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| Product | Description | |
|---|---|---|
| Iniparib | BSI-201 is a small-molecule prodrug inhibitor of the nuclear enzyme poly(ADP-ribose) polymerase-1 (PARP-1) with potential chemosensitizing, radiosensitizing and antineoplastic activities. In vivo, PARP-1 inhibitor BSI-201 is converted to the active drug, which selectively binds to PARP-1 and inhibits PARP-1- mediated DNA repair. Consequently, this agent may enhance the cytotoxicity of DNA-damaging agents and reverse tumor cell resistance to chemotherapy and radiation therapy. In addition, PARP-1 inhibitor BSI-201 may exhibit direct antineoplastic activity against cancers defective in DNA repair. PARP-1 catalyzes post-translational ADP-ribosylation of nuclear proteins and is activated by single-strand DNA (ssDNA) breaks. Uses: Poly(adp-ribose) polymerase inhibitors. Synonyms: BSI-201; BSI201; BSI 201; NSC746045; NSC-746045; NSC 746045; ND-71677; NIBA; INO-2BA; SAR-240550; IND-71677. IND 71677; IND71677; Iniparib. Grades: 99.82%. CAS No. 160003-66-7. Molecular formula: C7H5IN2O3. Mole weight: 292.032. |  |
| Iniparib | Iniparib is an irreversible PARP1 inhibitor. Studies show that potential therapeutic agent for the treatment of cancer, including triple-negative breast cancer. Group: Biochemicals. Alternative Names: 4-Iodo-3-nitrobenzamide; BSI 201. Grades: Highly Purified. CAS No. 160003-66-7. Pack Sizes: 5mg. US Biological Life Sciences. |  Worldwide |
| initiation-specific α-1,6-mannosyltransferase | Requires Mn2+. In Saccharomyces cerevisiae, this enzyme catalyses an essential step in the outer chain elongation of N-linked oligosaccharides. Man8GlcNAc and Man9GlcNAc are equally good substrates. Group: Enzymes. Synonyms: α-1,6-mannosyltransferase; GDP-mannose:oligosaccharide 1,6-α-D-mannosyltransferase; GDP-mannose:glycolipid 1,6-α-D-mannosyltransferase; glycolipid 6-α-mannosyltransferase; GDP-mannose:oligosaccharide 1,6-α-D-mannosyltransferase. Enzyme Commission Number: EC 2.4.1.232. CAS No. 346003-17-6. 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-2462; initiation-specific α-1,6-mannosyltransferase; EC 2.4.1.232; 346003-17-6; α-1,6-mannosyltransferase; GDP-mannose:oligosaccharide 1,6-α-D-mannosyltransferase; GDP-mannose:glycolipid 1,6-α-D-mannosyltransferase; glycolipid 6-α-mannosyltransferase; GDP-mannose:oligosaccharide 1,6-α-D-mannosyltransferase. Cat No: EXWM-2462. |  |
| Injection Bottles | Injection Bottles. Product ID: PM-010. Product Keywords: Packaging Materials; Glass Packaging; PM-010; Injection Bottles. Color: Clear/Amber. |  |
| Injection Vials | Injection Vials. Product ID: PM-029. Product Keywords: Packaging Materials; Glass Packaging; PM-029; Injection Vials. | |
| Innovating Science Instant Light Powder, 20 g | Notes: the amount of glow time depends upon solution concentration and the temperature of both the room and the water; supports 5 demonstrations. Storage Code: Green; general chemical storage. Uses: Demonstrate chemiluminescence by combining this instant light powder with water to produce blue light. Grades: chem-grade laboratory. Product ID: 872600. -- SOLD FOR EDUCATIONAL USE ONLY -- |  |
| Inobrodib | Inobrodib (CCS1477) is an orally active, potent, and selective inhibitor of the p300/CBP bromodomain. Inobrodib binds to p300 and CBP with K d values of 1.3 and 1.7 nM, respectively, and with 170/130-fold selectivity compared with BRD4 with a K d of 222 nM. CCS1477 inhibits cell proliferation in prostate cancer cell lines and decreases androgen receptor (AR)- and C-MYC-regulated gene expression [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CCS1477. CAS No. 2222941-37-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-111784. |  |
| Inobrodib | Inobrodib is an inhibitor of the histone acetyltransferase p300 and CREB-binding protein and has antineoplastic activity. Synonyms: (6S)-1-(3,4-difluorophenyl)-6-[5-(3,5-dimethyl-1,2-oxazol-4-yl)-1-(trans-4-methoxycyclohexyl)-1H-benzimidazol-2-yl]piperidin-2-one; (S)-1-(3,4-difluorophenyl)-6-(5-(3,5-dimethylisoxazol-4-yl)-1-((1R,4S)-4-methoxycyclohexyl)-1H-benzo[d]imidazol-2-yl)piperidin-2-one; CBP-IN-1; CCS-1477; (6S)-1-(3,4-Difluorophenyl)-6-[5-(3,5-dimethyl-4-isoxazolyl)-1-(trans-4-methoxycyclohexyl)-1H-benzimidazol-2-yl]-2-piperidinone; CCS 1477; CCS1477. Grades: >98%. CAS No. 2222941-37-7. Molecular formula: C30H32F2N4O3. Mole weight: 534.60. | |
