Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T23602 |
ABC99
ABC 99,ABC-99 |
Wnt/beta-catenin | Cytoskeletal Signaling; Stem Cells |
ABC99是 wnt 脱酰基酶的一种选择性不可逆抑制剂。ABC99抑制 NOTUM(IC50:13 nM)。它还显示了对丝氨酸水解酶家族的优良选择性。 | |||
T23601 |
ABC1183
ABC 1183,ABC-1183 |
GSK-3; CDK | Cell Cycle/Checkpoint; PI3K/Akt/mTOR signaling; Stem Cells |
ABC1183是一种抑制GSK3α, GSK3β和CDK9的新型二氨基噻唑。ABC1183通过诱导G2/M 阻滞和改变GSK3、糖原合成酶、β-catenin 磷酸化和MCL1表达降低细胞存活率来抑制多种癌细胞株的生长,并具有口服活性。 | |||
T6750 |
Opaganib
ABC294640 |
S1P Receptor | GPCR/G Protein |
Opaganib (ABC294640) 是选择性和竞争性的鞘氨醇激酶 2 (SK2) 抑制剂,Ki 为 9.8 μM。 | |||
T6367 |
Abacavir sulfate
Abacavir Hemisulfate,硫酸阿巴卡韦,1592U89,ABC sulfate,Ziagen |
Apoptosis; HIV Protease; Reverse Transcriptase | Apoptosis; Microbiology/Virology; Proteases/Proteasome |
Abacavir sulfate (Ziagen) 是一种核苷类似物逆转录酶抑制剂,可用于 HIV 和 AIDS。 | |||
T38316 |
ABC34
|
||
ABC34 is an inactive control probe for JJH260 , the inhibitor of androgen-induced gene 1 (AIG1), an enzyme that hydrolyzes fatty acid esters of hydroxy fatty acids (FAHFAs). ABC34 demonstrates an IC50 value greater than 25 μM for the inhibition of 9-PAHSA but is more potent in blocking the serine hydrolase ABHD6 and the palmitoyl-protein hydrolase PPT1, which are both off-targets of JJH260. | |||
T33648 |
Nestifylline
ABC 99,ABC99,ABC-99 |
||
Nestifylline is a biochemical. | |||
T68352 |
ABC294735
|
||
ABC294735 is a dual SK1/SK2 inhibitor with potential anticancer activity. | |||
T25611 |
Lanatoside
Lantoside,ABC lanatoside complex |
||
Lanatoside 是一种 FDA 批准的强心苷,已被确定为候选的抗登革热化合物。它也被发现可以促进脉粥样硬化,还具有抗肿瘤活性,可抑制结直肠癌细胞、肝癌细胞的生长。 | |||
T80903 |
Ulviprubart
ABC-008 |
||
Ulviprubart是一种Anti-KLRG1 mAb,适用于研究多种疾病。 | |||
T8596 |
Ceefourin 1
|
MRP | Immunology/Inflammation |
Ceefourin 1 是一种具有高度选择性的多药抗性蛋白 4 (MRP4) 抑制剂。它能够抑制多种 MRP4 底物的转运,但对其他 ABC 转运蛋白无影响。它是苯并噻唑,常作为高危神经母细胞瘤的化学增敏剂。 | |||
T16040 |
Mepazine
甲哌啶嗪,Pecazine |
Apoptosis; MALT | Apoptosis; Immunology/Inflammation |
Mepazine (Pecazine) 是一种有效的特异性 MALT1 抑制剂。 Mepazine 抑制 GSTMALT1 全长和 GSTMALT1 325-760,IC50 为 0.83 μM 和 0.42 μM。 Mepazine 增强细胞凋亡并影响细胞活力。 | |||
T71299 |
M-25
|
||
M-25 is a Smoothened antagonist and inhibitor of the Hedgehog pathway. | |||
T5354 |
IRAK4-IN-7
CA-4948 |
IRAK | Immunology/Inflammation; NF-κB |
IRAK4-IN-7 (CA-4948) 是白介素 1 受体相关激酶 4 (IRAK4) 的选择性抑制剂,口服有活性。它可用于研究癌症以及炎症疾病。 | |||
