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| Product | Description | |
|---|---|---|
| steroid sulfotransferase | Broad specificity resembling EC 2.8.2.2 alcohol sulfotransferase, but also acts on estrone. Group: Enzymes. Synonyms: steroid alcohol sulfotransferase. Enzyme Commission Number: EC 2.8.2.15. CAS No. 9032-76-2. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3373; steroid sulfotransferase; EC 2.8.2.15; 9032-76-2; steroid alcohol sulfotransferase. Cat No: EXWM-3373. |  |
| sterol 14α-demethylase | This heme-thiolate (P-450) enzyme acts on a range of steroids with a 14α-methyl group, such as obtusifoliol and lanosterol. The enzyme catalyses two successive hydroxylations of the 14α-methyl group, followed by elimination as formate, leaving a 14(15) double bond. Group: Enzymes. Synonyms: obtusufoliol 14-demethylase; lanosterol 14-demethylase; lanosterol 14α-demethylase; sterol 14-demethylase. Enzyme Commission Number: EC 1.14.13.70. CAS No. 60063-87-8. 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-0877; sterol 14α-demethylase; EC 1.14.13.70; 60063-87-8; obtusufoliol 14-demethylase; lanosterol 14-demethylase; lanosterol 14α-demethylase; sterol 14-demethylase. Cat No: EXWM-0877. | |
| sterol 22-desaturase | A heme-thiolate protein (P450). The enzyme, found in yeast and plants, catalyses the introduction of a double bond between the C-22 and C-23 carbons of certain sterols. In yeast the enzyme acts on ergosta-5,7,24(28)-trien-3β-ol, a step in the biosynthesis of ergosterol. The enzyme from the plant Arabidopsis thaliana acts on sitosterol and 24-epi-campesterol, producing stigmasterol and brassicasterol, respectively. Group: Enzymes. Synonyms: ERG5 (gene name); CYP710A (gene name). Enzyme Commission Number: EC 1.14.19.41. 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-1006; sterol 22-desaturase; EC 1.14.19.41; ERG5 (gene name); CYP710A (gene name). Cat No: EXWM-1006. | |
| sterol 24-C-methyltransferase | Requires glutathione. Acts on a range of sterols with a 24(25)-double bond in the sidechain. While zymosterol is the preferred substrate it also acts on desmosterol, 5α-cholesta-7,24-dien-3β-ol, 5α-cholesta-5,7,24-trien-3β-ol, 4α-methylzymosterol and others. S-Adenosyl-L-methionine attacks the Si-face of the 24(25) double bond and the C-24 hydrogen is transferred to C-25 on the Re face of the double bond. Group: Enzymes. Synonyms: Δ24-methyltransferase; Δ24-sterol methyltransferase; zymosterol-24-methyltransferase; S-adenosyl-4-methionine:sterol Δ24-methyltransferase; SMT1; 24-sterol C-methyltransferase; S-adenosyl-L-methionine:Δ24(23)-sterol methyltransferase; phytosterol methyltransferase. Enzyme Commission Number: EC 2.1.1.41. CAS No. 37257-07-1. 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-1945; sterol 24-C-methyltransferase; EC 2.1.1.41; 37257-07-1; Δ24-methyltransferase; Δ24-sterol methyltransferase; zymosterol-24-methyltransferase; S-adenosyl-4-methionine:sterol Δ24-methyltransferase; SMT1; 24-sterol C-methyltransferase; S-adenosyl-L-methionine:Δ24(23)-sterol methyltransferase; phytosterol methyltransferase. Cat No: EXWM-1945. | |
