109
56
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T4316 |
ML365
|
Potassium Channel | Membrane transporter/Ion channel |
ML365 是有效的,选择性的双孔结构域钾通道TASK1/KCNK3抑制剂,IC50为 4 nM。它可用于检查 TASK1 通道的特定作用。 | |||
T0280 |
Spiperone
螺哌隆,Spiroperidol,Spiropitan |
Dopamine Receptor | GPCR/G Protein; Neuroscience |
Spiperone (Spiropitan) 是多巴胺 D2、血清素5-HT1A 和血清素5-HT2A 拮抗剂。它是广泛使用的药理学工具。它具有研究神经系统疾病的潜力。 | |||
TP1088 |
N-Acetylcarnosine
N-Acetyl-L-carnosine,N-乙酰肌肽 |
Others | Others |
N-Acetylcarnosine (N-Acetyl-L-carnosine) 是一种含有组氨酸的天然二肽,是药理学上主要的 L-carnosine 的来源。它是一种眼科药物,对人类白内障具有潜在的应用价值。 | |||
T12146 |
N-Desmethyl-Apalutamide
N-Desmethyl Apalutamide,N-去甲基阿帕鲁胺杂质 |
P450; Androgen Receptor | Endocrinology/Hormones; Metabolism |
N-Desmethyl-Apalutamide 是一种 Apalutamide 的活性代谢产物,主要由 CYP2C8 和 CYP3A4 介导形成。它是一种低活性的雄激素受体拮抗剂,其作用力是 Apalutamide 活性的三分之一。它是中等至强的CYP3A4和CYP2B6诱导剂,并具有优异的血浆蛋白结合浓度。 | |||
T15233 |
Endovion
NS3728 |
Chloride channel | Membrane transporter/Ion channel |
Endovion (NS3728) 是阴离子通道抑制剂 和 Anoctamin-1 (ANO 1) 通道抑制剂,也是特异性的 VRAC/VSOAC 阻断剂。 | |||
T22416 |
RO495
CS-2667 |
Tyrosine Kinases; JAK | Angiogenesis; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells; Tyrosine Kinase/Adaptors |
RO495 (CS-2667) 是一种有效的非受体酪氨酸蛋白激酶2抑制剂。 | |||
TN6963 |
Hentriacontane
|
NF-κB | NF-κB |
Hentriacontane 是一种天然产物,具有多种药理作用,包括抗炎、抗肿瘤和抗菌活性。 | |||
T11016 |
DGAT-1 inhibitor 2
|
Transferase | Metabolism |
DGAT-1 inhibitor 2是有效的DGAT-1抑制剂,具有减肥功效。 | |||
T24932 |
Vatanidipine
AE-0047,AE 0047,AE0047 |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Vatanidipine (AE0047) 是一种新型的双氢吡啶(DHP)型钙通道阻滞剂,具有缓慢起效的药理作用。在各种实验性高血压模型中观察到缓慢起效和持久的降压作用。 | |||
T0797 |
Cimetidine
西米替汀,SKF-92334,西咪替丁 |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Cimetidine (SKF-92334) 是一种可口服的可逆组胺H2受体拮抗剂,Ki 为 0.6 μM。它抑制胃酸分泌,以及胃蛋白酶和胃泌素的输出,具有抗癌和抗炎活性。 | |||
T1540 |
Doxepin hydrochloride
Toruan,Doxepin HCl,Aponal,Novoxapin,盐酸多塞平 |
P450; Dopamine Receptor; 5-HT Receptor; Adrenergic Receptor; AChR; Norepinephrine; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Metabolism; Neuroscience |
Doxepin hydrochloride (Aponal) 是一种可口服的三环抗抑郁剂,是选择性组胺受体 H1拮抗剂。它也是 CYP450抑制剂,抑制 CYP450 2C19和 CYP450 1A2。 | |||
T12654 |
(Rac)-Acolbifene
(Rac)-EM-652,EM-343,阿考比芬 |
Estrogen Receptor/ERR | Endocrinology/Hormones |
(Rac)-Acolbifene (EM-343) 是 Acolbifene 的外消旋形式。Acolbifene 是一种 estrogen receptor 拮抗剂。(Rac)-Acolbifene 显示出抗雌激素和雌激素活性。 (Rac)-Acolbifene 包含哌啶环,显示出良好的药理作用,RBA=380。 | |||
T5159 |
Olodaterol hydrochloride
BI-1744 HCl,盐酸奥达特罗,BI 1744 hydrochloride |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Olodaterol hydrochloride (BI-1744 HCl) 是一种长效的、选择性 β2-adrenoceptor(β2-AR) 激动剂 (EC50=0.1 nM;pKi= 9.14 for human β2-adrenoceptor),可用于慢性阻塞性肺疾病 (COPD) 和肺纤维化的研究。 | |||
