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Search Results for " prostaglandin synthetase "

抑制剂 & 化合物

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Cat. No.	Product Name	Target	Signaling Pathways
T8356	FPL 62064	Lipoxygenase; COX	Immunology/Inflammation; Metabolism; Neuroscience
	FPL 62064 是 5-脂氧合酶和COX 双重抑制剂，具有抗炎活性，对 RBL-1 胞质 5-脂氧合酶和前列腺素合成酶 (环氧化酶) 的IC50值分别为 3.5 和 3.1 μM。
T0005	Aspirin 阿司匹林,Acetylsalicylate,Acetylsalicylic Acid,邻乙酰水杨酸,ASA	Mitophagy; Virus Protease; COX; Autophagy	Autophagy; Immunology/Inflammation; Microbiology/Virology; Neuroscience
	Aspirin (Acetylsalicylic Acid) 是一种选择性 COX 抑制剂，具有多种药理活性。它是组蛋白去乙酰化酶抑制剂，可上调细胞周期阻滞蛋白 p21，抑制携带 COX-1 的卵巢 Y 细胞。它还抑制 HUVEC 和新生大鼠心室心肌细胞中 COX-2 的表达，分别减少 PG 的产生和 ERK 和 NF-KB 的下调。
T10098	PGS-IN-1 KME-4	Lipoxygenase; Prostaglandin Receptor	GPCR/G Protein; Immunology/Inflammation; Metabolism
	PGS-IN-1 (KME-4)是一种前列腺素合成酶抑制剂，IC50=0.28 μM。它也可抑制5-脂肪氧合酶的活性，IC50=1.05 μM。
T0264	Zomepirac sodium salt Zomepirac Sodium,佐美酸钠,McN-2783-21-98	PGE Synthase; PDE	Immunology/Inflammation; Metabolism
	Zomepirac sodium salt (McN-2783-21-98) 是前列腺素合成酶抑制剂。它是一种非甾体抗炎药，但能够导致免疫介导的肝损伤。
T69424	Zomepirac free acid
	Zomepirac is a prostaglandin synthetase inhibitor. Zomepirac is an orally effective nonsteroidal anti-inflammatory drug (NSAID) that has antipyretic actions.
T69458	Pirprofen
	Pirprofen is an anti-inflammatory agent used in therapy of rheumatoid arthritis and a prostaglandin synthetase inhibitor.
T60431	Clopirac
	Clopirac 是有效的、口服活性的前列腺素合成酶 (prostaglandin synthetase) 抑制剂，是一种抗炎剂。
T61261	Isofezolac
	Isofezolac (LM 22070) is a non-steroidal anti-inflammatory drug (NSAID) known for its potent inhibition of prostaglandin-synthetase. This compound exhibits notable anti-inflammatory and antipyretic properties [1] [2].
T38327	Cryogenine
	Cryogenine is an alkaloid originally isolated from H. salicifolia that has anti-inflammatory activity.1 It inhibits prostaglandin synthetase (IC50 = 424 μM). Cryogenine (100 mg/kg per day, p.o.) reduces paw edema and the mean arthritic index in a rat model of adjuvant-induced polyarthritis.2 \|1. Lema, W.J., Blankenship, J.W., and Malone, M.H. Prostaglandin synthetase inhibition by alkaloids of Heimia salicifolia. J. Ethnopharmacol. 15(2), 161-167 (1986).\|2. Kosersky, D.S., Brown, J.K., and Malon...
T22581	Arachidonic Acid Leelamide	Others	Others
	Arachidonic acid leelamide is a phospholipase A2 inhibitor. Phospholipase A is a hydrolase responsible for the release of arachidonic acid from the sn2 position of phospholipids. The released arachidonic acid is then converted to mediators of inflammation

化合物

FPL 62064

Cat.No: T8356

Synonym:

Target: Lipoxygenase, COX

Aspirin

Cat.No: T0005

Synonym: 阿司匹林,Acetylsalicylate,Acetylsalicylic Acid,邻乙酰水杨酸,ASA

Target: Mitophagy, Virus Protease, COX, Autophagy

PGS-IN-1

Cat.No: T10098

Synonym: KME-4

Target: Lipoxygenase, Prostaglandin Receptor

Zomepirac sodium salt

Cat.No: T0264

Synonym: Zomepirac Sodium,佐美酸钠,McN-2783-21-98

Target: PGE Synthase, PDE

Arachidonic Acid Leelamide

Cat.No: T22581

Synonym:

Target: Others

Cat. No.	Product Name	Target	Signaling Pathways
TN1378	α-Viniferin ALPHA-VINIFERIN,Alpha-葡萄素	P450; NO Synthase; Prostaglandin Receptor	GPCR/G Protein; Immunology/Inflammation; Metabolism
	α-Viniferin 也称为2-芳基苯并呋喃类黄酮，是前列腺素H2合成酶抑制剂。具有抗阿尔茨海默病、抗结核、抗肿瘤、抗炎、抗糖尿病等多种药理活性

天然产物

α-Viniferin

Cat.No: TN1378

Synonym: ALPHA-VINIFERIN,Alpha-葡萄素

Target: P450, NO Synthase, Prostaglandin Receptor

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