139
22
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T10152 |
4-Methylamino antipyrine
|
COX; Drug Metabolite | Immunology/Inflammation; Metabolism; Neuroscience |
4-Methylamino antipyrine 是 Metamizole 的活性代谢产物,可用于疼痛和发烧的研究。Metamizole 是吡唑啉酮类非甾体抗炎药,可抑制COX。 | |||
T5449 |
Bamaquimast
F 10126,L 0042,巴马司特 |
Proton pump | Membrane transporter/Ion channel |
Bamaquimast (L 0042) 是一种抗哮喘药。 | |||
T4561 |
Tiaprofenic acid
Tiaprofensaeure,噻洛芬酸,Acido tiaprofenico,Surgam |
Others; COX | Immunology/Inflammation; Neuroscience; Others |
Tiaprofenic acid (Acido tiaprofenico) 是可口服的非甾体抗炎药,通过抑制环氧化酶抑制前列腺素合成,可用于风湿性疾病的研究。 | |||
T36683 |
Vedaprofen
Quadrisol,PM 150,维达洛芬,CERM 10202 |
COX; Antibacterial; Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation; Microbiology/Virology; Neuroscience |
Vedaprofen (PM 150) 抑制 COX-1 并通过抗炎活性减少前列腺素 H2 的合成。 Vedaprofen 是一种大肠杆菌滑动钳抑制剂,IC50 为 222 μM,Ki 为 131 μM。 | |||
T6540 |
Ibuprofen Lysine
布洛芬赖氨酸盐,Neoprofen |
COX | Immunology/Inflammation; Neuroscience |
Ibuprofen Lysine (Neoprofen) 是一种非甾体抗炎药。 | |||
T19679 |
Benoxaprofen
氧苯恶唑丙酸,NSC 299582,LY-90459,Benoxaphen. Compound 90459 |
COX | Immunology/Inflammation; Neuroscience |
Benoxaprofen (NSC-299582) 是长效的、强效的抗炎和解热化合物,在体外具有较弱的对环氧合酶的抑制作用,也可以抑制脂氧合酶,在一些炎症动物模型中抑制单核细胞迁移。 | |||
T1421 |
Aceclofenac
醋氯芬酸,Preservex,Airtal |
COX | Immunology/Inflammation; Neuroscience |
Aceclofenac (Preservex) 是一种可口服的非甾体抗炎药,可用于缓解疼痛、骨关节炎、强直性脊柱炎、类风湿性关节炎的研究。 | |||
T6498 |
Fenoprofen calcium hydrate
Feprona dihydrate,Fenoprofen calcium salt dihydrate,Progesic dihydrate,非诺洛芬钙二水合物 |
Apoptosis; Others; COX | Apoptosis; Immunology/Inflammation; Neuroscience; Others |
Fenoprofen calcium hydrate (Progesic dihydrate) 是一非甾体类抗炎症化合物。 | |||
T50025 |
Lonazolac
|
PPAR | DNA Damage/DNA Repair; Metabolism |
Lonazolac 是一种具有抗炎特性的非甾体抗风湿剂。 | |||
T17036 |
Tenidap
CP-66248 |
COX | Immunology/Inflammation; Neuroscience |
Tenidap is a non-steroidal anti-inflammatory drug and is a selective COX-1 inhibitor (IC50: 0.03 µM and 1.2 µM for COX-1 and COX-2, respectively). Tenidap is also a specific SLC26A3 inhibitor. | |||
T0321 |
Indoprofen
吲哚洛芬,(±)-Indoprofe,茚酮苯丙酸 |
COX | Immunology/Inflammation; Neuroscience |
Indoprofen ((±)-Indoprofe) 是非甾体类抗炎药, 可用于研究脊髓性肌萎缩。 | |||
T19636 |
Morniflumate
