68
24
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T5102 |
TGN-020
TGN020 |
Aquaporin; PROTAC Linker | Membrane transporter/Ion channel; PROTAC |
TGN-020 是一种属于 alkyl chain 类的 PROTAC linker,可用于 PROTAC 的合成分子。TGN020 是一种选择性水通道蛋白 4 (AQP4) 抑制剂,IC50为 3.1 μM。TGN020 减轻大鼠脊髓压迫损伤后的水肿并抑制神经胶质瘢痕的形成。 | |||
T6581 |
Methyclothiazide
Duretic,Enduron,甲氯噻嗪,Aquatensen |
Others; Carbonic Anhydrase | Metabolism; Others |
Methyclothiazide (Aquatensen) 是一种具有口服活性的利尿剂,也是一种降压剂。它能够拮抗体外的电压依赖性钙通道的 (VDCC) 活性,也可以抑制内源性血管收缩刺激导致的血管反应。 | |||
T4074 |
GSK-872
GSK872,GSK'872,GSK2399872A |
RIP kinase | Apoptosis; NF-κB |
GSK-872 (GSK2399872A) 是一种有效且特异性的 RIP3 激酶抑制剂,降低 RIPK3 介导的坏死和随后的 HMGB1 的细胞质易位和表达,可改善早期脑损伤中的脑水肿和神经功能缺损。它以高亲和力结合 RIP3 激酶结构域,IC50为1.8 nM,并抑制激酶活性,IC50为1.3 nM。 | |||
T14968 |
Cinanserin hydrochloride
SQ 10643 |
Influenza Virus; 5-HT Receptor | GPCR/G Protein; Microbiology/Virology; Neuroscience |
Cinanserin hydrochloride (SQ 10643) 是一种高亲和力拮抗剂,对 5-HT2 受体的Ki 值为 41 nM。它也是严重急性呼吸综合征冠状病毒的 3C 样蛋白酶抑制剂。 | |||
T23333 |
SC-58125
SC 58125,1-[(4-甲基磺酰基)苯基]-3-三氟甲基-5-(4-氟苯基)吡唑 |
COX | Immunology/Inflammation; Neuroscience |
SC-58125 是一种选择性的环氧合酶2 (COX-2)的抑制剂,IC50值为 0.04 μM。它在体内外均表现出抗肿瘤活性,还可抑制炎症部位的水肿并具有缓解疼痛作用。 | |||
T21412 |
Ketorolac
Toradol,Sprix,Acuvail,Macril,酮咯酸,Acular |
COX | Immunology/Inflammation; Neuroscience |
Ketorolac (Acuvail) 是非甾体抗炎剂,是非选择性的COX 抑制剂,对 COX-1 和 COX-2 的IC50值分别为 20 和 120 nM。 | |||
T34485 |
Safotibant
LF220542,LF 220542,LF 22-0542,LF-220542,LF-22-0542,LF22-0542 |
Bradykinin Receptor | GPCR/G Protein |
Safotibant (LF-22-0542) 是一种缓激肽 B1 受体拮抗剂,具有抗炎和镇痛活性,可用于局部治疗糖尿病性黄斑水肿。 | |||
T19286 |
Dixyrazine
UCB 3412 |
Others | Others |
Dixyrazine(UCB 3412) 具有短暂的降压作用,可预防注射硫酸鱼精蛋白引起的脑水肿,可用于研究与神经系统相关的疾病。 | |||
T16950 |
Sudoxicam
舒多昔康,4-Hydroxy-2-methyl-N-2-thiazolyl-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxide |
COX | Immunology/Inflammation; Neuroscience |
Sudoxicam (4-Hydroxy-2-methyl-N-2-thiazolyl-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxide) 是一种可逆的 COX 拮抗剂,具有抗炎、抗水肿和解热特性。 | |||
T8807 |
Benzydamine
|
Others | Others |
Benzydamine 是一种苄基吲唑,具有镇痛、解热和抗炎作用。 Benzydamine 用于减少手术后和创伤后的疼痛和水肿,并促进愈合。 | |||
T60351 |
Acetazolamide sodium
OT-302 sodium |
Carbonic Anhydrase | Metabolism |
Acetazolamide sodium (OT-302 sodium) 是一种高效的碳酸酐酶 (CA)IX抑制剂,具有利尿、抗淋球菌和降压活性,可用于癫痫、青光眼、水肿和高原反应等适应症。 | |||
T36619 |
Aligeron
|
Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation |
Aligeron 是一种非选择性的prostaglandin (PG)拮抗剂,对PGF2α和PGE2诱导的猫血压下降有抑制作用,可用于抑制PGF2α诱导的小鼠腹泻和PGE2诱导的大鼠爪水肿。Aligeron 对血管并发症具有抗氧化保护作用。 | |||
T12721 |
Rho-Kinase-IN-1
|
ROCK | Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells |
Rho-Kinase-IN-1 是一种 ROCK 抑制剂,对 ROCK1 和 ROCK2 的 Kis 分别为 30.5 nM 和 3.9 nM。 Rho-Kinase-IN-1 可用于细胞过度增殖、重塑、水肿和炎症疾病的研究。 | |||
T36534 |
SDZ 224-015
SDZ 224015 |
IL Receptor; Caspase | Apoptosis; Immunology/Inflammation; Proteases/Proteasome |
SDZ 224-015 是白细胞介素-1β(IL-1β)转化酶和 Caspase-1 的口服活性抑制剂。SDZ 224-015 具有抗 COVID-19 和抗炎活性,可减少角叉菜胶诱导的大鼠爪子水肿。 | |||
T0477 |
Zileuton
