Classification Term: 170856

Camphane monoterpenoids (ontology term: a22318c0872b9cb5c43cece69f5f937d)

found 211 associated metabolites at sub_class metabolite taxonomy ontology rank level.

Ancestor: Monoterpenoids

Child Taxonomies: There is no child term of current ontology term.

Camphor

Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-, (.+/-.)-

C10H16O (152.1201)


Camphor appears as a colorless or white colored crystalline powder with a strong mothball-like odor. About the same density as water. Emits flammable vapors above 150 °F. Used to make moth proofings, pharmaceuticals, and flavorings. Camphor is a cyclic monoterpene ketone that is bornane bearing an oxo substituent at position 2. A naturally occurring monoterpenoid. It has a role as a plant metabolite. It is a bornane monoterpenoid and a cyclic monoterpene ketone. Camphor is a natural product found in Xylopia aromatica, Xylopia sericea, and other organisms with data available. A bicyclic monoterpene ketone found widely in plants, especially CINNAMOMUM CAMPHORA. It is used topically as a skin antipruritic and as an anti-infective agent. A cyclic monoterpene ketone that is bornane bearing an oxo substituent at position 2. A naturally occurring monoterpenoid. C254 - Anti-Infective Agent > C28394 - Topical Anti-Infective Agent D000890 - Anti-Infective Agents relative retention time with respect to 9-anthracene Carboxylic Acid is 0.986 Camphor ((±)-Camphor) is a topical anti-infective and anti-pruritic and internally as a stimulant and carminative. However, Camphor is poisonous when ingested. Antiviral, antitussive, and anticancer activities[1]. Camphor is a TRPV3 agonist[2]. Camphor ((±)-Camphor) is a topical anti-infective and anti-pruritic and internally as a stimulant and carminative. However, Camphor is poisonous when ingested. Antiviral, antitussive, and anticancer activities[1]. Camphor is a TRPV3 agonist[2].

   

(2S,4R)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol

Bicyclo(2.2.1)heptan-2-ol, 1,7,7-trimethyl-, endo-(.+/-.)-

C10H18O (154.1358)


Borneol appears as a white colored lump-solid with a sharp camphor-like odor. Burns readily. Slightly denser than water and insoluble in water. Used to make perfumes. Borneol is a bornane monoterpenoid that is 1,7,7-trimethylbicyclo[2.2.1]heptane substituted by a hydroxy group at position 2. It has a role as a volatile oil component and a metabolite. Isoborneol is a natural product found in Xylopia sericea, Eupatorium capillifolium, and other organisms with data available. Both Borneol and Isoborneol and their acetates and formates are used as flavouring agents. 2-Bornanol is found in turmeric. Isoborneol ((±)-Isoborneol) is a monoterpenoid alcohol present in the essential oils of numerous medicinal plants and has antioxidant and antiviral properties. Isoborneol is a potent inhibitor of herpes simplex virus type 1 (HSV-1)[1][2]. Isoborneol ((±)-Isoborneol) is a monoterpenoid alcohol present in the essential oils of numerous medicinal plants and has antioxidant and antiviral properties. Isoborneol is a potent inhibitor of herpes simplex virus type 1 (HSV-1)[1][2].

   

Mecamylamine

N,2,3,3-tetramethylbicyclo[2.2.1]heptan-2-amine

C11H21N (167.1674)


A nicotinic antagonist that is well absorbed from the gastrointestinal tract and crosses the blood-brain barrier. Mecamylamine has been used as a ganglionic blocker in treating hypertension, but, like most ganglionic blockers, is more often used now as a research tool. [PubChem] C - Cardiovascular system > C02 - Antihypertensives > C02B - Antiadrenergic agents, ganglion-blocking > C02BB - Secondary and tertiary amines D018373 - Peripheral Nervous System Agents > D001337 - Autonomic Agents > D005730 - Ganglionic Blockers D018377 - Neurotransmitter Agents > D018678 - Cholinergic Agents > D018680 - Cholinergic Antagonists Acquisition and generation of the data is financially supported in part by CREST/JST. D002317 - Cardiovascular Agents > D000959 - Antihypertensive Agents KEIO_ID M039

   

Camphene

3,3-Dimethyl-2-methylidenebicyclo[2.2.1]heptane

C10H16 (136.1252)


Camphene, also known as 2,2-dimethyl-3-methylenebicyclo[2.2.1]heptane or 2,2-dimethyl-3-methylenenorbornane, is a member of the class of compounds known as bicyclic monoterpenoids. Bicyclic monoterpenoids are monoterpenoids containing exactly 2 rings, which are fused to each other. Monoterpenoids are terpenes that contain 10 carbon atoms and are comprised of two isoprene units. The biosynthesis of monoterpenes is known to occur mainly through the methyl-erythritol-phosphate (MEP) pathway in plastids (PMID:7640522 ). Geranyl diphosphate (GPP) is a key intermediate in the biosynthesis of cyclic monoterpenes. GPP undergoes several cyclization reactions to yield a diverse number of cyclic arrangements. Camphene is nearly insoluble in water but very soluble in common organic solvents. It volatilizes readily at room temperature and has a pungent smell. It exists as a flammable, white solid that has a minty, citrus, eucalyptus odor. It is produced industrially by catalytic isomerization of the more common alpha-pinene. Camphene is used in the preparation of fragrances and in food additives for flavouring. In the mid-19th century it was used as a fuel for lamps, but this was limited by its explosiveness. Camphene exists in all eukaryotes, ranging from yeast to plants to humans. Camphene can be found in a number of food items such as dill, carrots, caraway, hyssop, lemon, orange, nutmeg seed, parsley, sage, thyme, turmeric and fennel, which makes camphene a potential biomarker for the consumption of these food products. It is a minor constituent of many essential oils such as turpentine, cypress oil, camphor oil, citronella oil, neroli, ginger oil, and valerian. Camphene is one of several monoterpenes that are found in cannabis plants (PMID:6991645 ). Camphene, also known as 2,2-dimethyl-3-methylenebicyclo[2.2.1]heptane or 2,2-dimethyl-3-methylenenorbornane, is a member of the class of compounds known as bicyclic monoterpenoids. Bicyclic monoterpenoids are monoterpenoids containing exactly 2 rings, which are fused to each other. Camphene is a camphor, fir needle, and herbal tasting compound and can be found in a number of food items such as cardamom, yellow bell pepper, common thyme, and coriander, which makes camphene a potential biomarker for the consumption of these food products. Camphene can be found primarily in feces and saliva. Camphene exists in all eukaryotes, ranging from yeast to humans. Camphene is a bicyclic monoterpene. It is nearly insoluble in water, but very soluble in common organic solvents. It volatilizes readily at room temperature and has a pungent smell. It is a minor constituent of many essential oils such as turpentine, cypress oil, camphor oil, citronella oil, neroli, ginger oil, and valerian. It is produced industrially by catalytic isomerization of the more common alpha-pinene. Camphene is used in the preparation of fragrances and as a food additive for flavoring. Its mid-19th century use as a fuel for lamps was limited by its explosiveness .

   

Fenchol

Bicyclo[2.2.1]heptan-2-ol, 1,3,3-trimethyl-, (1R-endo)-

C10H18O (154.1358)


Fenchol is found in fennel. Fenchol is a flavouring ingredient with a bitter, lime-like flavour [DFC] (Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.). Fenchol is a natural product found in Kunzea salina, Hyptis goyazensis, and other organisms with data available. Flavouring ingredient with a bitter, lime-like flavour [DFC] Fenchyl alcohol is a monoterpene alcohol in the essential oils isolated from Douglas fir needles, acts as a fragrance. Fenchyl alcohol strongly inhibits the rumen microbial activity of both sheep and deer[1][2]. Fenchyl alcohol is a monoterpene alcohol in the essential oils isolated from Douglas fir needles, acts as a fragrance. Fenchyl alcohol strongly inhibits the rumen microbial activity of both sheep and deer[1][2].

   

(-)-Bornyl acetate

(1S,2R)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-yl acetic acid

C12H20O2 (196.1463)


(-)-Bornyl acetate is isolated from Blumea balsamifera, Jasonia sp., Salvia fruticosa, carrot, rosemary, sage and lavender oil. (-)-Bornyl acetate is a flavouring agent [CCD]. Isolated from Blumea balsamifera, Jasonia species, Salvia fruticosa, carrot, rosemary, sage and lavender oil. Flavouring agent [CCD] (-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1]. (-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1]. (-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1]. (-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1].

