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| Product | Description | |
|---|---|---|
| Gentamicin X2 | One of several different components found in standard grade Gentamicin. Gentamicin is an aminoglycoside antibiotic. Synonyms: O-2-Amino-2-deoxy-α-D-glucopyranosyl-(1?4)-O-[3-deoxy-4-C-methyl-3-(methylamino)-β-L-arabinopyranosyl-(1?6)]-2-deoxy-D-streptamine; Gentamicin X. Grades: ≥98.0%. CAS No. 36889-17-5. Molecular formula: C19H38N4O10. Mole weight: 482.53. |  |
| Gentamicin X2 | Gentamicin X2. Group: Biochemicals. Grades: Highly Purified. CAS No. 36889-17-5. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C19H38N4O10. US Biological Life Sciences. |  Worldwide |
| Gentamycin B | Gentamycin B is an aminoglycoside antibiotic coproduced as a minor component in the gentamicin fermentation. It was found to have the same antibacterial spectrum as gentamicin in vitro and in vivo. Synonyms: Sch-14342; Sch 14342. Molecular formula: C19H38N4O10. Mole weight: 482.5. | |
| Gentamycin (Gentamicin) (BSA) | Precursor: Gentamycin Sulfate. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Gentamycin (Gentamicin) (HRP) | Gentamicin is a broad-spectrum antibiotic derived from an actinomycete of the genus Micromonospora, used in its sulfate form to treat various infections. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Gentamycin (Gentamicin) Sulfate Solution 10mg/ml | Broad spectrum, cell culture antibiotic that is non toxic to viruses and mammalian cells at antibacterial levels. Inhibits growth of gram positive and negative bacteria, and mycoplasma. Inhibits normal protein synthesis by binding to L6 protein of 50S ribosomal subunit. Useful antibiotic for Baculovirus expression systems since mutations in rplF prevent Gentamycin from binding. Group: Biochemicals. Grades: Cell Culture Grade. CAS No. 1405-41-0. Pack Sizes: 20ml, 5x20ml, 10x20ml. Molecular Formula: C21H43N5O7 H2SO4, Molecular Weight: ~575.6. US Biological Life Sciences. | Worldwide |
| Gentamycin (Gentamicin) Sulfate Solution 50mg/ml | Broad spectrum, cell culture antibiotic that is non toxic to viruses and mammalian cells at antibacterial levels. Inhibits growth of gram positive and negative bacteria, and mycoplasma. Inhibits normal protein synthesis by binding to L6 protein of 50S ribosomal subunit. Useful antibiotic for Baculovirus expression systems since mutations in rplF prevent Gentamycin from binding. Group: Biochemicals. Alternative Names: Alcomici; Bristagen; Cidomycin; Duragentam; Garamycin; Garasol; Apogen, Gentiomycin C, Refobacin, NSC-82261; Gentamycin sulphate. Grades: Molecular Biology Grade. CAS No. 1405-41-0. Pack Sizes: 20ml, 5x20ml, 10x20ml. US Biological Life Sciences. | Worldwide |
| Gentamycin (Gentamicin) Sulfate USP | Broad spectrum, cell culture aminoglycoside antibiotic that is non toxic to viruses and mammalian cells at antibacterial levels. Inhibits growth of gram positive and negative bacteria, and mycoplasma. Inhibits normal protein synthesis by binding to L6 protein of 50S ribosomal subunit. Useful antibiotic for Baculovirus expression systems since mutations in rplF prevent Gentamycin from binding.Causes codon misreading by binding to the 30S ribosomal subunit, blocking the translocation of peptidyl-tRNA from the acceptor site to the donor site. Antibacterial against Gram-negative aerobic bacteria, Gram-positive bacteria and mycoplasmas. Used as a selection agent (gentamicin-resi...ption of the membrane. This increases the permeability of the cell envelope, leakage of cell contents, and leading to apoptosis and proteolysis (cell death). Causes also cell death by generation of free radicals, phospholipidosis, extracellular calcium-sensing recep- tor stimulation and energetic catastrophe. Source:Micromonospora sp. Group: Biochemicals. Alternative Names: Alcomici; Bristagen; Cidomycin; Duragentam; Garamycin; Garasol; Apogen, Gentiomycin C, Refobacin, NSC-82261; Gentamycin sulphate. Grades: Cell Culture Grade. CAS No. 1405-41-0. Pack Sizes: 5g, 25g, 100g, 500g, 1Kg. Molecular Formula: C21H43N5O7.H2SO4, Molecular Weight: ~575.6. US Biological Life Sciences. | Worldwide |