马尼氟酯,Niflam,UP 164,UP-164,Morniflu,UP164 |
Others | Others |
Morniflumate (Niflam) 是一种非甾体抗炎药。它用于治疗炎症。 | |||
T1280 |
Nepafenac
AL 6515,AHR 9434,奈帕芬胺 |
COX | Immunology/Inflammation; Neuroscience |
Nepafenac (AHR 9434) 是一种非甾体抗炎药,可抑制COX-2,是Amfenac 的原药。 | |||
T3608 |
Carbasalate calcium
Rheomin,Omegin,Alcacyl,Iromin,卡巴匹林钙,Solupsan,Carbasalate Calcium |
Platelet aggregation | Others |
Carbasalate calcium (Rheomin) 是抗炎和解热剂,可用于研究疼痛的缓解。 | |||
T1582 |
Naproxen
萘普生,(S)-Naproxen |
COX; Autophagy | Autophagy; Immunology/Inflammation; Neuroscience |
Naproxen ((S)-Naproxen) 是COX-1和COX-2的抑制剂,在细胞试验中IC50值分别为8.72 和5.15 μM。它是丙酸衍生物和非甾体抗炎药,具有抗炎、解热和镇痛活性。 | |||
T0258 |
Carsalam
恶喹二酮,卡沙仑,Carsalame,Carbonylsalicylamide,2H-1,3-Benzoxazine-2,4(3H)-dione |
Antibiotic | Microbiology/Virology |
Carsalam (2H-1,3-Benzoxazine-2,4(3H)-dione) 是非类固醇类的抗炎药。 | |||
T11340 |
Furprofen
|
Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation |
Furprofen, a non-steroidal anti-inflammatory drug (NSAID), exerts its effects by inhibiting the synthesis of prostaglandin (PGE). This compound demonstrates analgesic properties and can be conveniently administered orally to alleviate pain. | |||
T6387 |
Ampiroxicam
CP 65703,Flucam,安吡昔康 |
COX | Immunology/Inflammation; Neuroscience |
Ampiroxicam (Flucam) 是一种非选择性的环氧化酶抑制剂,有抗炎活性。 | |||
T0708 |
Oxaprozin
奥沙普秦,Oxaprozinum,Wy21743 |
NF-κB; COX | Immunology/Inflammation; Neuroscience; NF-κB |
Oxaprozin (Oxaprozinum) 是 COX-1和 COX-2的抑制剂,还能抑制 NF-κB 的活化,对人类血小板 COX-1 和 IL-1 刺激的人类滑膜细胞 COX-2 的 IC50值分别为 2.2 和 36 μM。 | |||
T0826 |
Meloxicam
美洛昔康,Movalis,Mobic,Metacam |
Apoptosis; COX; Autophagy | Apoptosis; Autophagy; Immunology/Inflammation; Neuroscience |
Meloxicam (Metacam) 是一种非甾体类抗炎剂,抑制COX 的活性,对 COX-2 和 COX-1 的IC50值分别为 0.49 µM 和 36.6 µM。 | |||
T0310 |
Actarit
阿克他利,4-acetylaminophenylacetic acid |
Others | Others |
Actarit (4-acetylaminophenylacetic acid) 是一种口服具有活性的化合物,可用于抗风湿研究以及 II 型胶原诱导性关节炎的研究。 | |||
T1325 |
Carprofen
卡洛芬,Ridamyl,Imadyl,Rimadyl |
FAAH; COX; Autophagy | Autophagy; Immunology/Inflammation; Metabolism; Neuroscience |
Carprofen (Ridamyl) 是多靶点FAAH/COX 抑制剂,能够抑制 COX-2,COX-1 和 FAAH 的活性,IC50值分别为 3.9 μM,22.3 μM 和 78.6 μM。它是一种丙酸衍生物和非甾体抗炎药,具有抗炎、镇痛和解热活性。 | |||
T2550 |
Tolmetin
Tolectin,托麦汀 |
COX | Immunology/Inflammation; Neuroscience |