Abbott 64077,齐留通,A 64077 |
Ferroptosis; Lipoxygenase; COX | Apoptosis; Immunology/Inflammation; Metabolism; Neuroscience |
Zileuton (A 64077) 是羟基脲的合成衍生物,是一种选择性的5-脂氧合酶抑制剂,具有平喘特性。 | |||
TP1168 |
N-Formyl-Met-Leu-Phe-Lys
fMLFK |
Others | Others |
N-Formyl-Met-Leu-Phe-Lys (fMLFK) 是一种多肽,是选择性FPR1激动剂,作用于 FPR1(IC50:3.5 nM),FPR2(IC50:6.7 nM) 和 FPR2-D2817.32G(IC50:0.88 nM) 。 | |||
T35336 |
Furosemide sodium
Frusemide Sodium,Lasix |
Na-K-Cl cotransporter | Membrane transporter/Ion channel |
Furosemide sodium (Frusemide Sodium) 是 Na+/K+/2Cl- (NKCC),NKCC1 和 NKCC2 共转运蛋白的有效的和具有口服活性抑制剂。Furosemide sodium 也是 GABAA 受体拮抗剂,对含 α6 受体的选择性是含 α1 受体的 100 倍。Furosemide sodium 用作利尿试剂,用于充血性心力衰竭,高血压和水肿的研究。 | |||
T0755 |
Carglumic Acid
Carbaglu,N-Carbamylglutamate,N-Carbamyl-L-glutamic acid,氨甲酰谷氨酸,Carbamylglutamic acid,Carbamino-L-glutamic acid,Ureidoglutaric acid |
Others | Others |
Carglumic Acid (Ureidoglutaric acid) 是一种 N-乙酰谷氨酸 (NAG) 的功能类似物和氨甲酰磷酸合成酶 1(CPS1)的活化剂,可用于与 N-乙酰谷氨酸合成酶 (NAGS) 缺陷相关的急性和慢性高氨血症的研究。 | |||
T6529 |
Halobetasol propionate
卤贝他索丙酸酯,Halobetasol Propionate,Ulobetasol propionate,BMY-30056,卤倍他索丙酸酯,CGP-14458 |
Phospholipase | Metabolism |
Halobetasol propionate (BMY-30056) 是一种在皮肤外使用的合成类固醇,具有抗炎,止痒和收缩血管的活性。 | |||
T0782 |
Benzthiazide
Aquatag,苄噻嗪,Lemazide,Dihydrex |
Carbonic Anhydrase | Metabolism |
Benzthiazide (Lemazide) 是长效利尿剂及抗高血压剂。它也是碳酸酐酶 9 的抑制剂,他对 CA9,CA2 和 CA1 的 Ki 分别为 8.0,8.8 和 10 nM。它对肿瘤细胞增殖具有抑制作用。 | |||
T31725 |
Etozolin
GO 687,W-2900A,W2900A,GO-687,W 2900A |
||
Ezozolin (Diulozin, W-2900A) is a diuretic used for the treatment of edema and hypertension. | |||
T33276 |
Mefruside
FDA1902,FDA-1902,FDA 1902,FBA-1500,FBA1500,FBA 1500 |
||
Mefruside is a diuretic indicated for the treatment of edema and hypertension. | |||
T33600 |
Naxifylline
CVT 124,CVT-124,CVT124,BG9719 |
||
Naxifylline is an A1 adenosine receptor antagonist that promotes urine volume to prevent the decline in renal function observed during diuretic therapy for the treatment of edema associated with congestive heart failure. | |||
T27391 |
FSBA
|
||
FSBA inhibits covalently anthrax edema factor. | |||
T33294 |
Mercaptomerin sodium
Diucardyn sodium,Mercaptomerine sodique,Thiomerin sodium,Letorin |
||
Mercaptomerin sodium can be used to treat cardiac edema. | |||
T38544 |
Fasitibant chloride
MEN16132 free base,Fasitibant chloride |
||
Fasitibant chloride (MEN16132 free base) is a powerful and specific nonpeptide antagonist of the bradykinin B2 receptor (B2R). This compound effectively reduces joint pain and mitigates joint edema in a rat model of Carrageenan-induced arthritis. | |||
T24950 |
VUF-10214
VUF 10214,VUF10214 |
||
VUF-10214 is an H4 receptor-ligand. VUF-10214 has significant anti-inflammatory properties in the carrageenan-induced paw edema model in vivo studies in the rat reveal. | |||
T27670 |
JNJ-26076713
JNJ26076713 |
||
JNJ-26076713, an orally active alpha V integrin antagonist, represents a potential therapeutic candidate for the treatment of macular edema, age-related macular degeneration, and proliferative diabetic retinopathy. | |||
