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Cat. No.	Product Name	Target	Signaling Pathways
T9110	Ceapin-A7	Others	Others
	Ceapin-A7 是内质网应激 ATF6α信号的选择性阻断剂(IC50:0.59 μM)，可用于探讨 ATF6α 促细胞活化的机制及其在病理环境中的作用。
T8903	Retro-2 Retro 2,2-{[(5-methyl-2-thienyl)methylene]amino}	Others; Virus Protease; Parasite; Autophagy	Autophagy; Microbiology/Virology; Others
	Retro-2 (2-{[(5-methyl-2-thienyl)methylene]amino}) 是一种植物毒素蓖麻毒素抑制剂，它保护 HeLa 细胞免受蓖麻毒素、Stx1 和 Stx2 的侵害，选择性地阻断早期内体蛋白质-高尔基体界面处的逆行毒素运输。
T22665	PD 128042 CI 976	Acyltransferase	Metabolism
	PD 128042 (CI 976) 是口服有效的ACAT (酰基辅酶 A: 胆固醇酰基转移酶)选择性抑制剂。它也是LPAT(溶血磷脂酰基转移酶) 抑制剂。它抑制高尔基体相关 LPAT 活性 (IC50=15 μM)。它抑制多种膜运输步骤，包括在内吞和分泌途径中发现的步骤。
T3135	KM11060	CFTR; Autophagy	Autophagy; Membrane transporter/Ion channel
	KM11060 是 F508del-CFTR 运输缺陷的新型校正剂，可纠正 F508del-CFTR 运输，增加质膜上功能性 CFTR 的数量。它可用于 F508del-CFTR 加工缺陷的研究和囊性纤维化治疗剂的开发。
T12711	Retro-2 cycl RN 1-001	Virus Protease	Microbiology/Virology
	Retro-2 cycl 是一种抗病毒剂，是一种逆行运输抑制剂，抑制 JCPyV（IC50s：54 μM）和 HPV16 假病毒（IC50s：160 μM）。
T2595	Lumacaftor 鲁玛卡托,VX-809,VRT 826809	CFTR; Autophagy	Autophagy; Membrane transporter/Ion channel
	Lumacaftor (VRT 826809) 是一种 CFTR 调节剂，可纠正 CFTR 蛋白的折叠和运输。它增强了 FRT 细胞中 F508del-CFTR 蛋白的成熟，EC50为100 nM。
T7130	Navarixin MK-7123,SCH 527123	CXCR	Autophagy; GPCR/G Protein; Immunology/Inflammation
	Navarixin (MK-7123) 是一种可口服的 CXCR1和 CXCR2变构拮抗剂，对猕猴 CXCR1的 Kd 值为 41 nM，对大小鼠和猕猴 CXCR2的 Kd 值分别为 0.20、0.20 和 0.08 nM。
T1844	KPT330,(E)- (E)-RN,KPT-330,KPT330,KPT 330	Others; CRM1	Membrane transporter/Ion channel; Others
	(E)-RN (KPT 330) 是一种 CRM1 选择性核输出抑制剂。它抑制细胞核中的蛋白质运输并诱导间皮瘤细胞中的细胞周期停滞和凋亡。
T14935	Elexacaftor VX-445	CFTR; Autophagy	Autophagy; Membrane transporter/Ion channel
	Elexacaftor (VX-445) 是一种囊性纤维化跨膜电导调节因子 (CFTR) 校正剂。它促进CFTR 的加工和转运，增加细胞表面CFTR 的数量。
T13254L	UNC10217938A HCl UNC10217938A HCl(1347749-97-6 Free base),UNC7938 HCl	Others	Others
	UNC10217938A HCl (UNC7938 HCl) 是具有寡核苷酸 (oligonucleotides) 增强作用的 3-deazapteridine 类似物，通过调节寡核苷酸在细胞内的运输和从内体中的释放来增强寡核苷酸的作用。UNC10217938A HCl 还增强了 siRN 和反义寡核苷酸的作用。
T67835	LKM38
	LKM38是一种新型的重氮烷基胆固醇探针，是一种有前途的胆固醇模拟物。LKM38既能维持抗胆固醇细胞的生长，又能适当地调节关键的胆固醇平衡途径。LKM38可以作为研究胆固醇蛋白相互作用和贩运的有力工具。
T23874	CESTRIN
	CESTRIN is a cellulose synthase trafficking probe that acts by inhibiting cellulose deposition and interferes with the trafficking of cellulose synthase complexes and their associated proteins KORRIGAN1 and POM2/CSI1.
T28228	Okicenone
	Okicenone is an antibiotic, interferring with HuR RNA binding, HuR trafficking, T-cell activation and cytokine expression.
T69069	Endosidin1
	Endosidin1 is a natural vesicle trafficking inhibitor.
T6266L	PP2 Analog PP2-Analog,CHEMBL-306012,CHEMBL306012,CHEMBL 306012
	PP2 Analog is an analog of PP2. It also acts as a protein trafficking modulator.
T15110	DHQZ 36	Others	Others
	DHQZ 36 is a potent retrograde trafficking inhibitor. It has potent anti-parasite activity. DHQZ 36 inhibits Leishmania amazonensis infection in macrophages (EC50: 13.63 μM).
T70320	GNLPT-IN-1
	GNLPT-IN-1 is an inhibitor of gram-negative lipoprotein trafficking.
T23006	MM-22	Others	Others
	biotinylated anandamide analog acts as a probe for visualizing the accumulation and intracellular trafficking of anandamide