| Gentamycin Impurity E | Gentamycin Impurity E is an important component of several aminocyclitol antibiotics. Synonyms: 2-Deoxystreptamine dihydrobromide; 2-DOS · 2HBr; 4t,6t-Diamino-cyclohexan-1r,2t,3c-triol; 2-Deoxy-1,3-myo-inosadiamine. Grades: > 95%. CAS No. 84107-26-6. Molecular formula: C6H16N2O3Br2. Mole weight: 324.01. | |
| Gentamycin sulfate | Gentamycin sulfate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: GENTAMICIN 2,5-SULFATE HYDRATE;genoptics.o.p.;gentalline;gentamicinsolution;nsc-82261;sch9724;gentamicin solution 10mg/ml sterile*filtered;gentamicin solution cell culture tested. Appearance: powder. CAS No. 1405-41-0. Molecular formula: C60H127N15O26S. Mole weight: 1506.8. Purity: 0.96. IUPACName: Gentamicin Sulfate. Product ID: ACM1405410-1. Alfa Chemistry ISO 9001:2015 Certified. Categories: Gentamcin Sulfate. |  |
| Gentamycin sulfate | Cas No. 1405-41-0. | |
| Gentamycin Sulfate | 5g Pack Size. Group: Antibiotics. Formula: C21H43N5O7H2So4. CAS No. 1405-41-0. Prepack ID 10336465-5g. Molecular Weight 575.68. See USA prepack pricing. |  |
| Gentamycin Sulfate | 25g Pack Size. Group: Antibiotics. Formula: C21H43N5O7H2So4. CAS No. 1405-41-0. Prepack ID 10336465-25g. Molecular Weight 575.68. See USA prepack pricing. | |
| Gentamycin Sulfate EP Impurity C | Synonyms: 4-O-(6-Amino-6,7-dideoxy-α-D-glycero-D-gluco-heptopyranosyl)-6-O-(4-methyl-3-methylamino-3-deoxy-β-L-arabinopyranosyl)-2-deoxy-D-streptamine; ; Gentamycin B1; D-Streptamine, o-6-amino-6,7-dideoxy-D-glycero-alpha-D-gluco-heptopyranosyl-(1-4)-o-(3-deoxy-4-C-me. Grades: > 95%. CAS No. 36889-16-4. Molecular formula: C20H40N4O10. Mole weight: 496.56. | |
| Gentamycin sulfate EP impurity D | Grades: > 95%. Molecular formula: C19H39N5O9. Mole weight: 481.55. | |
| Gentian Extract (Ratio) | Gentian Extract (Ratio). Group: Others. Purity: 4:1~20:1. Gentian Extract (Ratio). Cat No: EXTW-068. |  |
| Gentianose | Gentianose is a remarkable disaccharide derived from the gentian root, exhibiting its innate aptitude to suppress inflammatory processes. By integrating Gentianose into pharmaceutical compositions, manifold ailments including diabetes, liver maladies and gastrointestinal anomalies can be study. Synonyms: b-D-Glc-(1->6)-a-D-Glc-(1<->2)-b-D-Fru; b-D-fructofuranosyl 6-O-b-D-glucopyranosyl-a-D-glucopyranoside. CAS No. 25954-44-3. Molecular formula: C18H32O16. Mole weight: 504.45. | |
| Gentian Root P.E. 10:1 TLC | Gentian Root P.E. 10:1 TLC. |  CA, FL & NJ |
| Gentian Violet USP | Gentian Violet USP. CAS No. 548-62-9. Molecular formula: C25H30CIN3. |  |
| Gentiobiose | Gentiobiose. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Gentiobiose, beta-Gentiobiose, melibiose, MolPort-004-956-057, CPD-3605, CID441422, SBB012564, ZINC04097481, NCGC00142607-01, C08240, 554-91-6, 5996-00-9. Product Category: Heterocyclic Organic Compound. Appearance: WHITE TO OFF-WHITE POWDER. CAS No. 554-91-6. Molecular formula: C12H22O11. Mole weight: 342.3. Purity: >96.0%(LC). IUPACName: (2R,3R,4S,5S,6R)-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxane-2,3,4,5-tetrol. Canonical SMILES: C(C1C(C(C(C(O1)OCC(C(C(C(C=O)O)O)O)O)O)O)O)O. Density: 1.76 g/cm³. Product ID: ACM554916. Alfa Chemistry ISO 9001:2015 Certified. | |
