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抑制剂 & 化合物

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Cat. No.	Product Name	Target	Signaling Pathways
T15371	Gardiquimod	TLR; HIV Protease	Immunology/Inflammation; Microbiology/Virology; Proteases/Proteasome
	Gardiquimod 可抑制巨噬细胞和活化的外周血单个核细胞的HIV-1感染。它是一种咪唑喹啉类似物，是一种 TLR7/8 激动剂。
T24984	5J-4	Calcium Channel	Membrane transporter/Ion channel; Metabolism
	5J-4 是一种有效的钙释放激活钙通道 (CRAC) 和钙池操纵性钙内流(SOCE) 阻滞剂。 5J-4 减少 IL-17 的产生并降低 RORα 和 RORγt 的表达。
T6649	(S)-(+)-Rolipram (S)-Rolipram,(+)-Rolipram,盐酸环胞苷,S- (+)-Rolipram	Apoptosis; PDE	Apoptosis; Metabolism
	(S)-(+)-Rolipram ((+)-Rolipram) 是一种 cAMP 依赖性磷酸二酯酶 4 (PDE4) 抑制剂，IC50=1100 nM。它能够抑制人单核细胞产生的肿瘤坏死因子 α (TNFα)。
TQ0221	Rufloxacin hydrochloride MF-934 hydrochloride,盐酸芦氟沙星	Antibacterial	Microbiology/Virology
	Rufloxacin hydrochloride (MF-934 hydrochloride) 是一种氟喹诺酮类抗菌剂，可抑制拓扑异构酶。 Rufloxacin hydrochloride 抑制人单核细胞中的 B 细胞分化。
T8311	Obefazimod ABX-464,ABX464	HIV Protease	Microbiology/Virology; Proteases/Proteasome
	Obefazimod (ABX-464) 是一种抗HIV 剂。它抑制受刺激的外周血单核细胞中的 HIV-1 复制，IC50值为 0.1 μM 至 0.5 μM。
T9682	AZD-4877 AZD4877	Apoptosis; Kinesin	Apoptosis; Cytoskeletal Signaling
	AZD-4877 是一种高效的纺锤体驱动蛋白 (Eg5) 抑制剂，对其 IC50 值为 2 nM。 AZD-4877 是 Ispinesib 的另一种构型，能够抑制细胞有丝分裂，诱导形成单极纺锤体表型，介导细胞凋亡(Apoptosis)。 AZD-4877 具有抗肿瘤活性，对循环外周血单核细胞 (PBMC)有抑制作用。
T1639	Amlexanox 氨来呫诺,CHX3673,Amoxanox,氨来诺,AA673	IL Receptor; FGFR; Others; IκB/IKK	Angiogenesis; Immunology/Inflammation; NF-κB; Others; Tyrosine Kinase/Adaptors
	Amlexanox (AA673) 是一种特异性的 IKKε和 TBK1抑制剂，其 IC50=1-2 μM。
T21618L	Myelin Basic Protein (87-99) Acetate Myelin Basic Protein (87-99) Acetate (118506-26-6 Free base)	Others	Others
	Myelin Basic Protein (87-99) Acetate (Myelin Basic Protein (87-99) Acetate (118506-26-6 Free base)) 是一种致脑炎肽，可诱导碱性蛋白特异性 T 细胞增殖。它导致外周血单核细胞中的 Th1 极化，这与多发性硬化症 (MS) 有牵连。
T14381	AZD7624 AZD-7624	p38 MAPK; TNF	Apoptosis; MAPK
	AZD7624 是一种 p38 抑制剂，具有强大的抗炎活性。
T14374	AZD2906
	AZD2906, a selective glucocorticoid receptor (GR) agonist, demonstrates inhibitory concentrations (IC50s) of 2.2 nM in human GR, 0.3 nM in rat peripheral blood mononuclear cells (PBMC), 41.6 nM in human whole blood, and 7.5 nM in rat whole blood, respectively[1]. Additionally, it induces an increase in micronucleated immature erythrocytes within rat bone marrow.
T70881	Dolutegravir RR Isomer
	Dolutegravir RR Isomer is an isomer of Dolutegravir -- a second generation HIV-1 integrase strand transfer inhibitor. Dolutegravir has been shown to potently inhibit HIV replication in cells such as peripheral blood mononuclear cells (PBMCs), MT-4 cells and CIP4 cells infected with a self-inactivating PHIV lentiviral vector.
T37590	ML 3403
