Baccatin III is a precursor to the anti-cancer drug paclitaxel, it's a natural product isolated and purified from the barks of Taxus chinensis.

Kalii dehydrographolidi succinas is an immune system drug that can be used in viral upper respiratory infection.

Tryptanthrin is a natural alkaloidal compound having basic indoloquinazoline moiety. It has broad spectrum of biological activities including anticancer activity, anti-inflammatory, antiprotozoal, antiallergic, antioxidant, and antimicrobial.

Clonixin is a non steroidal anti inflammatory drug (NSAID) with analgesic properties.

Forsythoside H是从 Forsythia suspensa (Thunb.) Vahl 中分离出的咖啡酰基苯乙醇苷 (CPG)，具有抗炎作用。

Ferric maltol是一种口服活性的单一铁离子（Fe3+）复合物，可用于研究炎症性肠病中的缺铁性贫血。

Idramantone is use as an immune agonist.

α-Terpineol 从蓝桉 (Eucalyptus globulus Labill) 中分离出来，对牙周病和致龋菌具有很强的抗菌活性。

Eleutheroside E, a principal component of Eleutherococcus enticosus, has anti-inflammatory and protective effects in ischemia heart.

Hesperidin methylchalcone是一种来源于柑橘的化合物，具有强效的抗氧化和抗炎活性。它通过抑制氧化应激、细胞因子产生和 NF-κB 活化来减少炎症和疼痛，同时具有血管保护作用。Hesperidin methylchalcone 在心血管疾病、炎症性疾病和抗氧化保健品领域中具有潜在应用价值。

Sodium houttufonate是一种植物来源的化合物，具有显著的抗感染活性。它主要用于治疗脓毒性皮肤感染、呼吸道感染，包括老年患者的肺炎和慢性支气管炎。Sodium houttufonate 通过对抗感染和支持呼吸系统健康，在相关领域展示出治疗潜力。

Indirubin is a purple 3,2- bisindole and a stable isomer of indigo isolated from Indigo naturalis (Apiaceae) with anti-inflammatory and anticancer activities.

NPC 15199 is an anti-inflammatory agent. It increases intracellular Ca2+ levels.

Saikogenin D从 Bupleurum chinense 中分离，具有抗炎作用。它激活环氧合酶，将花生四烯酸转化为环氧二十烷酸和二羟基二十碳三烯酸，从而抑制前列腺素E2 (PGE2) 的生成。由于细胞内 Ca²⁺的释放，Saikogenin D 还会引起 Ca²⁺的升高。

Naringenin chalcone, found in peels of citrus maxima, has antiallergic and anti-inflammatory properties.

Skimmin 是从圆锥绣球的草本植物中分离和纯化的一种天然产物，具有抗炎活性。

Incensole acetate是卡氏乳香树脂的主要成分，对创伤性和缺血性颅脑损伤中的神经元损伤具有神经保护作用。Incensole acetate 减少了 hOBNSC 中由 Aβ 25-35 触发的细胞凋亡(apoptosis)。

Isoacteoside is a natural compound isolated and purified from the herb of Pedicularis striata Pall. which exhibit significant inhibition of advanced glycation end product formation with IC50 values of 4.6-25.7 μM, compared with those of aminoguanidine (IC50=1,056 μM) and quercetin (IC50=28.4 μM) as positive controls, and exhibits anti-inflammatory effects through blocking TLR4 dimerization.

Peimine can inhibit the production of inflammatory cytokines induced by LPS and block MAPK and NF-κB signaling pathways. It is purified from the bulbus of fritillaria thunbergii.

Oxysophocarpine, a natural product isolated and purified from the root of Styphnolobium japonicum (L.) Schott., can decrease the level of serum transaminase, improve lipid metabolism, reduce synthesis of inflammatory cytokines TNF-α, TGF-β1 and IL-6, activate protective adipocytokine adiponectin, and may be a drug for colonic inflammation and NASH.