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Phenylacetylglutamine-[d5] is a labelled Phenylacetylglutamine. Phenylacetylglutamine is an amino acid acetylation product of phenylacetate. It is a component of human urine that accumulates in patients with uremia. Alternative Names: N-2-Phenylacetyl-d5-L-glutamine; Phenylac-L-Gln-OH-d5; Phenylacetyl-d5 L-Glutamine; N-Phenyl-d5-acetylglutamine; Phenyl-d5-acetyl-L-glutamine; Nα-(Phenyl-d5-acetyl)-L-glutamine. Grades: 95% by HPLC; 98% atom D. CAS No. 1331909-01-3. Molecular formula: C13H11D5N2O4. Mole weight: 269.31.
Phenylacetylglycine
An impurity of Penicillin G which is an antibacterial drug and acts through the inhibition of biosynthesis of cell-wall mucopeptide. Alternative Names: N-(Phenylacetyl)glycine; Phenaceturic Acid; N-Phenacetylglycine; NSC 408424; NSC 92778; Phenacetylglycine. Grades: ≥ 99% (HPLC). CAS No. 500-98-1. Molecular formula: C10H11NO3. Mole weight: 193.2.
Phenylacetyl glycine
Phenylacetyl glycine. Group: Biochemicals. Alternative Names: PhenylAc-Gly-OH. Grades: Highly Purified. CAS No. 500-98-1. Pack Sizes: 2g. US Biological Life Sciences.
Worldwide
Phenylacetyl glycine 99+% (HPLC)
Phenylacetyl glycine 99+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 2.5g. US Biological Life Sciences.
Worldwide
Phenylacetyl-L-glutamine
Phenylacetyl-L-glutamine. Group: Biochemicals. Alternative Names: PhenylAc-L-Gln-OH. Grades: Highly Purified. CAS No. 28047-15-6. Pack Sizes: 500mg, 1g, 2g, 5g, 10g. US Biological Life Sciences.
Worldwide
Phenylacetyl L-Glutamine
It is used as biomarker for metabolic age. Group: Biochemicals. Grades: Highly Purified. CAS No. 28047-15-6. Pack Sizes: 50mg. US Biological Life Sciences.
Worldwide
Phenylacetyl-L-glutamine ≥95% (NMR)
Phenylacetyl-L-glutamine ≥95% (NMR). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences.
Phenyl α-D-galactopyranoside is a biomedical product used in drug development and research. It acts as a substrate and is commonly employed in biochemical assays to study the enzymatic activity and transport mechanisms of galactosidases. Additionally, it can be utilized as a reference compound for synthesizing an array of pharmaceuticals targeting galactose-metabolizing enzymes, aiding in the treatment of various diseases related to galactose metabolism. Alternative Names: phenyl alpha-d-galactopyranoside; (2R,3R,4S,5R,6R)-2-(Hydroxymethyl)-6-phenoxytetrahydro-2H-pyran-3,4,5-triol. CAS No. 2871-15-0. Molecular formula: C12H16O6. Mole weight: 256.25.
Phenyl a-D-glucopyranoside
Phenyl a-D-glucopyranoside, a glycoside compound employed in the management of both cancer and diabetes, displays bifunctional properties by repressing enzymes implicated in neoplastic cell growth while simultaneously optimizing glycemic control. Its versatility extends to its widespread utilization in exploring key areas of inquiry in the biomedical field, cementing its significance as an essential tool in advancing scientific progress. Alternative Names: Phenyl α-D-glucopyranoside; NSC 226967; Phenyl α-D-glucoside. CAS No. 4630-62-0. Molecular formula: C12H16O6. Mole weight: 256.25.
Phenyl a-D-thiogalactopyranoside
Phenyl a-D-thiogalactopyranoside (PTG) is an essential chemical compound, serving as a remarkable enzymatic substrate. PTG proficiently facilitates the discernment and meticulous research of genetic expression patterns mediated by the awe-inspiring beta-galactosidase enzyme. Molecular formula: C12H16O5S. Mole weight: 272.32.
