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FMK is a an irreversible RSK2 kinase inhibitor, that covalently modifies the C-terminal kinase domain of RSK. Uses: Scientific research. Group: Signaling pathways. CAS No. 821794-92-7. Pack Sizes: 10 mM * 1 mL; 2 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-52101A.
FMK 9a
FMK 9a is a covalent autophagin-1 inhibitor (IC50 = 80 and 73 μM in FRET and LRA assay). Synonyms: FMK-9a; FMK 9a; FMK9a; N-[(2S)-1-[(3-fluoro-2-oxopropyl)amino]-1-oxo-3-phenylpropan-2-yl]naphthalene-1-carboxamide. CAS No. 1955550-51-2. Molecular formula: C23H21FN2O3. Mole weight: 392.42.
FMK-MEA
FMK-MEA is a potent and selective p90 Ribosomal S6 Kinase (RSK) inhibitor. CAS No. 1414811-15-6. Molecular formula: C21H26FN5O2. Mole weight: 399.47.
FMK-MEA
FMK-MEA is a potent and selective p90 Ribosomal S6 Kinase (RSK) inhibitor. Uses: Scientific research. Group: Signaling pathways. CAS No. 1414811-15-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-52101C.
FMN hydrolase
Requires Mg2+. The enzyme, found in many isoforms purified from both bacteria and plants, is a member of the haloacid dehalogenase superfamily. Most of the isoforms have a wide substrate specificity, but isoforms specific for FMN also exist. Group: Enzymes. Synonyms: FMN phosphatase; AtcpFHy1. Enzyme Commission Number: EC 3.1.3.102. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3611; FMN hydrolase; EC 3.1.3.102; FMN phosphatase; AtcpFHy1. Cat No: EXWM-3611.
FMN Reductase from Escherichia coli (Fre), Recombinant
E.coli. Applications: Bacterial (e. coli) nad(p)h-dependent fmn-oxidoreductase is a recombinant protein of ca. 26kda overexpressed in e.coli. the sequence of cloned fre (swissprot accession number p0aen1) was confirmed by dna sequencing (100% identity). Group: Enzymes. Synonyms: NAD(P)H:flavin oxidoreduct. Enzyme Commission Number: EC 1.5.1.29. Mole weight: 26kDa. Activity: >2U/mg. Appearance: Coupling of bacterial luciferase to FMN-NAD(P)H oxidoreductase has been used to provide ultrasensitive analytical tools for thequantification of NADH and the substrates of NADH-, NADPH- dependent enzymes (e.g. glucose, lactate, malate, ethanol, sorbitol,oxaloacetate). Although FMN-reductase often present in luciferase enzyme preparations may be sufficient for producing light in the presence of NAD(P)H, highly purified and characterized Fre enzyme can offer some advantages such as an increased sensitivity,better control of the signal intensity and duration, and saving of the luciferase enzyme. Species: FMN Reductase. NAD(P)H:flavin oxidoreductase; NAD(P)H:flavin mono-nucleotide oxidoreductase; NAD(P)H(2):FMN oxidoreductase; NAD(P)H-FMN reductase; NAD(P)H-dependent FMN reductase; NAD(P)H:FMN oxidoreductase; riboflavin mononucleotide reductase; flavin mononucleotide reductase; EC 1.5.1.29. Pack: stable lyophilized form. Cat No: NATE-1744.
FMN reductase (NADH)
The enzyme often forms a two-component system with monooxygenases. Unlike EC 1.5.1.38, FMN reductase (NADPH), and EC 1.5.1.39, FMN reductase [NAD(P)H], this enzyme has a strong preference for NADH over NADPH, although some activity with the latter is observed.While FMN is the preferred substrate, FAD can also be used with much lower activity. Group: Enzymes. Synonyms: NADH-FMN reductase; NADH-dependent FMN reductase; NADH:FMN oxidoreductase; NADH:flavin oxidoreductase. Enzyme Commission Number: EC 1.5.1.42. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1523; FMN reductase (NADH); EC 1.5.1.42; NADH-FMN reductase; NADH-dependent FMN reductase; NADH:FMN oxidoreductase; NADH:flavin oxidoreductase. Cat No: EXWM-1523.
FMN reductase (NADPH)
The enzymes from bioluminescent bacteria contain FMN, while the enzyme from Escherichia coli does not. The enzyme often forms a two-component system with monooxygenases such as luciferase. Unlike EC 1.5.1.39, this enzyme does not use NADH as acceptor. While FMN is the preferred substrate, the enzyme can also use FAD and riboflavin with lower activity. Group: Enzymes. Synonyms: FRP; flavin reductase P; SsuE. Enzyme Commission Number: EC 1.5.1.38. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1519; FMN reductase (NADPH); EC 1.5.1.38; FRP; flavin reductase P; SsuE. Cat No: EXWM-1519.
