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| Product | Description | |
|---|---|---|
| Ingenol | Ingenol - Product ID: NST-10-168. Category: Terpenes. Alternative Names: (-)-Ingenol. Purity: 98%. Test method: HPLC. CAS No. 30220-46-3. Pack Sizes: 0,05g, 0,1g, 0,25g, 0,5g. Appearance: White powder. Molecular formula: C20H26O5. Mole weight: 348.19. Storage: +2 +8 °C. |  |
| Ingenol-3,4:5,20-diacetonide | Ingenol-3,4:5,20-diacetonide. Group: Biochemicals. Grades: Plant Grade. CAS No. 77573-44-5. Pack Sizes: 20mg. Molecular Formula: C26H36O5, Molecular Weight: 428.56. US Biological Life Sciences. |  Worldwide |
| Ingenol-3-angelate | ?95% (HPLC). Group: Fluorescence/luminescence spectroscopy. |  |
| Ingenol-3-angelate | Ingenol 3-Angelate is a diterpenoid ester isolated from Euphorbia peplus that induces rapid cell death with keratinocytes and some cancer cell lines. Ingenol 3-Angelate is a protein kinase C activator that displays potent antileukemic activity. Ingenol 3-Angelate (ingenol mebutate) is used for treatment of actinic keratosis.Source:Semi-synthetic, the starting material ingenol was isolated from Euphorbia latyris. Group: Biochemicals. Grades: Highly Purified. CAS No. 75567-37-2. Pack Sizes: 1mg, 5mg. Molecular Formula: C25H34O6. US Biological Life Sciences. | Worldwide |
| Ingenol 3-Angelate | Ingenol 3-Angelate. Group: Biochemicals. Alternative Names: (2Z)-2-Methyl-2-butenoic Acid (1aR, 2S, 5R, 5aS, 6S, 8aS, 9R, 10aR) -1a, 2, 5, 5a, 6, 9, 10, 10a-Octahydro-5, 5a-dihydroxy-4- (hydroxymethyl) -1, 1, 7, 9-tetramethyl-11-oxo-1H-2, 8a-methanocyclopenta [a]cyclopropa [e]cyclodecen-6-yl Ester; 3-Angeloylingenol; 3-Ingenyl angelate; Euphorbia factor An1; Euphorbia factor H1; Ingenol mebutate; PEP 005; Picato. Grades: Highly Purified. CAS No. 75567-37-2. Pack Sizes: 2.5mg. Molecular Formula: C25H34O6, Molecular Weight: 430.53. US Biological Life Sciences. | Worldwide |
| Ingenol-3-mebutate | Ingenol-3-mebutate is a substance found in the sap of the plant Euphorbia peplus and an inducer of cell death. It is effective for field treatment of actinic keratoses, significantly reduced head and non-head actinic keratosis lesions. Synonyms: PEP005; PEP-005; PEP 005; ingenol-3-angelate; Ingenol mebutate. Grade: >98%. CAS No. 75567-37-2. Molecular formula: C25H34O6. Mole weight: 430.53. |  |
| Ingenol-5,20-acetonide | Intermediate and starting material for the synthesis and preparation of ingenol 3-ester derivatives. For use in chemical synthesis see references. Has improved shelf life compared to ingenol. Source:Semi-synthetic. Group: Biochemicals. Grades: Highly Purified. CAS No. 77573-43-4. Pack Sizes: 1mg, 5mg. Molecular Formula: C23H32O5. US Biological Life Sciences. | Worldwide |
| Ingenol Mebutate | Ingenol Mebutate is an active ingredient in Euphorbia peplus , acts as a potent PKC modulator, with K i s of 0.3, 0.105, 0.162, 0.376, and 0.171 nM for PKC-α, PKC-β, PKC-γ, PKC-δ, and PKC-ε, respectively, and has antiinflammatory and antitumor activity. Uses: Scientific research. Group: Natural products. Alternative Names: Ingenol 3-angelate; PEP005. CAS No. 75567-37-2. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-B0719. |  |
| Ingrain blue 1 | Ingrain blue 1. Uses: Designed for use in research and industrial production. Additional or Alternative Names: ,n31,n32]-,tetrachloride;alcian;copper(4++),[[n,n',n'',n'''-[29h,31h-phthalocyaninetetrayltetrakis[methyleneth;io[(dimethylamino)methylidyne]]]tetrakis[n-methylmethanaminiumato]](2-)-n29,n39;INGRAIN BLUE;INGRAIN BLUE I;INGRAIN BLUE 1;CI NO 74240. Product Category: Heterocyclic Organic Compound. Appearance: solid. CAS No. 33864-99-2. Molecular formula: C56H68Cl4CuN16S4. Mole weight: 1298.86. Purity: Dye content >60%. Product ID: ACM33864992. Alfa Chemistry ISO 9001:2015 Certified. |  |
| INH1 | INH1. Group: Biochemicals. Grades: Purified. CAS No. 313553-47-8. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| Inhibitor Library | A unique collection of 5700 inhibitors for research in cell signaling, high throughput screening (HTS) and high content screening (HCS) for new drugs; - Bioactivity and safety confirmed by pre-clinical research and clinical trials, and some of them are approved by FDA; - Covers various major targets including MAPK, PI3K, JAK, HDAC, VEGFR, CDK, etc. ; - Detailed compound information with structure, target, activity, IC50 value, and biological activity description; - Structurally diverse, medicinally active, and cell permeable; - NMR and HPLC validated to ensure high purity and quality. Uses: Scientific use. Product Category: L2000. Categories: Inhibitor Libraries. |  |
