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| Product | Description | |
|---|---|---|
| Sulpride Impurity 8 | Sulpride Impurity 8. Uses: For analytical and research use. Molecular formula: C15H22N2O2. Mole weight: 262.35. Catalog: APB09522. |  |
| Sulpride Impurity B | Sulpride Impurity B. Uses: For analytical and research use. CAS No. 33045-52-2. Molecular formula: C9H11NO5S. Mole weight: 245.25. Catalog: APB33045522. | |
| Sulpride Impurity C | Sulpride Impurity C. Uses: For analytical and research use. CAS No. 33045-53-3. Molecular formula: C10H13NO5S. Mole weight: 259.28. Catalog: APB33045533. | |
| Sulpride Impurity D | Sulpride Impurity D. Uses: For analytical and research use. CAS No. 22117-85-7. Molecular formula: C8H9NO5S. Mole weight: 231.22. Catalog: APB22117857. | |
| Sulpride Impurity E | Sulpride Impurity E. Uses: For analytical and research use. CAS No. 52395-25-2. Molecular formula: C8H10N2O4S. Mole weight: 230.24. Catalog: APB52395252. | |
| Sulpride Impurity F | Sulpride Impurity F. Uses: For analytical and research use. CAS No. 2214214-03-4. Molecular formula: C15H23N3O5S. Mole weight: 357.43. Catalog: APB2214214034. | |
| Sulpride Impurity G | Sulpride Impurity G. Uses: For analytical and research use. CAS No. 67381-52-6. Molecular formula: C14H21N3O4S. Mole weight: 327.4. Catalog: APB67381526. | |
| 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. Category: 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. Group: Biochemicals. Grades: Highly Purified. CAS No. 76497-13-7. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. US Biological Life Sciences. | Worldwide |
| Sultamicillin impurity 2 | Sultamicillin impurity 2. Uses: For analytical and research use. Molecular formula: C25H34N4O11S2. Mole weight: 630.68. Catalog: APB11924. | |
| 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 |
| Sultiame | Sultiame is a carbonic anhydrase inhibitor, widely used as an antiepileptic agent. Uses: Scientific research. Category: Signaling pathways. CAS No. 61-56-3. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-108316. | |
| 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 |
| 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 ED50 of about 46 nM. Sumanirole plays an important role in the research of Parkinson's disease and restless leg syndrome[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: U-95666E; PNU-95666. CAS No. 179386-44-8. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-70081A. | |
| 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 | Sumatriptan (GR 43175) is an orally active 5-HT1 receptor agonist with IC50s of 7.3 nm, 9.3nm and 17.8 nm for 5-HT1D, 5-HT1B and 5-HT1F receptors, respectively. Sumatriptan can be used for migraine headache research[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: GR 43175 free base. CAS No. 103628-46-2. Pack Sizes: 10 mM * 1 mL in DMSO; 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] 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 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 EP Impurity A | Sumatriptan EP Impurity A. Uses: For analytical and research use. CAS No. 545338-89-4. Molecular formula: C27H37N5O2S. Mole weight: 495.69. Catalog: APB545338894. | |
| Sumatriptan EP Impurity B | Sumatriptan EP Impurity B. Uses: For analytical and research use. CAS No. 88919-51-1. Molecular formula: C13H19N3O2S. Mole weight: 281.37. Catalog: APB88919511. | |
| Sumatriptan EP Impurity C | Sumatriptan EP Impurity C. Uses: For analytical and research use. CAS No. 1797905-62-4. Molecular formula: C15H23N3O3S. Mole weight: 325.43. Catalog: APB1797905624. | |
| Sumatriptan EP Impurity D | Sumatriptan EP Impurity D. Uses: For analytical and research use. CAS No. 212069-94-8. Molecular formula: C14H21N3O3S. Mole weight: 311.4. Catalog: APB212069948. | |
| Sumatriptan EP Impurity E | Sumatriptan EP Impurity E. Uses: For analytical and research use. CAS No. 88919-22-6. Molecular formula: C12H17N3O2S. Mole weight: 267.35. Catalog: APB88919226. | |
| Sumatriptan EP Impurity F | Sumatriptan EP Impurity F. Uses: For analytical and research use. CAS No. 2074615-63-5. Molecular formula: C13H17N3O2S. Mole weight: 279.36. Catalog: APB2074615635. | |
| Sumatriptan EP Impurity G | Sumatriptan EP Impurity G. Uses: For analytical and research use. Molecular formula: C15H21N3O4S. Mole weight: 339.41. Catalog: APB09676. | |
| Sumatriptan EP Impurity H | Sumatriptan EP Impurity H. Uses: For analytical and research use. CAS No. 1391052-59-7. Molecular formula: C27H37N5O2S. Mole weight: 495.69. Catalog: APB1391052597. | |
| Sumatriptan Impurity 1 | Sumatriptan Impurity 1. Uses: For analytical and research use. Molecular formula: C14H20N4O3S. Mole weight: 324.4. Catalog: APB09677. | |
| Sumatriptan Impurity 2 | Sumatriptan Impurity 2. Uses: For analytical and research use. CAS No. 2250254-19-2. Molecular formula: C14H21N3O4S. Mole weight: 327.4. Catalog: APB2250254192. | |
| Sumatriptan Impurity 3 | Sumatriptan Impurity 3. Uses: For analytical and research use. CAS No. 4025-75-6. Molecular formula: C7H6ClNO4S. Mole weight: 235.64. Catalog: APB4025756. | |