| Gentiobiose octaacetate | Gentiobiose octaacetate reigns as an esteemed derivative of the intricate Gentiobiose, presenting itself as a disaccharide formed by the union of two glucose entities. Through acetylation, the resulting compound vastly augments the resilience and biogenic accessibility of the drugs. Synonyms: 1,2,3,4-Tetra-O-acetyl-6-O-(2,3,4,6-tetra-O-acetyl-b-D-glucopyranosyl)-D-glucopyranose. Molecular formula: C28H38O19. Mole weight: 678.59. | |
| Gentiobiulose | Gentiobiulose is a remarkable compound, applied in the research of conquering resilient bacterial infections. Its antibacterial potency transpires through the inhibition of diverse bacterial growth, encompassing the notorious strains such as Staphylococcus aureus and Escherichia coli. Synonyms: 6-O-(b-D-Glucopyranosyl)-D-fructose. CAS No. 132436-90-9. Molecular formula: C12H22O11. Mole weight: 342.30. | |
| Gentioheptaose | Gentioheptaose is an intricately structured carbohydrate, finding indispensable utility in the research of bacterial and viral infections. CAS No. 144448-00-0. Molecular formula: C42H72O36. Mole weight: 1153.00. | |
| Gentiohexaose | Gentiohexaose is an extensively employed carbohydrate compound, used for studying diverse ailments such as diabetes and cancer. CAS No. 37698-89-8. Molecular formula: C36H62O31. Mole weight: 990.86. | |
| Gentiooligosaccharides | Gentiooligosaccharides. Product ID: 5-02366. Mole weight: DP 2-4. Properties: ~10 mPas (5%). |  |
| Gentiopentaose | Gentiopentaose is a type of oligosaccharide used in the biomedical industry for its potential role in treating cancer and improving the immune system. Studies have shown that gentiopentaose has anti-tumor effects by inhibiting cancer cell growth and inducing apoptosis. It also has immunomodulatory properties by activating T cells and enhancing natural killer cell function. Gentipentaose shows great promise as a therapeutic agent for cancer and immune-related diseases. CAS No. 37796-54-6. Molecular formula: C30H52O26. Mole weight: 828.72. | |
| Gentiopicrin | Gentiopicrin. Group: Biochemicals. Grades: Plant Grade. CAS No. 20831-76-9. Pack Sizes: 20mg. Molecular Formula: C16H20O9, Molecular Weight: 356.32. US Biological Life Sciences. | Worldwide |
| Gentiopicroside | Gentiopicroside - Product ID: NST-10-165. Category: Glycosides. Alternative Names: Gentiopicrin. Purity: 98%. Test method: HPLC. CAS No. 20831-76-9. Pack Sizes: 0,05g, 0,1g, 0,25g, 0,5g. Appearance: White powder. Molecular formula: C16H20O9. Mole weight: 356.32. Storage: +2 +8 °C. |  |
| Gentiopicroside | Gentiopicroside. Group: Biochemicals. CAS No. 20831-76-9. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Gentiopicroside | Gentiopicroside, a naturally occurring iridoid glycoside, inhibits P450 activity, with an IC50 and a Ki of 61 μM and 22.8 μM for CYP2A6; Gentiopicroside has anti-inflammatoryand antioxidative effects. Uses: Designed for use in research and industrial production. Additional or Alternative Names: (5R-trans)-6-(beta-D-glucopyranosyloxy)-5,6-dihydro-5-vinyl-1H,3H-pyrano[3,4-c]pyran-1-one. Product Category: Inhibitors. Appearance: White powder. CAS No. 20831-76-9. Molecular formula: C16H20O9. Mole weight: 356.32. Purity: 0.98. IUPACName: (3S,4R)-4-ethenyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,6-dihydro-3H-pyrano[3,4-c]pyran-8-one. Canonical SMILES: C=C[C@H]1[C@@H](OC=C2C1=CCOC2=O)O[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O. Density: 1.52±0.1 g/ml. Product ID: ACM20831769. Alfa Chemistry ISO 9001:2015 Certified. Categories: Gentiopicrin. | |