   

Camphorquinone

1,7,7-trimethylbicyclo[2.2.1]heptane-2,3-dione bornane-2,3-dione

C10H14O2 (166.0994)


   

bornane-2,6-dione

1,7,7-trimethylbicyclo[2.2.1]heptane-2,6-dione

C10H14O2 (166.0994)


   

6-hydroxycamphor

(1S)-6-Hydroxy-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one

C10H16O2 (168.115)


   

(-)-Bornyl acetate

[(1R,2S,4R)-1,7,7-trimethyl-2-bicyclo[2.2.1]heptanyl] acetate

C12H20O2 (196.1463)


(-)-alpha-Fenchyl acetate is a flavouring ingredient, together with stereoisomers. Flavouring ingredient, together with stereoisomers Same as: D09740

   

(+)-Camphene

(1R,4S)-2,2-dimethyl-3-methylidenebicyclo[2.2.1]heptane

C10H16 (136.1252)


Camphene, also known as 2,2-dimethyl-3-methylenebicyclo[2.2.1]heptane or 2,2-dimethyl-3-methylenenorbornane, is a member of the class of compounds known as bicyclic monoterpenoids. Bicyclic monoterpenoids are monoterpenoids containing exactly 2 rings, which are fused to each other. Monoterpenoids are terpenes that contain 10 carbon atoms and are comprised of two isoprene units. The biosynthesis of monoterpenes is known to occur mainly through the methyl-eritritol-phosphate (MEP) pathway in plastids (PMID: 7640522). Geranyl diphosphate (GPP) is a key intermediate in the biosynthesis of cyclic monoterpenes. GPP undergoes several cyclization reactions to yield a diverse number of cyclic arrangements. Camphene is nearly insoluble in water but very soluble in common organic solvents. It volatilizes readily at room temperature and has a pungent smell. It exists as a flammable, white solid that has a minty, citrus, eucalyptus odor. It is produced industrially by catalytic isomerization of the more common alpha-pinene. Camphene is used in the preparation of fragrances and in food additives for flavouring. In the mid-19th century it was used as a fuel for lamps, but this was limited by its explosiveness. Camphene exists in all eukaryotes, ranging from yeast to plants to humans. Camphene can be found in a number of food items such as dill, carrots, caraway, hyssop, lemon, orange, nutmeg seed, parsley, sage, thyme, turmeric and fennel, which makes camphene a potential biomarker for the consumption of these food products. It is a minor constituent of many essential oils such as turpentine, cypress oil, camphor oil, citronella oil, neroli, ginger oil, and valerian. (+)-camphene is a member of the class of compounds known as bicyclic monoterpenoids. Bicyclic monoterpenoids are monoterpenoids containing exactly 2 rings, which are fused to each other. Thus, (+)-camphene is considered to be an isoprenoid lipid molecule (+)-camphene is a camphor, fir, and fresh tasting compound found in common sage and turmeric, which makes (+)-camphene a potential biomarker for the consumption of these food products.

   

(-)-camphene

(-)-camphene

C10H16 (136.1252)


A camphene (2,2-dimethyl-3-methylenebicyclo[2.2.1]heptane) that has S configuration at position 1 and R configuration at position 4.

   

(-)-Borneol

1,7,7-Trimethyl-(1R,2S,4R)-rel-bicyclo[2.2.1]heptan-2-ol

C10H18O (154.1358)


(-)-Borneol is found in common thyme and in turmeric. (-)-Borneol is a constituent of Blumea balsamifera (sambong). Both Borneol and Isoborneol and their acetates and formates are used as flavouring agents Constituent of Blumea balsamifera (sambong). (-)-Borneol is found in many foods, some of which are tea, coriander, common thyme, and cornmint. Isoborneol ((±)-Isoborneol) is a monoterpenoid alcohol present in the essential oils of numerous medicinal plants and has antioxidant and antiviral properties. Isoborneol is a potent inhibitor of herpes simplex virus type 1 (HSV-1)[1][2]. Isoborneol ((±)-Isoborneol) is a monoterpenoid alcohol present in the essential oils of numerous medicinal plants and has antioxidant and antiviral properties. Isoborneol is a potent inhibitor of herpes simplex virus type 1 (HSV-1)[1][2].

   

Isobornyl propionate

exo-1,7,7-trimethylbicyclo(2.2.1)Heptan-2-yl propanoate

C13H22O2 (210.162)


Isobornyl propionate is a flavouring agent. Flavouring agent

   

(+)-Isoborneol

(1S,2S,4S)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol

C10H18O (154.1358)


(+)-Isoborneol, also known as (S,S,S)-(+)-isoborneol, belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids containing exactly 2 rings, which are fused to each other. (+)-Isoborneol is a flavouring agent. Flavouring agent Isoborneol ((±)-Isoborneol) is a monoterpenoid alcohol present in the essential oils of numerous medicinal plants and has antioxidant and antiviral properties. Isoborneol is a potent inhibitor of herpes simplex virus type 1 (HSV-1)[1][2]. Isoborneol ((±)-Isoborneol) is a monoterpenoid alcohol present in the essential oils of numerous medicinal plants and has antioxidant and antiviral properties. Isoborneol is a potent inhibitor of herpes simplex virus type 1 (HSV-1)[1][2].

   

(-)-Isoborneol

(1R,2R,4R)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol

C10H18O (154.1358)


(-)-Isoborneol, also known as (R,R,R)-(-)-isoborneol, belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids containing exactly 2 rings, which are fused to each other. (-)-Isoborneol is a flavouring agent. Flavouring agent Isoborneol ((±)-Isoborneol) is a monoterpenoid alcohol present in the essential oils of numerous medicinal plants and has antioxidant and antiviral properties. Isoborneol is a potent inhibitor of herpes simplex virus type 1 (HSV-1)[1][2]. Isoborneol ((±)-Isoborneol) is a monoterpenoid alcohol present in the essential oils of numerous medicinal plants and has antioxidant and antiviral properties. Isoborneol is a potent inhibitor of herpes simplex virus type 1 (HSV-1)[1][2].

   

trans-beta-Santalol

(2E)-2-methyl-5-[(1S,2R,4R)-2-methyl-3-methylidenebicyclo[2.2.1]heptan-2-yl]pent-2-en-1-ol

C15H24O (220.1827)


trans-beta-Santalol is a flavouring ingredient. trans-beta-Santalol is a constituent of Santalum album (sandalwood). Flavouring ingredient. Constituent of Santalum album (sandalwood)

   

Camphane

1,7,7-trimethylbicyclo[2.2.1]heptane

C10H18 (138.1408)


   

Santalol

2-methyl-5-{2-methyl-3-methylidenebicyclo[2.2.1]heptan-2-yl}pent-2-en-1-ol

C15H24O (220.1827)


   

alpha-Fenchyl acetate

1,3,3-trimethylbicyclo[2.2.1]heptan-2-yl acetate

C12H20O2 (196.1463)


Fenchyl acetate, also known as fenchyl acetic acid, is a member of the class of compounds known as bicyclic monoterpenoids. Bicyclic monoterpenoids are monoterpenoids containing exactly 2 rings, which are fused to each other. Fenchyl acetate is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). Fenchyl acetate is a sweet, citrus, and fir tasting compound found in sweet basil, which makes fenchyl acetate a potential biomarker for the consumption of this food product.

   

Bornylene

Bicyclo[2.2.1]hept-2-ene,1,7,7-trimethyl-

C10H16 (136.1252)


Bornylene, also known as 1,7,7-trimethylbicyclo(2.2.1)hept-2-ene, is a member of the class of compounds known as polycyclic hydrocarbons. Polycyclic hydrocarbons are polycyclic organic compounds made up only of carbon and hydrogen atoms. Bornylene can be found in rosemary, which makes bornylene a potential biomarker for the consumption of this food product.

   

(+)-Angelicoidenol

1,7,7-Trimethylbicyclo[2.2.1]heptane-2,5-diol

C10H18O2 (170.1307)


(+)-angelicoidenol is a member of the class of compounds known as bicyclic monoterpenoids. Bicyclic monoterpenoids are monoterpenoids containing exactly 2 rings, which are fused to each other (+)-angelicoidenol is soluble (in water) and a very weakly acidic compound (based on its pKa). (+)-angelicoidenol can be found in ginger, which makes (+)-angelicoidenol a potential biomarker for the consumption of this food product.

