1,5-Dimethylcycloocta-2,4,6-trien-1-ol

Details

Top
Internal ID 743ce4df-5a8f-4d16-accb-8676e218317b
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Tertiary alcohols
IUPAC Name 1,5-dimethylcycloocta-2,4,6-trien-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H14O/c1-9-5-3-7-10(2,11)8-4-6-9/h3-7,11H,8H2,1-2H3
InChI Key AQTPUXMQWKOGLL-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C10H14O
Molecular Weight 150.22 g/mol
Exact Mass 150.104465066 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.20
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 1,5-Dimethylcycloocta-2,4,6-trien-1-ol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9950 99.50%
Caco-2 + 0.9752 97.52%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Lysosomes 0.6178 61.78%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9458 94.58%
OATP1B3 inhibitior + 0.9725 97.25%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8109 81.09%
P-glycoprotein inhibitior - 0.9849 98.49%
P-glycoprotein substrate - 0.9257 92.57%
CYP3A4 substrate - 0.5688 56.88%
CYP2C9 substrate - 0.8054 80.54%
CYP2D6 substrate - 0.7907 79.07%
CYP3A4 inhibition - 0.8147 81.47%
CYP2C9 inhibition - 0.8629 86.29%
CYP2C19 inhibition - 0.7325 73.25%
CYP2D6 inhibition - 0.9283 92.83%
CYP1A2 inhibition - 0.7515 75.15%
CYP2C8 inhibition - 0.9071 90.71%
CYP inhibitory promiscuity - 0.8905 89.05%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.6352 63.52%
Carcinogenicity (trinary) Non-required 0.5041 50.41%
Eye corrosion - 0.8775 87.75%
Eye irritation + 0.9890 98.90%
Skin irritation + 0.6076 60.76%
Skin corrosion - 0.8105 81.05%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8429 84.29%
Micronuclear - 0.8400 84.00%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation + 0.8718 87.18%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity - 0.6222 62.22%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity - 0.6277 62.77%
Acute Oral Toxicity (c) III 0.8202 82.02%
Estrogen receptor binding - 0.8551 85.51%
Androgen receptor binding - 0.9536 95.36%
Thyroid receptor binding - 0.8420 84.20%
Glucocorticoid receptor binding - 0.8214 82.14%
Aromatase binding - 0.8789 87.89%
PPAR gamma - 0.8910 89.10%
Honey bee toxicity - 0.9720 97.20%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity - 0.5870 58.70%

Targets

Top

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
CHEMBL4040 P28482 MAP kinase ERK2 91.82% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.69% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.38% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.51% 95.56%
CHEMBL4208 P20618 Proteasome component C5 82.31% 90.00%

Plants that contains it

Top
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.
Aegle marmelos

Cross-Links

Top
PubChem 162878377
LOTUS LTS0160536
wikiData Q104917072