T21777 |
VU0359595
VU0359595-1,CID-53361951,ML-270 |
Phospholipase | Metabolism |
VU0359595 (ML-270)是一种选择性磷脂酶 D1 (PLD1) 抑制剂,IC50 值为 3.7 nM。VU0359595 对 PLD1 的选择性比 PLD2 (IC50=6.4 μM) 高 1700 倍以上。VU0359595 可用于癌症、糖尿病、神经退行性疾病和炎性疾病等疾病研究。 | |||
T67917 |
ML353
VU0478006 |
Potassium Channel | Membrane transporter/Ion channel |
ML353 (VU0478006)是 TREK-1和 TREK-2的选择性激活剂,是 mGlu5 沉默变构调节剂 (SAM) 的选择性配体(Ki =18.2 nM)。 ML353 有作为解决 SAM 体内固有活性或药物阻断的潜力。 | |||
T4688 |
Pipequaline hydrochloride
PK-8165 hydrochloride,盐酸哌夸林 |
GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
Pipequaline hydrochloride (PK-8165 hydrochloride) 是一种苯二氮卓受体部分激动剂,有抗焦虑作用。 | |||
T14978 |
CL-82198
|
MMP | Proteases/Proteasome |
CL-82198 是 MMP-13选择性抑制剂。它能够与 MMP-13 的整个 S1' 口袋结合,这是其对 MMP-13 选择性和对其他 MMP 缺乏抑制活性的基础。它可用于研究骨关节炎。 | |||
T21720 |
GP-82996
Cdk4/6 Inhibitor IV,CINK4 |
CDK | Cell Cycle/Checkpoint |
GP-82996 (CINK4) (CINK4) 是 CDK4/6的药理学抑制剂。GP-82996 对 CDK4/cyclin D1、CDK6/cyclin D1 和 Cdk5/p35 的 IC50s 分别为 1.5、5.6 和 25 μM。GP-82996 诱导肿瘤细胞 U2OS 的凋亡,可用于癌症研究。 | |||
T35028 |
Valiglurax
VU2957,VU 0652957,VU 2957,VU-0652957,VU0652957,VU-2957 |
GluR | Neuroscience |
Valiglurax (VU2957),也称为 VU0652957和 VU2957,是一种强效、选择性、中枢神经系统渗透剂,可口服生物利用的 mGlu4正变构调节剂。VU2957具有良好的跨物种的体内外药理学和药代动力学性质。VU2957被评估为治疗帕金森病的临床前开发候选药物。 | |||
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。 | |||
T0455 |
Clozapine
氯氮平,HF 1854,LX 100-129 |
Dopamine Receptor; Adrenergic Receptor; AChR | GPCR/G Protein; Neuroscience |
Clozapine (HF 1854) 是一种三环二苯二氮卓类药物,属于非典型抗精神病药物。它结合几种类型的中枢神经系统受体,并显示出独特的药理学特征。 它是一种血清素拮抗剂,与 5-HT 2A/2C 受体亚型具有强结合力。它还对几种多巴胺能受体表现出很强的亲和力,但对多巴胺 D2 受体仅表现出较弱的拮抗作用,这种受体通常被认为可调节精神抑制活性。 | |||
T1787 |
Levobupivacaine
|
Sodium Channel | Membrane transporter/Ion channel |
Levobupivacaine 是一种氨基酰胺类局麻药,属于n-alkylsubstituted pipecoloxylidide 家族。它是bupivacaine 的 S-对映异构体。 | |||
Fr13587 |
7-Chloro-4-(piperazin-1-yl)quinoline
|
||
7-Chloro-4-(piperazin-1-yl)quinolone 结构是药物化学中的重要支架,它单独或与其他活性药效团混合显示出多种药理特性。7-Chloro-4-(piperazin-1-yl)quinolone 是有效的sirtuin 抑制剂,并且抑制 5-羟色胺的摄取,IC50值为 50 μM。7-Chloro-4-(piperazin-1-yl)quinolone 对恶性疟原虫 D10 和 K1 菌株表现出抗疟疾活性,IC50分别为 1.18 μM 和 0.97 μM。 | |||
T36520 |
COR659
|
Cannabinoid Receptor; GABA Receptor | GPCR/G Protein; Membrane transporter/Ion channel; Neuroscience |
COR659 是一种有效的 GABAB 的阳性变构调节剂。COR659具有缓解大鼠对酒精和巧克力成瘾的作用。 | |||
T36008 |
Nebentan potassium
|
||
