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| Product | Description | |
|---|---|---|
| Sulpiride | 25g Pack Size. Group: Bioactive Small Molecules, Research Organics & Inorganics. Formula: C15H23N3O4S. CAS No. 15676-16-1. Prepack ID 23728623-25g. Molecular Weight 341.43. See USA prepack pricing. |  |
| Sulpiride impurity 35 | Sulpiride impurity 35. Uses: For analytical and research use. Group: Impurity standards. CAS No. 124020-27-5. Molecular formula: C15H20D3N3O4S. Mole weight: 344.44. Catalog: APB124020275. |  |
| Sulprostone | ?95% (HPLC), oil. Group: Fluorescence/luminescence spectroscopy. | |
| Sulprostone | Sulprostone (SHB 286) is a potent and selective EP3 receptor agonist. Sulprostone (SHB 286) is a prostaglandin E2 (PGE2) analogue and has antiulcer and nonsteroidal abortifacient effects. Sulprostone has potential for the research of pregnancy termination and hemorrhages during delivery [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SHB 286; CP-34089; ZK-57671. CAS No. 60325-46-4. Pack Sizes: 1 mg (10.74 mM * 200 μL in Methyl acetate). Product ID: HY-19360. |  |
| Sulprostone | Sulprostone. Group: Biochemicals. Grades: Purified. CAS No. 60325-46-4. Pack Sizes: 1mg. US Biological Life Sciences. |  Worldwide |
| Sultamicillin | Sultamicillin is a broad-spectrum and orally active beta-lactamase inhibitor, an antibiotic with antibacterial activity [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 76497-13-7. Pack Sizes: 10 mM * 1 mL; 25 mg; 50 mg; 100 mg. Product ID: HY-N7115. | |
| Sultamicillin | Sultamicillin. Group: Biochemicals. Grades: Highly Purified. CAS No. 76497-13-7. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. US Biological Life Sciences. | Worldwide |
| Sultamicillin tosylate | Sultamicillin tosylate is a broad-spectrum and orally active beta-lactamase inhibitor, an antibiotic with antibacterial activity [1]. Uses: Scientific research. Group: Natural products. Alternative Names: Sultamicillin (tosilate). CAS No. 83105-70-8. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g. Product ID: HY-N7111. | |
| Sultamicillin tosylate | Sultamicillin tosylate. Group: Biochemicals. Grades: Highly Purified. CAS No. 83105-70-8. Pack Sizes: 100mg, 250mg, 500mg, 1g. US Biological Life Sciences. | Worldwide |
| Sultanene | Sultanene. CAS No. 15848-49-4. VIGON Item # 507536. Categories: Speciality Ingrdients Suppliers, Fragrances, Perfumers, ethyl-2-cyclopentenyl acetate. |  America & Internationally |
| Sulthiame | Sulthiame is a benzenesulfonamide derivative. Sulthiame acts as an inhibitor of the enzyme carbonic anhydrase. Sulthiame is used as an anticonvulsant in the treatment of benign and symptomatic focal epilepsy. Group: Biochemicals. Alternative Names: 4-(Tetrahydro-1,1-dioxido-2H-1,2-thiazin-2-yl)benzenesulfonamide; 4-(Tetrahydro-2H-1,2-thiazin-2-yl)benzenesulfonamide S,S-Dioxide; 2-(p-Sulfamoylphenyl)-tetrahydro-2H-1,2-thiazine 1,1-Dioxide; A 168; Bayer A 168; Conadil; Contravul; Elisal; Ospolot; Riker 594; Sulphenyltame; Sulphenytame; Sulphthiame; Sulthiam; Sulthiamine; Sultiam; Sultiame; Trolone; p-(Tetrahydro-2H-1,2-thiazin-2-yl)benzenesulfonamide Dioxide. Grades: Highly Purified. CAS No. 61-56-3. Pack Sizes: 25mg. US Biological Life Sciences. | Worldwide |
| Sultiame | Sultiame is a carbonic anhydrase inhibitor, widely used as an antiepileptic agent. Uses: Scientific research. Group: Signaling pathways. CAS No. 61-56-3. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-108316. | |
| Sultopride hydrochloride | Sultopride hydrochloride (LIN-1418 hydrochloride) is a selective antagonist of dopamine D2 receptor. Uses: Scientific research. Group: Signaling pathways. Alternative Names: LIN-1418 hydrochloride. CAS No. 23694-17-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-42849A. | |