Tolmetin (Tolectin) 是非甾体类抗炎药,是可口服的 COX 抑制剂,对人 COX-1 和 COX-2 的 IC50值分别为 0.35 和 0.82 µM。 | |||
T0319 |
Suxibuzone
琥布宗,Calibene,Suxibuzonum,Suxibuzona |
COX | Immunology/Inflammation; Neuroscience |
Suxibuzone (Suxibuzona) 是非甾体类抗炎药 Phenylbutazone 的前药,可用于关节和肌肉疼痛研究。 | |||
T20615 |
Olsalazine
奥沙拉嗪,Dipentium,Salicylic acid |
Others | Others |
Olsalazine (Dipentium) 是一种抗炎药,用于治疗炎症性肠病。它也是一种新型的 DNA 去甲基化剂。 | |||
T6424 |
Bromfenac Sodium
AHR 10282B,Bronuck,AHR 10282R,溴芬酸钠 |
COX | Immunology/Inflammation; Neuroscience |
Bromfenac Sodium (AHR 10282R) 是可口服的COX 抑制剂,抑制COX-1和COX-2的IC50值分别为 5.56 和 7.45 nM。它是溴化非甾体类抗炎药,通常用于白内障的术后炎症和疼痛以及假晶状体囊状黄斑水肿的研究。 | |||
T4966 |
Ufenamate
氟芬那酸丁酯,Flufenamic acid butyl ester,Butyl flufenamate,氟灭酸丁酯 |
Others | Others |
Ufenamate (Flufenamic acid butyl ester) 是一种基于邻氨基苯甲酸的抗炎药。它可用于皮肤疾病研究。 | |||
T0055 |
Glafenine
Glafenin,格拉非宁 |
COX | Immunology/Inflammation; Neuroscience |
Glafenine (Glafenin) 是一种可用于缓解疼痛研究的非甾体抗炎药。 | |||
T0159 |
Pranoprofen
普拉洛芬,Pyranoprofen |
Apoptosis; COX; PGE Synthase; Prostaglandin Receptor | Apoptosis; GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Pranoprofen (Pyranoprofen) 可抑制COX1/2酶,阻断花生四烯酸转化为二十烷醇,减少前列腺素的合成。它是一种用于眼科的非甾体抗炎试剂。 | |||
T1720 |
Amfenac Sodium Hydrate
一水氨芬酸钠,Amfenac Sodium Monohydrate,氨芬酸钠水合物 |
COX | Immunology/Inflammation; Neuroscience |
Amfenac Sodium Hydrate 是一种含有乙酸部分的非甾体镇痛抗炎药,是 COX-2抑制剂。 | |||
T0466 |
Celecoxib
塞来西布,塞来昔布,SC 58635 |
COX | Immunology/Inflammation; Neuroscience |
Celecoxib (SC 58635) 是一种非甾体抗炎药,是选择性的COX-2抑制剂,IC50为 40 nM。 | |||
T23403 |
Sulindac sulfone
|
Reductase; COX | Endocrinology/Hormones; Immunology/Inflammation; Metabolism; Neuroscience |
Sulindac sulfone 是非甾体抗炎药舒林酸 (sulindac) 的代谢物。 它是醛糖还原酶的抑制剂 (IC50 =367 nM)。 | |||
T0448 |
(S)-(+)-Ibuprofen
左旋布洛芬,Dexibuprofen,(S)-Ibuprofen,(S)-(+)-布洛芬 |
BCL; Thrombin; Cysteine Protease; COX; PPAR | Apoptosis; DNA Damage/DNA Repair; Immunology/Inflammation; Metabolism; Neuroscience; Proteases/Proteasome |
(S)-(+)-Ibuprofen (Dexibuprofen) 是 Ibuprofen 的 S(+)-对映异构体,能够有效的抑制COX-1(IC50:2.1 μM)和COX-2(IC50:1.6 μM),。它具有抗癌、退热、止痛,抗炎的效果。 | |||
T0498 |
Salsalate
Disalicylic acid,Salicylsalicylic acid,Sasapyrine,NSC-49171,双水杨酸酯 |
Reactive Oxygen Species; COX | Immunology/Inflammation; Metabolism; Neuroscience; NF-κB |