| Inolimomab | Inolimomab is an anti-interleukin-2 receptor ( IL-2R ) α chain monoclonal antibody. Inolimomab improves the survival rate in the early research of treating acute graft-versus-host disease (aGVHD) [1] [2]. Uses: Scientific research. Group: Inhibitory antibodies. CAS No. 152981-31-2. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99664. | |
| Inolitazone | Inolitazone is an orally bioavailable PAPR-gamma inhibitor with potential antineoplastic activity. Inolitazone binds to and activates peroxisome proliferation-activated receptor gamma (PPAR-gamma), which may result in the induction of tumor cell differentiation and apoptosis, and so a reduction in tumor cell proliferation. PPAR-gamma is a nuclear hormone receptor and ligand-activated transcription factor controlling gene expression involved in such cellular processes as differentiation, apoptosis, cell-cycle control, carcinogenesis, and inflammation. Synonyms: CS-7017, CS7017; CS 7017; RS5444; RS-5444; RS 5444; Efatutazone; PPAR-gamma agonist CS-7017, CS-7017, RS5444. Efatutazone. CAS No. 223132-37-4. Molecular formula: C27H26N4O4S. Mole weight: 502.58. | |
| Inolitazone dihydrochloride | In vitro, the IC50 for growth inhibition is approximately 0.8 nM while anaplastic thyroid carcinoma (ATC) tumor growth was inhibited three- to fourfold in nude mice. siRNA against PPARgamma and a pharmacological antagonist demonstrated that functional PPARgamma was required for growth inhibitory activity of RS5444. RS5444 upregulated the cell cycle kinase inhibitor, p21WAF1/CIP1. RS5444inhibited culture growth and caused irreversible G1 arrest, but did not induce apoptosis. In addition, RS5444 caused dramatic changes in cellular morphology which were associated with increased motility and diminished cellular adherence, but no increase in the ability of such cells to digest and invade Matrigel. Treatment with RS5444 leads to the up-regulation of RhoB and subsequent activation of p21, and that silencing of RhoB by RNAi blocks the ability of RS5444 to induce p21 and to inhibit ATC cells proliferation. The median peak efatutazone blood level was 8.6 ng/mL for 0.15-mg dosing vs 22.0 ng/mL for 0.3-mg twice daily dosing. Although efatutazone treatment did not reduce percentage of mice developing invasive cancer, it significantly reduced prevalence of noninvasive cancer and total number of cancers per mouse and increased prevalence of well-differentiated cancer subtypes not usually seen in this mouse model. Uses: Antineoplastic agents. Synonyms: Efatutazone; Efatutazone hydrochloride; CS 7017; CS-7017; CS7017 ;RS-5444; RS5444; UNII-76B44WEA8O. Grades: >98%. CAS No. 223132-38-5. Molecular formula: C27H28Cl2N4O4S. Mole weight: 575.51. | |
| Inonotus Obliquus Extract | Inonotus Obliquus Extract. Applications: It ues for treat diabetes. anticancer.prevent and cure aids,antiaging.inhibit infectious virus.prevent high blood pressure.relieve and prevent allergic cortex.have obvious curative effect on hepatitis, gastritis, duodenal ulcer, nephritis. Group: Others. Synonyms: Inonotus Obliquus Extract; Fuscoporia obliqua. Purity: 20%-30% Polysaccharides. Appearance: Brown fine powder. Storage: 2 years under well storage situation and stored away from direct sun light. Source: Fruit. Species: Fuscoporia obliqua. Inonotus Obliquus Extract; Fuscoporia obliqua; plant extract. Pack: 25KG/Drum with double plastic bag of foodstuff inside. Cat No: EXTW-171. | |
| Inophyllum b | Inophyllum B ((+)-Inophyllum B) is a potent HIV Reverse Transcriptase inhibitor with an IC50 value of 38 nM. Inophyllum B inhibits HIV-1 (IC50=1.4 μM) in vitro cell culture. Inophyllum B can be isolated from the acetone extract of the giant African snail, Achatina fulica. Group: Inhibitors. CAS No. 41135-06-2. Catalog: ACM41135062. |  |
| Inophyllum E | Inophyllum E is a natural product [1]. Uses: Scientific research. Group: Natural products. CAS No. 17312-31-1. Pack Sizes: 1 mg; 5 mg. Product ID: HY-N13645. | |
| inorganic diphosphatase | Specificity varies with the source and with the activating metal ion. The enzyme from some sources may be identical with EC 3.1.3.1 (alkaline phosphatase) or EC 3.1.3.9 (glucose-6-phosphatase). A form of this enzyme with a molecular mass of about 90 kDa is found in tonoplasts of plants and fungi, where it imports protons from the cytosol into the vacuolar lumen. Group: Enzymes. Enzyme Commission Number: EC 3.6.1.1. CAS No. 9024-82-2. Inorganic pyrophosphatase. 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-4593; inorganic diphosphatase; EC 3.6.1.1; 9024-82-2. Cat No: EXWM-4593. | |
