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Filtered Search Results

MEDCHEMEXPRESS LLC ARACHIDONIC ACID-10MM-1ML DMSO
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NC3310516 ARACHIDONIC ACID-10MM-1ML DMSO

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MEDCHEMEXPRESS LLC SAPANISERTIB IN DMSO
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NC3441661 SAPANISERTIB IN DMSO

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MEDCHEMEXPRESS LLC LY2090314 1ML IN DMSO
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NC3385760 LY2090314 1ML IN DMSO

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Medchemexpress LLC Cbl-b-IN-5 10mM x 1ml DMSO
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Cbl-b-IN-5 10mM x 1ml DMSO

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MEDCHEMEXPRESS LLC AFATINIB 10MM/1ML IN DMSO
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NC2892010 AFATINIB 10MM/1ML IN DMSO

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SELLECK CHEMICAL LLC FER-1 FERROSTATIN-1 10MM DMSO
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NC3071708 FER-1 FERROSTATIN-1 10MM DMSO

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Medchemexpress LLC IDASANUTLIN MM 1 ML IN DMSO
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Idasanutlin mM * 1 mL in DMSO ready for reconstitution

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ACCUSTANDARD INC AROMATICS QUANTIT CALI 5X10ML
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NC3037970 AROMATICS QUANTIT CALI 5X10ML

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MEDCHEMEXPRESS LLC MIPS521 10MM/1ML IN DMSO
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NC2880424 MIPS521 10MM/1ML IN DMSO

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Hampton Research 30% V/V DIMETHYL SULFOX 1ML
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HR2-428-28/Additive Screen 28 (C04), 1.0 ml - 30% v/v Dimethyl sulfoxide. Please note items from this supplier are non-returnable.

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Apexbio Technology LLC HTH-01-015 10MM IN 1ML DMSO
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HTH-01-015 (CAS 1613724-42-7) is a highly selective inhibitor targeting the NUAK1 kinase exhibiting potent inhibitory activity with an IC50 of approximately 100 nM It specifically blocks NUAK1-mediated phosphorylation of MYPT1 at Ser445 with negligible off-target effects among a comprehensive panel of 139 other kinases Cellular studies demonstrate that treatment with HTH-01-015 reduces migration of mouse embryonic fibroblasts (MEFs) suppresses proliferation in U2OS and MEF cell lines at concentrations around 10 M and significantly inhibits invasion of U2OS cells within 3D Matrigel transwell assays This compound serves as a useful research tool for investigating NUAK1-related signaling pathways in cancer biology and cellular dynamics

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Apexbio Technology LLC HYOSCYAMINE 10MM IN 1ML DMSO
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Hyoscyamine (CAS 101-31-5) is a small molecule antagonist targeting acetylcholine receptors (AChR) Acting via inhibition of cholinergic signaling it exhibits a potent inhibitory activity with an IC50 of approximately 7 5 nM By blocking AChRs hyoscyamine modulates neurotransmission pathways involved in autonomic regulation Research applications include studies exploring cholinergic function investigations into parasympathetic nervous system disorders and testing therapeutic strategies involving ACh modulation

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Apexbio Technology LLC GDC-0879 10MM IN 1ML DMSO
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GDC-0879 (CAS 905281-76-7) is a selective inhibitor of B-Raf kinase targeting the Raf/MEK/ERK signaling cascade implicated in tumorigenesis It specifically inhibits B-Raf harboring the V600E mutation demonstrating IC50 values of 0 13 nM against purified mutant B-Raf and 63 nM for phosphorylated ERK in MALME-3M cells In vitro assays using V600E mutant cell lines (A375 melanoma Colo205 colorectal cancer) illustrate the compound s selectivity towards B-Raf and related C-Raf kinases In mouse xenografts expressing human BRAFV600E tumors GDC-0879 treatment results in sustained ( 90%) inhibition of ERK phosphorylation and reduced tumor progression highlighting its research value in oncology studies involving Raf pathway modulation

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Apexbio Technology LLC CORTICOSTERONE 1ML DMSO
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Corticosterone (CAS 50-22-6) is an endogenous steroid hormone secreted by the adrenal cortex which exhibits affinity toward both glucocorticoid and mineralocorticoid receptors Its mechanism of action involves serum- and glucocorticoid-inducible kinase (SGK)-mediated phosphorylation of GDP dissociation inhibitor (GDI) at Ser-213 thereby promoting GDI-Rab4 complex assembly This activity enhances Rab4-dependent recycling of AMPA receptors to cortical neuron synapses leading to elevated synaptic excitatory responses Corticosterone thus serves as a useful biochemical tool for investigating stress-related modulation of synaptic transmission and plasticity

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Apexbio Technology LLC AM1241 10MM IN 1ML DMSO
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AM1241 (CAS number 444912-48-5) is a selective agonist of the cannabinoid receptor type 2 (CB2) a G protein-coupled receptor encoded by the CNR2 gene CB2 receptors modulate inflammation and neuropathic pain pathways outside the central nervous system In vitro studies suggest stereoisomer-dependent activities specifically the S-enantiomer demonstrates higher functional potency toward human and rodent CB2 receptors compared to the R-enantiomer In animal models AM1241 administration reduces neuropathic pain phenotypes including hyperalgesia and allodynia and shows potential for delaying disease progression in an ALS (amyotrophic lateral sclerosis) mouse model Currently AM1241 remains a valuable investigational tool in preclinical pain and neurodegeneration research

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