T23933	D011-2120 D0112120,D011 2120
	D011-2120 is an agent of antiviral that acts by blocking microtubule polymerization, disrupting the Golgi complex and inhibiting viral trafficking to the plasma membrane during virus egress.
T69436	Endosidin7
	Endosidin7 is a specific inhibitor for plant callose deposition during cytokinesis without affectting endomembrane trafficking during interphase or cytoskeletal organization.
T28443	PPQ-581
	PPQ-581 is an anti-influenza agent. PPQ-581 interrupts the crucial RNP trafficking, resulting in influenza replication inhibition, preventing virus-induced cytopathic effects.
T36519	Posenacaftor sodium
	Posenacaftor (PTI-801) sodium, a cystic fibrosis transmembrane regulator (CFTR) modulator, corrects CFTR protein folding and trafficking. It is utilized in researching cystic fibrosis (CF)[1].
T39187	Gliadin p31-43 Gliadin p31-43
	Gliadin p31-43, an undigested peptide derived from gliadin, prompts an innate immune response in the intestine and disrupts endocytic trafficking. Moreover, its utilization in celiac disease research has proven beneficial.
T10713	CCR4 antagonist 2	Calcium Channel	Membrane transporter/Ion channel; Metabolism
	CCR4 antagonist 2 (Compound 31) is a novel potent, orally bioavailable small molecule antagonists of CC chemokine receptor 4 (CCR4) that inhibits Treg trafficking into the Tumor Microenvironment without suppressing the number of Treg in healthy tissues. CCR4 antagonist 2 (Compound 31) exhibits IC50 values of Ca2+flux and (chemotaxis) CTX are 40 nM and 70 nM, respectively.
T35925	(R)-Posenacaftor sodium
	(R)-Posenacaftor ((R)-PTI-801) sodium, the R enantiomer of Posenacaftor, is a cystic fibrosis transmembrane regulator (CFTR) protein modulator. It corrects the folding and trafficking of the CFTR protein, and is utilized in the research of cystic fibrosis (CF)[1].
T11343	G0507	Others	Others
	G0507 is a pyrrolopyrimidinedione compound that serves as a potent inhibitor of Escherichia coli growth, effectively inducing the extracytoplasmic σE stress response. It acts as a valuable chemical probe, specifically designed to dissect lipoprotein trafficking in Gram-negative bacteria. Notably, G0507 demonstrates strong inhibitory activity against the LolCDE ABC Transporter.
T28838	SPM-242 SPM 242
	SPM-242 is an orthosteric agonist of Sphingosine 1-phosphate (S1P) and a bitopic antagonist. S1P is a lysophospholipid signaling molecule that regulates important biological functions, including vascular development and lymphocyte trafficking, by activat
T37858	Dehydroergosterol 9,11-dehydro Ergosterol,DHE
	Dehydroergosterol is a naturally occurring, fluorescent analog of cholesterol (ex/em = 324/375 nm) that mimics the properties of cholesterol in cell membranes.[1] It is readily bound by cholesterol-binding proteins and has been used for real-time probing of the sterol environment and to elucidate intracellular sterol trafficking in living organisms.[1]
T74435	Alicaforsen sodium
	Alicaforsen sodium为20个碱基长度的反义寡核苷酸，主要通过抑制ICAM-1的产生发挥作用，ICAM-1作为关键粘附分子，参与白细胞向炎症部位的迁移和转运。
T25365	EGA	Others	Others
	EGA 抑制致命毒素的中毒，并阻止多种其他酸依赖性细菌毒素和病毒进入哺乳动物细胞。EGA 是研究膜运输的有力工具，可用于治疗传染病。