Salsalate (Sasapyrine) 是一种有效的抗风湿药物,是一种非乙酰化水杨酸盐,可以绕过胃的吸收,也可以避免环氧合酶的抑制。它具有抗炎活性,降低血糖水平、胰岛素抵抗和细胞因子表达,可用于研究 2 型糖尿病。 | |||
T0285 |
Isoxicam
伊索昔康,Isoxicamum,Isoxicamo,Maxicam |
COX | Immunology/Inflammation; Neuroscience |
Isoxicam (Isoxicamum) 是可口服的非甾体抗炎剂,可通过抑制环氧合酶 1 和 2 来阻断前列腺素的合成,可用于关节炎的研究。 | |||
T1258 |
Nabumetone
BRL14777,萘丁美酮 |
COX; Glutathione Peroxidase | Immunology/Inflammation; Metabolism; Neuroscience |
Nabumetone (BRL14777) 是一种非甾体抗炎药,是选择性COX-2抑制剂,其活性代谢物 6MNA 可抑制环加氧酶 I 和 II。 | |||
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。 | |||
T0767 |
Sulfapyridine
磺胺吡啶,Sulfidine,Sulfidin,2-Sulfapyridine |
Antibacterial; Antibiotic; Autophagy | Autophagy; Microbiology/Virology |
Sulfapyridine (2-Sulfapyridine) 是一种磺酰胺类抗生素,是 Sulfasalazine 的代谢产物。它抑制重组 P. carinii 二氢蝶呤合成酶,IC50为 0.18 μM。它具有抗菌,抗炎和抗风湿作用。 | |||
T2553 |
Etofenamate
|
COX | Immunology/Inflammation; Neuroscience |
Etofenamate 是非甾体类抗炎小分子,也是非选择性的 COX 抑制剂,具有抗风湿和解热抗炎作用,可用于缓解疼痛、关节炎等炎症相关疾病的研究。 | |||
T28972 |
Tiaramide hydrochloride
FK-1160,NTA-194,FK 1160,FK1160,tiaramide |
Others | Others |
Tiaramide hydrochloride (FK-1160) 是一种抗炎药,可抑制肥大细胞释放的介质的作用,并具有直接的平滑肌松弛特性。 | |||
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。 | |||
T1394 |
Ibuprofen
Brufen,(±)-Ibuprofe,布洛芬,Motrin,Advil |
COX | Immunology/Inflammation; Neuroscience |
Ibuprofen (Advil) 是一种丙酸衍生物和非甾体抗炎药 (NSAID),具有抗炎、镇痛和解热作用。它是COX-1和COX-2的抑制剂,IC50值分别为 13 和 370 μM,导致前列腺素和血栓素前体的形成减少。 | |||
T0435 |
Sulfinpyrazone
(+/-)-Sulfinpyrazone,G-28315,苯磺保泰松,NSC 75925 |
COX | Immunology/Inflammation; Neuroscience |
Sulfinpyrazone (NSC-75925) 是一种口服有效的尿酸剂,具有抗血栓和血小板抑制作用。它可作用于慢性和间歇性痛风性关节炎。 | |||
T1191L |
Metamizole sodium
安乃近,Analgin,安乃近钠盐(诺瓦经),Dipyron |
COX | Immunology/Inflammation; Neuroscience |
Metamizole sodium (Analgin) 是一种环氧合酶-3 (COX-3) 抑制剂,具有良好的解热作用,可用于缓解疼痛的研究。 | |||
T0726 |
Benzydamine hydrochloride
Benzydamine HCl,盐酸苄达明,AF864 |
COX; PGE Synthase; Antibacterial | Immunology/Inflammation; Microbiology/Virology; Neuroscience |
Benzydamine hydrochloride (AF864) 是一种局部作用的非甾体抗炎药,具有局部麻醉和镇痛作用。它也是前列腺素合成酶抑制剂,有抗细菌活性。 | |||
T4542 |
Clonixin
Clonixic acid,氯尼辛 |
Others | Others |
Clonixin (Clonixic acid) 是一种非甾体抗炎药,具有口服活性。 | |||
T5843 |
Tarenflurbil
MPC7869,(R)-Flurbiprofen,R-flurbiprofen,氟比洛芬,R-氟比洛芬 |
