(+)-gamma-Pinene

Details

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Internal ID eb87c90c-5baa-4cbf-ab29-d8f99c9ed25e
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Bicyclic monoterpenoids
IUPAC Name 4,6,6-trimethylbicyclo[3.1.1]hept-2-ene
SMILES (Canonical) CC1C=CC2CC1C2(C)C
SMILES (Isomeric) CC1C=CC2CC1C2(C)C
InChI InChI=1S/C10H16/c1-7-4-5-8-6-9(7)10(8,2)3/h4-5,7-9H,6H2,1-3H3
InChI Key XJBOZKOSICCONT-UHFFFAOYSA-N
Popularity 300 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16
Molecular Weight 136.23 g/mol
Exact Mass 136.125200510 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.30
Atomic LogP (AlogP) 2.85
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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5947-71-7
3-pinene
2,6,6-Trimethylbicyclo[3.1.1]hept-3-ene
DTXSID60424021
XJBOZKOSICCONT-UHFFFAOYSA-N
DL-4,7,7-trimethylbicyclo[3.1.1]-2-heptene

2D Structure

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2D Structure of (+)-gamma-Pinene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9943 99.43%
Caco-2 + 0.5824 58.24%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.8714 87.14%
Subcellular localzation Lysosomes 0.7220 72.20%
OATP2B1 inhibitior - 0.8635 86.35%
OATP1B1 inhibitior + 0.9298 92.98%
OATP1B3 inhibitior + 0.9393 93.93%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9402 94.02%
P-glycoprotein inhibitior - 0.9652 96.52%
P-glycoprotein substrate - 0.9065 90.65%
CYP3A4 substrate - 0.5199 51.99%
CYP2C9 substrate - 0.8047 80.47%
CYP2D6 substrate - 0.7942 79.42%
CYP3A4 inhibition - 0.8067 80.67%
CYP2C9 inhibition - 0.8289 82.89%
CYP2C19 inhibition - 0.7988 79.88%
CYP2D6 inhibition - 0.9285 92.85%
CYP1A2 inhibition - 0.8402 84.02%
CYP2C8 inhibition - 0.9711 97.11%
CYP inhibitory promiscuity - 0.6561 65.61%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5700 57.00%
Carcinogenicity (trinary) Non-required 0.4505 45.05%
Eye corrosion - 0.5646 56.46%
Eye irritation + 0.7952 79.52%
Skin irritation + 0.6873 68.73%
Skin corrosion - 0.8462 84.62%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6064 60.64%
Micronuclear - 0.9641 96.41%
Hepatotoxicity + 0.6426 64.26%
skin sensitisation + 0.8809 88.09%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity - 0.5889 58.89%
Mitochondrial toxicity - 0.5934 59.34%
Nephrotoxicity - 0.7156 71.56%
Acute Oral Toxicity (c) III 0.7471 74.71%
Estrogen receptor binding - 0.8950 89.50%
Androgen receptor binding - 0.8188 81.88%
Thyroid receptor binding - 0.8785 87.85%
Glucocorticoid receptor binding - 0.8829 88.29%
Aromatase binding - 0.9035 90.35%
PPAR gamma - 0.9148 91.48%
Honey bee toxicity - 0.7569 75.69%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.8800 88.00%
Fish aquatic toxicity + 0.9808 98.08%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.06% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.76% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.01% 91.11%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 86.27% 82.69%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.91% 97.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.47% 92.94%
CHEMBL2996 Q05655 Protein kinase C delta 82.21% 97.79%
CHEMBL3045 P05771 Protein kinase C beta 82.10% 97.63%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Pilocarpus microphyllus

Cross-Links

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PubChem 6431006
LOTUS LTS0014368
wikiData Q82236422