89 Results for "

ABCG2

" in MedChemExpress (MCE) Product Catalog:
Products (89)

89 Results for "ABCG2" in MCE Product Catalog:

  • Targets Recommended:
Cat. No.: HY-146676
CAS No.: 2412461-98-2
Target:  

BCRP

Research Areas:  

Cancer

UR-MB108 is a selective ABCG2 inhibitor with an IC50 value of 79 nM. UR-MB108 acts as a potent inhibitor of ABCG2 transport and ATPase activity. UR-MB108 can be used in cancer-related research .
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Cat. No.: HY-113805
CAS No.: 1031367-64-2
Purity:  99.50%
Target:  

P-glycoprotein

Research Areas:  

Cancer

MC70 is a potent and non-selective P-glycoprotein (P-gp) inhibitor with an EC50 of 0.69 µM. MC70 is an ABC transporters inhibitor and anticancer agent. MC70 interacts with ABCB1, ABCG2 and ABCC1 [2].
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Cat. No.: HY-N3806
CAS No.: 917-13-5
Enniatin B is a Fusarium mycotoxin that acts as an ionophore to form cation-selective membrane channels, disrupt ion homeostasis and mitochondrial function, inhibit cell proliferation, and induce apoptosis, while modulating ERK, p38 MAPK, and STAT3 signaling pathways. Enniatin B is used in research on atherosclerosis, hypercholesterolemia, cervical cancer, and colon adenocarcinoma [2] .
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Cat. No.: HY-111678
CAS No.: 1776055-05-0
Purity:  99.65%
Synonyms: CID44640177; SID 88095709
Target:  

BCRP

Research Areas:  

Cancer

ML230 (CID44640177; SID 88095709) is a selective inhibitor of ATP-binding cassette (ABC) transporter ABCG2, and 36-fold selective for ABCG2 over ABCB1 with EC50s values of 0.13 μM and 4.65 μM, respectively .
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Cat. No.: HY-178226
CAS No.: 3003834-34-9
PBX-7016 is a DNA topoisomerase I inhibitor and DDX5 degrader. PBX-7016 induces DNA damage and downregulates Survivin, Mcl-1, and XIAP. PBX-7016 exerts a bystander killing effect. PBX-7016 can serve as an ADC payload for the synthesis of ADC. PBX-7016 is applicable to research related to head and neck cancer, non-small cell lung cancer, breast cancer, colorectal cancer, and ovarian cancer [2].
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Cat. No.: HY-RS00077
Research Areas:  

Others

ABCG2 Human Pre-designed siRNA Set A contains three designed siRNAs for ABCG2 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS00078
Research Areas:  

Others

Abcg2 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Abcg2 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS00079
Research Areas:  

Others

Abcg2 Rat Pre-designed siRNA Set A contains three designed siRNAs for Abcg2 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-174435
Target:  

P-glycoprotein

Research Areas:  

Cancer

ABCB1/ABCG2-IN-1 (Compound (S,Z)-4b) is an inhibitor of ABCB1 and ABCB2 transporters. ABCB1/ABCG2-IN-1 shows moderate activity in SW620M, -V, and –Mito variants (IC50 ≈ 50 μM). ABCB1/ABCG2-IN-1 affects methotrexate resistance in vitro. ABCB1/ABCG2-IN-1 can be studied in anticancer research .
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Cat. No.: HY-112505
CAS No.: 1776055-29-8
Purity:  ≥98.0%
Target:  

BCRP

Research Areas:  