T81449	PKC-ε translocation inhibitor peptide	PKC	Chromatin/Epigenetic; Cytoskeletal Signaling
	PKC-ε translocation inhibitor peptide，作为一种特定的PKC-ε易位抑制剂，能够特异性地调控FcγR介导的调理珠内化速率，而对FcαR运输不产生影响。
T79817	S1P1 agonist 6 hemicalcium	LPL Receptor	GPCR/G Protein
	S1P1 agonist 6 hemicalcium (Compound I) 为一S1P1激动剂，其通过抑制淋巴细胞迁移而降低免疫反应，适用于自身免疫性疾病研究中的免疫抑制剂。
T79816	S1P1 agonist 6	LPL Receptor	GPCR/G Protein
	S1P1 agonist 6 (Compound I) 是一种可以通过阻断淋巴细胞迁移来减弱免疫反应的S1P1激动剂，常用于研究自身免疫性疾病的免疫抑制剂。
T82311	Gliadin p31-43 TFA
	Gliadin p31-43 TFA 是一种未消化gliadin peptide，可诱导肠道先天性免疫反应并干扰内吞运输，用于乳糜泻研究。
T61265	Exo2
	Exo2 is a secretion inhibitor that hinders the trafficking of Shiga toxin from endosomes to the trans-Golgi network. It inhibits the exit of secretory cargo from the endoplasmic reticulum (ER) and disrupts the Golgi apparatus. Notably, Exo2 does not impact the morphology of the trans-Golgi network (TGN). Additionally, Exo2 has the ability to induce calcium-dependent exocytosis in permeabilized adrenal chromaffin cells [1] [2].
T70944	Carotegrast methyl HCl
	Carotegrast methyl, also known as AJM300 and PTC-100, is an orally-active small molecule that antagonises the α4 integrin receptor. AJM300 reduces inflammation by blocking leucocyte trafficking. Oral treatment with AJM300 dose-dependently inhibited lymphocyte homing to Peyer's patches and increased the peripheral lymphocyte count in the same dose range. AJM300 dose-dependently prevented the development of experimental colitis in mice.
T35947	17(S)-HDHA
	17(S)-HDHA is a primary mono-oxygenation product of docosahexaenoic acid in human whole blood, human leukocytes, and mouse brain. 17(S)-HDHA serves as a precursor to 17(S)-resolvins and has intrinsic biological activity, such as the inhibition of TNF-α-induced interleukin-1β expression in human glioma cells and inhibition of TNF-α-induced leukocyte trafficking to the mouse air pouch.
T81305	ReAsH-EDT2
	ReAsH-EDT2为膜透性红色荧光染料，专用于蛋白质标记。作为二砷化合物，其通过共价结合至四半胱氨酸序列实现蛋白质成像，并可监测其定位与转运。(λex=530 nm，λem=592 nm)。
T76156	Sphingomyelin phosphodiesterase
	Sphingomyelinphosphodiesterase 是一种水解酶，参与鞘磷脂代谢过程。Sphingomyelinphosphodiesterase 水解鞘磷脂，使其向磷酸胆碱和神经酰胺转化。Sphingomyelinphosphodiesterase 还在细胞分化、各种免疫和炎症反应以及细胞内胆固醇运输和代谢中发挥重要作用。
T76221	Leptin (116-130)
	Leptin(116-130)是一种生物活性的瘦素片段，能促进AMPA受体运输至突触并加强活动依赖性的海马突触可塑性。此外，Leptin(116-130)在抗淀粉样蛋白毒性模型中有效阻止海马突触损伤和神经元细胞死亡，显示出对研究阿尔茨海默病(AD)具有重要潜力。
T71174	PBT434 HBr
	PBT434 is a novel, brain-penetrant, small molecule inhibitor of α-synuclein aggregation. In transgenic animal models of Parkinson disease (A53T) and MSA (PLP-α-Syn), PBT434 reduced α-synuclein aggregation, preserved neurons and improved motor function. Glial cell inclusions were also reduced in a murine MSA model. PBT434 is thought to act by redistributing reactive iron across membranes, thereby blocking intracellular protein aggregation and oxidative stress. The affinity of PBT434 for iron is g...
T83937	Tricyclic cytosine tC
	Tricyclic cytosine tC 是一种用于在活细胞中成像 RNA 的荧光胞嘧啶类似物。当与共聚焦成像技术结合使用时，可用于研究单细胞分辨率下的 RNA 合成、降解和运输。激发/发射最大值 (λ) = 375/505 nm；消光系数 = 4000 M-1cm-1；量子产率 = 0.2。
T74553	YSK 05
