62
13
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TP1837 |
Acyl Carrier Protein (ACP) (65-74)
Acyl Carrier Protein (ACP) 65-74 |
||
Acyl Carrier Protein (ACP) (65-74) is an active acyl carrier protein (ACP) fragment.Acyl Carrier Protein (ACP) is a component of plastid-located plant fatty acid synthetase. It binds acyl groups covalently via the prosthetic group, 4-phosphopantetheine, d | |||
T8732 |
CTPI-2
|
Others; Mitochondrial Metabolism | Metabolism; Others |
CTPI-2 是一种特异性线粒体柠檬酸盐载体SLC25A1抑制剂,KD=3.5 μM,具有抗肿瘤作用。它能够抑制糖酵解、PPARγ 及其下游靶点葡萄糖转运蛋白 GLUT4。它阻断非酒精性脂肪性肝炎逆转脂肪变性的显著改变,防止演变为脂肪性肝炎,减少肝脏和脂肪组织中炎性巨噬细胞的浸润,并显著减轻由高脂肪饮食引起的肥胖。 | |||
T2607 |
MSDC 0160
CAY10415,Mitoglitazone,MSDC0160,MSDC-0160 |
Others; IGF-1R; Mitochondrial Metabolism | Metabolism; Others; Tyrosine Kinase/Adaptors |
MSDC 0160 (CAY10415) 是一种线粒体丙酮酸载体(MPC) 的调节剂,也是调节噻唑烷二酮的线粒体靶标 (mTOT) 的胰岛素增敏剂。它是一种噻唑烷二酮 (TZD),具有抗糖尿病和神经保护活性作用。它具有用于阿尔茨海默氏病的潜力。 | |||
T19507 |
Perfluamine
FTPA,Tris(perfluoropropyl)amine,Perfluorotripropylamine |
Others | Others |
Perfluamine (FTPA) 是一种疏水性载液,可用作血液替代品。 | |||
T83656 |
DLIN-MC4-DMA
|
Others | Others |
DLIN-MC4-DMA 是一种脂质膜,是一种潜在的核酸载体。 | |||
T19642 |
Nilofabicin
CG 0549,CG-0549,CG-400549,CG 400549,CG0549,CG400549 |
Antibacterial | Microbiology/Virology |
Nilofabicin (CG-400549) 是一种有效的烯酰-(酰基-载体-蛋白)还原酶下降(FabI)抑制剂,可用于治疗复杂急性疾病的研究。 | |||
T83655 |
DLIN-MC2-DMA
DLin-M-C2-DMA |
Others | Others |
DLIN-MC2-DMA (DLin-M-C2-DMA) 是一种脂质膜,是一种潜在的核酸载体。 | |||
TP1798 |
Pep-1 (uncapped)
Pep-1 uncapped |
Others | Others |
Pep-1 (uncapped) 是一种能够透过细胞的多肽。 | |||
T74233 |
Dlin-MeOH
|
Others | Others |
Dlin-MeOH 是一种脂质膜,是一种潜在的核酸载体,可用于合成 DLin-MC3-DMA。 | |||
T83654 |
Dilinoleyl Ketone
Bis(linoleyl) ketone |
Others | Others |
Dilinoleyl Ketone (Bis(linoleyl) ketone) 是一种脂质膜,是一种潜在的核酸载体。 | |||
T6834 |
FCCP
Carbonyl cyanide 4-(trifluoromethoxy)phenylhydrazone,Trifluoromethoxy carbonylcyanide phenylhydrazone |
ATPase; Mitochondrial Metabolism | Membrane transporter/Ion channel; Metabolism |
FCCP (Trifluoromethoxy carbonylcyanide phenylhydrazone) 是一种氧化磷酸化 (OXPHOS) 抑制剂,线粒体质子载体解偶联剂。FCCP 常被用作细胞凋亡诱导剂。 | |||
T11938L |
Macropa-NH2
|
Others | Others |
Macropa-NH2 是 macropa 双功能类似物,是一种常与抗体偶联的载体分子,常作为螯合剂使用,参与癌症研究。 | |||
T41324 |
L319
Di((Z)-Non-2-en-1-yl) 9-((4-(dimethylamino)butanoyl)oxy)heptadecanedioate |
Others | Others |
L319 (Di((Z)-Non-2-en-1-yl) 9-((4-(dimethylamino)butanoyl)oxy)heptadecanedioate) 是一种脂质膜,是一种潜在的核酸载体。 | |||
T9807 |
CPDS
|
