56
82
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T37859 |
SY-640
|
Endogenous Metabolite | Metabolism |
SY-640 是一种乙酰胺衍生物,显示出有效的保肝作用。SY-640 可缓解由脂多糖和痤疮丙酸杆菌诱导的小鼠肝损伤。 | |||
T21785 |
AG957
|
Bcr-Abl | Angiogenesis; Cytoskeletal Signaling; Tyrosine Kinase/Adaptors |
Tyrphostin AG957 是一种酪氨酸激酶抑制剂,具有抗BCR/ABL 酪氨酸激酶活性。它能够抑制p210bcr/abl 酶活性 (IC50:2.9 μM)。 | |||
T8235 |
L-732138
|
Neurokinin receptor | GPCR/G Protein; Neuroscience |
L-732138 是选择性有效和竞争性神经激肽-1受体拮抗剂,IC50为 2.3 nM,可减轻痛觉过敏并具有抗肿瘤作用。它在克隆的人 NK-1受体中的效力比在克隆大鼠 NK-1受体中高 200 倍,比人类 NK-2 和 NK-3 受体高 1000 倍以上。 | |||
T2923 |
Apremilast
阿普斯特,CC-10004,阿普司特 |
Apoptosis; TNF; PDE | Apoptosis; Metabolism |
Apremilast (CC-10004) 是一种口服有效的磷酸二酯酶 4 抑制剂,IC50为 74 nM。它抑制脂多糖释放TNF-α,IC50为 104 nM。 | |||
T16501 |
PF-3644022
|
p38 MAPK; Serine Protease; MAPK | MAPK; Proteases/Proteasome |
PF-3644022 是可口服的,具有 ATP 竞争性的MAPKAPK2 (MK2)选择性抑制剂,IC50为 5.2 nM,Ki 为 3 nM。它有效抑制 TNFα 的产生并具有抗炎作用,还抑制 MK3 和 p38 调节/激活激酶,IC50分别为 53 和 5.0 nM。 | |||
T0947 |
Dexamethasone acetate
Dexamethasone 21-acetate,醋酸地塞米松,Dexamethason acetate,NSC 39471 |
Glucocorticoid Receptor; Mitophagy; IL Receptor; Annexin A; NOS; Antibacterial; Autophagy | Autophagy; Endocrinology/Hormones; GPCR/G Protein; Immunology/Inflammation; Microbiology/Virology |
Dexamethasone acetate (NSC 39471) 是一种糖皮质素类甾体,有抗炎和免疫抑制活性。它可研究眼部感染。 | |||
T21233 |
Dihydrolipoic acid
Reduced thioctic acid,Reduced lipoic acid,DHLA,USAF XR-12,6,8-Dihydrothioctic acid,二氢硫辛酸 |
Antioxidant | oxidation-reduction |
Dihydrolipoic acid (USAF XR-12) 是高效的抗氧化剂,对所有以氧为中心的自由基都有很强的清除能力。它在多种疾病中表现出抗炎特性。在 LPS 诱导的疾病行为大鼠中,它通过 ERK/Nrf2/HO-1/ROS/NLRP3 通路发挥预防作用。它还可以可用于抑郁症的研究。 | |||
T5101 |
BW-A 78U
BW-A78U |
PDE | Metabolism |
BW-A 78U 抑制 PDE4,其 IC50值为 3 μM。 | |||
TP1050L |
Murepavadin acetate(944252-63-5 free base)
|
Antibacterial; Antibiotic | Microbiology/Virology |
Murepavadin acetate(944252-63-5 free base) 是一种有效且特异性的抗生素,用于治疗由铜绿假单胞菌引起的细菌感染。 Murepavadin acetate 靶向脂多糖转运蛋白 D。 | |||
T11348 |
G907
|
Antibiotic | Microbiology/Virology |
G907 是一种具有选择性和有效性的小分子ATP 结合盒 (ABC) 转运蛋白 MsbA 的拮抗剂,具有杀菌活性,可将 MsbA 捕获在朝内的脂多糖中。 G907 对大肠杆菌 MsbA 有抑制作用, IC50 值为 18 nM。 | |||
T60472 |
GSK-3β inhibitor 12
|
GSK-3 | PI3K/Akt/mTOR signaling; Stem Cells |
GSK-3β inhibitor 12 是一种选择性 GSK-3β 的抑制剂。GSK-3β inhibitor 12 抑制 49.11% 25 μM 的 GSK-3β 的活性和37.11% 50 μM 的 GSK-3β 的活性。GSK-3β inhibitor 12 可用于研究有脂多糖诱导的帕金森。 | |||
T23636 |
Adenosine N1-oxide
ANO,1-Oxoadenosine,Adenosine N1 oxide,Adenosine, 1-oxide,腺苷氮氧化物 |
Immunology/Inflammation related | Immunology/Inflammation |
Adenosine N1-oxide (1-Oxoadenosine) 是在蜂王浆中发现的腺苷 N1-氧化物,可抑制活化的巨噬细胞分泌炎症介质,并降低脂多糖 (LPS) 诱导的内毒素休克的致死率。 | |||
T60396 |
JMS-053
|
Phosphatase | Metabolism |
JMS-053 是一种具有有效性和选择性的磷酸酶 DUSP3 抑制剂, 抑制 PTP4A3、 PTP4A1 、 PTP4A2 和 CDC25B,抑制癌细胞迁移和球体生长,避免血管内皮生长因子或脂多糖对微血管内皮屏障功能的破坏。 | |||
T73286 |
SRI-42127
|
HuR | Chromatin/Epigenetic |
SRI-42127 是一种新型 RNA 调节因子 HuR 的小分子抑制剂,抑制肿瘤生长,可减弱脂多糖诱导的神经炎症模型中的神经胶质活化,通过抑制神经炎症反应来减轻神经损伤后的神经性疼痛。 | |||
T4062 |
CAY10602
|
Sirtuin | Chromatin/Epigenetic; DNA Damage/DNA Repair |
