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2-Chloro-4-nitrophenylphosphate, an indispensable compound in the field of biomedicine, possesses extraordinary capabilities in suppressing protein tyrosine phosphatases (PTPs). This fundamental trait renders it a promising avenue for therapeutic intervention against an array of ailments, encompassing malignancies and autoimmune disorders, by selectively targeting PTPs implicated in intricate signal transduction cascades. Synonyms: 2-Chloro-4-nitrophenyl dihydrogen phosphate; 14957-98-3; (2-chloro-4-nitrophenyl) dihydrogen phosphate; AGN-PC-0N3TPY; SCHEMBL1134003; DTXSID40439315; 2-Chloro-4-nitrophenyldihydrogenphosphate; (2-chloro-4-nitrophenoxy)phosphonic acid; A919724. CAS No. 14957-98-3. Molecular formula: C6H5ClNO6P. Mole weight: 253.53.
2-Nitrophenyl b-D-galactopyranoside-6-phosphate cyclohexylammonium salt
2-Nitrophenyl β-D-galactopyranoside-6-phosphate cyclohexylammonium salt is an indispensable compound extensively employed in the fields of biomedical inquiry and research assessments, assuming the role of a substrate designated for the detection and quantification of β-galactosidase functionality. Its implementation facilitates the comprehensive exploration of galactose metabolic pathways, lysosomal afflictions, as well as genetic irregularities correlating with the scarcity of galactosidase enzyme. Synonyms: o-Nitrophenyl b-D-galactopyranoside-6-phosphate cyclohexylammonium salt. CAS No. 25405-62-3. Molecular formula: C12H16NO11P.C6H13N. Mole weight: 480.4.
2-(N,N-Dimethylamino)-4-nitrophenylPhosphate Triethylamine Salt
Intermediate in the preparation of Adenosine derivatives. Group: Biochemicals. Grades: Highly Purified. CAS No. 55428-52-9. Pack Sizes: 100mg. US Biological Life Sciences.
2'-O-Methyluridine 3',5'-Bis(4-nitrophenyl)phosphate Diester can be obtained from 2'-O-Methyl Uridine (M338200) which is uridine analog and is used for preparation of antiviral nucleoside derivatives as inhibitors of subgenomic hepatitis C virus RNA replication. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg, 25mg. Molecular Formula: C22H22N4O16P2, Molecular Weight: 660.37. US Biological Life Sciences.
2'-O-Methyluridine 3',5'-Bis(4-nitrophenyl)phosphate Diester can be obtained from 2'-O-Methyl Uridine which is uridine analog and is used for preparation of antiviral nucleoside derivatives as inhibitors of subgenomic hepatitis C virus RNA replication. Molecular formula: C22H22N4O16P2. Mole weight: 660.37.
4-Nitrophenyl-b-D-glucopyranoside-6-phosphate
4-Nitrophenyl-b-D-glucopyranoside-6-phosphate is an indispensable compound, playing a pivotal role in exploring enzyme activities. Functioning as a substrate for diverse phosphatases, specifically alkaline phosphatase, it enables researchers to assess the enzymatic hydrolysis process. This compound enables insightful analysis of phosphatase activity, thereby facilitating comprehensive investigations into the correlation between such activity and afflictions like cancer, diabetes as well as metabolic disorders. Synonyms: 4-Nitrophenyl b-D-glucopyranoside-6-phosphate; 55196-70-8. CAS No. 55196-70-8. Molecular formula: C12H16NO11P. Mole weight: 381.23.
4-Nitrophenylphosphate
4-Nitrophenylphosphate is a crucial recompound utilized in the biomedical industry for the detection of alkaline phosphatase activity. It undergoes enzymatic hydrolysis by alkaline phosphatase, resulting in the release of a yellow compound that can be measured spectrophotometrically. This recompound finds applications in the research of various diseases, including liver diseases, bone disorders is and genetic abnormalities. Synonyms: PHOSPHORIC ACID MONO-(4-NITRO-PHENYL) ESTER. CAS No. 330-13-2. Molecular formula: C6H6NO6P. Mole weight: 219.09.