T33725 |
Norgestrienone
Planor,A-301,A301,Ogyline,A 301 |
||
Nogotrienone is an anabolic steroid with fertility and contraceptive activity that has been studied as a therapeutic agent for hereditary angioneurotic edema. | |||
T27042 |
Clobenoside
Ba-43853,Ba 43853,Ba43853 |
||
Clobenoside is a non-steroidal anti-inflammatory agent. Clobenoside also has an edema-protective effect while not influencing blood pressure nor heart rat and not producing any direct vasoactive effects. | |||
T68926 | Indomethacin salicylate | ||
Indomethacin salicylate is an antiinflammatory drug. It has shown remarkable inhibitory effects on carrageenin edema, ultraviolet erythema and adjuvant arthritis. | |||
T34107 |
Polythiazide
P2525,NSC-108161,NSC 108161,P-2525,NSC108161 |
||
Polythiazide (NSC-108161, P-2525) is used to treat fluid retention (edema) caused by a variety of causes, including congestive heart failure, severe liver disease (cirrhosis), kidney disease, or steroid or hormonal medication. | |||
T61403 |
Plasma kallikrein-IN-3
|
||
Plasma kallikrein-IN-3, a potent inhibitor ( IC 50 : 0.15 μM) of plasma kallikrein, finds application in research related to hereditary angioedema, diabetic macular edema, and diabetic retinopathy [1]. | |||
T33851 |
Ozolinone
W 3282,W3282,W-3282 |
||
Ozolinone is an active metabolite of etozoline which acts as a loop diuretic --- a diuretic that acts at the ascending limb of the loop of Henle in the kidney. Loop diuretics are primarily used in medicine to treat hypertension and edema often due to cong | |||
T72337 | Plasma kallikrein-IN-2 | ||
Plasma kallikrein-IN-2 是一个有效的 plasma kallikrein (PKal)抑制剂,IC50值为 0.1 nM。Plasma kallikrein-IN-2 可用于遗传性血管水肿、糖尿病性黄斑水肿、糖尿病视网膜病变的研究。 | |||
T15434 | GSK2798745 | TRP/TRPV Channel | Membrane transporter/Ion channel |
GSK2798745 is an orally active transient receptor potential vanilloid 4 (TRPV4) ion channel blocker (IC50s: 1.8 and 1.6 nM for hTRPV4 and rTRPV4). It is used in research for the treatment of pulmonary edema associated with congestive heart failure. | |||
T80502 |
P4pal10
|
||
P4pal10为PAR4拮抗剂,能在体内抑制凝血酶介导的小鼠血小板聚集,并显著减少Carrageenan引起的水肿及粒细胞浸润。 | |||
T61711 | COX-2-IN-14 | ||
COX-2-IN-14 (compound 2a) is a highly potent and selective inhibitor of COX-2 (cyclooxygenase-2), with strong binding affinity at the active site of COX-2 co-crystal. Demonstrating remarkable in vivo anti-inflammatory activity, COX-2-IN-14 effectively reduces ear edema and myeloperoxidase (MPO) activity in mice [1]. | |||
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... | |||
T83048 | Anti-inflammatory agent 64 | ROS Kinase | Tyrosine Kinase/Adaptors |
Anti-inflammatory agent 64(compound 4b)能抑制IL-6和TNF-α的分泌,具备抗氧化及抗炎活性,无论在体内外均有效,能显著减轻足跖水肿。 | |||
T78253 |
Faricimab
RG7716 |
VEGFR | Angiogenesis; Tyrosine Kinase/Adaptors |
Faricimab是一种双特异性抗体,针对angiopoietin-2和血管内皮生长因子-A (VEGF-A)。该化合物可应用于糖尿病黄斑水肿(DME)的研究。 | |||
T69990 |