| 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 succinate | Sumatriptan succinate. Group: Biochemicals. Grades: Purified. CAS No. 103628-48-4. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| Sumatriptan Succinate | Sumatriptan succinate is a serotonin1 (5-HT1) receptor agonist, which is effective in the acute treatment of migraine headache. Category: Active pharmaceutical ingredients. CAS No. 103628-48-4. Product ID: API103628484. Molecular formula: C18H27N3O6S. Mole weight: 341.426. Appearance: Powder. Standard: USP/EP. |  |
| 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 |
| Sumibox-Patacon | Sumibox-Patacon. |  |
| Sumiceller | Sumiceller. | |
| 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. | |
| SUMO Protease | SUMO Protease is highly specific for proteins containing small ubiquitin-like modifier (SUMO) tags. SUMO Protease can be used to regulates the proteins splicing, controlls protein structure and function in vitro[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1607459-82-4. Pack Sizes: 100 U; 500 U. Product ID: HY-E70372. | |
| 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. | |
| SUN11602 | SUN11602 is a novel aniline compound with basic fibroblast growth factor-like activity. Uses: Scientific research. Category: Signaling pathways. CAS No. 704869-38-5. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-101493. | |
| SUN 11602 | SUN 11602. Group: Biochemicals. Grades: Purified. CAS No. 704869-38-5. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| SUN B8155 | SUN B8155, a non-peptide agonist of calcitonin (CT) receptor, selectively mimics the biological actions of calcitonin. Calcitonin, a 32-amino acid peptide hormone secreted mainly from the thyroid gland, plays an important role in maintaining bone homeostasis[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 345893-91-6. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-103302. | |
| 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 Amindopropyl Dimethylamine | Sunflower Amindopropyl Dimethylamine is a hair conditioning agent that is derived from sunflower oil. It is commonly used in hair care products such as shampoos, conditioners, and hair masks due to its ability to improve the overall health and appearance of hair. This ingredient works by penetrating the hair shaft and forming a protective layer around each strand, helping to reduce damage from heat styling, chemical treatments, and environmental stressors. It also helps to detangle and smooth the hair, making it easier to comb and reducing frizz. Sunflower Amindopropyl Dimethylamine is a biodegradable and eco-friendly ingredient, making it a popular choice for natural and green beauty products. Product ID: CI-HC-0075. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| 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-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 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 | 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 | Sunflower oil is a type of vegetable oil that is derived from sunflower seeds through a process of pressing, refining, and extraction. It is commonly used for cooking, frying, baking, and as a salad dressing. Alternative Names: Helianthus annuus oil. CAS No. 8001-21-6. Product ID: CI-HC-0082. Alfa Chemistry - ISO 9001:32057 Certified. | |
| 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 | Sunflower seed oil. Alternative Names: Organic sunflower oil. CAS No. 8001-21-6. Purity: 0.98. Product ID: CI-EO-0056. Alfa Chemistry - ISO 9001:32057 Certified. | |
| 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 IC50s 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. Category: Signaling pathways. Alternative Names: SU 11248. CAS No. 557795-19-4. Pack Sizes: 10 mM * 1 mL in DMSO; 100 mg; 200 mg; 500 mg. Product ID: HY-10255A. | |
| Sunitinib | Sunitinib (SU 11248) is a multi-targeted receptor tyrosine kinase (RTK) inhibitor that inhibits VEGFR2 and PDGFRβ (IC50=80/2 nM). It exhibits antitumor activity and is used for treating kidney cancer and gastrointestinal tumors. Category: Active pharmaceutical ingredients. CAS No. 557795-19-4. Product ID: API557795194. Molecular formula: C22H27FN4O2. Mole weight: 398.47. | |
| 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 | Sunitinib D10 is a deuterium labeled Sunitinib. Sunitinib is a inhibitor of multi-targeted receptor tyrosine kinase(IC50s of 80 nM and 2 nM for VEGFR2 and PDGFRβ, respectively). Category: Active pharmaceutical ingredients. CAS No. 1126721-82-1. Product ID: API1126721821. Molecular formula: C22H27FN4O2. Mole weight: 408.54. | |
| 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-d4 | Sunitinib-d4 is a deuterated compound of Sunitinib. Category: Active pharmaceutical ingredients. CAS No. 1126721-79-6. Product ID: API1126721796. Molecular formula: C22H23D4FN4O2. Mole weight: 402.5. | |
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