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Search Results for " indomethacin "

20

抑制剂 & 化合物

3

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T0458	Indomethacin Indocin,Indometacine,吲哚美辛,Indomethacine,Indometacin	Phospholipase; COX; PDE; Autophagy	Autophagy; Immunology/Inflammation; Metabolism; Neuroscience
	Indomethacin (Indometacin) 是一种可透过血脑屏障的，非选择性的COX1和COX2抑制剂，在 CHO 细胞中，对人 COX-1 和 COX-2 的IC50值分别为 18 nM 和 26 nM。它通过干扰溶酶体的正常功能来破坏自噬流，是一种非甾体抗炎药。
T22092	Indomethacin heptyl ester	COX	Immunology/Inflammation; Neuroscience
	Indomethacin heptyl ester 是 COX-1 和 COX-2 的非选择性抑制剂。
T7882	Indomethacin farnesil 吲哚美辛法呢酯,Infree	Others; COX; Autophagy	Autophagy; Immunology/Inflammation; Neuroscience; Others
	Indomethacin farnesil (Infree) 是具有口服活性的 Indomethacin 前药，可通过干扰溶酶体的正常功能来破坏自噬流，有抗炎和抗风湿作用。它是一种可透过血脑屏障的，非选择性的 COX1和 COX2抑制剂，在 CHO 细胞中，对人 COX-1 和 COX-2 的IC50值分别为 18 nM 和 26 nM。
T22346	Indomethacin sodium hydrate Indometacin sodium hydrate	COX	Immunology/Inflammation; Neuroscience
	Indomethacin sodium hydrate (Indometacin sodium hydrate) 是一种口服活性、竞争性和可逆性的 COX1/2 抑制剂，具有潜在的抗炎活性，可诱发的偏头痛，诱导的胃肠道损伤，可用于研究成人继发于严重创伤性脑损伤的颅内压增高和类风湿性关节。
T36538	NO-Indomethacin
	NO-indomethacin is a hybrid molecule of indomethacin and a nitric oxide (NO) donor. This drug design combines the anti-inflammatory properties of a non-steroidal anti-inflammatory drug (NSAID) with the gastrointestinal protective effects of NO. Compounds of this class retain their anti-inflammatory and analgesic activity, but have reduced gastrointestinal and kidney toxicity compared to the NSAID alone. NO-indomethacin also enhances the cancer chemopreventative activity of indomethacin. NO-indom...
T37210	5-hydroxy Indomethacin
	5-hydroxy Indomethacin is a metabolite of indomethacin .1It is formed from indomethacin in rabbit hepatic microsomes. 1.Evans, M.A., Papazafiratou, C., Bhat, R., et al.Indomethacin metabolism in isolated neonatal and fetal rabbit hepatocytesPediatr. Res.15(11)1406-1410(1981)
T68926	Indomethacin salicylate
	Indomethacin salicylate is an antiinflammatory drug. It has shown remarkable inhibitory effects on carrageenin edema, ultraviolet erythema and adjuvant arthritis.
T11655	Indomethacin-D4 Indometacin-D4,吲哚美辛-D4	CDK	Cell Cycle/Checkpoint
	Indomethacin-D4 is a deuterium labeled Indomethacin. Indomethacin is a potent and nonselective inhibitor of COX1 and COX2, with IC50s of 18 nM and 26 nM for human COX-1 and COX-2, respectively, in CHO cells.
T36418	O-Desmethyl-N-deschlorobenzoyl Indomethacin
