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53

抑制剂 & 化合物

8

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T7776	ADH-503 GB1275	Complement System	Immunology/Inflammation
	ADH-503 (GB1275) 是一种可口服的变构CD11b 激动剂，可以导致与肿瘤相关的巨噬细胞重新极化，可减轻骨髓细胞的免疫抑制，并增强树突状细胞的反应。
T3100	GSK-J4 GSK J4 HCl	Apoptosis; Histone Demethylase	Apoptosis; Chromatin/Epigenetic
	GSK-J4 (GSK J4 HCl) 是 H3K27me3/me2 去甲基化酶JMJD3/KDM6B 和UTX/KDM6A 双抑制剂，IC50分别为 8.6 μM 和 6.6 μM。它是 GSK-J1 的细胞通透性前药，可诱导内质网应激相关的细胞凋亡。它抑制 LPS 诱导的人原代巨噬细胞产生 TNF-α，IC50值为 9 μM。
T4383	GSK-J4 Hydrochloride GSK J4 HCl,GSK J4 HCl (1373423-53-0 free base)	Histone Demethylase	Chromatin/Epigenetic
	GSK-J4 Hydrochloride (GSK J4 HCl) 是 H3K27me3/me2 去甲基化酶 JMJD3/KDM6B 和 UTX/KDM6A 双抑制剂，IC50分别为 8.6 和 6.6 μM。它是 GSK-J1 的乙酯衍生物，体外 IC50 值大于 50 μM。它抑制 LPS 诱导的人原代巨噬细胞产生 TNF-α，IC50值为 9 μM。
TP1540	Jagged-1 （188-204） Jagged-1 188-204	Gamma-secretase	Neuroscience; Proteases/Proteasome; Stem Cells
	Jagged-1 （188-204）是 JAG-1 蛋白的一个片段。其中 JAG-1 能够诱导单核细胞衍生的人树突状细胞成熟，是一种在培养的和原发性多发性骨髓瘤细胞中高度表达的 Notch 配体。
T13379	(Z)-Leukadherin-1 ADH-503 free base	Complement System	Immunology/Inflammation
	(Z)-Leukadherin-1 (ADH-503 free base) 是 CD11b 的变构激动剂。
T2018	Apilimod 阿匹莫德,阿吡莫德,STA 5326	IL Receptor; PI3K; Interleukin	Immunology/Inflammation; PI3K/Akt/mTOR signaling
	Apilimod (STA 5326) 是一种有效的、高度选择性的PIKfyve 抑制剂，是一种 IL-12/IL-23 的有效抑制剂，抑制人和猴的 PBMC 细胞中的 IL-12，IC50值为 1 nM 和 2 nM。
T25450L	GGTI 2147 FA GGTI2147 FA,GGTI-2147 FA,GGTI 2147 FA(191102-87-1 Free base)	Others	Others
	GGTI 2147 FA 是一种选择性 GGT 抑制剂，在海马体实验中双库林诱导的树突棘密度增加被消除，可能会降低小鼠的学习和记忆能力。
T72482	Dazostinag disodium	STING	Immunology/Inflammation
	Dazostinag disodium (TAK-676) 是一种新型干扰素基因刺激剂（STING）激动剂，也是一种免疫系统调节剂，具有抗肿瘤活性，可激活树突状细胞、自然杀伤细胞和 T 细胞。
T74874	CpG ODN 10101
	CpG ODN 10101为合成寡脱氧核苷酸(ODN)，作为Toll样受体9(TLR9)激动剂，在与HH2(VQLRIRVAVIRA-NH2)联用时，有效促进体外细胞因子/趋化因子表达。此化合物能诱导树突状细胞(DC)分泌IFN，刺激B细胞活化，展现抗病毒及免疫调节功能，对慢性HCV感染具影响。
T6964	Resiquimod R848,雷西莫特,S28463	HCV Protease; TLR	Immunology/Inflammation; Microbiology/Virology; Proteases/Proteasome
	Resiquimod (R848) 是一种 Toll 样受体7/8的激动剂，可诱导细胞因子上调。
TP1895L1	KYL acetate(676657-00-4 free base)	Ephrin Receptor	Tyrosine Kinase/Adaptors
	KYL acetate(676657-00-4 free base) 是EphA4受体酪氨酸激酶抑制剂（Kd = 0.8 μM）；抑制 EphA4-EphrinA5 相互作用 (IC50 = 6.34 μM)。防止 AβO 诱导的突触损伤、树突棘丢失并防止海马 CA3-CA1 传输中 LTP 的阻断。在细胞培养基中表现出较长的半衰期（在 PC3 和 C2C12 培养基中分别为 8 和 12 小时）。它有神经保护作用。
T27160	DG026 DG 026,DG-026
	DG026 is a IRAP inhibitor. DG026 ables to selectively downregulate IRAP-dependent cross-presentation by dendritic cells but leave ERAP1-dependent cross-presentation unaffected.
T40452	N-Acetylpsychosine N-Acetylpsychosine,C2 Galactosylceramide (d18:1/2:0)
	N-Acetylpsychosine, also known as α-galactosylated C2-ceramide (d18:1/2:0), exhibits immunostimulatory properties. This compound, N-Acetylpsychosine, holds potential as a valuable tool for studying the mechanisms of apoptosis and immune responses activated by dendritic cells (DCs).
