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| Product | Description | |
|---|---|---|
| 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. Grades: >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 | Sumanirole maleate, also referred as PNU 95666E or U95666E, is a high affinity D2 receptor full agonist that shows >200-fold selectivity over dopamine receptor subtypes (Ki values are 9.0, 1940, >2190 and >7140 for D2, D3, D4 and D1 receptors respectively) with an ED50 of about 46 nM. Sumanirole was developed for the treatment of Parkinson's disease and restless leg syndrome. While it has never been approved for medical use. Sumanirole is a highly valuable tool compound for basic research to identify neurobiological mechanisms that are based on a dopamine D2-linked (vs. D1, D3, D4, and D5-linked) mechanism of action. Synonyms: 5,6-dihydro-5-(methylamino)-4H-imidazo(4,5,1ij)-quinolin-2(1H)-one (Z)-2-butenedioate; PNU-95666; PNU95666; PNU 95666; Sumanirole; U 95666E; U-95666E; U95666E. CAS No. 179386-44-8. Molecular formula: C15H17N3O5. Mole weight: 319.31. | |
| 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 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: Sumatriptan is a medication used for the treatment of migraine headaches. Synonyms: Imitrex; Sumatran; Sumax; Sumatriptanum; 1-[3-[2-(Dimethylamino)ethyl]-1H-indol-5-yl]-N-methylmethanesulfonamide; (3-[2-(Dimethylamino)ethyl]-1H-indol-5-yl)-N-methylmethanesulfonamide; GR-43175; GR43175. Grades: 95%. CAS No. 103628-46-2. Molecular formula: C14H21N3O2S. Mole weight: 295.40. | |
| 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 | 2H Labeled Compounds. Alternative Names: 3-[2-(Dimethyl-d6-amino)-ethyl]-N-methyl-1H-indole-5-methanesulfonamide. CAS No. 1020764-38-8. Molecular formula: C14H15D6N3O2S. Mole weight: 301.44. Catalog: ACM1020764388. |  |
| 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 succinate | Heterocyclic Organic Compound. Alternative Names: 3-[2-(Dimethyl-d6-amino)ethyl]-N-methyl-1H-indole-5-methanesulfonamide, Succinate, Imigran, Imitrex. 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. Catalog: ACM1215621310. | |
| 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 (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. Group: Impurity standards. CAS No. 545338-89-4. Molecular Formula: C27H37N5O2S. Mole Weight: 495.69. Catalog: APB545338894. |  |
| Sumatriptan EP impurity B | One of the impurities of Sumatriptan that is a 5-HT receptro agonist. Synonyms: Monodesmethyl sumatriptan; N-Desmethyl SumatriptanDiscontinued; 88919-51-1; Sumatriptan EP Impurity B; Sumatriptan succinate specified impurity B [EP]. Grades: > 95%. CAS No. 88919-51-1. Molecular formula: C13H19N3O2S. Mole weight: 281.38. | |
| Sumatriptan EP Impurity B | Sumatriptan EP Impurity B. Uses: For analytical and research use. Group: Impurity standards. CAS No. 88919-51-1. Molecular Formula: C13H19N3O2S. Mole Weight: 281.37. Catalog: APB88919511. | |
| Sumatriptan EP impurity C | One of the impurities of Sumatriptan that is a 5-HT receptro agonist. Synonyms: Sumatriptan EP Impurity C; Sumatriptan USP Related Compound C; [3-[2-(Dimethylamino)ethyl]-1-(hydroxymethyl)-1H-indol-5-yl]- N-methylmethanesulphonamide. Grades: > 95%. Molecular formula: C15H23N3O3S. Mole weight: 325.43. | |
| Sumatriptan EP Impurity C | Sumatriptan EP Impurity C. Uses: For analytical and research use. Group: Impurity standards. 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. Group: Impurity standards. CAS No. 212069-94-8. Molecular Formula: C14H21N3O3S. Mole Weight: 311.4. Catalog: APB212069948. | |
| Sumatriptan EP impurity E | One of the impurities of Sumatriptan that is a 5-HT receptro agonist. Synonyms: 3-(2-Aminoethyl)-N-methyl-1H-indole-5-methanesulfonamide; 1-(3-(2-Aminoethyl)-1H-indol-5-yl)-N-methylmethanesulfonamide; Didesmethyl sumatriptan; 1-[3-(2-aminoethyl)-1H-indol-5-yl]-N-methylmethanesulfonamide. Grades: > 95%. CAS No. 88919-22-6. Molecular formula: C12H17N3O2S. Mole weight: 267.35. | |
