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81

抑制剂 & 化合物

23

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Cat. No. Product Name Target Signaling Pathways
T8477 IQ-3

JNK MAPK
IQ3 是c-JNK 家族选择性抑制剂,对JNK3 的选择性更好。它对JNK1、JNK2 和 JNK3 的Kd 值分别为0.24 μM、0.29 μM 和 0.066 μM。
T11636 IL-17A antagonist 3

IL Receptor Immunology/Inflammation
IL-17A antagonist 3 is an IL-17A antagonist.
T40127 IL-17 modulator 3

IL-17 modulator 3 (US20200247785A1) is a chemical compound that acts as an IL-17 modulator. It has potential applications in researching inflammation, cancer, and autoimmune diseases.
T9027 CA-4948

Emavusertib

IRAK; FLT Angiogenesis; Immunology/Inflammation; NF-κB; Tyrosine Kinase/Adaptors
CA-4948 (Emavusertib) 是一种IRAK4抑制剂,也是一种FLT3抑制剂,具有抗肿瘤作用。
T4602 Hydrocortisone hemisuccinate

Hydrocortisone 21-he,氢化可的松琥珀酸酯,hydrocortisone 21-hemisuccinate*free acid,Hydrocortisone 21-hemisuccinate

Glucocorticoid Receptor; Others; Interleukin Endocrinology/Hormones; Immunology/Inflammation; Others
Hydrocortisone hemisuccinate (hydrocortisone 21-hemisuccinate*free acid) 是糖皮质激素, 是口服有活性的甾体抗炎剂。它能够降低IL-6(IC50:6.7 μM)、IL-3(IC50:21.4 μM)的生物活性,可用于研究溃疡性结肠炎。
T22698 TLR3-IN-1

CU CPT 4a

TLR Immunology/Inflammation
TLR3-IN-1 (CU CPT 4a) 是一种选择性的TLR3信号抑制剂,在 RAW 264.7 细胞中 IC50 为 3.44 μM。它可以抑制 TLR3/dsRNA 复合物介导的下游信号通路,并抑制全细胞中 TNF-α 和 IL-1β 的产生。
T11670 IRAK inhibitor 3

IRAK Immunology/Inflammation; NF-κB
IRAK inhibitor 3 是白细胞介素-1受体相关激酶调节剂。
T72549 IL-17A modulator-3

IL-17Amodulator-3IL-17A 的调节剂。IL-17Amodulator-3 抑制 IL-17A/A,IC50值 <10 μM。IL-17Amodulator-3 可以用于炎症、癌症和自身免疫疾病的研究。
T38105 Ixekizumab

LY2439821

IL Receptor; Interleukin Immunology/Inflammation
Ixekizumab (LY2439821) 是一种人源化 IgG4 单克隆抗体,可选择性结合和中和白细胞介素 IL-17A ,Kd 值<3 pM。Ixekizumab 科阻断 IL-17A 与 IL-17RA 的结合,但不与其他 IL-17 家族成员结合。Ixekizumab 用于治疗中重度斑块型银屑病、银屑病关节炎和牛皮癣。
TP2008L Lyn peptide inhibitor acetate

Lyn peptide inhibitor acetate(222018-18-0 free base)

IL Receptor Immunology/Inflammation
Lyn peptide inhibitor acetate(222018-18-0 free base) 是一种有效的细胞渗透性 Lyn 偶联 IL-5 受体信号通路抑制剂,同时保持其他信号完整。它阻断 Lyn 活化并抑制 Lyn 酪氨酸激酶与 IL-3/GM-CSF/IL-5 受体的 βc 亚基的结合。它可用于哮喘、过敏和其他嗜酸性粒细胞疾病的研究。
T7606 Guanosine 5'-diphosphate disodium salt

5'-二磷酸鸟苷二钠,5'-GDP-Na2,鸟苷-5'-二磷酸二钠盐

Endogenous Metabolite Metabolism
Guanosine 5'-diphosphate disodium salt (5'-GDP-Na2) 是一种核苷二磷酸。它是一种潜在的铁动员剂,能够阻断铁调素-铁转运蛋白相互作用,也可以调节白 IL-6/stat-3 途径。
T5821 BC-1215

Others; Ligand for E3 Ligase Others; PROTAC
BC-1215 是一种 F-box protein 3 抑制剂。它能够稳定 TRAF1-TRAF6 来抑制 Fbxo3-TRAF 激活途径。它与 ApaG 相互作用,阻碍来自人 PBMC 广谱 TH1 细胞因子的分泌。
T2061 APY0201

PI3K; Interleukin Immunology/Inflammation; PI3K/Akt/mTOR signaling
APY0201 是PIKfyve 抑制剂,能够抑制 PtdIns3P 转化为PtdIns(3,5)P2 (IC50:5.2 nM),还能够抑制IL-12/IL-23产生。
T25150 BI-69A11

BI 69A11,(E)-3-(1H-Benzo[d]imidazol-2-yl)-1-(6-chloro-2-hydroxy-4-phenylquinolin-3-yl)prop-2-en-1-one