T26828	BIT225 BIT 225,BIT-225
	BIT-225 is a NCp7 zinc finger inhibitor. BIT225 inhibits HIV-1 replication in myeloid dendritic cells. BIT225 inhibits HIV-1 release from human macrophages. BIT225 inhibits bovine viral diarrhea virus in vitro and shows synergism with recombinant interfer
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。
T78079	NF546 hydrate	P2Y Receptor	GPCR/G Protein; Neuroscience
	NF546 (hydrate)为选择性非核苷酸P2Y11激动剂，具有pEC50值为6.27。该化合物可促进人单核细胞源性树突状细胞释放白细胞介素-8。
T37162	8-hydroxy Efavirenz
	8-hydroxy Efavirenz is a major oxidative metabolite of the non-nucleoside reverse transcriptase inhibitor efavirenz . 8-hydroxy Efavirenz is formed when efavirenz is metabolized by the cytochrome P450 (CYP) isoform CYP2B6. It induces apoptosis in rat primary hippocampal neurons and loss of dendritic spines in rat primary hippocampal neuronal cultures when used at a concentration of 0.01 μM.
T76767	Daxdilimab
	Daxdilimab 是一种 anti-ILT7单克隆抗体，ILT7 是 pDC 型树突状细胞特有的细胞表面分子。Daxdilimab 可用于 COVID-19 感染的急性肺损伤 (ALI) 的研究。
T38946	C8 Dihydroceramide C8 Dihydroceramide
	C8 Dihydroceramide acts as a negative control for C8 Ceramide, a cell-permeable analog of natural ceramides. C8 Ceramide, also known as N-Octanoyl-D-erythro-sphingosine, exhibits potent chemotherapeutic properties and anti-proliferation effects. Additionally, it stimulates dendritic cells to enhance T cell responses during viral infections. In vitro studies have also shown that C8 Ceramide induces a slight activation of protein kinase (PKC) [4].
T74706	Vidutolimod
	Vidutolimod 是一种CpG-A 类寡核苷酸，是TLR9的激动剂。Vidutolimod 激活浆细胞样树突状细胞(pDCs)并触发IFNα的释放，导致抗肿瘤免疫作用。
T80918	Tuparstobart Incagn-02385
	Tuparstobart (Incagn-02385)为针对LAG-3的IgG1κ抗体。LAG-3，作为一种免疫检查点受体蛋白，其主要存在于活化T细胞、NK细胞、B细胞及浆细胞树突细胞上。
T74969	Phospholipid PL1
	Phospholipid PL1 是一种磷脂衍生的纳米颗粒，能够向 T 细胞传递共刺激受体 mRNA (CD137 或 OX40)。Phospholipid PL1 可诱导多种免疫细胞的激活，包括T 细胞和树突状细胞 (DC)，以增强抗肿瘤免疫反应。
T37898	UDP-α-D-Glucose (sodium salt hydrate)
	UDP-α-D-Glucose is an endogenous nucleotide sugar involved in glycosyltransferase reactions in metabolism. It has been shown to bind the P2Y14receptor (EC50= 0.35 μM), an atypical P2Y receptor involved in the activation of dendritic cells and glial cells.1It can also bind to and activate GPR17, inducing oligodendrocyte differentiation at a maximal concentration of 100 μM.2 1.Jacobson, K.A., Ivanov, A.A., de Castro, S., et al.Development of selective agonists and antagonists of P2Y receptorsPurin...
T36868	4-oxo Docosahexaenoic Acid
	4-oxo Docosahexaenoic acid (4-oxo DHA) is a putative metabolite of DHA with antiproliferative and PPARγ agonist activity. It inhibits the growth of several triple negative breast cancer cell lines (MCF-10F, trMCF, bsMCF, MDA-MB-231, and BT549) at 50-100 μM, however it increased proliferation of MCF-7 cells. 4-oxo DHA binds covalently to PPARγ and activates gene transcription in luciferase reporter assays and in dendritic cells with EC50 values of approximately 8-16 μM.