| Gentiotetraose | Gentiotetraose is a distinctive biomedical compound with profound resemblance to endogenous glycoconjugates, thus used for studying autoimmune disorders and chronic inflammatory ailments. Synonyms: O-b-D-Glucopyranosyl-(1?6)-O-b-D-glucopyranosyl-(1?6)-O-b-D-glucopyranosyl-(1?6)-D-glucose. CAS No. 37796-39-7. Molecular formula: C24H42O21. Mole weight: 666.58. | |
| Gentiournoside D | Gentiournoside D. Group: Biochemicals. CAS No. 157722-21-9. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Gentiournoside D | Gentiournoside D is a compound of the iridoids found in the Gentiana urnula. Synonyms: (1S,4aS,6S,7R,7aS)-6-[(2,3-Dihydroxybenzoyl)oxy]-1-(beta-D-glucopyranosyloxy)-1,4a,5,6,7,7a-hexahydro-7-methylcyclopenta[c]pyran-4-carboxylic acid. Grades: >98%. CAS No. 157722-21-9. Molecular formula: C23H28O13. Mole weight: 512.46. | |
| gentisate 1,2-dioxygenase | Requires Fe2+. Group: Enzymes. Synonyms: gentisate oxygenase; 2,5-dihydroxybenzoate dioxygenase; gentisate dioxygenase; gentisic acid oxidase; gentisate:oxygen 1,2-oxidoreductase (decyclizing). Enzyme Commission Number: EC 1.13.11.4. CAS No. 9029-48-5. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0559; gentisate 1,2-dioxygenase; EC 1.13.11.4; 9029-48-5; gentisate oxygenase; 2,5-dihydroxybenzoate dioxygenase; gentisate dioxygenase; gentisic acid oxidase; gentisate:oxygen 1,2-oxidoreductase (decyclizing). Cat No: EXWM-0559. | |
| gentisate decarboxylase | This enzyme belongs to the family of lyases, specifically the carboxy-lyases, which cleave carbon-carbon bonds. This enzyme participates in tyrosine metabolism. Group: Enzymes. Synonyms: 2,5-dihydroxybenzoate decarboxylase; gentisate carboxy-lyase. Enzyme Commission Number: EC 4.1.1.62. CAS No. 37290-54-3. 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-4809; gentisate decarboxylase; EC 4.1.1.62; 37290-54-3; 2,5-dihydroxybenzoate decarboxylase; gentisate carboxy-lyase. Cat No: EXWM-4809. | |
| Gentisic acid | Gentisic acid. Group: Biochemicals. Alternative Names: 2,5-Dihydroxybenzoic acid. Grades: Plant Grade. CAS No. 490-79-9. Pack Sizes: 20mg. Molecular Formula: C7H6O4, Molecular Weight: 154.121. US Biological Life Sciences. | Worldwide |
| Gentisic Acid, Sodium Salt (Sodium Gentisate) | Gentisic acid (2,5-Dihydroxybenzoic acid; 5-hydroxysalicylic acid) is chemically related to salicylate and aspirin (acetylsalicylate) and shares with the latter agent analgesic and anti-inflammatory properties. Gentisic acid is an aromatic carboxylic acid used as a sample matrix in Matrix-assisted laser desorption/ionization Mass spectrometry. As a hydroquinone, it is readily oxidized and is used as an antioxidant excipient in some pharmaceutical preparations.In vitro stabilization of low-tin bone-imaging agents has previously been achieved with ascorbic acid. Gentisic acid is shown to be an equally effective antioxidant for the (1-hydroxyethylidene) diphosphonate (HEDP) and hydroxy methyl enediphosphonate (HMDP) skeletal agents. In vitro studies show less than 2% free sodium [99mTc] pertechnetate at 24 hr with the gentisic acid stabilizer. Studies in guinea pigs at 3 and 24 hrwhether with C-14- or H-3-labeled gentisic acid as stabilizershow no alteration in the biodistribution of either skeletal imaging agent by the addition of the gentisic acid.Gentisic acid is a safe and effective stabilizer, and clinical studies have shown bioequivalency with ascorbic acid. Gentisic acid has been shown to be one of the most commenly occurring aromatic acids of green plants. Group: Biochemicals. Alternative Names: 2,5-Dihydroxybenzoic acid, Sodium Salt; 5-Hydroxysalicylate sodium. Grades: Highly Purified. CAS No. 4955-90-2. Pack Sizes: 10g, 25g, 50g, 100g, 250g. Molecular Formula: C7H5O4Na, Molecular Weight: 176.1. US Biological Life Sciences. | Worldwide |