Ruboxistaurin mesylate monohydrate
|
||
Ruboxistaurin mesylate monohydrate is a PKC beta inhibitor potentially for the treatment of diabetic nephropathy and diabetic macular edema. Ruboxistaurin attenuates diabetic nephropathy via modulation of TGF-β1/Smad and GRAP pathways. Ruboxistaurin reduces oxidative stress and attenuates left ventricular hypertrophy and dysfunction in rats with streptozotocin-induced diabetes. Ruboxistaurin inhibits retinal neovascularization via suppression of phosphorylation of ERK1/2 and Akt. | |||
T36623 |
Antileukinate
|
||
Antileukinate is a synthetic hexapeptide with an acetylated amino terminus and an amidated carboxyl terminus that inhibits the binding of CXC chemokines to the chemokine receptor CXCR2. It inhibits IL-8 binding to neutrophils (Ki = 2.7-13 μM), prevents neutrophil chemotaxis and β-glucuronidase release, and blocks IL-8-induced skin edema in rabbits. At 53 mg/kg, antileukinate has been shown to protect mice against acute pancreatitis and associated lung injury. | |||
T11240 |
Ethacrynic acid D5
|
Others | Others |
Ethacrynic acid, a diuretic, functions as an inhibitor of L-type voltage-dependent and store-operated calcium channels, facilitating the relaxation of airway smooth muscle (ASM) cells. It exhibits anti-inflammatory effects, notably reducing retinoid-induced ear edema in mice, and inhibits glutathione S-transferases (GSTs), making it a potent suppressor of the NF-kB signaling pathway. Additionally, ethacrynic acid modulates leukotriene formation. A variant, Ethacrynic acid D5, is distinguished by... | |||
TP1408 |
Peptide 401
|
||
Peptide 401 is an antimicrobial peptide (AMP) derived from the venom of bees and wasps. Peptide 401 induces mast cell degranulation, activating histamine release from peritoneal mast cells. Additionally, peptide 401 exhibits some anti-inflammatory activit | |||
T71893 |
Clobetasol Propionate-d5
|
||
Clobetasol propionate-d5 is intended for use as an internal standard for the quantification of clobetasol propionate by GC- or LC-MS. Clobetasol propionate is a corticosteroid. It binds to glucocorticoid receptors in a cell-free assay and inhibits proliferation of primary human skin fibroblasts when used at a concentration of 5 µg/ml. Topical administration of clobetasol propionate reduces croton oil-induced ear edema in mice. Formulations containing clobetasol propionate have been used in the t... | |||
T69244 |
Betulonaldehyde
|
||
Betulonaldehyde is a pentacyclic triterpenoid and derivative of the cholesterol biosynthesis inhibitor betulin that has been found in Betula. It is active against P. falciparum (IC50 = 3.36 µg/ml) and cytotoxic to NCI H187 lung cancer cells and non-cancerous Vero cells (IC50s = 19.23 and 17.09 µg/ml, respectively). Topical application of betulonaldehyde (1 mg/ear) reduces ear edema induced by phorbol 12-myristate 13-acetate (TPA; Item No. 10008014) in mice. It has also been used a precursor in t... | |||
T68665 |
