xi-p-Mentha-1(7),2-dien-4-ol

Details

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Internal ID 010c49e1-5ce7-4368-a5a9-5db477424c8f
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Menthane monoterpenoids
IUPAC Name 4-methylidene-1-propan-2-ylcyclohex-2-en-1-ol
SMILES (Canonical) CC(C)C1(CCC(=C)C=C1)O
SMILES (Isomeric) CC(C)C1(CCC(=C)C=C1)O
InChI InChI=1S/C10H16O/c1-8(2)10(11)6-4-9(3)5-7-10/h4,6,8,11H,3,5,7H2,1-2H3
InChI Key BLCSHJQURBOXAI-UHFFFAOYSA-N
Popularity 4 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 2.20
Atomic LogP (AlogP) 2.28
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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4-methylidene-1-propan-2-ylcyclohex-2-en-1-ol
CHEBI:171982
p-Mentha-1(7),2-diene-4-ol
4-methylidene-1-(propan-2-yl)cyclohex-2-en-1-ol

2D Structure

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2D Structure of xi-p-Mentha-1(7),2-dien-4-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9949 99.49%
Caco-2 + 0.8180 81.80%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.8143 81.43%
Subcellular localzation Lysosomes 0.4690 46.90%
OATP2B1 inhibitior - 0.8574 85.74%
OATP1B1 inhibitior + 0.9599 95.99%
OATP1B3 inhibitior + 0.9309 93.09%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.9416 94.16%
P-glycoprotein inhibitior - 0.9851 98.51%
P-glycoprotein substrate - 0.9429 94.29%
CYP3A4 substrate - 0.6340 63.40%
CYP2C9 substrate - 0.7880 78.80%
CYP2D6 substrate - 0.7952 79.52%
CYP3A4 inhibition - 0.8515 85.15%
CYP2C9 inhibition - 0.8550 85.50%
CYP2C19 inhibition - 0.7895 78.95%
CYP2D6 inhibition - 0.9210 92.10%
CYP1A2 inhibition - 0.8655 86.55%
CYP2C8 inhibition - 0.9740 97.40%
CYP inhibitory promiscuity - 0.9008 90.08%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8028 80.28%
Carcinogenicity (trinary) Non-required 0.6285 62.85%
Eye corrosion - 0.8183 81.83%
Eye irritation + 0.9246 92.46%
Skin irritation + 0.7572 75.72%
Skin corrosion - 0.8474 84.74%
Ames mutagenesis - 0.7770 77.70%
Human Ether-a-go-go-Related Gene inhibition - 0.5945 59.45%
Micronuclear - 0.9500 95.00%
Hepatotoxicity + 0.6930 69.30%
skin sensitisation + 0.8815 88.15%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity - 0.6111 61.11%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity - 0.6402 64.02%
Acute Oral Toxicity (c) III 0.7988 79.88%
Estrogen receptor binding - 0.8958 89.58%
Androgen receptor binding - 0.7283 72.83%
Thyroid receptor binding - 0.8571 85.71%
Glucocorticoid receptor binding - 0.7217 72.17%
Aromatase binding - 0.8280 82.80%
PPAR gamma - 0.8303 83.03%
Honey bee toxicity - 0.9561 95.61%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.7271 72.71%

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 92.76% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.38% 96.09%
CHEMBL2581 P07339 Cathepsin D 85.37% 98.95%
CHEMBL4208 P20618 Proteasome component C5 84.91% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.80% 95.56%

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 argyi
Piper nigrum

Cross-Links

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PubChem 5319360
NPASS NPC87566