| Inhibitor removers | replacement packing, for removing tert-butylcatechol. Group: Lplc & flash columns; accessories. | |
| Inhibitor removers | replacement packing for removing hydroquinone and monomethyl ether hydroquinone. Group: Lplc & flash columns; accessories. | |
| Inhoffen lythgoe diol | Inhoffen lythgoe diol. Group: Biochemicals. Alternative Names: (b-S,1R,3aR,4S,7aR)-Octahydro-4-hydroxy-b,7a-dimethyl-1H-indene-1-ethanol; (1R,3aR,4S,7aR)-1-((S)-1-Hydroxypropan-2-yl)-7a-methyloctahydro-1H-inden-4-ol. Grades: Highly Purified. CAS No. 64190-52-9. Pack Sizes: 250mg, 500mg, 1g, 2g, 5g. Molecular Formula: C13H24O2. US Biological Life Sciences. | Worldwide |
| Inhoffen Lythgoe Diol. | A key intermediate for the preparation of Vitamin D metabolites and analogs. Group: Biochemicals. Alternative Names: ( βS,1R,3aR,4S,7aR)--Octahydro-4-hydroxy- β,7a-dimethyl- 1H-indene-1-ethanol. Grades: Highly Purified. CAS No. 64190-52-9. Pack Sizes: 500mg. US Biological Life Sciences. | Worldwide |
| Inhoffen lythgoe diol monotosylate | Inhoffen lythgoe diol monotosylate. Group: Biochemicals. Alternative Names: (b-S,1R,3aR,4S,7aR)-Octahydro-4-hydroxy-b,7a-dimethyl-1H-indene-1-ethanol 1- (4-Methyl Benzene sulfonate) . Grades: Highly Purified. CAS No. 66774-80-9. Pack Sizes: 100mg, 250mg, 500mg, 1g, 2g. Molecular Formula: C20H30O4S. US Biological Life Sciences. | Worldwide |
| INI-43 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| 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 |
| Iniparib | Iniparib (BSI-201) is an irreversible inhibitor of PARP1 , used in the research of triple negative breast cancer. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BSI-201; NSC-746045; IND-71677. CAS No. 160003-66-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg; 500 mg. Product ID: HY-12015. | |
| Iniparib | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| 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. | |
| Inner centromere protein (48-56) | A fragment of Inner centromere protein. Inner centromere protein (INCENP) is a component of the chromosomal passenger complex (CPC), which is an important regulator of mitosis. It can be used in Ovarian carcinoma research. | |
| INNO-206 | INNO-206 (Aldoxorubicin) is the 6-maleimidocaproyl hydrazone derivative prodrug of the anthracycline antibiotic doxorubicin (DOXO-EMCH) with antineoplastic activity. Uses: Adcs cytotoxin-linker. Synonyms: Doxorubicin-hydrazone-caproyl-maleimide; Aldoxorubicin; 2,5-Dihydro-2,5-dioxo-1H-pyrrole-1-hexanoic acid (2E)-2-[1-[(2S,4S)-4-[(3-amino-2,3,6-trideoxy-α-L-lyxo-hexopyranosyl)oxy]-1,2,3,4,6,11-hexahydro-2,5,12-trihydroxy-7-methoxy-6,11-dioxo-2-naphthacenyl]-2-hydroxyethylidene]hydrazide; 1H-Pyrrole-1-hexanoic acid, 2,5-dihydro-2,5-dioxo-, (2E)-2-[1-[(2S,4S)-4-[(3-amino-2,3,6-trideoxy-α-L-lyxo-hexopyranosyl)oxy]-1,2,3,4,6,11-hexahydro-2,5,12-trihydroxy-7-methoxy-6,11-dioxo-2-naphthacenyl]-2-hydroxyethylidene]hydrazide; INNO 206; INNO206. Grade: >98%. CAS No. 1361644-26-9. Molecular formula: C37H42N4O13. Mole weight: 750.75. | |
| 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. | |
| Inokosterone | Inokosterone. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Inokosterone. Product Category: Steroidal Compounds. CAS No. 15130-85-5. Molecular formula: C27H44O7. Mole weight: 480.64. Purity: 0.95. IUPACName: (2S,3R,5R,9R,10R,13R,14S,17S)-2,3,14-trihydroxy-10,13-dimethyl-17-[(2R,3R,6R)-2,3,7-trihydroxy-6-methylheptan-2-yl]-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one. Canonical SMILES: CC(CCC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O)CO. Density: 1.28g/cm³. Product ID: ACM15130855. Alfa Chemistry ISO 9001:2015 Certified. | |
| 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. | |
| 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. Uses: Designed for use in research and industrial production. Product Category: Inhibitors. CAS No. 41135-06-2. Product ID: ACM41135062. Alfa Chemistry ISO 9001:2015 Certified. | |
