2-Methyl-6-methylene-oct-3,7-dien-2-ol

Details

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Internal ID 52a5d6fc-ea05-469b-8a3a-f850367bc7d8
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Tertiary alcohols
IUPAC Name 2-methyl-6-methylideneocta-3,7-dien-2-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H16O/c1-5-9(2)7-6-8-10(3,4)11/h5-6,8,11H,1-2,7H2,3-4H3
InChI Key NOEQSPUVXRMJBW-UHFFFAOYSA-N
Popularity 8 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 2.70
Atomic LogP (AlogP) 2.45
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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2-methyl-6-methylene-oct-3,7-dien-2-ol
2-methyl-6-methylideneocta-3,7-dien-2-ol

2D Structure

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2D Structure of 2-Methyl-6-methylene-oct-3,7-dien-2-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9711 97.11%
Caco-2 + 0.8494 84.94%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Lysosomes 0.4163 41.63%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8635 86.35%
OATP1B3 inhibitior + 0.9491 94.91%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8969 89.69%
P-glycoprotein inhibitior - 0.9762 97.62%
P-glycoprotein substrate - 0.9746 97.46%
CYP3A4 substrate - 0.6340 63.40%
CYP2C9 substrate - 0.6141 61.41%
CYP2D6 substrate - 0.7761 77.61%
CYP3A4 inhibition - 0.7614 76.14%
CYP2C9 inhibition - 0.7737 77.37%
CYP2C19 inhibition - 0.6273 62.73%
CYP2D6 inhibition - 0.9375 93.75%
CYP1A2 inhibition - 0.8389 83.89%
CYP2C8 inhibition - 0.9270 92.70%
CYP inhibitory promiscuity - 0.6183 61.83%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) + 0.5483 54.83%
Carcinogenicity (trinary) Non-required 0.5885 58.85%
Eye corrosion + 0.6494 64.94%
Eye irritation + 0.8279 82.79%
Skin irritation + 0.7925 79.25%
Skin corrosion - 0.6079 60.79%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6391 63.91%
Micronuclear - 0.9500 95.00%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation + 0.8111 81.11%
Respiratory toxicity - 0.8444 84.44%
Reproductive toxicity - 0.9444 94.44%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity + 0.6461 64.61%
Acute Oral Toxicity (c) III 0.6193 61.93%
Estrogen receptor binding - 0.8486 84.86%
Androgen receptor binding - 0.9603 96.03%
Thyroid receptor binding - 0.8810 88.10%
Glucocorticoid receptor binding - 0.6979 69.79%
Aromatase binding - 0.8920 89.20%
PPAR gamma - 0.7988 79.88%
Honey bee toxicity - 0.8939 89.39%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity + 0.7356 73.56%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.18% 97.25%
CHEMBL5251 Q06187 Tyrosine-protein kinase BTK 89.19% 98.51%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 87.68% 89.34%
CHEMBL3401 O75469 Pregnane X receptor 83.57% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.82% 91.11%
CHEMBL2885 P07451 Carbonic anhydrase III 81.34% 87.45%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.92% 96.95%

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.
Artemisia salsoloides
Rhododendron groenlandicum

Cross-Links

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PubChem 81478
LOTUS LTS0025501
wikiData Q105182528