Retinoid Receptor; Autophagy | Autophagy; Metabolism |
Tarenflurbil ((R)-Flurbiprofen) 是 Flurbiprofen 的 R 型对映体,可抑制 [3H]9-cis-RA 结合到 RXRαLBD,IC50为 75 μM。它可研究阿尔兹海默症。 | |||
T8826 |
3-AMINO-1,2,4-TRIAZINE
|
Others | Others |
3-AMINO-1,2,4-TRIAZINE 是一种芳香族生物活性化合物,已用于合成各种药物,包括抗真菌药物氟康唑、抗炎药物布洛芬和抗癌药物紫杉醇;也被用于设计新药,如抗艾滋病药物齐多夫定和抗疟疾药物青蒿素;以及用于合成各种其他化合物,如抗糖尿病药物二甲双胍和抗高血压药物赖诺普利。 | |||
T7207 |
FK 3311
N-[4-乙酰基-2-(2,4-二氟苯氧基)苯基]-甲烷磺酰胺,FK-3311,COX-2 Inhibitor V |
COX | Immunology/Inflammation; Neuroscience |
FK 3311 (COX-2 Inhibitor V) 是一种细胞渗透性和口服磺胺类药物,可作为 COX-2 抑制剂和非甾体抗炎药。 | |||
T37482 |
Diclofenac methyl ester
|
Others | Others |
Diclofenac methyl ester 是双氯芬酸(diclofenac)的疏水性前药形式,它是一种非甾体抗炎药 (NSAID)。它比双氯芬酸更易溶于肉豆蔻酸异丙酯,但毒性更高。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T1468 |
Lornoxicam
Ro 13-9297,Chlortenoxicam,TS110,氯诺昔康 |
COX; Endogenous Metabolite | Immunology/Inflammation; Metabolism; Neuroscience |
Lornoxicam (Chlortenoxicam) 是一种新型非甾体抗炎药,是高活性 COX-1 和 COX-2 抑制剂,IC50 分别为 5 和 8 nM。 | |||
T2959 |
Ginsenoside Rh2
20(S)-Rh2,20S-Ginsenoside Rh2,人参皂苷Rh2,20(S)-Ginsenoside Rh2,人参皂苷 Rh2 |
Apoptosis; EGFR; Caspase; Endogenous Metabolite | Angiogenesis; Apoptosis; JAK/STAT signaling; Metabolism; Proteases/Proteasome; Tyrosine Kinase/Adaptors |
Ginsenoside Rh2 (20(S)-Ginsenoside Rh2) 诱导caspase-8和caspase-9活化。它以多途径方式诱导癌细胞凋亡。 | |||
T6S1683 |
Demethoxycurcumin
Curcumin II,去甲氧基姜黄素,Desmethoxycurcumin,脱甲氧姜黄,Monodemethoxycurcumin |
Apoptosis; Antioxidant; Antibacterial; Autophagy | Apoptosis; Autophagy; Microbiology/Virology; oxidation-reduction |
Demethoxycurcumin (Desmethoxycurcumin) 是姜黄素的主要活性成分,有抗炎和抗癌作用。 | |||
T6926 |
Palmitoylethanolamide
Mackpeart DR 14V,帕米醇,N-palmitoylethanolamine,Loramine P 256,Impulsin,AM 3112,Palmidrol |
Influenza Virus; Endogenous Metabolite; PPAR | DNA Damage/DNA Repair; Metabolism; Microbiology/Virology |
Palmitoylethanolamide (Impulsin) 是一种内源性脂肪酸酰胺。它有消炎药、降压药、神经保护剂和抗惊厥药的作用。在给药后,Palmitoylethanolamide 可抑制促炎介质从活化肥大细胞的释放。 | |||
T2787 |
Picroside I
6'-Cinnamoylcatalpol,胡黄连苦苷I |
MMP; STAT | JAK/STAT signaling; Proteases/Proteasome; Stem Cells |
Picroside I (6'-Cinnamoylcatalpol) 是胡黄连的一种天然产物,是有肝脏保护作用的代谢成分,可用于哮喘研究,有减轻炎症作用,还下调 pSTAT6 和 GATA3 表达。 | |||
T3S2296 |
Gardenoside
羟异栀子苷,栀子苷 |
Others | Others |
