(+)-3-Carene, 10-(acetylmethyl)-

Details

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Internal ID f2ae0830-a64e-48d5-9f54-6778fd0b0ece
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Bicyclic monoterpenoids
IUPAC Name 4-(7,7-dimethyl-3-bicyclo[4.1.0]hept-3-enyl)butan-2-one
SMILES (Canonical) CC(=O)CCC1=CCC2C(C1)C2(C)C
SMILES (Isomeric) CC(=O)CCC1=CCC2C(C1)C2(C)C
InChI InChI=1S/C13H20O/c1-9(14)4-5-10-6-7-11-12(8-10)13(11,2)3/h6,11-12H,4-5,7-8H2,1-3H3
InChI Key IGPRYTURJRKOCT-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C13H20O
Molecular Weight 192.30 g/mol
Exact Mass 192.151415257 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.30
Atomic LogP (AlogP) 3.35
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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IGPRYTURJRKOCT-UHFFFAOYSA-N
10-(acetylmethyl)-(+)-3-carene
4-(7,7-Dimethylbicyclo[4.1.0]hept-3-en-3-yl)-2-butanone #

2D Structure

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2D Structure of (+)-3-Carene, 10-(acetylmethyl)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9936 99.36%
Caco-2 + 0.7817 78.17%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.3860 38.60%
OATP2B1 inhibitior - 0.8481 84.81%
OATP1B1 inhibitior + 0.8911 89.11%
OATP1B3 inhibitior + 0.9356 93.56%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8680 86.80%
P-glycoprotein inhibitior - 0.9338 93.38%
P-glycoprotein substrate - 0.8477 84.77%
CYP3A4 substrate - 0.5191 51.91%
CYP2C9 substrate - 0.8039 80.39%
CYP2D6 substrate - 0.7758 77.58%
CYP3A4 inhibition - 0.9241 92.41%
CYP2C9 inhibition - 0.7716 77.16%
CYP2C19 inhibition - 0.7956 79.56%
CYP2D6 inhibition - 0.9451 94.51%
CYP1A2 inhibition - 0.5861 58.61%
CYP2C8 inhibition - 0.9396 93.96%
CYP inhibitory promiscuity - 0.7851 78.51%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6800 68.00%
Carcinogenicity (trinary) Non-required 0.5691 56.91%
Eye corrosion - 0.9123 91.23%
Eye irritation + 0.6753 67.53%
Skin irritation + 0.7251 72.51%
Skin corrosion - 0.9805 98.05%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7020 70.20%
Micronuclear - 0.8900 89.00%
Hepatotoxicity + 0.6510 65.10%
skin sensitisation + 0.8982 89.82%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity - 0.7000 70.00%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity + 0.6153 61.53%
Acute Oral Toxicity (c) III 0.7575 75.75%
Estrogen receptor binding - 0.9090 90.90%
Androgen receptor binding - 0.7736 77.36%
Thyroid receptor binding - 0.8099 80.99%
Glucocorticoid receptor binding - 0.6721 67.21%
Aromatase binding - 0.8097 80.97%
PPAR gamma - 0.8045 80.45%
Honey bee toxicity - 0.7915 79.15%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9716 97.16%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.71% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.43% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.55% 97.25%
CHEMBL4040 P28482 MAP kinase ERK2 92.69% 83.82%
CHEMBL2581 P07339 Cathepsin D 91.76% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.86% 94.45%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 83.74% 82.69%

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.
Mentha arvensis
Mentha canadensis

Cross-Links

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PubChem 561019
NPASS NPC84547