| Inorganic Diphosphatase (Crude Enzyme) | This enzyme belongs to the family of hydrolases, specifically those acting on acid anhydrides in phosphorus-containing anhydrides. This product with the indicated enzyme activity was briefly purified from engineered E. coli. Applications: Molecular biology; synthesis; drug development. Group: Enzymes. Enzyme Commission Number: EC 3.6.1.1. CAS No. 9024-82-2. Inorganic pyrophosphatase. Activity: Undetermined. Appearance: Clear to translucent yellow solution. Storage: at -20 °C or lower, for at least 1 month. Source: E. coli. Inorganic pyrophosphatase. Pack: 100ml. Cat No: NATE-1843. | |
| Inorganic perovskite quantum dots CsPbX3 | Inorganic perovskite quantum dots CsPbX3. Group: Inorganic perovskite quantum dots cspbx3. |  |
| Inorganic Pyrophosphatase from Escherichia coli, Recombinant | Pyrophosphatase (or inorganic pyrophosphatase) is an enzyme (EC 3.6.1.1) that catalyzes the conversion of one molecule of pyrophosphate to two phosphate ions. This is a highly exergonic reaction, and therefore can be coupled to unfavorable biochemical transformations in order to drive these transformations to completion. The functionality of this enzyme plays a critical role in lipid metabolism (including lipid synthesis and degradation), calcium absorption and bone formation, and DNA synthesis,as well as other biochemical transformations. Applications: Inorganic pyrophosphatase (ppase) is a ubiquitous enzyme catalyzing the reaction ppi + h2o ? 2pi. it plays an important role in protein, rna, and dna synthesis. Group: Enzymes. Synonyms: Pyrophosphate phosphohydrolase; inorganic pyrophosphatase; EC 3.6.1.1; 9024-82-2; iphosphate phosphohydrolase. Enzyme Commission Number: EC 3.6.1.1. CAS No. 9024-82-2. Purity: > 90%. Inorganic pyrophosphatase. Activity: > 800 units/mg protein. Storage: -20°C. Form: Lyophilized powder in Tris-buffered salts containing protease inhibitors. Source: E. coli. Species: Escherichia coli. Pyrophosphate phosphohydrolase; inorganic pyrophosphatase; EC 3.6.1.1; 9024-82-2; iphosphate phosphohydrolase. Cat No: NATE-0355. | |
| Inorganic Pyrophosphatase from Saccharomyces cerevisiae, Recombinant | Pyrophosphatase (or inorganic pyrophosphatase) is an enzyme (EC 3.6.1.1) that catalyzes the conversion of one molecule of pyrophosphate to two phosphate ions. This is a highly exergonic reaction, and therefore can be coupled to unfavorable biochemical transformations in order to drive these transformations to completion. The functionality of this enzyme plays a critical role in lipid metabolism (including lipid synthesis and degradation), calcium absorption and bone formation, and DNA synthesis,as well as other biochemical transformations. Inorganic pyrophosphatase (ppase) catalyzes the hydrolysis of inorganic pyrophosphate to form orthophosphate. a variety ...actions that can be pulled far in the synthesis direction by the action of inorganic pyrophosphatase. Applications: Enhancing yields of rna in transcription reactions. Group: Enzymes. Synonyms: Pyrophosphate phosphohydrolase; inorganic pyrophosphatase; EC 3.6.1.1; 9024-82-2; iphosphate phosphohydrolase. CAS No. 9024-82-2. Inorganic pyrophosphatase. Mole weight: 71 kDa. Storage: at -20°C. Form: 20 mM Tris-HCl (pH 8.0), 100 mM KCl, 0.1 mM EDTA, 1 mM dithiothreitol and 50% glycerol. Source: E. coli. Species: Saccharomyces cerevisiae. Pyrophosphate phosphohydrolase; inorganic pyrophosphatase; EC 3.6.1.1; 9024-82-2; iphosphate phosphohydrolase. Cat No: NATE-1281. | |
| Inorganic pyrophosphatase, Saccharomyces cerevisiae | Inorganic pyrophosphatase, Saccharomyces cerevisiae (PPase) converts pyrophosphate (PPi) to phosphate. Inorganic pyrophosphatase is an essential component of in vitro transcription reactions for RNA preparation, is often used in biochemical studies. Inorganic pyrophosphatase is critical for driving cellular processes such as nucleic acid and protein synthesis [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: PPase. CAS No. 9024-82-2. Pack Sizes: 100 U. Product ID: HY-P2992. | |
| Inorganic Silica Core/Shell Nanoparticles | Inorganic Silica Core/Shell Nanoparticles. Group: Core shell nanoparticles. 99.9%. | |
| Inosamycin A | Inosamycin A is a broad-spectrum antimicrobial antibiotic originally isolated from Str. hygroscopicus No. J296-21. Its antibacterial activity was comparable to that of neomycin, and about twice that of ribomycin. Synonyms: Bu 2659A; 6-Amino-2-{[3-O- (2, 6-diamino-2, 6-dideoxyhexopyranosyl) pentofuranosyl]oxy}-3, 4-dihydroxycyclohexyl 2,6-diamino-2,6-dideoxyhexopyranoside. CAS No. 91421-97-5. Molecular formula: C23H45N5O14. Mole weight: 615.63. | |