Gardenoside 是一种发现于栀子中的天然化合物,具有保肝作用。它对 FFA 诱导的细胞脂肪变性有抑制作用。它可以调节 P2X3 和 P2X7 受体来抑制慢性缩痛。 | |||
T4518 |
Licochalcone D
|
ERK; NF-κB | MAPK; NF-κB |
Licochalcone D 是一种 NF-κB p65的有效抑制剂,是一种存在于 Glycyrrhiza inflate 中的黄酮类化合物,具有抗氧化、抗炎、抗癌等作用。 | |||
T3S1471 |
Cucurbitacin IIA
葫芦素Iia,Dihydrocucurbitacin Q1,Hemslecin A,Curcurbitacin IIA |
Apoptosis; Survivin | Apoptosis |
Cucurbitacin IIA (Dihydrocucurbitacin Q1) 是从园果雪胆中分离得到的一种三萜烯,可诱导细胞凋亡和增强自噬,有助于葫芦素IIA 对炎症相关疾病的抗炎活性。它可降低癌细胞中生存素的表达,降低磷酸化组蛋白 H3 的水平,增加裂解的 PARP 的水平。 | |||
T4S1962 |
beta-Asarone
β-细辛脑,(Z)-1,2,4-三甲氧基-5-丙烯基苯;顺式细辛脑,Cis-Isoasarone,Cis-Asarone,Cis-Isoelemicin |
NF-κB; JNK | MAPK; NF-κB |
beta-Asarone (Cis-Isoelemicin) 是一种石菖蒲中的主要成分,具有免疫抑制、促进安定、中枢神经系统抑制、降温等功能。它可透过血脑屏障,能够预防帕金森病。 | |||
T10619 |
Bromelain
|
Apoptosis; Others | Apoptosis; Others |
Bromelain 是来源于菠萝茎的一种抗炎药,可诱导细胞凋亡,具有纤维蛋白溶解、抗癌、抗水肿和抗血栓形成活性。它通过下调血浆激肽原,抑制前列腺素 E2 表达,降解晚期糖基化终产物受体,在COX 途径上游发生抗氧化作用以及调节血管生成生物标志物而发挥作用。 | |||
T5S2357 |
Acetylcorynoline
(+)-Corynoline Acetate,O-Acetylcorynoline,乙酰紫堇灵 |
Antifungal | Microbiology/Virology |
Acetylcorynoline (O-Acetylcorynoline) 是提取自 Corydalis bungeana 中的一种主要生物碱成分,具有抗炎活性。 | |||
T5S1172 |
Tiliroside
银椴甙,Tribuloside,银椴苷;椴树苷 |
Antioxidant | oxidation-reduction |
Tiliroside (Tribuloside) 是糖苷类黄酮,是 α-淀粉酶的非竞争性抑制剂(Ki:84.2 μM)。它抑制胃肠道中碳水化合物的消化和葡萄糖的吸收,具有抗糖尿病作用。 | |||
T3794 |
Pentagalloylglucose
Penta-O-galloyl-β-D-glucose,1,2,3,4,6-O-Pentagalloylglucose,1,2,3,4,6-Penta-O-galloyl-beta-D-glucopyranose,1,2,3,4,6-五没食子酰葡萄糖 |
Influenza Virus | Microbiology/Virology |
1,2,3,4,6-O-Pentagalloylglucose (Penta-O-galloyl-β-D-glucose) 存在于多种植物中,具有重要的药理作用。Pentagalloylglucose 表现出显著的抗狂犬病病毒 (RABV) 活性。 | |||
T3417 |
Amentoflavone
Didemethyl-ginkgetin,穗花杉双黄酮,Amenthoflavone,3',8''-Biapigenin |
Apoptosis; P450; Phospholipase; Reactive Oxygen Species; Opioid Receptor; COX; Antibacterial; RSV; Antifungal | Apoptosis; Endocrinology/Hormones; GPCR/G Protein; Immunology/Inflammation; Metabolism; Microbiology/Virology; Neuroscience; NF-κB |
Amentoflavone (3',8''-Biapigenin) 是一种具有很多生物活性的双黄酮类天然产物,有抗炎、抗氧化和神经保护等作用。 | |||
T6S0077 |
Byakangelicol
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COX | Immunology/Inflammation; Neuroscience |
Byakangelicol 是一种分离自白芷的白三醇,能够抑制环加氧酶-2的表达及活性,从而减少白细胞介素-1β诱导的 A549 细胞中前列腺素 E2 的释放。它可用于研究气道炎症。 | |||
