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Chemical compound
Bisabolenes are a group of closely related natural chemical compounds which are classified as sesquiterpenes. Bisabolenes are produced from farnesyl pyrophosphate
Bisabolene
Enzyme
α-Bisabolene synthase (EC 4.2.3.38, bisabolene synthase) is an enzyme with systematic name (2E,6E)-farnesyl-diphosphate diphosphate-lyase ((E)-α-bisabolene-forming)
Alpha-bisabolene_synthase
Class of enzymes
(Z)-γ-bisabolene synthase (EC 4.2.3.40) is an enzyme with systematic name (2E,6E)-farnesyl-diphosphate diphosphate-lyase ((Z)-γ-bisabolene-forming). This
(Z)-gamma-bisabolene_synthase
Species of flowering plant
oil as camphor (32%), eucalyptol (19%), ⍺-bisabolene (17%), eugenol (14%), germacrene (11%) and β-bisabolene (11%).[better source needed] In addition,
Ocimum_tenuiflorum
Index of enzymes associated with the same name
Alpha-bisabolene synthase (Z)-gamma-bisabolene synthase Beta-farnesene synthase (3S,6E)-nerolidol synthase (3R,6E)-nerolidol synthase (S)-beta-bisabolene synthase
(2E,6E)-farnesyl-diphosphate diphosphate-lyase
(2E,6E)-farnesyl-diphosphate_diphosphate-lyase
Class of enzymes
(E)-γ-bisabolene synthase (EC 4.2.3.59) is an enzyme with systematic name (2E,6E)-farnesyl-diphosphate diphosphate-lyase ((E)-γ-bisabolene-forming). This
(E)-gamma-bisabolene_synthase
Class of enzymes
(S)-β-bisabolene synthase (EC 4.2.3.55) is an enzyme with systematic name (2E,6E)-farnesyl-diphosphate diphosphate-lyase ((S)-β-bisabolene-forming). This
(S)-beta-bisabolene_synthase
Resin and essential oil from Copaifera trees
also contains significant amounts of α-bergamotene, α-copaene, and β-bisabolene. It is also the primary source of copalic acid. The aroma of copaiba resin
Copaiba
Species of true bug
characterization, and functional expression of wound-inducible (E)-α-bisabolene synthase from grand fir (Abies grandis)". Proc Natl Acad Sci U S A. 95
Pyrrhocoris_apterus
Species of plant used as a spice
of fresh ginger, primarily consisting of sesquiterpenes, such as beta-bisabolene and zingiberene, zingerone, shogaols, and gingerols with [6]-gingerol
Ginger
Chemical compound
reproduction. The first sesquiterpene to be formed, (E)-α-bisabolene (formed by (E)-α-bisabolene synthase), can be further transformed into juvabione and
Juvabione
Species of flowering plant
include α-bisabolol (26%), β-caryophyllene (7%), germacrene D (7%), β-bisabolene (5%), and α-humulene (4%). Extracts from the root of Eleutherococcus senticosus
Eleutherococcus_senticosus
Class of oily organic compounds found in plants
α-Copaene Aromadendrene Eremophilene Longifolene β-Guaiene Valencene β-Bisabolene γ-Cadinene β-Selinene Neophytadiene Ferruginol Aristolone β-Amyrin Oleanene
Terpene
Class of enzymes
(decyclizing). This enzyme catalyses the following chemical reaction (S)-β-bisabolene ⇌ {\displaystyle \rightleftharpoons } (S)-β-macrocarpene The synthesis
(S)-beta-macrocarpene synthase
(S)-beta-macrocarpene_synthase
Cold-pressed essential oil
linalool, γ-terpinene and β-pinene, and in smaller quantities geranial and β-bisabolene. The main non-volatile compounds are coumarins (citropten,
Bergamot_essential_oil
Species of flowering plant
including cupacinoside, cupacinoxepin, scopoletin, caryophyllene oxide, two bisabolene sesquiterpenes, lichexanthone, gustastatin, lupenone, betulone, 17β,21β-epoxyhopan-3-one
Cupania_cinerea
Index of chemical compounds with the same molecular formula
C15H24 (molar mass : 204.35 g/mol) may refer to: Farnesene Bergamotene Bisabolene Elemene Germacrene Humulene Zingiberene Amorpha-4,11-diene Aristolochene
C15H24
Stereogenic group placed on a molecule to encourage stereoselectivity in reactions
leaving group. Biogenetic-type asymmetric synthesis of limonene and bisabolenes". Journal of the American Chemical Society. 105 (19): 6154–6155. Bibcode:1983JAChS
Chiral_auxiliary
epi-isozizaene synthase EC 4.2.3.38: α-bisabolene synthase EC 4.2.3.39: epi-cedrol synthase EC 4.2.3.40: (Z)-γ-bisabolene synthase EC 4.2.3.41: elisabethatriene
List_of_EC_numbers_(EC_4)
butyrate Benzyl cinnamate Benzyl propionate Benzyl salicylate Bergamot oil Bisabolene Black currant buds absolute Borneol Bornyl acetate Buchu leaf oil 1,3-Butanediol
List of additives in cigarettes
List_of_additives_in_cigarettes
American biologist
drop-in replacement for gasoline; pinene, a replacement for jet fuel; and bisabolene, a replacement for diesel fuel. Because isoprenoids add a methyl side
Jay_Keasling
Metabolic pathway
genes from different organisms, production of terpenoids like limonene, bisabolene and isoprene could be achieved in different microbial chassis. Studies
Non-mevalonate_pathway
Chemical compound
α-Copaene Aromadendrene Eremophilene Longifolene β-Guaiene Valencene β-Bisabolene γ-Cadinene β-Selinene Neophytadiene Ferruginol Aristolone β-Amyrin Oleanene
Valencene
Species of flowering plant
thymol/p-cymene/γ-terpinene, thymol/p-cymene/neral, thymol/p-cymene/γ-terpinene/β-bisabolene, thymol/p-cymene/isoborneol/γ-terpinene, thymol/linalyl acetate/γ-terpinene/α-cubebene
Thymus_pannonicus
Chemical compound
α-Copaene Aromadendrene Eremophilene Longifolene β-Guaiene Valencene β-Bisabolene γ-Cadinene β-Selinene Neophytadiene Ferruginol Aristolone β-Amyrin Oleanene
Cucurbitane
Chemical compound
α-Copaene Aromadendrene Eremophilene Longifolene β-Guaiene Valencene β-Bisabolene γ-Cadinene β-Selinene Neophytadiene Ferruginol Aristolone β-Amyrin Oleanene
Longifolene
Species of plant in the celery family
limonene, β-pinene, α-phellandrene, β-pinene, thujene, β-caryophyllene, β-bisabolene, germacrene D with oxygenated terpenes such as trans-carveol, β-caryophyllene
Angelica_glauca
Organic chemical compound, sesquiterpenoid
α-Copaene Aromadendrene Eremophilene Longifolene β-Guaiene Valencene β-Bisabolene γ-Cadinene β-Selinene Neophytadiene Ferruginol Aristolone β-Amyrin Oleanene
Echinopine
Mackie H, Overton K, Picken D, Swanson S (1984). "Biosynthesis of gamma-bisabolene in tissue-cultures of Andrographis paniculata". Can. J. Chem. 62 (10):
Farnesol_2-isomerase
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