| Sultopride Hydrochloride | Dopamine D2-receptor antagonist. An antipsychotic. Group: Biochemicals. Alternative Names: N-[(1-Ethyl-2-pyrrolidinyl)methyl]-5-(ethylsulfonyl)-2-methoxybenzamide. Grades: Highly Purified. CAS No. 23694-17-9. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Sultosilic acid piperazine salt | Sultosilic acid piperazine salt (Piperazine sultosylate; A-585) is a lipid-lowering agent. Sultosilic acid piperazine salt modifies the blood lipids levels, reduces platelet adhesiveness without promoting peroxisomal activity of hepatocytes or producing other adverse side-effects [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Piperazine sultosylate; A-585. CAS No. 57775-27-6. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-130587. | |
| Sultriecin | Sultriecin is a dominant analogue in the family of triene antibiotic isolated from Streptomyces. It is a phosphate ester of fostriecin and displays potent antifungal and antitumour activity. Synonyms: BU 3285T; (+)-Phostriecin; Phostriecin; (+)-Sultriecin; (5S)-5alpha-Hydroxy-6alpha-[(1E,4S,5S,6S,7Z,9Z,11E)-4-(sodiooxysulfonyloxy)-5-methyl-6-hydroxy-1,7,9,11-heptadecatetraenyl]-5,6-dihydro-2H-pyran-2-one sodium. Grade: >98% by HPLC. CAS No. 131774-59-9. Molecular formula: C23H33NaO8S. Mole weight: 492.56. |  |
| Sultriecin (Antibiotic BU 3285T) | Sultriecin is a dominant analogue in a family of sulfate esters of a triene antibiotic isolated from Streptomyces. Despite the structural similarity to fostriecin there is little comparative data to support a common mode of action. Sultriecin is reported to display potent antifungal and antitumor activity. Group: Biochemicals. Alternative Names: Antibiotic BU 3285T. Grades: Highly Purified. CAS No. 131774-59-9. Pack Sizes: 500ug. US Biological Life Sciences. | Worldwide |
| Sumanirole maleate | Sumanirole maleate (U-95666E; PNU-95666E) is a highly selective D2 receptor full agonist with an ED 50 of about 46 nM. Sumanirole plays an important role in the research of Parkinson's disease and restless leg syndrome [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: U-95666E; PNU-95666. CAS No. 179386-44-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-70081A. | |
| Sumanirole maleate | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Sumanirole Maleate | Sumanirole is a high affinity D2 receptor agonist (EC50 values are between 17 and 75 nM in cell-based assays). Sumanirole displays >200-fold selectivity for the D2 receptor against other dopamine receptor subtypes (Ki values are 9.0, 1940, >2190 and >7140 for D2, D3, D4 and D1 receptors respectively). Sumanirole exhibits anti-Parkinsonian activity similar to Ropinirole. Group: Biochemicals. Alternative Names: (5R)-5,6-Dihydro-5-(methylamino)-4H-imidazo[4,5,1-ij]quinolin-2(1H)-one (2Z)-2-Butenedioate; (R)-5,6-Dihydro-5-(methylamino)-4H-imidazo[4,5,1-ij]quinolin-2(1H)-one (2Z)-2-Butenedioate. Grades: Highly Purified. CAS No. 179386-43-7. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Sumatriptan | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Sumatriptan | Sumatriptan (GR 43175) is an orally active 5-HT1 receptor agonist with IC 50 s of 7.3 nm, 9.3nm and 17.8 nm for 5-HT 1D , 5-HT 1B and 5-HT 1F receptors, respectively. Sumatriptan can be used for migraine headache research [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: GR 43175 free base. CAS No. 103628-46-2. Pack Sizes: 10 mM * 1 mL; 25 mg; 50 mg; 100 mg. Product ID: HY-B0121B. | |