	p38 MAPK inhibitor (IC50 = 0.38 μM). Inhibits the release of IL-1β and TNF-α in a peripheral blood mononuclear cell (PBMC) assay (IC50 values are 0.039 and 0.16 μM respectively). Laufer et al (2003) Novel substituted pyridinyl imidazoles as potent anticytokine agents with low activity against hepatic cytochrome P450 enzymes. J.Med.Chem. 46 3230 PMID:12852754 \|Kammerer et al (2007) Pharmacokinetics of ML3403 ({4-[5-(4-fluorophenyl)-2-methylsulfanyl-3H-imidazol-4-yl]-pyridin-2-yl}-(1-phenylethyl)-...
T23585	5-Et-ddU ddEtUrd,D2EtU,5-Ethyl-2',3'-dideoxyuridine
	5-Et-ddU, Structure-activity relationships of pyrimidine nucleosides as antiviral agents for human immunodeficiency virus type 1 in peripheral blood mononuclear cells.
T27642	I-XW-053 sodium I-XW-053 Na,I XW 053 sodium,IXW053 sodium,I XW 053 Na,IXW053 Na
	I-XW-053 sodium inhibits the replication of a diverse panel of primary HIV-1 isolates in Peripheral blood mononuclear cell with no appreciable cytotoxicity.
T74915	ODN D-SL03
	ODN D-SL03是C类CpG寡核苷酸，能诱导PBMCs产生高水平IFN-α，激活人B细胞、NK细胞和单个核细胞，同时上调PBMCs亚群表面CD80、CD86和HLA-DR的表达，还能抑制肿瘤生长。ODN D-SL03序列：5'-tcgcgaacgttcgccgcgttcgaacgcgg-3'。
T27030	CK176 HIV-1 inhibitor-34,HIV-1 inhibitor 34,CK 176,CK-176,HIV-1 inhibitor34
	CK176 is a capsid targeted inhibitor of HIV-1 replication. CK176 shows an 11-fold improvement over I-XW-053 in blocking HIV-1 replication in primary human peripheral blood mononuclear cells (PBMCs).
T79749	TLR7 agonist 14
	TLR7 agonist14（compound 17b）作为一种TLR7激动剂，具有高效性，其EC50值为59 nM。在低纳摩尔级别浓度下，TLR7 agonist14能有效激活小鼠巨噬细胞以及hPBMC。
T82515	E104
	E104（compound 1）为一种高效且选择性的TLR7激动剂，适用于ADC合成，以激发显著的抗癌活性。该化合物能够诱导小鼠巨噬细胞与hPBMC的活化。
T40979	XJB-5-131
	XJB-5-131 is a synthetic, bi-functional antioxidant specifically designed to target mitochondria for the scavenging of reactive oxygen species (ROS) and electrons, thereby acting as a radical scavenger. Additionally, it serves as an effective protector and mitigator against ionizing irradiation for cord blood mononuclear cells (CB MNCs).
TP1962	Pam2CSK4
	Toll-like receptor 2/6 (TLR2/6) agonist. Induces TNF-α production in human mononuclear cells. Also induces proliferation and activation of mouse splenic B cells.
T36011	p38 MAP Kinase Inhibitor IV p38 MAPK Inhibitor IV
	p38 MAPK inhibitor IV is an ATP-competitive inhibitor of p38 MAP kinases with IC50 values of 0.13, 0.55, 5.47, and 8.63 μM for p38α, p38β, p38x, and p38δ, respectively, in vitro.[1] It also inhibits LPS-induced TNF-α and IL-1β cytokine production (IC50s = 22 and 44 nM, respectively) in human peripheral blood mononuclear cells.
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%。
T61574	PD-L1-IN-1
	PD-L1-IN-1, a powerful PD-L1 inhibitor, demonstrated an IC50 of 115 nM. By forming a robust bond with the PD-L1 protein, PD-L1-IN-1 effectively suppressed tumor growth by enhancing the antitumor immune activity of peripheral blood mononuclear cells in co-cultures with PD-L1 expressing cancer cells (PC9 and HCC827 cells). It significantly elevated the release of interferon γ and induced apoptosis in cancer cells, while exhibiting minimal cytotoxicity in healthy cells [1].
