Chk1 and MK2 Inhibitors set |
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A9908-1 |
ApexBio |
1 set |
EUR 294.4 |
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Description: Cell Cycle/Checkpoint|Chk |
Human IgG antibody Laboratories manufactures the medchemexpress inhibitors reagents distributed by Genprice. The Medchemexpress Inhibitors reagent is RUO (Research Use Only) to test human serum or cell culture lab samples. To purchase these products, for the MSDS, Data Sheet, protocol, storage conditions/temperature or for the concentration, please contact MedChemExpress Inc.. Other Medchemexpress products are available in stock. Specificity: Medchemexpress Category: Inhibitors
Human True Insulin ELISA Kit |
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MyBiosource |
5x96-Strip-Wells |
EUR 3420 |
Human True Insulin ELISA Kit |
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MyBiosource |
96-Strip-Wells |
EUR 765 |
Human True Insulin GENLISA ELISA |
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Krishgen |
1 x 96 wells |
EUR 286 |
Human True insulin ELISA kit |
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BlueGene |
96T |
EUR 700 |
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Description: ELISA |
Human True insulin ELISA kit |
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BlueGene |
192 tests |
EUR 1524 |
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Description: A competitive ELISA for quantitative measurement of Human True insulin in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species. |
Human True insulin ELISA kit |
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BlueGene |
1 plate of 48 wells |
EUR 624 |
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Description: A competitive ELISA for quantitative measurement of Human True insulin in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species. |
Human True insulin ELISA kit |
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BlueGene |
48 wells plate |
EUR 280 |
Chemicals information
KRAS inhibitor-21 |
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HY-151288 |
MedChemExpress |
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Description: KRAS inhibitor-21 (22b) is a KRAS G12C inhibitor with an IC50 value of <0.01 μM. KRAS inhibitor-21 can be used in cancer research[1]. |
HIV-1 inhibitor-49 |
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HY-151933 |
MedChemExpress |
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Description: HIV-1 inhibitor-49 is an orally active HIV-1 inhibitor, is a HEPT analog. HIV-1 inhibitor-49 possesses great pharmacokinetics profiles and potent non-nucleoside reverse transcriptase inhibitory activity (IC50=30 nM). HIV-1 inhibitor-49 exerts potential safety without acute toxicity in mouse model[1]. |
BRD4 Inhibitor-25 |
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HY-151972 |
MedChemExpress |
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Description: BRD4 Inhibitor-25 is a BRD4 inhibitor with IC50s of 0.82 μM, 1.94 μM for BD1 and BD2 domains of BRD4. BRD4 Inhibitor-25 induces apoptotic and autophagy cell death in ovarian cancer cells. BRD4 Inhibitor-25 can be used in the research of cancers, cardiovascular, neuromuscular and inflammatory disorders. |
HIV-1 inhibitor-52 |
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HY-152157 |
MedChemExpress |
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Description: HIV-1 inhibitor-52 is a potent broad-spectrum HIV-1 activity inhibitor with EC50s of 1.6 nM-6.4 nM for WT HIV-1, HIV-1 V370A, HIV-1 ΔV370, HIV-1 V362I/V370A, HIV-1 T332S/V362I/prR41G, HIV-1 A326T/V362I/V370A, HIV-1 R361K/V362I/L363M[1]. |
HIV-1 inhibitor-50 |
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HY-152160 |
MedChemExpress |
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Description: HIV-1 invistor-50 is a non-nucleoside reverse transcriptase inhibitor (NNRTI) that targets HIV-1 reverse transcriptase (RT) (IC50=50 nM). HIV-1 inhibitor-50 shows significant antiviral activity, with EC50s of 2.22-53.3nM against HIV-1 IIIB and its mutant strains[1]. |
HIV-1 inhibitor-51 |
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HY-152161 |
MedChemExpress |