| sterol 3β-glucosyltransferase | Not identical with EC 2.4.1.192 (nuatigenin 3β-glucosyltransferase) or EC 2.4.1.193 (sarsapogenin 3β-glucosyltransferase). Group: Enzymes. Synonyms: UDPG:sterol glucosyltransferase; UDP-glucose-sterol β-glucosyltransferase; sterol:UDPG glucosyltransferase; UDPG-SGTase; uridine diphosphoglucose-poriferasterol glucosyltransferase; uridine diphosphoglucose-sterol glucosyltransferase; sterol glucosyltransferase; sterol-β-D-glucosyltransferase; UDP-glucose-sterol glucosyltransferase. Enzyme Commission Number: EC 2.4.1.173. CAS No. 123940-38-5,9075-00-7. 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-2398; sterol 3β-glucosyltransferase; EC 2.4.1.173; 123940-38-5,9075-00-7; UDPG:sterol glucosyltransferase; UDP-glucose-sterol β-glucosyltransferase; sterol:UDPG glucosyltransferase; UDPG-SGTase; uridine diphosphoglucose-poriferasterol glucosyltransferase; uridine diphosphoglucose-sterol glucosyltransferase; sterol glucosyltransferase; sterol-β-D-glucosyltransferase; UDP-glucose-sterol glucosyltransferase. Cat No: EXWM-2398. | |
| sterol esterase | A group of enzymes of broad specificity, acting on esters of sterols and long-chain fatty acids, that may also bring about the esterification of sterols. Activated by bile salts. Group: Enzymes. Synonyms: cholesterol esterase; cholesteryl ester synthase; triterpenol esterase; cholesteryl esterase; cholesteryl ester hydrolase; sterol ester hydrolase; cholesterol ester hydrolase; cholesterase; acylcholesterol lipase. Enzyme Commission Number: EC 3.1.1.13. CAS No. 9026-00-0. Cholesterol Esterase. 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-3440; sterol esterase; EC 3.1.1.13; 9026-00-0; cholesterol esterase; cholesteryl ester synthase; triterpenol esterase; cholesteryl esterase; cholesteryl ester hydrolase; sterol ester hydrolase; cholesterol ester hydrolase; cholesterase; acylcholesterol lipase. Cat No: EXWM-3440. | |
| sterol O-acyltransferase | The animal enzyme is highly specific for transfer of acyl groups with a single cis double bond that is nine carbon atoms distant from the carboxy group. Group: Enzymes. Synonyms: cholesterol acyltransferase; sterol-ester synthase; sterol-ester synthetase; sterol-ester synthase; acyl coenzyme A-cholesterol-O-acyltransferase; acyl-CoA:cholesterol acyltransferase; ACAT; acylcoenzyme A:cholesterol O-acyltransferase; cholesterol ester synthase; cholesterol ester synthetase; cholesteryl ester synthetase. Enzyme Commission Number: EC 2.3.1.26. CAS No. 9027-63-8. 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-2203; sterol O-acyltransferase; EC 2.3.1.26; 9027-63-8; cholesterol acyltransferase; sterol-ester synthase; sterol-ester synthetase; sterol-ester synthase; acyl coenzyme A-cholesterol-O-acyltransferase; acyl-CoA:cholesterol acyltransferase; ACAT; acylcoenzyme A:cholesterol O-acyltransferase; cholesterol ester synthase; cholesterol ester synthetase; cholesteryl ester synthetase. Cat No: EXWM-2203. | |
| S-tert-Butyl-D-cysteine hydrochloride | S-tert-Butyl-D-cysteine hydrochloride. Group: Biochemicals. Alternative Names: D-Cys(tBu)-OH·HCl. Grades: Highly Purified. CAS No. 200353-65-7. Pack Sizes: 500mg, 1g, 2g, 5g, 10g. US Biological Life Sciences. |  Worldwide |
| S-tert-Butyl-D-cysteine hydrochloride | S-tert-Butyl-D-cysteine hydrochloride. Synonyms: D-Cys(tBu)-OH HCl; (S)-2-Amino-3-(Tert-Butylthio)Propanoic Acid Hydrochloride. Grade: ≥ 98% (HPLC). CAS No. 200353-65-7. Molecular formula: C7H15NO2S·HCl. Mole weight: 213.70. |  |
| S-tert-Butyl-D-cysteine hydrochloride 98+% (HPLC) | S-tert-Butyl-D-cysteine hydrochloride 98+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences. | Worldwide |
| S-(+)-teRt-Butyl glycidyl etheR | S-(+)-teRt-Butyl glycidyl etheR. Group: Biochemicals. Grades: Highly Purified. CAS No. 130232-97-2. Pack Sizes: 1g, 2g, 5g, 10g, 25g. US Biological Life Sciences. | Worldwide |
