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Tetrahydro-11-deoxycortisol is an endogenous urinary steroid metabolite supplied as a research reference standard for studies of 11β-hydroxylase deficiency and steroid metabolism. It is provided as a white to off-white solid suitable for analytical and biochemical applications.
High purity (>98.2% by HPLC).
Suitable as a reference standard for steroid metabolism and diagnostic research.
Solid form for accurate weighing and analytical preparation.
Molecular formula C21H34O4; molecular weight 350.49 g·mol⁻¹.
Available in small-quantity vials for method development and validation.
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This chemical is (S)-2-Aminopropanamide (hydrochloride), identified by CAS Number 33208-99-0. It has a molecular formula of C3H9ClN2O and a purity of ≥97.0%. It is a white to off-white solid.
CAS Number: 33208-99-0
Purity: ≥97.0%
Molecular formula: C3H9ClN2O
Molecular weight: 124.57
Appearance: White to off-white solid
Storage conditions for powder: -20°C for 3 years; 4°C for 2 years
Storage conditions in solvent: -80°C for 6 months; -20°C for 1 month
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3-Benzyl-6-bromo-1H-quinolin-2-one is a drug intermediate used for the synthesis of various active compounds. It is supplied as a white to off-white solid with a purity of 98.33%.
Purity of 98.33%
Molecular weight of 314.18
CAS number 924633-09-0
Solid appearance
White to off-white color
Stable as powder for 3 years at -20°C or 2 years at 4°C
Stable in solvent for 6 months at -80°C or 1 month at -20°C
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Broussonin E is a phenolic compound exhibiting anti-inflammatory activity. It suppresses inflammation by modulating the activation state of macrophages through inhibiting the ERK and p38 MAPK pathways, while enhancing the JAK2-STAT3 signaling pathway. This compound can be utilized for research related to inflammation-related diseases, such as atherosclerosis.
Inhibits LPS (lipopolysaccharides)-stimulated phosphorylation of ERK and p38 MAPK at 20 μM for 3 hours.
Activates janus kinase (JAK) 2 and signal transducer and activator of transcription (STAT) 3.
Suppresses LPS-induced pro-inflammatory production in RAW264.7 cells (0-20 μM, 3 h), including TNF-α, IL-1β, IL-6, COX-2, and iNOS.
Enhances the expression of anti-inflammatory mediators such as IL-10, CD206, and arginase-1 (Arg-1) in LPS-stimulated RAW264.7 cells.
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2'-Bromo-2'-deoxyuridine is a brominated deoxyuridine nucleoside analog supplied for research use. It is provided as a white to off-white solid and is commonly used as a thymidine analog for DNA incorporation, cell proliferation assays, and other biochemical studies.
White to off-white solid appearance.
Molecular formula C9H11BrN2O5; molecular weight 307.10 g/mol.
CAS number 4753-02-0.
Purity 96.9% (HPLC).
Storage: powder at -20°C for long-term stability.
Intended for research use only.
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2'-Bromo-2'-deoxyuridine is a brominated deoxyuridine nucleoside supplied for research use. It serves as a nucleoside analog for biochemical and molecular biology studies where modified nucleosides are required.
Brominated deoxyuridine nucleoside for incorporation in nucleic acid studies.
Molecular formula C9H11BrN2O5; molecular weight 307.10 g/mol.
Purity 96.9% by HPLC (certificate of analysis).
Available as a powder; storage recommended at -20°C for long-term stability.
CAS number 4753-02-0 for chemical identification.
Supplied in a 100 mg quantity suitable for lab-scale research.
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Tranylcypromine hydrochloride (CAS 1986-47-6) is a small molecule inhibitor that irreversibly targets monoamine oxidase (MAO) isoforms A and B demonstrating mechanism-based inhibition with Ki values of 101 9 M for MAO A and 16 M for MAO B and corresponding IC50 values of 2 3 M and 0 95 M Additionally tranylcypromine acts as a time-dependent irreversible inhibitor of lysine-specific demethylase 1 (LSD1) an amine oxidase homolog with structural similarities to MAOs exhibiting a Ki of 242 M and an IC50 of 20 7 M This compound is widely utilized in studies investigating MAO and LSD1 enzymatic functions epigenetic regulation and monoamine metabolism
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AZD-3463 (CAS 1356962-20-3) is an orally bioavailable small molecule inhibitor targeting anaplastic lymphoma kinase (ALK) and insulin-like growth factor 1 receptor (IGF1R) exhibiting a Ki of 0 75 nM ALK expression is predominantly neuronal and is upregulated in neuroblastoma where its activation promotes cell survival and proliferation In vitro AZD-3463 suppresses proliferation of neuroblastoma cell lines with wild-type or mutant ALK by inhibiting the ALK-mediated PI3K/AKT/mTOR signaling pathway leading to apoptosis and autophagy induction AZD-3463 also enhances the cytotoxicity of chemotherapeutic agents such as doxorubicin and temozolomide In vivo it has demonstrated efficacy in reducing neuroblastoma growth in xenograft mouse models
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N-Methylnicotinamide is an endogenous metabolite supplied as a high-purity solid for research use. It is provided as an analytical standard suitable for in vitro and in vivo studies, with recommended storage and formulation guidance for laboratory applications.