4-Nitrophenylphosphate bis(cyclohexylammonium) salt
4-Nitrophenylphosphate bis(cyclohexylammonium) salt, an invaluable compound utilized extensively in the biomedical field, serves as an exceptional substrate for the discernment of alkaline phosphatase activity within diverse biochemical assays. With its pivotal role in investigating enzyme kinetics, ascertaining liver and bone ailments, and exploring phosphatase-related disorders, this product assumes paramount significance. Moreover, it facilitates the advancement and assessment of therapeutic drugs that focus on ameliorating phosphatase-associated irregularities. CAS No. 52483-84-8.
4-Nitrophenylphosphate bis(tris(hydroxymethyl)amino methane) is an indispensable and highly significant recompound serving as a prominent substrate in enzyme-linked immunosorbent assays (ELISA) to precisely quantify and assess the alkaline phosphatase activity. Consequently, this exceptional compound assumes a pivotal function in research of diverse afflictions encompassing liver disorders, bone diseases and neoplasms. Synonyms: 4-Nitrophenylphosphate bis(tris) salt. CAS No. 68189-42-4. Molecular formula: C6H6NO6P.2C4H11NO3. Mole weight: 461.36.
4-Nitrophenylphosphate disodium salt hexahydrate
4-Nitrophenylphosphate disodium salt hexahydrate, a frequently employed compound, holds immense importance due to its multifaceted applications in the detection and quantification of alkaline phosphatase. This compound serves as an indispensable tool in the field of research pertaining to afflictions such as hepatic disorders and skeletal maladies. Synonyms: Sodium 4-nitrophenylphosphate hexahydrate; PNPP disodium hexahydrate. CAS No. 333338-18-4. Molecular formula: C6H6NO6P.2Na.6H2O. Mole weight: 371.142.
4-Nitrophenylphosphate disodium salt hexahydrate (PNPP)
1g Pack Size. Group: Analytical Reagents, Biochemicals, Diagnostic Raw Materials, Stains & Indicators. Formula: C6H4NO6P · 2Na · 6H2O. CAS No. 4264-83-9. Prepack ID 35359763-1g. Molecular Weight 371.14. See USA prepack pricing.
4-Nitrophenylphosphate disodium salt hexahydrate (PNPP)
25g Pack Size. Group: Analytical Reagents, Biochemicals, Diagnostic Raw Materials, Stains & Indicators. Formula: C6H4NO6P · 2Na · 6H2O. CAS No. 4264-83-9. Prepack ID 35359763-25g. Molecular Weight 371.14. See USA prepack pricing.
4-Nitrophenylphosphate disodium salt hexahydrate (PNPP)
5g Pack Size. Group: Analytical Reagents, Biochemicals, Diagnostic Raw Materials, Stains & Indicators. Formula: C6H4NO6P · 2Na · 6H2O. CAS No. 4264-83-9. Prepack ID 35359763-5g. Molecular Weight 371.14. See USA prepack pricing.
4-Nitrophenylphosphate di(tris) salt 99+% (HPLC)
4-Nitrophenylphosphate di(tris) salt 99+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 5g, 25g, 100g, 250g, 1Kg. US Biological Life Sciences.
Worldwide
4-Nitrophenylphosphate potassium salt
4-Nitrophenylphosphate potassium salt, an indispensable reagent in the field of biomedicine, plays a pivotal role in the study of protein phosphorylation. With its distinctive characteristics, this compound serves as a substrate for a diverse range of kinases, notably including alkaline phosphatases. Its multifunctionality extends to the exploration of signal transduction pathways and the elucidation of enzymatic activities implicated in afflictions such as cancer and metabolic disorders. Synonyms: pNP-Phos K. CAS No. 208651-58-5. Molecular formula: C6H5NO6P.K. Mole weight: 257.18.
Bis(4-nitrophenyl)hydrogen phosphate
Bis(4-nitrophenyl)hydrogen phosphate. Group: Biochemicals. Grades: Highly Purified. CAS No. 645-15-8. Pack Sizes: 1g, 2g, 5g, 10g. Molecular Formula: C12H9N2O8P. US Biological Life Sciences.
