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(1S)-(+)-3-Carene is used in the synthesis of compounds with various odoriferous properties. It is used by the perfume and fragrance industry or in perfume materials preparation. Group: Biochemicals. Grades: Highly Purified. CAS No. 498-15-7. Pack Sizes: 100mg, 250mg. Molecular Formula: C10H16, Molecular Weight: 136.229999999999. US Biological Life Sciences.
Worldwide
3-Carene
3-Carene is a bicyclic monoterpene in essential oils extracted from pine trees. 3-Carene inhibits nociceptive stimulus-induced inflammatory infiltrates and COX-2 overexpression, and with antinociceptive effect. 3-Carene stimulates the activity and expression of alkaline phosphatase that is an early phase marker of osteoblastic differentiation [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 13466-78-9. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-N6663.
3-Carene
3-Carene is a mutagenic compound that may be found in the fumes of heating freshly cut spruce and birch chips. 3-Carene is also found i many esential oils and it inhibits acetylcholinesterase activity. Group: Biochemicals. Grades: Highly Purified. CAS No. 13466-78-9. Pack Sizes: 100g, 250g. Molecular Formula: C10H16. US Biological Life Sciences.
Worldwide
3-Carene-D3
Deuterium labelled isotope of 3-Carene, which is a mutagenic compound that may be found in the fumes of heating freshly cut spruce and birch chips. 3-Carene is also found i many esential oils and it inhibits acetylcholinesterase activity. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 2.5mg. Molecular Formula: C10H13D3, Molecular Weight: 139.25. US Biological Life Sciences.
Worldwide
(-)-β-pinene synthase
Cyclase II of Salvia officinalis (sage) produces about equal parts (-)-α-pinene, (-)-β-pinene and (-)-camphene, plus traces of other monoterpenoids. The enzyme, which requires Mg2+ (preferred to Mn2+), can also use (3S)-Linalyl diphosphate (preferred to (3R)-linalyl diphosphate). The enzyme from Abies grandis (grand fir) produces roughly equal parts of (-)-α-pinene and (-)-β-pinene. Cyclase IV from Pinus contorta (lodgepole pine) produces 63% (-)-β-pinene, 26% 3-carene, and traces of α-pinene. Synthase III from Pinus taeda (loblolly pine) forms (-)-β-pinene with traces of α-pinene and requires Mn2+ and K+ (Mg2+ is ineffective). A clone...a spruce) forms 30% (-)-β-pinene and 70% (-)-α-pinene. See also EC 4.2.3.119, (-)-α-pinene synthase, EC 4.2.3.117, (-)-camphene synthase, and EC 4.2.3.107 (+)-3-carene synthase. Group: Enzymes. Synonyms: β-geraniolene synthase; (-)-(1S,5S)-pinene synthase; geranyldiphosphate diphosphate lyase (pinene forming). Enzyme Commission Number: EC 4.2.3.120. 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-5133; (-)-β-pinene synthase; EC 4.2.3.120; β-geraniolene synthase; (-)-(1S,5S)-pinene synthase; geranyldiphosphate diphosphate lyase (pinene forming). Cat No: EXWM-5133.
(+)-car-3-ene synthase
The enzyme reacts with (3S)-linalyl diphosphate twice as rapidly as geranyl diphosphate, but 25 times as rapidly as (3R)-linalyl diphosphate. It is assumed that (3S)-linalyl diphosphate is normally formed as an enzyme bound intermediate in the reaction. In the reaction the 5-pro-R hydrogen of geranyl diphosphate is eliminated during cyclopropane ring formation. In Picea abies (Norway spruce) and Picea sitchensis (Sitka spruce) terpinolene is also formed. See EC 4.2.3.113 terpinolene synthase. (+)-Car-3-ene is associated with resistance of Picea sitchensis (Sitka spruce) to white pine weevil. Group: Enzymes. Synonyms: 3-carene cyclase; 3-carene synthase; 3CAR; (+)-3-carene synthase. Enzyme Commission Number: EC 4.2.3.107. 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-5118; (+)-car-3-ene synthase; EC 4.2.3.107; 3-carene cyclase; 3-carene synthase; 3CAR; (+)-3-carene synthase. Cat No: EXWM-5118.
ipsdienol synthase
A cytochrome P-450 heme-thiolate protein. Involved in the insect aggregation pheromone production. Isolated from the pine engraver beetle, Ips pini. A small amount of (S)-ipsdienol is also formed. In vitro it also hydroxylated (+)- and (-)-α-pinene, 3-carene, and (+)-limonene, but not α-phellandrene, (-)-β-pinene, γ-terpinene, or terpinolene. Group: Enzymes. Synonyms: myrcene hydroxylase; CYP9T2; CYP9T3. Enzyme Commission Number: EC 1.14.14.31. 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-0929; ipsdienol synthase; EC 1.14.14.31; myrcene hydroxylase; CYP9T2; CYP9T3. Cat No: EXWM-0929.
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