Exact Mass: 136.1221

C10H16 (136.1252)

Terpinolene (TPO), also known as alpha-terpinolene or isoterpinene, belongs to the class of organic compounds known as menthane monoterpenoids. These are monoterpenoids with a structure based on the o-, m-, or p-menthane backbone. P-menthane consists of the cyclohexane ring with a methyl group and a (2-methyl)-propyl group at the 1 and 4 ring position, respectively. The o- and m- menthanes are much rarer, and presumably arise by alkyl migration of p-menthanes. Thus, terpinolene is considered to be an isoprenoid lipid molecule. Terpinolene is a very hydrophobic monoterpenoid, practically insoluble in water, and relatively neutral. Monoterpenoids are terpenes that contain 10 carbon atoms and are comprised of two isoprene units. The biosynthesis of monoterpenes in plants is known to occur mainly through the methyl-erythritol-phosphate (MEP) pathway in the 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. Terpinolene is one of the constituents of turpentine and an isomer of terpinene. It appears colourless to pale yellow liquid. Alpha-terpinolene has been identified as an abundant monoterpene in the essential oil of Cannabis sativa plants (PMID:6991645 ). There are more than 140 known terpenes in cannabis and the combination of these terepenoids produces the skunky, fruity odor characteristic of C. savita. Although common in cannabis cultivars, terpinolene is typically found in relatively low amounts. On the other hand, the concentration of terpinolene can be has high as 30\\% of the essential oil. It is thought that terpinolene offers a mildly sedative effect and can reduce anxiety (PMID:28826544 ). In particular, terpinolene is a central nervous system depressant that has been shown to induce drowsiness (PMID:23339024 ). Terpinolene has been demonstrated to prevent LDL oxidation and is of potential interest in the treatment of atherogenesis and coronary artery disease (PMID:28826544 ). Terpinolene exhibits antifungal and larvicidal properties (PMID:28826544 ). Terpinolene is also an effective anti-microbial agent, particularly against E coli and Staphylococcus bacteria (PMID:16402540 ). Terpinolene is also employed as a fragrence ingredient in lotions, insect repellents (similar to other terpenes), perfumes, and soaps. Terpinolene is also a constituent of many other essential oils e. g. Citrus, Mentha, Juniperus, Myristica species. Parsnip oil (Pastinaca sativa) in particular, is a major source (40-70\\%). Terpinolene is a sweet, citrus, and fresh tasting compound. It produces a floral, woody or herbal aroma reminiscent of pine needles. In addition to being found in various plant essential oils, terpinolene is found in a few different foods and spices, such as allspice, apples, sage, rosemary, parsnips, nutmegs, and wild carrots and in a lower concentration in sweet bay, star anises, turmerics, apricots, cumins, evergreen blackberries, red bell peppers, and caraway. Constituent of many essential oils e.g. Citrus, Mentha, Juniperus, Myristica subspecies Parsnip oil (Pastinaca sativa) is a major source (40-70\\%). Flavouring ingredient. Terpinolene is found in many foods, some of which are coriander, ceylon cinnamon, pine nut, and caraway.

(1R,5R)-4-methylidene-1-(propan-2-yl)bicyclo[3.1.0]hexane

C10H16 (136.1252)

(-)-beta-Phellandrene

(6R)-3-methylidene-6-(propan-2-yl)cyclohex-1-ene

C10H16 (136.1252)

(-)-beta-Phellandrene is found in pine nut. Phellandrene is the name for a pair of organic compounds that have a similar molecular structure and similar chemical properties. alpha-Phellandrene and beta-phellandrene are cyclic monoterpenes and are double-bond isomers. The phellandrenes are used in fragrances because of their pleasing aromas. (Wikipedia).

(+)-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.