NF-κB; Akt Cytoskeletal Signaling; NF-κB; PI3K/Akt/mTOR signaling
BI-69A11 ((E)-3-(1H-Benzo[d]imidazol-2-yl)-1-(6-chloro-2-hydroxy-4-phenylquinolin-3-yl)prop-2-en-1-one) 是一种双重 AKT 和 NFkB 通路抑制剂。它通过靶向 Akt 增强结肠癌细胞对 mda-7/IL-24 诱导的生长抑制的敏感性。
T76883 Talacotuzumab

CSL 362,JNJ 56022473

Immunology/Inflammation related; Interleukin Immunology/Inflammation
Talacotuzumab (JNJ 56022473) 是一种含有修饰的 Fc 结构的IgG1 型完全人源化的 CD123 中和单克隆抗体。Talacotuzumab 对 CD123、CD32b/c、CD16-158F、CD16-158V 具有很高的亲和力, KD 分别为 0.43 nM、188 nM、46 nM、16.8 nM。Talacotuzumab 通过抑制 IL-3 与 CD123 结合进而抑制靶细胞中的 IL-3 信号传导。Talacotuzumab 诱导 Fc 区发生突变以增加对 CD16 (FcγRIIIa) 的亲和力,从而加强抗体依赖性细胞介导的细胞毒性 (ADCC)。Talacotuzumab 急性髓性白血病 (AML) 异种移植小鼠模型中抑制白血病细胞生长。
T7123 AMG-47a

VEGFR; p38 MAPK; JAK; Src Angiogenesis; Chromatin/Epigenetic; JAK/STAT signaling; MAPK; Stem Cells; Tyrosine Kinase/Adaptors
AMG-47a 是具有口服活性的 Lck 抑制剂,IC50值为 0.2 nM。它具有抗炎作用,对 VEGF2、p38α、p38α、Jak3、MLR 和 IL-2的 IC50值分别为 1、3、72、30 和 21 nM。
T5416 T-5224

MMP Proteases/Proteasome
T-5224 是选择性的转录因子c-Fos/activator protein (AP)-1抑制剂,具有抗炎作用,能够特异性抑制 c-Fos/c-Jun 的 DNA 结合活性,但对其他转录因子的结合活性无影响。它抑制 IL-1β 诱导的 Mmp-3、Mmp-13、Adamts-5 转录上调。
T28599 Ro26-4550

Ro 26-4550,Ro-26-4550

Ro26-4550 is a competitive reversible inhibitor of interleukin-2 (IL-2) binding to IL-2R α-subunit (IC50 = 3 μM).
T76771 Pivekimab

Pivekimab为针对白介素3(IL-3)及CD123的人源IgG1型单克隆抗体。适用于母细胞浆细胞样树突状细胞肿瘤(BPDCN)研究。
T68182 3-Hydroxykynurenamine

3-Hydroxykynurenamine, also known as 3-Hydroxy-L-kynurenamine or 3-HKA, is a biogenic amine produced via an alternative pathway of tryptophan metabolism. In vitro, 3-HKA has an anti-inflammatory profile by inhibiting the IFN-γ mediated STAT1/NF-κΒ pathway in both mouse and human dendritic cells (DCs) with a consequent decrease in the release of pro-inflammatory chemokines and cytokines, most notably TNF, IL-6, and IL12p70. 3-HKA has protective effects in an experimental mouse model of psoriasis ...
T12752 RORγt Inverse agonist 3

Others Others
RORγt Inverse agonist 3 is a potent, selective and orally active inverse agonist of RORγ(EC50s of 0.22 μM and 0.15 μM for hRORγ and RORγt (human IL-17 cells), respectively).
T36517 Resveratrol-3-O-sulfate sodium

Resveratrol-3-O-sulfate is a metabolite of resveratrol . In U-937 cells stimulated with LPS, resveratrol-3-O-sulfate (1 μM) decreases the expression of IL-1α, IL-1β, and IL-6 by 61.2, 76.6, and 42.2%, respectively, and decreases the release of TNF-α and IL-6 to similar levels as resveratrol. It has antioxidant activity in a Trolox assay, dose-dependently decreases growth of Caco-2 colorectal adenocarcinoma cells when used at concentrations ranging from 10 to 100 μM, and induces apoptosis at conc...
T81895 Lysophosphatidylcholine C19:0

1-Nonadecanoyl-2-hydroxy-sn-glycero-3-phosphocholine

Lysophosphatidylcholine C19:0 (1-Nonadecanoyl-2-hydroxy-sn-glycero-3-phosphocholine)为具有C19:0酰基链的脂质。该化合物能促进IL-1beta的分泌。
TP2008 Lyn peptide inhibitor

Cell-permeable inhibitor of Lyn-dependent effects of the IL-5 receptor. Blocks binding of Lyn tyrosine kinase to βc subunit of IL-3/GM-CSF/IL-5 receptors, blocking Lyn activation. Inhibits IL-5 receptor-mediated eosinophil differentiation and survival in
T37443 Aspochalasin D

Aspochalasin D is a co-metabolite originally isolated from A. microcysticus with aspochalasins A, B, and C, that was initially thought to be inactive. It has antibacterial activity against Gram-positive and Gram-negative bacteria at a concentration of 1 mg/ml. Aspochalasin D is more cytotoxic, via apoptosis, to Ba/F3-V12 cells in an IL-3-free medium than in an IL-3-containing medium (IC50s = 0.49 and 1.9 μg/ml, respectively).
T75806 Lyn peptide inhibitor TFA