	O-Desmethyl-N-deschlorobenzoyl indomethacin is a metabolite of the non-steroidal anti-inflammatory drug (NSAID) and COX inhibitor indomethacin .1It is formed from indomethacin in isolated rabbit hepatocytes. O-Desmethyl-N-deschlorobenzoyl indomethacin (600 μM) decreases the viability of HL-60 leukemia cells when cultured with glucose oxidase.2It has also been used in the synthesis of prostaglandin D2receptor antagonists.3 1.Evans, M.A., Papazafiratou, C., Bhat, R., et al.Indomethacin metabolism ...
T6417	BML-190 2-[1-(4-氯苯甲酰基)-5-甲氧基-2-甲基-1H-吲哚-3-基]-1-(4-吗啉基)乙酮,Indomethacin morpholinylamide,吲哚美辛吗啉代酰胺,IMMA,BML 190	Cannabinoid Receptor	GPCR/G Protein
	BML-190 (Indomethacin morpholinylamide) 是一种 CB2 受体的配体，其对 CB2 受体 (Ki:435 nM) 和 CB1受体 (Ki> 2 μM)。
T61606	Indomethacin sodium
	Indomethacin sodium, a powerful and orally active inhibitor of COX1/2, exhibits IC50 values of 18 nM and 26 nM for COX-1 and COX-2, respectively. Apart from its potent anti-inflammatory effects, this compound possesses notable anticancer and anti-infective activities. Since it has such versatile attributes, it finds useful applicability in cancer, inflammation, and viral infection research [1] [2] [3].
T10355	Apyramide	COX	Immunology/Inflammation; Neuroscience
	Apyramide 是一种抗炎试剂 (NSAID)，是吲哚美辛的前药。Indomethacin 是一种强效的、血脑通透的、非选择性的 COX1 和 COX2 抑制剂。
T1467	Acemetacin 阿西美辛,K-708,TVX 1322	COX	Immunology/Inflammation; Neuroscience
	Acemetacin (TVX 1322) 是一种非甾体抗炎类的化合物。
T4313	Tinoridine hydrochloride 盐酸替诺立定,Nonflamin,Y-3642 hydrochloride	COX; Glutathione Peroxidase	Immunology/Inflammation; Metabolism; Neuroscience
	Tinoridine hydrochloride (Y-3642 hydrochloride) 是非甾体抗炎药，具有显著的自由基清除和抗过氧化物特性。
T70000	Ebopiprant HCl
	Ebopiprant, also known as OBE-022, is an Oral and Selective Prostaglandin F 2α Receptor Antagonist as an Effective and Safe Modality for the Treatment of Preterm Labor. OBE022 exhibits potent tocolytic effects on human tissues ex vivo and animal models in vivo without causing the adverse fetal side effects seen with indomethacin.
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.
T36214	16,16-dimethyl Prostaglandin E1 16,16-dimethyl Prostaglandin E1
	16,16-dimethyl Prostaglandin E1 是 PGE1 (T1626) 类似物，可诱导支气管收缩和血管平滑肌收缩，并抑制吲哚美辛诱导的细胞伸长。
T61674	COX-2/5-LOX-IN-1
	COX-2/5-LOX-IN-1 (compound 3a), a benzothiophen-2-yl pyrazole carboxylic acid derivative, is a potent and dual inhibitor of COX-2 / 5-LOX. It exhibits superior analgesic and anti-inflammatory properties compared to Celecoxib and Indomethacin. COX-2/5-LOX-IN-1 displays strong inhibitory activity against COX-1, COX-2, and 5-LOX, with IC50 values of 12.13 μM, 0.4 μM, and 4.96 μM, respectively [1].
T23676	AHR-10037
	AHR-10037是一种非甾体抗炎药，具有镇痛和解热特性以及高治疗指数，低胃毒性，它在抑制急性（伊文思蓝卡拉胶胸腔积液）和慢性（佐剂诱导的关节炎）炎症方面与吲哚美辛相当。研究表明，它在体内转化为环氧合酶抑制剂的前药。
T61910	COX-2/5-LOX-IN-2
	COX-2/5-LOX-IN-2 是苯并噻吩-2-基吡唑羧酸衍生物。COX-2/5-LOX-IN-2 (5b) 对COX-2和5-LOX 均有抑制作用。COX-2/5-LOX-IN-2 抑制 COX-1、COX-2 和 5-LOX 的IC50s 分别为 5.40、0.01 和 1.78 μM。COX-2/5-LOX-IN-2 显示出超过塞来昔布和吲哚美辛的镇痛和抗炎活性。

