20 Results for "

HeLa-S3 cells

" in MedChemExpress (MCE) Product Catalog:
Products (20)

20 Results for "HeLa-S3 cells" in MCE Product Catalog:

3
3 Cited Publications
Cat. No.: HY-13057
CAS No.: 382607-78-5
Purity:  ≥95.0%
Synonyms: Glucose-conjugated MGMT inhibitor
Target:  

DNA Methyltransferase

Research Areas:  

Cancer

O6BTG-octylglucoside is a potent O 6-methylguanine-DNAmethyl-transferase (MGMT) inhibitor, with IC50s of 32 nM in vitro (cell extracts) and 10 nM in HeLa S3 cells.
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Cat. No.: HY-101775A
CAS No.: 52238-35-4
Purity:  ≥99.0%
Target:  

Topoisomerase

9-Hydroxyellipticine hydrochloride is a inhibitor of Topo II and RyR. 9-Hydroxyellipticine hydrochloride exhibits antitumor, antioxidant and catecholamine-releasing activities. 9-Hydroxyellipticine hydrochloride exhibits IC50 values of 1.6 μM and 1.2μM in Hela S-3 and 293T cells, respectively .
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Cat. No.: HY-N9172
CAS No.: 476630-49-6
Eupaglehnin C is a germacrane-type sesquiterpenoi. Eupaglehnin C can be isolated from the MeOH extract of Eupatorium glehni (Compositae). Eupaglehnin C has cytotoxic activity against HeLa-S3 cancer cell lines .
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Cat. No.: HY-N10542
CAS No.: 151923-86-3
Aplyronine C is an active compound. Aplyronine C shows potent antitumor activity and has cytotoxicity against HeLa-S3 cells with an IC50 values of 22 nM. Aplyronine C can be used for the research of cancer .
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Cat. No.: HY-N10541
CAS No.: 151923-85-2
Aplyronine B is an active compound. Aplyronine B shows potent antitumor activity and has cytotoxicity against HeLa-S3 cells with an IC50 values of 2.9 nM. Aplyronine B can be used for the research of cancer .
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Cat. No.: HY-N14947
CAS No.: 190143-30-7
Pterulinic acid is a coenzyme I: Coenzyme Q oxidoreductase inhibitor. he IC50 (μg/mL) L1210 and HL60 of Pterulinic acid to mammalian cell lines are 50 and 20 respectively. HeLaS3 25; BHK is 100 .
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Cat. No.: HY-N13976
CAS No.: 189871-55-4
Target:  

Others

Belactosin C is found in the strain of Streptomyces sp. that inhibits HeLa S3 cells with the IC50 of 200 μM .
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Cat. No.: HY-N15297
CAS No.: 10092-04-3
Isotenulin inhibits the efflux function of P-glycoprotein by stimulation of P-glycoprotein ATPase, thereby overcoming the multidrug resistance (MDR) of cancer cells. Isotenulin exhibits cytotoxicity in multidrug-resistant cancer cell KB-vin and sensitive cancer cell HeLaS3. Isotenulin exhibits synergistic effect with Paclitaxel (HY-B0015), Vinblastine (HY-13780) and Doxorubicin (HY-15142) .
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Cat. No.: HY-N5186
CAS No.: 154277-21-1
Cypemycin is a linaridin antibiotic that can inhibit cancer cell activity, inhibits P388 leukemia cells with IC50 of 1.3 μg/mL. Cypemycin can inhibit human tumor cells such as HeLa S3, HHCC-1, HCCS-M and Slex with IC50 of >25 μg/mL .
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Cat. No.: HY-N8512
CAS No.: 129277-10-7
Asperfuran is an antifungal dihydrobenzofuran derivative produced by a strain of Aspergillus oryzae. Asperfuran weakly inhibits chitin synthase from Coprinus cinereus. Asperfuran shows weak cytotoxicity In HeLa S3 and L1210 cells with an IC50 of 25 μg/ml .
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Cat. No.: HY-13786
CAS No.: 793035-88-8
Target:  