T35420	(S)-p38 MAPK Inhibitor III (S)-p38 MAPK Inhibitor III
	(S)-p38 MAPK inhibitor III is a methylsulfanylimidazole that inhibits p38 MAP kinase (IC50 = 0.90 μM in vitro). It is cell-permeable, potently blocking the release of TNF-α and IL-1β from human peripheral blood mononuclear cells (IC50s = 0.37 and 0.044 μM, respectively).
T71009	Dolutegravir SR Isomer
	Dolutegravir SR Isomer is an isomeric derivative of Dolutegravir -- a second generation HIV-1 integrase strand transfer inhibitor. Dolutegravir has been shown to potently inhibit HIV replication in cells such as peripheral blood mononuclear cells (PBMCs), MT-4 cells and CIP4 cells infected with a self-inactivating PHIV lentiviral vector.
T74990	ICeD-2
	ICeD-2 是一种细胞死亡诱导剂，可诱导HIV-1感染的细胞死亡。 ICeD-2 介导的HIV-1感染细胞杀伤依赖于HIV-1蛋白酶活性。ICeD-2 可有效阻断二肽基肽酶DPP8和DPP9对 Gly-Pro-AMC 的水解。ICeD-2 显示 PBMC 中 DPP9 的强稳定性。
T39106	BMSpep-57
	BMSpep-57, a potent macrocyclic peptide inhibitor, competitively disrupts the PD-1/PD-L1 interaction, demonstrating a significant inhibitory concentration (IC50) of 7.68 nM. It exhibits binding affinity towards PD-L1 with dissociation constants (Kd) of 19 nM and 19.88 nM in MicroScale Thermophoresis (MST) and Surface Plasmon Resonance (SPR) assays, respectively. This compound enhances T cell functionality by promoting Interleukin-2 (IL-2) production within Peripheral Blood Mononuclear Cells (PBM...
T78755	PD-1/PD-L1-IN-31	PD-1/PD-L1	Apoptosis; Cell Cycle/Checkpoint; Immunology/Inflammation
	PD-1/PD-L1-IN-31为具高效PD-1/PD-L1抑制能力的化合物（IC50=2.2 nM），能激进IFN-γ分泌及激活外周血单核细胞（PBMC），进而抑制肿瘤细胞生长。
T69009	Gnidimacrin
	Gnidimacrin activated HIV-1 replication and killed persistently-infected cells at picomolar concentrations. In addition to its potential to purge HIV-1 from latently infected cells, gnidimacrin potently inhibited a panel of HIV-1 R5 virus infection of peripheral blood mononuclear cells (PBMCs) at an average concentration lower than 10 pM. These results suggest that gnidimacrin could activate latent HIV-1, specifically kill HIV-1 persistently infected cells, and inhibit R5 viruses at picomolar c...
T5499	gardiquimod TFA salt
	Gardiquimod diTFA，咪唑啉类似物TLR7/8激动剂，可特异性抑制巨噬细胞和活化外周血单个核细胞(PBMCs)的HIV-1感染。在浓度低于10 μM时，该化合物特异性激活TLR7。
T80964	Toxic Shock Syndrome Toxin-1 (TSST-1) (58-78)
	Toxic Shock Syndrome Toxin-1 (TSST-1) (58-78)为T细胞增殖激活剂，以剂量依赖性方式增强人外周血单核细胞(PBMC)的体外增殖，适用于癌症与炎症免疫研究。
T36109	L Moses dihydrochloride
