出潜在效用。
T72687	Keap1-Nrf2-IN-11
	Keap1-Nrf2-IN-11为Keap1-Nrf2抑制剂，KD2值达0.21 nM。该化合物可有效抑制ROS及NO的生成，并降低TNF-α的表达。通过促进Nrf2的核内转移，Keap1-Nrf2-IN-11对炎症具有调节作用，适用于抗炎研究。
T75763	TP508 TFA
	TP508 TFA为含23个氨基酸的非蛋白质水解凝血酶肽, 属凝血酶分子受体结合结构域部分。该化合物能激活内皮NO synthase(eNOS)，促进人内皮细胞内NO生成，进而通过激活内皮细胞及干细胞，促进血管及组织再生。
T79637	CIAC001
	CIAC001是一种丙酮酸激酶PKM2的抑制剂，它展现出了抗神经炎症活性。这种化合物能够抑制LPS诱导的一氧化氮(NO)产生(IC50=2.5 μM)，并保护BV-2免疫活性细胞。在小鼠模型中，CIAC001减轻了慢性吗啡引起的成瘾和神经炎症症状。
T79371	HDAC-IN-62	Autophagy	Autophagy
	HDAC-IN-62（Compound 5），是一款针对HDAC6/8/11的HDAC抑制剂，IC50分别为0.78、1.0、1.2μM。该化合物通过诱导自噬（Autophagy）来抑制微胶质细胞的激活，进而抑制一氧化氮产生，显示出抗炎和抗抑郁的效果。此外，HDAC-IN-62还能抑制实验小鼠大脑中的微胶质细胞活化。
T79619	Anti-inflammatory agent 54
	Anti-inflammatory agent 54 (compound 9c)，作为薏苡醇 (Coixol) 的衍生物，显示出显著的抗炎效果。它通过抑制NF-κB通路，降低iNOS、TNF-α、IL-6和IL-1β的表达，进而在LPS诱导的RAW264.7巨噬细胞中降低一氧化氮 (NO) 生成（IC50: 2.4 μM）。此外，该化合物在小鼠耳廓水肿模型中表现出了体内抗炎活性。
T71212	Lornoxicam-d4
	Lornoxicam-d4 is intended for use as an internal standard for the quantification of lornoxicam by GC- or LC-MS. Lornoxicam is a COX inhibitor and non-steroidal anti-inflammatory drug (NSAID) with anti-inflammatory and analgesic properties. It inhibits production of thromboxane B2 from arachidonic acid in HEL human erythroleukemic cells, which endogenously express COX-1, as well as inhibits LPS-induced formation of prostaglandin F1α from arachidonic acid in Mono-Mac-6 cells, which endogenously e...
T79620	Anti-inflammatory agent 55
	Anti-inflammatory agent 55 (compound 9j) 作为薏苡醇 (Coixol) 的衍生物，展现出显著的抗炎活性。该化合物通过抑制NF-κB途径，有效下调iNOS、TNF-α、IL-6及IL-1β的表达水平。其中，Anti-inflammatory agent 54 能够在RAW264.7巨噬细胞中通过抑制LPS诱导的NO产生（IC50: 0.8 μM）来发挥其抗炎作用，并在小鼠耳廓水肿模型中证实了其体内抗炎效果。
T62317	α7 nAchR-JAK2-STAT3 agonist 1
	α7 nAchR-JAK2-STAT3 agonist 1 是一种 α7 nAchR-JAK2-STAT3 通路的有效抑制剂，能够作用于一氧化氮 (NO) (IC50: 0.32 μM)。α7 nAchR-JAK2-STAT3 agonist 1 在小鼠巨噬细胞 RAW264.7 中对 iNOS、IL-1β 和 IL-6 的表达具有有效的抑制作用。α7 nAchR-JAK2-STAT3 agonist 1 对 LPS 诱导的 NO 释放、NF-κB 激活和细胞因子产生具有抑制作用。α7 nAchR-JAK2-STAT3 agonist 1 能够用于研究败血症。
T83895	NCI 126224 NSC 126224
	NCI 126224 是一种 toll-like receptor 4 (TLR4) 的拮抗剂。它在 RAW 264.7 巨噬细胞中，选择性抑制由 TLR4 激动剂 LPS 引起的一氧化氮 (NO) 产生（IC50 = 0.31 µM），而对 TLR7/8 激动剂 R-848、TLR1/2 激动剂 Pam3CSK4 以及 TLR3 激动剂 poly(I:C) 的影响较小；但对于相同细胞中由 TLR2/6 激动剂 FSL-1 引起的 NO 产生，其抑制作用在 0.6 µM 时亦显现。此外，NCI 126224 在 BV-2 微胶质细胞的报告实验中抑制了 LPS 引起的 NF-κB 活性，并在 RAW 264.7 巨噬细胞中降低了 LPS 引起的 IL-1β 和 TNF-α 水平（IC50s = 5.92, 0.42, 和 1.54 µM，分别）。
T83768	Zofenoprilat Zofenopril-SH,SQ 26,333
	Zofenoprilat是一种血管紧张素转换酶(ACE; IC50 = 8 nM for the rabbit lung enzyme)的抑制剂，同时也是前体药zofenopril的活性代谢产物。它能够抑制分离的豚鼠小肠中由血管紧张素I或缓激肽诱导的收缩(EC50s = 3 and 1 nM, respectively)。在人类脐静脉内皮细胞(HUVECs)中，Zofenoprilat (10 nM)降低基础内皮素-1分泌和一氧化氮(NO)生成，并阻止TNF-α诱导的活性氧种(ROS)增加以及谷胱甘肽(GSH)水平降低。Zofenoprilat (10 µM)保护初级人类心脏微血管内皮细胞免受多柔比星诱导的细胞毒性。此外，Zofenoprilat (10 µM)还能增加HUVECs中的硫化氢(H2S)生成，以及细胞的黏着、迁移和增殖。在以400 µM浓度使用时，它可以减少Langendorff分离的大鼠心脏灌流缺血再灌注损伤模型中的舒张末压和乳酸脱氢酶(LDH)释放。
T36176	AMK (hydrochloride)
	AMK is an active metabolite of the neurohormone melatonin .1,2,3,4It is formed from melatoninviathe metabolic intermediate AFMK that is then deformylated by catalase or formamidase.5,6AMK scavenges singlet oxygenin vitrowhen used at a concentration of 200 μM.1It inhibits the epinephrine- and arachidonic acid-induced production of prostaglandin E2and PGD2in ovine seminal vesicle microsomes in a concentration- and time-dependent manner, as well as LPS-induced increases in COX-2 levels in RAW 264.7...