Others | Others |
CPDS 是一种非渗透性硫醇剂,可影响多种线粒体功能。在大鼠肝线粒体中,它仅抑制 Pi/OH- 载体。它和丙二酸正丁酯都是完全抑制 Pi 进入所必需的。 | |||
T4105 |
AFN-1252
Debio 1452,API-1252 |
Others; Antibacterial; Antibiotic | Microbiology/Virology; Others |
AFN-1252 (Debio 1452)是一种FabI 的高效抑制剂,能抑制金黄色葡萄球菌。 | |||
T38715 |
MSDC-0602K
MSDC-0602K,Azemiglitazone potassium |
PPAR | DNA Damage/DNA Repair; Metabolism |
MSDC-0602K (Azemiglitazone potassium) (Azemiglitazone potassium) is a PPARγ-sparing thiazolidinedione (Ps-TZD) compound that binds to PPARγ with an IC50 of 18.25 μM. It also modulates the mitochondrial pyruvate carrier (MPC). This compound, MSDC-0602K, has potential applications in researching fatty liver conditions, including dysfunctional lipid metabolism, inflammation, and insulin resistance. MSDC-0602K acts as an insulin sensitizer, improving insulinemia and fatty liver disease in mice both ... | |||
T7081 |
CCCP
Carbonyl Cyanide m-Chlorophenylhydrazone,Carbonyl cyanide 3-chlorophenylhydrazone,羰基氰化氯苯腙 |
Apoptosis; IκB/IKK; COX; Mitochondrial Metabolism; STING; IFNAR; Antibacterial | Apoptosis; Immunology/Inflammation; Metabolism; Microbiology/Virology; Neuroscience; NF-κB |
CCCP (Carbonyl Cyanide m-Chlorophenylhydrazone) 是一种氧化磷酸化 (OXPHOS) 抑制剂,线粒体质子载体解偶联剂。CCCP 抑制 STING 及其下游信号分子 TBK1 和 IRF3 的激活。 | |||
T4441 |
UK-5099
UK 5099,PF-1005023,UK5099 |
Others; Mitochondrial Metabolism | Metabolism; Others |
UK-5099 (PF-1005023) 是一种有效的线粒体丙酮酸转运蛋白(MPC) 抑制剂, 抑制丙酮酸依赖性 O2消耗的 IC50值为50 nM。 | |||
T72968 |
ZINC00640089
|
Akt | Cytoskeletal Signaling; PI3K/Akt/mTOR signaling |
ZINC00640089 是一种选择性的脂质运载蛋白-2 (LCN2) 抑制剂。ZINC00640089 对细胞增殖、细胞活力有抑制作用,可减少 SUM149 细胞的 AKT 磷酸化水平。ZINC00640089 可用于研究炎症性乳腺癌 (IBC) 。 | |||
T9405 |
1,4-Dipierazino-2,3,5,6-tetrafluorobenzene
|
Others | Others |
1,4-Dipierazino-2,3,5,6-tetrafluorobenzene 是一种四氟苯衍生物,它的独特结构使其能够作为药物的载体,药物可以以可控的方式释放,使其能够用于开发靶向药物递送系统。 | |||
T6170 |
Elesclomol
伊利司莫,STA-4783 |
Apoptosis; HSP; Reactive Oxygen Species | Apoptosis; Cytoskeletal Signaling; Immunology/Inflammation; Metabolism; NF-κB |
Elesclomol (STA-4783) 是一种氧化应激诱导剂,也是一种高度亲脂性的铜离子载体。Elesclomol 可以诱导肿瘤细胞凋亡,用于铜死亡相关研究。Elesclomol 还可以抑制 FDX1 介导的 Fe-S 簇生物合成。 | |||
T6120 |
Pralatrexate
Folotyn,10-炔丙基-10-去氮杂氨基蝶呤,10-Propargyl-10-deazaaminopterin,普拉曲沙 |
Apoptosis; DHFR; Antifolate; TAM Receptor | Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism; Tyrosine Kinase/Adaptors |
Pralatrexate (10-Propargyl-10-deazaaminopterin) 是一种抗叶酸剂,也是二氢叶酸还原酶抑制剂,Ki 值为 13.4 pM。它具有抗肿瘤活性,可研究复发/难治性 T 细胞淋巴瘤。它是叶酰聚谷氨酸合成酶的底物,具有改善的细胞摄取和保留能力。 | |||