   

Angelicoidenol 2-O-beta-D-glucopyranoside

2-({5-hydroxy-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl}oxy)-6-(hydroxymethyl)oxane-3,4,5-triol

C16H28O7 (332.1835)


Angelicoidenol 2-o-beta-d-glucopyranoside is a member of the class of compounds known as terpene glycosides. Terpene glycosides are prenol lipids containing a carbohydrate moiety glycosidically bound to a terpene backbone. Angelicoidenol 2-o-beta-d-glucopyranoside is soluble (in water) and a very weakly acidic compound (based on its pKa). Angelicoidenol 2-o-beta-d-glucopyranoside can be found in ginger, which makes angelicoidenol 2-o-beta-d-glucopyranoside a potential biomarker for the consumption of this food product.

   

Camphene-hydrate

2,3,3-trimethylbicyclo[2.2.1]heptan-2-ol

C10H18O (154.1358)


Camphene-hydrate, also known as camphene-hydric acid, is a member of the class of compounds known as bicyclic monoterpenoids. Bicyclic monoterpenoids are monoterpenoids containing exactly 2 rings, which are fused to each other. Camphene-hydrate is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). Camphene-hydrate can be found in ginger, which makes camphene-hydrate a potential biomarker for the consumption of this food product.

   

Bornyl acetate

(1S,2R,4S)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl acetate

C12H20O2 (196.1463)


Bornyl acetate, also known as bornyl acetic acid, is a member of the class of compounds known as bicyclic monoterpenoids. Bicyclic monoterpenoids are monoterpenoids containing exactly 2 rings, which are fused to each other. Bornyl acetate is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). Bornyl acetate is a camphor, cedar, and herbal tasting compound and can be found in a number of food items such as nutmeg, rosemary, spearmint, and sunflower, which makes bornyl acetate a potential biomarker for the consumption of these food products. (-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1]. (-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1]. (-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1]. (-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1]. Bornyl acetate is a potent odorant, exhibiting one of the highest flavor dilution factor (FD factor). Bornyl acetate possesses anti-cancer activity[1][2]. Bornyl acetate is a potent odorant, exhibiting one of the highest flavor dilution factor (FD factor). Bornyl acetate possesses anti-cancer activity[1][2].

   

D-Camphor

1,7,7-Trimethylbicyclo[2.2.1]heptan-2-one

C10H16O (152.1201)


(+)-camphor, also known as formosa camphor or 2-bornanone, is a member of the class of compounds known as bicyclic monoterpenoids. Bicyclic monoterpenoids are monoterpenoids containing exactly 2 rings, which are fused to each other. Thus, (+)-camphor is considered to be an isoprenoid lipid molecule (+)-camphor is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). (+)-camphor is a bitter, camphor, and herbal tasting compound and can be found in a number of food items such as sugar apple, sunflower, fennel, and cardamom, which makes (+)-camphor a potential biomarker for the consumption of these food products. C254 - Anti-Infective Agent > C28394 - Topical Anti-Infective Agent D000890 - Anti-Infective Agents Camphor ((±)-Camphor) is a topical anti-infective and anti-pruritic and internally as a stimulant and carminative. However, Camphor is poisonous when ingested. Antiviral, antitussive, and anticancer activities[1]. Camphor is a TRPV3 agonist[2]. Camphor ((±)-Camphor) is a topical anti-infective and anti-pruritic and internally as a stimulant and carminative. However, Camphor is poisonous when ingested. Antiviral, antitussive, and anticancer activities[1]. Camphor is a TRPV3 agonist[2].

   

1,2,4-trichloro-5-(2-chloroethenyl)-1,5-dimethylcyclohexane

1,2,4-trichloro-5-(2-chloroethenyl)-1,5-dimethylcyclohexane

C10H14Cl4 (273.985)


   

1,7,7-Trimethylbicyclo[2.2.1]heptane-2,5-diol

1,7,7-Trimethylbicyclo[2.2.1]heptane-2,5-diol

C10H18O2 (170.1307)


   

Camphane

Bicyclo[2.2.1]heptane,1,7,7-trimethyl-

C10H18 (138.1408)


   

alpha-Fenchyl acetate

1,3,3-trimethylbicyclo[2.2.1]heptan-2-yl acetate

C12H20O2 (196.1463)


Fenchyl acetate, also known as fenchyl acetic acid, is a member of the class of compounds known as bicyclic monoterpenoids. Bicyclic monoterpenoids are monoterpenoids containing exactly 2 rings, which are fused to each other. Fenchyl acetate is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). Fenchyl acetate is a sweet, citrus, and fir tasting compound found in sweet basil, which makes fenchyl acetate a potential biomarker for the consumption of this food product.

   

Bornylene

Bicyclo[2.2.1]hept-2-ene,1,7,7-trimethyl-

C10H16 (136.1252)


   

Camphenilone

Camphenilone

C9H14O (138.1045)


   

Camphene hydrate

Camphene hydrate

C10H18O (154.1358)


   

Santalol

2-Penten-1-ol, 2-methyl-5-[(1S,2R,4R)-2-methyl-3-methylenebicyclo[2.2.1]hept-2-yl]-, (2Z)-

C15H24O (220.1827)


   

Bornyl 2-methylbutyrate

1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl 2-methylbutanoate

C15H26O2 (238.1933)


   

borneol

1,7,7-Trimethyl-(1R,2S,4R)-rel-bicyclo[2.2.1]heptan-2-ol

C10H18O (154.1358)


Flavouring agent. (±)-Borneol is found in many foods, some of which are pot marjoram, pepper (spice), saffron, and german camomile. Constituent of Curcuma aromatica and other plants. (+)-Borneol is found in nutmeg, herbs and spices, and ginger. Isoborneol ((±)-Isoborneol) is a monoterpenoid alcohol present in the essential oils of numerous medicinal plants and has antioxidant and antiviral properties. Isoborneol is a potent inhibitor of herpes simplex virus type 1 (HSV-1)[1][2]. Isoborneol ((±)-Isoborneol) is a monoterpenoid alcohol present in the essential oils of numerous medicinal plants and has antioxidant and antiviral properties. Isoborneol is a potent inhibitor of herpes simplex virus type 1 (HSV-1)[1][2].

   

trans-b-Santalol

(2E)-2-methyl-5-[(1S,2R,4R)-2-methyl-3-methylidenebicyclo[2.2.1]heptan-2-yl]pent-2-en-1-ol

C15H24O (220.1827)


   

Bornyl butyrate

1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl butanoate

C14H24O2 (224.1776)


   

2-Methylisoborneol

(2R,4R)-1,2,7,7-tetramethylbicyclo[2.2.1]heptan-2-ol

C11H20O (168.1514)


   

(+)-Borneol

(+)-Borneol

C10H18O (154.1358)


   

(-)-Borneol

(-)-Borneol

C10H18O (154.1358)


   

1,5,5-TRIMETHYLBICYCLO[2.2.1]HEPTAN-2-ONE

1,5,5-TRIMETHYLBICYCLO[2.2.1]HEPTAN-2-ONE

C10H16O (152.1201)


   

(+)-6-Endo-hydroxycamphor

(+)-6-Endo-hydroxycamphor

C10H16O2 (168.115)


   

3,3-Dimethylbicyclo[2.2.1]heptan-2-one

3,3-Dimethylbicyclo[2.2.1]heptan-2-one

C9H14O (138.1045)


   

(+)-Bornyl acetate

Bornyl acetate, (-)-

C12H20O2 (196.1463)


(-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1]. (-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1]. (-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1]. (-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1]. Bornyl acetate is a potent odorant, exhibiting one of the highest flavor dilution factor (FD factor). Bornyl acetate possesses anti-cancer activity[1][2]. Bornyl acetate is a potent odorant, exhibiting one of the highest flavor dilution factor (FD factor). Bornyl acetate possesses anti-cancer activity[1][2].

   

Bornyl acetate

(1R,2S,4R)-(+)-Bornyl acetate

C12H20O2 (196.1463)


Same as: D09740 (-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1]. (-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1]. (-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1]. (-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1]. Bornyl acetate is a potent odorant, exhibiting one of the highest flavor dilution factor (FD factor). Bornyl acetate possesses anti-cancer activity[1][2]. Bornyl acetate is a potent odorant, exhibiting one of the highest flavor dilution factor (FD factor). Bornyl acetate possesses anti-cancer activity[1][2].

   

D-CAMPHOR

(±)-Camphor

C10H16O (152.1201)


(+)-camphor, also known as formosa camphor or 2-bornanone, is a member of the class of compounds known as bicyclic monoterpenoids. Bicyclic monoterpenoids are monoterpenoids containing exactly 2 rings, which are fused to each other. Thus, (+)-camphor is considered to be an isoprenoid lipid molecule (+)-camphor is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). (+)-camphor is a bitter, camphor, and herbal tasting compound and can be found in a number of food items such as sugar apple, sunflower, fennel, and cardamom, which makes (+)-camphor a potential biomarker for the consumption of these food products. (+)-Camphor is a food additive used medicinally as a preservative. (+)-Camphor is a food additive used medicinally as a preservative. (+)-Camphor is a food additive used medicinally as a preservative. (+)-Camphor is a food additive used medicinally as a preservative.