| Inosamycin B | Inosamycin B is a broad-spectrum antimicrobial antibiotic originally isolated from Str. hygroscopicus No. J296-21. Its antibacterial activity is about half that of Inosamycin A. Synonyms: Bu 2659B; BMY-28163; 4-O-(2,6-Diamino-2,6-dideoxy-α-D-glucopyranosyl)-5-O-[3-O-(2,6-diamino-2,6-dideoxy-α-D-glucopyranosyl)-β-D-ribofuranosyl]-3-amino-2,3-dideoxy-D-myo-inositol. CAS No. 91465-52-0. Molecular formula: C23H45N5O14. Mole weight: 615.63. | |
| inosinate nucleosidase | This enzyme belongs to the family of hydrolases, specifically those glycosylases that hydrolyse N-glycosyl compounds. The systematic name of this enzyme class is 5'-inosinate phosphoribohydrolase. This enzyme participates in purine metabolism. Group: Enzymes. Synonyms: 5'-inosinate phosphoribohydrolase. Enzyme Commission Number: EC 3.2.2.12. CAS No. 37288-61-2. 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-3966; inosinate nucleosidase; EC 3.2.2.12; 37288-61-2; 5'-inosinate phosphoribohydrolase. Cat No: EXWM-3966. | |
| Inosine | Inosine. Categories: inosine; 58-63-9. |  CA, FL & NJ |
| Inosine | 100g Pack Size. Group: Biochemicals, Carbohydrates. Formula: C10H12N4O5. CAS No. 58-63-9. Prepack ID 51213659-100g. Molecular Weight 268.23. See USA prepack pricing. |  |
| Inosine | Inosine. Synonyms: (-)-Inosine, Hypoxanthine 9-β-D-ribofuranoside. CAS No. 58-63-9. Pack Sizes: 1, 5, 10, 25, 100 g in poly bottle. Product ID: CDC10-0576. Molecular formula: C10H12N4O5. Category: Skin protectants. Product Keywords: Cosmetic Ingredients; Active Ingredients; Skin protectants; Inosine; CDC10-0576; 58-63-9; C10H12N4O5; (-)-Inosine, Hypoxanthine 9-β-D-ribofuranoside; 200-390-4; MFCD00066770; 58-63-9. Purity: ≥99% (HPLC). EC Number: 200-390-4. Quality Level: 200. Melting Point: 222-226 °C (dec.) (lit.). | |
| Inosine | Inosine. Group: Biochemicals. Grades: Highly Purified. CAS No. 58-63-9. Pack Sizes: 100g, 250g, 500g, 1kg, 2kg. Molecular Formula: C10H12N4O5. US Biological Life Sciences. | Worldwide |
| Inosine | Inosine is an endogenous purine nucleoside produced by catabolism of adenosine. Inosine has anti-inflammatory, antinociceptive, immunomodulatory and neuroprotective effects. Inosine is an agonist for adenosine A 1 ( A 1 R ) and A 2A ( A 2A R ) receptors [1] [2] [3]. Uses: Scientific research. Group: Natural products. CAS No. 58-63-9. Pack Sizes: 10 mM * 1 mL; 500 mg; 25 g. Product ID: HY-N0092. | |
| Inosine | Inosine is a nucleoside that is formed when hypoxanthine is attached to a ribose ring (also known as a ribofuranose) via a β-N9-glycosidic bond. Uses: Coenzymes. Synonyms: 1,9-Dihydro-9-β-D-ribofuranosyl-6H-purin-6-one; 9-β-D-Ribofuranosylhypoxanthine; Hypoxanthine 9-β-D-ribofuranoside; Hypoxanthine Ribonucleoside; Hypoxanthine Riboside; Hypoxanthosine; Ribonosine; Atorel; Oxiamin; Trophicardyl; Selfer. Grades: ≥98% by HPLC. CAS No. 58-63-9. Molecular formula: C10H12N4O5. Mole weight: 268.23. | |
| Inosine-15N4 | Inosine is a non-canonical purine nucleoside commonly found in tRNAs. Uses: Biomolecular nmr, genetic therapy, metabolism, metabolomics. Group: 15n labeled compounds. Alternative Names: 9-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1H-purin-6-one; Hypoxanthosine; Hypoxanthine D-riboside. CAS No. 204634-01-5. Molecular formula: C10H1215N4O5. Mole weight: 272.2. Appearance: Individual. Canonical SMILES: O[C@H]1[C@] (O[C@@H] ([C@H]1O)CO) ([H])[15N]2C3=C (C ([15N]=C[15NH]3)=O)[15N]=C2. ECNumber: 200-390-4. Catalog: ACM204634015. | |
| Inosine 2',3'-cyclic monophosphate sodium salt | Inosine 2',3'-cyclic monophosphate sodium salt is an indispensable compound extensively employed in the biomedical field, manifesting its significance through the research of diverse afflictions including cardiovascular dysfunctions, malignant tumors and neurodegenerative ailments. Functioning as a facilitator of signal transduction regulation, this product remarkably orchestrates cellular reactions. Synonyms: 2',3' cyclic IMP. CAS No. 15569-30-9. Molecular formula: C10H11N4O7P. Mole weight: 330.19. | |
| Inosine, 2'-deoxy-, 3', 5'-diacetate(9ci) | Heterocyclic Organic Compound. Alternative Names: 3'-5'-DI-O-ACETYL-2'-DEOXYINOSINE. CAS No. 106568-79-0. Molecular formula: C14H16N4O6. Mole weight: 336.3. Purity: 0.96. IUPACName: 3-5-DI-O-ACETYL-2-DEOXYINOSINE. Catalog: ACM106568790. | |