CAY10602 是一种SIRT1激活剂,可剂量依赖性地抑制 THP-1 细胞中脂多糖对 TNF-α 的 NF-κB 依赖性诱导。 | |||
T24262 |
KL-1156
|
||
KL-1156 is an NF-κB inhibitor. It is also a lipopolysaccharide (LPS)-induced nitric oxide production inhibitor. | |||
T25846 | N-Acylkansosamine | ||
N-Acylkansosamine is a N-acylamino sugar isolated from trehalose-containing lipopolysaccharide antigens of Mycobacterium kansasii. | |||
T70354 |
E 5531
|
||
E 5531 is a novel synthetic lipopolysaccharide antagonist. | |||
T69210 | Chondrocurine | ||
Chondrocurine is a biochemical that Inhibits quick death of mice treated with bacillus Calmetta Guerin & elicited with lipopolysaccharide. | |||
T32948 |
Lumin
|
||
Lumin is a cyanine dye that enhances interleukin 12-dependent interferon gamma production by lipopolysaccharide-stimulated mouse splenocytes. | |||
T61157 |
ABAI-30
|
||
ABAI-30 is a highly potent and orally bioavailable anti-inflammatory compound that efficiently suppresses nitric oxide (NO) production in lipopolysaccharide (LPS) activated RAW264.7 cells [1]. | |||
T28681 |
SB220025
SB-220025,SB 220025 |
||
SB220025, a specific and potent inhibitor of human p38 mitogen-activated protein kinase, reduces the production of tumor necrosis factor induced by lipopolysaccharide. | |||
T10350 |
Apremilast-d5
Apremilast D5,CC-10004 D5 |
TNF; PDE | Apoptosis; Metabolism |
Apremilast D5 (CC-10004 D5) is a deuterium-labeled Apremilast. Apremilast is an orally available inhibitor of PDE-4 (IC50: 74 nM). Apremilast inhibits TNF-α release by lipopolysaccharide (IC50: 104 nM). | |||
T70367 | SNU-BP | ||
SNU-BP is an agonist of PPAR-gamma, inhibiting lipopolysaccharide (LPS)-induced NO production and pro-inflammatory cytokines. SNU-BP potentiates interleukin-4-induced arginase-1 expression, and promotes microglial polarization toward an M2 anti-inflammatory phenotype. | |||
T28241 |
Ono 3403
Ono3403,Ono-3403 |
||
Ono 3403 is a synthetic serine protease inhibitor. Ono 3403 inhibits lipopolysaccharide-induced tumor necrosis factor-alpha and nitric oxide production. ONO-3403 also has an antitumor effect on malignant tumors. | |||
T37901 |
UDP-N-acetyl-D-Glucosamine (sodium salt hydrate)
|
||
UDP-N-acetyl-D-Glucosamine is a natural nucleotide sugar that is used by glycosyltransferases to transfer N-acetyl-D-glucosamine residues to substrates.1It is an important component of antibiotic biosynthesis pathways in fungi and lipopolysaccharide production in bacteria.2,3 1.Roseman, S.Reflections on glycobiologyJ. Biol. Chem.276(45)41527-41542(2001) 2.Kudo, F., and Eguchi, T.Biosynthetic genes for aminoglycoside antibioticsJ. Antibiot. (Tokyo)62(9)471-481(2009) 3.Mulrooney, E.F., Poon, K.K.,... | |||
T40225 |
JH-X-119-01 hydrochloride
|
||
JH-X-119-01 hydrochloride is a potent and selective inhibitor of interleukin-1 receptor-associated kinases 1 (IRAK1). It effectively alleviates lipopolysaccharide (LPS)-induced sepsis in mice. | |||
T62339 | MsbA-IN-2 | ||
MsbA-IN-2 是一种脂多糖转运蛋白 MsbA 的有效抑制剂,能够作用于 E. coliMsbA (IC50: 2 nM)。 | |||