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Description: HIV-1 inhibitor-51, a non-nucleoside reverse transcriptase inhibitor (NNRTI), exhibits outstanding antiviral activity against WT HIV-1 (IIIB) and a panel of mutant strains. HIV-1 inhibitor-51 has high binding affinity (KD=2.50 μM) and inhibitory activity (IC50=0.03 μM) to WT HIV-1 RT. HIV-1 inhibitor-51 has EC50s of 2.22-53.3 nM for mutant strains (L100I, K103N, Y181C, Y188L, E138K, F227L + V106A, RES056)[1]. |
HIV-1 inhibitor-53 |
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HY-152200 |
MedChemExpress |
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Description: HIV-1 inhibitor-53 is a dual HIV-1 protease and reverse transcriptase inhibitor. HIV-1 inhibitor-53 inhibits HIV-1 protease (PR) and reverse transcriptase (RT) activity with IC50 values of 1.93 nM and 2.35 μM, respectively. HIV-1 inhibitor-53 can be used for the research of acquired immune deficiency syndrome (AIDS)[1]. |
BRD4 Inhibitor-26 |
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HY-152209 |
MedChemExpress |
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Description: BRD4 Inhibitor-26 is a bromodomain protein 4 (BRD4) inhibitor/nitric oxide-donator. BRD4 Inhibitor-26 inhibits BRD4 (BD1) and BRD4 (BD2) with IC50 values of 0.82 μM and 1.94 μM, respectively. BRD4 Inhibitor-26 can be used for the research of ovarian cancer[1]. |
iNOS inhibitor-10 |
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HY-152536 |
MedChemExpress |
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Description: iNOS inhibitor-10 is an iNOS inhibitor (IC50: 65 nM). iNOS inhibitor-10 has antiproliferative effect against triple negative breast cancer cells[1]. |
HIV-1 inhibitor-54 |
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HY-152539 |
MedChemExpress |
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Description: HIV-1 inhibitor-54 is a potent HIV-1 inhibitor. HIV-1 inhibitor-54 has anti-HIV activity in MT-4 cells against WT HIV-1 (strain IIIB) with an EC50 value of 0.032 μM. HIV-1 inhibitor-54 can be used for the research of virus infection[1]. |
HIV-1 inhibitor-55 |
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HY-152560 |
MedChemExpress |
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Description: HIV-1 inhibitor-55 (compound 4d) inhibits WT HIV-1 with an EC50 value of 8.6 nM. HIV-1 inhibitor-55 also shows inhibitory potency against single and double HIV-1 mutants. HIV-1 inhibitor-55 can be used for the research of virus infection[1]. |
KRAS inhibitor-22 |
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HY-153412 |
MedChemExpress |
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Description: KRAS inhibitor-22 (compound FB9/6B9) is a potent inhibitor of K-Ras. KRAS inhibitor-22 targets to Kras 4B(G12D) and (G12C), which can be used for cancer research[1]. |
HIV-1 inhibitor-60 |
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HY-108255 |
MedChemExpress |
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Description: HIV-1 inhibitor-60 (compound 45) is an HIV inhibitor with the potential for the research of infection diseases[1]. |
HIV-1 inhibitor-61 |
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HY-10891 |
MedChemExpress |
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Description: HIV-1 inhibitor-61 (2c) is a HIV-1 reverse transcriptase inhibitor, with an EC50 of 0.07 nM in NL4-3 wt MT-4 cells[1]. |
mTOR inhibitor-11 |
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HY-154957 |
MedChemExpress |
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Description: mTOR inhibitor-11 (Compound 9) is a brain-penetrant mTOR inhibitor (IC50: 21 nM for pS6). mTOR inhibitor-11 also inhibits pCHK1 and PDE4D with IC50s of 17.2 and 17.0 μM. mTOR inhibitor-11 can be used for research of CNS disease[1]. |
mTOR inhibitor-12 |
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HY-154958 |
MedChemExpress |
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Description: mTOR inhibitor-12 (Compound 11) is a selective brain penetrant mTOR inhibitor without genotoxicity risk. mTOR inhibitor-12 can be used for the research of CNS diseases[1]. |
BRD4 Inhibitor-27 |
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HY-155078 |
MedChemExpress |
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Description: BRD4 Inhibitor-27 (compound 6) is a BRD4 inhibitor with IC50 of 9.6 and 11.3 μM for BRD4 BD1 and BRD4 BD2, respectively. BRD4 Inhibitor-27 has the potential to study cancer[1]. |