Nebentan potassium (YM598) is a potent, selective and orally active non-peptide endothelin ETA receptor antagonist through the modification of Bosentan . Nebentan potassium inhibits [125I] endothelin-1 binding to cloned human endothelin ETA and ETB receptor, with Ki of 0.697 nM and 569 nM, respectively[1]. YM598 can ameliorate the progression of cor pulmonale and myocardial infarction in vivo[2]. Nebentan potassium inhibits the specific binding of [125I] endothelin-1 to endothelin ETA and ETB re... | |||
T14940 |
CGP11952
|
Others | Others |
CGP11952 is same the benzodiazepines in its pharmacological action and it also is an experimental benzodiazepine derivative. | |||
T31178 |
Dabequin
dabechin,G 800 |
||
Dabequin is a derivative of aminoquinoline. It is said to have pharmacological activity against Plasmodium fukiparum. | |||
T23710 | Watanidipine dihydrochloride | ||
Watanidipine dihydrochloride is a novel dihydropyridine (DHP)-type calcium channel blocker with slow-onset pharmacological actions. | |||
T20492 |
Tetragastrin
Cholecystokinin tetrapeptide,Gastrin tetrapeptide |
||
Tetragastrin is the C-terminal tetrapeptide of gastrin. It has the same physiological and pharmacological activity as gastrin. | |||
T29533 |
ABT-866
ABT 866,A 286666 |
||
ABT-866 is a novel alpha-adrenoceptor agent with mixed pharmacological properties. | |||
T28822 |
SNAP 398299
SNAP-398299,SNAP398299 |
||
SNAP 398299, a galanin receptor antagonist, is a potential novel pharmacological treatment for mood disorders. | |||
T23628 |
AD-2646
AD2646 |
||
AD-2646 is a new quinoline derivative. It also has similar pharmacological properties to tricyclic antidepressants. | |||
T19182 |
Afegostat D-Tartrate
Isofagomine D-Tartrate,D-Isofagomine D-Tartrate |
Others | Others |
Afegostat D-Tartrate is a pharmacological chaperone that specifically and reversibly binds acid-β-glucosidase (GCase) in the endoplasmic reticulum with high affinity. | |||
T25542 |
Isamfazone
Isamfazona,Isamfazonum |
||
Isamfazone is utilized in the chemical and pharmacological studies on substituted pyridazones, the discovery of novel anti-inflammatory agents by aligning screening. | |||
T11893L |
Lurasidone metabolite 14326 hydrochloride
Lurasidone metabolite 14326 hydrochloride (186204-33-1 free base) |
Others | Others |
Lurasidone metabolite 14326 hydrochloride, an active metabolite of the atypical antipsychotic Lurasidone, maintains its significant function in pharmacological efficacy. | |||
T71600 | Benazoline oxalate salt | ||
Benazoline oxalate salt is a pharmacological active compound that inhibits casein kinase Iε (CKIε) or CKIδ phosphorylation of the PER2 protein. | |||
T19181 |
Afegostat
D-Isofagomine,Isofagomine |
Others | Others |