T83049 | Anti-inflammatory agent 63 | ||
Anti-inflammatory agent 63,在RAW264.7细胞中对脂多糖 (LPS) 诱导的一氧化氮 (NO) 产生显示最佳抑制效果,其半抑制浓度(EC50)为5.33±0.57 μM。 | |||
T70268 |
3A-MPLA
|
||
Monophosphoryl lipid A (MPLA) is a natural agonist for the toll-like receptor-4 (TLR4). It is useful as an adjuvant in immunization. MPLA is a safe prophylactic agent and has immunotherapeutic applications. It induces tumor necrosis factor and interleukin (IL)-1β, however not as efficient as lipopolysaccharide (LPS). MPLA improves immune response during bacterial sepsis infection. | |||
T38945 |
Carboxy-PTIO
|
||
Carboxy-PTIO is a highly effective nitric oxide (NO) scavenger known for its rapid reaction rate with NO, resulting in the formation of nitric dioxide (NO2). Its direct scavenging action against NO plays a crucial role in preventing hypotension and endotoxic shock, particularly in lipopolysaccharide-stimulated rat models. | |||
T4186 |
AC-264613
AC264613 |
Protease-activated Receptor | GPCR/G Protein |
AC-264613 是一种选择性蛋白酶激活受体 (PAR-2) 激动剂,pEC50为 7.5。 | |||
T79981 |
Nitric oxide production-IN-1
|
NO Synthase | Immunology/Inflammation |
Nitric oxide production-IN-1(Compound 1)是从Tupistra chinensis中提取的一种NO产生抑制剂,能够抑制脂多糖诱导的大鼠腹腔巨噬细胞NO产量。 | |||
T75011 | STING-IN-5 | STING | Immunology/Inflammation |
STING-IN-5为有效STING抑制剂,IC50达1.15 μM,能在巨噬细胞内抑制LSP诱导之NO合成,从而抑制炎症反应,主用于抗炎疾病与败血症研究。 | |||
T74953 | Antimicrobial agent-7 | ||
Antimicrobial agent-7 (Compound 12) 为一化合物,对革兰氏阴性及革兰氏阳性菌展现出显著的抗菌能力,MIC值介于 2-8 μg/mL 之间。此外,该化合物还对脂多糖引发的炎症有着抗炎作用。 | |||
T37988 |
D-Ribulose-5-phosphate (sodium salt)
Ru5P,D-Ribulose-5-phosphate (sodium salt) |
||
D-Ribulose-5-phosphate is an intermediate in the pentose phosphate pathway. [1][2] It can be derived from 6-phosphogluconate by a dehydrogenase or from xylulose 5-phosphate by ribulose phosphate 3-epimerase. D-Ribulose-5-phosphate is also an intermediate in carbon fixation in photosynthetic organisms as well as in the biosynthesis of lipopolysaccharide, amino acids, secondary metabolites, and antibiotics.[3] | |||
T73667 | Motapizone | ||
Motapizone (NAT 05-239) 是一种选择性 PDE3抑制剂。Motapizone 适度抑制脂多糖 (LPS) 诱导的肺泡巨噬细胞中细胞因子的释放。Motapizone 还通过增加细胞内 cAMP 来抑制人血小板聚集。 | |||
T37989 |
D-Sedoheptulose-7-phosphate (barium salt)
|
||
D-Sedoheptulose-7-phosphate is an intermediate in the pentose phosphate pathway. [1] [2] In this pathway, transaldolase catalyzes the transfer of a three carbon dihydroxyacetone moiety from D-sedoheptulose-7-phosphate to glyceraldehyde-3-phosphate to generate D-fructose-6-phosphate . D-Sedoheptulose-7-phosphate is also an intermediate in carbon fixation in photosynthetic organisms, as well as in the biosynthesis of lipopolysaccharide, amino acids, secondary metabolites, and antibiotics. [3] | |||
T69451 | R-130823 | ||