Pinene

(1R,5R)-2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene

C10H16 (136.1252)

Pinene (is a bicyclic monoterpene chemical compound. There are two structural isomers of pinene found in nature: alpha-pinene and beta-pinene. As the name suggests, both forms are important constituents of pine resin; they are also found in the resins of many other conifers, as well as in non-coniferous plants. Both isomers are used by many insects in their chemical communication system.

β-Pinene

(1S,5S)-7,7-dimethyl-4-methylidene-bicyclo[3.1.1]heptane

C10H16 (136.1252)

2-Ethyl-3,(5 or 6)-dimethylpyrazine

C8H12N2 (136.1)

3-Ethyl-2,5-dimethylpyrazine is found in coffee and coffee products. 3-Ethyl-2,5-dimethylpyrazine is isolated from coffee. 2-Ethyl-3,(5 or 6)-dimethylpyrazine is a constituent of numerous cooked foods. 3-Ethyl-2,5-dimethylpyrazine is organoleptic agent with nutty roasted odour. Isolated from coffee. Constituent of numerous cooked foods. Organoleptic agent with nutty roasted odour. 3-Ethyl-2,5-dimethylpyrazine is found in tea, soft-necked garlic, and coffee and coffee products.

cis-Ocimene

(Z)-3,7-dimethylocta-1,3,6,-triene

C10H16 (136.1252)

Ocimene refers to several isomeric hydrocarbons. The ocimenes are monoterpenes found within a variety of plants and fruits. alpha-Ocimene and the two beta-ocimenes differ in the position of the isolated double bond: it is terminal in the alpha isomer. alpha-Ocimene is 3,7-dimethyl-1,3,7-octatriene. beta-Ocimene is 3,7-dimethyl-1,3,6-octatriene. beta-Ocimene exists in two stereoisomeric forms, cis and trans, with respect to the central double bond. The ocimenes are often found naturally as mixtures of the various forms. The mixture (as well as the pure compounds) is an oil with a pleasant odor. It is used in perfumery. cis-beta-Ocimene is found in many foods, some of which are cornmint, sweet orange, sweet basil, and common sage. cis-Ocimene is found in allspice. Ocimene refers to several isomeric hydrocarbons. The ocimenes are monoterpenes found within a variety of plants and fruits. alpha-Ocimene and the two beta-ocimenes differ in the position of the isolated double bond: it is terminal in the alpha isomer. alpha-Ocimene is 3,7-dimethyl-1,3,7-octatriene. beta-Ocimene is 3,7-dimethyl-1,3,6-octatriene. beta-Ocimene exists in two stereoisomeric forms, cis and trans, with respect to the central double bond. The ocimenes are often found naturally as mixtures of the various forms. The mixture (as well as the pure compounds) is an oil with a pleasant odor. It is used in perfumery. (Wikipedia

2,7,7-Trimethyl-bicyclo[2.2.1]hept-2-ene belongs to the class of organic compounds known as polycyclic hydrocarbons. These are polycyclic organic compounds made up only of carbon and hydrogen atoms.

3-Methylene-1,5,5-trimethylcyclohexene

1,5,5-trimethyl-3-methylidenecyclohex-1-ene

C10H16 (136.1252)

3-Methylene-1,5,5-trimethylcyclohexene belongs to the class of organic compounds known as cycloalkenes. These are compounds containing a non-aromatic closed ring of carbon atoms in which at least 2 atoms are connected by a double bond.

Adamantane

Tricyclo[3.3.1.1(3,7)]decane

C10H16 (136.1252)

Adamantane, a polycyclic cage molecule with high symmetry and remarkable properties. Adamantane can be incorporated into a lipophilic part of the lipid bilayer that constitutes membranes and as an anchor in the lipid bilayer of liposomes. Adamantane can be used in research of surface recognition and drug delivery[1]. Adamantane, a polycyclic cage molecule with high symmetry and remarkable properties. Adamantane can be incorporated into a lipophilic part of the lipid bilayer that constitutes membranes and as an anchor in the lipid bilayer of liposomes. Adamantane can be used in research of surface recognition and drug delivery[1].