| Inosine-3',5'-cyclic-monophosphate | Inosine-3',5'-cyclic-monophosphate, a multifaceted signaling molecule, participates in diverse physiological processes including muscle contraction, neurotransmission, and ion channel regulation. This intriguing biomolecule has captivated scientific attention for its prospective therapeutic applications in neurological disorders, cardiovascular pathologies, and malignant conditions. Its aptitude in promoting neuroprotection and augmenting synaptic plasticity renders it a fascinating candidate for tackling the symptoms of Alzheimer's and various other neurodegenerative afflictions. Synonyms: 3',5'-Cyclic IMP. CAS No. 3545-76-4. Molecular formula: C10H11N4O7P. Mole weight: 330.19. | |
| Inosine-3',5'-cyclic-monophosphate free acid | Inosine-3',5'-cyclic-monophosphate free acid. Group: Biochemicals. Grades: Highly Purified. CAS No. 3545-76-4. Pack Sizes: 1mg, 5mg, 10mg. Molecular Formula: C10H11N4O7P. US Biological Life Sciences. | Worldwide |
| Inosine-3',5'-cyclic Monophosphate Sodium Salt | Inosine-3',5'-cyclic monophosphate is a cyclic nucleotide that stimulates steroidogenesis by adrenocortical cells in rats. Inosine-3',5'-cyclic monophosphate also stimulates insulin secretion in hamster pancreas cells. Synonyms: Inosine Cyclic 3',5'-(Hydrogen Phosphate) Sodium Salt; Inosine 3',5'-Phosphate (Cyclic) Sodium Salt; Inosine Cyclic 3',5'-(Hydrogen Phosphate) Monosodium Salt; 4H-Furo[3,2-d]-1,3,2-dioxaphosphorin Inosine Deriv.; 3',5'-cIMP Sodium Salt. Grades: 95%. CAS No. 41092-64-2. Molecular formula: C10H10N4NaO7P. Mole weight: 352.17. | |
| Inosine-3',5'-cyclic-monophosphate triethylammonium | Inosine-3',5'-cyclic-monophosphate triethylammonium is an indispensable compound extensively employed in the biomedical sector, operating as a pivotal second messenger in manifold cellular pathways. Its paramount significance lies in its indispensable role in studying signal transduction, gene expression and cellular metabolism, thereby facilitating research endeavors concerning drug development, particularly focused on cardiovascular, neurological and immune-related maladies. Molecular formula: C10H11N4O7P·NC6H15. Mole weight: 431.38. | |
| Inosine-5'-diphosphate | Inosine-5-diphosphate is a nucleoside diphosphate that is indubitably vital to cellular energy metabolism. It serves as a crucial substrate for enzymes involved in purine salvage pathways and contributes to the biosynthesis of purine nucleotides. Additionally, IDP has been linked to an array of signal transduction pathways and has the ability to modulate the activity of ion channels. There is promising potential for IDP to become an effective therapy option for diseases characterized by purine metabolism imbalances. Synonyms: Inosine diphosphate; Riboxin; Inosine 5'-pyrophosphate; IDP; riboxine; Inosine pyrophosphate; Inosine 5'-(trihydrogen diphosphate); 9-{5-O-[Hydroxy(phosphonooxy)phosphoryl]-β-D-ribofuranosyl}-9H-purin-6-ol; 5'-IDP; Inosine 5'-diphosphoric acid. Grades: ≥98% by HPLC. CAS No. 86-04-4. Molecular formula: C10H14N4O11P2. Mole weight: 428.19. | |
| Inosine 5'-diphosphate disodium salt | Inosine 5'-diphosphate disodium salt, a pivotal biochemical compound sought after in the biomedical industry, assumes an indispensable function in the generation and modulation of intracellular signaling molecules. Given its implication in cellular energy metabolism and nucleotide biosynthesis, this particular product finds application in ameliorating distinct metabolic disorders and neurodegenerative ailments. Synonyms: Inosine 5'-(trihydrogen diphosphate), disodium salt. Grades: 95%. CAS No. 54735-61-4. Molecular formula: C10H12N4O11P2·2Na. Mole weight: 472.15. | |
| Inosine 5'-diphosphate disodium salt | Inosine 5'-diphosphate disodium salt. Group: Biochemicals. Grades: Highly Purified. CAS No. 54735-61-4. Pack Sizes: 25g, 50g, 100g, 250g, 500g. Molecular Formula: C10H12N4O11P2·2Na. US Biological Life Sciences. | Worldwide |
| Inosine 5-diphosphate sodium | Inosine 5-diphosphate sodium is a purine ribonucleoside 5-diphosphate with inosine as the nucleobase, which can participate in intracellular energy metabolism and signal transduction processes [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 81012-88-6. Pack Sizes: 25 mg; 50 mg; 100 mg. Product ID: HY-W749117. | |
| Inosine 5'-diphosphate trisodium salt | Inosine 5'-diphosphate trisodium salt is a pivotal constituent in the biomedical field, serving as a precursor for crucial molecules engaged in cellular processe. Its applied scope encompasses the synthesis of paramount compounds pertinent to studying viral invasions, immune disorders and select cancerous conditions. Synonyms: IDP 3Na; Inosine-5'-diphosphoric acid trisodium salt. Grades: ≥ 93% (HPLC). CAS No. 81012-88-6. Molecular formula: C10H11N4O11P2·3Na. Mole weight: 494.13. | |