化合物

Nitric oxide production-IN-1

Cat.No: T79981

Target: NO Synthase

Cat.No: T61157

Anti-inflammatory agent 63

Cat.No: T83049

Aminoguanidine hemisulfate

Cat.No: T78229

Target: Reactive Oxygen Species

Anti-inflammatory agent 60

Cat.No: T83052

Target: NF-κB

Akt/NF-κB/JNK-IN-1

Cat.No: T62078

Cat.No: T61821

1,2-Diaminoanthraquinone

Cat.No: T78439

Antitumor agent-49

Cat.No: T83002

Cat.No: T35864

Anti-inflammatory agent 45

Cat.No: T79478

Target: Apoptosis

Cat.No: T79304

Synonym: CPSI-2364,CNI-1493 free base

Keap1-Nrf2-IN-11

Cat.No: T72687

Cat.No: T75763

Cat.No: T79637

Cat.No: T79371

Target: Autophagy

Anti-inflammatory agent 54

Cat.No: T79619

Cat.No: T71212

Anti-inflammatory agent 55

Cat.No: T79620

α7 nAchR-JAK2-STAT3 agonist 1

Cat.No: T62317

Cat.No: T83895

Synonym: NSC 126224

Cat.No: T83768

Synonym: Zofenopril-SH,SQ 26,333

AMK (hydrochloride)