R-130823 is a ighly selective inhibition against mitogen-activated protein kinase p38alpha (IC50=22 nM). The release of tumor necrosis factor-alpha, interleukin-1beta, -6 and -8 was inhibited in lipopolysaccharide-stimulated human blood pretreated by R-130823 , with IC50 values of 0.089, 0.066, 0.95 and 0.16 microM, respectively. R-130823 reduced the established hind paw swelling in rat adjuvant-induced arthritis, while methotrexate showed no suppression. In the same model, R-130823 ameliorated ... | |||
T80361 |
SpHistin
|
||
SpHistin为一种抗菌肽(AMP)。该化合物能够结合LPS并增加细菌膜的透化性。SpHistin与利福平与阿奇霉素结合时,能够促进这些抗生素的细胞内摄取,从而提高对铜绿假单胞菌的杀菌效果。 | |||
TP1341 |
Polymyxin B nonapeptide
|
||
Polymyxin B nonapeptide, a cationic cyclic peptide derived by enzymatic processing from the naturally occurring peptide polymyxin B, is able to increase the permeability of the outer membrane of Gram-negative bacteria toward hydrophobic antibiotics probab | |||
T73497 |
GSK761
|
||
GSK761作为Sp 140核体蛋白(SP140)的选择性抑制剂,其IC50值达到77.79 nM。它有效减少了单核细胞向炎性巨噬细胞的分化及脂多糖(LPS)诱导的炎症反应。此外,GSK761通过阻断SP140活动,促进CD206+调节性巨噬细胞的形成。 | |||
T75996 |
Murepavadin TFA
|
||
Murepavadin (POL7080) (TFA),一种 14 个氨基酸的环肽,是一种高效的特异性抗生素。Murepavadin 对P. aeruginosa 表现出有效的抗菌活性。MIC50和MIC90值均为 0.12 mg/L。Murepavadin 还可以靶向脂多糖转运蛋白 D。Murepavadin 可用于细菌耐药性的研究。 | |||
T72414 |
Antimicrobial agent-8
|
||
Antimicrobial agent-8 是一种有效的抗菌剂,对革兰氏阴性和革兰氏阳性菌表现出强大的抗菌活性,MIC 范围为 2-8 μg/mL。Antimicrobial agent-8 对脂多糖引起的炎症表现出抗炎活性。 | |||
T22506 |
3,4-DAA
|
NOS | Immunology/Inflammation |
3,4-DAA 具有抗炎活性,可改善急性肝同种异体移植损伤,通过抑制肠道屏障功能障碍和 NF-κB 活化来缓解严重的急性胰腺炎。3,4-DAA 抑制由 IFN-γ 和脂多糖诱导的 EOC20 细胞诱导型一氧化氮合酶 (iNOS) 发挥作用。 | |||
T83226 | A3373 | Phospholipase | Metabolism |
A3373 是新型 PLD1 和 PLD2 抑制剂,对 PLD1 的 IC50 为 325 nM ,对 PLD2 的 IC50 为 15.15 µM,能够有效抑制 LPS 诱导的免疫反应,并在自身免疫性关节炎、骨脱矿及破骨细胞生成等方面发挥关键作用。 | |||
T72412 | Antimicrobial agent-5 | ||
Antimicrobial agent-5 是一种强效抗菌剂,对革兰氏阳性菌/阴性菌展示出良好的细胞选择性。通过阻断LPS与CD14/TLR4受体之间的交互作用,Antimicrobial agent-5 显示出抗炎活性并能缓解LPS引发的炎症反应。 | |||
T79484 |
Nrf2 activator-8
|
||
Nrf2 activator-8(化合物 10e)作为一种效能显著的Nrf2激活剂(EC50=37.9 nM),在BV-2微神经胶质细胞中展现出优异的抗氧化及抗炎效应。此外,Nrf2 activator-8可有效逆转脂多糖(LPS)诱导的小鼠神经炎症模型中的空间记忆缺失。 | |||
T78803 | SIRT5 inhibitor 7 | Sirtuin | Chromatin/Epigenetic; DNA Damage/DNA Repair |
SIRT5 inhibitor7 (compound 58) 是一种底物竞争性且选择性的SIRT5抑制剂,展现出抗炎活性。它在调节蛋白质琥珀酰化和抑制促炎细胞因子释放方面具有潜在的肾功能保护效果。此外,在LPS和CLP诱导的脓毒症相关急性肾损伤小鼠模型中,SIRT5 inhibitor7已证实具备体内有效性。 | |||
T71651 |
GSK1370319A
|
||
GSK1370319A is a potent P2X7 antagonist (IC50 = 3.2 nM). GSK1370319A inhibits ATP-induced increase in IL-1β release and caspase 1 activation in lipopolysaccharide (LPS)-primed mixed glia by blocking assembly of the inflammasome in a pannexin 1-dependent manner. GSK1370319A also inhibits ATP-induced subregion-specific neuronal loss in hippocampal organotypic slice cultures, which is dependent on its ability to prevent inflammasome assembly in glia. Significantly, GSK1370319A attenuates age-relate... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T41078 |
Lipopolysaccharides, Escherichiacoli (11C)
LPS E. coli O55:B5,Lipopolysaccharide, E. coli O111:B4 |
Others | Others |
Lipopolysaccharides, Escherichiacoli (11C) (LPS E. coli O55:B5)是革兰阴性菌外膜的大分子成分,由脂质a、寡糖核心和o -特异性多糖(O-antigen) 3个区域组成。 | |||
TN1291 |