| Sumatriptan-[d6] | Sumatriptan-[d6] is the labelled analogue of Sumatriptan. Sumatriptan is a Serotonin-1b and Serotonin-1d Receptor Agonist that acts selectively at 5HT1 receptors. It is a sulfonamide triptan with vasoconstrictor activity. It selectively binds to and activates serotonin 5-HT1D receptors in the central nervous system, thus constricts cerebral blood vessels. It may also relieve vascular headaches by decreasing the release of vasoactive neuropeptides from perivascular trigeminal axons in the dura mater. It is a medication used for the treatment of migraine headaches. Synonyms: Sumatriptan D6; 3-[2-(Dimethyl-d6-amino)-ethyl]-N-methyl-1H-indole-5-methanesulfonamide. Grade: 95% by HPLC; 98% atom D. CAS No. 1020764-38-8. Molecular formula: C14H15D6N3O2S. Mole weight: 301.44. | |
| Sumatriptan-d6 (3-[2-(Dimethyl-d6-amino)-ethyl]-N-methyl-1H-indole-5-methanesulfonamide) | A serotonin 5HT1-receptor agonist. Antimigraine. Group: Biochemicals. Alternative Names: 3-[2-(Dimethyl-d6-amino)-ethyl]-N-methyl-1H-indole-5-methanesulfonamide. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Sumatriptan-[d6] Hemisuccinate | Sumatriptan-[d6] Hemisuccinate is the labelled analogue of Sumatriptan. Sumatriptan is a Serotonin-1b and Serotonin-1d Receptor Agonist that acts selectively at 5HT1 receptors. It is a sulfonamide triptan with vasoconstrictor activity. It selectively binds to and activates serotonin 5-HT1D receptors in the central nervous system, thus constricts cerebral blood vessels. It may also relieve vascular headaches by decreasing the release of vasoactive neuropeptides from perivascular trigeminal axons in the dura mater. It is a medication used for the treatment of migraine headaches. Synonyms: Sumatriptan-d6 Hemisuccinate. Grade: 95% by HPLC; 95% atom D. CAS No. 1397195-80-0. Molecular formula: C32H36D12N6O8S2. Mole weight: 720.96. | |
| Sumatriptan-d6 succinate | Sumatriptan-d6 succinate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 3-[2-(Dimethyl-d6-amino)ethyl]-N-methyl-1H-indole-5-methanesulfonamide, Succinate, Imigran, Imitrex. Product Category: Heterocyclic Organic Compound. CAS No. 1215621-31-0. Molecular formula: C18H21D6N3O6S. Mole weight: 419.53. Purity: 0.96. IUPACName: 1-[3-[2-[bis(trideuteriomethyl)amino]ethyl]-1H-indol-5-yl]-N-methylmethanesulfonamide;butanedioic acid. Canonical SMILES: CNS(=O)(=O)CC1=CC2=C(C=C1)NC=C2CCN(C)C.C(CC(=O)O)C(=O)O. Product ID: ACM1215621310. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Sumatriptan-d6 succinate | Sumatriptan-d6 succinate is the deuterium labeled Sumatriptan succinate. Sumatriptan succinate is an orally active 5-HT1 receptor agonist with K i s of 17 nM, 27 nM and 100 nM for 5-HT1D , 5-HT1B and 5-HT1A receptors , respectively. Sumatriptan succinate can be used for migraine headache research [1] [2] [3]. Uses: Scientific research. Group: Isotope-labeled compounds. Alternative Names: GR 43175C-d6. CAS No. 1215621-31-0. Pack Sizes: 1 mg. Product ID: HY-B0121BS. | |
| Sumatriptan-[d6] Succinate | Sumatriptan-[d6] Succinate is the labelled analogue of Sumatriptan. Sumatriptan is a Serotonin-1b and Serotonin-1d Receptor Agonist that acts selectively at 5HT1 receptors. It is a sulfonamide triptan with vasoconstrictor activity. It selectively binds to and activates serotonin 5-HT1D receptors in the central nervous system, thus constricts cerebral blood vessels. It may also relieve vascular headaches by decreasing the release of vasoactive neuropeptides from perivascular trigeminal axons in the dura mater. It is a medication used for the treatment of migraine headaches. Uses: Labelled sumatriptan, a serotonin 5ht1-receptor agonist. Synonyms: Sumatriptan-D6 Succinate. Grade: 98% by HPLC; 99% atom D. CAS No. 1215621-31-0. Molecular formula: C18H21D6N3O6S. Mole weight: 419.53. | |
