(+)-cis-3-Pinen-2-ol

Details

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Internal ID 18becf0d-d2ee-4fad-aad7-50686f68715e
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Bicyclic monoterpenoids
IUPAC Name (1R,5R)-2,6,6-trimethylbicyclo[3.1.1]hept-3-en-2-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H16O/c1-9(2)7-4-5-10(3,11)8(9)6-7/h4-5,7-8,11H,6H2,1-3H3/t7-,8+,10?/m0/s1
InChI Key QBKKSIMANOEXOI-VLCSVPMDSA-N
Popularity 9 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16O
Molecular Weight 152.23 g/mol
Exact Mass 152.120115130 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 1.80
Atomic LogP (AlogP) 1.97
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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SCHEMBL7929001

2D Structure

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2D Structure of (+)-cis-3-Pinen-2-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9965 99.65%
Caco-2 + 0.5374 53.74%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.4901 49.01%
OATP2B1 inhibitior - 0.8627 86.27%
OATP1B1 inhibitior + 0.9543 95.43%
OATP1B3 inhibitior + 0.9526 95.26%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9516 95.16%
P-glycoprotein inhibitior - 0.9746 97.46%
P-glycoprotein substrate - 0.9362 93.62%
CYP3A4 substrate - 0.5652 56.52%
CYP2C9 substrate - 0.7740 77.40%
CYP2D6 substrate - 0.8090 80.90%
CYP3A4 inhibition - 0.8537 85.37%
CYP2C9 inhibition - 0.7581 75.81%
CYP2C19 inhibition - 0.6482 64.82%
CYP2D6 inhibition - 0.9285 92.85%
CYP1A2 inhibition - 0.8192 81.92%
CYP2C8 inhibition - 0.9343 93.43%
CYP inhibitory promiscuity - 0.8320 83.20%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8200 82.00%
Carcinogenicity (trinary) Non-required 0.6118 61.18%
Eye corrosion - 0.7878 78.78%
Eye irritation + 0.7398 73.98%
Skin irritation + 0.5986 59.86%
Skin corrosion - 0.6826 68.26%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6354 63.54%
Micronuclear - 0.9300 93.00%
Hepatotoxicity + 0.6460 64.60%
skin sensitisation + 0.6886 68.86%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.6444 64.44%
Mitochondrial toxicity - 0.7446 74.46%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.7857 78.57%
Estrogen receptor binding - 0.8363 83.63%
Androgen receptor binding - 0.7405 74.05%
Thyroid receptor binding - 0.8105 81.05%
Glucocorticoid receptor binding - 0.8403 84.03%
Aromatase binding - 0.9039 90.39%
PPAR gamma - 0.8599 85.99%
Honey bee toxicity - 0.8376 83.76%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity + 0.6700 67.00%
Fish aquatic toxicity + 0.9117 91.17%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.18% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.03% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.35% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.25% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.75% 100.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 80.72% 82.69%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.25% 94.45%

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.
Gutierrezia sarothrae

Cross-Links

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PubChem 57323151
LOTUS LTS0070318
wikiData Q105217859