T76023	Jagged-1 (188-204) (TFA)
	Jagged-1 (188-204) TFA 是 JAG-1 蛋白的一个片段，具有Notch 激动剂活性。JAG-1 是一种在培养的和原发性多发性骨髓瘤 (MM) 细胞中高度表达的Notch 配体。JAG-1 诱导单核细胞衍生的人树突状细胞成熟。
T71325	ANA-773
	ANA773 is a Toll-like Receptor 7 (TLR7) agonist prodrug with potential immunostimulating activity. Upon oral administration, ANA773 is metabolized into its active form that binds to and activates TLR7, thereby stimulating dendritic cells (DCs) and enhancing natural killer cell (NK) cytotoxicity. This activation results in the production of proinflammatory cytokines, including interferon alpha, and enhanced antibody-dependent cellular cytotoxicity (ADCC). TLR7 is a member of the TLR family, which...
TP1895	KYL peptide KYL
	EphA4 receptor tyrosine kinase inhibitor (Kd = 0.8 μM); inhibits EphA4-EphrinA5 interactions (IC50 = 6.34 μM). Prevents AβO induced synaptic damage, dendritic spine loss and prevents the blocking of LTP in hippocampal CA3-CA1 transmissions. Exhibits a lon
T63553	HPK1-IN-28
	HPK1-IN-28 是 HPK1 的有效抑制剂。其中造血祖细胞激酶 1 (HPK1) 是一种树突状细胞 (DC)、T 细胞和 B 细胞活化反应的负调节剂。HPK1-IN-28 能够有效提高人体的抗肿瘤免疫力，对免疫相关疾病，尤其是肿瘤表现出研究潜力。
T36452	1-Arachidonoyl Lysophosphatidic Acid (ammonium salt)
	1-Arachidonoyl lysophosphatidic acid is a phospholipid containing arachidonic acid at the sn-1 position. It has been found in rat brain as 37% of the arachidonic acid-containing lysophosphatidic acid (LPA) species and is a precursor to 1-arachidonoyl glycerol . 1-Arachidonoyl lysophosphatidic acid binds to the LPA2/EDG4 receptor with an EC50 value of approximately 10 nM. It prevents TNF-α and IL-6 secretion in wild-type but not Lpa2-/- dendritic cells stimulated by LPS. It also decreases differe...
T69944	NLG802 HCl
	NLG802 is an orally bioavailable prodrug of indoximod, a methylated tryptophan, with immune checkpoint inhibitory and antineoplastic activities. Upon oral administration, the indoximod prodrug NLG802 is converted to indoximod. Indoximod targets, binds to and inhibits the enzyme indoleamine 2,3-dioxygenase (IDO; IDO1), which converts the essential amino acid tryptophan into the immunosuppressive metabolite kynurenine. By increasing tryptophan levels and decreasing kynurenine levels, indoximod res...
T79707	Cholicamideβ	Necroptosis	Apoptosis
	Cholicamideβ（compound 6）为自组装小分子癌症疫苗佐剂，能够形成细胞毒性低的病毒样颗粒。该化合物与肽抗原结合，可增强树突状细胞的抗原呈递能力，并激活抗原特异性T细胞反应。Cholicamideβ还能引发细胞凋亡(apoptosis)和坏死(necrosis)。
T78596	CAD031
	CAD031，一种针对阿尔茨海默病 (AD) 的J147衍生物，展现了神经保护和记忆增强的特性。它能增强小鼠的记忆力，优化树突结构，并促进老年小鼠大脑生发区细胞的分裂。相较于J147，CAD031在人类神经干细胞测定中显示出更高的活性。
T79608	DPP	JAK	Angiogenesis; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells
	DPP，一种含紫檀芪衍生轴向配体的铂(IV)络合物，能够抑制乳腺癌(BC)细胞的JAK2-STAT3通路并显示出抗增殖特性。它通过激活caspase-3和裂解聚ADP-核糖聚合酶诱导细胞凋亡(apoptosis)，同时促进树突状细胞成熟及抗原呈现功能，并已证明体内具有安全性。
