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Search Results for " psoriatic "

Targets Recommended: Epigenetic Reader Domain Histone Acetyltransferase

22

抑制剂 & 化合物

1

天然产物

6

重组蛋白

1

同位素标记化合物

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Cat. No.	Product Name	Target	Signaling Pathways
T6668	SGC-CBP30	Epigenetic Reader Domain; Histone Acetyltransferase	Chromatin/Epigenetic
	SGC-CBP30 是高选择性CBP/p300溴结构域的有效抑制剂，对CBP 和p300的Kd 值分别为 21 和 32 nM。它强烈减少 Th17 细胞中 IL-17A 的分泌，具有抗炎作用。
T1159	Leflunomide SU101,RS-34821,HWA486,来氟米特	Others; Dehydrogenase; AhR	Immunology/Inflammation; Metabolism; Others
	Leflunomide (HWA486) 是嘧啶合成抑制剂，能够抑制二氢乳清酸脱氢酶，具有抗风湿的活性。
T76840	Vunakizumab Anti-Human IL17A Recombinant Antibody	IL Receptor	Immunology/Inflammation
	Vunakizumab 是一种靶向 IL-17A 的人源化 IgGκ 单克隆抗体，常与白细胞介素 22 链接形成 Vunakizumab-IL22 来研究流感病毒引起的肺免疫损伤。Vunakizumab 可用于研究银屑病关节炎，通过与IL-17A结合发挥作用。
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。
T38362	Guselkumab CNTO 1959	IL Receptor	Immunology/Inflammation
	Guselkumab (CNTO 1959) 是一种针对IL-23p19亚基的重组人IgG1单克隆抗体。Guselkumab 与人和食蟹猴IL-23结合，Kd 值分别为3.3和1.9 pmol/L。Guselkumab 对IL-23信号通路下游细胞因子的产生具有抑制作用，可用于银屑病关节炎的研究。
T77677	12R-LOX-IN-2	Lipoxygenase	Metabolism
	12R-LOX-IN-2 是一种 12R-脂氧合酶 (12R-LOX) 的抑制剂。12R-LOX-IN-2 抑制咪喹莫特 (IMQ) 诱导银屑病角质形成细胞过度增殖，并抑制细胞集落形成。12R-LOX-IN-2 还降低 IMQ 诱导细胞中 Ki67 的蛋白水平和 IL-17A 的 mRNA 表达。12R-LOX-IN-2 可用于牛皮癣和其他皮肤相关炎症性疾病的研究。
T76778	Risankizumab Risankizumab rzaa,SKYRIZI,ABBV 066,BI-655066	IL Receptor	Immunology/Inflammation
	Risankizumab (BI 655066) 是一种人源化靶向 IL-23 p19 亚基的 IgG 单克隆抗体(Kd <10 pM)。 Risankizumab 能抑制人 IL-23 在小鼠脾细胞中诱导的 IL-17 产生，IC50 值为 2 pM。Risankizumab 可用于预防和治疗如寻常型银屑病、银屑病关节炎、广泛性脓疱型银屑病和红皮病型银屑病类的免疫性和炎症性疾病。
T21043	Apremilast, (+/-)- Apremilast (+/-)-,	Others	Others
	Apremilast, (+/-)-, is a small molecule inhibitor of phosphodiesterase 4 (PDE4) with oral activity. It is used to treat psoriatic arthritis.
T76823	Perakizumab
	Perakizumab (RG4934)为针对IL-17A(Interleukin Related)的人源化IgG1κ单克隆抗体。适用于自身免疫性疾病（例如银屑病关节炎）的研究。
T40106	IL-17 modulator 1
	IL-17 modulator 1 is an orally active small molecule. It is highly efficacious in modulating IL-17 and can effectively prevent, treat, or ameliorate various diseases such as psoriasis, ankylosing spondylitis, and psoriatic arthritis.
T36525	IL-17 modulator 1 disodium	Others	Others
	IL-17 Modulator 1 (disodium) is a potent, orally active compound, known for its high efficacy in modulating IL-17. This compound is extensively utilized for researching various diseases such as psoriasis, ankylosing spondylitis, and psoriatic arthritis[1].
T36611	(±)13-HODE	Others	Others