| Inosine-5'-diphosphate trisodium salt | Synonyms: IDP; IDP, NA3; INOSINE 5'-DIPHOSPHATE SODIUM SALT; INOSINE-5'-DIPHOSPHORIC ACID, TRISODIUM; 5'-IDP 3NA; 5'-IDP-NA3; Inosine 5'-(trihydrogen diphosphate), trisodium salt; Inosine-5'-diphosphatetrisodiumsaltbyu.v. CAS No. 71672-86-1. Molecular formula: C10H11N4Na3O11P2. Mole weight: 494.13. | |
| Inosine-5'-diphosphate trisodium salt ≥93% (HPLC) | Inosine-5'-diphosphate trisodium salt ≥93% (HPLC). Group: Biochemicals. Grades: Reagent Grade. CAS No. 81012-88-6. Pack Sizes: 100mg, 250mg, 1g. US Biological Life Sciences. | Worldwide |
| Inosine 5'-monophosphate | Inosine 5'-monophosphate (IMP) is a profound molecular compound magnanimously entrusted with the profound responsibility of studying an extensive array of afflictions, encompassing neurologic dysfunctions, cardiac anomalies and immunological imperfections. Synonyms: Inosinic acid; IMP; 1-5'-P; inosinemonophosphate; [(2R,3S,4R,5R)-3,4-dihydroxy-5-(6-oxo-1H-purin-9-yl)oxolan-2-yl]methyl dihydrogen phosphate. Grades: ≥ 98%. CAS No. 131-99-7. Molecular formula: C10H13N4O8P. Mole weight: 348.20. | |
| Inosine 5'-monophosphate | Inosine 5'-monophosphate. Group: Biochemicals. Alternative Names: Inosinic acid; IMP. Grades: Highly Purified. CAS No. 131-99-7. Pack Sizes: 500mg, 1g, 2g, 5g. Molecular Formula: C10H13N4O8P. US Biological Life Sciences. | Worldwide |
| Inosine 5'-monophosphate disodium salt | Disodium inosinate (E631) is the disodium salt of inosinic acid with the chemical formula C10H11N4Na2O8P. It is used as a food additive and often found in instant noodles, potato chips, and a variety of other snacks. This salt is used as a flavor enhancer made from microbial fermentation growth media that are all-vegetable, usually consisting mainly of tapioca starch. Synonyms: Disodium 5'-inosinate; Disodium inosinate; Sodium Inosine 5'-Phosphate (2:1); 5'-Inosinic Acid Disodium Salt; 5'-IMP Disodium Salt; Disodium 5'-IMP; Disodium 5'-Inosinate; Disodium IMP; Disodium Inosinate; Disodium Inosine 5'-Monophosphate; Disodium Inosine 5'-Phosphate; IMP Disodium Salt; Inosine 5'-Monophosphate Disodium Salt; Inosine 5'-Monophosphoric Acid Disodium Salt. Grades: ≥97% by HPLC. CAS No. 4691-65-0. Molecular formula: C10H11N4Na2O8P. Mole weight: 392.17. | |
| Inosine-5'-monophosphate disodium salt heptahydrate | Inosine-5'-monophosphate disodium salt heptahydrate, an indispensable intermediate in purine biosynthesis, possesses a crucial role in nucleotide metabolism. Its applications primarily encompass functions such as treating gout and hyperuricemia while simultaneously enhancing the production of ribonucleotides. Synonyms: Sodium 5'-Inosinate hydrate (2:1:7). Grades: 98%. CAS No. 849725-39-9. Molecular formula: C10H25N4Na2O15P. Mole weight: 518.28. | |
| Inosine 5'-monophosphate disodium salt hydrate | Inosine 5'-monophosphate disodium salt hydrate. Group: Biochemicals. Grades: Highly Purified. CAS No. 4691-65-0,352195-40-5. Pack Sizes: 250g, 500g, 1kg, 2kg, 5kg. Molecular Formula: C10H11N4O8PNa2·xH2O. US Biological Life Sciences. | Worldwide |
| Inosine-5'-monophosphate disodium salt hydrate, 99-103% | Inosine-5'-monophosphate disodium salt hydrate, 99-103%. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 5g, 25g, 100g, 250g, 1Kg. US Biological Life Sciences. | Worldwide |
| Inosine-5-monophosphate disodium salt octahydrate | Inosine-5'-monophosphate disodium salt octahydrate is a purine nucleotide that can be used as an umami tastant as well as a precursor of GMP and AMP [1]. Uses: Scientific research. Group: Natural products. CAS No. 20813-76-7. Pack Sizes: 5 g. Product ID: HY-W010759. | |
| Inosine-5'-monophosphate disodium salt octahydrate | Inosine-5'-monophosphate disodium salt octahydrate, a pivotal compound in biomedicine, holds immense significance due to its involvement in the biosynthesis of purine and nucleoside derivatives. Synonyms: 5'-IMP-Na2; Disodium 5'-inosinate octahydrate. Grades: 98%. CAS No. 20813-76-7. Molecular formula: C10H27N4Na2O16P. Mole weight: 536.29. | |
| Inosine 5'-(tetrahydrogen triphosphate) | Inosine 5'-(tetrahydrogen triphosphate) is a bioactive organic molecule with immense therapeutic potential in addressing an array of ailments- from cancer, metabolic afflictions, to viral infections. It functions as an indispensable precursor for purine nucleotide synthesis, thereby stimulating ATP production, augmenting cellular energy reserves, and activating immune cells such as T-cells to ramp up response to various intruders. Synonyms: ITP; Hypoxanthine; Inosine-5'-Triphosphate. Grades: ≥98% by AX-HPLC. CAS No. 132-06-9. Molecular formula: C10H15N4O14P3. Mole weight: 508.10. | |