| Sumatriptan-d6 Succinate (3-[2-(Dimethyl-d6-amino)ethyl]-N-methyl-1H-indole-5-methanesulfonamide, Succinate, Imigran, Imitrex,) | Labelled Sumatriptan, a serotonin 5HT1-receptor agonist. Group: Biochemicals. Alternative Names: 3-[2-(Dimethyl-d6-amino)ethyl]-N-methyl-1H-indole-5-methanesulfonamide, Succinate, Imigran, Imitrex. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Sumatriptan Dimer Impurity-d4 | Sumatriptan Dimer Impurity-d4. Group: Biochemicals. Alternative Names: 1-[[3-[2-(Dimethylamino)ethyl]-1H-indol-5-yl]methyl]-3-[2-(Dimethylamino)ethyl]-N-methyl-indole-5-methanesulfonamide-d4. Grades: Highly Purified. Pack Sizes: 1mg. Molecular Formula: C27H33D4N5O2S, Molecular Weight: 499.7. US Biological Life Sciences. | Worldwide |
| Sumatriptan Hydroxy-Oxindole Impurity (Sumatriptan Impurity 1) | Sumatriptan Hydroxy-Oxindole Impurity (Sumatriptan Impurity 1). Uses: For analytical and research use. Group: Impurity standards. Pack Sizes: 5MG. Catalog: APS013024. Format: Neat. Shipping: Room Temperature. | |
| Sumatriptan N-oxide | Sumatriptan N-oxide. Group: Biochemicals. Alternative Names: 3-[2- (Dimethyloxidoamino) ethyl]-N-methyl-1H-indole-5-methanesulfonamide; GR 112504. Grades: Highly Purified. CAS No. 212069-94-8. Pack Sizes: 10mg, 25mg, 50mg, 100mg, 250mg. Molecular Formula: C14H21N3O3S. US Biological Life Sciences. | Worldwide |
| Sumatriptan N-Oxide | Sumatriptan N-Oxide. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: Ph Eur Sumatriptan Impurity Mixture, BP Sumatriptan Impurity D, Sumatriptan Test Mix for Impurity Identification Solution 2, GR 112504, Ph Eur Sumatriptan Impurity D, GR 112504X, Sumatriptan N-Oxide,3-[2-(Dimethyloxidoamino)ethyl]-N-methyl-1H-indole-5-methanesulfonamide, Sumatriptan N-oxide (GR 112504X). CAS No. 212069-94-8. Pack Sizes: 10MG. IUPAC Name: N,N-dimethyl-2-[5-(methylsulfamoylmethyl)-1H-indol-3-yl]ethanamine oxide. Molecular formula: C14H21N3O3S. Mole weight: 311.40. Catalog: APS212069948. SMILES: CNS(=O)(=O)Cc1ccc2[nH]cc(CC[N+](C)(C)[O-])c2c1. Format: Neat. Shipping: Room Temperature. | |
| Sumatriptan succinate | Sumatriptan succinate (GR 43175) is an orally active 5-HT1 receptor agonist with IC 50 s of 7.3 nm, 9.3nm and 17.8 nm for 5-HT 1D , 5-HT 1B and 5-HT 1F receptors, respectively. Sumatriptan succinate can be used for migraine headache research [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: GR 43175 succinate. CAS No. 103628-48-4. Pack Sizes: 10 mM * 1 mL; 10 mg; 25 mg; 50 mg; 100 mg; 500 mg. Product ID: HY-B0121. | |
| Sumatriptan succinate | Sumatriptan succinate. Group: Biochemicals. Grades: Purified. CAS No. 103628-48-4. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| Sumatriptan Succinate (3-[2-(Dimethylamino)ethyl]-N-methyl-1H-indole-5-methanesulfonamide, Succinate, Imigran, Imitrex,) | A serotonin 5HT1-receptor agonist. Group: Biochemicals. Alternative Names: 3-[2-(Dimethylamino)ethyl]-N-methyl-1H-indole-5-methanesulfonamide, Succinate, Imigran, Imitrex. Grades: Highly Purified. Pack Sizes: 50mg. US Biological Life Sciences. | Worldwide |
| Sumatriptan Succinate Related Compound A | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Sumatriptan succinate Related Compound C | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Sumatriptan succinate Related Impurities | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Sumibox-Patacon | Sumibox-Patacon. Group: Polymers. |  |
| Sumiceller | Sumiceller. Group: Polymers. | |
| Sumifix dark brown brs | Sumifix dark brown brs. Uses: Designed for use in research and industrial production. Additional or Alternative Names: C.I. Reactive Brown 21;Reactive Brown 21;Sumifix Dark Brown BRS. Product Category: Heterocyclic Organic Compound. CAS No. 154999-66-3. Mole weight: 0. Product ID: ACM154999663. Alfa Chemistry ISO 9001:2015 Certified. | |
| Sumilizer GA 80 | Sumilizer GA 80. Group: Biochemicals. Grades: Highly Purified. CAS No. 90498-90-1. Pack Sizes: 10mg, 25mg, 50mg, 100mg, 250mg. Molecular Formula: C43H64O10. US Biological Life Sciences. | Worldwide |