T67727 |
MCT1-IN-3
|
Monocarboxylate transporter | Membrane transporter/Ion channel |
MCT1-IN-3是一种单羧酸转运蛋白1 (MCT1)抑制剂。溶质载体(SLC)单羧酸转运蛋白1 (MCT1);SLC16A1)是治疗癌症的一个有希望的靶点。MCT1-IN-3(化合物24)对MCT1转运抑制作用强,IC50值为81.0 nM。MCT1-IN-3对多药转运体ABCB1也有明显的抑制作用。 | |||
T72054 |
SLC26A3-IN-1
|
transporter | Metabolism |
SLC26A3-IN-1 是一种阴离子交换蛋白 SLC26A3 的抑制剂 ,IC50值为340 nM。SLC26A3 属于溶质载体 (SLC) 蛋白,是 SLC26 家族成员之一。SLC26 家族对氯化物、碳酸氢盐、硫酸盐和草酸盐具有广泛的阴离子特异性。SLC26A3 在腺瘤 (DRA) 中下调,参与氯化物和草酸盐的肠道吸收且与氯离子丢失性腹泻有关。 | |||
T8637 |
DMNB
6-Nitroveratraldehyde,6-硝基藜芦醛 |
DNA-PK | DNA Damage/DNA Repair; PI3K/Akt/mTOR signaling |
DMNB (6-Nitroveratraldehyde) 可用于合成no-carrier-added 6-[18F]fluoro-L-DOPA (6-FDOPA)。它可用于研究多巴胺能系统的PET。 | |||
T0239 |
Lonidamine
AF1890,氯尼达明,DICA,Diclondazolic Acid |
Apoptosis; Hexokinase; Mitochondrial Metabolism | Apoptosis; Metabolism |
Lonidamine (Diclondazolic Acid) 是一种抗肿瘤药物,是己糖激酶、线粒体丙酮酸载体和质膜单羧酸转运蛋白抑制剂,同时也抑制线粒体复合物 II。 | |||
T30680 |
Cabiotraxetan
|
||
Cabiotraxetan is a therapeutic carrier. | |||
T32255 |
Jam 2-263
Jam 2 263l,Jam-2-263,Jam2263 |
||
Jam 2-263 is a spermidine-based catechol ferric carrier - carbocephalosporin. | |||
T28732 |
SCH-538415
|
||
SCH-538415 is an inhibitor of acyl carrier protein synthase from a microorganism. SCH-538415 exhibited inhibitory activity in the acyl carrier protein synthase (AcpS) assay with an IC(50) value of 4.19 microM and showed antibacterial activity against Stap | |||
T26184 |
Seproxetine HCl
(S)-Norfluoxetine hydrochloride,Seproxetine hydrochloride,(S)-Desmethylfluoxetine Hydrochloride |
||
Seproxetine HCl, a more active enantiomer of N-desmethyl metabolite fluoxetine, works by selectively inhibiting the serotonin uptake carrier. | |||
T33929 |
Perflubrodec
AF0144,AF-0144,AF 0144 |
||
Perflubrodec is a component of an intravascular temporary oxygen carrier to enhance oxygen transport. | |||
T32619 |
Lead phthalocyanine
|
||
Lead phthalocyanine, a selective carrier, can be used for the preparation of a cysteine-selective electrode. | |||
T24841 |
Sulfo-MBS Crosslinker
Sulfo-MBS Cross linker,Sulfo-MBS Cross-linker |
||
Sulfo-MBS Crosslinker is a non-cleavable, water-soluble, heterobifunctional protein crosslinking reagent. It is commonly used to crosslink haptens to carrier proteins and enzymes to antibodies. | |||
T32598 |
Lauroyl-coenzyme A
Dodecanoyl-coa,Coenzyme A, lauroyl-,Lauroyl-coa |
||