Afegostat is a pharmacological chaperone that specifically and reversibly binds acid-β-glucosidase (GCase) in the endoplasmic reticulum with high affinity. | |||
T68749 |
EBOV-IN-C31
|
||
EBOV-IN-C31 is a novel PP1-targeting Ebola Virus (EBOV) inhibitor with improved pharmacological properties. | |||
T30489 |
BMS 181101
BMS181101,BMS-181101 |
||
BMS-181101 is a novel antidepressant that has pharmacological characteristics as a serotonin reuptake inhibitor and a serotonin 5-HT receptor agonist. | |||
T22975 |
Methyl α-Linolenyl Fluorophosphonate
|
Others | Others |
Methyl α-Linolenyl Fluorophosphonate is an inhibitor of phospholipases. Methyl α-Linolenyl Fluorophosphonate (MLnFP), an analog of methyl Arachidonyl Fuorophosphonate (MAFP), has not been completely investigated for its pharmacological activity. | |||
T34819 |
Tetragastrin HCl
Trp-Met-Asp-Phe hydrochloride,Tetragastrin hydrochloride |
||
Tetragastrin HCl is the HCl salt of Tetragastrin, the C-terminal tetrapeptide of gastrin. It has the same physiological and pharmacological activity as gastrin. | |||
T33607 |
NBI-34041
NBI34041,SB 723620,SB-723620,SB723620 |
||
NBI-34041 is an effective and high-affinity CRF1 receptor antagonist that effectively reduces endocrine responses to CRF(1) receptor-mediated pharmacological and behavioral challenges. | |||
T23653 |
Afegostat HCl
Afegostat,AT-2101,Afegostat hydrochloride,AT2101 |
||
Afegostat is an acid β-glucosidase (GCase) active site inhibitor that acts as a pharmacological chaperone. Afegostat inhibits GCase with K(i) ~30 nM for wild-type and mutant enzymes. Afegostat was an experimental drug for the treatment of certain forms of | |||
T39795 |
Tricarbonyldichlororuthenium(II) dimer
CORM-2 |
||
Tricarbonyldichlororuthenium(II) dimer, a pharmacological CO donor, prevents ischemia/reperfusion (I/R)-induced oxidative damage to the gastric mucosa by enhancing gastric blood flow (GBF) and reducing DNA oxidation and systemic inflammatory response. | |||
T75002 | Antidepressant agent 3 | ||
Antidepressant agent 3, 一种具有口服活性的抗抑郁剂,具备抗抑郁、抗焦虑、性能增强及促智活性。 | |||
T68257 |
Hydromethylthionine HBr
|
||
Hydromethylthionine, also known as LMTM and Leucomethylene Blue, is a apotent tau aggregation inhibitor for the treatment of Alzheimer's disease (AD) and frontotemporal dementia. Hydromethylthionine showed pharmacological activity on brain structure and function as both monotherapy and as an add-on to symptomatic treatment in certain patients with Alzheimer’s disease. | |||
T78564 |
Depramine
GP 31406 |
||
Depramine (GP 31406) 是三环抗抑郁剂,具药理活性。该化合物可抑制乙酰胆碱酯酶、Mg2+-ATPase 与 Na+/K+ ATPase 活性。 | |||
T71160 |
Levomepromazine HCl
|
||