Lyn peptide inhibitor TFA 是一种有效的,可以细胞渗透的抑制剂,抑制Lyn 偶联的IL-5受体相关信号通路,同时保持其他信号的完整。Lyn peptide inhibitor TFA 可以阻断 Lyn 的激活,抑制 Lyn 酪氨酸激酶与 IL-3/GM-CSF/IL-5 受体的 βc 亚基结合。Lyn peptide inhibitor TFA 可用于哮喘、过敏等嗜酸性疾病的研究。
T73697 Denileukin diftitox

Denileukin diftitox (DAB 389IL-2) 是一种融合蛋白毒素,将白喉毒素 (DT) 与白细胞介素 2 (IL-2) 结合,专门针对表达高亲和力IL-2受体 (IL-2R)、CD25 的细胞。它通过与IL-2R阳性细胞结合并利用白喉毒素片段的内化作用来抑制蛋白质合成,从而达到耗尽目标细胞的效果。
T80959 Trabikibart

CSL311

Trabikibart(CSL311)为βc特异性的全人源单克隆抗体,专一性结合人βc受体的细胞因子结合位点表位,并展现高皮摩尔级别的结合亲和力。此抗体能有效抑制IL-3、GM-CSF和IL-5在嗜酸性粒细胞存活中的协同作用,显示出治疗慢性炎症性疾病的应用潜力。
T82373 FPR2 agonist 3

FPR2 agonist 3 能够抑制 LPS 刺激下的培养物中乳酸脱氢酶的释放,并减少促炎性因子IL-1β和IL-6的表达水平。此外,FPR2 agonist 3 还可以通过作用于 STAT3/SOCS3 信号通路来降低 STAT3 的磷酸化水平。
T37564 C4 Ceramide (d18:1/4:0)

C4 Ceramide (d18:1/4:0),Cer(d18:1/4:0)

C4 Ceramide is a bioactive sphingolipid and cell-permeable analog of naturally occurring ceramides. [1] [2] [3] It inhibits IL-4 production by 16% in EL4 T cells stimulated with phorbol 12-myristate 13-acetate when used at a concentration of 10 μM. [1] C4 Ceramide is cytotoxic to SK-BR-3 and MCF-7/Adr breast cancer cells (IC50s = 15.9 and 19.9 μM, respectively). [2] C4 Ceramide also increases maturation and stability of cystic fibrosis transmembrane conductance regulator (CFTR) proteins bearing...
T63287 HPK1-IN-3

HPK1-IN-3 是一种选择性的、有效的、ATP 竞争性的造血祖细胞激酶 1 (HPK1; MAP4K1) 抑制剂 (IC50: 0.25 nM)。HPK1-IN-3 具有 IL-2 细胞效力,能够作用于人外周血单核细胞 (PBMC),EC50 值为 108 nM。
T77096 Nemvaleukin alfa

Nemvaleukin alfa (ALKS 4230) 为一种IL-2融合蛋白,专门针对中等亲和力IL-2R进行选择性结合。该化合物作为NK及效应T细胞的活化剂,主要应用于癌症研究领域。
T35452 β-Defensin-3 (human) (trifluoroacetate salt)

β-Defensin-3 is a peptide with antimicrobial properties that protects the skin and mucosal membranes of the respiratory, genitourinary, and gastrointestinal tracts. It inhibits the growth of the periodontopathogenic and cariogenic bacteria F. nucleatum, S. mutans, S. sobrinus, S. salivarius, and L. casei (MICs = 12.5-100 mg/l). It also inhibits the growth of S. aureus, S. pyogenes, P. aeruginosa, E. coli, and C. albicans. β-Defensin-3 stimulates gene expression and production of IL-6, IL-10, CXC...
T23028 MRT67307 HCl (1190378-57-4 free base)

MRT67307 HCl

Others Others
MRT67307 is an inhibitor for TBK1, IKKε , MARK1-4 and NUAK1 with IC50 value of 19, 160, 27-52 and 230nM , respectively [1]. It is an inhibitor for ULK1and ULK2 with IC50 value of 45 and 38nM, respectively [2]. Also, it is a salt inducible kinase (SIK) inhibitor with IC50 value of 250, 67 and 430nM for SIK1, SIK2 and SIK3, respectively.<br />SIKs prevent the formation of regulatory macrophages and their inhibition induces increasing in some markers of regulatory macrophages, such as IL-10 and oth...
T21633 N-3-oxo-dodecanoyl-L-Homoserine lactone

N-3-oxo-dodecanoyl-L-Homoserine lactone (3-oxo-C12-HSL) 是由铜绿假单胞菌和洋葱状芽孢杆菌复合物菌株产生的细菌群体感应信号分子,群体感应是细菌用来控制基因表达以响应细胞密度增加的调节系统。N-3-oxo-dodecanoyl-L-Homoserine lactone 诱导 16HBE 人支气管上皮细胞产生 IL-8。
T62622 MRL-871

MRL-871 (compound 3) 是一种有效的异生维甲酸受体相关孤儿受体 γt (RORγt) 反向激动剂 (IC50: 264 nM)。MRL-871 表现出独特的异恶唑化学型,可有效减少 EL4 细胞中 IL-17a mRNA 的产生。
T83681 IRBP (1-20) (human, rat) TFA

