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42

抑制剂 & 化合物

3

天然产物

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Cat. No. Product Name Target Signaling Pathways
T15108 DG-041

Prostaglandin Receptor GPCR/G Protein; Immunology/Inflammation
DG-041 是高亲和力,选择性的,有效的 EP3受体拮抗剂,在结合和 FLIPR 试验中,IC50分别为 4.6 nM 和 8.1 nM。DG-041通过抑制 PGE2促进血小板聚集。DG-041具有血脑屏障渗透性。
T0328 Hexetidine

NSC-17764,海克替啶

Antibacterial; Antifungal Microbiology/Virology
Hexetidine (NSC-17764) 是一种口服活性的抗菌抗真菌试剂,可用于口腔感染的相关研究。
T14369 AZD-0284

ROR Metabolism
AZD-0284 是核受体 (RORγ) 的选择性反向激动剂。它对呼吸道疾病及斑块型寻常型银屑病具有潜在的应用价值。
T7657 Myelin Oligodendrocyte Glycoprotein Peptide (35-55), mouse, rat

髓鞘少突胶质细胞糖蛋白,MOG (35-55)

Others Others
Myelin Oligodendrocyte Glycoprotein Peptide (35-55), mouse, rat (MOG (35-55)) 是中枢神经鞘的一个次要成分。它能诱导强效的 T 细胞和 B 细胞反应,同时是高度脑源性的。它能够引发复发缓解性神经系统疾病,伴有广泛的斑块样脱髓鞘。
TP2045 CH 275

Potent somatostatin receptor 1 (sst1) agonist; displays selectivity for sst1 (IC50 values are 30.9 nM, 345 nM, > 1 μM, > 10 μM and > 10μM for human sst1, sst3, sst4, sst2 and sst5 respectively). Attenuates somatostatin release in the rat nucleus accumbens
T1000L Chlorhexidine diacetate

醋酸氯己定,Hibitane diacetate,Chlorhexidine Acetate,Bactigras

CAT; Antibacterial; Antibiotic; Antifection Microbiology/Virology; oxidation-reduction
Chlorhexidine diacetate (Bactigras) 是一种双胍类杀菌剂,能快速消灭革兰氏阳性菌和革兰氏阴性菌。它也用作漱口水以防止口腔菌斑。
T68006 Orilotimod potassium

APO805K1

Orilotimod potassium (APO805K1)可用于研究斑块状银屑病。
T1147 Chlorhexidine dihydrochloride

盐酸氯己定,Chlorhexidine hydrochloride,Chlorhexidine 2HCl,NSC-185

CAT; Cell wall; Antibacterial; Antibiotic; Antifection Immunology/Inflammation; Microbiology/Virology; oxidation-reduction
Chlorhexidine dihydrochloride (NSC-185) 是一种消毒剂和局部抗感染剂,也用作漱口水以防止口腔菌斑。
T9930 Secukinumab

IL Receptor Immunology/Inflammation
Secukinumab 是一种完全人源化的单克隆抗 IL-17A 抗体,是一个被美国食品和药物管理局批准用于治疗中度至重度斑块型银屑病的抗体。
T17038 Tepilamide fumarate

XP-23829

Others Others
Tepilamide fumarate (XP-23829) 是一种口服具有活性的延胡索酸酯,可用于研究中度到重度慢性斑块银屑病。
T37445 Etanercept

TNF Apoptosis
Etanercept is a dimeric fusion protein that serves as a competitive TNF inhibitor by binding to TNF. It effectively inhibits the binding of both TNF-α and TNF-β to the TNF receptors on cell surfaces, thereby rendering TNF biologically inactive. Etanercept has demonstrated efficacy in treating rheumatoid arthritis, juvenile idiopathic arthritis, and plaque psoriasis.
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。
T77170 Siplizumab

MEDI-507

Others Others
Siplizumab (MEDI-507) 是一种人源化靶向 CD2 的 IgG1 单克隆抗体。Siplizumab 在体外选择性地消耗效应记忆 T 细胞并促进同种异体反应性调节性 T 细胞的相对扩增。Siplizumab 可用于治疗斑块状银屑病。
T16094 MK-3328

Others Others
MK-3328 是对β-淀粉样蛋白 (β-Amyloid)具有很高的亲和力(IC50 为 10.5 nM),是一种可作为临床评估β-淀粉样斑块负荷的候选 PET 配体。MK-3328是治疗阿尔茨海默病的潜在药物。
T0305 Erythrosine B