T35773	Gliotoxin-13C13 Gliotoxin-13C13
	Gliotoxin-13C13is intended for use as an internal standard for the quantification of gliotoxin by GC- or LC-MS. Gliotoxin is an immunosuppressive mycotoxin produced by pathogenic strains ofAspergillusand other fungi with diverse biological activities.1,2,3,4,5,6,7,8It inhibits 20S proteasomal chymotrypsin activity (IC50= 10 μM), blocking the degradation of IκBα and preventing the activation of NF-κB.2,3Gliotoxin induces apoptosis in monocytes and dendritic cells and reduces phagocytosis by neutr...
T63270	HPK1-IN-29
	HPK1-IN-29 是 HPK1 有效的抑制剂，其中造血祖细胞激酶 1 (HPK1) 是一种树突状细胞 (DC)、T 细胞和 B 细胞活化反应的负调节剂。HPK1-IN-29 能够提高人体的抗肿瘤免疫力，表现出研究免疫相关疾病，尤其是肿瘤的潜力。
T69523	BMS-681
	BMS-681 is an orthosteric antagonist of chemokine receptor 2 (CCR2) that forms a ternary complex with CCR2 and its allosteric antagonist, CCR2-RA-[R]. Together, the complex inhibits chemokine binding with BVMS-681 in the orthosteric pocket and CCR2-RA-[R] in the intracellular allosteric G-protein binding site. When chemokine binding is inhibited, modulation responses implicated in several inflammatory and neurodegenerative diseases, including atherosclerosis, multiple sclerosis, asthma, neuropat...
T37273	BLX3887
	BLX3887 is an inhibitor of 15-lipoxygenase type 1 (15-LO-1; IC50 = 32 nM in a cell-free enzyme assay).1 It is selective for 15-LO-1 over 15-LO-2, which it does not inhibit, 5-LO (IC50 = 472 nM), and 12-LO (IC50 = 3,310 nM). BLX3887 inhibits the production of 15-LO metabolites selectively in eosinophils over neutrophils when used at a concentration of 10 μM. It also inhibits endocytosis in, and the migration of, isolated human peripheral blood mononuclear cell-derived dendritic cells in vitro. \|1...
T70174	Pirlindole-d4 HCl
	Pirlindole-d4 is intended for use as an internal standard for the quantification of pirlindole by GC- or LC-MS. Pirlindole is a selective and reversible monoamine oxidase A (MAO-A) inhibitor. It is selective for MAO-A over MAO-B. In rats, it reverses the depressive-like effects induced by chronic mild stress (CMS), increases proliferation of hippocampal neural progenitor cells, and reverses dendritic atrophy in granule neurons. Pirlindole is also an inhibitor of enterovirus-D68 and coxsackieviru...
T77090	Mitazalimab
	Mitazalimab（ADC-1013; JNJ-64457107）是一种FcγR依赖性CD40激动剂，以肿瘤导向活性为特征。该化合物通过激活抗原呈递细胞（如树突状细胞[DC]），启动肿瘤反应性T细胞，进而诱导肿瘤特异性T细胞浸润并杀死肿瘤，有效重塑肿瘤浸润性骨髓微环境。
T27051	CM-414 CM 414,CM414
	CM-414 is a dual inhibitor of HDACs and PDE5 for the Treatment of Alzheimer’s Disease (IC50 values of 60 nM, 310 nM, 490 nM, 322 nM, and 91 nM against PDE5, HDAC1, HDAC2, HDAC3, and HDAC6, respectively). Chronic treatment of Tg2576 mice with CM-414 dimini
T83846	HOXB7 (8-25) TFA Homeobox B7 (8-25)
	HOXB7 (8-25) 是 homeobox B7 (HOXB7) 的肽段，是细胞增殖的主要调控因子和肿瘤基因途径的激活剂。通过 HOXB7 (8-25) 肽脉冲的树突状细胞展示抗原，这些树突状细胞来源于分离的人类外周血单核细胞（PBMCs），刺激CD4+辅助T细胞的激活和IFN-γ的产生，从而引发特异性和多向性肿瘤反应性的抗肿瘤反应。