| Inosine 5'-(trihydrogendiphosphate),8-bromo-,disodium salt(9ci) | Heterocyclic Organic Compound. CAS No. 102185-44-4. Molecular formula: C10H13BrN4O11P2.2Na. Mole weight: 551.05. Catalog: ACM102185444. | |
| Inosine 5'-triphosphate disodium salt | Inosine 5'-triphosphate disodium salt, a nucleotide precursor to ATP, is a pivotal biochemistry molecule. Its utility in probing purine nucleotides' influence on enzyme activity, coupled with its broad applicability in enzymatic and biochemical assays, render it a versatile research tool. Its involvement in hindering leukemia occurrence through DNA incorporation and synthesis blockade further underscores its therapeutic potential. Synonyms: INOSINE-5-TRIPHOSPHORIC ACID SODIUM SALT; INOSINE-5'-TRIPHOSPHATE TRISODIUM SALT; sodium((2R,3S,4R,5R)-3,4-dihydroxy-5-(6-oxo-1H-purin-9(6H)-yl)tetrahydrofuran-2-yl)methyl dihydrogentriphosphate. Grades: ≥ 95%. CAS No. 36051-67-9. Molecular formula: C10H13N4O14P3·2Na. Mole weight: 552.13. | |
| Inosine 5'-triphosphate lithium salt | Inosine 5'-triphosphate lithium salt is a crucial element in the biomedical industry with antiviral properties. It plays a significant role in the research of various diseases, including viral infections and autoimmune disorders. Molecular formula: C10H15N4O14P3F. Mole weight: 527.16. | |
| Inosine 5'-triphosphate,periodate oxidized sodium salt | Heterocyclic Organic Compound. CAS No. 105208-87-5. Molecular formula: C10H12N4NaO14P3. Mole weight: 528.13. Catalog: ACM105208875. | |
| Inosine 5'-triphosphate trisodium salt | Inosine-5'-triphosphate, an inosine nucleotide, is an intermediate in the purine metabolism pathway. Synonyms: Inosine 5'-(Tetrahydrogen Triphosphate) Trisodium Salt; NSC 20266; Trisodium Inosine-5'-triphosphate; ITP; 9H-Purin-6-ol, 9-[5-O-[hydroxy[[hydroxy (phosphonooxy) phosphinyl]oxy]phosphinyl]-β -D-ribofuranosyl]-, sodium salt (1:3); Trisodium 5'-O-[ ({[ (hydroxyphosphinato) oxy]phosphinato}oxy) phosphinato]inosine. Grades: ≥97% by HPLC. CAS No. 35908-31-7. Molecular formula: C10H12N4O14P3.3Na. Mole weight: 574.11. | |
| Inosine-5'-triphosphate trisodium salt | Inosine-5'-triphosphate trisodium salt is a nucleoside triphosphate and functions as an substrate for ATPases and GTPases [1] [2] [3] [4]. Uses: Scientific research. Group: Natural products. CAS No. 35908-31-7. Pack Sizes: 50 mg; 100 mg. Product ID: HY-W013706. | |
| Inosine 5-Triphosphate Trisodium Salt | Inosine 5 Triphosphate Trisodium Salt is used in studies where ATP and GTP are deaminated by various enzymes and biological processes. This can help with kinetics studies of enzymes as well. Group: Biochemicals. Alternative Names: Inosine 5-(Tetrahydrogen Triphosphate) Trisodium Salt; NSC 20266; Trisodium Inosine-5-triphosphate. Grades: Highly Purified. CAS No. 35908-31-7. Pack Sizes: 100mg, 250mg, 500mg, 1g. Molecular Formula: C??H??N?Na?O??P?, Molecular Weight: 577.14. US Biological Life Sciences. | Worldwide |
| Inosine 99+% | Inosine 99+%. Group: Biochemicals. Grades: Reagent Grade. CAS No. 58-63-9. Pack Sizes: 5g, 25g, 100g, 250g, 1Kg. US Biological Life Sciences. | Worldwide |
| inosine diphosphate phosphatase | The human enzyme also hydrolyses GDP and dGDP, and to a lesser extent ITP, dITP and XTP. Group: Enzymes. Synonyms: (deoxy)inosine diphosphatase; NUDT16. Enzyme Commission Number: EC 3.6.1.64. 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-4637; inosine diphosphate phosphatase; EC 3.6.1.64; (deoxy)inosine diphosphatase; NUDT16. Cat No: EXWM-4637. | |
| inosine kinase | This enzyme belongs to the family of transferases, specifically those transferring phosphorus-containing groups (phosphotransferases) with an alcohol group as acceptor. The systematic name of this enzyme class is ATP:inosine 5'-phosphotransferase. Other names in common use include inosine-guanosine kinase, and inosine kinase (phosphorylating). This enzyme participates in purine metabolism. Group: Enzymes. Synonyms: inosine-guanosine kinase; inosine kinase (phosphorylating). Enzyme Commission Number: EC 2.7.1.73. CAS No. 37237-46-0. 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-3103; inosine kinase; EC 2.7.1.73; 37237-46-0; inosine-guanosine kinase; inosine kinase (phosphorylating). Cat No: EXWM-3103. | |