Erythrosine I,Erythrosin extra bluish,Erythrosin B,赤藓红B

Others Others
Erythrosine B (Erythrosine I) 是一种已被用于开发动物模型的新型光敏剂,在食品和纺织工业的人造染料中具有广泛的应用。
T0578 Erythrosin B

Iodeosin,Tetraiodofluorescein,藻红B

Others Others
Erythrosin B (Iodeosin) 是一种四碘荧光素,在某些食物(樱桃、鱼)中用作红色色素,用作某些细胞类型的染色剂,以及用作牙菌斑的披露物。其分子结构与甲状腺素相似。
T64167 Ifebemtinib

IN-10018,BI-853520

FAK Angiogenesis; Cytoskeletal Signaling; Tyrosine Kinase/Adaptors
Ifebemtinib (BI-853520) 是一种具有口服活性和强效性的粘附斑激酶 (FAK) 抑制剂 (IC50=1 nM),具有抗肿瘤活性,可抑制恶性胸膜间皮瘤中的球状体形成和原位肿瘤生长,可用于研究乳腺癌和卵巢癌。
T76924 Efalizumab

Hu1124,HU 1124

Integrin Cytoskeletal Signaling
Efalizumab 是一种新型针对 T 细胞的有效调节剂,是人源化 LFA-1 α 亚基(CD11a)单克隆抗体。Efalizumab 对 T 细胞激活、皮肤T细胞运输和T细胞粘附到角质形成细胞有抑制作用,可用于研究斑块银屑病和银屑病关节炎。
T0900 Cetylpyridinium chloride monohydrate

Hexadecylpyridinium chloride monohydrate,十六烷基氯化吡啶

Antibacterial; Antibiotic Microbiology/Virology
Cetylpyridinium chloride monohydrate (Hexadecylpyridinium chloride monohydrate) 是阳离子季铵, 是一种能杀死细菌和其他微生物的防腐剂, 用于某些类型的漱口水, 牙膏, 咽喉和鼻腔喷雾剂中, 可有效预防牙斑和减少牙龈炎。
T68705 Salifluor

Salifluor is a broad spectrum antimicrobial agent that has been investigated for its abilities to inhibit dental plaque formation.
TP1494 β-Amyloid (4-10)

β-Amyloid 4-10

Antibodies corresponding to beta-amyloid (4-10) are effective in vivo inhibitors of cytotoxicity, amyloid plaque formation and special memory disturbances in mice. This peptide does not elicit an inflammatory response.
T68494 Octenidine saccharin

Octenidine saccharin is a Dental Plaque Inhibitor
T1267L Abacavir acetate

KM-133,KM133,KM 133

Abacavir acetate (Prurisol) has the potential to be used in the treatment of plaque psoriasis.
T38175 MPro N3

Coronavirus main protease (Mpro) inhibitor (respective IC50 values are 2.7, 4 and 8.8 μM for MHV-A29, HCoV-229E and FOPV replication in vitro). Inhibits viral cell infection in an MHV plaque reduction assay. Also inhibits SARS-CoV-2 viral cell entry in a plaque reduction assay (IC50 = 16.8 μM).
T69456 Melagatran monohydrate

Melagatran monohydrate is a thrombin inhibitor. Melagatran prevents tissue factor expression in human platelet-monocyte heterotypic complexes. Melagatran reduces advanced atherosclerotic lesion size and may promote plaque stability in apolipoprotein E-deficient mice.
T76885 Sonelokimab

Sonelokimab (ALX 0761; M 1095) 是三价纳米抗体,特异性结合人白介素(IL)-17A、IL-17F及人血清白蛋白VHH,由单价骆驼来源纳米抗体构成,展现于斑块型银屑病研究中的应用潜力。
T21814 ONO 4817

ONO-4817 是一种广谱基质金属蛋白酶 (MMP) 抑制剂。抑制基质金属蛋白酶 (MMP) 有望抑制动脉粥样硬化新内膜增殖,从而限制动脉粥样硬化斑块的进展。ONO-4817 抑制实验性高脂血症兔主动脉内膜增生的发展。
TP2171 β-amyloid (12-28) (TFA) (107015-83-8 free base)

Amyloid β-Protein (12-28) (TFA),β-amyloid (12-28) (TFA)

Others Others
β-amyloid (12-28) TFA, a peptide fragment of β-amyloid protein (β1-42), is the major component of senile plaque cores. β-amyloid (12-28) has aggregation properties and the potential for Alzheimer’s disease research.
TP2135 cAC 253