N1,N1-Dimethylbenzene-1,2-diamine

C8H12N2 (136.1)

C10H16 (136.1252)

(+)-beta-Fenchene

(1R)-2,2-Dimethyl-5-methylenebicyclo[2.2.1]heptane

C10H16 (136.1252)

gamma-Fenchene

2-Methyl-5-(1-methylethyl)-1,3-cyclohexadiene

C10H16 (136.1252)

One of a pair of phellandrene cyclic monoterpene double-bond isomers in which both double bonds are endocyclic (cf. alpha-phellandrene, where one of them is exocyclic).

Beta-Phellandrene

Bornylene

Sabinene

Bicyclo[3.1.0]hexane, 4-methylene-1-(1-methylethyl)-

C10H16 (136.1252)

Sabinene is a thujene that is a bicyclic monoterpene isolated from the essential oils of various plant species. It has a role as a plant metabolite. Black pepper allergenic extract is used in allergenic testing. Laurus nobilis allergenic extract is used in allergenic testing. Nutmeg allergenic extract is used in allergenic testing. Sabinene is a natural product found in Teucrium montanum, Xylopia aromatica, and other organisms with data available. Carrot Seed Oil is the oil extracted from the seeds of Daucus carota. Carrot seed oil is primarily used in skin treatment preparations. A thujene that is a bicyclic monoterpene isolated from the essential oils of various plant species. 4(10)-thujene, also known as sabinen or 1-isopropyl-4-methylenebicyclo[3.1.0]hexane, 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. 4(10)-thujene is a citrus, pepper, and pine tasting compound and can be found in a number of food items such as sweet orange, green bell pepper, pot marjoram, and parsley, which makes 4(10)-thujene a potential biomarker for the consumption of these food products. Sabinene is an naturally occurring bicyclic monoterpene which can be used as flavorings, perfume additives, fine chemicals, and advanced biofuels. Sabinene is also an orally active compound to attenuates skeletal muscle atrophy and regulates ROS-mediated MAPK/MuRF-1 pathways[1][2]. Sabinene is an naturally occurring bicyclic monoterpene which can be used as flavorings, perfume additives, fine chemicals, and advanced biofuels. Sabinene is also an orally active compound to attenuates skeletal muscle atrophy and regulates ROS-mediated MAPK/MuRF-1 pathways[1][2].

γ-Terpinene

gamma-terpinene

C10H16 (136.1252)

γ-Terpinene, a monoterpene, is an orally active antioxidant compound which can scavenge radicals directly. γ-Terpinene has potent antinociception activity[1]. γ-Terpinene, a monoterpene, is an orally active antioxidant compound which can scavenge radicals directly. γ-Terpinene has potent antinociception activity[1].

(+)-limonene

C10H16 (136.1252)

Major constituent of oil of orange rind, dill oil, oil of cumin, bergamot, caraway, lemon balm and lemon. obtained comly. from orange oil on a large scale (ca. 50000 T/a). Flavouring agent. Nutriceutical with anticancer props. (R)-Limonene is found in many foods, some of which are citrus, nutmeg, guava, and cardamom.

Phenelzine

C8H12N2 (136.1)

N - Nervous system > N06 - Psychoanaleptics > N06A - Antidepressants > N06AF - Monoamine oxidase inhibitors, non-selective D002491 - Central Nervous System Agents > D011619 - Psychotropic Drugs > D000928 - Antidepressive Agents C78272 - Agent Affecting Nervous System > C265 - Antidepressant Agent D004791 - Enzyme Inhibitors > D008996 - Monoamine Oxidase Inhibitors C471 - Enzyme Inhibitor > C667 - Monoamine Oxidase Inhibitor

d-limonene

C10H16 (136.1252)

(R)-(+)-limonene

C10H16 (136.1252)