Cat.No: T36176

Cat. No.	Product Name	Target	Signaling Pathways
TN6985	Anhydronotoptol 4-{[(2E,5E)-3,7-dimethylocta-2,5,7-trien-1-yl]oxy}-7H-furo[3,2-g]chromen-7-one	NO Synthase	Immunology/Inflammation
	Anhydronotoptol (4-{[(2E,5E)-3,7-dimethylocta-2,5,7-trien-1-yl]oxy}-7H-furo[3,2-g]chromen-7-one) 是一种可从伞科植物羌活中提取得到的天然化合物。Anhydronotoptol 是一种有效的一氧化氮生成抑制剂，抑制 LPS 诱导的 RAW 264.7 细胞 NO 生成，其 IC50 值为 36.6 μM。
T5S2283	Sesamolin	p38 MAPK; Caspase; JNK	Apoptosis; MAPK; Proteases/Proteasome
	Sesaminol 是从Justicia orbiculata 中分离得到的一种天然产物，抑制脂质过氧化，具有神经保护作用和抗氧化活性。它通过抑制JNK、p38 MAPKs 和caspase-3磷酸化，抑制MAPK 的级联反应。
T6S1665	Irisflorentin	Others; NO Synthase	Immunology/Inflammation; Others
	Irisflorentin 是天然存在的异黄酮，是大量存在于 Rhizoma Belamcandae 中的活性成分。它明显抑制了诱导型一氧化氮合酶的转录和翻译以及 NO 产生。
T3S2259	Methyl eugenol 4-allylveratrole,eugenyl methyl ether,O-methyleugenol,Eugenol Methyl ether,丁香酚甲醚,丁子香酚甲醚	GABA Receptor	Membrane transporter/Ion channel; Neuroscience
	Methyl eugenol (4-allylveratrole) 是一种苯丙类化合物，存在于植物叶子、果实、根茎中，当植物相应的部位因食草动物进食而受损时，就会释放。它可用于消灭雄性东方果蝇。
T6S1487	Ginsenoside Rg5 人参皂苷Rg5,人参皂甙 Rg5	NF-κB; COX; IGF-1R	Immunology/Inflammation; Neuroscience; NF-κB; Tyrosine Kinase/Adaptors
	Ginsenoside Rg5 是红参的主要成分，可阻断IGF-1与其受体的结合，IC50约为90 nM。它还通过抑制NF-κB p65的 DNA 结合活性来抑制COX-2的 mRNA 表达。它可促进血管生成和改善高血压，具有抗炎和治疗阿尔茨海默病的潜力。
TN4182	Hannokinol	Others	Others
	(+)-Hannokinol and MESO-hannokinol can significantly inhibit lipopolysaccharide-induced nitric oxide production in BV2 microglial cells at concentrations ranging from 1 microM to 100 microM.
T81684	Neuroinflammatory-IN-1
	Neuroinflammatory-IN-1 (Compound 5)，作为一种抗神经炎剂，对NO生成表现出显著的抑制效果，其IC50为65.4 μM。
T79955	Schiarisanrin A Kadsulignan J	NO Synthase	Immunology/Inflammation
	Schiarisanrin A (Kadsulignan J) 作为一种木脂素，具有对 BV-2 细胞中 NO 产生的抑制活性，其IC50值为 9.6 μM。
T81408	Preleoheterin
	Preleoheterin（化合物3）为一类从L. japonicus分离得到的拉丹烷二萜。
T83553	(4S)-10-Nor-calamenen-10-one
	(4S)-10-Nor-calamenen-10-one（Compound 15）促进小胶质细胞通过LPS刺激产生的NO增强。该化合物为桉树倍半萜烯类，可从Alpinia oxyphylla中提取。
TMA1012	Ganoderiol F	Androgen Receptor; HIV Protease; Autophagy	Autophagy; Endocrinology/Hormones; Microbiology/Virology; Proteases/Proteasome
	Ganoderiol F has anti-inflammatory, cytotoxic and anti-HIV activity, it inhibits activity of topoisomerases in vitro, and it inhibits human immunodeficiency virus-1 protease with IC(50) values of 20-40 microM. It induced HO-1 expression, activation of the mitogen-activated protein kinase EKR and up-regulation of cyclin-dependent kinase inhibitor p16 and suppressed lipopolysaccharide (LPS)-induced nitric oxide (NO) production.
T79954	Kadsulignan H	NO Synthase	Immunology/Inflammation
	Kadsulignan H (compound 13)，作为一种木脂素类化合物，展现了对 NO 产生的显著抑制作用。在 BV-2 细胞中，该化合物通过 IC50 值为 14.1 μM 来表征其对 NO 生成的抑制活性。
T81987	Kanzonol D
	Kanzonol D为一种存在于Glycyrrhiza glabra的毛状根培养物中的类黄酮化合物。
T79930	Sanggenon A Sanggenone A	NF-κB	NF-κB
	Sanggenon A通过调控BV2和RAW264.7细胞中的NF-κB及HO-1/Nrf2信号途径，展现了抗炎效果。该化合物明显抑制了由脂多糖(LPS)引起的一氧化氮产生。
T81853	Marstenacisside F1
	Marstenacisside F1（化合物1）为从通关藤(Marsdenia tenacissima)分离的抗炎聚氧孕烷苷，能抑制脂多糖激活的RAW 264.7细胞产生一氧化氮(NO)，属Tenacigenin B衍生物。
T80713	α-Glucosidase-IN-37
	α-Glucosidase-IN-37（Compound 11）展示出中等水平的抑制作用，能够抑制LPS诱导的NO产生，并在巨噬细胞中表现出23.7 μM的IC50值。该化合物对α-Glucosidase的抑制活性相对较弱。
TN5011	Shizukaol B	ERK; IL Receptor; p38 MAPK; TNF; NOS; NF-κB; COX; HIV Protease; DNA/RNA Synthesis; Prostaglandin Receptor; JNK	Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; GPCR/G Protein; Immunology/Inflammation; MAPK; Microbiology/Virology; Neuroscience; NF-κB; Proteases/Proteasome
	Shizukaol B exerts anti-inflammatory effects in LPS-activated microglia partly by modulating JNK-AP-1 signaling pathway; it also shows significant anti-neuroinflammatory effects by inhibiting nitric-oxide (NO) production in lipopolysaccharide (LPS)-stimul
T38250	L-Sepiapterin
	L-Sepiapterin, also known as Sepiapterin, is a precursor compound crucial for the production of tetrahydrobiopterin (BH4), which serves as a coenzyme for endothelial nitric oxide synthase (eNOS). This compound demonstrates its efficacy by improving endothelial dysfunction in small mesenteric arteries from db/db mice and promoting angiogenesis. Moreover, L-Sepiapterin exerts inhibitory effects on cellular proliferation and migration in ovarian cancer cells through the down-regulation of p70S6K-de...
T36417	Nargenicin Antibiotic 47444
	Nargenicin is a macrolide antibiotic that selectively inhibits the growth of S. aureus, methicilin resistant S. aureus (MRSA), and M. luteus (MICs = 0.6, 0.3, and 2.5 μg/ml, respectively) over a panel of 11 Gram-positive and Gram-negative bacteria (MICs = >80 μg/ml). [1] It dose-dependently inhibits S. aureus DnaE in the presence of DNase I-activated DNA and E. coli DnaE when used at concentrations of 0.00001-0.1 and 0.01-100 μg/mL, respectively. [2] In murine BV-2 microglial cells, nargenicin (...
T37272	9(S),12(S),13(S)-TriHOME
	9(S),12(S),13(S)-TriHOME is a linoleic acid-derived oxylipin that has diverse biological activities.1,2,3,4It has been found in various plants and is produced in human eosinophils in a 15-lipoxygenase-dependent, soluble epoxide hydrolase-independent manner.1,59(S),12(S)13(S)-TriHOME inhibits antigen-induced β-hexosaminidase release from RBL-2H3 mast cells (IC50= 28.7 μg/ml).2It inhibits LPS-induced nitric oxide (NO) production in BV-2 microglia (IC50= 40.95 μM).3In vivo, 9(S),12(S),13(S)-TriHOME...
T38330	Collinin
	Collinin is a coumarin that has been found in Z. schinifolium and has diverse biological activities.1,2,3,4 It is active against drug-susceptible and -resistant strains of M. tuberculosis (MIC50s = 3.13-6.25 μg/ml).1 Collinin inhibits LPS-induced nitric oxide (NO) production (IC50 = 5.9 μM) and reduces COX-2 protein levels in RAW 264.7 cells.2 It completely inhibits aggregation of isolated rabbit platelets induced by arachidonic acid , collagen, or platelet activating factor (PAF) when used at a...