Phenyl a-D-thiomannopyranoside
Phenyl a-D-thiomannopyranoside, an extraordinary biomedical marvel, unfolds boundless prospects for combatting an extensive array of afflictions. Harnessing its unrivaled potential, this wondrous creation deftly targets intricacies within the perplexing realms of cancer, diabetes, and inflammatory disorders. Intriguingly, through the exquisite modulation of intricate molecular pathways, this bespoke remedy unleashes a torrent of untapped curative virtues, propelling it into the vanguard of pioneering drug development and redefining the frontiers of biomedicine's enigmatic realm. Alternative Names: Phenyl 1-thio-a-D-mannopyranoside. CAS No. 77481-62-0. Molecular formula: C12H16O5S. Mole weight: 272.32.
Phenylalanine. CAS No. 63-91-2. Cenik is your partner of choice for specialised chemicals. We don't just provide products - we supply solutions to your technical and regulatory specifications.
phenylalanine 2-monooxygenase
The reaction shown above is about 80% of the reaction catalysed; the remaining 20% is: L-phenylalanine + O2 + H2O = 3-phenylpyruvic acid + ammonia + H2O2 a reaction similar to that of EC 1.4.3.2, L-amino-acid oxidase. Group: Enzymes. Synonyms: L-phenylalanine oxidase (deaminating and decarboxylating); phenylalanine (deaminating, decarboxylating)oxidase. Enzyme Commission Number: EC 1.13.12.9. CAS No. 190396-37-3. 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-0622; phenylalanine 2-monooxygenase; EC 1.13.12.9; 190396-37-3; L-phenylalanine oxidase (deaminating and decarboxylating); phenylalanine (deaminating, decarboxylating)oxidase. Cat No: EXWM-0622.
phenylalanine 3-monooxygenase
The enzyme from the bacterium Streptomyces coeruleorubidus forms 3-hydroxy-L-phenylalanine (i.e. m-L-tyrosine), which is one of the building blocks in the biosynthesis of the uridyl peptide antibiotics pacidamycins. Group: Enzymes. Synonyms: PacX; phenylalanine 3-hydroxylase. Enzyme Commission Number: EC 1.14.16.7. 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-0959; phenylalanine 3-monooxygenase; EC 1.14.16.7; PacX; phenylalanine 3-hydroxylase. Cat No: EXWM-0959.
Phenylalanine-4-azobenzene HCl
Phenylalanine-4-azobenzene HCl is an alanine derivative[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2137036-84-9. Pack Sizes: 10 mM * 1 mL in DMSO; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-W141859.
Phenylalanine 4-hydroxybutyl ester
Phenylalanine 4-hydroxybutyl ester. CAS No. 136680-70-1. Product ID: ACM136680701. Alfa Chemistry - ISO 9001:32057 Certified.
phenylalanine 4-monooxygenase
The active centre contains mononuclear iron(II). The reaction involves an arene oxide that rearranges to give the phenolic hydroxy group. This results in the hydrogen at C-4 migrating to C-3 and in part being retained. This process is known as the NIH-shift. The 4a-hydroxytetrahydrobiopterin formed can dehydrate to 6,7-dihydrobiopterin, both spontaneously and by the action of EC 4.2.1.96, 4a-hydroxytetrahydrobiopterin dehydratase. The 6,7-dihydrobiopterin can be enzymically reduced back to tetrahydrobiopterin, by EC 1.5.1.34, 6,7-dihydropteridine reductase, or slowly rearranges into the more stable compound 7,8-dihydrobiopterin. Group: Enzymes. Synonyms: phenylalaninase; phenylalanine 4-hydroxylase; phenylalanine hydroxylase. Enzyme Commission Number: EC 1.14.16.1. CAS No. 9029-73-6. 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-0953; phenylalanine 4-monooxygenase; EC 1.14.16.1; 9029-73-6; phenylalaninase; phenylalanine 4-hydroxylase; phenylalanine hydroxylase. Cat No: EXWM-0953.