Lauroyl-coenzyme A can function as an acyl group carrier, acetyl-CoA. It can be used as an intermediate in lipid metabolism and is involved in lipid biosynthesis and fatty acid transport. | |||
T12635L |
Plevitrexed
BGC9331,ZD 9331 |
Others | Others |
Plevitrexed is taken up via the α-folate receptor as well as the reduced folate carrier. Plevitrexed is an orally active and effective thymidylate synthase (TS) inhibitor (Ki: 0.44 nM). Plevitrexed is used for gastric cancer in clinical. | |||
T26635 |
Antifolate C1
AGF 94,AGF94,AGF-94 |
||
Antifolate C1 is an inhibitor of de novo purine biosynthesis. Antifolate C1 has selectivity for cellular uptake by high affinity folate receptors and the proton-coupled folate transporter (PCFT) over the reduced folate carrier (RFC). | |||
T60313 | Sucistil | ||
Sucistil 是一种活性生化物质。hemoglobin sucistil (bovine) 是一种氧载体。 | |||
T25980 |
Pralatrexate, (R)-
|
||
Pralatrexate, (R)- is a folate analog dihydrofolate reductase (DHFR) inhibitor exhibiting high affinity for reduced folate carrier-1 (RFC-1) with antineoplastic and immunosuppressive activities. Pralatrexate selectively enters cells expressing RFC-1; intr | |||
T73990 | Lipid M | ||
Lipid M (pKa: 6.75) 可用于递送 mRNA 疫苗,引发强大的免疫反应并提高耐受性。 | |||
T34316 |
Rhizoferrin
|
Others | Others |
Rhizoferrin 是一种来自真菌Rhizopus microsporus var.rhizopodiformis 的新型铁载体,可用于研究植物缺铁引起的萎黄病。 | |||
T70499 |
Afabicin diolamine
|
||
Afabicin (formerly Debio 1450, AFN-1720) is a prodrug of afabicin desphosphono, an enoyl-acyl carrier protein reductase (FabI) inhibitor, and is a first-in-class antibiotic with a novel mode of action to specifically target fatty acid synthesis in Staphylococcus spp. | |||
T5137 |
Corn oil
玉米油 |
Others | Others |
Corn oil 是一种药物分子的载体,是一种从玉米胚芽中提取出来的油。 | |||
T25981 | Pralatrexate, (S)- | ||
Pralatrexate, (S)- is a folate analog dihydrofolate reductase (DHFR) inhibitor exhibiting high affinity for reduced folate carrier-1 (RFC-1) with antineoplastic and immunosuppressive activities. Pralatrexate selectively enters cells expressing RFC-1; intr | |||
T76568 |
Aminopeptidase N Ligand (CD13) NGR peptide
|
||
AminopeptidaseN Ligand (CD13) NGR peptide 是靶向CD13的多肽,常见于癌症研究中,用作细胞内传递的载体介质。 | |||
T37070 |
Pyridomycin
|
||
Pyridomycin is a structurally unusual antimycobacterial cyclodepsipeptide whose composition includes two rare moieties: 3-(3-pyridyl)-L-alanine and 2-hydroxy-3-methylpent-2-enoic acid. It inhibits NADH-dependent enoyl (Acyl-Carrier-Protein) reductase InhA, preventing mycolic acid synthesis in M. tuberculosis, including isoniazid-resistant strains (MICs = 0.31-0.63 μg/ml). | |||