   

(+)-Angelicoidenol

1,7,7-Trimethylbicyclo[2.2.1]heptane-2,5-diol

C10H18O2 (170.1307)


(+)-angelicoidenol is a member of the class of compounds known as bicyclic monoterpenoids. Bicyclic monoterpenoids are monoterpenoids containing exactly 2 rings, which are fused to each other (+)-angelicoidenol is soluble (in water) and a very weakly acidic compound (based on its pKa). (+)-angelicoidenol can be found in ginger, which makes (+)-angelicoidenol a potential biomarker for the consumption of this food product.

   

isobornyl formate

isobornyl formate

C11H18O2 (182.1307)


A bornane monoterpenoid that is isoborneol in which the hydroxy hydrogen has been replaced by a formyl group.

   

methylisoborneol

(1R,2R,4R)-1,2,7,7-tetramethylbicyclo[2.2.1]heptan-2-ol

C11H20O (168.1514)


   

Borneol

Bicyclo(2.2.1)heptan-2-ol, 1,7,7-trimethyl-, endo-(.+/-.)-

C10H18O (154.1358)


Borneol appears as a white colored lump-solid with a sharp camphor-like odor. Burns readily. Slightly denser than water and insoluble in water. Used to make perfumes. Borneol is a bornane monoterpenoid that is 1,7,7-trimethylbicyclo[2.2.1]heptane substituted by a hydroxy group at position 2. It has a role as a volatile oil component and a metabolite. Isoborneol is a natural product found in Xylopia sericea, Eupatorium capillifolium, and other organisms with data available. A bornane monoterpenoid that is 1,7,7-trimethylbicyclo[2.2.1]heptane substituted by a hydroxy group at position 2. Isoborneol ((±)-Isoborneol) is a monoterpenoid alcohol present in the essential oils of numerous medicinal plants and has antioxidant and antiviral properties. Isoborneol is a potent inhibitor of herpes simplex virus type 1 (HSV-1)[1][2]. Isoborneol ((±)-Isoborneol) is a monoterpenoid alcohol present in the essential oils of numerous medicinal plants and has antioxidant and antiviral properties. Isoborneol is a potent inhibitor of herpes simplex virus type 1 (HSV-1)[1][2].

   

(+)-Camphene

2,2-dimethyl-3-methylidenebicyclo[2.2.1]heptane

C10H16 (136.1252)


A monoterpene with a bicyclic skeleton that is bicyclo[2.2.1]heptane substituted by geminal methyl groups at position 2 and a methylidene group at position 3. It is a widespread natural product found in many essential oils.

   

mecamylamine

methyl(2,3,3-trimethyltrinorbornan-2-yl)amine

C11H21N (167.1674)


C - Cardiovascular system > C02 - Antihypertensives > C02B - Antiadrenergic agents, ganglion-blocking > C02BB - Secondary and tertiary amines D018373 - Peripheral Nervous System Agents > D001337 - Autonomic Agents > D005730 - Ganglionic Blockers D018377 - Neurotransmitter Agents > D018678 - Cholinergic Agents > D018680 - Cholinergic Antagonists D002317 - Cardiovascular Agents > D000959 - Antihypertensive Agents

   

(+)-Camphene

(+)-Camphene

C10H16 (136.1252)


A camphene (2,2-dimethyl-3-methylenebicyclo[2.2.1]heptane) that has R configuration at position 1 and S configuration at position 4.

   

Fenchyl acetate

2-Norbornanol, 1,3,3-trimethyl-, acetate

C12H20O2 (196.1463)


   

(1r,2s,4s,5s)-1,2,4-trichloro-5-[(1e)-2-chloroethenyl]-1,5-dimethylcyclohexane

(1r,2s,4s,5s)-1,2,4-trichloro-5-[(1e)-2-chloroethenyl]-1,5-dimethylcyclohexane

C10H14Cl4 (273.985)


   

1,7,7-trimethylbicyclo[2.2.1]heptane-2-carboxylic acid

1,7,7-trimethylbicyclo[2.2.1]heptane-2-carboxylic acid

C11H18O2 (182.1307)


   

(1r,4r,5r)-1,7,7-trimethyl-5-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}bicyclo[2.2.1]heptan-2-one

(1r,4r,5r)-1,7,7-trimethyl-5-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}bicyclo[2.2.1]heptan-2-one

C16H26O7 (330.1678)


   

1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl prop-2-enoate

1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl prop-2-enoate

C13H20O2 (208.1463)


   

1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl 2-methylbut-2-enoate

1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl 2-methylbut-2-enoate

C15H24O2 (236.1776)


   

(1s,2r,4s)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2e)-3-phenylprop-2-enoate

(1s,2r,4s)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2e)-3-phenylprop-2-enoate

C19H24O2 (284.1776)


   

(1s,2r,4s)-5,5-dimethyl-6-methylidenebicyclo[2.2.1]heptan-2-ol

(1s,2r,4s)-5,5-dimethyl-6-methylidenebicyclo[2.2.1]heptan-2-ol

C10H16O (152.1201)


   

(2s,3z,4s,6s)-6-bromo-3-(2-bromoethylidene)-2,4-dichloro-1,1-dimethylcyclohexane

(2s,3z,4s,6s)-6-bromo-3-(2-bromoethylidene)-2,4-dichloro-1,1-dimethylcyclohexane

C10H14Br2Cl2 (361.8839)


   

(1s,2s,4s)-1,2,7,7-tetramethylbicyclo[2.2.1]heptan-2-ol

(1s,2s,4s)-1,2,7,7-tetramethylbicyclo[2.2.1]heptan-2-ol

C11H20O (168.1514)


   

(1s,2s,4s)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2z)-2-methylbut-2-enoate

(1s,2s,4s)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2z)-2-methylbut-2-enoate

C15H24O2 (236.1776)


   

(1s,2s,4s,7s)-7-(hydroxymethyl)-1,7-dimethylbicyclo[2.2.1]heptan-2-ol

(1s,2s,4s,7s)-7-(hydroxymethyl)-1,7-dimethylbicyclo[2.2.1]heptan-2-ol

C10H18O2 (170.1307)


   

(1r,2s,4r)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl propanoate

(1r,2s,4r)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl propanoate

C13H22O2 (210.162)


   

2-{[(3,4,5-trihydroxyoxan-2-yl)oxy]methyl}-6-({1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl}oxy)oxane-3,4,5-triol

2-{[(3,4,5-trihydroxyoxan-2-yl)oxy]methyl}-6-({1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl}oxy)oxane-3,4,5-triol

C21H36O10 (448.2308)


   

4-bromo-2,6-dichloro-3-(2-chloroethylidene)-1,1-dimethylcyclohexane

4-bromo-2,6-dichloro-3-(2-chloroethylidene)-1,1-dimethylcyclohexane

C10H14BrCl3 (317.9344)


   

(1r,2r,5s,7r)-6,6,7-trimethyltricyclo[3.2.0.0²,⁷]heptane

(1r,2r,5s,7r)-6,6,7-trimethyltricyclo[3.2.0.0²,⁷]heptane

C10H16 (136.1252)


   

(1s,2r,4s)-5,5-dimethyl-6-methylidenebicyclo[2.2.1]heptan-2-yl acetate

(1s,2r,4s)-5,5-dimethyl-6-methylidenebicyclo[2.2.1]heptan-2-yl acetate

C12H18O2 (194.1307)


   

(1r,2r,5r,7z)-7-ethylidene-1,2,8,8-tetramethylbicyclo[3.2.1]octane

(1r,2r,5r,7z)-7-ethylidene-1,2,8,8-tetramethylbicyclo[3.2.1]octane

C14H24 (192.1878)


   

(1r,2r,4s,6s)-1,7,7-trimethylbicyclo[2.2.1]heptane-2,6-diol

(1r,2r,4s,6s)-1,7,7-trimethylbicyclo[2.2.1]heptane-2,6-diol

C10H18O2 (170.1307)


   

(1r,2s,4r)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

(1r,2s,4r)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

C20H26O4 (330.1831)


   

(1r,2s,4r)-1-(hydroxymethyl)-7,7-dimethylbicyclo[2.2.1]heptan-2-ol

(1r,2s,4r)-1-(hydroxymethyl)-7,7-dimethylbicyclo[2.2.1]heptan-2-ol

C10H18O2 (170.1307)


