1. Signaling Pathways
  2. Membrane Transporter/Ion Channel
  3. BCRP

BCRP (乳腺癌耐药蛋白)

Breast cancer resistance protein; ABCG2

Breast cancer resistance protein (BCRP/ABCG2/MXR/ABCP) is an ATP-dependent efflux transporter, which belongs to the large ATP-binding cassette (ABC) transporter family present on cell membranes, and it is classified into the G subfamily of these transporters. BCRP is expressed in a variety of normal cells and acts as a xenobiotic efflux transporter. BCRP is often associated with cancer chemotherapeutic resistance. BCRP confers multidrug resistance (MDR) to a series of antitumor agents such as Mitoxantrone, Daunorubicin, SN-38, and Topotecan, and often limits the efficacy of chemotherapy.

BCRP physiologically functions as a part of a self-defense mechanism for the organism. It enhances elimination of toxic xenobiotic substances and harmful agents in the gut and biliary tract, as well as through the blood-brain, placental, and possibly blood-testis barriers. BCRP recognizes and transports numerous anticancer drugs including conventional chemotherapeutic and targeted small therapeutic molecules relatively new in clinical use. Thus, BCRP expression in cancer cells directly causes MDR by active efflux of anticancer drugs. Because BCRP is also known to be a stem cell marker, its expression in cancer cells could be a manifestation of metabolic and signaling pathways that confer multiple mechanisms of drug resistance, self-renewal (stemness), and invasiveness (aggressiveness), and thereby impart a poor prognosis. Therefore, blocking BCRP-mediated active efflux may provide a therapeutic benefit for cancers.

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-132934
    Ac32Az19 Inhibitor 99.50%
    Ac32Az19 是一种有效、无毒、高选择性的BCRP抑制剂,在BCRP过度表达的HEK293/R2细胞中,EC50值为13 nM。
    Ac32Az19
  • HY-128685
    FD 12-9 Inhibitor
    FD 12-9 是一种类黄酮二聚体,为 P-gpBCRP 的双重抑制剂,EC50 值分别为 285 nM 和 0.9 nM。具有抗胶质细胞瘤活性。
    FD 12-9
  • HY-136450
    Triclabendazole sulfoxide

    三氯苯达唑亚砜

    Inhibitor 98.78%
    Triclabendazole sulfoxide (TCBZ-SO) 是 Triclabendazole 的主要血浆代谢产物,具有抗寄生虫作用。Triclabendazole sulfoxide 可以抑制膜转运蛋白 ABCG2/BCRP 的活性。
    Triclabendazole sulfoxide
  • HY-136450S
    Triclabendazole sulfoxide-d3

    三氯苯达唑亚砜-d3

    Inhibitor
    Triclabendazole sulfoxide-d3 是 Triclabendazole sulfoxide 的氘代物。Triclabendazole sulfoxide (TCBZ-SO) 是 Triclabendazole 的主要血浆代谢产物,具有抗寄生虫作用。Triclabendazole sulfoxide 可以抑制膜转运蛋白 ABCG2/BCRP 的活性。
    Triclabendazole sulfoxide-d<sub>3</sub>
  • HY-146676
    UR-MB108 Inhibitor
    UR-MB108 (Compound 57) 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。
    UR-MB108
  • HY-155652
    ABCG2-IN-1 Inhibitor
    ABCG2-IN-1(化合物 K2)是一种 Ko143 类似物,是一种具有口服活性的 ABCG2 抑制剂,IC50 为 0.13 μM。ABCG2-IN-1 在小鼠体内具有良好的口服药代动力学特征。
    ABCG2-IN-1
  • HY-144393
    P-gp/BCRP-IN-1 Inhibitor
    P-gp/BCRP-IN-1 (compound 19) 是一种潜在的、相对安全的、口服有效的外排转运蛋白(P-gpBCRP) 抑制剂。P-gp/BCRP-IN-1 通过抑制 P-gpBCRP 的外排功能产生耐药性逆转,P-gp/BCRP-IN-1可克服紫杉醇的耐药性,提高紫杉醇的口服生物利用度。
    P-gp/BCRP-IN-1
  • HY-129301
    CCTA-1523 Inhibitor
    CCTA-1523 是一种有效的、选择性的、可逆的和具有口服活性的 ABCG2 抑制剂。CCTA-1523 显示细胞毒性。CCTA-1523 显示出抗癌活性。
    CCTA-1523
  • HY-156092
    Antitumor photosensitizer-4 Inhibitor
    Antitumor photosensitizer-4 (compound 10b) 是一种有效的靶向 ABCG2 的酪氨酸激酶抑制剂 (TKI)。Antitumor photosensitizer-4 是一种光敏剂 (PS),由达沙替尼 (HY-10181) 和伊马替尼 (HY-15463) 的偶联物组成。Antitumor photosensitizer-4 诱导细胞凋亡 (apoptosis) 和 ROS 产生,对 HepG2 和 B16-F10 细胞表现出强光毒性。
    Antitumor photosensitizer-4
  • HY-155653
    ABCG2-IN-2 Inhibitor
    ABCG2-IN-2 是一种有效的 ABCG2 抑制剂,在小鼠体内具有良好的口服药代动力学特征。ABCG2-IN-2 可用于肿瘤多药耐药(MDR)和红细胞生成性原卟啉症(EPP)的研究。
    ABCG2-IN-2
  • HY-136450S1
    Triclabendazole sulfoxide-13C,d3