FMN reductase [NAD(P)H]
Contains FMN. The enzyme can utilize NADH and NADPH with similar reaction rates. Different from EC 1.5.1.42, FMN reductase (NADH) and EC 1.5.1.38, FMN reductase (NADPH). The luminescent bacterium Vibrio harveyi possesses all three enzymes. Also reduces riboflavin and FAD, but more slowly. Group: Enzymes. Synonyms: FRG. Enzyme Commission Number: EC 1.5.1.39. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1520; FMN reductase [NAD(P)H]; EC 1.5.1.39; FRG. Cat No: EXWM-1520.
Fmoc-10-adc-oh
Fmoc-10-adc-oh. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Fmoc-10-Adc-OH;N-(9-Fluorenylmethyloxycarbonyl)-10-amino-decanoic acid. CAS No. 143688-82-8. Molecular formula: C25H31NO4. Mole weight: 409.52. Purity: 0.96. IUPACName: 10-(9H-fluoren-9-ylmethoxycarbonylamino)decanoicacid. Canonical SMILES: C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)NCCCCCCCCCC(=O)O. Product ID: ACM143688828. Alfa Chemistry ISO 9001:2015 Certified.
Fmoc-10-Adc-OH
Fmoc-10-Adc-OH. Group: Biochemicals. Alternative Names: N- (9-Fluorenyl methoxycarbonyl ) -10-amino-decanoic acid. Grades: Highly Purified. CAS No. 143688-82-8. Pack Sizes: 100mg, 250mg, 500mg, 1g, 2g. Molecular Formula: C25H31NO4. US Biological Life Sciences.
Fmoc-15-amino-4,7,10,13-tetraoxapentadecanoic acid ≥97% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 100mg, 250mg, 1g, 5g. US Biological Life Sciences.
Worldwide
Fmoc-1,5-diaminopentane hydrochloride
Fmoc-1,5-diaminopentane hydrochloride. Group: Biochemicals. Alternative Names: Fmoc-NH(CH2)5NH2·HCl. Grades: Highly Purified. CAS No. 118119-32-7. Pack Sizes: 500mg, 1g, 2g, 5g, 10g. US Biological Life Sciences.
Worldwide
Fmoc-1,5-diaminopentane hydrochloride 99+% (HPLC)
Fmoc-1,5-diaminopentane hydrochloride 99+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. CAS No. 118119-32-7. Pack Sizes: 250mg, 1g, 5g, 25g. US Biological Life Sciences.
Worldwide
Fmoc-1,6-diaminohexane
Fmoc-1,6-diaminohexane is an analog of Osw-1 which has the potential for Alzheimer's disease and cancer treatment from patent US 20140135279 A1. Uses: Scientific research. Group: Signaling pathways. CAS No. 166410-37-3. Pack Sizes: 10 mM * 1 mL; 200 mg. Product ID: HY-103664.
Fmoc-1,6-diaminohexane hydrochloride
Fmoc-1,6-diaminohexane hydrochloride. Group: Biochemicals. Alternative Names: Fmoc-NH(CH2)6NH2·HCl. Grades: Highly Purified. CAS No. 166410-37-3. Pack Sizes: 1g, 2g, 5g, 10g, 25g. US Biological Life Sciences.
Worldwide
Fmoc-1,6-diaminohexane hydrochloride 99+% (HPLC)
Fmoc-1,6-diaminohexane hydrochloride 99+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences.
Fmoc-1-amino-1-cycloheptanecarboxylic acid 99+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. CAS No. 188751-56-6. Pack Sizes: 100mg, 250mg, 1g, 5g. US Biological Life Sciences.
Worldwide
Fmoc-1-amino-1-cyclooctanecarboxylic acid
Fmoc-1-amino-1-cyclooctanecarboxylic acid. Uses: Designed for use in research and industrial production. Additional or Alternative Names: FMOC-1-AMINO-1-CYCLOOCTANECARBOXYLIC ACID;Cyclooctanecarboxylic acid, 1-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]- (9CI);Fmoc-1-amino-cyclooctane carboxylic acid. Product Category: Heterocyclic Organic Compound. CAS No. 222166-38-3. Molecular formula: C24H27NO4. Mole weight: 393.48. Product ID: ACM222166383. Alfa Chemistry ISO 9001:2015 Certified.
Fmoc-1-amino-1-cyclooctanecarboxylic acid
Fmoc-1-amino-1-cyclooctanecarboxylic acid. Group: Biochemicals. Alternative Names: Fmoc-acoc-OH. Grades: Highly Purified. CAS No. 222166-38-3. Pack Sizes: 250mg, 500mg, 1g, 2g, 5g. US Biological Life Sciences.