   

(1r,2s,4r)-bornyl acetate

(1r,2s,4r)-bornyl acetate

C12H20O2 (196.1463)


   

(2r,3s,4s,5r,6r)-2-({[(2r,3r,4r)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-{[(1s,2r,4s,5s)-5-hydroxy-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl]oxy}oxane-3,4,5-triol

(2r,3s,4s,5r,6r)-2-({[(2r,3r,4r)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-{[(1s,2r,4s,5s)-5-hydroxy-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl]oxy}oxane-3,4,5-triol

C21H36O11 (464.2258)


   

(1s,2s,4r,5s)-1,2,4-trichloro-5-[(1e)-2-chloroethenyl]-1,5-dimethylcyclohexane

(1s,2s,4r,5s)-1,2,4-trichloro-5-[(1e)-2-chloroethenyl]-1,5-dimethylcyclohexane

C10H14Cl4 (273.985)


   

(1s,2r,4s)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl 3-(3,4,5-trimethoxyphenyl)prop-2-enoate

(1s,2r,4s)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl 3-(3,4,5-trimethoxyphenyl)prop-2-enoate

C22H30O5 (374.2093)


   

1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

C20H26O4 (330.1831)


   

(2s,5r)-1,7,7-trimethylbicyclo[2.2.1]heptane-2,5-diol

(2s,5r)-1,7,7-trimethylbicyclo[2.2.1]heptane-2,5-diol

C10H18O2 (170.1307)


   

(1r,2s,4s)-1,3,3-trimethylbicyclo[2.2.1]heptan-2-ol

(1r,2s,4s)-1,3,3-trimethylbicyclo[2.2.1]heptan-2-ol

C10H18O (154.1358)


   

2-(hydroxymethyl)-6-({1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl}oxy)oxane-3,4,5-triol

2-(hydroxymethyl)-6-({1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl}oxy)oxane-3,4,5-triol

C16H28O6 (316.1886)


   

(2r,3s,4s,5r,6r)-2-({[(2s,3r,4s,5r)-3,4,5-trihydroxyoxan-2-yl]oxy}methyl)-6-{[(1s,2s,4s)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl]oxy}oxane-3,4,5-triol

(2r,3s,4s,5r,6r)-2-({[(2s,3r,4s,5r)-3,4,5-trihydroxyoxan-2-yl]oxy}methyl)-6-{[(1s,2s,4s)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl]oxy}oxane-3,4,5-triol

C21H36O10 (448.2308)


   

2-chloro-1,7,7-trimethylbicyclo[2.2.1]heptane

2-chloro-1,7,7-trimethylbicyclo[2.2.1]heptane

C10H17Cl (172.1019)


   

(2s,3r,4r,5s,6s)-2-({[(2s,3s,4s)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-{[(1s,2r,4s,5s)-5-hydroxy-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl]oxy}oxane-3,4,5-triol

(2s,3r,4r,5s,6s)-2-({[(2s,3s,4s)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-{[(1s,2r,4s,5s)-5-hydroxy-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl]oxy}oxane-3,4,5-triol

C21H36O11 (464.2258)


   

1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl 3-(3,4-dihydroxyphenyl)prop-2-enoate

1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl 3-(3,4-dihydroxyphenyl)prop-2-enoate

C19H24O4 (316.1675)


   

[(2s,3ar,7as)-1,1,3a,7,7-pentamethyl-2,3,6,7a-tetrahydroinden-2-yl]methanol

[(2s,3ar,7as)-1,1,3a,7,7-pentamethyl-2,3,6,7a-tetrahydroinden-2-yl]methanol

C15H26O (222.1984)


   

(2s,3e,4s,6s)-6-bromo-3-(2-bromoethylidene)-2,4-dichloro-1,1-dimethylcyclohexane

(2s,3e,4s,6s)-6-bromo-3-(2-bromoethylidene)-2,4-dichloro-1,1-dimethylcyclohexane

C10H14Br2Cl2 (361.8839)


   

4,5,7,7-tetramethylbicyclo[2.2.1]heptane-2,3,5-triol

4,5,7,7-tetramethylbicyclo[2.2.1]heptane-2,3,5-triol

C11H20O3 (200.1412)


   

(-)-β-fenchyl alcohol

(-)-β-fenchyl alcohol

C10H18O (154.1358)


   

3-hydroxy-4-(hydroxymethyl)-7,7-dimethylbicyclo[2.2.1]heptan-2-one

3-hydroxy-4-(hydroxymethyl)-7,7-dimethylbicyclo[2.2.1]heptan-2-one

C10H16O3 (184.1099)


   

(1r,2r,4s,5r)-1,2,4-trichloro-5-[(1e)-2-chloroethenyl]-1,5-dimethylcyclohexane

(1r,2r,4s,5r)-1,2,4-trichloro-5-[(1e)-2-chloroethenyl]-1,5-dimethylcyclohexane

C10H14Cl4 (273.985)


   

1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl 3-phenylprop-2-enoate

1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl 3-phenylprop-2-enoate

C19H24O2 (284.1776)


   

1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl 3-(4-hydroxyphenyl)prop-2-enoate

1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl 3-(4-hydroxyphenyl)prop-2-enoate

C19H24O3 (300.1725)


   

2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-({5-hydroxy-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl}oxy)oxane-3,4,5-triol

2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-({5-hydroxy-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl}oxy)oxane-3,4,5-triol

C21H36O11 (464.2258)


   

2-methyl-5-[(1r,2r,4s)-2-methyl-3-methylidenebicyclo[2.2.1]heptan-2-yl]pent-2-en-1-ol

2-methyl-5-[(1r,2r,4s)-2-methyl-3-methylidenebicyclo[2.2.1]heptan-2-yl]pent-2-en-1-ol

C15H24O (220.1827)


   

(1r,2s,4r)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2e)-3-phenylprop-2-enoate

(1r,2s,4r)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2e)-3-phenylprop-2-enoate

C19H24O2 (284.1776)


   

2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-({1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl}oxy)oxane-3,4,5-triol

2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-({1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl}oxy)oxane-3,4,5-triol

C21H36O10 (448.2308)


   

(2r)-7-(hydroxymethyl)-1,7-dimethylbicyclo[2.2.1]heptan-2-ol

(2r)-7-(hydroxymethyl)-1,7-dimethylbicyclo[2.2.1]heptan-2-ol

C10H18O2 (170.1307)


   

2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-({6-hydroxy-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl}oxy)oxane-3,4,5-triol

2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-({6-hydroxy-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl}oxy)oxane-3,4,5-triol

C21H36O11 (464.2258)


   

1,6,6-trimethylbicyclo[2.1.1]hexane-5-carbaldehyde

1,6,6-trimethylbicyclo[2.1.1]hexane-5-carbaldehyde

C10H16O (152.1201)


   

{1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl}acetic acid

{1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl}acetic acid

C12H20O2 (196.1463)


   

2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-{[7-(hydroxymethyl)-1,7-dimethylbicyclo[2.2.1]heptan-2-yl]oxy}oxane-3,4,5-triol

2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-{[7-(hydroxymethyl)-1,7-dimethylbicyclo[2.2.1]heptan-2-yl]oxy}oxane-3,4,5-triol

C21H36O11 (464.2258)


   

2-{3-[(1r,2s,4s)-2-methyl-3-methylidenebicyclo[2.2.1]heptan-2-yl]propylidene}propane-1,3-diol

2-{3-[(1r,2s,4s)-2-methyl-3-methylidenebicyclo[2.2.1]heptan-2-yl]propylidene}propane-1,3-diol

C15H24O2 (236.1776)


   

(2r,3r,4s,5s,6r)-2-{[(1r,2r,4s)-3,3-dimethylbicyclo[2.2.1]heptan-2-yl]methoxy}-6-({[(5s,8r,9r)-9-hydroxy-2,2-dimethyl-1,3,7-trioxaspiro[4.4]nonan-8-yl]oxy}methyl)oxane-3,4,5-triol

(2r,3r,4s,5s,6r)-2-{[(1r,2r,4s)-3,3-dimethylbicyclo[2.2.1]heptan-2-yl]methoxy}-6-({[(5s,8r,9r)-9-hydroxy-2,2-dimethyl-1,3,7-trioxaspiro[4.4]nonan-8-yl]oxy}methyl)oxane-3,4,5-triol

C24H40O10 (488.2621)


   

5-(hydroxymethyl)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol

5-(hydroxymethyl)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol

C11H20O2 (184.1463)


   