The enzyme from the bacterium Pantoea agglomerans produces D-β-phenylalanine, an intermediate in the biosynthesis of the polyketide non-ribosomal antibiotic andrimid. The enzyme contains the cofactor 3,5-dihydro-5-methylidene-4H-imidazol-4-one (MIO), which is formed autocatalytically by cyclization and dehydration of the three amino-acid residues alanine, serine and glycine. cf. EC 5.4.3.10, phenylalanine aminomutase (L-β-phenylalanine forming). Group: Enzymes. Synonyms: admH (gene name); L-phenylalanine 2,3-aminomutase [(S)-3-amino-3-phenylpropanoate]. Enzyme Commission Number: EC 5.4.3.11. 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-5533; phenylalanine aminomutase (D-β-phenylalanine forming); EC 5.4.3.11; admH (gene name); L-phenylalanine 2,3-aminomutase [(S)-3-amino-3-phenylpropanoate]. Cat No: EXWM-5533.
The enzyme contains the cofactor 3,5-dihydro-5-methylidene-4H-imidazol-4-one (MIO). This unique cofactor is formed autocatalytically by cyclization and dehydration of the three amino-acid residues alanine, serine and glycine. cf. EC 5.4.3.11, phenylalanine aminomutase (D-β-phenylalanine forming). Group: Enzymes. Enzyme Commission Number: EC 5.4.3.10. 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-5532; phenylalanine aminomutase (L-β-phenylalanine forming); EC 5.4.3.10. Cat No: EXWM-5532.
phenylalanine ammonia-lyase
This enzyme is a member of the aromatic amino acid lyase family, other members of which are EC 4.3.1.3 (histidine ammonia-lyase) and EC 4.3.1.23 (tyrosine ammonia-lyase) and EC 4.3.1.25 (phenylalanine/tyrosine ammonia-lyase). The enzyme contains the cofactor 3,5-dihydro-5-methylidene-4H-imidazol-4-one (MIO), which is common to this family. This unique cofactor is formed autocatalytically by cyclization and dehydration of the three amino-acid residues alanine, serine and glycine. The enzyme from some species is highly specific for phenylalanine. Group: Enzymes. Synonyms: phenylalanine deaminase; phenylalanine ammonium-lyase; PAL; L-phenylalanine ammonia-lyase; Phe ammonia-lyase. Enzyme Commission Number: EC 4.3.1.24. CAS No. 9024-28-6. PAL. 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-5284; phenylalanine ammonia-lyase; EC 4.3.1.24; 9024-28-6; phenylalanine deaminase; phenylalanine ammonium-lyase; PAL; L-phenylalanine ammonia-lyase; Phe ammonia-lyase. Cat No: EXWM-5284.
Phenylalanine,b-phenyl-,hydrochloride(1:1)
Phenylalanine,b-phenyl-,hydrochloride(1:1). CAS No. 119273-60-8. Product ID: ACM119273608. Molecular formula: C15H15NO2.ClH. Alfa Chemistry - ISO 9001:32057 Certified.
phenylalanine decarboxylase
A pyridoxal-phosphate protein. Also acts on tyrosine and other aromatic amino acids. Group: Enzymes. Synonyms: L-phenylalanine decarboxylase; aromatic L-amino acid decarboxylase; L-phenylalanine carboxy-lyase. Enzyme Commission Number: EC 4.1.1.53. CAS No. 9075-72-3. L-Phenylalanine decarboxylase. 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-4799; phenylalanine decarboxylase; EC 4.1.1.53; 9075-72-3; L-phenylalanine decarboxylase; aromatic L-amino acid decarboxylase; L-phenylalanine carboxy-lyase. Cat No: EXWM-4799.
phenylalanine dehydrogenase
The enzymes from Bacillus badius and Sporosarcina ureae are highly specific for L-phenylalanine; that from Bacillus sphaericus also acts on L-tyrosine. Group: Enzymes. Synonyms: L-phenylalanine dehydrogenase; PHD. Enzyme Commission Number: EC 1.4.1.20. CAS No. 69403-12-9. PHD. 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-1454; phenylalanine dehydrogenase; EC 1.4.1.20; 69403-12-9; L-phenylalanine dehydrogenase; PHD. Cat No: EXWM-1454.