| Sumipanel | Sumipanel. Group: Polymers. | |
| SUMO-1 human | ?95% (SDS-PAGE), recombinant, expressed in E. coli (GST-tagged). Group: Fluorescence/luminescence spectroscopy. | |
| SUMO Protease 1 (GST-tagged) from Yeast, Recombinant | SUMO (Small Ubiquitin-like MOdifiers) Protease 1 (Ulp1, Ubl-specific protease 1 from Saccharomyces cerevisiae) is a highly active cysteine protease. It is highly specific as it recognizes the tertiary structure of the ubiquitin-like (UBL) protein, SUMO (Smt3), rather than its amino acid sequence. SUMO fusion tag, as an N-terminal fusion partner, has been shown to enhance functional protein production in prokaryotic and eukaryotic expression systems with significantly improved protein stability and solubility. The SUMO protease 1 can be used to cleave SUMO protein tag from recombinant SUMO-fusion proteins. The optimal temperature for cleavage is 30°C; however, the en...eaction by affinity chromatography using the Glutathione resin. Group: Enzymes. Synonyms: Ulp1 peptidase; SUMO Protease; SUMO Protease. Enzyme Commission Number: EC 3.4.22.68. Purity: > 90% by SDS-PAGE. Mole weight: 52.6 kDa (403-621 aa + N-terminal GST). Activity: >10,000 units/mg. Storage: Store at -80°C. Stable for at least 1 year as supplied. It may be further diluted to 0.1-0.5 mg/ml with 50 mM Tris-HCl, 100 mM NaCl, 5 mM DTT and 20% glycerol pH 8.0 and stored at -20°C in aliquots. Avoid repeated freezing and thawing cycles. Form: Liquid. Source: E. coli. Species: Yeast. Ulp1 peptidase; SUMO Protease; SUMO Protease; SUMO Protease 1; Protease. Cat No: NATE-1708. |  |
| SUMO Protease 1 (His-tagged) from Yeast, Recombinant | SUMO (Small Ubiquitin-like MOdifiers) Protease 1 (Ulp1, Ubl-specific protease 1 from Saccharomyces cerevisiae) is a highly active cysteine protease. It is highly specific as it recognizes the tertiary structure of the ubiquitin-like (UBL) protein, SUMO (Smt3), rather than its amino acid sequence. SUMO fusion tag, as an N-terminal fusion partner, has been shown to enhance functional protein production in prokaryotic and eukaryotic expression systems with significantly improved protein stability and solubility. The SUMO Protease 1 can be used to cleave SUMO protein tag from recombinant SUMO-fusion proteins. The optimal temperature for cleavage is 30°C; however, the en...finity chromatography using the Ni chelating resin. Group: Enzymes. Synonyms: Ulp1 peptidase; SUMO Protease; SUMO Protease. Enzyme Commission Number: EC 3.4.22.68. Purity: > 90% by SDS-PAGE. Mole weight: 28.7 kDa (403-621 aa + N-terminal Poly-His tag). Activity: 1 X 10^6 units/mg. Storage: Store at -80°C. Stable for at least 1 year as supplied. It may be further diluted to 0.01-0.05 mg/ml with 50 mM Tris-HCl, 100 mM NaCl, 5 mM DTT and 20% glycerol pH 8.0 and stored at -20°C in aliquots. Avoid repeated freezing and thawing cycles. Form: Liquid. Source: E. coli. Species: Yeast. Ulp1 peptidase; SUMO Protease; SUMO Protease; SUMO Protease 1; Protease. Cat No: NATE-1709. | |
| SUN | ?95% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| SUN 11602 | SUN 11602. Group: Biochemicals. Grades: Purified. CAS No. 704869-38-5. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| SUN-B 8155 | SUN-B 8155. Group: Biochemicals. Grades: Purified. CAS No. 345893-91-6. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| Sundew Dry Herb Extract 10:1 (Drosera rotundifolia) | Sundew Dry Herb Extract 10:1 (Drosera rotundifolia). |  CA, FL & NJ |
| Sunflower CO2 | Sunflower CO2 (Peanut Replacer). CAS No. 8001-21-6. Kosher: Y. VIGON Item # 507454. Categories: Speciality Ingrdients Suppliers. | America & Internationally |
