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tert-Butyl (4-(4-amino-3-iodo-1H-pyrazolo[3,4-d]pyrimidin-1-yl)butyl)carbamate is a chemical compound that serves as a valuable drug intermediate for the synthesis of various active compounds. It is strictly for research purposes and not for direct use with patients. The compound is presented in a solid form.
Drug intermediate for synthesizing active compounds.
For research use only.
Available in solid appearance.
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AMC Arachidonoyl Amide (AMC-AA) is an AMC-tagged fatty acid amide used as a fluorogenic substrate to measure fatty acid amide hydrolase (FAAH) activity in biochemical assays. It is supplied as a light yellow solid with high reported purity and requires low-temperature storage and dry-ice shipment.
High purity: 99.5%.
Molecular weight: 461.64 g/mol.
Chemical formula: C30H39NO3.
Suitable as a substrate for FAAH activity assays.
Stored at -80°C and shipped on dry ice.
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Fluorescein-PEG3-amine is a PEG-based PROTAC linker comprising a fluorescein fluorophore connected through a three-unit polyethylene glycol spacer to a terminal primary amine. It is supplied as a solid for research use and is intended for conjugation reactions in chemical biology and PROTAC synthesis; follow frozen storage recommendations for long-term stability.
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Hydrochloride salt of a small-molecule research compound (CAS 2380273-26-5) supplied as a white to yellow solid for laboratory use. COA and SDS report purity 98.59% and provide storage and hazard guidance.
Hydrochloride salt, solid form.
Purity 98.6% (LCMS, COA).
Molecular weight 481.05 g/mol.
Chemical formula C23H33ClN4O3S.
Recommended storage: -20°C; protect from moisture and light.
Hazard statements: harmful if swallowed; causes skin and eye irritation; may cause respiratory irritation.
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AMI-1 is a cell-permeable, reversible small-molecule inhibitor of protein arginine N-methyltransferases (PRMTs). It blocks peptide-substrate binding and is used in biochemical and cellular studies to probe arginine methylation and PRMT function.
Purity: 98.0%.
Molecular weight: 548.45 g·mol⁻1.
CAS number: 20324-87-2.
Chemical formula: C21H14N2Na2O9S2.
Pack size: 10 MG.
Storage: sealed, away from moisture; in solution, -80°C up to 2 years or -20°C up to 1 year.
Targets: inhibits PRMT1, PRMT3, PRMT4, PRMT6, PRMT5, and yeast Hmt1p.
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(2S,4S)-1-((S)-2-amino-3,3-dimethylbutanoyl)-4-hydroxy-N-((S)-1-(4-(4-methylthiazol-5-yl)phenyl)ethyl)pyrrolidine-2-carboxamide hydrochloride is a synthetic peptidomimetic intermediate used in pharmaceutical research and synthesis. It is supplied as a white to yellow solid with molecular weight 481.05 g/mol and CAS 2380273-26-5; batch COA reports LCMS purity 98.59%. Recommended storage is -20°C, sealed, protected from moisture and light.
Hydrochloride salt suitable for synthetic intermediates
High purity (98.6%) by LCMS
White to yellow solid appearance
Molecular weight 481.05 g/mol; CAS 2380273-26-5
Intended for use as a drug intermediate and research chemical
Store at -20°C, sealed, protect from moisture and light
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Thieno-CTP is a structural analog of cytidine triphosphate (CTP) that incorporates a thiophene-modified nucleobase allowing incorporation into RNA by RNA polymerases during transcription Following enzymatic incorporation into nascent RNA transcripts the introduced thienyl modification acts as a reactive site suitable for subsequent bioorthogonal labeling via selective chemical reactions This chemical feature enables detection visualization and analysis of newly synthesized RNA molecules within biological systems Hence Thieno-CTP is utilized to examine transcriptional dynamics RNA synthetic regulation RNA trafficking and RNA-protein interaction studies supporting research into RNA biology and related areas
Encompass Procurement Services Non-distribution item offered as a customer accommodation; additional freight charges may apply. Learn More
Thieno-CTP is a structural analog of cytidine triphosphate (CTP) that incorporates a thiophene-modified nucleobase allowing incorporation into RNA by RNA polymerases during transcription Following enzymatic incorporation into nascent RNA transcripts the introduced thienyl modification acts as a reactive site suitable for subsequent bioorthogonal labeling via selective chemical reactions This chemical feature enables detection visualization and analysis of newly synthesized RNA molecules within biological systems Hence Thieno-CTP is utilized to examine transcriptional dynamics RNA synthetic regulation RNA trafficking and RNA-protein interaction studies supporting research into RNA biology and related areas
Encompass Procurement Services Non-distribution item offered as a customer accommodation; additional freight charges may apply. Learn More
Thieno-CTP is a structural analog of cytidine triphosphate (CTP) that incorporates a thiophene-modified nucleobase allowing incorporation into RNA by RNA polymerases during transcription Following enzymatic incorporation into nascent RNA transcripts the introduced thienyl modification acts as a reactive site suitable for subsequent bioorthogonal labeling via selective chemical reactions This chemical feature enables detection visualization and analysis of newly synthesized RNA molecules within biological systems Hence Thieno-CTP is utilized to examine transcriptional dynamics RNA synthetic regulation RNA trafficking and RNA-protein interaction studies supporting research into RNA biology and related areas
Encompass Procurement Services Non-distribution item offered as a customer accommodation; additional freight charges may apply. Learn More
Thieno-CTP is a structural analog of cytidine triphosphate (CTP) that incorporates a thiophene-modified nucleobase allowing incorporation into RNA by RNA polymerases during transcription Following enzymatic incorporation into nascent RNA transcripts the introduced thienyl modification acts as a reactive site suitable for subsequent bioorthogonal labeling via selective chemical reactions This chemical feature enables detection visualization and analysis of newly synthesized RNA molecules within biological systems Hence Thieno-CTP is utilized to examine transcriptional dynamics RNA synthetic regulation RNA trafficking and RNA-protein interaction studies supporting research into RNA biology and related areas
Encompass Procurement Services Non-distribution item offered as a customer accommodation; additional freight charges may apply. Learn More