Amylin (AMY3) antagonist (IC50 = 0.3 μM). Protects neuronal cells from Aβ(1-42)-induced cytotoxicity in vitro. Brain penetrant. Improves spatial memory and reduces Aβ plaque number and total area in a mouse Alzheimer's disease model.
T77098 Netakimab

Netakimab为抗IL-17单克隆抗体。Nerelimomab适用于研究强直性脊柱炎、银屑病关节炎及中重度斑块状银屑病。
T71306 Gemfibrozil-d6

Gemfibrozil-d6 is intended for use as an internal standard for the quantification of gemfibrozil by GC- or LC-MS. Gemfibrozil is a peroxisome proliferator-activated reporter α and PPARγ agonist. In vivo, gemfibrozil reduces serum total cholesterol, triglyceride, and LDL levels in a rat model of high-cholesterol diet-induced hyperlipidemia. Gemfibrozil reduces atherosclerotic plaque area, superoxide production, and expression of the genes encoding the NF-κB subunit p65 and chemokine (C-C) motif l...
T78298 Alefacept

LFA 3TIP,Human LFA 3IgG fusion protein,BG 9273

Alefacept (BG 9273)为一种人类淋巴细胞功能相关抗原3/免疫球蛋白1融合蛋白,主要在慢性斑块状银屑病研究中使用。
T69664 Umibecestat HCl

Umibecestat, also known as CNP-520, is a beta-secretase inhibitor and is a drug candidate for prevention trials in Alzheimer's disease. CNP520 has a selectivity, pharmacodynamics, and distribution profile suitable for AD prevention studies. CNP520 reduced brain and cerebrospinal fluid (CSF) Aβ in rats and dogs, and Aβ plaque deposition in APP-transgenic mice. CNP520 reduces Aβ load and neuroinflammation in APP‐transgenic mice
T75779 β-Amyloid (12-28) (TFA)

β-Amyloid (12-28) (TFA)为β-淀粉样蛋白(β1-42)的肽片段,后者是由42个氨基酸组成,构成老年斑核心的关键蛋白。β-Amyloid (12-28) (TFA)展现出聚集性质,并可能对阿尔茨海默氏病研究具有潜在价值。
T38118 Zanamivir-13C,15N2

Zanamivir-13C,15N2

Zanamivir-13C,15N2is intended for use as an internal standard for the quantification of zanamivir by GC- or LC-MS. Zanamivir is a sialic acid analog that inhibits neuraminidase release of newly replicated influenza virus particles.1It has been shown to selectively inhibit the growth of influenza A and B viruses in plaque reduction assays with IC50values ranging from 5 to 14 nM and to directly inhibit influenza A and B virus neuraminidases with IC50values ranging from 0.6 to 7.9 nMin vitro. Intra...
T63558 IRAK4-IN-21

IRAK4-IN-21 是选择性的、口服具有活力的、强效的 IRAK4 抑制剂,能够作用于 IRAK4 (IC50: 5 nM) 和 TAK1 (IC50: 56 nM)。IRAK4-IN-21 对 IL-23 的产生表现出有效的抑制作用,其 IC50值为0.17 μM。IRAK4-IN-21 能够用于研究自身免疫性疾病,如斑块状银屑病和银屑病关节炎。
T72893 AChE/MAO-IN-2

Dual AChE-MAO B-IN-5 是一种茚满酮衍生物,是一种有效的双重 AChE/MAO-B 抑制剂,对 AChE、MAO-B 和 MAO-A 的IC50值分别为 0.0224、0.0412 和 0.1116 μM。Dual AChE-MAO B-IN-5 具有抗氧化活性,防止 β-淀粉样斑块聚集。Dual AChE-MAO B-IN-5 可用于阿尔茨海默病 (AD) 研究。
T78541 Myelin Oligodendrocyte Glycoprotein Peptide (35-55), mouse, rat TFA

MOG (35-55) (TFA)

Myelin Oligodendrocyte Glycoprotein Peptide (35-55), mouse, rat (MOG (35-55)) TFA 是一种具有致脑炎活性的化合物,能够诱导 T 细胞增殖和 Th1 细胞因子反应,并促使产生相对较高水平的 IgG 抗体。此化合物作为中枢神经鞘的次要成分,可触发带有广泛斑块样脱髓鞘的复发缓解性神经系统疾病。
T63559 IRAK4-IN-22

IRAK4-IN-22 是选择性的、口服具有活力的、强效的 IRAK4 抑制剂,能够作用于 IRAK4 (IC50: 3 nM) 和 TAK1 (IC50: 17 nM)。IRAK4-IN-21 对 IL-23 的产生表现出有效的抑制作用,其 IC50值为0.10 μM。IRAK4-IN-21 能够用于研究自身免疫性疾病,如斑块状银屑病和银屑病关节炎。
T78542 Myelin Oligodendrocyte Glycoprotein Peptide (35-55), mouse, rat acetate