IRBP1-20,Interphotoreceptor Retinoid-Binding Protein (1-20)

IRBP1-20(1-20)是IRBP的一个十二肽片段,亦称视黄醇结合蛋白3,负责运输视锥细胞中的视黄醇和视黄醛至视网膜色素上皮,参与色素再生。在携带H-2b等位基因型的C57BL/6小鼠中,IRBP1-20用于诱导自身免疫性葡萄膜视网膜炎。IRBP1-20(3 µM)能增加初级小鼠脾淋巴细胞分泌IL-4、IL-5和IL-6的水平。用IRBP1-20免疫并再次挑战,可增加IFN-γ缺乏小鼠的耳部肿胀、眼部血管炎症、免疫细胞浸润和视锥细胞层损伤,以及视网膜脱落。
T76878 Vobarilizumab

Vobarilizumab (ALX-0061) 是一种抗 IL-6R 单克隆抗体 (mAb) (Kd: 0.19 pM)。Vobarilizumab 由一个抗 IL-6R 结构域和一个抗人血清白蛋白结构域组成。Vobarilizumab 可用于炎症性自身免疫性疾病的研究,如类风湿性关节炎。
T79304 Semapimod

CPSI-2364,CNI-1493 free base

Semapimod是一种抑制促炎细胞因子产生的化合物,具有抑制TNF-α、IL-1β和IL-6功能。它通过抑制巨噬细胞的p38 MAPK以及一氧化氮的生成发挥作用,并且能够抑制TLR4信号传导(IC50约为0.3 μM)。Semapimod对于治疗各类炎症和自身免疫性疾病显示出潜在效用。
T63339 ALV1

ALV1 是 Ikaros 和 Helios 的有效降解剂,对 IKZF1/2/3 具有相似的降解活性。ALV1 可以明显减少 IKZF1-4、CK1α (酪蛋白激酶 1α,CSNK1A1) 和核糖体蛋白 RPL4 的蛋白丰度,并诱导 Helios/CRBN 二聚反应,促进了 IL-2 的分泌。
T64232 Agatolimod

Agatolimod (ODN 2006) 是一种TLR9激动剂,是 B 类 ODN (寡脱氧核苷酸),也是人类的 CpG 序列(序列:5'-tcgtcgttttgtcgttttgtcgtt-3')。Agatolimod 能够刺激 HD11 细胞产生 NO2 和 IL-6。Agatolimod 能够用于研究乳腺癌。
T68225 Fc 11a-2

Fc 11a-2 是一种苯并咪唑化合物,一种具有口服活性且有效的NLRP3炎症小体 (NLRP3inflammasome) 抑制剂。Fc 11a-2 通过抑制caspase-1的激活进而抑制 IL-1b/IL-18 的激活来抑制NLRP3炎性体的形成。Fc 11a-2 可防止Dextran sulfate sodium(DSS) 诱导的小鼠实验性结肠炎。
T41189 AY 254

AY 254 is a potent PAR2 biased agonist. Selectively activates ERK1/2 signaling (EC50= 2 nM for ERK1/2 phosphorylation versus 80 nM for Ca2+release). Reduces cytoKi ne-induced caspase 3/8 activation, promotes scratch-wound healing, and induces IL-8 secretion, in human colorectal cancer (HT29) cellsin vitro.
T79170 Immuno modulator-1

Immuno modulator-1 (compound 22) 在hPBMC中抑制TNFα和IL-2的分泌,IC50为4.7 nM和26 nM。同时,该化合物对hERG钾通道具阻断活性,3 μM浓度时抑制率达20%。
T76906 Anrukinzumab

Anrukinzumab (IMA-638),一种针对人IL-13的人源化单克隆抗体,展示了在食蟹猕猴肺部炎症模型中显著的疗效。Anrukinzumab 目前被用于溃疡性结肠炎(UC)和哮喘的研究中。
T60366 Epinastine

Epinastine (WAL801) 是一种抗组胺剂和肥大细胞稳定剂。Epinastine 是一种有效的,选择性的,口服活性的组胺 H1 受体 (histamine H1 receptor) 拮抗剂。Epinastine 还抑制人嗜酸性粒细胞释放 IL-8 并具有抗过敏作用。
T76803 Elsilimomab

Elsilimomab (B-E8) 是一种抗白介素-6 (IL-6) 的 IgG1单克隆抗体,其 KD 为 22 pM,IC50为 1.4 nM。Elsilimomab 可用于多发性骨髓瘤、肾细胞癌和类风湿性关节炎 (RA) 的研究。
T19883 Ac-YVAD-CHO

L 709049,L-709049,L709049

L 709049是一种生物活性化合物,它是白细胞介素-1β转化酶( Caspase-1)的选择性抑制剂。 Caspase 抑制剂可干扰细胞凋亡的启动,具有多种临床应用前景。
T74911 ODN 24987

ODN 24987,一种鸟嘌呤修饰的抑制性寡核苷酸(ODN),作用于TLR9,能够抑制IL-6和IFN-α的释放,适用于免疫紊乱研究。ODN 24987 序列为5’-C-C-T-G-G-C-c7G-G-G-G-3’。
T62680 (R)-MLT-985