Levomepromazine HCl is a phenothiazine with pharmacological activity similar to that of both CHLORPROMAZINE and PROMETHAZINE. It has the histamine-antagonist properties of the antihistamines together with CENTRAL NERVOUS SYSTEM effects resembling those of chlorpromazine. | |||
T76572 |
Acetyl neurotensin (8-13)
|
||
Acetyl neurotensin (8-13) 是神经降压素类似物,具有完全结合和药理活性。 | |||
T68822 |
Tyrphostin AG17
|
||
Tyrphostin AG17 is a biochemical that promotes adipocyte apoptosis in vivo and is an effective modulator of adipocyte differentiation and WAT hypertrophy in vitro and in vivo. It is thought to possibly be useful as a pharmacological obesity treatment. It is a tyrosine kinase antagonist that has also been found to inhibit tumor cell growth. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T5722 |
Nevadensin
Pedunculin,石吊兰素,5,7-二羟基-6,8,4'-三甲氧基黄酮 |
Anti-infection; Antibacterial | Microbiology/Virology |
Nevadensin 是一种重要的草本成分,可抑制雌二醇的生物活化。 它具有抗结核分枝杆菌、镇咳、抗炎、抗高血压等多种药理作用。 | |||
T4104 |
Ophiopojaponin C
麦冬皂苷C,Ophiopogonin C |
Others | Others |
Ophiopogonin C' pharmacological activities may be related to the substances in nucleus mainly. | |||
T2891 |
Ammonium glycyrrhizinate
Glycamil,Monoammonium glycyrrhizinate,Ammonium Glycyrrhizate,甘草酸单胺,Monoammonium glycyrrhizinate hydrate,Glycyrram |
Others | Others |
Ammonium glycyrrhizinate (Glycyrram) 具有抗炎、抗胃溃疡、抗过敏、抗肝炎等药理功能。 | |||
T3S1251 |
Neoruscogenin
|
ROR | Metabolism |
Neoruscogenin 是甾体 sapogenin 家族的成员,是一种可生物利用且具有高亲和力的核受体RORα (NR1F1)激动剂。 | |||
T4878 |
Hecogenin
海柯吉宁,Hocogenin |
Others; Antifungal | Microbiology/Virology; Others |
Hecogenin (Hocogenin), a steroid saponin derived from Agave sisalana, serves as a specific inhibitor for human UDP-glucuronosyltransferases. Notably, it exhibits a broad range of pharmacological activities, such as anti-inflammatory, antifungal, and gastroprotective effects[1]. | |||
T7324 |
Chelidonine hydrochloride
|
Others | Others |
Chelidonine hydrochloride 是 Chelidonium majus 的生物碱之一,具有广泛的药理活性。 | |||
TN7030 |
Heteroclitin G
|
Others | Others |
Heteroclitin G 被发现是 KIS 补血活性的潜在生物标志物,定量分析为进一步药理研究提供了研究基础。 | |||
T7443 |
4'-Methoxychalcone
4'-甲氧基查耳酮,4'-甲氧基查尔酮 |
PARP; PPAR | Chromatin/Epigenetic; DNA Damage/DNA Repair; Metabolism |
4'-Methoxychalcone 通过PPARγ活化调节脂肪细胞分化,并调节参与胰岛素敏感性的脂肪组织中各种脂肪因子的表达和分泌,具抗肿瘤和抗炎活性。 | |||
TQ0264 |
Nigakinone
苦木酮碱,苦木酮 |
Others | Others |
Nigakinone 是一种苦木中含量丰富的生物碱,具有重要的药理活性。 | |||
T3O2709 |
Bronze Red
808猩红,Scarlet 808 |
Others | Others |
Bronze Red 属于酰胺类有机物,可用于含量测定、鉴定、药理实验等。 | |||
T2837 |
Chrysin
5, 7-Dihydroxyflavone,NSC 407436,白杨素,5,7-Dihydroxyflavone |
Estrogen Receptor/ERR; Antioxidant | Endocrinology/Hormones; oxidation-reduction |