| S-tert-Butyl-L-cysteine hydrochloride | S-tert-Butyl-L-cysteine hydrochloride. Synonyms: L-Cys(tBu)-OH HCl; L-Cysteine, S-(1,1-dimethylethyl)-, hydrochloride (1:1); L-Cysteine, S-(1,1-dimethylethyl)-, monohydrochloride; Alanine, 3-(tert-butylthio)-, hydrochloride; Alanine, 3-(tert-butylthio)-, hydrochloride, L-; (2R)-2-Amino-3-(tert-butylsulfanyl)propanoic acid hydrochloride. Grade: ≥95%. CAS No. 2481-9-6. Molecular formula: C7H15NO2S.HCl. Mole weight: 213.73. | |
| S-tert-Butyl-L-cysteine hydrochloride | S-tert-Butyl-L-cysteine hydrochloride. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g, 100g, 250g. US Biological Life Sciences. | Worldwide |
| S-tert-Butyl-L-cysteine Hydrochloride | Intermediate in peptide syntheses. CAS No. 2481-9-6. Pack Sizes: 5g. Product ID: FR-1331. M.P. 197-198. Mole weight: 213.73. |  Frinton Laboratories |
| S-tert-Butylthio-L-cysteine | S-tert-Butylthio-L-cysteine. Synonyms: L-Cys(StBu)-OH; 3-(tert-Butyldithio)-L-alanine. Grade: ≥ 99% (TLC). CAS No. 30044-51-0. Molecular formula: C7H15NO2S2. Mole weight: 209.30. | |
| S-tert-Butylthio-L-cysteine | S-tert-Butylthio-L-cysteine. Group: Biochemicals. Alternative Names: L-Cys(StBu)-OH; 3-(tert-Butyldithio)-L-alanine. Grades: Highly Purified. CAS No. 30044-51-0. Pack Sizes: 2g, 5g, 10g, 25g. US Biological Life Sciences. | Worldwide |
| S-tert-Butylthio-L-cysteine 99+% (TLC) | S-tert-Butylthio-L-cysteine 99+% (TLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences. | Worldwide |
| steryl-β-glucosidase | Acts on glucosides of cholesterol and sitosterol, but not on some related sterols such as coprostanol. Group: Enzymes. Enzyme Commission Number: EC 3.2.1.104. CAS No. 69494-88-8. 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-3787; steryl-β-glucosidase; EC 3.2.1.104; 69494-88-8. Cat No: EXWM-3787. | |
| steryl-sulfatase | Also acts on some related steryl sulfates. Group: Enzymes. Synonyms: arylsulfatase; steroid sulfatase; sterol sulfatase; dehydroepiandrosterone sulfate sulfatase; arylsulfatase C; steroid 3-sulfatase; steroid sulfate sulfohydrolase; dehydroepiandrosterone sulfatase; pregnenolone sulfatase; phenolic steroid sulfatase; 3-β-hydroxysteroid sulfate sulfatase. Enzyme Commission Number: EC 3.1.6.2. CAS No. 9025-62-1. 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-3753; steryl-sulfatase; EC 3.1.6.2; 9025-62-1; arylsulfatase; steroid sulfatase; sterol sulfatase; dehydroepiandrosterone sulfate sulfatase; arylsulfatase C; steroid 3-sulfatase; steroid sulfate sulfohydrolase; dehydroepiandrosterone sulfatase; pregnenolone sulfatase; phenolic steroid sulfatase; 3-β-hydroxysteroid sulfate sulfatase. Cat No: EXWM-3753. | |
| S-(-)-Tetrahydrofurancarboxylic acid | Tetrahydrofurancarboxylic acid. CAS No. 87392-07-2. Categories: (s)-tetrahydrofuran-2-carboxylic acid. |  Pennsylvania PA |
| Stevia 90% Steviosides | Stevia 90% Steviosides. |  CA, FL & NJ |
| Stevia extract | secondary reference standard. Group: Sweetener standards. |  |
| Stevia Extract (Ratio) | Stevia Extract (Ratio). Group: Others. Purity: 4:1~20:1. Stevia Extract (Ratio). Cat No: EXTW-066. | |
| Stevia Leaf Extract | Stevia leaf extract is prepared from the sweet leaf, the sunflower family (asteraceae) and is related to lettuce and marigolds. Stevioside and rebaudioside are natural constituents of stevia leaf extract. Stevioside is 250 times sweeter than sucrose, and have the potential to serve as non-caloric sweeteners. Stevia leaf extract is already in use as a food sweetener in a number of South American and Asian countries. Group: Others. Mole weight: 318.45. Stevia Leaf Extract; Stevia Rebaudiana Bertoni. Cat No: EXTC-003. | |
