3-Methyl-3-propan-2-ylcyclohexa-1,5-dien-1-ol

Details

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Internal ID 9d6486c1-f680-497e-88b3-c7da1e6d9a91
Taxonomy Organic oxygen compounds > Organooxygen compounds > Enols
IUPAC Name 3-methyl-3-propan-2-ylcyclohexa-1,5-dien-1-ol
SMILES (Canonical) CC(C)C1(CC=CC(=C1)O)C
SMILES (Isomeric) CC(C)C1(CC=CC(=C1)O)C
InChI InChI=1S/C10H16O/c1-8(2)10(3)6-4-5-9(11)7-10/h4-5,7-8,11H,6H2,1-3H3
InChI Key RKCYNTWBUKXVLX-UHFFFAOYSA-N
Popularity 0 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 3.20
Atomic LogP (AlogP) 3.05
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-Methyl-3-propan-2-ylcyclohexa-1,5-dien-1-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9917 99.17%
Caco-2 + 0.9225 92.25%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.4714 47.14%
OATP2B1 inhibitior - 0.8601 86.01%
OATP1B1 inhibitior + 0.9170 91.70%
OATP1B3 inhibitior + 0.9615 96.15%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9478 94.78%
P-glycoprotein inhibitior - 0.9837 98.37%
P-glycoprotein substrate - 0.9361 93.61%
CYP3A4 substrate - 0.6338 63.38%
CYP2C9 substrate - 0.8054 80.54%
CYP2D6 substrate - 0.8347 83.47%
CYP3A4 inhibition - 0.7659 76.59%
CYP2C9 inhibition - 0.7940 79.40%
CYP2C19 inhibition - 0.7512 75.12%
CYP2D6 inhibition - 0.9074 90.74%
CYP1A2 inhibition - 0.7495 74.95%
CYP2C8 inhibition - 0.9785 97.85%
CYP inhibitory promiscuity - 0.7687 76.87%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7171 71.71%
Carcinogenicity (trinary) Non-required 0.6461 64.61%
Eye corrosion + 0.6172 61.72%
Eye irritation + 0.8813 88.13%
Skin irritation + 0.8315 83.15%
Skin corrosion + 0.5875 58.75%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6409 64.09%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.5623 56.23%
skin sensitisation + 0.8271 82.71%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity - 0.6667 66.67%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity + 0.6360 63.60%
Acute Oral Toxicity (c) III 0.7206 72.06%
Estrogen receptor binding - 0.9398 93.98%
Androgen receptor binding - 0.7884 78.84%
Thyroid receptor binding - 0.8462 84.62%
Glucocorticoid receptor binding - 0.9048 90.48%
Aromatase binding - 0.9079 90.79%
PPAR gamma - 0.8938 89.38%
Honey bee toxicity - 0.9578 95.78%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9270 92.70%

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 96.91% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.22% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.80% 94.45%
CHEMBL2581 P07339 Cathepsin D 86.66% 98.95%
CHEMBL4208 P20618 Proteasome component C5 85.14% 90.00%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 81.47% 93.10%
CHEMBL1937 Q92769 Histone deacetylase 2 81.27% 94.75%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 80.61% 99.15%

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.
Thymbra capitata

Cross-Links

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PubChem 163189860
LOTUS LTS0038148
wikiData Q105238313