| Gentisuric acid | Gentisuric acid, a metabolite of Aspirin (HY-14654), is a substrate of α-amidating monooxygenase (PAM). Gentisuric acid prevents DNA-damage by Mitomycin C (HY-13316) [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 25351-24-0. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg; 250 mg. Product ID: HY-W338852. |  |
| Gentisyl alcohol | Gentisyl alcohol is produced by the strain of Penicillium patulum and Pen. divergens. It has anti-staphylococcus aureus activity. Synonyms: 2,5-Dihydroxybenzyl alcohol; 3,6-Dihydroxybenzyl alcohol; Salirepol; gentisin alcohol. Grades: 95%. CAS No. 495-08-9. Molecular formula: C7H8O3. Mole weight: 140.14. | |
| Gentisyl Quinone Isovalerate | Gentisyl Quinone Isovalerate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Blattellaquinone. Product Category: Insect Pheromone. CAS No. 849762-24-9. Molecular formula: C12H14O4. Mole weight: 222.24. Purity: ?95%. IUPACName: (3,6-dioxocyclohexa-1,4-dien-1-yl)methyl3-methylbutanoate. Canonical SMILES: CC(C)CC(=O)OCC1=CC(=O)C=CC1=O. Density: 1.16g/cm³. Product ID: ACM849762249. Alfa Chemistry ISO 9001:2015 Certified. | |
| Genz-123346 | Genz-123346 is an inhibitor of GL1 synthase that blocks the conversion of ceramide to GL1. It does not inhibit α-glucosidase or glucocerebrosidase. It lowered glucose and A1C levels and improved glucose tolerance in the Zucker diabetic fatty rat. Synonyms: Genz-123346; Genz123346; Genz 123346. Grades: >98%. CAS No. 943344-58-9. Molecular formula: C52H82N4O14. Mole weight: 987.23. | |
| Genz-123346 Free base | Genz-123346 is a glucosylceramide synthase inhibitor with potential anticancer activity. Exposure of cells to Genz-123346 and to other GCS inhibitors at non-toxic concentrations can enhance the killing of tumor cells by cytotoxic anti-cancer agents. Genz-123346 and a few other GCS inhibitors are substrates for multi-drug resistance efflux pumps such as P-gp (ABCB1, gP-170). In cell lines selected to over-express P-gp or which endogenously express P-gp, chemosensitization by Genz-123346 was primarily due to the effects on P-gp function. Synonyms: Genz-123346; Genz123346; Genz 123346. CAS No. 491833-30-8. Molecular formula: C24H38N2O4. Mole weight: 418.57. | |
| GENZ-644282 | GENZ-644282. Group: Biochemicals. Alternative Names: 2, 3-Dimethoxy-12-[2- (methylamino) ethyl]benzo[c][1, 3]benzodioxolo[5, 6-h][1, 6]naphthyridin-13 (12H) -one. Grades: Highly Purified. CAS No. 529488-28-6. Pack Sizes: 5mg. Molecular Formula: C22H21N3O5, Molecular Weight: 407.42. US Biological Life Sciences. | Worldwide |
| GENZ-644282 | Genz-644282 is a non-camptothecin inhibitor of topoisomerase I with potential antineoplastic activity. Topoisomerase I inhibitor Genz-644282 binds to and inhibits the enzyme topoisomerase I, which may result in the inhibition of repair of single-strand DNA breaks, DNA replication, and tumor cell growth in susceptible tumor cell populations. Synonyms: GENZ-644282; GENZ644282; GENZ 644282. CAS No. 529488-28-6. Molecular formula: C24H22F3N3O7. Mole weight: 521.44. | |
| Geobacillin I | Geobacillin I is from the thermophilic bacterium Geobacillus thermodenitrificans NG80-2. The antimicrobial spectrum of geobacillin I was generally similar to that of nisin A, with increased activity against Streptococcus dysgalactiae, one of the causative agents of bovine mastitis. | |
| Geobacillin II | Geobacillin II is from the thermophilic bacterium Geobacillus thermodenitrificans NG80-2. Geobacillin II only demonstrated antimicrobial activity against Bacillus strains. | |