	(±)13-HODE is one of the two racemic monohydroxy fatty acids resulting from the non-enzymatic oxidation of linoleic acid. It is the principle hydroxylated fatty acid in human psoriatic skin scales, with a mean concentration of 17 ng/mg.[1]
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。
T81331	QL-1200186	JAK	Angiogenesis; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells
	QL-1200186为具备口服活性与选择性的TYK2抑制剂。经口服后，该药剂量依赖性抑制因interleukin-12刺激所诱导的interferon-γ产生，并在银屑病模型小鼠中显著改善皮肤病变状况。
T76872	Neihulizumab
	Neihulizumab (ALTB-168) 是一种免疫检查点激动性抗体，可与人 CD162 (PSGL-1)结合，导致活化的 T 细胞下调。Neihulizumab 可用于类固醇难治性急性移植物抗宿主病 (SR-aGVHD)、银屑病、银屑病关节炎和溃疡性结肠炎的研究。
T76675	Clazakizumab
	Clazakizumab是一种具有高亲和力和特异性的单克隆抗体，针对IL-6(白细胞介素-6)细胞因子。它可能对抑制COVID-19中因SARS-CoV-2引起的细胞因子反应有帮助。此外，Clazakizumab也被用于研究银屑病关节炎(PsA)和肾抗体介导的排斥反应。
T63558	IRAK4-IN-21	Others	Others
	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。
T83457	12R-LOX-IN-1	Others	Others
	12R-LOX-IN-1（Compound 4a）是一种效能为IC50: 28.25 μM的12R-LOX抑制剂。该化合物能够有效抑制Imiquimod诱导的银屑病角质形成细胞的异常增殖和集落形成能力，同时减少活性氧、Ki67、IL-17A、TNF-α和IL-6的生成，适用于抗银屑病研究。
T63559	IRAK4-IN-22	Others	Others
	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。
T36379	Halometasone	Others	Others
	Halometasone is a synthetic corticosteroid.1,2Formulations containing halometasone have been used in the treatment of psoriasis vulgaris and eczematous dermatoses. 1.de la Brassine, M., Kint, A., Lachapelle, J.M., et al.Halomethasone (C 48.401-Ba) for the topical treatment of common dermatosesJ. Int. Med. Res.12(5)307-309(1984) 2.Zhu, J.-W., Wu, X.-J., Lu, Z.-F., et al.Role of VEGF receptors in normal and psoriatic human keratinocytes: Evidence from irradiation with different UV sourcesPLoS One8...
T38309	LL-37 amide (trifluoroacetate salt)	Others	Others
	LL-37 is a cationic and α-helical antimicrobial peptide expressed in human bone marrow, testis, granulocytes, and gingival epithelium and is upregulated in psoriatic lesions. It inhibits growth of Gram-positive E. coli D21 and Gram-negative B. megatarium in a concentration-dependent manner and LL-37 expression is induced in A549 epithelial cells, alveolar macrophages, neutrophils, and monocyte-derived macrophages following M. tuberculosis infection. LL-37 binds sheep erythrocytes coated with S. ...
T35451	β-Defensin-2 (human) (trifluoroacetate salt)
	β-Defensin-2 is a peptide with antimicrobial properties that protects the skin and mucosal membranes of the respiratory, genitourinary, and gastrointestinal tracts.1It inhibits the growth of periodontopathogenic and cariogenic bacteria, includingP. gingivalisandS. salivarius.2β-Defensin-2 (30 μg/ml) stimulates gene expression and production of IL-6, IL-10, CXCL10, CCL2, MIP-3α, and RANTES by keratinocytes.3It also stimulates calcium mobilization, migration, and proliferation of keratinocytes whe...