Yonkenafil
Tunodafil |
||
Yonkenafil (Tunodafil) 是一种新型PDE5抑制剂,对脑梗塞、神经功能缺损、水肿及梗塞区域神经元损伤具有显著降低效果。通过调节神经发生,Yonkenafil 可改善认知功能,展现出在阿尔茨海默病研究中的潜在价值。 | |||
T26447 |
A 78773
A78773,A-78773 |
||
A 78773 is a potent, selective, direct, and reversible 5-lipoxygenase inhibitor. It has activity in a variety of purified cells and in more complex biological systems such as whole blood, lung fragments, and tracheal tissues. A 78773 acts against inflamma | |||
T76195 |
Stresscopin-related peptide (human)
|
||
Stresscopin-related peptide (human) 是 2 型 CRH 受体的特异性配体。Stresscopin-related peptide (human) 抑制食物摄入,延迟胃排空,并减少热引起的水肿。Stresscopin-related peptide (human) 在应激后维持体内平衡,可用于应激相关疾病的研究。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T5781 |
taraxasteryl acetate
蒲公英甾醇醋酸酯,醋酸蒲公英酯 |
Antibacterial | Microbiology/Virology |
Taraxasteryl acetate 是分离自矢状疟原虫中,具有广谱的抗炎活性。它能够改善右旋糖酐、酵母聚糖及花生四烯酸诱导的大鼠后爪水肿。它可用于研究局部炎症。 | |||
TN6706 |
3-demethylcolchicine
3-去甲秋水仙碱,3-去甲基秋水仙碱 |
Reactive Oxygen Species | Immunology/Inflammation; Metabolism; NF-κB |
3-Demethylcolchicine 是一种从金莲花中分离得到的天然产物,对纯化的牛脑微管蛋白的聚合有抑制作用。 | |||
T2978 |
Mogroside V
|
AMPK | Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
Mogroside V 是三萜糖苷,是非糖类甜味剂,甜度比蔗糖甜高300倍。它具有抗氧化,抗糖尿病和抗癌作用。 | |||
T5S1982 |
Periplocin
Periplocoside,杠柳毒苷 |
Apoptosis; Others | Apoptosis; Others |
Periplocin (Periplocoside) 是从黑龙骨中分离出的一种强心类固醇。它可促进肿瘤细胞凋亡并抑制肿瘤生长。它通过激活 Na/K-ATPase 介导的 Src/ERK 和 PI3K/Akt 途径,具有促进伤口愈合的潜力。 | |||
T4S0176 |
Alnustone
(4E,6E)-1,7-Diphenyl-4,6-heptadien-3-one,桤木酮 |
Others | Others |
Alnustone ((4E,6E)-1,7-Diphenyl-4,6-heptadien-3-one) 是一种非酚双苯庚烷类化合物,在草药和香料中发现,是姜黄的成分之一,具有抗吐、抗炎作用。 | |||
T3S0401 |
Piceatannol 3'-O-glucoside
白皮杉醇 3'-O-葡萄糖苷,Piceatannol 3-glycoside,Quzhaqigan,曲札茋苷、白皮杉醇-3'-O-葡萄糖苷 |
Arginase; NO Synthase | Immunology/Inflammation |
Piceatannol 3'-O-glucoside (Piceatannol 3-glycoside) 是大黄的一种活性成分,通过抑制精氨酸酶活性激活内皮细胞一氧化氮合酶,抑制Arginase I 和Arginase II,IC50值分别为 11.22 和 11.06 μM。它可增加肺血氧分压,减少肺间质水肿,从而保护肺损伤。 | |||
T0522 |
Diammonium Glycyrrhizinate
甘草酸二铵,Glycyrrhizin |
Dehydrogenase | Metabolism |
Diammonium Glycyrrhizinate (Glycyrrhizin) 是分离自甘草中的化合物,有抗炎作用。 | |||
T2798 |
Esculetin
秦皮乙素,二羟基香豆素,Aesculetin,Cichorigenin |
Lipoxygenase; Akt; PI3K | Cytoskeletal Signaling; Metabolism; PI3K/Akt/mTOR signaling |
Esculetin (Cichorigenin) 是主要提取自水曲柳的树皮中的活性成分。它能够抑制PI3K/Akt 途径,阻碍血小板衍生生长因子诱导的气道平滑肌细胞表型转换。它具有抗氧化,抗炎和抗肿瘤的活性。 | |||
TN4493 |
Mannioside A
|
||
Mannioside A has anti-inflammatory activity, inhibits carrageenan-induced paw edema in the rat. | |||
TN4406 |
Lamiide
|
||
Lamiide has anti-inflammatory activity in carrageenin-induced paw edema test. It shows lipid peroxidation inhibition on rat-brain phospholipid peroxidation. | |||
TN5151 | Tomentin | ||
Tomentin has anti-inflammatory effects, it can inhibit the formation of λ-carrageenan footpad edema at 58%. | |||
TN1191 |
16α-Hydroxytrametenolic acid
16 alpha-Hydroxytrametenolic acid |
Others | Others |
16 alpha-Hydroxytrametenolic acid can inhibit 12-O-tetradecanoylphorbol 13-acetate (TAP)-induced mouse ear edema. | |||