(1r,2r,4r,5s)-1,2,4-trichloro-5-[(1e)-2-chloroethenyl]-1,5-dimethylcyclohexane

(1r,2r,4r,5s)-1,2,4-trichloro-5-[(1e)-2-chloroethenyl]-1,5-dimethylcyclohexane

C10H14Cl4 (273.985)


   

(2r,3r,4s,5s,6r)-2-{[(1r,2s,4r,5r)-5-hydroxy-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

(2r,3r,4s,5s,6r)-2-{[(1r,2s,4r,5r)-5-hydroxy-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

C16H28O7 (332.1835)


   

5,5-dimethyl-6-methylidenebicyclo[2.2.1]heptan-2-yl acetate

5,5-dimethyl-6-methylidenebicyclo[2.2.1]heptan-2-yl acetate

C12H18O2 (194.1307)


   

borneol; cis-p-coumaric acid

borneol; cis-p-coumaric acid

C19H26O4 (318.1831)


   

1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl 3-(4-methoxyphenyl)prop-2-enoate

1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl 3-(4-methoxyphenyl)prop-2-enoate

C20H26O3 (314.1882)


   

(2r,3r,4r,5r,6s)-2-{[(2r,3s,4s,5r,6r)-6-{[(1r,2r,4s)-3,3-dimethylbicyclo[2.2.1]heptan-2-yl]methoxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-6-methyloxane-3,4,5-triol

(2r,3r,4r,5r,6s)-2-{[(2r,3s,4s,5r,6r)-6-{[(1r,2r,4s)-3,3-dimethylbicyclo[2.2.1]heptan-2-yl]methoxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-6-methyloxane-3,4,5-triol

C22H38O10 (462.2465)


   

4,7,7-trimethyl-5-oxobicyclo[2.2.1]heptan-2-yl benzoate

4,7,7-trimethyl-5-oxobicyclo[2.2.1]heptan-2-yl benzoate

C17H20O3 (272.1412)


   

(1s,3s,4r)-2,2,3-trimethylbicyclo[2.2.1]heptane

(1s,3s,4r)-2,2,3-trimethylbicyclo[2.2.1]heptane

C10H18 (138.1408)


   

(2r,3s,4s,5r,6r)-2-({[(2r,3r,4r,5s)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-{[(1r,2s,4r)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl]oxy}oxane-3,4,5-triol

(2r,3s,4s,5r,6r)-2-({[(2r,3r,4r,5s)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-{[(1r,2s,4r)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl]oxy}oxane-3,4,5-triol

C21H36O10 (448.2308)


   

1,5,5-trimethyl-3-oxabicyclo[4.2.2]decane

1,5,5-trimethyl-3-oxabicyclo[4.2.2]decane

C12H22O (182.1671)


   

2,8,8-trimethyl-3-oxatricyclo[4.1.1.0²,⁴]octan-7-one

2,8,8-trimethyl-3-oxatricyclo[4.1.1.0²,⁴]octan-7-one

C10H14O2 (166.0994)


   

(2r,5s)-1,7,7-trimethylbicyclo[2.2.1]heptane-2,5-diol

(2r,5s)-1,7,7-trimethylbicyclo[2.2.1]heptane-2,5-diol

C10H18O2 (170.1307)


   

(1r,2s,4r)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate

(1r,2s,4r)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate

C19H24O3 (300.1725)


   

borneol; cis-ferulic acid

borneol; cis-ferulic acid

C20H28O5 (348.1937)


   

1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl 2-methylpropanoate

1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl 2-methylpropanoate

C14H24O2 (224.1776)


   

(1r,2r,4r,5r)-1,2,4-trichloro-5-[(1e)-2-chloroethenyl]-1,5-dimethylcyclohexane

(1r,2r,4r,5r)-1,2,4-trichloro-5-[(1e)-2-chloroethenyl]-1,5-dimethylcyclohexane

C10H14Cl4 (273.985)


   

1-(hydroxymethyl)-7,7-dimethylbicyclo[2.2.1]heptane-2,3-diol

1-(hydroxymethyl)-7,7-dimethylbicyclo[2.2.1]heptane-2,3-diol

C10H18O3 (186.1256)


   

(1s,2r,4s)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

(1s,2r,4s)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

C20H26O4 (330.1831)


   

(1s,2r,4r,6s)-1,7,7-trimethylbicyclo[2.2.1]heptane-2,6-diol

(1s,2r,4r,6s)-1,7,7-trimethylbicyclo[2.2.1]heptane-2,6-diol

C10H18O2 (170.1307)


   

(1r,2s,4r,7s)-7-(hydroxymethyl)-1,7-dimethylbicyclo[2.2.1]heptan-2-ol

(1r,2s,4r,7s)-7-(hydroxymethyl)-1,7-dimethylbicyclo[2.2.1]heptan-2-ol

C10H18O2 (170.1307)


   

(1s,2r,4s,5r)-5-(hydroxymethyl)-6,6-dimethylbicyclo[2.2.1]heptan-2-ol

(1s,2r,4s,5r)-5-(hydroxymethyl)-6,6-dimethylbicyclo[2.2.1]heptan-2-ol

C10H18O2 (170.1307)


   

(1r,2s,3r,4s,5r)-4,5,7,7-tetramethylbicyclo[2.2.1]heptane-2,3,5-triol

(1r,2s,3r,4s,5r)-4,5,7,7-tetramethylbicyclo[2.2.1]heptane-2,3,5-triol

C11H20O3 (200.1412)


   

1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate

1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate

C19H24O3 (300.1725)


   

1,2,7,7-tetramethylbicyclo[2.2.1]hept-2-ene

1,2,7,7-tetramethylbicyclo[2.2.1]hept-2-ene

C11H18 (150.1408)


   

(1r,2s,4s,5r)-1,2,4-trichloro-5-[(1e)-2-chloroethenyl]-1,5-dimethylcyclohexane

(1r,2s,4s,5r)-1,2,4-trichloro-5-[(1e)-2-chloroethenyl]-1,5-dimethylcyclohexane

C10H14Cl4 (273.985)


   

(1s,2r,4s)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2e)-3-(3,4,5-trimethoxyphenyl)prop-2-enoate

(1s,2r,4s)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2e)-3-(3,4,5-trimethoxyphenyl)prop-2-enoate

C22H30O5 (374.2093)


   

1-(hydroxymethyl)-7,7-dimethylbicyclo[2.2.1]heptan-2-ol

1-(hydroxymethyl)-7,7-dimethylbicyclo[2.2.1]heptan-2-ol

C10H18O2 (170.1307)


   

6,6-dimethylbicyclo[3.1.1]heptane-2-carboxylic acid

6,6-dimethylbicyclo[3.1.1]heptane-2-carboxylic acid

C10H16O2 (168.115)


   

(2r,3s,4s,5r,6r)-2-({[(2r,3r,4r)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-{[(1s,2r,4s,7s)-7-(hydroxymethyl)-1,7-dimethylbicyclo[2.2.1]heptan-2-yl]oxy}oxane-3,4,5-triol

(2r,3s,4s,5r,6r)-2-({[(2r,3r,4r)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-{[(1s,2r,4s,7s)-7-(hydroxymethyl)-1,7-dimethylbicyclo[2.2.1]heptan-2-yl]oxy}oxane-3,4,5-triol

C21H36O11 (464.2258)


   

(1s,2s,4r,5r)-1,2,4-trichloro-5-[(1e)-2-chloroethenyl]-1,5-dimethylcyclohexane

(1s,2s,4r,5r)-1,2,4-trichloro-5-[(1e)-2-chloroethenyl]-1,5-dimethylcyclohexane

C10H14Cl4 (273.985)


   

(1s,2r,4s)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate

(1s,2r,4s)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate

C19H24O3 (300.1725)


   

4,7,7-trimethylbicyclo[2.2.1]hept-1-ene

4,7,7-trimethylbicyclo[2.2.1]hept-1-ene

C10H16 (136.1252)


   

(1r,3as,7as)-1-hydroxy-5,7,7-trimethyl-1,3,3a,7a-tetrahydro-2-benzofuran-4-one

(1r,3as,7as)-1-hydroxy-5,7,7-trimethyl-1,3,3a,7a-tetrahydro-2-benzofuran-4-one

C11H16O3 (196.1099)


   

bis({1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl}oxidanesulfonic acid)

bis({1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl}oxidanesulfonic acid)

C20H36O8S2 (468.1851)


   

1,7,7-trimethyl-2-methylidenebicyclo[2.2.1]heptane

1,7,7-trimethyl-2-methylidenebicyclo[2.2.1]heptane

C11H18 (150.1408)


   