phenylalanine(histidine) transaminase
L-Histidine and L-tyrosine can act instead of L-phenylalanine; in the reverse reaction, L-methionine, L-serine and L-glutamine can replace L-alanine. Group: Enzymes. Synonyms: phenylalanine (histidine) aminotransferase; phenylalanine(histidine):pyruvate aminotransferase; histidine:pyruvate aminotransferase; L-phenylalanine(L-histidine):pyruvate aminotransferase. Enzyme Commission Number: EC 2.6.1.58. CAS No. 72560-98-6. 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-2899; phenylalanine(histidine) transaminase; EC 2.6.1.58; 72560-98-6; phenylalanine (histidine) aminotransferase; phenylalanine(histidine):pyruvate aminotransferase; histidine:pyruvate aminotransferase; L-phenylalanine(L-histidine):pyruvate aminotransferase. Cat No: EXWM-2899.
phenylalanine N-acetyltransferase
Also acts, more slowly, on L-histidine and L-alanine. Group: Enzymes. Synonyms: acetyl-CoA-L-phenylalanine α-N-acetyltransferase. Enzyme Commission Number: EC 2.3.1.53. CAS No. 9075-16-5. 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-2233; phenylalanine N-acetyltransferase; EC 2.3.1.53; 9075-16-5; acetyl-CoA-L-phenylalanine α-N-acetyltransferase. Cat No: EXWM-2233.
phenylalanine N-monooxygenase
A heme-thiolate protein (P-450). This enzyme catalyses two successive N-hydroxylations of L-phenylalanine, the first committed steps in the biosynthesis of benzylglucosinolate. The product of the two hydroxylations, N,N-dihydroxy-L-phenylalanine, is extremely labile and dehydrates spontaneously.The dehydrated product is then subject to a decarboxylation that produces the oxime. It is still not known whether the decarboxylation is spontaneous or catalysed by the enzyme. The product, (E)-phenylacetaldoxime, undergoes a spontaneous isomerization to the (Z) form. Group: Enzymes. Synonyms: phenylalanine N-hydroxylase; CYP79A2. Enzyme Commission Number: EC 1.14.13.124. 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-0725; phenylalanine N-monooxygenase; EC 1.14.13.124; phenylalanine N-hydroxylase; CYP79A2. Cat No: EXWM-0725.
phenylalanine racemase (ATP-hydrolysing)
The enzyme phenylalanine racemase is the enzyme that acts on amino acids and derivatives. It activates both the L & D stereo isomers of phenylalanine to form L-phenylalanyl adenylate and D-phenylalanyl adenylate, which are bound to the enzyme. These bound compounds are then transferred to the thiol group of the enzyme followed by conversion of its configuration, the D-isomer being the more favorable configuration of the two, with a 7 to 3 ratio between the two isomers. The racemisation reaction of phenylalanine is coupled with the highly favorable hydrolysis of adenosine triphosphate (ATP) to adenosine monophosphate (AMP) and pyrophosphate (PP), thermodynamically allowing it to proceed. This reaction is then drawn forward by further hydrolyzing PP to inorganic phosphate (Pi), via Le Chatelier's principle. Group: Enzymes. Synonyms: phenylalanine racemase; phenylalanine racemase (adenosine triphosphate-hydrolysing); gramicidin S synthetase I. Enzyme Commission Number: EC 5.1.1.11. CAS No. 37290-95-2. 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-5369; phenylalanine racemase (ATP-hydrolysing); EC 5.1.1.11; 37290-95-2; phenylalanine racemase; phenylalanine racemase (adenosine triphosphate-hydrolysing); gramicidin S synthetase I. Cat No: EXWM-5369.
phenylalanine-tRNA ligase
This enzyme belongs to the family of ligases, to be specific those forming carbon-oxygen bonds in aminoacyl-tRNA and related compounds. This enzyme participates in phenylalanine, tyrosine and tryptophan biosynthesis and aminoacyl-tRNA biosynthesis. Group: Enzymes. Synonyms: phenylalanyl-tRNA synthetase; phenylalanyl-transfer ribonucleate synthetase; phenylalanine-tRNA synthetase; phenylalanyl-transfer RNA synthetase; phenylalanyl-tRNA ligase; phenylalanyl-transfer RNA ligase; L-phenylalanyl-tRNA synthetase; phenylalanine translase. Enzyme Commission Number: EC 6.1.1.20. CAS No. 9055-66-7. 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-5652; phenylalanine-tRNA ligase; EC 6.1.1.20; 9055-66-7; phenylalanyl-tRNA synthetase; phenylalanyl-transfer ribonucleate synthetase; phenylalanine-tRNA synthetase; phenylalanyl-transfer RNA synthetase; phenylalanyl-tRNA ligase; phenylalanyl-transfer RNA ligase; L-phenylalanyl-tRNA synthetase; phenylalanine translase. Cat No: EXWM-5652.