7,3',4'-Tri-O-methylluteolin
5-Hydroxy-3',4',7-trimethoxyflavone,木犀草素-7,3',4'-三甲醚 |
TNF; COX; Interleukin | Apoptosis; Immunology/Inflammation; Neuroscience |
7,3',4'-Tri-O-methylluteolin (5-Hydroxy-3',4',7-trimethoxyflavone) 是来自草药马鞭草科的一种类黄酮,具有抗炎,解热,镇咳,抗糖尿病、抗癌和抗黑素生成特性。它以浓度依赖方式明显抑制促炎细胞因子,可显著降低在转录水平的诱导型一氧化氮合酶和环加氧酶-2 的 mRNA 表达。 | |||
T11855 |
Lipopolysaccharides
脂多糖,LPS |
Others | Others |
Lipopolysaccharides (LPS) 属于天然产物,是一种来源于革兰氏阴性菌外膜外叶的内毒素。Lipopolysaccharides 是一种高免疫原性抗原,可以增强免疫反应,可以用于炎症模型构建。 | |||
TWS0704 |
N-Methylnuciferine
|
Others | Others |
N-Methylnuciferine 是一种从Lotus Plumule 提取的生物碱,可改善脂多糖诱导的抑郁样行为。 | |||
TN1021 |
Secologanic acid
|
NO Synthase | Immunology/Inflammation |
Secologanic acid 是裂环烯醚萜苷的一种。 | |||
TN1933 |
Mitraphylline
帽柱木菲碱,帽柱叶碱 |
IL Receptor; TNF; NF-κB | Apoptosis; Immunology/Inflammation; NF-κB |
Mitraphylline 是一种绒毛钩藤中主要的五环吲哚类生物碱,可阻碍脂多糖介导的原代人中性粒细胞活化。 | |||
T7053 |
p-Hydroxycinnamic acid
p-Coumaric acid,p-Cumaric acid,p-Hydroxy-cinnamic acid,对羟基肉桂酸,NSC 59260 |
Thrombin; Endogenous Metabolite; Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation; Metabolism; Proteases/Proteasome |
p-Hydroxycinnamic acid (NSC-59260) 是常见的食用酚,可抑制血小板活性,对血栓素 B2 和前列腺素 E2 的 IC50值分别为 371 和 126 μM。 | |||
T29352 |
2-Hydroxydecanoic acid
(±)-α-hydroxy Decanoic Acid,羟基癸酸,(±)-2-hydroxy Decanoic Acid,alpha-Hydroxydecanoic acid,2-hydroxy Decylic Acid,2-Hydroxydecanoate |
Others | Others |
2-Hydroxydecanoic acid ((±)-α-hydroxy Decanoic Acid) 是一种在好氧菌 P. ovalis 的脂多糖部分的亲脂部分中发现的脂肪酸。 | |||
T5798 |
Euphorbia Factor L2
千金子素L2,euphorbiafactor L2,大戟因子L2 |
Apoptosis; NF-κB | Apoptosis; NF-κB |
Euphorbia Factor L2 是从大戟种子中分离得到的一种赤藓烷二萜,显示强烈的细胞毒性并通过线粒体途径诱导细胞凋亡,具有抗癌活性。 | |||
TN2167 |
Rutaevin
|
Reactive Oxygen Species; NO Synthase | Immunology/Inflammation; Metabolism; NF-κB |
Rutaevin 从Euodia rutaecarpa 中分离。它对 Raw 264.7 巨噬细胞中 LPS 诱导的NO 产生具有抑制作用。 | |||
T3383 |
Cimifugin
升麻素,Cimitin |
Others | Others |
Cimifugin (Cimitin) 是中草药Saposhnikovia divaricate 的一种生物活性成分。它能够调节紧密连接减少上皮衍生的主动关键因子,对过敏性炎症产生抑制作用。 | |||
TN1553 |
Deacetyl ganoderic acid F
|
Others | Others |
Deacetyl ganoderic acid F (DeGA F) 是从灵芝 Ganoderma lucidum 中提取的三萜类化合物,在体外和体内对脂多糖(LPS)诱导的炎症有抑制作用。 | |||
T4S1616 |
Sanggenon D
桑根酮D,Sanggenone D |
NOS; COX; GABA Receptor | Immunology/Inflammation; Membrane transporter/Ion channel; Neuroscience |
Sanggenone D represents a new scaffold of positive GABAA receptor modulators, it also inhibits COX-2 activity (IC 50 = 73-100 μM). Sanggenone D has anti-inflammatory activity, it can inhibit NO production from lipopolysaccharide (LPS)-induced RAW 264.7 ce | |||
T2916 |
Patchouli alcohol
百秋李醇,Patchouli camphor,Patchoulol,(-)-Patchouli Alcohol,广藿香醇 |
Antibacterial; Antifungal | Microbiology/Virology |
Patchouli alcohol (Patchoulol) 是一种从广藿香中提取的天然三环倍半萜,有抗幽门螺杆菌和抗炎活性。 | |||
T5660 |
Menthone
|
IL Receptor; TNF; NF-κB; Parasite | Apoptosis; Immunology/Inflammation; Microbiology/Virology; NF-κB |
Menthone 是一种从植物和薄荷油中提取的单萜,是精油的主要挥发性成分,具有抗炎和抗氧化特性。 | |||
T3S1692 |
Octahydrocurcumin
|