1 micro litter of limonene (liquid) was placed on glass capillary.; (R)-(+)-Limonene was purchased from Wako 124-03892.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 16HP2005 to the Mass Spectrometry Society of Japan.; Direct analysis in real time (DART) is a method of atmospheric pressure chemical ionization (APCI). Protons, H+, generated by glow discharge ionization (-5 kV) of the He gas in the ionization chamber, DART-SVP (IonSense Inc., MA, USA), were major reactant ions for the chemical ionization of samples.; The interface introducing the product ions to the mass spectrometer was Vapur Interface (AMR. Inc., Tokyo, Japan). The pressure in the interface was 710 Torr (96.3 kPa). One micro litter of the liquid sample was dropped in a 10 mL glass vial. The vial was placed under the DART ion source.; (R)-(+)-Limonene was purchased from Wako 124-03892.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 16HP2005 to the Mass Spectrometry Society of Japan.; Direct analysis in real time (DART) is a method of atmospheric pressure chemical ionization (APCI). Protons, H+, generated by glow discharge ionization (- 5 kV) of the He gas in the ionization chamber, DART-SVP (IonSense Inc., MA, USA), were major reactant ions for the chemical ionization of samples.; The interface introducing the product ions to the mass spectrometer was Vapur Interface (AMR. Inc., Tokyo, Japan). The pressure in the interface was 710 Torr (96.3 kPa).

(-)-limonene

(S)-(−)-Limonene

C10H16 (136.1252)

(-)-Limonene ((S)-(-)-Limonene) is a monoterpene found in citrus plants like lemon, orange, and grape. (-)-Limonene can induce a mild bronchoconstrictive effect[1]. (-)-Limonene ((S)-(-)-Limonene) is a monoterpene found in citrus plants like lemon, orange, and grape. (-)-Limonene can induce a mild bronchoconstrictive effect[1]. (-)-Limonene ((S)-(-)-Limonene) is a monoterpene found in citrus plants like lemon, orange, and grape. (-)-Limonene can induce a mild bronchoconstrictive effect[1]. (-)-Limonene ((S)-(-)-Limonene) is a monoterpene found in citrus plants like lemon, orange, and grape. (-)-Limonene can induce a mild bronchoconstrictive effect[1].

DMPD

C8H12N2 (136.1)

d-LIMONENE_major

C10H16 (136.1252)

N,N-Dimethyl-1,4-benzenediamine

"N,N-DIMETHYL-1,4-PHENYLENEDIAMINE"

C8H12N2 (136.1)

betahistine

C8H12N2 (136.1)

N - Nervous system > N07 - Other nervous system drugs > N07C - Antivertigo preparations > N07CA - Antivertigo preparations D018377 - Neurotransmitter Agents > D018494 - Histamine Agents > D017442 - Histamine Agonists C78274 - Agent Affecting Cardiovascular System > C29707 - Vasodilating Agent D002317 - Cardiovascular Agents > D014665 - Vasodilator Agents Betahistine is an orally active histamine H1 receptor agonist and a H3 receptor antagonist[1]. Betahistine is used for the study of rheumatoid arthritis (RA)[3].

(+)-4-Carene

C10H16 (136.1252)

(Z)-beta-ocimene

3,7-Dimethyl-1,3Z,6-octatriene

(-)-3-Thujene

(1R,5S)-2-Methyl-5-(propan-2-yl)bicyclo[3.1.0]hex-2-ene

C10H16 (136.1252)

Ligustizine

2,3,5,6-Tetramethylpyrazine

(6R)-3-methylidene-6-(propan-2-yl)cyclohex-1-ene

Terpinolen

N-propylpyridin-3-amine

C8H12N2 (136.1)

mebanazine

C8H12N2 (136.1)

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

C10H16 (136.1252)

3,4-DIMETHYL-O-PHENYLENEDIAMINE

C8H12N2 (136.1)

2-sec-butylpyrazine

C8H12N2 (136.1)