Worldwide
Bis(4-nitrophenyl) phosphate
Bis(4-nitrophenyl) phosphate is a catalyst for metal micelles and can catalyze the hydrolysis of (4-nitrophenyl) phosphate. Bis(4-nitrophenyl) phosphate is also an effective catalyst for ring-opening polymerization (ROP), which can achieve controlled polymerization of β-butyrolactone (β-BL) ring-opening and can be used to prepare diembedded polymers without quenching. segment copolymer [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 645-15-8. Pack Sizes: 250 mg; 500 mg; 1 g. Product ID: HY-W013205.
Paraoxon (Diethyl p-NitrophenylPhosphate)
A cholinesterase inhibitor. Group: Biochemicals. Alternative Names: Diethyl p-NitrophenylPhosphate; Phosphoric Acid Diethyl 4-Nitrophenyl Ester; 4-Nitrophenyl Diethyl Phosphate; Chinorto; Diethyl 4-NitrophenylPhosphate; Mintacol; Miotisal; Paraoxon-ethyl; Phosphachole; Phosphakol. Grades: Highly Purified. CAS No. 311-45-5. Pack Sizes: 250mg, 1g. Molecular Formula: C10H14NO6P , Molecular Weight: 275.2. US Biological Life Sciences.
Worldwide
P-Nitrophenylphosphate disodium salt
PNPP, Disodium Salt is a colorimetric alkaline phosphatase soluble substrate, p-NitrophenylPhosphate (pNPP) is the substrate of choice for use with alkaline phosphatase in Enzyme Linked Immunosorbant Assay (ELISA) procedures. Synonyms: PNPP; Disodium 4-nitrophenylphosphate; sodium 4-nitrophenylphosphate; Phosphoric acid, mono(4-nitrophenyl) ester, disodium salt; 4-Nitrophenylphosphate disodium salt; Phosphoric Acid 4-Nitrophenyl Ester Disodium Salt; Disodium p-NitrophenylPhosphate; p-NPP Disodium Salt; Mono(p-nitrophenyl) Ester Phosphoric Acid Disodium Salt. Grades: ≥98% by HPLC. CAS No. 4264-83-9. Molecular formula: C6H4NNa2O6P. Mole weight: 263.05.
Thymidine-3',5'-di(p-nitrophenylPhosphate) Disodium Salt
It is an artificial chromophoric substrate, could be used as a synthetic substrate for bovine pancreatic deoxyribonuclease. Uses: An artificial chromophoric substrate. Synonyms: 3'-Thymidylic Acid Mono(4-nitrophenyl) Ester 5'-(4-Nitrophenyl Hydrogen Phosphate) Disodium Salt. CAS No. 24418-12-0. Molecular formula: C22H22N4Na2O15P2. Mole weight: 688.34.
3-Nitrophenyl disulfide (Bis(3-Nitrophenyl) disulfide) is an inhibitor of mannitol-1-phosphate dehydrogenase ( M1PDH ) with IC 50 of 3 μM. 3-Nitrophenyl disulfide has antiparasitic activity [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Bis(3-nitrophenyl) disulfide; Nitrophenide. CAS No. 537-91-7. Pack Sizes: 10 mM * 1 mL; 25 mg; 50 mg; 100 mg. Product ID: HY-W009213.
4-Nitrophenyl β-D-glucopyranoside
4-Nitrophenyl β-D-glucopyranoside is a chromogenic substrate for β-glucosidase. 4-Nitrophenyl β-D-glucopyranoside is converted to a colored product, p-nitrophenol that is easily detected spectrophotometrically at 405 nm when used in a β-glycosidase assay. 4-Nitrophenyl β-D-glucopyranoside is hydrolysed through intramolecular nucleophilic catalysis by the phosphate group in the 2-position. 4-Nitrophenyl β-D-glucopyranoside is promising for research of postmenopausal osteoporosis [1] [2] [3]. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 2492-87-7. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g; 5 g. Product ID: HY-15927.
