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| Product | Description | |
|---|---|---|
| Decenal trans-4 | Decenal trans-4. CAS No. 65405-70-1. FEMA No. 3264. Kosher: Y. VIGON Item # 500972. Categories: Speciality Ingrdients Suppliers, Flavors, Fragrances, Perfumers. |  America & Internationally |
| trans-2-Decenal | trans-2-Decenal is an important raw material and intermediate used in organic synthesis, medicine, pesticides and dyes. Uses: Scientific research. Group: Natural products. Alternative Names: (E)-Dec-2-enal. CAS No. 3913-81-3. Pack Sizes: 10 g; 25 g. Product ID: HY-W015551. |  |
| 2-Decenal | Aldehydes. Alternative Names: trans-2-Decenal. CAS No. 3913-81-3/3913-71-1. Mole weight: 154.25. Purity: 0.99. IUPACName: (E)-Dec-2-enal. Canonical SMILES: CCCCCCCC=CC=O. Density: 0.841 g/mL at 25 °C(lit.). |  |
| 10-Hydroxydecanoic acid | 10-Hydroxydecanoic acid (10-HDAA) is a saturated fatty acid derived from 10-hydroxy-trans-2-decenoic acid, which can be isolated from royal jelly. 10-Hydroxydecanoic acid exhibits various biological activities, including anti-inflammatory, insecticidal, anti-malarial, and anti-Leishmania properties, as well as enhancing antigen-specific immune responses. The anti-inflammatory effects of 10-Hydroxydecanoic acid are primarily mediated by inhibiting the activation of NF-κB and the translation of interferon regulatory factor 1 ( IRF-1 ), which reduces the production of interleukin 6 ( IL-6 ) and nitric oxide ( NO ) in inflammatory cells. Additionally, 10-Hydroxydecanoic acid alleviates neuroinflammatory responses through the p53-autophagy pathway and the p53-NLRP3 pathway. Finally, 10-Hydroxydecanoic acid enhances antigen-specific immune responses by promoting the effective uptake of antigens by microfold cells [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Natural products. Alternative Names: NSC 15139; 10-HDAA. CAS No. 1679-53-4. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-Y0148. | |
| 10-Oxo-trans-8-decenoic Acid | 10-Oxo-trans-8-decenoic Acid was found to be the major nonvolatile metabolite associated with the enzymic cleavage of linoleic acid to 1-octen-3-ol by mycelial homogenate of mushrooms. Group: Biochemicals. Grades: Highly Purified. CAS No. 69152-89-2. Pack Sizes: 5mg, 50mg. Molecular Formula: C10H16O3, Molecular Weight: 184.23. US Biological Life Sciences. |  Worldwide |
| 2-Decen-1-ol | Alcohols. Alternative Names: Trans-2-decenol. CAS No. 18409-18-2. Mole weight: 156.26. Purity: 95%+. IUPACName: (E)-Dec-2-en-1-ol. Canonical SMILES: CCCCCCCC=CCO. Density: 0.844 g/mL at 25 °C(lit.). | |
| 3-hydroxyacyl-[acyl-carrier-protein] dehydratase | This enzyme is responsible for the dehydration step of the dissociated (type II) fatty-acid biosynthesis system that occurs in plants and bacteria. The enzyme uses fatty acyl thioesters of ACP in vivo. Different forms of the enzyme may have preferences for substrates with different chain length. For example, the activity of FabZ, the ubiquitous enzyme in bacteria, decreases with increasing chain length. Gram-negative bacteria that produce unsaturated fatty acids, such as Escherichia coli, have another form (FabA) that prefers intermediate chain length, and also catalyses EC 5.3.3.14, trans-2-decenoyl-[acyl-carrier protein] isomerase. Despite the differences both forms...hydratase. Enzyme Commission Number: EC 4.2.1.59. CAS No. 9030-85-7. 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-5047; 3-hydroxyacyl-[acyl-carrier-protein] dehydratase; EC 4.2.1.59; 9030-85-7; fabZ (gene name); fabA (gene name); D-3-hydroxyoctanoyl-[acyl carrier protein] dehydratase; D-3-hydroxyoctanoyl-acyl carrier protein dehydratase; β-hydroxyoctanoyl-acyl carrier protein dehydrase; β-hydroxyoctanoyl thioester dehydratase; β-hydroxyoctanoyl-ACP-dehydrase; (3R)-3-hydroxyoctanoyl-[acyl-carrier-protein] hydro-lyase; (3R)-3-hydroxyoctanoyl-[acyl-carrier-protein] hyd |  |