| Steviol | Steviol is a major metabolite of the sweetening compound stevioside. Steviol slows renal cyst growth by reducing AQP2 expression and promoting AQP2 degradation [1]. Uses: Scientific research. Group: Natural products. CAS No. 471-80-7. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 20 mg. Product ID: HY-N2057. |  |
| Steviol | Botanical Source: Group: Biochemicals. Grades: Plant Grade. CAS No. 471-80-7. Pack Sizes: 10mg, 20mg. US Biological Life Sciences. | Worldwide |
| Steviol | Steviol is a diterpenoiic carboxylic alcohol and is isolated from the herbs of Stevia rebaudiana. It is the aglycon derivative of natural sweetener steviol glycosides and is found to be highly mutagenic compared to Stevioside. It inhibits the proliferation of the gastrointestinal cancer cells and the human osteosarcoma U2OS cell line in a dose- and time-dependent manner. It also inhibits human organic anion transporters (hOATs) in uptake assays using murine cells from the S2 segment of proximal tubules. It is selective for hOAT1 and hOAT3 over hOAT2 and hOAT4. It increases CYP3A29 expression and enhances pancreatic beta-cell function and taste sensation by potentiation of TRPM5 channel activity. It can be used to treat polycystic kidney disease. It can promote proteasome and lysosome-mediated AQP2 degradation and slow cyst growth by reducing AQP2 transcription. Synonyms: (4α)-13-Hydroxy-kaur-16-en-18-oic Acid; 13-Hydroxy-kaur-16-en-18-oic Acid; 13-Hydroxykaurenoic Acid; Ent-13-hydroxy-kauran-16-en-19-oic Acid; 1H-2,10a-Ethanophenanthrene; 13-O-Glucosylsteviol; Hydroxydehydrostevic Acid; (4R,4aS,6aR,9S,11aR,11bS)-9-hydroxy-4,11b-dimethyl-8-methylenetetradecahydro-6a,9-methanocyclohepta[a]naphthalene-4-carboxylic acid. Grade: 98.5%. CAS No. 471-80-7. Molecular formula: C20H30O3. Mole weight: 318.45. | |
| Steviol | analytical standard. Group: Application areasfood additives, flavours & adulterants. Alternative Names: NSC 226902,Kaur-16-en-18-oic acid, 13-hydroxy-, (4?)-, Ent-13-hydroxykauran-16-en-19-oic acid, Kaur-16-en-18-oic acid, 13-hydroxy- (7CI,8CI), Hydroxydehydrostevic acid, (-)-Steviol, (4?)-13-Hydroxykaur-16-en-18-oic acid, Steviol (6CI), 13-Hydroxykaurenoic acid. | |
| Steviolbioside | Botanical Source: Group: Biochemicals. Grades: Plant Grade. CAS No. 41093-60-1. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Steviol Glycosides System Suitability | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Steviol hydrate | ?98% (HPLC), powder. Group: Fluorescence/luminescence spectroscopy. | |
| Steviol methyl ester | Steviol methyl ester. Uses: Designed for use in research and industrial production. Additional or Alternative Names: (10S)-13-hydroxy-kaur-16-en-19-oic acid methyl ester; Steriol-methylester; (-)-steviol methyl ester; Steviol methyl ester; (10S)-13-Hydroxy-kaur-16-en-19-saeure-methylester; (4aR)-Hydroxy-4bt,8c-dimethyl-12-methylen-8t-methylcarbonyl-(4arH.8acH)-1.2.4.4a. Product Category: Heterocyclic Organic Compound. CAS No. 14364-16-0. Molecular formula: C21H32O3. Mole weight: 332.477. Purity: 0.96. IUPACName: methyl (5β,8α,9β,10α,13α)-13-hydroxykaur-16-en-18-oate. Product ID: ACM14364160. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Stevioside | Stevioside. Group: Biochemicals. Alternative Names: Eupatorin; Rebaudin; Stevin; Steviosin. Grades: Plant Grade. CAS No. 57817-89-7. Pack Sizes: 20mg. Molecular Formula: C38H60O18, Molecular Weight: 804.871999999999. US Biological Life Sciences. | Worldwide |