| Sunflower oil | Sunflower oil occurs as a clear, light yellow-colored liquid with a bland, agreeable taste. Synonyms: Helianthi annui oleum raffinatum; huile de tournesol; oleum helianthi; sunflowerseed oil. CAS No. 8001-21-6. Product ID: PE-0473. Category: Binder Excipients. Product Keywords: Pharmaceutical Excipients; Excipients for Solid Dosage Form; Sunflower oil; Binder Excipients; Binder Excipients; 8001-21-6; 8001-21-6. UNII: NA. Chemical Name: Sunflower oil. Grade: Pharmceutical Excipients. Stability and Storage Conditions: Sunflower oil should be stored in an airtight, well-filled container, protected from light. Stability may be improved by the addition of an antioxidant such as butylated hydroxytoluene. Source and Preparation: Sunflower oil is obtained from the fruits and seeds (achenes) of the sunflower, Helianthus annus (Compositae), by mechanical means or by extraction. Applications: Sunflower oil is widely used as an edible oil, primarily in oleomargarine. It is also used extensively in cosmetics and pharmaceutical formulations. Therapeutically, sunflower oil is used to provide energy and essential fatty acids for parenteral nutrition. Studies have shown that sunflower oil may be used in intramuscular injections without inducing tissue damage. Safety: Sunflower oil is widely used in food products and on its own as an edible oil. It is also used extensively in cosmetics and topical pharmaceutical formulations, and is g |  |
| Sunflower oil | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Sunflower oil | Sunflower oil occurs as a clear, light yellow-colored liquid with a bland, agreeable taste. Synonyms: Helianthi annui oleum raffinatum; huile de tournesol; oleum helianthi; sunflowerseed oil. CAS No. 8001-21-6. Product ID: PE-0552. Category: Diluent; emollient; Emulsifying Agents; Solvent; Tablet Binder. Product Keywords: Excipients for Liquid Dosage Form; Emulsifier Excipients; PE-0552; Sunflower oil; Diluent; emollient; Emulsifying Agents; Solvent; Tablet Binder; ; 8001-21-6. UNII: NA. Chemical Name: Sunflower oil. Grade: Pharmceutical Excipients. Stability and Storage Conditions: Sunflower oil should be stored in an airtight, well-filled container, protected from light. Stability may be improved by the addition of an antioxidant such as butylated hydroxytoluene. Source and Preparation: Sunflower oil is obtained from the fruits and seeds (achenes) of the sunflower, Helianthus annus (Compositae), by mechanical means or by extraction. Applications: Sunflower oil is widely used as an edible oil, primarily in oleomargarine. It is also used extensively in cosmetics and pharmaceutical formulations. Therapeutically, sunflower oil is used to provide energy and essential fatty acids for parenteral nutrition. Studies have shown that sunflower oil may be used in intramuscular injections without inducing tissue damage. Safety: Sunflower oil is widely used in food products and on its own as an edible oil. It is also used extens | |
| Sunflower Oil | Sunflower Oil. CAS No. 8001-21-6. Kosher: Y. VIGON Item # 502711. Categories: Speciality Ingrdients Suppliers, Flavors, Fragrances, Perfumers, Cosmetics, Aromatherapy, Essetial Oils. | America & Internationally |
| Sunflower Oil BP/USP | Sunflower Oil BP/USP. CAS No. 8001-21-6. |  |
| Sunflower Oil Powder 50% Load NG | Sunflower Oil Powder 50% Load NG. | CA, FL & NJ |
| Sunflower Phytosterol Ester 97% | Sunflower Phytosterol Ester 97%. | CA, FL & NJ |
| Sunflower seed oil | analytical standard. Group: Flavor and fragrance standards. | |
| Sunflower seed oil microencapsulated powder | Sunflower seed oil microencapsulated powder. Product ID: CDF4-0205. Molecular formula: NA. Category: Unsaturated fatty acid supplement. Product Keywords: Food Ingredients; Nutrients; CDF4-0205; Sunflower seed oil microencapsulated powder; Unsaturated fatty acid supplement. Appearance: White to light yellow powder. Color: White to light yellow. Physical State: powder. Source and Preparation: sunflower. Applications: Dietary supplements, nutritional supplements, cosmetic raw materials, etc. | |