	High affinity and selective cell-permeable p300/CBP-associated factor (PCAF) inhibitor (Ki = 47 nM). Exhibits no significant activity against a panel of 48 other bromodomains except GCN5 (Kd = 600 nM). Exhibits >4500-fold selectivity for PCAF over BRD4. Also exhibits metabolic stability in mouse and human liver microsomes and no observable cytotoxicity in peripheral blood mononuclear cells (PBMC). Moustakim et al (2017) Discovery of a PCAF bromodomain chemical probe. Angew.Chem.Int.Ed. 56 827 P...
T79751	TLR7 agonist 16
	TLR7 agonist16 (compound 16d)为一种高效的TLR7激动剂，具有EC50值为59 nM。在低纳摩尔水平上，它可以有效激活小鼠巨噬细胞和hPBMC。
T78370	Myelin Basic Protein(87-99) TFA
	Myelin Basic Protein(87-99) TFA 为诱导神经碱性蛋白特异性T细胞增殖的致脑肽。该化合物能在外周血单核细胞中诱导Th1极化，与多发性硬化症(MS)的发病机制相关。
T82254	GSK-LSD1	Histone Demethylase	Chromatin/Epigenetic
	GSK-LSD1是一种LSD1抑制剂，能够降低肥胖小鼠模型的摄食量和体重，同时提升胰岛素敏感性与血糖控制。此外，GSK-LSD1对NAFLD也有改善作用，并能抑制COVID-19患者PBMC中SARS-CoV-2诱导的细胞因子释放。GSK-LSD1对抑制癌症的生长与转移也显示出潜在效果。
T74718	STING modulator-5
	STINGmodulator-5（compound 38）为THP-1和外周血单个核细胞（PBMC）的拮抗剂，其在THP-1上的pIC50值为8.9，在PBMC上的pIC50值为8.1。此化合物适用于免疫性疾病研究。
T35929	O-Demethyl Apremilast
	O-Demethyl apremilast is an active metabolite of the phosphodiesterase 4 (PDE4) inhibitor apremilast .1It inhibits the activity of PDE4 isolated from U937 cells and LPS-induced TNF-α production in isolated human peripheral blood mononuclear cells (PBMCs; IC50s = 8.3 and 5.6 μM, respectively). O-Demethyl apremilast is also an oxidative degradation product of apremilast.2,3 1.Hoffmann, M., Kumar, G., Schafer, P., et al.Disposition, metabolism and mass balance of [14C]apremilast following oral admi...
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。
T80130	SDF-1α (human)	CXCR	Autophagy; GPCR/G Protein; Immunology/Inflammation
	SDF-1α (human) 是一种能够与CXCR4受体相结合的单核细胞趋化剂，它在心肌梗死模型中的干细胞归巢、维持、生存、增殖、心肌细胞修复、血管形成以及心室重构过程扮演关键角色。SDF-1α (human) 常用于心血管病研究。
T79770	FB49	Autophagy	Autophagy
	FB49是一种针对Bcl-2-associated athanogene 3 (BAG3)的高选择性抑制剂，具有Ki值为45 μM。在人类肿瘤细胞系中，FB49能够有效抑制细胞生长，同时对人外周单核细胞无明显毒性。此外，FB49能够在HD-MB03成神经管细胞瘤细胞中阻碍G1期的细胞周期进程，并诱导细胞凋亡(apoptosis)和自噬(autophagy)。
T74062	PROTAC IRAK4 degrader-2
	PROTACIRAK4 degrader-2 (Compound 9) 是一种 PROTACIRAK4降解剂，在外周血单个核细胞 (PBMC) 中，降解 IRAK4，DC50为 151 nM。PROTACIRAK4 Degrader-2 在 PBMC 细胞中诱导 IRAK4蛋白水平降低，DC50为 36 nM。PROTACIRAK4 degrader-2 还抑制 PBMC 中多种细胞因子释放。
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...
T37523	Tenofovir diphosphate (sodium salt)
	Tenofovir diphosphate is an inhibitor of HIV reverse transcriptase (Kis = 0.022 and 1.55 μM for RNA and DNA, respectively) and hepatitis B virus (HBV) polymerase (Ki = 0.18 μM). It is selective for these enzymes over DNA polymerase α and β, as well as mitochondrial DNA polymerase γ (Kis = 5.2, 81.7, and 59.5 μM, respectively). Tenofovir diphosphate is formed intracellularly through phosphorylation of the prodrugs tenofovir and tenofovir disoproxil by nucleotide kinases. Increased levels of tenof...
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。