| Stevioside | Application Areas; Herbal Medicinal Products Standards. Uses: For analytical and research use. Group: Reagents. CAS No. 57817-89-7. | |
| Stevioside | Stevioside is an orally active sweetener that can be isolated from Stevia rebaudiana , with antihypertensive, antihyperglycemic, antioxidant, anti-inflammatory and anti-tumor activities [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 57817-89-7. Pack Sizes: 10 mM * 1 mL; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N0669. | |
| Stevioside | It is a natural herbal sweetener that is 250-300 times sweeter than sucrose (though with a bitter aftertaste), extracted from the Stevia rebaudiana plant native to South America. It has a role as a sweetening agent, an antioxidant, an antineoplastic agent, a hypoglycemic agent, an anti-inflammatory agent and a plant metabolite. It is a diterpene glycoside, an ent-kaurane diterpenoid, a beta-D-glucoside, a tetracyclic diterpenoid and a bridged compound. It is functionally related to a steviol and a rubusoside. Alternative Names: Steviosin. CHEBI:9271. Rebaudin. CAS No. 57817-89-7. Product ID: PIPE-0727. Molecular formula: C38H60O18. Mole weight: 804.9. EINECS: 260-975-5. SMILES: C[C@@]12CCC[C@@]([C@H]1CC[C@]34[C@H]2CC[C@](C3)(C(=C)C4)O[C@H]5[C@@H]([C@H]([C@@H]([C@H](O5)CO)O)O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O)(C)C(=O)O[C@H]7[C@@H]([C@H]([C@@H]([C@H](O7)CO)O)O)O. Appearance: White to light yellow powder. Category: Natural Extract. |  |
| Stevioside | Pharmacopeia & Metrological Institutes Standards; Food Additives, Flavours & Adulterants. Uses: For analytical and research use. Group: Reagents. Alternative Names: E 960, (4?)-13-[(2-O-?-D-Glucopyranosyl-?-D-glucopyranosyl)oxy]kaur-16-en-18-oic Acid ?-D-Glucopyranosyl Ester, Stevian 50, Stevioside (6CI,7CI), ?-G-Sweet,Kaur-16-en-18-oic acid, 13-[(2-O-?-D-glucopyranosyl-?-D-glucopyranosyl)oxy]-, ?-D-glucopyranosyl ester, (4?)-, 1H-2,10a-Ethanophenanthrene, kaur-16-en-18-oic acid deriv., Steviosin. CAS No. 57817-89-7. Pack Sizes: 30MG. | |
| Stevioside | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardsfood additives, flavours & adulterants. Alternative Names: E 960, (4?)-13-[(2-O-?-D-Glucopyranosyl-?-D-glucopyranosyl)oxy]kaur-16-en-18-oic Acid ?-D-Glucopyranosyl Ester, Stevian 50, Stevioside (6CI,7CI), ?-G-Sweet,Kaur-16-en-18-oic acid, 13-[(2-O-?-D-glucopyranosyl-?-D-glucopyranosyl)oxy]-, ?-D-glucopyranosyl ester, (4?)-, 1H-2,10a-Ethanophenanthrene, kaur-16-en-18-oic acid deriv., Steviosin. | |
| Stevioside | Stevioside. Synonyms: beta-d-glucopyranosyl(1r, 4as, 7s, 8ar, 10as)-7-(2-o-(beta-d-glucopyranosyl)-alpha-d-glucopyranosyloxy)-1, 4a-dimethyl-12-methyleneperhydro-7, 8a-ethanophenanthren-1-carboxylate; beta-d-glucopyranosylester; kaur-16-en-18-oicacid, 13-((2-o-beta-d-glucopyranosyl-alpha-d-glucopyranosyl)o; steviosin; (4alpha)-beta-d-glucopyranosyl 13-[(2-o-beta-d-glucopyranosyl-beta-d-glucopyranosyl)oxy]kaur-16-en-18-oate;13-[(2-O-beta-D-Glucopyranosyl-alpha-D-glucopyranosyl)oxy]kaur-16-en-18-oic acid beta-D-glucopyranosyl ester. CAS No. 57817-89-7. Pack Sizes: 1 kg. Product ID: CDF4-0161. Molecular formula: C38H60O18. Category: Sweeteners. Product Keywords: Food Ingredients; Sweeteners; Stevioside; CDF4-0161; 57817-89-7; C38H60O18; 260-975-5; 57817-89-7. Purity: 0.99. Color: White. EC Number: 260-975-5. Physical State: Powder. Solubility: DMSO: soluble25mg/mL, clear. Quality Level: 100. Storage: Sealed in dry,2-8°C. Application: The product has a refreshing sweet taste, sweetness is about 200-300 times that of sucrose. Slightly bitter taste at high concentrations, sweet taste in the mouth is not easy to disappear. The product is one of the natural sweeteners closest to sucrose. As low alorie food sweetener, it can low pressure. Boiling Point: 963.3±65.0 °C(Predicted). Melting Point: 198°C. Density: 1.53±0.1 g/cm3(Predicted). |  |