2-amino-4,5-dimethylphenylamine

2,5-dimethylbenzol-1,4-diamin

2,5-Dimethylbenzene-1,4-diamine

Phenyltrimethylammonium

C9H14N+ (136.1126)

D019995 - Laboratory Chemicals > D007202 - Indicators and Reagents

Cyclopentylidenecyclopentane

C10H16 (136.1252)

Cyclodecyne

C10H16 (136.1252)

Fluoroethylcholine ion F-18

C6H15FNO+ (136.1138)

C1446 - Radiopharmaceutical Compound > C2124 - Radioconjugate

InChI=1\C10H16\c1-8(2)10-6-4-9(3)5-7-10\h4,7-8H,5-6H2,1-3H

C10H16 (136.1252)

6153-17-9

(6R)-3-methylidene-6-propan-2-yl-cyclohexene

C10H16 (136.1252)

Tereben

Dipentene Fluka specially purified fraction of terpene hydrocarbons

C10H16 (136.1252)

4,7,7-trimethylbicyclo[4.1.0]hept-2-ene

C10H16 (136.1252)

(+)-4-carene 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 (+)-4-carene can be found in rosemary, which makes (+)-4-carene a potential biomarker for the consumption of this food product (+)-4-carene can be found primarily in urine. (+)-4-Carene belongs to the family of Cycloalkenes. These are compounds containing a non-aromatic closed ring of carbon atoms in which at least 2 atoms are connected by a double bond

2,6-Dimethyl-2,4,6-octatriene

2,6-dimethyl-octa-2,4,6-triene

C10H16 (136.1252)

2,6-dimethyl-2,4,6-octatriene, also known as alloocimene, (e,z)-isomer or allo-ocimene, is a member of the class of compounds known as acyclic monoterpenoids. Acyclic monoterpenoids are monoterpenes that do not contain a cycle. 2,6-dimethyl-2,4,6-octatriene can be found in parsnip, sweet basil, and tarragon, which makes 2,6-dimethyl-2,4,6-octatriene a potential biomarker for the consumption of these food products. 2,6-dimethyl-2,4,6-octatriene can be found primarily in saliva. 2,6-Dimethyl-2,4,6-octatriene belongs to the class of organic compounds known as alkatrienes. These are hydrocarbons that contain exactly three carbon-to-carbon double bonds.

polylimonene

C10H16 (136.1252)

It is used as a food additive .

(S)-Limonene

(S)-(−)-Limonene

C10H16 (136.1252)

Constituent of pine needle oiland is) also present in ginger, nutmeg, pepper, mace, coriander and other herbs and spices. (S)-Limonene is found in many foods, some of which are fennel, caraway, cardamom, and herbs and spices. (-)-Limonene ((S)-(-)-Limonene) is a monoterpene found in citrus plants like lemon, orange, and grape. (-)-Limonene can induce a mild bronchoconstrictive effect[1]. (-)-Limonene ((S)-(-)-Limonene) is a monoterpene found in citrus plants like lemon, orange, and grape. (-)-Limonene can induce a mild bronchoconstrictive effect[1]. (-)-Limonene ((S)-(-)-Limonene) is a monoterpene found in citrus plants like lemon, orange, and grape. (-)-Limonene can induce a mild bronchoconstrictive effect[1]. (-)-Limonene ((S)-(-)-Limonene) is a monoterpene found in citrus plants like lemon, orange, and grape. (-)-Limonene can induce a mild bronchoconstrictive effect[1].

(-)-α-Pinene

(-)-alpha-Pinene

C10H16 (136.1252)

C10H16 (136.1252)

A beta-phellandrene in which the chiral centre has R configuration.

(+)-alpha-Phellandrene

(S)-(+)-alpha-Phellandrene

C10H16 (136.1252)

2-Carene

C10H16 (136.1252)

2-Methyl-5-propylpyrazine

C8H12N2 (136.1)

4,7,7-trimethylbicyclo[4.1.0]hept-2-ene

C10H16 (136.1252)

beta-terpinene

C10H16 (136.1252)

Isoterpinolene

C10H16 (136.1252)

A p-menthadiene with double bonds at positions 2 and 4(8).

