1,6-Octadiene-1,3-diol, 3,7-dimethyl-

Details

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Internal ID ad5fa653-cdb9-43ab-beb2-cbfd531a287d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Acyclic monoterpenoids
IUPAC Name 3,7-dimethylocta-1,6-diene-1,3-diol
SMILES (Canonical) CC(=CCCC(C)(C=CO)O)C
SMILES (Isomeric) CC(=CCCC(C)(C=CO)O)C
InChI InChI=1S/C10H18O2/c1-9(2)5-4-6-10(3,12)7-8-11/h5,7-8,11-12H,4,6H2,1-3H3
InChI Key LCRYKIFRBLQIAW-UHFFFAOYSA-N
Popularity 19 references in papers

Physical and Chemical Properties

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Molecular Formula C10H18O2
Molecular Weight 170.25 g/mol
Exact Mass 170.130679813 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.56
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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1,6-Octadiene-1,3-diol, 3,7-dimethyl-
256418-61-8
DTXSID20336994

2D Structure

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2D Structure of 1,6-Octadiene-1,3-diol, 3,7-dimethyl-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9703 97.03%
Caco-2 + 0.9350 93.50%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Nucleus 0.3374 33.74%
OATP2B1 inhibitior - 0.8526 85.26%
OATP1B1 inhibitior + 0.9169 91.69%
OATP1B3 inhibitior + 0.9535 95.35%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.6917 69.17%
P-glycoprotein inhibitior - 0.9814 98.14%
P-glycoprotein substrate - 0.9541 95.41%
CYP3A4 substrate - 0.6227 62.27%
CYP2C9 substrate - 0.7958 79.58%
CYP2D6 substrate - 0.8146 81.46%
CYP3A4 inhibition - 0.8523 85.23%
CYP2C9 inhibition - 0.7620 76.20%
CYP2C19 inhibition - 0.6941 69.41%
CYP2D6 inhibition - 0.9152 91.52%
CYP1A2 inhibition - 0.7133 71.33%
CYP2C8 inhibition - 0.9533 95.33%
CYP inhibitory promiscuity - 0.6051 60.51%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.6600 66.00%
Carcinogenicity (trinary) Non-required 0.6073 60.73%
Eye corrosion - 0.8826 88.26%
Eye irritation + 0.8962 89.62%
Skin irritation + 0.6956 69.56%
Skin corrosion - 0.8360 83.60%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5821 58.21%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.5392 53.92%
skin sensitisation + 0.6922 69.22%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity - 0.8333 83.33%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity + 0.6490 64.90%
Acute Oral Toxicity (c) III 0.6837 68.37%
Estrogen receptor binding - 0.8664 86.64%
Androgen receptor binding - 0.9396 93.96%
Thyroid receptor binding - 0.7499 74.99%
Glucocorticoid receptor binding - 0.7022 70.22%
Aromatase binding - 0.9019 90.19%
PPAR gamma - 0.8297 82.97%
Honey bee toxicity - 0.8546 85.46%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity - 0.7700 77.00%
Fish aquatic toxicity - 0.5252 52.52%

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
CHEMBL3401 O75469 Pregnane X receptor 88.92% 94.73%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 88.87% 96.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 87.87% 97.21%
CHEMBL2885 P07451 Carbonic anhydrase III 81.00% 87.45%

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.
Salvia sclarea

Cross-Links

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PubChem 537782
LOTUS LTS0147124
wikiData Q82104536