2,4,4-Trimethyl-3-methylidenehex-5-en-2-ol

Details

Top
Internal ID b89e2a6a-b163-4eb9-ab96-66c40bd9f48f
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Tertiary alcohols
IUPAC Name 2,4,4-trimethyl-3-methylidenehex-5-en-2-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/C10H18O/c1-7-9(3,4)8(2)10(5,6)11/h7,11H,1-2H2,3-6H3
InChI Key FTVTXSVUPHFUIT-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C10H18O
Molecular Weight 154.25 g/mol
Exact Mass 154.135765193 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.53
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 2,4,4-Trimethyl-3-methylidenehex-5-en-2-ol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9837 98.37%
Caco-2 + 0.6406 64.06%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.4159 41.59%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9397 93.97%
OATP1B3 inhibitior + 0.9534 95.34%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9333 93.33%
P-glycoprotein inhibitior - 0.9689 96.89%
P-glycoprotein substrate - 0.9775 97.75%
CYP3A4 substrate - 0.6840 68.40%
CYP2C9 substrate - 0.7707 77.07%
CYP2D6 substrate - 0.8067 80.67%
CYP3A4 inhibition - 0.7487 74.87%
CYP2C9 inhibition - 0.7895 78.95%
CYP2C19 inhibition - 0.6657 66.57%
CYP2D6 inhibition - 0.9477 94.77%
CYP1A2 inhibition - 0.8819 88.19%
CYP2C8 inhibition - 0.9601 96.01%
CYP inhibitory promiscuity - 0.7475 74.75%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) + 0.6383 63.83%
Carcinogenicity (trinary) Non-required 0.5688 56.88%
Eye corrosion + 0.8432 84.32%
Eye irritation + 0.9687 96.87%
Skin irritation + 0.8729 87.29%
Skin corrosion - 0.6049 60.49%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7468 74.68%
Micronuclear - 0.9500 95.00%
Hepatotoxicity + 0.7125 71.25%
skin sensitisation + 0.6282 62.82%
Respiratory toxicity - 0.8667 86.67%
Reproductive toxicity - 1.0000 100.00%
Mitochondrial toxicity - 0.8321 83.21%
Nephrotoxicity + 0.7252 72.52%
Acute Oral Toxicity (c) III 0.8114 81.14%
Estrogen receptor binding - 0.7115 71.15%
Androgen receptor binding - 0.8477 84.77%
Thyroid receptor binding - 0.7811 78.11%
Glucocorticoid receptor binding - 0.8728 87.28%
Aromatase binding - 0.7939 79.39%
PPAR gamma - 0.8532 85.32%
Honey bee toxicity - 0.8322 83.22%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.7051 70.51%

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 88.02% 83.82%
CHEMBL1977 P11473 Vitamin D receptor 85.81% 99.43%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.63% 97.25%
CHEMBL2581 P07339 Cathepsin D 80.44% 98.95%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 80.14% 89.34%

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 lancea

Cross-Links

Top
PubChem 162932178
LOTUS LTS0238699
wikiData Q105001346