Find where to buy products from suppliers in the USA, including: distributors, industrial manufacturers in America, bulk supplies and wholesalers of raw ingredients & finished goods.
Search for products or services, then visit the American suppliers website for prices, SDS or more information. You can also view suppliers in Australia, NZ or the UK.
| Product | Description | |
|---|---|---|
| Abietic Acid | Abietic Acid is the primary component of resin acid found commonly in rosin. Abietic Acid exhibited potent testosterone 5α-reductase inhibitory activity in vitro. Group: Biochemicals. Alternative Names: (1R, 4aR, 4bR, 10aR)-1, 2, 3, 4, 4a, 4b, 5, 6, 10, 10a-Decahydro-1, 4a-dimethyl-7-(1-methylethyl)-1-phenanthrenecarboxylic Acid; 13-Isopropylpodocarpa-7,13-dien-15-oic Acid; (-)-Abietic Acid; 7,13-Abietadien-18-oic Acid; Abietic Acid; NSC 25149; Odomit B 10; Sylvic Acid; ZAO; l-Abietic Acid. Grades: Highly Purified. CAS No. 514-10-3. Pack Sizes: 25g. US Biological Life Sciences. |  Worldwide |
| Abietic Acid | CAS No: 514-10-3 |  Sarchem Laboratories New Jersey NJ |
| Abietic Acid, >95% | Abietic Acid is the primary component of resin acid found commonly in rosin. Abietic Acid exhibited potent testosterone 5α-reductase inhibitory activity in vitro. Group: Biochemicals. Grades: Highly Purified. CAS No. 514-10-3. Pack Sizes: 10mg, 25mg. Molecular Formula: C20H30O2. US Biological Life Sciences. | Worldwide |
| Abietic acid | Abietic acid, an orally active diterpene isolated from Colophony, displays significant anti-proliferative, anti-inflammatory, anti-obesity effect, bacteriostatic, cell cycle arresting and pro-apoptotic activities. Abietic acid inhibits lipoxygenase activity for allergy. Abietic acid enhances cell migration and tube formation in HUVECs. Abietic acid induces significant angiogenic potential, which is associated with upregulation of extracellular signal-regulated kinase (ERK) and p38 expression. Abietic acid attenuates sepsis-induced lung injury by inhibiting nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) pathway to inhibit M1 macrophage polarization. Abietic acid exhibits a positive effect against liver injury by attenuating inflammation and ferroptosis. Abietic acid shows accelerated wound closure in a mouse model of cutaneous wounds. Abietic acid significantly reduces the proliferation and growth of NSCLC cells by IKKβ inhibition.Additionally, Abietic acid ameliorates psoriasis-like inflammation and modulates gut microbiota in mice. Abietic acid is promising for research in non-small-cell lung cancer (NSCLC), liver injury-related deseases and psoriasis [1] [2] [3] [4] [5] [6] [7]. Uses: Scientific research. Group: Natural products. CAS No. 514-10-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-N6871. |  |
| Neoabietic Acid | Neoabietic Acid is a derivative of Gum Rosin (G855500). It is an abietane-type of diterpene resin acid and reduces the consumption rate, feeding efficiency, and growth rate of the larch sawfly (Pristiphora erichsonii) when applied to their natural food. Group: Biochemicals. Grades: Highly Purified. CAS No. 471-77-2. Pack Sizes: 5mg, 50mg. Molecular Formula: C20H30O2, Molecular Weight: 302.45. US Biological Life Sciences. | Worldwide |