| Stevioside-d2 (90%) | Isotope labelled Stevioside (S686730) is a glycoside from the stevia plant. Stevioside is a natural sweetening agent with sweetness about 250 times that of sugar with negligible effect on blood glucose. Stevioside, much like other steviol glycoside is known for its application in treatment of many diseases like diabetes and high blood pressure. It is also used as a food additive and in dietary supplements. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 2.5mg, 5mg. Molecular Formula: C3713CH58D2O18, Molecular Weight: 807.88. US Biological Life Sciences. | Worldwide |
| Stevioside hydrate | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Stevioside hydrate (BRN 0077427, CCRIS 6116) | Noncaloric natural sweetener, 300 times more potent than sucrose. Antidiabetic. Antihyperglycaemic and antihypoglycaemic. Potentiates insulin secretion. Enhances acetyl-CoA carboxylase (ACC) gene expression. Increases insulin sensitivity. Antihypertensive. Ca2+ influx inhibitor. Anticancer compound. Chemopreventive. Anti-inflammatory. IKKbeta, NF-kappaB and MAPK signaling inhibitor. Induces TNF-alpha, IL-1beta and nitric oxide release. Immunomodulator. Increasees phagocytic activity, haemagglutination antibody titre, delayed type hypersensitivity. Increased proliferation in LPS and Con A stimulated B and T cells. Peripheral me-opioid receptors activator. Important for regulation of glucose homeostasis. Anti-atherosclerotic. Group: Biochemicals. Alternative Names: BRN 0077427, CCRIS 6116. Grades: Highly Purified. CAS No. 57817-89-7 (anhy). Pack Sizes: 10mg, 50mg. Molecular Formula: C38H60O18. xH2O. US Biological Life Sciences. | Worldwide |
| Steviosin | Steviosin. Synonyms: Steviosides. CAS No. 57817-89-7. Product ID: PE-0006. Molecular formula: C38H60O18. Mole weight: 804.872. Category: Sweetening agent; Corrective Excipients. Product Keywords: Pharmaceutical Excipients; Excipients for Liquid Dosage Form; Corrective Excipients; Steviosin; PE-0006; C38H60O18; 57817-89-7; 57817-89-7. Appearance: White powder. Storage: 0-6ºC. Boiling Point: 963.3ºC at 760 mmHg. Melting Point: 198ºC. Density: 1.53 g/cm3. | |
| STF 083010 | STF 083010. Group: Biochemicals. Alternative Names: N-[ (2-Hydroxy-1-naphthalenyl) methylene]-2-thiophenesulfonamide. Grades: Highly Purified. CAS No. 307543-71-1. Pack Sizes: 25mg. Molecular Formula: C15H11NO3S2, Molecular Weight: 317.38. US Biological Life Sciences. | Worldwide |
| STF-083010 | STF-083010 is a specific IRE1? inhibitor. STF-083010 inhibits Ire1 endonuclease activity, without affecting its kinase activity, after endoplasmic reticulum stress. Uses: Scientific research. Group: Signaling pathways. CAS No. 307543-71-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-15845. | |
| STF-083010 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| STF 118804 | STF 118804. Group: Biochemicals. Grades: Purified. CAS No. 894187-61-2. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| STF-118804 | STF-118804 is a highly specific NAMPT inhibitor. STF-118804 activates AMPK and inhibits mTOR pathways. STF-118804 has antitumor activity against pancreatic cancer [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 894187-61-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-12808. | |