T79609	STAT3-IN-18	JAK	Angiogenesis; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells
	STAT3-IN-18 (compound SPP)，一种带紫檀芪衍生轴向配体的铂(IV)络合物，能抑制乳腺癌(BC)细胞的JAK2-STAT3通路，显示出抗增殖活性。它激活caspase-3和裂解聚ADP-核糖聚合酶，诱导apoptosis。此外，STAT3-IN-18可促进树突状细胞成熟与抗原呈递，体现了良好的体内安全性。
T81360	PSMα3 TFA
	PSMα3 TFA 作为一种肽类化合物，主要用于诱导生成耐受性的树突细胞（DC），以应用于DC疫苗接种。该化合物能对TLR2和TLR4诱导的DC成熟过程进行调节，抑制促炎和消炎细胞因子的产生，降低抗原摄取，并影响人单核细胞来源DC的渗透和调节能力。此外，PSMα3 TFA 是耐甲氧西林金黄色葡萄球菌（MRSA）中最有毒株释放的关键毒素之一。
T64280	ODN 2216
	ODN 2216 是一种 TLR9 (toll-like receptor 9) 配体或激动剂，能够诱导产生大量的 IFN-α 和 IFN-β。ODN 2216 可以利用 pDC (浆细胞样 DC) 诱导 IFN-α，以及利用 DC (树突状细胞) 产生IL-12 (p40)。ODN 2216 能够间接的、在 IFN-α/β 介导下刺激外周血单核细胞 (PBMC) 产生 IFN-γ。ODN 2216 可以激活 NK 细胞，诱导 IFN-γ 产生 TCR 触发的 CD4+T 细胞。
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 ...
T79718	CaMKIIα-PHOTAC	CaMK	Neuroscience
	CaMKIIα-PHOTAC是一种靶向Ca2+/钙调蛋白依赖性蛋白激酶IIα（CaMKIIα）的光化学靶向嵌合体（PHOTAC）。该分子在特定波长光照射下实现靶蛋白的泛素化及通过蛋白酶体催化的降解。CaMKIIα-PHOTAC能在光照条件下显著降低小鼠海马区域的诱发LTP反应强度，减弱突触功能，并对维护亚细胞级别的树突结构域、长时程增强及记忆能力起到关键作用。
T36984	Cyclic di-IMP (sodium salt)
	Cyclic di-IMP (sodium salt) (c-di-IMP) is a synthetic second messenger structurally related to the bacterial second messengers cyclic di-GMP and cyclic di-AMP . C-di-IMP has adjuvant properties when co-administered with antigens in vitro and by mucosal routes in vivo. C-di-IMP enriches the population of MHC class I and II, CD80, CD86, CD40, and CD54 positive dendritic cells derived from murine bone marrow. It also stimulates macrophages at 500 ng/ml. Mice immunized with β-galactosidase (β-gal) p...
T37800	PF-04449613
	PF-04449613 is a phosphodiesterase 9A (PDE9A) inhibitor (IC50= 22 nM).1It is selective for PDE9A over PDE1C (IC50= >1,000 nM), as well as over a variety of other PDEs, inhibiting PDE2-8, -10, and -11 activity by less than 30% in a panel of enzymes, ion channels, and transporters at 1 μM but does inhibit the human dopamine transporter (DAT; Ki= 293 nM). PF-04449613 (0.1-100 mg/kg, s.c.) increases cerebrospinal fluid (CSF) levels of cyclic GMP (cGMP) in rats. Subcutaneous administration of PF-0444...
T83847	SP-A (196-215) (human) TFA Surfactant Protein A,SPA4
	表面活性蛋白A（SP-A）（196-215）是一种合成肽，与人类SP-A的C末端碳水化合物识别域的196至215氨基酸序列相对应。当浓度为1和10 µM时，它能抑制JAWSII鼠树突细胞中由LPS诱导的TNF-α释放。SP-A（196-215）（75 µM）促使JAWSII细胞吞噬P. aeruginosa。通过气管内给药，SP-A（196-215）（50 µg/动物）降低了小鼠P. aeruginosa感染模型的疾病严重程度和肺部形成菌落数。
T83852	EGFRvIII Peptide TFA PEGFRvIII (9-mer),Epidermal Growth Factor Receptor Variant III Peptide
	EGFRvIII peptide是一种合成肽，对应于特异性肿瘤、具有持续激活性的EGFR变体EGFRvIII的融合接头，该变体缺少野生型EGFR的第6至273个氨基酸。在25 µg/ml的浓度下，它能与MHC I类亚型HLA-A*0201阳性的T2细胞结合。在用于分离的人外周血单个核细胞（PBMCs）衍生的树突状细胞中，EGFRvIII peptide可诱导抗原呈递，进而刺激CD8+细胞毒性T淋巴细胞的激活和IFN-γ产生。与toll样受体5（TLR5）激动剂鞭毛蛋白B共同免疫EGFRvIII peptide（15 µg/动物），在正交GL261胶质母细胞瘤小鼠异种移植模型中，增加了CD8+ T细胞数量，减少了调节性T细胞（Tregs）数量，减少了肿瘤体积，并提高了生存率。