	YSK 05是一种对pH敏感的阳离子脂质，能够改善非病毒载体的胞内转运效率。YSK 05-MEND显示出显著的基因沉默活性和溶血性。通过聚乙二醇化处理，YSK 05有效克服了对内体逃逸的抑制，从而在体外和体内均显著增强了siRNA的传递效率。
T37028	PtdIns-(3,4,5)-P3 (1,2-dipalmitoyl) (sodium salt) PtdIns-(3,4,5)-P3 (1,2-dipalmitoyl) (sodium salt)
	The phosphatidylinositol phosphates represent a small percentage of total membrane phospholipids. However, they play a critical role in the generation and transmission of cellular signals. PtdIns-(3,4,5)-P3 can serve as an anchor for the binding of signal transduction proteins bearing pleckstrin homology (PH) domains. Centuarin α and the Akt-family of GTPase activating proteins are examples of PtdIns-(3,4,5)-P3-binding proteins. Protein-binding to PtdIns-(3,4,5)-P3 is important for cytoskeletal ...
T72280	PBT434 methanesulfonate
	PBT434 methanesulfonate 为一种有效、口服活性并能穿透血脑屏障的α-synuclein aggregation抑制剂，同时担任铁螯合剂和跨细胞铁运输的调节剂。该化合物抑制铁介导的氧化还原活性及α-synuclein聚集，可有效防止SNpc神经元丢失，显示出在PD研究中的应用潜力。
T81966	L17E
	L17E是一种针对晚期内体(LE)特异性膜裂解活性的内体溶解肽，归类为阳离子两亲肽。它通过细胞内吞作用进入细胞，并运输到LE。在LE酸性环境下，L17E能干扰并裂解LE膜，引发膜破裂及LE内容物释放至胞质溶胶。该肽用于探究内体蛋白运输路径。
T35491	3,5-dimethyl PIT-1
	PtdIns-(3,4,5)-P3 (PIP3) serves as an anchor for the binding of signal transduction proteins bearing pleckstrin homology (PH) domains such as phosphatidylinositol 3-kinase (PI3K) or PTEN. Protein binding to PIP3 is important for cytoskeletal rearrangement and membrane trafficking and initiates an intricate signaling cascade that has been implicated in cancer. 3,5-dimethyl PIT-1 is a dimethyl analog of PIT-1, the selective inhibitor of PIP3/Akt PH domain binding, that is designed for more favorab...
T36939	PtdIns-(3,4,5)-P3 (1,2-dihexanoyl) (ammonium salt) PtdIns-(3,4,5)-P3 (1,2-dihexanoyl) (ammonium salt)
	The phosphatidylinositol (PtdIns) phosphates represent a small percentage of total membrane phospholipids. However, they play a critical role in the generation and transmission of cellular signals. PtdIns-(3,4,5)-P3, also known as PIP3, is resistant to cleavage by PI-specific phospholipase C (PLC). Thus, it is likely to function in signal transduction as a modulator in its own right, rather than as a source of inositol tetraphosphates. PIP3 can serve as an anchor for the binding of signal transd...
T35790	Palmitic acid-1,2,3,4-13C4 Palmitic Acid-13C (C1, C2, C3, and C4 labeled)
	Palmitic acid-13C (C1, C2, C3, and C4 labeled) is intended for use as an internal standard for the quantification of palmitic acid by GC- or LC-MS. Palmitic acid is a common 16-carbon saturated fat that represents 10-20% of human dietary fat intake and comprises approximately 25 and 65% of human total plasma lipids and saturated fatty acids, respectively.1,2Acylation of palmitic acid to proteins facilitates anchoring of membrane-bound proteins to the lipid bilayer and trafficking of intracellula...
T36805	TPC2-A1-N TPC2-A1-N
	TPC2-A1-N is a novel, lipophilic, membrane permeable isoform-selective small molecule agonist of two-pore channel 2 (TPC2). TPC2-A1-N plays its role by mimicking the physiological actions of NAADP and PI(3,5)P2 through independent binding sites. TPC2-A1-N has inverse effects on key lysosomal activities and increases the pH in the lysosomal lumen in a TPC2-dependent manner[1].