T25271 |
Cortivazol
Dilaster |
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Cortivazol is an Anti-Inflammatory Drug. | |||
TMA0925 | Wilforlide A acetate | Others | Others |
Wilforlide A (T1) serves as a quality control standard of Tripterygium Glycosides that be listed in Drug Standard of Ministry of Public Health of the People's Republic of China. T1 has anti-inflammatory effects. | |||
TN1681 |
Gentianine
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Others; TNF; transporter; PPAR | Apoptosis; DNA Damage/DNA Repair; Metabolism; Others |
Gentianine 是一种有效的 Swertiamarin 衍生物,具有抗糖尿病、抗精神病、抗炎、降血压、利尿等作用,具有被开发成一种安全的降压药物的潜力。 | |||
TN5186 |
Triptoquinone A
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IL Receptor; NOS | Immunology/Inflammation |
Triptoquinone A may be a useful candidate for the development of a drug as a potent inhibitor of iNOS gene over-expression. Triptoquinone A has anti-inflammatory activity, it prevents ndotoxin-or interleukin-1 beta-promoted induction of nitric oxide synth | |||
TN3779 | De-O-methyllasiodiplodin | IL Receptor; TNF; ROS; Antifection | Apoptosis; Immunology/Inflammation; Microbiology/Virology |
De-O-methyllasiodiplodin exhibits radical scavenging, moderate antibacterial, and potential anti-inflammatory effects, it shows moderate suppression effects on induced NO production. De-O-methyllasiodiplodin effectively lowers the blood glucose level in d | |||
TN4490 | Manassantin B | ERK; BCL; p38 MAPK; TNF; NF-κB; JNK; STAT; Antifection | Apoptosis; JAK/STAT signaling; MAPK; Microbiology/Virology; NF-κB; Stem Cells |
Manassantin B is a potent inhibitor of NF-κB activation by the suppression of transciptional activity of RelA/p65 subunit of NF-κB. It also possesses anti-EBV lytic replication activity. Manassantin B inhibits interleukin-6-induced signal transducer and activator of transcription 3 activation in Hep3B cells, it has potential as a potent anti-inflammatory drug for use in pathological processes such as sepsis or acute lung injury. Manassantin B exerts antifibrotic activity in HSC-T6 cells, in pa... | |||
T38330 |
Collinin
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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... |