4-nitrophenylphosphatase
A number of other substances, including phenyl phosphate, 4-nitrophenyl sulfate, acetyl phosphate and glycerol phosphate, are not substrates. Group: Enzymes. Synonyms: nitrophenyl phosphatase; p-nitrophenylphosphatase; para-nitrophenyl phosphatase; K-pNPPase; NPPase; PNPPase; Ecto-p-nitrophenyl phosphatase; p-nitrophenylphosphate phosphohydrolase. Enzyme Commission Number: EC 3.1.3.41. CAS No. 9073-68-1. 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-3645; 4-nitrophenylphosphatase; EC 3.1.3.41; 9073-68-1; nitrophenyl phosphatase; p-nitrophenylphosphatase; para-nitrophenyl phosphatase; K-pNPPase; NPPase; PNPPase; Ecto-p-nitrophenyl phosphatase; p-nitrophenylphosphate phosphohydrolase. Cat No: EXWM-3645.
[acetyl-CoA carboxylase]-phosphatase
Simultaneously dephosphorylates and activates EC 6.4.1.2 acetyl-CoA carboxylase. Acts similarly on EC 1.1.1.88 (hydroxymethylglutaryl-CoA reductase), EC 2.4.1.1 (phosphorylase), EC 2.4.1.11 [glycogen(starch) synthase], and dephosphorylates phosphoprotamine and 4-nitrophenylphosphate. Not identical to EC 3.1.3.17 ([phosphorylase] phosphatase ) or EC 3.1.3.43 {[pyruvate dehydrogenase (acetyl-transferring)]-phosphatase}. Group: Enzymes. Enzyme Commission Number: EC 3.1.3.44. CAS No. 77000-10-3. 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-3648; [acetyl-CoA carboxylase]-phosphatase; EC 3.1.3.44; 77000-10-3. Cat No: EXWM-3648.
α-Galactosidase, positionally specific from Escherichia coli, Recombinant
Alpha-galactosidase is a glycoside hydrolase enzyme that hydrolyses the terminal alpha-galactosyl moieties from glycolipids and glycoproteins. It is encoded by the GLA gene. Two recombinant forms of alpha-galactosidase are called agalsidase alfa (INN) and agalsidase beta (INN). Activity using maltose as substrate at ph 6.0 at 25 deg c is ~2x > that obtained using p-nitrophenyl-α-d-glucoside as substrate at ph 6.8 at 37 oc. protein determined by biuret. Applications: Α-glucosidase is potential enzyme for the biosynthesis of complex carbohydrates. Group: Enzymes. Synonyms: Alpha-Galactosidase; Galactosidase; EC 3.2.1.22; GLA; GALA; melibiase; α-D-galactosidase; α-galactosidase A; α-galactoside galactohydrolase. Enzyme Commission Number: EC 3.2.1.22. CAS No. 9025-35-8. GLA. Activity: > 50 units/mg protein. Storage: 2-8°C. Form: Lyophilized powder containing potassium phosphate buffer salt. Source: E. coli. Species: Escherichia coli. Alpha-Galactosidase; Galactosidase; EC 3.2.1.22; GLA; GALA; melibiase; α-D-galactosidase; α-galactosidase A; α-galactoside galactohydrolase. Cat No: NATE-0293.
Berberine hydrogen sulphate
Berberine is a natural compound that has been shown to have anti-inflammatory and anticancer properties. It is the main component of berberine sulfate, which can be found in plants such as Coptis chinensis and goldenseal. Berberine sulfate has been shown to inhibit skin tumor formation by inhibiting nuclear DNA synthesis and tumor cell growth. Berberine sulfate also inhibits the production of p-nitrophenylphosphate, a chemical that is used as an indicator for bacterial growth. Berberine sulfate binds to DNA polymerase and inhibits its activity, thereby preventing transcription of DNA into RNA. This compound can be used in chromatographic analysis and optical sensor systems to detect bacterial infections. Group: Other alkaloids. Alternative Names: Natural Yellow 18. CAS No. 633-66-9. Molecular formula: C20H18NO4·HSO4. Mole weight: 433.43 g/mol. Canonical SMILES: COC1=C (C2=C[N+]3=C (C=C2C=C1)C4=CC5=C (C=C4CC3)OCO5)OC. OS (=O) (=O)[O-]. Catalog: ACM633669.