| 1,3-Bis[(1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,7,9,10,10a-decahydrophenanthrene-1-carbonyl)oxy]propan-2-yl1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,7,9,10,10a-decahydrophenanthrene-1-carboxylate | Heterocyclic Organic Compound. Alternative Names: Tridihexethyl iodide, HSDB 5607, CID31333, EINECS 204-761-1, Abietic acid, dihydro-, triester with glycerol, 1,2,3-Propanetriyl (1R-(1alpha,4abeta,4balpha,10aalpha))-1,2,3,4,4a,4b,5,6,7,9,10,10a-dodecahydro-7-isopropyl-1,4a-dimethylphenanthren-1-carboxylate, 1-Phenanthrenecarboxylic acid, 1,2,3,4,4a,4b,5,6,7,9,10,10a-dodecahydro-1,4a-dimethyl-7-(1-methylethyl)-, 1,1,1-(1,2,3-propanetriyl) ester, (. CAS No. 125-93-9. Molecular formula: C63H98O6. Mole weight: 951.449 g/mol. Purity: 0.96. IUPACName: 2,3-bis[(1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,7,9,10,10a-decahydrophenanthrene-1-carbonyl)oxy]propyl 1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,7,9,10,10a-decahydrophenanthrene-1-carboxylate. Canonical SMILES: CC (C)C1CCC2C (=C1)CCC3C2 (CCCC3 (C)C (=O)OCC (COC (=O)C4 (CCCC5 (C4CCC6=CC (CCC65)C (C)C)C)C)OC (=O)C7 (CCCC8 (C7CCC9=CC (CCC98)C (C)C)C)C)C. Density: 1.08g/cm³. ECNumber: 204-761-1. Catalog: ACM125939. |  |
| 2-(2-Hydroxyethoxy)ethyl(1r,4ar,4br,10ar)-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylate | Heterocyclic Organic Compound. Alternative Names: Diethylene glycol abietate, CID61481, Abietic acid, diethylene glycol ester, 1-Phenanthrenecarboxylic acid, 1,2,3,4,4a,4b,5,6,10,10a-decahydro-1,4a-dimethyl-7-(1-methylethyl)-, 2-(2-hydroxyethoxy)ethyl ester, (1R,4aR,4bR,10aR)-, 10107-99-0. CAS No. 10107-99-0. Molecular formula: C24H38O4. Mole weight: 390.556 g/mol. Purity: 0.96. IUPACName: 2-(2-hydroxyethoxy)ethyl (1R,4aR,4bR,10aR)-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylate. Density: 1.08g/cm³. Catalog: ACM10107990. | |
| abieta-7,13-dien-18-al dehydrogenase | Abietic acid is the principle component of conifer resin. This enzyme catalyses the last step of the pathway of abietic acid biosynthesis in Abies grandis (grand fir). The activity has been demonstrated in cell-free stem extracts of A. grandis, was present in the cytoplasm, and required NAD+ as cofactor. The enzyme is expressed constitutively at a high level, and is not inducible by wounding of the plant tissue. Group: Enzymes. Synonyms: abietadienal dehydrogenase (ambiguous). Enzyme Commission Number: EC 1.2.1.74. 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-1176; abieta-7,13-dien-18-al dehydrogenase; EC 1.2.1.74; abietadienal dehydrogenase (ambiguous). Cat No: EXWM-1176. |  |
| abieta-7,13-dien-18-ol hydroxylase | A heme-thiolate protein (P-450). This enzyme catalyses a step in the pathway of abietic acid biosynthesis. The activity has been demonstrated in cell-free stem extracts of Abies grandis (grand fir) and Pinus contorta (lodgepole pine), and the gene encoding the enzyme has been identified in Pinus taeda (loblolly pine). The recombinant enzyme catalyses the oxidation of multiple diterpene alcohol and aldehydes, including levopimaradienol, isopimara-7,15-dienol, isopimara-7,15-dienal, dehydroabietadienol and dehydroabietadienal. It is not able to oxidize abietadiene. Group: Enzymes. Synonyms: CYP720B1; PtAO; abietadienol hydroxylase (ambiguous). Enzyme Commission Number: EC 1.14.13.109. 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-0708; abieta-7,13-dien-18-ol hydroxylase; EC 1.14.13.109; CYP720B1; PtAO; abietadienol hydroxylase (ambiguous). Cat No: EXWM-0708. | |
