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| Product | Description | |
|---|---|---|
| Campesterol | ~65%. Group: Fluorescence/luminescence spectroscopy. |  |
| Campesterol | Campesterol. Group: Biochemicals. Grades: Highly Purified. CAS No. 474-62-4. Pack Sizes: 1mg, 2mg, 5mg, 10mg, 25mg. Molecular Formula: C28H48O. US Biological Life Sciences. |  Worldwide |
| Campesterol | Campesterol is a phytosterol, primarily found in nuts, fruits, legumes and seeds. It is poorly absorbed in humans and competitively inhibits the absorption of cholesterol. lt decreases the transcription of genes involved in cholesterol metabolism in hepatocytes and enterocytes and has positive impact in treatment of cardiovascular disease. lt was used as standard in GC1 and HPLC2 analysis of oil samples from plants. Synonyms: Campest-5-en-3beta-ol; Ergost-5-en-3beta-ol, (24R)-; Ergost-5-en-3-ol, (3beta,24R)-; 24α-Methyl-5-cholesten-3β-ol. Grades: >98%. CAS No. 474-62-4. Molecular formula: C28H48O. Mole weight: 400.68. |  |
| Campesterol | Campesterol is a plant sterol with cholesterol lowering and anticarcinogenic effects. Uses: Scientific research. Group: Natural products. CAS No. 474-62-4. Pack Sizes: 10 mM * 1 mL; 2 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-N1459. |  |
| campesterol-d6 | campesterol-d6. Group: Others. Synonyms: 26,27-hexadeuteriocampest-5-en-3ss-ol. Purity: >99%. Mole weight: 406.717. Stability: 6 Months. Storage: -20°C. Avanti Polar Lipids; lipid products; sterols; sterols products; singnal transduction; cell pathways; campesterol-d6; campesterol-d6; 26,27-hexadeuteriocampest-5-en-3ss-ol. Cat No: STEZ-060. |  |
| Campesterol-d7 (Mixture of Diastereomers) | Labeled Campesterol. A phytosterol, which may inhibit the intestinal absorption of cholesterol. Group: Biochemicals. Alternative Names: 5-Cholesten-24(RS)-methyl-d3-3 β-ol-d7. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Delta-7-Campesterol | an impurity of campesterol. Synonyms: Ergost-7-en-3-ol, (3β,?24R)?-. Grades: > 95%. CAS No. 70095-94-2. Molecular formula: C28H48O. Mole weight: 400.69. | |
| (3 β,5α,6 β,22R,24R)-6-Methoxy-3,5-Cycloergostan-22-ol | (3 β,5α,6 β,22R,24R)-6-Methoxy-3,5-Cycloergostan-22-ol is an intermediate in the synthesis of Campesterol (C155360), a phytosterol, which may inhibit the intestinal absorption of cholesterol. Group: Biochemicals. Grades: Highly Purified. CAS No. 71473-15-9. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| (3 β,5α,6 β,24R)-6-Methoxy-3,5-cycloergostane | (3 β,5α,6 β,24R)-6-Methoxy-3,5-cycloergostane is an intermediate in the synthesis of Campesterol (C155360), a phytosterol, which may inhibit the intestinal absorption of cholesterol. Group: Biochemicals. Alternative Names: (3α,5R,6 β,24R)-6-Methoxy-3.5-cycloergostane. Grades: Highly Purified. CAS No. 71496-86-1. Pack Sizes: 2.5mg. US Biological Life Sciences. | Worldwide |
| 3-O-tert-Butyldimethylsilyl-24-methyl-cholest-5-ene-3,24-diol-d7 | 3-O-tert-Butyldimethylsilyl-24-methyl-cholest-5-ene-3,24-diol-d7 is Cholesterol (C432501) derivative used in the preparation of labelled Campesterol (C155364). Group: Biochemicals. Alternative Names: 3-O-tert-Butyldimethylsilyl-24-methyl-24-hydroxy-cholest-5-ene-3-ol-d7. Grades: Highly Purified. Pack Sizes: 2.5mg. US Biological Life Sciences. | Worldwide |
| 3-O-tert-Butyldimethylsilyl-24-phenylsulfonyl-cholest-5-ene-3-ol-d7 | 3-O-tert-Butyldimethylsilyl-24-phenylsulfonyl-cholest-5-ene-3-ol-d7 is an intermediate in the preparation of labelled Campesterol (C155364). Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| 3-O-tert-Butyldimethylsilyl-cholest-5-ene-3-ol Phenyl Sulfinate | 3-O-tert-Butyldimethylsilyl-cholest-5-ene-3-ol Phenyl Sulfinate is an intermediate in the preparation of Campesterol (C155360). Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| 5-Cholesten-24α-methyl 3β-ol | 5-Cholesten-24α-methyl 3β-ol. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Campesterol; CAMPESTEROL. Product Category: Steroidal Compounds. CAS No. 474-62-4. Molecular formula: C28H48O. Mole weight: 400.68. Purity: 95%+. IUPACName: (8R,9S,10S,13R,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol. Canonical SMILES: CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CCC4C3(CC=C(C4)O)C)C. Density: 0.98g/cm³. Product ID: ACM474624. Alfa Chemistry ISO 9001:2015 Certified. |  |
| 6 β-Methoxy-3α,5-cyclo-5α-pregnane-20α-carboxaldehyde | 6 β-Methoxy-3α,5-cyclo-5α-pregnane-20α-carboxaldehyde is an intermediate in the synthesis of Campesterol (C155360), a phytosterol, which may inhibit the intestinal absorption of cholesterol. Group: Biochemicals. Alternative Names: (3 β,5α,6 β,20S)-6-Methoxy-3,5-cyclopregnane-20-carboxaldehyde; (3α,5R,6 β,20S)-6-Methoxy-3,5-cyclopregnane-20-carboxaldehyde. Grades: Highly Purified. CAS No. 25819-77-6. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Beta-Sitosterol (purity>80%) | Beta-Sitosterol (purity>80%) includes β-sitosterol (≥80%), stigmasterol, campesterol and brassicasterol mainly. Beta-Sitosterol is a plant sterol. Beta-Sitosterol (purity>80%) interfere with multiple cell signaling pathways, including cell cycle, apoptosis, proliferation, survival, invasion, angiogenesis, metastasis and inflammation [1]. Uses: Scientific research. Group: Natural products. CAS No. 83-46-5. Pack Sizes: 100 mg; 1 g; 5 g. Product ID: HY-N0171. | |
| diacylglycerol-sterol O-acyltransferase | Cholesterol, sitosterol, campesterol and diacylglycerol can act as acceptors. Transfers a number of long-chain fatty acyl groups. Group: Enzymes. Synonyms: 1,2-diacyl-sn-glycerol:sterol acyl transferase. Enzyme Commission Number: EC 2.3.1.73. CAS No. 79586-23-5. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2253; diacylglycerol-sterol O-acyltransferase; EC 2.3.1.73; 79586-23-5; 1,2-diacyl-sn-glycerol:sterol acyl transferase. Cat No: EXWM-2253. | |
| (S)-1-Bromo-2,3-dimethylbutane | (S)-1-Bromo-2,3-dimethylbutane is a reagent used in the synthesis of Campesterol (C155360), a phytosterol, which may inhibit the intestinal absorption of cholesterol. Group: Biochemicals. Grades: Highly Purified. CAS No. 15164-29-1. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| 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. | |
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