Chrysin (5,7-Dihydroxyflavone) 是一种雌激素阻断剂。 | |||
T2718 |
Palmatine chloride
|
Others; Indoleamine 2,3-Dioxygenase (IDO); Aurora Kinase | Cell Cycle/Checkpoint; Chromatin/Epigenetic; Metabolism; Others |
Palmatine chloride 是口服具有活力的不可逆 IDO-1抑制剂。它能够减轻结肠损伤,预防肠道菌群失调和调节色氨酸分解代谢,并改善 DSS 诱发的结肠炎。 | |||
T5749 |
10-Deacetyl-7-xylosyl paclitaxel
10-Deacetyl-7-xylosyltaxol,10-Deacetyltaxol 7-Xyloside,7-Xylosyl-10-deacetyltaxol,7-木糖甙-10-脱乙酰基紫杉醇,10-Deacetylpaclitaxel 7-Xyloside |
Others; Microtubule Associated | Cytoskeletal Signaling; Others |
10-Deacetyl-7-xylosyl paclitaxel (7-Xylosyl-10-deacetyltaxol) 是一种紫杉醇衍生物,具有改进的药理特性和更高的水溶性,用于治疗癌症。 | |||
T3362 |
Eupatilin
NSC 122413,异泽兰黄素 |
PPAR; Autophagy | Autophagy; DNA Damage/DNA Repair; Metabolism |
Eupatilin (NSC-122413) 是一种从青蒿中提取的黄酮,是一种 PPARα 激动剂,具有药理活性。 | |||
T5S1882 |
Songorine
准葛尔乌头碱,Napellonine,Zongorine,Bullatine G |
Others; GABA Receptor | Membrane transporter/Ion channel; Neuroscience; Others |
Songorine (Napellonine) 是从乌头属中分离出的一种二萜生物碱,具有抗癌、抗心律不齐和抗炎活性。它是大鼠脑中的GABAA 受体拮抗剂,有用于上皮性卵巢癌的研究潜力。 | |||
T2866 |
Echinocystic acid
|
Apoptosis; Antioxidant; Reactive Oxygen Species | Apoptosis; Immunology/Inflammation; Metabolism; NF-κB; oxidation-reduction |
Echinocystic acid 是从皂角的果实中提取出来的一种五环三萜,有抗氧化,抗炎症和抗肿瘤作用。 | |||
T4S1659 |
Xanthotoxol
8-Hydroxypsoralen,8-Hydroxyfuranocoumarin,Psoralen,花椒毒酚,8-Hydroxypsoralene |
Reactive Oxygen Species; 5-HT Receptor; Endogenous Metabolite | GPCR/G Protein; Immunology/Inflammation; Metabolism; Neuroscience; NF-κB |
Xanthotoxol (Psoralen) 是一种具有生物活性的线性呋喃香豆素,具有很强的抗炎、抗氧化、5-HT 拮抗和神经保护作用等药理活性。 | |||
T0595 |
Naringin
Naringoside,柚皮苷 |
Mitophagy; P450; Endogenous Metabolite; Autophagy | Autophagy; Metabolism |
Naringin (Naringoside) 是一种黄烷酮糖苷,有抗氧化活性、降血脂、抗癌和抑制细胞色素P450酶的药理作用。 | |||
TN1966 |
N-(3-Methoxybenzyl)Oleamide
N-Benzyloleamide,MAC 18:1 |
Antioxidant | oxidation-reduction |
N-(3-Methoxybenzyl)Oleamide (MAC 18:1) 是一种从 Lepidium meyenii 中分离出来的玛瑙酰胺,对运动引起的疲劳具有药理作用,可能与调节能量代谢和改善抗氧化状态有关。 | |||
T5737 |
euphol
|
Others; Lipase; Endogenous Metabolite | Metabolism; Others |
Euphol 是从Euphorbia tirucalli 的汁液中分离出来的四环三萜醇,具有抗炎和免疫调节作用,口服具有活力。 它通过能够逆机制抑制单酰基甘油脂肪酶 (MGL) 的特性,IC50=315 nM。 外周 MGL 抑制能够调节内源性大麻素系统从而阻止炎症性疼痛的发展。 | |||
T3373 |
Columbianadin
Zosimin,2-Butenoic acid,二氢欧山芹醇当归酸酯 |
Apoptosis | Apoptosis |
Columbianadin (Zosimin) 是来自当归的根的主要生物活性成分之一,是一种天然香豆素,具有抗炎和抗癌作用。 | |||
TN1046 |
Murrayone
|
Others | Others |
Murrayone 是一种提取自M. paniculata 中的含有香豆素的化合物。Murrayone 具有独特的药理特性,可用作防止癌症转移的化学预防剂。 | |||
T2817 |
Picroside II
胡黄连苷II,Vanilloyl catalpol,6-Vanilloylcatalpol,胡黄连苦苷II |