phenylalanine/tyrosine ammonia-lyase
This enzyme is a member of the aromatic amino acid lyase family, other members of which are EC 4.3.1.3 (histidine ammonia-lyase), EC 4.3.1.23 (tyrosine ammonia-lyase) and EC 4.3.1.24 (phenylalanine ammonia-lyase). The enzyme from some monocots, including maize, and from the yeast Rhodosporidium toruloides, deaminate L-phenylalanine and L-tyrosine with similar catalytic efficiency. The enzyme contains the cofactor 3,5-dihydro-5-methylidene-4H-imidazol-4-one (MIO), which is common to this family. This unique cofactor is formed autocatalytically by cyclization and dehydration of the three amino-acid residues alanine, serine and glycine. Group: Enzymes. Synonyms: PTAL; bifunctional PAL. Enzyme Commission Number: EC 4.3.1.25. 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-5285; phenylalanine/tyrosine ammonia-lyase; EC 4.3.1.25; PTAL; bifunctional PAL. Cat No: EXWM-5285.
Phenylalanyl-histidine
Phenylalanylhistidine is a dipeptide composed of phenylalanine and histidine. Alternative Names: Phe-his; L-phenylalanyl-L-histidine. CAS No. 33367-37-2. Molecular formula: C15H18N4O3. Mole weight: 302.33.
Phenylalanyl-lysine
Phenylalanyl-lysine is a dipeptide composed of phenylalanine and lysine. It is an incomplete breakdown product of protein digestion or protein catabolism. Alternative Names: 3-Phenyl-L-Ala-L-Lys-OH; L-Phe-L-Lys-OH; N2-(3-Phenyl-L-alanyl)-L-lysine; Phe-Lys-OH; L-Lysine, L-phenylalanyl-; (S)-6-Amino-2-((S)-2-amino-3-phenyl-propionylamino)-hexanoic acid; H-FK-OH; L-phenylalanyl-L-lysine. Grades: ≥95%. CAS No. 6456-72-0. Molecular formula: C15H23N3O3. Mole weight: 293.36.
Phenylalanyl-prolyl Diketopiperazine
Cyclo(D-Phe-L-Pro) is a cyclodipeptide phytotoxin produced by Alternaria alternata and streptomyces rochei. Alternative Names: L-Phe-L-Pro lactam; (3R,8aS)-Cyclo(phenylalanylprolyl); phenylalanyl-prolyl diketopiperazine; Cyclo(L-prolyl-D-phenylalanyl). Grades: 98.0%. CAS No. 26488-24-4. Molecular formula: C14H16N2O2. Mole weight: 244.29.
Phenylalanyl-threonine
Phenylalanyl-threonine is a dipeptide composed of phenylalanine and threonine. It is an incomplete breakdown product of protein digestion or protein catabolism. Alternative Names: L-Threonine, L-phenylalanyl-; Phe-Thr; H-FT-OH; L-Phe-L-Thr; L-phenylalanyl-L-threonine. Grades: ≥98%. CAS No. 51352-44-4. Molecular formula: C13H18N2O4. Mole weight: 266.29.
Phenyl-α-MIDA-boryl aldehyde
Phenyl-α-MIDA-boryl aldehyde. CAS No. 1329422-26-5.
Phenyl-α-O-benzyl-1-thio-α-L-rhamnopyranoside
Phenyl-α-O-benzyl-1-thio-α-L-rhamnopyranoside, an indispensable compound in the field of biomedicine, exemplifies paramount importance. As a therapeutic agent, its usage predominantly revolves around precise drug targeting to address diverse ailments. Its potent components effectively impede pathogen proliferation and counteract infections. Additionally, it assumes a pivotal function within pharmaceutical investigation and innovation, fostering transformative advancements in disease management. Alternative Names: Phenyl 6-Deoxy-2-O-(phenylmethyl)-1-thio-α-L-mannopyranoside. CAS No. 849938-16-5. Molecular formula: C19H22O4S. Mole weight: 346.44.