MOG (35-55) (acetate)

Myelin Oligodendrocyte GlycoproteinPeptide (35-55), mouse, rat (MOG (35-55)) acetate 是一中枢神经系统髓鞘的非主要成分,它显示出致脑炎活性,并能诱导 T 细胞增殖。此外,MOG (35-55) acetate 能够诱导 Th1 细胞因子反应,并促使相对高水平的 IgG 抗体生成。它也可能引起复发性和缓解性的神经系统疾病,并伴随广泛的斑块样脱髓鞘现象。
T83710 Gastric Inhibitory Peptide (22-51) (human) TFA

GIP (22-51),Glucose-dependent Insulinotropic Peptide (22-51)

胃抑制肽(GIP) (22-51) 是一种具有30个氨基酸的前动脉硬化肽,对应于GIP前体蛋白proGIP的第22至51个氨基酸残基,已在人类血浆中发现。在1 µM的浓度下使用,该肽能引起在巨峰细胞分化的THP-1细胞和分离的人类主动脉内皮细胞中IκB-α的降解和NF-κB的核转移。在体内,GIP (22-51) 增加了ApoE-/-小鼠的动脉粥样硬化病变面积和斑块形成。
T72454 AChE/BChE/MAO-B-IN-4

AChE/BChE/MAO-B-IN-4 是一种 1-茚满酮衍生物,是一种有效的MAO-B 抑制剂,对人MAO-B 的IC50为 0.0359 μM。AChE/BChE/MAO-B-IN-4 是一种有效的AChE 和BChE 酶抑制剂,对人AChE 和BChE 酶的IC50值分别为 0.0473 μM 和 0.0782 μM。AChE/BChE/MAO-B-IN-4 显示出显着的抗氧化活性,并防止β-淀粉样蛋白斑块聚集。AChE/BChE/MAO-B-IN-4 具有用于阿尔茨海默病 (AD) 研究的潜力。