Anti-infection; NF-κB; Reactive Oxygen Species; ROS | Immunology/Inflammation; Metabolism; Microbiology/Virology; NF-κB |
Octahydrocurcumin 是一种姜黄素的氢化衍生物,是姜黄素的代谢物。 | |||
T6S2023 |
Harpagoside
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Others; COX; NO Synthase | Immunology/Inflammation; Neuroscience; Others |
Harpagoside 是从爪钩草中分离出来的一种天然产物,可抑制COX-1和COX-2活性,并抑制 NO 的产生。 | |||
TN2091 |
Polygalacin D
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Apoptosis; IAP | Apoptosis |
Polygalacin D 是从桔梗中分离的一种天然产物,具有抗癌和抗增殖特性。它通过 PI3K/Akt 途径诱导凋亡。它抑制 IAP 蛋白家族的表达,并通过抑制 GSK3β,Akt 的磷酸化和 PI3K 的表达来阻断 PI3K/Akt 途径。 | |||
T5S0581 |
Sec-O-Glucosylhamaudol
亥茅酚苷,Hamaudol 3-glucoside |
Others; Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience; Others |
Sec-O-Glucosylhamaudol (Hamaudol 3-glucoside) 是从滨海前胡中分离得到的一种天然产物,能够降低 μ 阿片受体的蛋白水平,可用于缓解疼痛的研究。它通过调节脂多糖刺激的 RAW264.7 细胞系中的 p38 丝裂原活化蛋白激酶具有抗炎作用。 | |||
T2S0731 |
Trilobatin
三叶苷,三叶甙,P-Phlorizin |
Amylase | Metabolism |
Trilobatin (P-Phlorizin) 是源自Lithocarpus polystachyusRehd 的甜味剂,是一种HIV-1抑制剂,靶向 Gp41 包膜蛋白,具有神经保护作用。它还是SGLT1/2抑制剂,可选择性诱导人肝母细胞瘤细胞增殖。 | |||
T3676 |
Sesamol
1,3-Benzodioxol-5-ol,3,4-Methylenedioxyphenol,芝麻酚 |
Apoptosis; AMPK | Apoptosis; Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
Sesamol (1,3-Benzodioxol-5-ol) 是芝麻油的主要成分,具有抗氧化和抗肿瘤活性。它是一种自由基清除剂,在 DPPH 实验中,IC50为 5.95±0.56 μg/mL。 | |||
T5S2283 |
Sesamolin
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p38 MAPK; Caspase; JNK | Apoptosis; MAPK; Proteases/Proteasome |
Sesaminol 是从Justicia orbiculata 中分离得到的一种天然产物,抑制脂质过氧化,具有神经保护作用和抗氧化活性。它通过抑制JNK、p38 MAPKs 和caspase-3磷酸化,抑制MAPK 的级联反应。 | |||
T7033 |
Rosmanol
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Antioxidant; COX | Immunology/Inflammation; Neuroscience; oxidation-reduction |
Rosmanol 能够显著抑制脂多糖诱导的 INOS、COX-2 的表达,抑制低密度脂蛋白的氧化,并具有抗炎作用。 | |||
T2S2362 |
Dehydrocorydaline nitrate
去氢延胡索甲素硝酸盐,硝酸脱氢紫堇碱 |
BCL; Others; PARP; p38 MAPK; Caspase; Parasite; Autophagy | Apoptosis; Autophagy; Chromatin/Epigenetic; DNA Damage/DNA Repair; MAPK; Microbiology/Virology; Others; Proteases/Proteasome |
Dehydrocorydaline nitrate 是生物碱。Dehydrocorydaline 调节 Bax,Bcl-2蛋白表达,激活 caspase-7,caspase-8,并使 PARP 失活。它能增强 p38 MAPK 活化,具有抗炎、抗癌、抗疟疾等功效。 | |||
T4S0878 |
Prunetin
樱黄素,Prunusetin |
ERK; Dehydrogenase; NF-κB | MAPK; Metabolism; NF-κB |
Prunetin (Prunusetin) 是一种O-甲基化异黄酮,具有抗炎的作用。它是人醛脱氢酶的有效抑制剂。 | |||
TJS1779 |
Protosappanin A
原苏木素A,PTA |
NADPH-oxidase; IL Receptor; IκB/IKK; TNF; NF-κB; TLR; ROS; COX; HIV Protease; JAK; NO Synthase; STAT | Angiogenesis; Apoptosis; Chromatin/Epigenetic; Immunology/Inflammation; JAK/STAT signaling; Microbiology/Virology; Neuroscience; NF-κB; Proteases/Proteasome; Stem Cells |
Protosappanin A (PTA) 是从苏木中分离得到的免疫抑制成分和主要联苯化合物,通过下调 JAK2和 STAT3的磷酸化,抑制 JAK2/STAT3依赖的炎症通路。 | |||
TN2063 |
Physalin B
NSC-287088 |
Apoptosis; NF-κB; Akt; PI3K; Nrf2; NOD | Apoptosis; Cytoskeletal Signaling; Immunology/Inflammation; NF-κB; PI3K/Akt/mTOR signaling |