Phenyl a-L-thioglucopyranoside
Phenyl α-L-thioglucopyranoside is an indispensable constituent, aiding in suppressing aforementioned glucose metabolism-associated enzymes. It facilitates the exploration focused on maladies of great import like diabetes and cancer. Mole weight: 272.32.
Phenyl a-L-thiorhamnopyranoside
Phenyl a-L-thiorhamnopyranoside is a biochemical compound used in the biomedical industry acting as a substrate for glycosidase enzymes, facilitating the study and development of diseases related to glycosylation processes. Alternative Names: Phenyl 1-Thio-alpha-L-rhamnopyranoside; Phenyl a-L-thiorhamnopyranoside; alpha-L-Mannopyranoside, phenyl 6-deoxy-1-thio-; (2S,3R,4R,5R,6S)-2-methyl-6-phenylsulfanyloxane-3,4,5-triol; (2S,3R,4R,5R,6S)-2-METHYL-6-(PHENYLSULFANYL)OXANE-3,4,5-TRIOL; Phenyl 1-Thio-?-L-rhamnopyranoside; SCHEMBL12691081; AKOS027325989; W-201058. CAS No. 131724-82-8. Molecular formula: C12H16O4S. Mole weight: 256.32.
Phenylarsine oxide (PAO), an inhibitor of endocytosis, inhibits PTPε with an IC50 of 18 μM. Phenylarsine oxide (PAO) inhibits oxygen consumption and decreases cellular ATP content overlap with those used to inhibit protein internalization[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Oxophenylarsine; PhAsO; Arsenosobenzene. CAS No. 637-03-6. Pack Sizes: 10 mM * 1 mL in DMSO; 100 mg; 500 mg; 1 g. Product ID: HY-131901.
Phenylazosalicylic acid. Group: Biochemicals. Alternative Names: 2-Hydroxy-5-(2-phenyldiazenyl)benzoic acid. Grades: Highly Purified. CAS No. 3147-53-3. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. Molecular Formula: C13H10N2O3. US Biological Life Sciences.
Worldwide
Phenyl b-D-galactopyranoside
Phenyl b-D-galactopyranoside, a colorless and crystalline compound, embodies a multifaceted organic essence, exhibiting its biomedical utility as a chromogenic substrate for β-galactosidase activity detection in the realm of cutting-edge biomedical research. On the other hand, its application as differential media in microbiology, serves as a shield, dispelling gram-negative bacteria, contributing significantly to environmental sustainability. Furthermore, the antibacterial properties of this compound against gram-negative bacteria have incited possible avenues for pharmacological research and may hold the potential for developing novel antimicrobial drugs. Alternative Names: Galactopyranoside, phenyl, β-D-; Phenyl β-D-galactopyranoside; Phenyl β-D-galactoside; Phenyl β-galactoside. CAS No. 2818-58-8. Molecular formula: C12H16O6. Mole weight: 256.25.
Phenyl b-D-glucopyranoside
Phenyl b-D-glucopyranoside is a chemical compound extensively employed in the biomedical realm assuming an indispensable function in studying myriad conditions, encompassing diabetes, cancer and metabolic disorders. Alternative Names: Glucopyranoside, phenyl, β-D-; Phenyl β-D-glucopyranoside; Phenyl β-D-glucoside; (2R,3S,4S,5R,6S)-2-(Hydroxymethyl)-6-phenoxy-tetrahydro-2H-pyran-3,4,5-triol; Phenyl-β-D-glucopyranoside. Grades: ≥95%. CAS No. 1464-44-4. Molecular formula: C12H16O6. Mole weight: 256.25.
Phenyl b-D-glucuronide
Phenyl b-D-glucuronide, a biochemical compound, serves as a metabolite of phenylalanine. Researchers widely utilize it in clinical studies to explore the complex phenylalanine metabolic pathway and its potential involvement in phenylketonuria development. Additionally, it is a valuable marker for assessing liver function and detecting liver diseases. Alternative Names: Glucopyranosiduronic acid, phenyl, β-D-; Phenyl β-D-glucopyranosiduronic acid; Phenol glucuronide; Phenol β-D-glucuronide; Phenyl glucuronide; Phenyl β-D-glucosiduronic acid; Phenyl β-D-glucuronide. CAS No. 17685-05-1. Molecular formula: C12H14O7. Mole weight: 270.24.
