(3R,4S,5S)-3,7-dimethylocta-1,6-diene-3,4,5-triol

Details

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Internal ID b70949e1-4e1a-443d-ba2c-171825b989d4
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Acyclic monoterpenoids
IUPAC Name (3R,4S,5S)-3,7-dimethylocta-1,6-diene-3,4,5-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H18O3/c1-5-10(4,13)9(12)8(11)6-7(2)3/h5-6,8-9,11-13H,1H2,2-4H3/t8-,9-,10+/m0/s1
InChI Key UBKAPFPNNLGJBH-LPEHRKFASA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C10H18O3
Molecular Weight 186.25 g/mol
Exact Mass 186.125594432 g/mol
Topological Polar Surface Area (TPSA) 60.70 Ų
XlogP 0.60
Atomic LogP (AlogP) 0.61
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3R,4S,5S)-3,7-dimethylocta-1,6-diene-3,4,5-triol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9220 92.20%
Caco-2 - 0.7699 76.99%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.5349 53.49%
OATP2B1 inhibitior - 0.8597 85.97%
OATP1B1 inhibitior + 0.9410 94.10%
OATP1B3 inhibitior + 0.9571 95.71%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9156 91.56%
P-glycoprotein inhibitior - 0.9620 96.20%
P-glycoprotein substrate - 0.9501 95.01%
CYP3A4 substrate - 0.5941 59.41%
CYP2C9 substrate - 0.8062 80.62%
CYP2D6 substrate - 0.7853 78.53%
CYP3A4 inhibition - 0.7467 74.67%
CYP2C9 inhibition - 0.5384 53.84%
CYP2C19 inhibition - 0.7893 78.93%
CYP2D6 inhibition - 0.9310 93.10%
CYP1A2 inhibition - 0.8463 84.63%
CYP2C8 inhibition - 0.9307 93.07%
CYP inhibitory promiscuity - 0.6997 69.97%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.5523 55.23%
Carcinogenicity (trinary) Non-required 0.5970 59.70%
Eye corrosion - 0.8438 84.38%
Eye irritation + 0.6577 65.77%
Skin irritation + 0.5855 58.55%
Skin corrosion - 0.8391 83.91%
Ames mutagenesis - 0.7278 72.78%
Human Ether-a-go-go-Related Gene inhibition - 0.7244 72.44%
Micronuclear - 0.8200 82.00%
Hepatotoxicity + 0.6558 65.58%
skin sensitisation + 0.4903 49.03%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity - 0.9222 92.22%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity + 0.7504 75.04%
Acute Oral Toxicity (c) III 0.5731 57.31%
Estrogen receptor binding - 0.7999 79.99%
Androgen receptor binding - 0.7357 73.57%
Thyroid receptor binding - 0.7592 75.92%
Glucocorticoid receptor binding - 0.7935 79.35%
Aromatase binding - 0.8441 84.41%
PPAR gamma - 0.7656 76.56%
Honey bee toxicity - 0.6826 68.26%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.8800 88.00%
Fish aquatic toxicity + 0.6911 69.11%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.19% 85.14%
CHEMBL2581 P07339 Cathepsin D 91.14% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.88% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.15% 97.25%
CHEMBL3401 O75469 Pregnane X receptor 80.40% 94.73%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 80.00% 97.29%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 162933951
LOTUS LTS0053406
wikiData Q105269419