p-Mentha-1,4-dien-7-ol

Details

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Internal ID f441958c-4806-44dd-b188-c7599310b400
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Primary alcohols
IUPAC Name (4-propan-2-ylcyclohexa-1,4-dien-1-yl)methanol
SMILES (Canonical) CC(C)C1=CCC(=CC1)CO
SMILES (Isomeric) CC(C)C1=CCC(=CC1)CO
InChI InChI=1S/C10H16O/c1-8(2)10-5-3-9(7-11)4-6-10/h3,6,8,11H,4-5,7H2,1-2H3
InChI Key IRZQJXCCKXGQFV-UHFFFAOYSA-N
Popularity 16 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 1.50
Atomic LogP (AlogP) 2.28
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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22539-72-6
1,4-Cyclohexadiene-1-methanol, 4-(1-methylethyl)-
1,4-p-Menthadien-7-ol
SCHEMBL20541879
DTXSID50334206
IRZQJXCCKXGQFV-UHFFFAOYSA-N
(4-Isopropyl-1,4-cyclohexadien-1-yl)methanol #

2D Structure

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

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9907 99.07%
Caco-2 + 0.8722 87.22%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Lysosomes 0.6158 61.58%
OATP2B1 inhibitior - 0.8601 86.01%
OATP1B1 inhibitior + 0.9265 92.65%
OATP1B3 inhibitior + 0.9422 94.22%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.9227 92.27%
P-glycoprotein inhibitior - 0.9830 98.30%
P-glycoprotein substrate - 0.9187 91.87%
CYP3A4 substrate - 0.7007 70.07%
CYP2C9 substrate - 0.6591 65.91%
CYP2D6 substrate - 0.7543 75.43%
CYP3A4 inhibition - 0.7565 75.65%
CYP2C9 inhibition - 0.8022 80.22%
CYP2C19 inhibition - 0.8196 81.96%
CYP2D6 inhibition - 0.8672 86.72%
CYP1A2 inhibition - 0.7868 78.68%
CYP2C8 inhibition - 0.9912 99.12%
CYP inhibitory promiscuity - 0.6889 68.89%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7328 73.28%
Carcinogenicity (trinary) Non-required 0.6598 65.98%
Eye corrosion - 0.6543 65.43%
Eye irritation + 0.9080 90.80%
Skin irritation - 0.5132 51.32%
Skin corrosion - 0.6405 64.05%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6212 62.12%
Micronuclear - 0.9500 95.00%
Hepatotoxicity + 0.5171 51.71%
skin sensitisation + 0.7441 74.41%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity - 0.7222 72.22%
Mitochondrial toxicity - 0.8750 87.50%
Nephrotoxicity + 0.4850 48.50%
Acute Oral Toxicity (c) III 0.8308 83.08%
Estrogen receptor binding - 0.9646 96.46%
Androgen receptor binding - 0.8374 83.74%
Thyroid receptor binding - 0.9009 90.09%
Glucocorticoid receptor binding - 0.8715 87.15%
Aromatase binding - 0.8267 82.67%
PPAR gamma - 0.9183 91.83%
Honey bee toxicity - 0.9832 98.32%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.9582 95.82%

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 94.30% 96.09%
CHEMBL2581 P07339 Cathepsin D 92.17% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.34% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.89% 97.25%
CHEMBL4208 P20618 Proteasome component C5 80.92% 90.00%

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.
Conioselinum anthriscoides
Ligusticum officinale
Rhodiola crenulata
Rhodiola rosea

Cross-Links

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PubChem 519966
NPASS NPC166399
LOTUS LTS0142196
wikiData Q82099918