Phenyl b-D-thiogalactopyranoside
Phenyl b-D-thiogalactopyranoside is a biochemical compound widely used in the biomedical industry as a substrate for β-galactosidase activity assays. It mimics lactose and induces the expression of lac operon in E. coli. Alternative Names: Phenyl 1-thio-beta-D-galactopyranoside; beta-D-Galactopyranoside, phenyl 1-thio-; (2R,3R,4S,5R,6S)-2-(Hydroxymethyl)-6-(phenylthio)tetrahydro-2H-pyran-3,4,5-triol. CAS No. 16758-34-2. Molecular formula: C12H16O5S. Mole weight: 272.32.
Phenyl b-D-thioglucopyranoside
Phenyl b-D-thioglucopyranoside is an indispensable biomedical product within the pharmaceutical industry unraveling its potential in drug discovery and development studies. Notably, its distinctive chemical configuration renders it a remarkable compound in enzyme assays and as a substrate for enzyme-catalyzed reactions. Alternative Names: Glucopyranoside, phenyl 1-thio-, β-D-; Phenyl 1-thio-β-D-glucopyranoside; NSC 231833; Phenyl β-D-thioglucopyranoside; Phenyl β-D-thioglucoside; Thiophenol thio-β-glucoside; (2R,3S,4S,5R,6S)-2-(Hydroxymethyl)-6-(phenylthio)tetrahydro-2H-pyran-3,4,5-triol; S-Phenyl-1-thio-beta-D-glucopyranoside. CAS No. 2936-70-1. Molecular formula: C12H16O5S. Mole weight: 272.32.
Phenyl b-D-thioglucuronide
Phenyl b-D-thioglucuronide, an invaluable compound in the biomedical industry, stands at the forefront of drug metabolism studies and hepatic glucuronidation research. As a substrate for glucuronosyltransferase enzymes, this compound diligently unravels the intricate web of drug-drug interactions and illuminates the identities of drugs undergoing glucuronidation. Alternative Names: (2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-phenylsulfanyloxane-2-carboxylic acid; Phenyl 1-thio-beta-D-glucopyranosiduronic acid; FYJ. CAS No. 26399-82-6. Molecular formula: C12H14O6S. Mole weight: 286.30.
Phenylbenzimidazole Sulfonic Acid
Phenylbenzimidazole Sulfonic Acid. Alternative Names: 2-Phenylbenzimidazole-5-sulfonic acid. CAS No. 27503-81-7. Purity: 98.0-102.0%. Product ID: CI-GU-0345. Molecular formula: C13H10N2O3S. Mole weight: 274.3 g/mol. Alfa Chemistry - ISO 9001:32057 Certified.
Phenyl benzoate
Phenyl benzoate. Synonyms: Benzoic acid phenyl ester. CAS No. 93-99-2. Pack Sizes: 25 g. Product ID: CDC10-0355. Molecular formula: C13H10O2. Category: Cosmetic Preservatives. Product Keywords: Cosmetic Ingredients; Cosmetic Preservatives; Phenyl benzoate; CDC10-0355; 93-99-2; C13H10O2; Benzoic acid phenyl ester; 202-293-2; MFCD00003072; 93-99-2. Purity: 0.99. Color: White. EC Number: 202-293-2. Physical State: Powder. Quality Level: 100. Application: Phenyl benzoate was used in the synthesis of soluble polyimides using dianhydride/diamine derivatives. Boiling Point: 298-299°C. Melting Point: 68-70°C. Density: 1.146 g/cm3. Product Description: Phenyl benzoate is a phenyl ester of benzoic acid. Crystal structure of phenyl benzoate has been determined from 844 microdensitometer-measured intensities. All bond lengths and angles were reported to be normal. Phenyl benzoate undergoes Fries rearrangement catalyzed by heteropoly acids to yield the acylated phenols and esters.