化合物

Cat.No: T6668

Target: Epigenetic Reader Domain, Histone Acetyltransferase

Cat.No: T1159

Synonym: SU101,RS-34821,HWA486,来氟米特

Target: Others, Dehydrogenase, AhR

Cat.No: T76840

Synonym: Anti-Human IL17A Recombinant Antibody

Target: IL Receptor

Cat.No: T76924

Synonym: Hu1124,HU 1124

Target: Integrin

Cat.No: T38362

Synonym: CNTO 1959

Target: IL Receptor

Cat.No: T77677

Target: Lipoxygenase

Cat.No: T76778

Synonym: Risankizumab rzaa,SKYRIZI,ABBV 066,BI-655066

Target: IL Receptor

Apremilast, (+/-)-

Cat.No: T21043

Synonym: Apremilast (+/-)-,

Target: Others

Cat.No: T76823

IL-17 modulator 1

Cat.No: T40106

IL-17 modulator 1 disodium

Cat.No: T36525

Target: Others

Cat.No: T36611

Target: Others

Cat.No: T77098

Cat.No: T81331

Target: JAK

Cat.No: T76872

Cat.No: T76675

Cat.No: T63558

Target: Others

Cat.No: T83457

Target: Others

Cat.No: T63559

Target: Others

Cat.No: T36379

Target: Others

LL-37 amide (trifluoroacetate salt)

Cat.No: T38309

Target: Others

β-Defensin-2 (human) (trifluoroacetate salt)

Cat.No: T35451

Cat. No.	Product Name	Target	Signaling Pathways
T1068	Dithranol 1,8,9-trihydroxyanthracene,cignoline,蒽林,Anthralin	Others; DNA/RNA Synthesis	Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Others
	Dithranol (cignoline) 是蒽醌衍生物，可破坏线粒体功能和结构，用于治疗皮肤病。