| Geodin | An antibiotic produced by the strain of Aspergillus terreus, Geodin is resistant to gram-positive bacteria, negative bacteria (weak) and plant viruses. Synonyms: (+)-Estin; 5,7-dichloro-4-hydroxy-5'-methoxy-6-methyl-3,3'-dioxo-1'-spiro[benzofuran-2,6'-cyclohexa-1,4-diene]carboxylic acid methyl ester; (1'R)-5,7-dichloro-4-hydroxy-6'-methoxy-6-methyl-3,4'-dioxo-spiro[benzofuran-2(3H),1'-[2,5]cyclohexadiene]-2'-carboxylic acid, methyl ester. Grades: ≥95%. CAS No. 427-63-4. Molecular formula: C17H12Cl2O7. Mole weight: 399.18. | |
| Geodin | Plasminogen activator inhibitor (PAI-1). Glucose uptake stimulator. Group: Biochemicals. Alternative Names: (1'R)-5,7-dichloro-4-hydroxy-6'-methoxy-6-methyl-3,4'-dioxo-spiro[benzofuran-2(3H),1'-[2,5]cyclohexadiene]-2'-carboxylic acid, methyl ester, Erdin (+)-form methyl ester; Estin. Grades: Highly Purified. CAS No. 427-63-4. Pack Sizes: 1mg, 5mg. Molecular Formula: C??H??Cl?O?. US Biological Life Sciences. | Worldwide |
| Geosmin-13C2 | Geosmin-13C2. Group: Biochemicals. Alternative Names: (4S,4aS,8aR)-Octahydro-4,8a-dimethyl-4a(2H)-naphthalenol-13C2;[4S-(4α,4aα,8a β)]-Octahydro-4,8a-dimethyl-4a(2H)-naphthalenol-13C2; Octahydro-4α,8a β-dimethyl-4aα(2H)-naphthol-13C2; (-)-Geosmin-13C2. Grades: Highly Purified. Pack Sizes: 500ug. Molecular Formula: C1013C2H22O, Molecular Weight: 184.29. US Biological Life Sciences. | Worldwide |
| geosmin synthase | Requires Mg2+. Geosmin is the cause of the characteristic smell of moist soil. It is a bifunctional enzyme. The N-terminal part of the enzyme is EC 4.2.3.22, germacradienol synthase, and forms germacradienol from FPP. The C-terminal part of the enzyme catalyses the conversion of germacradienol to geosmin via (1S,4aS,8aS)-1,4a-dimethyl-1,2,3,4,4a,5,6,8a-octahydronaphthalene. Group: Enzymes. Enzyme Commission Number: EC 4.1.99.16. 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-4930; geosmin synthase; EC 4.1.99.16. Cat No: EXWM-4930. | |
| Gepirone | Gepirone is an antidepressant and anxiolytic drug of the azapirone group that has been under development for the treatment of depression for a number of years but has yet to be marketed. It acts as a selective partial agonist of the 5-HT1A receptor. Synonyms: 4,4-Dimethyl-1-[4-[4-(2-pyrimidinyl)-1-piperazinyl]butyl]-2,6-piperidinedione; 2,6-Piperidinedione, 4,4-dimethyl-1-(4-(4-(2-pyrimidinyl)-1-piperazinyl)butyl)-; Gepirona. Grades: ≥95%. CAS No. 83928-76-1. Molecular formula: C19H29N5O2. Mole weight: 359.48. | |
| Gepirone | Gepirone is a selective and affinitive 5-HT 1A agonist. Gepirone binds selectively to 5-HT 1A receptor binding site. Gepirone acts as an antidepressant agent can be used for anxiety and major depressive disorder research [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 83928-76-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-122422. | |
| Gepotidacin | Gepotidacin is a potent Type II DNA topoisomerase inhibitor. It is a novel antibacterial drug candidate. It is used for the treatment of gram positive bacterial infection of skin and skin structure. It is also used for the treatment of gonorrhea. It was developed by GlaxoSmithKline R & D and in clinic phase 2 trials. Uses: Gepotidacin is used for the treatment of gram positive bacterial infection of skin and skin structure. it is also used for the treatment of gonorrhea. Synonyms: GSK-2140944; GSK2140944; GSK 2140944; GSK-2140944E; GSK2140944E; GSK 2140944E; Gepotidacin;(2R)-2-[(4-{[(3,4-dihydro-2H-pyrano[2,3-c]pyridin- 6-yl)methyl]amino}piperidin-1-yl)methyl]-1,2-dihydro- 3H,8H-2a,5,8a-triazaacenaphthylene-3,8-dione. Grades: >98%. CAS No. 1075236-89-3. Molecular formula: C24H28N6O3. Mole weight: 448.53. | |
