2,7-Dimethyl-2,6-octadien-1-ol

Details

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Internal ID 0f3acf00-506a-45e1-a600-d63a768ef24f
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name (2E)-2,7-dimethylocta-2,6-dien-1-ol
SMILES (Canonical) CC(=CCCC=C(C)CO)C
SMILES (Isomeric) CC(=CCC/C=C(\C)/CO)C
InChI InChI=1S/C10H18O/c1-9(2)6-4-5-7-10(3)8-11/h6-7,11H,4-5,8H2,1-3H3/b10-7+
InChI Key JSMKSZJPQZMEHN-JXMROGBWSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H18O
Molecular Weight 154.25 g/mol
Exact Mass 154.135765193 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.67
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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2,6-Octadien-1-ol, 2,7-dimethyl-
22410-74-8
2,7-Dimethylocta-2,6-dienol
JSMKSZJPQZMEHN-JXMROGBWSA-N
2,7-Dimethyl-octa-2,6-dien-1-ol
(2E)-2,7-Dimethyl-2,6-octadiene-1-ol

2D Structure

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2D Structure of 2,7-Dimethyl-2,6-octadien-1-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9823 98.23%
Caco-2 + 0.9472 94.72%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Lysosomes 0.5576 55.76%
OATP2B1 inhibitior - 0.8525 85.25%
OATP1B1 inhibitior + 0.9506 95.06%
OATP1B3 inhibitior + 0.9480 94.80%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.8224 82.24%
P-glycoprotein inhibitior - 0.9897 98.97%
P-glycoprotein substrate - 0.9728 97.28%
CYP3A4 substrate - 0.6800 68.00%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7450 74.50%
CYP3A4 inhibition - 0.9088 90.88%
CYP2C9 inhibition - 0.9071 90.71%
CYP2C19 inhibition - 0.9026 90.26%
CYP2D6 inhibition - 0.9230 92.30%
CYP1A2 inhibition - 0.9046 90.46%
CYP2C8 inhibition - 0.9894 98.94%
CYP inhibitory promiscuity - 0.7650 76.50%
UGT catelyzed - 0.8000 80.00%
Carcinogenicity (binary) - 0.6600 66.00%
Carcinogenicity (trinary) Non-required 0.6507 65.07%
Eye corrosion + 0.5325 53.25%
Eye irritation + 0.9958 99.58%
Skin irritation + 0.8492 84.92%
Skin corrosion - 0.9100 91.00%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6774 67.74%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6375 63.75%
skin sensitisation + 0.9333 93.33%
Respiratory toxicity - 0.9222 92.22%
Reproductive toxicity - 0.9812 98.12%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity + 0.7426 74.26%
Acute Oral Toxicity (c) III 0.8552 85.52%
Estrogen receptor binding - 0.9571 95.71%
Androgen receptor binding - 0.9238 92.38%
Thyroid receptor binding - 0.8405 84.05%
Glucocorticoid receptor binding - 0.8596 85.96%
Aromatase binding - 0.9302 93.02%
PPAR gamma - 0.6997 69.97%
Honey bee toxicity - 0.8804 88.04%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.7800 78.00%
Fish aquatic toxicity + 0.9500 95.00%

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
CHEMBL2581 P07339 Cathepsin D 85.91% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 83.57% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.90% 96.09%

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.
Citrus × aurantium
Curcuma kwangsiensis
Curcuma phaeocaulis
Curcuma wenyujin
Curcuma zedoaria
Houttuynia cordata

Cross-Links

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PubChem 5365825
NPASS NPC289827