(1s,2s,4r,7r)-7-(hydroxymethyl)-1,7-dimethylbicyclo[2.2.1]heptan-2-ol

(1s,2s,4r,7r)-7-(hydroxymethyl)-1,7-dimethylbicyclo[2.2.1]heptan-2-ol

C10H18O2 (170.1307)


   

borneol; para-coumaric acid

borneol; para-coumaric acid

C19H26O4 (318.1831)


   

7,7-dimethylbicyclo[2.2.1]heptan-2-yl 2-methylpropanoate

7,7-dimethylbicyclo[2.2.1]heptan-2-yl 2-methylpropanoate

C13H22O2 (210.162)


   

d-bornyl isovalerate

d-bornyl isovalerate

C15H26O2 (238.1933)


   

1-hydroxy-5,7,7-trimethyl-1,3,3a,7a-tetrahydro-2-benzofuran-4-one

1-hydroxy-5,7,7-trimethyl-1,3,3a,7a-tetrahydro-2-benzofuran-4-one

C11H16O3 (196.1099)


   

(1r,2r,4r)-4,7,7-trimethyl-5-oxobicyclo[2.2.1]heptan-2-yl benzoate

(1r,2r,4r)-4,7,7-trimethyl-5-oxobicyclo[2.2.1]heptan-2-yl benzoate

C17H20O3 (272.1412)


   

1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate

1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate

C19H24O4 (316.1675)


   

(2z)-2-methyl-5-[(1r,2r,4s)-2-methyl-3-methylidenebicyclo[2.2.1]heptan-2-yl]pent-2-en-1-ol

(2z)-2-methyl-5-[(1r,2r,4s)-2-methyl-3-methylidenebicyclo[2.2.1]heptan-2-yl]pent-2-en-1-ol

C15H24O (220.1827)


   

2-methoxy-1,7,7-trimethylbicyclo[2.2.1]heptane

2-methoxy-1,7,7-trimethylbicyclo[2.2.1]heptane

C11H20O (168.1514)


   

(1r,2r,4r)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate

(1r,2r,4r)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate

C19H24O3 (300.1725)


   

(1r,2s,4r)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2e)-3-(2h-1,3-benzodioxol-5-yl)prop-2-enoate

(1r,2s,4r)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2e)-3-(2h-1,3-benzodioxol-5-yl)prop-2-enoate

C20H24O4 (328.1675)


   

(1r,2s,5r)-6,6-dimethylbicyclo[3.1.1]heptane-2-carboxylic acid

(1r,2s,5r)-6,6-dimethylbicyclo[3.1.1]heptane-2-carboxylic acid

C10H16O2 (168.115)


   

7-ethylidene-1,2,8,8-tetramethylbicyclo[3.2.1]octane

7-ethylidene-1,2,8,8-tetramethylbicyclo[3.2.1]octane

C14H24 (192.1878)


   

{2-hydroxy-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl}acetic acid

{2-hydroxy-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl}acetic acid

C12H20O3 (212.1412)


   

(1s,2r,3s,4r)-3-hydroxy-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl acetate

(1s,2r,3s,4r)-3-hydroxy-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl acetate

C12H20O3 (212.1412)


   

6-bromo-3-(2-bromoethylidene)-2,4-dichloro-1,1-dimethylcyclohexane

6-bromo-3-(2-bromoethylidene)-2,4-dichloro-1,1-dimethylcyclohexane

C10H14Br2Cl2 (361.8839)


   

2-({3,3-dimethylbicyclo[2.2.1]heptan-2-yl}methoxy)-6-[({9-hydroxy-2,2-dimethyl-1,3,7-trioxaspiro[4.4]nonan-8-yl}oxy)methyl]oxane-3,4,5-triol

2-({3,3-dimethylbicyclo[2.2.1]heptan-2-yl}methoxy)-6-[({9-hydroxy-2,2-dimethyl-1,3,7-trioxaspiro[4.4]nonan-8-yl}oxy)methyl]oxane-3,4,5-triol

C24H40O10 (488.2621)


   

(3z,6s)-4-bromo-2,6-dichloro-3-(2-chloroethylidene)-1,1-dimethylcyclohexane

(3z,6s)-4-bromo-2,6-dichloro-3-(2-chloroethylidene)-1,1-dimethylcyclohexane

C10H14BrCl3 (317.9344)


   

1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl 3-(2-methoxyphenyl)prop-2-enoate

1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl 3-(2-methoxyphenyl)prop-2-enoate

C20H26O3 (314.1882)


   

1,7,7-trimethylbicyclo[2.2.1]heptane-2,6-diol

1,7,7-trimethylbicyclo[2.2.1]heptane-2,6-diol

C10H18O2 (170.1307)


   

1,7-bis(hydroxymethyl)-7-methylbicyclo[2.2.1]heptan-2-ol

1,7-bis(hydroxymethyl)-7-methylbicyclo[2.2.1]heptan-2-ol

C10H18O3 (186.1256)


   

(1r,2r,4r,5s)-1,2,4-trichloro-5-(2-chloroethenyl)-1,5-dimethylcyclohexane

(1r,2r,4r,5s)-1,2,4-trichloro-5-(2-chloroethenyl)-1,5-dimethylcyclohexane

C10H14Cl4 (273.985)


   

(1r,5s)-1,8,8-trimethyl-3-azabicyclo[3.2.1]octane

(1r,5s)-1,8,8-trimethyl-3-azabicyclo[3.2.1]octane

C10H19N (153.1517)


   

5-(hydroxymethyl)-6,6-dimethylbicyclo[2.2.1]heptan-2-ol

5-(hydroxymethyl)-6,6-dimethylbicyclo[2.2.1]heptan-2-ol

C10H18O2 (170.1307)


   

(1r,2s,4r)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate

(1r,2s,4r)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate

C19H24O4 (316.1675)


   

(2r,3e,4r,6r)-6-bromo-3-(2-bromoethylidene)-2,4-dichloro-1,1-dimethylcyclohexane

(2r,3e,4r,6r)-6-bromo-3-(2-bromoethylidene)-2,4-dichloro-1,1-dimethylcyclohexane

C10H14Br2Cl2 (361.8839)


   

(1s,2r,4s)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate

(1s,2r,4s)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate

C19H24O4 (316.1675)


   

(1r,2s,4r,5s)-1,2,4-trichloro-5-[(1e)-2-chloroethenyl]-1,5-dimethylcyclohexane

(1r,2s,4r,5s)-1,2,4-trichloro-5-[(1e)-2-chloroethenyl]-1,5-dimethylcyclohexane

C10H14Cl4 (273.985)


   

(1s,2s,3r,4r)-1-(hydroxymethyl)-7,7-dimethylbicyclo[2.2.1]heptane-2,3-diol

(1s,2s,3r,4r)-1-(hydroxymethyl)-7,7-dimethylbicyclo[2.2.1]heptane-2,3-diol

C10H18O3 (186.1256)


   

1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

C20H26O4 (330.1831)


   

6,6-dimethyl-5-methylidenebicyclo[2.2.1]heptan-2-one

6,6-dimethyl-5-methylidenebicyclo[2.2.1]heptan-2-one

C10H14O (150.1045)


   

(2s,4r,7r)-7-(hydroxymethyl)-1,7-dimethylbicyclo[2.2.1]heptan-2-ol

(2s,4r,7r)-7-(hydroxymethyl)-1,7-dimethylbicyclo[2.2.1]heptan-2-ol

C10H18O2 (170.1307)


   

6,6-dimethyl-5-methylidenebicyclo[2.2.1]heptan-2-ol

6,6-dimethyl-5-methylidenebicyclo[2.2.1]heptan-2-ol

C10H16O (152.1201)


   

(2r,3s,4s,5r,6r)-2-({[(2r,3r,4r)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-{[(1r,2s,4r)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl]oxy}oxane-3,4,5-triol

(2r,3s,4s,5r,6r)-2-({[(2r,3r,4r)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-{[(1r,2s,4r)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl]oxy}oxane-3,4,5-triol

C21H36O10 (448.2308)


   

(1s,3as,7as)-1-hydroxy-5,7,7-trimethyl-1,3,3a,7a-tetrahydro-2-benzofuran-4-one

(1s,3as,7as)-1-hydroxy-5,7,7-trimethyl-1,3,3a,7a-tetrahydro-2-benzofuran-4-one

C11H16O3 (196.1099)


   

2-{[6-({3,3-dimethylbicyclo[2.2.1]heptan-2-yl}methoxy)-3,4,5-trihydroxyoxan-2-yl]methoxy}-6-methyloxane-3,4,5-triol