| Gepotidacin | Gepotidacin (GSK2140944) is a novel triazaacenaphthylene bacterial type II topoisomerase inhibitor. Uses: Scientific research. Group: Signaling pathways. Alternative Names: GSK2140944. CAS No. 1075236-89-3. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-16742. | |
| Gepotidacin mesylate hydrate | Gepotidacin mesylate hydrate is an orally active triazaacenaphthylene antibiotic and bacterial type II topoisomerase inhibitor. Gepotidacin mesylate hydrate inhibits bacterial DNA replication by blocking topoisomerase enzymes. Gepotidacin mesylate hydrate selectively inhibits topoisomerase IV and the B subunit of DNA gyrase [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1624306-20-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-16742B. | |
| Gepotidacin S enantiomer | Gepotidacin S enantiomer is an S enantionmer of gepotidacin which is a potent Type II DNA topoisomerase inhibitor and appears as a novel antibacterial drug candidate. Synonyms: Gepotidacin (S enantiomer). Molecular formula: C24H28N6O3. Mole weight: 448.52. | |
| Geptanolimab | Geptanolimab (CBT-501) is a humanized IgG4k monoclonal antibody against programmed death-1 (PD-1). Siplizumab inhibits the binding of PD-L1/L2 to PD-1 through a competitive action. Siplizumab can be used in research of cancer [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: Genolimzumab; APL-501; CBT-501; GB-226. CAS No. 2348469-43-0. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99639. | |
| Geraldol | Geraldol. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Geraldol;3'-Methoxy-3,7,4'-trihydroxyflavone. Product Category: Heterocyclic Organic Compound. Appearance: Powder. CAS No. 21511-25-1. Molecular formula: C16H12O6. Mole weight: 300.3. Purity: 0.98. IUPACName: 3,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)chromen-4-one. Canonical SMILES: COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C=C(C=C3)O)O)O. Density: 1.538 g/cm³. Product ID: ACM21511251. Alfa Chemistry ISO 9001:2015 Certified. Categories: Gerald Oliver Smith. | |
| Geraldol | Geraldol is a Flavonoids product that can be isolated from the herbs of Lotus corniculatus L. [1]. Uses: Scientific research. Group: Natural products. CAS No. 21511-25-1. Pack Sizes: 1 mg; 5 mg. Product ID: HY-N8742. | |
| Geranial | Geranial ((E)-3,7-Dimethylocta-2,6-dienal) is a derivative of geraniol with anti-inflammatory activity. Geranial can inhibit the secretion of TNF-α and IL-6 in macrophages. Furthermore, Geranial also inhibits the secretion of IL-1β mediated by the NLRP-3 inflammasome [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: (E)-3,7-Dimethylocta-2,6-dienal. CAS No. 141-27-5. Pack Sizes: 25 mg; 50 mg; 100 mg. Product ID: HY-W1000105. | |
| geranial dehydrogenase | Does not act on neral. Group: Enzymes. Synonyms: GaDH; geoB (gene name). Enzyme Commission Number: EC 1.2.1.86. 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-1189; geranial dehydrogenase; EC 1.2.1.86; GaDH; geoB (gene name). Cat No: EXWM-1189. | |
| Geraniin | Geraniin is a TNF-α releasing inhibitor with numerous activities including anticancer, anti-inflammatory, and anti-hyperglycemic activities, with an IC50 of 43 μM. Uses: Designed for use in research and industrial production. Additional or Alternative Names: B-D-Glucopyranose. Product Category: Inhibitors. Appearance: Powder. CAS No. 60976-49-0. Molecular formula: C41H28O27. Mole weight: 952.64. Purity: 0.98. IUPACName: (1,13,14,15,18,19,20,34,35,39,39-undecahydroxy-2,5,10,23,31-pentaoxo-6,9,24,27,30,40-hexaoxaoctacyclo[34.3.1.04,38.07,26.08,29.011,16.017,22.032,37]tetraconta-3,11,13,15,17,19,21,32,34,36-decaen-28-yl) 3,4,5-trihydroxybenzoate. Canonical SMILES: C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C6=C5C7C(=CC(=O)C(C7(O)O)(O6)O)C(=O)O3)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O. Density: 2.25 g/ml. Product ID: ACM60976490. Alfa Chemistry ISO 9001:2015 Certified. | |