天然产物

Anhydronotoptol

Cat.No: TN6985

Synonym: 4-{[(2E,5E)-3,7-dimethylocta-2,5,7-trien-1-yl]oxy}-7H-furo[3,2-g]chromen-7-one

Target: NO Synthase

Cat.No: T5S2283

Target: p38 MAPK, Caspase, JNK

Cat.No: T6S1665

Target: Others, NO Synthase

Cat.No: T3S2259

Synonym: 4-allylveratrole,eugenyl methyl ether,O-methyleugenol,Eugenol Methyl ether,丁香酚甲醚,丁子香酚甲醚

Target: GABA Receptor

Ginsenoside Rg5

Cat.No: T6S1487

Synonym: 人参皂苷Rg5,人参皂甙 Rg5

Target: NF-κB, COX, IGF-1R

Cat.No: TN4182

Target: Others

Neuroinflammatory-IN-1

Cat.No: T81684

Schiarisanrin A

Cat.No: T79955

Synonym: Kadsulignan J

Target: NO Synthase

Cat.No: T81408

(4S)-10-Nor-calamenen-10-one

Cat.No: T83553

Cat.No: TMA1012

Target: Androgen Receptor, HIV Protease, Autophagy

Cat.No: T79954

Target: NO Synthase

Cat.No: T81987

Cat.No: T79930

Synonym: Sanggenone A

Target: NF-κB

Marstenacisside F1

Cat.No: T81853

α-Glucosidase-IN-37

Cat.No: T80713

Cat.No: TN5011

Target: ERK, IL Receptor, p38 MAPK, TNF, NOS, NF-κB, COX, HIV Protease, DNA/RNA Synthesis, Prostaglandin Receptor, JNK

Cat.No: T38250

Cat.No: T36417

Synonym: Antibiotic 47444

9(S),12(S),13(S)-TriHOME

Cat.No: T37272

Cat.No: T38330

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