Apoptosis; Others; Influenza Virus; NF-κB; Reactive Oxygen Species | Apoptosis; Immunology/Inflammation; Metabolism; Microbiology/Virology; NF-κB; Others |
Picroside II (Vanilloyl catalpol) 是从胡黄连提取的一种环烯醚萜类,有神经保护作用,具有抗氧化、抗炎、抗细胞凋亡、免疫调节和抗病毒等药理活性。 | |||
TN1714 |
Grosvenorine
罗汉果黄素,Grosvenorin |
Antibacterial | Microbiology/Virology |
Grosvenorine (Grosvenorin) 具有良好的抗菌和抗氧化活性,是罗汉果中主要的黄酮类物质。 | |||
T2746 |
Sophocarpine monohydrate
槐果碱,Sophocarpine,槐果碱水合物 |
Apoptosis; Influenza Virus; Akt; PI3K; AMPK; Autophagy | Apoptosis; Autophagy; Chromatin/Epigenetic; Cytoskeletal Signaling; Microbiology/Virology; PI3K/Akt/mTOR signaling |
Sophocarpine monohydrate 是从传统草药苦参中提取的一种重要生物碱,具有抗肿瘤活性,可用于肝细胞癌,前列腺癌和结肠直肠癌。苦参具有抗病毒,抗肿瘤和抗炎等多种药理作用。 | |||
T6S1101 |
Astragalin
Kaempferol 3-D-glucoside,Kaempferol 3-O-glucoside,kaempferol-3-glucoside,3-Glucosylkaempferol,Astragaline,紫云英苷,Kaempferol 3-β-D-glucopyranoside |
Apoptosis; NF-κB | Apoptosis; NF-κB |
Astragalin (Kaempferol 3-O-glucoside) 是一种具有生物活性的天然黄酮类化合物。 它具有多种药理特性,包括抗氧化、抗炎、抗癌、神经保护和心脏保护特性。 | |||
T3920 |
Pseudoginsenoside F11
Ginsenoside A1,拟人参皂苷 F11,拟人参皂苷F11 |
Others; Endogenous Metabolite | Metabolism; Others |
Pseudoginsenoside F11 (Ginsenoside A1) 从人参根和叶中分离得到。PF11在一系列心血管和中枢神经系统疾病中具有广泛的保护作用。 | |||
T3S1250 |
Ophiogenin 3-O-α-L-rhamnopyranosyl-(1→2)-β-D-glucopyranoside
麦冬苷元-3-O-Α-L-吡喃鼠李糖基(1→2)-Β-D-吡喃葡萄糖苷,Ophiogenin-3-O-alpha-L-rhaMnopyranosyl-(1->2)-beta-D-glucopyranoside |
Others | Others |
Ophiogenin 3-O-α-L-rhamnopyranosyl-(1→2)-β-D-glucopyranoside (Ophiogenin-3-O-alpha-L-rhaMnopyranosyl-(1->2)-beta-D-glucopyranoside) 是一种从麦冬根中取得的萜类糖苷,对心血管系统有良好的药理作用。 | |||
T8250 |
2,6,6-Trimethyl-2,4-cycloheptadien-1-one
|
Others | Others |
2,6,6-Trimethyl-2,4-cycloheptadien-1-one 是一种萜类化合物,存在于许多植物中,包括香菜、莳萝和芹菜。它是精油的重要成分,具有多种药用和药理特性。 | |||
T1716 |
Echinacoside
|
Reactive Oxygen Species; Wnt/beta-catenin | Cytoskeletal Signaling; Immunology/Inflammation; Metabolism; NF-κB; Stem Cells |
Echinacoside 是一种从Cistanche salsa 中分离的苯乙醇类化合物,抑制Wnt/β-catenin 信号通路。它能够激活 Trk 受体及其下游信号通路而起到神经保护作用,还具有显著的抗骨质疏松作用。 | |||
T1516 |
Curcumin
Diferuloylmethane,Natural Yellow 3,姜黄素,Indian Saffron,Turmeric yellow |
Mitophagy; Epigenetic Reader Domain; Ferroptosis; Influenza Virus; Nrf2; Histone Acetyltransferase; HDAC; Autophagy | Apoptosis; Autophagy; Chromatin/Epigenetic; DNA Damage/DNA Repair; Immunology/Inflammation; Microbiology/Virology |
Curcumin (Natural Yellow 3) 属于酚类天然产物,是一种组蛋白乙酰化转移酶 p300/CREB 的抑制剂 (IC50=25 μM),具有特异性。Curcumin 具有抗肿瘤、抗炎和抗氧化等多种药理活性。 | |||
T2729 |
Scoparone
滨蒿内酯,Escoparone,Scoparon,Aesculetin dimethyl ether,6,7-dimethoxycoumarin,6,7-Dimethylesculetin |
Others | Others |
