35 Results for "

Inhibitor 12

" in MedChemExpress (MCE) Product Catalog:
Products (35)

35 Results for "Inhibitor 12" in MCE Product Catalog:

1
1 Cited Publications
Cat. No.: HY-18707
CAS No.: 1469337-95-8
Target:  

Ras Apoptosis

Research Areas:  

Cancer

K-Ras(G12C) inhibitor 12 is an irreversible inhibitor of K-Ras(G12C). K-Ras(G12C) inhibitor 12 can alter the nucleotide-binding preference of K-Ras and block its interaction with effector proteins. K-Ras(G12C) inhibitor 12 can reduce cell viability and induce apoptosis in lung cancer cell lines with G12C mutations. K-Ras(G12C) inhibitor 12 has anti-tumor activity .
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Cat. No.: HY-60298
CAS No.: 79762-54-2
6-Bromo-1H-indazole is an indazole derivative that serves as an intermediate for research related to organic synthesis. 6-Bromo-1H-indazole acts as a building block for the preparation of PI3Kδ inhibitors, and also functions as a synthetic intermediate for the preparation of colchicine site-targeted tubulin polymerization inhibitors[1][2].
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Cat. No.: HY-W844543
CAS No.: 721964-48-3
Target:  

Others

Research Areas:  

Neurological Disease

Protein Kinase Inhibitor 12 (compound 1-91) is a triazolopyridazine derivative and protein kinase inhibitor that can be utilized in research related to diseases associated with protein kinases .
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Cat. No.: HY-146533
CAS No.: 2230874-00-5
Target:  

Ras

Research Areas:  

Cancer

KRAS inhibitor-12 (compound 6-1) is a potent KRAS G12C inhibitor with an IC50 of 0.537 µM. KRAS inhibitor-12 shows p-ERK inhibition activities with IC50s of 1.3, 3.7 µM in MIA PaCA-2, A549 cells, respectively. KRAS inhibitor-12 has the potential for the research of pancreatic, colorectal, and lung cancers .
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Cat. No.: HY-143606
CAS No.: 2648552-54-7
Target:  

Ras

Research Areas:  

Cancer

KRAS G12D inhibitor 12 is a potent inhibitor of KRAS G12D. The Ras family of proteins is an important intracellular signaling molecule that plays an important role in growth and development. KRAS G12D inhibitor 12 has the potential for the research of KRAS G12D-mediated cancer (extracted from patent WO2021108683A1, compound 134) .
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Cat. No.: HY-N4024
CAS No.: 128397-09-1
Hyptadienic acid is a triterpene acid that can be isolated from the leaves of Perilla frutescens. Hyptadienic acid inhibits 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced inflammation in mice with an ID50 value of 0.13 mg/ear. Hyptadienic acid can be used for the research of inflammation .
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Cat. No.: HY-168592
CAS No.: 3044040-29-8
Target:  

DNA/RNA Synthesis

Research Areas:  

Cancer

WRN inhibitor 12 (compound 5) is an inhibitor of WRN helicase .
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Cat. No.: HY-151619
Target:  

Epoxide Hydrolase

Research Areas:  

Inflammation/Immunology

sEH inhibitor-12 (compound 34) is a sEH inhibitor with an IC50 value of 0.7 μM. sEH inhibitor-12 inhibits the 5-lipoxygenase-activating protein (FLAP)-mediated leukotriene (LT) biosynthesis with an IC50 value of 2.9 μM. sEH inhibitor-12 can be used for the research of inflammation .
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Cat. No.: HY-154958
CAS No.: 3033409-34-3
Target:  

mTOR

Research Areas:  

Neurological Disease

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 .
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Cat. No.: HY-153668
CAS No.: 2010124-06-6
Research Areas:  

Inflammation/Immunology

Bromodomain inhibitor-12 (example 303) is a bromodomain inhibitor that can be used in the research of autoimmune and inflammatory diseases .
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Cat. No.: HY-142468
Target:  

HIV

Research Areas:  

Infection

HIV-1 inhibitor-12 is potent HIV-1 inhibitor. HIV-1 inhibitor-12 inhibits HIV-1 capsid protein polymerization with an IC50 of 9 nM (WO2021104413A1, compound 1-1a) .
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Cat. No.: HY-P10837
Target:  

LAG-3

Research Areas:  

Inflammation/Immunology Cancer

LAG-3 cyclic peptide inhibitor 12 (Cyclic peptide 12) is an inhibitor of LAG-3 with an IC50 value of 4.45 μM and a Ki value of 2.66 µM .
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Cat. No.: HY-132128
CAS No.: 328956-24-7
Research Areas:  

Cancer

BRD4 Inhibitor-12 (Compound 9) is a BRD4 ligand, and can be used for research of cancer, infammation .
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Cat. No.: HY-153668A
CAS No.: 2010124-27-1
Research Areas:  

Inflammation/Immunology

Bromodomain inhibitor-12 edisylate (example 303) is a bromodomain inhibitor that can be used in the research of autoimmune and inflammatory diseases .
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Cat. No.: HY-149694
Target:  

Aurora Kinase

Research Areas:  

Cancer

Aurora kinase inhibitor-12 (Compound 1a ) is the inhibitor of aurora kinase which is a key enzyme that is implicated in tumor growth .
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Cat. No.: HY-152238
CAS No.: 2891692-83-2
Target:  

PI3K mTOR

Research Areas:  

Cancer

PI3K/mTOR Inhibitor-12 is a potent, orally active and selective PI3K/mTOR inhibitor with IC50 values of 0.06 nM and 3.12 nM for PI3Kα and mTOR, respectively. PI3K/mTOR Inhibitor-12 has antitumor activity. PI3K/mTOR Inhibitor-12 has lower liver toxicity .
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Cat. No.: HY-143250
CAS No.: 92575-00-3
Target:  

Microtubule/Tubulin

Research Areas:  

Cancer

Tubulin inhibitor 12 (Hit 9) is a novel tubulin inhibitor (IC50=25.3 μM). Tubulin inhibitor 12 shows anti-tumor activity and anti-proliferative activity .
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Cat. No.: HY-144743
CAS No.: 2771312-16-2
Research Areas:  

Others

ATX inhibitor 12 (compound 20) is an orally active and potent ATX (autotaxin) inhibitor, with an IC50 of 1.72 nM. ATX inhibitor 12 effectively alleviates lung structural damage with fewer fibrotic lesions at an oral dose of 60 mg/kg in C57Bl/6J mice. ATX inhibitor 12 can be uesd for idiopathic pulmonary fibrosis (IPF) research .
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Cat. No.: HY-168714
Research Areas:  

Cancer

Microtubule inhibitor 12 (Compound 2k) is an inhibitor for microtubule polymerization with an IC50 of 22.23 μM. Microtubule inhibitor 12 arrests the cell cycle of B16-F10 at G2/M phase, induces apoptosis in B16-F10, and inhibits cell migration. Microtubule inhibitor 12 inhibits the proliferation of cancer cells B16-f10, A549, HepG2 and MCF-7, with IC50s of 0.098, 0.135, 0.109, and 0.259 μM, respectively. Microtubule inhibitor 12 exhibits antitumor efficacy in mouse model .
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Cat. No.: HY-49071
CAS No.: 793729-44-9
Target:  

Bacterial

Research Areas:  

Infection

Tuberculosis inhibitor 12 (compound 12) is an oxadiazole derivative and an inhibitor of Mycobacterium tuberculosis. The inhibition rates of Tuberculosis inhibitor 12 (20 μM) on 7H9-Tw-OADC and 7H9-Tw-OADC reached 82% and 78% respectively .
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