| Sumatriptan EP Impurity E | Sumatriptan EP Impurity E. Uses: For analytical and research use. Group: Impurity standards. 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. Group: Impurity standards. CAS No. 2074615-63-5. Molecular Formula: C13H17N3O2S. Mole Weight: 279.36. Catalog: APB2074615635. | |
| Sumatriptan EP Impurity H | Sumatriptan EP Impurity H. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1391052-59-7. Molecular Formula: C27H37N5O2S. Mole Weight: 495.69. Catalog: APB1391052597. | |
| 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 Impurity 1 | One of the impurities of Sumatriptan that is a 5-HT receptro agonist. Synonyms: Sumatriptan Impurity 1; Sumatriptan Hydroxy-Oxindole Impurity; 1-(3-(2-(Dimethylamino)ethyl)-3-hydroxy-2-oxoindolin-5-yl)-N-methylmethane. Grades: > 95%. Molecular formula: C14H21N3O4S. Mole weight: 327.41. | |
| Sumatriptan Impurity 2 | One of the impurities of Sumatriptan that is a 5-HT receptro agonist. Synonyms: Sumatriptan Impurity 2. Grades: > 95%. Molecular formula: C14H22N3O3S. Cl. Mole weight: 347.86. | |
| Sumatriptan Impurity 2 | Sumatriptan Impurity 2. Uses: For analytical and research use. Group: Impurity standards. 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. Group: Impurity standards. CAS No. 4025-75-6. Molecular Formula: C7H6ClNO4S. Mole Weight: 235.64. Catalog: APB4025756. | |
| Sumatriptan Impurity 3 | One of the impurities of Sumatriptan that is a 5-HT receptro agonist. Synonyms: Sumatriptan Impurity 3; 1-(3-(2-(Dimethylamino)ethyl)-1-((5-((N-methylsulfamoyl)methyl)-1H-indol-3-yl)methyl)-1H-indol-5-yl)-N-methylmethanesulfonamide. Grades: > 95%. Molecular formula: C25H33N5O4S2. Mole weight: 531.70. | |
| Sumatriptan Impurity A | One of the impurities of Sumatriptan that is a 5-HT receptro agonist. Synonyms: Sumatriptan succinate specified impurity A [EP]; Sumatriptan succinate related compound A free base; (3-(2-(Dimethylamino)ethyl)-2-((3-(2-(dimethylamino)ethyl)-1H-indol-5-yl)methyl)-1H-indol-5-yl)-N-methylmethanesulfonamide. Grades: > 95%. CAS No. 545338-89-4. Molecular formula: C27H37N5O2S. Mole weight: 495.69. | |
| Sumatriptan Impurity F | One of the impurities of Sumatriptan that is a 5-HT receptro agonist. Synonyms: Sumatriptan Impurity F; N-Methyl-1-(2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-6-yl)methanesulfonamide Succinate. Grades: > 95%. Molecular formula: C13H17N3O2S. Mole weight: 279.36. | |
| Sumatriptan Impurity G | One of the impurities of Sumatriptan that is a 5-HT receptro agonist. Synonyms: Sumatriptan Impurity G; N-Methyl-1-(2-methyl-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-6-yl)methanesulfonamide. Grades: > 95%. Molecular formula: C14H19N3O2S. Mole weight: 293.39. | |
| Sumatriptan Impurity H | One of the impurities of Sumatriptan that is a 5-HT receptro agonist. Synonyms: Sumatriptan Related Compound H; Sumatriptan Dimer Impurity; Sumatriptan EP Impurity H; N-(3-(2-(dimethylamino)ethyl)-1-((3-(2-(dimethylamino)ethyl)-1H-indol-5-yl)methyl)-1H-indol-5-yl)-N-methylmethanesulfonamide. Grades: > 95%. CAS No. 1391052-59-7. Molecular formula: C27H37N5O2S. Mole weight: 495.69. | |
| 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 | Sumatriptan Succinate is a triptan sulfa drug containing a sulfonamide group for the treatment of migraine headaches. Uses: Vasoconstrictor agents. Synonyms: GR 43175; GR43175; GR-4317. Grades: >98%. CAS No. 103628-48-4. Molecular formula: C14H21N3O2S.C4H6O4. Mole weight: 413.49. | |
| 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 EP impurity D | One metabolite impurities of Sumatriptan that is a 5-HT receptro agonist. Synonyms: Sumatriptan N-Oxide; Sumatriptan Succinate EP Impurity D; N,N-dimethyl-2-[5-(methylsulfamoylmethyl)-1H-indol-3-yl]ethanamine oxide. Grades: > 95%. CAS No. 212069-94-8. Molecular formula: C14H21N3O3S. Mole weight: 311.41. | |
| Sumibox-Patacon | Sumibox-Patacon. Group: Polymers. |  |
| Sumiceller | Sumiceller. Group: Polymers. | |
| 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. | |