2-{[6-({3,3-dimethylbicyclo[2.2.1]heptan-2-yl}methoxy)-3,4,5-trihydroxyoxan-2-yl]methoxy}-6-methyloxane-3,4,5-triol

C22H38O10 (462.2465)


   

(1s,2r,4s,7s)-1,7-bis(hydroxymethyl)-7-methylbicyclo[2.2.1]heptan-2-ol

(1s,2r,4s,7s)-1,7-bis(hydroxymethyl)-7-methylbicyclo[2.2.1]heptan-2-ol

C10H18O3 (186.1256)


   

(1s,4s)-1,7,7-trimethylbicyclo[2.2.1]heptane-2,6-dione

(1s,4s)-1,7,7-trimethylbicyclo[2.2.1]heptane-2,6-dione

C10H14O2 (166.0994)


   

2-({[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-({1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl}oxy)oxane-3,4,5-triol

2-({[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-({1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl}oxy)oxane-3,4,5-triol

C21H36O10 (448.2308)


   

(1s,2r,4s)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2z)-2-methylbut-2-enoate

(1s,2r,4s)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2z)-2-methylbut-2-enoate

C15H24O2 (236.1776)


   

1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl 3-(4-hydroxy-2-methoxyphenyl)prop-2-enoate

1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl 3-(4-hydroxy-2-methoxyphenyl)prop-2-enoate

C20H26O4 (330.1831)


   

(2r,3s,4s,5r,6r)-2-({[(2r,3r,4r)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-{[(1r,2r,4s,6r)-6-hydroxy-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl]oxy}oxane-3,4,5-triol

(2r,3s,4s,5r,6r)-2-({[(2r,3r,4r)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-{[(1r,2r,4s,6r)-6-hydroxy-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl]oxy}oxane-3,4,5-triol

C21H36O11 (464.2258)


   

(1r,2r,4r,5r)-1,2,4-trichloro-5-(2-chloroethenyl)-1,5-dimethylcyclohexane

(1r,2r,4r,5r)-1,2,4-trichloro-5-(2-chloroethenyl)-1,5-dimethylcyclohexane

C10H14Cl4 (273.985)


   

(1r,2s,4s)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol

(1r,2s,4s)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol

C10H18O (154.1358)


   

(1s,6s)-1,5,5-trimethyl-3-oxabicyclo[4.2.2]decane

(1s,6s)-1,5,5-trimethyl-3-oxabicyclo[4.2.2]decane

C12H22O (182.1671)


   

(1r,2s,4r)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2e)-3-(4-hydroxy-2-methoxyphenyl)prop-2-enoate

(1r,2s,4r)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2e)-3-(4-hydroxy-2-methoxyphenyl)prop-2-enoate

C20H26O4 (330.1831)


   

(1s,2s,4s)-5,5-dimethyl-6-methylidenebicyclo[2.2.1]heptan-2-yl acetate

(1s,2s,4s)-5,5-dimethyl-6-methylidenebicyclo[2.2.1]heptan-2-yl acetate

C12H18O2 (194.1307)


   

(1s,2r,4s)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2z)-3-(4-hydroxyphenyl)prop-2-enoate

(1s,2r,4s)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2z)-3-(4-hydroxyphenyl)prop-2-enoate

C19H24O3 (300.1725)


   

(1r,3s,4s)-3-hydroxy-4-(hydroxymethyl)-7,7-dimethylbicyclo[2.2.1]heptan-2-one

(1r,3s,4s)-3-hydroxy-4-(hydroxymethyl)-7,7-dimethylbicyclo[2.2.1]heptan-2-one

C10H16O3 (184.1099)


   

(2r,3s,4s,5r,6r)-2-(hydroxymethyl)-6-{[(1s,2r,4s)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl]oxy}oxane-3,4,5-triol

(2r,3s,4s,5r,6r)-2-(hydroxymethyl)-6-{[(1s,2r,4s)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl]oxy}oxane-3,4,5-triol

C16H28O6 (316.1886)


   

1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl 3-(2h-1,3-benzodioxol-5-yl)prop-2-enoate

1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl 3-(2h-1,3-benzodioxol-5-yl)prop-2-enoate

C20H24O4 (328.1675)


   

(2r,3z,4s,6r)-4-bromo-2,6-dichloro-3-(2-chloroethylidene)-1,1-dimethylcyclohexane

(2r,3z,4s,6r)-4-bromo-2,6-dichloro-3-(2-chloroethylidene)-1,1-dimethylcyclohexane

C10H14BrCl3 (317.9344)


   

2-(3-{2-methyl-3-methylidenebicyclo[2.2.1]heptan-2-yl}propylidene)propane-1,3-diol

2-(3-{2-methyl-3-methylidenebicyclo[2.2.1]heptan-2-yl}propylidene)propane-1,3-diol

C15H24O2 (236.1776)


   

(1r,2s,4r)-7,7-dimethylbicyclo[2.2.1]heptan-2-yl 2-methylpropanoate

(1r,2s,4r)-7,7-dimethylbicyclo[2.2.1]heptan-2-yl 2-methylpropanoate

C13H22O2 (210.162)


   

(1s,2r,4s)-1-(hydroxymethyl)-7,7-dimethylbicyclo[2.2.1]heptan-2-ol

(1s,2r,4s)-1-(hydroxymethyl)-7,7-dimethylbicyclo[2.2.1]heptan-2-ol

C10H18O2 (170.1307)


   

6,6,7-trimethyltricyclo[3.2.0.0²,⁷]heptane

6,6,7-trimethyltricyclo[3.2.0.0²,⁷]heptane

C10H16 (136.1252)


   

7-(hydroxymethyl)-1,7-dimethylbicyclo[2.2.1]heptan-2-ol

7-(hydroxymethyl)-1,7-dimethylbicyclo[2.2.1]heptan-2-ol

C10H18O2 (170.1307)


   

(2r,3r,4s,5s,6r)-2-{[(1s,2r,4s,5s)-5-hydroxy-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

(2r,3r,4s,5s,6r)-2-{[(1s,2r,4s,5s)-5-hydroxy-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

C16H28O7 (332.1835)


   

(1r,2s,4r)-2-chloro-1,7,7-trimethylbicyclo[2.2.1]heptane

(1r,2s,4r)-2-chloro-1,7,7-trimethylbicyclo[2.2.1]heptane

C10H17Cl (172.1019)


   

1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2z)-2-methylbut-2-enoate

1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2z)-2-methylbut-2-enoate

C15H24O2 (236.1776)


   

(1s,2r,4s,5s)-1,7,7-trimethylbicyclo[2.2.1]heptane-2,5-diol

(1s,2r,4s,5s)-1,7,7-trimethylbicyclo[2.2.1]heptane-2,5-diol

C10H18O2 (170.1307)


   

5,5-dimethyl-6-methylidenebicyclo[2.2.1]heptan-2-ol

5,5-dimethyl-6-methylidenebicyclo[2.2.1]heptan-2-ol

C10H16O (152.1201)


   

2,2,3-trimethylbicyclo[2.2.1]heptane

2,2,3-trimethylbicyclo[2.2.1]heptane

C10H18 (138.1408)


   

(1s,2r,4r,5s)-5-(hydroxymethyl)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol

(1s,2r,4r,5s)-5-(hydroxymethyl)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol

C11H20O2 (184.1463)


   

1,7,7-trimethyl-5-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}bicyclo[2.2.1]heptan-2-one

1,7,7-trimethyl-5-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}bicyclo[2.2.1]heptan-2-one

C16H26O7 (330.1678)


   

(2r,6s)-1,7,7-trimethylbicyclo[2.2.1]heptane-2,6-diol

(2r,6s)-1,7,7-trimethylbicyclo[2.2.1]heptane-2,6-diol

C10H18O2 (170.1307)


   

(1r,2r,5r,7e)-7-ethylidene-1,2,8,8-tetramethylbicyclo[3.2.1]octane

(1r,2r,5r,7e)-7-ethylidene-1,2,8,8-tetramethylbicyclo[3.2.1]octane

C14H24 (192.1878)


   

(1r,2r,4s)-1,3,3-trimethylbicyclo[2.2.1]heptan-2-ol

(1r,2r,4s)-1,3,3-trimethylbicyclo[2.2.1]heptan-2-ol

C10H18O (154.1358)


   

(1,1,3a,7,7-pentamethyl-2,3,6,7a-tetrahydroinden-2-yl)methanol

(1,1,3a,7,7-pentamethyl-2,3,6,7a-tetrahydroinden-2-yl)methanol

C15H26O (222.1984)