| 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. 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 | 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. 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. Categories: inosine; 58-63-9. |  CA, FL & NJ |
| inosine-[1',2',3',4',5'-13C5] | Isotope labelled analogue of (-)-Inosine, compound that exhibits neuroprotective properties by improving axonal wiring and has also been used stroke patients treatment to restore neural function. Synonyms: [1',2',3',4',5'-13C5]inosine; inosine-1',2',3',4',5'-13C5. Grade: 98%; 99% atom 13C. Molecular formula: C5[13C]5H12N4O5. Mole weight: 273.19. | |
| Inosine-[13C2,15N] | Inosine-13C2, 15N is a labelled Inosine, which is used to treat stroke patients to restore neural function. Synonyms: Inosine-13C2,15N; (-)-Inosine-13C2,15N. Grade: > 95%. Molecular formula: C8[13C]2H12N3[15N]O5. Mole weight: 271.20. | |
| Inosine-[15N4] | Inosine-[15N4] is the labelled analogue of 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. It has a role as a human metabolite, a Saccharomyces cerevisiae metabolite, an Escherichia coli metabolite and a mouse metabolite. Synonyms: (-)-Inosine-15N4. Grade: 98% by CP; 95% atom 15N. Molecular formula: C10H12[15N]4O5. Mole weight: 272.20. | |
| 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 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 processes. Its applied scope encompasses the synthesis of paramount compounds pertinent to studying viral invasions, immune disorders, and select cancerous conditions. Synonyms: 5'-IDP Na3; Inosine-5'-diphosphate, trisodium salt; Inosine 5'-(trihydrogen diphosphate), sodium salt (1:3); Inosine 5'-(trihydrogen diphosphate), trisodium salt; Inosine diphosphate trisodium salt; Inosine pyrophosphate trisodium salt; 5'-IDP trisodium salt; IDP trisodium salt. Grade: ≥98% by HPLC. 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'-diphosphate trisodium salt monohydrate | Inosine 5'-diphosphate trisodium salt monohydrate is a pivotal constituent in the biomedical field, serving as a precursor for crucial molecules engaged in cellular processes. Its applied scope encompasses the synthesis of paramount compounds pertinent to studying viral invasions, immune disorders, and select cancerous conditions. Synonyms: Inosine 5'-(trihydrogen diphosphate), trisodium salt, monohydrate; Inosine 5'-(trihydrogen diphosphate), sodium salt, hydrate (1:3:1); Inosine diphosphate trisodium salt, monohydrate; Inosine pyrophosphate trisodium salt, monohydrate; 5'-IDP trisodium salt, monohydrate; IDP trisodium salt, monohydrate. Grade: ≥93% by HPLC. CAS No. 81012-88-6. Molecular formula: C10H11N4Na3O11P2.H2O. Mole weight: 512.15. | |
| 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 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'-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. Grade: ≥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 5'-triphosphate trisodium salt hydrate | Inosine 5'-triphosphate trisodium salt hydrate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: INOSINE 5-TRIPHOSPHATE SODIUM SALT; 5-ITP 3Na Hydrate; Trisodium Inosine 5-Triphosphate Hydrate; itp; TRISODIUM INOSINE 5-TRIPHOSPHATE HYDRATE; trisodium inosine 5-triphosphate; Inosine 5-Triphosphate Trisodium Salt Hydrate; 5-ITPNa3; ITP.Na3; Inosine-5-triphosphatetrisodiumsalt; Inosine 5-triphosphate trisodium salt; 5-ITP 3Na; ITP SODIUM SALT; INOSINE 5-TRIPHOSPHATE SODIUM SALT HYDRATE. Appearance: WHITE POWDER. CAS No. 35908-31-7. Molecular formula: C10H12N4Na3O14P3. Mole weight: 574.11. Purity: 95+%. IUPACName: trisodium;[[[(2R,3S,4R,5R)-3,4-dihydroxy-5-(6-oxo-3H-purin-9-yl)oxolan-2-yl]methoxy-oxidophosphoryl]oxy-oxidophosphoryl]hydrogenphosphate. Canonical SMILES: C1=NC(=O)C2=C(N1)N(C=N2)C3C(C(C(O3)COP(=O)([O-])OP(=O)([O-])OP(=O)(O)[O-])O)O.[Na+].[Na+].[Na+]. Density: 2.63g/cm³. Product ID: ACM35908317. Alfa Chemistry ISO 9001:2015 Certified. | |
| Inosine-8-14c | Inosine-8-14c. Uses: Designed for use in research and industrial production. Additional or Alternative Names: INOSINE-8-14C. Product Category: Heterocyclic Organic Compound. CAS No. 3926-71-4. Molecular formula: C10H12N4O5. Mole weight: 270.24. Product ID: ACM3926714. Alfa Chemistry ISO 9001:2015 Certified. | |
| 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. | |
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