Physalin B 是茄科植物的主要活性化合物之一,具有广泛的生物活性,可用于治疗炎症湿疹和疱疹等疾病。Physalin B 通过激活 PI3K/Akt 通路抑制 NF-κB 和 NLRP3,从而改善脂多糖诱导的急性肺损伤造成的炎症反应。Physalin B 通过激活 Nrf2 通路抑制 PDGF-BB 诱导的 VSMC 增殖、迁移和表型转化。Physalin B 通过抑制 LAP2α-HDAC1 介导的胶质瘤相关癌基因 1 的去乙酰化和肝星状细胞活化来发挥抗肿瘤活性。 | |||
T4479 |
Isomaculosidine
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Others | Others |
Isomaculosidine can significantly inhibit nitric oxide (NO) production in lipopolysaccharide (LPS)-stimulated BV2 cells. | |||
TN5302 |
Withaperuvin C
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Withaperuvin C may have anti-inflammatory activity with lipopolysaccharide (LPS)-activated murine macrophage RAW 264.7 cells. | |||
TN4409 |
Lansiumarin C
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TNF | Apoptosis |
Lansiumarin C can decrease nitric oxide (NO) and tumor necrosis factor-α (TNF-α) production in lipopolysaccharide (LPS)-induced macrophages. | |||
T82211 |
Herpotrichone B
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Herpotrichone B exhibits potent anti-neuroinflammatory activity in BV-2 microglial cells induced by lipopolysaccharide (LPS), with a half-maximal inhibitory concentration (IC50) of 0.11μM. | |||
TN4633 |
Neocryptotanshinone II
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NOS; NF-κB | Immunology/Inflammation; NF-κB |
Neocryptotanshinone inhibits lipopolysaccharide-induced inflammation in RAW264.7 macrophages by suppression of NF-κB and iNOS signaling pathways. | |||
TN3519 |
Bisdehydroneotuberostemonine
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Others | Others |
Bisdehydroneotuberostemonine shows significant inhibitory effect on lipopolysaccharide-induced nitric oxide production in BV2 microglia at 100 uM. | |||
TN3241 | 7-O-Acetylbonducellpin C | Others | Others |
7-O-Acetylbonducellpin C may exhibit significant inhibition of nitric oxide production of RAW264.7 macrophages stimulated by lipopolysaccharide (LPS). | |||
TN4827 |
Preskimmianine
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Others | Others |
Preskimmianine is the biogenetic precursor of skimmianine.It can significantly inhibit nitric oxide (NO) production in lipopolysaccharide (LPS)-stimulated BV2 cells. | |||
TN5247 |
Vogeloside
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Others | Others |
Vogeloside shows inhibition of nitric oxide production in lipopolysaccharide-activated macrophages; its activity is comparable to that of aminoguanidine, a classic inhibitor. | |||
TN4938 |
Samidin
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p38 MAPK; TNF; NF-κB; COX; DNA/RNA Synthesis; JNK | Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Immunology/Inflammation; MAPK; Neuroscience; NF-κB |
Samidin has anti-inflammatory properties through suppression of NF-κB and AP-1-mediated-genes in lipopolysaccharide (LPS)-stimulated RAW 264.7 cells. | |||
TN4182 |
Hannokinol
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Others | Others |
(+)-Hannokinol and MESO-hannokinol can significantly inhibit lipopolysaccharide-induced nitric oxide production in BV2 microglial cells at concentrations ranging from 1 microM to 100 microM. | |||
