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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T0090 |
Moroxydine hydrochloride
盐酸吗啉胍,ABOB hydrochloride,病毒灵,Moroxydine HCl |
Antiviral; Influenza Virus | Immunology/Inflammation; Microbiology/Virology |
Moroxydine hydrochloride (ABOB hydrochloride) 是一种合成的杂环双胍类抗病毒药物。 它具有抗病毒活性,有助于预防和治疗流感。 | |||
T17026 |
Tecovirimat
ST-246,特考韦瑞 |
Cysteine Protease | Proteases/Proteasome |
Tecovirimat 是一种核心蛋白半胱氨酸蛋白酶抑制剂,可能用于治疗天花感染。Tecovirimat 是一种新型抗病毒药物,对多种正痘病毒具有有效和选择性的活性(EC50:约 10 nM)。通过靶向病毒 p37 蛋白直系同源物来抑制正痘病毒的排出。迄今为止,Tecovirimat 已在所有小动物和非人类灵长类动物预防和治疗痘病毒引起的疾病模型中显示出功效。 | |||
T78455 |
Ru(bpy)2(mcbpy-O-Su-ester)(PF6)2
|
||
Ru(bpy)2(mcbpy-O-Su-ester)(PF6)2 是一款钌基化合物,既可作为量子点 (QDs) 荧光猝灭剂,也适用于捕获病毒抗原EV71的探针。此外,该化合物还用于作为灵敏的电致化学发光 (ECL) 试剂,用于基质金属蛋白酶 (MMP)[2] 的检测。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN1059 |
Ganoderic acid B
|
IL Receptor; HIV Protease; JAK; STAT | Angiogenesis; Chromatin/Epigenetic; Immunology/Inflammation; JAK/STAT signaling; Microbiology/Virology; Proteases/Proteasome; Stem Cells |
Ganoderic acid B 是从灵芝中分离的一种三萜类天然产物。它是端粒酶抑制剂,抑制 Epstein-Barr 病毒抗原的活化。它是 HIV-1 蛋白酶抑制剂。 | |||
T4S0998 |
Trifolirhizin
红车轴草根甙/三叶豆紫檀苷,三叶豆紫檀苷 |
TNF; Tyrosinase | Apoptosis; Proteases/Proteasome |
Trifolirhizin 是一种从苦参根中分离出的 pterocarpan 黄酮类化合物。它具有酪氨酸酶高抑制活性,IC50=506 μM。它具有抗炎和抗癌的潜能。 | |||
T1664 |
Meglutol
Dicrotalic acid,3-Hydroxy-3-methylglutaric acid,美格鲁托 |
Endogenous Metabolite; HMG-CoA Reductase; Autophagy | Autophagy; Metabolism |
Meglutol (3-Hydroxy-3-methylglutaric acid) 是一种抗血脂剂,可降低胆固醇、甘油三酯、血清 β-脂蛋白和磷脂。它抑制胆固醇生物合成中的限速酶羟甲基戊二酰辅酶 A 还原酶的活性。 | |||
T5687 |
WITHAFERIN A
醉茄素 A,醉茄素A |
Ferroptosis; NF-κB | Apoptosis; NF-κB |
Withaferin A 是从南非醉茄中分离到的一种甾体内酯,是内皮蛋白 C 受体脱落抑制剂,可以抑制NF-kB 的活性,具有抗炎,抗肿瘤等作用。它是一种新型 NFkappaB 抑制剂,有望成为治疗各种炎症性疾病和癌症的新型抗炎药。 | |||
T2770 |
Gentiopicroside
Gentiopicrin,龙胆苦甙,龙胆苦苷 |
P450; HCV Protease | Metabolism; Microbiology/Virology; Proteases/Proteasome |
Gentiopicroside (Gentiopicrin) 是天然环烯醚萜苷,具有抗炎和抗氧化活性。它抑制P450的活性,对 CYP2A6 的 IC50和 Ki 值分别为 61 µM 和 22.8 µM, | |||
T3233 |
Sophoricoside
Genistein sophoricoside,槐苷 |
Others | Others |
Sophoricoside (Genistein sophoricoside) 是一种异黄酮糖苷,从槐花中分离得到,具有抗炎,抗癌和免疫抑制作活性。 | |||
T2786 |
Oxysophocarpine
氧化槐树碱,氧卡地平 |
Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation |
Oxysophocarpine 是提取自海藻的生物碱。它抑制口腔鳞状细胞癌的生长和转移。它对中枢神经系统和周围神经系统具有神经保护作用和抗伤害感受作用。 | |||
TQ0089 |
Juglanin
|
Apoptosis; JNK; Autophagy | Apoptosis; Autophagy; MAPK |
Juglanin 是来自金鸡脚的一种黄酮类天然产物,是一种 JNK 的激活剂,能诱导人乳腺癌细胞的凋亡和自噬,具有炎症和抗肿瘤活性。 | |||
T6S0232 |
Eriodictyol
圣草酚,Huazhongilexone |
Influenza Virus; DNA/RNA Synthesis; Nrf2; Endogenous Metabolite | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Immunology/Inflammation; Metabolism; Microbiology/Virology |
Eriodictyol (Huazhongilexone) 是从中草药中得到的一种黄酮类天然产物,具有抗氧化、抗炎和抗糖尿病作用。它还是一种流感依赖 RNA 的RNA 聚合酶抑制剂,IC50为 18 nM。它可诱导Nrf2信号通路。 | |||
TN1108 |
Kaempferol 3-O-sophoroside
槐角黄酮苷,Kaempferol 3-O-beta-sophoroside,山奈酚-3-O-β-D-槐糖苷 |
Anti-infection | Microbiology/Virology |
Kaempferol 3-O-sophoroside (Kaempferol 3-O-beta-sophoroside) 是一种 Kaempferol 衍生物,从栽培山参 (Panax ginseng) 的叶子中分离得到,具有抗炎作用。 | |||