化合物

Cat.No: T0458

Synonym: Indocin,Indometacine,吲哚美辛,Indomethacine,Indometacin

Target: Phospholipase, COX, PDE, Autophagy

Indomethacin heptyl ester

Cat.No: T22092

Target: COX

Indomethacin farnesil

Cat.No: T7882

Synonym: 吲哚美辛法呢酯,Infree

Target: Others, COX, Autophagy

Indomethacin sodium hydrate

Cat.No: T22346

Synonym: Indometacin sodium hydrate

Target: COX

NO-Indomethacin

Cat.No: T36538

5-hydroxy Indomethacin

Cat.No: T37210

Indomethacin salicylate

Cat.No: T68926

Indomethacin-D4

Cat.No: T11655

Synonym: Indometacin-D4,吲哚美辛-D4

Target: CDK

O-Desmethyl-N-deschlorobenzoyl Indomethacin

Cat.No: T36418

Cat.No: T6417

Synonym: 2-[1-(4-氯苯甲酰基)-5-甲氧基-2-甲基-1H-吲哚-3-基]-1-(4-吗啉基)乙酮,Indomethacin morpholinylamide,吲哚美辛吗啉代酰胺,IMMA,BML 190

Target: Cannabinoid Receptor

Indomethacin sodium

Cat.No: T61606

Cat.No: T10355

Target: COX

Cat.No: T1467

Synonym: 阿西美辛,K-708,TVX 1322

Target: COX

Tinoridine hydrochloride

Cat.No: T4313

Synonym: 盐酸替诺立定,Nonflamin,Y-3642 hydrochloride

Target: COX, Glutathione Peroxidase

Cat.No: T70000

Cat.No: T33417

Synonym: MK-410,MK410

16,16-dimethyl Prostaglandin E1

Cat.No: T36214

Synonym: 16,16-dimethyl Prostaglandin E1

COX-2/5-LOX-IN-1

Cat.No: T61674

Cat.No: T23676

COX-2/5-LOX-IN-2

Cat.No: T61910

Cat. No.	Product Name	Target	Signaling Pathways
TN4223	Homopterocarpin	Antifection	Microbiology/Virology
	Homopterocarpin and Pterocarpus extract offer gastroprotection against indomethacin- induced ulcer by antioxidative mechanism and the modulation of gastric homeostasis, homopterocarpin may be responsible for, or contribute to the antiulcerogenic property
TN4322	Isopulegol	ATPase; Potassium Channel; GABA Receptor	Membrane transporter/Ion channel; Neuroscience
	Isopulegol presents depressant- and anxiolytic-like effects, it also has anticonvulsant and bioprotective effects against PTZ-induced convulsions are possibly related to positive modulation of benzodiazepine-sensitive GABAA receptors and to antioxidant properties.Isopulegol presents significant gastroprotective effects in both ethanol- and indomethacin-induced ulcer models, which appear to be mediated, at least in part, by endogenous prostaglandins, K(ATP) channel opening, and antioxidant proper...
TN1606	(-)-Epiafzelechin (-)-表阿夫儿茶精,表阿夫儿茶精	COX	Immunology/Inflammation; Neuroscience
	(-)-Epiafzelechin exhibits significant anti-inflammatory activity on carrageenin-induced mouse paw edema, it exhibits a dose-dependent inhibition on the COX activity with an IC50 value of 15 microM, it exhibits about 3-fold weaker inhibitory potency on th

天然产物

Homopterocarpin

Cat.No: TN4223

Target: Antifection

Cat.No: TN4322

Target: ATPase, Potassium Channel, GABA Receptor

(-)-Epiafzelechin

Cat.No: TN1606

Synonym: (-)-表阿夫儿茶精,表阿夫儿茶精

Target: COX

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