5-Isopropyl-6-methyl-hepta-3,5-dien-2-ol

Details

Top
Internal ID 387a1d77-7969-4a1f-bfc0-1c619acbe8d8
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name (3E)-6-methyl-5-propan-2-ylhepta-3,5-dien-2-ol
SMILES (Canonical) CC(C)C(=C(C)C)C=CC(C)O
SMILES (Isomeric) CC(C)C(=C(C)C)/C=C/C(C)O
InChI InChI=1S/C11H20O/c1-8(2)11(9(3)4)7-6-10(5)12/h6-8,10,12H,1-5H3/b7-6+
InChI Key YMAQXOPPAMCPRY-VOTSOKGWSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C11H20O
Molecular Weight 168.28 g/mol
Exact Mass 168.151415257 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.50
Atomic LogP (AlogP) 2.92
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

Top
YMAQXOPPAMCPRY-VOTSOKGWSA-N
(3E)-5-Isopropyl-6-methyl-3,5-heptadien-2-ol #

2D Structure

Top
2D Structure of 5-Isopropyl-6-methyl-hepta-3,5-dien-2-ol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9904 99.04%
Caco-2 + 0.6994 69.94%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.4347 43.47%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9344 93.44%
OATP1B3 inhibitior + 0.9658 96.58%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9471 94.71%
P-glycoprotein inhibitior - 0.9709 97.09%
P-glycoprotein substrate - 0.9519 95.19%
CYP3A4 substrate - 0.6999 69.99%
CYP2C9 substrate - 0.6250 62.50%
CYP2D6 substrate - 0.7859 78.59%
CYP3A4 inhibition - 0.8890 88.90%
CYP2C9 inhibition - 0.8701 87.01%
CYP2C19 inhibition - 0.8049 80.49%
CYP2D6 inhibition - 0.9416 94.16%
CYP1A2 inhibition - 0.8724 87.24%
CYP2C8 inhibition - 0.9830 98.30%
CYP inhibitory promiscuity - 0.7410 74.10%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) + 0.6383 63.83%
Carcinogenicity (trinary) Non-required 0.5731 57.31%
Eye corrosion + 0.8791 87.91%
Eye irritation + 0.9708 97.08%
Skin irritation + 0.8015 80.15%
Skin corrosion + 0.7073 70.73%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6915 69.15%
Micronuclear - 0.9500 95.00%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation + 0.4766 47.66%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity - 0.9889 98.89%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity + 0.4812 48.12%
Acute Oral Toxicity (c) III 0.7821 78.21%
Estrogen receptor binding - 0.9054 90.54%
Androgen receptor binding - 0.9461 94.61%
Thyroid receptor binding - 0.7757 77.57%
Glucocorticoid receptor binding - 0.8163 81.63%
Aromatase binding - 0.9158 91.58%
PPAR gamma - 0.9127 91.27%
Honey bee toxicity - 0.8302 83.02%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.9000 90.00%
Fish aquatic toxicity - 0.4924 49.24%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.46% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.25% 91.11%
CHEMBL2581 P07339 Cathepsin D 85.23% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.69% 96.09%

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.
Elsholtzia ciliata
Mosla chinensis

Cross-Links

Top
PubChem 5363138
NPASS NPC194396