31
5
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
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)。 | |||
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。 | |||
TQ0186 |
Ko 143
|
BCRP; ABC | Membrane transporter/Ion channel |
Ko 143 有效且选择性抑制 ATP 结合盒亚家族 G 成员 2 (ABCG2/BCRP) | |||
T4595 |
YHO-13177
YHO 13177,YHO13177 |
BCRP | Membrane transporter/Ion channel |
YHO-13177 是高活性乳腺癌耐药蛋白多药转运通道(BCRP)抑制剂,可增强SN-38活性。 | |||
T3581 |
KS176
|
Potassium Channel; BCRP | Membrane transporter/Ion channel |
KS176是选择性高活性乳腺癌耐药蛋白多药转运通道抑制剂,在Pheo A 和Hoechst 检测中,IC50值分别为0.59和1.39 μM。 | |||
T38400 |
Triclabendazole sulfoxide
TCBZ-SO,三氯苯达唑亚砜 |
BCRP; Parasite | Membrane transporter/Ion channel; Microbiology/Virology |
Triclabendazole sulfoxide (TCBZ-SO) 是 Triclabendazole 的主要血浆代谢产物。Triclabendazole sulfoxide 具有抗寄生虫活性。Triclabendazole sulfoxide 可以抑制膜转运蛋白ABCG2/BCRP 的活性。 | |||
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。 | |||
T4337 |
PCI 29732
PCI29732,PCI-29732 |
Others; BCRP; BTK | Angiogenesis; Membrane transporter/Ion channel; Others; Tyrosine Kinase/Adaptors |
PCI 29732 是一种有效的可逆BTK 抑制剂,对 BTK、Lck 和 Lyn 的Kiapp 值分别为 8.2、4.6 和 2.5 nM。它通过竞争性结合ABCG2 的 ATP 结合位点来抑制ABCG2的功能。 | |||
T13383 |
Zamicastat
BIA 5-1058 |
BCRP; Hydroxylase; P-gp | Membrane transporter/Ion channel; Metabolism; Neuroscience |
Zamicastat (BIA 5-1058) 是多巴胺 β-羟化酶 (DBH) 抑制剂,可透过血脑屏障引起中枢和周边效应,具有降血压作用。它也是一种浓度依赖性的双重 P-gp 和 BCRP 抑制剂,IC50值分别为 73.8 和 17.0 μM。 | |||
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。 | |||
T2657 |
Elacridar
GW0918,依克立达,GW120918,GF120918,GG918 |
BCRP; P-gp | Membrane transporter/Ion channel; Neuroscience |
Elacridar (GG918) 是一种有效的 P-糖蛋白和BCRP 的抑制剂。 | |||
T2590 |
Vismodegib
Erivedge,GDC-0449,RG 3616,维莫德吉 |
Hedgehog/Smoothened; ABC; Autophagy | Autophagy; GPCR/G Protein; Membrane transporter/Ion channel; Stem Cells |
Vismodegib (GDC-0449) 是一种刺猬抑制剂,IC50值为 3 nM。它还可抑制 P-gp 和ABCG2的活性,IC50值分别为 3.0 μM 和 1.4 μM。 | |||
T9587 |
CCTA-1523
|
Others; ABC | Membrane transporter/Ion channel; Others |
CCTA-1523 是 ABCG2 抑制剂的外排功能。 它选择性地逆转癌细胞中 ABCG2 介导的 MDR。 | |||
T16164 |
MY-5445
N-(3-chlorophenyl)-4-phenylphthalazin-1-amine |
PDE | Metabolism |
MY-5445 (N-(3-chlorophenyl)-4-phenylphthalazin-1-amine) 是特异性的 cGMP 磷酸二酯酶 PDE5抑制剂,其 Ki=1.3 μM。它是一种 ABCG2转运蛋白调节剂,具有抗增殖活性。它能抑制人血小板凝集。 | |||
T2024 |
A-803467
A 803467,A803467 |
Sodium Channel | Membrane transporter/Ion channel |
A-803467 是有效的、选择性的河豚毒素不敏感型Nav1.8 钠通道阻断剂 。它在炎症性疼痛和神经性疼痛模型中有缓解疼痛作用。它通过与 ATP-binding cassette subfamily G member 2 (ABCG2) 转运蛋白的相互作用,增强了传统抗癌物的化疗敏感性。 | |||
T5109 |
Avapritinib
BLU-285 |
PDGFR; c-Kit | Angiogenesis; Tyrosine Kinase/Adaptors |
Avapritinib (BLU-285) 是选择性的、高效的、具有口服活性的 KIT 和 PDGFRA 激活环突变激酶抑制剂,能够作用于 KIT D816V (IC50:0.27 nM) 和 PDGFRA D842V (IC50:0.24 nM)。它减弱 ABCB1 和 ABCG2 的传输功能。它与激酶的活性构象结合,并显示抗肿瘤活性。 | |||
T0055L |
Glafenine Hydrochloride
格拉非宁盐酸盐,Glafenin hydrochloride |
ABC | Membrane transporter/Ion channel |
Glafenine Hydrochloride 是非甾体抗炎药, 可用于研究疼痛的缓解。 | |||
T16107 |
ML230
CID44640177,SID 88095709 |
CGRP Receptor | GPCR/G Protein; Neuroscience |
ML230 is a selective ATP-binding cassette (ABC) transporter ABCG2 inhibitor. It 36-fold selective for ABCG2 over ABCB1 (EC50s: 0.13 μM and 4.65 μM, respectively). | |||
T24552 |
NSC636795
NSC 636795,NSC-636795 |
||
NSC636795 is an ABCG2 transporter function inhibitor. | |||
T37685 |
CAY10719
CAY10719 |
||
CAY10719 is a selective inhibitor of the breast cancer resistance protein ABCG2 (IC50 = 0.23 μM) with little activity at ABCG1. It has been shown to reverse the ABCG2-mediated resistance toward SN 38 and to inhibit ATPase activity. | |||