| STF-118804 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| STF 31 | STF 31. Group: Biochemicals. Grades: Purified. CAS No. 724741-75-7. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| STF-31 | STF-31 is a selective inhibitor of glucose transporter 1 (GLUT1), with an IC50 of 1 ?M. STF-31 is also a NAMPT inhibitor. STF-31 inhibits glucose uptake in renal cell carcinoma (RCC) 4 cells[1][2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 724741-75-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-18728. | |
| STF-31 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| STF-62247 | ?98% (HPLC), solid. Group: Fluorescence/luminescence spectroscopy. | |
| STF-62247 | STF-62247 is an autophagy inducer that selectively cytotoxic to VHL-deficient renal cell carcinoma ( IC 50 of 0.625 μM and 16 μM in RCC4 and RCC4/VHL cells, respectively) [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 315702-99-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-100746. | |
| STh | STh is a heat stable toxin of Escherichia coli. CAS No. 118447-40-8. Molecular formula: C79H112N22O30S6. Mole weight: 2042.25. | |
| STh | STh, an Escherichia coli heat-stable toxin, is a 19 amino acid polypeptide encompassing three disulfide bridges. STh is an antigen of interest in the search for a broad coverage enterotoxigenic Escherichia coli (ETEC) vaccine [1]. Uses: Scientific research. Group: Peptides. CAS No. 118447-40-8. Pack Sizes: 1 mg. Product ID: HY-P2695. | |
| st-Ht31 | st-Ht31 is the stearate form of Ht-31 peptide, which can inhibit the PKA/AKAP interaction. Cell permeable. Synonyms: AKOS032962858. CAS No. 188425-80-1. Molecular formula: C129H217N29O39. Mole weight: 2798.27. | |
| St-Ht31 P | Negative control for st-Ht31. Synonyms: stearoyl-Asp-Leu-Ile-Glu-Glu-Ala-Ala-Ser-Arg-Pro-Val-Asp-Ala-Val-Pro-Glu-Gln-Val-Lys-Ala-Ala-Gly-Ala-Tyr-OH; N-stearoyl-L-alpha-aspartyl-L-leucyl-L-isoleucyl-L-alpha-glutamyl-L-alpha-glutamyl-L-alanyl-L-alanyl-L-seryl-L-arginyl-L-prolyl-L-valyl-L-alpha-aspartyl-L-alanyl-L-valyl-L-prolyl-L-alpha-glutamyl-L-glutaminyl-L-valyl-L-lysyl-L-alanyl-L-alanyl-glycyl-L-alanyl-L-tyrosine. Grade: >98%. CAS No. 252869-81-1. Molecular formula: C127H209N29O39. Mole weight: 2766.19. | |
| Stichodactyla helianthus Neurotoxin (ShK) | Stichodactyla helianthus Neurotoxin, a toxin originally isolated from sea anemone Stichodactyla helianthus, inhibits the specific binding of dendrotoxin I to rat brain membranes. Because of its unique structure (containing three intramolecular disulfide bridges) and high affinity for some potassium channels, it may be a useful molecular probe for studying potassium channels. Synonyms: ShK; H-Arg-Ser-Cys-Ile-Asp-Thr-Ile-Pro-Lys-Ser-Arg-Cys-Thr-Ala-Phe-Gln-Cys-Lys-His-Ser-Met-Lys-Tyr-Arg-Leu-Ser-Phe-Cys-Arg-Lys-Thr-Cys-Gly-Thr-Cys-OH (Disulfide bridge: Cys3-Cys35, Cys12-Cys28, Cys17-Cys32); L-Arginyl-L-seryl-L-cysteinyl-L-isoleucyl-L-alpha-aspartyl-L-threonyl-L-isoleucyl-L-prolyl-L-lysyl-L-seryl-L-arginyl-L-cysteinyl-L-threonyl-L-alanyl-L-phenylalanyl-L-glutaminyl-L-cysteinyl-L-lysyl-L-histidyl-L-seryl-L-methionyl-L-lysyl-L-tyrosyl-L-arginyl-L-leucyl-L-seryl-L-phenylalanyl-L-cysteinyl-L-arginyl-L-lysyl-L-threonyl-L-cysteinylglycyl-L-threonyl-L-cysteine cyclic (3→35),(12→28),(17→32)-tris(disulfide); Toxin ShK (Stoichactis helianthus potassium-channel). Grade: ≥95% by HPLC. CAS No. 172450-46-3. Molecular formula: C169H274N54O48S7. Mole weight: 4054.83. | |
