(2Z,6R)-3-(hydroxymethyl)-7-methylocta-2,7-diene-1,6-diol

Details

Top
Internal ID 39282932-28b1-4852-b269-45fe2289d162
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name (2Z,6R)-3-(hydroxymethyl)-7-methylocta-2,7-diene-1,6-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H18O3/c1-8(2)10(13)4-3-9(7-12)5-6-11/h5,10-13H,1,3-4,6-7H2,2H3/b9-5-/t10-/m1/s1
InChI Key RDOGOMPUCIUOGB-HYHWUIIZSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C10H18O3
Molecular Weight 186.25 g/mol
Exact Mass 186.125594432 g/mol
Topological Polar Surface Area (TPSA) 60.70 Ų
XlogP 0.70
Atomic LogP (AlogP) 0.61
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 6

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (2Z,6R)-3-(hydroxymethyl)-7-methylocta-2,7-diene-1,6-diol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9548 95.48%
Caco-2 - 0.6028 60.28%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.5743 57.43%
OATP2B1 inhibitior - 0.8473 84.73%
OATP1B1 inhibitior + 0.9314 93.14%
OATP1B3 inhibitior + 0.9581 95.81%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.9250 92.50%
P-glycoprotein inhibitior - 0.9775 97.75%
P-glycoprotein substrate - 0.8810 88.10%
CYP3A4 substrate - 0.5742 57.42%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7295 72.95%
CYP3A4 inhibition - 0.8484 84.84%
CYP2C9 inhibition - 0.8965 89.65%
CYP2C19 inhibition - 0.8798 87.98%
CYP2D6 inhibition - 0.9063 90.63%
CYP1A2 inhibition - 0.8244 82.44%
CYP2C8 inhibition - 0.9750 97.50%
CYP inhibitory promiscuity - 0.8724 87.24%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7500 75.00%
Carcinogenicity (trinary) Non-required 0.7073 70.73%
Eye corrosion - 0.7566 75.66%
Eye irritation + 0.7643 76.43%
Skin irritation - 0.6907 69.07%
Skin corrosion - 0.9415 94.15%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6361 63.61%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5159 51.59%
skin sensitisation + 0.5284 52.84%
Respiratory toxicity - 0.8333 83.33%
Reproductive toxicity - 0.9000 90.00%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity + 0.5434 54.34%
Acute Oral Toxicity (c) IV 0.4955 49.55%
Estrogen receptor binding - 0.8758 87.58%
Androgen receptor binding - 0.8787 87.87%
Thyroid receptor binding - 0.8247 82.47%
Glucocorticoid receptor binding - 0.5000 50.00%
Aromatase binding - 0.8072 80.72%
PPAR gamma - 0.7732 77.32%
Honey bee toxicity - 0.8385 83.85%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity - 0.8500 85.00%
Fish aquatic toxicity + 0.7004 70.04%

Targets

Top

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.82% 96.09%
CHEMBL2581 P07339 Cathepsin D 85.84% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.03% 91.11%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 84.49% 97.29%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.56% 99.17%

Plants that contains it

Top
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.
There are no matching plants.

Cross-Links

Top
PubChem 163020490
LOTUS LTS0127085
wikiData Q105234349