    三氯苯达唑亚砜-13C,d3

    Inhibitor
    Triclabendazole sulfoxide-13C,d3 是一种 13C- 和氘代标记的 Triclabendazole sulfoxide。Triclabendazole sulfoxide (TCBZ-SO) 是 Triclabendazole 的主要血浆代谢产物,具有抗寄生虫作用。Triclabendazole sulfoxide 可以抑制膜转运蛋白 ABCG2/BCRP 的活性。
    Triclabendazole sulfoxide-<sup>13</sup>C,d<sub>3</sub>
  • HY-155152
    P-gp/BCRP-IN-2 Inhibitor
    P-gp/BCRP-IN-2 (compound 15) 是恶二唑衍生物,是 ABC 转运蛋白 P-glycoprotein (IC50: 1.6 nM) 和 BCRP (IC50: 600 nM) 的双抑制剂。P-gp/BCRP-IN-2 还能够增强 Doxorubicin (HY-15142A) 在耐药人腺癌结肠癌细胞系 HT29/DX 和 MDCK-MDR1 细胞中的抗增殖作用。
    P-gp/BCRP-IN-2
  • HY-122416
    6,8-Diprenylnaringenin

    6,8-二异戊二烯基柚皮素

    Inhibitor
    6,8-Diprenylnaringenin (Lonchocarpol A; Senegalensin) 是一种啤酒花异戊二烯黄酮类化合物,是乳腺癌抗性蛋白 (ABCG2) 的抑制剂。具有一定的雌激素作用,但其效力不到 8-Prenylnaringenin 的 1%。在 HEK293 细胞中抑制 ABCG2 介导的 Mitoxantrone 流出和 3H-Methotrexate 转运 (IC50=0.41 μM)。Prenylnaringenin 具有一定的雌激素作用,但其效力不到 8-Prenylnaringenin 的 1%。
    6,8-Diprenylnaringenin
  • HY-N2651
    5,7,3'-Trihydroxy-4'-Methoxy-8-prenylflavanone Inhibitor
    5,7,3'-Trihydroxy-4'-Methoxy-8-prenylflavanone (compound 1) 是一种类黄酮,是一种有效的 ABCG2 抑制剂,IC50 为 6.6 μM。
    5,7,3'-Trihydroxy-4'-Methoxy-8-prenylflavanone
  • HY-149469
    3,7,2',4'-Tetramethoxy-5-hydroxyflavone Inhibitor
    BCRP/ABCG2-IN-1 是乳腺癌耐药蛋白 (BCRP/ABCG2) 的抑制剂,IC50 为 5.98 μM,可用于乳腺癌的多药耐药研究。
    3,7,2',4'-Tetramethoxy-5-hydroxyflavone
目录号 产品名 / 同用名 应用 反应物种