6-Octene-1,3-diol, 3,7-dimethyl-, (3R)-

Details

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Internal ID 043eee51-ba71-476b-9c48-a03e71e6f3e7
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Acyclic monoterpenoids
IUPAC Name (3R)-3,7-dimethyloct-6-ene-1,3-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H20O2/c1-9(2)5-4-6-10(3,12)7-8-11/h5,11-12H,4,6-8H2,1-3H3/t10-/m1/s1
InChI Key ALSCIJYFFHQRBX-SNVBAGLBSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C10H20O2
Molecular Weight 172.26 g/mol
Exact Mass 172.146329876 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 1.80
Atomic LogP (AlogP) 1.87
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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76936-25-9
DTXSID20473055

2D Structure

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2D Structure of 6-Octene-1,3-diol, 3,7-dimethyl-, (3R)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9680 96.80%
Caco-2 + 0.9578 95.78%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Lysosomes 0.4882 48.82%
OATP2B1 inhibitior - 0.8483 84.83%
OATP1B1 inhibitior + 0.9098 90.98%
OATP1B3 inhibitior + 0.9423 94.23%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7067 70.67%
BSEP inhibitior - 0.7586 75.86%
P-glycoprotein inhibitior - 0.9791 97.91%
P-glycoprotein substrate - 0.9553 95.53%
CYP3A4 substrate - 0.6440 64.40%
CYP2C9 substrate - 0.8168 81.68%
CYP2D6 substrate - 0.7766 77.66%
CYP3A4 inhibition - 0.8959 89.59%
CYP2C9 inhibition - 0.7717 77.17%
CYP2C19 inhibition - 0.8000 80.00%
CYP2D6 inhibition - 0.8913 89.13%
CYP1A2 inhibition - 0.7264 72.64%
CYP2C8 inhibition - 0.9612 96.12%
CYP inhibitory promiscuity - 0.7389 73.89%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.7200 72.00%
Carcinogenicity (trinary) Non-required 0.6521 65.21%
Eye corrosion - 0.9133 91.33%
Eye irritation + 0.9874 98.74%
Skin irritation - 0.5398 53.98%
Skin corrosion - 0.9751 97.51%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6771 67.71%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5541 55.41%
skin sensitisation + 0.5302 53.02%
Respiratory toxicity - 0.9000 90.00%
Reproductive toxicity - 0.8778 87.78%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity + 0.5943 59.43%
Acute Oral Toxicity (c) III 0.7375 73.75%
Estrogen receptor binding - 0.9241 92.41%
Androgen receptor binding - 0.8716 87.16%
Thyroid receptor binding - 0.7096 70.96%
Glucocorticoid receptor binding - 0.7857 78.57%
Aromatase binding - 0.9002 90.02%
PPAR gamma - 0.8560 85.60%
Honey bee toxicity - 0.9082 90.82%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity - 0.8600 86.00%
Fish aquatic toxicity + 0.6941 69.41%

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
CHEMBL1977 P11473 Vitamin D receptor 86.87% 99.43%
CHEMBL2581 P07339 Cathepsin D 85.94% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 83.31% 94.73%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.98% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.06% 91.11%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 81.48% 89.34%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.37% 96.09%
CHEMBL2885 P07451 Carbonic anhydrase III 80.34% 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.
Rosa gallica

Cross-Links

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PubChem 11805222
LOTUS LTS0158334
wikiData Q82302232