T64082 | ABC44 | ||
ABC44 是丝氨酸水解酶 (serine hydrolase) 的有效抑制剂,对棕榈酰蛋白硫酯酶 1 (PPT1) 原位和体外的 IC50 分别为 0.1 μM 和 6.5 μM。ABC44 能够用于研究婴儿晚期神经元样脂褐质沉积症。 | |||
T8491 |
Vorolanib
CM082,X-82 |
VEGFR; PDGFR | Angiogenesis; Tyrosine Kinase/Adaptors |
Vorolanib (X-82) 是一种有效的 ATP 结合盒 (ABC) 转运蛋白抑制剂,是一种有效的、具有口服活性的 VEGFR/PDGFR 抑制剂,是一种血管生成抑制剂,与 ZD1839 联用具有抗肿瘤作用。 | |||
T3503 |
MC-Val-Cit-PABC-PNP
Maleimidocaproyl-L-valine-L-citrulline-p-aminobenzyl alcohol p-nitrophenyl carbonate,马来酰亚胺基己酰-L-缬氨酸-L-瓜氨酸对氨基苄醇 对硝基苯基碳酸脂 |
Others; AChR | Neuroscience; Others |
MC-Val-Cit-PABC-PNP 是一种组织蛋白酶可裂解的 ADC 肽接头,可用于合成抗体偶联药物。 | |||
T18962 |
Dabcyl acid, SE
Dabcyl, SE |
Others | Others |
Dabcyl acid, SE (Dabcyl, SE) 是Dabcyl acid (DABCYL)的氨基活性形式,普遍用于制备含有DABCYL 荧光探针。 | |||
T68135L |
(Rac)-Sabcomeline HCl
sabcomeline HCl(149156-36-5 Free base) |
AChR | Neuroscience |
Sabcomeline HCl 是一种 M1 receptor 激动剂,可用于研究阿尔茨海默病。 | |||
T76844 |
Abciximab
C7E3 |
Integrin | Cytoskeletal Signaling |
Abciximab (C7E3) 是一种小鼠/人嵌合单克隆抗体,是一种有效的糖蛋白 IIb/IIIa (glycoprotein IIb/IIIa) 抑制剂。 Abciximab 具有抗血小板聚集和白细胞粘附的作用,通过与糖蛋白 IIb/IIIa、vitronectin 和 Mac-1 受体结合发挥作用。 | |||
T40303 |
5-A-RU-PABC-Val-Cit-Fmoc
|
Others | Others |
5-A-RU-PABC-Val-Cit-Fmoc 是 5-A-RU 的前体物质之一。5-A-RU 是一种小分子粘膜相关的 MAIT 激活剂,是细菌合成核黄素的前体物质。 | |||
T18963 |
Dabcyl acid
DABCYL,4-二甲胺偶氮苯-4’-羧酸,Para-methyl red |
Others | Others |
Dabcyl acid (DABCYL) 是一种最早的深色荧光猝灭剂。 | |||
T18268 | Mal-PEG1-Val-Cit-PABC-OH | Others | Others |
Mal-PEG1-Val-Cit-PABC-OH is a 1 unit polyethylene glycol (PEG) ADC linker that possesses cleavable properties. This linker, commonly utilized in the synthesis of antibody-drug conjugates (ADCs), serves as a critical component facilitating the conjugation of drugs to antibodies[1]. | |||
T18721 | MAC-VC-PABC-ST7612AA1 | Others | Others |
MAC-VC-PABC-ST7612AA1 is a part of antibody drug conjugates (ADCs) charged with HDAC inhibitor by a linker, shows antitumor activity[1]. | |||
T79514 | ABCG2-IN-2 | BCRP | Membrane transporter/Ion channel |
ABCG2-IN-2为一有效ABCG2抑制剂,呈现小鼠良好口服药代动力学性质。适用于研究肿瘤多药耐药(MDR)与红细胞生成性原卟啉症(EPP)。 | |||
T68135 |
sabcomeline
SB-202026,SB-202026 ; Memric,Memric |
||
Sabcomeline 是一种有效的功能性选择性 M1 毒蕈碱受体受体 (muscarinic M1 receptor) 部分激动剂,可以改善认知功能。Sabcomeline 可用于阿尔茨海默症的研究。 | |||
T18332 |
MC-VC-PABC-Aur0101
