(3R,4R,5E,7E,9E,11R,12R,13E)-11,12-dimethylpentadeca-1,5,7,9,13-pentaene-3,4-diol

Details

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Internal ID b9c344ca-81aa-4e0d-ab75-066754de499a
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Long-chain fatty alcohols
IUPAC Name (3R,4R,5E,7E,9E,11R,12R,13E)-11,12-dimethylpentadeca-1,5,7,9,13-pentaene-3,4-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H26O2/c1-5-11-14(3)15(4)12-9-7-8-10-13-17(19)16(18)6-2/h5-19H,2H2,1,3-4H3/b8-7+,11-5+,12-9+,13-10+/t14-,15-,16-,17-/m1/s1
InChI Key MPGRCXRDQITIIJ-NRCSPXNUSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C17H26O2
Molecular Weight 262.40 g/mol
Exact Mass 262.193280068 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 3.60
Atomic LogP (AlogP) 3.41
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3R,4R,5E,7E,9E,11R,12R,13E)-11,12-dimethylpentadeca-1,5,7,9,13-pentaene-3,4-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9734 97.34%
Caco-2 + 0.6647 66.47%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.4797 47.97%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8550 85.50%
OATP1B3 inhibitior + 0.9595 95.95%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.5795 57.95%
P-glycoprotein inhibitior - 0.8400 84.00%
P-glycoprotein substrate - 0.9477 94.77%
CYP3A4 substrate - 0.6250 62.50%
CYP2C9 substrate - 0.6216 62.16%
CYP2D6 substrate - 0.7970 79.70%
CYP3A4 inhibition - 0.7766 77.66%
CYP2C9 inhibition - 0.8235 82.35%
CYP2C19 inhibition - 0.8590 85.90%
CYP2D6 inhibition - 0.9392 93.92%
CYP1A2 inhibition - 0.8706 87.06%
CYP2C8 inhibition - 0.9536 95.36%
CYP inhibitory promiscuity - 0.8777 87.77%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) + 0.5783 57.83%
Carcinogenicity (trinary) Non-required 0.6633 66.33%
Eye corrosion + 0.7948 79.48%
Eye irritation - 0.7414 74.14%
Skin irritation + 0.7198 71.98%
Skin corrosion + 0.5177 51.77%
Ames mutagenesis - 0.6237 62.37%
Human Ether-a-go-go-Related Gene inhibition - 0.3796 37.96%
Micronuclear - 0.8500 85.00%
Hepatotoxicity + 0.6678 66.78%
skin sensitisation + 0.6047 60.47%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity - 0.9000 90.00%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity + 0.6744 67.44%
Acute Oral Toxicity (c) III 0.8197 81.97%
Estrogen receptor binding + 0.7920 79.20%
Androgen receptor binding - 0.8093 80.93%
Thyroid receptor binding - 0.5141 51.41%
Glucocorticoid receptor binding - 0.5000 50.00%
Aromatase binding + 0.6948 69.48%
PPAR gamma - 0.5649 56.49%
Honey bee toxicity - 0.7128 71.28%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.8600 86.00%
Fish aquatic toxicity - 0.5517 55.17%

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 89.08% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.45% 85.14%
CHEMBL2885 P07451 Carbonic anhydrase III 85.97% 87.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.87% 96.09%
CHEMBL4246 P42680 Tyrosine-protein kinase TEC 81.42% 82.05%

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 162821043
LOTUS LTS0254537
wikiData Q105169507