Cancer

Efflux inhibitor-1 is a pyrazolo[1,5-a]pyrimidine-based efflux inhibitor that inhibits the efflux activity of ABCG2 (IC50 = 0.45 µM) and ABCB1 (IC50 = 2.17 µM). Efflux inhibitor-1 can be used in research related to drug-resistant ovarian cancer and leukemia .
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Cat. No.: HY-W049875
CAS No.: 1689-89-0
Nitroxynil is a broad-spectrum veterinary anthelmintic and a substrate of ABCG2. Nitroxynil inhibits ATP production by uncoupling the oxidative phosphorylation process of mitochondria, thereby disrupting the parasite body covering, impairing its motility, and ultimately inducing parasite death. Nitroxynil induces chromosomal aberrations, sister chromatid exchanges and abnormal sperm morphology, and interferes with spermatogenesis. Nitroxynil is widely applicable to studies on fascioliasis, myiasis, Haemonchus spp. infections, and Oestrus ovis infections [2] .
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Cat. No.: HY-168573
Target:  

BCRP

Research Areas:  

Cancer

AZ99 (compound 7) is a potent ABCG2 inhibitor. AZ99 inhibits ABCG2-mediated transport of estrone-3-sulfate (E1S) into proteoliposomes and ABCG2 ATPase activity .
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Cat. No.: HY-178386
CAS No.: 190323-50-3
Target:  

BCRP

Research Areas:  

Cancer

ABCG2-IN-5 (Compound 10) is a is a selective ABCG2 inhibitor, with an IC50 of 0.34 µM. ABCG2-IN-5 can be used for the study of ABCG2-overexpressing tumors such as non-small cell lung cancer (NSCLC) .
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Cat. No.: HY-155652
CAS No.: 2559759-40-7
Target:  

BCRP

Research Areas:  

Cancer

ABCG2-IN-1 (compound K2), a Ko143 analog, is an orally active ABCG2 inhibitor with an IC50 of 0.13 μM. ABCG2-IN-1 has favorable oral pharmacokinetic profiles in mice .
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Cat. No.: HY-17648
CAS No.: 1353747-12-2
Target:  

BCRP

Research Areas:  

Cancer

MBL-II-141 is potent ABCG2 inhibitor with an IC50 of 0.11 μM. MBL-II-141 inhibits the transport function of ABCG2 in a non-competitive manner, preventing ABCG2 from pumping substrates (such as Irinotecan (HY-16562)) out of the cells, thereby increasing the accumulation of drugs within the cells. MBL-II-141 has no effect on ABCB1 (P-gp) and ABCC1 (MRP1) and has extremely low cytotoxicity (IG50 > 100 μM). MBL-II-141 can be used for the study of multidrug resistance (MDR) cancers [2].
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Cat. No.: HY-178100
Target:  

PARP BCRP

Research Areas:  

Cancer

PARP1-IN-45 (Compound 15) is a PARP1 inhibitor with an IC50 of 17  nM. PARP1-IN-45 effectively stimulates ATPase activity of ABCG2. PARP1-IN-45 can be used for cancers like ovarian cancer research .
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Cat. No.: HY-119724
CAS No.: 1942919-63-2
Target:  

BCRP

Research Areas:  

Cancer

ABCG2-IN-3 (Compound 52) is a selective inhibitor for breast cancer resistance protein (ABCG2), with an IC50 of 0.238 µM. ABCG2-IN-3 reverses the ABCG2-mediated resistance toward SN-38 and inhibit the ATPase activity .
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Cat. No.: HY-155653
CAS No.: 2559759-59-8
Target:  

BCRP

Research Areas:  

Cancer

ABCG2-IN-2 is a potent ABCG2 inhibitor with favorable oral pharmacokinetic profiles in mice. ABCG2-IN-2 can be used for the research of tumor multidrug resistance (MDR) and erythropoietic protoporphyria (EPP) .
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Cat. No.: HY-170396
CAS No.: 2559759-63-4
Target:  

BCRP

Research Areas:  

Inflammation/Immunology

ABCG2-IN-4 (Compound K31) is an orally active inhibitor for ABCG2, which reduces the release of Protoporphyrin IX (PPIX) (HY-B1247) from erythrocytes into plasma, and prevents the reduces phototoxicity. ABCG2-IN-4 exhibits anti-inflammatory and antioxidant activity in mouse models .
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