Bis-(4-nitrophenyl)phosphoric acid calcium salt
Heterocyclic Organic Compound. Alternative Names: BIS(4-NITROPHENYL)PHOSPHORIC ACID CALCIUM SALT;CALCIUM BIS(4-NITROPHENYL)PHOSPHATE;DI(4-NITROPHENYL)PHOSPHORIC ACID CALCIUM SALT; bis (4-nitrophenyl) phosphoricacidcalciumsalt95+%; Bis[bis (4-nitrophenoxy) phosphinyloxy]calcium. CAS No. 10331-55-2. Molecular formula: C24H16CaN4O16P2. Mole weight: 718.43. Catalog: ACM10331552.
Fenitrooxone is an intricately formulated biomedical agent, used for studying inflammation, malignancies and autoimmune dysfunctions. Synonyms: 3-Methyl-4-nitrophenyl dimethyl phosphate;3-methyl-4-nitrophenyldimethylphosphate;4-nitro-m-cresodimethylphosphate; Accothion O-analog; accothiono-analog; BAY 42247; bay42247; Dimethyl 3-methyl-4-nitrophenylphosphate. Grades: >98%. CAS No. 2255-17-6. Molecular formula: C9H12NO6P. Mole weight: 261.17.
maltose-6'-phosphate glucosidase
Hydrolyses a variety of 6-phospho-α-D-glucosides, including α-maltose 6'-phosphate, α,α-trehalose 6-phosphate, sucrose 6-phosphate and p-nitrophenyl-α-D-glucopyranoside 6-phosphate (as a chromogenic substrate). The enzyme is activated by FeII, MnII, CoII and NiII. It is rapidly inactivated in air. Group: Enzymes. Synonyms: phospho-α-glucosidase; maltose-6'-phosphate 6-phosphoglucohydrolase. Enzyme Commission Number: EC 3.2.1.122. CAS No. 98445-08-0. 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-3805; maltose-6'-phosphate glucosidase; EC 3.2.1.122; 98445-08-0; phospho-α-glucosidase; maltose-6'-phosphate 6-phosphoglucohydrolase. Cat No: EXWM-3805.
Naphthol as-bs phosphate
Heterocyclic Organic Compound. Alternative Names: NAPHTHOL AS-BS PHOSPHATE;N-(3-nitrophenyl)-3-(phosphonooxy)naphthalene-2-carboxamide;NAPHTHOL AS-BS-PHOSPHATE FOR &;N-(3-Nitrophenyl)-3-(phosphonooxy)-2-naphthalenecarboxamide;Einecs 233-014-2. CAS No. 10019-03-1. Molecular formula: C17H13N2O7P. Mole weight: 388.27. Catalog: ACM10019031.
Native Bovine Deoxyribonuclease II
Deoxyribonuclease II, also called as acid DNAse, hydrolyzes deoxyribonucleotide linkages in native and denatured DNA yielding products with 3'-phosphates. In vitro, its optimum pH range is 4.5-5.0. It also acts upon p-nitrophenyl-phosphodiesters at pH 5.6-5.9. The molecular weight is approximately 38 kDa Da. Applications: Dnase ii from creative enzymes has been used in the dissociation medium during the preparation of embryonic cardiac myocytes from rat heart. deoxyribonuclease ii from bovine spleen has been used in a study that conducted a partial purification of deoxyribonucleases from eggs and liver of xenopus laevis. deoxyribonuclease ii from bovine spleen has also been used in a study to investigate nucleic acid and protein synthesis of splenic lymphocytes. Group: Enzymes. Synonyms: DNASE2; deoxyribonuclease II; EC 3.1.22.1; 9025-64-3; DNase II; pancreatic DNase II; deoxyribonucleate 3'-nucleotidohydrolase; DNase II; pancreati. Enzyme Commission Number: EC 3.1.22.1. CAS No. 9025-64-3. DNASE2. Activity: > 1,000 units/mg protein. Storage: -20°C. Form: essentially salt-free, lyophilized powder. Source: Bovine spleen. Species: Bovine. DNASE2; deoxyribonuclease II; EC 3.1.22.1; 9025-64-3; DNase II; pancreatic DNase II; deoxyribonucleate 3'-nucleotidohydrolase; DNase II; pancreatic DNase II; acid deoxyribonuclease; acid Dnase. Cat No: NATE-0201.