| Summer Lilac Extract | Extract obtained from Buddleja Davidii (Summer Lilac) flowers. Dissolved in water and glycerin. Rich in phenylethanoids, flavanoids, and iridoids. Active ingredient of choice helping to prevent the appearance of aging. Especially suitable for all types of anti-aging and protective formulations. Uses: Anti-aging, cell-protective formulations. Group: Skin actives. CAS No. 94465-67-5 / 56-81-5 / 7732-18-5 / 77-92-9 / 532-32-1 / 24634-61-5. Catalog: CI-SC-1033. | |
| Summer Lilac & Thyme Extract | Natural extract that is an innovative plant based approach based on traditional medicine to reduce skin aging to a minimum. Both plants are known for their antioxidant, anti-irritant and soothing properties. Uses: Anti-aging, moisturizing and anti-wrinkle products, soothing and anti-irritant treatments, body moisturizing and after-shaves products. Group: Skin actives. CAS No. 56-81-5 / 7732-18-5 / 94465-67-5 / 84929-51-1. Appearance: Clear to slightly opalescent, brown-colored liquid. Catalog: CI-SC-0699. | |
| 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, which mimics the neuroprotective mechanisms of basic fibroblast growth factor. In primary cultures of rat cerebrocortical neurons, SUN11602 and bFGF prevented glutamate-induced neuronal death. Synonyms: SUN11602; SUN-11602; SUN 11602. 4-[[4-[[2-(4-amino-2,3,5,6-tetramethylanilino)acetyl]-methylamino]piperidin-1-yl]methyl]benzamide. Grades: >98%. CAS No. 704869-38-5. Molecular formula: C26H37N5O2. Mole weight: 451.615. | |
| 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 is a non-peptide calcitonin (CT) receptor agonist increasing cAMP production in CHO/hCTR cells (EC50 = 21 μM). SUN-B 8155 has been shown to reduce serum calcium concentrations in vivo following i.p. administration. Synonyms: SUN-B 8155; SUN B 8155; SUNB 8155; SUNB8155; 5-[1-[(2-Aminophenyl)imino]ethyl]-1,6-dihydroxy-4-methyl-2(1H)-pyridone; (3Z)-3-[1-(2-aminoanilino)ethylidene]-1-hydroxy-4-methylpyridine-2,6-dione. CAS No. 345893-91-6. Molecular formula: C14H15N3O3. Mole weight: 273.29. | |
| 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 |
| Sunepitron hydrochloride | Sunepitron hydrochloride is a potent and selective serotonin 5-HT1A autoreceptor agonist, α2-adrenergic antagonist, and dopamine D2 agonist. The phase III clinical trial for the treatment of depression is discontinued. Synonyms: CP-93393-1; 1-[[(7S,9aS)-2-pyrimidin-2-yl-1,3,4,6,7,8,9,9a-octahydropyrido[1,2-a]pyrazin-7-yl]methyl]pyrrolidine-2,5-dione hydrochloride. Grades: 99%. CAS No. 148408-65-5. Molecular formula: C17H23N5O2.HCl. Mole weight: 365.86. | |
| 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 | 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 Extract | Extract obtained from Helianthus Annus (Sunflower) seeds. Contains 20% extract dissolved in water and glycerin. Has skin-softening, soothing and firming properties. Uses: Cleansers, creams, lotions and toners. Group: Skin actives. CAS No. 7732-18-5 / 56-81-5 / 84776-03-4 / 122-99-6. Appearance: Colorless to light yellow liquid, characteristic odor. Catalog: CI-SC-0860. | |
| Sunflower seed oil glycerides | Emollient; Emulsifying; Skin Conditioning. Group: Emulsifying agents. Alternative Names: Glycerides, sunflower-oil mono-, di- and tri-. CAS No. 91723-16-9. Catalog: ACM91723169. | |
| 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. | |
| Sunflower Wax | Natural vegetable wax obtained from the winterization of sunflower oil. Consists of long chain, saturated esters providing hardness and crystalline structure with a high melting point. Saponification value 78-92 mg KOH/g. Melting point 74-77°C (165-171°F). Uses: Creams, lotions, pomades, lip balms, ointments, lipsticks, deodorants. Group: Emollients/oils/wax. CAS No. 1286686-34-7. Appearance: Light yellow granules. Catalog: CI-SC-0392. | |
| Sunifiram | unifiram (DM-235) is a piperazine derived research chemical which has nootropic effects in animal studies with significantly higher potency than piracetam. Synonyms: DM-235; DM 235; DM235. Grades: >98%. CAS No. 314728-85-3. Molecular formula: C14H18N2O2. Mole weight: 246.3. | |
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