1,1-Dimethyl-2-(3-methyl-1,3-butadiene)-cyclo-propane

1,1-dimethyl-2-(3-methyl-1,3-butadiene)-cyclo-propane

1-methyl-4-(1-methylethyl)-Cyclohexen

C10H16 (136.1252)

{"Ingredient_id": "HBIN002776","Ingredient_name": "1-methyl-4-(1-methylethyl)-Cyclohexen","Alias": "NA","Ingredient_formula": "C10H16","Ingredient_Smile": "CC1=CCC(=C(C)C)CC1","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "37066","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}

1-methyl-4-methylethenylcyclohexene

C10H16 (136.1252)

{"Ingredient_id": "HBIN002782","Ingredient_name": "1-methyl-4-methylethenylcyclohexene","Alias": "NA","Ingredient_formula": "C10H16","Ingredient_Smile": "CC=CC1CCC(=CC1)C","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "14591","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}

1R-2,6,6- trimethyl-bicyclo [3.1.1]-2-heptene

C10H16 (136.1252)

{"Ingredient_id": "HBIN003028","Ingredient_name": "1R-2,6,6- trimethyl-bicyclo [3.1.1]-2-heptene","Alias": "NA","Ingredient_formula": "C10H16","Ingredient_Smile": "CC1=CCC2CC1C2(C)C","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "41602","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}

1R-α- pinene

1R-α-pinene

C10H16 (136.1252)

{"Ingredient_id": "HBIN007440","Ingredient_name": "3,4-Dimethyl-2,4,6-octatriene","Alias": "NA","Ingredient_formula": "C10H16","Ingredient_Smile": "CC=CC=C(C)C(=CC)C","Ingredient_weight": "136.23 g/mol","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "41027","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "5371124","DrugBank_id": "NA"}

a- pinene

C10H16 (136.1252)

{"Ingredient_id": "HBIN016488","Ingredient_name": "a- pinene","Alias": "NA","Ingredient_formula": "C10H16","Ingredient_Smile": "CC1=CCC2CC1C2(C)C","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "33496","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}

A-terpinolene

C10H16 (136.1252)

{"Ingredient_id": "HBIN017274","Ingredient_name": "A-terpinolene","Alias": "NA","Ingredient_formula": "C10H16","Ingredient_Smile": "CC1=CC=C(CC1)C(C)C","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "34457","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}

β-fenchene

beta-fenchene; beta-Fenchene

C10H16 (136.1252)

{"Ingredient_id": "HBIN018117","Ingredient_name": "\u03b2-fenchene","Alias": "beta-fenchene; beta-Fenchene","Ingredient_formula": "C10H16","Ingredient_Smile": "CC1(CC2CC1C(C2=C)(C)C)C","Ingredient_weight": "136.26","OB_score": "39.16065976","CAS_id": "NA","SymMap_id": "SMIT00571;SMIT07183","TCMID_id": "30957;7749","TCMSP_id": "MOL004721;MOL005422","TCM_ID_id": "6287","PubChem_id": "NA","DrugBank_id": "NA"}

(-)- β- pinene

C10H16 (136.1252)

{"Ingredient_id": "HBIN018240","Ingredient_name": "(-)- \u03b2- pinene","Alias": "NA","Ingredient_formula": "C10H16","Ingredient_Smile": "CC1(C2CCC(=C)C1C2)C","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "36845","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}

beta.-Thujene

C10H16 (136.1252)

{"Ingredient_id": "HBIN018342","Ingredient_name": "beta.-Thujene","Alias": "NA","Ingredient_formula": "C10H16","Ingredient_Smile": "CC1C=CC2(C1C2)C(C)C","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "38551","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}