(R)-MLT-985 (compound 11) 是一种 MALT1 蛋白酶的有效抑制剂 (IC50: 3 nM)。(R)-MLT-985 在 Jurkat 细胞中对 MALT1 依赖性 IL-2 的 IC50 值为 20 nM。(R)-MLT-985 对 ABC-DLBCL 细胞中的生长和异常 CARD11/BCL10/MALT1 复合物信号传导具有抑制作用。

化合物

IQ-3
Cat.No: T8477
Synonym:
Target: JNK
IL-17A antagonist 3
Cat.No: T11636
Synonym:
Target: IL Receptor
IL-17 modulator 3
Cat.No: T40127
Synonym:
Target:
CA-4948
Cat.No: T9027
Synonym: Emavusertib
Target: IRAK, FLT
Hydrocortisone hemisuccinate
Cat.No: T4602
Synonym: Hydrocortisone 21-he,氢化可的松琥珀酸酯,hydrocortisone 21-hemisuccinate*free acid,Hydrocortisone 21-hemisuccinate
Target: Glucocorticoid Receptor, Others, Interleukin
TLR3-IN-1
Cat.No: T22698
Synonym: CU CPT 4a
Target: TLR
IRAK inhibitor 3
Cat.No: T11670
Synonym:
Target: IRAK
IL-17A modulator-3
Cat.No: T72549
Synonym:
Target:
Ixekizumab
Cat.No: T38105
Synonym: LY2439821
Target: IL Receptor, Interleukin
Lyn peptide inhibitor acetate
Cat.No: TP2008L
Synonym: Lyn peptide inhibitor acetate(222018-18-0 free base)
Target: IL Receptor
Guanosine 5'-diphosphate disodium salt
Cat.No: T7606
Synonym: 5'-二磷酸鸟苷二钠,5'-GDP-Na2,鸟苷-5'-二磷酸二钠盐
Target: Endogenous Metabolite
BC-1215
Cat.No: T5821
Synonym:
Target: Others, Ligand for E3 Ligase
APY0201
Cat.No: T2061
Synonym:
Target: PI3K, Interleukin
BI-69A11
Cat.No: T25150
Synonym: BI 69A11,(E)-3-(1H-Benzo[d]imidazol-2-yl)-1-(6-chloro-2-hydroxy-4-phenylquinolin-3-yl)prop-2-en-1-one
Target: NF-κB, Akt
Talacotuzumab
Cat.No: T76883
Synonym: CSL 362,JNJ 56022473
Target: Immunology/Inflammation related, Interleukin
AMG-47a
Cat.No: T7123
Synonym:
Target: VEGFR, p38 MAPK, JAK, Src
T-5224
Cat.No: T5416
Synonym:
Target: MMP
Ro26-4550
Cat.No: T28599
Synonym: Ro 26-4550,Ro-26-4550
Target:
Pivekimab
Cat.No: T76771
Synonym:
Target:
3-Hydroxykynurenamine
Cat.No: T68182
Synonym:
Target:
RORγt Inverse agonist 3
Cat.No: T12752
Synonym:
Target: Others
Resveratrol-3-O-sulfate sodium
Cat.No: T36517
Synonym:
Target:
Lysophosphatidylcholine C19:0
Cat.No: T81895
Synonym: 1-Nonadecanoyl-2-hydroxy-sn-glycero-3-phosphocholine
Target:
Lyn peptide inhibitor
Cat.No: TP2008
Synonym:
Target:
Aspochalasin D
Cat.No: T37443
Synonym:
Target:
Lyn peptide inhibitor TFA
Cat.No: T75806
Synonym:
Target:
Denileukin diftitox
Cat.No: T73697
Synonym:
Target:
Trabikibart
Cat.No: T80959
Synonym: CSL311
Target:
FPR2 agonist 3
Cat.No: T82373
Synonym:
Target:
C4 Ceramide (d18:1/4:0)
Cat.No: T37564
Synonym: C4 Ceramide (d18:1/4:0),Cer(d18:1/4:0)
Target:
HPK1-IN-3
Cat.No: T63287
Synonym:
Target:
Nemvaleukin alfa
Cat.No: T77096
Synonym:
Target:
β-Defensin-3 (human) (trifluoroacetate salt)
Cat.No: T35452
Synonym:
Target:
MRT67307 HCl (1190378-57-4 free base)
Cat.No: T23028
Synonym: MRT67307 HCl
Target: Others
N-3-oxo-dodecanoyl-L-Homoserine lactone
Cat.No: T21633
Synonym:
Target:
MRL-871
Cat.No: T62622
Synonym:
Target:
IRBP (1-20) (human, rat) TFA
Cat.No: T83681
Synonym: IRBP1-20,Interphotoreceptor Retinoid-Binding Protein (1-20)
Target:
Vobarilizumab
Cat.No: T76878
Synonym:
Target:
Semapimod
Cat.No: T79304
Synonym: CPSI-2364,CNI-1493 free base
Target:
ALV1
Cat.No: T63339
Synonym:
Target:
Agatolimod
Cat.No: T64232
Synonym:
Target:
Fc 11a-2
Cat.No: T68225
Synonym:
Target:
AY 254
Cat.No: T41189
Synonym:
Target:
Immuno modulator-1
Cat.No: T79170
Synonym:
Target:
Anrukinzumab
Cat.No: T76906
Synonym:
Target:
Epinastine
Cat.No: T60366
Synonym:
Target:
Elsilimomab
Cat.No: T76803
Synonym:
Target:
Ac-YVAD-CHO
Cat.No: T19883
Synonym: L 709049,L-709049,L709049
Target:
ODN 24987
Cat.No: T74911
Synonym:
Target:
(R)-MLT-985
Cat.No: T62680
Synonym:
Target:
Cat. No. Product Name Target Signaling Pathways
T2893 Muscone