TN3635 |
Chlojaponilactone B
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IL Receptor; IκB/IKK; TNF; NOS; NF-κB | Apoptosis; Immunology/Inflammation; NF-κB |
Chlojaponilactone B has anti-inflammatory activity, it exhibits pronounced inhibition of nitric oxide (NO) production in lipopolysaccharide (LPS)-induced RAW 264.7 macrophages. | |||
TN2152 |
Rhaponticin 2′′-O-gallate
土大黄苷 2''-O-没食子酸酯,Rhaponticin 2''-O-gallate |
Others | Others |
Rhaponticin 2''-O-gallate showed inhibitory activity of NO production in lipopolysaccharide-activated macrophages, (IC50 = 11-69 microM). | |||
TN4726 | Oxyphyllenone A | Others | Others |
Oxyphyllenone A can inhibit the NO production in lipopolysaccharide-activated macrophages. | |||
T5768 | bruceine B | TNF; Parasite | Apoptosis; Microbiology/Virology |
Bruceine B 是一种有效的白细胞-内皮细胞粘附抑制剂,可抑制蛋白质和核酸合成。 | |||
TN4941 | Sanggenon N | Others | Others |
Sanggenon N shows protective effects on t-BHP-induced oxidative stress with the EC50 value of 23.45 ± 4.72 uM. It inhibits lipopolysaccharide-induced nitric oxide production in RAW 264.7 macrophages. | |||
TN5202 |
Undulatoside A
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Others | Others |
Undulatoside A has anti-inflammatory activity, it exhibits inhibition on nitric oxide production in lipopolysaccharide induced RAW 264.7 macrophages with the IC50 value of 49.8 uM. | |||
TN2153 |
Rhaponticin 6′′-O-gallate
土大黄苷 6''-O-没食子酸酯,Rhaponticin 6''-O-gallate |
Others | Others |
Rhaponticin 6''-O-gallate showed inhibitory activity of NO production in lipopolysaccharide-activated macrophages, (IC50 = 11-69 microM). | |||
TN4050 |
Fargesone A
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NOS | Immunology/Inflammation |
Fargesone A shows inhibitory effects on nitric oxide (NO) production in the lipopolysaccharide plus interferon-gamma activated-murine macrophage cell line, J774.1. | |||
T83056 | Anti-inflammatory agent 5 | ||
5 是一种抗炎剂,对由 LPS 诱导的 BV-2 小胶质细胞中 NO 的生成显示出显著的抑制活性。 | |||
T3P2855 | Chamigrenal | EGFR; NOS; PAFR; COX; Prostaglandin Receptor | Angiogenesis; GPCR/G Protein; Immunology/Inflammation; JAK/STAT signaling; Neuroscience; Tyrosine Kinase/Adaptors |
β-Chamigrenal has anti-inflammatory activity, it has inhibitory effects on lipopolysaccharide-induced nitric oxide and prostaglandin E2 production in RAW 264.7 macrophages. Chamigrenal shows platelet-activating factor antagonistic activity and the IC(50) | |||
TN4089 |
Futokadsurin C
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Others | Others |
Futokadsurin C can inhibit nitric oxide production by a murine macrophage-like cell line (RAW 264.7), which is activated by lipopolysaccharide and interferon-gamma. | |||
T80860 |
Vitisin B
(-)-Vitisin B,E-Vitisin B |
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Vitisin B,从Vitis thunbergii var. taiwaniana分离提取,对脂多糖(LPS)诱导的关节炎表现出抗炎活性。 | |||
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