Scoparone (Aesculetin dimethyl ether) 是分离自毛蒿中,具有抗凝血,抗血管舒张作用和抗炎活性。 | |||
T5764 |
Alliin
蒜氨酸,(S)-3-(Allylsulphinyl)-L-alanine |
NF-κB; PPAR | DNA Damage/DNA Repair; Metabolism; NF-κB |
Alliin ((S)-3-(Allylsulphinyl)-L-alanine) 是一种从大蒜中提取的亚砜化合物,具有口服活性,表现出降血糖、抗氧化和抗炎特性。 | |||
T6677 |
Sophocarpine
|
ERK; p38 MAPK; NF-κB; TLR; COX; HER; JNK; STAT | Angiogenesis; Immunology/Inflammation; JAK/STAT signaling; MAPK; Neuroscience; NF-κB; Stem Cells; Tyrosine Kinase/Adaptors |
Sophocarpine 是一种从传统草药苦参中提取的重要生物碱。苦参具有抗病毒、抗肿瘤和抗炎等多种药理作用。它通过多种机制显著抑制癌细胞的生长,具有抗肿瘤活性。 | |||
T2768 |
Saikosaponin A
柴胡皂苷A,柴胡皂苷 A |
NF-κB; Antibacterial; Liver X Receptor | Metabolism; Microbiology/Virology; NF-κB |
Saikosaponin A 是银柴胡中的主要活性成分,有抗炎活性,可上调 LXRα的表达。 | |||
T3030 |
L-Sophoridine
L-槐定碱,Sophoridine,Matridin-15-one |
Others | Others |
L-Sophoridine (Matridin-15-one) 一种从药用植物中提取的天然产物,具有多种药理作用,包括抗Y 作用,可在体外和体内选择性诱导多种人体Y 细胞凋亡;然而,其作用机制需要进一步阐述。 | |||
TN5888 |
Toddaculin
|
Others | Others |
Toddaculin 是一种天然香豆素,抑制过度的破骨细胞活性并增强成骨细胞分化和矿化。它可诱导白血病细胞分化和凋亡,具有抗炎活性。 | |||
T4749 |
Squalene
角鲨烯,Nikko Squalane EX,Super Squalene,AddaVax,all-trans-Squalene,trans-Squalene,Spinacene |
Reactive Oxygen Species; Endogenous Metabolite; Antifungal | Immunology/Inflammation; Metabolism; Microbiology/Virology; NF-κB |
Squalene (AddaVax) 是胆固醇合成的中间产物,具有降血脂、保肝、心脏保护、抗氧化和抗毒活性等多种药理特性。它还具有抗真菌活性,可用于毛癣菌治疗的相关研究。 | |||
T81907 | Lucenin 3 | ||
Lucenin 3,一种生物活性类黄酮,具备生物医学领域内的功能性特性。 | |||
T82318 | Ginsenoside Rs1 | ||
Ginsenoside Rs1为人参根中提取的一种人参皂苷类化合物。 | |||
T78504 |
Lavandoside
|
||
Lavandoside是一种活性化合物,源自薰衣草之花。 | |||
T81220 |
Salvileucantholide
|
||
Salvileucantholide为一种从S. leucantha中提取的二萜类化合物。 | |||
T38479 |
3-Hydroxypyridine
|
||
3-Hydroxypyridine, extracted from Bamboo grass, is a structural analogue of vitamin B6. It exhibits diverse pharmacological properties, including antioxidant activity. | |||
T83601 |
(+)-Diasyringaresinol
|
||
(+)-Diasyringaresinol 是从 Aquilaria agallocha 提取的一种木质素化合物。 | |||
T82336 |
Ganoderic acid T
|
||
Ganoderic acid T为ganoderma lucidum中的一种天然化合物。 | |||
TN6584 |
Pallidol
|
||
Pallidol is a potent and selective singlet oxygen quencher in aqueous systems, it may be used in singlet oxygen-mediated diseases as a pharmacological agent. | |||
T81055 | Szechenyin A | ||
Szechenyin A 是Gentianae Szechenyii Spray 成分中的一种化学化合物。 | |||
T81195 |
Schiarisanrin E
|
||
Schiarisanrin E (compound 5),一种从松台五味子分离出的木脂素。 | |||
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 | |||
T79948 |
Kadsurenin B
|
||
Kadsurenin B为PAF(platelet-activating factor)拮抗剂,展现出神经保护作用。该化合物在药理学领域显示出广泛的研究潜力,包括抗菌、抗炎、神经保护、抗氧化、抗血小板聚集、细胞毒性和抗寄生虫等效能。 | |||
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