3-Methylcyclopentadecanone,Methylexaltone,麝香酮

MMP; TNF; NF-κB; NOD-like Receptor (NLR); P-gp; Interleukin Apoptosis; Immunology/Inflammation; Membrane transporter/Ion channel; Neuroscience; NF-κB; Proteases/Proteasome
Muscone (3-Methylcyclopentadecanone) 是中药麝香的一种主要活性单体。它抑制NF-κB 和NLRP3炎性小体的活化,显著降低炎性细胞因子水平,并最终改善心脏功能和存活率。
TN1787 Isomucronulatol 7-O-glucoside

Isomucronulatol 7-O-beta-glucoside,黄芪紫檀烷苷,3-羟基-9,10-二甲氧基紫檀烷

Others Others
Isomucronulatol 7-O-glucoside 具有潜在的抗炎活性,在体外对 LPS 刺激产生的 IL-12 p40 表现出微弱的抑制作用。
T4S0795 Berberrubine chloride

9-Berberoline Chloride,Beroline,Beroline Chloride,小檗红碱,Berberrubine,9-Berberoline

IL Receptor Immunology/Inflammation
Berberrubine chloride (9-Berberoline Chloride) 是一种黄连素的有效代谢物,能够改善动物模型中溃疡性结肠炎的症状。
T6S0139 Neobavaisoflavone

Apoptosis; DNA/RNA Synthesis Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair
Neobavaisoflavone 是一种从Psoralea corylifolia 的种子中分离出来的类黄酮。它具有抗炎,抗癌和抗氧化的作用。它在中至高浓度下可抑制 DNA 聚合酶,也可抑制血小板聚集。
T3859 Isomucronulatol

7,2'-Dihydroxy-3',4'-dimethoxyisoflavan,7,2'-二羟基-3',4'-二甲氧基异黄烷,异短尖剑豆酚

Others Others
Isomucronulatol (7,2'-Dihydroxy-3',4'-dimethoxyisoflavan) 是一种黄酮类化合物,分离自 A. membranaceus 根。它在体外对 LPS 刺激产生的 IL-12 p40 有抑制作用,具有潜在的抗炎作用。
T6S1597 Mulberroside A

桑皮苷 A,桑皮苷A

TNF; Tyrosinase; Interleukin Apoptosis; Immunology/Inflammation; Proteases/Proteasome
Mulberroside A 是桑中的一种主要活性成分,可降低TNF-α、IL-1β和IL-6的表达,抑制 NALP3、caspase-1 和 NF-κB 的激活以及 ERK、JNK 和 p38 的磷酸化 。它抑制蘑菇酪氨酸酶,具有抗炎和抗细胞凋亡作用。
TC0036 Compound Lup-20(29)-en-3-yl acetate

IL Receptor; VEGFR; Others; TNF; COX Angiogenesis; Apoptosis; Immunology/Inflammation; Neuroscience; Others; Tyrosine Kinase/Adaptors
Lup-20(29)-en-3-yl acetate 是 Lupeol 的衍生物,通过下调 TNF-α、IL-1β、MCP-1、COX-2、VEGF 和颗粒酶 B 来抑制类风湿性关节炎的进展。
T7210 Guanosine 5'-diphosphate

GDP,鸟苷-5ˊ-二磷酸

Endogenous Metabolite Metabolism
Guanosine 5'-diphosphate (GDP) 是核苷二磷酸,是潜在的铁动员剂,能够阻断铁调素-铁转运蛋白相互作用并调节白细胞介素-6 (IL-6)/stat-3 途径。
T5S1981 alpha-Cyperone

(+)-α-Cyperone,α-香附酮,α-Cyperone

Others; Endogenous Metabolite Metabolism; Others
alpha-Cyperone (α-Cyperone) 与 IL-6, Cox-2, Cdc42, Nck-2, Rac1 的表达下调相关,从而能够抑制炎症反应。
T2993 Cordycepin

3'-Deoxyadenosine,虫草素

MMP; TNF; Antibacterial; Antibiotic; Autophagy Apoptosis; Autophagy; Microbiology/Virology; Proteases/Proteasome
Cordycepin (3'-Deoxyadenosine) 是一种核苷衍生物,在类风湿性关节炎滑膜成纤维细胞中,剂量依赖性抑制 IL-1β 诱导的 MMP-1和 MMP-3表达。它也抑制细菌的腺苷激酶从而抗结核分枝杆菌。
T4S0145 Corylifol A

Corylinin,补骨脂异黄酮A

hCE; STAT; UGT JAK/STAT signaling; Metabolism; Stem Cells
Corylifol A (Corylinin) 是补骨脂中的一种天然产物,可抑制IL-6 诱导的STAT3激活和磷酸化,IC50值为0.81 μM。
T2795 Amygdalin