T25884 |
NSC103054
NSC-103054,NSC 103054 |
||
NSC103054 is an ABCG2 transporter function inhibitor. | |||
T33753 |
NSC265473
NSC-265473,NSC-305458,NSC305458,NSC 265473,NSC 305458 |
||
NSC265473 is an ABCG2 substrate. | |||
T33749 |
NSC107392
NSC 107392,NSC-107392 |
||
NSC107392 is a substrate of ABCG2. | |||
T25798 |
Methyl Streptonigrin
NSC 45384,NSC45384,NSC-45384 |
||
Methyl Streptonigrin is an ABCG2 transporter function inhibitor. | |||
T72521 | Efflux inhibitor-1 | ||
Efflux inhibitor-1为一种吡唑啉[1,5-a]嘧啶类外排抑制剂,具有对ABCG2/BCRP和ABCB1的选择性靶向性,优先靶向ABCG2,其IC50值分别为0.45 μM与2.17 μM。 | |||
T73369 |
UR-MB108
|
||
UR-MB108 是一种有效的、选择性的ABCG2 (BCRP)抑制剂,IC50值为 79 nM。UR-MB108 在血浆中很稳定。 | |||
T80245 |
LL-37(17-32)
|
||
LL-37(17-32)为具有生物活性的肽段,为LL-37抗菌肽C末端结构域源自的活性片段。报道显示,LL-37(17-32)能逆转癌细胞系中ABCG2介导的多药耐药性。 | |||
T79711 |
Antitumor photosensitizer-4
|
Apoptosis | Apoptosis |
Antitumor photosensitizer-4 (compound 10b) 是靶向ABCG2酪氨酸激酶抑制剂(TKI)的有效代表,由达沙替尼与伊马替尼构成的光敏剂(PS)。该化合物能够诱发细胞凋亡(apoptosis)及ROS生成,在HepG2和B16-F10细胞上展现出显著的光毒性作用。 | |||
T62432 | KPH2f | ||
KPH2f 是一种安全、口服有效的 URAT1/GLUT9双抑制剂,对 URAT1和 GLUT9 的 IC50分别为 0.24 μM 和 9.37 μM。KPH2f 对 OAT1 和 ABCG2 几乎没有影响 (IC50分别为 32.14 和 26.74 μM)。 | |||
T36485 |
Becatecarin
|
||
Becatecarin is a water-soluble, diethylaminoethyl analog of the antineoplastic antibiotic rebeccamycin. It intercalates into DNA, stabilizing the DNA-topoisomerase complex. This results in the potent catalytic inhibition of both topoisomerases I and II, initiating DNA cleavage and apoptosis. Becatecarin, alone or in combination with other compounds, has anti-cancer as well as myelosuppressive effects in vivo. It is also a transport substrate of the ATP-binding cassette (ABC) transporter ABCG2. | |||
T36807 |
Estradiol 17-(β-D-Glucuronide) (sodium salt hydrate)
|
||
Estradiol 17-(β-D-glucuronide) (E217G) is an estrogen metabolite formed in the liver and subsequently excreted in bile.1It acts as a substrate of the multidrug resistance protein 2 (MRP2; Km= 75 μM), and through MRP2-mediated transport, functions as a cholestatic agent, decreasing bile flow.1,2In addition to binding to the MRP2 transport site, E217G has been shown to bind to an allosteric site that through positive cooperativity activates its own transportviaMRP2 and the transport of other MRP2 ... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN3150 |
6,8-Diprenylnaringenin
6,8-二异戊二烯基柚皮素,Senegalensin,Lonchocarpol A |
BCRP; ABC | Membrane transporter/Ion channel |
6,8-Diprenylnaringenin (Senegalensin) 是来自蛇麻草 Humulus lupulus 的天然产物。 6,8-Diprenylnaringenin 是一种乳腺癌耐药蛋白 (BCRP) 抑制剂,具有一定雌激素作用。 | |||
T20003 |
Acridone
|
Antibacterial; ABC | Membrane transporter/Ion channel; Microbiology/Virology |
Acridone 具有抗菌、抗疟、抗病毒和抗肿瘤活性。它可诱导细胞凋亡,抑制 ABCG2 蛋白,并调节激素水平。 | |||
T3S1775 |
Tectochrysin
NSC 80687,Techtochrysine,Techtochrysin,柚木柯因 |
NF-κB; STAT | JAK/STAT signaling; NF-κB; Stem Cells |
Tectochrysin (Techtochrysine) 是Alpinia oxyphylla 的主要黄酮类化合物之一,能够抑制NF-κB 活性。 | |||
TN7124 |
5-Hydroxy-2′,3,4′,7-tetramethoxyflavone
|
ABC | Membrane transporter/Ion channel |
5-Hydroxy-2',3,4',7-tetramethoxyflavone 显示出较弱的 ABCG2 抑制效力,在 Hoechst 33342 和脱镁叶绿素 A 测定中 IC50 分别为 3.27 和 3.89 µM。 | |||
T15355 |
Fumitremorgin C
烟曲霉毒素c,12α-Fumitremorgin C |
BCRP; Antibacterial; Antibiotic; ABC | Membrane transporter/Ion channel; Microbiology/Virology |
Fumitremorgin C (12α-Fumitremorgin C) 是ABCG2/BRCP 的选择性抑制剂。 |