| Geraniin | Geraniin Inhibitor. Uses: Scientific use. Product Category: T6S2099. CAS No. 60976-49-0. |  |
| Geraniin | Geraniin. Group: Biochemicals. Grades: Plant Grade. CAS No. 60976-49-0. Pack Sizes: 10mg. Molecular Formula: C41H28O27, Molecular Weight: 952.64. US Biological Life Sciences. | Worldwide |
| Geraniin | Geraniin is a TNF-α releasing inhibitor with numerous activities including anticancer, anti-inflammatory, and anti-hyperglycemic activities, with an IC 50 of 43 μM. Uses: Scientific research. Group: Natural products. CAS No. 60976-49-0. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-N0472. | |
| GERANINE G | GERANINE G. Uses: Designed for use in research and industrial production. Additional or Alternative Names: GERANINE G;disodium 1-hydroxy-2-[[4-(6-methyl-2-benzothiazol-1-yl)phenyl]azo]naphthalenedisulphonate;ThiazineRed,Cl14930;2,?-Naphthalenedisulfonic acid, 4-hydroxy-3-4-(6-methyl-2-benzothiazolyl)phenylazo-, disodium salt;Direct Red 48;C.I. Direct Red 48;4. Product Category: Acid Dyes. CAS No. 8003-84-7. Molecular formula: C24H15N3Na2O7S3. Mole weight: 599.57. Product ID: ACM8003847. Alfa Chemistry ISO 9001:2015 Certified. Categories: Geraine Greear. | |
| Geraniol | Geraniol. Group: Biochemicals. Alternative Names: (2E)-3,7-Dimethyl-2,6-octadien-1-ol; (E)-3,7-Dimethyl-2,6-octadien-1-ol; (E)-3,7-Dimethyl-2,6-octadienol; (E)-Geraniol; (E)-Nerol; 3,7-Dimethyl-trans-2,6-octadien-1-ol; Geraniol BJ; Geranyl alcohol; Lemonol; MosquitoSafe; NSC 9279; trans-3,7-Dimethyl-2,6-octadien-1-ol; trans-Geraniol; β-Geraniol. Grades: Highly Purified. CAS No. 106-24-1. Pack Sizes: 10g. Molecular Formula: C10H18O, Molecular Weight: 154.25. US Biological Life Sciences. | Worldwide |
| Geraniol | Liquid with pleasant odor, d20 0.89. CAS No. 106-24-1. Pack Sizes: 250g. Product ID: FR-0188. B.P. 116-119/17 mm. Mole weight: 154.25. |  Frinton Laboratories |
| Geraniol | analytical standard. Uses: For analytical and research use. Group: Chemical class; pharma & vet compounds & metabolites; standards for environmental regulatory methods; pharma & vet compounds & metabolites. Alternative Names: Geraniol, Geraniol 60, (E)-3,7-Dimethyl-2,6-octadienol, NSC 9279, β-Geraniol, Geraniol 980, (E)-Nerol, trans-Geraniol,2,6-Octadien-1-ol, 3,7-dimethyl-, (2E)-, 3,7-Dimethyl-trans-2,6-octadien-1-ol, trans-3,7-Dimethyl-2,6-octadien-1-ol, (2E)-3,7-Dimethyl-2,6-octadien-1-ol, TT 4228, (E)-3,7-Dimethyl-2,6-octadien-1-ol, 2,6-Octadien-1-ol, 3,7-dimethyl-, (E)- (8CI), Geraniol BJ, TT 4302, (E)-Geraniol, trans-1-Hydroxy-3,7-dimethyl-2,6-octadiene, Geranyl alcohol, Lemonol, MosquitoSafe. Grades: analytical standard. CAS No. 106-24-1. Pack Sizes: 1ML, 5ML. IUPAC Name: (2E)-3,7-dimethylocta-2,6-dien-1-ol. Molecular Formula: C10H18O. Mole Weight: 154.25. EC Number: 203-377-1. Catalog: APS106241A. Assay: ≥98.5% (GC). SMILES: CC(=CCC\C(=C\CO)\C)C. Format: Neat. Shipping: Room Temperature. |  |
| Geraniol | Geraniol (CAS# 106-24-1) is used in the synthesis of insect repellant. It is also used in the synthesis of Angelicoin A and Herecinone J, which inhibit collagen-induced platelet aggregation. Uses: Anti-inflammatory, anti-angiogenic, anti-cell proliferative. Synonyms: (2E)-3,7-dimethylocta-2,6-dien-1-ol. Grades: 98 %. CAS No. 106-24-1. Molecular formula: C10H18O. Mole weight: 154.25. | |
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