T74304 | C16 PEG-Ceramide | ||
C16 PEG-Ceramide为一种聚乙二醇化神经酰胺,具备脂质载体传递功能,并能诱导自噬(autophagy),在癌症研究中有应用。 | |||
T73085 |
Talotrexin
PT523 |
||
Talotrexin (PT523) 是一种 Aminopterin 的类似物,是一种非聚谷氨酸化的经典抗叶酸剂 (antifolate)。 Talotrexin 是一种 RFC(还原型叶酸载体)的特异性抑制剂,可选择性地抑制 RFC 转运。Talotrexin 通过靶向 DHFR 抑制肿瘤生长显示出抗肿瘤活性。 | |||
T74859 | SLC7A11-IN-1 | ||
SLC7A11-IN-1 是一种有效的 SLC7A11抑制剂。SLC7A11-IN-1 显示出抗增殖活性。SLC7A11-IN-1 抑制细胞侵袭和转移。SLC7A11-IN-1 诱导细胞凋亡 (Apoptosis) 和细胞周期停滞在 S 期。SLC7A11-IN-1 具有抗肿瘤活性。 | |||
T35957 |
PBD-BODIPY
|
||
PBD-BODIPY is a probe for the spectrophotometric measurement of autoxidation reactions. Co-autoxidation of the PBD-BODIPY signal carrier and a hydrocarbon co-substrate can be quantified by monitoring loss of absorbance at 591 nm. PBD-BODIPY has been used to measure the activity of radical-trapping antioxidants in cell-free assays. It has also been used as a fluorescent probe for the detection of epoxidation activity. | |||
T73032 | MtInhA-IN-1 | ||
MtInhA-IN-1是一种口服活性的选择性结核分枝杆菌NADH依赖性烯酰基载体蛋白还原酶(MtInhA)抑制剂,IC50值为0.23 μM。对结核分枝杆菌H37Rv菌株,其MIC为0.4 μM。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T10857 |
Coenzyme A
|
Endogenous Metabolite | Metabolism |
Coenzyme A 是所有活细胞中必需的辅助因子,由泛酸,三磷酸腺苷和半胱氨酸合成的。Coenzyme A 与过氧化物酶 5 共价结合导致其过氧化物酶活性完全抑制,通过 DTT 还原能够逆转。Coenzyme A 及其硫酯衍生物是主要分解代谢,合成代谢途径和基因表达调控的关键参与者。 | |||
T15717 |
Lasalocid
Lasalocid-A,Antibiotic X-537A,Ionophore X-537A |
Antibacterial | Microbiology/Virology |
Lasalocid (Lasalocid-A) 是一种由链霉菌产生的离子载体抗生素,具有抗菌和寄生虫作用,常添加进饲料中。 | |||
T8170 |
Carboxyatractyloside
羧基苍术苷,Gummiferin,Carboxyatractyloside tripotassium salt |
Others | Others |
Carboxyatractyloside (Carboxyatractyloside tripotassium salt) tripotassium salt 是一种 ADP/ATP 载体蛋白 (ADP/ATP carrier) 抑制剂,抑制线粒体 ADP/ATP 的转运。它是一种具有毒性的天然产物, | |||
T2796 |
Coenzyme Q10
Ubiquinone-10,辅酶Q10,CoQ10 |
Ferroptosis; Reactive Oxygen Species; Endogenous Metabolite | Apoptosis; Immunology/Inflammation; Metabolism; NF-κB |
Coenzyme Q10 (CoQ10)是来自藤仓赤霉菌的一种天然产物,在线粒体呼吸链中充当电子载体。 | |||
T1609 |
NAD+
烟酰胺腺嘌呤二核苷酸,Cozymase,煙酸胺,β-DPN,DPN,β-Nicotinamide Adenine Dinucleotide,β-NAD |
NADPH; Endogenous Metabolite | Metabolism |
NAD+ (β-Nicotinamide Adenine Dinucleotide) 即烟酰胺腺嘌呤二核苷酸,是转递氢离子的辅酶。 | |||
T22446 |
NADP disodium salt
Disodium NADP,Triphosphopyridine nucleotide disodium salt,beta-烟酰胺腺嘌呤二核苷酸磷酸二钠盐 |