苦杏仁苷,Laetrile

Others Others
Amygdalin (Laetrile) 是一种植物葡萄糖苷,分离自蔷薇果实的果核中,如杏,桃,杏仁,樱桃和李子。
T6S1141 Ganoderic acid A

灵芝酸 A,灵芝酸A

Apoptosis; NF-κB; Endogenous Metabolite; Autophagy Apoptosis; Autophagy; Metabolism; NF-κB
Ganoderic acid A 能够抑制 JAK-STAT3信号通路,也能抑制细胞增殖,存活率和 ROS。 它对人骨肉瘤 HOS 和MG-63细胞具有增殖抑制、凋亡和侵袭抑制作用。
T38373 2-heptyl-3-hydroxy-4(1H)-Quinolone

2-heptyl-3-hydroxy-4(1H)-Quinolone,PQS,Pseudomonas Quinolone Signal

Others Others
2-heptyl-3-hydroxy-4(1H)-Quinolone (Pseudomonas Quinolone Signal) 是一种铜绿假单胞菌为应对细胞密度增加而产生的一种法定人数感应信号分子。 它增加了铜绿假单胞菌中lasB 基因的表达,增加代谢物焦蓝蛋白和凝集素PA-IL 的分泌,以及增加铜绿假单胞菌种群的生物膜生产。当使用浓度为40 μM 时,它还会降低铜绿假单胞菌生长介质中的铁含量,并在硫酸铁溶液中充当一种铁螯合剂。
T6S1579 Monotropein

水晶兰苷,Monotropeine

Others Others
Monotropein (Monotropeine) 是从Morinda officinalis 中获得,能够抑制硫酸葡聚糖硫酸钠诱导的结肠炎小鼠模型中炎性因子的表达。
T4S2063 Tetrahydrocoptisine

人血草碱,STYLOPINE

ERK; p38 MAPK; NF-κB MAPK; NF-κB
Tetrahydrocoptisine (STYLOPINE) 具有抑制炎症的有效作用。它通过抑制 NF-κB 信号通路对 LPS 诱导的 ALI 具有保护作用,这可能涉及抑制肺部炎症过程。它具有胃保护活性,归因于减少 NO 产生和调节促炎细胞因子,抑制中性粒细胞积累和 NF-κB 表达。它是一种活性抗炎成分,通过下调 NF-κB 活化、磷酸化 ERK1/2 和磷酸化-p38MAPK 信号通路抑制 TNF-α、IL-6 和 NO 的产生。
T2S0843 Negletein

黄芩素-7-甲醚,7-O-Methylbaicalein,Baicalein-7-methylether

IL Receptor; TNF; NOS; Interleukin Apoptosis; Immunology/Inflammation
Negletein (7-O-Methylbaicalein) 一种神经保护剂,可增强神经生长因子的作用并诱导 PC12 细胞中的神经突生长。它通过抑制TNF-α和IL-1β表现出抗炎活性,其 IC50值分别为 16.4 和 10.8 μM。它还具有抗菌、抗缺氧和抗阿尔茨海默病活性。
T6S1917 Schisandrol B

Gomisin A,TJN-101,Besigomsin,五味子醇乙,Gamma-Schisandrin,戈米辛A,Schizandrol B,Wuweizi alcohol-B

P450; Reactive Oxygen Species; Autophagy Autophagy; Immunology/Inflammation; Metabolism; NF-κB
Schisandrol B (Besigomsin) 是华中五味子的主要活性成分,具有保肝、抗炎、抗糖尿病和抗氧化的作用。它抑制活性氧的产生,也抑制 P-糖蛋白和CYP3A 的活性。
T6S1315 Oroxylin A

千层纸素A,6-Methoxybaicalein,Baicalein 6-methyl ether

Virus Protease; HIF/HIF Prolyl-Hydroxylase; Autophagy Autophagy; Chromatin/Epigenetic; Metabolism; Microbiology/Virology
Oroxylin A (Baicalein 6-methyl ether) 是一种有活性的黄酮,具有较强的抗癌作用。
T2S2264 Linalool

Linalol,(±)-Linalool,Phantol,沉香醇

Apoptosis; IL Receptor; TNF; Endogenous Metabolite; iGluR Apoptosis; Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism; Neuroscience
Linalool (Linalol) 是存在芫荽等植物中的单萜类天然产物,是竞争性NMDA 受体拮抗剂,具有抗肿瘤和抗心脏毒性的作用。它通过激活 Nrf2 诱导抗氧化防御和通过抑制 NF-κB 减少炎症反应来保护其免受 LPS/GalN 诱导的肝损伤,具有镇痛、抗菌和抗炎的特性。
TN5033 Skullcapflavone I

IL Receptor; Caspase; Prostaglandin Receptor Apoptosis; GPCR/G Protein; Immunology/Inflammation; Proteases/Proteasome
Skullcapflavone I has anti-inflammatory and anti-allergic potential, it can significantly inhibit LPS stimulated NO and PGE(2) release in J774A.1 macrophages and inhibit LPS induced IL-6 production in a concentration dependent manner. Skullcapflavone I se
TN5912 Macluraxanthone