|
Others | Others |
MC-VC-PABC-Aur0101 is a potent anticancer drug-linker conjugate designed for Antibody-Drug Conjugates (ADCs), comprising Aur0101, an auristatin microtubule inhibitor, connected through the MC-VC-PABC linker to enhance antitumor efficacy. | |||
T17357 |
AcLys-PABC-VC-Aur0101
|
Others | Others |
AcLys-PABC-VC-Aur0101 is a drug-linker conjugate for anti-CXCR4 ADC with potent antitumor activity, comprising the auristatin microtubule inhibitor Aur0101, connected through the cleavable linker AcLys-PABC-VC[1]. | |||
T76067 |
Dabcyl-KTSAVLQSGFRKME-Edans TFA
|
||
Dabcyl-KTSAVLQSGFRKME-Edans TFA 是一种用于测量蛋白酶酶促活性的荧光肽,具有研究2019-nCoV (COVID-19) 感染潜力的特性。该化合物作为底物,用于相关蛋白酶活性的测定。 | |||
T78763 |
ABCB1-IN-1
|
||
ABCB1-IN-1 (compound 3) 为高效ABCB1抑制剂,可诱导细胞凋亡。含1-苯甲基咪唑基团,其对Colo205与Colo320细胞系展现出的IC50分别为1.26 μM与2.21 μM。 | |||
T81832 |
MC-VC-PABC-C6-alpha-Amanitin
|
||
MC-VC-PABC-C6-alpha-Amanitin是一款针对HER2受体的ADC,包含致癌毒素alpha-Amanitin及单克隆抗体MC-VC-PABC-C6。alpha-Amanitin主要抑制RNA聚合酶IIα。该化合物专一性地靶向HER2阳性肿瘤细胞,主要应用于乳腺癌与胃癌的研究领域。 | |||
T17815 |
DBCO-Val-Cit-PABC-OH
|
Others | Others |
DBCO-Val-Cit-PABC-OH is a cleavable linker employed in the synthesis of antibody-drug conjugates (ADCs) [1]. | |||
T40342 |
MC-VC-PABC-amide-PEG1-CH2-CC-885
MC-VC-PABC-amide-PEG1-CH2-CC-885 |
||
MC-VC-PABC-amide-PEG1-CH2-CC-885 is an Antibody-Drug Conjugate (ADC) utilizing a protein-degrading agent (protac molecular glue, etc.). | |||
T75369 |
DABCYL-Glu-Arg-Nle-Phe-Leu-Ser-Phe-Pro-EDANS
|
||
DABCYL-Glu-Arg-Nle-Phe-Leu-Ser-Phe-Pro-EDANS 为一种用于人类疟原虫天冬氨酰蛋白酶的荧光底物,属于荧光染料类。储存条件:需避光。 | |||
T77848 |
vc-PABC-DM1
|
||
vc-PABC-DM1用于合成基于二硫键的ADC分子,且可探索其血清稳定性。 | |||
T18754 |
TCO-PEG1-Val-Cit-PABC-OH
|
Others | Others |
TCO-PEG1-Val-Cit-PABC-OH, a cleavable 1-unit PEG ADC linker, is employed in the synthesis of antibody-drug conjugates (ADCs)[1]. | |||
T81714 | N3-PEG8-Phe-Lys-PABC-Gefitinib | ||
N3-PEG8-Phe-Lys-PABC-Gefitinib是一种结合了抗癌活性分子Gefitinib(口服活性的抑制剂)与可降解的ADC linker N3-PEG8-Phe-Lys-PABC的点击化学试剂。该化合物具备Azide基团,能够通过铜催化的叠氮-炔环加成反应(CuAAc)与含Alkyne基团的分子反应,也可与含DBCO或BCN基团的分子进行菌株促进的炔-叠氮环加成反应(SPAAC)。 | |||
T17816 | DBCO-Val-Cit-PABC-PNP | Others | Others |
DBCO-Val-Cit-PABC-PNP is a cleavable linker for antibody-drug conjugate (ADC) synthesis[1]. | |||
T77822 | Mal-PEG8-Val-Ala-PABC | ||