| Stichodactyla helianthus neurotoxin (ShK) amide | Stichodactyla helianthus Neurotoxin, a toxin originally isolated from sea anemone Stichodactyla helianthus, inhibits the specific binding of dendrotoxin I to rat brain membranes. Because of its unique structure (containing three intramolecular disulfide bridges) and high affinity for some potassium channels, it may be a useful molecular probe for studying potassium channels. Synonyms: Arg-Ser-Cys-Ile-Asp-Thr-Ile-Pro-Lys-Ser-Arg-Cys-Thr-Ala-Phe-Gln-Cys-Lys-His-Ser-Met-Lys-Tyr-Arg-Leu-Ser-Phe-Cys-Arg-Lys-Thr-Cys-Gly-Thr-Cys-NH2 (Disulfide bond Cys3/Cys35, Cys12/Cys28, Cys17/Cys32). Molecular formula: C169H275N55O47S7. Mole weight: 4053.78. | |
| Stictic acid | Stictic acid. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Scopularic acid. Appearance: Light tan solid. CAS No. 549-06-4. Molecular formula: C19H14O9. Mole weight: 386.3. Purity: 0.95. Product ID: ACM549064. Alfa Chemistry ISO 9001:2015 Certified. | |
| Stigmast-4-ene-3β,6β-diol | Stigmast-4-ene-3β,6β-diol is a natural steroid found in the barks of Ailanthus altissima. Synonyms: (3S,6R,8S,9S,10R,13R,14S,17R)-17-((2R,5R)-5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene-3,6-diol. Grade: >97%. CAS No. 113626-76-9. Molecular formula: C29H50O2. Mole weight: 430.7. | |
| Stigmasta-4,22-dien-3-one | Stigmasta-4,22-dien-3-one can be found in the flower of Magnolia biondii. It has antioxidant activity. Uses: Antioxidant. Synonyms: 4,22-Cholestadien-24-ethyl-3-one. Grade: >98%. CAS No. 55722-32-2. Molecular formula: C29H46O. Mole weight: 410.7. | |
| Stigmasta-4,22-dien-3-one | Stigmasta-4,22-dien-3-one is an antitubercular agent. Stigmasta-4,22-dien-3-one shows cytotoxicity against human HT1080 tumoral cell line with an IC 50 of 0.3 mM [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 20817-72-5. Pack Sizes: 1 mg; 5 mg. Product ID: HY-N9596. | |
| Stigmasta-4,22-dien-3-one | Stigmasta-4,22-dien-3-one. Group: Biochemicals. Grades: Highly Purified. CAS No. 55722-32-2. Pack Sizes: 10g, 25g, 50g, 100g. Molecular Formula: C29H46O. US Biological Life Sciences. | Worldwide |
| Stigmastane-3,6-dione,(5a)- | Stigmastane-3,6-dione usually comes from the roots of Piper nigrum. Synonyms: 5α-Stigmastane-3,6-dione. Grade: >98%. CAS No. 22149-69-5. Molecular formula: C29H48O2. Mole weight: 428.7. | |
| Stigmastane-3β,5α,6β-triol | Stigmastane-3β,5α,6β-triol isolated from the fruits of Evodia rutaecarpa. Synonyms: alpha-stigmastane-3 beta,5,6 beta-triol 3-monobenzoate. Grade: 0.98. CAS No. 20835-91-0. Molecular formula: C29H52O3. Mole weight: 448.7. | |
| Stigmastanol | Stigmastanol. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 24-ALPHA-ETHYLCHOLESTANOL. Appearance: White Solid. CAS No. 83-45-4. Molecular formula: C29H52O. Mole weight: 416.72. Purity: 0.99. Product ID: ACM83454. Alfa Chemistry ISO 9001:2015 Certified. | |
| Stigmastanol | Stigmastanol is the 6-amino derivative isolated from Hypericum riparium. Hypericum riparium A. Chev. is a Cameroonian medicinal plant belonging to the family Guttiferae [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 83-45-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-113494. | |
| Stigmasterol | Stigmasterol - Product ID: NST-10-57. Category: Sterols. Purity: 98%. Test method: GC. CAS No. 83-48-7. Pack Sizes: 10g, 20g, 50g, 100g. Appearance: White to beige coloured Powder. Molecular formula: C29H48O. Mole weight: 412.69. Storage: +2 +8 °C. |  |
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