T40634 |
Perilla ketone
|
||
Perilla ketone is a naturally occurring xenobiotic compound that undergoes activation by pulmonary P450 cytochrome enzymes within the lung. This activation leads to the manifestation of severe pulmonary damage and the development of diffuse pulmonary edema. | |||
TN4185 |
Hautriwaic acid
|
||
Hautriwaic acid shows anti-inflammatory activity in 12-O-tetradecanoylphorbol 13-acetate (TPA) mice ear edema models, it diminishes the joint edema induced by this mixture of polysaccharides (carrageenan), possibly by acting as immunomodulator of the infl | |||
T21893 |
Luffariellolide
|
||
Luffariellolide 是人滑膜蛋白磷脂酶A2 (HSF-PLA2) 抑制剂 (IC50=5 μM)。Luffariellolide (ED50=50 μg/耳)可有效抑制佛波酯 (PMA) 引起的耳水肿。 | |||
T81975 |
Kopsininic acid
|
||
Kopsininic acid, 源自Kopsia hainanensis的天然产物,主要用于类风湿性关节炎、咽炎、扁桃体炎和水肿的研究。 | |||
TN1080 |
Kaji-ichigoside F1
蔷薇苷 |
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Kaji-ichigoside F1 shows antiinflammatory/antinociceptive action in acetic acid-induced writhing and hot plate testing and in a carrageenan-induced paw edema model in mice and rats. Kaji-ichigoside F1 exhibits in vivo hepatoprotective effects, it inhibite | |||
TN1623 |
Escin IIB
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Others; NOS | Immunology/Inflammation; Others |
Escin IIB has positive effects on acute inflammation in animals, it can inhibit the induced by serotonin in rats, the hind paw edema induced by carrageenin, and the scratching behavior induced by compound 48/80 in mice. | |||
TN3447 |
Arjunglucoside I
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Arjunglucoside I has anti-inflammatory activity, it exhibits significant activity against carrageenan-induced paw edema in rat. It also shows antiproliferative activity against the A2780 human ovarian cancer cell line with an IC(50) value of 1.2 microM. | |||
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 | |||
T73066 |
Thielavin B
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Thielavin B为Thielavin terricola产生的前列腺素生物合成抑制剂。该化合物能有效抑制内过氧物酶介导的前列腺素E2合成,并在静脉注射后显著降低大鼠因角叉菜胶引发的水肿。 | |||
T81324 |
Quercetin-3-O-(2′′-O-galloyl)-β-D-glucopyranoside
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Quercetin-3-O-(2′′-O-galloyl)-β-D-glucopyranoside 是一种从天竺葵属植物中分离的酚类化合物,具有口服活性和抗炎特性,可能在治疗水肿和改善主动脉内皮依赖性舒张损伤方面有应用潜力。 | |||
TN3395 |
Alpinone 3-acetate
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IFNAR | Immunology/Inflammation |
Alpinone 3-acetate 具有抗炎作用,可抑制12-O-tetradecanophenol 13-acetate 所致小鼠耳部水肿模型的炎症反应。Alpinone 3-acetate 是Alpinone 衍生物 。Alpinone 是一种具有活性的天然化合物,来源于向日葵,具有免疫调节和抗病毒活性 。 | |||
TN4505 | Masticadienolic acid | Others | Others |
Masticadienolic acid is a specific competitive inhibitor of secreted phospholipase A2, it not only protects the active site histidine from alkylation but also inhibits the action of secreted from pancreas, synovial fluid, and bee venom. Masticadienolic ac |