Mal-PEG8-Val-Ala-PABC是用于合成Tesirine的可剪切Tesirine linker,Tesirine是一种ADC用的drug-linker conjugate。 | |||
T79877 |
MTvkPABC-P5
|
||
MTvkPABC-P5d,作为TLR7激动剂,属于免疫刺激剂类。该化合物主要应用于合成免疫刺激抗体偶联物(ISAC)。 | |||
T77853 |
MC-VA-PABC-MMAE
|
||
MC-VA-PABC-MMAE是一种ADC(Linker为peptide MC-VA-PABC)的活性分子,由Linker与高效微管蛋白抑制剂MMAE通过偶联反应形成。 | |||
T77849 |
Val-Ala-PABC-Exatecan
|
||
Val-Ala-PABC-Exatecan 为药物-连接体(Drug-Linker Conjugates for ADC),包含可裂解的 Tesirine linker 及 Exatecan(topoisomerase I 抑制剂)。它适用于合成 Mal-PEGn-amide-va-Exatecan(ADC 分子)。 | |||
T28654 |
Sabcomeline hydrochloride
BCI224,BRL-55473,BCI-224,CEB-2424,SB-202026A,Sabcomeline HCl |
||
Sabcomeline is a selective M1 receptor partial agonist. | |||
T79513 | ABCG2-IN-1 | BCRP | Membrane transporter/Ion channel |
ABCG2-IN-1(化合物K2)为Ko143类似物,该口服活性ABCG2抑制剂IC50值为0.13 μM,显示出优良的小鼠体内口服药代动力学特性。 | |||
T74076 | MC-VC-PABC-SP 141 | ||
MC-VC-PABC-SP 141 是抗体-活性分子偶联物的一部分,由有效的 MDM2抑制剂 SP 141 和可降解的 ADC linkerMC-VC-PABC 连接而成。 | |||
T17351 |
Acetylene-linker-Val-Cit-PABC-MMAE
LCB14-0602 |
Others | Others |
Acetylene-linker-Val-Cit-PABC-MMAE (LCB14-0602) is a drug-linker conjugate for antibody-drug conjugates (ADCs) that combines the ADC linker (Acetylene-linker-Val-Cit-PABC) with the potent tubulin inhibitor MMAE. | |||
T18737 |
AcLysValCit-PABC-DMAE-SW-163D
|
Others | Others |
AcLysValCit-PABC-DMAE-SW-163D is a drug-linker conjugate for antibody-drug conjugates (ADCs), featuring a natural bis-intercalator, SW-163D, attached through an AcLysValCitPABC-DMAE linker[1]. | |||
T18875 |
(Ac)Phe-Lys(Alloc)-PABC-PNP
|
Others | Others |
'(Ac)Phe-Lys(Alloc)-PABC-PNP serves as a valuable cleavable linker in the development of antibody-drug conjugates.' | |||
T18331 |
MC-VC-PABC-DNA31
|
Others | Others |
MC-VC-PABC-DNA31 is a drug-linker conjugate designed for Antibody-Drug Conjugates (ADC) that demonstrates potent antitumor activity. It employs DNA31, an effective inhibitor of RNA polymerase, connected through the MC-VC-PABC ADC linker. | |||
T77856 |
Ac-Lys-Val-Cit-PABC-MMAE
|
||
Ac-Lys-Val-Cit-PABC-MMAE作为一种抗体偶联药物(ADC)的活性分子部分,由ADC连接子(肽 Ac-Lys-Val-Cit-PABC)与微管蛋白聚合抑制剂MMAE经偶联形成。 | |||
T77857 |
Ac-Lys-Val-Cit-PABC-MMAE formic
|
||
Ac-Lys-Val-Cit-PABC-MMAE (formic) 为一种抗体药物偶联物(ADC)的活性组分。该化合物是由ADC链接子(肽类Ac-Lys-Val-Cit-PABC)与微管蛋白聚合抑制剂Monomethylauristatin E (MMAE) 结合而得。 |