3-Hydroxyblancoxanthone

Antioxidant; TNF Apoptosis; oxidation-reduction
Macluraxanthone (3-Hydroxyblancoxanthone) 具有许多生物活性,包括抗胆碱酯酶、抗氧化、抗癌、抗疟疾、抗炎和免疫调节作用。Macluraxanthone 通过增加表达CD86的巨噬细胞的百分比,同时减少其CD14、CD11b 和CD80的表达,来促进M1类促炎症巨噬细胞的极化。Macluraxanthone 在促炎症刺激物脂多糖的存在下明显减少了TNF-α和IL-10细胞因子的产生。
T35741 Gliovirin

Gliovirin is a fungal metabolite that has been found inT. harzianumand has fungicidal, antimicrobial and anti-inflammatory activities.1It is active against the plant pathogenic fungusP. ultimum(MIC = 60 ng/ml) and the parasiteT. brucei brucei(IC50= 90 ng/ml), but has no effect on the plant pathogenic fungiR. solani,P. omnivorum,T. basicola,R. arrhizus, andV. dahliaeor the bacteriaB. thuringiensis,P. fluorescens, andX. malvacearumwhen used at concentrations up to 1,000 ng/ml.2,3Gliovirin decrease...

天然产物

Muscone
Cat.No: T2893
Synonym: 3-Methylcyclopentadecanone,Methylexaltone,麝香酮
Target: MMP, TNF, NF-κB, NOD-like Receptor (NLR), P-gp, Interleukin
Isomucronulatol 7-O-glucoside
Cat.No: TN1787
Synonym: Isomucronulatol 7-O-beta-glucoside,黄芪紫檀烷苷,3-羟基-9,10-二甲氧基紫檀烷
Target: Others
Berberrubine chloride
Cat.No: T4S0795
Synonym: 9-Berberoline Chloride,Beroline,Beroline Chloride,小檗红碱,Berberrubine,9-Berberoline
Target: IL Receptor
Neobavaisoflavone
Cat.No: T6S0139
Synonym:
Target: Apoptosis, DNA/RNA Synthesis
Isomucronulatol
Cat.No: T3859
Synonym: 7,2'-Dihydroxy-3',4'-dimethoxyisoflavan,7,2'-二羟基-3',4'-二甲氧基异黄烷,异短尖剑豆酚
Target: Others
Mulberroside A
Cat.No: T6S1597
Synonym: 桑皮苷 A,桑皮苷A
Target: TNF, Tyrosinase, Interleukin
Compound Lup-20(29)-en-3-yl acetate
Cat.No: TC0036
Synonym:
Target: IL Receptor, VEGFR, Others, TNF, COX
Guanosine 5'-diphosphate
Cat.No: T7210
Synonym: GDP,鸟苷-5ˊ-二磷酸
Target: Endogenous Metabolite
alpha-Cyperone
Cat.No: T5S1981
Synonym: (+)-α-Cyperone,α-香附酮,α-Cyperone
Target: Others, Endogenous Metabolite
Cordycepin
Cat.No: T2993
Synonym: 3'-Deoxyadenosine,虫草素
Target: MMP, TNF, Antibacterial, Antibiotic, Autophagy
Corylifol A
Cat.No: T4S0145
Synonym: Corylinin,补骨脂异黄酮A
Target: hCE, STAT, UGT
Amygdalin
Cat.No: T2795
Synonym: 苦杏仁苷,Laetrile
Target: Others
Ganoderic acid A
Cat.No: T6S1141
Synonym: 灵芝酸 A,灵芝酸A
Target: Apoptosis, NF-κB, Endogenous Metabolite, Autophagy
2-heptyl-3-hydroxy-4(1H)-Quinolone
Cat.No: T38373
Synonym: 2-heptyl-3-hydroxy-4(1H)-Quinolone,PQS,Pseudomonas Quinolone Signal
Target: Others
Monotropein
Cat.No: T6S1579
Synonym: 水晶兰苷,Monotropeine
Target: Others
Tetrahydrocoptisine
Cat.No: T4S2063
Synonym: 人血草碱,STYLOPINE
Target: ERK, p38 MAPK, NF-κB
Negletein
Cat.No: T2S0843
Synonym: 黄芩素-7-甲醚,7-O-Methylbaicalein,Baicalein-7-methylether
Target: IL Receptor, TNF, NOS, Interleukin
Schisandrol B
Cat.No: T6S1917
Synonym: Gomisin A,TJN-101,Besigomsin,五味子醇乙,Gamma-Schisandrin,戈米辛A,Schizandrol B,Wuweizi alcohol-B
Target: P450, Reactive Oxygen Species, Autophagy
Oroxylin A
Cat.No: T6S1315
Synonym: 千层纸素A,6-Methoxybaicalein,Baicalein 6-methyl ether
Target: Virus Protease, HIF/HIF Prolyl-Hydroxylase, Autophagy
Linalool
Cat.No: T2S2264
Synonym: Linalol,(±)-Linalool,Phantol,沉香醇
Target: Apoptosis, IL Receptor, TNF, Endogenous Metabolite, iGluR
Skullcapflavone I
Cat.No: TN5033
Synonym:
Target: IL Receptor, Caspase, Prostaglandin Receptor
Macluraxanthone
Cat.No: TN5912
Synonym: 3-Hydroxyblancoxanthone
Target: Antioxidant, TNF
Gliovirin
Cat.No: T35741
Synonym:
Target:
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