| abieta-7,13-diene hydroxylase | A heme-thiolate protein (P-450). This enzyme catalyses a step in the pathway of abietic acid biosynthesis. The activity has been demonstrated in cell-free stem extracts of Abies grandis (grand fir) and Pinus contorta (lodgepole pine). The enzyme is localized in the microsomal fraction and requires both oxygen and NADPH. Inhibition by carbon monoxide and several substituted N-heterocyclic inhibitors suggests that the enzyme is a cytochrome P-450-dependent monooxygenase. Activity is induced by wounding of the plant tissue. Group: Enzymes. Synonyms: abietadiene hydroxylase (ambiguous). Enzyme Commission Number: EC 1.14.13.108. 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-0707; abieta-7,13-diene hydroxylase; EC 1.14.13.108; abietadiene hydroxylase (ambiguous). Cat No: EXWM-0707. | |
| Methyl Abietate | Methyl Abietate was used as an antiplasticizer for polycarbonates. Group: Biochemicals. Alternative Names: Abietic Acid Methyl Ester (6CI,7CI); Methyl abietate; NSC 2141; (1R, 4aR, 4bR, 10aR)-1, 2, 3, 4, 4a, 4b, 5, 6, 10, 10a-decahydro-1, 4a-dimethyl-7-(1-methylethyl)-1-Phenanthrenecarboxylic Acid Methyl Ester. Grades: Highly Purified. CAS No. 127-25-3. Pack Sizes: 2.5g. US Biological Life Sciences. | Worldwide |
| 3, 5-Bis (tert-butyldimethylsiloxyl) benzoic Acid Methyl Ester | Protected 3,5-Dihydroxybenzoic Acid Methyl Ester (D451715), with potential antifeedant activity for pine weevil, Hylobius abietis. Group: Biochemicals. Alternative Names: 3, 5-Bis [ [ (1, 1-dimethylethyl) dimethylsilyl] oxy] benzoic Acid Methyl Ester; Methyl 3,5-Bis(tert-butyldimethylsiloxyl) Benzoate. Grades: Highly Purified. CAS No. 103929-83-5. Pack Sizes: 500mg. US Biological Life Sciences. | Worldwide |
| 3,5-Dihydroxybenzoic Acid Methyl Ester | The methyl ester of 3,5-Dihydroxybenzoic Acid with potential antifeedant activity for pine weevil, Hylobius abietis. Group: Biochemicals. Alternative Names: α-Resorcinol Carboxylic Acid Methyl Ester; 3,5-Dihydroxy Methyl Benzoate; 3,5-Dihydroxybenzoic Acid Methyl Ester; Methyl 3,5-dihydroxybenzoate; Methyl α-Resorcylate; NSC 146458. Grades: Highly Purified. CAS No. 2150-44-9. Pack Sizes: 5g. US Biological Life Sciences. | Worldwide |
| Copper abietate | Fungicide. Group: Agriculture. Alternative Names: 1-Phenanthrenecarboxylic acid, 1,2,3,4,4a,4b,5,6,10,10a-decahydro-1,4a-dimethyl-7-(1-methylethyl)-, copper salt (2:1), (1R,4aR,4bR,10aR)-. CAS No. 25986-23-6. Molecular formula: C40H58CuO4. Mole weight: 666.43. IUPACName: Copper;(1R,4aR,4bR,10aR)-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylate. Canonical SMILES: CC (C)C1=CC2=CC[C@@H]3[C@@] ([C@H]2CC1) (CCC[C@@]3 (C)C (=O)[O-])C. CC (C)C1=CC2=CC[C@@H]3[C@@] ([C@H]2CC1) (CCC[C@@]3 (C)C (=O)[O-])C. [Cu+2]. Catalog: ACM25986236. | |
| ferruginol synthase | The enzyme is found in some members of the Lamiaceae (mint family). The enzyme from Rosmarinus officinalis (rosemary) is involved in biosynthesis of carnosic acid, while the enzyme from the Chinese medicinal herb Salvia miltiorrhiza is involved in the biosynthesis of the tanshinones, abietane-type norditerpenoid naphthoquinones that are the main lipophilic bioactive components found in the plant. Group: Enzymes. Synonyms: miltiradiene oxidase (incorrect); CYP76AH1; miltiradiene,NADPH:oxygen oxidoreductase (ferruginol forming) (incorrect). Enzyme Commission Number: EC 1.14.13.190. 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-0790; ferruginol synthase; EC 1.14.13.190; miltiradiene oxidase (incorrect); CYP76AH1; miltiradiene,NADPH:oxygen oxidoreductase (ferruginol forming) (incorrect). Cat No: EXWM-0790. | |
Our database is helping our users find suppliers everyday.