化合物

Cat.No: T7776

Synonym: GB1275

Target: Complement System

Cat.No: T3100

Synonym: GSK J4 HCl

Target: Apoptosis, Histone Demethylase

GSK-J4 Hydrochloride

Cat.No: T4383

Synonym: GSK J4 HCl,GSK J4 HCl (1373423-53-0 free base)

Target: Histone Demethylase

Jagged-1 （188-204）

Cat.No: TP1540

Synonym: Jagged-1 188-204

Target: Gamma-secretase

(Z)-Leukadherin-1

Cat.No: T13379

Synonym: ADH-503 free base

Target: Complement System

Cat.No: T2018

Synonym: 阿匹莫德,阿吡莫德,STA 5326

Target: IL Receptor, PI3K, Interleukin

Cat.No: T25450L

Synonym: GGTI2147 FA,GGTI-2147 FA,GGTI 2147 FA(191102-87-1 Free base)

Target: Others

Dazostinag disodium

Cat.No: T72482

Target: STING

Cat.No: T74874

Cat.No: T6964

Synonym: R848,雷西莫特,S28463

Target: HCV Protease, TLR

KYL acetate(676657-00-4 free base)

Cat.No: TP1895L1

Target: Ephrin Receptor

Cat.No: T27160

Synonym: DG 026,DG-026

N-Acetylpsychosine

Cat.No: T40452

Synonym: N-Acetylpsychosine,C2 Galactosylceramide (d18:1/2:0)

Cat.No: T26828

Synonym: BIT 225,BIT-225

Cat.No: T76771

Cat.No: T78079

Target: P2Y Receptor

8-hydroxy Efavirenz

Cat.No: T37162

Cat.No: T76767

C8 Dihydroceramide

Cat.No: T38946

Synonym: C8 Dihydroceramide

Cat.No: T74706

Cat.No: T80918

Synonym: Incagn-02385

Phospholipid PL1

Cat.No: T74969

UDP-α-D-Glucose (sodium salt hydrate)

Cat.No: T37898

4-oxo Docosahexaenoic Acid

Cat.No: T36868

Jagged-1 (188-204) (TFA)

Cat.No: T76023

Cat.No: T71325

Cat.No: TP1895

Synonym: KYL

Cat.No: T63553

1-Arachidonoyl Lysophosphatidic Acid (ammonium salt)

Cat.No: T36452

Cat.No: T69944

Cat.No: T79707

Target: Necroptosis

Cat.No: T78596

Cat.No: T79608

Target: JAK

Gliotoxin-13C13

Cat.No: T35773

Synonym: Gliotoxin-13C13

Cat.No: T63270

Cat.No: T69523

Cat.No: T37273

Pirlindole-d4 HCl

Cat.No: T70174

Cat.No: T77090

Cat.No: T27051

Synonym: CM 414,CM414

HOXB7 (8-25) TFA

Cat.No: T83846

Synonym: Homeobox B7 (8-25)

Cat.No: T79609

Target: JAK

Cat.No: T81360

Cat.No: T64280

3-Hydroxykynurenamine

Cat.No: T68182

CaMKIIα-PHOTAC

Cat.No: T79718

Target: CaMK

Cyclic di-IMP (sodium salt)