Others | Others |
NADP disodium salt (Disodium NADP) 是一种氧化还原辅助因子,是一种烟酰胺腺嘌呤二核苷酸。它是代谢中电子转移的关键辅因子,可以被交替氧化 (NADP+) 和还原 (NADPH)。 | |||
T3092 |
Nigericin sodium salt
尼日利亚菌素,尼日利亚菌素钠盐 |
Potassium Channel; NOD-like Receptor (NLR); Antibacterial; Antibiotic; NOD | Immunology/Inflammation; Membrane transporter/Ion channel; Microbiology/Virology; NF-κB |
Nigericin sodium salt 属于抗生素,是一种 NLRP3 激活剂,也是一种阳离子离子载体。Nigericin sodium 可以触发 NALP3 炎性体的激活,可抑制高尔基体功能并抑制革兰氏阳性菌的生长。 | |||
TWA2417 |
Sodium taurocholate
牛黄胆酸钠(牛胆酸钠,牛胆酸钠盐,牛磺膽酸鈉,牛磺胆酸钠,牛磺胆酸钠盐,牛胆酸钠水合物,水合牛磺胆酸钠,牛胆酸钠(混合物),牛黄胆酸钠(水合),牛磺胆酸钠(标准品)),Taurocholate Sodium |
Others | Others |
Sodium taurocholate (Taurocholate Sodium) hydrate 具有显著的生物学效应,例如通过上调 VEGF-A 的表达抑制肝动脉结扎所致的胆道损伤。对免疫系统具有一定的调节作用。 | |||
T0326 |
DL-Glutamine
Glutamin,DL-Gl,(±)-Glutamine,DL-谷氨酰胺,2-amino-4-carbamoylbutanoic acid |
Ferroptosis; Amino Acids and Derivatives; Endogenous Metabolite | Apoptosis; Metabolism |
DL-Glutamine (2-amino-4-carbamoylbutanoic acid) 是一种非必需氨基酸,大量存在于全身并参与许多代谢过程。 它由谷氨酸和氨合成,是体内氮的主要载体,是许多细胞的重要能量来源,用于制药和供生物化学研究。 | |||
T38499 | κ-Carrageenan | ||
κ-Carrageenan, a natural polymer found predominantly in red seaweeds, can serve as an effective drug carrier for delivering curcumin to cancer cells and inducing apoptosis. Additionally, κ-Carrageenan holds promise as a potential inflammatory agent, amplifying existing intestinal inflammation. | |||
T38069 |
Aquastatin A
|
||
Aquastatin A is a fungal metabolite originally isolated fromF. aquaeductuumthat has diverse biological activities.1It is active againstS. aureus(MIC = 32 μg/ml) and inhibits enoyl-acyl carrier protein reductase (Fabl; IC50= 3.2 μM) andS. aureusfatty acid synthesis (IC50= 3.5 μM).2Aquastatin A also inhibits the Na+/K+-ATPase and H+/K+-ATPase (IC50s = 7.1 and 6.2 μM, respectively), as well as protein tyrosine phosphatase 1B (PTP1B; IC50= 0.19 μM).1,3 1.Hamano, K., Kinoshita-Okami, M., Minagawa, K.... | |||
T78465 |
H-γ-Glu-Gln-OH
γ-Glutamylglutamine,γ-Glu-Gln |
||
H-γ-Glu-Gln-OH 是一种水溶性肽类化合物,用于药物结合。该载体特征为高溶解度、药物负载效能、优良生物相容性、低毒性,并能增强抗癌药物对肿瘤的靶向作用及疗效。 | |||
T36439 |
Gramicidin A
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Antibacterial; HIF; Parasite | Angiogenesis; Chromatin/Epigenetic; Microbiology/Virology |
Gramicidin A 是一种从从 B. brevis 分离出来的多肽类抗生素。Gramicidin A 是一种高度疏水的通道形成离子载体,在人工膜中形成一价阳离子可渗透的通道。Gramicidin A 诱导缺氧诱导因子 1α (HIF-1α) 的降解,并能降低人肾细胞癌小鼠异种移植模型的生长。Gramicidin A 具有抗菌、抗疟活性以及溶血活性。 |