TN6709 |
6,7-DIMETHOXY-3,4-DIHYDRO-2H-ISOQUINOLIN
|
Others | Others |
6,7-DIMETHOXY-3,4-DIHYDRO-2H-ISOQUINOLIN 是一种从毛豆中分离出来的天然产物。 | |||
T6S1768 |
Narcissin
水仙苷,Isorhamnetin 3-Rutinoside,Narcissoside |
Antioxidant | oxidation-reduction |
Narcissin (Isorhamnetin 3-Rutinoside) 是一种黄连糖苷,能够清除 ONOO-(IC50:3.5 μM)和 SIN-1 衍生的 ONOO-(IC50:9.6 μM),具有抗氧化作用。 | |||
TN1327 | 7,22,25-Stigmastatrienol | Others | Others |
7,22,25-Stigmastatrienol is a natural product | |||
TN2223 |
Soyacerebroside I
大豆脑苷 I |
IL Receptor; NOS; COX | Immunology/Inflammation; Neuroscience |
Soyacerebroside I demonstrates a potent tyrosinase inhibitory activity. | |||
TN4515 |
Melilotigenin C
|
Others | Others |
Melilotigenin C是一种天然产物,属于豆科草木樨属,其产品编号为 TN4515,CAS号为 188970-21-0。Melilotigenin C可用作对照参考。 | |||
T32551 | Lamprolobine | ||
Lamprolobine is a bioactive chemical. | |||
TN4425 |
Lehmannine
Lemannine |
Others | Others |
Lehmannine是一种天然产物,属于豆科厚果槐属,其产品编号为 TN4425,CAS号为 58480-54-9。Lehmannine可用作对照参考。 | |||
TN1347 |
8-Prenylkaempferol
去甲脱水淫羊藿黄素 |
p38 MAPK; NF-κB; PI3K | MAPK; NF-κB; PI3K/Akt/mTOR signaling |
8-Prenylkaempferol is an effective agent for attenuating pro-inflammatory NO induction, it may be an anti-inflammatory agent for suppressing influenza A virus-induced RANTES production acts by blocking PI3K-mediated transcriptional activation of NF-κB and | |||
T2S0118 | Daurinoline | Calcium Channel; 5-HT Receptor; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism; Neuroscience |
Daurinoline is a non-competitive antagonist, it exerts marked relaxation effect on basilar artery of rabbits through non-competitive antagonism, it would have a protective function on microcirculation of cerebral pia mater, which may be beneficial to relieve cerebral ischemic injury. Daurinoline could significantly reverse noradrenaline induced constriction of pial arterioles and venules, and increase the number of blood vessels which were decreased by noradrenaline. | |||
TN5139 |
Thalifoline
|
Antifection | Microbiology/Virology |
Thalifoline shows antifungal activity, with 100 ug against Fusarium oxysporum f. sp. lycopersici. | |||
TN1158 |
(-)-Sparteine
Sparteine,(-)-Lupinidine,鹰爪豆碱 |
Others | Others |
Sparteine is a natural product | |||
TQ0072 |
Warangalone
Scandenolone,攀登鱼藤异黄酮 |
PKA | Tyrosine Kinase/Adaptors |
Warangalone is an anti-malarial compound that can inhibit the growth of both strains of parasite 3D7 (chloroquine-sensitive) and K1 (chloroquine-resistant) with IC50s of 4.8 μg/mL and 3.7 μg/mL, respectively. | |||
TN6686 |
Cyclo(Pro-Pro)
|
||
Cyclo(Pro-Pro) tasted bitter.Verpacamides A-D, a sequence of C11N5 diketopiperazines relating cyclo(Pro-Pro) to cyclo(Pro-Arg), from the marine sponge Axinella vaceleti is possible biogenetic precursors of pyrrole-2-aminoimidazole alkaloids. | |||
TMA0132 | Dihydrophaseic acid | Others | Others |
Dihydrophaseic acid 3'-O-b-D-glucopyranoside (D3G) can increase the proliferation and differentiation of osteoblast cells and enhance bone formation, suggests that D3G may be a good candidate for the treatment of osteoporosis. |