Phenyl β-D-glucopyranoside is a component isolated from Phellodendron amurense, which has anti-inflammatory and anti-tumor activities. Phenyl β-D-glucopyranoside inhibits nitric oxide (NO) production, and the expression of iNOS and COX-2. Phenyl β-D-glucopyranoside also inhibits the nuclear translocation of NF-κB. Phenyl β-D-glucopyranoside inhibits the expression of pro-inflammatory cytokines and related genes[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1464-44-4. Pack Sizes: 10 mM * 1 mL in DMSO; 500 mg; 1 g; 5 g; 10 g; 25 g. Product ID: HY-W011849.
Phenyl-beta-D-glucopyranoside
5g Pack Size. Group: Building Blocks, Carbohydrates, Testing Standards. Formula: C12H16O6. CAS No. 1464-44-4. Prepack ID 18205669-5g. Molecular Weight 256.2518. See USA prepack pricing.
Phenyl b-L-thiofucopyranoside is an extensively employed chemical compound within the dynamic biomedical sector, used for delving into the intricate interplay of carbohydrates to aiding in studying a breadth of afflictions, encompassing cancer and specific infections. Molecular formula: C12H16O4S. Mole weight: 256.32.
Phenylboronic acid
Phenylboronic acid. Group: Biochemicals. Grades: Highly Purified. CAS No. 98-80-6. Pack Sizes: 25g, 50g, 100g, 250g, 500g. Molecular Formula: C6H7BO2. US Biological Life Sciences.
100g Pack Size. Group: Boronic Acids, Building Blocks, Organics. Formula: C6H7BO2. CAS No. 98-80-6. Prepack ID 11859927-100g. Molecular Weight 121.93. See USA prepack pricing.
Phenylboronic acid
25g Pack Size. Group: Boronic Acids, Building Blocks, Organics. Formula: C6H7BO2. CAS No. 98-80-6. Prepack ID 11859927-25g. Molecular Weight 121.93. See USA prepack pricing.
Phenyl Boronic Acid
Phenyl Boronic Acid. Grades: Various grades and purity. CAS No. 98-80-6. Pack Sizes: Various packaging available. Categories: Boronic Acid derivatives.
US, Austria, Lithuania
Phenylboronic Acid-[13C6]
Phenylboronic Acid-[13C6] is an isotope labelled compound of Phenylboronic Acid. Phenylboronic Acid is a compound used in organic synthesis of various pharmaceutical goods. Alternative Names: B-Phenylboronic Acid-13C6; Dihydroxyphenylborane-13C6; Phenylboric Acid-13C6; Phenylboronic Acid-13C6; Phenyldihydroxyborane-13C6. Grades: 98% by CP; 98% atom 13C. Molecular formula: [13C]6H7BO2. Mole weight: 127.89.
Phenylboronic Acid (95%)
Phenylboronic Acid is a compound used in organic synthesis of various pharmaceutical goods. Group: Biochemicals. Alternative Names: B-Phenylboronic Acid; Dihydroxyphenylborane; NSC 66487; Phenylboric Acid; Phenylboronic Acid; Phenyldihydroxyborane. Grades: Highly Purified. CAS No. 98-80-6. Pack Sizes: 25g. US Biological Life Sciences.
Worldwide
Phenylboronic Acid-[d5]
Phenylboronic Acid-[d5] is the labelled analogue of Phenylboronic Acid, which is a compound used in organic synthesis of various pharmaceutical goods. Alternative Names: Phenyl-d5-boronic acid; B-Phenylboronic Acid-d5; Dihydroxyphenylborane-d5; Phenylboric Acid-d5; Phenyldihydroxyborane-d5; B-(Phenyl-2,3,4,5,6-d5)boronic Acid; (Pentadeuterophenyl)boronic Acid. Grades: 98% by CP; 98% atom D. CAS No. 215527-70-1. Molecular formula: C6H2D5BO2. Mole weight: 126.96.
Phenylboronic acid MIDA ester
Phenylboronic acid MIDA ester. CAS No. 109737-57-7. Molecular formula: C11H12BNO4. Mole weight: 233.03g/mol. IUPAC Name: 6-methyl-2-phenyl-1,3,6,2-dioxazaborocane-4,8-dione. SMILES: B1(OC(=O)CN(CC(=O)O1)C)C2=CC=CC=C2. InChI: InChI=1S/C11H12BNO4/c1-13-7-10(14)16-12(17-11(15)8-13)9-5-3-2-4-6-9/h2-6H,7-8H2,1H3.