Cat.No: T36984

Cat.No: T37800

SP-A (196-215) (human) TFA

Cat.No: T83847

Synonym: Surfactant Protein A,SPA4

EGFRvIII Peptide TFA

Cat.No: T83852

Synonym: PEGFRvIII (9-mer),Epidermal Growth Factor Receptor Variant III Peptide

Cat. No.	Product Name	Target	Signaling Pathways
TN1445	Bisabolangelone	p38 MAPK; MAPK	MAPK
	Bisabolangelone 是从没药中分离出来的一种倍半萜衍生物，具有抗炎作用。它通过阻断巨噬细胞内的NF-kappaB 和MAPK 通路抑制脂多糖刺激的炎症，具有抗溃疡作用。
T6S1027	Tussilagone	Others	Others
	Tussilagone 是Tussilago farfara 的主要活性成分，具有抗炎作用。它抑制盲肠结扎和穿刺导致脓毒症的小鼠的炎症反应，提高其生存率。它改善葡聚糖硫酸钠诱导的小鼠结肠炎的炎症反应。
T5S2357	Acetylcorynoline (+)-Corynoline Acetate,O-Acetylcorynoline,乙酰紫堇灵	Antifungal	Microbiology/Virology
	Acetylcorynoline (O-Acetylcorynoline) 是提取自 Corydalis bungeana 中的一种主要生物碱成分，具有抗炎活性。
T4A2399	Cinobufotalin 华蟾毒它灵,华蟾素	IL Receptor; Akt; MRP; P-gp	Cytoskeletal Signaling; Immunology/Inflammation; Membrane transporter/Ion channel; Neuroscience; PI3K/Akt/mTOR signaling
	Cinobufotalin 是一种从蟾蜍的皮肤分泌物中提取的强心类固醇或丁二烯内酯。它已被用作强心药，利尿药和止血药，也是潜在的抗肺癌药物。
T16733	Resolvin E1 RvE1	Others	Others
	Resolvin E1 is an effective endogenous pro-resolving mediator of inflammation. Resolvin E1 has unique counterregulatory actions that inhibit PMN transendothelial migration. Resolvin E1 also acts as an effective inhibitor of leukocyte infiltration, dendrit
TN1663	Ganoderic acid DM 灵芝酸DM,灵芝酸 DM	PARP; Androgen Receptor; CDK	Cell Cycle/Checkpoint; Chromatin/Epigenetic; DNA Damage/DNA Repair; Endocrinology/Hormones
	Ganoderic acid DM is an antiandrogenic osteoclastogenesis inhibitor, it especially suppresses the expression of c-Fos and nuclear factor of activated T cells c1 (NFATc1), this suppression leads to the inhibition of dendritic cell-specific transmembrane pr
T38394	PSMα3
	PSMα3 is a peptide compound that can be utilized to induce tolerance in dendritic cells (DCs) for DC vaccination strategies. It effectively penetrates and modulates human monocyte-derived DCs by modifying the maturation process induced by TLR2 or TLR4. Additionally, PSMα3 inhibits the production of both pro- and anti-inflammatory cytokines and decreases antigen uptake. Notably, PSMα3 is a significant virulence factor released by the most pathogenic strains of methicillin-resistant Staphylococcus...
T14063	7α,25-Dihydroxycholesterol 7α,25-OHC	EBI2/GPR183; Endogenous Metabolite	GPCR/G Protein; Metabolism
	7α,25-Dihydroxycholesterol 是一种孤儿 GPCR 受体EBI2 (GPR183)的内源性配体和有效选择性激动剂。它对激活 EBI2 有很强的作用 (EC50=140 pM;Kd=450 pM)。它能够作为一种趋化因子，指导 B 细胞、T 细胞和树突状细胞的迁移。

天然产物

Bisabolangelone

Cat.No: TN1445

Target: p38 MAPK, MAPK

Cat.No: T6S1027

Target: Others

Acetylcorynoline

Cat.No: T5S2357

Synonym: (+)-Corynoline Acetate,O-Acetylcorynoline,乙酰紫堇灵

Target: Antifungal

Cat.No: T4A2399

Synonym: 华蟾毒它灵,华蟾素

Target: IL Receptor, Akt, MRP, P-gp

Cat.No: T16733

Synonym: RvE1

Target: Others

Ganoderic acid DM

Cat.No: TN1663

Synonym: 灵芝酸DM,灵芝酸 DM

Target: PARP, Androgen Receptor, CDK

Cat.No: T38394

7α,25-Dihydroxycholesterol

Cat.No: T14063

Synonym: 7α,25-OHC

Target: EBI2/GPR183, Endogenous Metabolite

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