| Sunitinib | Sunitinib (SU 11248) is a multi-targeted receptor tyrosine kinase inhibitor with IC 50 s of 80 nM and 2 nM for VEGFR2 and PDGFRβ , respectively [1]. Sunitinib, an ATP-competitive inhibitor, effectively inhibits autophosphorylation of Ire1α by inhibiting autophosphorylation and consequent RNase activation [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SU 11248. CAS No. 557795-19-4. Pack Sizes: 10 mM * 1 mL; 100 mg; 200 mg; 500 mg. Product ID: HY-10255A. | |
| Sunitinib | Sunitinib (as the malate salt) is the active ingredient in the drug sold under the trade name Sutent. This drug is a small molecule receptor tyrosine kinase inhibitor that has been approved in at least one country for the treatment of patients having gastrointestinal stromal tumors or renal cell carcinomas. Group: Biochemicals. Alternative Names: N-[2-(Diethylamino)ethyl]-5-[(Z)-(5-fluoro-1,2-dihydro-2-oxo-3H-indol-3-ylidene)methyl]-2,4-dimethyl-1H-pyrrole-3-carboxamide; SU-11248; Sutent; PHA-290940AD; PNU-290940AD. Grades: Highly Purified. CAS No. 557795-19-4. Pack Sizes: 10mg, 100mg. Molecular Formula: C22H27FN4O2, Molecular Weight: 398.47. US Biological Life Sciences. | Worldwide |
| Sunitinib-d10 | Labeled Sunitinib, a multi-kinase inhibitor targeting several receptor tyrosine kinases (RTK). Group: Biochemicals. Grades: Highly Purified. CAS No. 1126721-82-1. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Sunitinib-[d10] | One of the isotopic labelled form of Sunitinib, which is a receptor tyrosine kinases inhibitor. Synonyms: N-[2-(Diethyl-d10)aminoethyl]-5-[(Z)-(5-fluoro-1,2-dihydro-2-oxo-3H-indol-3-ylidene)methyl]-2,4-dimethyl-1H-pyrrole-3-carboxamide; Sutent-d10; SU-11248-d10. Grade: >95%. CAS No. 1126721-82-1. Molecular formula: C22H17D10FN4O2. Mole weight: 408.47. | |
| Sunitinib Impurity 6 | Sunitinib Impurity 6. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1691223-83-2. Molecular formula: C22H27FN4O2. Mole weight: 398.48. Catalog: APB1691223832. | |
| Sunitinib Impurity 61 | Sunitinib Impurity 61. Uses: For analytical and research use. Group: Impurity standards. CAS No. 100487-78-3. Molecular formula: C8H6ClN3O. Mole weight: 195.61. Catalog: APB100487783. | |
| Sunitinib malate | Sunitinib (marketed as Sutent by Pfizer, and previously known as SU11248) is an oral, small-molecule, multi-targeted receptor tyrosine kinase (RTK) inhibitor that was approved by the FDA for the treatment of renal cell carcinoma (RCC) and imatinib-resistant gastrointestinal stromal tumor (GIST) on January 26, 2006. Sunitinib was the first cancer drug simultaneously approved for two different indications. Uses: Angiogenesis inhibitors. Synonyms: Sunitinib malate; SU011248 L-malate salt; N-[2-(diethylamino)ethyl]-5-[(Z)-(5-fluoro-2-oxo-1H-indol-3-ylidene)methyl]-2,4-dimethyl-1H-pyrrole-3-carboxamide; (2S)-2-hydroxybutanedioic acid. Grade: >98%. CAS No. 341031-54-7. Molecular formula: C22H27FN4O2.C4H6O5. Mole weight: 532.56. | |
| Sunitinib malate | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Sunitinib Malate | Sunitinib Malate (SU 11248 Malate) is a multi-targeted receptor tyrosine kinase inhibitor with IC 50 s of 80 nM and 2 nM for VEGFR2 and PDGFRβ , respectively [1]. Sunitinib Malate, an ATP-competitive inhibitor, effectively inhibits autophosphorylation of Ire1α by inhibiting autophosphorylation and consequent RNase activation [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SU 11248 Malate. CAS No. 341031-54-7. Pack Sizes: 10 mM * 1 mL; 100 mg; 200 mg; 500 mg. Product ID: HY-10255. | |
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