Bioactive Small Molecules
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Filtered Search Results
Cayman Chemical ANTIBODY CAY10717 5mg
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A multi-targeted kinase inhibitor; exhibits greater than 40% inhibition of 34 of 104 kinases in an enzymatic assay at a concentration of 100 nM; has activity at multiple oncogenic kinases (IC50 values less than 50 nM); highly cytotoxic against a cancer cell panel that includes chemotherapy-sensitive and -resistant cell lines (EC50s = 0.4-158 nM); inhibits the growth of HUVECs (EC50 = 34 nM)
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TARGETMOL CHEMICALS INC PJ34 50MG
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Also available in 10 mg 25 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. PJ34 HCl is the hydrochloride salt of PJ34 which is a PARP inhibitor with EC50 of 20 nM and is equally potent to PARP1/2. purity: 99%
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TARGETMOL CHEMICALS INC AMPIROXICAM 50MG
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Also available in 5 mg 10 mg 25 mg 100 mg 200 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Ampiroxicam (Flucam) is a nonselective cyclooxygenase inhibitor uesd as anti-inflammatory drug. purity: 99%
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eMolecules 1415562-82-1 | Medchem Express | PF-543 | 5mg | 415687519 | HY-15425 | MFCD23098794 | 465.61 | C27H31NO4S
AstaTech | ETHYL 2-(METHYLAMINO)-2-OXOACETATE | 0.25g | 296387275 | W11374 | 95.000 | 18522-95-7 | MFCD02859930 | 131.131 | C5H9NO3
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TARGETMOL CHEMICALS INC FV-100 5MG
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Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 500 mg and bulk. Please contact Fisher for quotes. FV-100 (Valnivudine HCl) is a potent selective and orally active anti-vaxx-zoster agent.FV-100 is the API for CF-1743.FV-100 exhibits very low toxicity in vivo.FV-100 is a potent selective and orally active anti-vaxx-zoster agent.FV-100 is the API for CF-1743.FV-100 exhibits very low toxicity in vivo. purity: 99%
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Medchemexpress LLC N-Desethyl amodiaquine-d5 | 1173023-19-2 | 99.9% | 1 MG
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N-Desethyl amodiaquine-d5 is the deuterium labeled N-Desethyl amodiaquine, which is the major biologically active metabolite of Amodiaquine. It is an antiparasitic agent with IC50 values for strains V1/S and 3D7 at 97 nM and 25 nM, respectively.
- Can be used as a tracer.
- Can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.
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BIOSYNTH INTERNATIONAL INC L-DEHYDROASCORBIC ACID 1 GR
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NC2251799 L-DEHYDROASCORBIC ACID 1 GR
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Cayman Chemical MetformIn-d6hydrochlorIde 5mg
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An internal standard for the quantification of metformin by GC- or LC-MS
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Cayman Chemical ANTIBODY ActInonIn 5mg
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A peptidomimetic antibiotic produced by Actinomyces that inhibits aminopeptidases, including MMP-1 (Ki = 300 nM), MMP-3 (Ki = 1,700 nM), MMP-8 (Ki = 130 nM), and MMP-9 (Ki = 330 nM); also targets peptide deformylase and meprin α (Ki = 20 nM)
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Cayman Chemical ANTIBODY PelItInIb 25mg
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A cyanoquinoline that irreversibly inhibits the receptor tyrosine kinases EGFR (IC50 = 39 nM) and HER2 (IC50 = 1.2 μM); disrupts Akt and MAPK pathways, inducing apoptosis and suppressing the growth of tumor cell lines
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Medchemexpress LLC B-catenin-IN-37 10mg | 1783856-40-5 | 307.27 g·mol⁻¹ | C13H9N9O | 10 MG
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β-catenin-IN-37 is a small-molecule inhibitor of the β-catenin/T-cell factor protein-protein interaction that suppresses canonical Wnt signaling and reduces proliferation of Wnt-activated colorectal cancer cell lines in vitro.
- Selective β-catenin/Tcf PPI inhibitor.
- Reported IC50 values: 20 μM (SW480) and 31 μM (HCT116).
- Molecular formula C13H9N9O; molecular weight 307.27 g·mol⁻¹.
- High reported purity (99.13%).
- Supplied as a 10 mg research reagent for in vitro assays.
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Abcam Formoterol hemifumarate, beta2 adrenoceptor agonist, 50MG
MW 402.45 g/mol, Purity >99%. Potent long-acting β₂ adrenoceptor agonist. Ki values are 27 and 2400 nM for adrenergic receptor subtypes β₂ and β₁, respectively. Trachea muscle relaxant.
The product is subject to the following: Abcam Restricted Use Statement
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Cayman Chemical L-GlutamIn-d5 5mg
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An internal standard for the quantification of L-glutamine by GC- or LC-MS
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Medchemexpress LLC Methyl 4-ethoxy-3-oxobutanoate | 415678-65-8 | MFCD24693495 | 250mg
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Methyl 4-ethoxy-3-oxobutanoate is a drug impurity
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Cayman Chemical ANTIBODY ApremIlast 25mg
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An orally active inhibitor of PDE4 with an IC50 value of 74 nM when tested in U937 cell lysates with 1 mM cAMP; decreases epidermal thickness in a mouse model of psoriasis, reduces both TNF-α and MMP-3 production in gut cells from patients with IBD, and improves clinical score in mouse models of arthritis
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