天然产物

Cat.No: T1068

Synonym: 1,8,9-trihydroxyanthracene,cignoline,蒽林,Anthralin

Target: Others, DNA/RNA Synthesis

Species：

Expression System：

Tag：

Cat. No.	Product Name	Species	Expression System
TMPY-02153	TNF beta Protein, Human, Recombinant LT,TNF β,TNFSF1,肿瘤坏死因子,TNFB,lymphotoxin alpha,lymphotoxin α	Human	E. coli
	Lymphotoxin-alpha, also known as LT-alpha, TNF-beta, Tumor necrosis factor ligand superfamily member 1, LTA TNFSF1, and TNFB, is a secreted protein that belongs to the tumor necrosis factor family. TNF-beta/TNFSF1/Lymphotoxin alpha is highly inducible, secreted, and exists as a homotrimeric molecule. It is a cytokine that in its homotrimeric form binds to TNFRSF1A / TNFR1, TNFRSF1B / TNFBR, and TNFRSF14 / HVEM. In its heterotrimeric form with LTB, TNF-beta/TNFSF1/Lymphotoxin alpha binds to TNFRS...
TMPK-01057	CLEC9A Protein, Human, Recombinant (hFc) CD370,UNQ9341,DNGR-1,HEEE9341,9830005G06Rik,CLEC9A	Human	HEK293 Cells
	CLEC9A expression was significantly higher in psoriatic skin compared with healthy donor. In psoriatic skin and PsA ST, CLEC9A() cells were in close proximity to TUNEL() cells. SF CLEC9A levels were significantly lower compared with paired PsA serum. Adalimumab treatment did not affect CLEC9A serum level and skin expression. The downregulation of synovial CLEC9A might be associated with a novel mechanism by which anti-TNF therapy might reduce CD8-mediated inflammation in PsA patients.
TMPJ-01292	Chemerin/RARRES2 Protein, Human, Recombinant (His) RAR-responsive protein TIG2,RARRES2,Chemerin,Tazarotene-indu...	Human	HEK293 Cells
	Retinoic acid receptor responder protein 2(RARRES2) is a secreted protein that in humans is encoded by the RARRES2 gene. It is highly expressed in skin, also found in pancreas, liver, spleen, prostate, ovary, small intestine and colon. It is a chemoattractant protein that acts as a ligand for the G protein-coupled receptor CMKLR1. RARRES2 is secreted in an inactive form as prochemerin and is activated through cleavage of the C-terminus by inflammatory and coagulation serine proteases. It is thou...
TMPJ-01073	FABP5 Protein, Human, Recombinant (His) Fatty Acid-Binding Protein Epidermal,PA-FABP,FABP5,Psoriasis...	Human	E. coli
	Fatty acid-binding protein 5 (FABP5) is a cytoplasm protein that belongs to the fatty-acid binding protein (FABP) family of calycin superfamily. Fatty acid binding proteins are a family of small, highly conserved, cytoplasmic proteins that bind long-chain fatty acids. FABP5 can be expressed in keratinocytes, and is highly expressed in psoriatic skin. FABP5 has been shown to be involved in keratinocyte differentiation. FABP5 has high specificity for fatty acids, the highest affinity for C18 chain...
TMPY-02117	Marapsin Protein, Human, Recombinant (His) UNQ1884/PRO4327,protease, serine 27,CAPH2,MPN	Human	HEK293 Cells
	The name "Pancreasin" because it is transcribed strongly in the pancreas. This secreted, tryptic serine protease, also known as Marapsin or PRSS27 (Protease, serine, 27), is a member of the peptidase S1 family. Pancreasin is inhibited by benzamidine and leupeptin but resists several classic inhibitors of trypsin. Marapsin was constitutively expressed in nonkeratinizing stratified squamous epithelia of human esophagus, tonsil, cervix, larynx, and cornea. In fact, marapsin was the second most stro...
TMPJ-01312	TWEAKR/TNFRSF12A Protein, Mouse, Recombinant (hFc) Fibroblast growth factor-regulated protein 2,TNFRSF12,Tumor ...	Mouse	HEK293 Cells
	Tumor necrosis factor receptor superfamily member 12A(Tnfrsf12a) is a single-pass type I membrane protein and contains 1 TNFR-Cys repeat. It is weak inducer of apoptosis in some cell types.It promotes angiogenesis and it is the proliferation of endothelial cells. It may modulate cellular adhesion to matrix proteins.TNFR binds specifically to tumor necrosis factor (TNF) and blocks its interaction with cell surface TNF receptors. TNF is a naturally occurring cytokine that is involved in normal inf...

重组蛋白

TNF beta Protein, Human, Recombinant

Cat.No: TMPY-02153

Species: Human

Expression System: E. coli

CLEC9A Protein, Human, Recombinant (hFc)

Cat.No: TMPK-01057

Species: Human

Expression System: HEK293 Cells

Chemerin/RARRES2 Protein, Human, Recombinant (His)

Cat.No: TMPJ-01292

Species: Human

Expression System: HEK293 Cells

FABP5 Protein, Human, Recombinant (His)

Cat.No: TMPJ-01073

Species: Human

Expression System: E. coli

Marapsin Protein, Human, Recombinant (His)

Cat.No: TMPY-02117

Species: Human

Expression System: HEK293 Cells

TWEAKR/TNFRSF12A Protein, Mouse, Recombinant (hFc)

Cat.No: TMPJ-01312

Species: Mouse

Expression System: HEK293 Cells

Cat. No.	Product Name	Target	Signaling Pathways
TMID-0237	Leflunomide-d4
	Leflunomide-d4 是 Leflunomide 的氘代化合物。Leflunomide 的 CAS 号为 75706-12-6。Leflunomide 是嘧啶合成抑制剂，能够抑制二氢乳清酸脱氢酶，具有抗风湿的活性。

同位素标记化合物

Cat.No: TMID-0237

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