| (E)-2-Decenoic acid | trans-2-Decenoic Acid is isolated along with 10-hydroxy-trans-2-decenoic acid, a fatty acid unique to royal jelly.(E)-2-decanoic acid(trans-2-Decenoic Acid) and 10-hydroxy-trans-2-decenoic acid are both described to demonstrate estrogenic activity, where the fatty acids demonstrate inhibition of 17β-estradiol binding to estrogen receptor-&beta. Synonyms: trans-2-Decenoic acid. Grades: >98%. CAS No. 334-49-6. Molecular formula: C10H18O2. Mole weight: 170.25. |  |
| (E)-3-Decenol | Heterocyclic Organic Compound. Alternative Names: 3-Decen-1-ol, trans-3-Decen-1-ol, (E)-3-Decenol, 3-Decen-1-ol, (E)-, 3-Decen-1-ol, (Z)-, 3-Decen-1-ol, (3E)-, EINECS 233-733-1, CID5352493, 10339-60-3, 69093-74-9. CAS No. 10339-60-3. Molecular formula: C10H20O. Mole weight: 156.265200 [g/mol]. Purity: 0.96. IUPACName: (E)-dec-3-en-1-ol. Catalog: ACM10339603. | |
| trans-2-Decen-1-ol | trans-2-Decen-1-ol is an antibiotic essential oil with nematicidal properties. Group: Biochemicals. Grades: Highly Purified. CAS No. 18409-18-2. Pack Sizes: 5g, 10g. Molecular Formula: C10H20O, Molecular Weight: 156.27. US Biological Life Sciences. | Worldwide |
| TRANS-2-DECENOIC ACID | TRANS-2-DECENOIC ACID. Synonyms: RARECHEM AL BK 0166;T2 DECENOIC ACID;TRANS-2-DECYLENIC ACID;TRANS-2-DECENOIC ACID;FEMA NUMBER 3913;2-DECYLENIC ACID;2-DECENOIC ACID;(E)-dec-2-enoic acid. CAS No. 334-49-6. Pack Sizes: 1 kg. Product ID: CDF4-0087. Molecular formula: C10H18O2. Category: Flavor Enhancers. Product Keywords: Food Ingredients; Flavor Enhancers; TRANS-2-DECENOIC ACID; CDF4-0087; 334-49-6; C10H18O2; 206-378-5; 334-49-6. Purity: 0.99. Color: Colorless to Light yellow. EC Number: 206-378-5. Physical State: Clear Liquid. Storage: 2-8°C. Boiling Point: 135-121 °C (2.5 mmHg). Melting Point: 18.83°C (estimate). Density: 0.925 g/mL. |  |
| trans-2-Decenoic acid ethyl ester | trans-2-Decenoic acid ethyl ester. Group: Biochemicals. Grades: Highly Purified. CAS No. 7367-88-6. Pack Sizes: 100g, 250g, 500g, 1kg. Molecular Formula: C12H22O2. US Biological Life Sciences. | Worldwide |
| trans-2-decenoyl-[acyl-carrier protein] isomerase | While the enzyme from Escherichia coli is highly specific for the 10-carbon enoyl-ACP, the enzyme from Streptococcus pneumoniae can also use the 12-carbon enoyl-ACP as substrate in vitro but not 14- or 16-carbon enoyl-ACPs. ACP can be replaced by either CoA or N-acetylcysteamine thioesters. The cis-3-enoyl product is required to form unsaturated fatty acids, such as palmitoleic acid and cis-vaccenic acid, in dissociated (or type II) fatty-acid biosynthesis. Group: Enzymes. Synonyms: β-hydroxydecanoyl thioester dehydrase; trans-2-cis-3-decenoyl-ACP isomerase; trans-2,cis-3-decenoyl-ACP isomerase; trans-2-decenoyl-ACP isomerase; FabM;decenoyl-[acyl-carrier-protein] Δ2-trans-Δ3-cis-isomerase. Enzyme Commission Number: EC 5.3.3.14. CAS No. 9030-80-2. 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-5494; trans-2-decenoyl-[acyl-carrier protein] isomerase; EC 5.3.3.14; 9030-80-2; β-hydroxydecanoyl thioester dehydrase; trans-2-cis-3-decenoyl-ACP isomerase; trans-2,cis-3-decenoyl-ACP isomerase; trans-2-decenoyl-ACP isomerase; FabM;decenoyl-[acyl-carrier-protein] Δ2-trans-Δ3-cis-isomerase. Cat No: EXWM-5494. | |
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