化合物

DG-041
Cat.No: T15108
Synonym:
Target: Prostaglandin Receptor
Hexetidine
Cat.No: T0328
Synonym: NSC-17764,海克替啶
Target: Antibacterial, Antifungal
AZD-0284
Cat.No: T14369
Synonym:
Target: ROR
Myelin Oligodendrocyte Glycoprotein Peptide (35-55), mouse, rat
Cat.No: T7657
Synonym: 髓鞘少突胶质细胞糖蛋白,MOG (35-55)
Target: Others
CH 275
Cat.No: TP2045
Synonym:
Target:
Chlorhexidine diacetate
Cat.No: T1000L
Synonym: 醋酸氯己定,Hibitane diacetate,Chlorhexidine Acetate,Bactigras
Target: CAT, Antibacterial, Antibiotic, Antifection
Orilotimod potassium
Cat.No: T68006
Synonym: APO805K1
Target:
Chlorhexidine dihydrochloride
Cat.No: T1147
Synonym: 盐酸氯己定,Chlorhexidine hydrochloride,Chlorhexidine 2HCl,NSC-185
Target: CAT, Cell wall, Antibacterial, Antibiotic, Antifection
Secukinumab
Cat.No: T9930
Synonym:
Target: IL Receptor
Tepilamide fumarate
Cat.No: T17038
Synonym: XP-23829
Target: Others
Etanercept
Cat.No: T37445
Synonym:
Target: TNF
Ixekizumab
Cat.No: T38105
Synonym: LY2439821
Target: IL Receptor, Interleukin
Siplizumab
Cat.No: T77170
Synonym: MEDI-507
Target: Others
MK-3328
Cat.No: T16094
Synonym:
Target: Others
Erythrosine B
Cat.No: T0305
Synonym: Erythrosine I,Erythrosin extra bluish,Erythrosin B,赤藓红B
Target: Others
Erythrosin B
Cat.No: T0578
Synonym: Iodeosin,Tetraiodofluorescein,藻红B
Target: Others
Ifebemtinib
Cat.No: T64167
Synonym: IN-10018,BI-853520
Target: FAK
Efalizumab
Cat.No: T76924
Synonym: Hu1124,HU 1124
Target: Integrin
Cetylpyridinium chloride monohydrate
Cat.No: T0900
Synonym: Hexadecylpyridinium chloride monohydrate,十六烷基氯化吡啶
Target: Antibacterial, Antibiotic
Salifluor
Cat.No: T68705
Synonym:
Target:
β-Amyloid (4-10)
Cat.No: TP1494
Synonym: β-Amyloid 4-10
Target:
Octenidine saccharin
Cat.No: T68494
Synonym:
Target:
Abacavir acetate
Cat.No: T1267L
Synonym: KM-133,KM133,KM 133
Target:
MPro N3
Cat.No: T38175
Synonym:
Target:
Melagatran monohydrate
Cat.No: T69456
Synonym:
Target:
Sonelokimab
Cat.No: T76885
Synonym:
Target:
ONO 4817
Cat.No: T21814
Synonym:
Target:
β-amyloid (12-28) (TFA) (107015-83-8 free base)
Cat.No: TP2171
Synonym: Amyloid β-Protein (12-28) (TFA),β-amyloid (12-28) (TFA)
Target: Others
cAC 253
Cat.No: TP2135
Synonym:
Target:
Netakimab
Cat.No: T77098
Synonym:
Target:
Gemfibrozil-d6
Cat.No: T71306
Synonym:
Target:
Alefacept
Cat.No: T78298
Synonym: LFA 3TIP,Human LFA 3IgG fusion protein,BG 9273
Target:
Umibecestat HCl
Cat.No: T69664
Synonym:
Target:
β-Amyloid (12-28) (TFA)
Cat.No: T75779
Synonym:
Target:
Zanamivir-13C,15N2
Cat.No: T38118
Synonym: Zanamivir-13C,15N2
Target:
IRAK4-IN-21
Cat.No: T63558
Synonym:
Target:
AChE/MAO-IN-2
Cat.No: T72893
Synonym:
Target:
Myelin Oligodendrocyte Glycoprotein Peptide (35-55), mouse, rat TFA
Cat.No: T78541
Synonym: MOG (35-55) (TFA)
Target:
IRAK4-IN-22
Cat.No: T63559
Synonym:
Target:
Myelin Oligodendrocyte Glycoprotein Peptide (35-55), mouse, rat acetate
Cat.No: T78542
Synonym: MOG (35-55) (acetate)
Target:
Gastric Inhibitory Peptide (22-51) (human) TFA
Cat.No: T83710
Synonym: GIP (22-51),Glucose-dependent Insulinotropic Peptide (22-51)
Target:
AChE/BChE/MAO-B-IN-4
Cat.No: T72454
Synonym:
Target:
Cat. No. Product Name Target Signaling Pathways
T5244 Aminomalonic acid

2-Aminopropanedioic Acid,氨基丙二酸,Aminomalonate

Others; Endogenous Metabolite Metabolism; Others
Aminomalonic acid (Aminomalonate) 是氨基内源性代谢产物,在体外能作为来源 Leukemia 5178Y/AR 和小鼠胰腺的 L- 天冬酰胺合成酶的高效抑制剂 (Leukemia 5178Y/AR:Ki= 0.0023 M,小鼠胰腺:Ki= 0.0015 M)。它有潜力用作区分黑素瘤转移的不同阶段生物标志物。
T4723 D-Tagatose

塔格糖,D-(-)-Tagatose,D-塔格糖,d-tagatos

Others; Endogenous Metabolite Metabolism; Others
D-Tagatose (D-(-)-Tagatose) 是自然界中发现的一种罕见的单糖,具有益生元特性。它是研究II 型糖尿病的潜在抗糖尿病药物,也是帮助提升结肠有益细菌、预防结肠癌和抑制胆固醇的益生元。它是蔗糖的替代品,也是口香糖、果汁和饮料等食品中的低热量甜味剂。
T38015 Herquline A

Herquline A is an alkaloid fungal metabolite originally isolated from P. herquei. It inhibits cell death induced by influenza A strain A/PR/8/34 in MDCK cells with an IC50 value of 10 μg/ml and inhibits viral replication in a plaque assay in a concentration-dependent manner. Herquline A also inhibits platelet aggregation induced by ADP and platelet-activating factor (PAF) in vitro (IC50s = 180 and 240 μM, respectively).

天然产物

Aminomalonic acid
Cat.No: T5244
Synonym: 2-Aminopropanedioic Acid,氨基丙二酸,Aminomalonate
Target: Others, Endogenous Metabolite
D-Tagatose
Cat.No: T4723
Synonym: 塔格糖,D-(-)-Tagatose,D-塔格糖,d-tagatos
Target: Others, Endogenous Metabolite
Herquline A
Cat.No: T38015
Synonym:
Target:
TargetMol Loading
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