Carvotanacetone

Details

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Internal ID 3f12683e-06b4-4c52-8c19-b21ba58edbf0
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Menthane monoterpenoids
IUPAC Name (5S)-2-methyl-5-propan-2-ylcyclohex-2-en-1-one
SMILES (Canonical) CC1=CCC(CC1=O)C(C)C
SMILES (Isomeric) CC1=CC[C@@H](CC1=O)C(C)C
InChI InChI=1S/C10H16O/c1-7(2)9-5-4-8(3)10(11)6-9/h4,7,9H,5-6H2,1-3H3/t9-/m0/s1
InChI Key WPGPCDVQHXOMQP-VIFPVBQESA-N
Popularity 11 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) 17.10 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.57
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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2-Cyclohexen-1-one, 2-methyl-5-(1-methylethyl)-, (S)-
(5S)-2-methyl-5-propan-2-ylcyclohex-2-en-1-one
p-Menth-6-en-2-one, (S)-(+)-
499-71-8
(+)-Carvotanacetone
Carvotanacetone, (+)-
SCHEMBL11902533
CHEBI:171922
WPGPCDVQHXOMQP-VIFPVBQESA-N
(A+/-)-p-menth-6-en-2-one
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Carvotanacetone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.8509 85.09%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.7016 70.16%
OATP2B1 inhibitior - 0.8514 85.14%
OATP1B1 inhibitior + 0.9644 96.44%
OATP1B3 inhibitior + 0.9474 94.74%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.8709 87.09%
P-glycoprotein inhibitior - 0.9724 97.24%
P-glycoprotein substrate - 0.9394 93.94%
CYP3A4 substrate - 0.6410 64.10%
CYP2C9 substrate - 0.8078 80.78%
CYP2D6 substrate - 0.8631 86.31%
CYP3A4 inhibition - 0.9511 95.11%
CYP2C9 inhibition - 0.9068 90.68%
CYP2C19 inhibition - 0.7438 74.38%
CYP2D6 inhibition - 0.9175 91.75%
CYP1A2 inhibition - 0.7903 79.03%
CYP2C8 inhibition - 0.9876 98.76%
CYP inhibitory promiscuity - 0.7696 76.96%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6727 67.27%
Carcinogenicity (trinary) Non-required 0.6312 63.12%
Eye corrosion - 0.6194 61.94%
Eye irritation + 0.9360 93.60%
Skin irritation + 0.7723 77.23%
Skin corrosion - 0.9144 91.44%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5955 59.55%
Micronuclear - 0.8500 85.00%
Hepatotoxicity + 0.7500 75.00%
skin sensitisation + 0.9390 93.90%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.6222 62.22%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity + 0.7249 72.49%
Acute Oral Toxicity (c) III 0.5634 56.34%
Estrogen receptor binding - 0.9787 97.87%
Androgen receptor binding - 0.8044 80.44%
Thyroid receptor binding - 0.9052 90.52%
Glucocorticoid receptor binding - 0.9231 92.31%
Aromatase binding - 0.9089 90.89%
PPAR gamma - 0.8875 88.75%
Honey bee toxicity - 0.8781 87.81%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9307 93.07%

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
CHEMBL2581 P07339 Cathepsin D 92.09% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.78% 95.56%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 88.97% 90.71%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.63% 96.09%
CHEMBL1907 P15144 Aminopeptidase N 83.95% 93.31%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.95% 97.25%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.73% 95.89%

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.
Artemisia arborescens
Artemisia sericea
Aucklandia costus
Croton eluteria
Echinophora tenuifolia
Pelargonium quercifolium

Cross-Links

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PubChem 6432475
NPASS NPC264644
LOTUS LTS0083143
wikiData Q104253813