Native Human β-N-Acetylglucosaminidase
This enzyme, sometimes called β-N-acetylhexosaminidase, is reported to liberate terminal β-linked N-acetylglucosamine and N-acetylgalactosamine from a variety of substrates. The activity of β-N-actylglucosaminidase may be determined with the chromogenic substrate p-nitrophenyl-N-acetyl-β-D-glucosaminide. β-N-actylglucosaminidase hydrolyzes the terminal nonreducing N-acetyl-D-hexosamine residues. This enzyme contains two predominant isozymes, Hex A, a heterodimer, and Hex B, a homodimer. N-acetylglucosamine, acetamide, N-2-acetamido-2-deoyglucosylamine, N-acetylnojirimycin, and N-acetyldeoxynojirmycin are known inhibitors. Applications: Β-n-...etylhexosaminidase; β-D-hexosaminidase; 9012-33-3; EC 3.2.1.52. Enzyme Commission Number: EC 3.2.1.52. CAS No. 9012-33-3. β-N-Acetylhexosaminidase. Activity: 6-20 units/mg protein. Storage: 2-8°C. Form: ammonium sulfate suspension. Suspension in 2.4 M (NH4)2SO4 containing 0.15 M NaCl and 0.1 M sodium phosphate, pH 6.0. Source: Human placenta. Species: Human. hexosaminidase; β-acetylaminodeoxyhexosidase; N-acetyl-β-D-hexosaminidase; N-acetyl-beta-hexosaminidase; β-hexosaminidase; β-acetylhexosaminidinase; β-D-N-acetylhexosaminidase; β-N-acetyl-D-hexosaminidase; β-N-acetylglucosaminidase; hexosaminidase A; N-acetylhexosaminidase
Native Porcine Deoxyribonuclease II
Deoxyribonuclease II, also called as acid DNAse, hydrolyzes deoxyribonucleotide linkages in native and denatured DNA yielding products with 3'-phosphates. In vitro, its optimum pH range is 4.5-5.0. It also acts upon p-nitrophenyl-phosphodiesters at pH 5.6-5.9. The molecular weight is approximately 38 kDa Da. Applications: Dnase ii from creative enzymes has been used to treat transformed cells during the purification of β-lactamase. it has also been used for the preparation of adenoma tissue in a study that investigated the effect of somatoprim on growth hormone secretion in human adenoma cell cultures (hsa). deoxyribonuclease ii from porcine spleen has been used in an immunohistological study of the immune system cells in paraffin-embedded tissues. deoxyribonuclease ii from porcine spleen has also been used in a study to investigate its reassociation with the lysosomal membrane. Group: Enzymes. Synony. Enzyme Commission Number: EC 3.1.22.1. CAS No. 9025-64-3. DNASE2. Activity: 2,000-6,000 Kunitz units/mg protein (biuret). Storage: -20°C. Form: lyophilized powder. Contains sodium chloride. Source: Porcine spleen. Species: Porcine. DNASE2; deoxyribonuclease II; EC 3.1.22.1; 9025-64-3; DNase II; pancreatic DNase II; deoxyribonucleate 3'-nucleotidohydrolase; DNase II; pancreatic DNase II; acid deoxyribonuclease; acid Dnase. Cat No: NATE-0202.
nucleotidase
A wide specificity for 2', 3'- and 5'- nucleotides; also hydrolyses glycerol phosphate and 4-nitrophenylphosphate. Group: Enzymes. Synonyms: nucleotide phosphatase; nucleotide-specific phosphatase; NSP I; NSP II; deoxyribonucleoside-activated nucleotidase (DAN); deoxyinosine-activated nucleotidase (DIAN); acid nucleotidase. Enzyme Commission Number: EC 3.1.3.31. CAS No. 9033-33-4. 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-3634; nucleotidase; EC 3.1.3.31; 9033-33-4; nucleotide phosphatase; nucleotide-specific phosphatase; NSP I; NSP II; deoxyribonucleoside-activated nucleotidase (DAN); deoxyinosine-activated nucleotidase (DIAN); acid nucleotidase. Cat No: EXWM-3634.