化合物

Cat.No: T9110

Target: Others

Cat.No: T8903

Synonym: Retro 2,2-{[(5-methyl-2-thienyl)methylene]amino}

Target: Others, Virus Protease, Parasite, Autophagy

Cat.No: T22665

Synonym: CI 976

Target: Acyltransferase

Cat.No: T3135

Target: CFTR, Autophagy

Cat.No: T12711

Synonym: RN 1-001

Target: Virus Protease

Cat.No: T2595

Synonym: 鲁玛卡托,VX-809,VRT 826809

Target: CFTR, Autophagy

Cat.No: T7130

Synonym: MK-7123,SCH 527123

Target: CXCR

Cat.No: T1844

Synonym: (E)-RN,KPT-330,KPT330,KPT 330

Target: Others, CRM1

Cat.No: T14935

Synonym: VX-445

Target: CFTR, Autophagy

UNC10217938A HCl

Cat.No: T13254L

Synonym: UNC10217938A HCl(1347749-97-6 Free base),UNC7938 HCl

Target: Others

Cat.No: T67835

Cat.No: T23874

Cat.No: T28228

Cat.No: T69069

Cat.No: T6266L

Synonym: PP2-Analog,CHEMBL-306012,CHEMBL306012,CHEMBL 306012

Cat.No: T15110

Target: Others

Cat.No: T70320

Cat.No: T23006

Target: Others

Cat.No: T23933

Synonym: D0112120,D011 2120

Cat.No: T69436

Cat.No: T28443

Posenacaftor sodium

Cat.No: T36519

Cat.No: T39187

Synonym: Gliadin p31-43

CCR4 antagonist 2

Cat.No: T10713

Target: Calcium Channel

(R)-Posenacaftor sodium

Cat.No: T35925

Cat.No: T11343

Target: Others

Cat.No: T28838

Synonym: SPM 242

Dehydroergosterol

Cat.No: T37858

Synonym: 9,11-dehydro Ergosterol,DHE

Alicaforsen sodium

Cat.No: T74435

Cat.No: T25365

Target: Others

PKC-ε translocation inhibitor peptide

Cat.No: T81449

Target: PKC

S1P1 agonist 6 hemicalcium

Cat.No: T79817

Target: LPL Receptor

Cat.No: T79816

Target: LPL Receptor

Gliadin p31-43 TFA

Cat.No: T82311

Cat.No: T61265

Carotegrast methyl HCl

Cat.No: T70944

Cat.No: T35947

Cat.No: T81305

Sphingomyelin phosphodiesterase

Cat.No: T76156

Leptin (116-130)

Cat.No: T76221

Cat.No: T71174

Tricyclic cytosine tC

Cat.No: T83937

Cat.No: T74553

PtdIns-(3,4,5)-P3 (1,2-dipalmitoyl) (sodium salt)

Cat.No: T37028

Synonym: PtdIns-(3,4,5)-P3 (1,2-dipalmitoyl) (sodium salt)

PBT434 methanesulfonate

Cat.No: T72280

Cat.No: T81966

3,5-dimethyl PIT-1

Cat.No: T35491

PtdIns-(3,4,5)-P3 (1,2-dihexanoyl) (ammonium salt)

Cat.No: T36939

Synonym: PtdIns-(3,4,5)-P3 (1,2-dihexanoyl) (ammonium salt)

Palmitic acid-1,2,3,4-13C4

Cat.No: T35790

Synonym: Palmitic Acid-13C (C1, C2, C3, and C4 labeled)

Cat.No: T36805

Synonym: TPC2-A1-N

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