Hydrocarbons
Apexbio Technology LLC ML162-YNE-10MG
ML162-yne (CAS No 2883115-46-4) is a compound predominantly used in biomedical research as a kinase inhibitor Originating in specialized laboratories focused on signal transduction pathways ML162-yne acts by targeting specific kinases involved in cellular signaling thereby modulating critical biochemical pathways Its in vitro activity is observed in the nanomolar to low micromolar range making it a potent agent for studies investigating kinase-mediated processes Researchers commonly utilize ML162-yne in both cellular and animal models to elucidate its effect on cell proliferation apoptosis and other vital cellular functions This compound is frequently used in drug screening assays to discover and optimize new therapeutic agents targeting kinase pathways Experimental concentrations of ML162-yne typically depend on the specific research design allowing flexibility in its application across various investigational contexts
Apexbio Technology LLC ML162-YNE-25MG
ML162-yne (CAS No 2883115-46-4) is a compound predominantly used in biomedical research as a kinase inhibitor Originating in specialized laboratories focused on signal transduction pathways ML162-yne acts by targeting specific kinases involved in cellular signaling thereby modulating critical biochemical pathways Its in vitro activity is observed in the nanomolar to low micromolar range making it a potent agent for studies investigating kinase-mediated processes Researchers commonly utilize ML162-yne in both cellular and animal models to elucidate its effect on cell proliferation apoptosis and other vital cellular functions This compound is frequently used in drug screening assays to discover and optimize new therapeutic agents targeting kinase pathways Experimental concentrations of ML162-yne typically depend on the specific research design allowing flexibility in its application across various investigational contexts
Medchemexpress LLC ML162-yne | 2883115-46-4 | C25H22Cl2N2O3S | 5 MG
ML162-yne is a potent GPX4-inhibitor affinity probe and a click chemistry reagent. It contains an Alkyne group, enabling it to undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
- Potent GPX4-inhibitor affinity probe
- Click chemistry reagent
- Contains an Alkyne group for CuAAc reactions
- High purity: 99.06%
- Molecular weight: 501.42
- Appearance: Solid, white to off-white
- Soluble in DMSO (100 mg/mL)
- Targets GPX4
Strem, An Ascensus Company CAS# 12289-94-0. 5G. Bis(2-methylallyl)(1,5-cyclooctadiene)ruthenium(II), min. 97%. MFCD00216965
CAS# 12289-94-0. 5G. Bis(2-methylallyl)(1,5-cyclooctadiene)ruthenium(II), min. 97%. MFCD00216965. Molecular Formula: (C4H7)2(C8H12)Ru. Molecular Weight: 319.45. Color/Form: tan to brown pwdr. Stability: store cold (-18°C). Strem# 44-0046. www.strem.com/catalog/v3/44-0046/
Medchemexpress LLC ML162-yne | 2883115-46-4 | C25H22Cl2N2O3S | 50 MG
ML162-yne is a potent GPX4-inhibitor affinity probe and a click chemistry reagent. It contains an alkyne group, enabling it to undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing azide groups.
- Potent GPX4 inhibitor
- Affinity probe
- Click chemistry reagent
- Contains alkyne group
- Enables copper-catalyzed azide-alkyne cycloaddition (CuAAc)
- Purity of 99.06% (LCMS)
- Appearance: white to off-white solid
- Used in cancer research
- Targeted therapy for cancer
- Relevant to cancer metabolism and metastasis studies
- Involved in apoptosis research
- Acts as a metabolic enzyme/protease inhibitor
- Inhibits glutathione peroxidase
Aobchem Phenylmethyl 3-cyclopentene-1-carboxylate | 95% | CAS 130762-09-3 | C13H14O2 | 1g
Phenylmethyl 3-cyclopentene-1-carboxylate | 95% | CAS 130762-09-3 | C13H14O2 | 1g
Aobchem Phenylmethyl 3-cyclopentene-1-carboxylate | 95% | CAS 130762-09-3 | C13H14O2 | 250mg
Phenylmethyl 3-cyclopentene-1-carboxylate | 95% | CAS 130762-09-3 | C13H14O2 | 250mg
Medchemexpress LLC VE-821 | 1232410-49-9 | 99.7% | 368.41 | 10 MM 1 ML
VE-821 is a potent ATP-competitive inhibitor of ATR with a Ki/IC50 of 13 nM/26 nM. It exhibits excellent selectivity for ATR with minimal cross-reactivity against related PIKKs. This compound significantly enhances the sensitivity of pancreatic cancer cells to radiation and Gemcitabine, making it suitable for studies on DNA damage response and cancer therapy.
- Potent ATP-competitive inhibitor of ATR.
- Exhibits excellent selectivity for ATR.
- Enhances sensitivity of pancreatic cancer cells to radiation and Gemcitabine.
- Inhibits radiation-induced G2/M arrest in cancer cells.
- Soluble in DMSO (50 mg/mL).
Aobchem Phenylmethyl 3-cyclopentene-1-carboxylate | 95% | CAS 130762-09-3 | C13H14O2 | 10g
Phenylmethyl 3-cyclopentene-1-carboxylate | 95% | CAS 130762-09-3 | C13H14O2 | 10g
Aobchem Phenylmethyl 3-cyclopentene-1-carboxylate | 95% | CAS 130762-09-3 | C13H14O2 | 25g
Phenylmethyl 3-cyclopentene-1-carboxylate | 95% | CAS 130762-09-3 | C13H14O2 | 25g
eMolecules 16004-75-4 | Ambeed | 1357-Tetraphenyladamantane | 5g | 591800469 | A321985 | 440.63 | C34H32
Medchem Express | XPC-6444 | 5mg | 654490215 | HY-128772 | 2230144-21-3 | 498.580 | C22H25F3N4O2S2
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