T68321	AS1940477
	AS1940477 is p38 MAPK inhibitor. AS1940477 inhibited the enzymatic activity of recombinant p38α and β isoforms but showed no effect against other 100 protein kinases including p38γ and δ isoforms. In human peripheral blood mononuclear cells, AS1940477 inhibited lipopolysaccharide (LPS)- or phytohemagglutinin A (PHA)-induced production of proinflammatory cytokines, including TNFα, IL-1β, and IL-6 at low concentrations (LPS/TNFα, IC(50)=0.45n M; PHA/TNFα, IC(50)=0.40 nM). In addition, equivalent c...
T37355	CAY10703
	Dichloroacetate (DCA) is an inhibitor of all pyruvate dehydrogenase kinase (PDHK) isoforms, which are enzymes that phosphorylate and inhibit PDH in mitochondria. Inhibition of PDHK shifts cell metabolism from glycolysis to mitochondrial glucose oxidation, an effect that has relevance to cancer, type 2 diabetes, and other diseases. CAY10703 is a DCA trimer that is at least 10-fold more cytotoxic against leukemia cell lines than DCA. It is approximately 3-fold less cytotoxic than DCA against perip...
T70313	Indoxyl Sulfate-d5 potassium salt
	Indoxyl sulfate-d5 is intended for use as an internal standard for the quantification of indoxyl sulfate by GC- or LC-MS. Indoxyl sulfate is a uremic toxin and a metabolite of tryptophan. It is formed via sulfation of indole, an intermediate generated from tryptophan by intestinal bacteria, by the sulfotransferase (SULT) isoform 1A1 variant 2 (SULT1A1*2) in the liver. Indoxyl sulfate activates the aryl hydrocarbon receptor (AhR) in HepG2 40/6 hepatoma cells (EC50 = 12.1 nM in a reporter assay). ...
T69081	KRH-1636
	KRH-1636 is an orally active, selective and extremely potent CXC chemokine receptor 4 antagonist. KRH-1636 exhibits a potent and selective anti-HIV-1 activity. KRH-1636 efficiently blocked replication of various T cell line-tropic (X4) HIV type 1 (HIV-1) in MT-4 cells and peripheral blood mononuclear cells through the inhibition of viral entry and membrane fusion via the CXC chemokine receptor (CXCR)4 coreceptor but not via CC chemokine receptor 5. KRH-1636 also inhibits binding of the CXC chem...
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。
T36862	Ganglioside GT1b Mixture (sodium salt) Ganglioside GT1b Mixture (sodium salt),Ganglioside G1 Mixture
	Ganglioside GT1b is a trisialoganglioside that is characterized by having two sialic residues linked to the inner galactose unit. It binds to the neurotoxins botulinum toxin serotype A (BTxA), BTxA heavy chain, and tetanus toxin with IC50 values of 11, 0.74, and 7.2 μM, respectively.[1] Ganglioside GT1b-containing liposomes bind to the major coat protein VP1 from Merkel cell polyomavirus (MCPyV), which has been identified in Merkel cell carcinomas, identifying ganglioside GT1b as a putative MCP...

