4-Ethenyl-2,5-dimethylhexa-1,5-dien-3-ol

Details

Top
Internal ID 21631384-bde2-46f5-b757-f714a523e40e
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Secondary alcohols
IUPAC Name 4-ethenyl-2,5-dimethylhexa-1,5-dien-3-ol
SMILES (Canonical) CC(=C)C(C=C)C(C(=C)C)O
SMILES (Isomeric) CC(=C)C(C=C)C(C(=C)C)O
InChI InChI=1S/C10H16O/c1-6-9(7(2)3)10(11)8(4)5/h6,9-11H,1-2,4H2,3,5H3
InChI Key YAATZFSMWSSRHJ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
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) 2.30
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

Top
4-Ethenyl-2,5-dimethylhexa-1,5-dien-3-ol
96203-74-6
DTXSID70616470
YAATZFSMWSSRHJ-UHFFFAOYSA-N

2D Structure

Top
2D Structure of 4-Ethenyl-2,5-dimethylhexa-1,5-dien-3-ol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9885 98.85%
Caco-2 - 0.6660 66.60%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.3936 39.36%
OATP2B1 inhibitior - 0.8602 86.02%
OATP1B1 inhibitior + 0.9488 94.88%
OATP1B3 inhibitior + 0.9667 96.67%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9620 96.20%
P-glycoprotein inhibitior - 0.9524 95.24%
P-glycoprotein substrate - 0.9648 96.48%
CYP3A4 substrate - 0.6998 69.98%
CYP2C9 substrate - 0.8012 80.12%
CYP2D6 substrate - 0.7460 74.60%
CYP3A4 inhibition - 0.7896 78.96%
CYP2C9 inhibition - 0.9228 92.28%
CYP2C19 inhibition - 0.6463 64.63%
CYP2D6 inhibition - 0.9441 94.41%
CYP1A2 inhibition - 0.8310 83.10%
CYP2C8 inhibition - 0.9767 97.67%
CYP inhibitory promiscuity - 0.8032 80.32%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) + 0.7083 70.83%
Carcinogenicity (trinary) Non-required 0.6659 66.59%
Eye corrosion + 0.9161 91.61%
Eye irritation + 0.9350 93.50%
Skin irritation + 0.7643 76.43%
Skin corrosion + 0.6023 60.23%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7046 70.46%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.7925 79.25%
skin sensitisation + 0.7366 73.66%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity - 0.9667 96.67%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity + 0.6753 67.53%
Acute Oral Toxicity (c) III 0.4677 46.77%
Estrogen receptor binding - 0.9045 90.45%
Androgen receptor binding - 0.9294 92.94%
Thyroid receptor binding - 0.7545 75.45%
Glucocorticoid receptor binding - 0.9340 93.40%
Aromatase binding - 0.8146 81.46%
PPAR gamma - 0.7672 76.72%
Honey bee toxicity - 0.6874 68.74%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.8700 87.00%
Fish aquatic toxicity - 0.3853 38.53%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.33% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.80% 91.11%
CHEMBL2581 P07339 Cathepsin D 82.21% 98.95%

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.
Artemisia arbuscula

Cross-Links

Top
PubChem 21630873
LOTUS LTS0113777
wikiData Q82518368