DNA Methyltransferase

Research Areas:  

Cancer

O6BTG-C8-αGlu is an O6-methylguanine-DNA methyltransferase (MGMT) inhibitor with an IC50 of 0.45 μM. At a concentration of 0.1 μM, O6BTG-C8-αGlu can completely inhibit MGMT in HeLaS3 cells. Even when applied chronically at high doses (up to 20 μM), it does not exhibit cytotoxicity. O6BTG-C8-αGlu is suitable for research on MGMT-related cancer diseases .
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Cat. No.: HY-101775
CAS No.: 51131-85-2
Target:  

Topoisomerase

Research Areas:  

Cardiovascular Disease Cancer

9-hydroxyellipticine is an inhibitor of Topo II and RyR, exhibiting high affinity for DNA with a Pka value of 9.8 at pH 7.4. It has antitumor, antioxidant, and catecholamine-releasing activities, with IC50 values of 1.6 μM and 1.2 μM for Hela S-3 and 293T cells, respectively. It also demonstrates anticancer effects in L1210 leukemia mice .
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Cat. No.: HY-P10596
CAS No.: 1242413-05-3
Target:  

Bacterial Fungal

Research Areas:  

Infection Cancer

Lasioglossin-III is an antimicrobial peptide that can be isolated from the venom of wild bees. Lasioglossin-III has high antibacterial activity against Gram-positive and Gram-negative bacteria, antifungal activity and antitumor activity. Lasioglossin-III has certain cytotoxicity against three cancer cell lines (HeLa S3, CRC SW 480 and CCRF-CEM T) with IC50 values ​​of 4, 18 and 5 μM, respectively .
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Cat. No.: HY-101775AR
CAS No.: 52238-35-4
9-Hydroxyellipticine (hydrochloride) (Standard) is the analytical standard of 9-Hydroxyellipticine (hydrochloride). This product is intended for research and analytical applications. 9-Hydroxyellipticine hydrochloride is a inhibitor of Topo II and RyR. 9-Hydroxyellipticine hydrochloride exhibits antitumor, antioxidant and catecholamine-releasing activities. 9-Hydroxyellipticine hydrochloride exhibits IC50 values of 1.6 μM and 1.2μM in Hela S-3 and 293T cells, respectively .
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Cat. No.: HY-N13975
CAS No.: 189871-53-2
Target:  

Others

Belactosin A is found in the strain of Streptomyces sp. that inhibits HeLa S3 cells with the IC50 of 51 μM .
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Cat. No.: HY-N14438
CAS No.: 125108-66-9
Furaquinocin A can kill HeLa S3 and B16 melanoma cells, but has no antibacterial activity .
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Cat. No.: HY-N14439
CAS No.: 125224-54-6
Furaquinocin B can kill HeLa S3 and B16 melanoma cells, but has no antibacterial activity .
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Cat. No.: HY-N14440
CAS No.: 134984-98-8
Furaquinocin CA can kill HeLa S3 and B16 melanoma cells, but has no antibacterial activity .
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Cat. No.: HY-181804
Target:  

BCRP P-glycoprotein

Research Areas:  

Cancer

MRS8288 is a ABCG2 and P-glycoprotein inhibitor, with an IC50 of 0.96 μM against ABCG2 and an IC50 of 1.39 μM against P-glycoprotein. MRS8288 inhibits the ATPase activity of ABCG2 and P-glycoprotein, and suppresses ABCG2-mediated substrate transport. MRS8288 is applicable for cancer research .
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Cat. No.: HY-181802
Target:  

BCRP

Research Areas:  

Cancer

MRS8431 is an ABCG2 inhibitor with a IC50 of 160 nM against human ABCG2. MRS8432 partially inhibits ABCG2-mediated substrate transport. MRS8432 is applicable to research related to cancer multidrug resistance .
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