化合物

Cat.No: T15371

Target: TLR, HIV Protease

Cat.No: T24984

Target: Calcium Channel

(S)-(+)-Rolipram

Cat.No: T6649

Synonym: (S)-Rolipram,(+)-Rolipram,盐酸环胞苷,S- (+)-Rolipram

Target: Apoptosis, PDE

Rufloxacin hydrochloride

Cat.No: TQ0221

Synonym: MF-934 hydrochloride,盐酸芦氟沙星

Target: Antibacterial

Cat.No: T8311

Synonym: ABX-464,ABX464

Target: HIV Protease

Cat.No: T9682

Synonym: AZD4877

Target: Apoptosis, Kinesin

Cat.No: T1639

Synonym: 氨来呫诺,CHX3673,Amoxanox,氨来诺,AA673

Target: IL Receptor, FGFR, Others, IκB/IKK

Myelin Basic Protein (87-99) Acetate

Cat.No: T21618L

Synonym: Myelin Basic Protein (87-99) Acetate (118506-26-6 Free base)

Target: Others

Cat.No: T14381

Synonym: AZD-7624

Target: p38 MAPK, TNF

Cat.No: T14374

Dolutegravir RR Isomer

Cat.No: T70881

Cat.No: T37590

Cat.No: T23585

Synonym: ddEtUrd,D2EtU,5-Ethyl-2',3'-dideoxyuridine

I-XW-053 sodium

Cat.No: T27642

Synonym: I-XW-053 Na,I XW 053 sodium,IXW053 sodium,I XW 053 Na,IXW053 Na

Cat.No: T74915

Cat.No: T27030

Synonym: HIV-1 inhibitor-34,HIV-1 inhibitor 34,CK 176,CK-176,HIV-1 inhibitor34

TLR7 agonist 14

Cat.No: T79749

Cat.No: T82515

Cat.No: T40979

Cat.No: TP1962

p38 MAP Kinase Inhibitor IV

Cat.No: T36011

Synonym: p38 MAPK Inhibitor IV

Immuno modulator-1

Cat.No: T79170

Cat.No: T61574

(S)-p38 MAPK Inhibitor III

Cat.No: T35420

Synonym: (S)-p38 MAPK Inhibitor III

Dolutegravir SR Isomer

Cat.No: T71009

Cat.No: T74990

Cat.No: T39106

PD-1/PD-L1-IN-31

Cat.No: T78755

Target: PD-1/PD-L1

Cat.No: T69009

gardiquimod TFA salt

Cat.No: T5499

Toxic Shock Syndrome Toxin-1 (TSST-1) (58-78)

Cat.No: T80964

L Moses dihydrochloride

Cat.No: T36109

TLR7 agonist 16

Cat.No: T79751

Myelin Basic Protein(87-99) TFA

Cat.No: T78370

Cat.No: T82254

Target: Histone Demethylase

STING modulator-5

Cat.No: T74718

O-Demethyl Apremilast

Cat.No: T35929

Cat.No: T63287

SDF-1α (human)

Cat.No: T80130

Target: CXCR

Cat.No: T79770

Target: Autophagy

PROTAC IRAK4 degrader-2

Cat.No: T74062

Cat.No: T37273

Tenofovir diphosphate (sodium salt)

Cat.No: T37523

Cat.No: T64280

Cat.No: T68321

Cat.No: T37355

Indoxyl Sulfate-d5 potassium salt

Cat.No: T70313

Cat.No: T69081

HOXB7 (8-25) TFA

Cat.No: T83846

Synonym: Homeobox B7 (8-25)

Ganglioside GT1b Mixture (sodium salt)

Cat.No: T36862

Synonym: Ganglioside GT1b Mixture (sodium salt),Ganglioside G1 Mixture

Cat. No.	Product Name	Target	Signaling Pathways
TN1520	Isoforskolin Coleonol B	IL Receptor; TNF	Apoptosis; Immunology/Inflammation
	Isoforskolin 源自毛喉鞘蕊花，可减少人单核白细胞中 TNF-α、IL-1β、IL-6 和 IL-8 的分泌。Isoforskolin 可用于治疗莱姆关节炎的研究。
T7009	Soyacerebroside II	IL Receptor; Calcium Channel	Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism
	Soyacerebroside II exhibits ionophoretic activity for Ca2+ ion. Soyacerebrosides I and II have modulating the cellular immune response effects, they show obvious inhibitory activity on IL-18 secretion in human peripheral blood mononuclear cells (PBMC).
TN6054	Norglaucine hydrochloride
	(+)-Norglaucine shows cytotoxic activity toward the tumor cell lines B16-F10 (mouse melanoma), HepG2 (human hepatocellular carcinoma), K562 (human chronic myelocytic leukemia) and HL-60 (human promyelocytic leukemia) and non-tumor peripheral blood mononuc

天然产物

Cat.No: TN1520

Synonym: Coleonol B

Target: IL Receptor, TNF

Soyacerebroside II

Cat.No: T7009

Target: IL Receptor, Calcium Channel

Norglaucine hydrochloride

Cat.No: TN6054

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