PC Amino-Modifier Phosphoramidite
PC Amino-Modifier Phosphoramidite is can be incorporated into DNA and RNA with both phosphate and phosphorothioate linkages, used to prepare 5'-amino-modified oligonucleotides suitable for subsequent photocleavage. Synonyms: [ (6-Trifluoroacetylamidocaproamido methyl ) -1- (2-nitrophenyl) -ethyl] -2-cyanoethyl- (N, N-diisopropyl ) -phosphoramidite. Molecular formula: C26H39F3N5O6P. Mole weight: 605.59.
PC Spacer Phosphoramidite
PC Spacer phosphoramidite can be used as an intermediate to link any modification reagent (which can be used as phosphoramidite) to the end of the oligonucleotide. After light cleavage, 5'-phosphate is generated on the DNA, making it suitable for further biotransformation, such as gene construction and cloning after ligation. Synonyms: [4-(4,4'-Dimethoxytrityloxy)butyramidomethyl)-1-(2-nitrophenyl)-ethyl]-2-cyanoethyl-(N,N-diisopropyl)-phosphoramidite. Molecular formula: C43H53N4O8P. Mole weight: 784.88.
PD 168368
PD 168368 is a competitive antagonist of neuromedin B (NMB) receptors. It blocks the elevation of intracellular calcium and release of inositol phosphate induced by NMB in cells expressing NMB receptors. Synonyms: (2S)-3-(1H-indol-3-yl)-2-methyl-2-[(4-nitrophenyl)carbamoylamino]-N-[(1-pyridin-2-ylcyclohexyl)methyl]propanamide. Grades: ≥95%. CAS No. 204066-82-0. Molecular formula: C31H34N6O4. Mole weight: 554.6.
PNPP disodium
PNPP (Para-nitrophenylphosphate) disodium is a non-proteinaceous chromogenic substrate for alkaline and acid phosphatases used in ELISA and conventional spectrophotometric assays. Uses: Scientific research. Group: Fluorescent dye. Alternative Names: Para-nitrophenylphosphate disodium. CAS No. 4264-83-9. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g; 5 g. Product ID: HY-15928.
Ribavirin Impurity 12
Ribavirin Impurity 12. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: methyl bis(4-nitrophenyl) phosphate. CAS No. 799-87-1. Molecular Formula: C13H11N2O8P. Mole Weight: 354.21. Catalog: APB799871.
PHPS1 is a cell-permeable inhibitor of the protein tyrosine phosphatase Shp2, a positive modulator of growth factor signaling. It is selective for Shp2 over ECPTP, PTP1B, Shp1, and mycobacterium MptpA. Synonyms: 4-[2-[1,5-Dihydro-3-(4-nitrophenyl)-5-oxo-1-phenyl-4H-pyrazol-4-ylidene]hydrazinyl]benzenesulfonic acid sodium salt. Grades: ≥98% by HPLC. Molecular formula: C21H14N5O6SNa. Mole weight: 487.42.
SMI 481
SMI 481 is a small-molecule inhibitor (SMI) of the yeast phosphatidylinositol transfer proteins (PITP) Sec14 (IC50 values of 211 nM and 2.87 μM for Sec14 mediated [3H]PtdIns transfer in vitro, and Sec14 dependent cell growth inhibition of WT (CTY182, gray) strains, respectively). SMI 481 exhibits exquisite pathway selectivity in inhibiting phosphoinositide signaling in cells with >200-fold selectivity over other yeast Sec14-like transfer activities. Synonyms: SMI481; SMI-481 SMI 481; NPPM 6748-481; NPPM 6748481; NPPM6748481; NPPM-6748-481; (4-Chloro-3-nitrophenyl)(4-(2-fluorophenyl)piperazin-1-yl)methanone; 1-(4-chloro-3-nitrobenzoyl)-4-(2-fluorophenyl)piperazine; (4-chloro-3-nitrophenyl)[4-(2-fluorophenyl)piperazin-1-yl]methanone. Grades: 99%. CAS No. 432020-20-7. Molecular formula: C17H15ClFN3O3. Mole weight: 363.77.
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