1,7-Nonadien-4-ol, 4,8-dimethyl-

Details

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Internal ID ab1fb55d-4ded-494e-88e7-37322e2c79eb
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Acyclic monoterpenoids
IUPAC Name 4,8-dimethylnona-1,7-dien-4-ol
SMILES (Canonical) CC(=CCCC(C)(CC=C)O)C
SMILES (Isomeric) CC(=CCCC(C)(CC=C)O)C
InChI InChI=1S/C11H20O/c1-5-8-11(4,12)9-6-7-10(2)3/h5,7,12H,1,6,8-9H2,2-4H3
InChI Key PWEXDCWJSFTGOP-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H20O
Molecular Weight 168.28 g/mol
Exact Mass 168.151415257 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.06
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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PWEXDCWJSFTGOP-UHFFFAOYSA-N
4,8-Dimethyl-1,7-nonadiene-4-ol
1,7-Nonadien-4-ol, 4,8-dimethyl-
4,8-Dimethyl-1,7-nonadien-4-ol #

2D Structure

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2D Structure of 1,7-Nonadien-4-ol, 4,8-dimethyl-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9888 98.88%
Caco-2 + 0.9446 94.46%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Lysosomes 0.3683 36.83%
OATP2B1 inhibitior - 0.8533 85.33%
OATP1B1 inhibitior + 0.9313 93.13%
OATP1B3 inhibitior + 0.9550 95.50%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.7377 73.77%
P-glycoprotein inhibitior - 0.9752 97.52%
P-glycoprotein substrate - 0.9598 95.98%
CYP3A4 substrate - 0.6012 60.12%
CYP2C9 substrate - 0.7899 78.99%
CYP2D6 substrate - 0.7511 75.11%
CYP3A4 inhibition - 0.7932 79.32%
CYP2C9 inhibition - 0.8146 81.46%
CYP2C19 inhibition - 0.8095 80.95%
CYP2D6 inhibition - 0.9390 93.90%
CYP1A2 inhibition - 0.6968 69.68%
CYP2C8 inhibition - 0.9557 95.57%
CYP inhibitory promiscuity - 0.8135 81.35%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.5900 59.00%
Carcinogenicity (trinary) Non-required 0.6290 62.90%
Eye corrosion - 0.7875 78.75%
Eye irritation + 0.9578 95.78%
Skin irritation + 0.8196 81.96%
Skin corrosion - 0.9436 94.36%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6538 65.38%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5924 59.24%
skin sensitisation + 0.8922 89.22%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity - 0.9053 90.53%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity + 0.6028 60.28%
Acute Oral Toxicity (c) III 0.8717 87.17%
Estrogen receptor binding - 0.9247 92.47%
Androgen receptor binding - 0.9135 91.35%
Thyroid receptor binding - 0.7043 70.43%
Glucocorticoid receptor binding - 0.7140 71.40%
Aromatase binding - 0.8632 86.32%
PPAR gamma - 0.8166 81.66%
Honey bee toxicity - 0.7789 77.89%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.7300 73.00%
Fish aquatic toxicity + 0.8754 87.54%

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 86.71% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.04% 97.25%
CHEMBL3401 O75469 Pregnane X receptor 85.89% 94.73%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 84.55% 89.34%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.73% 91.11%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.06% 96.95%
CHEMBL1977 P11473 Vitamin D receptor 81.99% 99.43%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.54% 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.
Schisandra chinensis

Cross-Links

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PubChem 536461
NPASS NPC307371