| Inosine Monophosphate Dehydrogenase from Staphylococcus aureus, Recombinant | E.coli. Applications: Impdh is a recombinant protein of ca. 53kda cloned by pcr amplification of guab gene of staphylococcus aureus and expressed in e.coli. Group: Enzymes. Synonyms: inosine-5'-phosphate dehydrogenase; inosinic acid dehydrogenase; inosinate dehydrogenase; inosine 5'-monophosphate dehydrogenase; inosine monophosphate dehydrogenase; IMP oxidoreductase; inosine monophosphate oxidoreductase; IMP dehydrogenase; IMP:NAD+ oxidoreductase; EC 1.1.1.205; IMPDH. Enzyme Commission Number: EC 1.1.1.205. CAS No. 9028-93-7. IMPDH2. Mole weight: 53kDa. Activity: ≥ 0.3 unit/mg protein. Source: S. aureus. Species: IMPDH2. inosine-5'-phosphate dehydrogenase; inosinic acid dehydrogenase; inosinate dehydrogenase; inosine 5'-monophosphate dehydrogenase; inosine monophosphate dehydrogenase; IMP oxidoreductase; inosine monophosphate oxidoreductase; IMP dehydrogenase; IMP:NAD+ oxidoreductase; EC 1.1.1.205; IMPDH. Pack: stable lyophilized form. Cat No: NATE-1739. | |
| Inosine Monophosphate Dehydrogenase Type II from Human, Recombinant | Type II is the predominant IMPDH isoform and is specifically linked to a wide range of cancers and lymphocyte proliferation. Group: Enzymes. Synonyms: inosine-5'-phosphate dehydrogenase; inosinic acid dehydrogenase; inosinate dehydrogenase; inosine 5'-monophosphate dehydrogenase; inosine monophosphate dehydrogenase; IMP oxidoreductase; inosine monophosphate oxidoreductase; IMP dehydrogenase; IMP:NAD+ oxidoreductase; EC 1.1.1.205; IMPDH II; IMPDH2; IMPD 2. Enzyme Commission Number: EC 1.1.1.205. CAS No. 231-791-2. IMPDH2. Storage: -70°C. Form: Solution in 20 mM Tris-HCl, pH 8.0, containing 0.5 mM EDTA and 1 mM DTT. Source: E. coli. Species: Human. inosine-5'-phosphate dehydrogenase; inosinic acid dehydrogenase; inosinate dehydrogenase; inosine 5'-monophosphate dehydrogenase; inosine monophosphate dehydrogenase; IMP oxidoreductase; inosine monophosphate oxidoreductase; IMP dehydrogenase; IMP:NAD+ oxidoreductase; EC 1.1.1.205; IMPDH II; IMPDH2; IMPD 2. Pack: vial of > 0.002 unit. Cat No: NATE-0352. | |
| inosine nucleosidase | This enzyme belongs to the family of hydrolases, specifically those glycosylases that hydrolyse N-glycosyl compounds. The systematic name of this enzyme class is inosine ribohydrolase. Other names in common use include inosinase, and inosine-guanosine nucleosidase. This enzyme participates in purine metabolism. Group: Enzymes. Synonyms: inosinase; inosine-guanosine nucleosidase. Enzyme Commission Number: EC 3.2.2.2. CAS No. 9030-95-9. 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-3973; inosine nucleosidase; EC 3.2.2.2; 9030-95-9; inosinase; inosine-guanosine nucleosidase. Cat No: EXWM-3973. | |
| Inosine pranobex | Inosine pranobex is an orally active immunomodulator. Inosine pranobex has broad-spectrum antiviral activity. Inosine pranobex inhibits human immunodeficiency virus (HIV), herpes simplex virus (HSV), vaccinia virus (VACV), human tumor virus (HPV), Cytomegalovirus, influenza virus (INFV), parainfluenza virus (PIV), and Epstein-Barr virus [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Imunovir; Delimmun; Groprinosin. CAS No. 36703-88-5. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g; 5 g. Product ID: HY-107801. | |
| Inosinic acid | Inosinic acid is an endogenous metabolite. Inosinic acid is used as umami tastant, or as the dietary supplement to improve the yield and meat quality of pigs [1]. Uses: Scientific research. Group: Natural products. Alternative Names: 5'-IMP; IMP; Inosine 5'-(dihydrogen phosphate). CAS No. 131-99-7. Pack Sizes: 25 mg; 50 mg; 100 mg. Product ID: HY-108213. | |
| Inositol | Inositol is revered as vitamin B8, used for studying diabetes mellitus. Synonyms: Cyclohexane-1,2,3,4,5,6-hexaol; Hexahydroxycyclohexane; Inosite; NSC 25142; NSC 55551; NSC 8101. Grades: ≥95%. CAS No. 6917-35-7. Molecular formula: C6H12O6. Mole weight: 180.16. | |
| Inositol | Inositol is a unique new botanical complex which is processed from the fruits of Ceratonia Siliqua (carob tree). It is a multi-action tanning compound, which activates the main melanogenesis pathway thus intensifying and maintaining a suntan longer. Since it stimulates both immediate and delayed tanning, it can be applied to 'before-tanning' formulations such as sunscreens, tan accelerators, day facial creams and 'after-tanning' formulations such as tan-prolonging products, after-sun creams and lotions. Uses: Tan-prolonging products, after-sun creams and lotions. Alternative Names: Meso-inositol. CAS No. 87-89-8. Molecular formula: C6H12O6. Mole weight: 180.16. Appearance: Solid. Purity: 0.98. IUPACName: Cyclohexane-1,2,3,4,5,6-hexol. Canonical SMILES: C1(C(C(C(C(C1O)O)O)O)O)O. Density: 1.75 g/cm³. Catalog: ACM87898. | |
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