6-Methoxy-3-methyl-6-prop-1-en-2-ylcyclohex-2-en-1-one

Details

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Internal ID ff2a0528-3652-46de-95ab-4cfeae360301
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Menthane monoterpenoids
IUPAC Name 6-methoxy-3-methyl-6-prop-1-en-2-ylcyclohex-2-en-1-one
SMILES (Canonical) CC1=CC(=O)C(CC1)(C(=C)C)OC
SMILES (Isomeric) CC1=CC(=O)C(CC1)(C(=C)C)OC
InChI InChI=1S/C11H16O2/c1-8(2)11(13-4)6-5-9(3)7-10(11)12/h7H,1,5-6H2,2-4H3
InChI Key BRTZDCQNZKKULS-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H16O2
Molecular Weight 180.24 g/mol
Exact Mass 180.115029749 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.26
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6-Methoxy-3-methyl-6-prop-1-en-2-ylcyclohex-2-en-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9948 99.48%
Caco-2 + 0.8618 86.18%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.6786 67.86%
OATP2B1 inhibitior - 0.8552 85.52%
OATP1B1 inhibitior + 0.9310 93.10%
OATP1B3 inhibitior + 0.9309 93.09%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9427 94.27%
P-glycoprotein inhibitior - 0.9827 98.27%
P-glycoprotein substrate - 0.9301 93.01%
CYP3A4 substrate + 0.5088 50.88%
CYP2C9 substrate - 0.7759 77.59%
CYP2D6 substrate - 0.8609 86.09%
CYP3A4 inhibition - 0.7405 74.05%
CYP2C9 inhibition - 0.9372 93.72%
CYP2C19 inhibition - 0.7303 73.03%
CYP2D6 inhibition - 0.9256 92.56%
CYP1A2 inhibition - 0.7453 74.53%
CYP2C8 inhibition - 0.9528 95.28%
CYP inhibitory promiscuity - 0.8993 89.93%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7491 74.91%
Carcinogenicity (trinary) Non-required 0.4960 49.60%
Eye corrosion - 0.9387 93.87%
Eye irritation + 0.6844 68.44%
Skin irritation + 0.6190 61.90%
Skin corrosion - 0.9821 98.21%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7333 73.33%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.6348 63.48%
skin sensitisation + 0.7017 70.17%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity - 0.5556 55.56%
Mitochondrial toxicity - 0.8750 87.50%
Nephrotoxicity + 0.5662 56.62%
Acute Oral Toxicity (c) III 0.8256 82.56%
Estrogen receptor binding - 0.9266 92.66%
Androgen receptor binding + 0.6116 61.16%
Thyroid receptor binding - 0.7592 75.92%
Glucocorticoid receptor binding - 0.7498 74.98%
Aromatase binding - 0.7696 76.96%
PPAR gamma - 0.8474 84.74%
Honey bee toxicity - 0.6944 69.44%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.8581 85.81%

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 94.17% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.34% 95.56%
CHEMBL2581 P07339 Cathepsin D 89.59% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 88.69% 91.49%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.77% 96.09%
CHEMBL1937 Q92769 Histone deacetylase 2 85.56% 94.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.68% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.49% 94.00%

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 spicata subsp. condensata

Cross-Links

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PubChem 86225234
LOTUS LTS0064563
wikiData Q104945010